Multi-layer membrane, separator, battery, and method

Abstract

To provide a new and improved multi-layer microporous membrane, a base film, or a battery separator that exceeds a previous or typical membrane, base film, or battery separator, and a method for producing the multi-layer microporous membrane.SOLUTION: A microporous membrane includes two outer layers and a plurality of inner layers. Each outer layer includes a polyolefin. Each inner layer includes the polyolefin. Each of the outer layers is laminated to the inner layer, and each of the plurality of inner layers is laminated to at least another inner layer.SELECTED DRAWING: Figure 1

Description

[Technical field]

[0001] Related Applications This application claims priority to U.S. Provisional Patent Application No. 62 / 732,089, filed September 17, 2018, which is incorporated herein by reference.

[0002] Technical Field According to at least selected embodiments, the present application, disclosure or invention relates to improved membranes, separator films, separators, battery separators, lithium secondary battery separators, multilayer membranes, multilayer separator membranes, multilayer separators, multilayer battery separators, multilayer lithium secondary battery separators, multilayer battery separators, batteries, capacitors, fuel cells, lithium batteries, lithium ion batteries, lithium secondary batteries and / or lithium ion secondary batteries, and / or methods of making and / or using such membranes, separator films, separators, battery separators, lithium secondary battery separators, batteries, capacitors, fuel cells, lithium batteries, lithium ion batteries, lithium secondary batteries and / or lithium ion secondary batteries, and / or devices, vehicles or articles of manufacture comprising same, and / or methods of testing, quantifying, characterizing and / or analyzing such membranes, separator films, separators, battery separators and the like. According to at least certain embodiments, the present disclosure or invention relates to membrane layers, membranes or separator films, battery separators comprising such membranes, and / or related methods. According to at least certain selected embodiments, the disclosure or the present invention relates to a porous polymeric membrane or separator membrane comprising such membrane, a battery separator, and / or related methods. According to at least certain embodiments, the disclosure or the present invention relates to a microporous polyolefin membrane or separator membrane, a microlayer membrane, a multilayer membrane comprising one or more microlayers or nanolayer membranes, a battery separator comprising such membrane, and / or related methods. According to at least very certain embodiments, the disclosure or the present invention relates to a microporous stretched polymeric membrane or separator membrane having one or more outer and / or inner layers, a microlayer membrane, a multilayer microporous membrane or separator membrane having outer and / or inner layers, some of these layers or sublayers are produced by coextrusion and then laminated to form a membrane or separator membrane. In some embodiments, a particular layer, microlayer or nanolayer can comprise a homopolymer, a copolymer, a block copolymer, an elastomer, and / or a polymer blend.In selected embodiments, at least certain layers, microlayers or nanolayers may comprise different or separate polymers, homopolymers, copolymers, block copolymers, elastomers and / or polymer blends. The disclosure or invention also relates to methods of making such membranes, separator membranes or separators and / or methods of using such membranes, separator membranes or separators, for example as lithium battery separators. According to at least selected embodiments, the application or invention is directed to multi-layer and / or micro-layer porous or microporous membranes, separator membranes, separators, composites, electrochemical devices and / or batteries, and / or methods of making and / or using such membranes, separators, composites, devices and / or batteries. According to at least certain selected embodiments, the application or invention is directed to multi-layer separator membranes, where one or more layers of the multi-layer structure are produced in a multi-layer or micro-layer co-extrusion die using multiple extruders. The membranes, separator membranes or separators may demonstrate improved shutdown, improved strength, improved dielectric breakdown strength and / or reduced tendency to split. [Background technology]

[0003] Many batteries, such as lithium-ion batteries, use a system of electrodes to separate electrodes, hold electrolytes, and transfer charge. To improve the performance of batteries, and for other roles, single or multi-layer (2+ layer) membrane separators are incorporated. One conventional separator membrane design is a tri-layer polyolefin-based separator by Celgard, LLC, Charlotte, North Carolina, USA. While these conventional tri-layer designs have been effective in many lithium and other batteries, particularly lithium-ion secondary batteries, they may not work effectively in certain newer battery designs because the balance of strength and / or performance properties may not be fully optimized for certain newer applications of primary and / or secondary batteries, such as lithium-ion rechargeable batteries, in a particular battery technology. This is especially true as battery separator requirements become more demanding as customers desire thinner and stronger battery separators. For example, a microporous tri-layer membrane formed by co-extrusion of the tri-layers may in some cases lose strength when manufactured to thinner specifications. Separators formed by lamination of the monolayers may in some cases be unable to meet the never-ending demand for new thinner and stronger separators in certain new applications. Summary of the Invention [Problem to be solved by the invention]

[0004] Thus, a need exists for new and improved multi-layer microporous membranes, base films, or battery separators that have a variety of improvements over previous or typical membranes, base films, or battery separators. [Means for solving the problem]

[0005] According to at least selected embodiments, the present application, disclosure or invention may address previous needs, challenges or problems and may provide new or improved membranes, separator membranes, separators, battery separators, lithium secondary battery separators, multilayer (or multiple layer) membranes, multilayer separator membranes, multilayer separators, multilayer battery separators, multilayer lithium secondary battery separators, multilayer battery separators, batteries, capacitors, supercapacitors, bilayer supercapacitors, fuel cells, lithium batteries, lithium ion batteries, lithium secondary batteries and / or lithium ion secondary batteries, and / or methods of making and / or using such membranes, separator membranes, separators, battery separators, lithium secondary battery separators, batteries, capacitors, fuel cells, lithium batteries, lithium ion batteries, lithium secondary batteries and / or lithium ion secondary batteries, and / or devices, vehicles or articles of manufacture comprising same, and / or methods of testing, quantitating, characterizing and / or analyzing such membranes, separator membranes, separators, battery separators, and the like. According to at least certain embodiments, the disclosure or the invention relates to a membrane layer, a membrane or separator membrane, a battery separator, and / or related methods comprising such membranes. According to at least certain selected embodiments, the disclosure or the invention relates to a porous polymeric membrane or separator membrane, a battery separator, and / or related methods comprising such membranes. According to at least certain embodiments, the disclosure or the invention relates to a microporous polyolefin membrane or separator membrane, a microlayer membrane, a multilayer membrane comprising one or more microlayers or nanolayer membranes, a battery separator comprising such membranes, and / or related methods. According to at least very certain embodiments, the disclosure or the invention relates to a microporous stretched polymeric membrane or separator membrane having one or more outer and / or inner layers, a microlayer membrane, a multilayer microporous membrane or separator membrane having outer and / or inner layers, some of these layers or sublayers being produced by coextrusion and then laminated to form a membrane or separator membrane.In some embodiments, a particular layer, microlayer, or nanolayer can comprise a homopolymer, copolymer, block copolymer, elastomer, and / or polymer blend. In selected embodiments, at least a particular layer, microlayer, or nanolayer can comprise different or separate polymers, homopolymers, copolymers, block copolymers, elastomers, and / or polymer blends. The present disclosure or invention relates to methods of making such membranes, separator membranes, or separators. and / or methods of using such membranes, separator membranes, or separators, for example as lithium battery separators. According to at least selected embodiments, the present application or invention is directed to multilayer and / or microlayer porous or microporous membranes, separator membranes, separators, composites, electrochemical devices, and / or batteries, and / or methods of making and / or using such membranes, separators, composites, devices, and / or batteries. According to at least certain selected embodiments, the present application or invention is directed to multilayer separator membranes, where one or more layers of the multilayer structure are produced in a multilayer or microlayer coextrusion die, for example a coextrusion die using multiple extruders. The membranes, separator membranes, or separators can demonstrate improved shutdown, improved strength, improved dielectric breakdown strength, and / or reduced tendency to split.

[0006] In an aspect, the membrane described herein is a multilayer membrane. In some embodiments, the multilayer membrane comprises two outer layers, each of which comprises a polyolefin; and two or more inner layers, each of which comprises a polyolefin; each of the outer layers is laminated to one inner layer, and each of the two or more inner layers is laminated to at least one of the other inner layers. The polyolefin composition of each of the outer layers can include polypropylene, a polypropylene blend, a polypropylene copolymer, polyethylene, a polyethylene blend, a polyethylene copolymer, or any combination thereof. In some embodiments, the polyolefin composition of each of the outer layers can include polypropylene, a polypropylene blend, a polypropylene copolymer, polyethylene, a polyethylene blend, a polyethylene copolymer, or any combination thereof. In some embodiments, the polyolefin composition of each of the inner layers can include polypropylene, a polypropylene blend, a polypropylene copolymer, polyethylene, a polyethylene blend, a polyethylene copolymer, or any combination thereof.

[0007] In some cases, the two or more inner layers comprise a plurality of inner layers, such as two, three, four, five, six, or more inner layers. In some cases, the plurality of inner layers comprises two, three, or more layers. In one particular embodiment, the plurality of inner layers comprises three layers. In another embodiment, there are four inner layers, or five inner layers, or six inner layers, or seven inner layers, or eight inner layers, or nine inner layers, or ten inner layers. In a preferred embodiment, there are two or more, or three or more inner layers, such that three or more or four or more lamination interfaces are formed when the inner and outer layers are laminated to produce a microporous membrane.

[0008] Several new and improved multi-layer microporous membranes are disclosed, for example, in WO 2017 / 083633, but even better products than these may be needed as the manufacturing industry becomes more demanding, the disclosure of which is incorporated herein by reference in its entirety.

[0009] In some cases, the microporous membrane can be a five-layer membrane comprising a first outer layer, a first inner layer, a second inner (or intermediate) layer, a third inner layer, and a second outer layer. The first outer layer can be laminated to the first inner layer, the first inner layer can be laminated to the second inner (or intermediate) layer, the second inner (or intermediate) layer can be laminated to the third inner layer, and the third inner layer can be laminated to the second outer layer to form four lamination interfaces between the five layers. The composition of the first and second outer layers and the second inner (or intermediate) layer can include polypropylene, a polypropylene blend, a polypropylene copolymer, or any combination thereof. The composition of the first and second inner layers can include polyethylene, a polyethylene blend, a polyethylene copolymer, or any combination thereof. In some embodiments, the layers can include polyethylene, a polyethylene blend, a polyethylene copolymer, or any combination thereof.

[0010] In some embodiments, the multilayer films described herein are PP / PE / PP / P The present invention comprises a five-layer membrane having a structure of E / PP, where PP is polypropylene, a polypropylene blend, a polypropylene copolymer, or any combination thereof, and PE is polyethylene, a polyethylene blend, a polyethylene copolymer, or any combination thereof, and optionally each of the five layers is laminated to its respective adjacent layer.

[0011] In some embodiments, each of the layers of the multilayer film can comprise two, three, four, five, or six, or seven, or eight, or nine, or more sublayers. In some preferred cases, each layer comprises two, three, or more sublayers, and in some preferred cases, each layer comprises three sublayers. In some preferred embodiments, each of the sublayers of the layers can be coextruded together. Each sublayer can have a maximum average thickness of 6 μm or less, 5 μm or less, 4 μm or less, 3 μm or less, or 2 μm or less, or 1 μm or less.

[0012] In some cases, each layer in the multilayer film can have a maximum average thickness before stretching. For example, in some cases, each layer in the multilayer film can have a maximum average thickness of 1.2 mils or less, 1.1 mils or less, 1 mils or less, or 0.9 mils or less, 0.8 mils or less, 0.75 mils or less, 0.5 mils or less, 0.4 mils or less, 0.3 mils or less, or 0.2 mils or less before stretching. Based on the number of layers in the multilayer film, the film has a maximum average thickness in the range of 1 to 50 microns. Each layer in the multilayer film can have a maximum average thickness of 33% or less, 32% or less, 31% or less, 30% or less, 29% or less, 28% or less, 27% or less, 26% or less, 25% or less, 24% or less, 23% or less, 22% or less, 21% or less, 20% or less, 19% or less, 18% or less, or 17% or less than the total average thickness of the film.

[0013] The laminated multilayer film can be stretched uniaxially or biaxially, in some embodiments. In some embodiments, the multilayer film can be stretched in the machine direction (MD), in the transverse direction (TD), or in both MD and TD. When the multilayer film is stretched in both MD and TD, the stretching can be sequential or simultaneous. Furthermore, in some cases, the multilayer film can be rolled after stretching, such as rolling after TD stretching.

[0014] In some embodiments, the multilayer film can include additives such as functional polymers, ionomers, cellulose nanofibers, inorganic particles, smoothing agents, nucleating agents, cavitation promoters, fluorinated polymers, crosslinking agents, X-ray detectable materials, polymer processing agents, high temperature melt index (HTMI) polymers, electrolyte additives, energy dissipating immiscible additives, or any combination thereof. The additives can be part of a coating on the first outer layer, the second outer layer, or both layers. In some embodiments, the additives can be incorporated into one or more of the outer layers. If the outer layer comprises two or more sublayers, the additives can be incorporated into any one, some, or all of the sublayers.

[0015] In some embodiments, the multilayer membrane is a microporous multilayer membrane. In some cases, the first and second outer layers and the second inner (or intermediate) layer can have an average polypropylene pore size of 0.01 to 1.0 microns, in some cases 0.02 to 0.06 μm. In some cases, the first and third inner layers can have an average polyethylene pore size of 0.01 to 1.0 microns, in some cases 0.03 to 0.1 μm. Pore size may be measured, for example, using Aquapore or water or mercury porosimetry.

[0016] Multilayer membranes can exhibit improved physical properties compared to similar trilayer membranes. For example, in some cases, a multilayer membrane can exhibit improved physical properties, such as a 15% improvement over a PP / PE / PP trilayer microporous membrane or a (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) multilayer "trilayer" microporous membrane having the same thickness, Gurley, porosity, and / or layer composition as the membrane. It may have increased or improved elasticity at or above 0°C. In some embodiments, the multilayer membrane may have increased or improved puncture resistance, for example, compared to a PP / PE / PP trilayer microporous membrane or a (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) multilayer "trilayer" microporous membrane having the same thickness, Gurley, porosity, and / or layer composition as the membrane. The membrane has increased or improved longitudinal tensile strength at break, for example, compared to a PP / PE / PP trilayer microporous membrane or a (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) multilayer "trilayer" microporous membrane having the same thickness, Gurley, porosity, and / or layer composition as the membrane. In some cases, the multilayer membrane has increased or improved TD elongation compared to, for example, a PP / PE / PP trilayer microporous membrane or a (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) multilayer "trilayer" microporous membrane having the same thickness, Gurley, porosity, and / or layer composition as the membrane.

[0017] For lithium ion batteries, in some cases the improvements include the multilayer films described herein. For devices, the improvements in some examples include the multilayer films described herein. For textiles, the improvements in some examples include the multilayer films described herein.

[0018] In another embodiment, a method for producing a multi-layer microporous membrane is described herein. The method includes extruding a non-porous polypropylene precursor with multiple sublayers; extruding a non-porous polyethylene precursor with multiple sublayers; laminating an extruded polypropylene precursor layer with an extruded polyethylene precursor layer to produce a first intermediate precursor having a polyethylene layer and / or a polypropylene layer, in some embodiments, alternating a polyethylene layer with a polypropylene layer; simultaneously or separately / sequentially laminating an extruded polypropylene or polyethylene precursor, in a preferred embodiment a first outer layer comprising a polypropylene precursor, to a first surface of the intermediate precursor, and laminating an extruded polypropylene or polyethylene precursor, in a preferred embodiment a second outer layer comprising a polypropylene precursor, to a second surface of the first intermediate precursor opposite to the first surface, to produce a second intermediate precursor; annealing the second intermediate precursor to produce an annealed multi-layer membrane; uniaxially or biaxially stretching the annealed multi-layer membrane to produce a microporous multi-layer membrane; and optionally rolling the microporous multi-layer membrane. In some preferred embodiments, rolling is performed.

[0019] In some embodiments, the extruded polypropylene precursor is a structure containing a majority of polypropylene, and the extruded polyethylene precursor is a structure containing a majority of polyethylene. For example, the polypropylene precursor may have the structure "PP" or (PP / PP) or (PP / PE), or (PP / PE / PP) or (PP / PE / PP / PP), or (PP / PP / PE / PP / PP) or (PP / PE / PE / PP) so long as it contains a majority of polypropylene. The polyethylene precursor may have the structure PE (PE / PE), (PP / PE), (PE / PP / PE), (PE / PP / PP / PE), (PE / PE / PP / PP), etc. so long as it contains a majority of polyethylene. For example, the polypropylene or polyethylene precursor may have the structure (PP / PE), but for the polypropylene precursor, the PP sublayer may be thicker than the PE sublayer, and for the polyethylene precursor, the PE sublayer may be thicker than the PP sublayer. The thickness of each layer of the precursor may be different. For example, in some embodiments, the outer layer may be thinner than the inner layer, the inner layer may be thinner than the outer layer, the layer thicknesses may alternate between thick and thin layers, or all layers may have different thicknesses.

[0020] In some embodiments, the first intermediate precursor comprises a three-layer multilayer film having a structure of PE / PP / PE. In some cases, the second intermediate precursor comprises a five-layer film having a structure of PP / PE / PP / PE / PP. In any case, each layer of the three-layer multilayer structure preferably has two or more sublayers. For example, PP can be (PP / PP / PP), (PP / PE / PP), (PP / PP), or (PP / PE), where "PP" is the thicker or layer with three sublayers.

[0021] The uniaxial stretching can be in the machine direction or the transverse direction, and the biaxial stretching can be in the machine direction or the transverse direction. In the case of biaxial stretching, the machine direction and the transverse direction stretching can be sequential or simultaneous. In a preferred embodiment, at least MD stretching is performed to form pores.

[0022] The extruded precursor may optionally include multiple sublayers. For example, an extruded polypropylene precursor may optionally include two, three, four, or more sublayers, and an extruded polyethylene precursor may optionally include two, three, four, or more sublayers. In some embodiments, the second intermediate precursor may include a five-layer membrane having a structure of PP / PE / PP / PE / PP, with each layer having three sublayers. This structure may be represented by (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PP / PE) / (PP / PP / PE) / (PP / PE / PP) or, for example, (PP / PP / PE) / (PE / PP / PE) / (PE / PP / PE) / (PE / PP / PE) / (PE / PP / PP). In the second or third structure, PP or PE may be the majority polymer in either (PP / PE / PP) or (PE / PP / PE) or (PP / PE / PE) or (PE / PE / PP).

[0023] In some embodiments, the extruded polypropylene and polyethylene precursors are non-porous. In some cases, micropores can be formed in a uniaxial or biaxial stretching step. In a preferred embodiment, pores or micropores can be formed in at least the MD stretching step of a uniaxial or biaxial process. In some cases, the method can further include coating one or more of the first and second outer layers.

[0024] In another aspect, a method for making a five-layer microporous membrane is described herein, the method including extruding a plurality of polypropylene and polyethylene membranes; laminating one of the polyethylene membranes to a first side of the polypropylene membrane and another of the polyethylene membranes to an opposite second side of the polypropylene membrane to produce an inverted three-layer multilayer membrane having a PE / PP / PE or (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) structure; laminating one of the polypropylene layers to one of the polyethylene membranes in the inverted three-layer multilayer membrane and another of the polypropylene layers to the other of the polyethylene membranes in the inverted three-layer multilayer membrane to produce a five-layer multilayer membrane having a PP / PE / PP / PE / PP or (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) structure; annealing the five-layer multilayer membrane; uniaxially or biaxially stretching the annealed multilayer membrane to produce a microporous multilayer membrane; and, optionally, calendering the microporous multilayer membrane. In some preferred embodiments, the stretching is biaxial. In embodiments, the microporous membranes produced by the methods described herein include battery separators. In some cases, the microporous membranes produced by the methods described herein include lithium ion battery separators. In some cases, the microporous membranes produced by the methods described herein include devices. In some cases, the microporous membranes produced by the methods described herein include textiles. [Brief description of the drawings]

[0025] [Figure 1] 1 is an SEM of a second five-layer film according to certain embodiments described herein. [Figure 2A] 1 is an SEM of a second five-layer film according to certain embodiments described herein. [Figure 2B] 1 is an SEM of a second five-layer film according to certain embodiments described herein. [Figure 2C] 1 is an SEM of a second five-layer film according to certain embodiments described herein. [Diagram 3] FIG. 3 (a) is a schematic diagram of a three-layer membrane according to some embodiments described herein, (b) a schematic diagram of a five-layer membrane according to some embodiments described herein, and (c) a schematic diagram of a three-layer membrane according to some embodiments described herein. [Figure 4] FIG. 2 is a schematic diagram of three layers according to some embodiments described herein. [Diagram 5] FIG. 2 is a schematic diagram of three layers according to some embodiments described herein. [Figure 6] FIG. 2 is a schematic diagram of five layers according to some embodiments described herein. [Figure 7] 5A-5D show SEM images of the first five layers described herein at various processing steps. [Figure 8] 1 is a graph showing puncture strength as a function of ln(BW*Thickness) for example membranes described herein. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0026] The embodiments described herein can be more readily understood by reference to the following detailed specification and examples. However, the elements, devices and methods described herein are not limited to the specific embodiments shown in the detailed specification and examples. It should be recognized that these embodiments are merely illustrative of the principles of the present disclosure. Many modifications and adaptations will be readily apparent to those skilled in the art without departing from the spirit and scope of the present disclosure.

[0027] Additionally, all ranges disclosed herein are to be understood to encompass any and all subranges subsumed therein. For example, a stated range of "1.0 to 10.0" should be deemed to include any and all subranges beginning with a minimum value of 1.0 or greater and ending with a maximum value of 10.0 or less, such as 1.0 to 5.3, or 4.7 to 10.0, or 3.6 to 7.9, etc.

[0028] All ranges disclosed herein are to be construed as including the endpoints of the range unless expressly stated otherwise. For example, the ranges "5 to 10 (between 5 and 10)," "5 to 10 (from 5 to 10)," or "5 to 10 (5-10)" should generally be construed as including the endpoints 5 and 10.

[0029] Additionally, when the phrase "up to" is used in connection with an amount or quantity, it is to be understood that the amount is at least a detectable amount or quantity. For example, a material indicated as having an amount "up to" a particular amount may be present in an amount up to and including the detectable amount of the particular amount.

[0030] I. Multilayer membrane (or membrane separator) In aspects, improved multi-layer membranes, membranes, or separators are disclosed. In some embodiments, multi-layer microporous membranes, membranes, or separators are disclosed. Although the term "membrane" is used throughout this specification for simplicity purposes, it should be understood that the term refers to either "membrane" or "separator."

[0031] In some embodiments, the multilayer film comprises two outer layers and multiple inner layers, the multiple inner layers being 2 or more, 3 or more, 4 or more, 5 or more, 6 or more, 7 or more, 8 or more, 9 or more, 11 or more, 12 or more, 13 or more, 14 or more, 15 or more, 15 or more, 16 or more, 17 or more, 18 or more, 19 or more, 20 or more, 21 or more, 22 or more, 23 or more, 24 or more, 25 or more, 26 or more, It may include 27 or more, 28 or more, 29 or more, 30 or more, 40 or more, 50 or more, 60 or more, 70 or more, 80 or more, 90 or more, or 100 or more layers. The term "layer" includes layers having a maximum average thickness of 0.01 to 2.0, 25, or 3.0 mils before stretching. In some embodiments, the maximum average thickness is 0.1 to 1.5, 2.0, 2.5, or 3.0 mils before stretching, or 0.2 to 1.5, 2.0, 2.5, or 3.0 mils before stretching, or 0.2 to 1.2, 1.5, 2.0, 2.5, or 3.0 mils before stretching. In some preferred embodiments, the maximum average thickness of the layer is from 0.1 to 0.5, 1.0, 1.5, 2.0, 25, or 3.0 mils before being stretched.

[0032] Each layer can be mono-extruded, there are no sublayers, and the layer is extruded by itself. Alternatively, each layer can comprise multiple co-extruded sublayers. In a preferred embodiment, each layer comprises multiple, or more than two, co-extruded sublayers. For example, co-extruded bi-layer (having two sublayers), tri-layer (having three sublayers), or multi-layer (having two or more, three or more, or four or more sublayers) films are each collectively considered to be a "layer". The number of sublayers in a co-extruded bi-layer will be two, the number of layers in a co-extruded tri-layer will be three, the number of layers in a co-extruded multi-layer film will be two or more, three or more, four or more, five or more, etc. The exact number of sublayers in a co-extruded layer is determined by the design and not necessarily by the co-extruded materials that make up the co-extruded layer. For example, a co-extruded bi-, tri-, or multi-sublayer film can be made using the same material in each of the two, three, or four or more sublayers, and these sublayers would still be considered to be separate sublayers even if each sublayer is made from the same material. Each bath containing a coextruded two-, three-, or multi-sublayer membrane can have a pre-stretch thickness of 3.0 mils or less, 2.5 mils or less, 2.0 mils or less, 1.5 mils or less, 1.2 mils or less, 1.1 mils or less, 1 mils or less, or 0.9 mils or less, 0.8 mils or less, 0.75 mils or less, 0.5 mils or less, 0.4 mils or less, 0.3 mils or less, or 0.2 mils or less prior to stretching.

[0033] In some embodiments, the multi-layer microporous membrane or the multi-layer microporous membrane disclosed herein comprises two, three, four, or five or more coextruded layers. A coextruded layer is a layer produced by a coextrusion process. In some cases, the layers can be produced by the same or different coextrusion processes. Successive layers can be produced by the same coextrusion process, or two or more layers can be coextruded by one process. Two or more layers can be coextruded by different processes, and two or more layers produced by one process can be laminated to two or more layers produced by different processes to combine into four or more successive coextruded layers. In some embodiments, the coextruded layers are produced by the same coextrusion process. For example, two or more, or three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more, fifteen or more, twenty or more, twenty-five or more, thirty or more, thirty-five or more, forty or more, forty-five or more, fifty or more, fifty-five or more, or sixty or more coextruded layers can be produced by the same coextrusion process. Extrusion processes can also be performed by extruding a mixture of two or more polymers, which may be the same or different, with or without a solvent. In some cases, the coextrusion process is a dry process, such as the Celgard® dry process, which does not use a solvent.

[0034] In some embodiments, the multilayer film described herein is manufactured by forming a coextruded bilayer (two coextruded layers), trilayer (three coextruded layers), or multilayer (two, three, or more than three coextruded layers) film, and then laminating the bilayer, trilayer, or multilayer film to at least one or at least two other films. The other film can be a nonwoven or woven film, a monoextruded film, or a coextruded film. In some preferred embodiments, the other film is a coextruded film, including a coextruded film having the same number of coextruded layers as the coextruded bilayer, trilayer, or multilayer film. Furthermore, each of the coextruded layers can comprise two, three, four, or more sublayers, as described herein above.

[0035] Laminating a bi-layer, tri-layer, or multi-layer coextruded film to at least one other mono-layer film or bi-layer, tri-layer, or multi-layer film can include the use of heat, pressure, or heat and pressure.

[0036] The polymers or copolymers that can be used in the present battery separator are those that are extrudable. Such polymers are commonly referred to as thermoplastic polymers.

[0037] In some embodiments, one or more of the layers of the multi-layer microporous membrane or multi-layer membrane comprises a polymer or copolymer or a polymer blend or copolymer blend, a polyolefin or a polyolefin blend. As understood by those skilled in the art, a polyolefin blend can include a mixture of two or more different polyolefins, such as polyethylene and polypropylene, a blend of two or more homogeneous polyolefins, each polyolefin having different properties, such as a mixture of an ultra-high molecular weight polyolefin and a low molecular weight or ultra-low molecular weight polyolefin, or a polyolefin and another polymer or copolymer. Additives, drugs, fillers, and / or the like may be added to the polymer or polymer blend described herein. For example, elastomers, lubricants, antioxidants, colorants, crosslinking agents, and / or the like.

[0038] Polyolefins include, but are not limited to, polyethylene, polypropylene, polybutylene, polymethylpentene, copolymers thereof, and blends thereof. In some embodiments, the polyolefin can be an ultra-low molecular weight, low molecular weight, medium molecular weight, high molecular weight, or ultra-high molecular weight polyolefin, such as medium molecular weight or high molecular weight polyethylene (PE) or polypropylene (PP). For example, the ultra-high molecular weight polyolefin can have a molecular weight of 450,000 (450k) or more, such as 500k or more, 650k or more, 700k or more, 800k or more, 1 million or more, 2 million or more, 3 million or more, 4 million or more, 5 million or more, 6 million or more, etc. The high molecular weight polyolefin can have a molecular weight in the range of 250k to 450k, such as 250k to 400k, 250k to 350k, or 250k to 300k. The medium molecular weight polyolefins can have a molecular weight of 150k to 250k, such as 100k, 125k, 130k, 140k, 150 to 225k, 150k to 200k, 150k to 200k, etc. The low molecular weight polyolefins can have a molecular weight in the range of 100k to 150k, such as 100k to 125k. The ultra-low molecular weight polyolefins can have a molecular weight of less than 100k. The aforementioned values ​​are weight average molecular weights. In some embodiments, higher molecular weight polyolefins can be used to improve the strength or other properties of the microporous multilayer membranes described herein or batteries comprising the same. In some embodiments, lower molecular weight polymers, such as intermediate molecular weight, low molecular weight, or ultra-low molecular weight polymers, can be beneficial. Without wishing to be bound by a particular theory, it is believed that, for example, the crystallization behavior of lower molecular weight polyolefins can result in microporous multilayer membranes with smaller pores resulting from the pore-forming MD stretching process.

[0039] Exemplary thermoplastic polymers, blends, blends or copolymers other than polyolefin polymers, blends or blends can include, but are not limited to, thermoplastic polymers such as polyacetal (or polyoxymethylene), polyamides, polyesters, polysulfides, polyvinyl alcohol, polyvinyl esters, and polyvinylidenes such as polyvinylidene fluoride (PVDF), poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF:HFP), polytetrafluoroethylene (PTFE), polyethylene oxide (PEO), polyvinyl alcohol (PVA) polyacrylonitrile (PAN). Polyamides (nylons) include, but are not limited to, polyamide 6, polyamide 66, nylon 10,10, polyphthalamide (PPA), copolymers thereof, and blends thereof. Polyesters include, but are not limited to, polyterephthalic acid esters. , polybutyl terephthalate, copolymers thereof, and blends thereof. Polysulfides include, but are not limited to, polyphenyl sulfide, copolymers thereof, and blends thereof. Polyvinyl alcohols include, but are not limited to, ethylene-vinyl alcohol, copolymers thereof, and blends thereof. Polyvinyl esters include, but are not limited to, polyvinyl acetate, ethylene-vinyl acetate, copolymers thereof, and blends thereof. Polyvinylidenes include, but are not limited to, polyvinylidene fluorides (such as polyvinylidene chloride and polyvinylidene fluoride), copolymers thereof, and blends thereof. Various materials can be added to the polymer. In some cases, these materials are added to modify or enhance the performance or properties of individual layers or the entire membrane. Such materials include, but are not limited to, materials that lower the melting point of the polymer. For example, if the multilayer membrane is a battery separator, the multilayer separator will include layers designed to close its pores at a certain temperature that blocks ion flow between the electrodes of the battery. This function is usually called a shutdown.

[0040] In some embodiments, each layer or sublayer of each layer of the multilayer membrane comprises, consists of, or consists essentially of a different polymer or copolymer or polymer blend or copolymer blend. In some embodiments, each layer comprises, consists of, or consists essentially of the same polymer or copolymer or polymer blend or copolymer blend. In some embodiments, alternating layers of the multilayer microporous membrane or multilayer membrane comprise, consist of, or consist essentially of the same polymer or copolymer or polymer blend or copolymer blend. In other embodiments, some of the layers and / or sublayers of the multilayer membrane or microporous multilayer membrane comprise, consist of, or consist essentially of the same polymer or polymer blend, and some do not comprise, consist of, or consist essentially of the same polymer or polymer blend.

[0041] In some embodiments, a layer or sublayer of the multilayer film comprises, consists of, or consists essentially of a polyolefin (PO), such as PP or PE or PE+PP blends, blends, copolymers, or the like, and may further comprise other polymers (PY), and may include or employ additives, agents, materials, fillers, and / or particles (M) and / or the like to form a layer or microlayer, such as PP+PY, PE+PY, PP+M, PE+M, PP+PE+PY, PE+PP+M, PP+PY+M, PE+PY+M, PP+PE+PY+M, or blends, blends, copolymers, and / or the like.

[0042] The same, similar, separate, or different PP or PE or PE+PP polymers, homopolymers, copolymers, molecular weights, blends, mixtures, interpolymers, or the like can also be used. For example, the same, similar, separate, or different molecular weight PP or PE or PE+PP polymers, homopolymers, copolymers, multipolymers, blends, mixtures, and / or the like can be used in each layer or sub-layer. As such, configurations can include various combinations and subcombinations of PP, PE, PP+PE, PP1, PP2, PP3, PE1, PE2, PE3, PP1+PP2, PE1+PE2, PP1+PP2+PP3, PE1+PE2+PE3, PP1+PP2+PE, PP+PE1+PE2, PP1 / PP2, PP1 / PP2 / PP1, PE1 / PE2, PE1 / PE2 / PP1, PE1 / PE2 / PE3, PP1+PE / PP2, or other combinations or configurations.

[0043] In some embodiments, one or more additives can be added to the outermost layer of the multilayer microporous membrane or multilayer membrane to improve its properties or the properties of a battery separator or battery comprising the same. The outermost layer or any of the outermost sublayers of the outermost layer, including the outermost sublayer, In addition to additives, PE, PP, or PE+PP can be included, for example, lithium stearate, calcium stearate, PE beads, siloxanes, and polysiloxanes can be added to improve pin removal (i.e., to reduce the membrane or membrane's coefficient of friction).

[0044] In addition, certain polymers, copolymers, or polymer or copolymer blends can be used in the outermost layers of the multilayer film (such as the first and second outermost layers or outermost sublayers or other sublayers of any of these first and second outermost layers) to improve the properties or properties of the battery separator or battery comprising same. For example, the addition of an ultra-high molecular weight polymer or copolymer to the outermost layer can improve puncture strength.

[0045] In a further embodiment, additives to improve oxidation resistance can be added to the multi-layer microporous membrane or to the outermost layer of the membrane. The additives can be organic or inorganic additives or polymeric or non-polymeric additives.

[0046] In some embodiments, the outermost layer of the multilayer film or film comprises, consists of, or consists essentially of polyethylene, polypropylene, or a mixture thereof.

[0047] As mentioned above, the multilayer film can comprise two outer layers (a first outer layer and a second outer layer) and multiple inner layers. The multiple inner layers can be mono-extruded or co-extruded layers. A laminate barrier or interface can be formed between each of the inner layers and / or between each of the outer and one of the inner layers. A laminate barrier or interface is formed when two surfaces, such as two surfaces of different films or layers, are laminated using heat, pressure, or heat and pressure. In some embodiments, the layers of the film region have the following non-limiting configurations: PP, PE, PP / PP, PP / PE, PE / PP, PE / PE, PP / PP / PP, PP / PP / PE, PP / PE / PE, PP / PE / PP, PE / PP / PP / PP, PP / PE / PE / PP, PP / PP / PP / PP, PP / PE / PP / PP, PE / PP / PP / PE, PP / PE / PP / PP, PE / PE / PP / PP, PE / PE / PP / PP, PE / PE / PP / PP, PP / PE / PE / PE / PP , PE / PP / PP / PP / PE, PP / PP / PE / PP / PP, PE / PE / PP / PP / PE / PE, PP / PE / PP / PE / PP, PP / PP / PE / PE / PP / PP, PE / PE / PP / PP / PE / PE, P E / PP / PE / PP / PE / PP, PP / PE / PP / PE / PP / PE, PP / PP / PP / PE / PP / PP / PP, PE / PE / PE / PP / PE / PE / PE, PP / PE / PP / PE / PP / PE / PP, PE / P P / PE / PP / PE / PP / PE, PE / PP / PE / PP / PE / PP / PE / PP, PP / PE / PP / PE / PP / PE / PP / PE, PP / PP / PE / PE / PP / PP / PE / PE, PP / PE / PE / PE / PE / PE / PE / PP, PE / PP / PP / PP / PP / PP / PP / PE, PP / PP / PE / PE / PEPE / PP / PP, PP / PP / PP / PP / PE / PE / PE / PE, PP / PP / PP / PP / PE / PP / P P / PP / PP, PE / PE / PE / PE / PP / PE / PE / PE / PE, PP / PE / PP / PE / PP / PE / PP / PE / PP, PE / PP / PE / PP / PE / PP / PE / PP / PE, PE / PE / PE / PE / PE / PP / PP / PP / PP, PP / PP / PP / PP / PP / PE / PE / PE / PE, PP / PP / PP / PP / PP / PE / PE / PE / PE / PE, PE / PE / PE / PE / PE / PP / PP / PP / PP / PP,PP / PE / PP / PE / PP / PE / PP / PE / PP / PE, PE / PP / PE / PP / PE / PP / PE / PP / PE / PP, PE / PP / PP / PP / PP / PP / PP / PP / PP / PP / PE, PP / PE / PE / PE / PE / PE / PE / PE / PE / PE / P P, PP / PP / PE / PE / PP / PP / PE / PE / PP / PP, PE / PE / PP / PP / PP / PP / PP / PP / PP / PE / PE, PP / PP / PP / PE / PE / PP / PP / PP / PP / PE, PE / PE / PE / PP / PP / PE / PE / PE / PP / PP. For purposes herein, PE includes, consists of, By PP is meant a single layer (including, in preferred embodiments, a sublayer) in a multilayer film that comprises, consists of, or consists essentially of PP. Similarly, PP means a single layer (including, in preferred embodiments, a sublayer) in a multilayer film that comprises, consists of, or consists essentially of PP.

[0048] The PE or PP composition in each of the different layers may be the same type or different type of the PE or PP composition in the other layers. For example, the coextrusion precursor can have the structure (PP1 / PP2 / PP3), (PP3 / PP2 / PP1), (PP3 / PP3 / PP2 / PP1 / PP1), (PP3 / PP3 / PP2 / PP2 / PP1 / PP1), (PP3 / PP3 / PP3 / PP2 / PP2 / PP2 / PP1 / PP1 / PP1), etc. PP1 can be made from homopolymer PP and additives that modify the surface friction coefficient, including any anti-slip or anti-block additives, such as polysiloxane or siloxane. PP2 can be made from PP homopolymer and copolymers of PP, which may be the same or different from PP1, and the PP copolymer can be any propylene-ethylene or ethylene-propylene random copolymer, block copolymer, or elastomer. PP3 can be made from a PP homopolymer that may be the same or different than PP1 and PP2, and also contains an additive to modify the surface coefficient of friction that may be the same or different than that used in PP1. Stated differently, a multilayer film having the general structure of PP / PE / PP / PE / PP can include PP1 / PE1 / PP2 / PE2 / PP3, where each of the PP layers has a different polypropylene composition than the other two PP layers, and similarly for the two PE layers.

[0049] In another embodiment, the coextrusion precursor can have the structure (PP1 / PP2 / PP3), (PP3 / PP2 / PP1), (PP3 / PP3 / PP2 / PP1 / PP1), (PP3 / PP3 / PP2 / PP2 / PP1 / PP1), (PP3 / PP3 / PP3 / PP2 / PP2 / PP2 / PP1 / PP1 / PP1), etc. PP1 can be any polypropylene blend. PP2 can be made from any polypropylene block copolymer, including those described herein. PP3 can be made from any polypropylene block copolymer different from that used in PP2.

[0050] An individual layer in a multilayer film can comprise multiple sublayers, where individual monoextruded sublayers can be coextruded or laminated, e.g., laminated, to produce an individual layer of the multilayer film. With a multilayer film having a structure of PP / PE / PP / PE / PP, each individual PP or PE layer can comprise two or more coextruded sublayers. For example, if each individual PP or PE layer comprises three sublayers, each individual PP layer can be represented as PP=(PP1, PP2, PP3) and each individual PE layer can be represented as PE=(PE1, PE2, PE3). Thus, the structure of PP / PE / PP / PE / PP can be represented as (PP1,PP2,PP3) / (PE1,PE2,PE3) / (PP1,PP2,PP3) / (PE1,PE2,PE3) / (PP1,PP2,PP3) or (PP1 / PP2 / PP3) / (PE1 / PE2 / PE3) / (PP1 / PP2 / PP3) / (PE1 / PE2 / PE3) / (PP1 / PP2 / PP3). The composition of each of the PP1, PP2, and PP3 sublayers can be the same, or each sublayer can have a different polypropylene composition than one or both of the other polypropylene sublayers. Similarly, the composition of each of the PE1, PE2, and PE3 sublayers can be the same, or each sublayer can have a different polyethylene composition than one or both of the other polyethylene sublayers. This principle also applies to other multilayer membranes having layers of roughly the above exemplary five-layer membrane. The above improved or inventive five-layer multilayer membrane has four lamination interfaces. A similar six-layer multilayer would have five lamination interfaces, and a similar four-layer multilayer would have three lamination interfaces. It is hypothesized herein that multilayers having three or more, and in some preferred embodiments, four or more lamination interfaces, will have improved properties. For example, they may be compared to a particular microlayer three-layer (or trilayer) multilayer having only two lamination interfaces, or compared to a conventional trilayer. would have improved properties compared to

[0051] The maximum average thickness of each sublayer in a layer can be less than 50 microns, less than 40 microns, less than 30 microns, less than 25 microns, less than 20 microns, less than 19 microns, less than 18 microns, less than 17 microns, less than 16 microns, less than 15 microns, less than 14 microns, less than 13 microns, less than 12 microns, less than 11 microns, less than 10 microns, less than 9 microns, less than 8 microns, less than 7 microns, less than 6 microns, less than 5 microns, less than 4 microns, less than 3 microns, less than 2 microns, or less than 1 micron. The thickness of each layer in the microporous membrane can be less than 50 microns, less than 40 microns, less than 30 microns, less than 25 microns, less than 20 microns, less than 19 microns, less than 18 microns, less than 17 microns, less than 16 microns, less than 15 microns, less than 14 microns, less than 13 microns, less than 12 microns, less than 11 microns, less than 10 microns, less than 9 microns, less than 8 microns, less than 7 microns, less than 6 microns, less than 5 microns, less than 4 microns, less than 3 microns, less than 2 microns, or less than 1 micron. The thickness of the microporous membrane can be less than 50 microns, less than 40 microns, less than 30 microns, less than 25 microns, less than 20 microns, less than 19 microns, less than 18 microns, less than 17 microns, less than 16 microns, less than 15 microns, less than 14 microns, less than 13 microns, less than 12 microns, less than 11 microns, less than 10 microns, less than 9 microns, less than 8 microns, less than 7 microns, less than 6 microns, less than 5 microns, less than 4 microns, less than 3 microns, less than 2 microns, or less than 1 micron. This is the thickness of the multilayer or film before any coatings or treatments have been applied to it.

[0052] As used herein, microporous means that the average pore size of the membrane or coating is 2 microns or less, 1 micron or less, 0.9 microns or less, 0.8 microns or less, 0.7 microns or less, 0.6 microns or less, 0.5 microns or less, 0.4 microns or less, 0.3 microns or less, 0.2 microns or less, 0.1 microns or less, 0.09 microns or less, 0.08 microns or less, 0.07 microns or less, 0.06 microns or less, 0.05 microns or less, 0.04 microns or less, 0.03 microns or less, 0.02 microns or less, or 0.01 microns or less. In some embodiments, the pores can be formed, for example, by subjecting the precursor membrane to a stretching treatment, such as occurs in the Celgard® dry process.

[0053] In some embodiments, one or more layers of the multilayer membrane comprise, consist of, or consist essentially of microporous PE, and the average pore size of the PE layer is 0.03-0.1, 0.05-0.09, 0.05-0.08, 0.05-0.07, or 0.05-0.06.

[0054] In some embodiments, one or more layers of the multilayer membrane comprise, consist of, or consist essentially of microporous PP, and the average pore size of the PP layer is 0.02-0.06, 0.03-0.05, and even 0.04-0.05, or 0.03-0.04.

[0055] The multi-layer microporous membrane or membrane comprises a layer comprising, consisting of, or consisting essentially of PP and another layer comprising, consisting of, or consisting essentially of PE, where the average pore size of the PP layer is smaller than the average pore size of the PE layer.

[0056] The microporous multilayer membrane can have a Gurley consistent with the objectives of the present disclosure, such as a Gurley acceptable for use as a battery separator. In some embodiments, the microporous multilayer membrane or film described herein has a JIS Gurley of 150 or more, 160 or more, 170 or more, 180 or more, 190 or more, 200 or more, 210 or more, 220 or more, 230 or more, 240 or more, 250 or more, 260 or more, 270 or more, 280 or more, 290 or more, 300 or more, 310 or more, 320 or more, 330 or more, 340 or more, or 350 or more. The Gurley has a Gurley (sec / 100cc). The Gurley can be less than 150 sec / 100cc and can be as high as 500 sec / 100cc or more. The Gurley is not limited as long as the membrane functions as a battery separator.

[0057] The porosity of the microporous multilayer membrane can be any porosity that is consistent with the goals of the present disclosure. For example, any porosity that can produce an acceptable battery separator is acceptable. In some embodiments, the porosity of the membrane or membranes can be 10-60%, 20-60%, 30-60%, or 40-60%. The porosity of the membrane can be 65% or more, or 70% or more. The porosity of the membrane is not limited, so long as the membrane functions as a battery separator.

[0058] The microporous multilayer film or membrane can have a puncture strength of uncoated, 200gf or more, 210gf or more, 220gf or more, 230gf or more, 240gf or more, 250gf or more, 260gf or more, 270gf or more, 280gf or more, 290gf or more, 300gf or more, 310gf or more, 320gf or more, 330gf or more, 340gf or more, 350gf or more, or as high as 400gf or more. In some embodiments, the puncture strength may be less than 200gf, especially for thinner membranes, and in some embodiments, the puncture may be as high as 500gf or more.

[0059] In some embodiments, the multi-layer microporous membranes described herein can include one or more additives in at least one layer of the multi-layer microporous membrane. In some embodiments, at least one layer or sub-layer of the multi-layer microporous membrane includes more than one additive, such as two, three, four, five, or more. The additive can be present in one or both of the outermost layers of the multi-layer microporous membrane, one or more inner layers, all of the inner layers, or both of the inner layers and the outermost layer. In some embodiments, the additive can be present in one or more outermost layers and one or more innermost layers. In such embodiments, the additive can be released from the outermost layer or both outermost layers, and the additive supply of the outermost layer or both outermost layers can be replenished by migration of the additive from the inner layer to the outermost layer. In some embodiments, each layer of the multi-layer microporous membrane can include a different additive or combination of additives than the adjacent layer or layers of the multi-layer microporous membrane.

[0060] In some embodiments, the additive is, comprises, consists of, or consists essentially of a functional polymer. As will be appreciated by those skilled in the art, a functional polymer is a polymer having functional groups pendant from the polymer backbone. Exemplary functional groups include: In some embodiments, the functional polymer is a maleic anhydride functional polymer. In some embodiments, the maleic anhydride modified polymer is a maleic anhydride homopolymer polypropylene, copolymer polypropylene, high density polypropylene, low density polypropylene, very high density polypropylene, very low density polypropylene, homopolymer polyethylene, copolymer polyethylene, high density polyethylene, low density polyethylene, very high density polyethylene, very low density polyethylene. In some embodiments, the additive comprises, consists of, or consists essentially of an ionomer. As will be understood by those skilled in the art, an ionomer is a copolymer that contains both ionic-containing and non-ionic repeating groups. The ionic-containing repeating groups can make up less than 25%, less than 20%, or less than 15% of the ionomer. In some embodiments, the ionomer can be a Li-based, Na-based, or Zn-based ionomer.

[0061] In some embodiments, the additive comprises cellulose nanofibers.

[0062] In some embodiments, the additive comprises inorganic particles having a narrow particle size distribution. For example, the difference between D10 and D90 in the distribution is less than 100 nanometers, less than 90 nanometers, less than 80 nanometers, less than 70 nanometers, less than 60 nanometers, less than 50 nanometers, etc. In some embodiments, the inorganic particles are SiO, Ti O2, or a combination thereof.

[0063] In some embodiments, the additive can comprise, consist of, or consist essentially of a lubricant. The lubricants or lubricants described herein are not limited. As understood by those skilled in the art, lubricants are compounds that act to reduce friction between a variety of different surfaces, including the following: polymer:polymer; polymer:metal; polymer:organic materials; and polymer:inorganic materials. Specific examples of the lubricants or lubricants described herein are compounds that contain siloxy functional groups, including siloxanes and polysiloxanes, and fatty acid salts, including metal stearates.

[0064] Compounds containing 2 or more, 3 or more, 4 or more, 5 or more, 6 or more, 7 or more, 8 or more, 9 or more, or 10 or more siloxy groups can be used as lubricants as described herein. As will be understood by those skilled in the art, siloxanes are a class of molecules that have a backbone of alternating silicon (Si) and oxygen (O) atoms, with each silicon atom having a bonded hydrogen (H) or a saturated or unsaturated alkyl group, such as -CH3 or -C2H5. It may have organic groups. Polysiloxanes are polymerized siloxanes that are usually of higher molecular weight. In some embodiments described herein, the polysiloxanes may be of high molecular weight, such as ultra-high molecular weight polysiloxanes. In some embodiments, the high molecular weight and ultra-high molecular weight polysiloxanes may have a weight average molecular weight in the range of 500,000 to 1,000,000.

[0065] The fatty acid salts described herein are not limited to, but may be any fatty acid salt that acts as a lubricant. The fatty acid of the fatty acid salt may be a fatty acid having 12 to 22 carbon atoms. For example, the metal fatty acid may be selected from the group consisting of lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, palmitoleic acid, behenic acid, erucic acid, and arachidic acid. The metal may be any metal not inconsistent with the objectives of the present disclosure. In some cases, the metal is an alkali metal or an alkaline earth metal, such as Li, Be, Na, Mg, K, Ca, Rb, Sr, Cs, Ba, Fr, and Ra. In some embodiments, the metal is Li, Be, Na, Mg, K, or Ca.

[0066] The fatty acid salt can be lithium stearate, sodium stearate, lithium oleate, sodium oleate, sodium palmitate, lithium palmitate, potassium stearate, or potassium oleate.

[0067] Lubricants containing fatty acid salts as described herein may have melting points of 200°C or more, 210°C or more, 220°C or more, 230°C or more, or 240°C or more. Fatty acid salts such as lithium stearate (melting point of 220°C) or sodium stearate (melting point 245-255°C) have such melting points. Fatty acid salts such as calcium stearate (melting point 155°C) do not have such melting points. The present inventors have found that calcium stearate is less ideal from a process standpoint than other fatty acid metal salts such as metal stearates that have higher melting points. In particular, they have found that calcium stearate is not believed to be able to be added in amounts greater than 800 ppm without the occurrence of what is referred to as the "dusty effect" where the wax separates and becomes ubiquitous during the cooking extrusion process. While not wishing to be bound by any particular theory, it is believed that with fatty acid metal salts having the above melting points, cooking extrusion temperatures will solve this "dusty" problem. Fatty acid salts with higher melting points than calcium stearate, especially those with melting points above 200° C., can be incorporated in amounts greater than 1% or greater than 1,000 ppm without "dusting." Amounts greater than 1% may improve wetting and pin removal. It has been found that this is important to obtain desired properties such as improved

[0068] In some embodiments, the additive can comprise, consist, or consist essentially of one or more nucleating agents. As will be appreciated by those skilled in the art, in some embodiments, a nucleating agent is a material, an inorganic material, that aids, enhances, or promotes crystallization of polymers, including semi-crystalline polymers.

[0069] In some embodiments, the additive can comprise, consist, or consist essentially of a cavitation promoter. As will be understood by those skilled in the art, a cavitation promoter is a material that forms, aids in, enhances, or promotes the formation of bubbles or voids in a polymer.

[0070] In some embodiments, the additive can comprise, consist, or consist essentially of a fluorinated polymer, which is not limited to such, but in some embodiments is PVDF.

[0071] In some embodiments, the additive can comprise, consist, or consist essentially of a crosslinking agent.

[0072] In some embodiments, the additive can comprise, consist of, or consist essentially of an X-ray detectable material. The X-ray detectable material is not so limited, but can be any material, such as those disclosed in U.S. Patent No. 7,662,510, which is incorporated herein by reference in its entirety. Suitable X-ray detectable materials or elements are also disclosed in the '510 patent, but in some embodiments, 50% or less, 40% or less, 30% or less, 20% or less, 10% or less, 5% or less, or 1% or less by weight can be used, based on the total weight of the microporous membrane or membrane. In an embodiment, the additive is barium sulfate.

[0073] In some embodiments, the additive can comprise, consist of, or consist essentially of a lithium halide. The lithium halide can be lithium chloride, lithium fluoride, lithium bromide, or lithium iodide. The lithium halide can be lithium iodide, which is both ionically conductive and electrically insulating. In some cases, a material that is both ionically conductive and electrically insulating can be used as part of the battery separator.

[0074] In some embodiments, the additives can comprise, consist of, or consist essentially of polymer processing agents. As understood by those skilled in the art, polymer processing agents or additives are added to improve the processing efficiency and quality of polymeric compounds. In some embodiments, the polymer processing agent can be an antioxidant, stabilizer, lubricant, processing aid, nucleating agent, colorant, antistatic agent, plasticizer, or filler.

[0075] In some embodiments, the additive can comprise, consist, or consist essentially of a high temperature melt index (HTMI) polymer, which can be at least one selected from the group consisting of, but not limited to, PMP, PMMA, PET, PVDF, aramid, syndiotactic polystyrene, and combinations thereof.

[0076] In some embodiments, the additive can comprise, consist of, or consist essentially of an electrolyte additive. The electrolyte additives as described herein are not limited so long as they are consistent with the goals set forth herein. Electrolyte additives typically have the potential to improve battery performance. The electrolyte additive may be any additive added by a battery manufacturer, particularly a lithium battery manufacturer, to improve the electrolyte performance. The electrolyte additive should preferably be blendable, e.g., miscible with the polymer used for the polymeric microporous membrane or compatible with the coating slurry. The compatibility of the additive may also be aided or improved by coating or partially coating the additive. For example, exemplary electrolyte additives are disclosed in A Review of Electrolyte Additives for Lithium-Ion Batteries, J. of Power Sources, vol. 162, issue 2, 2006 pp. 1379-1394, the contents of which are incorporated herein by reference. In some preferred embodiments, the electrolyte additive may also be a solid electrolyte interphase (SEI) modifier, a cathode protectant, a flame retardant additive, a LiPF6 salt stabilizer, an overcharge inhibitor, an aluminum corrosion inhibitor, a lithium precipitation agent, or the like. or at least one selected from the group consisting of a precipitation modifier, or a solvation promoter, an aluminum corrosion inhibitor, a wetting agent, and a viscosity modifier. In some embodiments, an additive may have more than one property, for example, it may be a wetting agent and a viscosity modifier.

[0077] Exemplary SEI modifiers include VEC (vinyl ethylene carbonate), VC (vinylene carbonate), FEC (fluoroethylene carbonate), and LiBOB (lithium bis(oxalato)borate). Exemplary cathodic protectants include N,N'-dicyclohexylcarbodiimide, N,N-diethylaminotrimethylsilane, and LiBOB. Exemplary flame retardant additives include TTFP (tris(2,2,2-trifluoroethyl) phosphate), fluorinated propylene carbonate, and MFE (methyl nonafluorobutyl ether). Exemplary LiPF6 salt stabilizers include LiF, TTFP, and LiF6. (tris(2,2,2-trifluoroethyl)phosphate), 1-methyl-2-pyrrolidinone, fluorinated carbamates, hexamethylphosphoramide. Exemplary overcharge inhibitors include xylene, cyclohexylbenzene, biphenyl, 2,2-diphenylpropane, phenyl tert-butyl carbonate. Exemplary Li precipitation modifiers include AlI3, SnI2, cetyltrimethylammonium chloride, perfluoropolyethers, tetraalkylammonium chlorides with long alkyl chains. Exemplary ionic solvation promoters include 12-crown-4, TFPPB (tris(pentafluorophenyl)). Exemplary Al corrosion inhibitors include borates, LiBOB, LiODFB. Exemplary wetting agents and viscosity reducers include cyclohexane and P2O5.

[0078] In some embodiments, the electrolyte additive is air stable or oxidation resistant. Battery separators containing the electrolyte additives disclosed herein can have a shelf life of several weeks to several months, for example, 1 week to 11 months.

[0079] In some embodiments, the additive can comprise, consist, or consist essentially of an energy dissipative immiscible additive, where immiscible means that the additive is not miscible with the polymer used to manufacture the multi-layer microporous membrane or layers of the membrane that contain the additive.

[0080] In some embodiments, the membrane or film has or exhibits increased or improved puncture strength compared to a three-layer microporous membrane or a three-layer (tri-layer) multi-layer microporous membrane. For example, the puncture strength may be greater than 250g, greater than 260g, greater than 270g, greater than 280g, greater than 290g, greater than 300g, or greater than 310g. In preferred embodiments, the puncture is 300g or greater or 310g or greater. The multi-layer membranes described herein may have improved MD shrinkage at 120°C for 1 hour compared to a three-layer microporous membrane or a three-layer (tri-layer) multi-layer microporous membrane. For example, the MD shrinkage at 120°C for 1 hour may be less than 25%, less than 24%, less than 23%, less than 22%, less than 21%, or less than 20%. In preferred embodiments, the MD shrinkage at 120°C for 1 hour is less than 24% or less than 20%. The MD shrinkage at 120° C. for 1 hour can be less than 15%. The multilayer films described herein can also have improved MD tensile strength at break. For example, the MD tensile strength at break can be greater than 900 kg / cm 2 or over 1,000 kg / cm 2 or over 1,100 kg / cm 2 These properties may be due to the membrane itself, i.e. , a membrane without any coating or other treatment. In some embodiments, these properties may be exhibited in TD stretched products.

[0081] In some embodiments, at least one layer of the multilayer film or film described herein comprises a polymeric additive. The polymeric additive is added in an amount less than the main polymer that constitutes the film. For example, in some embodiments, the main polymer can be a polyolefin. This is another way of saying that at least one layer of the multilayer film or film described herein comprises or is composed of a polymeric blend. In some embodiments, the layer can comprise or be composed of one or more of the polymeric blend or polymeric blend and other additives described herein.

[0082] In some embodiments, the layer comprising the polymer blend is an outer layer, such as the first outer layer or the opposite second outer layer. In some embodiments, both the first outer layer and the second outer layer comprise the polymer blend. In some embodiments, the inner layer comprises the polymer blend. In some cases, at least one inner layer and at least one outer layer comprise the polymer blend, and in some embodiments, all of the inner layers and all of the outer layers comprise the polymer blend.

[0083] In some embodiments, the polymer blend comprises, consists of, or consists essentially of at least two different polyolefins, such as at least two different polyethylenes, at least two different polypropylenes, or a combination of at least one polyethylene and one polypropylene. In some embodiments, the polymer blend comprises, consists of, or consists essentially of a polyolefin and a non-polyolefin, i.e., a polymer that is not a polyolefin.

[0084] In some embodiments, each layer of the multilayer film or film has a different composition than its adjacent layers. For example, one layer may contain two different polyolefin polymer blends, one adjacent layer may contain a polyolefin and a non-polyolefin polymer blend, and another adjacent layer does not contain a polymer blend.

[0085] The multilayer film can be stretched in the machine direction (MD) to produce a microporous multilayer film. In some cases, the microporous multilayer film is produced by stretching the MD-stretched microporous multilayer film in the transverse direction (TD). In addition to sequential MD-TD stretching, the multilayer film can also be simultaneously biaxially MD-TD stretched. Furthermore, the simultaneous or sequential MD-TD stretched microporous multilayer film can be followed by a rolling step to reduce the film thickness, reduce the roughness, reduce the porosity%, increase the TD tensile strength, increase the uniformity, and / or reduce the TD splittability. In some embodiments, the multilayer film is TD stretched 1x, 2x, 3x, 4x, 5x, 6x, 7x, 8x, 9x, 10x, or more than 10x.

[0086] In embodiments, multilayer membranes can be made using exemplary methods including stretching and subsequent rolling steps, such as longitudinal stretching followed by transverse stretching (with or without longitudinal relaxation) and subsequent rolling steps, as a method to reduce the thickness of such stretched membranes, e.g., to reduce the % porosity of such stretched membranes in a controlled manner, e.g., to improve the strength, properties, and / or performance of such stretched membranes in a controlled manner, e.g., to improve the puncture strength, longitudinal and / or transverse tensile strength, uniformity, wettability, coatability, runnability, compression, return, tortuosity, permeability, thickness, pin removal force, mechanical strength, surface roughness, hot tip hole propagation, and / or combinations thereof, of such stretched membranes. and / or produce unique structures, pore structures, materials, membranes, base membranes, and / or separators in a controlled manner, for example, multi-layer porous membranes.

[0087] In some cases, the TD tensile strength of the multilayer membrane can be further improved by adding a rolling step after TD stretching. The rolling method usually involves heat and pressure, which can reduce the thickness of the porous membrane. The rolling process step can restore the loss of MD and TD tensile strength caused by TD stretching. Furthermore, the observed enhancement in MD and TD tensile strength by rolling can create a more balanced MD and TD tensile strength ratio, which can be beneficial to the overall mechanical performance of the multilayer membrane.

[0088] The rolling method may use uniform or non-uniform heat, pressure, and / or speed to selectively densify the heat-sensitive material, to provide uniform or non-uniform rolling conditions (such as by using smooth rolls, rough rolls, patterned rolls, micropatterned rolls, nanopatterned rolls, speed changes, temperature changes, pressure changes, humidity changes, double roll processes, multiple roll processes, or combinations thereof), to obtain improved, desired or unique structure, properties, and / or performance, to obtain or control the resulting structure, properties, and / or performance, etc. In embodiments, rolling temperatures of 50° C. to 70° C. and line speeds of 40 to 80 ft / min may be used, with rolling pressures of 50 to 200 psi. In some cases, higher pressures provide thinner separators and lower pressures provide thicker separators. All of these exemplary processing conditions are non-limiting.

[0089] In some embodiments, one or more coating layers can be applied to one or both sides of the multilayer membrane. In some embodiments, one or more of the coatings can be a ceramic coating comprising, consisting of, or consisting essentially of a polymeric binder and organic and / or inorganic particles. In some embodiments, only the ceramic coating is applied to one or both sides of the microporous membrane. In other embodiments, a different coating can be applied to the microporous membrane before or after application of the ceramic coating. A different additional coating can be applied to one or both sides of the membrane or thin film. In some embodiments, the different polymeric coating layer can comprise, consist of, or consist essentially of at least one of polyvinylidene fluoride (PVdF) or polycarbonate (PC).

[0090] In some embodiments, the thickness of the coating layer is less than about 12 μm, sometimes less than 10 μm, sometimes less than 9 μm, sometimes less than 8 μm, sometimes less than 7 μm, and sometimes less than 5 μm. In at least certain selected embodiments, the coating layer is less than 4 μm, less than 2 μm, or less than 1 μm.

[0091] The coating method is not limited, and the coating layer described herein can be coated on the porous substrate by at least one of the following coating methods: extrusion coating, roll coating, gravure coating, printing, knife coating, air knife coating, spray coating, dip coating, or curtain coating. The coating method can be performed at room temperature or at an elevated temperature.

[0092] The coating layer can be any one of non-porous, nanoporous, microporous, mesoporous, or macroporous. The coating layer can have a JIS Gurley of 700 or less, sometimes 600 or less, 500 or less, 400 or less, 300 or less, 200 or less, or 100 or less.

[0093] One or more layers, treatments, materials, or coatings (CT) and / or nets, meshes, mats, wovens, or nonwovens (NW) may be added onto one or both sides of or within the multilayer films or membranes (M) described herein. Examples of suitable axial tension couplings include, but are not limited to, CT / M, CT / M / CT, NW / M, NW / M / NW, CT / M / NW, CT / NW / M / NW / CT, and CT / M / NW / CT.

[0094] II. Battery separator In some embodiments, the battery separator herein consists of, or consists essentially of, a (i.e., one or more) multilayer or multilayer microporous membrane, and optionally including a coating layer on one or both sides of the membrane. The membrane itself, i.e., without a coating or other additional components, exhibits the above-mentioned improved properties. The performance of the membrane can be further enhanced by the addition of a coating or other additional components, such as nonwovens, nets, meshes, with or without a coating, on one or both sides, and / or by MD, MD-TD, or MD-TD-C stretching and rolling as described.

[0095] III. Composites, Vehicles, or Devices In an embodiment, the composite comprises a multilayer membrane or battery separator as described in Sections I and II, and one or more electrodes, such as an anode, a cathode, or an anode and a cathode, provided in direct contact therewith. The type of the electrode is not limited. For example, the electrode may be one suitable for use in a lithium ion secondary battery.

[0096] Suitable anodes can have an energy capacity of greater than or equal to 372 mAh / g, preferably ≧700 mAh / g, most preferably ≧1000 mAh / g. The anodes are made from lithium metal or lithium alloy foils (e.g., lithium aluminum alloys), or mixtures of lithium metal and / or lithium alloys and materials such as carbon (e.g., coke, graphite), nickel, copper, etc. The anodes are not made solely from lithium-containing intercalation compounds or lithium-containing insertion compounds.

[0097] A suitable cathode can be any cathode compatible with the anode, and can include intercalation compounds, insertion compounds, or electrochemically active polymers. Suitable intercalation materials include, for example, MoS2, FeS2, MnO2, TiS2, NbSe3, LiCo O2, LiNiO2, LiMn2O4, V6O 13 , V2O5, and CuCl2. Suitable polymers include, for example, polyacetylene, polypyrrole, polyaniline, and polythiopene.

[0098] Any of the separators described herein above can be incorporated into any vehicle or device, such as an e-vehicle, or device, such as a cell phone or laptop, that is fully or partially battery powered.

[0099] IV.Textiles In some embodiments, a textile is described that comprises, consists of, or consists essentially of a multi-layer microporous membrane or film as described herein. In some preferred embodiments, the textile comprises a multi-layer microporous membrane or film as described herein and a nonwoven or woven material. The nonwoven may be a staple nonwoven, a meltblown nonwoven, a spunbond nonwoven, a flash-spun nonwoven, a near-laid nonwoven, or a nonwoven made by any other method. In some preferred embodiments, the nonwoven or woven is attached to the multi-layer microporous membrane or film. In some embodiments, the textile comprises, consists of, or consists essentially of a woven or nonwoven multi-layer microporous membrane or film as described herein, and another woven or nonwoven, in that order. In some embodiments, the textile comprises, consists of, or consists essentially of a multi-layer microporous membrane or film as described herein, a nonwoven or woven, and a multi-layer microporous membrane or film as described herein, in that order. Become.

[0100] V. Multilayer Film Manufacturing Method In some embodiments, the physical properties of the multilayer films described herein are a result, at least in part, of the method by which the multilayer films are manufactured.

[0101] In an embodiment, the method includes co-extruding at least two or more polymer mixtures to produce a first co-extruded bi-, tri-, or multi-layer membrane, co-extruding two or more other polymer mixtures to produce a second co-extruded bi-, tri-, or multi-layer membrane, and co-extruding two or more additional polymer mixtures to produce a third co-extruded bi-, tri-, or multi-layer membrane. The polymer mixtures used to produce each layer of the first, second, and third bi-, tri-, or multi-layer membranes can be the same or different. The mixtures can include only one polymer, or more than one polymer, such as a polymer blend. Also, more than three bi-, tri-, or multi-layer membranes can be produced. After producing the first, second, and third bi-, tri-, or multi-layer membranes, the membranes are laminated with two of the membranes formed on the opposite side of one of the membranes to produce the microporous battery separator described herein. The laminated multi-layer membranes can be uniaxially or biaxially stretched and, in some cases, rolled.

[0102] Each layer of the multilayer film can comprise one or more sublayers, microlayers, or plies produced by extrusion or coextrusion. Coextrusion typically involves the use of a coextrusion die with one or more extruders feeding the die (usually one extruder for each layer of a bilayer, trilayer, or multilayer film). An exemplary coextrusion process is shown in FIG. 4, and a coextrusion die is shown in FIG. 5.

[0103] In some embodiments, the coextrusion process is carried out using a coextrusion die with one or more extruders feeding the die. Typically, there is one extruder for each desired layer or microlayer of the final coextruded thin film produced. For example, if the desired coextruded thin film comprises three microlayers, three extruders are used with the coextrusion die. In at least one embodiment, the multilayer film can be constructed from many sublayers, microlayers, or nanolayers, and the final product can include two, three, four, five, six, seven, eight, nine, ten, or more layers of individual sublayers, microlayers, or nanolayers that together comprise the layer in the multilayer film. In at least certain embodiments, the sublayer technology can be produced by a preencapsulation feedblock before entering the cast or blown thin film die.

[0104] In some embodiments, the coextrusion is an air bubble coextrusion process, and the blow-up ratio can vary between 0.5 to 2.0, 0.7 to 1.8, or 0.9 to 1.5. After coextrusion using this blow-up ratio, the film can be MD stretched, MD stretched and then TD stretched (with or without MD relaxation), or simultaneously MD and TD stretched, as described in more detail below. The film can then be calendered as needed to further control the porosity.

[0105] Benefits of coextrusion include, but are not limited to, an increase in the number of layers (interfaces), which is believed to improve puncture strength, without wishing to be bound by any particular theory. It is believed that coextrusion leads to observed DB improvement, without wishing to be bound by any particular theory. In particular, DB improvement may be related to the PP pore size reduction observed when using coextrusion methods. Coextrusion allows for more material selection by incorporating blends within the microlayers. Coextrusion also allows for the formation of tri-layer or multi-layer films (coextruded films). For example, tri-layer coextruded films with thicknesses of 8 or 10 microns or less can be produced. Coextrusion allows for higher MD elongation, various pore structures (smaller PP, larger PE). Coextrusion can be combined with lamination to produce multi-layer structures of the invention. For example, the structures produced in the examples.

[0106] The lamination process involves bringing a surface of the coextruded thin film together with a surface of at least one other thin film and using heat, pressure, and / or heat and pressure to secure the two surfaces together. For example, heat can be used to increase the tackiness of either or both surfaces of the coextruded film and at least one other thin film, to stick the two surfaces together, or to better bond them together, to facilitate lamination. The number of lamination steps is not so limited. For example, all of the layers of the film may be laminated, or two layers may be laminated at once. For example, two layers may be laminated to make a laminate, then another layer may be laminated with this laminate to make a second laminate, then another layer may be laminated with this second laminate to make a third laminate, and so on.

[0107] In some embodiments, the laminate produced by laminating the coextruded thin film with at least one other thin film is a precursor for a subsequent MD and / or TD stretching step, with or without relaxation. In some embodiments, the coextruded thin film is stretched before lamination.

[0108] The additional steps can include, consist of, or consist essentially of MD, TD, or sequential or simultaneous MD and TD stretching steps. The stretching steps can occur before or after the lamination step. Stretching can occur with or without MD and / or TD relaxation. Co-pending, commonly owned, U.S. Patent Application Publication No. 2017 / 0084898(A1), published March 23, 2017, is hereby incorporated by reference in its entirety.

[0109] Other additional steps can include rolling. For example, in some embodiments, rolling can be performed as a means to reduce the thickness of the porous biaxially stretched membrane precursor, to reduce pore size and / or porosity, and / or to further improve transverse direction (TD) tensile strength and / or puncture strength. Rolling can also improve strength, wettability, and / or uniformity, and can also reduce surface layer defects introduced during the manufacturing process, for example, during MD and TD stretching. Rolled thin films or membranes can have improved coating properties (using smooth rolling rolls or multiple rolls). In addition, the use of textured rolling rolls can help improve coating adhesion to thin films or membranes.

[0110] The rolling can be cold (below room temperature), ambient (room temperature), or hot (e.g., 90° C.) and can include the application of pressure or the application of heat and pressure to reduce the thickness of the film or thin film in a controlled manner. In one or more steps, the rolling can be, for example, low pressure rolling followed by higher pressure rolling, cold calendering followed by hot calendering, etc. In addition, the rolling method can use at least one of heat, pressure, and densification speed of the heat-sensitive material. In addition, the rolling method can use uniform or non-uniform heat, pressure, and / or speed to selectively densify the heat-sensitive material, to provide uniform or non-uniform rolling conditions (such as by using smooth rolls, rough rolls, patterned rolls, micropatterned rolls, nanopatterned rolls, speed changes, temperature changes, pressure changes, humidity changes, double roll steps, multiple roll steps, or combinations thereof), to obtain improved, desired or unique structure, properties, and / or performance, to obtain or control the resulting structure, properties, and / or performance, etc.

[0111] Another exemplary method for making a multi-layer microporous membrane includes the steps of co-extruding a non-porous polypropylene precursor having a plurality of sublayers; co-extruding a non-porous polyethylene precursor having a plurality of sublayers; laminating a plurality of co-extruded polypropylene precursor layers with an extruded polyethylene precursor layer to produce a first intermediate precursor having alternating polyethylene and polypropylene layers; depositing a first outer layer comprising the co-extruded polypropylene precursor on a first side of the intermediate precursor and a second outer layer comprising the co-extruded polypropylene precursor on a side opposite the first side of the first intermediate precursor. The method includes laminating the first intermediate precursor to the second surface of the precursor to produce a second intermediate precursor; annealing the second intermediate precursor to produce an annealed multilayer film; uniaxially or biaxially stretching the annealed multilayer film to produce a microporous multilayer film; and optionally rolling the microporous multilayer film. In some preferred embodiments, rolling is performed. This method is not limited. For example, the first intermediate precursor may include all polyethylene or all polypropylene precursor.

[0112] In some cases, the first intermediate precursor comprises a three-layer film having a PE / PP / PE or (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) structure, and the second intermediate precursor comprises a five-layer film having a PP / PE / PP / PE / PP or (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) structure.

[0113] Each of the coextruded polypropylene precursor layers can have one monolayer or two, three, four, or more sublayers, and each of the extruded polyethylene precursors can have one monolayer or two, three, four, or more sublayers. In one embodiment, the second intermediate precursor comprises a five-layer membrane having a structure of PP / PE / PP / PE / PP, with each layer having three sublayers. For example, the structure is (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP).

[0114] The coextruded polypropylene and polyethylene precursors are non-porous and can be made microporous by the stretching process. The uniaxial stretching can be in the machine direction or transverse direction, and the biaxial stretching can be in the machine direction or transverse direction. The biaxial machine direction and transverse direction stretching can be sequential or simultaneous.

[0115] In some embodiments, there is a rolling step, which may involve the application of heat, pressure, or heat and pressure.

[0116] In some embodiments, the method further includes coating one or more of the first and second outer layers, for example when the membrane is a battery separator.

[0117] In another embodiment of the method for producing a five-layer membrane having a general structure of PP / PE / PP / PE / PP or (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) and, in some embodiments, a specific structure of (PP1,PP2,PP3) / (PE1,PE2,PE3) / (PP1,PP2,PP3) / (PE1,PE2,PE3) / (PP1,PP2,PP3), where each layer comprises three sublayers or plies, the method includes steps 1 and 2 shown in FIG.

[0118] FIG. 1 shows an exemplary method for producing a five-layer membrane with the general structure of PP / PE / PP / PE / PP or (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP). The three-layer component may have the structure PE / PP / PE or (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE). This is a two-step process, but the five layers may be produced in a one-step process of laminating all five layers. Methods using more than two steps are also possible.

[0119] In step 1, an inverted trilayer membrane is produced by laminating a first layer of polyethylene to a first side of the intermediate polypropylene and a second layer of polyethylene to a second side of the intermediate polypropylene layer to obtain a trilayer having the structure PE / PP / PE. A non-inverted trilayer PP / PE / PP may also be produced. The first and second polyethylene layers and the intermediate polypropylene of the trilayer may each be a single monolayer or may have multiple sublayers as described in section 1 above. In a preferred embodiment, each layer may comprise a sub-layer. In step 2, the three layers are used as intermediate layers, and a first polypropylene outer layer (or polyethylene) is laminated to one side of the first or third layer of polyethylene, and a second polypropylene outer layer (or polyethylene) is laminated to the opposite side of the second or third layer of polyethylene to obtain a five-layer membrane with a structure of PP / PE / PP / PE / PP. Furthermore, the first and second outer layers of polypropylene (or polyethylene) can each be a single monolayer, or can have multiple sub-layers as described in Section I above. When the first and second outer layers have multiple sub-layers (2 or more), the thickness of the outermost layer and the exposed sub-layers can be thicker, thinner, or the same as the inner sub-layers. In one embodiment, each layer of the five-layer membrane comprises three sub-layers, for a total of 15 sub-layers. The structure is (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP).

[0120] In yet another exemplary method for producing a five-layer microporous membrane, the method includes the steps of extruding a plurality of polypropylene and polyethylene films; laminating one of the polyethylene films to a first side of the polypropylene film and another of the polyethylene films to an opposite second side of the polypropylene film to produce an inverted tri-layer membrane having a PE / PP / PE or (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) structure; laminating one of the polypropylene layers to one of the polyethylene films in the tri-layer membrane and another of the polypropylene layers to the other polyethylene film in the tri-layer membrane to produce a five-layer membrane having a PP / PE / PP / PE / PP or (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) structure; uniaxially or biaxially stretching the annealed multi-layer membrane to produce a microporous multi-layer membrane; and, optionally, calendering the microporous multi-layer membrane. In some embodiments, the three layers can be PP / PE / PP or (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) and the five layer structure can be (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE). The three layers can be all PP or all PE, e.g., PP / PP / PP or PE / PE / PE or (PP / PP / PP) / (PP / PP / PP) / (PP / PP / PP) / (PE / PE / PE) / (PE / PE / PE) / (PE / PE / PE). The five layers may be PE / PP / PP / PP / PE or PP / PE / PE / PE / PP or (PE / PE / PE) / (PP / PP / PP) / (PP / PP / PP) / (PP / PP / PP) / (PE / PE / PE) or (PP / PP / PP) / (PE / PE / PE) / (PE / PE / PE) / (PE / PE / PE) / (PP / PP / PP). EXAMPLES

[0121] Example 1 Experimental five-layer composition The composition of the experimental five-layer membrane was (PP1 / PP1 / PP1) / (PE1 / PE1 / PE1) / (PP1 / PP1 / PP1) / (PE1 / PE1 / PE1) / (PP1 / PP1 / PP1), where PP1 is homopolymer PP, 0.90-0.92 g / cm 3 Density range of 0. The MFR ranges from 5MFR to 2MFR. The entire PE1 layer has a melt index of 0.25 to 0.5 g / 10 min at 2.16 kg and 190 °C, and a viscosity of 0.95 to 0.97 g / cm 3 The polyethylene has a density range of 100 to 200 mm.

[0122] Five layers: (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) manufacturing method The five-layer membrane of Example 9 having a structure of (PP1 / PP1 / PP2) / (PE2 / PE2 / PE2) / (PP1 / PP2 / PP1) / (PE2 / PE2 / PE2) / (PP2 / PP1 / PP1) was subjected to a test using a layer having a structure (PP1 / PP1 / PP2), a layer having a structure (PE2 / PE2 / PE2), a layer having a structure (PP1 / PP2 / PP1) and a layer having a structure (PP2 / PP The coextruded layers were then laminated to produce an intermediate product having a structure of (PP1 / PP1 / PP2) / (PE2 / PE2 / PE2) / (PP1 / PP2 / PP1) / (PE2 / PE2 / PE2) / (PP2 / PP1 / PP1), which was stretched in the MD and TD directions and then rolled.

[0123] The five layers are shown diagrammatically in Figure 6 and Figure 3(b). The PP1:PP2:PP1 ratio is 1:1:1. The PP1:PP1:PP2 ratio is 1:1:1. The PP:PE:PP:PE:PP ratio is 15:10:15:10:15. The total PE content is 30%.

[0124] SEM images of MD, TD, and TDC FIG. 7 shows a scanning electron microscope (SEM) image of a pentalayer membrane with a general structure of PP / PE / PP / PE / PP, where each layer (e.g., PP in the structure PP / PE / PP / PE / PP is considered a layer) has three sublayers (total of 15 sublayers combined). See, e.g., FIG. 3(b) and FIG. 6. The SEM micrograph in FIG. 7 marked "MD" is of the pentalayer membrane after uniaxial stretching in the MD direction. The pores are square slit-like. The SEM micrograph in FIG. 7 marked "TD" is of the pentalayer membrane after sequential stretching in the MD-TD directions. As shown in the SEM micrograph in FIG. 7 marked "TD", there is a larger open porous structure of the PE microporous layer sandwiched between the PP microporous layers, and the pores have a roughly circular appearance. The SEM micrograph labeled "TDC" in Figure 7 is of a five-layer membrane after a combination of TD stretching and subsequent rolling (TDC) of the MD stretched membrane in the SEM micrograph in Figure 7 labeled "MD." The rolling process involves heat and pressure, which allows for a controlled reduction in the thickness of the membrane.

[0125] Example 2 (three layers 1) First trilayer composition (Trilayer 1): PP1 / PE1 / PP1 All PP layers are 0.90-0.92g / cm 3 Density range: 0.5MFR~2MF The entire PE1 layer is made of homopolymer PP having a MFR in the range of 0.25-0.5 g / 10 min at 2.16 kg and 190 °C, and a melt index of 0.95-0.97 g / cm 3 The polyethylene has a density range of 100 to 200 mm.

[0126] Three-layer 1: PP1 / PE1 / PP1 manufacturing method The first layer of Example 5 was produced by extruding two PP and PE monolayers. The monolayers were then laminated such that two PP monolayers were laminated on one side of the PE monolayer to produce an intermediate product, which was then stretched in MD and TD directions and then rolled. The monolayers could all be laminated together, or one PP layer could be laminated to the PE monolayer and then the other PP layer. The PP:PE:PP ratio was 2:1:2, with a total amount of PE of 20%.

[0127] The first trilayer is shown diagrammatically in FIG. 4 and FIG. 3(c).

[0128] Example 3 (three layers 2) Composition of the three layers 2 The composition of the second five layers is (PP1 / PP2 / PP1) / (PE2 / PE2 / PE2) / (PP1 / PP2 / PP1), where PP1 is homopolymer PP and has a density of 0.90-0.92 g / cm 3 and MFR in the range of 0.5MFR to 2MFR. It is a blend consisting of 90% homopolymer PP of PP1 and 10% propylene-ethylene elastomer. PE1 has a melt index of 0.25-0.5 g / 10 min and a viscosity of 0.95-0.97 g / cm at 2.16 kg and 190°C. 3 It has a density range of The material consists of a blend of 95% high density polyethylene, 5% mLLDPE, and 5% PE.

[0129] Manufacturing method of the third layer 2 Tri-layer 2 was produced by co-extruding a PP-containing layer having the composition described in Example 7 above (i.e., PP1 / PP2 / PP1) and a PE-containing layer having the composition described in Example 7 above (i.e., PE2 / PE2 / PE2), each of which had three sub-layers as shown in Figure 3(a). The two PP-containing layers were then laminated to one side of the PE-containing layer to produce an intermediate product. The intermediate product was then MD and TD stretched and then rolled.

[0130] The three layers 2 are shown diagrammatically in Figure 5 and Figure 3(a). The PP1:PP2:PP1 ratio is 1:1:1. The PP:PE:PP ratio is 2:1:2. The total PE is 20%.

[0131] Example 4 (Second Five Layers) Composition of the second five layers The second pentalayer has the structure PP1 / PE1 / PP1 / PE1 / PP1, where PP1 and PE1 are as described herein.

[0132] Manufacturing method of the second five layers The second five layers are produced by extruding monolayers of PP1 and PE1, respectively, and then laminating these monolayers to form the structure PP1 / PE1 / PP1 / PE1 / PP1. The laminate is MD and TD oriented and then calendered.

[0133] Example 5 (Collapsed Bubble Coextrusion) composition The composition of Example 5 has the structure PP1 / PP2 / PE1 / PE1 / PP2 / PP1, where PP1, PP2 and PE1 are as described herein.

[0134] Manufacturing method Example 5 was produced by co-extrusion of three layers PP1 / PP2 / PE1 using bubble extrusion method, collapsing the bubbles and laminating the PE1 layer on one side of the bubble to the other.The laminate was then MD and TD stretched and then rolled.This embodiment has one lamination interface, which is the PE / PE lamination interface.

[0135] Example 6 (Multi-laminate) Composition of Example 5 Example 6 has the structure PP1 / PP2 / PE1 / PE1 / PP2 / PP1, where PP1, PP2, and PE1 are as described herein.

[0136] Manufacturing method of Example 6 Six monolayers were coextruded (two PP1, two PP2, and two PE1 monolayers) and laminated to produce the structure of Example 6 with five lamination interfaces (only two PP / PE lamination interfaces). The laminate was then MD and TD stretched and then rolled.

[0137] Example 7 (Multi-laminate) composition Example 7 has the structure PP1 / PE1 / PP2 / PP2 / PE1 / PP1, where PP, PP2, and PE1 are as described herein.

[0138] Manufacturing method of Example 7 Six monolayers (two PP1 monolayers, two PE1 monolayers, and two PP2 monolayers) were extruded and laminated to produce the above structure. The laminate was then MD and TD stretched before The laminate has 5 lamination interfaces. It has 4 PP / PE lamination interfaces.

[0139] result Comparison of MD-stretched five-layer membrane of Example 1 Table 1 below shows comparative properties of a uniaxially MD-stretched five-layer membrane 1 (Example 1) having the composition and structure (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) shown in FIG. 3(b) compared to a first MD-stretched three-layer membrane (Example 2) having the composition and structure (PP / PE / PP) shown in FIG. 3(c) and a second three-layer membrane (Example 3) having the composition and structure (PP / PE / PP) shown in FIG. 3(a). As shown below, each of the layers in FIG. 3(b) comprises three sublayers, and the second three-layer layer in FIG. 3(a) also comprises sublayers. It is noted that FIGS. 3(a)-3(c) are not drawn to scale, but rather are drawn to show that the first and second three-layer membranes correspond to portions of a five-layer membrane. As shown in Tables 1-3, the overall thickness of the first and second tri-layers is roughly equivalent to the overall thickness of the penta-layer membrane (with some differences as disclosed in Tables 1-3). Thus, each sub-layer in the penta-layer membrane has an average thickness that is less than the average thickness of the corresponding sub-layer in the first and second tri-layers. The PP and PE materials used in the penta-layer membrane and the second tri-layer membrane are the same.

[0140] [Table 1]

[0141] Table 2 below shows the results of the TD stretched first trilayer membrane having the composition and structure (PP / PE / PP) shown in FIG. 3(c) and the composition and structure (PP / PP / PP) shown in FIG. 3(a). 3(b) shows the comparative properties of a TD stretched five-layer membrane with the composition and structure (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP), compared to a second three-layer membrane with the composition and structure (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP).

[0142] [Table 2]

[0143] Table 3 below shows the comparative properties of a TD stretched and rolled pentalayer membrane with the composition and structure (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) shown in FIG. 3(b) compared to a TD stretched and rolled trilayer membrane with the composition and structure (PP / PE / PP) shown in FIG. 3(c) and a second trilayer membrane with the composition and structure (PP / PP / PP) / (PE / PE / PE) / (PP / PP / PP) shown in FIG. 3(a).

[0144] [Table 3]

[0145] As can be seen by comparing a five-layer embodiment (Example 1) with two three-layer embodiments (Examples 2 and 3), the five-layer embodiment, for example, exhibits improved puncture. This is believed to be at least partially due to the lamination interfaces compared to a first three-layer having no lamination interfaces and / or an increased number of lamination interfaces compared to a second three-layer having two lamination interfaces. It is hypothesized that three or more lamination interfaces improve the properties of the microporous membrane. Four lamination interfaces have been found to improve the properties of the microporous thin film.

[0146] [Table 4]

[0147] [Table 5]

[0148] [Table 6]

[0149] Thus, Tables 4-6 show the improvement of a product having four lamination interfaces (a second five-ply, Example 4) compared to a product having two lamination interfaces (three-ply 1, Example 2). In these examples, each of the lamination interfaces is a PP / PE lamination interface where the layer or sub-layer at the interface is PP on one side of the interface and PE on the other side.

[0150] The normalized puncture strength for Examples 1-7 is shown in FIG. 8. In FIG. 8, the "a" value is the normalized puncture strength value calculated as shown in the figure. From the results in FIG. 8, some conclusions are that the number of PP / PE interfaces has a strong effect on the obtained strength of the examples. Example 2, which has two PP / PE lamination interfaces, is compared to Example 4, which has four PP / PE lamination interfaces. Example 4, which has four lamination interfaces, is compared to Example 7, which has five lamination interfaces. Example 2 is compared to Example 6, which have two and five lamination interfaces, respectively, but have the same number of PP / PE lamination interfaces.

[0151] In at least another embodiment, the porous membrane can be a base thin film for coating, dipping or impregnation, for example, a gradient or controlled impregnation or coating (e.g., a partially pre-wetted membrane is coated with a PO dipping solution). In this case, the coating will only partially impregnate the membrane. For example, there can be a controlled impregnation, where the dipping material is a blend of two polymer resins, one that penetrates the membrane more easily than the other.

[0152] The membrane or separator may be cut, slit, leaf, sleeve, pocket, envelope, wrap, Z-fold, zigzag, and / or the like. The membrane or separator may be flat sheet, tape, slit, nonwoven, woven, mesh, knit, hollow fiber, and / or the like. The membrane or separator may be applied for use in electrochemical devices, batteries, cells, ESS, UPS, capacitors, supercapacitors, double layer capacitors, fuel cells (PEM, humidity control membrane, ...), catalyst supports, supports, pancakes (anode, separator, cathode), base membranes, coated base membranes, textiles, barrier layers in textiles, protective clothing, barrier layers in protective clothing, blood barriers, water barriers, filtration media, blood, blood components, blood oxygenators, disposable lighters, and / or the like.

[0153] The battery separator may be a coextruded multi-layer battery separator. Coextrusion refers to a process in which polymers come together simultaneously in an extrusion die and exit the die in a shape, e.g., a generally planar structure, with at least two separate layers bonded at the interface of the separate layers by mixing the polymers that form the interface of the separate layers. The extrusion die may be either a planar sheet (or slot) die or a blown thin film (or annular) die. Coextrusion processes are described in more detail below. Multi-layer refers to a separator having at least two layers. Multi-layer may refer to a structure having three, four, five, six, seven, or more layers. Each layer is formed by a separate polymer feed stream into the extrusion die. The layers may be of different thicknesses. Often most often, at least two feed streams are of different polymers. Different polymers refer to: polymers with different chemical properties (e.g. PE and PP, or copolymers of PE and PE are polymers with different chemical properties); and / or polymers with the same chemical properties but different properties (e.g. two PEs with different properties (e.g. density, molecular weight, molecular weight distribution, rheology, additives (composition and / or percentage), etc.)). However, the polymers may be the same or identical.

[0154] Polymers that may be used in the battery separator are those that are extrudable. Such polymers are commonly referred to as thermoplastic polymers. Exemplary thermoplastic polymers include, but are not limited to: polyolefins, polyacetals (or polyoxymethylenes), polyamides, polyesters, polysulfides, polyvinyl alcohols, polyvinyl esters, and polyvinylidenes. Polyolefins include, but are not limited to, polyethylene (including, for example, LDPE, LLDPE, HDPE, UHDPE), polypropylene, polybutylene, polymethylpentane, copolymers thereof, and blends thereof. Polyamides (nylons) include, but are not limited to, polyamide 6, polyamide 66, nylon 10,10, polyphthalamide (PPA), copolymers thereof, and blends thereof. Polyesters include, but are not limited to, polyterephthalate esters, polybutyl terephthalate, copolymers thereof, and blends thereof. Polysulfides include, but are not limited to, polyphenyl sulfide, copolymers thereof, and blends thereof. Polyvinyl alcohols include, but are not limited to, ethylene-vinyl alcohol, copolymers thereof, and blends thereof. Polyvinyl esters include, but are not limited to, polyvinyl acetate, ethylene-vinyl acetate, copolymers thereof, and blends thereof. Polyvinylidenes include, but are not limited to, polyvinylidene fluorides (e.g., polyvinylidene chloride, polyvinylidene fluoride), copolymers thereof, and blends thereof.

[0155] Various materials may be added to the polymer to modify or enhance the performance or properties of the individual layers or the separator as a whole. Materials that lower the melting point of the polymer may be added. Usually, multi-layer separators have layers designed to close their pores at a certain temperature that blocks the flow of ions between the electrodes of the battery. This function is usually called "shutdown". In one embodiment, a three-layer separator has a central shutdown layer. To lower the shutdown temperature of the layers, materials that have a lower melting point than the polymers with which they are mixed may be added to the polymer. Such materials include, but are not limited to: materials with a melting point lower than 125°C, such as polyolefins or polyolefin oligomers. Such materials include, but are not limited to: polyolefin waxes (polyethylene wax, polypropylene wax, polybutene wax, and blends thereof). These materials may be introduced into the polymer in a proportion of 5 to 50% by weight of the polymer. Shutdown temperatures lower than 140°C can be obtained in one embodiment. Shutdown temperatures lower than 130°C can be obtained in another embodiment. It can be obtained in this state.

[0156] Materials may be added to improve the melt integrity of the membrane. Melt integrity refers to the ability of the membrane to limit its loss or degradation of its physical dimensions at high temperatures so that the electrodes remain physically separated. Such materials include inorganic fillers. Inorganic fillers include, but are not limited to: talc, blue phosphorus, synthetic silica, diatomaceous earth, mica, nanoclay, boron nitride, silicon dioxide, titanium dioxide, barium sulfate, calcium carbonate, aluminum hydroxide, magnesium hydroxide, and the like, and blends thereof. Such materials may also include, but are not limited to, fine fibers. Fine fibers include glass fibers and chopped polymer fibers. The loading ratio ranges from 1 to 60% by weight of the polymer of the layer. Such materials may also include high melting point or high viscosity organic materials, such as PTFE and UHMWPE. Such materials may also include crosslinking or coupling agents.

[0157] Materials may be added to improve the strength or toughness of the membrane. Such materials include elastomers. Elastomers include, but are not limited to: ethylene-propylene (EPR), ethylene-propylene-diene (EPDM), styrene-butadiene (SBR), styrene-isoprene (SIR), ethylidene norbornene (ENB), epoxy, and polyurethane and blends thereof. Such materials may also include, but are not limited to, fine fibers. Fine fibers include glass fibers and chopped polymer fibers. The loading rate ranges from 2 to 30% by weight of the polymer of the layer. Such materials may also include crosslinking or coupling agents or high viscosity or high melting point materials. Materials may be added to improve the antistatic properties of the membrane. Such materials include, for example, antistatic agents, including, but not limited to, glycerol monostearate, ethoxylated amines, polyethers (e.g., Pelestat 300, available from Sanyo Chemical Industries, Japan), and the loading ratio is in the range of 0.001-10% by weight of the layer polymer.

[0158] Materials may be added to improve the surface wettability of the separator. Such materials include, for example, wetting agents. Wetting agents include, but are not limited to: ethoxylated alcohols, primary polymeric carboxylic acids, glycols (e.g., polypropylene glycol and polyethylene glycol), maleic anhydride functionalized polyolefins, acrylic acid, glycidyl methacrylate. The loading ratio ranges from 0.01 to 10% by weight of the layer polymer.

[0159] Materials for improving the surface tribological performance of the separator may be added. Such materials include lubricants. Examples of lubricants include fluorinated polymers (e.g., polyvinylidene fluoride, polytetrafluoroethylene, low molecular weight fluorinated polymers), slip agents (e.g., oleamide, stearamide, erucic acid amide, Kemamide®, calcium stearate, and silicones. The loading ratio is in the range of 0.001 to 10% by weight of the layer polymer.

[0160] Materials may be added to improve polymer processability. Examples of such materials include fluorinated polymers, boron nitride, and polyolefin waxes. The dosage ratio ranges from 100 ppm to 10% by weight of the layer polymer.

[0161] Materials may be added to improve the flame retardancy of the membrane, including, for example, brominated flame retardants, ammonium phosphate, ammonium hydroxide, alumina trihydrate, and phosphate esters.

[0162] Materials that promote the nucleation of the polymer may be added. Such materials include nucleating agents, including but not limited to sodium benzoate, dibenzylidene sorbitol (DBS) and its chemical derivatives. The dosing ratios are conventional.

[0163] Materials may be added to color the layer. Such colorants are conventional.

[0164] In the manufacture of the battery separator, polymers are co-extruded to produce a multi-layer non-porous precursor, which is then processed to form the micropores. The micropores may be formed by a "wet" or "dry" process. A wet process (also called solvent extraction, phase inversion, thermally induced phase separation (TIPS), or gel extraction) generally involves the addition of a removable material prior to the formation of the precursor, followed by the removal of this material, for example, by an extraction process, to form the pores. A dry process (also called the Celgard process) generally involves extracting the precursor (without removing material to form the pores); annealing the precursor, and extruding the precursor to form the micropores. Hereinafter, the invention will be described with respect to the dry process.

[0165] One way to describe a potentially preferred five-layer structure is an inverted three-layer (PE / PP / PE) laminated between two polypropylene layers.

[0166] Additional illustrative data on top of that In accordance with at least selected embodiments, aspects or objectives, the present application, disclosure or invention relates to improved membranes, separator membranes, separators, battery separators, lithium secondary battery separators, multilayer membranes, multilayer separator membranes, multilayer separators, multilayer battery separators, multilayer lithium secondary battery separators, multilayer battery separators, batteries, capacitors, supercapacitors, bilayer supercapacitors, fuel cells, lithium batteries, lithium ion batteries, lithium secondary batteries and / or lithium ion secondary batteries, and / or methods of making and / or using such membranes, separator membranes, separators, battery separators, lithium secondary battery separators, batteries, capacitors, fuel cells, lithium batteries, lithium ion batteries, lithium secondary batteries and / or lithium ion secondary batteries, and / or devices, vehicles or articles of manufacture comprising same, and / or the like.

[0167] In accordance with at least selected embodiments, the application, disclosure or invention relates to improved membranes, separator membranes, separators, battery separators, lithium secondary battery separators, multilayer membranes, multilayer separator membranes, multilayer separators, multilayer battery separators, multilayer lithium secondary battery separators, multilayer battery separators, electrochemical cells, batteries, capacitors, supercapacitors, bilayer supercapacitors, fuel cells, lithium batteries, lithium ion batteries, lithium secondary batteries and / or lithium ion secondary batteries, and / or methods of making and / or using such membranes, separator membranes, separators, battery separators, lithium secondary battery separators, electrochemical cells, batteries, capacitors, fuel cells, lithium batteries, lithium ion batteries, lithium secondary batteries and / or lithium ion secondary batteries, and / or devices, vehicles or articles of manufacture comprising same, and / or the like.

[0168] Various embodiments of the present invention have been described as fulfilling various objectives of the present invention. It should be recognized that these embodiments are merely illustrative of the principles of the present invention. Numerous modifications and adaptations will be readily apparent to those skilled in the art without departing from the spirit and scope of the invention.

[0169] As used in this specification and the appended claims, the singular forms "a," "an," and "the" include the plural unless the context clearly dictates otherwise. Ranges may be expressed herein as from "about" or "approximately" one particular value and / or to "about" or "approximately" another particular value. When such a range is expressed, another embodiment includes from the one particular value and / or to the other particular value. Similarly, when values ​​are expressed as approximations, by use of the antecedent "about," it will be understood that the particular value constitutes another embodiment. It will be further understood that the endpoints of each of the ranges are significant both in relation to the other endpoint, and independently of the other endpoint. "Optionally" or "optionally" means that the sequentially described events or circumstances may or may not occur, and that the description includes instances in which said events or circumstances occur and instances in which said events or circumstances do not occur.

[0170] Throughout the specification and claims of this specification, the word "comprise" and variations of this word, such as "comprising" and "comprises," mean "including but not limited to," and are not intended to exclude, for example, other additives, components, integers, or steps. The terms "consisting essentially of" and "consisting of" can be used in place of "comprising" and "including" to provide and disclose more specific embodiments of the invention. "Exemplary" or "for example" means "example of" and is not intended to convey an indication of a preferred or ideal embodiment. Similarly, "such as" is not used in a limiting sense, but is used for descriptive or exemplary purposes.

[0171] Unless otherwise noted, all numbers expressed as shapes, dimensions, and the like used in the specification and claims, should at the very least be understood as being in light of the number of significant digits and ordinary rounding approaches, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims.

[0172] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the disclosed invention belongs. References cited herein and the materials for which they are cited are incorporated herein by reference.

Claims

1. A microporous membrane, comprising: two outer layers, each outer layer comprising a polyolefin; a plurality of inner layers, each inner layer comprising a polyolefin; Including, Each of the outer layers is laminated to an inner layer, and each of the inner layers is laminated to at least one other inner layer. Microporous membrane.

2. 10. The microporous membrane of claim 1, wherein each of the outer layers comprises polypropylene, a polypropylene blend, a polypropylene copolymer, polyethylene, a polyethylene blend, a polyethylene copolymer, or any combination thereof.

3. 10. The microporous membrane of claim 1, wherein each of the outer layers comprises polypropylene, a polypropylene blend, a polypropylene copolymer, or any combination thereof.

4. 10. The microporous membrane of claim 1, wherein each of the plurality of inner layers comprises polypropylene, a polypropylene blend, a polypropylene copolymer, polyethylene, a polyethylene blend, a polyethylene copolymer, or any combination thereof.

5. 10. The microporous membrane of claim 1, wherein there are 2, 3, 4, 5, 6 or more inner layers.

6. 10. The microporous membrane of claim 1, wherein there are two, three, or more inner layers.

7. 10. The microporous membrane of claim 1, wherein there are three inner layers.

8. 10. The microporous membrane of claim 1, wherein the microporous membrane is a five-layer membrane comprising a first outer layer, a first inner layer, a second inner (or middle) layer, a third inner layer, and a second outer layer.

9. the first outer layer is laminated to the first inner layer; the first inner layer is laminated to the first outer layer and to the second inner (or intermediate) layer; the second inner (or intermediate) layer is laminated to the first inner layer and to the third inner layer; 9. The microporous membrane of claim 8, wherein the third inner layer is laminated to the second inner (or intermediate) layer and the second outer layer.

10. 9. The microporous membrane of claim 8, wherein the first and second outer layers and the second inner (or intermediate) layer comprise polypropylene, a polypropylene blend, a polypropylene copolymer, or any combination thereof.

11. 11. The microporous membrane of claim 10, wherein the first and third inner layers comprise polyethylene, a polyethylene blend, a polyethylene copolymer, or any combination thereof.

12. 2. The microporous membrane of claim 1, comprising a five-layer membrane comprising a structure of PP / PE / PP / PE / PP, where PP is polypropylene, a polypropylene blend, a polypropylene copolymer, or any combination thereof, and PE is polyethylene, a polyethylene blend, a polyethylene copolymer, or any combination thereof.

13. Each of the five layers (inner or outer layers) of the five-layer membrane is The microporous membrane of claim 12 laminated to a layer (inner layer or outer layer).

14. The microporous membrane of any one of claims 1 to 13, wherein each layer (inner or outer) comprises two, three, four, five or more sublayers.

15. The microporous membrane of any one of claims 1 to 13, wherein each layer (inner or outer) comprises two, three or more sublayers.

16. The microporous membrane of any one of claims 1 to 13, wherein each layer (inner or outer) comprises three sublayers.

17. 17. The microporous membrane of claim 16, wherein each sublayer has a maximum average thickness of 6 μm or less, 5 μm or less, 4 μm or less, 3 μm or less, 2 μm or less, or 1 μm or less.

18. The microporous membrane of claim 14, wherein each of the sublayers is coextruded.

19. 20. The microporous membrane of claim 18, wherein each of the layers has a maximum average thickness, prior to stretching, of 1.2 mils or less, 1.1 mils or less, 1 mil or less, 0.9 mils or less, 0.8 mils or less, 0.75 mils or less, 0.5 mils or less, 0.4 mils or less, 0.3 mils or less, or 0.2 mils or less.

20. The microporous membrane of any one of claims 1 to 13, wherein the membrane has a maximum average thickness in the range of 1 to 50 microns.

21. 14. The microporous membrane of any one of claims 1-13, wherein each layer comprises a maximum average thickness of less than 33%, 32%, 31%, 30%, 29%, 28%, or 28% of the total average thickness of the membrane.

22. The microporous membrane of any one of claims 1 to 13, wherein the membrane is stretched in the longitudinal direction.

23. The microporous membrane of any one of claims 1 to 13, wherein the membrane is stretched in the transverse direction.

24. The microporous membrane of any one of claims 1 to 13, wherein the membrane is stretched in both the longitudinal and transverse directions.

25. The microporous membrane of any one of claims 1 to 13, wherein the microporous membrane is stretched in the transverse direction and rolled.

26. The microporous membrane of any one of claims 1 to 13, further comprising an additive.

27. 27. The microporous membrane of claim 26, wherein the additive comprises a functional polymer, an ionomer, a cellulose nanofiber, an inorganic particle, a smoothing agent, a nucleating agent, a cavitation promoter, a fluorinated polymer, a crosslinking agent, an X-ray detectable material, a polymer processing agent, a high temperature melt index (HTMI) polymer, an electrolyte additive, an energy dissipating immiscible additive, or any combination thereof.

28. 27. The microporous membrane of claim 26, wherein the additive is a coating on the first outer layer, on the second outer layer, or on both the first and second layers.

29. The first and second outer layers and the second inner (or intermediate) layer have a thickness of 0.02 to 0.06 μm. The microporous membrane of any one of claims 10 to 13, having an average polypropylene pore size in the range of

30. The microporous membrane of any one of claims 10 to 13, wherein the first and third inner layers have an average polyethylene pore size in the range of 0.03 to 1.0 μm.

31. 14. The microporous membrane of any one of claims 1 or 10-13, wherein the membrane has increased or improved elasticity at 150°C or higher compared to a PP / PE / PP trilayer microporous membrane having the same thickness, same Gurley, same porosity, and / or same layer component configuration as the membrane.

32. 14. The microporous membrane of any one of claims 1 or 10-13, wherein the membrane has increased or improved puncture resistance compared to a PP / PE / PP trilayer microporous membrane having the same thickness, same Gurley, same porosity, and / or same layer component configuration as the membrane.

33. 14. The microporous membrane of any one of claims 1 or 10-13, wherein the membrane has increased or improved longitudinal tensile strength at break compared to a PP / PE / PP trilayer microporous membrane having the same thickness, same Gurley, same porosity, and / or same layer composition as the membrane.

34. 14. The microporous membrane of any one of claims 1 or 10-13, wherein the membrane has increased or improved TD elongation compared to a PP / PE / PP trilayer microporous membrane having the same thickness, same Gurley, same porosity, and / or same layer component configuration as the membrane.

35. A lithium ion battery comprising the microporous membrane according to any one of claims 1 to 34.

36. A device, comprising the microporous membrane according to any one of claims 1 to 34.

37. A woven fabric, characterized in that it comprises the microporous membrane according to any one of claims 1 to 34.

38. 1. A method for making a multi-layer, microporous membrane, the method comprising: extruding a polypropylene precursor comprising a plurality of sublayers; extruding a polyethylene precursor comprising a plurality of sublayers; laminating the extruded polypropylene precursor layer with the extruded polyethylene precursor layer to produce a first intermediate precursor having an alternating polyethylene and polypropylene precursor structure; laminating, simultaneously or separately, a first outer layer comprising one of the extruded polypropylene precursors to a first side of the intermediate precursor and a second outer layer comprising one of the extruded polypropylene precursors to a second side of the first intermediate precursor opposite the first side to produce a second intermediate precursor; annealing the second intermediate precursor to produce an annealed multilayer film; uniaxially or biaxially stretching the annealed multilayer film to produce a microporous multilayer film; optionally rolling the microporous multilayer film; A method comprising:

39. 38. The first intermediate precursor comprises a three-layer structure of PE / PP / PE or PP / PE / PP, or a four-layer structure of PP / PE / PE / PP or PE / PP / PP / PE. The method according to

40. 39. The method of claim 38, wherein the second intermediate precursor comprises a five-layer structure of PP / PE / PP / PE / PP or PE / PP / PE / PP / PE or a six-layer structure of PP / PP / PE / PE / PE / PP / PP, PE / PE / PP / PP / PE / PE, PP / PE / PE / PE / PE / PE / PP, or PE / PP / PP / PP / PP / PE / PE.

41. 39. The method of claim 38, wherein the uniaxial stretching is in the machine direction or the transverse direction.

42. 39. The method of claim 38, wherein the biaxial stretching is in the machine direction and the transverse direction.

43. 43. The method of claim 42, wherein the machine direction and transverse direction stretching is sequential or simultaneous.

41. 40. The method of claim 38, wherein the oriented polypropylene precursor comprises two, three, four, or more sublayers.

42. 39. The method of claim 38, wherein the expanded polyethylene precursor comprises two, three, four, or more sublayers.

43. 40. The method of claim 38, wherein the second intermediate precursor comprises a five-layer structure of PP / PE / PP / PE / PP, and each of the polyethylene and polypropylene precursors comprises three sublayers.

44. 39. The method of claim 38, wherein the extruded polypropylene precursor and the extruded polyethylene precursor are non-porous.

45. 40. The method of claim 38, further comprising coating one or more of the first outer layer and the second outer layer.

46. 1. A method for making a five-layer microporous membrane, the method comprising: extruding a plurality of polypropylene and polyethylene films; laminating one of the polyethylene films to a first surface of a polypropylene film and another of the polyethylene films to an opposite second surface of the polypropylene film to produce an inverted tri-layer film having a PE / PP / PE structure; laminating one of the polypropylene films to one of the polyethylene films of the inverted tri-layer film and another of the polypropylene films to the other polyethylene film of the inverted tri-layer film simultaneously or separately to produce a five-layer film having a structure of PP / PE / PP / PE / PP; annealing the pentalayer film; stretching the annealed five-layer membrane uniaxially or biaxially to produce the microporous membrane, or stretching and optionally rolling the annealed five-layer membrane to produce the microporous membrane; A method comprising:

47. A battery separator comprising a microporous membrane produced by the method of any one of claims 38 to 46.

48. A lithium ion battery separator comprising a microporous membrane produced by the method of any one of claims 38 to 46.

49. A device comprising a microporous membrane manufactured by the method according to any one of claims 38 to 46. Vice.

50. A woven fabric comprising a microporous membrane produced by the method of any one of claims 38 to 46.

51. A multi-layer, microporous membrane having three or more lamination interfaces and exhibiting a puncture strength of 150 g or more, 260 g or more, 270 g or more, 280 g or more, 290 g or more, 300 g or more, 310 g or more, 400 g or more, or 500 g or more.

52. 52. The multi-layer, microporous membrane of claim 51, wherein the puncture strength is 300 g or greater.

53. 52. The multi-layer, microporous membrane of claim 51, wherein the puncture strength is 310 g or greater.

54. 52. The multi-layer, microporous membrane of claim 51, wherein the puncture strength is greater than or equal to 290 g.

55. 52. The multi-layer, microporous membrane of claim 51 comprising three lamination interfaces.

56. 52. The multi-layer, microporous membrane of claim 51 comprising four lamination interfaces.

57. 52. The multi-layer, microporous membrane of claim 51 comprising five or more laminated surfaces.

58. 58. The multi-layer, microporous membrane of any one of claims 51-57, wherein the membrane comprises four or more layers, each layer comprising two or more sub-layers produced by a coextrusion process.

59. 58. An electrochemical cell, battery, capacitor, supercapacitor, bilayer supercapacitor, fuel cell, lithium battery, lithium ion battery, lithium secondary battery and / or lithium ion secondary battery comprising the microporous membrane of any one of claims 1 to 34 or the multilayer microporous membrane of any one of claims 51 to 57.

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