1723 results about "Polyethylene terephthalate" patented technology

One aspect is a method for producing a first intermediate product. A feedstock is provided that comprises a first polyester. The feedstock is contacted with a first amount of a first organic compound in a volume section V1 to obtain a first initial mixture. The first amount is in the form of a liquid. The first polyester is transported, and at least a fraction of the first amount of the first organic compound, from the volume section V1 to a volume section V2. The volume section V2 is at least partially filled with the first organic compound. A level of the first organic compound in the volume section V1 is at a height H1 from a floor, and a level of the first organic compound in the volume section V2 is at a height H2 from the floor. The first polyester is contacted with a further organic compound in a volume section V3, to obtain a further initial mixture. A weight average molar mass of the first polyester is reduced in the volume section V3, to obtain a first intermediate mixture. The first intermediate mixture comprisesa first intermediate product,the further organic compound.H1<H2.

One aspect is a method for producing a first intermediate product. A feedstock is provided that comprises a first polyester. The feedstock is contacted with a first amount of a first organic compound in a volume section V1 to obtain a first initial mixture. The first amount is in the form of a liquid. The first polyester is contacted with a further organic compound to obtain a further initial mixture. A weight average molar mass of the first polyester is reduced to obtain a first intermediate mixture. The first intermediate mixture has a first intermediate product, the further organic compound. A mass ratio of the feedstock to the first organic compound in the volume section V1 is in the range of 0.02 to 3.

The invention relates to an antistatic MLCC release film base film and a preparation method thereof. The antistatic MLCC release film base film is prepared by melt blending and biaxial stretching of PET master batch, an antistatic composition and a nano filler, wherein the antistatic composition is prepared by compounding modified PET-PEG and thiophene modified aromatic polyamide; the nano filler is prepared by carrying out melt extrusion on KH550 modified talcum powder and MAH-g-PET (maleic anhydride-grafted polyethylene terephthalate). The antistatic composition disclosed by the invention has the beneficial effects that the antistatic composition is formed by interweaving two polymers, and a stable three-dimensional conductive network is constructed in the PET film, so that the antistatic performance is more efficient, lasting and stable. In addition, through chemically bonded modified talcum powder, the smoothness and low roughness are provided, and meanwhile reinforcing and toughening are achieved; and the single-layer extrusion process can realize ultrathin thin film, the production process is simplified, and the production cost is greatly reduced.

The invention relates to the technical field of PET optical films, and particularly discloses a high-light-transmittance blue-light-resistant PET optical film and a preparation method thereof, and the high-light-transmittance blue-light-resistant PET optical film is prepared from the following raw materials by weight: 70-85% of a polyethylene glycol terephthalate resin matrix; 3%-8% of a benzotriazole anti-blue light agent; 5%-12% of a silicon dioxide nano anti-reflection agent; 2%-6% of nano zinc oxide or nano cerium oxide; 1.5% to 4% of a polycarbodiimide cross-linking agent; 0.5%-3% of an anti-blocking agent; 0.4%-1.5% of an antioxidant; 0.4%-1.0% of an ultraviolet light absorber; the balance is a processing aid; the preparation method comprises the following steps: S1, pretreating the raw materials; s2, a mixing procedure; and S3, extruding and coating. The PET optical film provided by the invention has high optical properties of high light transmittance, blue light resistance and low haze, and has the advantages of high light transmittance and blue light blocking rate of the optical film and improvement of the application range of the optical film.

The invention relates to the technical field of polyester fibers, and discloses a preparation method of antibacterial modified polyester hollow fibers, which comprises the following steps: by taking nitrilotriacetic acid, thionyl chloride, epoxy chloropropane, eugenol and the like as raw materials, carrying out acylating chlorination reaction, quaternization reaction and esterification reaction to obtain eugenol epoxy quaternary ammonium salt. The preparation method comprises the following steps: carrying out ring-opening reaction on carboxyl groups in graphene oxide and epoxy groups in eugenol epoxy quaternary ammonium salt to obtain modified graphene, uniformly mixing the modified graphene with polyethylene glycol terephthalate, and carrying out a series of steps to finally obtain the antibacterial modified polyester hollow fiber. Eugenol and quaternary ammonium salt are utilized to improve the antibacterial property of the polyester hollow fiber, and graphene is utilized to improve the mechanical property of the polyester hollow fiber. The polyester hollow fiber prepared by the invention has excellent mechanical properties and antibacterial properties.

The invention belongs to the technical field of high polymer materials, and particularly relates to a high-strength papermaking forming net fiber. Comprising the following raw materials in parts by weight: 75-90 parts of polyethylene glycol terephthalate, 5-15 parts of polybutylene terephthalate, 3-10 parts of a modified fiber filler, 2-5 parts of modified graphene, 2-8 parts of silicon dioxide, 0.5-2 parts of a silane coupling agent KH-560, 1-3 parts of an anti-hydrolysis agent, 0.5-1.5 parts of an antioxidant and 0.3-1 part of a lubricant. Wherein the modified fiber filler is prepared by sequentially carrying out modification processes such as silane coupling agent, citric acid-glycerol esterification, iron bismuth oxide loading and the like on glass fibers; the modified graphene is prepared by introducing dopamine, cerium ions and glycidyl methacrylate for modification. The mechanical strength, the hydrolysis resistance and the wear resistance of the fiber are remarkably improved through the synergistic effect of all the components and the melt spinning-multi-stage stretching process, and the fiber is particularly suitable for a forming net of a high-speed paper machine.

Provided is an exterior material for a power storage device which excels in formability and heat resistance.　The exterior material for a power storage device is composed of a multilayer body that comprises a base material layer, a barrier layer, and a heat-fusible resin layer, in that order. The base material layer is a polyester film containing polyethylene terephthalate and polybutylene terephthalate at a mass ratio of 65 / 35 to 90 / 10. The tensile elongation at break of the polyester film in the width direction is 90 to 155%.

The invention relates to the technical field of polyester, in particular to a flame-retardant and antibacterial dual-function fiber and a preparation method thereof. The flame-retardant antibacterial fiber overcomes the defects that existing fibers are poor in flame retardance and antibacterial property. According to the invention, PET resin, a composite modified auxiliary agent master batch and a composite flexibilizer are used as raw materials, and the bifunctional fiber is prepared through melting and spinning; wherein the composite modified additive master batch is prepared from the following raw materials: PET (Polyethylene Terephthalate) resin, aluminum diethylphosphinate, modified halloysite nanotubes, modified zinc oxide nanowires and zinc borate; the modified halloysite nanotube is prepared from the following raw materials: a halloysite nanotube, KH560 and phosphoric acid; the modified zinc oxide nanowire is prepared from the following raw materials: zinc nitrate hexahydrate, hexamethylenetetramine and sodium hypophosphite. By controlling the dosage of each component and processing technological parameters, the finally prepared difunctional fiber has good flame retardance and good antibacterial property, and is suitable for manufacturing curtains.

The present invention provides a polyester heat-shrinkable film containing recycled materials and a preparation method thereof, belonging to the technical field of polymer synthetic films. The raw materials of the polyester heat-shrinkable film include recycled PET polyester particles, PET polyester chips, and a modified masterbatch; the modified masterbatch is prepared from polyethylene terephthalate-1,4-cyclohexanedimethanol ester, triphenyl phosphite, polyethylene glycol block copolymer, nano-silica, and hyperbranched polyester amine; the polyethylene glycol block copolymer is prepared from polyethylene glycol and γ-valerolactone under the action of a catalyst; the hyperbranched polyester amine is prepared from trimethylolpropane, methyl crotonate, and diethylenetriamine. The product of the present invention has excellent properties such as excellent unidirectional anti-shrinkage performance and low haze.

This invention discloses a method for catalytically depolymerizing polyethylene terephthalate (PET) to prepare terephthalate. Under catalyst-free conditions or with a salt as a catalyst, PET or its composite system is treated in diester carbonate to achieve chemical depolymerization of PET, yielding PET monomers terephthalate and ethylene carbonate, and achieving complete depolymerization of PET in the composite. This invention, through the reaction of diester carbonate with PET, enables the depolymerization of PET under mild conditions, and further facilitates the research and development of related technologies for the chemical recovery of PET monomers from PET composite or mixed systems. The method provided by this invention has advantages such as high efficiency, environmental friendliness, and mild reaction conditions, and can catalyze the depolymerization of PET to generate its monomer terephthalate, possessing strong industrial application value.

The invention discloses a batch processing technology of micro-fluidic chips, and relates to the technical field of chip processing. The method comprises the following steps: firstly, providing at least two layers of polymer coiled materials, namely a first coiled material for forming a micro-channel structure and a second coiled material for closing a micro-channel, the coiled materials are continuous coiled materials selected from polyethylene glycol terephthalate (PET), cycloolefin polymer (COP), polycarbonate (PC) or polymethyl methacrylate (PMMA), and the coiled materials are continuous coiled materials selected from polyethylene glycol terephthalate (PET), cycloolefin polymer (COP), polycarbonate (PC) or polymethyl methacrylate (PMMA); the thickness of the coiled material is 50-500 microns; secondly, carrying out continuous compression molding processing on the surface of the first coiled material through a roll-to-roll processing platform; through a roll-to-roll continuous process, micro-channel mold pressing, functional deposition, precise alignment bonding and online cutting are integrated, high-efficiency, high-consistency and high-integration-level batch manufacturing of the micro-fluidic chip is realized, and manual intervention and production cost are remarkably reduced.

The invention discloses a platinum-tungsten bimetallic catalyst for PET depolymerization and a method for directional depolymerization of PET by the platinum-tungsten bimetallic catalyst, and belongs to the technical field of solid waste recycling, the platinum-tungsten bimetallic catalyst for PET depolymerization is prepared by a deposition-precipitation method, a mesoporous molecular sieve MCM-48 is used as a carrier to load platinum-tungsten bimetallic, the molar ratio of platinum to tungsten is 1: (0.5-2), the molecular sieve MCM-48 is a mesoporous molecular sieve MCM-48, and the mesoporous molecular sieve MCM-48 is a mesoporous molecular sieve MCM-48 carrier. And the platinum loading capacity is 4-6 wt%. By utilizing the platinum-tungsten bimetallic catalyst, one-pot depolymerization of PET can be realized to prepare p-toluic acid and p-xylene, the platinum-tungsten bimetallic catalyst can be used for multiple times through reduction regeneration, the catalytic activity is high, and the PET depolymerization method under catalysis of the platinum-tungsten bimetallic catalyst is suitable for recycling and upgrading of PET wastes in various forms and has wide application prospects. The technical problems of efficient depolymerization and directional conversion of the waste PET are solved, and a sustainable technical path is provided for resource recycling of the PET.

A protective barrier affixable to a curved substrate comprises a stack of two or more lenses, each of the two or more lenses including a polyethylene terephthalate (PET) film, a hard coat on a first side of the PET film, and an adhesive layer on a second side of the PET film opposite the first side. The stack of two or more lenses may have a modulation transfer function that exhibits a contrast value greater than 75% for a spatial resolution of one line-pair per 0.0003 radians at 65 degrees angle of incidence. Heat and pressure may be applied to conform the stack of two or more lenses to the shape of the curved substrate.

An insulated shipping container and method of forming and loading an insulated container utilizing sustainable materials including recycled post-industrial, pre-consumer natural fiber, plant-based fiber and synthetic fiber to include recycled polyethylene terephthalate (PET).

The invention provides a method for alcoholysis of polyethylene glycol terephthalate, and relates to the technical field of PET degradation. The PET alcoholysis method provided by the invention comprises the following steps: mixing PET, ethylene glycol, a cosolvent and a composite catalyst, and carrying out alcoholysis reaction to obtain bis (hydroxyethyl) terephthalate (BHET). According to the invention, dimethyl sulfoxide is taken as a cosolvent, zinc acetate and 1, 8-diazabicyclo [5.4. 0] undec-7-ene are taken as a composite catalyst, catalysis and solvent effect driving are combined, and ethylene glycol alcoholysis of PET is carried out under the synergistic effect of the composite catalyst and the cosolvent. According to the method, effective decomposition of PET can be achieved at the low temperature (140-155 DEG C) and within the short reaction time (60-100 min), and the yield of BHET is high (66% or above and can reach 80% or above). The method provided by the invention can realize high-efficiency alcoholysis of PET with ethylene glycol.

A composite membrane for desalination includes a polyethylene terephthalate (PET) nonwoven layer having a fibrous structure, and has an average thickness of about 30 to 200 micrometers (μm). A polysulfone (PS) layer having an average thickness of about 30 to 100 μm is disposed on a surface of the PET nonwoven layer. Further, a polyamide layer is disposed on a surface of the PS layer including reacted units of an acyl compound, a phenylenediamine monomer, and a poly-(DADMAC-co-DADA). The polyamide layer has a rough surface including a plurality of irregular-sized ridge-and-valley structures of polyamide. The poly-(DADMAC-co-DADA) has a formula (I), and n is a positive integer.

The invention discloses a production method of a PET composite current collector base film with high mechanical property. The base film comprises an outer surface layer, a middle core layer and an inner surface layer, the outer surface layer is composed of PET, fumaric acid, hydroxyl-terminated polybutadiene and an antioxidant; the middle core layer consists of PET (Polyethylene Terephthalate), furandicarboxylic acid, an antioxidant and a stabilizer; the inner surface layer is composed of dimethyl terephthalate, ethylene glycol, spiro diol, ethylene glycol antimony and zinc acetate. The PET composite current collector base film prepared by the preparation method disclosed by the invention has relatively high mechanical properties.

The invention relates to the technical field of polyester fibers, in particular to a negative ion polyester fiber which is prepared from the following raw materials in percentage by mass: 85-92% of polyethylene glycol terephthalate, 3-8% of nano tourmaline composite powder, 2-5% of a titanium dioxide / graphene composite carrier, 0.5-1.5% of a coupling agent and 0.3-0.8% of an antioxidant. The invention also discloses a preparation method of the composition. According to the invention, the core-shell structure optimization design is adopted, the core layer ensures the high loading capacity of the tourmaline composite powder, the shell layer has the synergistic effect of the titanium dioxide / graphene composite carrier, the negative ion release efficiency is obviously enhanced, the particle size of the nanoscale tourmaline is controlled to be 50-100nm, the nanoscale tourmaline is uniformly dispersed, the nanoscale tourmaline and graphene form a heterojunction structure, and the electron transmission capability is greatly improved; the negative ion release amount meets the JIS standard, a chemical bonding interface is formed through transesterification, the structural stability is enhanced, and the retention rate of the negative ion release performance is still high even after multiple times of washing.

A protective lens stack comprises a base layer including a polyethylene terephthalate (PET) film containing a UV blocking additive and one or more removable lens layers stacked on top of the base layer. Each of the removable lens layers may include a PET film and a first adhesive disposed on a bottom surface of the PET film. Refractive indices of the base layer and the one or more removable lens layers may be matched to within 0.2. Each layer of the protective lens stack, including the base layer and each of the removable lens layer(s), may have less than 0.5% haze. The protective lens stack may be used as a face shield or may be surface mountable using a second adhesive disposed on a bottom surface of the PET film containing the UV blocking additive.

The invention provides a low-melting-point PET short fiber, and relates to the technical field of fiber production. The low-melting-point PET short fiber comprises a high-strength low-melting-point PET short fiber, the short fiber is of a skin-core composite structure, a skin layer of the skin-core composite structure is modified low-melting-point polyester and is prepared by melt copolymerization of PET, 10-30% of rigid comonomers and 5-15% of flexible chain segments, the melting point is 110-160 DEG C, and the glass-transition temperature (Tg) is larger than or equal to 60 DEG C. The gradient interface enhancement technology is adopted, the PET-g-PE grafting layer is introduced between the skin layer and the core layer, the grafting rate reaches 5-8% through melt blending, a transition layer of 1-3 microns is formed, the peel strength is improved to 1.5 N / cm or above, and the problem of interface stripping of traditional composite fibers is solved.

The invention relates to the field of fiber processing, and particularly discloses a processing technology of colored superfine flat elastic polyester interlaced yarn, which comprises the following steps: S1, carrying out oxygen plasma treatment on PET (polyethylene terephthalate) slices, then adding maleic anhydride coated nano whiskers at 60-70 DEG C, gradually heating to 200-210 DEG C, pre-crystallizing for 24-28 hours, and then drying at 155-165 DEG C, so as to obtain the colored superfine flat elastic polyester interlaced yarn; crystallization slices are obtained; s2, performing melt spinning on the crystal slices to obtain cellosilk; s3, performing circular blowing cooling, spinning on an oil frame and elasticizing treatment on the cellosilk to obtain a finished product terylene interlaced yarn; meanwhile, the super-fine fiber has the advantages of being good in dyeing effect, stable in color and luster, super-fine, high in strength, good in elasticity, easy in flatness control and good in stability.

The present disclosure provides variant enzymes for use in the enzymatic degradation of polyethylene terephthalate (PET).

The utility model belongs to the technical field of resin film production, and particularly relates to a PET (Polyethylene Terephthalate) resin film trimming device which comprises a compression roller assembly for dynamically clamping a PET resin film during trimming, cutter assemblies mounted at two axial ends of the compression roller assembly and used for trimming the PET resin film, and a winding roller for winding the PET resin film after trimming, a plurality of guide rollers are arranged on the two sides, in the conveying direction of the PET resin film, of the pressing roller assembly; the pressing roller assembly is adopted, and the cutter assemblies are installed at the two axial ends of the pressing roller assembly, so that dynamic clamping is conducted during edge cutting of the PET resin film, the stability of the PET resin film at the cutting point can be guaranteed, the edge cutting accuracy and consistency of the PET resin film are effectively guaranteed, and it is guaranteed that the edge of the PET resin film after edge cutting is neat and flawless.

The present application relates to the technical field of current collectors, and specifically relates to a multilayer composite film and a current collector prepared from same. The present application provides a preparation method for the multilayer composite film. The multilayer composite film comprises a layer X, a layer Y and a layer Z from top to bottom; the layer X and the layer Z are made of polyimide, and the polyimide is a polycondensation reactant of carboxylic acid anhydride and diamine; and the material of the layer Y is any one or more of polypropylene, polyethylene, polyethylene terephthalate, polybutylene terephthalate, polyvinylidene fluoride, polytetrafluoroethylene, polyphenylene sulfide, polyphenyl ether, polyester, polystyrene and derivatives thereof. The polyimide prepared in the present application solves the problems of low solubility and poor processability of conventional fully aromatic polyimides, and a composite current collector is prepared by using heat resistance and improved surface polarity of polyimides, thereby improving the bonding force between a composite current collector film and a metal layer, and improving the tensile strength of a finished product.

The invention relates to the technical field of coatings, in particular to an antistatic film material and a preparation method thereof.The antistatic film material comprises a film base material layer and a photocuring antistatic coating coated on the film base material layer, and the film base material layer is a polyethylene glycol terephthalate film; the light-cured antistatic coating is prepared from the following raw materials: water-soluble polyurethane acrylic resin, water-soluble acrylic resin, modified polyhedral oligomeric silsesquioxane, a composite conductive material, a photoinitiator, a flatting agent, a defoaming agent and water; the modified polyhedral oligomeric silsesquioxane and the composite conductive material are added into the coating base material to modify the coating base material, the coating has excellent antistatic performance and good mechanical property after being cured by ultraviolet light, and the special structure of the composite conductive filler and the compounding of the composite conductive filler and the modified polyhedral oligomeric silsesquioxane have excellent antistatic performance and good mechanical property. The anti-static performance reduction caused by low humidity and organic matter migration is avoided.

The invention relates to the technical field of biological materials, in particular to a pillararene-based photoresponse MOF-based ion gating nanochannel and a preparation method thereof. According to the pillararene-based photoresponse MOF-based ion gating nano-channel, a bullet-shaped nano-channel is prepared by taking PET (Polyethylene Terephthalate) as a substrate, and the substrate can provide structural support; p5A-MOF-1 based on pillararene is used as a core functional layer, and the core functional layer can provide a stable cavity environment; a P5A-MOF-1 cavity is filled with an organic aromatic azo compound, so that the light response structure change is realized. And the effective volume of the P5A-MOF-1 cavity is regulated and controlled through the photoisomerization effect of the azo group, so that precise gating of ion transmission is achieved. The preparation method provided by the invention is simple and convenient to operate, mild and controllable in condition and beneficial to large-scale production.

The present invention relates to a process for depolymerizing a polyester feedstock comprising opaque PET, which comprises: a) a conditioning step; b) a step of glycolysis, operated at between 180 and 400° C., a residence time of from 0.1 to 10 h in the presence of diol; c) a diol separation step, at a temperature of between 100 and 250° C., a pressure lower than that of step b) and producing a diol effluent and an effluent rich in monomers; d) a step of separating into a heavy impurities effluent and a prepurified monomers effluent, at a temperature of less than 250° C. and a pressure of less than 0.001 MPa and a residence time of less than 10 min; e) a step of decolourizing the prepurified monomers effluent, by adsorption of a mixture comprising between 20% and 90% by weight of the prepurified monomers effluent and a solvent, at a temperature of between 100 and 200° C., a pressure of between 0.1 and 1.0 MPa and in the presence of at least one adsorbent.

The invention belongs to the technical field of textile materials, and discloses an easy-to-dye composite polyester fiber and a preparation method thereof. The preparation method comprises the following steps: by taking polyethylene glycol terephthalate as a core layer and low-melting-point polyester as a skin layer, carrying out melt spinning to prepare skin-core composite fibers; after heating and melting a skin layer, bombarding by using a titanium dioxide nano particle flow to obtain roughened fibers; after plasma treatment, dipping with an activating solution of triethylamine and 4-methylbenzenesulfonyl chloride to obtain activated fibers; carrying out ultrasonic reaction on the activated fiber and a modifier under the catalysis of tetrabutyl titanate, and washing and drying to obtain the easy-to-dye composite polyester fiber. The prepared composite polyester fiber not only has the advantage of being easy to dye, but also has excellent antibacterial performance and flame retardant performance, and the quality of the composite polyester fiber is effectively guaranteed.

The invention discloses a marine-derived carboxylesterase and an application of the marine-derived carboxylesterase in degradation of PET (Polyethylene Terephthalate) plastics. The amino acid sequence of the enzyme is as shown in SEQ ID NO.1, experiments show that Tm of RbCE1 is 79.5 DEG C, 40 mM of depolymerization monomers can be generated after the enzyme treats low-crystallinity PET powder at 60 DEG C for 4 hours, the catalytic activity is equivalent to that of LCC, and good degradation activity is shown. Through escherichia coli heterologous expression, 0.4 g / L high expression quantity can be achieved in a shake flask, and the potential of remarkably reducing the enzyme production cost is achieved. Therefore, the novel carboxylesterase RbCE1 is suitable for degrading PET plastics and composite materials thereof, and is a potential enzyme preparation for efficient biological catalysis of a waste PET plastic waste enzymatic depolymerization recovery treatment process.

Provided are: an optical laminate which uses a biaxially stretched polyethylene terephthalate film as a base material, has bending resistance, and in which iris irregularities are suppressed; and an image display device which uses the optical laminate. This optical laminate is used in an image display device, and is provided with: a light-transmitting base material which is formed from a biaxially stretched polyethylene terephthalate film and which has in-plane birefringence; and an optical functional layer provided on one surface of the light-transmitting substrate, the arithmetic average roughness Ra of the surface of the optical functional layer being 0.04 [mu] m or more, the average inclination angle [theta] a of unevenness present on the surface of the optical functional layer being 0.30 DEG or more, and the in-plane retardation Re of the light-transmitting substrate defined by formula (1): Re = (nx-ny) * d being 2,000 nm to 7500 nm (inclusive). Here, nx is the refractive index in the slow axis direction, ny is the refractive index in the in-phase axis direction, and d is the thickness of the translucent substrate.