Ethylene vinyl alcohol copolymer composition, single layer film and multilayer structure containing the same

Abstract

To provide an ethylene-vinyl alcohol copolymer composition, a monolayer film and a multilayer structure each including the same.SOLUTION: An ethylene-vinyl alcohol copolymer composition includes an ethylene-vinyl alcohol copolymer, an antioxidant, and a fluorine-containing compound. A ratio of an antioxidant content to a fluorine content is 0.5 to 65. A film including the ethylene-vinyl alcohol copolymer composition not only has good heat resistance but also can avoid mass outbreak of gel particles in a preparation process.SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present invention relates primarily, but not exclusively, to ethylene-vinyl alcohol (EVOH) copolymer compositions, and more particularly to ethylene-vinyl alcohol copolymer compositions and monolayer films and multilayer structures containing the same. [Background technology]

[0002] Ethylene-vinyl alcohol (EVOH) copolymer compositions have properties such as good transparency, gas barrier properties, solvent / oil resistance, and mechanical strength, and are widely used in laminate sheets capable of preserving perishable items. For example, EVOH copolymer compositions and laminate sheets are widely used in the food packaging industry, medical device and accessory industry, pharmaceutical industry, electronics industry, and agricultural chemical industry. Specifically, EVOH copolymer compositions are commonly used to form a separate layer in laminate sheets as an oxygen barrier layer.

[0003] The manufacturing process of ethylene-vinyl alcohol copolymers is often carried out under high-temperature conditions. Because of the large number of reactive groups in the molecule, the stability of the material is easily affected under high-temperature processing conditions. Specifically, this can lead to carbon buildup on the molds (dies) used in the manufacturing process, gel formation in the samples, and even deterioration of the final product. Therefore, heat resistance is undoubtedly one of the most important properties in the preparation of ethylene-vinyl alcohol copolymers.

[0004] Current technology usually employs the addition of various heat stabilizers or auxiliaries to solve the above problems, such as adding a certain content of antioxidants to the material. Summary of the Invention [Problem to be solved by the invention]

[0005] This summary is intended to provide a brief summary of the invention to provide the reader with a basic understanding of the invention. It is not a complete description of the invention, nor is it intended to identify key or critical elements of embodiments of the invention or to delineate the scope of the invention.

[0006] The inventors of the present invention discovered that, based on the prior art, adding a specific antioxidant to an ethylene-vinyl alcohol copolymer material can effectively improve the heat resistance of the preparation, but at the same time, it also generates a large amount of gel particles (also known as fish eyes) in the ethylene-vinyl alcohol copolymer material. Regarding this problem, the inventors conducted further experiments and found that adding a specific antioxidant and a fluorine-containing compound simultaneously prevents the material from adhering to hot metal surfaces, and also enhances the mixing effect of the ethylene-vinyl alcohol copolymer and the antioxidant. This solves the problem of generating a large amount of gel particles when an antioxidant is added to an ethylene-vinyl alcohol copolymer material. [Means for solving the problem]

[0007] Specifically, one embodiment of the present invention provides an ethylene-vinyl alcohol copolymer composition comprising an ethylene-vinyl alcohol copolymer, an antioxidant, and a fluorine-containing compound, wherein the ratio of the antioxidant content to the fluorine content contained in the ethylene-vinyl alcohol copolymer composition is 0.5 to 65.

[0008] According to one embodiment of the present invention, the content of the antioxidant is 250 ppm to 3200 ppm.

[0009] According to one embodiment of the present invention, the antioxidant is selected from the group consisting of hindered phenol-based antioxidants, hindered amine-based antioxidants, phosphite-based antioxidants, thioester-based antioxidants, benzotriazole-based antioxidants, and diphenyl ketone-based antioxidants.

[0010] According to one embodiment of the present invention, the fluorine content of the ethylene-vinyl alcohol copolymer composition is 40 ppm to 700 ppm.

[0011] According to one embodiment of the present invention, the fluorine-containing compound is selected from the group consisting of vinylidene fluoride (VDF), hexafluoropropylene (HFP), and tetrafluoroethylene (TFE), or a combination thereof.

[0012] According to one embodiment of the present invention, the boron content in the ethylene-vinyl alcohol copolymer composition is 10 to 450 ppm.

[0013] According to one embodiment of the present invention, the alkali metal content in the ethylene-vinyl alcohol copolymer composition is 10 to 450 ppm.

[0014] According to one embodiment of the present invention, the fluorine-containing compound has a particulate form, the size of which is 20 μm or less.

[0015] In another aspect of the present invention, there is provided a monolayer film comprising the ethylene-vinyl alcohol copolymer composition, wherein the monolayer film has less than 200 gel particles having a particle size of 100 μm or less within an area of ​​1 m2.

[0016] According to one embodiment of the present invention, the ethylene content in the ethylene-vinyl alcohol copolymer composition constituting the monolayer film is 20 to 35 mol %, and the heat resistance time at 150° C. is 110 hours or more.

[0017] According to one embodiment of the present invention, the ethylene content in the ethylene-vinyl alcohol copolymer composition constituting the monolayer film is 36 to 50 mol %, and the heat resistance time at 150° C. is 80 hours or more.

[0018] According to a further embodiment of the present invention, there is provided a multilayer structure comprising at least one layer formed from the ethylene-vinyl alcohol copolymer composition, the multilayer structure comprising at least one polymer layer and at least one adhesive layer.

[0019] According to one embodiment of the present invention, the polymer layer is selected from the group consisting of a polyethylene layer, a maleic anhydride grafted polyethylene layer, a polypropylene layer, a nylon layer, and combinations thereof. [Effects of the Invention]

[0020] The features of the present invention are as follows: The ethylene-vinyl alcohol copolymer composition provided by the present invention contains an antioxidant and a fluorine-containing compound in a specific content ratio range, which not only has excellent heat resistance but also prevents the generation of large amounts of gel particles during the production process. DETAILED DESCRIPTION OF THE INVENTION

[0021] In order to explain the present invention in more detail and without omission, the following describes embodiments and specific examples of the present invention, but these are not the only forms of specific examples for carrying out or applying the present invention. In this specification and claims, unless otherwise specified, the terms "one" and "the" can be interpreted as meaning "plural." Furthermore, in this specification and claims, unless otherwise specified, "placed on an object" can be considered to be attached to the surface of an object directly or indirectly or to be in contact with the surface of an object in some other way, and the definition of the surface should be determined by the implication of the preceding and following paragraphs / paragraphs of the content of the specification and common knowledge in the field to which this specification pertains.

[0022] Although the numerical ranges and parameters defining the present invention are approximate, the relevant numerical values ​​in the specific examples are presented as precisely as possible. However, any numerical value inherently contains standard deviations resulting from individual testing methods. In this regard, "about" generally means that the actual numerical value is within ±10%, 5%, 1%, or 0.5% of the specified value or range. Alternatively, the term "about" may mean that the actual numerical value is within an acceptable standard error of the mean, as considered and determined by one of ordinary skill in the art to which the present invention pertains. Thus, unless otherwise specified, all numerical parameters disclosed in the present specification and claims are approximate and may vary as necessary. At the very least, these numerical parameters should be interpreted as values ​​obtained using the indicated number of significant digits and ordinary rounding techniques.

[0023] The present invention relates to an ethylene-vinyl alcohol copolymer (EVOH) composition. The EVOH composition simultaneously contains an ethylene-vinyl alcohol copolymer, an antioxidant, and a fluorine-containing compound, and the ratio of the antioxidant content to the fluorine content is within a specific range. The EVOH composition can be used to produce a monolayer film or a multilayer structure.

[0024] One aspect of the present invention provides an ethylene-vinyl alcohol copolymer composition containing an ethylene-vinyl alcohol copolymer, an antioxidant, and a fluorine-containing compound, wherein the ratio of the antioxidant content to the fluorine content in the ethylene-vinyl alcohol copolymer composition is 0.5 to 65, for example, 0.52, 0.53, 4.25, 4.80, 4.87, 5.13, 5.50, 7.58, 8.57, 8.64, 9.86, 10.21, 10.47, 10.67, 27.23, 50.28, or 63.50.

[0025] The term "antioxidant" as used herein refers to a compound used to capture free radicals generated by degradation of an ethylene-vinyl alcohol copolymer. According to at least one embodiment of the present invention, the antioxidant is selected from the group consisting of hindered phenol-based antioxidants, hindered amine-based antioxidants, phosphite-based antioxidants, thioester-based antioxidants, benzotriazole-based antioxidants, and diphenyl ketone-based antioxidants. In a preferred embodiment, the content of the antioxidant is 250 ppm to 3200 ppm of the ethylene-vinyl alcohol copolymer composition, such as, but not limited to, 250 ppm, 500 ppm, 750 ppm, 1000 ppm, 1250 ppm, 1500 ppm, 1750 ppm, 2000 ppm, 2250 ppm, 2500 ppm, 2750 ppm, 3000 ppm, 3200 ppm, or a value between any two of the above values. The present invention includes an antioxidant in the ethylene-vinyl alcohol copolymer composition, which can capture free radicals generated during the process of the ethylene-vinyl alcohol copolymer being exposed to heat, thereby reducing the deterioration of the ethylene-vinyl alcohol copolymer.

[0026] The fluorine-containing compounds described herein are also referred to as fluoropolymers. According to at least one embodiment of the present invention, the fluorine-containing compounds may be selected from polyvinylidene fluoride (PVDF), polytetrafluoroethylene, polyhexafluoropropylene, polychlorotrifluoroethylene (PCTFE), 2-chloropentafluoropropene, dichlorodifluoroethylene, and 1,1-dichlorofluoroethylene, or a combination thereof. Further, the fluorine-containing compounds may be derived from a copolymer of at least two selected from vinylidene fluoride (VDF), hexafluoropropylene (HFP), and tetrafluoroethylene (TFE). In some embodiments, the fluoropolymer can include a copolymer derived from two or more of VDF, HFP, and TFE. For example, the fluoropolymer can include a copolymer derived from VDF and HFP, a copolymer derived from TFE and HFP, a copolymer derived from VDF and TFE, and / or a copolymer derived from VDF, HFP, and TFE.

[0027] The fluorine content of the ethylene-vinyl alcohol copolymer composition is 40 ppm to 700 ppm relative to the ethylene-vinyl alcohol copolymer composition. According to some embodiments of the present invention, the fluorine content may be 40 to 100 ppm, 101 to 200 ppm, 201 to 300 ppm, 301 to 400 ppm, 401 to 500 ppm, 501 to 600 ppm, or 601 to 700 ppm. According to at least one embodiment of the present invention, the fluorine-containing compound has a particulate form. Preferably, the particulate form may be fine particles. According to the International Union of Pure and Applied Chemistry (IUPAC), fine particles are defined as 10-7 to 10-4 meters. In the present invention, particle size is expressed by the diameter or the length of the major axis of the cross-sectional area. The size of the fluorine-containing compound can be controlled by adjusting the type or kind of fluoropolymer, the amount of fluoropolymer, and the ethylene content in the ethylene-vinyl alcohol copolymer composition. When the fluorine-containing compound particles are spherical, whether or not they have a desired particle size is determined by their cross-sectional diameter. When the fluorine-containing compound particles are not spherical and / or the cross-sectional shape of the fluorine-containing compound particles is not circular (e.g., elliptical or blocky), whether the fluorine-containing compound particles have a desired particle size is determined by the length of the major axis of the cross-section of the fluorine-containing compound particles. The major axis is defined as the axis with the longest length. In some embodiments, the size of all fluorine-containing compound particles evaluated on the cross-section of the EVOH composition is 20 μm or less, for example, 19 μm or less, 18 μm or less, 16 μm or less, 14 μm or less, or 12 μm or less. An appropriate amount of fluorine-containing compound particles can not only reduce the generation of carbon residue in the mold (die) when the ethylene-vinyl alcohol copolymer composition of the present invention is subjected to heat, but also reduce the number of gels during extrusion molding of the ethylene-vinyl alcohol copolymer composition, thereby facilitating the manufacturing process of the product and improving quality.

[0028] In the prior art, antioxidants are commonly added to ethylene-vinyl alcohol copolymers to enhance their heat resistance, but the present inventors have discovered that adding a larger amount of antioxidant to enhance heat resistance results in aggregation and gel formation. In the present invention, the addition of a fluorine-containing compound enables the ethylene-vinyl alcohol copolymer composition to be stably heated during processing, and the presence of the antioxidant significantly improves heat resistance and reduces gel formation. In other words, in the present invention, the presence of a fluorine-containing compound improves the performance of the antioxidant, and the simultaneous presence of both improves the processability of the ethylene-vinyl alcohol copolymer composition.

[0029] In another aspect of the present invention, the inventors discovered that when an ethylene-vinyl alcohol copolymer composition simultaneously contains an ethylene-vinyl alcohol copolymer, an antioxidant, and a fluorine-containing compound, the fluorine-containing compound prevents the ethylene-vinyl alcohol copolymer composition from adhering to hot metal in machinery, thereby achieving an external effect related to physical properties, and also that this allows the ethylene-vinyl alcohol copolymer to be more easily mixed with the antioxidant, thereby enabling the antioxidant's effect to be exerted, thereby achieving an internal effect related to chemical reactions. Therefore, the internal and external additive effects achieved by the ethylene-vinyl alcohol copolymer composition of the present invention are superior to those achieved when only one of these is added.

[0030] According to some embodiments of the present invention, the ethylene-vinyl alcohol copolymer composition further comprises a boron compound, and the content thereof is 10 to 450 ppm. Specifically, the boron content is 10 to 450 ppm, 10 to about 400 ppm, 10 to about 350 ppm, 10 to about 300 ppm, 10 to about 275 ppm, 10 to about 250 ppm, 10 to about 225 ppm, 10 to about 200 ppm, 10 to about 175 ppm, about 20 to 450 ppm, about 20 to about 400 ppm, about 20 to about 350 ppm, or about 20 to about 300 ppm, based on the total weight of the ethylene-vinyl alcohol copolymer composition. ppm, about 20 to about 275ppm, about 20 to about 250ppm, about 20 to about 225ppm, about 20 to about 200ppm, about 20 to about 175ppm, about 60 to 450ppm, about 60 to about 400ppm, about 60 to about Approximately 350ppm, approximately 60 to approximately 300ppm, approximately 60 to approximately 275ppm, approximately 60 to approximately 250ppm, approximately 60 to approximately 225ppm, approximately 60 to approximately 200ppm, approximately 60 to approximately 175ppm, approximately 100 to 450ppm, Approximately 100 to approximately 400ppm, approximately 100 to approximately 350ppm, approximately 100 to approximately 300ppm, approximately 100 to approximately 275ppm, approximately 100 to approximately 250ppm, approximately 100 to approximately 225ppm, approximately 100 to approximately 200ppm, Approximately 100 to approximately 175ppm, approximately 140 to 450ppm, approximately 140 to approximately 400ppm, approximately 140 to approximately 350ppm, approximately 140 to approximately 300ppm, approximately 140 to approximately 275ppm, approximately 140 to approximately 250ppm, approximately 1 The boron content may be 40 to about 225 ppm, about 140 to about 200 ppm, about 180 to about 450 ppm, about 180 to about 400 ppm, about 180 to about 350 ppm, about 180 to about 300 ppm, about 180 to about 275 ppm, about 180 to about 250 ppm, about 180 to about 225 ppm, about 220 to about 450 ppm, about 220 to about 400 ppm, about 220 to about 350 ppm, about 220 to about 300 ppm, or about 220 to about 275 ppm. When the boron content in the ethylene-vinyl alcohol copolymer composition is within a certain range, its viscosity increases, the chance of adhesion to the screw is reduced, and the material can have a self-cleaning function. As a result, the uniformity of the film thickness can be further improved.

[0031] In some circumstances, the boron compound may include boric acid or its metal salts. Examples of metal salts include calcium borate, cobalt borate, zinc borate (e.g., zinc tetraborate, zinc metaborate), aluminum potassium borate, ammonium borates (e.g., ammonium metaborate, ammonium tetraborate, ammonium pentaborate, ammonium octaborate), cadmium borates (e.g., cadmium orthoborate, cadmium tetraborate), potassium borates (e.g., potassium metaborate, potassium tetraborate, potassium pentaborate, potassium hexaborate, potassium octaborate), silver borates (e.g., silver metaborate, silver tetraborate), copper borates (e.g., cupric borate, copper metaborate, copper tetraborate), sodium borates (e.g., sodium metaborate, sodium diborate, sodium tetraborate, sodium pentaborate, sodium hexaborate, sodium octaborate). sodium borate, etc.), lead borate (lead metaborate, lead hexaborate, etc.), nickel borate (nickel orthoborate, nickel diborate, nickel tetraborate, nickel octaborate, etc.), barium borate (barium orthoborate, barium metaborate, barium diborate, barium tetraborate, etc.), bismuth borate, magnesium borates (magnesium orthoborate, magnesium diborate, magnesium metaborate, trimagnesium tetraborate, pentamagnesium tetraborate, etc.), manganese borates (manganese borate, manganese metaborate, manganese tetraborate, etc.), lithium borates (lithium metaborate, lithium tetraborate, lithium pentaborate, etc.), salts thereof, or combinations thereof. For example, borate minerals such as borax, kernite, inyoite, cottolite, seiberite / suanite, and szaibelyite may be included, among which borax, boric acid, and sodium borate (sodium metaborate, sodium diborate, sodium tetraborate, sodium pentaborate, sodium hexaborate, sodium octaborate, etc.) are preferably used.

[0032] Under certain circumstances, the ethylene-vinyl alcohol copolymer composition may contain not only 10 to 450 ppm of boron but also cinnamic acid, alkali metal, conjugated polyene, lubricant, alkaline earth metal, salts thereof, and / or mixtures thereof. The above substances can be used to impart better properties to the ethylene-vinyl alcohol copolymer composition. According to some embodiments of the present invention, when the content of the conjugated polyene structure compound per unit weight in the ethylene-vinyl alcohol copolymer composition is 1 to 30,000 ppm, coloration after heating can be further suppressed, resulting in better thermal stability. When the content of the alkali metal compound or alkaline earth metal compound per unit weight in the ethylene-vinyl alcohol copolymer composition is 1 to 1,000 ppm, preferably 10 to 450 ppm, calculated as metal, long-run moldability can be improved. Furthermore, when the content of the lubricant per unit weight in the ethylene-vinyl alcohol copolymer composition is 1 to 300 ppm, processability can be improved. According to at least one preferred embodiment, the alkali metal content in the ethylene-vinyl alcohol copolymer composition is 10 to 450 ppm, for example, but not limited to, 10 ppm, 50 ppm, 100 ppm, 150 ppm, 200 ppm, 250 ppm, 300 ppm, 350 ppm, 400 ppm, 450 ppm, or a range between any two of the foregoing values.

[0033] In another embodiment, the present invention further provides a monolayer film comprising the ethylene vinyl alcohol copolymer composition, the monolayer film having a thickness of 1 m. 2 The number of gel particles having a particle size of 100 μm or less is less than 200 within an area of ​​100 μm. Specifically, the number of gel particles was measured using an FSA-100 designed with a charged coupled device (CCD) sensor and FSA-100 V.8 software.

[0034] According to at least one embodiment of the present invention, the thickness of the monolayer film is 50 to 150 μm, preferably 100 μm. In another embodiment, the ethylene-vinyl alcohol copolymer contained in the monolayer film has a predetermined ethylene content, for example, about 20 to about 50 mol%, about 25 to about 45 mol%, about 28 to about 42 mol%, or about 30 to about 40 mol%. The ethylene-vinyl alcohol copolymer composition can also be formed from two or more ethylene-vinyl alcohol copolymers having different ethylene contents. For example, the ethylene content of one ethylene-vinyl alcohol copolymer may be within the range of about 20 to about 35 mol%, for example, about 24 to about 35 mol%, about 28 to about 35 mol%, about 20 to about 32 mol%, about 24 to about 32 mol%, about 28 to about 32 mol%, about 20 to about 30 mol%, or about 24 to about 30 mol%. Furthermore, the ethylene-vinyl alcohol copolymer composition has a heat resistance time of 110 hours or more at a temperature of 150°C. Further, according to some embodiments of the present invention, the ethylene-vinyl alcohol copolymer may have an ethylene content of about 36 to about 50 mol%, e.g., about 40 to about 50 mol%, about 44 to about 50 mol%, about 36 to about 45 mol%, or about 40 to about 45 mol%. Furthermore, the ethylene-vinyl alcohol copolymer composition has a heat resistance time of 80 hours or more at a temperature of 150°C.

[0035] The present invention also provides a multilayer structure comprising at least one layer formed from the ethylene-vinyl alcohol copolymer composition of the present invention, at least one polymer layer, and at least one adhesive layer. The polymer layer can be selected from a polyethylene layer, a maleic anhydride-grafted polyethylene layer, a polypropylene layer, a nylon layer, and combinations thereof. The adhesive layer can be a tie layer, such as ARKEMA OREVAC 18729 from ARKEMA. [Example]

[0036] Example

[0037] The non-limiting examples of each aspect of the present invention provided below are primarily intended to clarify each aspect of the present invention and the advantages achieved thereby.

[0038] Preparation of ethylene vinyl alcohol copolymer

[0039] According to at least one embodiment of the present invention, ethylene-vinyl alcohol copolymer is prepared by saponifying an ethylene-vinyl acetate copolymer (hereinafter referred to as "EVAC") having an ethylene content of 29 or 44 mol% to prepare an ethylene-vinyl alcohol copolymer with a saponification degree of 99.5%. The ethylene-vinyl alcohol copolymer is then dissolved in a solution containing methanol and water (ratio 70:30). After that, the solid content of the ethylene-vinyl alcohol copolymer in the solution becomes 41 wt% and the solution is kept at 60°C.

[0040] Next, the above-mentioned solution of methanol, water, and ethylene-vinyl alcohol copolymer was pelletized by underwater pelletization. Specifically, using a pump, the above-mentioned solution of methanol, water, and ethylene-vinyl alcohol copolymer was sent to a supply pipe at a flow rate of 120 L / min, then sent to a suction pipe with a diameter of 2.8 mm, and cut at 1500 rpm using a rotary knife. Water at 5°C was added to cool the ethylene-vinyl alcohol copolymer pellets. Next, the ethylene-vinyl alcohol copolymer pellets were centrifuged to separate the ethylene-vinyl alcohol copolymer particles. The separated ethylene-vinyl alcohol copolymer particles were washed with water and then dried to obtain ethylene-vinyl alcohol copolymer pellets.

[0041] Preparation of fluorine-containing compound A

[0042] An autoclave was used as a batch reactor to prepare fluorine-containing compound A. The autoclave had an internal volume of approximately 20 L and was equipped with an electromagnetic induction stirrer. The autoclave was thoroughly filled with nitrogen gas (N2), and then filled with reduced-pressure nitrogen gas five times.

[0043] The autoclave was decompressed and 6,960 g of deoxygenated pure water, 3,204 g of 1,1,2-trichloro-1,2,2-trifluoroethane, and 3.5 g of methyl cellulose were added to the autoclave. The methyl cellulose had a viscosity of 50 cp and was stirred into the composition in the autoclave at 450 rpm as a suspension stabilizer. The composition in the autoclave was kept in a temperature environment of 52°C.

[0044] A monomer mixture consisting of 25.3 wt% vinylidene fluoride (VDF), 68.6 wt% hexafluoropropylene (HFP), and 6.1 wt% tetrafluoroethylene (TFE) was mixed into the batch as a fill gas and filled to 10 kg / cm². Then, 45.6 g of a solution containing approximately 90 wt% 1,1,2-trichloro-1,2,2-trifluoroethane and 10 wt% diisopropyl peroxydicarbonate was added as a catalyst to initiate the polymerization reaction. Diisopropyl peroxydicarbonate was used as an initiator to initiate the polymerization reaction. During the polymerization process, the pressure decreased, so a monomer mixture containing 44.7 wt% VDF, 32.5 wt% HFP, and 22.8 wt% TFE was added to raise the pressure to 10 kg / cm². After the polymerization reaction was completed, the remaining mixed monomer was removed, and the resulting suspension was dehydrated using a centrifuge, washed with deionized water, and then vacuum dried at 100° C. to obtain 7.5 kg of a fluorine-containing compound A.

[0045] Preparation of fluorine-containing compound B

[0046] A similar autoclave was used to prepare fluorine-containing compound B and was set up in the same manner as for fluorine-containing compound A. The autoclave was similarly evacuated and filled with nitrogen gas five times.

[0047] The autoclave was decompressed and simultaneously charged with 7,200 g of deoxygenated pure water, 3,250 g of 1,1,2-trichloro-1,2,2-trifluoroethane, and 4 g of methylcellulose. The methylcellulose had a viscosity of 50 cp and was stirred into the batch in the autoclave at 500 rpm as a suspension stabilizer. The batch in the autoclave was kept at a temperature of 52°C.

[0048] A monomer mixture consisting of 25 wt% VDF, 55 wt% HFP, and 20 wt% TFE was filled to a pressure of 20 kg / cm² as the fill gas. Then, 40 g of a solution containing approximately 85 wt% 1,1,2-trichloro-1,2,2-trifluoroethane and 15 wt% diisopropyl peroxydicarbonate was added as a catalyst to initiate the polymerization reaction. Diisopropyl peroxydicarbonate was used as an initiator to initiate the polymerization reaction. Because the pressure decreased during the polymerization reaction, a monomer mixture consisting of 40 wt% VDF, 35 wt% HFP, and 25 wt% TFE was added to raise the pressure to 20 kg / cm². After the polymerization reaction was completed, the remaining monomer mixture was removed, and the resulting suspension was dehydrated using a centrifuge, washed with deionized water, and then vacuum-dried at 100°C to obtain 6 kg of fluorine-containing compound B.

[0049] Preparation of ethylene vinyl alcohol copolymer composition

[0050] The ethylene-vinyl alcohol copolymer composition of the present invention is prepared by using the above-mentioned essential components, i.e., the ethylene-vinyl alcohol copolymer, the fluorine-containing compound, and the antioxidant, and, if necessary, separately blending the above-mentioned optional components. The production method may be a known method such as a dry blending method, a melt mixing method, a solution mixing method, or an impregnation method, or any combination of these methods.

[0051] According to some embodiments of the present invention, ethylene-vinyl alcohol copolymer composition particles can be prepared by a method of dry-blending ethylene-vinyl alcohol copolymer pellets, an antioxidant, and a fluorine-containing compound directly together in a dry mixer or the like, or by a melt-kneading method.

[0052] According to some other embodiments of the present invention, the ethylene-vinyl alcohol copolymer composition particles can be prepared by a method such as separately kneading ethylene-vinyl alcohol copolymer pellets with a fluorine-containing compound and an antioxidant to form two masterbatches, and then dry-blending the two masterbatches.

[0053] Preparation of monolayer films

[0054] According to some embodiments of the present invention, the ethylene-vinyl alcohol copolymer composition particles prepared above are further fed into a single-layer T-die cast film extruder (optical control system MEV4) to produce a film, specifically, the extruder temperature was set to 220°C, the mold (i.e., T-die) temperature was set to 230°C, and the screw rotation speed was 7 rpm (rotations / minutes).

[0055] Analysis and evaluation methods

[0056] Antioxidant content analysis

[0057] According to some embodiments of the present invention, the analytical method involves first uniformly grinding 200 g of the final product particles, then taking a 5 g powder sample from it and extracting it with 10 ml of an organic solvent (a solvent capable of dissolving antioxidants, such as toluene, dichlorotoluene, or acetone), diluting the extract, and then analyzing it by LC-Q-TOF. Alternatively, a standard curve can be prepared using a standard solution of the antioxidant, and the antioxidant content can be quantified using the absolute calibration curve method.

[0058] Total fluorine content analysis

[0059] The total fluorine content was analyzed using ion chromatography (IC). Meter: Metrohm 930 Compact IC Flex / Ses / PP / Deg Detection method: NIEA W415.54B (detection method for anions in water) Pretreatment: 20g of sample was combusted in an oxygen bomb, then extracted with water and chemically analyzed. Samples were randomly sampled, and 10 samples were analyzed, and the average value of the 10 tests was calculated.

[0060] Analysis and evaluation of gel particles

[0061] After preparing a film sheet from the ethylene-vinyl alcohol copolymer composition, gel particles were measured and analyzed using an FSA-100 designed with a charge-coupled device (CCD) sensor and FSA-100 V.8 software. Specifically, if the number of gel particles with a size of 100 μm or less per 1 m2 was less than 200, it was indicated by "O," and if the number of gel particles with a size of 100 μm or less per 1 m2 was more than 200, it was indicated by "X."

[0062] Analysis and evaluation of heat resistance

[0063] A film sheet with a thickness of 100 μm was prepared from the ethylene-vinyl alcohol copolymer composition, and the aging state was measured at a standard test temperature of 150°C using DIN EN ISO 2578:1998-10. The tensile test method used was ASTM D882. Specifically, ethylene-vinyl alcohol copolymers with an ethylene content of 20 to 35 mol% were evaluated as "O" if their heat resistance time was longer than 110 hours, and as "X" if not. Ethylene-vinyl alcohol copolymers with an ethylene content of 36 to 50 mol% were evaluated as "O" if their heat resistance time was longer than 80 hours, and as "X" if not.

[0064] Examples 1 to 17

[0065] The present invention prepared the ethylene-vinyl alcohol copolymer compositions of Examples 1 to 17 using the same or similar preparation methods as described above. For details of variables and preparation parameters, see Tables 1-1 and 1-2. [Table 1] [Table 2]

[0066] Specifically, among Examples 1 to 17, the production method of Example 1 involves directly melt-kneading ethylene-vinyl alcohol copolymer pellets with an antioxidant and a fluorine-containing compound to prepare ethylene-vinyl alcohol copolymer composition particles. Regarding the specific production method of Example 1, the ethylene-vinyl alcohol copolymer pellets, the antioxidant, and the fluorine-containing compound were kneaded in a Zenix ZPT-32HT twin-screw extruder (purchased from Zenix Industrial Co., Ltd.), with an aspect ratio of 20:1 (20 mm / mm), a twin-screw rotation speed of 100 rpm, and a hopper rotation speed of 15 rpm.

[0067] The manufacturing methods of Examples 2 to 17 were as follows: in Step 1, ethylene-vinyl alcohol copolymer pellets were added to an antioxidant to prepare masterbatch MB-A; the ethylene-vinyl alcohol copolymer pellets were added to a fluorine-containing compound to prepare masterbatch MB-B; and then, in Step 2, the two masterbatches (MB-A and MB-B) were dry-blended to form ethylene-vinyl alcohol copolymer composition particles. Specifically, in Examples 2 to 17, the same extruder as in Example 1 was used, with an aspect ratio of 20:1 (20 mm / mm) and a twin-screw rotation speed of 10 rpm. EVOH was kneaded with the antioxidant and the fluorine-containing compound, respectively, to prepare MB-A and MB-B separately. The EVOH was then mixed with the prepared MB-A and MB-B in a dry mixer at a rotation speed of 30 rpm for 30 minutes.

[0068] In addition, the content parameters in Tables 1-1 and 1-2 represent parts by weight, and the units used are all weight percentages (%); EV29 represents an ethylene-vinyl alcohol copolymer composition with an ethylene content of 29 mol%, and EV44 represents an ethylene-vinyl alcohol copolymer composition with an ethylene content of 44 mol%; and the antioxidants used here are hindered phenol type (product code: IRGANOX 1010; Antioxidant CA; IRGANOX 1098), hindered amine type (product code: Naugard (R) 445), phosphite type (product code: IRGANOX 168), thioester type (product code: Naugard (R) 412S) is used as the fluorine-containing compound, and the fluorine-containing compounds used are the above-mentioned fluorine-containing compounds A and B, respectively.

[0069] Comparative Examples 1 to 15

[0070] The present invention used the same or similar preparation methods as described above to prepare ethylene-vinyl alcohol copolymer compositions of Comparative Examples 1 to 15. For details of variables and preparation parameters, see Tables 2-1 and 2-2. [Table 3] [Table 4]

[0071] Specifically, among Comparative Examples 1 to 15, Comparative Examples 1 and 2 did not contain any antioxidant or fluorine-containing compound. The production method of Comparative Example 3 was similar to that of Example 1, in which ethylene-vinyl alcohol copolymer pellets and an antioxidant were directly melt-kneaded together to produce ethylene-vinyl alcohol copolymer composition particles. The production methods of Comparative Examples 4 to 15 were similar to those of Examples 2 to 17, in which, in step 1, ethylene-vinyl alcohol copolymer pellets were added to the antioxidant or fluorine-containing compound, respectively, to produce two masterbatches (MB-A and MB-B, respectively), and in step 2, the two masterbatches were dry-blended to produce ethylene-vinyl alcohol copolymer composition particles (among which, the masterbatch in Comparative Example 6 contained only MB-A, and the masterbatch in Comparative Example 15 contained only MB-B).

[0072] In addition, it should be understood that the content parameters in Tables 2-1 and 2-2 represent parts by weight, and the units used are all weight percentages (%); EV29 represents an ethylene-vinyl alcohol copolymer composition having an ethylene content of 29 mol%, and EV44 represents an ethylene-vinyl alcohol copolymer composition having an ethylene content of 44 mol%; antioxidants here are divided into hindered phenol types (product code: IRGANOX 1010; Antioxidant CA; IRGANOX 1098) and phosphite ester types (product code: IRGANOX 168); and the fluorine-containing compounds used are the above-mentioned fluorine-containing compounds A and B, respectively.

[0073] Analysis and evaluation results

[0074] The present invention further analyzed the antioxidant content, total fluorine concentration, and the ratio of the two for Examples 1 to 17 and Comparative Examples 1 to 15. Furthermore, the monolayer films prepared from the ethylene-vinyl alcohol copolymer compositions of Examples 1 to 17 and Comparative Examples 1 to 15 were analyzed and evaluated for "gel particle generation" and "heat resistance." NA indicates that the content was 0 or the content was too low to be detected. For details of the results, see Tables 3-1 and 3-2, respectively. [Table 5] [Table 6]

[0075] By comparison, when the ratio of the antioxidant and fluorine-containing compound contents in the ethylene-vinyl alcohol copolymer composition was 0.5 to 65 (e.g., Examples 1 to 17), the films produced not only had ideal heat resistance, but also avoided the generation of large amounts of gel particles during the preparation process. Conversely, in Comparative Examples 1 and 2, in which no antioxidant or fluorine-containing compound was added, the heat resistance performance was not ideal. Comparative Examples 3 and 6 contained only an antioxidant, but the film performance characteristics of Comparative Examples 3 and 6 only had good heat resistance, but the gel particle performance was unsatisfactory. Comparative Example 15 contained only a fluorine-containing compound, but the film performance characteristics of both heat resistance and gel particle performance were unsatisfactory. Furthermore, in the remaining Comparative Examples, although an antioxidant and a fluorine-containing compound were both added, the ratio of the contents was not within the range of 0.5 to 65, and therefore, none of them were able to simultaneously achieve ideal heat resistance and avoid the generation of large amounts of gel particles.

[0076] Therefore, by controlling the content ratio of the antioxidant to the fluorine compound in the ethylene-vinyl alcohol copolymer composition, the present invention not only imparts excellent heat resistance to the ethylene-vinyl alcohol copolymer composition and a film containing the same, but also prevents a large amount of gel particles from being generated during the film production process.

[0077] Although the present invention has been described in detail above, the above description is merely a preferred embodiment of the present invention and does not limit the scope of the present invention. Any equivalent changes or modifications based on the scope of the claims of the present invention are also within the scope of the claims of the present invention.

Claims

1. An ethylene-vinyl alcohol copolymer composition comprising an ethylene-vinyl alcohol copolymer, an antioxidant, and a fluorine-containing compound, the fluorine-containing compound is polyvinylidene fluoride (PVDF), polychlorotrifluoroethylene (PCTFE), or a combination thereof, or a copolymer of at least two selected from the group consisting of vinylidene fluoride (VDF), hexafluoropropylene (HFP), and tetrafluoroethylene (TFE); The content of the antioxidant is 250 ppm to 3200 ppm, The fluorine content is 40 ppm to 700 ppm, An ethylene-vinyl alcohol copolymer composition, wherein the ratio of the antioxidant content to the fluorine content contained in the ethylene-vinyl alcohol copolymer composition is 0.5 to 65.

2. 2. The ethylene-vinyl alcohol copolymer composition according to claim 1, wherein the antioxidant is selected from the group consisting of hindered phenol-based antioxidants, hindered amine-based antioxidants, phosphite-based antioxidants, thioester-based antioxidants, benzotriazole-based antioxidants, and diphenyl ketone-based antioxidants.

3. 3. The ethylene-vinyl alcohol copolymer composition according to claim 1, having a boron content of 10 to 450 ppm.

4. 3. The ethylene-vinyl alcohol copolymer composition according to claim 1, having an alkali metal content of 10 to 450 ppm.

5. 3. The ethylene-vinyl alcohol copolymer composition according to claim 1, wherein the fluorine-containing compound is in the form of particles having a size of 20 μm or less.

6. A monolayer film comprising the ethylene-vinyl alcohol copolymer composition of claim 1, ２ A monolayer film having less than 200 gel particles with a particle size of 100 μm or less within an area of ​​the monolayer film.

7. 7. The monolayer film according to claim 6, wherein the ethylene-vinyl alcohol copolymer composition has an ethylene content of 20 to 35 mol % and a heat resistance time at 150° C. of 110 hours or more.

8. 7. The monolayer film according to claim 6, wherein the ethylene content in the ethylene-vinyl alcohol copolymer composition is 36 to 50 mol % and the heat resistance time at 150° C. is 80 hours or more.

9. At least one layer formed from the ethylene-vinyl alcohol copolymer composition of claim 1; at least one polymer layer; at least one adhesive layer; A multilayer structure comprising:

10. 10. The multilayer structure of claim 9, wherein the polymer layer is selected from the group consisting of a polyethylene layer, a maleic anhydride grafted polyethylene layer, a polypropylene layer, a nylon layer, and combinations thereof.

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