BRPI1004649B1 - superfície polimérica para impressão, artigo e processo de impressão - Google Patents
superfície polimérica para impressão, artigo e processo de impressão Download PDFInfo
- Publication number
- BRPI1004649B1 BRPI1004649B1 BRPI1004649-6A BRPI1004649A BRPI1004649B1 BR PI1004649 B1 BRPI1004649 B1 BR PI1004649B1 BR PI1004649 A BRPI1004649 A BR PI1004649A BR PI1004649 B1 BRPI1004649 B1 BR PI1004649B1
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- Brazil
- Prior art keywords
- printing
- polymer
- composition
- polymeric
- molecular weight
- Prior art date
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- 238000007639 printing Methods 0.000 title claims abstract description 65
- 238000000034 method Methods 0.000 title claims abstract description 61
- 230000008569 process Effects 0.000 title claims abstract description 41
- 229920000642 polymer Polymers 0.000 claims abstract description 122
- 239000000203 mixture Substances 0.000 claims abstract description 121
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims abstract description 67
- 239000004014 plasticizer Substances 0.000 claims abstract description 54
- 125000005250 alkyl acrylate group Chemical group 0.000 claims abstract description 47
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims abstract description 40
- 239000000178 monomer Substances 0.000 claims abstract description 38
- 125000005395 methacrylic acid group Chemical group 0.000 claims abstract description 36
- 229920000058 polyacrylate Polymers 0.000 claims abstract description 9
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical group COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 25
- 239000002356 single layer Substances 0.000 claims description 23
- -1 alkyl methacrylate Chemical compound 0.000 claims description 18
- 229920001577 copolymer Polymers 0.000 claims description 17
- 239000004593 Epoxy Substances 0.000 claims description 14
- 150000002148 esters Chemical class 0.000 claims description 13
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 10
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 8
- QZCLKYGREBVARF-UHFFFAOYSA-N Acetyl tributyl citrate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)(OC(C)=O)CC(=O)OCCCC QZCLKYGREBVARF-UHFFFAOYSA-N 0.000 claims description 8
- PYGXAGIECVVIOZ-UHFFFAOYSA-N Dibutyl decanedioate Chemical compound CCCCOC(=O)CCCCCCCCC(=O)OCCCC PYGXAGIECVVIOZ-UHFFFAOYSA-N 0.000 claims description 8
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 8
- 239000003973 paint Substances 0.000 claims description 8
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- 239000005977 Ethylene Substances 0.000 claims description 6
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 6
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 5
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 5
- 239000011976 maleic acid Substances 0.000 claims description 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 5
- 150000001860 citric acid derivatives Chemical class 0.000 claims description 3
- 239000010696 ester oil Substances 0.000 claims 1
- 239000000976 ink Substances 0.000 description 72
- 239000000654 additive Substances 0.000 description 30
- 238000012360 testing method Methods 0.000 description 21
- 238000010348 incorporation Methods 0.000 description 18
- 239000010410 layer Substances 0.000 description 16
- 238000000576 coating method Methods 0.000 description 15
- 239000000463 material Substances 0.000 description 15
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 14
- 239000011248 coating agent Substances 0.000 description 13
- 238000001125 extrusion Methods 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- 239000000758 substrate Substances 0.000 description 10
- 235000012424 soybean oil Nutrition 0.000 description 9
- 239000003549 soybean oil Substances 0.000 description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 230000000996 additive effect Effects 0.000 description 8
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical class CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- 238000011049 filling Methods 0.000 description 7
- 230000009477 glass transition Effects 0.000 description 7
- 238000003475 lamination Methods 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 239000012530 fluid Substances 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
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- 238000004806 packaging method and process Methods 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 5
- 239000006057 Non-nutritive feed additive Substances 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 239000005033 polyvinylidene chloride Substances 0.000 description 5
- 239000003981 vehicle Substances 0.000 description 5
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
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- 239000000944 linseed oil Substances 0.000 description 4
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- 235000015112 vegetable and seed oil Nutrition 0.000 description 4
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- 239000001993 wax Substances 0.000 description 4
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
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- 239000000314 lubricant Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000005056 compaction Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000007580 dry-mixing Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 2
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 238000007647 flexography Methods 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical class [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
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- 229920006254 polymer film Polymers 0.000 description 2
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- 235000020238 sunflower seed Nutrition 0.000 description 2
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- 150000003626 triacylglycerols Chemical class 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 229920001959 vinylidene polymer Polymers 0.000 description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
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- 241000269319 Squalius cephalus Species 0.000 description 1
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- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
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- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
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- 230000015556 catabolic process Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
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- 238000002425 crystallisation Methods 0.000 description 1
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- 238000006731 degradation reaction Methods 0.000 description 1
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- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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- 238000010438 heat treatment Methods 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
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- RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
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- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 238000001542 size-exclusion chromatography Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M1/00—Inking and printing with a printer's forme
- B41M1/26—Printing on other surfaces than ordinary paper
- B41M1/30—Printing on other surfaces than ordinary paper on organic plastics, horn or similar materials
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/08—Homopolymers or copolymers of vinylidene chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08J2327/08—Homopolymers or copolymers of vinylidene chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0016—Plasticisers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/08—Homopolymers or copolymers of acrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
- C08L33/12—Homopolymers or copolymers of methyl methacrylate
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Laminated Bodies (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Printing Methods (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26315709P | 2009-11-20 | 2009-11-20 | |
| US61/263,157 | 2009-11-20 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BRPI1004649A2 BRPI1004649A2 (pt) | 2012-07-31 |
| BRPI1004649B1 true BRPI1004649B1 (pt) | 2021-03-02 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI1004649-6A BRPI1004649B1 (pt) | 2009-11-20 | 2010-11-11 | superfície polimérica para impressão, artigo e processo de impressão |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9828475B2 (OSRAM) |
| EP (1) | EP2325251B1 (OSRAM) |
| JP (1) | JP5632266B2 (OSRAM) |
| CN (1) | CN102070862B (OSRAM) |
| BR (1) | BRPI1004649B1 (OSRAM) |
| ES (1) | ES2681798T3 (OSRAM) |
| RU (1) | RU2560430C2 (OSRAM) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11396595B2 (en) | 2012-10-05 | 2022-07-26 | Sk Saran Americas Llc | Vinylidene chloride copolymer composition for barrier film |
| BR112018002522A2 (pt) * | 2015-08-31 | 2018-09-18 | Dow Global Technologies Llc | métodos de preparar composições de polímero de cloreto de vinilideno |
| JP6795350B2 (ja) * | 2016-08-08 | 2020-12-02 | 株式会社クレハ | 塩化ビニリデン系樹脂フィルム、それを用いたラップフィルム、及び当該樹脂フィルムの製造方法 |
| US12005725B2 (en) * | 2016-12-15 | 2024-06-11 | Ricoh Company, Ltd. | Method of forming a surface covering with substrate, phase transition liquid and plasticizer |
| JP2018177849A (ja) * | 2017-04-04 | 2018-11-15 | 大同化成株式会社 | 塩化ビニリデン樹脂組成物、及び樹脂ブレンド物 |
| CN112552623B (zh) * | 2019-09-26 | 2023-03-10 | 旭化成株式会社 | 保鲜膜 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR741657A (OSRAM) | 1931-09-25 | 1933-02-17 | ||
| US2075429A (en) | 1934-06-15 | 1937-03-30 | Union Carbide & Carbon Corp | Process for producing vinyl resins |
| US3007903A (en) | 1956-04-16 | 1961-11-07 | Dow Chemical Co | Continuous polymerization process |
| US2968651A (en) | 1957-02-08 | 1961-01-17 | Dow Chemical Co | Process for preparing normally crystalline vinylidene chloride polymers |
| US3275716A (en) | 1962-07-17 | 1966-09-27 | Dow Chemical Co | Vinylidene chloride polymer compositions and films therefrom |
| US3642743A (en) | 1966-10-14 | 1972-02-15 | Dow Chemical Co | Controlled polymerization of mixtures of vinylidene chloride and vinyl chloride in aqueous suspension |
| US3662028A (en) * | 1970-03-02 | 1972-05-09 | Dow Chemical Co | Vinylidene chloride polymer compositions containing plasticized polyvinyl chloride |
| US3879359A (en) | 1972-04-11 | 1975-04-22 | Dow Chemical Co | High vinylidene chloride polymer content coating resins and method of preparation |
| JPS6024812B2 (ja) | 1979-11-09 | 1985-06-14 | 呉羽化学工業株式会社 | 塩化ビニリデン系樹脂ケ−シング |
| WO1991008260A1 (en) * | 1989-11-27 | 1991-06-13 | Viskase Corporation | Hot extrudable blend, thermoplastic body and its manufacture |
| EP0450247B1 (en) * | 1990-04-04 | 1995-02-08 | American National Can Company | Packages with controlled easy-open features |
| NZ244002A (en) | 1991-08-23 | 1996-03-26 | Grace W R & Co | Extrudable composition containing plasticiser, acrylate/styrene polymer and vinylidene chloride copolymer; multilayer polymeric films |
| US5202188A (en) | 1991-08-23 | 1993-04-13 | W. R. Grace & Co.-Conn. | Vinylidene chloride film |
| CA2104625A1 (en) | 1992-12-17 | 1994-06-18 | Cryovac, Inc. | Extrudable vinylidene chloride polymeric film |
| NZ280151A (en) | 1994-10-04 | 1997-12-19 | Grace W R & Co | Heat-shrinkable, multilayer packaging film which maintains transparency after shrinking |
| US5538770A (en) | 1994-11-18 | 1996-07-23 | W. R. Grace & Co. -Conn. | Vinylidene chloride film with controlled gas permeability |
| US5679465A (en) | 1995-10-03 | 1997-10-21 | W. R. Grace & Co.-Conn. | Vinylidene chloride composition and film with high thermal stability |
| US6045924A (en) | 1996-06-19 | 2000-04-04 | Cryovac, Inc. | Film from a vinylidene chloride copolymer containing blend |
| KR100622292B1 (ko) | 1998-08-18 | 2006-09-11 | 다우 글로벌 테크놀로지스 인크. | 염화비닐리덴 또는 염화비닐 중합체 조성물, 이의 제조방법 및 이를 포함하는 단층 또는 다층 구조물 |
| US6713105B1 (en) | 2000-10-12 | 2004-03-30 | Cryovac, Inc. | Vinylidene chloride film having reduced protein adhesion |
| JP3967173B2 (ja) | 2001-05-09 | 2007-08-29 | 株式会社クレハ | ポリ塩化ビニリデン系樹脂組成物及びその製造方法 |
| US6673406B2 (en) * | 2001-10-15 | 2004-01-06 | Cryovac, Inc. | High barrier polyvinylidene chloride composition and film |
| US6761969B2 (en) * | 2002-08-21 | 2004-07-13 | Avery Dennison Corporation | Labels and labeling process |
| ES2633237T3 (es) * | 2004-04-08 | 2017-09-20 | Dow Global Technologies Llc | Estructuras de multi-componente que tienen adhesión mejorada entre componentes |
| US7754300B2 (en) * | 2004-10-12 | 2010-07-13 | Dow Global Technologies Inc. | Plasticzer in alkyl acrylate vinylidene chloride polymer |
| US8309634B2 (en) * | 2008-08-27 | 2012-11-13 | Dow Global Technologies Llc | Polyvinylidene chloride compositions and their use in monofilament structures |
-
2010
- 2010-11-08 US US12/941,609 patent/US9828475B2/en active Active
- 2010-11-09 RU RU2010145600/05A patent/RU2560430C2/ru active
- 2010-11-11 BR BRPI1004649-6A patent/BRPI1004649B1/pt active IP Right Grant
- 2010-11-12 EP EP10191042.0A patent/EP2325251B1/en active Active
- 2010-11-12 ES ES10191042.0T patent/ES2681798T3/es active Active
- 2010-11-18 JP JP2010257935A patent/JP5632266B2/ja active Active
- 2010-11-19 CN CN201010557878.7A patent/CN102070862B/zh active Active
Also Published As
| Publication number | Publication date |
|---|---|
| EP2325251B1 (en) | 2018-04-18 |
| ES2681798T3 (es) | 2018-09-17 |
| RU2010145600A (ru) | 2012-05-20 |
| RU2560430C2 (ru) | 2015-08-20 |
| CN102070862B (zh) | 2015-04-22 |
| JP2011122149A (ja) | 2011-06-23 |
| EP2325251A1 (en) | 2011-05-25 |
| BRPI1004649A2 (pt) | 2012-07-31 |
| JP5632266B2 (ja) | 2014-11-26 |
| US20110124780A1 (en) | 2011-05-26 |
| US9828475B2 (en) | 2017-11-28 |
| CN102070862A (zh) | 2011-05-25 |
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| B03A | Publication of a patent application or of a certificate of addition of invention [chapter 3.1 patent gazette] | ||
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Owner name: DOW GLOBAL TECHNOLOGIES LLC (US) |
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Owner name: SK SARAN AMERICAS LLC (US) |
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| B06U | Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette] | ||
| B06A | Patent application procedure suspended [chapter 6.1 patent gazette] | ||
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