CA1090938A - Latex polymerique de type chlorure de vinylidene - Google Patents

Latex polymerique de type chlorure de vinylidene

Info

Publication number: CA1090938A
Authority: CA; Canada
Prior art keywords: parts; weight; vinylidene chloride; latices; latex
Prior art date: 1977-08-29
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA310,160A

Other languages

English (en)

Inventor

Masaoki Koyama

Hiroyuki Kigo

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Asahi Dow Ltd

Original Assignee

Asahi Dow Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1977-08-29

Filing date

1978-08-28

Publication date

1980-12-02

1978-08-28 Application filed by Asahi Dow Ltd filed Critical Asahi Dow Ltd

1980-12-02 Application granted granted Critical

1980-12-02 Publication of CA1090938A publication Critical patent/CA1090938A/fr

Status Expired legal-status Critical Current

Links

229920000126 latex Polymers 0.000 title claims abstract description 44
239000004816 latex Substances 0.000 title claims abstract description 25
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 title claims abstract description 23
229920000642 polymer Polymers 0.000 title claims description 12
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims abstract description 16
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 13
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 10
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract 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 abstract description 6
239000008199 coating composition Substances 0.000 claims abstract description 5
239000000839 emulsion Substances 0.000 claims abstract description 5
230000000379 polymerizing effect Effects 0.000 claims abstract description 3
150000001735 carboxylic acids Chemical class 0.000 claims description 8
239000000203 mixture Substances 0.000 claims description 8
125000005395 methacrylic acid group Chemical class 0.000 claims description 7
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 6
239000000178 monomer Substances 0.000 claims description 5
239000000758 substrate Substances 0.000 claims description 5
150000001408 amides Chemical class 0.000 claims description 4
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 3
125000005907 alkyl ester group Chemical group 0.000 claims description 3
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 3
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
150000002825 nitriles Chemical class 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims 1
238000007789 sealing Methods 0.000 abstract description 15
230000000903 blocking effect Effects 0.000 abstract description 10
230000003247 decreasing effect Effects 0.000 abstract 1
238000000576 coating method Methods 0.000 description 15
238000000034 method Methods 0.000 description 11
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
239000011248 coating agent Substances 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
230000000996 additive effect Effects 0.000 description 3
-1 alkali metal bisulfite Chemical class 0.000 description 3
239000012298 atmosphere Substances 0.000 description 3
239000011127 biaxially oriented polypropylene Substances 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000000314 lubricant Substances 0.000 description 3
239000005022 packaging material Substances 0.000 description 3
238000004806 packaging method and process Methods 0.000 description 3
JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 3
239000000377 silicon dioxide Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
229920000298 Cellophane Polymers 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
238000002156 mixing Methods 0.000 description 2
238000009840 oxygen flask method Methods 0.000 description 2
150000002978 peroxides Chemical class 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
239000002985 plastic film Substances 0.000 description 2
229920006255 plastic film Polymers 0.000 description 2
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
239000011347 resin Substances 0.000 description 2
229920005989 resin Polymers 0.000 description 2
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 2
230000003068 static effect Effects 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000001993 wax Substances 0.000 description 2
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
IEVADDDOVGMCSI-UHFFFAOYSA-N 2-hydroxybutyl 2-methylprop-2-enoate Chemical compound CCC(O)COC(=O)C(C)=C IEVADDDOVGMCSI-UHFFFAOYSA-N 0.000 description 1
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 1
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
238000002835 absorbance Methods 0.000 description 1
230000032683 aging Effects 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
230000004888 barrier function Effects 0.000 description 1
229920006378 biaxially oriented polypropylene Polymers 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000004203 carnauba wax Substances 0.000 description 1
229940082483 carnauba wax Drugs 0.000 description 1
235000013869 carnauba wax Nutrition 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000003851 corona treatment Methods 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
230000002950 deficient Effects 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
230000003292 diminished effect Effects 0.000 description 1
229910001873 dinitrogen Inorganic materials 0.000 description 1
BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
238000007720 emulsion polymerization reaction Methods 0.000 description 1
SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
239000004744 fabric Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
230000000977 initiatory effect Effects 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
239000000463 material Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
229940057952 methanol Drugs 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
229940065472 octyl acrylate Drugs 0.000 description 1
ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
230000035882 stress Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
238000004448 titration Methods 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F214/00—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
- C08F214/02—Monomers containing chlorine
- C08F214/04—Monomers containing two carbon atoms
- C08F214/08—Vinylidene chloride
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/04—Monomers containing three or four carbon atoms
- C08F210/06—Propene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—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 a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—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 a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Paints Or Removers (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Compositions Of Macromolecular Compounds (AREA)

CA310,160A 1977-08-29 1978-08-28 Latex polymerique de type chlorure de vinylidene Expired CA1090938A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
JP52-102,623		1977-08-29
JP52102623A JPS5941467B2 (ja)	1977-08-29	1977-08-29	コ−テイング樹脂組成物

Publications (1)

Publication Number	Publication Date
CA1090938A true CA1090938A (fr)	1980-12-02

Family

ID=14332361

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA310,160A Expired CA1090938A (fr)	1977-08-29	1978-08-28	Latex polymerique de type chlorure de vinylidene

Country Status (5)

Country	Link
JP (1)	JPS5941467B2 (fr)
CA (1)	CA1090938A (fr)
DE (1)	DE2837296C2 (fr)
FR (1)	FR2401966A1 (fr)
GB (1)	GB2003489B (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4296013A (en) *	1978-09-15	1981-10-20	The Dow Chemical Co.	Vinylidene chloride polymer microgels
US4457969A (en) *	1982-12-16	1984-07-03	Union Oil Company Of California	Fire-resistant, light stable textile structure
JPS61103465A (ja) *	1984-10-26	1986-05-21	太陽電子株式会社	パチンコ式組合せゲ−ム機における規定数の打玉自動供給装置
JPS61130280U (fr) *	1985-01-31	1986-08-14
JPS62246913A (ja) *	1986-04-18	1987-10-28	Kureha Chem Ind Co Ltd	塩化ビニリデン共重合体ラテツクスの製造法
JPH0165079U (fr) *	1987-10-20	1989-04-26

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE586366A (fr) *	1959-01-12
DE1915682A1 (de) *	1969-03-27	1970-10-08	Bayer Ag	Niedermolekulare,halogenhaltige Copolymerisate

1977
- 1977-08-29 JP JP52102623A patent/JPS5941467B2/ja not_active Expired
1978
- 1978-08-25 GB GB7834624A patent/GB2003489B/en not_active Expired
- 1978-08-26 DE DE2837296A patent/DE2837296C2/de not_active Expired
- 1978-08-28 CA CA310,160A patent/CA1090938A/fr not_active Expired
- 1978-08-28 FR FR7824834A patent/FR2401966A1/fr active Granted

Also Published As

Publication number	Publication date
DE2837296A1 (de)	1979-03-15
FR2401966A1 (fr)	1979-03-30
JPS5941467B2 (ja)	1984-10-06
DE2837296C2 (de)	1987-02-19
FR2401966B1 (fr)	1981-01-30
JPS5437134A (en)	1979-03-19
GB2003489A (en)	1979-03-14
GB2003489B (en)	1982-01-13

Legal Events

Date	Code	Title	Description
1997-12-02	MKEX	Expiry

Publication	Publication Date	Title
EP0629642B1 (fr)	1998-05-06	Composition interpolymère de chlorure de vinylidène en émulsion
US3696082A (en)	1972-10-03	Vinylidene chloride-long chain alkyl ester polymer
US3215678A (en)	1965-11-02	Copolymers of ethylene with vinyl esters and alpha-beta ethylenically unsaturated acids
US3041208A (en)	1962-06-26	Coating polyolefin film and coating method
US3819557A (en)	1974-06-25	Polymeric pigments and method for preparation thereof
US3309330A (en)	1967-03-14	Coated particles of vinylidene chloride copolymers
US3968319A (en)	1976-07-06	Plastic pigments for paper coatings
FI95584B (fi)	1995-11-15	Ei-tertiaarisia butyyli(met)akrylaatteja sisältävien kopolymeraattien, joiden lasiutumislämpötila on alle -10 C, dispersioita
US4211684A (en)	1980-07-08	Vinylidene chloride polymer latex
US2824025A (en)	1958-02-18	Thermoplastic polymeric films
Roberge et al.	2006	The effect of particle size and composition on the performance of styrene/butyl acrylate miniemulsion-based PSAs
CA1088817A (fr)	1980-11-04	Pellicule de polyolefines revetue
CA1090938A (fr)	1980-12-02	Latex polymerique de type chlorure de vinylidene
US4350622A (en)	1982-09-21	Aqueous dispersions of vinylidene chloride resins
CA1055628A (fr)	1979-05-29	Polymerisation en emulsion d'acrylate ou d'autres monomeres vinyliques a l'aide de melanges choisis de sels solubles de certains monoesters de l'acide sulfosuccinique
US4151149A (en)	1979-04-24	Vinylidene chloride polymer latices
US2805963A (en)	1957-09-10	Coating of polyethylene terephthalate film
US3353991A (en)	1967-11-21	Crystalline polypropylene coated with a vinylidene chloride copolymer
US3696067A (en)	1972-10-03	Vinylidene chloride copolymer latex coating composition
US5858524A (en)	1999-01-12	Flexible laminates bonded with water-based laminating ink vehicles and laminating adhesives
US2819985A (en)	1958-01-14	Regenerated cellulose packaging materials and process
US3988500A (en)	1976-10-26	Non-blocking, oxygen-resistant vinylidene chloride polymer coatings and composite articles prepared therefrom
MXPA96002779A (en)	1998-04-01	Adhesive mixtures of packaging with controlled barrier properties
US3753940A (en)	1973-08-21	Method for preparing vinylidene chloride copolymer latex coating compositions
US3557041A (en)	1971-01-19	Vinylidene chloride interpolymers