CA1142673A - Elastomeres thermoplastiques - Google Patents

Elastomeres thermoplastiques

Info

Publication number: CA1142673A
Authority: CA; Canada
Prior art keywords: copolymer; composition; weight; blend; molecular weight
Prior art date: 1980-04-03
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

CA000349157A

Other languages

English (en)

Inventor

Samuel C. Temin

Kishore R. Shah

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.)

Kendall Co

Original Assignee

Kendall Co

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.)

1980-04-03

Filing date

1980-04-03

Publication date

1983-03-08

1980-04-03 Application filed by Kendall Co filed Critical Kendall Co

1980-04-03 Priority to CA000349157A priority Critical patent/CA1142673A/fr

1983-03-08 Application granted granted Critical

1983-03-08 Publication of CA1142673A publication Critical patent/CA1142673A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 60
229920001169 thermoplastic Polymers 0.000 title claims abstract description 6
239000004416 thermosoftening plastic Substances 0.000 title claims abstract description 6
229920001577 copolymer Polymers 0.000 claims abstract description 42
229920002554 vinyl polymer Polymers 0.000 claims abstract description 19
239000000178 monomer Substances 0.000 claims abstract description 16
229920000642 polymer Polymers 0.000 claims abstract description 16
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims abstract description 9
-1 vinyl lactam Chemical class 0.000 claims abstract description 9
239000002253 acid Substances 0.000 claims abstract description 7
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 7
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 4
229920003169 water-soluble polymer Polymers 0.000 claims abstract description 3
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 10
230000009477 glass transition Effects 0.000 claims description 3
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 3
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 2
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 6
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
239000000243 solution Substances 0.000 description 6
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
230000002378 acidificating effect Effects 0.000 description 4
238000004132 cross linking Methods 0.000 description 4
238000000034 method Methods 0.000 description 4
238000002156 mixing Methods 0.000 description 4
239000007787 solid Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
238000006116 polymerization reaction Methods 0.000 description 3
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
239000004820 Pressure-sensitive adhesive Substances 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
229920001971 elastomer Polymers 0.000 description 2
239000000806 elastomer Substances 0.000 description 2
239000000945 filler Substances 0.000 description 2
239000003921 oil Substances 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
HQGPZXPTJWUDQR-UHFFFAOYSA-N 1-ethenyl-5-methylpyrrolidin-2-one Chemical compound CC1CCC(=O)N1C=C HQGPZXPTJWUDQR-UHFFFAOYSA-N 0.000 description 1
JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 1
PRAMZQXXPOLCIY-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethanesulfonic acid Chemical compound CC(=C)C(=O)OCCS(O)(=O)=O PRAMZQXXPOLCIY-UHFFFAOYSA-N 0.000 description 1
PYKCEDJHRUUDRK-UHFFFAOYSA-N 2-(tert-butyldiazenyl)-2-methylpropanenitrile Chemical compound CC(C)(C)N=NC(C)(C)C#N PYKCEDJHRUUDRK-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
102100024133 Coiled-coil domain-containing protein 50 Human genes 0.000 description 1
229920008712 Copo Polymers 0.000 description 1
101000910772 Homo sapiens Coiled-coil domain-containing protein 50 Proteins 0.000 description 1
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
239000000654 additive Substances 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000013329 compounding Methods 0.000 description 1
LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
230000007423 decrease Effects 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000010528 free radical solution polymerization reaction Methods 0.000 description 1
229940071826 hydroxyethyl cellulose Drugs 0.000 description 1
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
239000003999 initiator Substances 0.000 description 1
238000004255 ion exchange chromatography Methods 0.000 description 1
150000003951 lactams Chemical class 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
239000002245 particle Substances 0.000 description 1
230000035699 permeability Effects 0.000 description 1
239000000049 pigment Substances 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
239000000047 product Substances 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000005060 rubber Substances 0.000 description 1
239000002195 soluble material Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000007858 starting material Substances 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
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
238000004073 vulcanization Methods 0.000 description 1

Landscapes

Compositions Of Macromolecular Compounds (AREA)

CA000349157A 1980-04-03 1980-04-03 Elastomeres thermoplastiques Expired CA1142673A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA000349157A CA1142673A (fr)	1980-04-03	1980-04-03	Elastomeres thermoplastiques

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA000349157A CA1142673A (fr)	1980-04-03	1980-04-03	Elastomeres thermoplastiques

Publications (1)

Publication Number	Publication Date
CA1142673A true CA1142673A (fr)	1983-03-08

Family

ID=4116630

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000349157A Expired CA1142673A (fr)	1980-04-03	1980-04-03	Elastomeres thermoplastiques

Country Status (1)

Country	Link
CA (1)	CA1142673A (fr)

1980
- 1980-04-03 CA CA000349157A patent/CA1142673A/fr not_active Expired

Legal Events

Date	Code	Title	Description
2000-03-08	MKEX	Expiry

Publication	Publication Date	Title
EP1081161B1 (fr)	2004-07-28	Procede de production d'emulsion de resine d'acetate de vinyle et d'adhesif a base d'eau
US4508885A (en)	1985-04-02	Elastomer of acrylic ester type copolymer
US4370380A (en)	1983-01-25	Pressure-sensitive adhesive
US4337325A (en)	1982-06-29	Pressure-sensitive adhesive
US4952638A (en)	1990-08-28	Process for producing macromonomers
US5700873A (en)	1997-12-23	Method of preparation of water-soluble copolymer
US5198501A (en)	1993-03-30	In-situ polymerized blends of vinyl acetate/ethylene copolymar and poly(vinyl chloride)
US4902745A (en)	1990-02-20	Rubber-like thermoplastic polymer mixtures
EP1919968A1 (fr)	2008-05-14	Copolymeres d'ethylene et acide insature
US4306039A (en)	1981-12-15	Thermoplastic elastomeric compositions
US6084032A (en)	2000-07-04	Carboxylated polymer composition
JPH06287360A (ja)	1994-10-11	ポリクロロプレンラテックス及びその組成物
EP0013087B1 (fr)	1984-06-06	Compositions à base de copolymères de chlorure de vinylidène modifiées par du caoutchouc polyacrylate sous forme de mélanges de poudre ou de latex et procédé de préparation des compositions de mélange
IE49518B1 (en)	1985-10-16	Thermoplastic elastomeric composition
GB2073209A (en)	1981-10-14	Pressure sensitive adhesives
IE51292B1 (en)	1986-11-26	Water-absorptive compositions
JP2004300193A (ja)	2004-10-28	水性エマルジョン
US5061761A (en)	1991-10-29	Polyvinyl ester macromonomer and its uses
JP2996419B2 (ja)	1999-12-27	乳化重合用安定剤
US4758628A (en)	1988-07-19	Thermoplastic elastomeric blends of polyethylene and polychloroprene gel
US6620874B1 (en)	2003-09-16	Method of making ionomeric particulates by suspension polymerization
NO800824L (no)	1981-09-22	Termoplastiske elastomersammensetning.
US5231141A (en)	1993-07-27	Process for producing macromonomers
JPH0525898B2 (fr)	1993-04-14
CA1137680A (fr)	1982-12-14	Adhesif autocollant