NL8301462A - Vinylchloridepolymeren. - Google Patents

Vinylchloridepolymeren. Download PDF

Info

Publication number: NL8301462A
Authority: NL; Netherlands
Prior art keywords: vinyl chloride; weight; polyvinyl; polymerization; solvolysis
Prior art date: 1983-04-26

Application number

NL8301462A

Other languages

English (en)

Dutch (nl)

Original Assignee

Stamicarbon

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.)

1983-04-26

Filing date

1983-04-26

Publication date

1984-11-16

1983-04-26 Application filed by Stamicarbon filed Critical Stamicarbon

1983-04-26 Priority to NL8301462A priority Critical patent/NL8301462A/nl

1984-04-24 Priority to AT84200582T priority patent/ATE39702T1/de

1984-04-24 Priority to EP84200582A priority patent/EP0124176B1/de

1984-04-24 Priority to DE8484200582T priority patent/DE3475913D1/de

1984-04-25 Priority to ES531893A priority patent/ES531893A0/es

1984-04-25 Priority to CA000452765A priority patent/CA1243795A/en

1984-04-25 Priority to NO841641A priority patent/NO164908C/no

1984-04-26 Priority to JP59083079A priority patent/JPS6042408A/ja

1984-11-16 Publication of NL8301462A publication Critical patent/NL8301462A/nl

Links

BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims abstract description 25
229920000642 polymer Polymers 0.000 title claims abstract description 18
239000000375 suspending agent Substances 0.000 claims abstract description 27
238000006116 polymerization reaction Methods 0.000 claims abstract description 20
238000003797 solvolysis reaction Methods 0.000 claims abstract description 20
239000000178 monomer Substances 0.000 claims abstract description 18
229920001290 polyvinyl ester Polymers 0.000 claims abstract description 12
-1 aromatic carboxylic acids Chemical class 0.000 claims abstract description 7
239000003999 initiator Substances 0.000 claims abstract description 7
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 4
125000001931 aliphatic group Chemical group 0.000 claims abstract description 3
229920001567 vinyl ester resin Polymers 0.000 claims abstract description 3
238000000034 method Methods 0.000 claims description 13
229920002554 vinyl polymer Polymers 0.000 claims description 9
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 6
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 2
238000002360 preparation method Methods 0.000 claims description 2
239000002002 slurry Substances 0.000 claims 1
238000010557 suspension polymerization reaction Methods 0.000 abstract description 5
238000004519 manufacturing process Methods 0.000 abstract 1
229920002451 polyvinyl alcohol Polymers 0.000 description 14
235000019422 polyvinyl alcohol Nutrition 0.000 description 14
239000000203 mixture Substances 0.000 description 11
229920000915 polyvinyl chloride Polymers 0.000 description 11
239000004800 polyvinyl chloride Substances 0.000 description 11
239000004372 Polyvinyl alcohol Substances 0.000 description 10
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
230000000052 comparative effect Effects 0.000 description 7
238000002474 experimental method Methods 0.000 description 7
239000002245 particle Substances 0.000 description 6
241000251468 Actinopterygii Species 0.000 description 5
238000011049 filling Methods 0.000 description 5
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
230000001476 alcoholic effect Effects 0.000 description 4
239000001913 cellulose Substances 0.000 description 4
229920002678 cellulose Polymers 0.000 description 4
229920001577 copolymer Polymers 0.000 description 4
230000007062 hydrolysis Effects 0.000 description 4
238000006460 hydrolysis reaction Methods 0.000 description 4
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
239000011976 maleic acid Substances 0.000 description 3
239000002609 medium Substances 0.000 description 3
239000004014 plasticizer Substances 0.000 description 3
238000012545 processing Methods 0.000 description 3
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-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
108010010803 Gelatin Proteins 0.000 description 2
229920002153 Hydroxypropyl cellulose Polymers 0.000 description 2
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
229920000159 gelatin Polymers 0.000 description 2
239000008273 gelatin Substances 0.000 description 2
235000019322 gelatine Nutrition 0.000 description 2
235000011852 gelatine desserts Nutrition 0.000 description 2
239000001863 hydroxypropyl cellulose Substances 0.000 description 2
235000010977 hydroxypropyl cellulose Nutrition 0.000 description 2
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
239000011118 polyvinyl acetate Substances 0.000 description 2
229920002689 polyvinyl acetate Polymers 0.000 description 2
238000012360 testing method Methods 0.000 description 2
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 1
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
ZACVGCNKGYYQHA-UHFFFAOYSA-N 2-ethylhexoxycarbonyloxy 2-ethylhexyl carbonate Chemical compound CCCCC(CC)COC(=O)OOC(=O)OCC(CC)CCCC ZACVGCNKGYYQHA-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
AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
244000215068 Acacia senegal Species 0.000 description 1
244000007835 Cyamopsis tetragonoloba Species 0.000 description 1
229920000084 Gum arabic Polymers 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000003926 acrylamides Chemical class 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
239000003513 alkali Substances 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
238000006243 chemical reaction 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
BSVQJWUUZCXSOL-UHFFFAOYSA-N cyclohexylsulfonyl ethaneperoxoate Chemical compound CC(=O)OOS(=O)(=O)C1CCCCC1 BSVQJWUUZCXSOL-UHFFFAOYSA-N 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
SXOCZLWARDHWFQ-UHFFFAOYSA-N dioxathiirane 3,3-dioxide Chemical class O=S1(=O)OO1 SXOCZLWARDHWFQ-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000000605 extraction Methods 0.000 description 1
239000011888 foil Substances 0.000 description 1
VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical class [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
150000002688 maleic acid derivatives Chemical class 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 1
230000035515 penetration Effects 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
RGBXDEHYFWDBKD-UHFFFAOYSA-N propan-2-yl propan-2-yloxy carbonate Chemical compound CC(C)OOC(=O)OC(C)C RGBXDEHYFWDBKD-UHFFFAOYSA-N 0.000 description 1
238000005029 sieve analysis Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000000725 suspension Substances 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-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
239000000052 vinegar Substances 0.000 description 1
235000021419 vinegar Nutrition 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
229940082509 xanthan gum Drugs 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
- C08F14/00—Homopolymers and 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
- C08F14/02—Monomers containing chlorine
- C08F14/04—Monomers containing two carbon atoms
- C08F14/06—Vinyl chloride

Landscapes

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

NL8301462A 1983-04-26 1983-04-26 Vinylchloridepolymeren. NL8301462A (nl)

Priority Applications (8)

Application Number	Priority Date	Filing Date	Title
NL8301462A NL8301462A (nl)	1983-04-26	1983-04-26	Vinylchloridepolymeren.
AT84200582T ATE39702T1 (de)	1983-04-26	1984-04-24	Vinylchlorid-polymere.
EP84200582A EP0124176B1 (de)	1983-04-26	1984-04-24	Vinylchlorid-Polymere
DE8484200582T DE3475913D1 (en)	1983-04-26	1984-04-24	Vinyl chloride polymers
ES531893A ES531893A0 (es)	1983-04-26	1984-04-25	Procedimiento para preparar polimeros de cloruro de vinilo por polimerizacion en suspension
CA000452765A CA1243795A (en)	1983-04-26	1984-04-25	Vinyl chloride polymers
NO841641A NO164908C (no)	1983-04-26	1984-04-25	Fremgangsmaate ved fremstilling av vinylkloridpolymerer.
JP59083079A JPS6042408A (ja)	1983-04-26	1984-04-26	塩化ビニル重合体の製法

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
NL8301462		1983-04-26
NL8301462A NL8301462A (nl)	1983-04-26	1983-04-26	Vinylchloridepolymeren.

Publications (1)

Publication Number	Publication Date
NL8301462A true NL8301462A (nl)	1984-11-16

Family

ID=19841760

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8301462A NL8301462A (nl)	1983-04-26	1983-04-26	Vinylchloridepolymeren.

Country Status (8)

Country	Link
EP (1)	EP0124176B1 (de)
JP (1)	JPS6042408A (de)
AT (1)	ATE39702T1 (de)
CA (1)	CA1243795A (de)
DE (1)	DE3475913D1 (de)
ES (1)	ES531893A0 (de)
NL (1)	NL8301462A (de)
NO (1)	NO164908C (de)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL7714034A (nl) *	1977-12-19	1979-06-21	Stamicarbon	Vinylchloridepolymeren.
NL8000707A (nl) *	1980-02-05	1981-09-01	Stamicarbon	Vinylchloridepolymeren.

1983
- 1983-04-26 NL NL8301462A patent/NL8301462A/nl not_active Application Discontinuation
1984
- 1984-04-24 AT AT84200582T patent/ATE39702T1/de not_active IP Right Cessation
- 1984-04-24 DE DE8484200582T patent/DE3475913D1/de not_active Expired
- 1984-04-24 EP EP84200582A patent/EP0124176B1/de not_active Expired
- 1984-04-25 NO NO841641A patent/NO164908C/no unknown
- 1984-04-25 ES ES531893A patent/ES531893A0/es active Granted
- 1984-04-25 CA CA000452765A patent/CA1243795A/en not_active Expired
- 1984-04-26 JP JP59083079A patent/JPS6042408A/ja active Pending

Also Published As

Publication number	Publication date
DE3475913D1 (en)	1989-02-09
NO164908C (no)	1990-11-28
CA1243795A (en)	1988-10-25
ES8502135A1 (es)	1984-12-16
JPS6042408A (ja)	1985-03-06
ES531893A0 (es)	1984-12-16
NO164908B (no)	1990-08-20
EP0124176A1 (de)	1984-11-07
EP0124176B1 (de)	1989-01-04
ATE39702T1 (de)	1989-01-15
NO841641L (no)	1984-10-29

Legal Events

Date	Code	Title
1984-11-16	A1B	A search report has been drawn up
1985-01-01	A85	Still pending on 85-01-01
1986-12-01	BV	The patent application has lapsed

Publication	Publication Date	Title
EP0281210B1 (de)	1997-04-23	Verfahren zur Herstellung von Vinylchloridpolymeren
EP0705847B1 (de)	1999-03-03	Suspendiermittel für die Suspensionspolymerisation von Vinylverbindungen
RU2021292C1 (ru)	1994-10-15	Способ получения привитого сополимера
US5342910A (en)	1994-08-30	Process for preparing vinylidene chloride or vinyl chloride polymer by suspension polymerization
US4143224A (en)	1979-03-06	Process for the manufacture of suspension polymers of vinyl chloride
NL8301463A (nl)	1984-11-16	Vinylchloridepolymeren.
NL8301462A (nl)	1984-11-16	Vinylchloridepolymeren.
EP0195522B1 (de)	1991-12-27	Vinylchlorid-Polymerzusammensetzung
JP2005522538A (ja)	2005-07-28	重合反応の間の有機開始剤及び保護コロイドの同時計量供給
JPH0428704A (ja)	1992-01-31	塩化ビニル系化合物の懸濁重合用分散安定剤
US3772226A (en)	1973-11-13	Suspension polymerization of vinyl chloride
NL8000707A (nl)	1981-09-01	Vinylchloridepolymeren.
US4659794A (en)	1987-04-21	Process for the polymerization of polymers of vinyl chloride
KR930004274B1 (ko)	1993-05-22	수성 중합에 의한 저분자량 비닐 할라이드/비닐 에스테르 공중합체의 제조방법
JP2003238606A (ja)	2003-08-27	塩化ビニル系樹脂の製造方法
EP0433754B1 (de)	1994-06-08	Verfahren zur Suspensionspolymerisation von Vinylchloridmonomeren
JPH05125105A (ja)	1993-05-21	塩化ビニル系樹脂の製造方法
IE45992B1 (en)	1983-01-26	Preparation of dispersions
JPH0539310A (ja)	1993-02-19	塩化ビニル系重合体の製造方法
JPH10231305A (ja)	1998-09-02	塩化ビニル系重合体の製造方法
NO156453B (no)	1987-06-15	Fremgangsmaate ved fremstilling av vinylkloridpolymerer.
JPH06107734A (ja)	1994-04-19	耐熱塩化ビニル系共重合体の製造方法
JPH05255410A (ja)	1993-10-05	ビニル系化合物の懸濁重合用分散安定剤
JPH09110906A (ja)	1997-04-28	塩化ビニル系重合体の製造方法