DE2636931A1 - Verfahren zur herstellung von pastenfaehigen vinylchloridpolymerisaten - Google Patents
Verfahren zur herstellung von pastenfaehigen vinylchloridpolymerisatenInfo
- Publication number
- DE2636931A1 DE2636931A1 DE19762636931 DE2636931A DE2636931A1 DE 2636931 A1 DE2636931 A1 DE 2636931A1 DE 19762636931 DE19762636931 DE 19762636931 DE 2636931 A DE2636931 A DE 2636931A DE 2636931 A1 DE2636931 A1 DE 2636931A1
- Authority
- DE
- Germany
- Prior art keywords
- monomers
- vinyl chloride
- weight
- carbon atoms
- chain length
- Prior art date
- 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.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims description 16
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims description 14
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 239000000178 monomer Substances 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- -1 alkyl radicals Chemical class 0.000 claims description 9
- 239000003995 emulsifying agent Substances 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 5
- 239000000084 colloidal system Substances 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 5
- 230000001681 protective effect Effects 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 4
- 235000011837 pasties Nutrition 0.000 claims description 4
- 150000002976 peresters Chemical class 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 3
- 125000005634 peroxydicarbonate group Chemical group 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- 150000003254 radicals Chemical class 0.000 claims 4
- 239000004816 latex Substances 0.000 description 8
- 229920000126 latex Polymers 0.000 description 8
- 229920000915 polyvinyl chloride Polymers 0.000 description 8
- 239000004800 polyvinyl chloride Substances 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 238000006116 polymerization reaction Methods 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 description 3
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 3
- FPVVYTCTZKCSOJ-UHFFFAOYSA-N Ethylene glycol distearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCCCC FPVVYTCTZKCSOJ-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 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 3
- KYBDAUNESKLXAZ-UHFFFAOYSA-N didodecyl oxalate Chemical compound CCCCCCCCCCCCOC(=O)C(=O)OCCCCCCCCCCCC KYBDAUNESKLXAZ-UHFFFAOYSA-N 0.000 description 3
- 229940100608 glycol distearate Drugs 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-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
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 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 description 1
- ZVUNTIMPQCQCAQ-UHFFFAOYSA-N 2-dodecanoyloxyethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCC ZVUNTIMPQCQCAQ-UHFFFAOYSA-N 0.000 description 1
- IKVCSHRLYCDSFD-UHFFFAOYSA-N 2-hexadecanoyloxyethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCC IKVCSHRLYCDSFD-UHFFFAOYSA-N 0.000 description 1
- RAWISQFSQWIXCW-UHFFFAOYSA-N 2-methylbutan-2-yl 2,2-dimethyloctaneperoxoate Chemical compound CCCCCCC(C)(C)C(=O)OOC(C)(C)CC RAWISQFSQWIXCW-UHFFFAOYSA-N 0.000 description 1
- AMOSICMEJHNLEP-UHFFFAOYSA-N 2-tetradecanoyloxyethyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCC AMOSICMEJHNLEP-UHFFFAOYSA-N 0.000 description 1
- QILMKHPBHSTXSI-UHFFFAOYSA-N 4-dodecanoyloxybutyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCOC(=O)CCCCCCCCCCC QILMKHPBHSTXSI-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 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
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- 239000000337 buffer salt Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- JBJMZCVEBLDYCA-UHFFFAOYSA-N didodecyl butanedioate Chemical compound CCCCCCCCCCCCOC(=O)CCC(=O)OCCCCCCCCCCCC JBJMZCVEBLDYCA-UHFFFAOYSA-N 0.000 description 1
- GOAUNPQUDWQWCP-UHFFFAOYSA-N didodecyl carbonate Chemical compound CCCCCCCCCCCCOC(=O)OCCCCCCCCCCCC GOAUNPQUDWQWCP-UHFFFAOYSA-N 0.000 description 1
- LMBSJQLSUSUWQR-UHFFFAOYSA-N dihexadecyl butanedioate Chemical compound CCCCCCCCCCCCCCCCOC(=O)CCC(=O)OCCCCCCCCCCCCCCCC LMBSJQLSUSUWQR-UHFFFAOYSA-N 0.000 description 1
- XMQXMOKIYVQDNL-UHFFFAOYSA-N dioctadecyl oxalate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(=O)OCCCCCCCCCCCCCCCCCC XMQXMOKIYVQDNL-UHFFFAOYSA-N 0.000 description 1
- QZTCMCYWQLXVRK-UHFFFAOYSA-N ditetradecyl butanedioate Chemical compound CCCCCCCCCCCCCCOC(=O)CCC(=O)OCCCCCCCCCCCCCC QZTCMCYWQLXVRK-UHFFFAOYSA-N 0.000 description 1
- VNTSIWKMTCHTHF-UHFFFAOYSA-N ditetradecyl oxalate Chemical compound CCCCCCCCCCCCCCOC(=O)C(=O)OCCCCCCCCCCCCCC VNTSIWKMTCHTHF-UHFFFAOYSA-N 0.000 description 1
- LMSGSHBFYQRPBM-UHFFFAOYSA-N dodecyl ethyl carbonate Chemical compound CCCCCCCCCCCCOC(=O)OCC LMSGSHBFYQRPBM-UHFFFAOYSA-N 0.000 description 1
- HAWBZAVPHSULBJ-UHFFFAOYSA-N dodecyl methyl carbonate Chemical compound CCCCCCCCCCCCOC(=O)OC HAWBZAVPHSULBJ-UHFFFAOYSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- IXFVFNWPPCEKMG-UHFFFAOYSA-N ethoxycarbonyl acetate Chemical compound CCOC(=O)OC(C)=O IXFVFNWPPCEKMG-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 1
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 239000003999 initiator Substances 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
- XWTZFWZIPNGCGO-UHFFFAOYSA-N methoxycarbonyl acetate Chemical compound COC(=O)OC(C)=O XWTZFWZIPNGCGO-UHFFFAOYSA-N 0.000 description 1
- NNBBVUXGGBWVQP-UHFFFAOYSA-N octan-3-yl octan-3-yloxycarbonyloxy carbonate Chemical compound CCCCCC(CC)OC(=O)OOC(=O)OC(CC)CCCCC NNBBVUXGGBWVQP-UHFFFAOYSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 150000002889 oleic acids Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- KQYLUTYUZIVHND-UHFFFAOYSA-N tert-butyl 2,2-dimethyloctaneperoxoate Chemical compound CCCCCCC(C)(C)C(=O)OOC(C)(C)C KQYLUTYUZIVHND-UHFFFAOYSA-N 0.000 description 1
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 238000010626 work up procedure Methods 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)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762636931 DE2636931A1 (de) | 1976-08-17 | 1976-08-17 | Verfahren zur herstellung von pastenfaehigen vinylchloridpolymerisaten |
| GB3046777A GB1527711A (en) | 1976-08-17 | 1977-07-20 | Manufacture of vinyl chloride polymers |
| FR7725104A FR2362166A1 (fr) | 1976-08-17 | 1977-08-17 | Procede de preparation de polymeres du chlorure de vinyle pour fabrication de pates |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762636931 DE2636931A1 (de) | 1976-08-17 | 1976-08-17 | Verfahren zur herstellung von pastenfaehigen vinylchloridpolymerisaten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2636931A1 true DE2636931A1 (de) | 1978-02-23 |
Family
ID=5985614
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19762636931 Withdrawn DE2636931A1 (de) | 1976-08-17 | 1976-08-17 | Verfahren zur herstellung von pastenfaehigen vinylchloridpolymerisaten |
Country Status (3)
| Country | Link |
|---|---|
| DE (1) | DE2636931A1 (enExample) |
| FR (1) | FR2362166A1 (enExample) |
| GB (1) | GB1527711A (enExample) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB978875A (enExample) * | 1963-03-29 | Ici Ltd | ||
| DE2220477C3 (de) * | 1972-04-26 | 1985-03-21 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von Vinylchlorid-Polymerisaten |
-
1976
- 1976-08-17 DE DE19762636931 patent/DE2636931A1/de not_active Withdrawn
-
1977
- 1977-07-20 GB GB3046777A patent/GB1527711A/en not_active Expired
- 1977-08-17 FR FR7725104A patent/FR2362166A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| FR2362166B1 (enExample) | 1979-03-30 |
| GB1527711A (en) | 1978-10-11 |
| FR2362166A1 (fr) | 1978-03-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8139 | Disposal/non-payment of the annual fee |