CZ154294A3 - Homopolymers or copolymers of vinyl chloride containing alpha-olefins - Google Patents
Homopolymers or copolymers of vinyl chloride containing alpha-olefins Download PDFInfo
- Publication number
- CZ154294A3 CZ154294A3 CZ941542A CZ154294A CZ154294A3 CZ 154294 A3 CZ154294 A3 CZ 154294A3 CZ 941542 A CZ941542 A CZ 941542A CZ 154294 A CZ154294 A CZ 154294A CZ 154294 A3 CZ154294 A3 CZ 154294A3
- Authority
- CZ
- Czechia
- Prior art keywords
- oligomer
- polymerization
- polymer
- vinyl chloride
- olefin
- Prior art date
Links
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims abstract description 32
- 229920001577 copolymer Polymers 0.000 title claims abstract description 5
- 239000004711 α-olefin Substances 0.000 title abstract description 3
- 229920001519 homopolymer Polymers 0.000 title 1
- 229920000642 polymer Polymers 0.000 claims abstract description 36
- 239000000203 mixture Substances 0.000 claims abstract description 15
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims abstract description 4
- 238000006116 polymerization reaction Methods 0.000 claims description 47
- -1 carbon atom olefin Chemical class 0.000 claims description 7
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000013638 trimer Substances 0.000 claims description 5
- GGQQNYXPYWCUHG-RMTFUQJTSA-N (3e,6e)-deca-3,6-diene Chemical compound CCC\C=C\C\C=C\CC GGQQNYXPYWCUHG-RMTFUQJTSA-N 0.000 claims description 3
- 239000000539 dimer Substances 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 239000000725 suspension Substances 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 abstract description 5
- 239000004800 polyvinyl chloride Substances 0.000 description 12
- 229920000915 polyvinyl chloride Polymers 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000003999 initiator Substances 0.000 description 9
- 239000000178 monomer Substances 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- IQFVPQOLBLOTPF-HKXUKFGYSA-L congo red Chemical compound [Na+].[Na+].C1=CC=CC2=C(N)C(/N=N/C3=CC=C(C=C3)C3=CC=C(C=C3)/N=N/C3=C(C4=CC=CC=C4C(=C3)S([O-])(=O)=O)N)=CC(S([O-])(=O)=O)=C21 IQFVPQOLBLOTPF-HKXUKFGYSA-L 0.000 description 6
- 239000000314 lubricant Substances 0.000 description 6
- 239000002270 dispersing agent Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- AQSPWOCSGZUTBB-UHFFFAOYSA-N carbonic acid;1-hexadecylperoxyhexadecane Chemical compound OC(O)=O.CCCCCCCCCCCCCCCCOOCCCCCCCCCCCCCCCC AQSPWOCSGZUTBB-UHFFFAOYSA-N 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000000375 suspending agent Substances 0.000 description 2
- 238000010557 suspension polymerization reaction Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical class CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 1
- LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 1
- PTCHOCKDDCIPGX-UHFFFAOYSA-N 1-hexadecylperoxyhexadecane Chemical class CCCCCCCCCCCCCCCCOOCCCCCCCCCCCCCCCC PTCHOCKDDCIPGX-UHFFFAOYSA-N 0.000 description 1
- CHZCERSEMVWNHL-UHFFFAOYSA-N 2-hydroxybenzonitrile Chemical compound OC1=CC=CC=C1C#N CHZCERSEMVWNHL-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 239000004610 Internal Lubricant Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- BSVQJWUUZCXSOL-UHFFFAOYSA-N cyclohexylsulfonyl ethaneperoxoate Chemical compound CC(=O)OOS(=O)(=O)C1CCCCC1 BSVQJWUUZCXSOL-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 125000004836 hexamethylene group Chemical class [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- PIJPYDMVFNTHIP-UHFFFAOYSA-L lead sulfate Chemical compound [PbH4+2].[O-]S([O-])(=O)=O PIJPYDMVFNTHIP-UHFFFAOYSA-L 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 150000002825 nitriles Chemical class 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
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadecene Natural products CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 125000004817 pentamethylene group Chemical class [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 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
-
- 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
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/18—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
- C08L23/20—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
- C08L23/22—Copolymers of isobutene; Butyl rubber; Homopolymers or copolymers of other iso-olefins
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI916190A FI95474C (fi) | 1991-12-31 | 1991-12-31 | Vinyylikloridipolymeeri |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CZ154294A3 true CZ154294A3 (en) | 1994-11-16 |
Family
ID=8533759
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CZ941542A CZ154294A3 (en) | 1991-12-31 | 1992-12-23 | Homopolymers or copolymers of vinyl chloride containing alpha-olefins |
Country Status (20)
| Country | Link |
|---|---|
| EP (1) | EP0619828A1 (enExample) |
| JP (1) | JPH07506847A (enExample) |
| KR (1) | KR940703867A (enExample) |
| CN (1) | CN1074913A (enExample) |
| AU (1) | AU3161093A (enExample) |
| BR (1) | BR9207003A (enExample) |
| CA (1) | CA2127104A1 (enExample) |
| CZ (1) | CZ154294A3 (enExample) |
| EE (1) | EE9400235A (enExample) |
| FI (1) | FI95474C (enExample) |
| HU (1) | HUT68309A (enExample) |
| LT (1) | LT3070B (enExample) |
| LV (1) | LV10115B (enExample) |
| NO (1) | NO942384L (enExample) |
| RU (1) | RU94031216A (enExample) |
| SI (1) | SI9200419A (enExample) |
| SK (1) | SK78294A3 (enExample) |
| TW (1) | TW254960B (enExample) |
| WO (1) | WO1993013144A1 (enExample) |
| YU (1) | YU112492A (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5780549A (en) * | 1996-07-29 | 1998-07-14 | General Electric Company | Polybutene polymers as modifiers for PVC |
| CN101747459B (zh) * | 2008-12-02 | 2011-09-07 | 卢金永 | 化学改性聚乙烯醇分散剂的制备方法 |
| EP3617503A1 (en) * | 2017-04-28 | 2020-03-04 | Panasonic Appliances Refrigeration Devices Singapore | Hermetically sealed refrigerant compressor and refrigeration device using same |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3560462A (en) * | 1967-09-15 | 1971-02-02 | Tenneco Chem | Vinyl chloride copolymers and process for preparing same |
| JPS5812286B2 (ja) | 1974-11-22 | 1983-03-07 | リヨウニチ カブシキガイシヤ | エンカビニルジユシノ セイゾウホウホウ |
| US4031299A (en) * | 1975-04-11 | 1977-06-21 | Stauffer Chemical Company | Process for forming a polyvinyl chloride extender resin by incorporating in the suspension polymerization medium a prehomogenized solution of a polyallyl compound and a low molecular polymer of propylene |
| US4508863A (en) * | 1983-07-06 | 1985-04-02 | Argus Chemical Corporation | Stabilization of polyvinyl chloride |
| JPS61155401A (ja) | 1984-12-27 | 1986-07-15 | Mitsubishi Chem Ind Ltd | 塩化ビニル重合体の製造法 |
-
1991
- 1991-12-31 FI FI916190A patent/FI95474C/fi not_active IP Right Cessation
-
1992
- 1992-12-23 BR BR9207003A patent/BR9207003A/pt not_active Application Discontinuation
- 1992-12-23 RU RU94031216/04A patent/RU94031216A/ru unknown
- 1992-12-23 CA CA002127104A patent/CA2127104A1/en not_active Abandoned
- 1992-12-23 LT LTIP254A patent/LT3070B/lt not_active IP Right Cessation
- 1992-12-23 WO PCT/FI1992/000360 patent/WO1993013144A1/en not_active Ceased
- 1992-12-23 SK SK782-94A patent/SK78294A3/sk unknown
- 1992-12-23 HU HU9401946A patent/HUT68309A/hu unknown
- 1992-12-23 CZ CZ941542A patent/CZ154294A3/cs unknown
- 1992-12-23 JP JP5511464A patent/JPH07506847A/ja active Pending
- 1992-12-23 AU AU31610/93A patent/AU3161093A/en not_active Abandoned
- 1992-12-23 EP EP93900211A patent/EP0619828A1/en not_active Ceased
- 1992-12-23 KR KR1019940702278A patent/KR940703867A/ko not_active Withdrawn
- 1992-12-29 SI SI19929200419A patent/SI9200419A/sl unknown
- 1992-12-30 LV LVP-92-565A patent/LV10115B/lv unknown
- 1992-12-31 YU YU112492A patent/YU112492A/sh unknown
- 1992-12-31 CN CN92113843A patent/CN1074913A/zh active Pending
-
1993
- 1993-01-07 TW TW082100066A patent/TW254960B/zh active
-
1994
- 1994-06-22 NO NO942384A patent/NO942384L/no unknown
- 1994-11-22 EE EE9400235A patent/EE9400235A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| RU94031216A (ru) | 1996-04-20 |
| EE9400235A (et) | 1996-02-15 |
| TW254960B (enExample) | 1995-08-21 |
| KR940703867A (ko) | 1994-12-12 |
| BR9207003A (pt) | 1995-12-05 |
| HUT68309A (en) | 1995-06-28 |
| CA2127104A1 (en) | 1993-07-08 |
| FI916190L (fi) | 1993-07-01 |
| FI916190A0 (fi) | 1991-12-31 |
| FI95474C (fi) | 1996-02-12 |
| SI9200419A (en) | 1993-06-30 |
| AU3161093A (en) | 1993-07-28 |
| LTIP254A (lt) | 1994-03-25 |
| YU112492A (sh) | 1995-10-03 |
| LV10115A (lv) | 1994-05-10 |
| LT3070B (en) | 1994-10-25 |
| NO942384L (no) | 1994-06-22 |
| CN1074913A (zh) | 1993-08-04 |
| FI95474B (fi) | 1995-10-31 |
| HU9401946D0 (en) | 1994-09-28 |
| LV10115B (en) | 1995-02-20 |
| NO942384D0 (enExample) | 1994-06-22 |
| EP0619828A1 (en) | 1994-10-19 |
| WO1993013144A1 (en) | 1993-07-08 |
| SK78294A3 (en) | 1995-02-08 |
| JPH07506847A (ja) | 1995-07-27 |
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