GB816252A - Improvements in or relating to emulsion polymerization of unsaturated compounds - Google Patents
Improvements in or relating to emulsion polymerization of unsaturated compoundsInfo
- Publication number
- GB816252A GB816252A GB913/57A GB91357A GB816252A GB 816252 A GB816252 A GB 816252A GB 913/57 A GB913/57 A GB 913/57A GB 91357 A GB91357 A GB 91357A GB 816252 A GB816252 A GB 816252A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenyl
- cyclohexyl
- cyclohexane
- methyl
- rosin
- 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.)
- Expired
Links
- 150000001875 compounds Chemical class 0.000 title 1
- 238000007720 emulsion polymerization reaction Methods 0.000 title 1
- -1 butadiene-1 Chemical class 0.000 abstract 22
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 abstract 5
- 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 abstract 5
- 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 abstract 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 3
- IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical class C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 239000000344 soap Substances 0.000 abstract 3
- QMCKTOHWNLWTCG-UHFFFAOYSA-N (1-bromocyclohexyl)benzene Chemical compound C=1C=CC=CC=1C1(Br)CCCCC1 QMCKTOHWNLWTCG-UHFFFAOYSA-N 0.000 abstract 2
- XSBHLHKJNKIZPF-UHFFFAOYSA-N (1-chlorocyclohexyl)benzene Chemical compound C=1C=CC=CC=1C1(Cl)CCCCC1 XSBHLHKJNKIZPF-UHFFFAOYSA-N 0.000 abstract 2
- IOJZDLAYKWBDNU-UHFFFAOYSA-N (1-ethoxycyclohexyl)benzene Chemical compound C=1C=CC=CC=1C1(OCC)CCCCC1 IOJZDLAYKWBDNU-UHFFFAOYSA-N 0.000 abstract 2
- WQQSDYPOAXHFDZ-UHFFFAOYSA-N (1-ethylcyclohexyl)benzene Chemical compound C=1C=CC=CC=1C1(CC)CCCCC1 WQQSDYPOAXHFDZ-UHFFFAOYSA-N 0.000 abstract 2
- QCRRJEABYLEFAE-UHFFFAOYSA-N (1-hydroperoxycyclohexyl)benzene Chemical compound C=1C=CC=CC=1C1(OO)CCCCC1 QCRRJEABYLEFAE-UHFFFAOYSA-N 0.000 abstract 2
- WCBHWEUIZQCQIK-UHFFFAOYSA-N (1-methoxycyclohexyl)benzene Chemical compound C=1C=CC=CC=1C1(OC)CCCCC1 WCBHWEUIZQCQIK-UHFFFAOYSA-N 0.000 abstract 2
- RATMDIXKNCIQOD-UHFFFAOYSA-N (1-methylcyclohexyl)benzene Chemical compound C=1C=CC=CC=1C1(C)CCCCC1 RATMDIXKNCIQOD-UHFFFAOYSA-N 0.000 abstract 2
- HDSAFUWBFABACP-UHFFFAOYSA-N (1-propylcyclohexyl)benzene Chemical compound C=1C=CC=CC=1C1(CCC)CCCCC1 HDSAFUWBFABACP-UHFFFAOYSA-N 0.000 abstract 2
- UAJRSHJHFRVGMG-UHFFFAOYSA-N 1-ethenyl-4-methoxybenzene Chemical compound COC1=CC=C(C=C)C=C1 UAJRSHJHFRVGMG-UHFFFAOYSA-N 0.000 abstract 2
- ZGHFDIIVVIFNPS-UHFFFAOYSA-N 3-Methyl-3-buten-2-one Chemical compound CC(=C)C(C)=O ZGHFDIIVVIFNPS-UHFFFAOYSA-N 0.000 abstract 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 abstract 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 2
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- 229910052783 alkali metal Inorganic materials 0.000 abstract 2
- 150000001340 alkali metals Chemical class 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000000460 chlorine Chemical group 0.000 abstract 2
- 229910052801 chlorine Chemical group 0.000 abstract 2
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 2
- 239000003995 emulsifying agent Substances 0.000 abstract 2
- 229930195729 fatty acid Natural products 0.000 abstract 2
- 239000000194 fatty acid Substances 0.000 abstract 2
- 150000004665 fatty acids Chemical class 0.000 abstract 2
- 229910001385 heavy metal Inorganic materials 0.000 abstract 2
- 125000001867 hydroperoxy group Chemical group [*]OO[H] 0.000 abstract 2
- FQPQJXVSQZUUQU-UHFFFAOYSA-N n,n-dimethyl-1-phenylcyclohexan-1-amine Chemical compound C=1C=CC=CC=1C1(N(C)C)CCCCC1 FQPQJXVSQZUUQU-UHFFFAOYSA-N 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000002023 wood Substances 0.000 abstract 2
- JOGWEGRCMAWPBA-UHFFFAOYSA-N (2,2-dimethylcyclohexyl)benzene Chemical compound CC1(C)CCCCC1C1=CC=CC=C1 JOGWEGRCMAWPBA-UHFFFAOYSA-N 0.000 abstract 1
- TXQRNCINXFEKQB-UHFFFAOYSA-N (2-bromo-1-chlorocyclohexyl)benzene Chemical compound BrC1C(CCCC1)(C1=CC=CC=C1)Cl TXQRNCINXFEKQB-UHFFFAOYSA-N 0.000 abstract 1
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 abstract 1
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 abstract 1
- ZTVPQIPXQQZRFG-UHFFFAOYSA-N 1-ethyl-2,2,3,3,4-pentamethyl-1-phenylcyclohexane Chemical compound CC1C(C(C(CC1)(C1=CC=CC=C1)CC)(C)C)(C)C ZTVPQIPXQQZRFG-UHFFFAOYSA-N 0.000 abstract 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 abstract 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical group S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 abstract 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 abstract 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 abstract 1
- PSCTZWAMEIDXRF-UHFFFAOYSA-N N-ethyl-1-hydroperoxy-N-methyl-2-phenylcyclohexan-1-amine Chemical class C1(=CC=CC=C1)C1C(CCCC1)(N(CC)C)OO PSCTZWAMEIDXRF-UHFFFAOYSA-N 0.000 abstract 1
- FSWVVVJTTURSIF-UHFFFAOYSA-N N-ethyl-2-methyl-1-phenylcyclohexan-1-amine Chemical compound CC1C(CCCC1)(C1=CC=CC=C1)NCC FSWVVVJTTURSIF-UHFFFAOYSA-N 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 abstract 1
- 239000012190 activator Substances 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 230000002528 anti-freeze Effects 0.000 abstract 1
- FNXLCIKXHOPCKH-UHFFFAOYSA-N bromamine Chemical group BrN FNXLCIKXHOPCKH-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 abstract 1
- 239000000920 calcium hydroxide Substances 0.000 abstract 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000003638 chemical reducing agent Substances 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 abstract 1
- 150000001993 dienes Chemical class 0.000 abstract 1
- 229960001484 edetic acid Drugs 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 239000011790 ferrous sulphate Substances 0.000 abstract 1
- 235000003891 ferrous sulphate Nutrition 0.000 abstract 1
- 239000007789 gas Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 abstract 1
- SNVLJLYUUXKWOJ-UHFFFAOYSA-N methylidenecarbene Chemical group C=[C] SNVLJLYUUXKWOJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000003607 modifier Substances 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- MGDJUVKRKGOTEA-UHFFFAOYSA-N n-ethyl-n-methyl-1-phenylcyclohexan-1-amine Chemical compound C=1C=CC=CC=1C1(N(C)CC)CCCCC1 MGDJUVKRKGOTEA-UHFFFAOYSA-N 0.000 abstract 1
- 150000002894 organic compounds Chemical class 0.000 abstract 1
- 150000002978 peroxides Chemical class 0.000 abstract 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- VYGBQXDNOUHIBZ-UHFFFAOYSA-L sodium formaldehyde sulphoxylate Chemical compound [Na+].[Na+].O=C.[O-]S[O-] VYGBQXDNOUHIBZ-UHFFFAOYSA-L 0.000 abstract 1
- 239000001488 sodium phosphate Substances 0.000 abstract 1
- 239000003784 tall oil Substances 0.000 abstract 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 abstract 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 abstract 1
- 235000019801 trisodium phosphate Nutrition 0.000 abstract 1
- SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 abstract 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
- C08F4/00—Polymerisation catalysts
- C08F4/28—Oxygen or compounds releasing free oxygen
- C08F4/32—Organic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Organic compounds containing the CH2=C< group are polymerized in aqueous emulsion at temperatures below 10 DEG C. in the presence of a catalyst comprising a phenylcyclohexyl hydroperoxide in which the hydroperoxy group is attached to the carbon atom in the cyclohexyl ring which is attached to the phenyl ring, an activator comprising a water-soluble heavy metal salt and sodium formaldehyde sulphoxylate, and an emulsifier comprising an alkali metal soap of an unmodified rosin, rosin acid or rosin acid containing material. Specified monomers are conjugated dienes, e.g. butadiene-1,3, isoprene, 2,3-dimethyl butadiene-1,3, chloroprene, piperylene, mixtures thereof with styrene, p-chlorostyrene, p-methoxystyrene, vinyl naphthalene, acrylic acid, acrylonitrile, methacrylonitrile, methyl acrylate, methyl methacrylate, methyl vinyl ketone, methyl isopropenyl ketone and methyl vinyl ether; and vinyl acetate, styrene, methyl methacrylate, vinyl chloride, vinylidene chloride and vinyl pyridine. The peroxide may be phenylcyclohexyl hydroperoxide or its alkyl, alkoxy, amino, bromine or chlorine substituted derivatives, e.g. methylphenylcyclohexyl, ethylphenylcyclohexyl, n-propylphenylcyclohexyl, phenyl(methyl)cyclohexyl, phenyl(ethyl)cyclohexyl, phenyl(propyl)-cyclohexyl, tert.-butylphenylcyclohexyl, phenyl-(dimethyl)cyclohexyl, pentamethylethylphenyl-cyclohexyl, bromophenylcyclohexyl, phenyl-(bromo)cyclohexyl chlorophenylcyclohexyl, phenyl(chloro)cyclohexyl, bromochlorophenylcyclohexyl, phenyl(bromochloro)cyclohexyl, methoxyphenylcyclohexyl, ethoxyphenylcyclohexyl, phenyl(methoxy)cyclohexyl, phenyl(ethoxy)cyclohexyl, dimethylaminophenylcyclohexyl, methylethylaminophenylcyclohexyl, phenyl(dimethylamino)cyclohexyl and phenyl-(methylethylamino)cyclohexyl hydroperoxides. The rosin soaps may be derived from N wood rosin, FF wood rosin, abietic and other C20H30O2 rosin acids, neoabietic, levopimaric, dextropimaric and isodextropimaric acids, mixtures of natural rosins and fatty acids, and tall oil. The preferred heavy metal salt is ferrous sulphate, preferably associated with an alkali metal, e.g. trisodium, salt of ethylenediamine tetracetic acid. Additional emulsifiers, e.g. fatty acid soaps and sodium alkylaryl sulphonates, modifiers, e.g. primary and tertiary mercaptans such as tert.-dodecyl mercaptan, viscosity reducers, e.g. trisodium phosphate, and antifreezes, e.g. methanol, ethanol, ethylene glycol, glycerol, acetone and methyl acetate, may be present.ALSO:Phenylcyclohexyl hydroperoxides in which the hydroperoxy group is attached to the carbon atom in the cyclohexyl ring which is attached to the phenyl ring may be prepared by passing oxygen or a mixture of gases containing oxygen, e.g. air, through the corresponding phenylcyclohexanes at 50 DEG to 150 DEG C. in the presence of alkali, e.g. aqueous sodium hydroxide or anhydrous calcium hydroxide. The reaction may be initiated with ultra-violet light. The phenylcyclohexanes may be of the form <FORM:0816252/IV (b)/1> wherein R1 and R2 may represent H, X, XO, X2N, Br or Cl, where X is an alkyl radical, e.g. phenylcyclohexane, methylphenylcyclohexane, ethylphenylcyclohexane, n - propylphenylcyclohexane, phenyl(methyl)cyclohexane, phenyl(ethyl)cyclohexane, phenyl(propyl)-cyclohexane, tert. - butylphenylcyclohexane, phenyl(dimethyl)cyclohexane, pentamethylethylphenylcyclohexane, bromophenylcyclohexane, phenyl(bromo)cyclohexane, chlorophenylcyclohexane, phenyl(chloro)cyclohexane, bromochlorophenylcyclohexane, phenyl(bromochloro)cyclohexane, methoxyphenylcyclohexane, ethoxyphenylcyclohexane, phenyl(methoxy)cyclohexane, phenyl(ethoxy)cyclohexane, dimethylaminophenylcyclohexane, methylethylaminophenylcyclohexane, phenyl(dimethylamino)cyclohexane and phenyl(methylethylamino)cyclohexane.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US816252XA | 1956-02-01 | 1956-02-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB816252A true GB816252A (en) | 1959-07-08 |
Family
ID=22165321
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB913/57A Expired GB816252A (en) | 1956-02-01 | 1957-01-09 | Improvements in or relating to emulsion polymerization of unsaturated compounds |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB816252A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012016869A1 (en) | 2010-08-02 | 2012-02-09 | Wacker Chemie Ag | Process for preparing vinyl acetate-ethylene copolymers by means of emulsion polymerization |
-
1957
- 1957-01-09 GB GB913/57A patent/GB816252A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012016869A1 (en) | 2010-08-02 | 2012-02-09 | Wacker Chemie Ag | Process for preparing vinyl acetate-ethylene copolymers by means of emulsion polymerization |
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