CA1090950A - Process for the production of copolymer powders - Google Patents
Process for the production of copolymer powdersInfo
- Publication number
- CA1090950A CA1090950A CA243,314A CA243314A CA1090950A CA 1090950 A CA1090950 A CA 1090950A CA 243314 A CA243314 A CA 243314A CA 1090950 A CA1090950 A CA 1090950A
- Authority
- CA
- Canada
- Prior art keywords
- maleic acid
- olefin
- acid anhydride
- copolymer
- mol
- 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
- 229920001577 copolymer Polymers 0.000 title claims abstract description 38
- 238000000034 method Methods 0.000 title claims abstract description 31
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- 239000000843 powder Substances 0.000 title abstract description 28
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims abstract description 50
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 41
- 239000006185 dispersion Substances 0.000 claims abstract description 40
- 239000000203 mixture Substances 0.000 claims abstract description 26
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 11
- 238000006243 chemical reaction Methods 0.000 claims abstract description 10
- 239000000945 filler Substances 0.000 claims abstract description 8
- 150000008064 anhydrides Chemical group 0.000 claims abstract description 6
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 claims description 26
- 125000004432 carbon atom Chemical group C* 0.000 claims description 22
- -1 ethylene, propylene, butylene, isobutylene Chemical group 0.000 claims description 13
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 12
- 239000002612 dispersion medium Substances 0.000 claims description 12
- 229920006395 saturated elastomer Polymers 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 7
- 239000000178 monomer Substances 0.000 claims description 3
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 claims description 3
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 claims 2
- 239000002245 particle Substances 0.000 abstract description 20
- 239000000725 suspension Substances 0.000 abstract description 14
- 150000001412 amines Chemical class 0.000 abstract description 10
- 229920003052 natural elastomer Polymers 0.000 abstract description 7
- 229920001194 natural rubber Polymers 0.000 abstract description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract description 6
- 238000000227 grinding Methods 0.000 abstract description 6
- 229920000089 Cyclic olefin copolymer Polymers 0.000 abstract description 5
- 229920003051 synthetic elastomer Polymers 0.000 abstract description 5
- 239000011248 coating agent Substances 0.000 abstract description 4
- 229910021529 ammonia Inorganic materials 0.000 abstract description 3
- 239000005061 synthetic rubber Substances 0.000 abstract 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 8
- 150000001298 alcohols Chemical class 0.000 description 8
- 239000011976 maleic acid Substances 0.000 description 8
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 8
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 230000009435 amidation Effects 0.000 description 6
- 238000007112 amidation reaction Methods 0.000 description 6
- 230000032050 esterification Effects 0.000 description 5
- 238000005886 esterification reaction Methods 0.000 description 5
- 239000012442 inert solvent Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 150000001408 amides Chemical class 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 description 2
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- PCJGHYSTCBLKIA-UHFFFAOYSA-N (1-acetylcyclohexyl)sulfonyloxy 1-acetylcyclohexane-1-sulfonate Chemical compound C1CCCCC1(C(C)=O)S(=O)(=O)OOS(=O)(=O)C1(C(=O)C)CCCCC1 PCJGHYSTCBLKIA-UHFFFAOYSA-N 0.000 description 1
- WRXCBRHBHGNNQA-UHFFFAOYSA-N (2,4-dichlorobenzoyl) 2,4-dichlorobenzenecarboperoxoate Chemical compound ClC1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1Cl WRXCBRHBHGNNQA-UHFFFAOYSA-N 0.000 description 1
- OXYKVVLTXXXVRT-UHFFFAOYSA-N (4-chlorobenzoyl) 4-chlorobenzenecarboperoxoate Chemical compound C1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1 OXYKVVLTXXXVRT-UHFFFAOYSA-N 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- STGNLGBPLOVYMA-TZKOHIRVSA-N (z)-but-2-enedioic acid Chemical compound OC(=O)\C=C/C(O)=O.OC(=O)\C=C/C(O)=O STGNLGBPLOVYMA-TZKOHIRVSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- XSZYESUNPWGWFQ-UHFFFAOYSA-N 1-(2-hydroperoxypropan-2-yl)-4-methylcyclohexane Chemical compound CC1CCC(C(C)(C)OO)CC1 XSZYESUNPWGWFQ-UHFFFAOYSA-N 0.000 description 1
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- WCVOGSZTONGSQY-UHFFFAOYSA-N 2,4,6-trichloroanisole Chemical compound COC1=C(Cl)C=C(Cl)C=C1Cl WCVOGSZTONGSQY-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- MKTOIPPVFPJEQO-UHFFFAOYSA-N 4-(3-carboxypropanoylperoxy)-4-oxobutanoic acid Chemical compound OC(=O)CCC(=O)OOC(=O)CCC(O)=O MKTOIPPVFPJEQO-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 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
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- PLZVEHJLHYMBBY-UHFFFAOYSA-N Tetradecylamine Chemical compound CCCCCCCCCCCCCCN PLZVEHJLHYMBBY-UHFFFAOYSA-N 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 238000011938 amidation process Methods 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 239000010692 aromatic oil Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 150000001470 diamides Chemical class 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- JGEMYUOFGVHXKV-UPHRSURJSA-N malealdehyde Chemical compound O=C\C=C/C=O JGEMYUOFGVHXKV-UPHRSURJSA-N 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- SZEGKVHRCLBFKJ-UHFFFAOYSA-N n-methyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNC SZEGKVHRCLBFKJ-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 239000004482 other powder Substances 0.000 description 1
- 150000002976 peresters Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- HCTVWSOKIJULET-LQDWTQKMSA-M phenoxymethylpenicillin potassium Chemical compound [K+].N([C@H]1[C@H]2SC([C@@H](N2C1=O)C([O-])=O)(C)C)C(=O)COC1=CC=CC=C1 HCTVWSOKIJULET-LQDWTQKMSA-M 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 229940095068 tetradecene Drugs 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene 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
- C08F222/00—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 carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/04—Anhydrides, e.g. cyclic anhydrides
- C08F222/06—Maleic anhydride
-
- 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
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- 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
- C08F212/00—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 an aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/06—Hydrocarbons
- C08F212/08—Styrene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L21/00—Compositions of unspecified rubbers
Landscapes
- Chemical & Material Sciences (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)
- Polymerisation Methods In General (AREA)
- Paper (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEP2501123.8 | 1975-01-14 | ||
| DE2501123A DE2501123C2 (de) | 1975-01-14 | 1975-01-14 | Verfahren zur Herstellung von Suspensions-Copolymerisaten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1090950A true CA1090950A (en) | 1980-12-02 |
Family
ID=5936352
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA243,314A Expired CA1090950A (en) | 1975-01-14 | 1976-01-12 | Process for the production of copolymer powders |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US4048422A (enExample) |
| JP (1) | JPS5930723B2 (enExample) |
| AT (1) | AT340137B (enExample) |
| BE (1) | BE837475A (enExample) |
| BR (1) | BR7600166A (enExample) |
| CA (1) | CA1090950A (enExample) |
| CH (1) | CH601366A5 (enExample) |
| CS (1) | CS183834B2 (enExample) |
| DE (1) | DE2501123C2 (enExample) |
| ES (1) | ES444247A1 (enExample) |
| FI (1) | FI760051A7 (enExample) |
| FR (1) | FR2297866A1 (enExample) |
| GB (1) | GB1528992A (enExample) |
| IT (1) | IT1053368B (enExample) |
| NL (1) | NL178168C (enExample) |
| NO (1) | NO754384L (enExample) |
| SE (1) | SE7600277L (enExample) |
| SU (1) | SU576324A1 (enExample) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2750070A1 (de) * | 1977-11-09 | 1979-05-10 | Huels Chemische Werke Ag | Papierleimungsmittel |
| DE2840502A1 (de) * | 1978-09-18 | 1980-03-27 | Basf Ag | Verfahren zur herstellung von terpolymeren |
| DE2840501A1 (de) * | 1978-09-18 | 1980-03-27 | Basf Ag | Verfahren zur herstellung von copolymerisaten aus maleinsaeureanhydrid und alkenen |
| NO792863L (no) * | 1978-09-19 | 1980-03-20 | Bayer Ag | Skumfattig overflatelimingsmiddel for papir |
| GB2065674B (en) | 1979-12-21 | 1983-03-30 | Ici Ltd | Sterically stabilised non-aqueous dispersions of styrene copolymers |
| NL8002689A (nl) * | 1980-05-09 | 1981-12-01 | M & T Chemicals Bv | Polymeren met biocide eigenschappen. |
| US4358573A (en) * | 1981-05-29 | 1982-11-09 | S. C. Johnson & Son, Inc. | Waxy maleic anhydride alpha olefin terpolymers |
| US4604221A (en) * | 1982-07-06 | 1986-08-05 | The Lubrizol Corporation | Nitrogen-containing esters and lubricants containing them |
| JPS6016851A (ja) * | 1983-07-08 | 1985-01-28 | 花王株式会社 | セメント混和剤 |
| US4594378A (en) * | 1985-03-25 | 1986-06-10 | The Lubrizol Corporation | Polymeric compositions, oil compositions containing said polymeric compositions, transmission fluids and hydraulic fluids |
| DE3628247A1 (de) * | 1986-08-20 | 1988-02-25 | Huels Chemische Werke Ag | Verfahren zur herstellung von pulverfoermigen olefin-maleinsaeureanhydrid-copolymeren |
| JPS63291905A (ja) * | 1987-05-25 | 1988-11-29 | Kao Corp | オレフィン−無水マレイン酸共重合体粒子の製造方法 |
| DE3827631A1 (de) * | 1988-08-16 | 1990-02-22 | Hoechst Ag | Selbsttragendes flaechengebilde mit wenigstens einer strukturierten oberflaeche |
| DE3930141A1 (de) * | 1989-09-09 | 1991-03-21 | Bayer Ag | Vernetzte perlpolymerisate und ihre herstellung |
| DE4131142A1 (de) * | 1991-09-19 | 1993-03-25 | Bayer Ag | Elektroviskose fluessigkeit |
| DE4205839A1 (de) * | 1992-02-26 | 1993-09-02 | Basf Ag | Verwendung von umsetzungsprodukten von homo- oder copolymerisaten auf basis monoethylenisch ungesaettigter dicarbonsaeureanhydride mit aminen oder alkoholen zum fetten und fuellen von leder oder pelzfellen |
| US5453476A (en) * | 1993-08-23 | 1995-09-26 | Rohm And Haas Company | High solids copolymerization via in-situ isomerization |
| DE19621573A1 (de) * | 1996-05-29 | 1997-12-04 | Basf Ag | Thermisch härtbare, wäßrige Zusammensetzungen |
| DE19824532A1 (de) | 1998-06-03 | 1999-12-09 | Basf Ag | Verfahren zur Herstellung von Schalenkatalysatoren für die katalytische Gasphasenoxidation von aromatischen Kohlenwasserstoffen und so erhältliche Katalysatoren |
| US7126037B2 (en) | 1999-11-08 | 2006-10-24 | Nippon Petrochemicals Co., Lt. | Butene oligomer derivatives having terminal 1,4-butanediol functional groups |
| WO2008152018A1 (de) | 2007-06-13 | 2008-12-18 | Basf Se | Verfahren zur herstellung von formkörpern |
| JP5134351B2 (ja) * | 2007-12-07 | 2013-01-30 | 花王株式会社 | 電子材料用油中分散剤組成物 |
| CN102171258B (zh) * | 2008-07-31 | 2014-10-15 | 卢布里佐尔公司 | 共聚物及其润滑组合物 |
| CN102510886B (zh) | 2009-07-22 | 2015-04-29 | 巴斯夫欧洲公司 | 成膜聚合物和有机中空粒子用于涂层剂的用途 |
| US9574100B2 (en) | 2011-06-22 | 2017-02-21 | Basf Se | Coated polymer foils with oxygen barrier properties |
| BR112013032551A2 (pt) | 2011-06-22 | 2017-01-17 | Basf Se | folha fina polimérica, uso de uma composição aquosa, e, processo para a produção ou reforço de um efeito de barreira a oxigênio em um substrato de suporte |
| CN102344526B (zh) * | 2011-07-12 | 2013-07-17 | 江南大学 | 一种支化型聚苯乙烯马来酸酐的制备方法及其用途 |
| CA2921773A1 (en) | 2013-08-22 | 2015-02-26 | Basf Se | Method for producing emulsion polymerisates |
| KR20160045702A (ko) | 2013-08-22 | 2016-04-27 | 헨켈 아이피 앤드 홀딩 게엠베하 | 높은 올레핀 함량을 갖는 높은 분자량의 중합체 |
| WO2015024882A1 (de) | 2013-08-22 | 2015-02-26 | Basf Se | Verfahren zur herstellung von emulsionspolymerisaten |
| WO2017139572A1 (en) | 2016-02-11 | 2017-08-17 | Henkel IP & Holding GmbH | Olefin-acrylate copolymers with pendant hydroxyl functionality and use thereof |
| EP3414270B1 (en) | 2016-02-11 | 2022-09-14 | Henkel AG & Co. KGaA | Olefin-acrylate copolymers with pendant hydroxyl functionality and use thereof |
| MX2019003825A (es) | 2016-10-07 | 2019-11-18 | Basf Se | Metodo para producir dispersiones acuosas. |
| US20210214709A1 (en) | 2017-11-09 | 2021-07-15 | Basf Se | Coatings of enzyme particles comprising organic white pigments |
| KR20240130084A (ko) * | 2021-12-27 | 2024-08-28 | 카오카부시키가이샤 | 축전 디바이스 전극용 분산제 |
| WO2024245300A1 (zh) * | 2023-05-29 | 2024-12-05 | 江苏扬农化工集团有限公司 | 一种以连续进料的方式合成烯烃功能聚合物的方法和基于烯烃功能聚合物的用途 |
| CN119119770B (zh) * | 2024-09-05 | 2025-07-01 | 重庆市化工研究院有限公司 | 一种还原染料分散剂及其应用和液体预还原还原染料的制备方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2921928A (en) * | 1957-11-29 | 1960-01-19 | Monsanto Chemicals | Preparation of copolymer diamides |
| US2979487A (en) * | 1960-02-25 | 1961-04-11 | Monsanto Chemicals | Suspension polymerization process |
| US3553183A (en) * | 1969-03-27 | 1971-01-05 | Gaf Corp | Interpolymeric anti-clumping additives |
| US3729451A (en) * | 1972-07-10 | 1973-04-24 | Gulf Research Development Co | Process for copolymerization of maleic anhydride with 1-olefins |
-
1975
- 1975-01-14 DE DE2501123A patent/DE2501123C2/de not_active Expired
- 1975-10-30 GB GB44919/75A patent/GB1528992A/en not_active Expired
- 1975-12-23 NO NO754384A patent/NO754384L/no unknown
-
1976
- 1976-01-07 SU SU7602310602A patent/SU576324A1/ru active
- 1976-01-08 US US05/647,502 patent/US4048422A/en not_active Expired - Lifetime
- 1976-01-12 CA CA243,314A patent/CA1090950A/en not_active Expired
- 1976-01-12 CS CS7600000191A patent/CS183834B2/cs unknown
- 1976-01-12 AT AT13176A patent/AT340137B/de not_active IP Right Cessation
- 1976-01-12 BE BE163437A patent/BE837475A/xx unknown
- 1976-01-12 FI FI760051A patent/FI760051A7/fi not_active Application Discontinuation
- 1976-01-12 IT IT47586/76A patent/IT1053368B/it active
- 1976-01-12 NL NLAANVRAGE7600262,A patent/NL178168C/xx not_active IP Right Cessation
- 1976-01-12 JP JP51002159A patent/JPS5930723B2/ja not_active Expired
- 1976-01-13 ES ES444247A patent/ES444247A1/es not_active Expired
- 1976-01-13 SE SE7600277A patent/SE7600277L/xx unknown
- 1976-01-13 BR BR7600166A patent/BR7600166A/pt unknown
- 1976-01-14 FR FR7600849A patent/FR2297866A1/fr active Granted
- 1976-01-14 CH CH41676A patent/CH601366A5/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE2501123A1 (de) | 1976-07-15 |
| CH601366A5 (enExample) | 1978-07-14 |
| AT340137B (de) | 1977-11-25 |
| SE7600277L (sv) | 1976-07-15 |
| NL178168C (nl) | 1986-02-03 |
| US4048422A (en) | 1977-09-13 |
| NL178168B (nl) | 1985-09-02 |
| JPS5930723B2 (ja) | 1984-07-28 |
| DE2501123C2 (de) | 1984-02-09 |
| FR2297866B1 (enExample) | 1980-02-22 |
| IT1053368B (it) | 1981-08-31 |
| NL7600262A (nl) | 1976-07-16 |
| BR7600166A (pt) | 1976-08-31 |
| ATA13176A (de) | 1977-03-15 |
| ES444247A1 (es) | 1977-05-01 |
| FR2297866A1 (fr) | 1976-08-13 |
| CS183834B2 (en) | 1978-07-31 |
| FI760051A7 (enExample) | 1976-07-15 |
| JPS5195489A (enExample) | 1976-08-21 |
| BE837475A (fr) | 1976-07-12 |
| NO754384L (enExample) | 1976-07-15 |
| SU576324A1 (ru) | 1977-10-15 |
| GB1528992A (en) | 1978-10-18 |
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