PL106061B1 - Sposob polimeryzacji etylenowo-nienasyconych monomerow - Google Patents
Sposob polimeryzacji etylenowo-nienasyconych monomerow Download PDFInfo
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- PL106061B1 PL106061B1 PL1976191794A PL19179476A PL106061B1 PL 106061 B1 PL106061 B1 PL 106061B1 PL 1976191794 A PL1976191794 A PL 1976191794A PL 19179476 A PL19179476 A PL 19179476A PL 106061 B1 PL106061 B1 PL 106061B1
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- compounds
- compound
- dyes
- polymerization
- acid
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- 238000000034 method Methods 0.000 title claims description 76
- 238000006116 polymerization reaction Methods 0.000 title claims description 57
- 239000000178 monomer Substances 0.000 title claims description 35
- 150000001875 compounds Chemical class 0.000 claims description 92
- -1 polyene compounds Chemical class 0.000 claims description 62
- 239000002253 acid Substances 0.000 claims description 29
- 239000000975 dye Substances 0.000 claims description 26
- 150000002894 organic compounds Chemical class 0.000 claims description 23
- 230000008569 process Effects 0.000 claims description 23
- 239000000203 mixture Substances 0.000 claims description 21
- 239000011248 coating agent Substances 0.000 claims description 15
- 238000000576 coating method Methods 0.000 claims description 15
- 239000000243 solution Substances 0.000 claims description 15
- YCUVUDODLRLVIC-VPHDGDOJSA-N sudan black b Chemical compound C1=CC(=C23)NC(C)(C)NC2=CC=CC3=C1\N=N\C(C1=CC=CC=C11)=CC=C1\N=N\C1=CC=CC=C1 YCUVUDODLRLVIC-VPHDGDOJSA-N 0.000 claims description 12
- 239000002585 base Substances 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 8
- 239000000987 azo dye Substances 0.000 claims description 7
- 239000007800 oxidant agent Substances 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 239000011734 sodium Substances 0.000 claims description 7
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 6
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 6
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 6
- 239000001000 anthraquinone dye Substances 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 6
- 230000009471 action Effects 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- 239000006185 dispersion Substances 0.000 claims description 4
- 150000002823 nitrates Chemical class 0.000 claims description 4
- 230000001590 oxidative effect Effects 0.000 claims description 4
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 claims description 4
- 150000004057 1,4-benzoquinones Chemical class 0.000 claims description 3
- 229930192627 Naphthoquinone Natural products 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 239000003638 chemical reducing agent Substances 0.000 claims description 3
- 150000002791 naphthoquinones Chemical class 0.000 claims description 3
- 150000004053 quinones Chemical class 0.000 claims description 3
- 150000003568 thioethers Chemical class 0.000 claims description 3
- 239000001018 xanthene dye Substances 0.000 claims description 3
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 claims description 2
- 235000000177 Indigofera tinctoria Nutrition 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 2
- 150000001299 aldehydes Chemical class 0.000 claims description 2
- 229910021529 ammonia Inorganic materials 0.000 claims description 2
- 150000008064 anhydrides Chemical class 0.000 claims description 2
- 150000001491 aromatic compounds Chemical class 0.000 claims description 2
- 150000007514 bases Chemical class 0.000 claims description 2
- 229910052728 basic metal Inorganic materials 0.000 claims description 2
- 150000001720 carbohydrates Chemical class 0.000 claims description 2
- 235000014633 carbohydrates Nutrition 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 150000004678 hydrides Chemical class 0.000 claims description 2
- 229940097275 indigo Drugs 0.000 claims description 2
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 claims description 2
- 229910000000 metal hydroxide Inorganic materials 0.000 claims description 2
- 150000004692 metal hydroxides Chemical class 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 150000002828 nitro derivatives Chemical class 0.000 claims description 2
- 239000001005 nitro dye Substances 0.000 claims description 2
- 150000001451 organic peroxides Chemical class 0.000 claims description 2
- 150000004893 oxazines Chemical class 0.000 claims description 2
- 150000002978 peroxides Chemical class 0.000 claims description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 claims description 2
- 239000000985 reactive dye Substances 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 2
- 239000001017 thiazole dye Substances 0.000 claims description 2
- 150000003557 thiazoles Chemical class 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
- 239000000370 acceptor Substances 0.000 claims 2
- 239000000984 vat dye Substances 0.000 claims 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims 1
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 claims 1
- 239000000980 acid dye Substances 0.000 claims 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 239000003518 caustics Substances 0.000 claims 1
- 150000002429 hydrazines Chemical class 0.000 claims 1
- 229910010276 inorganic hydride Inorganic materials 0.000 claims 1
- 229910001959 inorganic nitrate Inorganic materials 0.000 claims 1
- 229910052920 inorganic sulfate Inorganic materials 0.000 claims 1
- 229910052945 inorganic sulfide Inorganic materials 0.000 claims 1
- 239000001006 nitroso dye Substances 0.000 claims 1
- 150000007524 organic acids Chemical class 0.000 claims 1
- 235000005985 organic acids Nutrition 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 239000001007 phthalocyanine dye Substances 0.000 claims 1
- 125000003367 polycyclic group Chemical group 0.000 claims 1
- 230000000379 polymerizing effect Effects 0.000 claims 1
- 229920000137 polyphosphoric acid Polymers 0.000 claims 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 claims 1
- 229930185107 quinolinone Natural products 0.000 claims 1
- 150000004897 thiazines Chemical class 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 description 30
- 229920000642 polymer Polymers 0.000 description 27
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 13
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
- 239000003921 oil Substances 0.000 description 12
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 11
- 238000000151 deposition Methods 0.000 description 10
- 229920002554 vinyl polymer Polymers 0.000 description 10
- 230000008021 deposition Effects 0.000 description 9
- 238000010557 suspension polymerization reaction Methods 0.000 description 9
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 9
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
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- 239000004816 latex Substances 0.000 description 5
- 229910001220 stainless steel Inorganic materials 0.000 description 5
- 239000010935 stainless steel Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 4
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 4
- 150000004056 anthraquinones Chemical class 0.000 description 4
- CUFNKYGDVFVPHO-UHFFFAOYSA-N azulene Chemical compound C1=CC=CC2=CC=CC2=C1 CUFNKYGDVFVPHO-UHFFFAOYSA-N 0.000 description 4
- 150000001993 dienes Chemical class 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 229920003002 synthetic resin Polymers 0.000 description 4
- 239000000057 synthetic resin Substances 0.000 description 4
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 3
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 3
- 241001436793 Meru Species 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 239000004115 Sodium Silicate Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
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- 150000002170 ethers Chemical class 0.000 description 3
- 235000019239 indanthrene blue RS Nutrition 0.000 description 3
- UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 description 3
- 230000001678 irradiating effect Effects 0.000 description 3
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- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 2
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- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
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- YOCIQNIEQYCORH-UHFFFAOYSA-M chembl2028361 Chemical compound [Na+].OC1=CC=C2C=C(S([O-])(=O)=O)C=CC2=C1N=NC1=CC=CC=C1 YOCIQNIEQYCORH-UHFFFAOYSA-M 0.000 description 1
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- 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 1
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- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 description 1
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- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
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- FTZLWXQKVFFWLY-UHFFFAOYSA-L disodium;2,5-dichloro-4-[3-methyl-5-oxo-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazol-1-yl]benzenesulfonate Chemical group [Na+].[Na+].CC1=NN(C=2C(=CC(=C(Cl)C=2)S([O-])(=O)=O)Cl)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 FTZLWXQKVFFWLY-UHFFFAOYSA-L 0.000 description 1
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- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
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- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical class C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
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- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexamethylene diamine Natural products NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- SURQXAFEQWPFPV-UHFFFAOYSA-L iron(2+) sulfate heptahydrate Chemical compound O.O.O.O.O.O.O.[Fe+2].[O-]S([O-])(=O)=O SURQXAFEQWPFPV-UHFFFAOYSA-L 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229940107698 malachite green Drugs 0.000 description 1
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
- JGEMYUOFGVHXKV-UPHRSURJSA-N malealdehyde Chemical compound O=C\C=C/C=O JGEMYUOFGVHXKV-UPHRSURJSA-N 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- COTNUBDHGSIOTA-UHFFFAOYSA-N meoh methanol Chemical compound OC.OC COTNUBDHGSIOTA-UHFFFAOYSA-N 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- OOFZXICLQFOHEN-UHFFFAOYSA-N methanol Chemical compound OC.OC.OC OOFZXICLQFOHEN-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 239000000983 mordant dye Substances 0.000 description 1
- SHXOKQKTZJXHHR-UHFFFAOYSA-N n,n-diethyl-5-iminobenzo[a]phenoxazin-9-amine;hydrochloride Chemical compound [Cl-].C1=CC=C2C3=NC4=CC=C(N(CC)CC)C=C4OC3=CC(=[NH2+])C2=C1 SHXOKQKTZJXHHR-UHFFFAOYSA-N 0.000 description 1
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- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
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- 150000002927 oxygen compounds Chemical class 0.000 description 1
- CUOYSVTWECOPNA-UHFFFAOYSA-N pentacyclo[11.7.0.02,10.03,8.015,20]icosa-1(13),2(10),3,5,7,11,15,17,19-nonaene Chemical compound C1C2=CC=CC=C2C2=C1C=CC1=C2C2=CC=CC=C2C1 CUOYSVTWECOPNA-UHFFFAOYSA-N 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
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- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- YPCZIDDPJRHZIZ-UHFFFAOYSA-N phosphoric acid;decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.OP(O)(O)=O YPCZIDDPJRHZIZ-UHFFFAOYSA-N 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
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- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 229940043267 rhodamine b Drugs 0.000 description 1
- 229940074386 skatole Drugs 0.000 description 1
- XFMZNMJZQJDSHM-UHFFFAOYSA-M sodium 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-phenylphenyl)phenyl]phenyl]phenyl]phenyl]phenyl]phenyl]phenyl]phenyl]phenyl]benzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)c1ccccc1-c1ccccc1-c1ccccc1-c1ccccc1-c1ccccc1-c1ccccc1-c1ccccc1-c1ccccc1-c1ccccc1-c1ccccc1-c1ccccc1-c1ccccc1 XFMZNMJZQJDSHM-UHFFFAOYSA-M 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- FLOMHNPVJPAASA-UHFFFAOYSA-M sodium;3-[[4-(dimethylamino)phenyl]-[4-[methyl-[(3-sulfonatophenyl)methyl]amino]phenyl]methylidene]-6-dimethylazaniumylidenecyclohexa-1,4-diene-1-sulfonate Chemical compound [Na+].C1=CC(N(C)C)=CC=C1C(\C=1C=CC(=CC=1)N(C)CC=1C=C(C=CC=1)S([O-])(=O)=O)=C\1C=C(S([O-])(=O)=O)C(=[N+](C)C)C=C/1 FLOMHNPVJPAASA-UHFFFAOYSA-M 0.000 description 1
- 241000894007 species Species 0.000 description 1
- JMCKWTQLJNQCTD-UHFFFAOYSA-N spirit blue Chemical compound Cl.C=1C=C(C(=C2C=CC(C=C2)=NC=2C=CC=CC=2)C=2C=CC(NC=3C=CC=CC=3)=CC=2)C=CC=1NC1=CC=CC=C1 JMCKWTQLJNQCTD-UHFFFAOYSA-N 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 description 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
- BNKODMWOYPLRKR-UHFFFAOYSA-N tetrahydroxy silicate Chemical compound OO[Si](OO)(OO)OO BNKODMWOYPLRKR-UHFFFAOYSA-N 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 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
- 229940086542 triethylamine Drugs 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- 229940048102 triphosphoric acid Drugs 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
- C08F2/00—Processes of polymerisation
- C08F2/002—Scale prevention in a polymerisation reactor or its auxiliary parts
- C08F2/004—Scale prevention in a polymerisation reactor or its auxiliary parts by a prior coating on the reactor walls
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50098784A JPS5223187A (en) | 1975-08-14 | 1975-08-14 | Process for polymerizing vinyl monomers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL106061B1 true PL106061B1 (pl) | 1979-11-30 |
Family
ID=14228982
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1976191794A PL106061B1 (pl) | 1975-08-14 | 1976-08-13 | Sposob polimeryzacji etylenowo-nienasyconych monomerow |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US4105839A (en, 2012) |
| JP (1) | JPS5223187A (en, 2012) |
| AT (1) | AT351257B (en, 2012) |
| BE (1) | BE845168A (en, 2012) |
| BR (1) | BR7605327A (en, 2012) |
| CA (1) | CA1118144A (en, 2012) |
| DE (1) | DE2635780A1 (en, 2012) |
| DK (1) | DK152436C (en, 2012) |
| ES (1) | ES450547A1 (en, 2012) |
| FR (1) | FR2320952A1 (en, 2012) |
| GB (1) | GB1562290A (en, 2012) |
| HU (1) | HU174386B (en, 2012) |
| IT (1) | IT1062554B (en, 2012) |
| NL (1) | NL7609027A (en, 2012) |
| NO (1) | NO151414C (en, 2012) |
| PL (1) | PL106061B1 (en, 2012) |
| PT (1) | PT65475B (en, 2012) |
| SE (1) | SE7608915L (en, 2012) |
| SU (1) | SU1003759A3 (en, 2012) |
| TR (1) | TR19676A (en, 2012) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2960426D1 (en) * | 1978-02-24 | 1981-10-01 | Ici Plc | Coating product for use in a reactor for vinyl halide polymerisation process, the reactor and the process |
| US4228130A (en) * | 1978-10-23 | 1980-10-14 | The B. F. Goodrich Company | Coating polymerization reactors with oligomers derived from polyhydric phenols plus a bleach |
| JPS55155001A (en) * | 1979-05-21 | 1980-12-03 | Shin Etsu Chem Co Ltd | Polymerization of vinyl monomer |
| JPS568490U (en, 2012) * | 1979-07-03 | 1981-01-24 | ||
| JPS59202201A (ja) * | 1983-04-28 | 1984-11-16 | Shin Etsu Chem Co Ltd | 重合体スケ−ル付着防止剤およびそれを使用する方法 |
| IT1190641B (it) * | 1986-05-16 | 1988-02-16 | Enichem Polimeri | Procedimento per la polimerizzazione in sospensione acquosa di monomeri vinilici contenenti alogeno |
| DE3815397C2 (de) * | 1988-05-05 | 1998-02-26 | Wacker Chemie Gmbh | Verfahren zur Herstellung einer Autoklavenbeschichtung |
| PH26338A (en) * | 1988-08-10 | 1992-04-29 | Shinetsu Chemical Co | Method of preventing polymer scale formation |
| US5053466A (en) * | 1988-12-07 | 1991-10-01 | Shin-Ftsu Chemical Co., Ltd. | Method of preventing polymer scale deposition |
| JPH0739445B2 (ja) * | 1988-12-07 | 1995-05-01 | 信越化学工業株式会社 | 重合体スケールの付着防止方法 |
| JPH0615566B2 (ja) * | 1989-02-02 | 1994-03-02 | 信越化学工業株式会社 | 重合体スケールの付着防止方法 |
| US4963592A (en) * | 1989-11-20 | 1990-10-16 | The B. F. Goodrich Company | Super porous low molecular weight vinyl halide resins |
| JPH0450203A (ja) * | 1990-06-19 | 1992-02-19 | Shin Etsu Chem Co Ltd | 重合体スケール付着防止剤および重合体スケールの付着防止方法 |
| DE69209672T2 (de) * | 1991-01-22 | 1996-09-26 | Shinetsu Chemical Co | Beschichtungslösung zur Verhinderung von Polymeransatzbildung und Verfahren zu ihrem Gebrauch |
| JP2764660B2 (ja) * | 1991-05-17 | 1998-06-11 | 信越化学工業株式会社 | 重合体スケール付着防止剤および重合体スケールの付着防止方法 |
| JP2678702B2 (ja) * | 1992-02-20 | 1997-11-17 | 信越化学工業株式会社 | 重合体スケール付着防止剤及びそれを使用する重合体製造方法 |
| JP2966198B2 (ja) * | 1992-06-04 | 1999-10-25 | 信越化学工業株式会社 | 重合体スケール付着防止剤、重合体スケールの付着を防止する重合器及びそれを使用する重合体製造方法 |
| CA2097570A1 (en) * | 1992-06-04 | 1993-12-05 | Toshihide Shimizu | Polymer scale preventive agent |
| US5393857A (en) * | 1992-06-04 | 1995-02-28 | Shin-Etsu Chemical Co., Ltd. | Polymer scale preventive agent |
| ATE315052T1 (de) | 1999-07-14 | 2006-02-15 | Johnson Polymer Inc | Verfahren zur kontinuierlichen herstellung von epoxy - (meth)acryl - styrolpolymeren und ihre verwendung in beschichtungsmassen |
| US6605681B1 (en) | 2000-07-12 | 2003-08-12 | Johnson Polymer, Inc. | Process for the continuous production of epoxylated addition polymers, and powder and liquid coating applications containing epoxylated addition polymers |
| US8324329B2 (en) * | 2007-08-07 | 2012-12-04 | Bridgestone Corporation | Process for producing functionalized polymers |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2775625A (en) * | 1953-06-17 | 1956-12-25 | Dow Chemical Co | Inhibiting polymerization of monomeric vinylidene chloride |
| US2761864A (en) * | 1955-01-17 | 1956-09-04 | Phillips Petroleum Co | Stabilization of heterocyclic nitrogen compounds |
| DE1236200B (de) * | 1963-05-10 | 1967-03-09 | Huels Chemische Werke Ag | Verfahren zum Verringern und Beseitigen von Ablagerungen in Reaktionsgefaessen fuer die Olefin-Niederdruckpolymerisation nach Ziegler |
| US3515709A (en) * | 1967-08-02 | 1970-06-02 | Dow Chemical Co | Process for eliminating polymer build-up on reactor walls during polymerization of water-insoluble monoethylenically unsaturated liquid monomers |
| JPS4814437B1 (en, 2012) * | 1969-12-15 | 1973-05-07 | ||
| DE91560C (en, 2012) * | 1970-05-07 | |||
| US3778423A (en) * | 1971-06-28 | 1973-12-11 | Universal Pvc Resins | Method for reducing polymer deposit in polymerization of vinyl chloride |
| GB1439339A (en) * | 1972-11-20 | 1976-06-16 | Ici Ltd | Vinyl chloride polymerisation process |
| US3849179A (en) * | 1973-08-27 | 1974-11-19 | Goodrich Co B F | Internally coated reaction vessel and process for coating the same |
| JPS5113881A (en) * | 1974-07-24 | 1976-02-03 | Kanegafuchi Chemical Ind | Enkabiniruno jugohoho |
| JPS5150887A (ja) * | 1974-09-18 | 1976-05-04 | Goodrich Co B F | Jugotaifuchakuohaijosuruhoho |
| US3962196A (en) * | 1974-10-29 | 1976-06-08 | Continental Oil Company | Technique for reducing polymer deposit during polymerization in aqueous dispersion |
| JPS5157791A (ja) * | 1974-11-18 | 1976-05-20 | Ryonichi Kk | Jugokinadonokihekimenniryukasenryo oyobi * mataha ryukatatezomesenryootofusuru hoho |
| US4024301A (en) * | 1975-05-02 | 1977-05-17 | The B. F. Goodrich Company | Internally coated reaction vessel for use in olefinic polymerization |
| JPS5224953A (en) * | 1975-08-22 | 1977-02-24 | Osaka Transformer Co Ltd | Arc welding machine |
| JPS536025A (en) * | 1976-07-06 | 1978-01-20 | Mamoru Koshi | Projector with intermittently irradiating light source |
| JPS594061B2 (ja) * | 1976-08-30 | 1984-01-27 | 日本電気株式会社 | 補間演算回路 |
-
1975
- 1975-08-14 JP JP50098784A patent/JPS5223187A/ja active Granted
-
1976
- 1976-08-06 ES ES450547A patent/ES450547A1/es not_active Expired
- 1976-08-09 DE DE19762635780 patent/DE2635780A1/de active Granted
- 1976-08-10 NO NO762767A patent/NO151414C/no unknown
- 1976-08-10 HU HU76SI1535A patent/HU174386B/hu unknown
- 1976-08-10 SE SE7608915A patent/SE7608915L/ unknown
- 1976-08-12 CA CA000258970A patent/CA1118144A/en not_active Expired
- 1976-08-12 FR FR7624626A patent/FR2320952A1/fr active Granted
- 1976-08-12 US US05/713,894 patent/US4105839A/en not_active Expired - Lifetime
- 1976-08-12 AT AT602176A patent/AT351257B/de not_active IP Right Cessation
- 1976-08-13 IT IT26274/76A patent/IT1062554B/it active
- 1976-08-13 PL PL1976191794A patent/PL106061B1/pl unknown
- 1976-08-13 NL NL7609027A patent/NL7609027A/xx not_active Application Discontinuation
- 1976-08-13 BE BE169792A patent/BE845168A/xx not_active IP Right Cessation
- 1976-08-13 DK DK365576A patent/DK152436C/da not_active IP Right Cessation
- 1976-08-13 PT PT65475A patent/PT65475B/pt unknown
- 1976-08-13 SU SU762387317A patent/SU1003759A3/ru active
- 1976-08-13 TR TR19676A patent/TR19676A/xx unknown
- 1976-08-13 BR BR7605327A patent/BR7605327A/pt unknown
- 1976-08-13 GB GB33721/76A patent/GB1562290A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NO762767L (en, 2012) | 1977-02-15 |
| BR7605327A (pt) | 1977-08-09 |
| IT1062554B (it) | 1984-10-20 |
| PT65475B (en) | 1978-02-11 |
| NO151414B (no) | 1984-12-27 |
| CA1118144A (en) | 1982-02-09 |
| SU1003759A3 (ru) | 1983-03-07 |
| DK365576A (da) | 1977-02-15 |
| FR2320952B1 (en, 2012) | 1979-09-28 |
| US4105839A (en) | 1978-08-08 |
| HU174386B (hu) | 1979-12-28 |
| NO151414C (no) | 1985-04-10 |
| AT351257B (de) | 1979-07-10 |
| FR2320952A1 (fr) | 1977-03-11 |
| DK152436B (da) | 1988-02-29 |
| NL7609027A (nl) | 1977-02-16 |
| PT65475A (en) | 1976-09-01 |
| JPS5346235B2 (en, 2012) | 1978-12-12 |
| DE2635780A1 (de) | 1977-02-24 |
| ATA602176A (de) | 1978-12-15 |
| DK152436C (da) | 1988-07-25 |
| TR19676A (tr) | 1979-10-05 |
| SE7608915L (sv) | 1977-02-15 |
| JPS5223187A (en) | 1977-02-21 |
| DE2635780C2 (en, 2012) | 1989-03-09 |
| GB1562290A (en) | 1980-03-12 |
| BE845168A (fr) | 1976-12-01 |
| ES450547A1 (es) | 1977-08-16 |
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