JP2732551B2 - ポリ（アリーレンスルフィド）ポリマーの調製方法 - Google Patents
ポリ（アリーレンスルフィド）ポリマーの調製方法Info
- Publication number
- JP2732551B2 JP2732551B2 JP16643792A JP16643792A JP2732551B2 JP 2732551 B2 JP2732551 B2 JP 2732551B2 JP 16643792 A JP16643792 A JP 16643792A JP 16643792 A JP16643792 A JP 16643792A JP 2732551 B2 JP2732551 B2 JP 2732551B2
- Authority
- JP
- Japan
- Prior art keywords
- polymer
- poly
- arylene sulfide
- polymerization
- molecular weight
- 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 - Lifetime
Links
- -1 poly (arylene sulfide Chemical compound 0.000 title claims description 122
- 229920000642 polymer Polymers 0.000 title claims description 120
- 238000000034 method Methods 0.000 title claims description 73
- 238000006116 polymerization reaction Methods 0.000 claims description 120
- 239000002699 waste material Substances 0.000 claims description 83
- 239000000203 mixture Substances 0.000 claims description 35
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 33
- 150000002894 organic compounds Chemical class 0.000 claims description 25
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 19
- 229910052717 sulfur Inorganic materials 0.000 claims description 18
- 239000011593 sulfur Substances 0.000 claims description 18
- 229910052783 alkali metal Inorganic materials 0.000 claims description 15
- 239000011541 reaction mixture Substances 0.000 claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 14
- 238000011084 recovery Methods 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical group [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- 125000004122 cyclic group Chemical group 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 150000001491 aromatic compounds Chemical class 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 239000001632 sodium acetate Substances 0.000 claims description 5
- 235000017281 sodium acetate Nutrition 0.000 claims description 5
- 150000007942 carboxylates Chemical class 0.000 claims description 4
- 150000003950 cyclic amides Chemical class 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 230000000977 initiatory effect Effects 0.000 claims description 4
- 229910052744 lithium Inorganic materials 0.000 claims description 4
- 238000000746 purification Methods 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 2
- 229910001508 alkali metal halide Inorganic materials 0.000 claims 3
- 150000008045 alkali metal halides Chemical class 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 2
- 238000010438 heat treatment Methods 0.000 claims 1
- 229920006158 high molecular weight polymer Polymers 0.000 claims 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 86
- 238000002474 experimental method Methods 0.000 description 79
- 229920000069 polyphenylene sulfide Polymers 0.000 description 62
- 239000000047 product Substances 0.000 description 41
- 239000000706 filtrate Substances 0.000 description 36
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 27
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- 208000005156 Dehydration Diseases 0.000 description 19
- 230000018044 dehydration Effects 0.000 description 19
- 238000006297 dehydration reaction Methods 0.000 description 19
- 239000000463 material Substances 0.000 description 19
- 238000005227 gel permeation chromatography Methods 0.000 description 18
- 238000009826 distribution Methods 0.000 description 15
- 239000002002 slurry Substances 0.000 description 15
- 238000004458 analytical method Methods 0.000 description 13
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000000155 melt Substances 0.000 description 9
- 239000000376 reactant Substances 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000006227 byproduct Substances 0.000 description 7
- 229910052977 alkali metal sulfide Inorganic materials 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 150000002430 hydrocarbons Chemical group 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
- 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 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 239000008367 deionised water Substances 0.000 description 3
- 229910021641 deionized water Inorganic materials 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
- 230000002411 adverse Effects 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 229910052979 sodium sulfide Inorganic materials 0.000 description 2
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 1
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 1
- OFHDZEYCBJGZEF-UHFFFAOYSA-N 1,4-dibromo-2-(4-methylphenyl)benzene Chemical compound C1=CC(C)=CC=C1C1=CC(Br)=CC=C1Br OFHDZEYCBJGZEF-UHFFFAOYSA-N 0.000 description 1
- GHVFWFCIYIGDCX-UHFFFAOYSA-N 1,4-dibromo-2-butyl-5-cyclohexylbenzene Chemical compound C1=C(Br)C(CCCC)=CC(Br)=C1C1CCCCC1 GHVFWFCIYIGDCX-UHFFFAOYSA-N 0.000 description 1
- KZHZSALFKRDIBQ-UHFFFAOYSA-N 1,4-dibromo-2-ethyl-5-propan-2-ylbenzene Chemical compound CCC1=CC(Br)=C(C(C)C)C=C1Br KZHZSALFKRDIBQ-UHFFFAOYSA-N 0.000 description 1
- SWJPEBQEEAHIGZ-UHFFFAOYSA-N 1,4-dibromobenzene Chemical compound BrC1=CC=C(Br)C=C1 SWJPEBQEEAHIGZ-UHFFFAOYSA-N 0.000 description 1
- PTIQIITULDNGAF-UHFFFAOYSA-N 1,4-dichloro-2,3,5,6-tetramethylbenzene Chemical compound CC1=C(C)C(Cl)=C(C)C(C)=C1Cl PTIQIITULDNGAF-UHFFFAOYSA-N 0.000 description 1
- UTGSRNVBAFCOEU-UHFFFAOYSA-N 1,4-dichloro-2,5-dimethylbenzene Chemical group CC1=CC(Cl)=C(C)C=C1Cl UTGSRNVBAFCOEU-UHFFFAOYSA-N 0.000 description 1
- WKDOCYUWLREIQL-UHFFFAOYSA-N 1,4-dichloro-2-(3-methylcyclopentyl)-5-octylbenzene Chemical compound C1=C(Cl)C(CCCCCCCC)=CC(Cl)=C1C1CC(C)CC1 WKDOCYUWLREIQL-UHFFFAOYSA-N 0.000 description 1
- KFAKZJUYBOYVKA-UHFFFAOYSA-N 1,4-dichloro-2-methylbenzene Chemical compound CC1=CC(Cl)=CC=C1Cl KFAKZJUYBOYVKA-UHFFFAOYSA-N 0.000 description 1
- ULYZMNKNGHNAIE-UHFFFAOYSA-N 1,4-diiodo-2-octadecylbenzene Chemical compound CCCCCCCCCCCCCCCCCCC1=CC(I)=CC=C1I ULYZMNKNGHNAIE-UHFFFAOYSA-N 0.000 description 1
- LFMWZTSOMGDDJU-UHFFFAOYSA-N 1,4-diiodobenzene Chemical compound IC1=CC=C(I)C=C1 LFMWZTSOMGDDJU-UHFFFAOYSA-N 0.000 description 1
- AZAMPMUEKXNYFW-UHFFFAOYSA-N 1-[2-(2-oxopyrrolidin-1-yl)ethyl]pyrrolidin-2-one Chemical compound O=C1CCCN1CCN1C(=O)CCC1 AZAMPMUEKXNYFW-UHFFFAOYSA-N 0.000 description 1
- NHDODQWIKUYWMW-UHFFFAOYSA-N 1-bromo-4-chlorobenzene Chemical compound ClC1=CC=C(Br)C=C1 NHDODQWIKUYWMW-UHFFFAOYSA-N 0.000 description 1
- UCCUXODGPMAHRL-UHFFFAOYSA-N 1-bromo-4-iodobenzene Chemical compound BrC1=CC=C(I)C=C1 UCCUXODGPMAHRL-UHFFFAOYSA-N 0.000 description 1
- GWQSENYKCGJTRI-UHFFFAOYSA-N 1-chloro-4-iodobenzene Chemical compound ClC1=CC=C(I)C=C1 GWQSENYKCGJTRI-UHFFFAOYSA-N 0.000 description 1
- JTPNRXUCIXHOKM-UHFFFAOYSA-N 1-chloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1 JTPNRXUCIXHOKM-UHFFFAOYSA-N 0.000 description 1
- YDUZJJVOMVPPMD-UHFFFAOYSA-N 2,5-dichloro-1-dodecyl-3-hexylbenzene Chemical compound CCCCCCCCCCCCC1=CC(Cl)=CC(CCCCCC)=C1Cl YDUZJJVOMVPPMD-UHFFFAOYSA-N 0.000 description 1
- ZXONXKTYRSSVKY-UHFFFAOYSA-N 2-benzyl-1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C(CC=2C=CC=CC=2)=C1 ZXONXKTYRSSVKY-UHFFFAOYSA-N 0.000 description 1
- SHJDOXMERQRWDJ-UHFFFAOYSA-N 4-bromo-1-chloro-2-phenylbenzene Chemical compound ClC1=CC=C(Br)C=C1C1=CC=CC=C1 SHJDOXMERQRWDJ-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000002547 anomalous effect Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- QTNDMWXOEPGHBT-UHFFFAOYSA-N dicesium;sulfide Chemical compound [S-2].[Cs+].[Cs+] QTNDMWXOEPGHBT-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- GLNWILHOFOBOFD-UHFFFAOYSA-N lithium sulfide Chemical compound [Li+].[Li+].[S-2] GLNWILHOFOBOFD-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- IHYNKGRWCDKNEG-UHFFFAOYSA-N n-(4-bromophenyl)-2,6-dihydroxybenzamide Chemical compound OC1=CC=CC(O)=C1C(=O)NC1=CC=C(Br)C=C1 IHYNKGRWCDKNEG-UHFFFAOYSA-N 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- DPLVEEXVKBWGHE-UHFFFAOYSA-N potassium sulfide Chemical compound [S-2].[K+].[K+] DPLVEEXVKBWGHE-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- AHKSSQDILPRNLA-UHFFFAOYSA-N rubidium(1+);sulfide Chemical compound [S-2].[Rb+].[Rb+] AHKSSQDILPRNLA-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- HYHCSLBZRBJJCH-UHFFFAOYSA-M sodium hydrosulfide Chemical compound [Na+].[SH-] HYHCSLBZRBJJCH-UHFFFAOYSA-M 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical class S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 1
- 150000003556 thioamides Chemical class 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J11/00—Recovery or working-up of waste materials
- C08J11/04—Recovery or working-up of waste materials of polymers
- C08J11/06—Recovery or working-up of waste materials of polymers without chemical reactions
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/688—Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/025—Preparatory processes
- C08G75/0259—Preparatory processes metal hydrogensulfides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2381/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen, or carbon only; Polysulfones; Derivatives of such polymers
- C08J2381/02—Polythioethers; Polythioether-ethers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/62—Plastics recycling; Rubber recycling
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Sustainable Development (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71985291A | 1991-06-24 | 1991-06-24 | |
| US719852 | 1991-06-24 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05186593A JPH05186593A (ja) | 1993-07-27 |
| JP2732551B2 true JP2732551B2 (ja) | 1998-03-30 |
Family
ID=24891619
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16643792A Expired - Lifetime JP2732551B2 (ja) | 1991-06-24 | 1992-06-24 | ポリ（アリーレンスルフィド）ポリマーの調製方法 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US5354841A (enExample) |
| EP (1) | EP0520370A3 (enExample) |
| JP (1) | JP2732551B2 (enExample) |
| KR (1) | KR100189767B1 (enExample) |
| CA (1) | CA2072165C (enExample) |
| TW (1) | TW224475B (enExample) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69222997T2 (de) * | 1991-08-06 | 1998-04-30 | Tosoh Corp | Verfahren zur Herstellung von Polyarylensulfid |
| CA2111404A1 (en) * | 1992-12-31 | 1994-07-01 | Jon F. Geibel | Process for preparing poly(arylene sulfide) polymers using high molecular weight poly(arylene sulfide) polymer as a reactant |
| US5869599A (en) * | 1995-04-10 | 1999-02-09 | Hay; Allan S. | Free radical ring opening for polymerization of cyclic oligomers containing an aromatic sulfide linkage |
| US7312196B2 (en) * | 1997-01-08 | 2007-12-25 | Amylin Pharmaceuticals, Inc. | Formulations for amylin agonist peptides |
| US6201097B1 (en) * | 1998-12-31 | 2001-03-13 | Phillips Petroleum Company | Process for producing poly (arylene sulfide) |
| US6380347B1 (en) | 1999-04-09 | 2002-04-30 | Honeywell International Inc. | Nanoporous polymers comprising macrocycles |
| JP2003252610A (ja) * | 2001-12-27 | 2003-09-10 | Idemitsu Petrochem Co Ltd | 硫化リチウムの再生方法及びポリアリーレンスルフィドの製造方法 |
| JP3898542B2 (ja) * | 2002-03-22 | 2007-03-28 | 日本ジーイープラスチックス株式会社 | 重縮合系樹脂のリサイクル法 |
| WO2003082953A1 (en) * | 2002-03-22 | 2003-10-09 | General Electric Company | Recycle process for polycondensation resins |
| JP2004131602A (ja) * | 2002-10-10 | 2004-04-30 | Idemitsu Petrochem Co Ltd | ポリアリーレンスルフィド系樹脂の製造方法 |
| US8329832B2 (en) * | 2007-02-28 | 2012-12-11 | Toray Industries, Inc. | Process for producing cyclic polyarylene sulfide |
| US8263734B2 (en) * | 2009-02-13 | 2012-09-11 | Chevron Phillips Chemical Company Lp | System and method for reducing off-gassing of polyphenylene sulfide |
| KR101410407B1 (ko) * | 2010-10-29 | 2014-06-20 | 도레이 카부시키가이샤 | 폴리아릴렌술피드의 제조 방법 및 폴리아릴렌술피드 |
| US20130317159A1 (en) | 2012-05-22 | 2013-11-28 | Chevron Phillips Chemical Company Lp | Reinforced Poly(Arylene Sulfide) Compositions |
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| US9617387B2 (en) | 2013-09-25 | 2017-04-11 | Ticona Llc | Scrubbing process for polyarylene sulfide formation |
| US9403948B2 (en) | 2013-09-25 | 2016-08-02 | Ticona Llc | Salt byproduct separation during formation of polyarylene sulfide |
| JP6797687B2 (ja) | 2013-09-25 | 2020-12-09 | ティコナ・エルエルシー | ポリアリーレンスルフィド結晶化方法 |
| JP2016536376A (ja) | 2013-09-25 | 2016-11-24 | ティコナ・エルエルシー | 低ハロゲン含量のポリアリーレンスルフィドを形成する方法 |
| JP6797686B2 (ja) | 2013-09-25 | 2020-12-09 | ティコナ・エルエルシー | ポリアリーレンスルフィドを形成するための多段階プロセス |
| US20150175748A1 (en) * | 2013-12-19 | 2015-06-25 | Chevron Phillips Chemical Company Lp | Process for Production of Poly(Arylene Sulfide) |
| WO2016133739A1 (en) | 2015-02-19 | 2016-08-25 | Ticona Llc | Method for forming a high molecular weight polyarylene sulfide |
| JP6803844B2 (ja) | 2015-02-19 | 2020-12-23 | ティコナ・エルエルシー | 低粘度のポリアリーレンスルフィドを形成する方法 |
| WO2016133740A1 (en) | 2015-02-19 | 2016-08-25 | Ticona Llc | Method of polyarylene sulfide precipitation |
| JP6783242B2 (ja) | 2015-03-25 | 2020-11-11 | ティコナ・エルエルシー | 高溶融粘度のポリアリーレンスルフィドを形成する方法 |
| US11407861B2 (en) | 2019-06-28 | 2022-08-09 | Ticona Llc | Method for forming a polyarylene sulfide |
| CN115279734A (zh) | 2019-12-20 | 2022-11-01 | 提克纳有限责任公司 | 形成聚芳硫醚的方法 |
| JP2024535216A (ja) | 2021-09-08 | 2024-09-30 | ティコナ・エルエルシー | ポリアリーレンスルフィド廃棄汚泥から有機溶媒を回収するための逆溶媒技術 |
| WO2023038889A1 (en) | 2021-09-08 | 2023-03-16 | Ticona Llc | Extraction technique for recovering an organic solvent from a polyarylene sulfide waste sludge |
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| US3354129A (en) | 1963-11-27 | 1967-11-21 | Phillips Petroleum Co | Production of polymers from aromatic compounds |
| US3607843A (en) * | 1969-05-16 | 1971-09-21 | Phillips Petroleum Co | Process for making poly (phenylene sulfide) polymers of increased molecular weight |
| US3919177A (en) | 1973-11-19 | 1975-11-11 | Phillips Petroleum Co | P-phenylene sulfide polymers |
| US4415729A (en) | 1982-06-04 | 1983-11-15 | Phillips Petroleum Company | Recovering granular poly(arylene sulfide) particles from a poly(arylene sulfide) reaction mixture |
| US4405767A (en) * | 1982-06-22 | 1983-09-20 | Phillips Petroleum Company | Treatment of poly(arylene sulfide) |
| US4645826A (en) | 1984-06-20 | 1987-02-24 | Kureha Kagaku Kogyo Kabushiki Kaisha | Process for production of high to ultra-high molecular weight linear polyarylenesulfides |
| DE3527492C2 (de) * | 1984-07-31 | 1997-09-11 | Dainippon Ink & Chemicals | Verfahren zur Herstellung eines Polyarylensulfidpolymeren |
| JPS6153325A (ja) * | 1984-08-23 | 1986-03-17 | Toyo Soda Mfg Co Ltd | ポリアリ−レン・サルフアイド反応液スラリ−より溶媒の回収蒸留精製法 |
| JPH0651794B2 (ja) * | 1986-04-28 | 1994-07-06 | 呉羽化学工業株式会社 | Ｎ−メチルピロリドンの回収法 |
| US4730034A (en) * | 1987-01-23 | 1988-03-08 | Phillips Petroleum Company | Recovering poly(arylene sulfide) oligomers from a poly(arylene sulfide) reaction mixture |
| JPH0722645B2 (ja) * | 1988-10-18 | 1995-03-15 | 出光石油化学株式会社 | ポリアリーレンスルフィド製造溶媒の回収方法 |
| JPH0672185B2 (ja) * | 1989-07-17 | 1994-09-14 | 出光石油化学株式会社 | ポリアリーレンスルフィドの製造方法 |
| EP0413257A3 (en) * | 1989-08-14 | 1992-06-03 | The Dow Chemical Company | Cyclic poly(aryl ether) oligomers, a process for preparation thereof, and polymerization of cyclic poly (aryl ether) oligomers |
-
1992
- 1992-06-23 EP EP19920110561 patent/EP0520370A3/en not_active Withdrawn
- 1992-06-23 CA CA 2072165 patent/CA2072165C/en not_active Expired - Fee Related
- 1992-06-23 KR KR1019920010912A patent/KR100189767B1/ko not_active Expired - Fee Related
- 1992-06-24 JP JP16643792A patent/JP2732551B2/ja not_active Expired - Lifetime
- 1992-06-24 TW TW81104971A patent/TW224475B/zh active
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1993
- 1993-08-09 US US08/103,847 patent/US5354841A/en not_active Expired - Fee Related
- 1993-09-13 US US08/120,305 patent/US6281326B1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| KR930000564A (ko) | 1993-01-15 |
| CA2072165C (en) | 2000-09-19 |
| KR100189767B1 (ko) | 1999-06-01 |
| JPH05186593A (ja) | 1993-07-27 |
| TW224475B (enExample) | 1994-06-01 |
| US5354841A (en) | 1994-10-11 |
| EP0520370A2 (en) | 1992-12-30 |
| EP0520370A3 (en) | 1993-01-27 |
| CA2072165A1 (en) | 1992-12-25 |
| US6281326B1 (en) | 2001-08-28 |
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