JPH0541651B2 - - Google Patents
Info
- Publication number
- JPH0541651B2 JPH0541651B2 JP61501268A JP50126886A JPH0541651B2 JP H0541651 B2 JPH0541651 B2 JP H0541651B2 JP 61501268 A JP61501268 A JP 61501268A JP 50126886 A JP50126886 A JP 50126886A JP H0541651 B2 JPH0541651 B2 JP H0541651B2
- Authority
- JP
- Japan
- Prior art keywords
- polymers
- polymer
- bis
- examples
- biphenyl
- 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
- 229920000642 polymer Polymers 0.000 claims abstract 54
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims abstract 23
- 235000010290 biphenyl Nutrition 0.000 claims abstract 14
- 239000004305 biphenyl Substances 0.000 claims abstract 14
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims 14
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims 14
- 238000000034 method Methods 0.000 claims 11
- 239000002904 solvent Substances 0.000 claims 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 9
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims 9
- -1 4-chlorophenylsulfonyl Chemical group 0.000 claims 8
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 claims 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 6
- 229920000110 poly(aryl ether sulfone) Polymers 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 6
- 125000006267 biphenyl group Chemical group 0.000 claims 5
- 238000006243 chemical reaction Methods 0.000 claims 5
- 150000001875 compounds Chemical class 0.000 claims 5
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical group [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims 5
- OZUNPRDEUXITBO-UHFFFAOYSA-N 1-(4-chlorophenyl)sulfonyl-4-[4-(4-chlorophenyl)sulfonylphenyl]benzene Chemical group C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC=C(C=2C=CC(=CC=2)S(=O)(=O)C=2C=CC(Cl)=CC=2)C=C1 OZUNPRDEUXITBO-UHFFFAOYSA-N 0.000 claims 4
- 230000015271 coagulation Effects 0.000 claims 4
- 238000005345 coagulation Methods 0.000 claims 4
- 238000001914 filtration Methods 0.000 claims 4
- 239000003880 polar aprotic solvent Substances 0.000 claims 4
- 238000006116 polymerization reaction Methods 0.000 claims 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
- 229910000288 alkali metal carbonate Inorganic materials 0.000 claims 3
- 150000008041 alkali metal carbonates Chemical class 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 235000011181 potassium carbonates Nutrition 0.000 claims 3
- 239000011541 reaction mixture Substances 0.000 claims 3
- 150000003457 sulfones Chemical class 0.000 claims 3
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 claims 2
- BXAVKNRWVKUTLY-UHFFFAOYSA-N 4-sulfanylphenol Chemical compound OC1=CC=C(S)C=C1 BXAVKNRWVKUTLY-UHFFFAOYSA-N 0.000 claims 2
- 229930185605 Bisphenol Natural products 0.000 claims 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 239000006227 byproduct Substances 0.000 claims 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 claims 2
- 229920001577 copolymer Polymers 0.000 claims 2
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 claims 2
- 239000011521 glass Substances 0.000 claims 2
- 230000009477 glass transition Effects 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 229920002492 poly(sulfone) Polymers 0.000 claims 2
- 229910000027 potassium carbonate Inorganic materials 0.000 claims 2
- 239000012429 reaction media Substances 0.000 claims 2
- 235000012239 silicon dioxide Nutrition 0.000 claims 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims 2
- 239000011877 solvent mixture Substances 0.000 claims 2
- HHVIBTZHLRERCL-UHFFFAOYSA-N sulfonyldimethane Chemical compound CS(C)(=O)=O HHVIBTZHLRERCL-UHFFFAOYSA-N 0.000 claims 2
- MBDUIEKYVPVZJH-UHFFFAOYSA-N 1-ethylsulfonylethane Chemical compound CCS(=O)(=O)CC MBDUIEKYVPVZJH-UHFFFAOYSA-N 0.000 claims 1
- ZDULHUHNYHJYKA-UHFFFAOYSA-N 2-propan-2-ylsulfonylpropane Chemical compound CC(C)S(=O)(=O)C(C)C ZDULHUHNYHJYKA-UHFFFAOYSA-N 0.000 claims 1
- GPAPPPVRLPGFEQ-UHFFFAOYSA-N 4,4'-dichlorodiphenyl sulfone Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC=C(Cl)C=C1 GPAPPPVRLPGFEQ-UHFFFAOYSA-N 0.000 claims 1
- 229910021532 Calcite Inorganic materials 0.000 claims 1
- 229920000049 Carbon (fiber) Polymers 0.000 claims 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 229920000742 Cotton Polymers 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- 229910000831 Steel Inorganic materials 0.000 claims 1
- 239000012963 UV stabilizer Substances 0.000 claims 1
- 238000002441 X-ray diffraction Methods 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001447 alkali salts Chemical class 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000005037 alkyl phenyl group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- 239000000010 aprotic solvent Substances 0.000 claims 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- WYLQRHZSKIDFEP-UHFFFAOYSA-N benzene-1,4-dithiol Chemical compound SC1=CC=C(S)C=C1 WYLQRHZSKIDFEP-UHFFFAOYSA-N 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 claims 1
- IFVTZJHWGZSXFD-UHFFFAOYSA-N biphenylene Chemical group C1=CC=C2C3=CC=CC=C3C2=C1 IFVTZJHWGZSXFD-UHFFFAOYSA-N 0.000 claims 1
- 230000005587 bubbling Effects 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- QXJJQWWVWRCVQT-UHFFFAOYSA-K calcium;sodium;phosphate Chemical compound [Na+].[Ca+2].[O-]P([O-])([O-])=O QXJJQWWVWRCVQT-UHFFFAOYSA-K 0.000 claims 1
- 239000004917 carbon fiber Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000004927 clay Substances 0.000 claims 1
- 229910052570 clay Inorganic materials 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 230000000052 comparative effect Effects 0.000 claims 1
- 230000006835 compression Effects 0.000 claims 1
- 238000007906 compression Methods 0.000 claims 1
- 238000007796 conventional method Methods 0.000 claims 1
- 238000002425 crystallisation Methods 0.000 claims 1
- 230000008025 crystallization Effects 0.000 claims 1
- CCAFPWNGIUBUSD-UHFFFAOYSA-N diethyl sulfoxide Chemical compound CCS(=O)CC CCAFPWNGIUBUSD-UHFFFAOYSA-N 0.000 claims 1
- 239000010459 dolomite Substances 0.000 claims 1
- 229910000514 dolomite Inorganic materials 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 239000000835 fiber Substances 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 239000003365 glass fiber Substances 0.000 claims 1
- 239000012760 heat stabilizer Substances 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 229920006158 high molecular weight polymer Polymers 0.000 claims 1
- 239000012510 hollow fiber Substances 0.000 claims 1
- 150000002430 hydrocarbons Chemical group 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 229940050176 methyl chloride Drugs 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000010445 mica Substances 0.000 claims 1
- 229910052618 mica group Inorganic materials 0.000 claims 1
- 239000012764 mineral filler Substances 0.000 claims 1
- 238000000465 moulding Methods 0.000 claims 1
- 125000004957 naphthylene group Chemical group 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 235000006408 oxalic acid Nutrition 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 239000004014 plasticizer Substances 0.000 claims 1
- 238000006068 polycondensation reaction Methods 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011736 potassium bicarbonate Substances 0.000 claims 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims 1
- 235000015497 potassium bicarbonate Nutrition 0.000 claims 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims 1
- 238000005381 potential energy Methods 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 238000003825 pressing Methods 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000010453 quartz Substances 0.000 claims 1
- 238000011084 recovery Methods 0.000 claims 1
- 238000010992 reflux Methods 0.000 claims 1
- 239000012783 reinforcing fiber Substances 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 150000004760 silicates Chemical class 0.000 claims 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 1
- 235000011182 sodium carbonates Nutrition 0.000 claims 1
- 238000000935 solvent evaporation Methods 0.000 claims 1
- 239000010959 steel Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 239000000454 talc Substances 0.000 claims 1
- 229910052623 talc Inorganic materials 0.000 claims 1
- ISXOBTBCNRIIQO-UHFFFAOYSA-N tetrahydrothiophene 1-oxide Chemical compound O=S1CCCC1 ISXOBTBCNRIIQO-UHFFFAOYSA-N 0.000 claims 1
- 239000004408 titanium dioxide Substances 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- 239000010456 wollastonite Substances 0.000 claims 1
- 229910052882 wollastonite Inorganic materials 0.000 claims 1
- 239000008096 xylene Substances 0.000 claims 1
- 229920000090 poly(aryl ether) Polymers 0.000 abstract 1
- 125000001174 sulfone group Chemical group 0.000 abstract 1
Classifications
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
-
- 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
-
- 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
- C08G75/20—Polysulfones
- C08G75/23—Polyethersulfones
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyethers (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Polyesters Or Polycarbonates (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Insulating Materials (AREA)
- Materials For Medical Uses (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US70123485A | 1985-02-13 | 1985-02-13 | |
| US701234 | 1991-05-16 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62502407A JPS62502407A (ja) | 1987-09-17 |
| JPH0541651B2 true JPH0541651B2 (OSRAM) | 1993-06-24 |
Family
ID=24816541
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61501268A Granted JPS62502407A (ja) | 1985-02-13 | 1986-02-12 | ポリアリ−ルエ−テルスルホン重合体 |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP0213179B1 (OSRAM) |
| JP (1) | JPS62502407A (OSRAM) |
| KR (1) | KR870700228A (OSRAM) |
| AT (1) | ATE51880T1 (OSRAM) |
| CA (1) | CA1250693A (OSRAM) |
| DE (1) | DE3670302D1 (OSRAM) |
| WO (1) | WO1986004906A1 (OSRAM) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4755556A (en) * | 1985-02-13 | 1988-07-05 | Amoco Corporation | Thermoplastic composites comprising a polyaryl ether sulphone matrix resin |
| RU2007134432A (ru) * | 2005-02-16 | 2009-03-27 | СОЛВЕЙ ЭДВАНСТ ПОЛИМЕРС, Эл.Эл.Си. (US) | Материал на основе простого полиэфира арилсульфона и его применение |
| US7273919B1 (en) | 2005-11-21 | 2007-09-25 | General Electric Company | High heat polyethersulfone compositions |
| JP5703645B2 (ja) * | 2009-09-29 | 2015-04-22 | 住友化学株式会社 | 芳香族ポリスルホン樹脂及びその膜 |
| CN101704951B (zh) * | 2009-10-27 | 2012-01-25 | 金发科技股份有限公司 | 聚联苯砜醚与聚醚砜三元共聚物的制备方法 |
| CN101735459B (zh) * | 2009-12-23 | 2012-01-25 | 金发科技股份有限公司 | 聚联苯醚砜与聚联苯醚联苯砜三元共聚物的制备方法 |
| BR112013030102A2 (pt) * | 2011-05-25 | 2016-09-20 | Solvay Specialty Polymers Usa | polímeros com atividade estrogênica reduzida |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1348630A (en) * | 1970-08-19 | 1974-03-20 | Ici Ltd | Aromatic polymers |
| CH555382A (de) * | 1971-04-26 | 1974-10-31 | Inventa Ag | Verfahren zur herstellung von polymeren verbindungen. |
| GB1569603A (en) * | 1976-07-28 | 1980-06-18 | Ici Ltd | Production of aromatic polyethers |
| GB1588331A (en) * | 1977-03-14 | 1981-04-23 | Ici Ltd | Production of aromatic polyethers |
| EP0010868A3 (en) * | 1978-10-27 | 1980-06-11 | Imperial Chemical Industries Plc | Production of aromatic polyethers |
| US4331798A (en) * | 1979-01-18 | 1982-05-25 | Imperial Chemical Industries Limited | Production of aromatic polyethers with infusible particulate substance |
-
1986
- 1986-01-28 CA CA000500510A patent/CA1250693A/en not_active Expired
- 1986-02-12 AT AT86901610T patent/ATE51880T1/de active
- 1986-02-12 EP EP86901610A patent/EP0213179B1/en not_active Expired - Lifetime
- 1986-02-12 JP JP61501268A patent/JPS62502407A/ja active Granted
- 1986-02-12 DE DE8686901610T patent/DE3670302D1/de not_active Revoked
- 1986-02-12 KR KR1019860700702A patent/KR870700228A/ko not_active Withdrawn
- 1986-02-12 WO PCT/US1986/000293 patent/WO1986004906A1/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| KR870700228A (ko) | 1987-05-30 |
| EP0213179B1 (en) | 1990-04-11 |
| ATE51880T1 (de) | 1990-04-15 |
| EP0213179A1 (en) | 1987-03-11 |
| CA1250693A (en) | 1989-02-28 |
| DE3670302D1 (en) | 1990-05-17 |
| WO1986004906A1 (en) | 1986-08-28 |
| JPS62502407A (ja) | 1987-09-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP4842434B2 (ja) | 改良されたポリ（ビフェニルエーテルスルホン） | |
| EP0113112B1 (en) | Use of an aromatic amorphous thermoplastic polymer | |
| JPS6328927B2 (OSRAM) | ||
| EP0121257B1 (en) | Polyarylnitrile polymers and a method for their production | |
| US20050113558A1 (en) | Polyethersulfone composition, method of making and articles therefrom | |
| JP2664180B2 (ja) | 結晶質ボリアリールエーテルおよびその製造法 | |
| JPS61221227A (ja) | ポリ（アリールエーテルケトン）の改良製造方法 | |
| US4794155A (en) | Process for forming arylether polymers | |
| AU600441B2 (en) | Block polymers containing a poly(aryl ether ketone) | |
| JPH0541651B2 (OSRAM) | ||
| EP1773913B1 (en) | Polysulfone-polyether blockcopolymers, process to synthesize it, membranes made therefrom | |
| EP0303337A2 (en) | Thermoplastic composites comprising a polyaryl ether sulphone matrix resin | |
| JPS62116628A (ja) | アルカリ若しくはアルカリ土類金属塩の存在でのポリ（アリ−ルエ−テルケトン）の製造 | |
| US4785072A (en) | Polyaryl ether sulphones | |
| EP0047999B1 (en) | Use of aromatic amorphous thermoplastic polymers for the production of molded articles | |
| US3939119A (en) | Aromatic polyether-polythioether-polysulfone thermoplastics | |
| EP0213178B1 (en) | Polyaryl ether sulphone polymers | |
| JPS6040454B2 (ja) | ポリアリ−レンポリエ−テルスルホンの改良重合方法 | |
| JP2657827B2 (ja) | 熱安定性の優れた芳香族ポリエーテル | |
| JPS6227434A (ja) | ケト基含有の単一−および共重合体ポリアリ−レンスルフイド並びにその製造方法 | |
| EP0555290B1 (en) | Aryl-ether-sulphone monomers and aryl-ether-ketone-sulphone polymers | |
| JPH0269527A (ja) | 新規の芳香剤ポリエーテルスルホン、その製造方法およびその使用 | |
| JPH02173120A (ja) | 芳香族ポリエーテルケトンの製造方法 | |
| US4912192A (en) | Polyarylnitrile polymers and a method for their production | |
| JPH01141912A (ja) | 芳香族ポリエーテルスホンの製造方法 |