JP3164218B2 - 静電気に用いるための連鎖延長された低分子量ポリオキシラン - Google Patents
静電気に用いるための連鎖延長された低分子量ポリオキシランInfo
- Publication number
- JP3164218B2 JP3164218B2 JP50333691A JP50333691A JP3164218B2 JP 3164218 B2 JP3164218 B2 JP 3164218B2 JP 50333691 A JP50333691 A JP 50333691A JP 50333691 A JP50333691 A JP 50333691A JP 3164218 B2 JP3164218 B2 JP 3164218B2
- Authority
- JP
- Japan
- Prior art keywords
- polymer
- electrostatic dissipative
- molecular weight
- moles
- low molecular
- 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
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- -1 vinyl halide Chemical class 0.000 claims description 14
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- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 claims 1
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- 239000011159 matrix material Substances 0.000 abstract 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 16
- 239000000463 material Substances 0.000 description 16
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 15
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- 125000004432 carbon atom Chemical group C* 0.000 description 7
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 7
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- 239000005059 1,4-Cyclohexyldiisocyanate Substances 0.000 description 2
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- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
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- XJELOQYISYPGDX-UHFFFAOYSA-N ethenyl 2-chloroacetate Chemical compound ClCC(=O)OC=C XJELOQYISYPGDX-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229920005621 immiscible polymer blend Polymers 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 238000004377 microelectronic Methods 0.000 description 1
- UTSYWKJYFPPRAP-UHFFFAOYSA-N n-(butoxymethyl)prop-2-enamide Chemical compound CCCCOCNC(=O)C=C UTSYWKJYFPPRAP-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229940065472 octyl acrylate Drugs 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical compound C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229940100474 polyethylene glycol 1450 Drugs 0.000 description 1
- 229940057838 polyethylene glycol 4000 Drugs 0.000 description 1
- 229940057847 polyethylene glycol 600 Drugs 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010558 suspension polymerization method Methods 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/16—Anti-static materials
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4833—Polyethers containing oxyethylene units
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or 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 halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or 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 halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or 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 halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S524/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S524/91—Antistatic compositions
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/932—Blend of matched optical properties
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyesters Or Polycarbonates (AREA)
- Epoxy Compounds (AREA)
- Polyurethanes Or Polyureas (AREA)
- Polyethers (AREA)
- Laminated Bodies (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 |
|---|---|---|---|
| US46160690A | 1990-01-05 | 1990-01-05 | |
| US461,606 | 1990-01-05 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05506464A JPH05506464A (ja) | 1993-09-22 |
| JP3164218B2 true JP3164218B2 (ja) | 2001-05-08 |
Family
ID=23833253
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50333691A Expired - Lifetime JP3164218B2 (ja) | 1990-01-05 | 1991-01-02 | 静電気に用いるための連鎖延長された低分子量ポリオキシラン |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US5342889A (https=) |
| EP (1) | EP0507873B1 (https=) |
| JP (1) | JP3164218B2 (https=) |
| AT (1) | ATE121115T1 (https=) |
| BR (1) | BR9105924A (https=) |
| CA (1) | CA2073171C (https=) |
| DE (1) | DE69108895T2 (https=) |
| DK (1) | DK0507873T3 (https=) |
| ES (1) | ES2073736T3 (https=) |
| GR (1) | GR3015761T3 (https=) |
| NO (1) | NO922646L (https=) |
| TW (1) | TW203082B (https=) |
| WO (1) | WO1991009906A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20140027283A (ko) * | 2011-04-21 | 2014-03-06 | 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 | 정전기 소산성 폴리카보네이트 조성물 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5574104A (en) * | 1990-01-05 | 1996-11-12 | The B. F. Goodrich Company | Chain extended low molecular weight polyoxiranes and electrostatic dissipating blend compositions based thereon |
| ATE148718T1 (de) * | 1991-06-20 | 1997-02-15 | Goodrich Co B F | Kettenverlängerte polyethylenglycole mit einem niedrigen molekulargewicht als antistatika in polymeren zusammensetzungen |
| US5298558A (en) * | 1991-06-25 | 1994-03-29 | The Geon Company | Electrostatic dissipative blends of PVC, polyetheramides and an impact modifier |
| CA2085266A1 (en) * | 1991-12-20 | 1993-06-21 | Biing-Lin Lee | Chain extended low molecular weight polyoxirane salt complexes for electrostatic applications |
| CA2088338A1 (en) * | 1992-01-29 | 1993-07-30 | Peter Malcolm Goman | Anti-static agent for thermoplastic polymers |
| US5785049A (en) | 1994-09-21 | 1998-07-28 | Inhale Therapeutic Systems | Method and apparatus for dispersion of dry powder medicaments |
| WO1996006875A1 (en) * | 1994-09-01 | 1996-03-07 | W.L. Gore & Associates, Inc. | Hydrophilic polyurethane |
| US6284839B1 (en) | 1995-12-29 | 2001-09-04 | The B.F. Goodrich Company | Blends of thermoplastic polymers, electrostatic dissipative polymers and electrostatic dissipative enhancers |
| US5914191A (en) * | 1996-05-03 | 1999-06-22 | Eastman Chemical Company | Multilayered packaging materials for electrostatic applications |
| JP3546614B2 (ja) | 1996-10-07 | 2004-07-28 | ソニー株式会社 | ディスクカートリッジ |
| US5863466A (en) * | 1997-02-06 | 1999-01-26 | Mor; Ebrahim | Electrostatic dissipative composition |
| US6140405A (en) * | 1998-09-21 | 2000-10-31 | The B. F. Goodrich Company | Salt-modified electrostatic dissipative polymers |
| US6440540B1 (en) | 1998-12-03 | 2002-08-27 | Eastman Kodak Company | Electrophotographic toner receiving material |
| DE69906367T2 (de) | 1998-12-03 | 2003-12-18 | Eastman Kodak Co., Rochester | Elektrofotografisches Tonerempfangsmaterial |
| US6730401B2 (en) | 2001-03-16 | 2004-05-04 | Eastman Chemical Company | Multilayered packaging materials for electrostatic applications |
| US6740410B2 (en) * | 2001-05-16 | 2004-05-25 | Noveon Ip Holdings Corp. | Electrostatic dissipating polymeric multi-layer article or laminate |
| US20040176537A1 (en) * | 2001-10-16 | 2004-09-09 | Armentrout Rodney Scott | Inherently electrostatic dissipating block copolymer compositions |
| DE60329921D1 (de) * | 2002-09-13 | 2009-12-17 | Cerex Advanced Fabrics Inc | Verfahren zur reduzierung von statischen ladungen in einem spunbondverfahren |
| US7175904B2 (en) * | 2003-08-28 | 2007-02-13 | Congoleum Corporation | Non-vinyl flooring and method for making same |
| KR20080043424A (ko) * | 2006-11-14 | 2008-05-19 | 삼성전자주식회사 | 대전방지제 조성물 및 이를 이용한 반송용 롤러 제조방법 |
| US8357766B2 (en) | 2008-10-08 | 2013-01-22 | Evonik Stockhausen Gmbh | Continuous process for the production of a superabsorbent polymer |
| US8063121B2 (en) * | 2008-10-08 | 2011-11-22 | Evonik Stockhausen Gmbh | Process for the production of a superabsorbent polymer |
| US8048942B2 (en) * | 2008-10-08 | 2011-11-01 | Evonik Stockhausen Gmbh | Process for the production of a superabsorbent polymer |
| US8413914B2 (en) | 2010-03-04 | 2013-04-09 | Hanson Group, Llc | Electrostatic fast-set sprayable polymer system and process |
| US8980415B2 (en) | 2010-12-03 | 2015-03-17 | Benoit Ambroise | Antistatic films and methods to manufacture the same |
| US8861167B2 (en) | 2011-05-12 | 2014-10-14 | Global Plasma Solutions, Llc | Bipolar ionization device |
| CN102585479B (zh) * | 2011-12-26 | 2014-04-09 | 金发科技股份有限公司 | 一种耐磨无卤阻燃弹性体复合物及其制备方法 |
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| US2353228A (en) * | 1941-08-01 | 1944-07-11 | Bakelite Corp | Polystyrene molding composition |
| US2948691A (en) * | 1951-05-10 | 1960-08-09 | Mobay Chemical Corp | High molecular weight polyether urethane polymers |
| NL82533C (https=) * | 1952-11-19 | |||
| US3049505A (en) * | 1958-09-24 | 1962-08-14 | Borg Warner | Mechanical blend of a polyurethane rubber with blends of a graft copolymer of polybutadiene, styrene, and acrylonitrile |
| US3425981A (en) * | 1965-02-12 | 1969-02-04 | Union Carbide Corp | Olefin polymer compositions containing ethylene oxide polymers having a molecular weight of from 100,000 to 10 million |
| GB1154800A (en) * | 1967-02-17 | 1969-06-11 | Monsanto Soc | Resin Compositions |
| CA938388A (en) * | 1969-04-24 | 1973-12-11 | Kimura Isao | Synthetic thermoplastic fiber-forming polymer having durable anti-electrostatic and hydrophilic properties and its fibers |
| US3660010A (en) * | 1969-12-17 | 1972-05-02 | Nat Starch Chem Corp | Treating textiles with soil release agents |
| US3706710A (en) * | 1970-12-31 | 1972-12-19 | Hooker Chemical Corp | Process for preparing discoloration-resistant curable polyurethane coatings |
| US4093676A (en) * | 1971-09-01 | 1978-06-06 | Basf Wyandotte Corporation | Antistatic agents for melt-formed polymers |
| US3923924A (en) * | 1973-03-14 | 1975-12-02 | Allied Chem | Antistatic fiber containing chain-extended tetrols based on diamines |
| US3876725A (en) * | 1973-03-14 | 1975-04-08 | Allied Chem | Antistatic fiber containing chain-extended tetrols based on diamines |
| US3887644A (en) * | 1973-10-18 | 1975-06-03 | Allied Chem | Antistatic polyamide fiber |
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| US4051196A (en) * | 1975-05-27 | 1977-09-27 | Allied Chemical Corporation | Antistatic fiber containing chain-extended tetrols based on diamines |
| JPS5318656A (en) * | 1976-08-05 | 1978-02-21 | Mitsui Toatsu Chem Inc | Vinyl chloride resin composition |
| DE2656927C2 (de) * | 1976-12-16 | 1983-03-03 | Akzo Gmbh, 5600 Wuppertal | Gleitmittel aus Polyalkylenoxiden für die formgebende Verarbeitung von Kunststoffen |
| US4230827A (en) * | 1978-12-06 | 1980-10-28 | Rohm And Haas Company | Ethylene oxide polymers as impact modifiers for PVC |
| US4499124A (en) * | 1978-12-15 | 1985-02-12 | Hospal-Sodip, S.A. | Process of coating consisting of a mixture of vinyl chloride polymer and polyurethane with tertiary amine and/or ammonium groups |
| DE2916668A1 (de) * | 1979-04-25 | 1980-11-13 | Basf Ag | Formmassen, enthaltend styrolacrylnitril-copolymerisate und aethylenoxid-/pro- pylenoxid-dreiblockcopolymerisate, verwendung derselben und formteile aus solchen mischungen |
| JPS58157861A (ja) * | 1982-03-16 | 1983-09-20 | Toyo Rubber Chem Ind Co Ltd | 無帯電性合成樹脂 |
| US4379913A (en) * | 1982-05-04 | 1983-04-12 | Diamond Shamrock Corporation | Compositions useful as internal antistatic additives for polymeric structures |
| US4408013A (en) * | 1982-05-24 | 1983-10-04 | The B. F. Goodrich Company | Epihalohydrin polymer cure systems |
| US4543390A (en) * | 1984-12-20 | 1985-09-24 | Toray Industries, Inc. | Antistatic resinous compositions |
| US4588773A (en) * | 1984-12-21 | 1986-05-13 | Borg-Warner Chemicals, Inc. | Antistatic thermoplastic composition |
| JPS61146802A (ja) * | 1984-12-21 | 1986-07-04 | ダイヤゴム株式会社 | 透湿性且つ耐油性作業用手袋およびその製造方法 |
| US4775716A (en) * | 1984-12-21 | 1988-10-04 | Borg-Warner Chemicals, Inc. | Antistatic thermoplastic composition |
| US4719263A (en) * | 1985-05-10 | 1988-01-12 | The B. F. Goodrich Company | Antistatic plastic materials containing epihalohydrin polymers |
| ATE75709T1 (de) * | 1985-08-20 | 1992-05-15 | Smith & Nephew | Beschichtete gegenstaende und verfahren zu ihrer herstellung. |
| US4751118A (en) * | 1985-08-26 | 1988-06-14 | The B. F. Goodrich Company | Clear polyvinyl chloride articles and compositions |
| EP0282985A3 (en) * | 1987-03-20 | 1990-09-19 | The B.F. Goodrich Company | A polymer of ethylene oxide and epihalohydrin as an antistatic additive |
| US4931506A (en) * | 1987-03-20 | 1990-06-05 | The B. F. Goodrich Company | Ethylene oxide/epihalohydrin copolymer antistatic additive for chlorine-containing polymers |
| US4912142A (en) * | 1987-04-15 | 1990-03-27 | The Dow Chemical Company | Antistatic phase-segregated polyurethanes |
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| JPH0725976B2 (ja) * | 1987-06-16 | 1995-03-22 | 東レ株式会社 | 熱可塑性樹脂組成物 |
| US4906681A (en) * | 1987-07-22 | 1990-03-06 | Sherex Chemical Company, Inc. | Anti-stat for polyvinyl chloride polymers |
| US5096995A (en) * | 1987-08-13 | 1992-03-17 | Toray Industries, Inc. | Polyether-ester amide and permanently antistatic resin composition |
| AU2812389A (en) * | 1987-10-14 | 1989-05-23 | Tyndale Plains-Hunter Ltd. | Moisture sensitive elastomer compositions |
| US5077330A (en) * | 1988-08-29 | 1991-12-31 | Armstrong World Industries, Inc. | Conductive polyurethane-urea/polyethylene oxide |
| US4990357A (en) * | 1989-05-04 | 1991-02-05 | Becton, Dickinson And Company | Elastomeric segmented hydrophilic polyetherurethane based lubricious coatings |
-
1991
- 1991-01-02 CA CA002073171A patent/CA2073171C/en not_active Expired - Lifetime
- 1991-01-02 WO PCT/US1991/000047 patent/WO1991009906A1/en not_active Ceased
- 1991-01-02 DK DK91903022.1T patent/DK0507873T3/da active
- 1991-01-02 JP JP50333691A patent/JP3164218B2/ja not_active Expired - Lifetime
- 1991-01-02 BR BR919105924A patent/BR9105924A/pt not_active Application Discontinuation
- 1991-01-02 ES ES91903022T patent/ES2073736T3/es not_active Expired - Lifetime
- 1991-01-02 DE DE69108895T patent/DE69108895T2/de not_active Expired - Lifetime
- 1991-01-02 AT AT91903022T patent/ATE121115T1/de not_active IP Right Cessation
- 1991-01-02 EP EP91903022A patent/EP0507873B1/en not_active Expired - Lifetime
- 1991-07-10 US US07/729,865 patent/US5342889A/en not_active Expired - Lifetime
-
1992
- 1992-07-03 NO NO92922646A patent/NO922646L/no unknown
- 1992-07-27 TW TW081105917A patent/TW203082B/zh not_active IP Right Cessation
-
1995
- 1995-04-13 GR GR940402417T patent/GR3015761T3/el unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20140027283A (ko) * | 2011-04-21 | 2014-03-06 | 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 | 정전기 소산성 폴리카보네이트 조성물 |
| KR102040086B1 (ko) | 2011-04-21 | 2019-11-04 | 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 | 정전기 소산성 폴리카보네이트 조성물 |
Also Published As
| Publication number | Publication date |
|---|---|
| ATE121115T1 (de) | 1995-04-15 |
| DK0507873T3 (da) | 1995-07-03 |
| EP0507873A1 (en) | 1992-10-14 |
| NO922646L (no) | 1992-08-27 |
| JPH05506464A (ja) | 1993-09-22 |
| NO922646D0 (no) | 1992-07-03 |
| WO1991009906A1 (en) | 1991-07-11 |
| EP0507873B1 (en) | 1995-04-12 |
| BR9105924A (pt) | 1992-11-10 |
| DE69108895T2 (de) | 1995-08-24 |
| DE69108895D1 (de) | 1995-05-18 |
| CA2073171A1 (en) | 1991-07-06 |
| CA2073171C (en) | 2002-10-29 |
| US5342889A (en) | 1994-08-30 |
| ES2073736T3 (es) | 1995-08-16 |
| TW203082B (https=) | 1993-04-01 |
| GR3015761T3 (en) | 1995-07-31 |
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