DE60017068T2 - Verfahren zur Herstellung von amorphen anisotrope Schmelzen bildenden Polymeren mit hoher Dehnbarkeit und nach diesem Verfahren hergestellte Polymere - Google Patents
Verfahren zur Herstellung von amorphen anisotrope Schmelzen bildenden Polymeren mit hoher Dehnbarkeit und nach diesem Verfahren hergestellte Polymere Download PDFInfo
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- DE60017068T2 DE60017068T2 DE60017068T DE60017068T DE60017068T2 DE 60017068 T2 DE60017068 T2 DE 60017068T2 DE 60017068 T DE60017068 T DE 60017068T DE 60017068 T DE60017068 T DE 60017068T DE 60017068 T2 DE60017068 T2 DE 60017068T2
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- XBNGYFFABRKICK-UHFFFAOYSA-N 2,3,4,5,6-pentafluorophenol Chemical compound OC1=C(F)C(F)=C(F)C(F)=C1F XBNGYFFABRKICK-UHFFFAOYSA-N 0.000 description 2
- DNUYOWCKBJFOGS-UHFFFAOYSA-N 2-[[10-(2,2-dicarboxyethyl)anthracen-9-yl]methyl]propanedioic acid Chemical compound C1=CC=C2C(CC(C(=O)O)C(O)=O)=C(C=CC=C3)C3=C(CC(C(O)=O)C(O)=O)C2=C1 DNUYOWCKBJFOGS-UHFFFAOYSA-N 0.000 description 2
- AULKDLUOQCUNOK-UHFFFAOYSA-N 3,5-dichloro-4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC(Cl)=C(O)C(Cl)=C1 AULKDLUOQCUNOK-UHFFFAOYSA-N 0.000 description 2
- QGNLHMKIGMZKJX-UHFFFAOYSA-N 3-chloro-4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C(Cl)=C1 QGNLHMKIGMZKJX-UHFFFAOYSA-N 0.000 description 2
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- 238000009835 boiling Methods 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- IJFXRHURBJZNAO-UHFFFAOYSA-N meta--hydroxybenzoic acid Natural products OC(=O)C1=CC=CC(O)=C1 IJFXRHURBJZNAO-UHFFFAOYSA-N 0.000 description 2
- 238000000386 microscopy Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachloro-phenol Natural products OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
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- 238000002360 preparation method Methods 0.000 description 2
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- JMSVCTWVEWCHDZ-UHFFFAOYSA-N syringic acid Chemical compound COC1=CC(C(O)=O)=CC(OC)=C1O JMSVCTWVEWCHDZ-UHFFFAOYSA-N 0.000 description 2
- CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 2
- AUFZRCJENRSRLY-UHFFFAOYSA-N 2,3,5-trimethylhydroquinone Chemical compound CC1=CC(O)=C(C)C(C)=C1O AUFZRCJENRSRLY-UHFFFAOYSA-N 0.000 description 1
- CZAZXHQSSWRBHT-UHFFFAOYSA-N 2-(2-hydroxyphenyl)-3,4,5,6-tetramethylphenol Chemical compound OC1=C(C)C(C)=C(C)C(C)=C1C1=CC=CC=C1O CZAZXHQSSWRBHT-UHFFFAOYSA-N 0.000 description 1
- LPADJMFUBXMZNL-UHFFFAOYSA-N 4-hydroxy-3-phenylbenzoic acid Chemical compound OC(=O)C1=CC=C(O)C(C=2C=CC=CC=2)=C1 LPADJMFUBXMZNL-UHFFFAOYSA-N 0.000 description 1
- VARPGHCVZGMTLL-UHFFFAOYSA-N 5,7-dichloro-6-hydroxynaphthalene-2-carboxylic acid Chemical compound ClC1=C(O)C(Cl)=CC2=CC(C(=O)O)=CC=C21 VARPGHCVZGMTLL-UHFFFAOYSA-N 0.000 description 1
- MIBYFOLNIIUGNA-UHFFFAOYSA-N 5-chloro-6-hydroxynaphthalene-2-carboxylic acid Chemical compound ClC1=C(O)C=CC2=CC(C(=O)O)=CC=C21 MIBYFOLNIIUGNA-UHFFFAOYSA-N 0.000 description 1
- RHXQHKDRWDVLBY-UHFFFAOYSA-N 6-hydroxy-5-methoxynaphthalene-2-carboxylic acid Chemical compound OC(=O)C1=CC=C2C(OC)=C(O)C=CC2=C1 RHXQHKDRWDVLBY-UHFFFAOYSA-N 0.000 description 1
- XKFNZRZICQABOD-UHFFFAOYSA-N 6-hydroxy-5-methylnaphthalene-2-carboxylic acid Chemical compound OC(=O)C1=CC=C2C(C)=C(O)C=CC2=C1 XKFNZRZICQABOD-UHFFFAOYSA-N 0.000 description 1
- RAAPMEWYFAUSOB-UHFFFAOYSA-N 6-hydroxy-5-phenylnaphthalene-2-carboxylic acid Chemical compound OC=1C=CC2=CC(C(=O)O)=CC=C2C=1C1=CC=CC=C1 RAAPMEWYFAUSOB-UHFFFAOYSA-N 0.000 description 1
- JHXIMYHYJSQGGB-UHFFFAOYSA-N 7-chloro-6-hydroxynaphthalene-2-carboxylic acid Chemical compound C1=C(O)C(Cl)=CC2=CC(C(=O)O)=CC=C21 JHXIMYHYJSQGGB-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- GGWCZBGAIGGTDA-UHFFFAOYSA-N CC(c1ccc(cc(cc2)OC)c2c1)=O Chemical compound CC(c1ccc(cc(cc2)OC)c2c1)=O GGWCZBGAIGGTDA-UHFFFAOYSA-N 0.000 description 1
- LYIIIJNIEDNXSL-UHFFFAOYSA-N CC(c1ccc(cc(cc2)OC)c2c1)=[O-] Chemical compound CC(c1ccc(cc(cc2)OC)c2c1)=[O-] LYIIIJNIEDNXSL-UHFFFAOYSA-N 0.000 description 1
- GGWCZBGAIGGTDA-UHFFFAOYSA-O CC(c1ccc(cc(cc2)OC)c2c1)=[OH+] Chemical compound CC(c1ccc(cc(cc2)OC)c2c1)=[OH+] GGWCZBGAIGGTDA-UHFFFAOYSA-O 0.000 description 1
- NLOAYRCEHHUTDL-UHFFFAOYSA-N C[NH+](CCN[NH+](C)[O-])[O-] Chemical compound C[NH+](CCN[NH+](C)[O-])[O-] NLOAYRCEHHUTDL-UHFFFAOYSA-N 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical class [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000001010 compromised effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000008358 core component Substances 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000009477 glass transition Effects 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
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N hydroquinone methyl ether Natural products COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical class [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
- 239000011654 magnesium acetate Chemical class 0.000 description 1
- 229940069446 magnesium acetate Drugs 0.000 description 1
- 235000011285 magnesium acetate Nutrition 0.000 description 1
- 238000010128 melt processing Methods 0.000 description 1
- QLNWXBAGRTUKKI-UHFFFAOYSA-N metacetamol Chemical compound CC(=O)NC1=CC=CC(O)=C1 QLNWXBAGRTUKKI-UHFFFAOYSA-N 0.000 description 1
- MNZMMCVIXORAQL-UHFFFAOYSA-N naphthalene-2,6-diol Chemical compound C1=C(O)C=CC2=CC(O)=CC=C21 MNZMMCVIXORAQL-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000001632 sodium acetate Chemical class 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- WKOLLVMJNQIZCI-UHFFFAOYSA-N vanillic acid Chemical compound COC1=CC(C(O)=O)=CC=C1O WKOLLVMJNQIZCI-UHFFFAOYSA-N 0.000 description 1
- TUUBOHWZSQXCSW-UHFFFAOYSA-N vanillic acid Natural products COC1=CC(O)=CC(C(O)=O)=C1 TUUBOHWZSQXCSW-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/60—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds
- C08G63/605—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds the hydroxy and carboxylic groups being bound to aromatic rings
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
- Polyamides (AREA)
- Laminated Bodies (AREA)
- Artificial Filaments (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Multicomponent Fibers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US484120 | 2000-01-14 | ||
| US09/484,120 US6132884A (en) | 2000-01-14 | 2000-01-14 | Process for producing amorphous anisotrophic melt-forming polymers having a high degree of stretchability and polymers produced by same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60017068D1 DE60017068D1 (de) | 2005-02-03 |
| DE60017068T2 true DE60017068T2 (de) | 2006-04-20 |
Family
ID=23922825
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60017068T Expired - Lifetime DE60017068T2 (de) | 2000-01-14 | 2000-11-09 | Verfahren zur Herstellung von amorphen anisotrope Schmelzen bildenden Polymeren mit hoher Dehnbarkeit und nach diesem Verfahren hergestellte Polymere |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US6132884A (enExample) |
| EP (1) | EP1116736B1 (enExample) |
| JP (1) | JP4679721B2 (enExample) |
| DE (1) | DE60017068T2 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6294640B1 (en) * | 2000-01-14 | 2001-09-25 | Ticona Llc | Stretchable polymers and shaped articles produced by same |
| US6660182B2 (en) | 2000-09-01 | 2003-12-09 | Ticona Llc | Blends of stretchable liquid crystal polymers with thermoplastics |
| US6666990B2 (en) * | 2001-02-14 | 2003-12-23 | Ticona Llc | Stretchable liquid crystal polymer composition |
| ES2389027T3 (es) * | 2001-06-20 | 2012-10-22 | Daiichi Sankyo Company, Limited | Derivados de diamina |
| US6514611B1 (en) | 2001-08-21 | 2003-02-04 | Ticona Llc | Anisotropic melt-forming polymers having a high degree of stretchability |
| US6989194B2 (en) * | 2002-12-30 | 2006-01-24 | E. I. Du Pont De Nemours And Company | Flame retardant fabric |
| JP4245969B2 (ja) * | 2003-04-24 | 2009-04-02 | ポリプラスチックス株式会社 | 非晶質全芳香族ポリエステルアミド及びその組成物 |
| JP2006008964A (ja) * | 2004-01-22 | 2006-01-12 | Polyplastics Co | 熱可塑性樹脂組成物 |
| WO2005116141A1 (ja) * | 2004-05-26 | 2005-12-08 | Polyplastics Co., Ltd. | 熱可塑性樹脂組成物 |
| KR101595121B1 (ko) * | 2008-12-31 | 2016-02-17 | 심천 워트 어드밴스드 머티리얼즈 주식회사 | 방향족 폴리에스테르 아미드 공중합체, 상기 방향족 폴리에스테르 아미드 공중합체를 채용한 프리프레그와 프리프레그 적층체, 및 상기 프리프레그 또는 프리프레그 적층체를 채용한 금속박 적층판과 프린트 배선판 |
| JP7578505B2 (ja) * | 2021-02-24 | 2024-11-06 | 上野製薬株式会社 | 非晶質ポリエステル樹脂 |
| CN116836374B (zh) * | 2023-02-28 | 2025-03-18 | 珠海万通特种工程塑料有限公司 | 一种液晶聚合物、lcp纤维及其制备方法和应用 |
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| US4318841A (en) * | 1980-10-06 | 1982-03-09 | Celanese Corporation | Polyester of 6-hydroxy-2-naphthoic acid, para-hydroxy benzoic acid, terephthalic acid, and resorcinol capable of readily undergoing melt processing to form shaped articles having increased impact strength |
| US4351918A (en) * | 1981-04-06 | 1982-09-28 | Celanese Corporation | Poly(ester-amide) capable of forming an anisotropic melt phase derived from 6-hydroxy-2-naphthoic acid, other aromatic hydroxyacid, carbocyclic dicarboxylic acid, and aromatic monomer capable of forming an amide linkage |
| US4522974A (en) * | 1982-07-26 | 1985-06-11 | Celanese Corporation | Melt processable polyester capable of forming an anisotropic melt comprising a relatively low concentration of 6-oxy-2-naphthoyl moiety-4-benzoyl moiety, 1,4-dioxyphenylene moiety, isophthaloyl moiety and terephthaloyl moiety |
| US4473682A (en) * | 1982-07-26 | 1984-09-25 | Celanese Corporation | Melt processable polyester capable of forming an anisotropic melt comprising a relatively low concentration of 6-oxy-2-naphthoyl moiety, 4-oxybenzoyl moiety, 4,4'-dioxybiphenyl moiety, and terephthaloyl moiety |
| NL8303028A (nl) * | 1983-08-31 | 1985-03-18 | Stamicarbon | Winning van caprolactam uit caprolactam-bevattend destillatie-residu. |
| JP2664406B2 (ja) * | 1988-04-13 | 1997-10-15 | ポリプラスチックス 株式会社 | 溶融時に光学的異方性を示すポリエステル樹脂及び樹脂組成物 |
| DE3542856A1 (de) * | 1985-12-04 | 1987-06-11 | Basf Ag | Vollaromatische mesomorphe polyesteramide, deren herstellung und verwendung |
| JP2664405B2 (ja) * | 1988-04-13 | 1997-10-15 | ポリプラスチックス 株式会社 | 溶融時に光学的異方性を示すポリエステル樹脂及び樹脂組成物 |
| JP2664404B2 (ja) * | 1988-04-13 | 1997-10-15 | ポリプラスチックス 株式会社 | 溶融時に光学的異方性を示すポリエステル樹脂及び樹脂組成物 |
| JPH0216120A (ja) * | 1988-07-05 | 1990-01-19 | Polyplastics Co | 溶融時に光学的異方性を示すポリエステル樹脂及び樹脂組成物 |
| ES2010297A6 (es) * | 1988-07-27 | 1989-11-01 | Cables Comunicaciones | Un procedimiento para la preparacion de nuevas copoliesteramidas termotropas aromaticas. |
| US5025082A (en) * | 1988-08-24 | 1991-06-18 | Mitsubishi Kasei Corporation | Aromatic polyester, aromatic polyester-amide and processes for producing the same |
| US5089594A (en) * | 1988-10-11 | 1992-02-18 | Amoco Corporation | Wholly aromatic polyester of isophthalic acid, terephthalic acid, p-hydroxybenzoic acid, hydroquinone and an arylene diol |
| JP2847188B2 (ja) * | 1988-11-04 | 1999-01-13 | 住友化学工業株式会社 | 芳香族ポリエステルの製造方法 |
| JPH02276819A (ja) * | 1988-12-29 | 1990-11-13 | Kawasaki Steel Corp | 芳香族ポリエステルおよび芳香族ポリエステルアミドならびにそれらを用いた繊維、樹脂組成物 |
| US5066767A (en) * | 1989-03-01 | 1991-11-19 | Amoco Corporation | Wholly aromatic polyesters comprising isophthalic acid, terephthalic acid, p-hydroxybenzoic acid, hydroquinone and an arylene diol |
| DE3923294A1 (de) * | 1989-07-14 | 1991-01-24 | Bayer Ag | Hochwaermeformbestaendige thermotrope polyester mit guter schlagzaehigkeit, verfahren zu ihrer herstellung sowie ihrer verwendung zur herstellung von formkoerpern, filamenten und folien |
| US5015722A (en) * | 1990-04-04 | 1991-05-14 | Hoechst Celanese Corporation | Melt-processable polyester capable of forming an anisotropic melt which exhibits a highly attractive balance between its molding and heat deflection temperatures |
| KR930005104B1 (ko) * | 1990-08-30 | 1993-06-15 | 한국과학기술연구원 | 액정 폴리에스테르 펄프상 단섬유 |
| JP3099455B2 (ja) * | 1990-10-08 | 2000-10-16 | 住友化学工業株式会社 | 芳香族ポリエステルおよびその製造方法 |
| US5204443A (en) * | 1991-04-19 | 1993-04-20 | Hoechst Celanese Corp. | Melt processable poly(ester-amide) capable of forming an anisotropic melt containing an aromatic moiety capable of forming an amide linkage |
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| US5656714A (en) * | 1995-06-02 | 1997-08-12 | Hoechst Celanese Corp. | Polyester from terephthalic acid, 6-hydroxy-2-naphthoic acid, 4-hydroxybenzoic acid, 4,4'-biphenol and resorcinol |
| US5798432A (en) * | 1996-03-22 | 1998-08-25 | Hoechst Celanese Corp. | Method of making thermotropic liquid crystalline polymers containing hydroquinone |
| DE19612973A1 (de) * | 1996-04-01 | 1997-10-02 | Hoechst Ag | LCP-Blends |
| US6312772B1 (en) * | 1997-10-20 | 2001-11-06 | Hoechst Celanese Corporation | Multilayer laminate formed from a substantially stretched non-molten wholly aromatic liquid crystalline polymer and non-polyester thermoplastic polymer |
| US6268026B1 (en) * | 1997-10-20 | 2001-07-31 | Hoechst Celanese Corporation | Multilayer laminate formed from a substantially stretched non-molten wholly aromatic liquid crystalline polymer and non-liquid crystalline polyester and method for forming same |
| US6426128B1 (en) * | 1998-01-06 | 2002-07-30 | Hna Holdings, Inc. | Co-processable multi-layer laminates for forming high strength, haze-free, transparent articles and methods of producing same |
| WO2000068291A1 (en) * | 1999-05-07 | 2000-11-16 | Kabushiki Kaisha Ueno Seiyaku Oyo Kenkyujo | Liquid-crystal polymer |
-
2000
- 2000-01-14 US US09/484,120 patent/US6132884A/en not_active Expired - Lifetime
- 2000-11-09 DE DE60017068T patent/DE60017068T2/de not_active Expired - Lifetime
- 2000-11-09 EP EP00309971A patent/EP1116736B1/en not_active Expired - Lifetime
- 2000-12-27 JP JP2000396452A patent/JP4679721B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP1116736A3 (en) | 2001-11-07 |
| US6132884A (en) | 2000-10-17 |
| EP1116736A2 (en) | 2001-07-18 |
| JP2001226471A (ja) | 2001-08-21 |
| JP4679721B2 (ja) | 2011-04-27 |
| EP1116736B1 (en) | 2004-12-29 |
| DE60017068D1 (de) | 2005-02-03 |
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