ZA200300760B - Compositions adapted for chain linking. - Google Patents
Compositions adapted for chain linking. Download PDFInfo
- Publication number
- ZA200300760B ZA200300760B ZA200300760A ZA200300760A ZA200300760B ZA 200300760 B ZA200300760 B ZA 200300760B ZA 200300760 A ZA200300760 A ZA 200300760A ZA 200300760 A ZA200300760 A ZA 200300760A ZA 200300760 B ZA200300760 B ZA 200300760B
- Authority
- ZA
- South Africa
- Prior art keywords
- polymer
- chain
- temperature
- linking
- composition
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 157
- 229920000642 polymer Polymers 0.000 claims abstract description 272
- 238000000034 method Methods 0.000 claims abstract description 58
- 125000003118 aryl group Chemical group 0.000 claims abstract description 40
- 230000008569 process Effects 0.000 claims abstract description 36
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- 239000002131 composite material Substances 0.000 claims abstract description 17
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- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 14
- 238000006243 chemical reaction Methods 0.000 claims description 46
- 239000002904 solvent Substances 0.000 claims description 46
- 229920005989 resin Polymers 0.000 claims description 40
- 239000011347 resin Substances 0.000 claims description 40
- 239000000243 solution Substances 0.000 claims description 31
- 239000000835 fiber Substances 0.000 claims description 24
- 239000000178 monomer Substances 0.000 claims description 24
- 238000012545 processing Methods 0.000 claims description 24
- 150000001412 amines Chemical class 0.000 claims description 22
- 238000007493 shaping process Methods 0.000 claims description 21
- 239000000047 product Substances 0.000 claims description 20
- 239000002243 precursor Substances 0.000 claims description 19
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- 239000000126 substance Substances 0.000 claims description 17
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- RXNYJUSEXLAVNQ-UHFFFAOYSA-N 4,4'-Dihydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1 RXNYJUSEXLAVNQ-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
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- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
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- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
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- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
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- MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
- 125000006836 terphenylene group Chemical group 0.000 description 1
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- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
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Classifications
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- 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
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
-
- 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
-
- 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
- C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L81/00—Compositions 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; Compositions of polysulfones; Compositions of derivatives of such polymers
- C08L81/06—Polysulfones; Polyethersulfones
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Reinforced Plastic Materials (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Lubricants (AREA)
- Graft Or Block Polymers (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Fertilizers (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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GBGB0020620.1A GB0020620D0 (en) | 2000-08-22 | 2000-08-22 | Compostions adapted for chain linking |
Publications (1)
Publication Number | Publication Date |
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ZA200300760B true ZA200300760B (en) | 2004-04-28 |
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ID=9898045
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ZA200300760A ZA200300760B (en) | 2000-08-22 | 2003-01-28 | Compositions adapted for chain linking. |
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Country | Link |
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US (1) | US7084213B2 (no) |
EP (1) | EP1311570B1 (no) |
JP (1) | JP5081364B2 (no) |
KR (1) | KR100849280B1 (no) |
CN (1) | CN1250606C (no) |
AT (1) | ATE316109T1 (no) |
AU (2) | AU2001279963B2 (no) |
BR (1) | BR0113433A (no) |
CA (1) | CA2420341C (no) |
DE (1) | DE60116777T2 (no) |
DK (1) | DK1311570T3 (no) |
ES (1) | ES2257426T3 (no) |
GB (1) | GB0020620D0 (no) |
IL (2) | IL154399A0 (no) |
MX (1) | MXPA03001411A (no) |
MY (1) | MY123932A (no) |
NO (1) | NO20030758L (no) |
RU (1) | RU2278126C2 (no) |
WO (1) | WO2002016456A2 (no) |
ZA (1) | ZA200300760B (no) |
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US20060240239A1 (en) * | 2003-05-22 | 2006-10-26 | Mcgrail Patrick T | Compositions adapted for chain linking |
WO2010041909A2 (ko) * | 2008-10-09 | 2010-04-15 | 한양대학교 산학협력단 | 고분자 및 이의 제조방법 |
ES2368865T3 (es) * | 2008-10-15 | 2011-11-23 | Evonik Degussa Gmbh | Agente auxiliar de tratamiento para poliuretanos termoplásticos. |
KR101096855B1 (ko) | 2009-03-24 | 2011-12-22 | 도레이 카부시키가이샤 | 섬유 강화 복합 재료용 에폭시 수지 조성물, 프리프레그 및 섬유 강화 복합 재료 |
CN102822227B (zh) | 2010-03-23 | 2014-11-05 | 东丽株式会社 | 碳纤维增强复合材料用环氧树脂组合物、预浸料以及碳纤维增强复合材料 |
GB201009851D0 (en) * | 2010-06-14 | 2010-07-21 | Hexcel Composites Ltd | Improvements in composite materials |
EP2596947B1 (en) * | 2010-07-21 | 2019-02-06 | Toray Industries, Inc. | Prepreg, fiber-reinforced composite material, and process for producing prepreg |
WO2012039456A1 (ja) | 2010-09-24 | 2012-03-29 | 東レ株式会社 | 繊維強化複合材料用エポキシ樹脂組成物、プリプレグおよび繊維強化複合材料 |
GB201101302D0 (en) | 2011-01-25 | 2011-03-09 | Cytec Tech Corp | Benzoxazine resins |
GB201113196D0 (en) * | 2011-08-01 | 2011-09-14 | Cytec Tech Corp | Thermoset resin compositions with increased toughness |
CN103987770B (zh) | 2011-12-22 | 2016-01-20 | 塞特工业公司 | 马来酰亚胺树脂 |
GB201122296D0 (en) * | 2011-12-23 | 2012-02-01 | Cytec Tech Corp | Composite materials |
FR2991331B1 (fr) * | 2012-06-01 | 2015-05-15 | Arkema France | Materiau composite thermoplastique a base de fibres naturelles |
WO2014017340A1 (ja) | 2012-07-25 | 2014-01-30 | 東レ株式会社 | プリプレグおよび炭素繊維強化複合材料 |
EP2862893B1 (en) | 2012-07-25 | 2018-02-28 | Toray Industries, Inc. | Prepreg and carbon-fiber-reinforced composite material |
WO2014050264A1 (ja) | 2012-09-28 | 2014-04-03 | 東レ株式会社 | プリプレグおよび炭素繊維強化複合材料 |
MX371000B (es) | 2012-11-15 | 2020-01-13 | Cytec Ind Inc | Materiales de compuestos de resinas termoestables que comprenden partículas de endurecimiento entre las láminas. |
US9920197B2 (en) * | 2012-12-20 | 2018-03-20 | Cytec Technology Corp. | Liquid binder composition for binding fibrous materials |
JP5800031B2 (ja) | 2013-01-15 | 2015-10-28 | 東レ株式会社 | エポキシ樹脂組成物、プリプレグおよび炭素繊維強化複合材料 |
RU2536969C2 (ru) * | 2013-04-18 | 2014-12-27 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Кабардино-Балкарский государственный университет им. Х.М. Бербекова" | Полимерный композиционный материал и способ его получения |
KR20160030208A (ko) | 2013-07-11 | 2016-03-16 | 도레이 카부시키가이샤 | 에폭시 수지 조성물, 프리프레그 및 탄소 섬유 강화 복합 재료 |
CN105408386B (zh) | 2013-07-26 | 2017-07-21 | 东丽株式会社 | 环氧树脂组合物、预浸料坯及纤维增强复合材料 |
EP3031860B1 (en) | 2013-08-07 | 2019-09-25 | Toray Industries, Inc. | Prepreg based on an epoxy resin composition, and fiber-reinforced composite material |
WO2015081831A1 (zh) * | 2013-12-02 | 2015-06-11 | 天津键凯科技有限公司 | 多臂聚乙二醇-叠氮衍生物 |
JP5831668B1 (ja) | 2014-03-24 | 2015-12-09 | 東レ株式会社 | プリプレグおよび繊維強化複合材料 |
WO2015179426A1 (en) * | 2014-05-19 | 2015-11-26 | MegaMatter Inc. | Large molecule and polymer flame retardants |
BR112017012644B1 (pt) | 2014-12-18 | 2022-04-19 | Cytec Industries Inc | Processo de fabricação para produzir um artigo moldado por infusão de resina líquida, composição curável, artigo moldado curado, e, uso de uma composição curável |
FR3030548B1 (fr) | 2014-12-22 | 2018-03-30 | Rhodia Operations | Composition thermoplastique a haute fluidite |
US11027856B2 (en) | 2015-11-30 | 2021-06-08 | Cytec Industries Inc. | Surfacing materials for composite structures |
RU2019114198A (ru) | 2016-10-21 | 2020-11-24 | Торэй Индастриз, Инк. | Композиции эпоксидных смол и армированные волокном композитные материалы, полученные из них |
WO2018135594A1 (ja) | 2017-01-19 | 2018-07-26 | 東レ株式会社 | プリプレグおよびその製造方法、スリットテーププリプレグ |
EP3604407B1 (en) | 2017-03-24 | 2024-10-16 | Toray Industries, Inc. | Prepreg and carbon fiber-reinforced composite material |
KR20200034967A (ko) | 2017-07-28 | 2020-04-01 | 도레이 카부시키가이샤 | 프리프레그 및 탄소섬유 강화 복합 재료 |
US11590742B2 (en) | 2017-12-21 | 2023-02-28 | Cytec Industries Inc. | UV protective surfacing materials for composite parts |
US12109789B2 (en) | 2017-12-26 | 2024-10-08 | Cytec Industries Inc. | Self-releasing, UV blocking surfacing materials for composite parts |
EP3842481A4 (en) | 2018-08-22 | 2022-06-08 | Toray Industries, Inc. | PREPREGNATED |
EP3853283A4 (en) | 2018-09-21 | 2022-07-27 | Toray Industries, Inc. | EPOXY RESIN COMPOSITION, PREPREG AND FIBER REINFORCED COMPOSITES |
WO2020131946A1 (en) | 2018-12-18 | 2020-06-25 | Cytec Industries Inc. | Flame-retardant epoxy composition and method of using the same |
CN113396254B (zh) * | 2019-02-08 | 2024-03-15 | Ppg工业俄亥俄公司 | 涂覆含纤维的材料的方法和经过涂覆的含纤维的材料 |
EP3946925A1 (en) | 2019-03-29 | 2022-02-09 | Cytec Industries, Inc. | Permeable materials capable of lightning strike protection and use thereof in resin infusion processing |
WO2021133972A1 (en) | 2019-12-27 | 2021-07-01 | Cytec Industries Inc. | Uv resistant surfacing materials for composite parts |
US20240043636A1 (en) | 2020-12-04 | 2024-02-08 | Toray Composite Materials America, Inc. | Prepreg and carbon fiber-reinforced composite material |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4156771A (en) | 1977-06-20 | 1979-05-29 | General Electric Company | Process of forming heterocyclic-coupled block polymers of polyphenylene oxide |
JPS60166326A (ja) * | 1984-02-10 | 1985-08-29 | Showa Denko Kk | 共重合体及びその製造方法 |
EP0226637A1 (en) | 1985-06-12 | 1987-07-01 | Amoco Corporation | Chain-extended poly(aryl ether ketones) |
JPH0768379B2 (ja) * | 1986-02-12 | 1995-07-26 | 東レ株式会社 | プリプレグ用樹脂組成物の製法 |
JP2506920B2 (ja) * | 1988-03-31 | 1996-06-12 | ダイセル化学工業株式会社 | ポリエ―テルスルホンオリゴマ―及びポリエ―テルスルホンイミド |
US4972031A (en) * | 1988-10-05 | 1990-11-20 | Imperial Chemical Industries Plc | Plastic moulding composition comprising an uncured or partly cured thermoset resin precursor and a polyarylsulphone |
DE3900674A1 (de) * | 1989-01-12 | 1990-07-19 | Basf Ag | Hochtemperaturbestaendige polysulfon-polyimid-blockcopolykondensate, verfahren zu ihrer herstellung und ihre verwendung |
US5068286A (en) * | 1989-02-27 | 1991-11-26 | Ge Plastics Japan Ltd. | Copolymers from nucleophilic olefin polymers and epoxytriazine-capped polyphenylene ethers |
US5266610A (en) * | 1991-03-11 | 1993-11-30 | Ici Composites Inc. | Toughened cocontinuous resin system |
WO1994002537A1 (en) | 1992-07-20 | 1994-02-03 | Allied-Signal Inc. | Process for preparing chain extended polymers and graft and block copolymers |
JP3265407B2 (ja) * | 1993-04-07 | 2002-03-11 | 住友化学工業株式会社 | 熱可塑性樹脂組成物 |
EP0653455B1 (en) * | 1993-05-19 | 1997-10-01 | Teijin Limited | Film for metal lamination |
DE69401919C5 (de) * | 1994-06-01 | 2010-08-26 | Sabic Innovative Plastics Ip B.V. | Thermoplastische Zusammensetzung aus kompatibilisiertem Polyphenylenether-Polyamidharz und elektrisch leitender Russ |
-
2000
- 2000-08-22 GB GBGB0020620.1A patent/GB0020620D0/en not_active Ceased
-
2001
- 2001-08-09 MY MYPI20013746 patent/MY123932A/en unknown
- 2001-08-20 DE DE60116777T patent/DE60116777T2/de not_active Expired - Lifetime
- 2001-08-20 CN CNB018145264A patent/CN1250606C/zh not_active Expired - Lifetime
- 2001-08-20 US US10/362,502 patent/US7084213B2/en not_active Expired - Lifetime
- 2001-08-20 MX MXPA03001411A patent/MXPA03001411A/es active IP Right Grant
- 2001-08-20 CA CA2420341A patent/CA2420341C/en not_active Expired - Lifetime
- 2001-08-20 AU AU2001279963A patent/AU2001279963B2/en not_active Expired
- 2001-08-20 BR BR0113433-7A patent/BR0113433A/pt not_active Application Discontinuation
- 2001-08-20 RU RU2003107848/04A patent/RU2278126C2/ru active
- 2001-08-20 AT AT01958238T patent/ATE316109T1/de active
- 2001-08-20 IL IL15439901A patent/IL154399A0/xx active IP Right Grant
- 2001-08-20 KR KR1020037002638A patent/KR100849280B1/ko active IP Right Grant
- 2001-08-20 ES ES01958238T patent/ES2257426T3/es not_active Expired - Lifetime
- 2001-08-20 AU AU7996301A patent/AU7996301A/xx active Pending
- 2001-08-20 EP EP01958238A patent/EP1311570B1/en not_active Expired - Lifetime
- 2001-08-20 JP JP2002521550A patent/JP5081364B2/ja not_active Expired - Lifetime
- 2001-08-20 DK DK01958238T patent/DK1311570T3/da active
- 2001-08-20 WO PCT/GB2001/003729 patent/WO2002016456A2/en active IP Right Grant
-
2003
- 2003-01-28 ZA ZA200300760A patent/ZA200300760B/en unknown
- 2003-02-11 IL IL154399A patent/IL154399A/en not_active IP Right Cessation
- 2003-02-18 NO NO20030758A patent/NO20030758L/no not_active Application Discontinuation
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MXPA03001411A (es) | 2003-08-29 |
NO20030758D0 (no) | 2003-02-18 |
US7084213B2 (en) | 2006-08-01 |
DE60116777D1 (de) | 2006-04-06 |
GB0020620D0 (en) | 2000-10-11 |
JP5081364B2 (ja) | 2012-11-28 |
WO2002016456A2 (en) | 2002-02-28 |
WO2002016456A3 (en) | 2003-02-06 |
JP2004506789A (ja) | 2004-03-04 |
ATE316109T1 (de) | 2006-02-15 |
BR0113433A (pt) | 2003-07-15 |
CN1468276A (zh) | 2004-01-14 |
EP1311570B1 (en) | 2006-01-18 |
DK1311570T3 (da) | 2006-03-06 |
CA2420341C (en) | 2011-04-05 |
MY123932A (en) | 2006-07-31 |
NO20030758L (no) | 2003-04-08 |
AU7996301A (en) | 2002-03-04 |
AU2001279963B2 (en) | 2006-04-27 |
CN1250606C (zh) | 2006-04-12 |
KR20030036720A (ko) | 2003-05-09 |
US20040044141A1 (en) | 2004-03-04 |
IL154399A (en) | 2007-03-08 |
IL154399A0 (en) | 2003-09-17 |
ES2257426T3 (es) | 2006-08-01 |
RU2278126C2 (ru) | 2006-06-20 |
EP1311570A2 (en) | 2003-05-21 |
DE60116777T2 (de) | 2006-08-10 |
KR100849280B1 (ko) | 2008-07-29 |
CA2420341A1 (en) | 2002-02-28 |
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