NO319699B1 - Polymerblandinger, fremstilling og anvendelse av disse - Google Patents
Polymerblandinger, fremstilling og anvendelse av disse Download PDFInfo
- Publication number
- NO319699B1 NO319699B1 NO19990256A NO990256A NO319699B1 NO 319699 B1 NO319699 B1 NO 319699B1 NO 19990256 A NO19990256 A NO 19990256A NO 990256 A NO990256 A NO 990256A NO 319699 B1 NO319699 B1 NO 319699B1
- Authority
- NO
- Norway
- Prior art keywords
- weight
- polymer mixture
- polymer
- aromatic
- mixture according
- Prior art date
Links
- 229920002959 polymer blend Polymers 0.000 title claims description 49
- 229920000647 polyepoxide Polymers 0.000 claims description 50
- 239000003822 epoxy resin Substances 0.000 claims description 47
- 125000003118 aryl group Chemical group 0.000 claims description 35
- 229920001169 thermoplastic Polymers 0.000 claims description 25
- 229920000768 polyamine Polymers 0.000 claims description 23
- 229920001601 polyetherimide Polymers 0.000 claims description 20
- 238000006243 chemical reaction Methods 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 15
- 229920002492 poly(sulfone) Polymers 0.000 claims description 15
- 239000000853 adhesive Substances 0.000 claims description 10
- 230000001070 adhesive effect Effects 0.000 claims description 10
- 229920001955 polyphenylene ether Polymers 0.000 claims description 9
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 8
- 150000001412 amines Chemical class 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 239000004593 Epoxy Substances 0.000 claims description 6
- 125000003277 amino group Chemical group 0.000 claims description 6
- 125000003700 epoxy group Chemical group 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 238000003786 synthesis reaction Methods 0.000 claims description 5
- 239000002131 composite material Substances 0.000 claims description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 4
- 240000005428 Pistacia lentiscus Species 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 3
- 150000004982 aromatic amines Chemical class 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 229920001643 poly(ether ketone) Polymers 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 239000002318 adhesion promoter Substances 0.000 claims description 2
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims description 2
- 239000012760 heat stabilizer Substances 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- 150000003141 primary amines Chemical group 0.000 claims description 2
- 239000004734 Polyphenylene sulfide Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 229920000069 polyphenylene sulfide Polymers 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 72
- 229910000831 Steel Inorganic materials 0.000 description 16
- 239000010959 steel Substances 0.000 description 16
- 238000000576 coating method Methods 0.000 description 13
- 229920000642 polymer Polymers 0.000 description 12
- 239000004697 Polyetherimide Substances 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 9
- 238000005259 measurement Methods 0.000 description 8
- 239000013535 sea water Substances 0.000 description 8
- 230000035882 stress Effects 0.000 description 8
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 230000000930 thermomechanical effect Effects 0.000 description 7
- 238000010521 absorption reaction Methods 0.000 description 6
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229920004738 ULTEM® Polymers 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 229920012287 polyphenylene sulfone Polymers 0.000 description 5
- UFFBMTHBGFGIHF-UHFFFAOYSA-N 2,6-dimethylaniline Chemical compound CC1=CC=CC(C)=C1N UFFBMTHBGFGIHF-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 229920003295 Radel® Polymers 0.000 description 4
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 4
- 238000007654 immersion Methods 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- -1 polypropylene Polymers 0.000 description 4
- 230000009257 reactivity Effects 0.000 description 4
- VIOMIGLBMQVNLY-UHFFFAOYSA-N 4-[(4-amino-2-chloro-3,5-diethylphenyl)methyl]-3-chloro-2,6-diethylaniline Chemical compound CCC1=C(N)C(CC)=CC(CC=2C(=C(CC)C(N)=C(CC)C=2)Cl)=C1Cl VIOMIGLBMQVNLY-UHFFFAOYSA-N 0.000 description 3
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 238000005266 casting Methods 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 230000009477 glass transition Effects 0.000 description 3
- 239000008240 homogeneous mixture Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920013636 polyphenyl ether polymer Polymers 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- WKBALTUBRZPIPZ-UHFFFAOYSA-N 2,6-di(propan-2-yl)aniline Chemical compound CC(C)C1=CC=CC(C(C)C)=C1N WKBALTUBRZPIPZ-UHFFFAOYSA-N 0.000 description 2
- FOYHNROGBXVLLX-UHFFFAOYSA-N 2,6-diethylaniline Chemical compound CCC1=CC=CC(CC)=C1N FOYHNROGBXVLLX-UHFFFAOYSA-N 0.000 description 2
- WFGHUOGOUOTVBO-UHFFFAOYSA-N 2,6-dipropylaniline Chemical compound CCCC1=CC=CC(CCC)=C1N WFGHUOGOUOTVBO-UHFFFAOYSA-N 0.000 description 2
- RJBSWZGPNTZBSJ-UHFFFAOYSA-N 3-chloro-2,6-di(propan-2-yl)aniline Chemical compound CC(C)C1=CC=C(Cl)C(C(C)C)=C1N RJBSWZGPNTZBSJ-UHFFFAOYSA-N 0.000 description 2
- FGMXFOTYCHZCLA-UHFFFAOYSA-N 3-chloro-2,6-dimethylaniline Chemical compound CC1=CC=C(Cl)C(C)=C1N FGMXFOTYCHZCLA-UHFFFAOYSA-N 0.000 description 2
- AYAICOKIGVUDTA-UHFFFAOYSA-N 3-chloro-2,6-dipropylaniline Chemical compound C(CC)C1=C(N)C(=CC=C1Cl)CCC AYAICOKIGVUDTA-UHFFFAOYSA-N 0.000 description 2
- NWIVYGKSHSJHEF-UHFFFAOYSA-N 4-[(4-amino-3,5-diethylphenyl)methyl]-2,6-diethylaniline Chemical compound CCC1=C(N)C(CC)=CC(CC=2C=C(CC)C(N)=C(CC)C=2)=C1 NWIVYGKSHSJHEF-UHFFFAOYSA-N 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 2
- 229920000265 Polyparaphenylene Polymers 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- 239000003129 oil well Substances 0.000 description 2
- 239000005077 polysulfide Substances 0.000 description 2
- 229920001021 polysulfide Polymers 0.000 description 2
- 150000008117 polysulfides Polymers 0.000 description 2
- 238000001542 size-exclusion chromatography Methods 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- 150000003568 thioethers Chemical class 0.000 description 2
- OUPZKGBUJRBPGC-UHFFFAOYSA-N 1,3,5-tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound O=C1N(CC2OC2)C(=O)N(CC2OC2)C(=O)N1CC1CO1 OUPZKGBUJRBPGC-UHFFFAOYSA-N 0.000 description 1
- SHWYYYOHLLKLNJ-UHFFFAOYSA-N 1,3-diethyl-5-methyl-2,4-dinitrobenzene Chemical compound CCC1=CC(C)=C([N+]([O-])=O)C(CC)=C1[N+]([O-])=O SHWYYYOHLLKLNJ-UHFFFAOYSA-N 0.000 description 1
- BLPURQSRCDKZNX-UHFFFAOYSA-N 2,4,6-tris(oxiran-2-ylmethoxy)-1,3,5-triazine Chemical compound C1OC1COC(N=C(OCC1OC1)N=1)=NC=1OCC1CO1 BLPURQSRCDKZNX-UHFFFAOYSA-N 0.000 description 1
- HGXVKAPCSIXGAK-UHFFFAOYSA-N 2,4-diethyl-6-methylbenzene-1,3-diamine;4,6-diethyl-2-methylbenzene-1,3-diamine Chemical compound CCC1=CC(CC)=C(N)C(C)=C1N.CCC1=CC(C)=C(N)C(CC)=C1N HGXVKAPCSIXGAK-UHFFFAOYSA-N 0.000 description 1
- VDJBIPLKIGSVRG-UHFFFAOYSA-N 3-chloro-2,6-diethylaniline Chemical compound CCC1=CC=C(Cl)C(CC)=C1N VDJBIPLKIGSVRG-UHFFFAOYSA-N 0.000 description 1
- RQEOBXYYEPMCPJ-UHFFFAOYSA-N 4,6-diethyl-2-methylbenzene-1,3-diamine Chemical compound CCC1=CC(CC)=C(N)C(C)=C1N RQEOBXYYEPMCPJ-UHFFFAOYSA-N 0.000 description 1
- OMHOXRVODFQGCA-UHFFFAOYSA-N 4-[(4-amino-3,5-dimethylphenyl)methyl]-2,6-dimethylaniline Chemical compound CC1=C(N)C(C)=CC(CC=2C=C(C)C(N)=C(C)C=2)=C1 OMHOXRVODFQGCA-UHFFFAOYSA-N 0.000 description 1
- FLNVGZMDLLIECD-UHFFFAOYSA-N 4-[(4-amino-3-methyl-5-propan-2-ylphenyl)methyl]-2-methyl-6-propan-2-ylaniline Chemical compound CC1=C(N)C(C(C)C)=CC(CC=2C=C(C(N)=C(C)C=2)C(C)C)=C1 FLNVGZMDLLIECD-UHFFFAOYSA-N 0.000 description 1
- KZTROCYBPMKGAW-UHFFFAOYSA-N 4-[[4-amino-3,5-di(propan-2-yl)phenyl]methyl]-2,6-di(propan-2-yl)aniline Chemical compound CC(C)C1=C(N)C(C(C)C)=CC(CC=2C=C(C(N)=C(C(C)C)C=2)C(C)C)=C1 KZTROCYBPMKGAW-UHFFFAOYSA-N 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000003679 aging effect Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000002270 exclusion chromatography Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 229960004279 formaldehyde Drugs 0.000 description 1
- 235000019256 formaldehyde Nutrition 0.000 description 1
- 238000001033 granulometry Methods 0.000 description 1
- 238000013038 hand mixing Methods 0.000 description 1
- 230000008642 heat stress Effects 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000002076 thermal analysis method Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
- C08G59/5033—Amines aromatic
-
- 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
- Y10T428/249921—Web or sheet containing structurally defined element or component
- Y10T428/249924—Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
- Y10T428/24994—Fiber embedded in or on the surface of a polymeric matrix
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Reinforced Plastic Materials (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9800757A FR2773809B1 (fr) | 1998-01-22 | 1998-01-22 | Compositions de polymeres, leurs preparations et leurs utilisations |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO990256D0 NO990256D0 (no) | 1999-01-21 |
| NO990256L NO990256L (no) | 1999-07-23 |
| NO319699B1 true NO319699B1 (no) | 2005-09-05 |
Family
ID=9522123
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19990256A NO319699B1 (no) | 1998-01-22 | 1999-01-21 | Polymerblandinger, fremstilling og anvendelse av disse |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US6239232B1 (de) |
| EP (1) | EP0931803B1 (de) |
| JP (1) | JPH11323128A (de) |
| DE (1) | DE69824385T2 (de) |
| FR (1) | FR2773809B1 (de) |
| HK (1) | HK1021542A1 (de) |
| NO (1) | NO319699B1 (de) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2822100B1 (fr) * | 2001-03-13 | 2004-04-23 | Inst Francais Du Petrole | Methode de fabrication en grande longueur d'elements tubulaires en composite |
| FR2842206B1 (fr) * | 2002-07-11 | 2007-03-23 | Inst Francais Du Petrole | Compositions pour nouveaux revetements pour conduites hautes temperatures |
| EP2176355A1 (de) * | 2007-08-02 | 2010-04-21 | Dow Global Technologies Inc. | Dämpfender duroplast |
| CN104334611B (zh) * | 2012-03-28 | 2017-05-10 | 巴斯夫欧洲公司 | 用于输送气体的由聚联苯基醚砜聚合物制成的管道和连接件 |
| US9677372B2 (en) | 2013-06-06 | 2017-06-13 | Halliburton Energy Services, Inc. | Well system cementing plug |
| DE202013009991U1 (de) * | 2013-11-04 | 2014-05-12 | Korupp Gmbh | Struktur, insbesondere Gründungsstruktur für eine Windenergieanlage, Windenergieanlage, Arbeitsplattform oder Spundwand, sowie Einrichtung auf See oder an der Küste damit |
| JP2019212664A (ja) * | 2018-05-31 | 2019-12-12 | 住友ベークライト株式会社 | 磁性部材成形用の樹脂組成物、磁性部材、コイル、磁性部材の製造方法および磁性部材成形用キット |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH637150A5 (de) * | 1978-10-30 | 1983-07-15 | Ciba Geigy Ag | Epoxidharzformmasse. |
| US4528346A (en) * | 1982-09-17 | 1985-07-09 | Dainippun Ink and Chemicals, Inc. | Resin composition |
| CH660358A5 (de) * | 1984-07-06 | 1987-04-15 | Lonza Ag | Substituierte p,p'-methylen-bisaniline. |
| JPS6282023A (ja) * | 1985-10-04 | 1987-04-15 | Nitto Electric Ind Co Ltd | 鋼材の防食方法 |
| US4808441A (en) * | 1987-05-15 | 1989-02-28 | Ford Motor Company | Metal articles having corrosion-resistant epoxy coatings |
| EP0455755B1 (de) * | 1989-08-10 | 1997-04-02 | Fiberite Inc. | Mit polyimid-thermoplastischem harz gehärtete epoxydmatrize |
| JPH05132540A (ja) * | 1991-04-18 | 1993-05-28 | Nippon Kayaku Co Ltd | エポキシ樹脂用硬化剤及びそれを用いるエポキシ樹脂の硬化法 |
| JPH05239238A (ja) * | 1991-08-26 | 1993-09-17 | Matsushita Electric Works Ltd | プリプレグの製造法及び該プリプレグを用いた積層板 |
| EP0583224B1 (de) * | 1992-08-11 | 1999-01-20 | Hexcel Corporation | Mit Sulfonpolymeren zäher gemachte hitzehärtbare Harze |
| US5840793A (en) * | 1993-03-08 | 1998-11-24 | General Electric Company | Modified high heat amorphous crystalline blends |
| US5502102A (en) * | 1994-08-09 | 1996-03-26 | General Electric Company | Epoxy modified blends of poly(arylenesulfide) and polyetherimide resins |
| US5985431A (en) * | 1994-12-02 | 1999-11-16 | Toray Industries, Inc. | Prepreg, and a fiber reinforced composite material |
| FR2753978B1 (fr) * | 1996-09-30 | 1999-05-14 | Inst Francais Du Petrole | Composition thermodurcissable, ses utilisations et preforme souple depliable comprenant cette composition |
-
1998
- 1998-01-22 FR FR9800757A patent/FR2773809B1/fr not_active Expired - Fee Related
- 1998-12-23 EP EP19980403277 patent/EP0931803B1/de not_active Expired - Lifetime
- 1998-12-23 DE DE1998624385 patent/DE69824385T2/de not_active Expired - Fee Related
-
1999
- 1999-01-21 NO NO19990256A patent/NO319699B1/no unknown
- 1999-01-22 JP JP1367699A patent/JPH11323128A/ja active Pending
- 1999-01-22 US US09/235,336 patent/US6239232B1/en not_active Expired - Fee Related
-
2000
- 2000-01-24 HK HK00100434A patent/HK1021542A1/xx not_active IP Right Cessation
-
2001
- 2001-04-20 US US09/838,264 patent/US6548608B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20010021753A1 (en) | 2001-09-13 |
| NO990256L (no) | 1999-07-23 |
| EP0931803B1 (de) | 2004-06-09 |
| HK1021542A1 (en) | 2000-06-16 |
| EP0931803A1 (de) | 1999-07-28 |
| FR2773809A1 (fr) | 1999-07-23 |
| JPH11323128A (ja) | 1999-11-26 |
| NO990256D0 (no) | 1999-01-21 |
| US6239232B1 (en) | 2001-05-29 |
| DE69824385T2 (de) | 2004-10-28 |
| FR2773809B1 (fr) | 2000-03-17 |
| DE69824385D1 (de) | 2004-07-15 |
| US6548608B2 (en) | 2003-04-15 |
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