CN105713179A - 聚噁唑烷酮树脂 - Google Patents
聚噁唑烷酮树脂 Download PDFInfo
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- CN105713179A CN105713179A CN201610034163.0A CN201610034163A CN105713179A CN 105713179 A CN105713179 A CN 105713179A CN 201610034163 A CN201610034163 A CN 201610034163A CN 105713179 A CN105713179 A CN 105713179A
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- Prior art keywords
- epoxy
- oxazolidone
- resin
- epoxy resin
- present
- Prior art date
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- 229920005989 resin Polymers 0.000 title claims description 70
- 239000011347 resin Substances 0.000 title claims description 70
- 239000000203 mixture Substances 0.000 claims abstract description 122
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 claims abstract description 102
- 239000004593 Epoxy Substances 0.000 claims abstract description 96
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 90
- 239000003822 epoxy resin Substances 0.000 claims abstract description 87
- 239000003054 catalyst Substances 0.000 claims abstract description 49
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 34
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 34
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 31
- 238000000034 method Methods 0.000 claims abstract description 30
- 229920001187 thermosetting polymer Polymers 0.000 claims description 30
- -1 alicyclic carboxylic acid Chemical class 0.000 claims description 25
- 239000000126 substance Substances 0.000 claims description 21
- 150000002460 imidazoles Chemical class 0.000 claims description 11
- 239000000654 additive Substances 0.000 claims description 10
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 238000007711 solidification Methods 0.000 claims description 9
- 230000008023 solidification Effects 0.000 claims description 9
- 239000011248 coating agent Substances 0.000 claims description 8
- 238000000576 coating method Methods 0.000 claims description 8
- 239000002131 composite material Substances 0.000 claims description 8
- 230000009477 glass transition Effects 0.000 claims description 8
- 150000003839 salts Chemical group 0.000 claims description 8
- 239000002841 Lewis acid Substances 0.000 claims description 7
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical class P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 7
- 125000001931 aliphatic group Chemical group 0.000 claims description 7
- 150000007517 lewis acids Chemical class 0.000 claims description 7
- 230000000996 additive effect Effects 0.000 claims 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 claims description 6
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 5
- 239000002648 laminated material Substances 0.000 claims description 5
- 150000002989 phenols Chemical class 0.000 claims description 5
- 150000003512 tertiary amines Chemical class 0.000 claims description 5
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- 239000011353 cycloaliphatic epoxy resin Substances 0.000 claims description 4
- 238000000113 differential scanning calorimetry Methods 0.000 claims description 4
- AFEQENGXSMURHA-UHFFFAOYSA-N oxiran-2-ylmethanamine Chemical compound NCC1CO1 AFEQENGXSMURHA-UHFFFAOYSA-N 0.000 claims description 4
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 3
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 claims description 3
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Chemical class 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 229940106691 bisphenol a Drugs 0.000 claims description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
- 239000005011 phenolic resin Substances 0.000 claims description 3
- 229920001568 phenolic resin Polymers 0.000 claims description 3
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 3
- 150000005846 sugar alcohols Polymers 0.000 claims description 3
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 2
- 150000008065 acid anhydrides Chemical class 0.000 claims description 2
- 150000004982 aromatic amines Chemical class 0.000 claims description 2
- 239000004841 bisphenol A epoxy resin Substances 0.000 claims description 2
- XUCHXOAWJMEFLF-UHFFFAOYSA-N bisphenol F diglycidyl ether Chemical compound C1OC1COC(C=C1)=CC=C1CC(C=C1)=CC=C1OCC1CO1 XUCHXOAWJMEFLF-UHFFFAOYSA-N 0.000 claims description 2
- 239000004845 glycidylamine epoxy resin Substances 0.000 claims description 2
- 239000010409 thin film Substances 0.000 claims description 2
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- 239000011342 resin composition Substances 0.000 claims 7
- YDIZFUMZDHUHSH-UHFFFAOYSA-N 1,7-bis(ethenyl)-3,8-dioxatricyclo[5.1.0.02,4]oct-5-ene Chemical compound C12OC2C=CC2(C=C)C1(C=C)O2 YDIZFUMZDHUHSH-UHFFFAOYSA-N 0.000 abstract description 28
- 239000000047 product Substances 0.000 abstract description 14
- 230000008569 process Effects 0.000 abstract description 7
- 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 abstract description 3
- 150000001728 carbonyl compounds Chemical class 0.000 abstract description 2
- 239000007795 chemical reaction product Substances 0.000 abstract description 2
- 238000002360 preparation method Methods 0.000 description 19
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 17
- 150000001875 compounds Chemical class 0.000 description 15
- 239000012948 isocyanate Substances 0.000 description 14
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 14
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 13
- 150000002118 epoxides Chemical class 0.000 description 13
- 229910052787 antimony Inorganic materials 0.000 description 10
- 150000002513 isocyanates Chemical class 0.000 description 9
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 8
- ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 2-phenyl-1h-imidazole Chemical compound C1=CNC(C=2C=CC=CC=2)=N1 ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 0.000 description 7
- 125000003700 epoxy group Chemical group 0.000 description 7
- 238000012545 processing Methods 0.000 description 7
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 6
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 229920003986 novolac Polymers 0.000 description 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 5
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 5
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 150000004945 aromatic hydrocarbons Chemical group 0.000 description 4
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 125000000623 heterocyclic group Chemical group 0.000 description 4
- 125000001261 isocyanato group Chemical group *N=C=O 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
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- RKHXQBLJXBGEKF-UHFFFAOYSA-M tetrabutylphosphanium;bromide Chemical compound [Br-].CCCC[P+](CCCC)(CCCC)CCCC RKHXQBLJXBGEKF-UHFFFAOYSA-M 0.000 description 4
- 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
- 239000005058 Isophorone diisocyanate Substances 0.000 description 3
- 235000010290 biphenyl Nutrition 0.000 description 3
- MPMBRWOOISTHJV-UHFFFAOYSA-N but-1-enylbenzene Chemical compound CCC=CC1=CC=CC=C1 MPMBRWOOISTHJV-UHFFFAOYSA-N 0.000 description 3
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- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Natural products OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 3
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- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 3
- DUNKXUFBGCUVQW-UHFFFAOYSA-J zirconium tetrachloride Chemical compound Cl[Zr](Cl)(Cl)Cl DUNKXUFBGCUVQW-UHFFFAOYSA-J 0.000 description 3
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 2
- JIABEENURMZTTI-UHFFFAOYSA-N 1-isocyanato-2-[(2-isocyanatophenyl)methyl]benzene Chemical class O=C=NC1=CC=CC=C1CC1=CC=CC=C1N=C=O JIABEENURMZTTI-UHFFFAOYSA-N 0.000 description 2
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- WAEOXIOXMKNFLQ-UHFFFAOYSA-N 1-methyl-4-prop-2-enylbenzene Chemical group CC1=CC=C(CC=C)C=C1 WAEOXIOXMKNFLQ-UHFFFAOYSA-N 0.000 description 2
- ILSRXKFYTXYKJS-UHFFFAOYSA-N 2,4-bis(ethenyl)-3,6-dioxatetracyclo[6.4.0.02,4.05,7]dodeca-1(12),8,10-triene Chemical compound C=CC12OC1(C=C)C1=CC=CC=C1C1C2O1 ILSRXKFYTXYKJS-UHFFFAOYSA-N 0.000 description 2
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 2
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- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
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- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 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
- 239000012745 toughening agent Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000000080 wetting agent Substances 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
- 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
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
-
- 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
- C08G18/003—Polymeric products of isocyanates or isothiocyanates with epoxy compounds having no active hydrogen
-
- 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
- C08G59/20—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 epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/26—Di-epoxy compounds heterocyclic
-
- 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
- C08G59/20—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 epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/28—Di-epoxy compounds containing acyclic nitrogen atoms
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)
- Polyurethanes Or Polyureas (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26066709P | 2009-11-12 | 2009-11-12 | |
| US61/260,667 | 2009-11-12 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201080051377.XA Division CN102666633B (zh) | 2009-11-12 | 2010-10-15 | 聚噁唑烷酮树脂 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN105713179A true CN105713179A (zh) | 2016-06-29 |
Family
ID=43856160
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201610034163.0A Pending CN105713179A (zh) | 2009-11-12 | 2010-10-15 | 聚噁唑烷酮树脂 |
| CN201080051377.XA Expired - Fee Related CN102666633B (zh) | 2009-11-12 | 2010-10-15 | 聚噁唑烷酮树脂 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201080051377.XA Expired - Fee Related CN102666633B (zh) | 2009-11-12 | 2010-10-15 | 聚噁唑烷酮树脂 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8871892B2 (https=) |
| EP (1) | EP2499180A2 (https=) |
| JP (2) | JP5706437B2 (https=) |
| KR (1) | KR20120097511A (https=) |
| CN (2) | CN105713179A (https=) |
| BR (1) | BR112012010870A2 (https=) |
| TW (1) | TWI515215B (https=) |
| WO (1) | WO2011059633A2 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111057219A (zh) * | 2018-10-16 | 2020-04-24 | 沙特基础工业全球技术有限公司 | 热固性低聚物、包含其的热固性组合物、热固性材料和制品、及其制备方法 |
| CN113166368A (zh) * | 2018-10-30 | 2021-07-23 | 科思创知识产权两合公司 | 生产热塑性聚噁唑烷酮聚合物的方法 |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20140000282A (ko) * | 2010-11-22 | 2014-01-02 | 다우 글로벌 테크놀로지스 엘엘씨 | 강인화제로서 다이비닐벤젠 다이옥사이드의 부가물을 포함하는 에폭시 수지 |
| WO2013070393A1 (en) * | 2011-11-08 | 2013-05-16 | Dow Global Technologies Llc | Curable compositions |
| CN104271667B (zh) * | 2012-04-27 | 2018-01-26 | 陶氏环球技术有限责任公司 | 可固化环氧树脂组合物和由其制造的复合材料 |
| US9371417B2 (en) * | 2012-06-15 | 2016-06-21 | Blue Cube Ip Llc | Curable compositions |
| US9617413B2 (en) * | 2012-10-01 | 2017-04-11 | Dow Global Technologies Llc | Curable epoxy resin compositions |
| WO2014062475A2 (en) * | 2012-10-17 | 2014-04-24 | Dow Global Technologies Llc | Toughened, curable epoxy compositions for high temperature applications |
| CN104837921B (zh) * | 2012-11-07 | 2018-04-13 | 陶氏环球技术有限公司 | 可固化环氧树脂组合物和由其制成的复合物 |
| BR112016002599A2 (pt) * | 2013-08-16 | 2017-08-01 | Dow Global Technologies Llc | composição de epóxi termofixa 1k |
| CN103834168B (zh) | 2014-02-25 | 2016-09-07 | 广东生益科技股份有限公司 | 一种无卤阻燃型树脂组合物 |
| US20170081459A1 (en) * | 2014-05-12 | 2017-03-23 | Covestro Deutschland Ag | Method for the production of polyoxazolidinone polymer compounds |
| DE102014226842A1 (de) | 2014-12-22 | 2016-06-23 | Henkel Ag & Co. Kgaa | Katalysator-Zusammensetzung zur Härtung von Epoxidgruppen-haltigen Harzen |
| DE102014226838A1 (de) * | 2014-12-22 | 2016-06-23 | Henkel Ag & Co. Kgaa | Oxazolidinon- und Isocyanurat-vernetzte Matrix für faserverstärktes Material |
| CN105778414B (zh) | 2014-12-26 | 2018-05-29 | 广东生益科技股份有限公司 | 一种环氧树脂组合物以及使用它的预浸料和层压板 |
| ES2731925T3 (es) * | 2015-02-13 | 2019-11-19 | Covestro Deutschland Ag | Procedimiento para la síntesis de compuestos de polioxazolidinona con alta estabilidad |
| CN106916282B (zh) | 2015-12-28 | 2019-07-26 | 广东生益科技股份有限公司 | 一种环氧树脂组合物以及使用其的预浸料和层压板 |
| CN106519185B (zh) * | 2016-11-16 | 2020-03-31 | 苏州太湖电工新材料股份有限公司 | 一种聚噁唑烷酮树脂、其制备方法及在绝缘漆中的应用 |
| WO2018167228A1 (de) * | 2017-03-17 | 2018-09-20 | Basf Se | Verfahren zur herstellung von oxazolidinongruppen aufweisenden verbindungen |
| JP7365096B2 (ja) * | 2017-09-29 | 2023-10-19 | ビーエーエスエフ ソシエタス・ヨーロピア | ジイソシアネートおよび２－フェニル－１，３－プロパンジオールのジグリシジルエーテル誘導体からの熱可塑性ポリオキサゾリドン |
| JP7286678B2 (ja) * | 2018-05-18 | 2023-06-05 | ダウ グローバル テクノロジーズ エルエルシー | ポリイソシアネート成分、ポリウレタン発泡系、およびそれから製造される物品 |
| JP7512249B2 (ja) * | 2018-07-18 | 2024-07-08 | ビーエーエスエフ ソシエタス・ヨーロピア | ポリオキサゾリドンのバルク重合 |
| CN112638973B (zh) * | 2018-07-30 | 2023-03-31 | 陶氏环球技术有限责任公司 | 可固化的树脂组合物 |
| KR102510064B1 (ko) | 2021-06-03 | 2023-03-14 | 한국화학연구원 | 지속 가능한 자원과 이산화탄소를 이용한 폴리옥사졸리돈의 제조방법, 이를 이용하여 제조된 폴리옥사졸리돈 및 이를 포함하는 성형체 |
| CN118308011B (zh) * | 2024-05-14 | 2026-01-20 | 络合高新材料(上海)股份有限公司 | 一种高延伸率石油管道修补涂料环氧树脂组合物 |
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| US4658007A (en) * | 1985-05-07 | 1987-04-14 | The Dow Chemical Company | Polyisocyanurate-based polyoxazolidone polymers and process for their preparation |
| WO2009058715A2 (en) * | 2007-10-31 | 2009-05-07 | Dow Global Technology Inc. | Non-sintering isocyanate modified epoxy resin for fusion bonded epoxy applications |
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-
2010
- 2010-10-15 US US13/498,709 patent/US8871892B2/en not_active Expired - Fee Related
- 2010-10-15 KR KR1020127015002A patent/KR20120097511A/ko not_active Ceased
- 2010-10-15 BR BR112012010870A patent/BR112012010870A2/pt not_active IP Right Cessation
- 2010-10-15 CN CN201610034163.0A patent/CN105713179A/zh active Pending
- 2010-10-15 JP JP2012538829A patent/JP5706437B2/ja not_active Expired - Fee Related
- 2010-10-15 WO PCT/US2010/052767 patent/WO2011059633A2/en not_active Ceased
- 2010-10-15 CN CN201080051377.XA patent/CN102666633B/zh not_active Expired - Fee Related
- 2010-10-15 EP EP10768164A patent/EP2499180A2/en not_active Withdrawn
- 2010-11-11 TW TW099138801A patent/TWI515215B/zh not_active IP Right Cessation
-
2014
- 2014-12-05 JP JP2014246774A patent/JP6073284B2/ja active Active
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| US3198851A (en) * | 1961-02-23 | 1965-08-03 | Union Carbide Corp | Polyurethanes from non-hydroxyl polyepoxides, bf3-amine catalyst and alternatively avinyl chloride containing resin |
| US3334110A (en) * | 1965-08-16 | 1967-08-01 | Baker Chem Co J T | Method for preparing epoxyoxazolidinones |
| US3737406A (en) * | 1971-03-22 | 1973-06-05 | Alelio G D | Reactive epoxy-onium catalysts for synthesis of polyoxazolidones |
| US4658007A (en) * | 1985-05-07 | 1987-04-14 | The Dow Chemical Company | Polyisocyanurate-based polyoxazolidone polymers and process for their preparation |
| WO2009058715A2 (en) * | 2007-10-31 | 2009-05-07 | Dow Global Technology Inc. | Non-sintering isocyanate modified epoxy resin for fusion bonded epoxy applications |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111057219A (zh) * | 2018-10-16 | 2020-04-24 | 沙特基础工业全球技术有限公司 | 热固性低聚物、包含其的热固性组合物、热固性材料和制品、及其制备方法 |
| CN111057219B (zh) * | 2018-10-16 | 2022-12-06 | 高新特殊工程塑料全球技术有限公司 | 热固性低聚物、包含其的热固性组合物、热固性材料和制品、及其制备方法 |
| CN113166368A (zh) * | 2018-10-30 | 2021-07-23 | 科思创知识产权两合公司 | 生产热塑性聚噁唑烷酮聚合物的方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| TWI515215B (zh) | 2016-01-01 |
| BR112012010870A2 (pt) | 2019-09-24 |
| CN102666633B (zh) | 2016-02-17 |
| TW201124437A (en) | 2011-07-16 |
| WO2011059633A2 (en) | 2011-05-19 |
| WO2011059633A3 (en) | 2011-09-29 |
| JP5706437B2 (ja) | 2015-04-22 |
| US8871892B2 (en) | 2014-10-28 |
| JP2013510924A (ja) | 2013-03-28 |
| EP2499180A2 (en) | 2012-09-19 |
| CN102666633A (zh) | 2012-09-12 |
| KR20120097511A (ko) | 2012-09-04 |
| JP2015061925A (ja) | 2015-04-02 |
| JP6073284B2 (ja) | 2017-02-01 |
| US20120214958A1 (en) | 2012-08-23 |
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