CN111454431A - 一类耐高温黄变的环氧树脂固化剂及其制备方法 - Google Patents
一类耐高温黄变的环氧树脂固化剂及其制备方法 Download PDFInfo
- Publication number
- CN111454431A CN111454431A CN202010305004.6A CN202010305004A CN111454431A CN 111454431 A CN111454431 A CN 111454431A CN 202010305004 A CN202010305004 A CN 202010305004A CN 111454431 A CN111454431 A CN 111454431A
- Authority
- CN
- China
- Prior art keywords
- epoxy resin
- curing agent
- resin curing
- reaction
- temperature yellowing
- 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.)
- Pending
Links
- 239000003795 chemical substances by application Substances 0.000 title claims abstract description 65
- 239000003822 epoxy resin Substances 0.000 title claims abstract description 58
- 229920000647 polyepoxide Polymers 0.000 title claims abstract description 58
- 238000004383 yellowing Methods 0.000 title claims abstract description 53
- 238000002360 preparation method Methods 0.000 title abstract description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 4
- 238000006243 chemical reaction Methods 0.000 claims description 41
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 27
- 150000003141 primary amines Chemical class 0.000 claims description 22
- 238000010438 heat treatment Methods 0.000 claims description 17
- 239000002904 solvent Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 238000004821 distillation Methods 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- 238000006845 Michael addition reaction Methods 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 150000004985 diamines Chemical class 0.000 claims description 2
- 238000004128 high performance liquid chromatography Methods 0.000 claims description 2
- 238000004809 thin layer chromatography Methods 0.000 claims description 2
- -1 alicyclic amine Chemical class 0.000 abstract description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 24
- 238000003756 stirring Methods 0.000 description 19
- 230000032683 aging Effects 0.000 description 14
- 238000000576 coating method Methods 0.000 description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 12
- 150000001412 amines Chemical class 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 12
- 229910052739 hydrogen Inorganic materials 0.000 description 12
- 239000001257 hydrogen Substances 0.000 description 12
- 229910052742 iron Inorganic materials 0.000 description 12
- 230000001678 irradiating effect Effects 0.000 description 12
- 238000011056 performance test Methods 0.000 description 12
- QTKDDPSHNLZGRO-UHFFFAOYSA-N 4-methylcyclohexane-1,3-diamine Chemical compound CC1CCC(N)CC1N QTKDDPSHNLZGRO-UHFFFAOYSA-N 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 238000003786 synthesis reaction Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 5
- GZDFHIJNHHMENY-UHFFFAOYSA-N Dimethyl dicarbonate Chemical compound COC(=O)OC(=O)OC GZDFHIJNHHMENY-UHFFFAOYSA-N 0.000 description 5
- SSJXIUAHEKJCMH-UHFFFAOYSA-N cyclohexane-1,2-diamine Chemical compound NC1CCCCC1N SSJXIUAHEKJCMH-UHFFFAOYSA-N 0.000 description 5
- VKIRRGRTJUUZHS-UHFFFAOYSA-N cyclohexane-1,4-diamine Chemical compound NC1CCC(N)CC1 VKIRRGRTJUUZHS-UHFFFAOYSA-N 0.000 description 5
- 235000010300 dimethyl dicarbonate Nutrition 0.000 description 5
- 239000000047 product Substances 0.000 description 4
- ZDQNWDNMNKSMHI-UHFFFAOYSA-N 1-[2-(2-prop-2-enoyloxypropoxy)propoxy]propan-2-yl prop-2-enoate Chemical compound C=CC(=O)OC(C)COC(C)COCC(C)OC(=O)C=C ZDQNWDNMNKSMHI-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- 238000004321 preservation Methods 0.000 description 3
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 2
- 231100000053 low toxicity Toxicity 0.000 description 2
- FZZMTSNZRBFGGU-UHFFFAOYSA-N 2-chloro-7-fluoroquinazolin-4-amine Chemical compound FC1=CC=C2C(N)=NC(Cl)=NC2=C1 FZZMTSNZRBFGGU-UHFFFAOYSA-N 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 230000035484 reaction time Effects 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
- C08G59/18—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
- C08G59/5026—Amines cycloaliphatic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/04—Formation of amino groups in compounds containing carboxyl groups
- C07C227/06—Formation of amino groups in compounds containing carboxyl groups by addition or substitution reactions, without increasing the number of carbon atoms in the carbon skeleton of the acid
- C07C227/08—Formation of amino groups in compounds containing carboxyl groups by addition or substitution reactions, without increasing the number of carbon atoms in the carbon skeleton of the acid by reaction of ammonia or amines with acids containing functional groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C229/06—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton
- C07C229/10—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
- C07C229/14—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings to carbon atoms of carbon skeletons containing rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Abstract
Description
Claims (10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010305004.6A CN111454431A (zh) | 2020-04-17 | 2020-04-17 | 一类耐高温黄变的环氧树脂固化剂及其制备方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010305004.6A CN111454431A (zh) | 2020-04-17 | 2020-04-17 | 一类耐高温黄变的环氧树脂固化剂及其制备方法 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN111454431A true CN111454431A (zh) | 2020-07-28 |
Family
ID=71676435
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202010305004.6A Pending CN111454431A (zh) | 2020-04-17 | 2020-04-17 | 一类耐高温黄变的环氧树脂固化剂及其制备方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN111454431A (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112624932A (zh) * | 2020-12-02 | 2021-04-09 | 深圳飞扬兴业科技有限公司 | 一种聚脲预聚体的合成方法及其应用 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6172129B1 (en) * | 1999-01-29 | 2001-01-09 | Sartomer Technologies, Inc. | Cyclic amine acrylate monomers and polymers |
US20040072979A1 (en) * | 2002-10-15 | 2004-04-15 | Ashland, Inc. | Oligomers from multifunctional acrylates |
US20080146381A1 (en) * | 2006-12-18 | 2008-06-19 | Kondos Constantine A | Golf balls comprising (meth)acrylated amine curatives |
WO2013104564A1 (de) * | 2012-01-09 | 2013-07-18 | Bayer Intellectual Property Gmbh | Beta-aminosäureester und deren verwendung |
US20180319936A1 (en) * | 2015-07-10 | 2018-11-08 | Université De Haute-Alsace | Polymerization system using double click michael addition and photopolymerization |
CN109852310A (zh) * | 2018-12-27 | 2019-06-07 | 漳州丽都化工有限公司 | 低粘度常温固化双组分环氧胶水及其制备方法 |
CN110240693A (zh) * | 2019-07-10 | 2019-09-17 | 深圳市前海博扬研究院有限公司 | 多胺固化剂及制备方法和环氧树脂组合物 |
-
2020
- 2020-04-17 CN CN202010305004.6A patent/CN111454431A/zh active Pending
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6172129B1 (en) * | 1999-01-29 | 2001-01-09 | Sartomer Technologies, Inc. | Cyclic amine acrylate monomers and polymers |
US20040072979A1 (en) * | 2002-10-15 | 2004-04-15 | Ashland, Inc. | Oligomers from multifunctional acrylates |
US20080146381A1 (en) * | 2006-12-18 | 2008-06-19 | Kondos Constantine A | Golf balls comprising (meth)acrylated amine curatives |
WO2013104564A1 (de) * | 2012-01-09 | 2013-07-18 | Bayer Intellectual Property Gmbh | Beta-aminosäureester und deren verwendung |
US20180319936A1 (en) * | 2015-07-10 | 2018-11-08 | Université De Haute-Alsace | Polymerization system using double click michael addition and photopolymerization |
CN109852310A (zh) * | 2018-12-27 | 2019-06-07 | 漳州丽都化工有限公司 | 低粘度常温固化双组分环氧胶水及其制备方法 |
CN110240693A (zh) * | 2019-07-10 | 2019-09-17 | 深圳市前海博扬研究院有限公司 | 多胺固化剂及制备方法和环氧树脂组合物 |
Non-Patent Citations (2)
Title |
---|
何宏伟: "《碳纤维/环氧树脂复合材料改性处理》", 30 November 2014, 国防工业出版社 * |
张凤翻 等: "《热固性树脂基复合材料预浸料使用手册》", 30 June 2019, 中国建材工业出版社 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112624932A (zh) * | 2020-12-02 | 2021-04-09 | 深圳飞扬兴业科技有限公司 | 一种聚脲预聚体的合成方法及其应用 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103694892B (zh) | 一种含氟聚硅氧烷离型剂及其制备方法 | |
KR100748375B1 (ko) | 실리콘 이형 피막 조성물 | |
US4347346A (en) | Silicone release coatings and inhibitors | |
CN108676189B (zh) | 一种光学显示用紫外光固化氟硅离型膜的制备方法 | |
FI73236B (fi) | Loesningsmedelsfria vidhaeftningshindrande kompositioner och med denna komposition belagda produkter. | |
CA1188023A (en) | Vinyl gum cure accelerators for addition-cure silicone | |
CN104726052B (zh) | 一种uv/底涂双重固化液态光学胶及其制备方法 | |
JPS6126665A (ja) | (メト)アクリル酸エステル改質オルガノポリシロキサン混合物 | |
CN111454431A (zh) | 一类耐高温黄变的环氧树脂固化剂及其制备方法 | |
CN110373109A (zh) | 一种高耐候型粉末涂料及其生产工艺 | |
CN106752741A (zh) | 紫外光固化耐碱性涂料组合物 | |
CN110382598A (zh) | 有机硅防粘涂料组合物 | |
CN111732887A (zh) | 一种溶剂型喷涂光固化抗菌涂料及其制备方法和应用 | |
JPS62277470A (ja) | 合成樹脂用改質剤 | |
CN111978544B (zh) | 一种甲基苯基高沸硅油及其制备方法 | |
CN108753182A (zh) | 一种性能优异的oca光学胶、光学胶带及其制备方法 | |
CN109134825A (zh) | 改性环氧树脂及其制备和应用 | |
CN108276950A (zh) | 一种无酸体系、高耐候、uv固化的oca胶及其制备方法 | |
CN112322251B (zh) | 一种热固化耐黄变的全贴合专用材料及其制备方法和应用 | |
CN108102036A (zh) | 水性丙烯酸改性聚氨酯树脂及其制备方法和水性热封胶 | |
CN102212309B (zh) | 不饱和聚酯聚氨酯嵌段共聚物无溶剂涂料的制备方法 | |
CN103965431A (zh) | 合成树脂、制备方法及利用该合成树脂制备的背涂液 | |
CN116083049A (zh) | 一种聚氨酯改性的oca光学胶、光学胶膜及其制备方法 | |
CN112574704B (zh) | 一种抗静电压敏胶及其制备方法 | |
CN111423843A (zh) | 一种有机硅压敏胶及其制备方法与应用 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
TA01 | Transfer of patent application right | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20230118 Address after: 518000 805, building B, Feiyang science and Technology Innovation Park, No. 8, Longchang Road, district 67, Xingdong community, Xin'an street, Bao'an District, Shenzhen, Guangdong Province Applicant after: SHENZHEN FEIYANG JUNYAN NEW MATERIAL CO.,LTD. Address before: 8 / F, building B, Feiyang, No.8, Longchang Road, Baocheng 67 District, Bao'an District, Shenzhen, Guangdong 518000 Applicant before: SHENZHEN QIANHAI BOYANG RESEARCH INSTITUTE CO.,LTD. |
|
RJ01 | Rejection of invention patent application after publication | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20200728 |