CN108675996B - 一种电子级异氰尿酸三缩水甘油酯的制备方法 - Google Patents
一种电子级异氰尿酸三缩水甘油酯的制备方法 Download PDFInfo
- Publication number
- CN108675996B CN108675996B CN201810593466.5A CN201810593466A CN108675996B CN 108675996 B CN108675996 B CN 108675996B CN 201810593466 A CN201810593466 A CN 201810593466A CN 108675996 B CN108675996 B CN 108675996B
- Authority
- CN
- China
- Prior art keywords
- vacuum
- parts
- kettle
- steps
- water
- 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.)
- Active
Links
- 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 title claims abstract description 58
- 238000002360 preparation method Methods 0.000 title claims abstract description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 57
- 238000000034 method Methods 0.000 claims abstract description 39
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 30
- LRWZZZWJMFNZIK-UHFFFAOYSA-N 2-chloro-3-methyloxirane Chemical compound CC1OC1Cl LRWZZZWJMFNZIK-UHFFFAOYSA-N 0.000 claims abstract description 24
- 238000002425 crystallisation Methods 0.000 claims abstract description 20
- 230000008025 crystallization Effects 0.000 claims abstract description 20
- 235000011121 sodium hydroxide Nutrition 0.000 claims abstract description 19
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000000463 material Substances 0.000 claims abstract description 17
- 238000007363 ring formation reaction Methods 0.000 claims abstract description 15
- 239000007790 solid phase Substances 0.000 claims abstract description 12
- 238000001035 drying Methods 0.000 claims abstract description 11
- 238000003756 stirring Methods 0.000 claims abstract description 10
- 239000007791 liquid phase Substances 0.000 claims abstract description 6
- 239000012452 mother liquor Substances 0.000 claims abstract description 6
- 238000002156 mixing Methods 0.000 claims abstract description 5
- 150000003839 salts Chemical class 0.000 claims abstract description 5
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 13
- 238000001816 cooling Methods 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 12
- 238000004821 distillation Methods 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 239000002994 raw material Substances 0.000 claims description 7
- 230000035484 reaction time Effects 0.000 claims description 4
- 150000007530 organic bases Chemical class 0.000 claims description 3
- 238000001914 filtration Methods 0.000 claims description 2
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 claims 2
- KYVBNYUBXIEUFW-UHFFFAOYSA-N 1,1,3,3-tetramethylguanidine Chemical compound CN(C)C(=N)N(C)C KYVBNYUBXIEUFW-UHFFFAOYSA-N 0.000 claims 1
- 239000000047 product Substances 0.000 abstract description 19
- 239000003054 catalyst Substances 0.000 abstract description 11
- 230000008569 process Effects 0.000 abstract description 11
- 239000003513 alkali Substances 0.000 abstract description 10
- 238000004519 manufacturing process Methods 0.000 abstract description 10
- 239000002585 base Substances 0.000 abstract description 7
- 239000006227 byproduct Substances 0.000 abstract description 6
- 238000007142 ring opening reaction Methods 0.000 abstract description 6
- 229910052736 halogen Inorganic materials 0.000 abstract description 5
- 239000000126 substance Substances 0.000 abstract description 5
- 239000012467 final product Substances 0.000 abstract description 4
- 230000007062 hydrolysis Effects 0.000 abstract description 4
- 238000006460 hydrolysis reaction Methods 0.000 abstract description 4
- 238000005265 energy consumption Methods 0.000 abstract description 3
- 150000002367 halogens Chemical class 0.000 abstract description 3
- 238000001704 evaporation Methods 0.000 abstract description 2
- 239000007788 liquid Substances 0.000 abstract description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 42
- HTZCNXWZYVXIMZ-UHFFFAOYSA-M benzyl(triethyl)azanium;chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC1=CC=CC=C1 HTZCNXWZYVXIMZ-UHFFFAOYSA-M 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 8
- 239000004593 Epoxy Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 6
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 238000007599 discharging Methods 0.000 description 3
- -1 heterocyclic organic compound Chemical class 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 238000000967 suction filtration Methods 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000003507 refrigerant Substances 0.000 description 2
- 239000012086 standard solution Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- IEWXGNMLWRMTTJ-UHFFFAOYSA-N 1,3,5-tris(3-chloro-2-hydroxypropyl)-1,3,5-triazinane-2,4,6-trione Chemical compound ClCC(O)CN1C(=O)N(CC(O)CCl)C(=O)N(CC(O)CCl)C1=O IEWXGNMLWRMTTJ-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000012824 chemical production Methods 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- HPOKESDSMZRZLC-UHFFFAOYSA-N propan-2-one;hydrochloride Chemical compound Cl.CC(C)=O HPOKESDSMZRZLC-UHFFFAOYSA-N 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
Abstract
Description
组别 | 平均环氧值 | 合格率 |
组1 | 1.02 | 100% |
组2 | 1.04 | 100% |
组3 | 1.03 | 100% |
组4 | 1.05 | 100% |
组5 | 1.03 | 100% |
组6 | 1.03 | 100% |
组7 | 1.05 | 100% |
组8 | 1.04 | 100% |
组9 | 1.03 | 100% |
组10 | 1.03 | 100% |
组11 | 1.03 | 100% |
组12 | 1.06 | 66.7% |
组13 | 1.03 | 100% |
组14 | 1.04 | 100% |
组15 | 1.05 | 100% |
组16 | 1.04 | 100% |
组17 | 1.06 | 66.7% |
组18 | 1.04 | 100% |
组19 | 1.03 | 100% |
组20 | 1.04 | 100% |
组21 | 1.03 | 100% |
组22 | 1.03 | 100% |
组23 | 1.05 | 100% |
对比例1 | 1.06 | 66.7% |
对比例2 | 1.04 | 100% |
Claims (7)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810593466.5A CN108675996B (zh) | 2018-06-11 | 2018-06-11 | 一种电子级异氰尿酸三缩水甘油酯的制备方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810593466.5A CN108675996B (zh) | 2018-06-11 | 2018-06-11 | 一种电子级异氰尿酸三缩水甘油酯的制备方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN108675996A CN108675996A (zh) | 2018-10-19 |
CN108675996B true CN108675996B (zh) | 2020-05-15 |
Family
ID=63810756
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201810593466.5A Active CN108675996B (zh) | 2018-06-11 | 2018-06-11 | 一种电子级异氰尿酸三缩水甘油酯的制备方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN108675996B (zh) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114315809B (zh) * | 2020-09-29 | 2023-12-15 | 湖南云科化工有限公司 | 一种异氰尿酸三缩水甘油酯的制备方法 |
CN114315810B (zh) * | 2020-09-29 | 2023-12-15 | 湖南云科化工有限公司 | 一种异氰尿酸三缩水甘油酯的纯化方法 |
CN113105438A (zh) * | 2021-04-09 | 2021-07-13 | 河南易交联新材料科技有限公司 | 一种高纯度三(环氧丙基)异氰尿酸酯的合成方法 |
CN113278014B (zh) * | 2021-06-04 | 2024-07-05 | 黄山华惠科技有限公司 | 一种低氯电子级tgic及其制备方法 |
CN113307802B (zh) * | 2021-06-10 | 2023-10-27 | 黄山友谊南海新材料有限公司 | 一种高纯度异氰脲酸三缩水甘油酯的加工方法 |
CN113549205B (zh) * | 2021-07-22 | 2023-02-28 | 黄山嘉恒科技有限公司 | 一种低成本的耐高温型粉末涂料用聚酯树脂及其制备方法 |
CN114957225B (zh) * | 2021-07-31 | 2024-05-10 | 安徽诗雅涤科技有限公司 | 一种led电子封装专用环氧树脂的制备方法及其环氧树脂 |
CN114989150B (zh) * | 2022-03-21 | 2024-05-17 | 安徽工业大学 | 一种异氰尿酸三缩水甘油酯及其制备方法和应用 |
CN115403734A (zh) * | 2022-10-08 | 2022-11-29 | 安徽泓泽新材料科技有限公司 | 一种呔哔克基聚酯固化剂及其制备方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101177478A (zh) * | 2006-11-09 | 2008-05-14 | 西北工业大学 | 线型双酚f酚醛环氧树脂及其制备方法 |
CN101333285A (zh) * | 2008-07-24 | 2008-12-31 | 中昊晨光化工研究院 | 制备苯酚甲醛型环氧树脂的方法 |
-
2018
- 2018-06-11 CN CN201810593466.5A patent/CN108675996B/zh active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101177478A (zh) * | 2006-11-09 | 2008-05-14 | 西北工业大学 | 线型双酚f酚醛环氧树脂及其制备方法 |
CN101333285A (zh) * | 2008-07-24 | 2008-12-31 | 中昊晨光化工研究院 | 制备苯酚甲醛型环氧树脂的方法 |
Non-Patent Citations (1)
Title |
---|
季铵碱催化体系下异氰尿酸三缩水甘油酯的合成及性能;艾武全,等;《电镀与涂饰》;20131231;第35卷(第22期);第1180页以及表1 * |
Also Published As
Publication number | Publication date |
---|---|
CN108675996A (zh) | 2018-10-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN108675996B (zh) | 一种电子级异氰尿酸三缩水甘油酯的制备方法 | |
CN108947987B (zh) | 一种高品质的电子级异氰尿酸三缩水甘油酯 | |
CN103319469B (zh) | 一种异氰脲酸三缩水甘油酯生产方法 | |
CN100560630C (zh) | 一种低粘度双酚a环氧树脂的生产方法 | |
CN106832284B (zh) | 聚苯硫醚树脂的生产方法及其精馏残液的回收方法 | |
CN106008482B (zh) | 一种制备电子级异氰脲酸三缩水甘油酯的方法 | |
CN111056977A (zh) | 一种双氰胺的制备方法 | |
CN107739330A (zh) | 一种四甲基哌啶醇的绿色制备方法 | |
CN106750302B (zh) | 一种耐热、耐腐蚀的高分子量聚芳硫醚砜的制备方法 | |
CN113105438A (zh) | 一种高纯度三(环氧丙基)异氰尿酸酯的合成方法 | |
CN102794185B (zh) | 制备1,3-二氧戊环的方法及所用催化剂和装置 | |
CN113278014B (zh) | 一种低氯电子级tgic及其制备方法 | |
CN116041703A (zh) | 一种高白度低杂质含量的聚芳醚及其制备方法 | |
CN113788823B (zh) | 一种基于香草醛的生物基环氧树脂及其制备方法 | |
CN115160261A (zh) | 一种环氧树脂的制备方法 | |
CN111286027B (zh) | 低共价结合氯的聚苯硫醚的生产方法 | |
CN108217698B (zh) | 一种从pps催化剂废渣中回收锂的方法 | |
CN112979923A (zh) | 一种含有三嗪环的三官能度的环氧化合物及其制备方法 | |
CN111534143A (zh) | 一种环保型水性催干剂的制备方法 | |
CN113307714B (zh) | 一种派瑞林n的制备方法 | |
CN110526880B (zh) | 逆向分离法精制促进剂m(2-巯基苯并噻唑)的方法 | |
CN114957225B (zh) | 一种led电子封装专用环氧树脂的制备方法及其环氧树脂 | |
CN111592478B (zh) | 一种降低季戊四醇酯色度的方法 | |
CN117430486B (zh) | 一种tmbp的制备方法及应用 | |
CN117417274B (zh) | 一种3-氯-2-羟基丙基磺酸钠的制备方法 |
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 | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
PE01 | Entry into force of the registration of the contract for pledge of patent right | ||
PE01 | Entry into force of the registration of the contract for pledge of patent right |
Denomination of invention: A preparation method of electronic grade triglycidyl isocyanurate Effective date of registration: 20221010 Granted publication date: 20200515 Pledgee: Huizhou Mount Huangshan rural commercial bank Limited by Share Ltd. Pledgor: HUANGSHAN JINFENG INDUSTRIAL Co.,Ltd. Registration number: Y2022980017848 |
|
PC01 | Cancellation of the registration of the contract for pledge of patent right | ||
PC01 | Cancellation of the registration of the contract for pledge of patent right |
Date of cancellation: 20231009 Granted publication date: 20200515 Pledgee: Huizhou Mount Huangshan rural commercial bank Limited by Share Ltd. Pledgor: HUANGSHAN JINFENG INDUSTRIAL Co.,Ltd. Registration number: Y2022980017848 |
|
PE01 | Entry into force of the registration of the contract for pledge of patent right | ||
PE01 | Entry into force of the registration of the contract for pledge of patent right |
Denomination of invention: A Preparation Method of Electronic Grade Isocyanuric Acid Triglycidyl Ester Effective date of registration: 20231016 Granted publication date: 20200515 Pledgee: Huizhou Mount Huangshan rural commercial bank Limited by Share Ltd. Pledgor: HUANGSHAN JINFENG INDUSTRIAL Co.,Ltd. Registration number: Y2023980061263 |