JPH0362171B2 - - Google Patents
Info
- Publication number
- JPH0362171B2 JPH0362171B2 JP27815584A JP27815584A JPH0362171B2 JP H0362171 B2 JPH0362171 B2 JP H0362171B2 JP 27815584 A JP27815584 A JP 27815584A JP 27815584 A JP27815584 A JP 27815584A JP H0362171 B2 JPH0362171 B2 JP H0362171B2
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- parts
- hours
- epichlorohydrin
- epoxy
- 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.)
- Expired
Links
- 125000002947 alkylene group Chemical group 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 239000003822 epoxy resin Substances 0.000 description 31
- 229920000647 polyepoxide Polymers 0.000 description 31
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 239000000203 mixture Substances 0.000 description 14
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 13
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 8
- 238000001723 curing Methods 0.000 description 8
- 229920003986 novolac Polymers 0.000 description 8
- 235000011121 sodium hydroxide Nutrition 0.000 description 8
- 239000004593 Epoxy Substances 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- 230000007935 neutral effect Effects 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 230000002378 acidificating effect Effects 0.000 description 4
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 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 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 2
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 2
- 229910015900 BF3 Inorganic materials 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical group CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000007514 bases Chemical class 0.000 description 2
- 229930003836 cresol Natural products 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 2
- NGFPWHGISWUQOI-UHFFFAOYSA-N 2-sec-butylphenol Chemical compound CCC(C)C1=CC=CC=C1O NGFPWHGISWUQOI-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical group CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Phenolic Resins Or Amino Resins (AREA)
- Epoxy Resins (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27815584A JPS61152718A (ja) | 1984-12-26 | 1984-12-26 | 新規エポキシ樹脂 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27815584A JPS61152718A (ja) | 1984-12-26 | 1984-12-26 | 新規エポキシ樹脂 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61152718A JPS61152718A (ja) | 1986-07-11 |
JPH0362171B2 true JPH0362171B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1991-09-25 |
Family
ID=17593352
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27815584A Granted JPS61152718A (ja) | 1984-12-26 | 1984-12-26 | 新規エポキシ樹脂 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61152718A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5237926B2 (ja) * | 2008-12-26 | 2013-07-17 | 三洋化成工業株式会社 | 多官能エポキシ樹脂及びその製造方法 |
-
1984
- 1984-12-26 JP JP27815584A patent/JPS61152718A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS61152718A (ja) | 1986-07-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP3533577B2 (ja) | 新規なシクロヘキシル基含有グリシジルエーテル | |
JP2952094B2 (ja) | エポキシ化合物 | |
JP3206778B2 (ja) | 環状ホスファゼン化合物、樹脂組成物及びその硬化物 | |
JPS5839677A (ja) | 新規ポリエポキシ化合物 | |
US2910455A (en) | Glycidyl polyethers from an epihalohydrin and a bis(4-hydroxy-3 allyl phenyl) alkane | |
JPH0362171B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
US3632555A (en) | Preparation of epoxylated phenolic resins by reacting polymers fro aralkyl ethers and phenols with epihalohydrin | |
CN1479760A (zh) | 环氧树脂、其制造方法、环氧树脂组合物及固化物 | |
JP3074013B2 (ja) | エポキシ樹脂組成物及びその硬化物 | |
CA1105042A (en) | Epoxy resins and process for producing the same | |
JPH0364532B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
JP2008031343A (ja) | 接着用樹脂組成物 | |
US3383432A (en) | Epoxide composition containing the polyglycidyl ethers of 2, 4-bis-(4-hydroxycumyl)-phenol, bis-(4-hydroxy cumyl)-bis-(4-hydroxy-phenyl) 2, 2-propane and 2, 2-bis-(4-hydroxy phenyl)-propane | |
US3544517A (en) | Amino-ethylated novolaks as curing agents for epoxy resins | |
JPS629128B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
JP3080448B2 (ja) | ノボラック型樹脂の製造法 | |
JP2865439B2 (ja) | エポキシ樹脂及びその硬化物 | |
JPH0468313B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
JP2823056B2 (ja) | エポキシ樹脂組成物及びその硬化物 | |
US3060140A (en) | Polyglycidyl ethers of hydroxyphenylated-phenyletherated polymers | |
JP3403178B2 (ja) | フェノール性化合物及びその製造方法 | |
JPH07330645A (ja) | ポリフェノール類化合物、エポキシ樹脂、エポキシ樹脂組成物及びその硬化物 | |
JP3165678B2 (ja) | エポキシ化合物の製造方法 | |
JP2870710B2 (ja) | 新規化合物、樹脂、樹脂組成物及び硬化物 | |
JPH0428712B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |