GB806447A - Epoxy polymerizable and polymerized compositions and a process for their preparation - Google Patents
Epoxy polymerizable and polymerized compositions and a process for their preparationInfo
- Publication number
- GB806447A GB806447A GB17284/57A GB1728457A GB806447A GB 806447 A GB806447 A GB 806447A GB 17284/57 A GB17284/57 A GB 17284/57A GB 1728457 A GB1728457 A GB 1728457A GB 806447 A GB806447 A GB 806447A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diol
- methyl
- bis
- epoxycyclohexanecarboxylate
- hexane
- 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
- 238000000034 method Methods 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- 238000002360 preparation method Methods 0.000 title abstract 2
- 239000004593 Epoxy Substances 0.000 title 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 13
- -1 diol carboxylates Chemical class 0.000 abstract 11
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract 10
- 150000002009 diols Chemical class 0.000 abstract 10
- SXFJDZNJHVPHPH-UHFFFAOYSA-N 3-methylpentane-1,5-diol Chemical compound OCCC(C)CCO SXFJDZNJHVPHPH-UHFFFAOYSA-N 0.000 abstract 6
- 239000002253 acid Substances 0.000 abstract 4
- 150000007513 acids Chemical class 0.000 abstract 4
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- XRVCFZPJAHWYTB-UHFFFAOYSA-N prenderol Chemical compound CCC(CC)(CO)CO XRVCFZPJAHWYTB-UHFFFAOYSA-N 0.000 abstract 3
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 abstract 3
- UNVGBIALRHLALK-UHFFFAOYSA-N 1,5-Hexanediol Chemical compound CC(O)CCCCO UNVGBIALRHLALK-UHFFFAOYSA-N 0.000 abstract 2
- KQWPPKFUTRANJS-UHFFFAOYSA-N 2-(methoxymethyl)-2,4-dimethylpentane-1,5-diol Chemical compound COCC(C)(CO)CC(C)CO KQWPPKFUTRANJS-UHFFFAOYSA-N 0.000 abstract 2
- RWLALWYNXFYRGW-UHFFFAOYSA-N 2-Ethyl-1,3-hexanediol Chemical compound CCCC(O)C(CC)CO RWLALWYNXFYRGW-UHFFFAOYSA-N 0.000 abstract 2
- SLBYAVDWXWDQRW-UHFFFAOYSA-N 2-[2-(3-methyl-7-oxabicyclo[4.1.0]heptane-3-carbonyl)oxyethoxy]ethyl 3-methyl-7-oxabicyclo[4.1.0]heptane-3-carboxylate Chemical compound CC1(CC2C(CC1)O2)C(=O)OCCOCCOC(=O)C2(CC1C(CC2)O1)C SLBYAVDWXWDQRW-UHFFFAOYSA-N 0.000 abstract 2
- LAIUFBWHERIJIH-UHFFFAOYSA-N 3-Methylheptane Chemical compound CCCCC(C)CC LAIUFBWHERIJIH-UHFFFAOYSA-N 0.000 abstract 2
- AVBDVHVPMHLINW-UHFFFAOYSA-N 6-(5-methyl-7-oxabicyclo[4.1.0]heptane-3-carbonyl)oxyhexyl 5-methyl-7-oxabicyclo[4.1.0]heptane-3-carboxylate Chemical compound CC1C2C(CC(C1)C(=O)OCCCCCCOC(=O)C1CC3C(C(C1)C)O3)O2 AVBDVHVPMHLINW-UHFFFAOYSA-N 0.000 abstract 2
- URRZEEWQOJPKID-UHFFFAOYSA-N 6-(7-oxabicyclo[4.1.0]heptane-4-carbonyloxy)hexyl 7-oxabicyclo[4.1.0]heptane-4-carboxylate Chemical compound C1CC2OC2CC1C(=O)OCCCCCCOC(=O)C1CC2OC2CC1 URRZEEWQOJPKID-UHFFFAOYSA-N 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 abstract 2
- DBIWHDFLQHGOCS-UHFFFAOYSA-N piperidine;trifluoroborane Chemical compound FB(F)F.C1CCNCC1 DBIWHDFLQHGOCS-UHFFFAOYSA-N 0.000 abstract 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 abstract 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 abstract 2
- ORTVZLZNOYNASJ-UPHRSURJSA-N (z)-but-2-ene-1,4-diol Chemical compound OC\C=C/CO ORTVZLZNOYNASJ-UPHRSURJSA-N 0.000 abstract 1
- 229940043375 1,5-pentanediol Drugs 0.000 abstract 1
- IHJUECRFYCQBMW-UHFFFAOYSA-N 2,5-dimethylhex-3-yne-2,5-diol Chemical compound CC(C)(O)C#CC(C)(C)O IHJUECRFYCQBMW-UHFFFAOYSA-N 0.000 abstract 1
- ZWNMRZQYWRLGMM-UHFFFAOYSA-N 2,5-dimethylhexane-2,5-diol Chemical compound CC(C)(O)CCC(C)(C)O ZWNMRZQYWRLGMM-UHFFFAOYSA-N 0.000 abstract 1
- GHTVHGGJFHMYBA-UHFFFAOYSA-N 2-(7-oxabicyclo[4.1.0]heptane-4-carbonyloxy)ethyl 7-oxabicyclo[4.1.0]heptane-4-carboxylate Chemical compound C1CC2OC2CC1C(=O)OCCOC(=O)C1CC2OC2CC1 GHTVHGGJFHMYBA-UHFFFAOYSA-N 0.000 abstract 1
- YTLHXFVJMRDAMC-UHFFFAOYSA-N 2-[2-(3-methyl-7-oxabicyclo[4.1.0]heptane-4-carbonyl)oxyethoxy]ethyl 3-methyl-7-oxabicyclo[4.1.0]heptane-4-carboxylate Chemical compound C1C2OC2CC(C)C1C(=O)OCCOCCOC(=O)C1CC2OC2CC1C YTLHXFVJMRDAMC-UHFFFAOYSA-N 0.000 abstract 1
- HAIVWDGLCRYQMC-UHFFFAOYSA-N 4-methylpentane-1,4-diol Chemical compound CC(C)(O)CCCO HAIVWDGLCRYQMC-UHFFFAOYSA-N 0.000 abstract 1
- OBZZBKAKHCSTNG-UHFFFAOYSA-N 5-methyl-7-oxabicyclo[4.1.0]heptane-4-carboxylic acid Chemical compound C1CC(C(O)=O)C(C)C2OC21 OBZZBKAKHCSTNG-UHFFFAOYSA-N 0.000 abstract 1
- HKCPDPSBVNMCBM-UHFFFAOYSA-N 5-methylcyclohex-3-ene-1-carboxylic acid Chemical class CC1CC(C(O)=O)CC=C1 HKCPDPSBVNMCBM-UHFFFAOYSA-N 0.000 abstract 1
- CMXLPMFCQMQFCI-UHFFFAOYSA-N 6-methyl-7-oxabicyclo[4.1.0]heptane-3-carboxylic acid Chemical compound C1CC(C(O)=O)CC2OC21C CMXLPMFCQMQFCI-UHFFFAOYSA-N 0.000 abstract 1
- CYZXJGWRCHEHPR-UHFFFAOYSA-N 6-methyl-7-oxabicyclo[4.1.0]heptane-4-carboxylic acid Chemical compound C1C(C(O)=O)CCC2OC21C CYZXJGWRCHEHPR-UHFFFAOYSA-N 0.000 abstract 1
- OXQXGKNECHBVMO-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptane-4-carboxylic acid Chemical class C1C(C(=O)O)CCC2OC21 OXQXGKNECHBVMO-UHFFFAOYSA-N 0.000 abstract 1
- 229910015900 BF3 Inorganic materials 0.000 abstract 1
- CVZKVLLSYYFCRX-UHFFFAOYSA-N CC1C(CCC2C1O2)C(=O)OCCC(CCOC(=O)C2C(C1C(CC2)O1)C)C Chemical compound CC1C(CCC2C1O2)C(=O)OCCC(CCOC(=O)C2C(C1C(CC2)O1)C)C CVZKVLLSYYFCRX-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 abstract 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- 239000004642 Polyimide Substances 0.000 abstract 1
- DUFKCOQISQKSAV-UHFFFAOYSA-N Polypropylene glycol (m w 1,200-3,000) Chemical class CC(O)COC(C)CO DUFKCOQISQKSAV-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 abstract 1
- NINDUEPLZFQYGQ-UHFFFAOYSA-N [3-methyl-5-(1-methyl-7-oxabicyclo[4.1.0]heptane-3-carbonyl)oxypentyl] 1-methyl-7-oxabicyclo[4.1.0]heptane-3-carboxylate Chemical compound CC12CC(CCC1O2)C(=O)OCCC(CCOC(=O)C2CC1(C(CC2)O1)C)C NINDUEPLZFQYGQ-UHFFFAOYSA-N 0.000 abstract 1
- NIYNIOYNNFXGFN-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol;7-oxabicyclo[4.1.0]heptane-4-carboxylic acid Chemical compound OCC1CCC(CO)CC1.C1C(C(=O)O)CCC2OC21.C1C(C(=O)O)CCC2OC21 NIYNIOYNNFXGFN-UHFFFAOYSA-N 0.000 abstract 1
- 239000003377 acid catalyst Substances 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- DLDJFQGPPSQZKI-UHFFFAOYSA-N but-2-yne-1,4-diol Chemical compound OCC#CCO DLDJFQGPPSQZKI-UHFFFAOYSA-N 0.000 abstract 1
- ITMIAZBRRZANGB-UHFFFAOYSA-N but-3-ene-1,2-diol Chemical compound OCC(O)C=C ITMIAZBRRZANGB-UHFFFAOYSA-N 0.000 abstract 1
- BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 abstract 1
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 239000000470 constituent Substances 0.000 abstract 1
- VUSWCWPCANWBFG-UHFFFAOYSA-N cyclohex-3-ene-1-carboxylic acid Chemical compound OC(=O)C1CCC=CC1 VUSWCWPCANWBFG-UHFFFAOYSA-N 0.000 abstract 1
- 150000002118 epoxides Chemical class 0.000 abstract 1
- 125000003700 epoxy group Chemical group 0.000 abstract 1
- 239000003822 epoxy resin Substances 0.000 abstract 1
- JDVIRCVIXCMTPU-UHFFFAOYSA-N ethanamine;trifluoroborane Chemical compound CCN.FB(F)F JDVIRCVIXCMTPU-UHFFFAOYSA-N 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 239000010408 film Substances 0.000 abstract 1
- 150000002334 glycols Chemical class 0.000 abstract 1
- 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 1
- QVTWBMUAJHVAIJ-UHFFFAOYSA-N hexane-1,4-diol Chemical compound CCC(O)CCCO QVTWBMUAJHVAIJ-UHFFFAOYSA-N 0.000 abstract 1
- OHMBHFSEKCCCBW-UHFFFAOYSA-N hexane-2,5-diol Chemical compound CC(O)CCC(C)O OHMBHFSEKCCCBW-UHFFFAOYSA-N 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 150000003949 imides Chemical class 0.000 abstract 1
- 150000002466 imines Chemical class 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 229910001507 metal halide Inorganic materials 0.000 abstract 1
- 150000005309 metal halides Chemical class 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 235000010755 mineral Nutrition 0.000 abstract 1
- 238000000465 moulding Methods 0.000 abstract 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 abstract 1
- KHLCTMQBMINUNT-UHFFFAOYSA-N octadecane-1,12-diol Chemical compound CCCCCCC(O)CCCCCCCCCCCO KHLCTMQBMINUNT-UHFFFAOYSA-N 0.000 abstract 1
- GTCCGKPBSJZVRZ-UHFFFAOYSA-N pentane-2,4-diol Chemical compound CC(O)CC(C)O GTCCGKPBSJZVRZ-UHFFFAOYSA-N 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 229920000647 polyepoxide Polymers 0.000 abstract 1
- 229920001721 polyimide Polymers 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 229920006295 polythiol Polymers 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 229950006800 prenderol Drugs 0.000 abstract 1
- 150000003141 primary amines Chemical class 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 abstract 1
- 239000011592 zinc chloride Substances 0.000 abstract 1
- 235000005074 zinc chloride Nutrition 0.000 abstract 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
- C08G59/62—Alcohols or phenols
- C08G59/625—Hydroxyacids
-
- 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
- C08G59/24—Di-epoxy compounds carbocyclic
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Compounds (AREA)
- Epoxy Resins (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US806447XA | 1956-06-01 | 1956-06-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB806447A true GB806447A (en) | 1958-12-23 |
Family
ID=22158681
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB17284/57A Expired GB806447A (en) | 1956-06-01 | 1957-05-31 | Epoxy polymerizable and polymerized compositions and a process for their preparation |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE557990A (enrdf_load_stackoverflow) |
| DE (1) | DE1112637B (enrdf_load_stackoverflow) |
| FR (1) | FR1176406A (enrdf_load_stackoverflow) |
| GB (1) | GB806447A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115028804A (zh) * | 2022-06-16 | 2022-09-09 | 深圳市恒纬祥科技有限公司 | 一种用于半导体灌封胶的脂环环氧树脂及其合成方法 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL235520A (enrdf_load_stackoverflow) * | 1958-01-29 | |||
| DE19534668A1 (de) * | 1995-09-19 | 1997-03-20 | Thera Ges Fuer Patente | Kettenverlängerte Epoxidharze enthaltende, vorwiegend kationisch härtende Masse |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE580075C (de) * | 1925-07-14 | 1933-07-05 | I G Farbenindustrie Akt Ges | Verfahren zur Herstellung von Glykolmonoalkylaethern |
| DE578722C (de) * | 1931-05-12 | 1933-06-16 | I G Farbenindustrie Akt Ges | Verfahren zur Herstellung von Glykolaethern |
| DE575750C (de) * | 1931-08-06 | 1933-08-22 | Georg Frank Dr | Verfahren zur Herstellung von Polyglyciden |
| DE659879C (de) * | 1934-11-09 | 1938-05-12 | Carbide & Carbon Chem Corp | Verfahren zur Herstellung von Glykoldialkylaethern |
| US2609357A (en) * | 1950-11-13 | 1952-09-02 | Rohm & Haas | Preparation of thermoset resins |
-
0
- BE BE557990D patent/BE557990A/xx unknown
-
1957
- 1957-05-28 DE DEU4561A patent/DE1112637B/de active Pending
- 1957-05-31 GB GB17284/57A patent/GB806447A/en not_active Expired
- 1957-06-01 FR FR1176406D patent/FR1176406A/fr not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115028804A (zh) * | 2022-06-16 | 2022-09-09 | 深圳市恒纬祥科技有限公司 | 一种用于半导体灌封胶的脂环环氧树脂及其合成方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| BE557990A (enrdf_load_stackoverflow) | |
| DE1112637B (de) | 1961-08-10 |
| FR1176406A (fr) | 1959-04-10 |
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