NO117394B - - Google Patents
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- Publication number
- NO117394B NO117394B NO147829A NO14782963A NO117394B NO 117394 B NO117394 B NO 117394B NO 147829 A NO147829 A NO 147829A NO 14782963 A NO14782963 A NO 14782963A NO 117394 B NO117394 B NO 117394B
- Authority
- NO
- Norway
- Prior art keywords
- mixture
- pressure
- epoxy
- rollers
- tetrakis
- Prior art date
Links
- 239000000203 mixture Substances 0.000 claims description 50
- 229920000647 polyepoxide Polymers 0.000 claims description 24
- 239000003822 epoxy resin Substances 0.000 claims description 16
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 239000007787 solid Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 4
- 238000004898 kneading Methods 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims 1
- 238000009736 wetting Methods 0.000 claims 1
- 239000004593 Epoxy Substances 0.000 description 12
- 239000000463 material Substances 0.000 description 12
- 239000000843 powder Substances 0.000 description 10
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000002245 particle Substances 0.000 description 9
- 229920000768 polyamine Polymers 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 7
- 150000008064 anhydrides Chemical class 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 239000000945 filler Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 230000006835 compression Effects 0.000 description 6
- 238000007906 compression Methods 0.000 description 6
- 229920003986 novolac Polymers 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 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 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 230000002028 premature Effects 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- -1 0.5-0.8 Chemical compound 0.000 description 3
- 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 3
- 239000002253 acid Substances 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 229930003836 cresol Natural products 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 125000003700 epoxy group Chemical group 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 239000012764 mineral filler Substances 0.000 description 3
- 230000001376 precipitating effect Effects 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 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 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229910052570 clay Inorganic materials 0.000 description 2
- 238000005056 compaction Methods 0.000 description 2
- 238000007033 dehydrochlorination reaction Methods 0.000 description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical group C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- 150000002118 epoxides Chemical group 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000012778 molding material Substances 0.000 description 2
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
- 238000010944 pre-mature reactiony Methods 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- PTDNSWDSFRYEJE-UHFFFAOYSA-N 1-[1,4,4-tris(2-hydroxynaphthalen-1-yl)butyl]naphthalen-2-ol Chemical compound OC1=C(C2=CC=CC=C2C=C1)C(CCC(C1=C(C=CC2=CC=CC=C12)O)C1=C(C=CC2=CC=CC=C12)O)C1=C(C=CC2=CC=CC=C12)O PTDNSWDSFRYEJE-UHFFFAOYSA-N 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- JVLSSVPWICWNKS-UHFFFAOYSA-N 2-[1,10,10-tris(2-hydroxyphenyl)decyl]phenol Chemical compound OC1=CC=CC=C1C(C=1C(=CC=CC=1)O)CCCCCCCCC(C=1C(=CC=CC=1)O)C1=CC=CC=C1O JVLSSVPWICWNKS-UHFFFAOYSA-N 0.000 description 1
- UBVXRQAPDRCBOE-UHFFFAOYSA-N 2-[1,2,2-tris(2-hydroxyphenyl)ethyl]phenol Chemical compound OC1=CC=CC=C1C(C=1C(=CC=CC=1)O)C(C=1C(=CC=CC=1)O)C1=CC=CC=C1O UBVXRQAPDRCBOE-UHFFFAOYSA-N 0.000 description 1
- ILNIOUMONWGNAQ-UHFFFAOYSA-N 2-[1,3,3-tris(2-hydroxyphenyl)-2-nitropropyl]phenol Chemical compound OC1=CC=CC=C1C(C=1C(=CC=CC=1)O)C([N+]([O-])=O)C(C=1C(=CC=CC=1)O)C1=CC=CC=C1O ILNIOUMONWGNAQ-UHFFFAOYSA-N 0.000 description 1
- GVKSCCNBFCEGAF-UHFFFAOYSA-N 2-[1,3,3-tris(2-hydroxyphenyl)propyl]phenol Chemical compound OC1=CC=CC=C1C(C=1C(=CC=CC=1)O)CC(C=1C(=CC=CC=1)O)C1=CC=CC=C1O GVKSCCNBFCEGAF-UHFFFAOYSA-N 0.000 description 1
- GBWAFSJFKVFIIW-UHFFFAOYSA-N 2-[1,4,4-tris(2-hydroxyphenyl)butyl]phenol Chemical compound OC1=CC=CC=C1C(C=1C(=CC=CC=1)O)CCC(C=1C(=CC=CC=1)O)C1=CC=CC=C1O GBWAFSJFKVFIIW-UHFFFAOYSA-N 0.000 description 1
- VNOQDTZSURHRQH-UHFFFAOYSA-N 2-[1,5,5-tris(2-hydroxyphenyl)-3-methylpentyl]phenol Chemical compound C=1C=CC=C(O)C=1C(C=1C(=CC=CC=1)O)CC(C)CC(C=1C(=CC=CC=1)O)C1=CC=CC=C1O VNOQDTZSURHRQH-UHFFFAOYSA-N 0.000 description 1
- RIAQEKNMIWPIPJ-UHFFFAOYSA-N 2-[1,8,8-tris(2-hydroxyphenyl)octyl]phenol Chemical compound OC1=CC=CC=C1C(C=1C(=CC=CC=1)O)CCCCCCC(C=1C(=CC=CC=1)O)C1=CC=CC=C1O RIAQEKNMIWPIPJ-UHFFFAOYSA-N 0.000 description 1
- GWJGDZZDCHGKRV-UHFFFAOYSA-N 2-[2,3-dibromo-1,4,4-tris(2-hydroxyphenyl)butyl]phenol Chemical compound OC1=CC=CC=C1C(C=1C(=CC=CC=1)O)C(Br)C(Br)C(C=1C(=CC=CC=1)O)C1=CC=CC=C1O GWJGDZZDCHGKRV-UHFFFAOYSA-N 0.000 description 1
- KPULBHABQXWIPQ-UHFFFAOYSA-N 2-[2-chloro-1,3,3-tris(2-hydroxyphenyl)propyl]phenol Chemical compound OC1=CC=CC=C1C(C=1C(=CC=CC=1)O)C(Cl)C(C=1C(=CC=CC=1)O)C1=CC=CC=C1O KPULBHABQXWIPQ-UHFFFAOYSA-N 0.000 description 1
- ZLFXBKJTASKDHP-UHFFFAOYSA-N 2-[3-[bis(2-hydroxyphenyl)methyl]-1-(2-hydroxyphenyl)pentyl]phenol Chemical compound C=1C=CC=C(O)C=1C(C=1C(=CC=CC=1)O)C(CC)CC(C=1C(=CC=CC=1)O)C1=CC=CC=C1O ZLFXBKJTASKDHP-UHFFFAOYSA-N 0.000 description 1
- XRLGXAZWNNQDCK-UHFFFAOYSA-N 2-chloro-4-[1,6,6-tris(3-chloro-4-hydroxyphenyl)hexyl]phenol Chemical compound ClC=1C=C(C=CC1O)C(CCCCC(C1=CC(=C(C=C1)O)Cl)C1=CC(=C(C=C1)O)Cl)C1=CC(=C(C=C1)O)Cl XRLGXAZWNNQDCK-UHFFFAOYSA-N 0.000 description 1
- GRWFFFOEIHGUBG-UHFFFAOYSA-N 3,4-Epoxy-6-methylcyclohexylmethyl-3,4-epoxy-6-methylcyclo-hexanecarboxylate Chemical compound C1C2OC2CC(C)C1C(=O)OCC1CC2OC2CC1C GRWFFFOEIHGUBG-UHFFFAOYSA-N 0.000 description 1
- BDVJEFYOBPFHBG-UHFFFAOYSA-N 3,5-ditert-butyl-4-[1,3,3-tris(2,6-ditert-butyl-4-hydroxyphenyl)propyl]phenol Chemical compound OC1=CC(=C(C(=C1)C(C)(C)C)C(CC(C1=C(C=C(C=C1C(C)(C)C)O)C(C)(C)C)C1=C(C=C(C=C1C(C)(C)C)O)C(C)(C)C)C1=C(C=C(C=C1C(C)(C)C)O)C(C)(C)C)C(C)(C)C BDVJEFYOBPFHBG-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- XRPAXETZYYVFHX-UHFFFAOYSA-N 4-methyl-2-[1,2,2-tris(2-hydroxy-5-methylphenyl)ethyl]phenol Chemical compound OC1=C(C=C(C=C1)C)C(C(C1=C(C=CC(=C1)C)O)C1=C(C=CC(=C1)C)O)C1=C(C=CC(=C1)C)O XRPAXETZYYVFHX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 150000002334 glycols Chemical group 0.000 description 1
- 239000005337 ground glass Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- YOURXVGYNVXQKT-UHFFFAOYSA-N oxacycloundecane-2,11-dione Chemical compound O=C1CCCCCCCCC(=O)O1 YOURXVGYNVXQKT-UHFFFAOYSA-N 0.000 description 1
- 125000000466 oxiranyl group Chemical group 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000006069 physical mixture Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 150000003141 primary amines Chemical group 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000010125 resin casting Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000009941 weaving Methods 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
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)
- Compositions Of Macromolecular Compounds (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US178571A US3390123A (en) | 1962-03-09 | 1962-03-09 | Molding compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO117394B true NO117394B (es) | 1969-08-04 |
Family
ID=22653074
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO147829A NO117394B (es) | 1962-03-09 | 1963-03-08 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US3390123A (es) |
| BE (1) | BE629380A (es) |
| CH (1) | CH445117A (es) |
| DE (1) | DE1545187B2 (es) |
| DK (1) | DK107060C (es) |
| FI (1) | FI41873C (es) |
| GB (1) | GB1033514A (es) |
| NL (2) | NL138957B (es) |
| NO (1) | NO117394B (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4146525A (en) * | 1977-06-20 | 1979-03-27 | Minnesota Mining And Manufacturing Company | High strength ceramic-polymer composites |
| DE3026455A1 (de) * | 1980-07-12 | 1982-02-11 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur herstellung von haertern fuer epoxidharze aus monosalzen von aromatischen polycarbonsaeuren |
| DE3424700A1 (de) * | 1984-07-05 | 1986-02-06 | Basf Ag, 6700 Ludwigshafen | Faserverbundwerkstoffe auf basis von epoxidharzen |
| GB8503882D0 (en) * | 1985-02-15 | 1985-03-20 | Raychem Ltd | Heat curable composition |
| JP2501154B2 (ja) * | 1990-11-26 | 1996-05-29 | 三井東圧化学株式会社 | テトラキスキシレノ―ルエタンの製造方法 |
| WO1997028203A1 (en) * | 1996-02-02 | 1997-08-07 | Ciba Specialty Chemicals Holding Inc. | Storage-stable moulding powder based on epoxy resins |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2899407A (en) * | 1959-08-11 | Xcuming o of epoxy resins | ||
| BE476967A (es) * | 1945-07-13 | 1900-01-01 | ||
| US2773048A (en) * | 1952-08-25 | 1956-12-04 | Honeywell Regulator Co | Epoxy resin composition containing para, para' diamino diphenylmethane |
| US2934520A (en) * | 1954-10-04 | 1960-04-26 | Aries Lab Inc | Epoxy resin compositions |
| US2806016A (en) * | 1954-11-01 | 1957-09-10 | Shell Dev | Polyglycidyl ethers of tetraphenols |
| BE543822A (es) * | 1954-12-23 | |||
| US2866768A (en) * | 1955-03-18 | 1958-12-30 | Honeywell Regulator Co | Epoxy molding composition and method of molding with same |
| NL218575A (es) * | 1956-07-03 | |||
| NL219578A (es) * | 1956-08-03 | 1900-01-01 | ||
| US3025263A (en) * | 1957-07-31 | 1962-03-13 | Jr Henry L Lee | Epoxy carboxylic acid dianhydride compositions |
| US2965930A (en) * | 1957-08-21 | 1960-12-27 | Union Carbide Corp | Process for preparing polyepoxide solder |
| US3159595A (en) * | 1960-08-11 | 1964-12-01 | Shell Oil Co | Blending crystalline 2, 2-bis(2, 3-epoxypropoxyphenyl) propane with curing agent |
-
0
- BE BE629380D patent/BE629380A/xx unknown
- NL NL289911D patent/NL289911A/xx unknown
-
1962
- 1962-03-09 US US178571A patent/US3390123A/en not_active Expired - Lifetime
-
1963
- 1963-02-26 GB GB7651/63A patent/GB1033514A/en not_active Expired
- 1963-03-07 NL NL63289911A patent/NL138957B/xx not_active IP Right Cessation
- 1963-03-07 DE DE1963W0034046 patent/DE1545187B2/de active Granted
- 1963-03-08 CH CH298763A patent/CH445117A/de unknown
- 1963-03-08 FI FI630452A patent/FI41873C/fi active
- 1963-03-08 NO NO147829A patent/NO117394B/no unknown
- 1963-03-09 DK DK110463AA patent/DK107060C/da active
Also Published As
| Publication number | Publication date |
|---|---|
| FI41873C (fi) | 1970-03-10 |
| DE1545187B2 (de) | 1976-11-11 |
| BE629380A (es) | |
| FI41873B (es) | 1969-12-01 |
| NL289911A (es) | |
| DK107060C (da) | 1967-04-17 |
| US3390123A (en) | 1968-06-25 |
| DE1545187A1 (de) | 1969-11-27 |
| NL138957B (nl) | 1973-05-15 |
| GB1033514A (en) | 1966-06-22 |
| CH445117A (de) | 1967-10-15 |
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