NO833538L - Fremgangsmaate for fremstilling av gjenstander av termoherdet harpiks - Google Patents

Fremgangsmaate for fremstilling av gjenstander av termoherdet harpiks

Info

Publication number: NO833538L
Authority: NO; Norway
Prior art keywords: mold; curing; temperature; epoxy; resin
Prior art date: 1982-09-30

Application number

NO833538A

Other languages

English (en)

Norwegian (no)

Inventor

Richard Gordon Angell

Kenneth Elton Hobbs

John Martin Konrad

Original Assignee

Union Carbide Corp

Priority date (The priority date 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 date listed.)

1982-09-30

Filing date

1983-09-29

Publication date

1984-04-02

1983-09-29 Application filed by Union Carbide Corp filed Critical Union Carbide Corp

1984-04-02 Publication of NO833538L publication Critical patent/NO833538L/no

Links

238000000034 method Methods 0.000 title claims abstract description 27
238000004519 manufacturing process Methods 0.000 title claims description 6
229920005989 resin Polymers 0.000 title description 25
239000011347 resin Substances 0.000 title description 25
239000000463 material Substances 0.000 claims abstract description 29
239000011368 organic material Substances 0.000 claims abstract description 17
239000007788 liquid Substances 0.000 claims abstract description 16
239000004634 thermosetting polymer Substances 0.000 claims abstract description 11
238000010438 heat treatment Methods 0.000 claims abstract description 8
230000000977 initiatory effect Effects 0.000 claims abstract description 6
239000004593 Epoxy Substances 0.000 claims description 20
238000009825 accumulation Methods 0.000 claims description 4
239000000203 mixture Substances 0.000 abstract description 20
150000002118 epoxides Chemical class 0.000 abstract 1
229920005862 polyol Polymers 0.000 description 21
150000003077 polyols Chemical class 0.000 description 21
239000003054 catalyst Substances 0.000 description 20
238000002360 preparation method Methods 0.000 description 14
238000005266 casting Methods 0.000 description 12
-1 2-ethylhexyl Chemical group 0.000 description 10
239000002253 acid Substances 0.000 description 10
150000001875 compounds Chemical class 0.000 description 10
150000002924 oxiranes Chemical class 0.000 description 10
150000007513 acids Chemical class 0.000 description 9
238000009472 formulation Methods 0.000 description 9
239000004632 polycaprolactone Substances 0.000 description 9
229920000647 polyepoxide Polymers 0.000 description 9
239000002518 antifoaming agent Substances 0.000 description 8
125000003700 epoxy group Chemical group 0.000 description 8
239000003822 epoxy resin Substances 0.000 description 8
229920001610 polycaprolactone Polymers 0.000 description 8
229920001187 thermosetting polymer Polymers 0.000 description 8
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
125000002947 alkylene group Chemical group 0.000 description 7
125000004432 carbon atom Chemical group C* 0.000 description 7
239000004848 polyfunctional curative Substances 0.000 description 7
MUTGBJKUEZFXGO-UHFFFAOYSA-N hexahydrophthalic anhydride Chemical compound C1CCCC2C(=O)OC(=O)C21 MUTGBJKUEZFXGO-UHFFFAOYSA-N 0.000 description 6
150000008064 anhydrides Chemical class 0.000 description 5
239000001257 hydrogen Substances 0.000 description 5
229910052739 hydrogen Inorganic materials 0.000 description 5
238000005303 weighing Methods 0.000 description 5
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
238000002347 injection Methods 0.000 description 4
239000007924 injection Substances 0.000 description 4
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
150000007519 polyprotic acids Polymers 0.000 description 4
238000007789 sealing Methods 0.000 description 4
239000000126 substance Substances 0.000 description 4
PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 4
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000000945 filler Substances 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
239000003999 initiator Substances 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 description 2
ARXKVVRQIIOZGF-UHFFFAOYSA-N 1,2,4-butanetriol Chemical compound OCCC(O)CO ARXKVVRQIIOZGF-UHFFFAOYSA-N 0.000 description 2
LDMRLRNXHLPZJN-UHFFFAOYSA-N 3-propoxypropan-1-ol Chemical compound CCCOCCCO LDMRLRNXHLPZJN-UHFFFAOYSA-N 0.000 description 2
YXALYBMHAYZKAP-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-4-ylmethyl 7-oxabicyclo[4.1.0]heptane-4-carboxylate Chemical compound C1CC2OC2CC1C(=O)OCC1CC2OC2CC1 YXALYBMHAYZKAP-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
RREGISFBPQOLTM-UHFFFAOYSA-N alumane;trihydrate Chemical compound O.O.O.[AlH3] RREGISFBPQOLTM-UHFFFAOYSA-N 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
235000013405 beer Nutrition 0.000 description 2
DJUWPHRCMMMSCV-UHFFFAOYSA-N bis(7-oxabicyclo[4.1.0]heptan-4-ylmethyl) hexanedioate Chemical compound C1CC2OC2CC1COC(=O)CCCCC(=O)OCC1CC2OC2CC1 DJUWPHRCMMMSCV-UHFFFAOYSA-N 0.000 description 2
NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
125000002843 carboxylic acid group Chemical group 0.000 description 2
QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 2
238000010586 diagram Methods 0.000 description 2
150000001991 dicarboxylic acids Chemical class 0.000 description 2
239000000539 dimer Substances 0.000 description 2
239000012530 fluid Substances 0.000 description 2
150000002430 hydrocarbons Chemical group 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
150000003022 phthalic acids Chemical class 0.000 description 2
WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
229920001451 polypropylene glycol Polymers 0.000 description 2
239000000047 product Substances 0.000 description 2
YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
235000012239 silicon dioxide Nutrition 0.000 description 2
230000003068 static effect Effects 0.000 description 2
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
KQTIIICEAUMSDG-UHFFFAOYSA-N tricarballylic acid Chemical compound OC(=O)CC(C(O)=O)CC(O)=O KQTIIICEAUMSDG-UHFFFAOYSA-N 0.000 description 2
IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 1
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
RWLALWYNXFYRGW-UHFFFAOYSA-N 2-Ethyl-1,3-hexanediol Chemical compound CCCC(O)C(CC)CO RWLALWYNXFYRGW-UHFFFAOYSA-N 0.000 description 1
GTEXIOINCJRBIO-UHFFFAOYSA-N 2-[2-(dimethylamino)ethoxy]-n,n-dimethylethanamine Chemical compound CN(C)CCOCCN(C)C GTEXIOINCJRBIO-UHFFFAOYSA-N 0.000 description 1
LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 2-phenyl-1h-imidazole Chemical compound C1=CNC(C=2C=CC=CC=2)=N1 ZCUJYXPAKHMBAZ-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
QULBZCRWOMFYMS-UHFFFAOYSA-N 4-methyl-7-oxabicyclo[4.1.0]heptane-4-carboxylic acid Chemical compound C1C(C)(C(O)=O)CCC2OC21 QULBZCRWOMFYMS-UHFFFAOYSA-N 0.000 description 1
IUPVBNDTWKQQRC-UHFFFAOYSA-N 5-methyl-7-oxabicyclo[4.1.0]heptane-3-carboxylic acid Chemical compound CC1CC(C(O)=O)CC2OC12 IUPVBNDTWKQQRC-UHFFFAOYSA-N 0.000 description 1
MWSKJDNQKGCKPA-UHFFFAOYSA-N 6-methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1CC(C)=CC2C(=O)OC(=O)C12 MWSKJDNQKGCKPA-UHFFFAOYSA-N 0.000 description 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 description 1
LHFIAMMRYGQCJH-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-4-yl 7-oxabicyclo[4.1.0]heptane-4-carboxylate Chemical compound C1CC2OC2CC1C(=O)OC1CC2OC2CC1 LHFIAMMRYGQCJH-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
229920003319 Araldite® Polymers 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
HEBKCHPVOIAQTA-QWWZWVQMSA-N D-arabinitol Chemical compound OC[C@@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-QWWZWVQMSA-N 0.000 description 1
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LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
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229930195725 Mannitol Natural products 0.000 description 1
229920000459 Nitrile rubber Polymers 0.000 description 1
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 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 description 1
239000012190 activator Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
WTEPWWCRWNCUNA-UHFFFAOYSA-M benzyl(triphenyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)CC1=CC=CC=C1 WTEPWWCRWNCUNA-UHFFFAOYSA-M 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
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XFUOBHWPTSIEOV-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) cyclohexane-1,2-dicarboxylate Chemical compound C1CCCC(C(=O)OCC2OC2)C1C(=O)OCC1CO1 XFUOBHWPTSIEOV-UHFFFAOYSA-N 0.000 description 1
LMMDJMWIHPEQSJ-UHFFFAOYSA-N bis[(3-methyl-7-oxabicyclo[4.1.0]heptan-4-yl)methyl] hexanedioate Chemical compound C1C2OC2CC(C)C1COC(=O)CCCCC(=O)OCC1CC2OC2CC1C LMMDJMWIHPEQSJ-UHFFFAOYSA-N 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
235000019437 butane-1,3-diol Nutrition 0.000 description 1
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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229920002678 cellulose Polymers 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
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238000010276 construction Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
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235000014113 dietary fatty acids Nutrition 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
238000005485 electric heating Methods 0.000 description 1
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125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
JHYNXXDQQHTCHJ-UHFFFAOYSA-M ethyl(triphenyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CC)C1=CC=CC=C1 JHYNXXDQQHTCHJ-UHFFFAOYSA-M 0.000 description 1
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239000011737 fluorine Substances 0.000 description 1
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238000001879 gelation Methods 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
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238000002156 mixing Methods 0.000 description 1
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125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
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239000000049 pigment Substances 0.000 description 1
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ILVXOBCQQYKLDS-UHFFFAOYSA-N pyridine N-oxide Chemical compound [O-][N+]1=CC=CC=C1 ILVXOBCQQYKLDS-UHFFFAOYSA-N 0.000 description 1
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239000011342 resin composition Substances 0.000 description 1
150000004756 silanes Chemical class 0.000 description 1
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239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000004071 soot Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
239000013638 trimer Substances 0.000 description 1
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
XMQSELBBYSAURN-UHFFFAOYSA-M triphenyl(propyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CCC)C1=CC=CC=C1 XMQSELBBYSAURN-UHFFFAOYSA-M 0.000 description 1
239000000811 xylitol Substances 0.000 description 1
HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
235000010447 xylitol Nutrition 0.000 description 1
229960002675 xylitol Drugs 0.000 description 1

Classifications

- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C39/00—Shaping by casting, i.e. introducing the moulding material into a mould or between confining surfaces without significant moulding pressure; Apparatus therefor
- B29C39/003—Shaping by casting, i.e. introducing the moulding material into a mould or between confining surfaces without significant moulding pressure; Apparatus therefor characterised by the choice of material
- B29C39/006—Monomers or prepolymers
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C39/00—Shaping by casting, i.e. introducing the moulding material into a mould or between confining surfaces without significant moulding pressure; Apparatus therefor
- B29C39/22—Component parts, details or accessories; Auxiliary operations
- B29C39/40—Compensating volume change, e.g. retraction
- B29C39/405—Compensating volume change, e.g. retraction by applying pressure to the casting composition
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C39/00—Shaping by casting, i.e. introducing the moulding material into a mould or between confining surfaces without significant moulding pressure; Apparatus therefor
- B29C39/22—Component parts, details or accessories; Auxiliary operations
- B29C39/42—Casting under special conditions, e.g. vacuum
- 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
- 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
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
- C08G59/4284—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof together with other curing agents
- 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
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2063/00—Use of EP, i.e. epoxy resins or derivatives thereof, as moulding material

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Mechanical Engineering (AREA)
Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Reinforced Plastic Materials (AREA)
Injection Moulding Of Plastics Or The Like (AREA)
Moulds For Moulding Plastics Or The Like (AREA)
Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
Heating, Cooling, Or Curing Plastics Or The Like In General (AREA)

NO833538A 1982-09-30 1983-09-29 Fremgangsmaate for fremstilling av gjenstander av termoherdet harpiks NO833538L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US43036682A	1982-09-30	1982-09-30

Publications (1)

Publication Number	Publication Date
NO833538L true NO833538L (no)	1984-04-02

Family

ID=23707250

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO833538A NO833538L (no)	1982-09-30	1983-09-29	Fremgangsmaate for fremstilling av gjenstander av termoherdet harpiks

Country Status (8)

Country	Link
EP (1)	EP0107104B1 (fr)
JP (1)	JPS59131416A (fr)
AT (1)	ATE43532T1 (fr)
AU (1)	AU567305B2 (fr)
CA (1)	CA1213114A (fr)
DE (1)	DE3379942D1 (fr)
MX (1)	MX168310B (fr)
NO (1)	NO833538L (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS61130015A (ja) *	1984-11-30	1986-06-17	Sumitomo Bakelite Co Ltd	光デイスク用基板の成形方法
US6730244B1 (en)	1986-01-28	2004-05-04	Q2100, Inc.	Plastic lens and method for the production thereof
US6201037B1 (en)	1986-01-28	2001-03-13	Ophthalmic Research Group International, Inc.	Plastic lens composition and method for the production thereof
US5415816A (en)	1986-01-28	1995-05-16	Q2100, Inc.	Method for the production of plastic lenses
EP0318164A3 (fr) *	1987-10-29	1990-11-22	Techna Vision, Inc.	Dispositif de moulage de lentilles
KR970008322B1 (en) *	1988-01-07	1997-05-23	Varian Associates	Method and apparatus fro thermal transfer with a semiconductor wafer in vacuum
GB8806299D0 (en) *	1988-03-17	1988-04-13	Glynwed Consumer & Building	Process of manufacturing thin-walled plastics moulding
GB8916751D0 (en) *	1989-07-21	1989-09-06	Babcock Transformers Limited	Producing moulded castings in polymer materials
FR2730662B1 (fr) *	1995-02-17	1997-05-09	Robin Christian	Procede et dispositif pour la fabrication de pieces moulees en matiere synthetique
US6022498A (en)	1996-04-19	2000-02-08	Q2100, Inc.	Methods for eyeglass lens curing using ultraviolet light
US6280171B1 (en)	1996-06-14	2001-08-28	Q2100, Inc.	El apparatus for eyeglass lens curing using ultraviolet light
GB0200313D0 (en) *	2002-01-08	2002-02-20	Mining & Chemical Products Ltd	Moulded plastics articles

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1069374B (de) *		1961-10-26	Ankerwerk Gebr Goller Nürnberg	Spritzgießmaschine zur Verarbeitung thermoplastischer Kunst stoffe
DD43934A (fr) *
DD64881A (fr) *
US3169945A (en) *	1956-04-13	1965-02-16	Union Carbide Corp	Lactone polyesters
US2921925A (en) *	1956-12-20	1960-01-19	Union Carbide Corp	Polyepoxide compositions
CH509139A (de) *	1969-06-19	1971-06-30	Ciba Geigy Ag	Verfahren zur Herstellung von gehärteten Kunststoff-Formkörpern
JPS5414777Y2 (fr) *	1977-08-06	1979-06-16
DD149339A1 (de) *	1980-02-27	1981-07-08	Peter Siegert	Verfahren zum spritzgiessen von verformbaren werkstoffen,insbesondere thermoplasten
JPS574718A (en) *	1980-06-12	1982-01-11	Janome Sewing Mach Co Ltd	Casting method of synthetic resin

1983
- 1983-09-09 CA CA000436368A patent/CA1213114A/fr not_active Expired
- 1983-09-29 MX MX198938A patent/MX168310B/es unknown
- 1983-09-29 EP EP83109779A patent/EP0107104B1/fr not_active Expired
- 1983-09-29 NO NO833538A patent/NO833538L/no unknown
- 1983-09-29 JP JP58179469A patent/JPS59131416A/ja active Granted
- 1983-09-29 AT AT83109779T patent/ATE43532T1/de not_active IP Right Cessation
- 1983-09-29 DE DE8383109779T patent/DE3379942D1/de not_active Expired
- 1983-09-29 AU AU19743/83A patent/AU567305B2/en not_active Ceased

Also Published As

Publication number	Publication date
ATE43532T1 (de)	1989-06-15
EP0107104A2 (fr)	1984-05-02
AU567305B2 (en)	1987-11-19
EP0107104B1 (fr)	1989-05-31
CA1213114A (fr)	1986-10-28
MX168310B (es)	1993-05-17
DE3379942D1 (en)	1989-07-06
AU1974383A (en)	1984-04-05
JPH032043B2 (fr)	1991-01-14
JPS59131416A (ja)	1984-07-28
EP0107104A3 (en)	1984-10-24

Publication	Publication Date	Title
US2949441A (en)	1960-08-16	Process for curing materials possessing internal epoxy groups
US4066625A (en)	1978-01-03	Unitary curable resin compositions
CN104250427B (zh)	2016-08-17	铸塑成形用环氧树脂组合物、以及使用了其的高电压设备用模制品及其制造方法
EP0107104B1 (fr)	1989-05-31	Procédé pour fabriquer des objets en matière plastique durcissable à chaud
US3507831A (en)	1970-04-21	Process for curing epoxy resins with polycarboxylic anhydrides in presence of n-alkyl imidazoles
AU669230B2 (en)	1996-05-30	Moulding process
US5612424A (en)	1997-03-18	Fiber-reinforced resin composition
JP6137407B2 (ja)	2017-05-31	繊維強化複合材料用２液型エポキシ樹脂組成物および繊維強化複合材料
KR20100100668A (ko)	2010-09-15	에폭시드-기재 조성물
CN106459376A (zh)	2017-02-22	用于制造环氧/酸酐玻状体树脂的包括有机催化剂的组合物
US2993920A (en)	1961-07-25	Resins and method of making the same
NO169450B (no)	1992-03-16	Stoepepreparat paa basis av et cykloalifatisk epoksyd
JPWO2017221542A1 (ja)	2019-05-09	繊維強化複合材料用２液型エポキシ樹脂組成物および繊維強化複合材料
JPS5928221B2 (ja)	1984-07-11	樹脂形成均質溶液
JPH11507978A (ja)	1999-07-13	硬化性組成物
EP0107103A2 (fr)	1984-05-02	Moule pour fabriquer des objets allongés
JP2013118338A (ja)	2013-06-13	フィルムコンデンサ用樹脂組成物及びフィルムコンデンサ
JPS6053523A (ja)	1985-03-27	エポキシド樹脂成形物質の製造方法
JPH04227621A (ja)	1992-08-17	重合可能な液状組成物
KR20140061446A (ko)	2014-05-21	액체 메틸렌디아닐린 조성물
RU2652251C1 (ru)	2018-04-25	Эпоксидный состав для исправления дефектов технологической оснастки
JPS63213516A (ja)	1988-09-06	新規なエポキシ硬化剤
SU413680A3 (ru)	1974-01-30	Отверждаемая эпоксидная композиция
JPH0464602B2 (fr)	1992-10-15
CA2201584A1 (fr)	1997-10-04	Fabrication de produits moules par la technique de gelification sous pression automatique