PH26975A - Epoxide advancement - Google Patents
Epoxide advancement Download PDFInfo
- Publication number
- PH26975A PH26975A PH37864A PH37864A PH26975A PH 26975 A PH26975 A PH 26975A PH 37864 A PH37864 A PH 37864A PH 37864 A PH37864 A PH 37864A PH 26975 A PH26975 A PH 26975A
- Authority
- PH
- Philippines
- Prior art keywords
- formula
- group
- epoxy
- dispersion
- bad
- Prior art date
Links
- 150000002118 epoxides Chemical class 0.000 title 1
- 239000004593 Epoxy Substances 0.000 claims description 62
- 239000006185 dispersion Substances 0.000 claims description 49
- 238000000034 method Methods 0.000 claims description 36
- 150000001875 compounds Chemical class 0.000 claims description 32
- 229920000647 polyepoxide Polymers 0.000 claims description 18
- -1 propane-2,2-diyl Chemical group 0.000 claims description 18
- 239000002253 acid Substances 0.000 claims description 16
- 239000003381 stabilizer Substances 0.000 claims description 12
- 125000003700 epoxy group Chemical group 0.000 claims description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 9
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 8
- 239000003822 epoxy resin Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 239000005062 Polybutadiene Substances 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 229920003986 novolac Polymers 0.000 claims description 7
- 229920002857 polybutadiene Polymers 0.000 claims description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 4
- 238000009835 boiling Methods 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 4
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 4
- 229920005989 resin Polymers 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 4
- 229920001519 homopolymer Polymers 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 claims description 2
- 239000000203 mixture Substances 0.000 description 49
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 27
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 25
- 238000010992 reflux Methods 0.000 description 21
- 239000002904 solvent Substances 0.000 description 16
- 239000000126 substance Substances 0.000 description 16
- 239000002270 dispersing agent Substances 0.000 description 15
- 150000002924 oxiranes Chemical class 0.000 description 15
- 150000002009 diols Chemical class 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 9
- 235000019439 ethyl acetate Nutrition 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 8
- 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 8
- 239000000047 product Substances 0.000 description 8
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 7
- 239000000758 substrate Substances 0.000 description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 6
- 238000004821 distillation Methods 0.000 description 6
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000002184 metal Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 229940114072 12-hydroxystearic acid Drugs 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- 229920000058 polyacrylate Polymers 0.000 description 4
- 239000001294 propane Substances 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 3
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 3
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- 239000004342 Benzoyl peroxide Substances 0.000 description 3
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 3
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 3
- 235000019400 benzoyl peroxide Nutrition 0.000 description 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- XXUJMEYKYHETBZ-UHFFFAOYSA-N ethyl 4-nitrophenyl ethylphosphonate Chemical compound CCOP(=O)(CC)OC1=CC=C([N+]([O-])=O)C=C1 XXUJMEYKYHETBZ-UHFFFAOYSA-N 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 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 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 238000010561 standard procedure Methods 0.000 description 2
- SRNFODIJXVPXHO-FSJWMSIRSA-N (4r,4ar,5'r,7r,8r,8as)-5'-(furan-3-yl)-4,7-dimethylspiro[1,3,4,4a,5,6,7,8a-octahydronaphthalene-8,3'-oxolane]-2,2'-dione Chemical compound C=1([C@H]2C[C@@]3(C(O2)=O)[C@H](C)CC[C@H]2[C@@H]3CC(=O)C[C@H]2C)C=COC=1 SRNFODIJXVPXHO-FSJWMSIRSA-N 0.000 description 1
- BUZMJVBOGDBMGI-UHFFFAOYSA-N 1-phenylpropylbenzene Chemical compound C=1C=CC=CC=1C(CC)C1=CC=CC=C1 BUZMJVBOGDBMGI-UHFFFAOYSA-N 0.000 description 1
- CQOZJDNCADWEKH-UHFFFAOYSA-N 2-[3,3-bis(2-hydroxyphenyl)propyl]phenol Chemical compound OC1=CC=CC=C1CCC(C=1C(=CC=CC=1)O)C1=CC=CC=C1O CQOZJDNCADWEKH-UHFFFAOYSA-N 0.000 description 1
- CNPVJWYWYZMPDS-UHFFFAOYSA-N 2-methyldecane Chemical compound CCCCCCCCC(C)C CNPVJWYWYZMPDS-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- SRNFODIJXVPXHO-UHFFFAOYSA-N Crotonin Natural products CC1CC(=O)CC2C1CCC(C)C2(C(O1)=O)CC1C=1C=COC=1 SRNFODIJXVPXHO-UHFFFAOYSA-N 0.000 description 1
- 241001649012 Cypselea humifusa Species 0.000 description 1
- 101710096246 Dihydroorotate dehydrogenase (fumarate) Proteins 0.000 description 1
- 101710175803 Dihydroorotate dehydrogenase (quinone) Proteins 0.000 description 1
- 101710084265 Dihydroorotate dehydrogenase (quinone), mitochondrial Proteins 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 101150034680 Lis-1 gene Proteins 0.000 description 1
- 101150084844 PAFAH1B1 gene Proteins 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
- 101100099943 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) TOP2 gene Proteins 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 208000024780 Urticaria Diseases 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- RICLFGYGYQXUFH-UHFFFAOYSA-N buspirone hydrochloride Chemical compound [H+].[Cl-].C1C(=O)N(CCCCN2CCN(CC2)C=2N=CC=CN=2)C(=O)CC21CCCC2 RICLFGYGYQXUFH-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
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- GELSOTNVVKOYAW-UHFFFAOYSA-N ethyl(triphenyl)phosphanium Chemical compound C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CC)C1=CC=CC=C1 GELSOTNVVKOYAW-UHFFFAOYSA-N 0.000 description 1
- HZZUMXSLPJFMCB-UHFFFAOYSA-M ethyl(triphenyl)phosphanium;acetate Chemical compound CC([O-])=O.C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CC)C1=CC=CC=C1 HZZUMXSLPJFMCB-UHFFFAOYSA-M 0.000 description 1
- SLAFUPJSGFVWPP-UHFFFAOYSA-M ethyl(triphenyl)phosphanium;iodide Chemical compound [I-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CC)C1=CC=CC=C1 SLAFUPJSGFVWPP-UHFFFAOYSA-M 0.000 description 1
- SBPGGGVNZLWFGE-UHFFFAOYSA-N ethylphosphanium;acetate Chemical compound CC[PH3+].CC([O-])=O SBPGGGVNZLWFGE-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- HOMBCMTVOCZMMX-UHFFFAOYSA-N panal Natural products CC1CC(=O)C(C2C=C(CC(O)C12)C(=O)O)C(=C)C=O HOMBCMTVOCZMMX-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- LSMAIBOZUPTNBR-UHFFFAOYSA-N phosphanium;iodide Chemical compound [PH4+].[I-] LSMAIBOZUPTNBR-UHFFFAOYSA-N 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000120 polyethyl acrylate Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000010959 steel Substances 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
- 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
-
- 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
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/04—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
- C08G59/06—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
- C08G59/066—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols with chain extension or advancing agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31511—Of epoxy ether
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)
- Paints Or Removers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP87402769 | 1987-12-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PH26975A true PH26975A (en) | 1992-12-28 |
Family
ID=8198280
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PH37864A PH26975A (en) | 1987-12-04 | 1988-11-28 | Epoxide advancement |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US4952456A (fr) |
| EP (1) | EP0321088B1 (fr) |
| JP (1) | JPH0618851B2 (fr) |
| CN (1) | CN1021450C (fr) |
| AU (1) | AU609226B2 (fr) |
| CA (1) | CA1333313C (fr) |
| DE (1) | DE3887485T2 (fr) |
| DK (1) | DK674788A (fr) |
| ES (1) | ES2061686T3 (fr) |
| GB (1) | GB8826915D0 (fr) |
| MY (1) | MY103478A (fr) |
| NO (1) | NO172498C (fr) |
| NZ (1) | NZ227035A (fr) |
| PH (1) | PH26975A (fr) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9013678D0 (en) * | 1990-06-19 | 1990-08-08 | Ici Plc | Curable composition comprising a crystallisable polymer |
| GB9013679D0 (en) * | 1990-06-19 | 1990-08-08 | Ici Plc | Curable composition comprising a crystallisable polymer |
| US5252637A (en) * | 1992-06-12 | 1993-10-12 | The Glidden Company | Low VOC, high molecular weight epoxy emulsion coatings |
| DE4423309A1 (de) * | 1994-07-02 | 1996-01-04 | Basf Lacke & Farben | Verfahren zur Herstellung einer sterisch stabilisierten, nichtwäßrigen Dispersion eines Polyepoxids und diese Dispersion enthaltende Beschichtungsmittel |
| DE4441684A1 (de) * | 1994-11-23 | 1996-05-30 | Basf Lacke & Farben | Beschichtungsmittel auf der Basis einer sterisch stabilisierten, nichtwäßrigen Dispersion, Verfahren zu deren Herstellung sowie ihre Verwendung zur Beschichtung von Emallagen |
| DE19607435A1 (de) * | 1996-02-28 | 1997-09-04 | Basf Lacke & Farben | Sterisch stabilisierte, nicht-wäßrige Dispersion, und Beschichtungsmittel auf deren Basis |
| CN100418302C (zh) * | 2002-08-23 | 2008-09-10 | 国际商业机器公司 | 用于控制面板的可插拔无线远程控制机构 |
| WO2022019309A1 (fr) * | 2020-07-21 | 2022-01-27 | 株式会社日本触媒 | Composition de résine |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3297784A (en) * | 1964-12-17 | 1967-01-10 | Union Carbide Corp | Alpha olefin polymer modified thermoplastic polyhydroxyether compositions |
| US3931109A (en) * | 1972-03-13 | 1976-01-06 | The Dow Chemical Company | Process for coating substrates with high molecular weight epoxy resins |
| US4122067A (en) * | 1977-10-07 | 1978-10-24 | Celanese Polymer Specialties Company | Process of reacting a polyepoxide compound with a phenol in aqueous medium |
| US4341682A (en) * | 1980-12-23 | 1982-07-27 | Mobil Oil Corporation | Composition comprising ester of epoxy, carbonyl containing polybutadiene polymer and acid containing addition polymer, and aqueous coating compositions prepared therefrom |
| GB8420816D0 (en) * | 1984-08-16 | 1984-09-19 | Dow Chemical Rheinwerk Gmbh | Epoxy resins |
| US4579887A (en) * | 1985-02-26 | 1986-04-01 | The Dow Chemical Company | Non-aqueous dispersions of relatively high molecular weight epoxy resins |
| US4684700A (en) * | 1986-02-14 | 1987-08-04 | The Dow Chemical Company | Advanced epoxy resins prepared from triglycidyl ethers and dihydri phenols |
-
1988
- 1988-11-09 EP EP19880310512 patent/EP0321088B1/fr not_active Expired - Lifetime
- 1988-11-09 ES ES88310512T patent/ES2061686T3/es not_active Expired - Lifetime
- 1988-11-09 DE DE3887485T patent/DE3887485T2/de not_active Expired - Fee Related
- 1988-11-17 MY MYPI88001307A patent/MY103478A/en unknown
- 1988-11-17 GB GB8826915A patent/GB8826915D0/en active Pending
- 1988-11-22 NZ NZ22703588A patent/NZ227035A/xx unknown
- 1988-11-28 PH PH37864A patent/PH26975A/en unknown
- 1988-12-01 AU AU26454/88A patent/AU609226B2/en not_active Ceased
- 1988-12-02 JP JP30425088A patent/JPH0618851B2/ja not_active Expired - Lifetime
- 1988-12-02 NO NO885378A patent/NO172498C/no unknown
- 1988-12-02 DK DK674788A patent/DK674788A/da not_active Application Discontinuation
- 1988-12-03 CN CN88108369A patent/CN1021450C/zh not_active Expired - Fee Related
- 1988-12-05 US US07/279,618 patent/US4952456A/en not_active Expired - Fee Related
- 1988-12-05 CA CA 584953 patent/CA1333313C/fr not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02627A (ja) | 1990-01-05 |
| DK674788D0 (da) | 1988-12-02 |
| AU2645488A (en) | 1989-06-08 |
| CA1333313C (fr) | 1994-11-29 |
| CN1033816A (zh) | 1989-07-12 |
| NO172498C (no) | 1993-07-28 |
| MY103478A (en) | 1993-06-30 |
| EP0321088B1 (fr) | 1994-01-26 |
| ES2061686T3 (es) | 1994-12-16 |
| NO885378L (no) | 1989-06-05 |
| GB8826915D0 (en) | 1988-12-21 |
| DE3887485T2 (de) | 1994-09-08 |
| NO885378D0 (no) | 1988-12-02 |
| EP0321088A3 (en) | 1989-06-28 |
| AU609226B2 (en) | 1991-04-26 |
| NO172498B (no) | 1993-04-19 |
| US4952456A (en) | 1990-08-28 |
| EP0321088A2 (fr) | 1989-06-21 |
| NZ227035A (en) | 1990-09-26 |
| DE3887485D1 (de) | 1994-03-10 |
| DK674788A (da) | 1989-06-05 |
| CN1021450C (zh) | 1993-06-30 |
| JPH0618851B2 (ja) | 1994-03-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3781379A (en) | Powdered coating compositions containing glycidyl methacrylate copolymers with anhydride crosslinking agents and flow control agent | |
| CA2018423C (fr) | Composition de revetement a base de poudre thermodurcissable contenant un melange de polymeres a tg faibles et elevees, avec des groupes fonctionnels acides | |
| US5098955A (en) | Powder coating composition low Tg and high Tg polymers with acid groups | |
| KR100430728B1 (ko) | 원자 전이 라디칼 중합에 의해 제조된 카복실산 작용성중합체 및 에폭시 작용성 중합체 함유 열경화성 조성물 | |
| JP2899832B2 (ja) | 新規熱硬化性樹脂組成物 | |
| EP0249201A2 (fr) | Revêtement à base d'époxyde cycloaliphatique résistant à l'affaissement, ayant une haute teneur en matières solides qui contient un polymère à bas poids moléculaire et à haute Tg comme additif résistant à l'affaissement | |
| US4374954A (en) | Powder paint with epoxy and hydroxy copolymer and anhydride | |
| JPS6358866B2 (fr) | ||
| US5264503A (en) | Phenol-terminated epoxy resin with functional elastomer | |
| NO139091B (no) | Varmeherdbart, pulverformig belegningsmateriale, inneholdende tverrbindingsmidler med frie carboxylgrupper | |
| JPS5824464B2 (ja) | カルボキシ アクリルジユウゴウタイ オ ユウスル フンタイコ−テイングソセイブツ | |
| JPH04224818A (ja) | 粉末被覆組成物用のエラストマー改質エポキシ樹脂 | |
| US3787520A (en) | Powdered coating compositions containing a glycidyl ester copolymer,a phenolic hydroxy crosslinking agent,and a flow control agent | |
| EP1213334B1 (fr) | Compositions de revêtement aqueuses comprenant des composés de l'acide phosphonique | |
| US5523336A (en) | Aqueous, one-component coating composition and use thereof in processes for repair lacquer coating of plastic substrates | |
| PH26975A (en) | Epoxide advancement | |
| JP3476436B2 (ja) | 原子移動ラジカル重合によって調製されるカルボン酸官能性ポリマーを含む熱硬化性組成物 | |
| JP2002523579A (ja) | 原子移動ラジカル重合によって調製されるエポキシ官能性ポリマーを含む熱硬化性組成物 | |
| US4777207A (en) | Aqueous dispersion of film forming polymer and process of preparing same | |
| JPS6123952B2 (fr) | ||
| EP0299421B1 (fr) | Resines époxydes modifieés par une imide | |
| JP2002501561A (ja) | 変性エポキシ樹脂および熱硬化性組成物、特に粉末塗料の構成成分としてのその使用 | |
| JPH04227748A (ja) | 安定なアクリル共重合体分散液 | |
| US4095002A (en) | Heat-curable pulverulent coating agent of a mixture of copolymers containing glycidyl groups and an adduct of aliphatic dicarboxylic acid and 2,4,6-tris(N',N",N'"-dimethylaminomethyl)-phenol | |
| US4039627A (en) | Heat-curable pulverulent coating agent of a mixture of a copolymer containing glycidyl groups and an adduct of aliphatic dicarboxylic acid and 2,4,6-tris-(N',N",N'"-dimethylaminomethyl)-phenol |