IL100117A - Resin preparations that can be cross-linked with an amino group, cross-linked solid polymer preparations prepared from them and processes for their preparation - Google Patents

Resin preparations that can be cross-linked with an amino group, cross-linked solid polymer preparations prepared from them and processes for their preparation

Info

Publication number: IL100117A
Authority: IL; Israel
Prior art keywords: composition; crosslinking agent; acid; carbon atoms; polymer
Prior art date: 1990-12-19

Application number

IL10011791A

Other languages

English (en)

Hebrew (he)

Other versions

IL100117A0 (en

Original Assignee

Exxon Chemical Patents Inc

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.)

1990-12-19

Filing date

1991-11-21

Publication date

1994-10-07

1991-11-21 Application filed by Exxon Chemical Patents Inc filed Critical Exxon Chemical Patents Inc

1992-08-18 Publication of IL100117A0 publication Critical patent/IL100117A0/xx

1994-10-07 Publication of IL100117A publication Critical patent/IL100117A/en

Links

239000000203 mixture Substances 0.000 title claims description 105
238000000034 method Methods 0.000 title claims description 15
230000008569 process Effects 0.000 title claims description 10
238000002360 preparation method Methods 0.000 title description 8
239000007787 solid Substances 0.000 title description 8
239000011342 resin composition Substances 0.000 title description 5
229920006037 cross link polymer Polymers 0.000 title description 4
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 claims description 54
229920000642 polymer Polymers 0.000 claims description 42
238000000576 coating method Methods 0.000 claims description 38
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 34
239000003431 cross linking reagent Substances 0.000 claims description 31
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 23
150000005690 diesters Chemical class 0.000 claims description 22
229920000728 polyester Polymers 0.000 claims description 22
125000004432 carbon atom Chemical group C* 0.000 claims description 21
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 20
239000011248 coating agent Substances 0.000 claims description 19
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims description 19
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 19
239000001361 adipic acid Substances 0.000 claims description 17
235000011037 adipic acid Nutrition 0.000 claims description 17
150000002009 diols Chemical class 0.000 claims description 17
229920000180 alkyd Polymers 0.000 claims description 15
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 14
125000001931 aliphatic group Chemical group 0.000 claims description 12
239000008199 coating composition Substances 0.000 claims description 12
229920000515 polycarbonate Polymers 0.000 claims description 12
239000004417 polycarbonate Substances 0.000 claims description 12
239000004645 polyester resin Substances 0.000 claims description 12
229920001225 polyester resin Polymers 0.000 claims description 12
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 10
125000004849 alkoxymethyl group Chemical group 0.000 claims description 10
KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 claims description 10
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
229940090248 4-hydroxybenzoic acid Drugs 0.000 claims description 7
238000010438 heat treatment Methods 0.000 claims description 7
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
229910052799 carbon Inorganic materials 0.000 claims description 6
239000000758 substrate Substances 0.000 claims description 6
BNCADMBVWNPPIZ-UHFFFAOYSA-N 2-n,2-n,4-n,4-n,6-n,6-n-hexakis(methoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical group COCN(COC)C1=NC(N(COC)COC)=NC(N(COC)COC)=N1 BNCADMBVWNPPIZ-UHFFFAOYSA-N 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 5
238000001035 drying Methods 0.000 claims description 5
239000007859 condensation product Substances 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000004925 Acrylic resin Substances 0.000 claims description 3
229920000178 Acrylic resin Polymers 0.000 claims description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
150000002431 hydrogen Chemical class 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims description 3
239000001301 oxygen Substances 0.000 claims description 3
229910052760 oxygen Inorganic materials 0.000 claims description 3
229910052717 sulfur Inorganic materials 0.000 claims description 3
239000011593 sulfur Substances 0.000 claims description 3
239000004215 Carbon black (E152) Substances 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
239000007795 chemical reaction product Substances 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
150000002367 halogens Chemical class 0.000 claims description 2
229930195733 hydrocarbon Natural products 0.000 claims description 2
239000003960 organic solvent Substances 0.000 claims 1
229920005668 polycarbonate resin Polymers 0.000 claims 1
239000004431 polycarbonate resin Substances 0.000 claims 1
229930185605 Bisphenol Natural products 0.000 description 33
239000002904 solvent Substances 0.000 description 31
229920005989 resin Polymers 0.000 description 30
239000011347 resin Substances 0.000 description 30
239000003054 catalyst Substances 0.000 description 29
238000006243 chemical reaction Methods 0.000 description 20
238000009472 formulation Methods 0.000 description 19
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 17
239000000047 product Substances 0.000 description 17
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 17
150000002148 esters Chemical class 0.000 description 14
239000010408 film Substances 0.000 description 14
-1 aromatic dicarboxylic acids Chemical class 0.000 description 13
238000004132 cross linking Methods 0.000 description 13
239000000463 material Substances 0.000 description 13
239000002253 acid Substances 0.000 description 11
125000003118 aryl group Chemical group 0.000 description 11
239000003921 oil Substances 0.000 description 11
239000000178 monomer Substances 0.000 description 10
235000019198 oils Nutrition 0.000 description 10
VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 9
125000004356 hydroxy functional group Chemical group O* 0.000 description 9
238000006068 polycondensation reaction Methods 0.000 description 9
229940106691 bisphenol a Drugs 0.000 description 8
150000001875 compounds Chemical class 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 6
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 6
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
239000000654 additive Substances 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 6
239000003822 epoxy resin Substances 0.000 description 6
239000003925 fat Substances 0.000 description 6
235000019197 fats Nutrition 0.000 description 6
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 6
229920000647 polyepoxide Polymers 0.000 description 6
239000000126 substance Substances 0.000 description 6
229920003270 Cymel® Polymers 0.000 description 5
150000007513 acids Chemical class 0.000 description 5
238000012360 testing method Methods 0.000 description 5
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
229920006243 acrylic copolymer Polymers 0.000 description 4
230000000996 additive effect Effects 0.000 description 4
239000003849 aromatic solvent Substances 0.000 description 4
229920005601 base polymer Polymers 0.000 description 4
239000011230 binding agent Substances 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 4
229920001971 elastomer Polymers 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
150000004665 fatty acids Chemical class 0.000 description 4
CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 4
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
125000005395 methacrylic acid group Chemical class 0.000 description 4
239000000049 pigment Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
239000004593 Epoxy Substances 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
101710113246 Pectinesterase 3 Proteins 0.000 description 3
239000003377 acid catalyst Substances 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
150000008064 anhydrides Chemical group 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
239000000806 elastomer 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
230000006872 improvement Effects 0.000 description 3
125000005647 linker group Chemical group 0.000 description 3
230000007246 mechanism Effects 0.000 description 3
229940098779 methanesulfonic acid Drugs 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000003973 paint Substances 0.000 description 3
230000009467 reduction Effects 0.000 description 3
239000007921 spray Substances 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 2
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 2
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GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 2
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
URFNSYWAGGETFK-UHFFFAOYSA-N 4,4'-Dihydroxybibenzyl Chemical compound C1=CC(O)=CC=C1CCC1=CC=C(O)C=C1 URFNSYWAGGETFK-UHFFFAOYSA-N 0.000 description 2
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150000005691 triesters Chemical class 0.000 description 2
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150000004670 unsaturated fatty acids Chemical class 0.000 description 2
235000021122 unsaturated fatty acids Nutrition 0.000 description 2
235000015112 vegetable and seed oil Nutrition 0.000 description 2
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BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical class CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 1
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125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
239000002861 polymer material Substances 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920000166 polytrimethylene carbonate Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
239000001294 propane Substances 0.000 description 1
229960004063 propylene glycol Drugs 0.000 description 1
235000013772 propylene glycol Nutrition 0.000 description 1
LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
230000005855 radiation Effects 0.000 description 1
239000002994 raw material Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
238000007761 roller coating Methods 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
229920002050 silicone resin Polymers 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
230000007928 solubilization Effects 0.000 description 1
238000005063 solubilization Methods 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
241000894007 species Species 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
239000010959 steel Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
235000011044 succinic acid Nutrition 0.000 description 1
150000003444 succinic acids Chemical class 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
239000003784 tall oil Substances 0.000 description 1
239000003760 tallow Substances 0.000 description 1
ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
238000010998 test method Methods 0.000 description 1
150000000000 tetracarboxylic acids Chemical class 0.000 description 1
UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
239000010409 thin film Substances 0.000 description 1
YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
229950006389 thiodiglycol Drugs 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
150000004072 triols Chemical class 0.000 description 1
235000019871 vegetable fat Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D169/00—Coating compositions based on polycarbonates; Coating compositions based on derivatives of polycarbonates
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08L61/32—Modified amine-aldehyde condensates

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Paints Or Removers (AREA)
Polyesters Or Polycarbonates (AREA)
Phenolic Resins Or Amino Resins (AREA)
Macromonomer-Based Addition Polymer (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
Compositions Of Macromolecular Compounds (AREA)

IL10011791A 1990-12-19 1991-11-21 Resin preparations that can be cross-linked with an amino group, cross-linked solid polymer preparations prepared from them and processes for their preparation IL100117A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US07/630,298 US5166289A (en)	1990-12-19	1990-12-19	Thermoset coating composition having improved hardness

Publications (2)

Publication Number	Publication Date
IL100117A0 IL100117A0 (en)	1992-08-18
IL100117A true IL100117A (en)	1994-10-07

Family

ID=24526613

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL10011791A IL100117A (en)	1990-12-19	1991-11-21	Resin preparations that can be cross-linked with an amino group, cross-linked solid polymer preparations prepared from them and processes for their preparation

Country Status (19)

Country	Link
US (2)	US5166289A (fr)
EP (1)	EP0563274B1 (fr)
JP (1)	JPH06503375A (fr)
KR (1)	KR0167362B1 (fr)
CN (1)	CN1062915A (fr)
AR (1)	AR247906A1 (fr)
AT (1)	ATE126259T1 (fr)
AU (1)	AU648629B2 (fr)
BR (1)	BR9107219A (fr)
CA (1)	CA2096961C (fr)
DE (1)	DE69112081T2 (fr)
DK (1)	DK0563274T3 (fr)
ES (1)	ES2075680T3 (fr)
GR (1)	GR3017095T3 (fr)
IL (1)	IL100117A (fr)
MX (1)	MX174554B (fr)
NO (1)	NO932184D0 (fr)
NZ (1)	NZ240652A (fr)
WO (1)	WO1992011329A1 (fr)

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US5210155A (en) *	1990-08-24	1993-05-11	Exxon Chemical Patents Inc.	Phenol terminated diester compositions derived from dicarboxylic acids, polyester polymers or alkyd polymers, and curable compositions containing same
US5166289A (en) *	1990-12-19	1992-11-24	Exxon Chemical Patents Inc.	Thermoset coating composition having improved hardness
AU665346B2 (en) *	1991-03-20	1996-01-04	North Dakota State University	Compounds with liquid crystalline properties and coating binders based thereon
US5574103A (en) *	1992-12-29	1996-11-12	Cytec Technology Corp.	Aminoresin based coatings containing 1,3,5-triazine tris-carbamate co-crosslinkers
CA2129720A1 (fr) *	1993-08-10	1995-02-11	Tadahiko Nishi	Composition de revetement aqueux et procede utilisant ce revetement
AU1733395A (en) *	1994-01-25	1995-08-08	Eastern Michigan University	Polymeric vehicle effective for providing solventless coating compositions
US5610263A (en) *	1994-01-25	1997-03-11	Eastern Michigan University	Water thinned polymeric vehicle for coating compositions with low amounts of volatile oragnic compounds
WO1995020004A1 (fr) *	1994-01-25	1995-07-27	Eastern Michigan University	Vehicule polymere pour revetements a haute teneur en solides
US5910563A (en) *	1994-01-25	1999-06-08	Exxon Chemical Patents, Inc.	Water thinned polymeric vehicle for coating compositions with low amounts of volatile organic compounds
US5955550A (en) *	1994-01-25	1999-09-21	Exxon Chemical Patents, Inc.	Polymeric vehicle for providing solventless coating compositions
US5969085A (en) *	1994-01-25	1999-10-19	Exxon Chemical Patents, Inc.	Polymeric vehicle for high solids coatings
US5458920A (en) *	1994-05-20	1995-10-17	Exxon Chemical Patents, Inc.	Gloss reduction agent for solvent based pigmented coating formulations
US6051674A (en) *	1996-08-26	2000-04-18	Exxon Chemical Patents, Inc.	Polymeric vehicles which include a phenol blocked isocyanate having aliphatic hydroxyl fucntionality
US6103826A (en) *	1995-04-19	2000-08-15	Eastern Michigan University	Clearcoat compositions containing phenolic ester compounds
US5973072A (en) *	1996-03-21	1999-10-26	Exxon Chemical Patents, Inc.	Polymeric vehicles which include a phenolic urethane reactive diluent
US5681906A (en) *	1995-04-19	1997-10-28	Exxon Chemical Patents Inc.	Thermoset coating compositions having improved hardness
US5780556A (en) *	1995-06-07	1998-07-14	Exxon Chemical Patents Inc	Thermoset coating compositions having improved hardness and curing properties
JPH09100439A (ja) *	1995-10-05	1997-04-15	Kansai Paint Co Ltd	上塗用ベースコート塗料組成物及びその塗装方法
US5817722A (en) *	1995-10-10	1998-10-06	Exxon Chemical Patents Inc.	Low viscosity, high solids polyesterdiols and compositions containing same
US6005135A (en) *	1996-03-21	1999-12-21	Exxon Chemical Patents Inc.	Water-borne polymeric vehicle for coating compositions containing an amine or ammonium salt of phenolic ester alcohols
DE69734060T2 (de)	1996-05-24	2006-06-29	Angiotech Pharmaceuticals, Inc., Vancouver	Zubereitungen und verfahren zur behandlung oder prävention von krankheiten der körperpassagewege
US7037402B2 (en)	2002-10-15	2006-05-02	National Starch & Chemical Investment Holding Corporation	Reactive hot melt adhesive with non-polymeric aromatic difunctionals
EP1615966B2 (fr)	2003-04-02	2019-10-09	Swimc Llc	Dispersions aqueuses et revetements
US8664330B2 (en)	2003-04-04	2014-03-04	Henkel US IP LLC	Reactive hot melt adhesive with improved hydrolysis resistance
PL3037488T3 (pl)	2004-10-20	2022-11-14	Swimc Llc	Kompozycje powlekające dla pojemników i sposoby powlekania
US7666951B2 (en) *	2005-02-24	2010-02-23	Ppg Industries Ohio, Inc.	Coating compositions that include a polyester polyol, related coated substrates, multi-layer coating and methods
US7910170B2 (en) *	2005-10-18	2011-03-22	Valspar Sourcing, Inc.	Coating compositions for containers and methods of coating
CN101033365B (zh) *	2006-03-09	2010-06-16	上海威肯化学品有限公司	水性烤漆
AU2007259036B2 (en) *	2006-06-15	2012-09-13	Croda International Plc	UV absorbing composition
US7655737B2 (en) *	2006-11-16	2010-02-02	Sabic Innovative Plastics Ip B.V.	Polycarbonate-polyester blends, methods of manufacture, and methods of use
KR101115230B1 (ko) *	2007-07-10	2012-03-13	세키스이가가쿠 고교가부시키가이샤	벤족사진 구조를 갖는 열경화성 수지 및 그의 제조 방법
MX338773B (es)	2009-04-09	2016-05-02	Valspar Sourcing Inc	Polimero que tiene funcionalidad cicloalifatica insaturada y composiciones de recubrimiento formadas de este.
US8747979B2 (en)	2009-07-17	2014-06-10	Valspar Sourcing, Inc.	Coating compositions and articles coated therewith
US9011999B2 (en)	2009-09-18	2015-04-21	Valspar Sourcing, Inc.	Coating composition including an unsaturated polymer
JP6209103B2 (ja) *	2014-02-25	2017-10-04	富士フイルム株式会社	感活性光線性又は感放射線性樹脂組成物、それを用いたレジスト膜、レジスト塗布マスクブランクス、レジストパターン形成方法、及び、フォトマスク

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US4216298A (en) *	1976-11-12	1980-08-05	Bayer Aktiengesellschaft	Process for the preparation of carbonic acid bis-diphenol esters of polyester-diols and their use for the preparation of high-molecular segmented polyester/polycarbonates which can be processed as thermoplastics
US4297455A (en) *	1977-03-22	1981-10-27	Bayer Aktiengesellschaft	Process for the preparation of carbonic acid aryl esters of polyester-diols lengthened via carbonate groups and their use for the preparation of polyester-diol bis-diphenol carbonates and polyester/polycarbonates
DE2827325A1 (de) *	1978-06-22	1980-01-10	Bayer Ag	Verfahren zur herstellung von aliphatisch-aromatischen polycarbonaten mit diphenolcarbonat-endgruppen und ihre verwendung zur herstellung von thermoplastisch verarbeitbaren, hochmolekularen, segmentierten, aliphatisch-aromatischen polycarbonat-elastomeren
US4365039A (en) *	1980-12-15	1982-12-21	Ashland Oil, Inc.	Vapor permeation curable polyester resin coating compositions for flexible substrates
DE3320260A1 (de) *	1983-06-04	1984-12-06	Bayer Ag, 5090 Leverkusen	Diphenolmonoester von carbonsaeuren, ein verfahren zu ihrer herstellung, ihre verwendung zur herstellung von polyestercarbonaten, die erfindungsgemaess erhaeltlichen polyestercarbonate sowie flammwidrige formmassen enthaltend diese polyestercarbonate
US4535132A (en) *	1983-12-12	1985-08-13	Ppg Industries, Inc.	Thermosetting high solids solvent-based polyester polyol coating compositions
GB8519290D0 (en) *	1985-07-31	1985-09-04	Dow Chemical Rheinwerk Gmbh	Resin composition
US5210289A (en) *	1990-06-18	1993-05-11	Eastman Kodak Company	Carboxy containing monomers
US5166289A (en) *	1990-12-19	1992-11-24	Exxon Chemical Patents Inc.	Thermoset coating composition having improved hardness

1990
- 1990-12-19 US US07/630,298 patent/US5166289A/en not_active Expired - Fee Related
1991
- 1991-11-19 NZ NZ240652A patent/NZ240652A/en unknown
- 1991-11-21 IL IL10011791A patent/IL100117A/en not_active IP Right Cessation
- 1991-12-10 ES ES92903275T patent/ES2075680T3/es not_active Expired - Lifetime
- 1991-12-10 AT AT92903275T patent/ATE126259T1/de not_active IP Right Cessation
- 1991-12-10 KR KR1019930701606A patent/KR0167362B1/ko not_active Expired - Fee Related
- 1991-12-10 WO PCT/US1991/009271 patent/WO1992011329A1/fr not_active Ceased
- 1991-12-10 JP JP4503697A patent/JPH06503375A/ja active Pending
- 1991-12-10 DK DK92903275.3T patent/DK0563274T3/da active
- 1991-12-10 EP EP92903275A patent/EP0563274B1/fr not_active Expired - Lifetime
- 1991-12-10 DE DE69112081T patent/DE69112081T2/de not_active Expired - Fee Related
- 1991-12-10 CA CA002096961A patent/CA2096961C/fr not_active Expired - Fee Related
- 1991-12-10 AU AU91533/91A patent/AU648629B2/en not_active Ceased
- 1991-12-10 BR BR919107219A patent/BR9107219A/pt not_active Application Discontinuation
- 1991-12-18 MX MX9102664A patent/MX174554B/es not_active IP Right Cessation
- 1991-12-18 CN CN91111301A patent/CN1062915A/zh active Pending
- 1991-12-19 AR AR91321456A patent/AR247906A1/es active
1993
- 1993-06-14 NO NO932184A patent/NO932184D0/no unknown
1994
- 1994-12-27 US US08/364,059 patent/US5536794A/en not_active Expired - Fee Related
1995
- 1995-08-10 GR GR950402027T patent/GR3017095T3/el unknown

Also Published As

Publication number	Publication date
CA2096961A1 (fr)	1992-06-20
DE69112081D1 (de)	1995-09-14
BR9107219A (pt)	1993-11-16
KR0167362B1 (ko)	1999-05-01
MX174554B (es)	1994-05-25
IL100117A0 (en)	1992-08-18
AU9153391A (en)	1992-07-22
AR247906A1 (es)	1995-04-28
DE69112081T2 (de)	1996-02-29
JPH06503375A (ja)	1994-04-14
US5166289A (en)	1992-11-24
MX9102664A (es)	1992-06-01
EP0563274A1 (fr)	1993-10-06
CA2096961C (fr)	2000-03-28
ES2075680T3 (es)	1995-10-01
ATE126259T1 (de)	1995-08-15
WO1992011329A1 (fr)	1992-07-09
CN1062915A (zh)	1992-07-22
NO932184L (no)	1993-06-14
AU648629B2 (en)	1994-04-28
NO932184D0 (no)	1993-06-14
EP0563274B1 (fr)	1995-08-09
GR3017095T3 (en)	1995-11-30
US5536794A (en)	1996-07-16
NZ240652A (en)	1995-03-28
DK0563274T3 (da)	1995-12-27

Legal Events

Date	Code	Title	Description
1998-11-26	RH	Patent void

Publication	Publication Date	Title
AU648629B2 (en)	1994-04-28	Thermoset coating compositions having improved hardness
US5334671A (en)	1994-08-02	Phenol terminated diester compositions derived from dicarboxylic acids, polyester polymers or alkyd polymers, and curable compositions containing same
US5453469A (en)	1995-09-26	Liquid polymer and polyol compositions, and process for preparing phenol-functional polymer
US5681906A (en)	1997-10-28	Thermoset coating compositions having improved hardness
US5334652A (en)	1994-08-02	Polyester-based coating compositions having high pigment-to-binder ratios
US5458920A (en)	1995-10-17	Gloss reduction agent for solvent based pigmented coating formulations
US5322884A (en)	1994-06-21	Polyester-based coating compositions having high pigment-to-binder ratios
AU715220B2 (en)	2000-01-20	Thermoset coating compositions having improved hardness and curing properties
JP3122122B2 (ja)	2001-01-09	液体ポリマー組成物及びその製造方法
MXPA97007985A (en)	1998-01-01	Coating compositions thermofraguadasteniendo better hardness