DE1302319C2 - Durch multiveresterung haertbare ueberzugsmasse - Google Patents

Durch multiveresterung haertbare ueberzugsmasse

Info

Publication number: DE1302319C2
Authority: DE; Germany
Prior art keywords: water; maleic anhydride; weight; phv; molecular weight
Prior art date: 1961-04-12
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

DENDAT1302319D

Other languages

German (de)

English (en)

Other versions

DE1302319U (da

DE1302319B (da

Inventor

Herbert Dr Graz Honel (Oster reich)

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Allnex Austria GmbH

Original Assignee

Vianova Resins AG

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.)

1961-04-12

Publication date

1973-07-12

1971-10-14 Publication of DE1302319B publication Critical patent/DE1302319B/de

1973-07-12 Application granted granted Critical

1973-07-12 Publication of DE1302319C2 publication Critical patent/DE1302319C2/de

Status Expired legal-status Critical Current

Links

239000011248 coating agent Substances 0.000 title claims description 6
238000000576 coating method Methods 0.000 title claims description 4
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 27
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 25
150000001875 compounds Chemical class 0.000 claims description 23
238000005886 esterification reaction Methods 0.000 claims description 20
239000000203 mixture Substances 0.000 claims description 17
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 16
229920005862 polyol Polymers 0.000 claims description 16
229920001225 polyester resin Polymers 0.000 claims description 14
239000004645 polyester resin Substances 0.000 claims description 14
150000003077 polyols Chemical class 0.000 claims description 14
239000002253 acid Substances 0.000 claims description 12
229910052757 nitrogen Inorganic materials 0.000 claims description 9
239000000047 product Substances 0.000 claims description 9
229920003180 amino resin Polymers 0.000 claims description 8
-1 polyol ester Chemical class 0.000 claims description 7
150000002989 phenols Chemical class 0.000 claims description 6
239000010685 fatty oil Substances 0.000 claims description 4
239000003960 organic solvent Substances 0.000 claims description 3
125000001931 aliphatic group Chemical group 0.000 claims description 2
239000007795 chemical reaction product Substances 0.000 claims description 2
238000006386 neutralization reaction Methods 0.000 claims description 2
150000003138 primary alcohols Chemical class 0.000 claims description 2
125000005313 fatty acid group Chemical group 0.000 claims 1
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 42
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 42
241000150258 Prospect Hill orthohantavirus Species 0.000 description 39
229920000218 poly(hydroxyvalerate) Polymers 0.000 description 39
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 27
238000000034 method Methods 0.000 description 20
239000000243 solution Substances 0.000 description 20
239000000126 substance Substances 0.000 description 19
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 17
238000007792 addition Methods 0.000 description 17
150000008064 anhydrides Chemical class 0.000 description 16
239000002585 base Substances 0.000 description 15
235000014113 dietary fatty acids Nutrition 0.000 description 14
230000032050 esterification Effects 0.000 description 14
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239000008149 soap solution Substances 0.000 description 14
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 13
229910021529 ammonia Inorganic materials 0.000 description 13
239000003921 oil Substances 0.000 description 13
235000019198 oils Nutrition 0.000 description 13
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
238000006243 chemical reaction Methods 0.000 description 12
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125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 10
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 10
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 10
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239000011347 resin Substances 0.000 description 10
239000002904 solvent Substances 0.000 description 8
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 7
238000003756 stirring Methods 0.000 description 7
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KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
239000000654 additive Substances 0.000 description 6
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230000003197 catalytic effect Effects 0.000 description 6
150000002148 esters Chemical class 0.000 description 6
238000010438 heat treatment Methods 0.000 description 6
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 6
239000000944 linseed oil Substances 0.000 description 6
235000021388 linseed oil Nutrition 0.000 description 6
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 6
239000003549 soybean oil Substances 0.000 description 6
235000012424 soybean oil Nutrition 0.000 description 6
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 5
230000015572 biosynthetic process Effects 0.000 description 5
238000006266 etherification reaction Methods 0.000 description 5
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 5
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
239000004640 Melamine resin Substances 0.000 description 4
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 4
125000005456 glyceride group Chemical group 0.000 description 4
239000003973 paint Substances 0.000 description 4
239000002023 wood Substances 0.000 description 4
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
230000001476 alcoholic effect Effects 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
238000009835 boiling Methods 0.000 description 3
239000004359 castor oil Substances 0.000 description 3
235000019438 castor oil Nutrition 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
238000009833 condensation Methods 0.000 description 3
230000005494 condensation Effects 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
238000001035 drying Methods 0.000 description 3
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
230000009257 reactivity Effects 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000003784 tall oil Substances 0.000 description 3
150000003512 tertiary amines Chemical class 0.000 description 3
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 3
229910052725 zinc Inorganic materials 0.000 description 3
239000011701 zinc Substances 0.000 description 3
SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 2
HCGFUIQPSOCUHI-UHFFFAOYSA-N 2-propan-2-yloxyethanol Chemical compound CC(C)OCCO HCGFUIQPSOCUHI-UHFFFAOYSA-N 0.000 description 2
QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
229930185605 Bisphenol Natural products 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
235000011037 adipic acid Nutrition 0.000 description 2
239000001361 adipic acid Substances 0.000 description 2
229920000180 alkyd Polymers 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
239000011230 binding agent Substances 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
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
239000011575 calcium Substances 0.000 description 2
239000003518 caustics Substances 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
150000001993 dienes Chemical class 0.000 description 2
125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 2
125000000524 functional group Chemical group 0.000 description 2
238000001879 gelation Methods 0.000 description 2
235000011187 glycerol Nutrition 0.000 description 2
238000000265 homogenisation Methods 0.000 description 2
239000011133 lead Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
238000005809 transesterification reaction Methods 0.000 description 2
239000002966 varnish Substances 0.000 description 2
230000003313 weakening effect Effects 0.000 description 2
KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical class C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
SQHKJSPPFSVNDF-UHFFFAOYSA-N 1,2,2,3-tetrakis(hydroxymethyl)cyclohexan-1-ol Chemical compound OCC1CCCC(O)(CO)C1(CO)CO SQHKJSPPFSVNDF-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
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
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 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical group [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
235000013162 Cocos nucifera Nutrition 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-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
229930040373 Paraformaldehyde Natural products 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
241001125046 Sardina pilchardus Species 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
238000007259 addition reaction Methods 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
230000000903 blocking effect Effects 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
238000005352 clarification Methods 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
238000006482 condensation reaction Methods 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
210000003298 dental enamel Anatomy 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
230000007717 exclusion Effects 0.000 description 1
235000019197 fats Nutrition 0.000 description 1
229940013317 fish oils Drugs 0.000 description 1
150000002314 glycerols Chemical class 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
230000035876 healing Effects 0.000 description 1
TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 description 1
150000004678 hydrides Chemical class 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
230000003993 interaction Effects 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
239000002609 medium Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000004492 methyl ester group Chemical group 0.000 description 1
238000002156 mixing Methods 0.000 description 1
IJDIONYCFIJYLK-UHFFFAOYSA-N n,n-diethylethanamine;propan-2-ol Chemical compound CC(C)O.CCN(CC)CC IJDIONYCFIJYLK-UHFFFAOYSA-N 0.000 description 1
239000004006 olive oil Substances 0.000 description 1
235000008390 olive oil Nutrition 0.000 description 1
229920002866 paraformaldehyde Polymers 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 1
229940031826 phenolate Drugs 0.000 description 1
239000006069 physical mixture Substances 0.000 description 1
238000004321 preservation Methods 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
239000001294 propane Substances 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
229920003987 resole Polymers 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
235000019512 sardine Nutrition 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
150000003384 small molecules Chemical class 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
241000894007 species Species 0.000 description 1
230000002269 spontaneous effect Effects 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
229940014800 succinic anhydride Drugs 0.000 description 1
230000009897 systematic effect Effects 0.000 description 1
230000008719 thickening Effects 0.000 description 1
238000004448 titration Methods 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
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SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09F—NATURAL RESINS; FRENCH POLISH; DRYING-OILS; OIL DRYING AGENTS, i.e. SICCATIVES; TURPENTINE
- C09F7/00—Chemical modification of drying oils
- C09F7/10—Chemical modification of drying oils by re-esterification
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/46—Polyesters chemically modified by esterification
- C08G63/48—Polyesters chemically modified by esterification by unsaturated higher fatty oils or their acids; by resin acids
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/52—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/52—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
- C08G63/54—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation the acids or hydroxy compounds containing carbocyclic rings
- C08G63/553—Acids or hydroxy compounds containing cycloaliphatic rings, e.g. Diels-Alder adducts
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/08—Polyesters modified with higher fatty oils or their acids, or with resins or resin acids
- 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
- C09D155/00—Coating compositions based on homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C09D123/00 - C09D153/00
- C09D155/04—Polyadducts obtained by the diene synthesis
- 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
- C09D191/00—Coating compositions based on oils, fats or waxes; Coating compositions based on derivatives thereof
- C09D191/005—Drying oils
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/78—Preparation processes
- C08G63/82—Preparation processes characterised by the catalyst used

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Polymers & Plastics (AREA)
Medicinal Chemistry (AREA)
Oil, Petroleum & Natural Gas (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Engineering & Computer Science (AREA)
Life Sciences & Earth Sciences (AREA)
General Chemical & Material Sciences (AREA)
Polyesters Or Polycarbonates (AREA)
Compositions Of Macromolecular Compounds (AREA)
Macromonomer-Based Addition Polymer (AREA)

DENDAT1302319D 1961-04-12 Durch multiveresterung haertbare ueberzugsmasse Expired DE1302319C2 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
AT293061A AT268675B (de)	1961-04-12	1961-04-12	Verfahren zur Herstellung einer vorzugsweise als Überzugsmittel geeigneten Lösung eines Kunstharzgemisches, welches durch erhöhte Temperatur und/oder Katalysatoren härtbar ist

Publications (2)

Publication Number	Publication Date
DE1302319B DE1302319B (da)	1971-10-14
DE1302319C2 true DE1302319C2 (de)	1973-07-12

Family

ID=3542549

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DENDAT1302319D Expired DE1302319C2 (de)	1961-04-12		Durch multiveresterung haertbare ueberzugsmasse

Country Status (8)

Country	Link
US (1)	US3300424A (da)
AT (1)	AT268675B (da)
BE (1)	BE616311A (da)
CH (1)	CH459567A (da)
DE (1)	DE1302319C2 (da)
DK (1)	DK119785B (da)
ES (1)	ES276225A1 (da)
GB (1)	GB1007163A (da)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AT267185B (de) *	1964-04-13	1968-12-10	Vianova Kunstharz Ag	Verfahren zur Herstellung eines den unlöslichen Zustand überführbaren Stoffgemisches aus einer Additionsverbindung aus Maleinsäureanhydrid und ungesättigte Ölfettsauren enthaltenden Polyolestern und einer Polyhydroxylverbindung
US3878145A (en) *	1965-03-13	1975-04-15	Reichhold Albert Chemie Ag	Process for producing water-dilutable coating compositions suitable for electrocoating
US3950286A (en) *	1965-09-21	1976-04-13	Vianova Kunstharz, A.G.	Coating process and composition
AT281229B (de) *	1966-10-06	1970-05-11	Vianova Kunstharz Ag	Verfahren zur Herstellung wasserlöslicher Bindemittel für elektrophoretische Oberflächenbeschichtung
NL129446C (da) *	1967-03-09	1900-01-01
US3867323A (en) *	1973-06-06	1975-02-18	Union Carbide Corp	Water-dilutable coating compositions containing maleinized oil and resole
AT328587B (de) *	1973-08-20	1976-03-25	Vianova Kunstharz Ag	Verfahren zur herstellung von wasserigen uberzugsmitteln
CH592737A5 (da) *	1973-10-05	1977-11-15	Ciba Geigy Ag
USRE30660E (en) *	1975-10-21	1981-06-30		Water soluble insulating varnish
US4179420A (en) *	1975-10-21	1979-12-18	Schenectady Chemicals, Inc.	Water soluble insulating varnish
DE2851962A1 (de) *	1978-03-18	1980-06-19	Hoechst Ag	Verwendung eines wasserloeslichen reaktiven bindemittels fuer klebstoffe
DE2914299C3 (de) *	1979-04-09	1982-03-25	Hoechst Ag, 6000 Frankfurt	Pigmentpräparate, Verfahren zu ihrer Herstellung und ihre Verwendung
US4248745A (en) *	1979-05-01	1981-02-03	Schenectady Chemicals, Inc.	Water soluble insulating varnish
US4511682A (en) *	1983-06-28	1985-04-16	Union Carbide Corporation	Water-dispersible coating compositions and process

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2306281A (en) *		1942-12-22		Peocess of making fatty oil
US2033132A (en) *	1931-08-07	1936-03-10	Ellis Foster Co	Diene type reaction product and method of making same
US2188883A (en) *	1936-12-22	1940-01-30	Edwin T Clocker	Condensation product and method
GB500348A (en) *	1937-05-06	1939-02-06	Pinchin Johnson & Co Ltd	Improvements in or relating to synthetic resinous compositions
US2188888A (en) *	1938-10-15	1940-01-30	Edwin T Clocker	Condensation product and method
US2312732A (en) *	1938-10-19	1943-03-02	Standard Oil Dev Co	Process and agent for breaking petroleum emulsions
US2444328A (en) *	1943-12-31	1948-06-29	Petrolite Corp	Composition of matter
US2941968A (en) *	1954-11-03	1960-06-21	Pittsburgh Plate Glass Co	Water dispersible interpolymers
US2909496A (en) *	1955-07-19	1959-10-20	Devoe & Raynolds Co	Reaction products of polyepoxides and monomeric partial esters of polyhydric alcohols with maleic anhydrideunsaturated organic acid adducts, and methods and compositionsfor producing the same
US3012485A (en) *	1959-03-30	1961-12-12	Shell Oil Co	Bituminous compositions
BE622310A (da) *	1961-10-09

0
- BE BE616311D patent/BE616311A/xx unknown
- DE DENDAT1302319D patent/DE1302319C2/de not_active Expired
1961
- 1961-04-12 AT AT293061A patent/AT268675B/de active
1962
- 1962-04-06 ES ES276225A patent/ES276225A1/es not_active Expired
- 1962-04-09 GB GB13617/62A patent/GB1007163A/en not_active Expired
- 1962-04-10 CH CH436062A patent/CH459567A/de unknown
- 1962-04-12 DK DK167862AA patent/DK119785B/da unknown
- 1962-04-12 US US187133A patent/US3300424A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
DK119785B (da)	1971-02-22
US3300424A (en)	1967-01-24
CH459567A (de)	1968-07-15
GB1007163A (en)	1965-10-13
BE616311A (da)	1900-01-01
DE1302319B (da)	1971-10-14
AT268675B (de)	1969-02-25
ES276225A1 (es)	1962-09-16

Legal Events

Date	Code	Title	Description
1977-12-31	E77	Valid patent as to the heymanns-index 1977

Publication	Publication Date	Title
DE1595278C3 (de)	1980-10-09	Verfahren zur Herstellung von wasserdispergierbaren Alkydharzen und deren Verwendung
DE1302319C2 (de)	1973-07-12	Durch multiveresterung haertbare ueberzugsmasse
DE2416658C3 (de)	1979-09-27	Verfahren zur Herstellung von wasserlöslichen und wasserdispergierbaren Alkydharzen und ihre Verwendung
EP0029145A2 (de)	1981-05-27	Verfahren zur Herstellung von verbesserten wässrigen Emulsionen von luft- und ofentrocknenden Alkydharzen
DE2928552A1 (de)	1981-01-29	Waessrige dispersionen urethanmodifizierter polyester, verfahren zu ihrer herstellung und ihre verwendung zur herstellung von lacken
EP0167962B1 (de)	1989-09-27	Ungesättigte Polyester
DE3246618A1 (de)	1984-07-05	Alkydharze, enthaltend ringoeffnungsprodukte epoxidierter fettalkohole oder fettsaeurederivate als hydroxylverbindungen
DE2601618A1 (de)	1976-07-29	Beschichtungsmittel auf basis eines mit wasser verduennbaren maleinatoeles
DE887413C (de)	1953-08-24	Verfahren zur Herstellung von oel-, wachs- oder harzartigen Um-wandlungsprodukten von AEthergruppen enthaltenden Kondensations-produkten aus Aminotriazinen, Formaldehyd und Alkoholen
EP0002488A1 (de)	1979-06-27	Verfahren zur Herstellung von wasseremulgierbaren lufttrocknenden Lackbindemitteln
DE2204140A1 (de)	1973-08-02	Haertbares wasserloesliches polyesteramid und verfahren zu dessen herstellung
DE1570461C3 (de)	1978-10-26	Verfahren zur Herstellung von mit Wasser verdünnbaren Bindemitteln
DE2013702B2 (de)	1974-10-24	Überzugsmittel
DE2439548A1 (de)	1976-03-04	Wassermischbare reaktivverduenner
EP0062786B1 (de)	1984-07-18	Verfahren zur Herstellung phenolharzmodifizierter Bindemittel
EP0259681A2 (de)	1988-03-16	Verfahren zur Herstellung wasserverdünnbarer, phosphorsäuremodifizierter Bindemittel für Einbrennlacke
DE2555732A1 (de)	1976-06-24	Verfahren zur herstellung von wasserverduennbaren lackbindemitteln
DE1805189C3 (de)	1981-05-14	Überzugsmittel
DE2161253A1 (de)	1973-06-28	Verfahren zur herstellung von alkydharzen
DE3507505A1 (de)	1986-09-04	Polyetherpolyester
DE1520747C (de)		Verfahren zur Herstellung von Alkydharzen
DE1298224B (de)	1969-06-26	Waessrige UEberzugsmittel
DE2119161C3 (de)	1976-09-09	Verfahren zur Herstellung von Alkyd harzen und deren Verwendung
CH460350A (de)	1968-07-31	Verfahren zur Herabsetzung der Säurezahl von Alkydharzen
DE868349C (de)	1953-02-23	Verfahren zur Herstellung von Kondensationsprodukten