NL8702018A - Harssamenstelling op basis van een polymeer en een ester. - Google Patents

Harssamenstelling op basis van een polymeer en een ester. Download PDF

Info

Publication number: NL8702018A
Authority: NL; Netherlands
Prior art keywords: resin composition; ester; polymer; composition according; carbon atoms
Prior art date: 1987-08-28

Application number

NL8702018A

Other languages

English (en)

Dutch (nl)

Original Assignee

Dsm Resins Bv

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.)

1987-08-28

Filing date

1987-08-28

Publication date

1989-03-16

1987-08-28 Application filed by Dsm Resins Bv filed Critical Dsm Resins Bv

1987-08-28 Priority to NL8702018A priority Critical patent/NL8702018A/nl

1988-08-23 Priority to EP19880201788 priority patent/EP0305006A3/fr

1989-03-16 Publication of NL8702018A publication Critical patent/NL8702018A/nl

1989-08-18 Priority to US07/395,719 priority patent/US5064892A/en

Links

239000011342 resin composition Substances 0.000 title claims description 44
229920000642 polymer Polymers 0.000 title claims description 32
150000002148 esters Chemical class 0.000 claims description 43
229920000180 alkyd Polymers 0.000 claims description 21
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 18
125000004432 carbon atom Chemical group C* 0.000 claims description 17
239000003973 paint Substances 0.000 claims description 14
239000000203 mixture Substances 0.000 claims description 13
150000001875 compounds Chemical class 0.000 claims description 11
239000008199 coating composition Substances 0.000 claims description 9
ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical group C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 claims description 8
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 5
229920005989 resin Polymers 0.000 claims description 5
150000004670 unsaturated fatty acids Chemical class 0.000 claims description 4
235000021122 unsaturated fatty acids Nutrition 0.000 claims description 4
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
238000007605 air drying Methods 0.000 claims description 3
125000000962 organic group Chemical group 0.000 claims description 3
229920005862 polyol Polymers 0.000 claims description 3
150000003077 polyols Chemical class 0.000 claims description 3
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical group OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 2
238000010526 radical polymerization reaction Methods 0.000 claims description 2
235000014113 dietary fatty acids Nutrition 0.000 description 18
239000000194 fatty acid Substances 0.000 description 18
229930195729 fatty acid Natural products 0.000 description 18
150000004665 fatty acids Chemical class 0.000 description 17
239000002904 solvent Substances 0.000 description 16
238000001035 drying Methods 0.000 description 12
239000002253 acid Substances 0.000 description 10
239000003921 oil Substances 0.000 description 9
235000019198 oils Nutrition 0.000 description 9
239000003085 diluting agent Substances 0.000 description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
235000010469 Glycine max Nutrition 0.000 description 6
-1 dicyclopentyl oxyalkyl ester Chemical class 0.000 description 6
230000032050 esterification Effects 0.000 description 6
238000005886 esterification reaction Methods 0.000 description 6
238000009835 boiling Methods 0.000 description 5
239000007787 solid Substances 0.000 description 5
229920002554 vinyl polymer Polymers 0.000 description 5
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
150000001252 acrylic acid derivatives Chemical group 0.000 description 4
150000008064 anhydrides Chemical class 0.000 description 4
238000009833 condensation Methods 0.000 description 4
230000005494 condensation Effects 0.000 description 4
238000000034 method Methods 0.000 description 4
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
239000011347 resin Substances 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
244000068988 Glycine max Species 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
239000000178 monomer Substances 0.000 description 3
150000005846 sugar alcohols Polymers 0.000 description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 2
VHVMXWZXFBOANQ-UHFFFAOYSA-N 1-Penten-3-ol Chemical compound CCC(O)C=C VHVMXWZXFBOANQ-UHFFFAOYSA-N 0.000 description 2
LZDXRPVSAKWYDH-UHFFFAOYSA-N 2-ethyl-2-(prop-2-enoxymethyl)propane-1,3-diol Chemical compound CCC(CO)(CO)COCC=C LZDXRPVSAKWYDH-UHFFFAOYSA-N 0.000 description 2
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 2
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 2
239000000020 Nitrocellulose Substances 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
150000001335 aliphatic alkanes Chemical class 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
JQRRFDWXQOQICD-UHFFFAOYSA-N biphenylen-1-ylboronic acid Chemical compound C12=CC=CC=C2C2=C1C=CC=C2B(O)O JQRRFDWXQOQICD-UHFFFAOYSA-N 0.000 description 2
MKUWVMRNQOOSAT-UHFFFAOYSA-N but-3-en-2-ol Chemical compound CC(O)C=C MKUWVMRNQOOSAT-UHFFFAOYSA-N 0.000 description 2
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 description 2
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
230000007613 environmental effect Effects 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
239000000944 linseed oil Substances 0.000 description 2
235000021388 linseed oil Nutrition 0.000 description 2
150000002734 metacrylic acid derivatives Chemical group 0.000 description 2
238000002156 mixing Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000012986 modification Methods 0.000 description 2
229920001220 nitrocellulos Polymers 0.000 description 2
ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
229920001296 polysiloxane Polymers 0.000 description 2
239000000600 sorbitol Substances 0.000 description 2
239000003549 soybean oil Substances 0.000 description 2
235000012424 soybean oil Nutrition 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
239000008096 xylene Substances 0.000 description 2
YAXKTBLXMTYWDQ-UHFFFAOYSA-N 1,2,3-butanetriol Chemical compound CC(O)C(O)CO YAXKTBLXMTYWDQ-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
DGFTWPLUNSGYME-UHFFFAOYSA-N 3-ethylundec-2-enoic acid Chemical compound CCCCCCCCC(CC)=CC(O)=O DGFTWPLUNSGYME-UHFFFAOYSA-N 0.000 description 1
LDMIYOHXGMOTJI-UHFFFAOYSA-N 5-ethyltridec-2-enoic acid Chemical compound CCCCCCCCC(CC)CC=CC(O)=O LDMIYOHXGMOTJI-UHFFFAOYSA-N 0.000 description 1
239000004859 Copal Substances 0.000 description 1
239000004971 Cross linker Substances 0.000 description 1
241000782205 Guibourtia conjugata Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
240000006240 Linum usitatissimum Species 0.000 description 1
235000004431 Linum usitatissimum Nutrition 0.000 description 1
229920000877 Melamine resin Polymers 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
235000004443 Ricinus communis Nutrition 0.000 description 1
235000019486 Sunflower oil Nutrition 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 1
125000000746 allylic group Chemical group 0.000 description 1
229940121363 anti-inflammatory agent Drugs 0.000 description 1
239000002260 anti-inflammatory agent Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
238000010533 azeotropic distillation Methods 0.000 description 1
239000011575 calcium Substances 0.000 description 1
FKYAWWVVKRUUFY-UHFFFAOYSA-L calcium;decanoate Chemical compound [Ca+2].CCCCCCCCCC([O-])=O.CCCCCCCCCC([O-])=O FKYAWWVVKRUUFY-UHFFFAOYSA-L 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
235000013877 carbamide Nutrition 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
CTIHZTFULZJBGQ-UHFFFAOYSA-L cobalt(2+);decanoate Chemical compound [Co+2].CCCCCCCCCC([O-])=O.CCCCCCCCCC([O-])=O CTIHZTFULZJBGQ-UHFFFAOYSA-L 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
238000001816 cooling Methods 0.000 description 1
PQANGXXSEABURG-UHFFFAOYSA-N cyclohex-2-en-1-ol Chemical compound OC1CCCC=C1 PQANGXXSEABURG-UHFFFAOYSA-N 0.000 description 1
238000007865 diluting Methods 0.000 description 1
229910001873 dinitrogen Inorganic materials 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000003912 environmental pollution Methods 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
235000004426 flaxseed Nutrition 0.000 description 1
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 1
238000010438 heat treatment Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
239000004922 lacquer Substances 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
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000003607 modifier Substances 0.000 description 1
150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
LGRFSURHDFAFJT-UHFFFAOYSA-N phthalic anhydride Chemical compound C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
239000003505 polymerization initiator Substances 0.000 description 1
150000007519 polyprotic acids Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
241000894007 species Species 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000002600 sunflower oil Substances 0.000 description 1
239000003784 tall oil Substances 0.000 description 1
229920005992 thermoplastic resin Polymers 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
239000004408 titanium dioxide Substances 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
KHDNXEYJITXOKI-UHFFFAOYSA-N undec-4-enoic acid Chemical compound CCCCCCC=CCCC(O)=O KHDNXEYJITXOKI-UHFFFAOYSA-N 0.000 description 1
239000002023 wood Substances 0.000 description 1
NVKSAUAQUPYOPO-UHFFFAOYSA-L zinc;decanoate Chemical compound [Zn+2].CCCCCCCCCC([O-])=O.CCCCCCCCCC([O-])=O NVKSAUAQUPYOPO-UHFFFAOYSA-L 0.000 description 1
229910052845 zircon Inorganic materials 0.000 description 1
GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
- C08F299/04—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polyesters
- C08F299/0478—Copolymers from unsaturated polyesters and low molecular monomers characterised by the monomers used
- 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
- C09D167/08—Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Oil, Petroleum & Natural Gas (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Paints Or Removers (AREA)
Macromonomer-Based Addition Polymer (AREA)
Polyesters Or Polycarbonates (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

NL8702018A 1987-08-28 1987-08-28 Harssamenstelling op basis van een polymeer en een ester. NL8702018A (nl)

Priority Applications (3)

Application Number	Priority Date	Filing Date	Title
NL8702018A NL8702018A (nl)	1987-08-28	1987-08-28	Harssamenstelling op basis van een polymeer en een ester.
EP19880201788 EP0305006A3 (fr)	1987-08-28	1988-08-23	Composition de résine à base d'un polymère et d'un ester
US07/395,719 US5064892A (en)	1987-08-28	1989-08-18	Resin composition based on a polymer and an ester

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
NL8702018A NL8702018A (nl)	1987-08-28	1987-08-28	Harssamenstelling op basis van een polymeer en een ester.
NL8702018		1987-08-28

Publications (1)

Publication Number	Publication Date
NL8702018A true NL8702018A (nl)	1989-03-16

Family

ID=19850513

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8702018A NL8702018A (nl)	1987-08-28	1987-08-28	Harssamenstelling op basis van een polymeer en een ester.

Country Status (2)

Country	Link
EP (1)	EP0305006A3 (fr)
NL (1)	NL8702018A (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5173113A (en) *	1991-03-12	1992-12-22	Topez Company	Composition for ink vehicles and protective coatings
NL9200506A (nl) *	1992-03-19	1993-10-18	Dsm Nv	Bindmiddelsamenstelling voor poedercoatings.
FR2711659B1 (fr) *	1993-10-25	1995-12-29	Cray Valley Sa	Composition de revêtement pour accrochage direct sur matériaux thermodurcissables et stratifiés utilisant une telle composition.
WO2004111143A2 (fr)	2003-06-12	2004-12-23	Valspar Sourcing, Inc.	Compositions de revetement contenant des diluants reactifs et procedes associes

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1084203A (fr) *	1960-06-27
DE1161014B (de) *	1961-12-09	1964-01-09	Basf Ag	Polyester-Form- oder -UEberzugsmassen
US3423319A (en) *	1966-08-18	1969-01-21	Us Agriculture	Bis(trimethylolpropane diallyl ether) dilinoleate and its phosphonates and lubricant compositions

1987
- 1987-08-28 NL NL8702018A patent/NL8702018A/nl unknown
1988
- 1988-08-23 EP EP19880201788 patent/EP0305006A3/fr not_active Withdrawn

Also Published As

Publication number	Publication date
EP0305006A2 (fr)	1989-03-01
EP0305006A3 (fr)	1990-12-05

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EP1194493B2 (fr)	2009-03-04	Revetements a haute teneur en solides, a sechage rapide a base de resines alkydes modifiees
US4071489A (en)	1978-01-31	Coating compositions from dicyclopentenyl acrylate and/or methacrylate
NL9200506A (nl)	1993-10-18	Bindmiddelsamenstelling voor poedercoatings.
US3806480A (en)	1974-04-23	Esters of melamine resins
US4294735A (en)	1981-10-13	Coating compositions
JPH0586435B2 (fr)	1993-12-13
DE602004009820T2 (de)	2008-08-14	Strahlenhärtbare wässrige zusammensetzung
US4997480A (en)	1991-03-05	Alkyd resins and the use thereof for high solids coatings
US2627508A (en)	1953-02-03	Long oil alkyd resins
NL8702018A (nl)	1989-03-16	Harssamenstelling op basis van een polymeer en een ester.
US9540538B2 (en)	2017-01-10	Drier for alkyd resin compositions
US5064892A (en)	1991-11-12	Resin composition based on a polymer and an ester
EP0357128A1 (fr)	1990-03-07	Diluant réactif pour compositions de peinture
NL8702017A (nl)	1989-03-16	Harssamenstelling op basis van een polymeer en een ester.
WO1996013558A1 (fr)	1996-05-09	Composition de liant insature
US5370939A (en)	1994-12-06	Yellowing resistant, air-drying coating composition containing allyloxypropoxylate
JPH11507639A (ja)	1999-07-06	改良された硬度及び硬化特性を有する熱硬化性被塗組成物
EP0685543B1 (fr)	1999-08-04	Composition de résine contenant une résine alkyde et un diluent réactif
US4720522A (en)	1988-01-19	Water reducible alkyd vinyl copolymer resins
US4100119A (en)	1978-07-11	Greater water resistance and shorter drying time in water soluble enamel paints
NL8802321A (nl)	1990-04-17	Reactieve verdunner voor verfsamenstellingen.
WO2007074333A2 (fr)	2007-07-05	Compositions de revetement et diluants reactifs pour leur preparation
US3333977A (en)	1967-08-01	Water-dispersible coating compositions and phenolic wood bases coated therewith
WO2007074332A2 (fr)	2007-07-05	Compositions de revetement et diluants reactifs pour leur preparation