SU655322A3 - Лакокрасочна композици - Google Patents

Лакокрасочна композици

Info

Publication number: SU655322A3
Authority: SU; USSR - Soviet Union
Prior art keywords: water; pigment; soluble; pigments; resin
Prior art date: 1974-06-07

Application number

SU752140018A

Other languages

English (en)

Russian (ru)

Inventor

Галатик Вальтер

Дворак Герт

Original Assignee

Вианова Кунстхарц Аг (Фирма)

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.)

1974-06-07

Filing date

1975-06-02

Publication date

1979-03-30

1975-06-02 Application filed by Вианова Кунстхарц Аг (Фирма) filed Critical Вианова Кунстхарц Аг (Фирма)

1979-03-30 Application granted granted Critical

1979-03-30 Publication of SU655322A3 publication Critical patent/SU655322A3/ru

Links

239000002966 varnish Substances 0.000 title claims description 33
239000000203 mixture Substances 0.000 title claims description 30
239000000049 pigment Substances 0.000 claims description 53
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 31
229920005989 resin Polymers 0.000 claims description 14
239000011347 resin Substances 0.000 claims description 14
229920000180 alkyd Polymers 0.000 claims description 10
239000004925 Acrylic resin Substances 0.000 claims description 8
229920000178 Acrylic resin Polymers 0.000 claims description 7
239000003973 paint Substances 0.000 claims description 6
239000003960 organic solvent Substances 0.000 claims description 4
125000001931 aliphatic group Chemical group 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
150000005690 diesters Chemical class 0.000 claims description 2
-1 ether polyol Chemical class 0.000 claims description 2
229920005862 polyol Polymers 0.000 claims description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 1
150000005846 sugar alcohols Polymers 0.000 claims 1
239000002253 acid Substances 0.000 description 17
239000011230 binding agent Substances 0.000 description 14
239000004922 lacquer Substances 0.000 description 11
125000002887 hydroxy group Chemical group [H]O* 0.000 description 10
239000000243 solution Substances 0.000 description 10
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
239000006185 dispersion Substances 0.000 description 9
238000001035 drying Methods 0.000 description 9
239000002904 solvent Substances 0.000 description 9
238000000576 coating method Methods 0.000 description 7
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 6
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 6
238000010992 reflux Methods 0.000 description 6
239000013049 sediment Substances 0.000 description 6
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 5
239000000945 filler Substances 0.000 description 5
238000005189 flocculation Methods 0.000 description 5
230000016615 flocculation Effects 0.000 description 5
239000007787 solid Substances 0.000 description 5
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 4
239000011248 coating agent Substances 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-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
CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000001361 adipic acid Substances 0.000 description 3
235000011037 adipic acid Nutrition 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
239000008367 deionised water Substances 0.000 description 3
229910021641 deionized water Inorganic materials 0.000 description 3
239000000975 dye Substances 0.000 description 3
239000001023 inorganic pigment Substances 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
239000000463 material Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
239000012860 organic pigment Substances 0.000 description 3
239000002245 particle Substances 0.000 description 3
238000012545 processing Methods 0.000 description 3
239000004576 sand Substances 0.000 description 3
238000004062 sedimentation Methods 0.000 description 3
238000000926 separation method Methods 0.000 description 3
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 3
SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 2
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 compound COCN(COC)C1=NC(N(COC)COC)=NC(N(COC)COC)=N1 BNCADMBVWNPPIZ-UHFFFAOYSA-N 0.000 description 2
SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
229920000877 Melamine resin Polymers 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
239000011324 bead Substances 0.000 description 2
125000002091 cationic group Chemical group 0.000 description 2
238000004132 cross linking Methods 0.000 description 2
WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
238000000227 grinding Methods 0.000 description 2
238000006386 neutralization reaction Methods 0.000 description 2
230000019612 pigmentation Effects 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
238000003860 storage Methods 0.000 description 2
239000000725 suspension Substances 0.000 description 2
HGTUJZTUQFXBIH-UHFFFAOYSA-N (2,3-dimethyl-3-phenylbutan-2-yl)benzene Chemical group C=1C=CC=CC=1C(C)(C)C(C)(C)C1=CC=CC=C1 HGTUJZTUQFXBIH-UHFFFAOYSA-N 0.000 description 1
229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 description 1
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 1
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
ZFJCQQPFHVYVKC-UHFFFAOYSA-N C(C)(C)O.CN(CCO)C Chemical compound C(C)(C)O.CN(CCO)C ZFJCQQPFHVYVKC-UHFFFAOYSA-N 0.000 description 1
235000003385 Diospyros ebenum Nutrition 0.000 description 1
241000792913 Ebenaceae Species 0.000 description 1
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
239000004640 Melamine resin Substances 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
229920006243 acrylic copolymer Polymers 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
230000000740 bleeding effect Effects 0.000 description 1
239000007767 bonding agent Substances 0.000 description 1
229910052796 boron Inorganic materials 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
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Natural products CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
125000001142 dicarboxylic acid group Chemical group 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000007865 diluting Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000007720 emulsion polymerization reaction Methods 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
RMALEVVYWOZIFD-UHFFFAOYSA-N ethene;hexyl prop-2-enoate Chemical compound C=C.CCCCCCOC(=O)C=C RMALEVVYWOZIFD-UHFFFAOYSA-N 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000008394 flocculating agent Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
230000003993 interaction Effects 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
238000005259 measurement Methods 0.000 description 1
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
239000011164 primary particle Substances 0.000 description 1
239000010802 sludge Substances 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
238000012360 testing method Methods 0.000 description 1
230000009974 thixotropic effect Effects 0.000 description 1
239000003232 water-soluble binding agent Substances 0.000 description 1
238000005303 weighing Methods 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 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
- C09D167/06—Unsaturated polyesters having carbon-to-carbon 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2606—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
- C08G65/2609—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups containing aliphatic hydroxyl groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- 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
- 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
- C09D17/00—Pigment pastes, e.g. for mixing in paints
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Paints Or Removers (AREA)

SU752140018A 1974-06-07 1975-06-02 Лакокрасочна композици SU655322A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
AT474874A AT335019B (de)	1974-06-07	1974-06-07	Verfahren zur herstellung von pigmentierten wasserverdunnbaren einbrennlacken

Publications (1)

Publication Number	Publication Date
SU655322A3 true SU655322A3 (ru)	1979-03-30

Family

ID=3567861

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU752140018A SU655322A3 (ru)	1974-06-07	1975-06-02	Лакокрасочна композици

Country Status (5)

Country	Link
AT (1)	AT335019B (de)
DE (1)	DE2516386A1 (de)
FR (1)	FR2273852A1 (de)
GB (1)	GB1501926A (de)
SU (1)	SU655322A3 (de)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
RU2484113C2 (ru) *	2008-04-16	2013-06-10	Сайтек Серфейс Спешиэлтиз Аустриа Гмбх	Пастообразующая смола для универсальной пигментной пасты
RU2520439C2 (ru) *	2008-08-19	2014-06-27	Эвоник Рем ГмбХ	Способ окрашивания поли(мет)акрилатов жидкими красками на водной основе и жидкие краски на водной основе
RU2650141C2 (ru) *	2016-05-23	2018-04-09	Наталья Александровна Мельник	Способ получения водоразбавляемого алкидного пентафталевого лака впф-050

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2710993C3 (de) *	1977-03-14	1981-05-14	Henkel KGaA, 4000 Düsseldorf	Wäßrige Dispersion von als Überzugsmittel bzw. Lackbindemittel geeigneten Harzen
DK378479A (da) *	1978-10-02	1980-04-03	Henkel & Cie Gmbh	Fremgangsmaade til fremstilling af modoficerede alkydharpikser og harpiksernes anvendelse som lakbindemiddel
JPS59124922A (ja) *	1982-12-31	1984-07-19	Nippon Paint Co Ltd	顔料分散用樹脂
EP2873703A1 (de) *	2013-11-18	2015-05-20	BASF Coatings GmbH	Mischsystem zur Herstellung sowohl von Decklackzusammensetzungen als auch von als Spachtel eingesetzten Beschichtungszusammensetzungen

1974
- 1974-06-07 AT AT474874A patent/AT335019B/de not_active IP Right Cessation
1975
- 1975-04-15 DE DE19752516386 patent/DE2516386A1/de not_active Withdrawn
- 1975-05-22 GB GB22325/75A patent/GB1501926A/en not_active Expired
- 1975-06-02 SU SU752140018A patent/SU655322A3/ru active
- 1975-06-02 FR FR7517144A patent/FR2273852A1/fr active Granted

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
RU2484113C2 (ru) *	2008-04-16	2013-06-10	Сайтек Серфейс Спешиэлтиз Аустриа Гмбх	Пастообразующая смола для универсальной пигментной пасты
RU2520439C2 (ru) *	2008-08-19	2014-06-27	Эвоник Рем ГмбХ	Способ окрашивания поли(мет)акрилатов жидкими красками на водной основе и жидкие краски на водной основе
RU2520439C9 (ru) *	2008-08-19	2015-02-20	Эвоник Рем ГмбХ	Способ окрашивания поли(мет)акрилатов жидкими красками на водной основе и жидкие краски на водной основе
RU2650141C2 (ru) *	2016-05-23	2018-04-09	Наталья Александровна Мельник	Способ получения водоразбавляемого алкидного пентафталевого лака впф-050

Also Published As

Publication number	Publication date
DE2516386A1 (de)	1975-12-18
FR2273852B3 (de)	1978-12-29
FR2273852A1 (fr)	1976-01-02
GB1501926A (en)	1978-02-22
ATA474874A (de)	1975-08-15
AT335019B (de)	1977-02-25

Publication	Publication Date	Title
EP0068044B1 (de)	1985-01-23	Wässrige Pigmentpasten und deren Verwendung
EP0485441A1 (de)	1992-05-20	Neue pigmentzubereitungen auf basis von perylenverbindungen.
WO2015021933A1 (zh)	2015-02-19	一种超支化聚酯树脂颜料分散剂、制备方法及其色浆和色浆的应用
JPH0753889A (ja)	1995-02-28	銅フタロシアニン顔料の製造方法および該製造方法より得られる銅フタロシアニン顔料を含む印刷インキもしくは塗料組成物
CN109337536A (zh)	2019-02-15	一种水性丙烯酸-醇酸涂料及其制备方法
JPH06122835A (ja)	1994-05-06	細分された顔料分散液、水性顔料懸濁液、分散液の製造方法及びこの分散液を含有する耐水性インク
CN111019442B (zh)	2022-06-28	一种高浓缩通用色浆及其制备方法和应用
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SU655322A3 (ru)	1979-03-30	Лакокрасочна композици
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