FR1155644A - Procédé de fabrication d'une résine alkyde pouvant être mise en dispersion dans l'eau - Google Patents
Procédé de fabrication d'une résine alkyde pouvant être mise en dispersion dans l'eauInfo
- Publication number
- FR1155644A FR1155644A FR1155644DA FR1155644A FR 1155644 A FR1155644 A FR 1155644A FR 1155644D A FR1155644D A FR 1155644DA FR 1155644 A FR1155644 A FR 1155644A
- Authority
- FR
- France
- Prior art keywords
- mono
- styrene
- iii
- glycol
- water
- Prior art date
- 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
Links
- 229920000180 alkyd Polymers 0.000 title abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title abstract 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 2
- HXGDTGSAIMULJN-UHFFFAOYSA-N acenaphthylene Chemical compound C1=CC(C=C2)=C3C2=CC=CC3=C1 HXGDTGSAIMULJN-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 abstract 2
- 238000001035 drying Methods 0.000 abstract 2
- 235000019198 oils Nutrition 0.000 abstract 2
- -1 poly-oxyalkylene glycol Chemical compound 0.000 abstract 2
- 229920001223 polyethylene glycol Polymers 0.000 abstract 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 abstract 2
- 150000005846 sugar alcohols Polymers 0.000 abstract 2
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 abstract 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 abstract 1
- SZTBMYHIYNGYIA-UHFFFAOYSA-N 2-chloroacrylic acid Chemical class OC(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-N 0.000 abstract 1
- KBKNKFIRGXQLDB-UHFFFAOYSA-N 2-fluoroethenylbenzene Chemical compound FC=CC1=CC=CC=C1 KBKNKFIRGXQLDB-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- 235000017060 Arachis glabrata Nutrition 0.000 abstract 1
- 244000105624 Arachis hypogaea Species 0.000 abstract 1
- 235000010777 Arachis hypogaea Nutrition 0.000 abstract 1
- 235000018262 Arachis monticola Nutrition 0.000 abstract 1
- 244000025254 Cannabis sativa Species 0.000 abstract 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 abstract 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 abstract 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 abstract 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 abstract 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 abstract 1
- 244000068988 Glycine max Species 0.000 abstract 1
- 235000010469 Glycine max Nutrition 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- 240000006240 Linum usitatissimum Species 0.000 abstract 1
- 235000004431 Linum usitatissimum Nutrition 0.000 abstract 1
- 229930195725 Mannitol Natural products 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- 235000008753 Papaver somniferum Nutrition 0.000 abstract 1
- 235000010678 Paulownia tomentosa Nutrition 0.000 abstract 1
- 240000002834 Paulownia tomentosa Species 0.000 abstract 1
- 235000004347 Perilla Nutrition 0.000 abstract 1
- 244000124853 Perilla frutescens Species 0.000 abstract 1
- 239000004698 Polyethylene Substances 0.000 abstract 1
- 239000002202 Polyethylene glycol Substances 0.000 abstract 1
- 235000004443 Ricinus communis Nutrition 0.000 abstract 1
- 235000003434 Sesamum indicum Nutrition 0.000 abstract 1
- 244000000231 Sesamum indicum Species 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthalene Natural products C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 abstract 1
- 150000001242 acetic acid derivatives Chemical class 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 125000005907 alkyl ester group Chemical group 0.000 abstract 1
- 235000009120 camo Nutrition 0.000 abstract 1
- 235000005607 chanvre indien Nutrition 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 abstract 1
- 235000012343 cottonseed oil Nutrition 0.000 abstract 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical class C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 abstract 1
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 1
- 230000032050 esterification Effects 0.000 abstract 1
- 238000005886 esterification reaction Methods 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 238000002474 experimental method Methods 0.000 abstract 1
- 239000000194 fatty acid Substances 0.000 abstract 1
- 229930195729 fatty acid Natural products 0.000 abstract 1
- 150000004665 fatty acids Chemical class 0.000 abstract 1
- 235000004426 flaxseed Nutrition 0.000 abstract 1
- 235000011187 glycerol Nutrition 0.000 abstract 1
- 239000011487 hemp Substances 0.000 abstract 1
- 229940051250 hexylene glycol Drugs 0.000 abstract 1
- SVTBMSDMJJWYQN-UHFFFAOYSA-N hexylene glycol Natural products CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 abstract 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 abstract 1
- HTUMBQDCCIXGCV-UHFFFAOYSA-N lead oxide Chemical compound [O-2].[Pb+2] HTUMBQDCCIXGCV-UHFFFAOYSA-N 0.000 abstract 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N lead(II) oxide Inorganic materials [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 abstract 1
- 239000000594 mannitol Substances 0.000 abstract 1
- 235000010355 mannitol Nutrition 0.000 abstract 1
- 125000005395 methacrylic acid group Chemical group 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- 239000003973 paint Substances 0.000 abstract 1
- 235000020232 peanut Nutrition 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- 229920001451 polypropylene glycol Polymers 0.000 abstract 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical class C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 239000000600 sorbitol Substances 0.000 abstract 1
- 235000010356 sorbitol Nutrition 0.000 abstract 1
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 1
- 235000020238 sunflower seed Nutrition 0.000 abstract 1
- 239000000454 talc Substances 0.000 abstract 1
- 229910052623 talc Inorganic materials 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 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
- C09D167/08—Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
-
- 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
- C08F242/00—Copolymers of drying oils with other monomers
-
- 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
- C08G63/66—Polyesters containing oxygen in the form of ether groups
- C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
-
- 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
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/08—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
-
- 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
- C08F212/00—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 an aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/06—Hydrocarbons
- C08F212/08—Styrene
-
- 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
- C08F212/00—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 an aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/06—Hydrocarbons
- C08F212/12—Monomers containing a branched unsaturated aliphatic radical or a ring substituted by an alkyl radical
-
- 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
- C08F220/00—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 a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
-
- 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
- C08F220/00—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 a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/42—Nitriles
- C08F220/44—Acrylonitrile
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Polyesters Or Polycarbonates (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB351405X | 1955-07-15 | ||
| GB100756X | 1956-07-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| FR1155644A true FR1155644A (fr) | 1958-05-06 |
Family
ID=26247242
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR1155644D Expired FR1155644A (fr) | 1955-07-15 | 1956-07-13 | Procédé de fabrication d'une résine alkyde pouvant être mise en dispersion dans l'eau |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3001961A (fr) |
| BE (1) | BE549546A (fr) |
| CH (1) | CH351405A (fr) |
| DE (1) | DE1231433B (fr) |
| FR (1) | FR1155644A (fr) |
| GB (1) | GB845861A (fr) |
| NL (2) | NL208940A (fr) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0000087A1 (fr) * | 1977-06-13 | 1978-12-20 | Unilever N.V. | Dispersions aqueuses de résines alkydes séchant à l'air et leur utilisation |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3223658A (en) * | 1958-07-21 | 1965-12-14 | Tenneco Chem | Stable aqueous alkyd resin emulsions |
| NL268270A (fr) * | 1960-08-23 | |||
| US3297605A (en) * | 1961-01-10 | 1967-01-10 | Textron Inc | Water dispersible condensation products of a drying oil glyceride ester and a polyethylene glycol |
| US3333977A (en) * | 1961-12-15 | 1967-08-01 | Textron Inc | Water-dispersible coating compositions and phenolic wood bases coated therewith |
| US3333978A (en) * | 1961-12-15 | 1967-08-01 | Textron Inc | Water-dispersible coating compositions and phenolic wood bases coated therewith |
| BE632501A (fr) * | 1962-05-18 | |||
| US3254040A (en) * | 1962-12-07 | 1966-05-31 | Interchem Corp | Thixotropic syrups containing polyamide-modified unsaturated polyesters and styrene |
| US3280057A (en) * | 1963-02-12 | 1966-10-18 | Allied Chem | Water thinned industrial baking enamels comprising an adduct of an alkylene oxide and a polyhydroxy compound containing at least three hydroxyl groups |
| US3442835A (en) * | 1965-08-19 | 1969-05-06 | Ashland Oil Inc | Water-dispersible polyalkylene glycol modified drying oil alkyd |
| US3457206A (en) * | 1966-05-16 | 1969-07-22 | Staley Mfg Co A E | Water dispersible alkyd resins comprising esterified units of an alkoxypolyoxyethylene glycol |
| US3485781A (en) * | 1968-01-05 | 1969-12-23 | Ashland Oil Inc | Cross-linking of water soluble or water-dispersible polyesters with dichromates |
| US4051089A (en) * | 1975-04-21 | 1977-09-27 | Mobil Oil Corporation | Water reducible short oil alkyd resins and process of making same |
| GB1580044A (en) * | 1976-04-07 | 1980-11-26 | Coates Brothers & Co | Oleoresinous paint binders |
| US4116903A (en) * | 1977-03-02 | 1978-09-26 | P.R.A. Laboratories Incorporated | Alkyd-supported emulsion interpolymers and methods for preparation |
| US4410687A (en) * | 1982-11-29 | 1983-10-18 | Ppg Industries, Inc. | Polyester dispersants for coating compositions |
| US6172159B1 (en) * | 2000-01-18 | 2001-01-09 | Accures Corporation | Water-reducible polyester resins and urethane coatings produced therefrom |
| WO2014087418A1 (fr) * | 2012-12-05 | 2014-06-12 | Asian Paints Ltd. | Dispersions aqueuses d'alkyde acrylé |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2092713A (en) * | 1927-05-23 | 1937-09-07 | Ellis Foster Co | Synthetic product and process of making same |
| US2155639A (en) * | 1935-08-30 | 1939-04-25 | American Cyanamid Co | Rubber-like material and method of producing same |
| US2166542A (en) * | 1937-09-24 | 1939-07-18 | American Cyanamid Co | Oxygen-convertible compositions |
| GB629490A (en) * | 1947-08-13 | 1949-09-21 | Donald Atherton | Improvements in or relating to the manufacture of oil-modified alkyd resins |
| US2634245A (en) * | 1950-04-27 | 1953-04-07 | Pittsburgh Plate Glass Co | Water dispersible alkyd type resins |
| US2919254A (en) * | 1954-03-22 | 1959-12-29 | Pittsburgh Plate Glass Co | Acrylamide and aromatic hydrocarbon monomer modified interpolymers of maleinized oils |
| NL195778A (fr) * | 1954-03-22 | |||
| US2919253A (en) * | 1954-08-27 | 1959-12-29 | American Cyanamid Co | Styrenated oil-modified alkyd resins modified with divinyl benzene and the process of preparing same |
-
0
- NL NL101563D patent/NL101563C/xx active
- BE BE549546D patent/BE549546A/xx unknown
- NL NL208940D patent/NL208940A/xx unknown
-
1955
- 1955-07-15 GB GB20626/55A patent/GB845861A/en not_active Expired
-
1956
- 1956-07-12 US US597326A patent/US3001961A/en not_active Expired - Lifetime
- 1956-07-13 CH CH351405D patent/CH351405A/fr unknown
- 1956-07-13 FR FR1155644D patent/FR1155644A/fr not_active Expired
- 1956-07-14 DE DEB41042A patent/DE1231433B/de active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0000087A1 (fr) * | 1977-06-13 | 1978-12-20 | Unilever N.V. | Dispersions aqueuses de résines alkydes séchant à l'air et leur utilisation |
Also Published As
| Publication number | Publication date |
|---|---|
| CH351405A (fr) | 1961-01-15 |
| NL101563C (fr) | |
| NL208940A (fr) | |
| DE1231433B (de) | 1966-12-29 |
| BE549546A (fr) | |
| GB845861A (en) | 1960-08-24 |
| US3001961A (en) | 1961-09-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| FR1155644A (fr) | Procédé de fabrication d'une résine alkyde pouvant être mise en dispersion dans l'eau | |
| US4983716A (en) | Non-aqueous dispersions | |
| CN100376644C (zh) | 抗污涂料 | |
| CN106478896A (zh) | 一种综合型聚羧酸减水剂的制备方法 | |
| CN110511388B (zh) | 一种用于水性印铁涂料的改性羟基丙烯酸乳液及其制备方法 | |
| US3719619A (en) | Quick drying coatings containing copolymers having t-aliphatic hydrocarbon groups and t-aliphatic alkyd resins | |
| CN105802433A (zh) | 一种速干环保涂料及其制作方法 | |
| US2992197A (en) | Modified oil copolymer emulsions and process of preparing the same | |
| JPS6210269B2 (fr) | ||
| CN104693371B (zh) | 一种新型水性双组份聚氨酯涂料用丙烯酸改性树脂 | |
| US4309321A (en) | Aqueous coating composition | |
| CN111499805A (zh) | 腰果油改性的水性丙烯酸改性醇酸树脂分散体的制备方法 | |
| CN114773970A (zh) | 一种水性高体积固含钢结构常温防腐漆及其制备方法 | |
| CN110563889A (zh) | 一种稀土改性丙烯酸共聚水性醇酸树脂及其制备方法 | |
| CN1224643C (zh) | 树脂组合物、含硼聚合物的生产方法和防污涂料 | |
| GB989252A (en) | Improvements in or relating to water-dispersible drying oil compositions | |
| JPH0588275B2 (fr) | ||
| CN111171244A (zh) | 一种聚丙烯酸酯改性醇酸树脂复合乳液的制备方法 | |
| GB962974A (en) | Process for preparing oil-containing binders suitable for the preparation of water-based binder compositions | |
| JP2763790B2 (ja) | 酸化架橋性水稀釈性結合剤及びその製造方法 | |
| CN105754461A (zh) | 一种水性预混乳液及其抗污涂料 | |
| JPS6223790B2 (fr) | ||
| DE1794223C3 (de) | Einbrennlacke auf Basis von wäßrigen Dispersionen Von reaktive Gruppen enthaltenden Acrylestermischpolymerisaten | |
| DE916906C (de) | Verfahren zur Herstellung von harzartigen Terpolymeren | |
| AT394566B (de) | Verfahren zur herstellung von wasserverduennbaren ueberzugsmaterialien auf basis von mit fettsaeuren oder oel modifizierten harzen und einer waessrigen polymerdispersion |