WO2000040659A2 - Aqueous resin compositions - Google Patents

Aqueous resin compositions Download PDF

Info

Publication number
WO2000040659A2
WO2000040659A2 PCT/US2000/000162 US0000162W WO0040659A2 WO 2000040659 A2 WO2000040659 A2 WO 2000040659A2 US 0000162 W US0000162 W US 0000162W WO 0040659 A2 WO0040659 A2 WO 0040659A2
Authority
WO
WIPO (PCT)
Prior art keywords
ethylene glycol
composition
resin
ether
water
Prior art date
Application number
PCT/US2000/000162
Other languages
French (fr)
Other versions
WO2000040659A3 (en
Inventor
Scott Patrick Christensen
Brian T. Keen
Original Assignee
Union Carbide Chemicals & Plastics Technology Corporation
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.)
Filing date
Publication date
Application filed by Union Carbide Chemicals & Plastics Technology Corporation filed Critical Union Carbide Chemicals & Plastics Technology Corporation
Priority to CA002358919A priority Critical patent/CA2358919A1/en
Priority to JP2000592360A priority patent/JP2002534554A/en
Priority to EP00901391A priority patent/EP1194488A2/en
Priority to BR0008356-9A priority patent/BR0008356A/en
Priority to MXPA01006924A priority patent/MXPA01006924A/en
Priority to KR1020017008568A priority patent/KR20010101396A/en
Priority to AU22239/00A priority patent/AU2223900A/en
Publication of WO2000040659A2 publication Critical patent/WO2000040659A2/en
Publication of WO2000040659A3 publication Critical patent/WO2000040659A3/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/20Diluents or solvents
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/02Emulsion paints including aerosols
    • C09D5/024Emulsion paints including aerosols characterised by the additives
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D167/00Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/08Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids

Definitions

  • This invention relates to aqueous resin compositions which contain a novel coupling solvent and are useful in architectural or industrial coating compositions such as paints and protective coating formulations.
  • Coupling power efficiency may be quantified as a "coupling number", which number represents the minimum mole percent of solvent required to ensure a single phase system at any ratio of water to resin.
  • Glycol ethers have been recognized as useful coupling solvents.
  • D. Pollock and R. J. LaTulip The Dow Chemical Company, presented at Proceedings of the ESD/ASM, Advanced Coatings Technology Conference, June 10-12, 1991, Dearborn, Michigan , the coupling efficiency of glycol ethers prepared from ethylene oxide and propylene oxide having an alkyl group of one to four carbon atoms were evaluated in various hydrocarbon/water mixtures.
  • Ethylene glycol ethers in particular ethylene glycol butyl ether, was found to perform satisfactorily as a coupling agent in mixtures of lower hydrocarbons such as cyclohexane or decane and water.
  • the present invention relates to water-borne resin compositions which comprise a resin component, water and a coupling solvent comprising a predominately normal or straight chain ethylene glycol pentyl ether composition containing at least 90% by weight, based on the total weight of the glycol ether composition of ethylene glycol n-pentyl ether.
  • the water-borne resin compositions of the present invention comprise (a) a resin component, (b) water and (c) a novel glycol ether coupling solvent component whose coupling efficiency has heretofore gone unrecognized in the art.
  • the coupling solvent component which applicants have discovered exhibits unexpectedly good coupling efficiency when tested in hexadecane/water mixtures is a predominately normal or straight chain ethylene glycol pentyl ether composition containing at least 90% by weight, based on the total weight of the component of ethylene glycol n-pentyl ether.
  • the presence of higher amounts of ethylene glycol n-pentyl ether appears to improve coupling efficiency and particularly good results are obtained when the coupling solvent component contains at least 95% by weight of ethylene glycol n-pentyl ether.
  • the ethylene glycol pentyl ether coupling solvent component containing at least 90% by weight of ethylene glycol n-pentyl ether may be obtained using known processes and techniques. Such a product is advantageously prepared by reacting pentanol containing at least 90% n-pentanol with ethylene oxide in the presence of a basic or acidic catalyst. Pentanol containing at least 90% n-pentanol may be prepared directly utilizing oxo technology disclosed in U.S. Patent Nos.
  • ethylene glycol n-pentyl ether product used in the present invention contains minor amounts, i.e. 10% or less of the ethylene glycol 2-methylbutyl ether isomer but is otherwise essentially free of isomers including highly toxic species such as ethylene glycol 3- methylbutyl ether.
  • the amount of ethylene glycol n-pentyl ether present in the water-borne resin compositions of the present invention will vary depending on the type and amount of resin present with the optimum amount easily being determined by the skilled formulator.
  • the ethylene glycol n-pentyl ether component will be present in an amount of from about 0.2 to about 50% by weight, based on the total weight of the water-borne resin composition.
  • the water-borne resin compositions of the present invention may contain other organic solvents in addition to the ethylene glycol n- pentyl ether.
  • Suitable compounds which may be useful as cosolvents with ethylene glycol n-pentyl ether are well known and may be selected from alcohols, glycols, glycol ethers, glycol ether esters, ketones, esters, aliphatic and aromatic hydrocarbons, halogenated hydrocarbons, nitriles, amides and carbonates.
  • Examples of such compounds include, without limitation, ethanol, butanol, ethylene glycol, ethylene glycol ethyl ether, ethylene glycol propyl ether, ethylene glycol butyl ether, ethylene glycol hexyl ether, diethylene glycol ethyl ether, diethylene glycol butyl ether, propylene glycol t- butyl ether and mixtures thereof.
  • Resins useful in the compositions of the present invention tend to be hydrophobic and may be any of the resins known in the art to be suitable for use in paints and protective coatings.
  • examples of such resins include, but are not limited to alkyds, epoxies, polyesters, polyurethanes, acrylics, vinyl resins, styrene resins, styrene-acrylic resins, styrene-butadiene resins, vinyl acetate resins and mixtures thereof.
  • the amount of resin present in the aqueous resin compositions of the present invention will be in the range of about 10 to about 75% by weight based on the total weight of the composition.
  • the ethylene glycol n-pentyl ether coupling solvents are particularly useful with alkyd resins.
  • the water-borne resin compositions of this invention may include any of the well- known and conventional additives such as flow-control agents, adhesion promoters, wetting agents, cross-linking agents, surfactants, plasticizers, drying retarders, biocides, anti-foaming agents, rheology modifiers, pigments, fillers and the like. Selection and use of such additives is well within the capabilities of the skilled formulator.
  • the amount of water present in the water-borne resin compositions of this invention will depend upon the type and amount of resin present and the intended use of such composition. Typically, the amount of water used in such compositions will be in the range of about 5 to about 75% by weight, based on the total weight of the composition. Selection of the appropriate amount of water and the manner in which the various ingredients are combined to prepare the resin compositions of this invention are within the skill of a knowledgeable formulator. - b -
  • ethylene glycol hexyl ether ethylene glycol hexyl ether
  • EGPE ethylene glycol pentyl ether compound of the present invention
  • ternary phase diagrams were prepared for the water- EGHE- hexadecane and water-EGPE-hexadecane from phase composition measurements obtained at 25°C by compositional analysis of phases equilibrated in a constant temperature bath for at least 24 hours.
  • Water composition was determined by Karl Fisher titration: glycol ether and hexadecane compositions were determined by gas chromatography.
  • Phase boundaries for the ternary systems are drawn through the data points plotted in the ternary phase diagrams.
  • the coupling number for a particular glycol ether which is the minimum mole percent of that glycol ether required to ensure a single phase system at any ratio of water to hexedecane, is determined from the phase boundary curve of the relevant ternary phase diagram.
  • ethylene glycol pentyl ether would have a coupling number of at least 50 or higher for hexadecane mixtures.
  • the coupling number of the ethylene glycol pentyl ether of the present invention is at least 20% lower than what might be expected for a pentyl glycol ether.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Paints Or Removers (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Novel water-borne resin compositions useful in architectural or industrial coatings comprising: (a) a resin, (b) a coupling solvent comprising ethylene glycol pentyl ether which contains at least about 90 % by weight of ethylene glycol n-pentyl ether, and (c) water.

Description

AQUEOUS RESIN COMPOSITIONS
Field of the Invention
This invention relates to aqueous resin compositions which contain a novel coupling solvent and are useful in architectural or industrial coating compositions such as paints and protective coating formulations.
Background of the Invention
The paints and coatings industry is continually looking for new formulations which meet demands for better product performance. In addition, the industry is faced with increasing pressure from regulatory efforts to reduce the release of volatile organic solvents into the environment when coating formulations are applied to a substrate. This has led the industry to step up efforts to develop high performance, resin-based architectural coating formulations in which the resin is water-borne, i.e. dispersed or emulsified in water, thus reducing the amount of volatile organic solvents present.
It is well known that a suitable coupling solvent needs to be present in water-borne resin coating compositions to achieve acceptable film forming and other properties when applied to a substrate. The resins used in coating compositions are normally not dissolved by water. The coupling solvent increases the mutual solubility between the resin and the water thus increasing the homogeneity of a coating composition and improving its performance when applied as a protective coating. Normally, sufficient coupling solvent must be present to maintain a single phase resin/water mixture for any ratio of water to resin. Because compounds useful as coupling solvents are relatively expensive and in light of the effort to reduce the presence of volatile organic compounds in coating compositions, there is a need to find solvents having a high degree of coupling power or coupling efficiency so as to achieve the desired results with a minimum amount of solvent present. Coupling power efficiency may be quantified as a "coupling number", which number represents the minimum mole percent of solvent required to ensure a single phase system at any ratio of water to resin.
Glycol ethers have been recognized as useful coupling solvents. In an article titled "Fundamentals of Glycol Ethers in Coupling Solvents", D. Pollock and R. J. LaTulip, The Dow Chemical Company, presented at Proceedings of the ESD/ASM, Advanced Coatings Technology Conference, June 10-12, 1991, Dearborn, Michigan , the coupling efficiency of glycol ethers prepared from ethylene oxide and propylene oxide having an alkyl group of one to four carbon atoms were evaluated in various hydrocarbon/water mixtures. Ethylene glycol ethers, in particular ethylene glycol butyl ether, was found to perform satisfactorily as a coupling agent in mixtures of lower hydrocarbons such as cyclohexane or decane and water. However, all of the ethylene oxide based glycol ethers tested, including ethylene glycol butyl ether, were found to be too hydrophilic to perform satisfactorily as a coupling solvent in mixtures of water and higher hydrocarbons such as hexadecane.
USP 5,753,738 describes certain alkoxy ethoxyethanol compounds which are useful as coupling solvents. The coupling efficiency of these diethylene glycol ethers was tested in mixtures of heptane and water and in aqueous resin systems and compared to commercially available coupling solvents such as ethylene glycol butyl ether, ethylene glycol hexyl ether and diethylene glycol butyl ether. The data in tables 1 to 5 of this patent suggests that among the commercially available coupling solvents tested ethylene glycol butyl ether has the best coupling efficiency followed by diethylene glycol butyl ether with ethylene glycol hexyl ether being the least effective.
Summary of the Invention
According to the present invention, applicants have discovered a specific glycol ether composition which is useful as a coupling solvent as demonstrated by coupling efficiency tests performed in hexadecane and water mixtures. More specifically, the present invention relates to water-borne resin compositions which comprise a resin component, water and a coupling solvent comprising a predominately normal or straight chain ethylene glycol pentyl ether composition containing at least 90% by weight, based on the total weight of the glycol ether composition of ethylene glycol n-pentyl ether.
Description of the Invention
The water-borne resin compositions of the present invention comprise (a) a resin component, (b) water and (c) a novel glycol ether coupling solvent component whose coupling efficiency has heretofore gone unrecognized in the art. The coupling solvent component which applicants have discovered exhibits unexpectedly good coupling efficiency when tested in hexadecane/water mixtures is a predominately normal or straight chain ethylene glycol pentyl ether composition containing at least 90% by weight, based on the total weight of the component of ethylene glycol n-pentyl ether. The presence of higher amounts of ethylene glycol n-pentyl ether appears to improve coupling efficiency and particularly good results are obtained when the coupling solvent component contains at least 95% by weight of ethylene glycol n-pentyl ether.
The ethylene glycol pentyl ether coupling solvent component containing at least 90% by weight of ethylene glycol n-pentyl ether may be obtained using known processes and techniques.. Such a product is advantageously prepared by reacting pentanol containing at least 90% n-pentanol with ethylene oxide in the presence of a basic or acidic catalyst. Pentanol containing at least 90% n-pentanol may be prepared directly utilizing oxo technology disclosed in U.S. Patent Nos. 3,527,809; 4,283,562; 4,593,011; 4,762,817; 4,769,498; 5,113,022; 5,180,854 and 5,364,950 or by appropriate refining of a pentanol product containing more than 10% isomers using known techniques. The ethylene glycol n-pentyl ether product used in the present invention contains minor amounts, i.e. 10% or less of the ethylene glycol 2-methylbutyl ether isomer but is otherwise essentially free of isomers including highly toxic species such as ethylene glycol 3- methylbutyl ether.
The amount of ethylene glycol n-pentyl ether present in the water-borne resin compositions of the present invention will vary depending on the type and amount of resin present with the optimum amount easily being determined by the skilled formulator. Typically, the ethylene glycol n-pentyl ether component will be present in an amount of from about 0.2 to about 50% by weight, based on the total weight of the water-borne resin composition.
The water-borne resin compositions of the present invention may contain other organic solvents in addition to the ethylene glycol n- pentyl ether. Suitable compounds which may be useful as cosolvents with ethylene glycol n-pentyl ether are well known and may be selected from alcohols, glycols, glycol ethers, glycol ether esters, ketones, esters, aliphatic and aromatic hydrocarbons, halogenated hydrocarbons, nitriles, amides and carbonates. Examples of such compounds include, without limitation, ethanol, butanol, ethylene glycol, ethylene glycol ethyl ether, ethylene glycol propyl ether, ethylene glycol butyl ether, ethylene glycol hexyl ether, diethylene glycol ethyl ether, diethylene glycol butyl ether, propylene glycol t- butyl ether and mixtures thereof.
Resins useful in the compositions of the present invention tend to be hydrophobic and may be any of the resins known in the art to be suitable for use in paints and protective coatings. Examples of such resins include, but are not limited to alkyds, epoxies, polyesters, polyurethanes, acrylics, vinyl resins, styrene resins, styrene-acrylic resins, styrene-butadiene resins, vinyl acetate resins and mixtures thereof. Typically, the amount of resin present in the aqueous resin compositions of the present invention will be in the range of about 10 to about 75% by weight based on the total weight of the composition. The ethylene glycol n-pentyl ether coupling solvents are particularly useful with alkyd resins.
When used in paints and protective coatings, the water-borne resin compositions of this invention may include any of the well- known and conventional additives such as flow-control agents, adhesion promoters, wetting agents, cross-linking agents, surfactants, plasticizers, drying retarders, biocides, anti-foaming agents, rheology modifiers, pigments, fillers and the like. Selection and use of such additives is well within the capabilities of the skilled formulator.
The amount of water present in the water-borne resin compositions of this invention will depend upon the type and amount of resin present and the intended use of such composition. Typically, the amount of water used in such compositions will be in the range of about 5 to about 75% by weight, based on the total weight of the composition. Selection of the appropriate amount of water and the manner in which the various ingredients are combined to prepare the resin compositions of this invention are within the skill of a knowledgeable formulator. - b -
Examples
Coupling numbers for commercially available, ethylene glycol hexyl ether (EGHE) and an ethylene glycol pentyl ether compound of the present invention (EGPE) were determined in a hexadecane/water system. The ether compound of the present invention which was tested contained about 99% by weight of ethylene glycol n-pentyl ether.
To obtain the coupling numbers for the glycol ethers tested, ternary phase diagrams were prepared for the water- EGHE- hexadecane and water-EGPE-hexadecane from phase composition measurements obtained at 25°C by compositional analysis of phases equilibrated in a constant temperature bath for at least 24 hours. Water composition was determined by Karl Fisher titration: glycol ether and hexadecane compositions were determined by gas chromatography. Phase boundaries for the ternary systems are drawn through the data points plotted in the ternary phase diagrams. The coupling number for a particular glycol ether, which is the minimum mole percent of that glycol ether required to ensure a single phase system at any ratio of water to hexedecane, is determined from the phase boundary curve of the relevant ternary phase diagram.
The coupling numbers for EGHE and EGPE obtained from the hexadecane ternary diagrams are shown in Table 1 and compared with the coupling number determined for EGBE in the article titled "Fundamentals of Glycol Ethers in Coupling Solvents" (the "Dow Article") discussed earlier. Table 1
Figure imgf000009_0001
invention
When a higher hydrocarbon such as hexadecane is present in an aqueous mixture, it might be expected that a glycol ether having a longer alkyl chain would have a lower coupling number than a glycol ether with a shorter alkyl chain. This does in fact prove to be the case as shown by the coupling numbers for ethylene glycol butyl ether and ethylene glycol hexyl ether in Table 1. However, the coupling number for the ethylene glycol n-pentyl ether compound of the present invention shown in Table 1 is suprisingly low as compared to the other ethers. The data from the Dow article and that in Table 1 suggests that ethylene glycol pentyl ether would have a coupling number of at least 50 or higher for hexadecane mixtures. The coupling number of the ethylene glycol pentyl ether of the present invention is at least 20% lower than what might be expected for a pentyl glycol ether.

Claims

- o -What is claimed is:
1. An aqueous composition useful in paints and protective coatings comprising:
(a) a resin,
(b) a coupling solvent comprising ethylene glycol pentyl ether which contains at least about 90% by weight of ethylene glycol n-pentyl ether, and
(c) water.
2 The composition of claim 1 wherein said resin is selected from the group consisting of alkyds, epoxies, polyesters, polyurethanes, acrylics, vinyl resins, styrene resins, styrene-acrylic resins, styrene- butadiene resins, vinyl acetate resins and mixtures thereof.
3. The composition of claim 2 wherein the resin is an alkyd resin.
4. The composition of claim 1 wherein said ethylene glycol pentyl ether contains at least about 95% ethylene glycol n-pentyl ether.
5. The composition of claim 1 wherein the resin is present in an amount of from about 10 to about 75% by weight, based on the total weight of the composition.
6. The composition of claim 5 wherein the ethylene glycol pentyl ether is present in an amount of from about 0.2 to about 50% by weight.
7. An architectural or industrial coating composition containing the aqueous resin composition of claim 1.
8. A method of improving the film forming properties of an architectural coating composition by adding thereto an effective amount of the aqueous resin composition of claim 1.
PCT/US2000/000162 1999-01-06 2000-01-05 Aqueous resin compositions WO2000040659A2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
CA002358919A CA2358919A1 (en) 1999-01-06 2000-01-05 Aqueous resin compositions
JP2000592360A JP2002534554A (en) 1999-01-06 2000-01-05 Aqueous resin composition
EP00901391A EP1194488A2 (en) 1999-01-06 2000-01-05 Aqueous resin compositions
BR0008356-9A BR0008356A (en) 1999-01-06 2000-01-05 Aqueous resin compositions and their use
MXPA01006924A MXPA01006924A (en) 1999-01-06 2000-01-05 Aqueous resin compositions.
KR1020017008568A KR20010101396A (en) 1999-01-06 2000-01-05 Aqueous resin compositions
AU22239/00A AU2223900A (en) 1999-01-06 2000-01-05 Aqueous resin compositions

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/226,450 US6242517B1 (en) 1999-01-06 1999-01-06 Aqueous resin compositions
US09/226,450 1999-01-06

Publications (2)

Publication Number Publication Date
WO2000040659A2 true WO2000040659A2 (en) 2000-07-13
WO2000040659A3 WO2000040659A3 (en) 2002-01-24

Family

ID=22848953

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2000/000162 WO2000040659A2 (en) 1999-01-06 2000-01-05 Aqueous resin compositions

Country Status (10)

Country Link
US (1) US6242517B1 (en)
EP (1) EP1194488A2 (en)
JP (1) JP2002534554A (en)
KR (1) KR20010101396A (en)
CN (1) CN1339053A (en)
AU (1) AU2223900A (en)
BR (1) BR0008356A (en)
CA (1) CA2358919A1 (en)
MX (1) MXPA01006924A (en)
WO (1) WO2000040659A2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102993845A (en) * 2012-11-29 2013-03-27 陈容太 Wooden floor care agent
US9902895B2 (en) 2014-10-31 2018-02-27 Chevron U.S.A. Inc. Polymer compositions
CA2997138C (en) 2015-09-02 2022-07-26 Chevron U.S.A. Inc. Enhanced oil recovery compositions and methods thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0009526A1 (en) * 1978-10-10 1980-04-16 Mobil Oil Corporation Water-solubilizable epoxy resin and coating composition comprising the resin for metal food contact surfaces
WO1995017461A1 (en) * 1993-12-23 1995-06-29 Bp Chemicals Limited Ether cosolvents for resin formulations

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3446764A (en) 1965-04-23 1969-05-27 Scm Corp Solvent composition for water reducible resin dispersions
US4131585A (en) 1976-11-15 1978-12-26 Sybron Corporation Leveling agent for floor polishes
GB8306530D0 (en) 1983-03-09 1983-04-13 Bp Chem Int Ltd Coalescing agents
US5238987A (en) 1991-01-11 1993-08-24 Arco Chemical Technology, L.P. Propoxylated PTB coalescing agents for water-borne protective coatings

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0009526A1 (en) * 1978-10-10 1980-04-16 Mobil Oil Corporation Water-solubilizable epoxy resin and coating composition comprising the resin for metal food contact surfaces
WO1995017461A1 (en) * 1993-12-23 1995-06-29 Bp Chemicals Limited Ether cosolvents for resin formulations

Also Published As

Publication number Publication date
MXPA01006924A (en) 2003-06-04
CN1339053A (en) 2002-03-06
US6242517B1 (en) 2001-06-05
AU2223900A (en) 2000-07-24
BR0008356A (en) 2001-10-09
CA2358919A1 (en) 2000-07-13
EP1194488A2 (en) 2002-04-10
WO2000040659A3 (en) 2002-01-24
KR20010101396A (en) 2001-11-14
JP2002534554A (en) 2002-10-15

Similar Documents

Publication Publication Date Title
CA2439083C (en) Coating compositions containing low voc compounds
US8440752B2 (en) Coating compositions containing low VOC compounds
KR101758397B1 (en) Fluorine-containing compound, fluorine-containing surfactant and compositions containing same
EP2097476A1 (en) Amine neutralizing agents for low volatile compound organic paints
EP2424833B1 (en) Polyhydroxy-diamines as multi-functional additives for paints, coatings and expoxies
AU2007313927A1 (en) Aqueous film-forming compositions containing reduced levels of volatile organic compounds
CA2510554A1 (en) Hydrophilicized blocked polyisocyanates
US8329634B2 (en) Water based paint thinner
EP0551378A1 (en) Method of activating n-methyl-2-pyrrolidone (nmp) and/or gamma-butyrolactone (blo) varnish and paint remover solvents
CN101735682A (en) Use of adducts of ethylene and/or propylene oxide with fatty alcohols as coalescents
US20050272842A1 (en) Antiskinning compound and compositions containing them
SE512220C2 (en) Aqueous concentrate of an associative thickening polymer and use of a nonionic surfactant to reduce the viscosity of the concentrate
US5238987A (en) Propoxylated PTB coalescing agents for water-borne protective coatings
US6583104B1 (en) Aqueous cleaning compositions
US5186744A (en) Propoxylated PTB coalescing agents for water-borne protective coatings
EP0119026A2 (en) Coalescing agents
US6242517B1 (en) Aqueous resin compositions
WO2018004473A2 (en) Coalescing agent derived from dioxolane derivatives
CN113121319A (en) Compound and coating composition comprising same
JP2016132771A (en) Wetting agent for aqueous coating
JP3778222B2 (en) Orthophthalaldehyde stabilization solution
CN115052481B (en) Tebuconazole formulations
US20040219350A1 (en) Polyfluorinated compounds useful as surfactants, foam control agents and/or rheology modifiers
EP4282859A1 (en) Triazine carbamate crosslinker
CN112010739A (en) Film forming additive and preparation method thereof

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 00803499.0

Country of ref document: CN

AK Designated states

Kind code of ref document: A2

Designated state(s): AL AU BA BB BG BR CA CN CU CZ EE GE HU ID IL IN IS JP KR KZ LC LK LR LT LV MG MK MN MX NO NZ PL RO RU SG SI SK TR TT UA UZ VN ZA

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): GH GM KE LS MW SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: 2000901391

Country of ref document: EP

ENP Entry into the national phase

Ref document number: 2358919

Country of ref document: CA

Ref document number: 2358919

Country of ref document: CA

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 1020017008568

Country of ref document: KR

ENP Entry into the national phase

Ref document number: 2000 592360

Country of ref document: JP

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: PA/a/2001/006924

Country of ref document: MX

WWP Wipo information: published in national office

Ref document number: 1020017008568

Country of ref document: KR

AK Designated states

Kind code of ref document: A3

Designated state(s): AL AU BA BB BG BR CA CN CU CZ EE GE HU ID IL IN IS JP KR KZ LC LK LR LT LV MG MK MN MX NO NZ PL RO RU SG SI SK TR TT UA UZ VN ZA

AL Designated countries for regional patents

Kind code of ref document: A3

Designated state(s): GH GM KE LS MW SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

WWP Wipo information: published in national office

Ref document number: 2000901391

Country of ref document: EP

WWW Wipo information: withdrawn in national office

Ref document number: 2000901391

Country of ref document: EP

WWW Wipo information: withdrawn in national office

Ref document number: 1020017008568

Country of ref document: KR