WATERBORNE COATING COMPOSITIONS
This is a division of copending Canadian Patent Application Serial No.
2,430,496 with a national phase entry date of May 28, 2003 based on PCT/LTSO1/44891 filed November 30, 2001.
BACKGROUND OF THE INVENTION
This invention relates to a waterborne coating produced using all liquid slurry raw materials and an all liquid blend process for making the coatings. The process of this invention reproducibly produces waterborne coating formulations having predetermined quality such as viscosity, pH, NVM, and the like, and reproducible color and gloss. The present invention utilizes novel raw material slurry compositions whereby each raw material, including titanium dioxide, p a~ment extenders, thickeners, etc., is prefbrmulated as liquid slurries to have substantially the same viscosity.
According to this invention, each raw material slurry typically has substantially the same viscosity as that desired of the final waterborne coating product. The slurries are admixed and blended, by volumetric and gravimetric methods, to form coating formulations having predetermined quality and specifications.
Conventional waterborne paint manufacturing processes consist of mixing or blending pigments and various liquid and dry additives with latex resins, and then processing or grinding using high speed Cowles dispensers. Dry raw materials commonly used in waterborne coatings include prime hiding, e~rtender and prime colored pigments and hydroxyethylcellulose thickeners.
?0 Typically, waterborne formulations contain high levels of these hard-to-Qrind pigments, which are dispersed with lov volume extenders, pigments, and additives in a high speed Cowles dispenser. The dispersion paste. is then thinned down by adding other raw materials such as water based vehicles and defoamers, and then subsequently adding other raw materials such as liquid pigment slurries and thickeners to obtain the final unshaded product. Liquid components commonly used in waterborne coatings include additives such as wetting agents, dispersants, defoamers, glycols, mildeweides, bactericides, coalescents, ammonium hydroxide, amines, etc. as well as pigment slurries and late.
WO 02l-1~28G PCT/USO1/-t~891 Multiple additions of the required shading bases are then necessary to achieve the final color. Other adjustments to the final product to meet specifications for gloss, viscosity, pH, ete., are common.
Thus, the raw materials used in waterborne paint formulations typically contain high levels of materials having extremely narrow compatibility tolerances, due to incompatibilities of the components in the mixing. Of particular concern in any system is the ability to reproducibly and consistently obtain the same quality of product . Also, pigments in colorant dispersions and conventional pigment slurries have a tendency to settle, which require agitators that can maintain the dispersions as a reasonably uniform mixture. It is sometimes also necessary to add materials that are incompatible with materials already in the process stream. Such additives, as well as their order of addition, may cause problems associated with stability, seeding and/or settling typically due to these iilcompatibilities.
Thus, there is a need for a process to overcome the incompatibilities between raw materials in formulation. There is also a need to produce waterborne coatings with reproducible quality and characteristics, without the need for making adjustments to the final waterborne coating products that do not meet quality specifications. W accordance with the teachings of the present invention, paint manufacturing process steps can be significantly reduced by first consolidating or interblending the raw materials into liquid blends or slurries, and then continuously, simultaneously, or sequentially admixing the liquid slurries to obtain a final waterborne coating. The waterborne coatings produced according to this invention do not require rebalancing or adjustments to pH, viscosity;
color, etc. Thus, in the present invention, a waterborne product can be achieved having predetermined quality and physical properties such as color, viscosity, pH, NVivI, and gloss by cross-blending the liquid blends or slurries.
SLiYMARY OF TIC IvVENTION
The present invention is directed to a waterborne coating composition comprising (a) about 0 to 70 percent by weight, based on the total weight of the composition, of a titanium dioxide slurry;
WO 02/.1a28C PCT/USI)1/~-1891 (b) about 0 to 75 percent by weight, based on the total weight of the composition, of at least one extender pigment slurry that can be selected from the group consisting of, but not limited to, calcium carbonate slurry, silica slurry, and kaolin clay slurry; and (c) about 1 to 20 percent by weight, based on the total weight of the composition, of at least one thickener slurry that can be selected from the group consisting of polyacrylates, hydroxyethylcellulose, alkali soluble emulsions, hydrophobic ethoxylated urethane resins, and hydrophobically-modified alkali soluble emulsions; and (d) about I
to 10 percent by weight of a glycol slurry; and (e) at least one latex binder.
The viscosity of the coating composition produced according to this invention can be predetermined and substantially the same as the viscosity of the raw material slurries, and which is preferably within the range of 70-125 hrebs units. A process for producing the waterborne coating composition is also provided.
This invention is also directed to pigment slurries comprising (a) about 20 to 90 percent by .
weight, based on the total weight of the slurry, of titanium dioxide pigment;
(b) about 0.5 to 10 percent by weight, based on the total weight of the slurry, of a glycol; and (c) about 0.1 to 10 percent by weight, based on the total weight of the slurry, of at least one thickener that can be selected from the group consisting of polyacrylates, hydroxyethylcellulose, alkali soluble emulsions, hydrophobic ethoxylated urethane resins, and hydrophobically-modified alkali soluble emulsions. The pigment can be selected from the group consisting of titanium dioxide, calcium carbonate, kaolin clay and silica. The Stormer viscosity of said pigment slurry is in the range of about 70-125 Krebs units. A
process for producing the slurry is also provided.
Another object is to provide a process for producing a waterborne coating composition having predetermined viscosity characteristics utilizing a total liquid blend process, comprising: (a) providing a plurality of reservoirs containing liquid blend~slurries of raw materials, said liquid blend slurries of raw materials have substantially the same viscosities; (b) continuously, simultaneously, or sequentially mixing a latex binder with a controlled amount of the liquid blend slurries from said reservoirs to WO 02/-1.128Cr PCT/USO1/1.1891 produce the waterborne coating. The final waterborne coating product has substantially the same viscosity as the liquid blend slurries and does not require additional adjustments for viscosity. The process comprises providing suitable liquid blends of raw materials, such as titanium dioxide slurries or other pigment slurries, such as extender pigment slurries of calcium carbonate, kaolin clay, silica, glycol slurries, and the like, or mixtures thereof.
DETA.II,ED DESCRIPTION OF THE INVENTION
According to this invention, the raw materials of waterborne coatings which are typically incompatible with each other, are made into compatible liquid blends or slurries prior to formulation.
The liquid blends and slurries can then be combined together to obtain a final liquid blend waterborne coating via a continuous, simultaneous or sequential dosing process. The process of making the waterborne coating of this invention uses preferred raw material slurries, such as titanium dioxide slurries and pigment extender slurries, that are preformulated at a viscosity similar to the final paint product. All other liquid blend raw materials, including additives to the formulation, particularly those with narrow compatibility tolerances, such as thickeners, organic solvents, and powders, are l~ prefonnulated and pre-dispersed in a liquid slurry and preformulated to obtain the desired viscosity characteristics. As used herein, "slurries" is synonymous with intermediates, mixtures, blends, or composites of raw materials, and these terms are used interchangeably.
In particular; non-settling titanium dioxide slurries and other rav material slurries, are utilized in this invention, having viscosities substantially the same as the desired final waterborne coating.
Typically, aqueous slurries of titanium dioxide pigment are prepared by mixing titanium dioxide pigment powder with dispersants and other additives with water in a batch mixer and stirred for a long time until the required percentage of solids and degree of dispersion is achieved in the slurry. Storage tanks hold the mi~Yed slurry, but there must always be a high degree of agitation occurring in the tanks to prevent the titanium dioxide pigments in tile slurry from settling. Due to the non-settling nature of the slurries WO 02/1.1286 PCT/USO1/~~891 of this invention, high agitation is not required. All other liquid raw material slurries or blends are also preformulated at the desired final waterborne coating viscosity. Ultimately, ease of manufacture occurs through the total liquid blending process of this invention. In contrast to a conventional latex process where a large number of raw materials are utilized, and adjustments to pH, viscosity, etc. are usually required, the process of the present invention minimizes the number of raw materials required due to consolidation of raw material components in a liquid blend. This process also eliminates the problems associated with settling and seedilig in the final blend. Colored shading bases can also be added during the blending process by accurate dispensing and/or metering. The system allows for the greatest fonnulation flexibility, as well as the best process and quality control designed system, and also minunizes raw materials while maintaining product mix and lowest effective total operation cost.
Titanium Dioxide Slurries The titanium dioxide slurries of this invention have a viscosity of a desired final waterborne coating product. The titanium dioxide slurry can be utilized in a liquid blend paint manufacturing system. The predispersed slurry may be stored for considerable periods of time without settling, although occasional agitation in a storage tank is preferred. The present predispersed titanium dioxide slurry has been found to remain free from agglomerates and remain stable in a storage tank for extended periods of time. This process is repeated for all other dry components such as other pigments and pigment extenders. Said dry components are processed into liquid slurries and stored in the same fashion. Thus, all components utilized by this process are converted to an all liquid system prior to the manufacturing process.
Preferably, the titanium dioxide slurry comprises (a) about 50 to 90 percent by weight, based on the total weight of the slurry, of titanium dioxide pigment; (b) about 0.5 to 10 percent by weight, based on the total weight of the slurry, of a glycol; and (c) about 0.1 to 10 percent by weight; based on the total weight of the slurry, of at least one thickener. The thickener can be selected from the WO 02/-1-1286 PCT/USO1/.1-1891 group consisting of polyacrylates, hydroxyethylcellulose, alkali soluble emulsions, hydrophobic ethoxylated urethane resins, and hydrophobically-modified alkali soluble emulsions. Examples of alkali-soluble emulsions and polyacrylates include, but are not limited to, ACRYSOL~ ASE-60, ACRYSOL~ G-I 11, ASE-75, and ASE-95NP, all commercially available from Rohm &
Haas Company. Hydrophobically-modified alkali soluble emulsions and hydrophobic ethoxylated urethane resins are generally known as associated thickeners. Hydrophobically-modified alkali soluble emulsions are generally copolymers of high levels of (meth)acrylic acid with hydrophobic monomers, and hydrophobic ethoxylated urethane resins are generally the reaction products of polyethylene glycols with diisocyanates. Examples of hydrophobically-modified alkali soluble emulsions include, but are not limited to, ACRYSOL~ RM-5, RM-6, TT-615, and TT-(commercially available from Rolun & Haas). Examples of hydrophobic ethoxylated urethane resins include, but are not limited to, ACRYSOL~ RM-825, RM-8W, RM-2020NPR, SCT-275, and RM-12W (commercially available from Rohm & Haas). Glycols useful for the titanium dioxide slurry, as well as any other slurry of this invention, can be any glycol that can provide wettability to the slurry 1 ~ and help prevent the seeding and/or settling of raw material particulates.
Useful glycols can include, but are not limited to, ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, and the like. Weight percents of the thickeners are adjusted in order to obtain a viscosity of the titanium dioxide slurry in the range of about 70-125 Krebs units.
Extender Slurries ?0 The pigment e~-tender slurries such as the calcium carbonate and clay slurries each comprise (a) about ~0 to 90 percent by weight, based on the total weight of the slurry, of the extender pigment;
(b) about 0.~ to 10 percent by weight, based on the total weight of the slurry, of a glycol; and (c) about 0.1 to 10 percent by weight, based on the total weight of the slurry, of at least one thickener selected from the group consisting of polyacrylates, hydroxyethylcellulose, alkali soluble emulsions, hydrophobic ethoxylated urethane resins, and hydrophobically-modified alkali soluble emulsions.
The thickeners and glycols useful for this slurry is as defined under the titanium dioxide slurries.
Weight percents of the thickeners are adjusted in order to obtain a viscosity of the extender slurry in the range of about 70-125 Krebs units.
The silica pigment extender slurry comprises (a) about 20 to 50 percent by weight, based on the total weight of the slurry, of the silica; (b) about 0.5 to 10 percent by weight, based on the total weight of the slurry, of a glycol; and (c) about 0.1 to_ 10-percent by weight, based on the total weight of the slurry, of at least one thickener selected from the group consisting of polyacrylates, hydroxyethylcellulose, alkali soluble emulsions, liydrophobic ethoxylated urethane resins, and hydrophobically-modified alkali soluble emulsions. The thickeners and glycols useful for this slurry is as defined under the titanium dioxide slurries. Weight percents of the thickeners are adjusted in order to obtain a viscosity of the silica slurry in the range of about 70-125 Krebs units.
Preferably, the pigment and pigment extender slurries will also contain one or more dispersants, present in an amount between about 0.1 to 5%, based on the weight of the slurry. Useful dispersants include organic polyelectrolytes such as 2-amino-2-methyl-1-propanol, triethanolamine, sorbitol, mannitol, water soluble sodium salts, for example, alkali polyphosphates, aliphatic carboxylic acids and alkali salts thereof, poiyacrylic acids and alkali salts thereof, polyhydroxy alcohols, amino alcohols, sodium salt of polymeric carboxylic acids, such as Tamol~ 963, sold by Rohm & Haas, and mixtures thereof. For some applications, the preferred range of dispersants can be in an amount of about 0.1 to 2.0 weight percent, based on the weight of the slurry.
It has been found advantageous to further add to the slurry up to about 10% by weight, based on the total weight of the slurry, of a glycol. A preferred glycol for this invention is ethylene glycol.
For some applications, ethylene glycol is present in an amount of about 0.~ to 3 weight percent, based on the weight of the slurry.
In addition, other conventional additives may be incorporated into the slurry, such as bactericides, preservatives, defoamers, surfactants, and coalescents. Common bactericides include Proxel~GXL, manufactured by ICI, used at a concentration of from about 0.01 to about 2 weight percent of the slurry. Defoamers include Nopco~8034, manufactured by the Nopco Division of Diamond Shamrock Corporation. Surfactants include nonylphenoIs. Coalescents include Texanols manufactured by Eastman Chemical Company, Kingsport, Tennessee.
Glycol Slurry Glycol slurries useful for this invention comprises (a) about 5 to 50 percent by weight, based oa the total weight of the slurry, of a glycol selected from the group consisting of ethylene glycol, propylene glycol, etc.; and (b) about 1 and 50 percent by weight, based on the total weight of the slurry, of at least one thickener selected from the group consisting of polyacrylates, hydroxyethylcellulose, alkali soluble emulsions, hydrophobic ethoxylated urethane resins, and hydrophobically-modified alkali soluble emulsions. Examples of the thickeners are the same as provided under the titanium dioxide slurries. Weight percents of the thickeners are adjusted in order to obtain a viscosity of the glycol slurry in the range of about 70-125 Krebs units.
The slurry is made by admi.Ying a glycol, such as ethylene glycol, with at least one thickener, dispersing with a high speed mixer, then admi.~cing defoamer, coalescent, and cosolvent. Mixing is maintained as thickener and buffer are added to complete the slurry.
Thickener Slurry The thickener slurry useful for this invention comprises about ~ to 30% by weight. based on the total weight of the slurry, of at least one thickener selected from the group consisting of polyacrylates, hydroxyethylcellulose, alkali soluble emulsions, hydrophobic ethoxylated urethane resins, and hydrophobicalIy-modifed alkali soluble emulsions. Examples of the thickeners are the same as provided under the titanium dioxide slurries. Most preferred is the alkali-soluble emulsions WO 02/.l-t28G PCT/USO1/~~891 and the hydrophobically-modifted alkali-soluble emulsions. Polyacrylates, hydroxyethylcellulose, though a possible thickener, is least desirable due to its dry form and di~culty to incorporate into the slurry. It is essential that the pH of the thickener slurry be in the range of about 5.5 to 6.5. The viscosity of the thickener slurry is in the range of about 70-125 IC.rebs units.
Coating Composition According to this invention, various waterborne coating compositions can be prepared by blending the above-referenced slurries with at least one latex binder having substantially the same viscosity as the desired final waterborne product. The waterborne coating composition can comprise about 0-70 weight percent of the titanium dioxide dioxide slurry, 0 to 50 weight percent of at least one pigment extender slurry selected from the group consisting of calcium carbonate slurry, clay slurry, and silica slurry; 0.5 to 10 weight percent of a glycol slurry; and about 1 to 20 weight percent of a thickener slurry, and the remaining amount being a latex binder. The thickener can be selected from the group consisting of po(yacrylates, hydroxyethyIceIIulose, alkali soluble emulsions, hydrophobic ethoxylated urethane resins, and hydrophobically-modified alkali soluble emulsions, all based on the total weight ofthe coating composition. The slurries are admixed and blended with at least one latex binder to form a final waterborne coating composition. The latex can be any commercially available latex polymer. The latex binder may be a dispersed polymer having polymer particles dispersed ut an aqueous evaporabie carrier or.it may be either a water soluble polymer, a water-reducible polymer, a mixture of the water soluble and water-reducible polymers in the aqueous evaporable carrier, or a mixture of the dipsersed, water-reducible and water soluble polymers in the aqueous evaporable carrier. If desired, the latex binder may include a mixture of a dispersed polymer with a water soluble or a water-reducible polymer.
The latex polymer suitable for use in the present invention includes an emulsion polymer of mono- or poly-ethylenically unsaturated olefinic, vinyl or acrylic monomers, including WO 02/~.128G PCT/USI)1/~.1891 homopolymers and copolymers of such monomers. Specifically, the dispersed polymer may include polyvinyl acetate) and copolymers of vinyl acetate with one or more of vinyl chloride, vinylidene chloride, styrene, vinyltoluene, acryluonitrile, methacrylonitrile, acrylamide, methacrylamide, malefic acid and esters thereof, or one or more of the acrylic and methacrylic acid esters, which polymers are well-known as the film-forming component of aqueous base paints; homopolymers of C2-C40 alpha-olefins such as ethylene, isobutylene, octene, nonene, and styrene; copolymers of one or more of these hydrocarbons with one or more esters, nitrites, or amides of acrylic acid or of methacrylic acid or with vinyl esters, such as vinyl acetate and vinyl chloride, or with vinylidene chloride; and diene polymers, such as copolymers of butadiene with one or more of styrene, vinyl tolutene, acry(onitrile, methacrylonitrile, and esters of acrylic acid or methacrylic acid. The vinyl acetate copolymers are well-known and include copolymers such as vinyl acetate/butyl _acryiate/Z-ethylhexyl acrylate, vinyl acetate/butyl maleate, vinyl acetate/ethylene, vinyl acetate/vinyl chloride/butyl acrylate and vinyl acetate/vinyl chloride/ethylene.
Other suitable monomers from which the latex binder may be polymerized from include at 1 ? least one or more of the following monomers, such as, for example, acrylic and methacrylic ester monomers including methyl (meth) abrylate, ethyl (meth)acrylate, butyl (meth)acry(ate, ?-ethylhexyl (meth)acrylate, decyl (meth)acrylate, lauryl (meth)acrylate, isobornyl (meth)acrylate, isodecyl (meth)acrylate, oleyl (metli)acrylate, palmityl (meth)acrylate, stearyl (meth)acrylate, hydroxyethyl (meth)acrylate, and hydroxypropyl (meth)acrylate; acid functional monomers, such as acrylic acid, methaerylic acid, crotonic acid, itaconic acid, famuric acid and malefic acid;
monomethyl fumarate;
munobutyl fumarate; malefic anhydride, acrylamide or substituted acrylamides;
sodium vinyl sulfonate; phosphoethyl (meth)acrylate; acrylamido propane sulfonate;
diacetone acrylamide;
glycidyl methacrylate; acetoacetyl ethylmethacrylate; acrolein and methacrolein; dicyclopentadienyl methacrylate; dimethyt meta-isopropenyl benzyl isocyanate; isocyanato ethyl-methacrylate; styrene WO 02/x-t286 PCT/USI)1/~.1891 or substituted styrenes; butadiene; ethyleen; vinyl acetate or other vinyl esters, N-vinyl pyrrolidone;
amino monomers, such as for example, N, N'-dimethylamino and (meth)acrylate.
Preferably, the final waterborne product will have a viscosity substantially the same as each of the slurries, and preferably in the range of about 70-125 ICrebs units.
Preservatives, defoamers, freeze-thaw agents, and fungicides/mildewcides may be used in the coating composition at concentrations from about 0.1 to about 10 weight percent, based on the total weight of the coating composition. Shading bases may be added to the coating composition and further blended.
Tlie waterborne coating composition of this invention, having predetermined viscosity characteristics can be prepared utilizing a total liquid blend process. A
plurality of liquid blend raw materials can be admixed to produce the waterborne coating product. The process can include providing a plurality of reservoirs containing liquid blends of raw materials, each liquid blend of raw materials have substantially the same viscosities, then admixing a controlled amount of the liquid blends from said reservoirs in a mix tank having an appropriate agitation means, such as an impeller or other agitation means known in the art, and then producing a final liquid blend waterborne coating product by exposing the liquid blend slurries in said mix tank with said agitation means. The liquid blend raw materials can include latex binders, titanium dioxide slurries, extender pio vent slurries, thickener slurries, and the like, and mixtures thereof The thickener can be selected from the group consisting of polyacrylates, hydroxyethylcellulose, alkali soluble emulsions, hydrophobic ethoxylated urethane resins, and hydrophobically-modified alkali soluble emulsions. Preferably, the pH of the thickener slurry is in the ran?e of bet~veen 5.5 to 6.5. Preferably, the viscosity of the final waterborne coating is in the range of about 70-125 Iu~ebs units.
The following examples illustrate the invention but are not intended to limit it thereto.
Eh',A,MPLES
The pigment slurries are generally prepared by subjecting a pigment with dispersing treatment using a high speed mixer, admixing the dispersed pio~ment slurry with a glycol, adding at least one thickener which can be selected from the group consisting of polyacrylates, S hydroxyethylcellulose, alkali soluble emulsions, hydrophobic ethoxylated urethane resins, and hydrophobically-modified alkali soluble emulsions; and forming an aqueous pigment slurry by dispersing with a mixer.
E.YAZYBLE 1 Titanium Dioxide Slurry An aqueous titanium dioxide slurry can be made according to the formula in Table I.
The aqueous Ti02 slurry is prepared by subjecting Ti02 with a water and dispersant mixture, dispersing with a high speed mixer, then admixing defoamer, a glycol, and cosolvent.
Mixing is maintained as thickener, buffer, and biocide are added to complete the slurry. (TiPure~
titanium dioxide is manufactured by E.I, duPont deNemours & Company.) A
titanium dioxide slurry at 61 % solids can be prepared according to the following formula listed in the following table:
Weight Weight Description (Ibs/100 salt in Slurrv Water Solvent S 14 34.67 Thl'P (Potassium TriPolyPhosphate)Dispersant 2 I.3 Tamol~ 963 Dispersant 18 1.21 Nonylphenol Surfactant 3 2.0 Ti-Pure~ 8931 titanium dio;cidePigment S90 60.0 2s Nopco~8034 Defoamer 1 0.07 Ethylene Glycol 27 I.S2 Texanol~ Coalescent 13.5 0.91 Acrysol~ TT-935 Thickener . 6 0.40 Acrysol~ TT-615 Thickener 2 0.13 Ammonia Buffer 5 0.34 $ Proxel~ GXL Biocide 1 0.07 The titanium dioxide slurry may further comprise an extender selected from the group consisting of calcium carbonate, clay, silica, and others. The titanium dioxide slurry is dispersed at high shear having an impeller sufficient to deagglomerate the titanium dioxide. The dispersed slurry has a Krebs Stormer viscosity in the range of about 70-125 Krebs units, and a solids content of about 60-75%.
Calcium Carbonate Slurry The aqueous calcium carbonate slurry can be prepared by subjecting precipated calcium carbonate 325 mesh with a water and dispersant mixture, dispersing with a high speed mixer, then admixing defoamer, a glycol, and cosolvent. Mixing is maintained as thickener, buffer, and biocide are added to complete the slurry.
Weight Description (lbs/100 salt % in Slum Water Solvent 410.41 25.00 Tamol~ 963 Dispersant 10.8 7.4 N onylpheno l S urfactant 3 2.1 Calcium Carbonate Pigment 99~ 65.0 Nopco~ 8034 Defoamer 1 0.07 2~ Ethylene Glycol 20 1.37 Texanol~ Coalescent 10 0.68 Acrysol~ TT-935 Thickener 8.6 0.59 Acrysol~ TT-615 2.9 0,20 Thickener Proxel~ GXL, Biocide 1 0.07 The dispersed slurry has a IGebs Stormer viscosity in the range of about 70-125 Krebs units, and a solids content of about 60-75%.
. EXAMPLE 3 Silica Slurry The silica slurry is prepared by subjecting Celite~ diatomaceous earth with a water and dispersant mixture, dispersing with a high speed mixer, then admixing defoamer, a glycol, and cosolvent. Ivfixing is maintained as thickener, buffer, and biocide are added to complete the slurry. .
Weight Description ,~lbs/100 eal) % in Slurry Water Solvent 678 63.0 TKPP (Potassium TriPolyPhosphate)Dispersant 2 0.2 Tatnol~ 963 Dispersant 6 0.6 Nonylphenol Surfactant 1 0.1 Celite~ 400P Pigment 262 27.0 Nopco~ 8034 Defoamer 1 0.10.
Ethylene Glycol 6 0.62 Te:canol Coalescent 3 0.31 Acrysol~ TT-935 Thickener 8.4 0.86 Acrysol~ TT-615 Thickener 2.8 0.29 Ammonia Buffer 1 0.10 Proxel~ GXL Biocide 1 0.10 The dispersed slurry has a ICrebs Stormer viscosity in the range of about 70-125 Ktebs units, and a solids content of about 20-35%.
EXAI~.'LE 4 Thickener Slurry The aqueous thickener slurry is prepared by admixing the following raw materials with a high speed mixer:
Weight Description (lbs/100 Qal) % in Slurry Water Solvent 651.6 77.8 Nopco~ 8034 Defoamer 5- 0.60 Acrysol~TT-93S . Thickener 130 O.1S
Acrysol~TT-61S Thickener 43:3 5.17 Ammonia Buffer 6.5 0.78 Proxel~ GXI, Biocide 1 0.12 It is critical to this invention that the pH of the thickener solution be in the range of about 5.5 to 6.5.
The thickener slurry has a Krebs Stormer viscosity in the range of about 70-125 Krebs units, and a solids content of about 5-10%.
E~'Al~'LE 5 Glycol Slurry The aqueous glycol slurry is prepared by admixing the following raw materials with a high speed mixer:
Weight Description ~lbs/100 gall % in Slurry Water Solvent 506.6 36.84 Nonylphenol Surfactant 7.5 0.55 Nopco~ 8034 Defoamer 44.9 3.26 Ethylene Glycol 506.6 36:84 Texanol~ Coalescent 252 18.32 Acrysol~ TT-935 Thickener 1 40 2.91 Acrysol~ TT-615 Thickener 13 0.95 Ammonia Buffer 4.6 0.33 The glycol slurry has a Krebs Stormer viscosity in the range of about 70-125 Krebs units, and a solids content of about 5-10%.
One or more of the above slurries, having the desired viscosity characteristics, can be used to produce the waterborne coatings of this invention having substantially the same viscosity characteristics.
The slurries can be stored in respective reservoirs, and then directly blended within a processing vessel equipped with mining means, without the need for grinding or high shear miming. The manufacturing process can be controlled through computer means or manually dispensed. A
typical computer control system can control pump speeds, rates, and quantities of additions of components, and measurements taken on-line by various instrumentation.
The order of addition of the liquid raw material slurries/blends is not critical to this invention.
Shading bases can also be blended during the raw material blending process to form a finished product.
The color shading bases are added after formula blending has occurred by accurate dispensing or -m etering.
COMPARATIVE EXAMPLES
As a comparison e:cample, a batch of latex paint was formulated using a conventional paint making process. The formulation is listed in Table I.
Conventional Process Formula Grind: The following pigment dispersion is prepared using the ingredients in the following order, and subjected to a dispersing treatment by using a high speed disperser.
Weight Description (lbs/100 eal) % Weight Water Solvent 142.5164 13.3726 TKPP (Tetrapotassium Pyrophospahte) Dispersant 0.7073 0.5554 Tamol~ 963 Dispersant 5.2948 2.0903 Nonylphenol Surfactant 1.3953 0.5975 Nopco~ 8034 Defoamer 1.2600 0.6283 Ti-Pure~U 8931 Pigment 223;0941 25.5306 325 Nlesh PPT CaC03 Pigment Extender 61.2491 10.2714 Ethylene Glycol 37.2989 15.2659 Texanol~ Coalescent 18.5734 s.ssao 2~ Water 120.0000 54.7292 The above grind is then pumped to a letdown tank, and the following raw materials are then added:
Rovace~ 661 Vinyl Acrylic Later 425.000 39.8785 Nopco 8034 Defoamer 2.000 0.1877 Acrysol~ TT-935 Thickener 13.OS44 1.2277 Acrysol~TT-615 Thickener 4.3394 0.4072 Ammonia Buffer 2.9731 0.2790 Omacide~ IPBC 40% Mildeweide 1.0000 0.0935 Proxel~ GXI, Biocide 0.9500 0.0891 The batch is adjusted for pH, color, and viscosity.
COMPARATIVE EXAMPLE 2:
A second batch of he same latex paint was d process t formulated using the of the slurries an present invention:
Weight (Ibs/100 eal) % Weieht Water 33.1965 3.1149 Titanium Dioxide Slurry 380.0000 35.661 (Example 1 ) Calcium Carbonate Slurry 120.0000 11.298 (Example 2) Glycol Slurry 50.0000 4.6916 (Example 5) 2~ Thickener Slurry 5.0000 x.1605 (Example 4) Rovace~ 661 425.0000 39.S785 Omacide IPBC40% 1.0000 0.0938 Proxel~ GXL, 0.5400 0.0507 Ammonia ' 1.0000 0.0938 The above slurries are blended together into a mix tank or container, with no dispersion necessary. The product does not require adjustments for pH, color, or viscosity.