υη I MM ϋθΜΐ\υ ι π ιζικ ΓΙ ΙΖΓ Ι I I U I

Field

The present invention relates to a new process for making polyurethane/ acryl ic hybrid dispersions useful in high PVC coatings, the polyurethane/ acryl ic hybrid dispersions made thereof, and the coating composition comprising the polyurethane/ acryl ic hybrid dispersions. Background

υ ν σ I cbci ι ι u co, ii ici c ι ι α uca ι a υι ι ν_ ;ι icu ci ι υι ι ιυ ι iu c an 1 1 υο ι id ι pol lution caused by volatile solvents which are em itted during painting processes. Due to environmental concerns, volati le organic compounds (VOCs) have come under strict regulation by the government. Therefore, one of the major goals of the coating industry is to m inim ize the use of organic solvents by formulating w at erborne coating compositions which provide a smooth, high gloss appearance, as well as good physical properties including resistance to acid rain. While the solvent- type coatings provide many benefits, such as that they are fast-drying, have a high hardness, a high abrasion-resistance, a high water-resistance, a high chem ical- resistance and a low price, the waterborne coatings have environment-friendly benefits in that they are not flammable or explosive. The waterborne coatings use water as the system solvent and contain no poisonous chem icals. They require no or low amounts of volatile organic com pounds.

The unique advantage of polyurethane dispersions (PUDs) in relation to surface coatings is their abi lity to form coherent film and to control the m iaophase morphology by control ling the relative amounts of soft and hard segments in polymer chain. These features allow PU Ds to be employed in a wide variety of surface coating appl ications where mechanical properties are particularly crucial. H iah abrasion resistance suoerior touahness elastomeric Drooerties and hiah extensibi lity at low temperature are typical benefits. H owever, relatively high raw material cost in comparison with a typical acrylic emulsion has restricted its use in many industrial appl ications. To overcome this, polyurethane dispersions have been combined with other relatively inexpensive polymers to obtain a cost/ performance balance because the properties of polyurethane (PU) and the polyacrylate (PA) complement each other. The composite materials of PU and PA are more outstanding in terms of adhesion, film-formability, non-stickiness, weather- resistance, elongation and strength of the film with excellent cost-performance balance. Accordingly, since the development of PU, the modification of PU by PA has been an active research topic in the art.

Two methods can be used to modify PU with PA: physical methods and chemical methods. In the physical method, aqueous PA and PU dispersions (emulsions) are independently prepared first, and then both dispersions are mixed together under mechanical mixing. It is a very convenient method that makes it easy to control the composition of thefinal product. However, in such blends the superior performance properties may be compromised because of the incompatibility of the two materials, PU and PA. Such blended dispersions may suffer from instability.

For these reasons, chemical modification technology currently plays a more important role. The chemical method is achieved by post-polymerization of acrylates. In the chemical method, the PU dispersion can be prepared first, and then acrylates and other vinyl monomers can be polymerized in the PU dispersion. In most cases, core-shell emulsion polymerization is adopted. PU particles are used as seed particles and the acrylates are polymerized within the PU particles due to high hydrophobicity of the acrylates. These hybrid dispersions are expected to provide the advantages of PA, such as excellent weather resistance, affinity to pigments as well as lower cost, and the advantages of PU, such as better mechanical stability, excellent adhesion, solvent and chemical resistance, and toughness.However, when polyurethane/ acrylic hybrid dispersions made according to the prior art are formulated into paints with a pigment volume concentration (PVC) exceeding 40%, the elongation of coatings made therewith drops dramatically.

The present inventors have sought to solve the problem of providing polyurethane/ acrylic hybrid dispersions that when formulated into coatings provide improved binder affinity to pigments so that the PVC content in the formulated coating composition can be high while the performance of coatings made therefrom will not be adversely affected. Summary

The present invention provides a process for making polyurethane/ acrylic hybrid dispersions comprising the following continuous steps: i) adding at least one polyol into a reactor; ii) adding Dimethylolpropionic Acid (DM PA)simultaneously with/ after step i), but before step iii), as a water dispersibility enhancing agent, at a temperature of from 115°Cto 140°C to obtain a homogeneous solution; iii) adding at least one polyisocyanate at a temperature of from 75°C to 95°C, until the NCO content reaches a constant value, to prepare the polyurethane prepolymer; iv) adding at least one acrylate monomer(s), at least one styrenic monomer(s), or mixtures thereof, as diluent to the polyurethane prepolymer, at a temperature of from 40°C to 65°C; v) adding a neutralizing agent; vi) dispersing and extending the polyurethane prepolymer in the presence of the acrylate monomer, and/ or the styrenic monomer of step iv); and vii) feeding the emulsified mixture of at least one ethylenically unsaturated nonionic monomer(s), and based on the total weight of the ethylenically unsaturated nonionic monomer(s) including the acrylate monomer, and/ or the styrenic monomer of step iv), from 1 wt.% to 3 wt.% acid monomer(s), and co-polymerizing them together, at a pH value from 7.2 to 8.6 in the presence of a buffer reagent, to get the polyurethane/ acrylate hybrid dispersion.

The present invention further provides a process for making polyurethane/ acrylic hybrid dispersions further comprising cold-blending the polyurethane/ acrylic hybrid dispersions with polyacrylate dispersion under agitation. The process further comprises modifying the polyurethane/ acrylic hybrid dispersion and the polyacrylate dispersion by copolymerization with diacetone acrylamideor acetoacetoxy ethyl methacrylate; and adding adipicacid dihydrazide, asacrosslinker.

The present invention further provides a high pigment volume concentrate (PVC) coating composition comprising a polyurethane/ acrylic hybrid dispersion comprising a polyurethane prepolymer, and an acrylic polymer comprising in polymerized form, ethylenically unsaturated nonionic monomer(s), and from 1 wt.% to 3 wt.%, based on the total weight of ethylenically unsaturated nonionic monomer(s), of an acid monomer(s) and one or more pigments and/ or fillers having a PVC of 25 to 55, or, 30 to 55, or, more preferably, 35 to 50, or, even more preferably, 38 or more.

Detailed Description

In the present invention, the term "polyurethane" or"PU" describes polymers including oligomers (e.g., prepolymers) which contain multiple urethane groups, i.e., — O— C(=0)— NH— , regardless of how they are made. As is well known, polyurethanes can contain additional groups such as urea, allophanate, biuret, carbodiimide, oxazolidinyl, isocyanurate, uretdione, ether, ester, carbonate, etc., in addition to urethane groups. Typically, the prepolymers will be above 1,000 or 2,000 Daltons in number average molecular weight and if the chain is extended during processing, can reach number average molecular weights in the millions of Daltons.

The term " polyacrylate" or "PA" as used herein means those polymers or resins resulting from the polymerization of one or more acrylates such as, for example, methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, etc. as well as the methacrylates such as, for instance, methyl methacrylate, ethyl methaaylate, butyl methacrylate, hexyl methacrylate, etc. Copolymers of the above acrylateand methacrylate monomers are also included within theterm "polyacrylate" as it appears herein. The polymerization of the monomeric acrylates and methacrylates to provide the PA dispersions useful in the practice of the invention may be accomplished by any of the well known polymerization techniques.

Asused herein, theterm "wt.%" refers to weight percent.

The polyurethane/ acrylic hybrid dispersion (PUA) of the present invention is prepared by a) PU prepolymer preparation; b) dispersing and extending PU prepolymer in water; and c) adding and polymerizing at least one ethylenically unsaturated nonionic monomer(s) and one or more acid monomers. The PU prepolymer preparation of the present invention may be made under decreasing temperature by adding one or more polyol(s) into a reaction vessel under N ₂ purging and heating to a high temperature, preferably from 115°C to 140°C, more preferably from 120°C to 130°C, simultaneously or thereafter adding Dimethylolpropionic Acid (DM PA), as a water-dispersibility enhancing agent so that a homogeneous solution is obtained, lowering the composition temperature to 75°C - 95°C, more preferably from 80°C to 85°C, adding polyisocyanate(s), and reacting until the NCO content reaches a constant value, then adjusting the temperature to from 40°C to 65°C, more preferably from 55°C to 60°C, and adding at least one acrylate monomer(s), at least one styrenic monomer(s), or the mixture thereof as a reactive diluent. The weight ratio of acrylate and/ or styrenic monomers in the prepolymer may range from 10 wt.% to 50 wt.%, preferably from 10 wt.% to 30 wt.%. Finally, adding a neutralizing agent, such asatriethyl amine (TEA). The molar ratio of TEA to DM PA ranges from 0.9:1 to 1.1:1, preferably from 0.9:1 to 1:1.

In b), after a short (several minutes, such as, from 5 to 15 minutes, etc.) mixing time, pouring gradually the prepolymer into Dl water under agitation to form a dispersion. Several minutes later, adding dropwise to above dispersion, a chain extender with a molar ratio to NCO as 0.9:1 to 1.1:1, preferably from 0.9:1 to 1:1.

In polymerizing the ethylenically unsaturated nonionic monomer(s) in c), the total amount of ethylenically unsaturated nonionic monomer(s), including the acrylate and/ or styrenic monomers, is from 10 wt.% to 80 wt.%, preferably from 30 wt.% to 50 wt.% based on the total weight of the PU A polymer.

Dispersing b) may also be conducted by pouring the PU prepolymer into a PA dispersion under agitation followed by chain extension.

In c), adding from 1 wt.% to 3 wt.%, preferably, from 1.5% to 2.0% based on the total weight of the ethylenically unsaturated nonionic monomer(s), at least one acid monomer(s) as polymerization unit, and co-polymerizing with the ethylenically unsaturated nonionic monomer(s), the acrylate monomer, and/ or the styrenic monomer via radical polymerization, at a pH value from 6.8 to 8.6, preferably from 6.9-8.0, more preferably from 7.2-7.8, in the presence of a buffer reagent, a initiator, and at elevated temperature to get the polyurethane/ acrylate hybrid dispersion.

Suitable acid monomers for use in the present invention are selected from the group consisting of (methyl) acrylic acid, phosphoethyl methacrylate, itaconic acid, crotonic acid, 2-acrylamido-2-methyl propane sulfonic acid, 2-carboxyethyl acrylate, maleic acid and its anhydride fumaric acid and its anhydridemaleic anhydride, citraconic acid and its anhydride, and the mixture thereof. Preferably, it is (methyl) acrylic acid, phosphoethyl methacrylate, or the mixture thereof. Suitable buffer reagents for use in the present invention are selected from the group consisting of NaHC03, sodium bitartrate, N a ₂ H P0 ₄ / N aH ₂ P0 ₄ , KHC0 ₃ , NaAC or the mixture thereof. Preferably, it isNaHC03.

Optionally, the PUA dispersion prepared according to the above process can be mixed with PA dispersion under agitation to make a PUA dispersion with high PA content.

Optionally, the PUA dispersion and PA dispersion may be separately modified by copolymerization with di acetone-based monomer, preferably, with DAAm or AAEM and other acrylate monomer(s). The amount of DAAm or AAEM ranges from 0 to 3 wt%, based on the total weight of monomers used to make the acrylic/ styrenic portion of the PUA, preferably from 1 to3wt.%.

Adipic acid dihydrazide (ADH), as crosslinker, may be added into to the blend of PUA and PA dispersions. The content of polyacrylate, including those in both PA and PUA, may range from 10 wt. % to 80 wt. % in the total weight based on the total solids of PA and PUA.

Polyols, including polyether diols, polyester diols or multi-functional polyols, are used to prepare the PU prepolymer. "Polyols" means any product having two or more hydroxyl groups per molecule. Non-limiting examples of the polyols useful herein include polyether polyols, polyester polyols such as alkyds, polycarbonate polyols, polyhydroxy polyester amides, hydroxyl-containing polycaprolactones, hydroxyl-containing acrylic polymers, hydroxyl-containing epoxides, polyhydroxy polycarbonates, polyhydroxy polyacetals, polyhydroxy polythioethers, polysiloxane polyols, ethoxylated polysiloxane polyols, polybutadiene polyols and hydrogenated polybutadiene polyols, polyisobutylene polyols, polyacrylate polyols, polyols derived from halogenated polyesters and polyethers, and the like, and mixtures thereof. The polyether polyols, polyester polyols, and polycarbonate polyols are preferred.

The polyether polyols that can be used as the active hydrogen-containing compound according to the present invention contain the --C--O--C-- group. They can be obtained in a known manner by the reaction of starting compounds that contain reactive hydrogen atoms such as water or diols, and alkylene oxides such as ethylene oxide, propylene oxide, butylene oxide, styrene oxide, tetrahydrofuran, epichlorohydrin and mixtures thereof. Preferred polyethers include poly(propylene glycol) with molecular weight of 400 to 3000, polytetrahydrofuran and copolymers of poly(ethylene glycol) and poly(propylene glycol). The diols used in the preparation of the polyether polyols include alkylene glycols, preferably ethylene glycol, diethylene glycol and butylene glycol.

The polyester polyols are typically esterifi cation products prepared by the reaction of organic polycarboxylic acids or their anhydrides with a stoichiometric excess of a diol or diols. Non-limiting examples of suitable polyols for use in the reaction include poly(glycol adipate), poly(ethylene terephthalate) polyols, polycaprolactone polyols, alkyd polyols, orthophthalic polyols, sulfonated and phosphonated polyols, and mixtures thereof. The diols used in making the polyester polyols are as set forth for preparing the polyether polyols. Suitable carboxylic acids used in making the polyester polyols include, but are not limited to, dicarboxylic acids, tricarboxylic acids and anhydrides, e.g., maleic acid, maleic anhydride, succinic acid, glutaric acid, glutaric anhydride, adipicacid, suberic acid, pimelicacid, azelaic acid, sebacic acid, chlorendic acid, 1,2,4-butane-tricarboxylic acid, phthalic acid, the isomers of phthalic acid, phthalic anhydride, fumaric acid, dimeric fatty acids such as oleic acid, and the like, and mixtures thereof. Preferred polycarboxylic acids used in making the polyester polyols include aliphatic and/ or aromatic dibasic acids.

Particularly interesting polyols are the polyester diols containing -C(=0)-0- group. Non-limiting examples include poly(butanediol adipate), cap rol acton es, acid- containing polyols, polyesters made from hexane diol, adipic acid and isophthalic acid such as hexane adipate isophthalate polyester, hexane diol neopentyl glycol adipicacid polyester diols, as well as propylene glycol maleic anhydride adipic acid polyester diols, and hexanediol neopentyl glycol fumaric acid polyester diols.

Polyisocyanates have two or more isocyanate groups on average, preferably two to four isocyanate groups per molecule. Polyisocyanates typically comprise about 5 to 20 carbon atoms and include aliphatic, cycloaliphatic, ary I -aliphatic, and aromatic polyisocyanates, as well as products of their oligomerization, used alone or in mixtures of two or more. Diisocyanates are preferred. Toluene diisocyanate, hexamethylene isocyanate and/ or isophorone isocyanate may preferably be used in the embodiment of the present invention. Non-limiting examples of suitable aliphatic polyisocyanates include alpha, omega-alky I en e diisocyanates having from 5 to 20 carbon atoms, such as hexamethylene-1,6-diisocyanate, 1,12-dodecane diisocyanate, 2,2,4-trimethyl- hexamethylene diisocyanate, 2,4,4-trimethyl-hexamethylene diisocyanate, 2-methyl- 1,5-pentamethylene diisocyanate, and the like. Preferred aliphatic polyisocyanates include hexamethylene-1,6-diisocyanate, 2,2,4-trimethyl-hexamethylene- diisocyanate, and 2,4,4-trimethyl-hexamethylene diisocyanate.

Non-limiting examples of suitable cycloaliphatic polyisocyanates include dicyclohexylmethane diisocyanate (commercially available as Desmodur™ from Bayer Corporation), isophorone diisocyanate, 1,4-cyclohexane diisocyanate, 1,3-bis- (isocyanatomethyl)cyclohexane, and the like. Preferred cycloaliphatic polyisocyanates include dicyclohexylmethane diisocyanate and isophorone diisocyanate.

Non-limiting examples of suitable araliphatic polyisocyanates include m- tetramethyl xylylene diisocyanate, p-tetramethyl xylylene diisocyanate, 1,4-xylylene diisocyanate, 1,3-xylylene diisocyanate, and the like. A preferred araliphatic polyisocyanate is tetramethyl xylylene diisocyanate.

Non-limiting examples of suitable aromatic polyisocyanates include 4,4'- diphenylmethylene diisocyanate, toluene diisocyanate, their isomers, naphthalene diisocyanate, their oligomeric forms and the like. A preferred aromatic polyisocyanate is toluene diisocyanate.

The PU prepolymer may be formed without using a catalyst if desired, but using a catalyst may be preferred in some embodiments of the present invention.

Non-limiting examples of suitable catalysts include stannous octoate, dibutyl tin dilaurate, and tertiary amine compounds such as triethylamine and bis-

(dimethylaminoethyl)ether, morpholine compounds, bismuth carboxylate, zinc bismuth carboxylate and diazabicyclo[2.2.2]octane. Organic tin catalysts are preferred.

In the present invention, organic solvents are preferably not used, so the solvent-removing stage is omitted.

Chain extenders used in the preparation of thePU dispersion are employed in the dispersion step b). Non-limiting examples of chain extenders useful in this regard include any of inorganic or organic polyamines having an average of about 2 or more primary and/ or secondary amine groups, amine functional polyols, ureas, or combinations thereof, and their mixtures. Suitable organic amines for use as a chain extender include, but are not limited to, diethylene triamine (DETA), ethylene diamine (EDA), meta-xylylenediamine (MXDA), aminoethyl ethanolamine (AEEA), 2-methyl pentane diamine, and the like, and mixtures thereof. Also suitable for the present invention are propylene diamine, butylene diamine, hexamethylene diamine, cydohexylene diamine, phenylene diamine, tolylene diamine, 3,3-dichlorobenzidene, 4,4' -methylene-bis-(2-chloroaniline), 3,3-dichloro-4,4-diamino diphenylmethane, sulfonated primary and/ or secondary amines, and the like, and mixtures thereof. Suitable inorganic amines include hydrazine, substituted hydrazines, and hydrazine reaction products, and the like, and mixtures thereof. Suitable ureas include urea and its derivatives, and the like, and mixtures thereof. Ethylene diamine is preferably used. The amount of chain extender, which can be added before or after dispersion, typically ranges from about 0.5 to about 1.1 equivalents based on available equivalents of isocyanate.

The PA dispersion of the present invention may comprise a homopolymer of acrylates, a copolymer of acrylates, a copolymer of acrylates with other vinyl monomers, and/ or mixtures thereof. With the consideration of properties and prices of the products, all traditional co-monomers may be used to prepare the polymers and copolymers.

Non-limiting examples of suitable acrylate monomer(s) include esters of (meth)acrylic acid containing 1 to 18 carbon atoms in the alcohol radical, such as methyl methacrylate, butyl methacrylate, ethyl acrylate, butyl acrylate, cyclohexyl acrylate, 2-ethylhexyl acrylate and stearyl acrylate; di(meth)acrylic acid esters of diols, e.g. ethylene glycol, 1,4-butanediol or 1,6-hexanediol. The monomers including methyl (meth)acrylate, ethyl acrylate, butyl acrylate, hexyl acrylate, 2-ethylhexyl acrylate, hydroxyethyl (meth)acrylate, hydroxypropyl (meth)acrylate and glycidyl methacrylate, are preferable.

The ethylenically unsaturated nonionic monomers include, for example,

(meth)acrylic ester monomers, where (meth)acrylic ester designates methacrylic ester or acrylic ester, including methyl acrylate, ethyl acrylate, butyl acrylate, 2- ethylhexyl acrylate, decyl acrylate, lauryl acrylate, methyl methacrylate, butyl methaaylate, isodecyl methacrylate, lauryl methacrylate, hydroxyethyl methacrylate, hydroxypropyl methacrylate; (meth)acrylonitrile; (meth)acrylamide; amino- functional and ureido-functional monomers; monomers bearing acetoacetate- functional groups; styreneand substituted styrenes; butadiene; ethylene, propylene, a-olefins such as 1-decene; vinyl acetate, vinyl butyrate, vinyl versatate and other vinyl esters; and vinyl monomers such as vinyl chloride, vinylidene chloride.

Herein, "nonionic monomer" meansthat the copolymerized monomer residue does not bear an ionic charge between pH =1-14.

For the polymerization of monomers, initiators that may be used include, but are not limited to, peroxides such as potassium peroxy-disulphate, ammonium peroxydi sulphate, organic peroxides, organic hydroperoxides and hydrogen peroxide. Redox systems are preferably used, such as water-soluble, radical- producing non-ionogenic peroxides, e.g. t-butyl hydroperoxide, as the oxidation component, and reduction components such as formaldehyde sulphoxylate or ascorbic acid. Ammonium peroxydi sulphate, also called ammonium persulfate, is preferably used.

The polymerization can be carried out using any technical method for preparing an aqueous emulsion polymerization, employing non-ionic and/ or an ionic surfactants. Thedesignsfor theformulationsand thereaction technology can be utilized to obtain specific particle morphologies and reactive functionalities so that the PA can match the PU prepolymer/ dispersion and/ or PUA dispersion to give good film properties. Preferably, the polymerization is carried out with the previously mentioned monomers and is initiated with radical initiators. In one embodiment of the present invention, the mixture of monomers pre-emulsion and the initiator solution are respectively fed into a reactor over a defined period of time, such as 0.8 to 6 hours, preferably 3.5 hours. The initiator solution may comprise an initiator and water. The pre-emulsion comprises monomer mixture, surfactant/ emulsifier and water. The polymerization time span is dependent on the reaction conditions, such as temperature, initiator type and dosage, monomer dosage (solid content) and the reactivity of the monomers. Emulsion polymerization is generally conducted at temperatures of about 55°C to about 90°C, preferably 60°C to 85°C, and more preferably 75°C to 80°C. After the completion of the polymerization reaction, the polymer emulsion is allowed to cool to ambient temperature.

The obtained aqueous polymer emulsion has an average particle diameter of

30 to 300 nanometers (nm), preferably 40 to 90 nm, more preferably 50 to 80 nm.

The PUA dispersion of the present invention can be used for preparing coating compositions comprising one or more pigments, and/ or fillers , especially for high pigment volume concentration (PVC) coating compositions having a PVC of 25 to 55, or, 30 to 55, or, more preferably, 35 to 50 or, even more preferably, of 38 or more suitably for high PVC roof coatings. PVC is a percentage calculated by the equation PVC = (total volume of pigments, and fillers in a coating/ total volume of coating solids in the coating, including polymer solids) X 100%.

During application, the total amount of the pigments and fillers are typically from 10% to 60%, preferably from 20% to 50%, more preferably from 25% to 46%, most preferably from 33% to 45% by dry weight based on the total weight of the coating composition.

Examples of pigments that can be used in the invention include, but are not limited to, titanium dioxide (Ti0 ₂ ), zinc sulfide, lithopone, iron oxides, feldspar, and mixed metal oxides. Preferred pigments aretitanium dioxide (Ti0 ₂ ), and zinc oxide.

Examples of fillers which may be used in the high PVC roof coatings of the present invention are carbonates such as calcium carbonate in the form of dolomite, calcite, or chalk, silicates such as magnesium silicate in theform of talc, or aluminum silicates, such as loam and clays; powered quartz, quartz sand, finely divided silica, feldspar, barite, and calcium sulfate. Fibrous fillers are also suitable. Use is often made industrially of mixtures of various fillers, for example mixtures of fillers of different particlesize, or mixtures of carbonaceous and si I icaceous fillers. Preferably, thefiller is calcium carbonate (CaC0 ₃ ).

Additional ingredients of the coating composition include, but are not limited to, stabilizers, dispersants, surfactants, paraffins, waxes, UV light stabilizers, rheology modifiers, mildewcides, biocides, fungicides, and other conventional additives. I n the present specification, the technical features in each preferred technical solution and more preferred technical solution can be combined with each other to form new technical solutions unless indicated otherwise. For brevity, the applicant omits descriptions of these combinations. H owever, all the technical solutions obtained by combining these technical features should be deemed as being literally described in the present specification in an explicit manner.

Examples

Unless otherwise indicated, all pressures are atmospheric or ambient pressure and all temperatures are room temperature.

Raw materials used in the Examples include those listed in the following Tables:

Formulation materials:

ZnO Pigment Snopharm Chemical Reagent Company

Teaxanol Coalescent2,2,4-Trimethyl- Eastman

1,3-pentanediol

monoisobutyrate

Propyleneglycol Solvent Snopharm Chemical Reagent Company

N atrosol 250H BR Thickener, Ashland

hydroxy ethyl cellulose is a

n on i on i c,w ater-sol u bl e

hydroxy ethyl cellulose

surface-treated with glyoxal

SkaneM-8 M ildewcide, formaldehyde- Dow Chemical Company

free mildew cide

having active ingredient is

identified as2-n-octyl-4- isothiazdin-3-one

Test Methods used in the Examples include:

1. Dirt Pickup Resistance: (according to GB/ T 9755-2011 by General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China) a) Drawing down coating films on asbesto cement panels (wet film thickness 120um+80um by wiring bar applicator);

b) Curing 7daysin constant temperature room (CTR) (Temperature: 23 °C, humidity: 50%);

c) Checking the initial reflectance of coating films (described asY^;

d) Brushing formulated ash dispersion onto coating filmsthoroughly, and then dried 2hrsin CTR;

e) Rinsing off dirt from coating films by tap water for 1 min;

f) Repeating above evaluation cyclefor 5 times; and

g) Checking the final reflectance (Y ₂ ) and calculating loss rate of Y value: loss% = (Y ₁ -Y ₂ )/Y _r

2. Tensile strength and elongation rate: (according to JG/ T172-2005 by Ministry of Housing and Urban-Rural Development of PRC China)

a) Draw -downing on release paper (dry film thickness is 1mm);

b) Curing 14days in CTR (Temperature: 23 °C, humidity: 50%; after 7days, need to turn over);

c) Cutting paint films into a dumb bell shape; and

d) Using Gotech-AI 7000M Universal Testing Machinewith acrosshead speed of 200 mm/ min to test elongation and tensile at room temperature. 3. Water swelling performance:

a) Measuring cured coating film weight asm^g);

b) Immersing above coating films into water as described in GB/ T 6682-2008(by General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China) for 168hrs;

c) Removing excess water with a tissue paper, then determining the weight of the absorbed water on coating film is m ₂ (g);

d) Calculating water swelling as%. Water swelling % = (rr^-m / m ₁

Comparative .Example 1: Pure acrylic latex with a solid content, 54.5-55.5%; pH 9.0- 9.6; Brookfield viscosity, max.140 cPs, by Brookfield viscometer, 2# spindle, 60rpm; Density (wet), 1.04 g/ cm ³ ;

Glass transition temperature (Tg), -40.0 °C; by Differential scanning calorimetry (DSC) as a heating rate of 10 °CI min in the range of -30 °C ~ 100 °C under nitrogen atmosphere.

Comparative .Example 2: PUA hybrid dispersion.

A mixture of 200g PCL2K and 0.1g DBTDL were added into a 1L three-necked flask under stirring. Theflask was then heated to 115°C while purging thesystem with N ₂ for 15 min.80g IPDI was added into theflask slowly and the reaction was kept for 1 hour after cooling the system to 85 °C. 16.5 g DM PA was added afterwards for another 2 hour reaction period at the same temperature. Mixture of 40 g MMA and 12.3g ΤΕΞΑ were added into the flask after cooling the temperature to 65°C under stirring for 10 minutes.

The above pre-polymer was poured slowly into 680 g Dl water in another container under vigorous stirring for 10 minutes.9.6 g PDA was added dropwise into above emulsion under stirring for additional 10 minutes. Above emulsion was filtered with 100-mesh filter cloth to get the PU pre-polymer dispersion.

The emulsion dispersion was transferred into another flask which was equipped with a condenser, a mechanical stirrer and inlet for N ₂ . Solution of KPSin Dl water as initiator was poured into the flask. Monomer emulsion containing MMA and BA (mole rat io=2 3) was added into the flask under mild stirring under a nitrogen atmosphere. Temperature was increased to 75 °C to initiate the polymerization reaction for a period of two hours. Afterwards the temperature was lowered to 58 °C for residual monomer chasing process.0.10g t-BHP was added into above emulsion. After that a solution of 0.10g SFSin 3 mL Dl water was fed into the emulsion over 5 minutes. The system was cooled to room temperature after reaction period of 50 minutes. PUA emulsion was obtained by filtering through 100 mesh (0.15 mm) filtering cloth.

Example 1:

An aqueous dispersion was prepared by: adding a mixture of 200g PCL2K and 0.1g DBTDL catalyst into a 1L three-necked flask under stirring. The flask was then heated to 120°C while purging the system with N ₂ for 15 min.80g IPDI was added into the flask slowly and the reaction was kept for 1 hour after cooling the system to 85 °C.16.5 g DM PA was added afterwardsfor another 2h reaction period at the same temperature. Mixture of 40 g MMA and 12.3g TEA were added into the flask after cooling the temperature to 50 °C under stirring for 10 minutes.

The above prepolymer was poured slowly into 680 g Dl water in another container under vigorous stirring for 10 minutes.9.6 g PDA was added dropwise into above emulsion under stirring for additional 10 minutes. Above emulsion was filtered with 100-mesh filter cloth to get the PU-prepolymer dispersion.

The emulsion dispersion was transferred into another flask which was equipped with a condenser, a mechanical stirrer and inlet for N ₂ . Solution of KPSin Dl water as initiator was poured into the flask. 1.5% MAA, together with MMA and BA monomers, was fed into above dispersions. NaHC0 ₃ solution was added together with the monomer feeding to control the emulsion pH at around 7.2. Temperature was increased to 75°C to initiate the polymerization reaction for a period of two hours. Afterwards the temperature was lowered to 58 °C for residual monomer chasing process.0.10g t-BH P was added into above emulsion. After that a solution of 0.10g SFS in 3 mL Dl water was fed into the emulsion over 5 minutes. The system was cooled to room temperature after reaction period of 50 minutes. PUA emulsion was obtained by filtering through 100 mesh (0.15 mm) filtering cloth. Comparative Example 1, Comparative Example 2 as well as Example 1 were formulated into ERC paints at a PVC level (35%) and high PVC level (43%) separately with thefollowing ingredients:

As shown in Table 6, below, the acid monomer (MAA etc.) copolymerized into the acrylic backbone dramatically enhanced the mechanical performance especially elongation rate of coatings at high PVC levels (higher than 40% PVC). Also, the water swelling performance results of Example 1, compared with C.Ex.1 and C.Ex.2, were listed in Table 5 below. The less water swelling ration means better water resistance property after one week soak in water. Example 1 outperformed C.Ex.1 and C.Ex.2 at relative low PVC and high PVC levels. Table 5 Water Sw el ling

The tensile strength and elongation rate results were summarized in Table 6. Comparative example 1 has higher elongation rate but lower tensile elongation at both PVC levels due to the intrinsic elastic property of soft acrylic segment in pure acrylic emulsions. As for PUA hybrid emulsions, there is always d rop rate for the elongation rate for pigmented coati ng fi lms especially at high PVC levels (See C.Ex.2). After acid monomer was copolymerized into PUA polymer backbone, the i nterface and d ispersity of bi nder w ith pigments was improved because of better affi nity the carboxyl group with i norganic pigments, leadi ng to enhanced elasticity property. Example 1 has more balanced mechanical property and better elongation rate at high PVC level (43%).

Table 6 Tensile/ Elongation performance of pigmented coating films

As shown i n table 7, below , the d irt pickup resistance equates w ith a lower loss of reflectance. Example 1 has much better d irt resistance than C.Ex.1 both at 35% and 43% PVC levels, even comparable with C.Ex.2 w ithi n national standard requi rement ( <20%).

Table 7 Dirt Pickup Resistance

Example 2:

An aqueous dispersion was prepared as following process: mixture of 200g PCL2K and 0.1g DBTDL catalyst were added into a 1L three-necked flask under stirring. The flask was then heated to 115°C while purging the system with N ₂ for 15 min.80g IPDI was added into the flask slowly and the reaction was kept for 1 hour after cooling the system to 80 °C. 16.5 g DM PA was added afterwards for another 2h reaction period at the same temperature. Mixture of 40 g MMA and 12.3g TEA were added into the flask after cooling the temperature to 55°C under stirring for 10 minutes.

The above prepolymer was poured slowly into 680 g Dl water in another container under vigorous stirring for 10 minutes.9.6 g PDA was added dropwise into above emulsion under stirring for additional 10 minutes. Above emulsion was filtered with 100-mesh filter cloth to get the PU-prepolymer dispersion.

The emulsion dispersion was transferred into another flask which was equipped with a condenser, a mechanical stirrer and inlet for N ₂ . Solution of KPSin Dl water as initiator was poured into the flask.1.5% A A, together with St and BA (moleratio= 2/3) monomers, was fed into above dispersions. Na ₂ C0 ₃ solution was added together with the monomer emulsion and feeded to control the emulsion pH at around 7.8. Temperature was increased to 75 °C to initiate the polymerization reaction for a period of two hours. Afterwards the temperature was lowered to 58 °C for residual monomer chasing process.0.10g t-BHP was added into above emulsion. After that a solution of 0.10g SFSin 3 mL Dl water was fed into the emulsion over 5 minutes. The system was cooled to room temperature after reaction period of 50 minutes. PUA emulsion was obtained by filtering through 100 mesh (0.15 mm) filtering cloth.

Example 3:

An aqueous dispersion was prepared as following process as depicted in the following Table: A mixture of 200g PCL2K and 0.1g DBTDL catalyst were added into a 1L three-necked flask under stirring. The flask was then heated to 125°C while purging thesystem with N ₂ for 15min.80g IPDI was added intotheflask slowly and the reaction was kept for 1 hour after cooling the system to 75 °C.16.5 g DM PA was added afterwards for another 2h reaction period at the same temperature. Mixture of 40 g MMA and 12.3g TEA were added into the flask after cooling the temperature to 65 °C under stirring for 10 minutes.

The above prepolymer was poured slowly into 680 g Dl water in another container under vigorous stirring for 10 minutes.9.6 g PDA was added dropwise into above emulsion under stirring for additional 10 minutes. Above emulsion was filtered with 100-mesh filter cloth to get the PU pre-polymer dispersion.

The emulsion dispersion was transferred into another flask which was equipped with a condenser, a mechanical stirrer and inlet for N ₂ . Solution of KPSin Dl water as initiator was poured into the flask.1.5% PEM, together with MMA and BA (mole ratio= 2 3) monomers, was fed into above dispersions. Na ₂ C0 ₃ solution was feeded together with monomer emulsion to control the emulsion pH at around 7.5. Temperature was increased to 80 °C to initiate the polymerization reaction for a period of two hours. Afterwards the temperature was lowered to 58 °C for residual monomer chasing process.0.10g t-BHP was added into above emulsion. After that a solution of 0.10g SFSin 3ml_ Dl water was fed into the emulsion over 5 minutes. The system was cooled to room temperature after reaction period of 50 minutes. PUA emulsion was obtained by filtering through 100 mesh (0.15 mm) filtering cloth.

KTPP 0.57 0.57 0.57 0.57

Nopco N XZ 0.95 0.95 0.95 0.95

B. CaC0 ₃ CC700 171.92 171.92 171.92 171.92

TiO ₂ Ti-pure R-902 28.67 28.67 28.67 28.67

ZnO 19.10 19.095 19.10 19.10

Letdown

C. Latex 266.33 395.85 385.48 357.27

Nopco N XZ 0.95 0.95 0.95 0.95

Texanol 3.97 3.97 3.97 3.97

Skane M -8 1.05 1.05 1.05 1.05

Ammonia 0.5 0.5 0.5 0.50

Propylene Glycol 12.2 12.2 12.2 12.20

N astrosol 250 H BR 2.1 2.1 2.1 2.10

Thewater swelling performance results of Example 2 and Example 3, compared with C.Ex.1 and C.Ex.2, were listed in Table 8 below . Example 2 and 3 outperformed C.Ex.1 and C. Ex.2 with lower water swelling ratio means better water resistance.

Table 8 Water Sw el ling

The tensile strength and elongation rate results were summarized in Table9. Example 2 and 3 have more balanced tensile strength and elongation rate performance compared with comparative examples 1 and 2.

Table 9 Tensile/ Elongation performance of pigmented coating films

The dirt pickup resistance was shown in Table 10 where Example 2 and 3 has much better dirt resistance than C.Ex.1 and comparable with C.Ex.2 within national standard requirement ( <20%).

Table 10 Dirt Pickup Resistance Example 3 14.3