AU2005248959A1 - Surfactant free aqueous emulsions - Google Patents

Description

P/00/011 SRegulation 3.2

AUSTRALIA

Patents Act 1990 00 N COMPLETE SPECIFICATION 'N FOR A DIVISIONAL PATENT

ORIGINAL

TO BE COMPLETED BY APPLICANT Name of Applicant: E. I. DU PONT DE NEMOURS AND COMPANY Actual Inventor: Josef Huybrechts Address for Service: CALLINAN LAWRIE, 711 High Street, Kew, Victoria 3101, Australia Invention Title: SURFACTANT FREE AQUEOUS EMULSIONS The following statement is a full description of this invention, including the best method of performing it known to us:- 29/12/05,ckl 5458dec29.front,1 -la- O SURFACTANT FREE AQUEOUS EMULSIONS O This application is a divisional of application 13702/01, the disclosures of which are deemed to be incorporated herein.

0O 5 Background of the Invention This invention relates to aqueous copolymer compositions and in particular to self-stabilized aqueous copolymer emulsions. The aqueous copolymer compositions are stabilized by block and/or graft copolymers derived from the copolymerization of a water 00 soluble or dispersible macromonomer with a monomer or blend which is water insoluble.

Conventional emulsion copolymerization is a process in which a copolymer is Sformed directly in water using surfactants compounds which are able to form micelles in the aqueous phase), which stabilize the copolymer particles in the emulsion. Surfactants may be non-ionic alkyl or alkylphenol ethoxylated derivatives); anionic salts of alkyl sulfates, phosphates or sulfonates); or cationic quaternary ammonium salts of alkyl amines). Using such surfactants, which remain in the free form as a water soluble species in the emulsion, can cause problems when the emulsions are used as coating compositions, such as poor humidity and corrosion performance. It would therefore be an advantage if such copolymer emulsions could be prepared without the use of the monomeric, water sensitive surfactants.

US 5,936,026 is directed to surfactant-free emulsions and coating compositions containing same. The emulsion is prepared by emulsion copolymerization of a monomer blend in the presence of a water soluble or water dispersible macromonomer with at least of unsaturated monomers all having acid or all having amine groups in an ionized form.

At least 2% and preferably 10-40% of macromonomer is needed to prepare stable emulsions, based on the overall ionized acid or amine content in the macromonomer. Such copolymer emulsions do still have a high overall level of water sensitive groups. The macromonomers do not form micelles like conventional surfactants, which is why the higher levels of macromonomer are needed to sufficiently stabilize the overall copolymer emulsion.

US 5,362,826 discloses a method of preparing macromonomers from oligomers with a terminal unsaturated end-group. The oligomers are prepared by cobalt catalytic chain transfer polymerization as described in US 4,680,352 and US 4,722,984. There is no teaching in those references that the macromonomers can be used as surfactants in an emulsion copolymerization process.

29/12/05,ck 15458dec29.speci, PCT/US95/00376 teaches aqueous branched copolymers having hydrophobic Smacromonomer arms and a hydrophilic backbone. These copolymers are prepared in solvent and then inverted into water. There is no teaching or C suggestion that such copolymers are suitable for use in emulsion coatings.

US 5,231,131 relates to pigment dispersions in an aqueous carrier Scontaining a graft copolymer having a polymeric backbone which is Shydrophobic in nature as compared to the side chains which are hydrophilic.

The side chains consists of hydrophilic macromonomers with 20-50 of polymerized acid functional co-monomer which are neutralized with an amine 0. 10 or inorganic base. There is no teaching of using such graft copolymers as 0 0 surfactants in an emulsion copolymerization.

SSummary of the Invention An emulsion useful for forming coating compositions comprising a) an aqueous carrier; b) a polymer mixture comprising: 40-99.5 by weight of a copolymer with a weight average molecular weight of at least 3000; and 0.5-60 by weight of a stabilizing copolymer dispersed in water, said stabilizing copolymer comprising a hydrophobic portion and a hydrophilic portion, wherein said stabilizing polymer is selected from the group consisting of: polymers comprising 5-95% by weight of a hydrophilic macromonomer having at least by weight of an acid functional monomer and 5-90% by weight of at least one hydrophobic monomer polymerized in the presence of the macromonomer; (ii) polymers comprising 5-95% by weight of a hydrophobic macromonomer and 5-95% by weight of hydrophilic copolymer comprising at least 10% by weight of an acid functional monomer polymerized in the presence of the macromonomer.

The stabilizing copolymer can comprise a graft copolymer having a hydrophobic backbone with hydrophilic macromonomer arms, a hydrophilic backbone with hydrophobic macromonomer arms, or can comprise an AB block -2copolymer having a hydrophobic or hydrophilic macromonomer as the A block t¢ and a hydrophilic or hydrophobic copolymer as the B block.

The macromonomers preferably comprise the polymerization product of at least 50% by weight of monomers selected from methacrylate, methacrylonitrile, methacrylamide and derivatives and mixtures thereof with a weight average molecular weight of 500 to 10000 and prepared by cobalt N, catalytic chain transfer polymerization.

The process for making the emulsion and coating compositions based on the emulsion are also part of this invention.

In a most preferred embodiment, the acid value of the emulsion is oO less than 32.

Detailed Description of the Invention CI Emulsion copolymerization is a process of forming a copolymer from ethylenically unsaturated compounds directly in water. In the prior art, small amounts of surfactants were used in the process. By "surfactants" we mean organic compounds capable of forming micelles in water. These surfactants are monomer or low molecular weight derivatives which are water sensitive and can be non-ionic, anionic or cationic. Using the emulsion copolymers prepared in the presence of the surfactants in water borne coating formulations ofte:r to problems such as poor humidity and corrosion resistance because ot the presence of free surfactants which remain in the final film.

In an effort to solve these problems in the prior art, the present inventors discovered that certain structured polymers polymers with a well defined architecture, such as AB block copolymers and graft copolymers) prepared by cobalt catalytic chain transfer polymerization act as surfactants in an emulsion copolymerization process by stabilizing the emulsion. However, unlike the surfactants used in prior art processes, the stabilizing polymers do not present disadvantages in coatings containing the emulsion and indeed can become part of the cross-linked network that forms the coating, depending on the functional groups present in the stabilizing polymer and the type of crosslinking agent used.

In the research leading up to the present invention, it was discovered that AB block copolymers prepared by the so-called Group Transfer Polymerization process taught in Webster, US 4,508,880, having at least 2% content in either block, were not as effective at stabilizing the emulsions. More specifically, the present inventor found that the GTP AB -3block copolymers with an acid content of at least 10% in either block were not Sable to stabilize emulsions with high solid content greater than O solids), unless relatively large amounts of the GTP polymer were used. The C increased amount of the GTP polymer needed to stabilize the high solids

O

d 5 emulsions, in turn, raised the acid value of the overall emulsion to greater than 32.

Chain transfer agents employing cobalt II or III chelates such as disclosed in US Patent Nos. 4,680,352 and 4,694,054 allow the synthesis of low mole :ular weight (meth)acrylate based macrtmonomers with a terminally ethylenically unsaturated group. The term "macromonomers" as understood in 0 0 the art and used herein means a polymer terminating at one end with N1 -C-(COOR)=CH 2 Low molecular weight oligomers prepared from such chain Stransfer agents act themselves as chain transfer agents for methacrylate C, monomers through an addition-fragmentation process allowing the synthesis of semi-block copolymers as disclosed in US Patent No. 5,371,151. The terminal unsaturated end group on the macromonomer can also co-polymerize with vinyl and acrylate type monomers to form a graft copolymer.

Block or graft copolymers can so be synthesized from a hydrophilic macromonomer via copolymerization of the macromonomer with hydrophobic co-monomers or from a hydrophobic macromonomer by copolymerization of the hydrophobic macromonorn-r with a hydrophilic monomer blend. By "hydrophilic" we mean that the monomer, macromonomer or copolymer is water soluble or water dispersible. By hydrophobic we mean that the monomer, macromonomer or copolymer is not water soluble or water dispersible. Such hydrophilic macromonomers can be prepared from methacrylate monomers in the presence of a cobalt chain transfer agent. As an example, methacrylic acid monomers polymerized in the presence of the cobalt chain transfer agent can be used to form an anionic hydrophilic macromonomer which can be neutralized with a base and inverted into an aqueous solution. Similarly, a non-ionic hydrophilic macromonomer can be prepared from polyethyleneoxide derivatives of hydroxy functional methacrylates like 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate and 4-hydroxybutyl methacrylate polymerized in the presence of the cobalt chain transfer agent. And, of course, cationic macromonomers can be prepared by copolymerization of amino functional methacrylates monomers like dimethylaminoethyl methacrylate, diethylaminoethyl methacrylate, and t-butylaminoethyl methacrylate with a cobalt chain tran ''er agent, followed by neutralization with an acid or quaternization with alkylchloride, dialkylsulfate, or dialkylcarbonate.

-4- The hydrophilic macromonomer is typically prepared in a solvent V or solvent blend, however, it can also be prepared in water or water/solvent Smixture provided the formed macromonomer is soluble in the medium. The hydrophobic macromonomer is typically prepared in a solvent blend in which it is soluble. Typical solvents that can be used to form the macromonomer and further the graft or block copolymer are alcohols as methanol, ethanol, Sisopropanol, n-butanol, t-butanol, isobutanol, 2-butanol, 2-ethylhexylalcohol, etc.; ketones as acetone, methylethyl ketone, isobutyl methyl ketone, 0> diactone alcohc etc.; esters as ethyl acetate, butyl acetate, propyl acetate, isopropyl acetate, pentyl acetate, hexyl acetate, 2-ethylhexyl acetate, etc.; 0 glycols as ethylene glycol, propylene glycol, etc.; ethers as ethylene glycol ,I monobutyl ether, diethylene glycol mono butyl ether, etc.; aromatic solvents as 0 toluene, xylene, Solvesso® 100 (Exxon Chemicals), Solvesso® 150 C1 (Exxon Chemicals), Solvesso® 200 (Exxon Chemicals), etc.

To ensure that the macromonomer only has one terminal ethylenically unsaturated group to form the graft or block copolymer, the macromonomer is polymerized by using a catalytic chain transfer agent that contains cobalt II or III such as described in US Patent Nos. 4,680,352 and 4,722,984. Most preferred are pentacyanocobaltate (ii), diaquabis(borondifluorodimethyl-glyoxymato)cobaltate (ii) and diaquabis(borondifluorophenylglyoximae") cobaltate Typically these transfer agents are used at concentration or about 5 to 5000 parts per million depending on the monomers used. The polymerization of the monomers in the presence of the cobalt chain transfer agent is done with initiators as peroxides and azo derivatives. Most preferred are azo initiators such as 2,2'-azobis(2-methylbutanenitrile),4,4'-azobis(4-cyanovaleric acid) and 2-(t-butylazo)-2-cyanopropane. The peroxide initiators include peroxyesters as t-butylperoxipivalate, t-butylperoxiacetate; peroxides as dicumyl peroxide, di-tertiary butyl peroxide, di tertiary amyl peroxide; peroxicarbonates as di(n-propyl)preoxidicarbonate and peroxi salts as ammonium peroxide. Such polymerization initiators may be activated thermally, photochemically or via redox reaction.

The polymerization process can be carried out as either batch, semibatch, continuous or feed process at the boiling point of the solvent or below at ambient or at higher pressures. The monomer blend used in the synthesis of the hydrophilic or hydrophobic macromonomer has to contain at least 50% of methacrylate, methacryloni rile or methacrylamide monomers or derivatives thereof.

Examples of hydrophobic methacrylate monomers are methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, tbutyl methacrylate, 2-ethyihexyl methacrylate, lauryl methacrylate, stearyl N methacrylate, cyclohexyl methacrylate, trimethylcyclohexyl methacrylate, -isobornyl methacrylate, t-butylcyclohexyl methacrylate and benzyl methacrylate. Examples of hydrophilic methacrylate monomers include C hydroxy functional monomers like 2-hydroxyethyl methacrylate, 2hydroxypropyl methacrylate, 4-hydroxybutyl mlethacrylate as well as ethoxylated or propoxylatd derivatives thereof; acid functional monomers as methacrylic acid, 2-sulfoethyl methacrylate; amino functional monomers as 00 dimethylaminoethyl methacrylate, diethylaminoethyl methacrylate, tbutylaminoethyl methacrylate, morpholinoethyl methacrylate and quaternary ammonium salts thereof. Other functional methacrylate monomers include N acetoacetoxyethyl methacrylate, furfuryl fiethacrylate, glycidylmethacrylate, allyl methacrylate, n-(2-methacryloxyethyl)ethyleneurea, 2-cyanoethyl methacrylate and trimethoxysilylpropyl methacrylate.

Examples of methacrylonitrile and methacrylamide type monomers include alkyl or cycloalkyl methacrylamide, n-methylol methacrylamide, methoxymethyl methacrylamide, n-butoxymethyl methacrylamide, -isobutoxymethyl methacrylamide, t-butylaminopropyl methacrylamide and dimethylaninopropyl methacrylamide.

The remainder of the macromonomer composition can be prepared from other polymerizable ethylinically unsaturated monomers such as alkenes, vinyl, vinylaromatic, acrylates, acrylonitrile, acrylamide and their derivatives.

Examples of alkene and vinyl derivatives include dodecene, styrene, tbutylstyrene, methylstyrene, vinylacetate, vinylpropionate, versatic acid esters of vinylalcohol and vinylsilane. Examples of hydrophobic acrylates are methyl acrylate, ethyl acrylate, n-butyl acrylate, isobutyl acrylate, t-butyl acrylate, 2ethyihexyl acrylate, lauryl acrylate, stearyl acrylate, cyclohexyl acrylate, trimethylcyclohexyl acrylate, isobomyl acrylate, t-butylcyclohexyl acrylate, benzyl acrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, 4hydroxybuty acrylate as well as ethoxylated or propoxylated derivatives thereof; acid functional monomers as acrylic acid, itaconic acid; amino functional monomers as dimethylaminoethyl acrylate, diethylaminoethyl acrylate, t-butylaminoethyl acrylate, morpholinoethyl acrylate and quatemary ammonium salts thereof. Other functional acrylate monomers like furfuryl acrylate, glycidyl acrylate, allyl acrylhae and trimethoxysilylpropyl acrylate, acrylonitrile and acrylamide and derivatives as alkyl or cycloalkyl acrylamide, n-methylol acrylamide, methoxymethyl icrylamide, n-butoxymethyl t acrylamide, isobutoxymethyl acrylamide, t-butylaminopropyl acrylamide and Sdimethylaminopropyl acrylamide, and/or other unsaturated derivatives can be C copolymerized as maleates, fumarates, maleic anhydride and acid, fumaric U 5 acid, etc. may also be used.

The macromonomer can be chemically modified before or after N copolymerization by reaction of functional groups of the macromonomer with other chemicals. Acid functional groups on the macromonomer for example can be reacted with mono epoxy deri atives as butylene oxide, cyclohexeneoxide, Cardura® El0 a C10 versatic acid glycidyl ester from 0 0 Shell). Hydroxy functional groups can for examples be reacted with cyclic lactones as epsilon caprolactone. Epoxy functional groups can be modified Swith acid or amino functional derivatives.

The macromonomer is then further copolymerized with hydrophobic or hydrophilic monomers to form the structured block or graft) stabilizing copolymer. A low molecular weight macromonomer will form a block stabilizing copolymer when mostly methacrylate based monomers are used in this step via an addition-fragmentation process. Acrylate and other vinyl monomers will form a graft copolymer through reaction of the terminally unsaturated group.

One portion of the structured stabilizing copolymrnr either the backbone or arms of a graft copolymer or the A or B block of a block copolymer) must be hydrophilic, that is water soluble or water dispersible.

Thus, at least 10% by weight of either the macromonomer or the copolymerizing co-monomers must be acid functional. Methacrylic acid is preferred, but other acid functional monomers, acrylic acid, itaconic acid, maleic acid, fumaric acid, 2-sulfoethyl methacrylate, acrylamido propane sulfonic acid, can be used to advantage. The acid functionality in the block or graft copolymer is typically neutralized with a base to make it water soluble or dispersible. Examples of bases are alkali metal (potassium, sodium, lithium) hydroxides, or ammonia, or amines. Preferred are amines as e.g. triethylamine, dimethylamino ethanol, 2-amino-2-methyl-1 -propanol, 2-(dimethylamino)-2methyl-1-propanol, diethanolamine and diisopropanolamine, for example.

The process of forming the graft or block copolymer from the macromonomer is comparable to the typical process of forming the macromonomer in which the macromonomer is used as a co-monomer. The neutralization of the acid groups of the block or aft copolymer is preferably done after the formation of the copolymer before the inversion into water.

After the inversion step, the solvents used in the synthesis of the graft or block Scopolymer can be distilled off.

O

SThe stabilizing copolymer dispersion is then used in lieu of a surfactant in the formation of a copolymer emulsion. The amount of stabilizing d 5 copolymer used in the emulsion can be between 0.5-60% by weight, more preferably between 2-15% by weight and all ranges encompassed therein.

C Typical monomers used in the emulsion copolymerization step are the monomers used in the synthesis of the block copolymer. Preferably water soluble thermal initiators such as ammonium pe.sulfate, potassium persulfate, or 4,4'-azo bis (4-cyano pentanoic acid) are used. Redox initiators can also be Sused such as t-butylhydroperoxide, cumyhydroperoxide with ascorbic used such as t-butylhydroperoxide, cumylhydroperoxide with ascorbic N acid, sodium formaldehyde sulfoxylate as reducing agent.

SThe surfactant free emulsions stabilized by the block or graft 1 copolymers can be used in water borne coating compositions such as automotive primers, primer surfacers, pigmented topcoats and clear coats. Any kind of pigments used in waterborne paints such as metallic oxides like titanium dioxide, colored iron oxides, zinc oxide, talc, china clay, barium sulfate, aluminum silicates etc. and a wide variety of organic pigments such as quinacridones, phthalocyanines, perylenes, idanthrones, carbazoles and flake pigments as aluminum and pearlescent flakes may be used. The compositions can also be used in other water borne applications as inks, adhesives, cr nts and UV curable formulations.

The coating compositions preferably are based on (meth)acrylate vinylaromatic copolymers. The copolymers can be high molecular weight to be used in only thermoplastic formulations or can be of lower molecular weight with functional groups present to be crosslinked. Examples of crosslinkable formulations are hydroxy functional copolymers crosslinked with etherified melamine, benzoguanamine or urea formaldehyde adducts. The etherifications in those crosslinkers is typically done with mono alcohols as methanol, isobutanol or n-butanol. The crosslinking can also be done with blocked or unblocked polyisocyanates. Examples of polyisocyanates are urethane adducts, biurets and cyclotrimers of hexamethylenediisocyanate, tetramethyl xylylenediisocyanate, toluenediisocyanate and isophoronediisocyanate.

Examples of blocking groups are methylethyl ketoxime, caprolactam, alcohols, malonates and dimethyl pyrazole. The crosslinking can be performed at room temperature to higher temperatures up to 240 0 C. Typically the curing temperature is from ambient up to 80 0 C for compositions caed with unblocked polyisocyanates while 80 0 C to 180 0 C is used for formaldehyde adducts or blocked polyisocyanates. If those crosslinkers are not water soluble or Sdispersible, the graft copolymer emulsion can act as emulsifier. The crosslinkers can also be hydrophilically modified to make them water soluble or dispersible. An example ofhydrophilic modified crosslinkers are adducts of polyisocyanates with polyethylene glycol.

It may be desirable to add other optional ingredients to the paint Sformulations as antioxidants, flow modifiers, UV stabilizers, rheology control agents and/or other film forming binders can be added to the overall formulations such as binders derived from epoxy, phenolir, urethanes, polyester, polyamides, polyureas, polyacrylic or hybrids thereof.

00 Examples O The following examples illustrate the invention. All parts and CN percentages are on a weight basis. Molecular weights are determined by gel permeation chromatography using polystyrene as the standard and tetrahydrofuran as the carrier solvent.

Example 1: Macromonomer A macromonomer was prepared by mixing the following constituents into a 2 liter flask equipped with a thermometer, stirrer, dropping funnels, reflux condenser and a means for maintaining a nitrogen blanket over the reactants: Part 1 isopropanol 200 Part 2 methacrylic acid 400 isopropanol 106 Part 3 methyl ethyl ketone 209.6 diaquabis(borondifluorodiphenyl-glyoximato) cobalt(ii) (co(dpg- 0.4 bf2) 2,2'-azobis(2,4-dimethylpentanenitrile) (Vazo® 52, DuPont Co.) 4 Part 4 isopropanol methyl ethyl ketone Part Vazo® 52 methyl ethyl ketone 49.5 Part 6 methyl ethyl ketone Part 7 methyl ethyl ketone -9- Part 1 was heated in the reactor to its reflux temperature (±82 0

C)

i followed by the simultaneous addition of Parts 2 and 3 with a dropping funnel 8 over a 4 hour period. Part 4 was next added to rinse the dropping funnels and N1 the contents of the reactor was held at reflux for 15 minutes. Next was added Part 5 over a 30 minute period followed by Part 6 to rinse the funnel after which the reactor contents were held 1 hour at reflux. Finally Part 7 was added.

The macromonomer had the following properties: Solids contents 1 hour drying at 105 0 C) 36.2% Gardner Holdt viscosity Z2 t Number average molecular weight (MN) 1700 00 Weight average molecular weight (MW) 3000 0Examples 2-5: Block Oligomers Following the procedure of Example 1, the following block oligomers were prepared by starting with Part 1, adding Part 2 over 4 hours, followed by a rinsing step with Part 3. After a reflux hold period of 30 minutes, Part 4 was added as a shot followed by a rinsing step with Part 5 and a hold period at reflux for 1 hour. Finally Part 6 was added.

Examples 2 3 4 Part 1 Example 1 1000 500 1000 500 isopropanol 200 166.6 200 166.6 Part 2 methyl methacrylate 600 520 n-butyl methacrylate 600 520 2-hydroxyethyl methacrylate 280 280 2,2'-azo bis(2,-methylpropanonitrile) 6 8 6 8 (Vazo® 64 from DuPont) methyl ethyl ketone 94 92 94 92 Part 3 methyl ethyl ketone 20 20 20 Part 4 Vazo® 64 10 10 10 methyl ethyl ketone 90 90 90 Part methyl ethyl ketone 10 10 10 Part 6 methyl ethyl ketone 60 460 60 460 Properties: Solids 49.6 51 47.4 51 Gardner Holdt viscosity Z1+1/2 X Z4+1/2 MN 4000 6800 4000 6900 MW 8000 11900 7500 12300 i Examples 6-9: Copolymer Emulsions Stabilized With The Block Oligomers 0From Examples Copolymer emulsion stabilized with the block oligomers from 5 examples 2-5 were prepared by mixing the following constituents in a 2 liter flask equipped with a thermometer, stirrer, dropping funnels, reflux condenser C and a means for maintaining a nitrogen blanket over the reactants: Example 6 .7 8 9 Itn Part 1 ON dimethylamino ethanol 6 6 12 12 00 methyl methacrylate oligomer (70% 35.7 35.7 35.7 35.7 N1 solution in methyl ethyl ketone) oligomer from Example 2 oligomer from Example 4 oligomer from Example 3 120 oligomer from Example 5 120 deionized water 274 274 268 268 Part 2 styrene -125 125 125 125 2-ethylhexyl acrylate 75 75 70 2-ethylhexyl methacrylate 125 125 100 100 2-hydroxypropyl methacrylate 120 120 105 105 t-butylaminoethyl methacrylate 15 15 15 propyleneglycol methylether acetate 3 3 3 3 Part 3 4,4'-azobis (4-cyanopentanoic) acid 8.9 8.9 8.9 8.9 dimethylamino ethanol 6.6 6.6 6.6 '6.6 deionized water 170 170 170 170 Part 4 deionized water 3 3 3 3 propyleneglycol methylether acetate 2 2 2 2 Part 4,4'-azobis (4-cyanopentanoic) acid 0.9 0.9 0.9 0.9 dimethylamino ethanol 0.6 0.6 0.6 0.6 deionized water 10 10 10 Part 6 deionized water 5 5 5 Part 7 deionized water 10 10 10 The contents of Part 1 were brought in the reactor and heated till 92 0 C while the volatiles (methyl ethyl ketone-isopropanol) were distilled off.

Part 2 and 3 were added simultaneously to the reactor at 92 0 C over 4 hours followed by Part 4 to rinse the addition funnels and a hold period of 15 minutes.

-11-

I

Next were added Part 5 over 30 minutes, followed by Part 6 as rinse and a hold tt for 1 hour. Finally part 7 was added.

O

C

1 Properties: SExample 6 7 8 9 solids 50.8 51.6 50.4 50.6 0 Brookfield viscosity (centipoise) 9500 1740 53000 12000 N pH 8.6 8.5 8.7 8.6 MN 7500 22600 15300 22000 MW 36200 45100 58400 59000 00 Example 10: Macromonomer CThe procedure of example 1 was followed in making the following composition.

Part 1 isopropanol 200 Part 2 methacrylic acid 400 isopropanol 156 Part 3 methyl ethyl ketone 239.5 diaquabis(borondifluorodiphenyl-glyoximato) cobalt(ii) (co(dpg-bf2) Vazo® 52 4 Part 4 isopropanol methyl ethyl ketone Part Vazo® 52 0.3 methyl ethyl ketone 19.7 Part 6 methyl ethyl ketone Part 7 methyl ethyl ketone Properties: solids 34.8% Gardner Holdt viscosity T MN 1750 MW 2410 Examples 11 13: Block Oligomers The procedure of Examples 2-5 was followed using the ingredients below: 12- Examples 11 12 13 tn Part 1 SExample 10 525 1050 525 isopropanol 75 141.6 SPart 2 n-butyl methacrylate 200 300 500 2-hydroxyethyl methacrylate 580 280 280 O t-butylaminoethyl methacrylate 20 20 C Vazo®64 6 8 6 methyl ethyl ketone 192 132 192 Part 3 n methyl ethyl ketone 20 20 SPart 4 00 Vazo( 64 10 10 N methyl ethyl ketone 90 90 Part methyl ethyl ketone 10 10 (N Part 6 methyl ethyl ketone 20 20 Properties: solids 51.2 52.3 51.8 Gardner Holdt viscosity Z5-1/4 Z6-1/4 Z+1/2 MN 5100 3600 5300 MW 7600 5200 8500 Examples 14-16: Copolymer Emulsions Stabilized With The Block Oligomers From Examples 11-13.

The procedure of Examples 6-9 was followed in making the following compositions.

Example 14 15 16 Part 1 dimethylamino ethanol 6 6 6 methyl methacrylate oligomer (70% 35.7 35.7 35.7 solution in methyl ethyl ketone) oligomer from Example 11 300 oligomer from Example 12 300 oligomer from Example 13 300 deionized water 274 274 274 Part 2 styrene 125 125 125 2-ethylhexyl acrylate 75 75 2-ethylhexyl methacrylate 125 125 125 2-hydroxypropyl methacrylate 120 120 120 t-butylaminoethyl methacrylate 15 15 propyleneglycol methylether acetate 3 3 3 Part 3 4,4'-azobis (4-cyanopentanoic) acid 8.9 8.9 8.9 13dimethylamino ethanol 6.6 6.6 6.6 deionized water 170 170 170 Part 4 deionized water 3 3 3 propyleneglycol methylether acetate 2 2 2 SPart 4,4'-azobis (4-cyanopentanoic) acid 0.9 0.9 0.9 dimethylamino ethanol 0.6 0.6 0.6 N deionized water 10 10 Part 6 deionized water 5 5 Part 7 deionized water 10 10 00 Properties: solids 49.3 50 49.1 Brookfield viscosity (centipoise) 1960 3950 6700 pH 8.4 8.3 8.6 MN 20500 21500 23000 MW 107700 105200 110800 Example 17: Amide Functional Copolymer Emulsion Stabilized With Block Oligomer From Example 2.

The procedure of example 6-9 was followed for following composition: Part 1 Deionized water 331.2 2-Amino-2-methyl-1-propanol 90% in water 13.8 Oligomer from Example 2 Part 2 Styrene 100 Methyl methacrylate 42 2-Ethyihexyl acrylate 200 2-Hydroxyethyl acrylate 12 Isopropanol 3 Part 3 4,4'-azobis (4-cyanopentanoic) acid 1 2-Amino-2-methyl-l -propanol 90% in water 0.8 Methacrylamide 16 Deionized water 168.2 Part 4 isopropanol 2 Deionized water Part 4,4'-azobis (4-cyanopentanoic) acid 19.1 2-Amino-2-methyl-1 -propanol 90% in water Deionized water Part 6 Deionized water Part 7 Deionized water -14- 0 Test results: Solids 38.4 Viscosity 110 cps pH 6.4 Molecular weight: unknown (polymer not soluble in THF.) Example 18: Acetoacetoxy Functional Copolymer Emulsion Stabilized With Block Olinomer From Example 2.

The procedure of example 6-9 was followed for following composition: (N Part 1 Deionized water 280.9 Dimethylamino ethanol 6 N Oligomer from Example 2 27.3 Part 2 Acetoacetoxyethyl methacrylate 110 Methyl methacrylate 185 2-Ethylhexyl acrylate 150 2-Hydroxypropyl methacrylate Propyleneglycol methylether acetate 3 Part 3 4,4'-azobis (4-cyanopentanoic) acid 8.9 Dimethylamino ethanol 6.6 Deionized water 170 Part 4 Propyleneglycol methylether acetate 2 Deionized water 3 Part 4,4'-azobis (4-cyanopentanoic) acid 0.9 2-Amino-2-methyl-1 -propanol 90% in water 0.6 Deionized water Part 6 Deionized water Part 7 Deionizeq water Test results: Solids 48.1 Viscosity 175 cps pH 7.4 MN 82000 MW 800000 Example 19: Water Borne Basecoat Based On Example 17.

SFollowing ingredients were mixed: Deionized water 60.14 N Balab 3056a (Witco) 0.1 Emulsion from Example 17. 32.16 Dynol 604 (Air Products) 0.15 C n-pentanol 4 ammonia in deionized water 1.05 acrysol ase 60 (Rohm and Haas) 2.4 00 Of this first step, the pH was 8.36 and the viscosity 368 cps. To 45.12 5 parts of this first step were added under stirring: SAquapaste 3141-c33 (Silberline) 27.62 Aquapaste e2585 (Silberline) 26.2 Titanium dioxide paste MT-500-HD (Tayca) 0.46 Carbon black paste Raven 1170 (Columbian Chemicals) 0.36 Paste of a transparent red b rt333d (Ciba Chemicals) 0.24 The viscosity was adjusted to 2800 cps with deionized water and microns of this water borne silver metallic basecoat were sprayed over a standard 2-component primer surfacer which was first sanded. A standard 2component clear coat was applied at 50 microns film build over the basecoat and the overall system was baked 30 minutes at 60 0

C.

The adhesion, humidity and chip resistance were very good as well as the appearance and metallic flake control.

Comparative Example 1: Macromonomer According To Us Patent 5,936,026 With Composition From Example A macromonomer was prepared from methyl methacrylate, 2hydroxyethyl methacrylate and methacrylic acid (52/28/20 by weight) according US 5,936,026 using the cobalt chain transfer agent as used to prepare the methacrylic acid macromonomer in Example 1. Such a macromonomer is a random copolymer while Example 5 is a block copolymer with a ratio of methyl methacrylate/ 2-hydroxyethyl methacrylate (A-block)//methacrylic acid (Bblock) of 52/28//20.

-16- Cnmnarative F.YmnIe 9 Cnnnlvmpr Fmnli;nn With nnrn-c;t; n nfv. .a 9 Based On Comparative Example 1.

0The procedure of Example 9 was followed but in Part 1, the block oligomer of Example 5 was replaced with the iandom macromonomer of Comparative Example 1. During the step of adding Part 2 and Part 3, the emulsion phase separated and was unstable.

Comparative Example 3: Water Soluble Macromonomer With Less Than By Weight Of Acid.

10 The procedure of Example 1 was followed to prepare a 00 Smacromonomer with a monomer weight ratio 2-hydroxyethyl methacrylate/ methacrylic acid of 94/6.

Part 1 methyl ethyl ketone 2-hydroxyethyl methacrylate 13.16 methacrylic acid 0.84 co(dpg-bf2) 0.007 Part 2 methyl ethyl ketone 18.965 2-hydroxyethyl methacrylate 52.64 methacrylic acid 3.36 co(dpg-bc2) 0.028 Vazo® Part 3 methyl ethyl ketone 1 Part 1 was heated at reflux and Part 2 was added over 4 hours followed by a rinsing step with Part 3. The reactor contents were held 1 hour at reflux.

Properties: solids 65.6 Gardner Holdt viscosity 1+1/4 MN 980 MW 1450 Comparative Example 4: Block Oligomer From Macromonomer Example 3.

Following the procedure of Examples 11-13, a block oligomer was prepared as follows: -17- Part 1 macromonomer from comparative example 3 914.3 Part 2 n-butyl methacrylate 340 t-butylaminoethyl methacrylate Vazo®64 2 methyl ethyl ketone 28 Part 3 C methyl ethyl ketone 9 Part 4 Vazo® 64 1 methyl ethyl ketone 9 Part 0 0 methyl ethyl ketone SPart 6 methyl ethyl ketone 0Properties: solids 81.5 Gardner Holdt viscosity >Z6 MN 1530 MW 3600 Comparative Example 5: Copolymer Emulsion Stabilized By Block Copolymer Example 4.

The r1-- edure of Example 14 was followed, but in Part 1 block copolymer from Example 11 was replaced by block copolymer from Comparative Example 4. After 3 hours feeding of Parts 2 and 3, the emulsion' phase separated in two layers. This Comparative Example shows more than 6% acid groups are needed in the hydrophilic part of the block oligomer to enable to stabilize a copolymer emulsion.

Comparative Example 6: Block Oligomer By Group Transfer Polymerization According US 5 085 698 To a stirred solution of 34.5 grams of dimethyl ketene 2 trimethylsiloxyethyl trimethylsilylacetal and 0.3 ml of a 0.1 molar solution of tetrabutylammonium acetate in 375 grams of tetrahydrofuran was added 177.5 grams of n-butyl methacrylate (BMA). 45 minutes after the exother, a mixture of 88.8 grams n-butylmethacrylate and 199.4 grams of trimethylsilyl methacrylate was added. After 3 hours, the resulting block copolymer was refluyed for two hours with 420 grams of methanol to hydrolyze the trimethylsilyl methacrylate to methacrylic acid (MAA) after which the solvent was stripped off. The resulting AB block copolymer BMA//BMA/MAA 18- 47.5//23.7/28.8 by weight had MN=3960 and MW=4920 and an acid value of i 175.9.

1 Comparative Example 7: Copolvmer Emulsion Stabilized By Block Copolvmer From Example 6.

The procedure of example 6-9 was followed for following composition: O Part 1 Deionized water Sodium metabisulfite 0.25 Copolymer from Comparative Example 6 (25% solution in 3.13 VI) deionized water neutralized with dimethylamino ethanol) Part 2 00 n-butyl methacrylate 160 Sn-butyl acrylate 2-hydroxypropyl methacrylate ammonium persulfate Oligomer from Comparative Example 6 (25% solution in 15.21 deionized water neutralized with dimethylamino ethanol) sodium phosphate deionized water 131.25 Part 3 t-butylhydroperoxide 0.61 Deionized water Part 4 sodium formaldehyde sulfoxylate 0.61 Deionized water Part 2 was added over 3 hours to part 1 which was first brought to 80 0 C. Part 3 was then added and the reactor contents held for 10 minutes, followed by the addition of Part 4 over 30 minutes and a hold period of 60 minutes at 80 0

C.

The resulting latex was not stable.

Where the terms "comprise", "comprises", "comprised" or "comprising" are used in this specification, they are to be interpreted as specifying the presence of the stated features, integers, steps or components referred to, but not to preclude the presence or addition of one or more other feature, integer, step, component or group thereof.

-19-

Claims (1)

1. 40-99.5 by weight of a copolymer with a weight Saverage molecular weight of at least 3000; and 0.5-60 by weight of a stabilizing copolymer dispersed in water, said stabilizing copolymer comprising a t 10 hydrophobic portion and a hydrophilic portion, wherein 00 said stabilizing polymer is selected from the group Sconsisting of: polymers comprising 5-95% by weight of a hydrophilic macromonomer having at least by weight of an acid functional monomer and by weight of at least one hydrophobic monomer polymerized in the presence of the macromonomer; (ii) polymers comprising 5-95% by weight of a hydrophobic macromonomer and 5-95% by weight of hydrophilic copolymer comprising at least 10% by weight of an acid functional monomer polymerized in the presence of the macromonomer. 2. The emulsion of claim 1, wherein the macromonomer comprises at least 50% by weight of monomers selected from the group consisting of methacrylate, methacrylonitrile, methacrylamide and derivatives and mixtures thereof with a weight average molecular weight of 500 to 10000 and is prepared by cobalt catalytic chain transfer polymerization. 3( 3. The emulsion of claim 2, wherein the stabilizing copolymer comprises a AB block copolymer having a hydrophilic macromonomer as the A block and a hydrophobic copolymer as the B block. 4. The emulsion of claim 2, wherein the stabilizing polymer comprises a graft copolymer having a hydrophobic backbone and at least one hydrophobic macromonomer attached at a terminal end to the backbone. The emulsion of claim 2, wherein the stabilizing copolymer comprises 2-15% by weight of the polymer mixture. 6. The emulsion of claim 1 having an acid value of less than 32. I 7. A water borne coating composition comprising an aqueous V¢ emulsion, said emulsion comprising: 0a) an aqueous carrier; b) a polymer mixture comprising: 40-99.5 by weight of a copolymer with a weight average molecular weight of at least 3000; and 1 0.5-60 by weight of a stabilizing copolymer dispersed in water, said stabilizing copolymer comprising a h: drophobic portion and a hydrophilic portion, wherein 10 said stabilizing polymer is selected from the group consisting of: polymers comprising 5-95% by weight of a Shydrophilic macromonomer having at least N by weight of an acid functional monomer and 90% by weight of at least one hydrophobic monomer polymerized in the presence of the macromonomer; (ii) polymers comprising 5-95% by weight of a hydrophobic macromonomer and 5-95% by weight of hydrophilic copolymer comprising at least 10% by weight of an acid functional monomer polymerized in the presence of the macromonomer. 8. The coating composition of claim 7, wherein the macromonomer comprises at least 50% by weight of monomers selected from the group consisting of methacrylate, methacrylonitrile, methacrylamide and derivatives and mixtures thereof with a weight average molecular weight of 500 to 10000 and is prepared by cobalt catalytic chain transfer polymerization. 9. The coating composition of claim 8, wherein the stabilizing copolymer comprises a AB block copolymer having a hydrophilic macromonomer as the A block and a hydrophobic copolymer as the B block. The coating composition of claim 8, wherein the stabilizing polymer comprises a graft copolymer having a hydrophobic backbone and at least one hydrophobic macromonomer attached at a terminal end to the backbone. 11. The coating composition of claim 8, wherein the stabilizing copolymer comprises 2-15% by weight of the emulsion. 12. The coating compos'. on of claim 7, wherein said composition further comprises at least one additive selected from the group consisting of cross- -21 -22- O linking agents, pigments, antioxidants, flow modifiers, UV stabilizers, rheology control agents and film forming binders. 13. The coating composition of claim 7, wherein the acid value of the C emulsion is less than 32. 14. An emulsion, or coating composition incorporating said emulsion, substantially as hereinbefore described with reference to any one of the Examples 1 to 19. 00 DATED this 2 9 t h day of December, 2005 E. I. DU PONT DE NEMOURS AND COMPANY By their Patent Attorneys: CALLINAN LAWRIE /1 29/12/05,ck 5458dec29.claims,22