FLUOROPOLYMERS FOR COATING APPLICATIONS

Abstract

Copolymers formed by copolymerization of: (1) one or more hydrofluoroolefin monomer(s) selected from the group consisting of hydrofluoroethylenes, hydrofluoropropenes, hydrofluorobutenes, hydrofluoropentenes and combinations of these; (2) one or more aromatic vinyl ester monomer(s); (3) one or more vinyl ester monomer(s); and (4) one or more vinyl ether monomer(s), wherein at least a portion of said vinyl ether monomer is a hydroxyl group-containing vinyl ether monomer.

Claims

1. A fluorocopolymer formed by copolymerization of: (1) one or more hydrofluoroolefin monomer(s) selected from the group consisting of hydrofluoroethylenes, hydrofluoropropenes, hydrofluorobutenes, hydrofluoropentenes and combinations of these; (2) one or more aromatic vinyl ester monomer(s); (3) one or more vinyl ester monomer(s); and (4) one or more vinyl ether monomer(s), wherein at least a portion of said vinyl ether monomer is a hydroxyl group-containing vinyl ether monomer.

2. The fluorocopolymer of claim 1, wherein the one or more aromatic vinyl ester monomers comprises a monomer represented by the formula CH.sub.2CHO(CO)-(A), wherein (A) represents a phenyl group with or without a side group.

3. The fluorocopolymer of claim 1, wherein the one or more aromatic vinyl ester monomers comprises vinyl benzoate.

4. The fluorocopolymer of claim 1, wherein the one or more hydrofluoroolefin monomer(s) is selected from hydrofluoropropenes.

5. The fluorocopolymer of claim 4, wherein the one or more hydrofluoroolefin monomer(s) is selected from 2,3,3,3-tetrafluoropropene, 1,3,3,3-tetrafluoropropene, and combinations thereof.

6. The fluorocopolymer of claim 5, wherein the one or more hydrofluoroolefin monomer(s) is 1,3,3,3-tetrafluoropropene.

7. The fluorocopolymer of claim 6, wherein the 1,3,3,3-tetrafluoropropene comprises trans-1,3,3,3-tetrafluoropropene.

8. A fluorocopolymer formed by copolymerization of: (1) from about 40 mol % to about 60 mol % hydrofluoropropene monomers; (2) from about 2 mol % to about 40 mol % aromatic vinyl ester monomers; (3) from about 5 mol % to 45 mol % of vinyl ester, vinyl ether or a mixture thereof; wherein the vinyl ester has the formula CH.sub.2CR.sup.1O(CO).sub.xR.sup.2 wherein x is 1, R.sup.1 is a hydrogen or a methyl group, and R.sup.2 is selected from the group consisting of an unsubstituted straight-chain, branched-chain or alicyclic alkyl group having 1 to 12 carbon atoms; and wherein the vinyl ether has the formula CH.sub.2CR.sup.3OR.sup.4, wherein R.sup.3 is a hydrogen or a methyl group, and R.sup.4 is selected from the group consisting of an unsubstituted straight-chain, branched-chain or alicyclic alkyl group having 1 to 12 carbon atoms; and (4) from about 3 mol % to about 30 mol % of hydroxyalkyl vinyl ether having the formula CH.sub.2CR.sup.3OR.sup.5OH, where R.sup.3 is a hydrogen or a methyl group, and R.sup.5 is selected from the group consisting of a C2 to C12 unsubstituted straight-chain, branched-chain or alicyclic alkyl group having from 3 to 5 carbons; wherein the mol % are based on the total of the monomers.

9. The fluorocopolymer of claim 8, comprising from about 45 mol % to about 55 mol % of hydrofluoropropene monomers.

10. The fluorocopolymer of claim 8, comprising about 50 mol % of hydrofluoropropene monomers.

11. The fluorocopolymer of claim 8, wherein the hydrofluoropropene monomers are selected from the group consisting of HFO-1234ze, HFO-1234yf and combinations of these.

12. The fluorocopolymer of claim 8, wherein the hydrofluoropropene monomers are trans-HFO-1234ze.

13. The fluorocopolymer of claim 8, comprising from about 5 mol % to about 20 mol % of aromatic vinyl ester monomers.

14. The fluorocopolymer of claim 8, wherein the aromatic vinyl ester monomers comprise a monomer represented by the formula CH.sub.2CHO(CO)-(A), wherein (A) represents a phenyl group with or without a side group.

15. The fluorocopolymer of claim 8, wherein the aromatic vinyl ester monomers comprise vinyl benzoate.

16. The fluorocopolymer of claim 8, comprising from about 10 mol % to about 40 mol % of vinyl ester, vinyl either or a mixture thereof.

17. The fluorocopolymer of claim 8, comprising from about 20 mol % to about 40 mol % of vinyl ester, vinyl either or a mixture thereof.

18. The fluorocopolymer of claim 8, comprising from about 3 mol % to about 20 mol % of the hydroxyalkyl vinyl ether.

19. The fluorocopolymer of claim 8, comprising from about 3 mol % to about 10 mol % of the hydroxyalkyl vinyl ether.

20. A fluorocopolymer coating composition comprising: (i) one or more fluorocopolymers formed by the copolymerization of (1) first monomer(s) consisting essentially of trans-HFO-1234ze in an amount of from about 40 mol % to about 60 mol %, (2) second monomer(s) consisting essentially of vinyl benzoate in an amount of from about 2 mol % to about 40 mol %, (3) third monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2CR.sup.1O(CO).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is either hydrogen or a methyl group and wherein R.sup.2 is an unsubstituted branched-chain alkyl group having 6 to 8 carbon atoms including at least one tertiary or at least one quaternary carbon atom, wherein said vinyl ester monomer is present in an amount of from about 5 mol % to about 45 mol; and B) vinyl ether monomer(s), represented by formula CH.sub.2CR.sup.3OR.sup.4, wherein R.sup.3 is either hydrogen or a methyl group and wherein R.sup.4 is selected from the group consisting of a substituted or unsubstituted straight-chain or branched-chain alkyl group having 1 to 3 carbon atoms, said vinyl ether monomer(s) preferably being present in amounts of from about 10 mol % to about 40 mol %; and (4) fourth monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2CR.sup.3OR.sup.5OH, where R.sup.3 is either hydrogen or a methyl group and R.sup.5 is selected from the group consisting of a substituted or unsubstituted straight-chain or branched-chain C3 to C5 alkyl, wherein the amount of said fourth monomer is preferably from about 3 mol % to about 30 mol %; and (ii) a carrier comprising one or more VOC compounds; wherein the coating composition comprises not greater than about 30% by weight of said carrier.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0074] FIG. 1 shows a graph comparing the QUV-B durability of FPVE-VBZ to that of FPVE.

[0075] FIG. 2 shows a graph comparing the QUV-B durability of FPVE-VBZ (30% VBZ) and FPVE-VBZ (5% VBZ) to that of FPVE.

DETAILED DESCRIPTION OF THE INVENTION

[0076] As described above, preferred aspects of the present invention involve coating methods that provide reduced VOC emissions while at the same time providing effective and efficient protective coatings on substrates. As those skilled in the art will appreciate, the quality of a protective coating applied to a substrate can be measured by a variety of coating properties that, depending on the particular application, are important for achieving a commercially successful coating on a given substrate. These properties include but are not limited to: (1) viscosity, (2) gloss retention and (3) substrate adhesion.

[0077] Viscosity as used herein is measured according the ASTM Standard Test Method for Measuring Solution Viscosity of Polymers with Differential Viscometer, Designation D5225-14. According to this method as used herein, the viscometer used is a Brookfield viscometer (DV-II+Pro) using spindles S18/S31 using torque values from between 40% and 80% at room temperatures of about 232 C. If a solvent is used for the measurements, it is butyl acetate.

[0078] According to certain preferred embodiments, the coating compositions formed according to the present methods exhibit: (1) a solid concentration of at least about 70% by weight; (2) a viscosity, as measured by the ASTM Standard Test Method for Measuring Solution Viscosity of Polymers with Differential Viscometer, Designation D5225-14, of not greater than about 1700 mPa-s at about 232 C.; (3) a VOC content of not greater than about 450 g/l, more preferably not greater than about 400 g/l, and even more preferably not greater than about 350 g/1; and (4) a color change of below 2% after 600 hours of QUV-B testing.

[0079] In preferred embodiments, the polymers of the present invention have a hydroxyl value of greater than about 70, and in other preferred embodiments have a hydroxyl value of greater than about 90. As mentioned above, the ability to achieve such a method resides, in part, on the judicious selection of the type and the amounts of the various components that are used to form the fluoropolymer and the coating compositions of the present invention.

[0080] Monomers

[0081] Hydrofluoroolefins

[0082] The hydrofluoroolefin monomers according to the methods of the present invention can include in certain preferred embodiments hydrofluoroethylene monomer, that is, compounds having the formula CX.sup.1X.sup.2CX.sup.3X.sup.4; wherein X.sup.1, X.sup.2, X.sup.3, X.sup.4 are each independently selected from H or F or Cl atom, but at least one of them is a hydrogen atom. Examples of hydrofluoroethylene monomers include, among others:

[0083] CH.sub.2CHF,

[0084] CHFCHF,

[0085] CH.sub.2CF.sub.2, and

[0086] CHFCF.sub.2.

[0087] The hydrofluoroolefin monomers according to certain preferred aspects of the methods of the present invention include, and preferably consists essentially of or consist of hydrofluoropropenes having the formula CX.sup.5X.sup.6CX.sup.7CX.sup.8X.sup.9X.sup.10; wherein X.sup.5, X.sup.6, X.sup.7, X.sup.8, X.sup.9 and X.sup.10 are independently selected from H or F or Cl atom, but at least one of them is a hydrogen atom and another is a fluorine atom. Examples of hydrofluoropropene monomers include, among others:

[0088] CH.sub.2CFCF.sub.3 (HFO-1234yf),

[0089] trans-CHFCHCF.sub.3 (trans-HFO-1234ze),

[0090] CHClCFCF.sub.3 and

[0091] CH.sub.2CHCF.sub.3.

[0092] In preferred embodiments, the hydrofluoroolefin comprises, consists essentially of or consists of HFO-1234yf and/or HFO-1234ze. In preferred embodiments, the hydrofluoroolefin comprises, consists essentially of or consists of HFO-1234ze, with said HFO-1234ze preferably comprising, consisting essentially of or consisting of trans-HFO-1234ze.

[0093] The hydrofluoroolefin monomers according to certain preferred aspects of the methods of the present invention include hydrofluorobutene according to the following formula: CX.sup.11X.sup.12CX.sup.13CX.sup.14X.sup.15CX.sup.16X.sup.17X.sup.18; wherein X.sup.11, X.sup.12, X.sup.13, X.sup.14, X.sup.15, X.sup.16, X.sup.17 and X.sup.18 are independently selected from H or F or Cl atom, but at least one of them is a hydrogen atom and at least one is a fluorine atom. Examples of hydrofluorobutene include, among others, CF.sub.3CHCHCF.sub.3.

[0094] Vinyl Esters

[0095] The copolymers in accordance with the present invention preferably are also formed from vinyl ester monomer units, preferably in amounts of from about 5 mol % to about 45 mol %, more preferably from about 10 mol % to about 30 mol %, and even more preferably from about 10 mol % to about 20 mol %. In preferred embodiments, the vinyl ester monomer(s) are represented by the formula CH.sub.2CR.sup.1O(CO).sub.xR.sup.2, wherein x is 1 and wherein R.sup.1 is either hydrogen or a methyl group, and wherein R.sup.2 is selected from the group consisting of a substituted or unsubstituted, preferably unsubstituted, straight-chain or branched-chain, preferably branched chain, alkyl group having 5 to 12 carbon atoms, more preferably having from 5 to 10 carbon atoms, and even more preferably 8 to 10 carbon atoms. In preferred embodiments, the alkyl group includes at least one tertiary or quaternary carbon atom. In highly preferred embodiments, the vinyl ester includes at least one quaternary carbon according to the following formula:

##STR00001##

where each of R.sup.7 and R.sup.8 are alkyl groups, preferably branched alkyl groups, that together contain from 5 to about 8, more preferably from 6 to 7, carbon atoms.

[0096] Examples of vinyl ester monomers that are preferred according to certain preferred embodiments include vinyl acetate, vinyl propionate, vinyl butyrate, vinyl pivalate, vinyl capronate, vinyl laurate, VEOVA-9 (vinyl versatate ester formed from a C9 carbocylic acid, produced by Momentive), VEOVA-10 (vinyl versatate ester formed from a C10 carbocyclic acid, produced by Momentive) and vinyl cyclohexanecarboxylate. Each of VEOVA-9 and VEOVA-10 contain at least one quaternary carbon according to Formula A above. According to preferred embodiments, the vinyl ester comprises vinyl versatate ester having from 11 to 12 carbon atoms in the molecule, preferably with at least one quaternary carbon according to Formula A above.

[0097] Vinyl Ethers

[0098] The copolymers in accordance with the present invention preferably are also formed from vinyl ether monomer units, preferably in amounts of from about 5 mol % to about 45 mol %, more preferably from about 10 mol % to about 30 mol %, and even more preferably from about 10 mol % to about 20 mol %. In preferred embodiments, the vinyl ester monomer(s) are represented by the formula CH.sub.2CR.sup.3OR.sup.4, wherein R.sup.3 is independently either hydrogen or a methyl group and wherein R.sup.4 is selected from the group consisting of a substituted or unsubstituted, preferably unsubstituted, straight-chain or branched-chain, preferably straight chain, alkyl group having 1 to 5 carbon atoms, more preferably 1 to 3 carbon atoms. Examples of vinyl ether monomers that are preferred according to certain preferred embodiments include alkyl vinyl ethers such as methyl vinyl ether, ethyl vinyl ether, propyl vinyl ether, n-butyl vinyl ether, isobutyl vinyl ether, hexyl vinyl ether, octyl vinyl ether, decyl vinyl ether and lauryl vinyl ether. Vinyl ethers including an alicyclic group can also be used, for example, cyclobutyl vinyl ether, cyclopentyl vinyl ether and cyclohexyl vinyl ether. According to preferred embodiments, the vinyl ether comprises, consists essentially of, or consists of ethyl vinyl ether.

[0099] Preferably in those embodiments in which vinyl ether and vinyl ester monomers are both present, the amount of vinyl ether and vinyl ester monomers together comprise from about 25 mol % to about 45 mol % of the total monomers.

[0100] Hydroxy Vinyl Ethers

[0101] The copolymers in accordance with the present invention preferably are also formed from hydroxyl vinyl ether monomer units, preferably in amounts of from about 3 mol % to about 60 mol % of hydroxy vinyl ether monomer, preferably in an amount of from about 3 mol % to about 30 mol %, more preferably from about 3 mol % to about 20 mol %, and even more preferably from about 3 mol % to about 10 mol %. In preferred embodiments, the hydroxyl vinyl ether monomer(s) are represented by the formula CH.sub.2CR.sup.3OR.sup.5OH, where R.sup.3 is as defined above, preferably hydrogen, and where R.sup.5 is selected from the group consisting of a C2 to C6 substituted or unsubstituted, preferably unsubstituted, straight-chain or branched-chain, prefeethrably straight chain, alkyl group. Examples of preferred hydroxyalkyl vinyl ether monomers include hydroxyl-ethyl vinyl ether, hydroxypropyl vinyl ether, hydroxybutyl vinyl ether, hydroxypentyl vinyl ether and hydroxyhexyl vinyl ether. In certain embodiments, the copolymer is formed from about 5 mol % to about 20 mol % of hydroxyalkyl vinyl ether monomers, based on the total weight of the monomer.

[0102] In preferred embodiments, the co-monomers according to the fluorocopolymer formation step (b)(i) (as described above) comprise, and preferably consist essentially of: [0103] (1) first monomer consisting essentially of HFO-1234ze, preferably in an amount of from about 20 mol % to about 30 mol %, and even more preferably from about 22 mol % to about 27 mol %, and even more preferably about 25 mol %, [0104] (2) second monomer consisting essentially of vinyl benzoate, preferably in an amount of from about 1 mol % to about 40 mol %, and even more preferably from about 2 mol % to about 30 mol %, and even more preferably from about 5 mol % to about 20 mol %, [0105] (3) third monomer(s) comprising: [0106] A) vinyl ester monomer represented by formula CH.sub.2CR.sup.1O(CO).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is either hydrogen or a methyl group, preferably hydrogen, and wherein R.sup.2 is a substituted or unsubstituted branched or straight-chain alkyl group having 6 to 8 carbon atoms, preferably an unsubstituted branched-chain alkyl group having 6 to 8 carbon atoms, wherein said alkyl group preferably includes at least one tertiary or quaternary carbon atom, wherein said vinyl ester monomer is present in an amount of from about 5 mol % to about 45 mol %, more preferably from about 10 mol % to about 30 mol %, and even more preferably from about 10 mol % to about 20 mol %; and [0107] B) vinyl ether monomer(s), represented by formula CH.sub.2CR.sup.3OR.sup.4 respectively, wherein R.sup.3 is independently either hydrogen or a methyl group, preferably hydrogen, and wherein R.sup.4 is selected from the group consisting of a substituted or unsubstituted straight-chain or branched-chain, preferably straight chain, alkyl group having 1 to 3 carbon atoms, preferably 2 carbon atoms, said vinyl ether monomer(s) preferably being present in amounts of from about 10 mol % to about 40 mol %, more preferably from about 5 mol % to about 45 mol %, more preferably from about 10 mol % to about 30 mol %, and even more preferably from about 10 mol % to about 20 mol %; and [0108] (4) fourth monomer(s) consisting of hydroxyalkyl vinyl ether represented by formula CH.sub.2CR.sup.3OR.sup.5OH, where R.sup.3 is methyl or hydrogen, preferably hydrogen, and R.sup.5 is selected from the group consisting of a substituted or unsubstituted straight-chain or branched-chain C3 to C5 alkyl, preferably C4, unsubstituted straight-chain alkyl group, wherein the amount of said fourth monomer is preferably present in an amount of from about 3 mol % to about 30 mol %.

Copolymer Formation Methods

[0109] It will be appreciated by those skilled in the art, based on the teachings contained herein, that copolymers of the present invention may be formed to achieve the preferred characteristics described herein using a variety of techniques, and all such techniques are within the scope of the present invention.

[0110] In preferred embodiments, the fluorocopolymer is preferably produced in a polymerization system that utilizes a carrier for the monomer/polymer during and/or after formation. According to one preferred embodiment the carrier acts as a solvent and/or dispersant for the monomer and/or polymer, and such operations include dispersion, emulsion and solution polymerization. Examples of carriers in such systems, including preferably solvents for solution polymerization, include: esters, such as methyl acetate, ethyl acetate, propyl acetate and butyl acetate; ketones, such as acetone, methyl ethyl acetone and cyclohexanone; aliphatic hydrocarbons, such as hexane, cyclohexane, octane, nonane, decane, undecane, dodecane and mineral spirits; aromatic hydrocarbons, such as benzene, toluene, xylene, naphthalene, and solvent napthta; alcohols, such as methanol, ethanol, tert-butanol, iso-propanol, ethylene glycol monoalkyl ethers; cyclic ethers, such as tetrahydrofuran, tetrahydropyran, and dioxane; fluorinated solvents, such as HCFC-225 and HCFC-141b; dimethyl sulfoxide; and the mixtures thereof.

[0111] It is contemplated that the temperature conditions used in the polymerization process of the present invention can be varied according to the particular equipment and applications involved and all such temperatures are within the scope of the present invention. Preferably, the polymerization is conducted at a temperature in a range of from about 30 C. to about 150 C., more preferably from about 40 C. to about 100 C., and even more preferably from about 50 C. to about 70 C., depending on factors such as the polymerization initiation source and type of the polymerization medium.

[0112] In certain preferred embodiments, it is preferred that the solution polymerization is conducted under conditions under which the total amount of the solvent used in the copolymerization process, based on the weight of the solvent and monomer in the solution, is from about 10 wt % to about 40 wt %, more preferably in amounts of from about 10 wt % to about 30 wt %, and more preferably in certain embodiments in an amount of from about 15% to about 25%. In certain of such embodiments, the solvent used in the solution copolymerization process comprises, preferably consists essentially of, and more preferably in certain embodiments consists of C2-C5 alkyl acetate, and even more preferably butyl acetate.

[0113] In preferred embodiments, the copolymer as formed in accordance with the preferred methods described herein is prepared by copolymerizing those monomers under conditions effective to achieve a copolymer having a number average molecular weight of 5000 to 50,000, or in some embodiments 5000 to 10,000 as measured by gel phase chromatography (GPC) according to the method described in Skoog, D. A., Principles of Instrumental Analysis, 6th ed.; Thompson Brooks/Cole: Belmont, Calif., 2006, Chapter 28, which is incorporated herein by reference. In certain embodiments, the copolymer has a number average molecular weight that is greater than about 10,000, and even more preferably from 10,000 to about 14,000. According to certain preferred embodiments, the copolymer has a molecular weight distribution of 2 to 10, more preferably 2.5 to 8, and most preferably 3 to 6. Applicants have found that in certain embodiments the use of copolymers having a molecular weight less than 5000 produces weatherability and chemical resistance of the protective coating that is less than is desired for some applications, and that when the polymers have a molecular weight of more than 50,000, coating compositions having viscosities that may negatively impact the spreading or coating properties of the coating compositions and hence difficulties in the coating operations result.

[0114] In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: [0115] (i) providing one or more fluorocopolymers by copolymerization of [0116] (1) first monomer consisting essentially of HFO-1234ze, with said HFO-1234ze preferably comprising, consisting essentially of or consisting of trans-HFO-1234ze, preferably in an amount of from about 20 mol % to about 30 mol %, and even more preferably from about 22 mol % to about 27.5 mol %, and even more preferably about 25 mol %; [0117] (2) second monomer(s) consisting essentially of vinyl benzoate, preferably in an amount of from about 1 mol % to about 40 mol %, and even more preferably from about 2 mol % to about 30 mol %, and even more preferably from about 5 mol % to about 20 mol %; [0118] (3) third monomers comprising: [0119] A) vinyl ester monomer represented by formula CH.sub.2CR.sup.1O(CO).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is either hydrogen or a methyl group, preferably hydrogen, and wherein R.sup.2 is an unsubstituted branched-chain alkyl group having 6 to 8 carbon atoms, wherein said alkyl group preferably includes at least one tertiary or quaternary carbon atom, wherein said vinyl ester monomer is present in an amount of from about 5 mol % to about 45 mol %, more preferably from about 10 mol % to about 30 mol %, and even more preferably from about 10 mol % to about 20 mol %; and [0120] B) vinyl ether monomer(s), represented by formula CH.sub.2CR.sup.3OR.sup.4, wherein R.sup.3 is either hydrogen or a methyl group, preferably hydrogen, and wherein R.sup.4 is selected from the group consisting of a substituted or unsubstituted straight-chain or branched-chain, preferably straight chain, alkyl group having 1 to 3 carbon atoms, preferably 2 carbon atoms, said vinyl ether monomer(s) preferably being present in amounts of from about 10 mol % to about 40 mol %, more preferably from about 5 mol % to about 45 mol %, more preferably from about 10 mol % to about 30 mol %, and even more preferably from about 10 mol % to about 20 mol %; and [0121] (4) fourth monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2CR.sup.3OR.sup.5OH, where R.sup.3 is methyl or hydrogen, preferably hydrogen, and R.sup.5 is selected from the group consisting of a C3 to C5, preferably C4, unsubstituted straight-chain alkyl group, wherein the amount of said third monomer is preferably from about 3 mol % to about 30 mol %; [0122] and at the end of the copolymerization of these monomers, optionally reacting a radical transfer agent, preferably methanol, with the fluorocopolymer, preferably at an increased temperature from the copolymerization temperature, to produce an endcapped fluorocopolymer, preferably containing ether end groups; [0123] (ii) providing a carrier for said one or more fluorocopolymers, said carrier comprising one or more VOC compounds and preferably selected from aromatic hydrocarbons such as xylene and toluene; alcohols such as n-butanol; esters such as butyl acetate; ketones such as methyl isobutyl ketone, and glycol ethers such as ethyl cellusolve, with C2-C5 alkyl acetate being preferred, and even more preferably comprising, consisting essentially of, or consisting of butyl acetate; and [0124] (iii) combining said one or more fluorocopolymers with said carrier to produce a polymeric composition comprising not greater than about 30% by weight of said carrier, preferably with a solids content of at least about 70% by weight. According to preferred embodiments, the fluorocopolymer composition of the present invention, and in particular the fluorocopolymer formed as described in the preceding sentence, has a polymer number average molecular weight as measured by gel phase chromatography (GPC) according to the method described in Skoog, D. A., Principles of Instrumental Analysis, 6th ed.; Thompson Brooks/Cole: Belmont, Calif., 2006, Chapter 28, which is incorporated herein by reference, of from about 5000 to 50,000, more preferably from about 7000 to about 15000, and has a solids content of from about 70% to about 90% by weight, and even more preferably from about 70% to about 85% by weight, and preferably a VOC content of less than about 400 g/l, more preferably from about 400 g/l to about 100 g/l, and even more preferably from about 350 g/l to about 200 g/l. It is also preferred in such embodiments as described in the present application in general, and in this paragraph in particular, that the coating compositions of the present invention have a viscosity at 25 C. of less than about 1900 mPa-s, more preferably less than about 1800 mPa-s and even more preferably of less than about 1700 mPa-s as measured by Ford Cup at least at one of 12 revolutions per minutes (r/m), 30 r/m and 60 r/m, and preferably at all three speeds, preferably as measured according to ASTM D1200-10(2014) or ASTM D2196 as appropriate.

[0125] In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: [0126] (i) providing one or more fluorocopolymers by copolymerization of [0127] (1) first monomer consisting essentially of HFO-1234ze, with said HFO-1234ze preferably comprising, consisting essentially of or consisting of trans-HFO-1234ze in an amount of from about 40 mol % to about 60 mol %, and even more preferably from about 45 mol % to about 55 mol %, and even more preferably about 50 mol %, [0128] (2) second monomer(s) consisting essentially of vinyl benzoate, preferably in an amount of from about 1 mol % to about 40 mol %, and even more preferably from about 2 mol % to about 30 mol %, and even more preferably from about 5 mol % to about 20 mol %, [0129] (3) third monomer(s) comprising: [0130] A) vinyl ester monomer represented by formula CH.sub.2CR.sup.1O(CO).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is either hydrogen or a methyl group, preferably hydrogen, and wherein R.sup.2 is an unsubstituted branched-chain alkyl group having 6 to 8 carbon atoms including at least one tertiary carbon atom, wherein said vinyl ester monomer is present in an amount of from about 5 mol % to about 45 mol %, more preferably from about 10 mol % to about 30 mol %, and even more preferably from about 10 mol % to about 20 mol %; and [0131] B) vinyl ether monomer(s), represented by formula CH.sub.2CR.sup.3OR.sup.4, wherein R.sup.3 is either hydrogen or a methyl group, preferably hydrogen, and wherein R.sup.4 is selected from the group consisting of a substituted or unsubstituted straight-chain or branched-chain, preferably straight chain, alkyl group having 1 to 3 carbon atoms, preferably 2 carbon atoms, said vinyl ether monomer(s) preferably being present in amounts of from about 10 mol % to about 40 mol %, more preferably from about 5 mol % to about 45 mol %, more preferably from about 10 mol % to about 30 mol %, and even more preferably from about 10 mol % to about 20 mol %; and [0132] (4) fourth monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2CR.sup.3OR.sup.5OH, where R.sup.3 is either hydrogen or a methyl group and R.sup.5 is selected from the group consisting of a substituted or unsubstituted straight-chain or branched-chain C3 to C5 alkyl, preferably C4, unsubstituted straight-chain alkyl group, wherein the amount of said forth monomer is preferably from about 3 mol % to about 30 mol %; [0133] and at the end of the copolymerization of these monomers, optionally reacting a radical transfer agent, preferably methanol, with the fluorocopolymer, preferably at an increased temperature from the copolymerization temperature, to produce an endcapped fluorocopolymer, preferably containing ether end groups; and [0134] (ii) providing a carrier for said one or more fluorocopolymers, said carrier comprising one or more VOC compounds selected from aromatic hydrocarbons such as xylene and toluene; alcohols such as n-butanol; esters such as butyl acetate; ketones such as methyl isobutyl ketone, and glycol ethers such as ethyl cellusolve, with C2-C5 alkyl acetate being preferred, and even more preferably comprising, consisting essentially of, or consisting of butyl acetate; and [0135] (iii) combining said one or more fluorocopolymers with said carrier to produce a polymeric composition comprising not greater than about 30% by weight of said carrier, preferably with a solids content of at least about 70% by weight.

Coating Composition Formation Methods

[0136] The copolymers as formed in accordance with the procedures described herein may then be used to form various coating compositions that have the substantial advantages described above. For example, various solvents can be used for the preparation of solution-type paints or coatings by adding those solvents to the fluorocopolymer of the present invention formed as described herein. In certain embodiments, preferred solvents for formation of the coating composition include aromatic hydrocarbons such as xylene and toluene; alcohols such as n-butanol; esters such as butyl acetate; ketones such as methyl isobutyl ketone, and glycol ethers such as ethyl cellusolve and various commercial thinners.

[0137] In certain embodiments, the coating composition of the present invention has a solid content of from about 70% to about 90% by weight based on the total weight of the coating composition, and more preferably in certain embodiments from about 75% to about 85% by weight of solids. In certain preferred embodiments, the solids comprise and preferably consist essentially of the copolymers of the present invention and/or cross-linked copolymers formed using the copolymers of the present invention. Although it is contemplated that those skilled in the art will be able to form coatings using the present compositions according to any one of known methods, in preferred embodiments the coating is formed by brushing, a rolling, air spraying, airless spraying, flow coating, roller coating, a spin coating, and the like, and any combination of these may be used. Furthermore, the coating can be applied on various substrates. The coating film can be formed directly on a substrate or via a primer or if necessary, via an undercoating layer. Although all thicknesses are within the scope of the present invention, in preferred embodiments the outermost cured coating film layer has a layer thickness of from about 20 to about 30 m.

EXAMPLES

[0138] The present invention is further illustrated by the following non-limiting examples.

Example 1Fluoropolymer Preparation

[0139] A solution polymerization operation is carried out by charging into a 1000 ml stainless steel autoclave equipped with a stirrer the components as indicated in the following Table 1:

TABLE-US-00001 TABLE 1 Wt Mono- % of Mono- mer, COMPONENT Weight, solu- mer mol % of TYPE NAME grams tion Moles polymer Solvent butyl acetate 61.6 9.2 First trans-1,3,3,3- 253 37.8 2.22 50 Monomer tetrafluoropropene (HFO) (trans-HFO-1234ze) Second vinyl benzoate 118.4 17.7 0.8 18 Monomer Third VEOVA-10 157.4 23.5 0.8 18 Monomer (vinyl ester) Fourth hydroxybutylvinyl 72.2 10.8 0.62 14 Monomer ether (alkylhy- droxy ether) Initiator tert-Butyl 6.5 1.0 peroxypivalate

[0140] The butyl acetate, the vinyl benzoate monomer, the vinyl ester monomer (VEOVA-10), the hydroxybutyl vinyl ether, the initiator and 15 grams of zinc oxide were charged into the vessel. The mixture was solidified with liquid nitrogen, and deaerated to remove the dissolved air. Then, the trans-1,3,3,3-tetrafluoropropene (trans-HFO-1234ze) was added to the mixture in the autoclave, and the mixture was then gradually heated to about 57 C. The mixture was then stirred (at about 300 rpm) for about 0.5 hours to carry-out solution copolymerization of the monomers.

[0141] Then, at the end of copolymerization, 50 grams of methanol (as a radical transfer agent) was added into the autoclave to react with the fluorocopolymer. During the copolymerization of the fluorocopolymer, the end group should be a CH.sub.2* radical group or a CFH* radical group. Thus, addition of a radical transfer agent (i.e., a reagent capable of reacting with a CH.sub.2* radical group or a CFH* radical group, such as for example, an alcohol, an amine, or a hydrogen) should serve to endcap the end groups of the fluorocopolymer, and the resulting endgroups should preferably be ether groups (from an alcohol) and/or alkyl groups (from a hydrogen). Both ether groups and alkyl groups are much more thermally stable than the existing carboxylic acid end groups of the fluorocopolymer, and thus will result in a more thermally stable, endcapped fluorocopolymer. Although the endcapping process should greatly improve the thermal stability of the fluorocopolymer, it should not have an effect on the UV-light stability of the fluorocopolymer. In order to increase the yield of the endcapping reaction, the temperature of the mixture was increased from about 57 C. to about 130 C. after addition of the methanol. The mixture was then stirred (at about 300 rpm) for about 4 hours to carry out the endcapping reaction and produce a final, endcapped fluorocopolymer.

[0142] After the autoclave was cooled to room temperature, any unreacted monomers were purged and then the autoclave was opened and a vacuum was applied to the autoclave for a sufficient period of time to remove sufficient excess solvent to achieve a solid content (copolymer content) in the autoclave of about 67% by weight. The final fluorocopolymer had a weight of 821 grams, and a yield of 92%. The final fluorocopolymer (without solvent) was tested and found to have: a number average molecular weight in the range of about 12,000; a hydroxyl value of about 60 mg KOH/g; and a fluorine content of about 21 wt %. After post-treatment (filtering the zinc oxide and concentrating to a solid content of about 70%), the resulting final fluorocopolymer plus solvent combination was in the form of a clear solution having a solid, that is, copolymer, content of about 70%.

Example 2Coating Composition Preparation

[0143] A coating composition was then prepared using the final fluorocopolymer from Example 1 above. The coating composition was prepared from the following components:

TABLE-US-00002 Weight Component Name (g) Supplier Fluoroco- final fluorocopolymer 58.6 polymer from Example 1 above, 70% solid content Pigment carbon black FW200 2.5 Orion Engineered Carbons Pigment R-960 titanium dioxide 15.6 DuPont Ti-Pure Dispersant SOLSPERSE-32500 3 Lubrizol Corp. Solvent butyl acetate 20.3 Curing agent Desmodur N 3900 12.4 Covestro (NCO 19.6%)

[0144] The coating composition was prepared as follows. A pigment paste mixture was made by mixing the fluorocopolymer, the pigments and the dispersant in a high-speed dispersion machine with glass beads to disperse the mixture and reduce the size of the pigment. The mixture was dispersed for about 3 hours at 3000 RPM, until the fineness of the composition was less than about 20 m. The mixture was then filtered to remove the glass beads.

[0145] Next, the solvent was added to the pigment paste mixture, and the resulting mixture was well mixed by the high-speed dispersion machine for about 30 minutes at 1500 RPM. Then, the curing agent was added to the mixture, and the resulting mixture was again well mixed by the high-speed dispersion machine for about 30 minutes at 1500 RPM, thus forming the coating composition.

[0146] In order to form the coating film, conventional methods such as a brush, a roller, an air spray, an airless spray, a flow coater, a roll coater, a spin coater, and the like may be utilized, and the coating can be applied on various substrates. In addition, the coating film can be formed directly on a substrate or on a primer layer, or if necessary on an undercoating layer. In the present case, the coating film was applied to a substrate and the outermost cured coating film layer had a layer thickness of about 20-30 m.

[0147] After coating was complete, the coated substrate was kept at room temperature (about 20-25 C.) for about one week to ensure that the outermost coating film layer was completely cured.

[0148] QUV-B durability testing was then performed on the coating composition having the final fluorocopolymer described above (denoted as FPVE-VBZ), and the results were compared to another coating composition having a fluorocopolymer that was prepared exactly the same way as FPVE-VBZ except that the vinyl benzoate monomer was not included in the fluorocopolymer (denoted as FPVE). The QUV-B is measured according to ASTM D 7251, which is QUV Accelerated Weathering Tester Operating Procedure by which accelerated testing is performed in an accelerated testing cabinet sold under the trade mark QUV manufactured by Q-Lab Corporation of Cleveland, Ohio. Two lamps are used in this testing cabinet: A lamps (UVA-340) have a normal output of 0.69 W/m.sup.2 @ 340 nm m and a maximum output of 1.38 W/m.sup.2 @ 340 nm m; and B lamps (UVB-313) have a normal output of 0.67 W/m.sup.2 @ 310 nm m and a maximum output of 1.23 W/m.sup.2 @ 310 nm m. As used herein, the designation QUV-A refers to tests using the A lamps and QUV-B refers to tests using the B lamps. The procedure is accomplished using the following steps: [0149] 1. Measure the initial gloss of the coating film three times and obtain the average of the measurements, which is designated in the following calculations as A. [0150] 2. Place the test plate containing the coating in the panel holder in the cabinet and power the cabinet on. [0151] 3. Set the PROGRAM button in the control panel and select the desired program operation. [0152] 4. Engage the RUN button to start test. [0153] 5. Record down the exposure time indicated on the LED panel. [0154] 6. Stop the machine after the indicated hours, remove the test plate, and measure the gloss three times to get an average result for the indicated exposure time, and record this value as B for use in the calculation below. [0155] 7. Determine Gloss retention using the formula: Gloss Retention=B/A

[0156] As can be seen in FIG. 1, the QUV-B durability of FPVE-VBZ is much better than that of FPVE. For example, after approximately 240 hours of exposure under UV-B light, the actual gloss of FPVE is around 15 while that of FPVE-VBZ is around 60 (wherein the actual gloss is the B value as described in the preceding paragraph). Similarly, after approximately 400 hours of exposure under UV-B light, the actual gloss of FPVE is around 5 while that of FPVE-VBZ is around 47. Thus, these results show that inclusion of the aromatic vinyl ester monomer in the fluorocopolymer as described herein leads to an improvement in the QUV-B durability of the resulting fluorocopolymer.

[0157] Additional coating compositions and fluorocopolymers were also produced and subjected to QUV-B durability testing, in accordance with the procedures described above in Examples 1 and 2. Specifically, two additional coating compositions having a fluorocopolymer were produced in accordance with the procedure described above in Examples 1 and 2, except that different amounts of the vinyl benzoate monomer were employed in the fluorocopolymer. One fluorocopolymer was produced with 30 mol % of the vinyl benzoate monomer (coating composition denoted as FPVE-VBZ (30% VBZ)), and another fluorocopolymer was produced with 5 mol % of the vinyl benzoate monomer (coating composition denoted as FPVE-VBZ (5% VBZ)). As can be seen in FIG. 2, the QUV-B durability of both FPVE-VBZ (30% VBZ) and FPVE-VBZ (5% VBZ) is much better than that of FPVE. For example, after approximately 600 hours of exposure under UV-B light, the gloss retention of FPVE-VBZ (30% VBZ) is around 80% and the gloss retention of FPVE-VBZ (5% VBZ) is around 58%, while that of FPVE is around 8%. Similarly, after approximately 300 hours of exposure under UV-B light, the gloss retention of FPVE-VBZ (30% VBZ) is around 83% and the gloss retention of FPVE-VBZ (5% VBZ) is around 65%, while that of FPVE is around 18%. Thus, these results also show that inclusion of the aromatic vinyl ester monomer in the fluorocopolymer as described herein leads to an improvement in the QUV-B durability of the resulting fluorocopolymer.

[0158] In addition, although no QUV-A testing was done, because QUV-A testing generally has a much lower dosage of UV-light than does QUV-B testing, we would expect the color change and gloss retention in QUV-A testing to be better than those in QUV-B testing.