Gloss retentive fluorocopolymers for coating applications

Abstract

Disclosed are protective coating compositions having enhanced gloss retention properties formed by steps comprising: (i) providing one or more fluorocopolymers 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 vinyl ester monomer(s), and (3) 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, wherein the copolymer preferably has a number average molecular weight of greater than about 10,000; (ii) providing a VOC containing carrier for said one or more fluorocopolymers; and (iii) providing a stabilizing agent comprising: a) a radical scavenger and b) an absorber of UV light; and (iv) combining said one or more fluorocopolymers with said carrier and said stabilizing agent to produce a polymeric coating composition.

Claims

1. A protective coating composition having enhanced gloss retention properties comprising: (i) one or more fluorocopolymers comprising the copolymerization product 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 vinyl ester monomer(s), and (3) 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, wherein the fluorocopolymer has a number average molecular weight of greater than about 10,000; (ii) a carrier comprising one or more volatile organic compounds; and (iii) a stabilizing agent comprising a) a radical scavenger; and b) an absorber of UV light; wherein the coating composition comprises not greater than about 30% by weight of said carrier, and wherein said coating composition has a volatile organic compound content of less than about 450 g/l.

2. The protective coating of claim 1, wherein the one or more hydrofluoroolefin monomer(s) are selected from hydrofluoropropenes.

3. The protective coating of claim 1, wherein the one or more hydrofluoroolefin monomer(s) are selected from 2,3,3,3-tetrafluoropropene, 1,3,3,3-tetrafluoropropene, and combinations thereof.

4. The protective coating of claim 1, wherein the one or more hydrofluoroolefin monomer(s) are selected from trans-1,3,3,3-tetrafluoropropene.

5. The protective coating of claim 1, wherein the vinyl ester has the formula CH.sub.2═CR.sup.1—O(C═O).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.

6. The protective coating of claim 1, wherein the vinyl ether comprises a vinyl ether of the formula CH.sub.2═CR.sup.3—OR.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.

7. The protective coating of claim 1, wherein the radical scavenger is a hindered amine radical scavenger.

8. A protective coating composition having enhanced gloss retention properties comprising: (i) a fluorocopolymer comprising the copolymerization product of: (1) from about 40 mol % to about 60 mol % of hydrofluoroolefin monomer(s), selected from the group consisting of hydrofluoroethylenes, hydrofluoropropenes, hydrofluorobutenes and hydrofluoropentenes; (2) 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.2═CR.sup.1—O(C═O).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, wherein the vinyl ether has the formula CH.sub.2═CR.sup.3—OR.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 (3) from about 3 mol % to about 30 mol % of hydroxyalkyl vinyl ether represented by formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, wherein R.sup.3 is a hydrogen or a methyl group, and R.sup.5 is selected from the group consisting of an C2 to C12 unsubstituted straight-chain, branched-chain or alicyclic alkyl group, wherein the mol % are based on the total of the monomers in the copolymer; (ii) a carrier comprising one or more volatile organic compounds; and (iii) a stabilizing agent comprising a) a radical scavenger; and b) an absorber of UV light; wherein the coating composition comprises not greater than about 30% by weight of said carrier, and wherein said coating composition has a volatile organic compound content of less than about 450 g/l.

9. The protective coating of claim 8, comprising from about 45 mol % to about 55 mol % of hydrofluoroolefin monomers.

10. The protective coating of claim 8, wherein the one or more hydrofluoroolefin monomer(s) are selected from hydrofluoropropenes.

11. The protective coating of claim 8, wherein the one or more hydrofluoroolefin monomer(s) are selected from 2,3,3,3-tetrafluoropropene, 1,3,3,3-tetrafluoropropene, and combinations thereof.

12. The protective coating of claim 8, wherein the one or more hydrofluoroolefin monomer(s) are selected from trans-1,3,3,3-tetrafluoropropene.

13. The protective coating of claim 8, comprising about 10 mol % to about 40 mol % of vinyl ester, vinyl ether or a mixture thereof.

14. The protective coating of claim 8, comprising about 20 mol % to about 40 mol % of vinyl ester, vinyl ether or a mixture thereof.

15. The protective coating of claim 8, comprising from about 3 mol % to about 20 mol % of hydroxyalkyl vinyl ether.

16. The protective coating of claim 8, comprising from about 3 mol % to about 10 mol % of hydroxyalkyl vinyl ether.

17. A protective coating composition having enhanced gloss retention properties comprising: (i) a fluorocopolymer comprising the copolymerization product of: (1) first monomer consisting essentially of about 40 mol % to about 60 mol % trans-HFO-1234ze, (2) second monomer(s) comprising: A) from about 5 mol % to about 45 mol % vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is hydrogen, and wherein R.sup.2 is an unsubstituted branched-chain alkyl group having 6 to 8 carbon atoms, wherein said alkyl group includes at least one quaternary carbon atom; and B) from about 10 mol % to about 40 mol % vinyl ether monomer(s) represented by formula CH.sub.2═CR.sup.3—O—R.sup.4, wherein R.sup.3 is hydrogen and R.sup.4 is selected from the group consisting of a substituted or unsubstituted branched-chain alkyl group having 1 to 3 carbon atoms; and (3) from about 3 mol % to about 30 mol % of third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, where R.sup.3 is hydrogen, and R.sup.5 is a C4 unsubstituted straight-chain alkyl group, wherein the amount of said third monomer is preferably; and (ii) a carrier comprising at least about 50% by weight of a C2-C5 alkyl acetate; and (iii) a stabilizing agent comprising: a) a radical scavenger selected from the group consisting of bis(1,2,2,6,6-pentamethyl-4-piperidinyl)-sebacate; 1-(methyl)-8-(1,2,2,6,6-pentamethyl-4-piperidinyl)-sebacate; bis (1-octyloxy-2,2,6-tetramethyl-4-piperidyl) sebacate and combinations of these; and b) an absorber of UV light comprising at least one compounds selected from the group of consisting of beta-[3-(2-H-benzotriazole-2-yl)-4-hydroxy-5-tert-butylphenyl]-propionic acid poly(ethylene glycol) 300-ester; bis{b-[3-(2-H-benzotriazole-2-yl)-4-hydroxy-5-tert-butylphenyl]-propionic acid}-poly(ethylene glycol) 300-ester; and the combination of these; wherein the coating composition comprises not greater than about 30% by weight of said carrier, and wherein said coating composition has a volatile organic compound content of less than about 450 g/1.

18. The protective coating composition of claim 17 wherein the at least one fluorocopolymer has a number average molecular weight of from 10,000 to 50,000.

19. The protective coating composition of claim 1 wherein the at least one fluorocopolymer has a number average molecular weight of from 10,000 to 50,000.

20. The protective coating composition of claim 8 wherein the at least one fluorocopolymer has a number average molecular weight of from 10,000 to 50,000 and wherein said coating composition has a volatile organic compound content of from about 100 g/l to about 450 g/l.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows the gloss retention of the coating films.

DETAILED DESCRIPTION OF THE INVENTION

(2) 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) color retention and gloss retention.

(3) 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 to 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 23±2° C. If a solvent is used for the measurements, it is butyl acetate.

(4) 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 23±2° C. and a color change after about 1000 hours, of not greater than 2.0, more preferably not greater than about 1.5, and even more preferably not greater than about 1.2, as measured in comparison to the initial color, each as measured by ASTM D 7251, QUV-A; and 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/l.

(5) The QUV-A is measured as indicated above 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 (UVA-313) have a normal output of 0.67 W/m.sup.2 @ 310 nm 0.67 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 QUA-B refers to tests using the B lamps. The procedure is accomplished using the following steps: 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.” 2. Place the test plate containing the coating in the panel holder in the cabinet and power the cabinet on. 3. Set the PROGRAM button in the control panel and select the desired program operation. 4. Engage the RUN button to start test. 5. Record down the exposure time indicated on the led panel 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. 7. Determine Gloss retention using the formula Gloss Retention=B/A

(6) 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.

(7) Monomers

(8) Hydrofluoroolefins

(9) 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.2═CX.sup.3X.sup.4; wherein X′, 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:

(10) CH.sub.2═CHF,

(11) CHF═CHF,

(12) CH.sub.2═CF.sub.2, and

(13) CHF═CF.sub.2.

(14) The hydrofluoroolefin monomers according to certain preferred aspects of the methods of the present invention include, and preferably consists essentially of or consist of hydrofluoropropene having the formula CX.sup.5X.sup.6═CX.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. Examples of hydrofluoro-propene monomers include, among others:

(15) CH.sub.2═CFCF.sub.3 (HFO-1234y1),

(16) trans-CHF═CHCF.sub.3 (trans-HFO-1234ze),

(17) CHCl═CFCF.sub.3 and

(18) CH.sub.2═CHCF.sub.3.

(19) In preferred embodiments, the hydrofluoroolefin comprises, consists essentially of or consist of HFO-1234yf and/or HFO-1234ze. In preferred embodiments, the hydrofluoroolefin comprises, consists essentially of or consist of HFO-1234ze, with said HFO-1234ze preferably comprising, consisting essentially of or consisting of trans-HFO-1234ze.

(20) 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.12═C.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 another is a fluorine atom. Examples of hydrofluorobutene include, among others, CF.sub.3CH═CHCF.sub.3.

(21) Vinyl Esters

(22) 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.2═CR.sup.1—O(C═O) xR.sup.2, wherein x is 1 and wherein IV 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 is compound which includes at least one quaternary carbon according to the following formula:

(23) ##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.

(24) 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 carbocylic 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.

(25) Vinyl Ethers

(26) 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.2═CR.sup.3—OR.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, 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.

(27) 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.

(28) Hydroxy Vinyl Ethers

(29) 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 represented by formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, where R.sup.3 is as defined above, preferably hydrogen, and where R.sup.5 is selected from the group consisting of an C2 to C6 substituted or unsubstituted, preferably unsubstituted, straight-chain or branched-chain, preferably 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.

(30) In preferred embodiments, the co-monomers according to the fluorocopolymer formation step (b)(i) comprise, and preferably consist essentially of:

(31) (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 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 %,

(32) (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O) 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 B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—OR.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

(33) (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, where R.sup.3 is methyl or hydrogen, preferably hydrogen, and R.sup.5 is selected from the group consisting of an C3 to C5, preferably C4, unsubstituted straight-chain alkyl group, wherein the amount of said third monomer is preferably present in an amount of from about 3 mol % to about 30 mol %.

(34) Stabilizing Agent

(35) As described above, the protective coating compositions of the present invention preferably comprise a light stabilizer comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers; and b) an absorber of UV light. Applicants have found, as demonstrated by the Examples hereinafter, that the combination of these types of stabilizing agents produces unexpected advantages when used in coating formulations of the present invention.

(36) With respect to the radical scavenger, it is contemplated that a variety of such compounds can be used effectively in view of the teachings contained herein. However, it is preferred that the radical scavenger comprises, consists essentially of, or consist of hinder amine compounds. Examples of such hindered amine radical scavengers include: bis(1,2,2,6,6-pentamethyl-4-piperidinyl)-sebacate; 1-(methyl)-8-(1,2,2,6,6-pentamethyl-4-piperidinyl)-sebacate; bis (1-octyloxy-2,2,6-tetramethyl-4-piperidyl) sebacate and combinations of these. An example of a preferred combination of bis(1,2,2,6,6-pentamethyl-4-piperidinyl)-sebacate and 1-(methyl)-8-(1,2,2,6,6-pentamethyl-4-piperidinyl)-sebacate is available from Ciba Chemicals under the trademark TNUVIN 292. An example of the preferred bis (1-octyloxy-2,2,6-tetramethyl-4-piperidyl) sebacate is available from the Ciba Chemicals Division of BASF under the trademark TNUVIN 123.

(37) With respect to the UV absorber, it is contemplated that a variety of such compounds can be used effectively in view of the teachings contained herein. However, it is preferred that the UV absorber comprises, consists essentially of, or consists of one or more UV absorbers of the hydroxyphenylbenzotriazole class. In certain preferred embodiments, the UV absorber comprises: beta-[3-(2-H-benzotriazole-2-yl)-4-hydroxy-5-tert-butylphenyl]-propionic acid poly(ethylene glycol) 300-ester; bis{b-[3-(2-H-benzotriazole-2-yl)-4-hydroxy-5-tert-butylphenyl]-propionic acid}-poly(ethylene glycol) 300-ester; and the combination of these. An examples of a UV absorber that is a combination of beta-[3-(2-H-benzotriazole-2-yl)-4-hydroxy-5-tert-butylphenyl]-propionic acid poly(ethylene glycol) 300-ester and bis{beta-[3-(2-H-benzotriazole-2-yl)-4-hydroxy-5-tert-butylphenyl]-propionic acid}-poly(ethylene glycol) 300-ester is sold under the trade designation TINUVIN 1130 by Ciba Chemicals division of BASF.

(38) CoPolymer Formation Methods

(39) 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 broad scope of the present invention.

(40) 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.

(41) 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.

(42) 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.

(43) In preferred embodiments, the copolymer as formed 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 is 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 10000, 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.

(44) In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: (i) providing one or more fluorocopolymers by copolymerization of (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 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 %, (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).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 substituted or unsubstituted, branched or unbranched, 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 B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—O—R.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 (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, 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 third monomer is preferably from about 3 mol % to about 30 mol %; and (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 (iii) providing a stabilizing agent comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers; and b) an absorber of UV light; and (iv) combining said one or more fluorocopolymers with said carrier and said light stabilizer 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 and 50,000, more preferably from about 7000 to about 15,000 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 as 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.

(45) In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: (i) providing one or more fluorocopolymers by copolymerization of (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 %, (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).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 B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—O—R.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 (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, 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 third monomer is preferably from about 3 mol % to about 30 mol %; and (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; (iii) providing a stabilizing agent comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers; and b) an absorber of UV light; and (iv) 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.

(46) In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of:

(47) (i) providing one or more fluorocopolymers by copolymerization of (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 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 %, (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is 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 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 B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—O—R.sup.4, wherein R.sup.3 is a 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, 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 (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, where R.sup.3 is methyl or hydrogen, preferably hydrogen, and R.sup.5 is selected from the group consisting of an 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 third monomer is preferably from about 3 mol % to about 30 mol %; and (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; (iii) providing a stabilizing agent comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers; and b) an absorber of UV light; and (iv) 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.

(48) In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: (i) providing one or more fluorocopolymers by copolymerization of (1) first monomer consisting essentially 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 %, (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).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 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 B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—O—R.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 (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, 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 third monomer is preferably from about 3 mol % to about 30 mol %; and (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 (iii) providing a stabilizing agent comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers; and b) an absorber of UV light; and (iv) combining said one or more fluorocopolymers with said carrier and said light stabilizer 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.

(49) In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: (i) providing one or more fluorocopolymers by copolymerization of (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 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 %, (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is a methyl group, 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 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 B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—O—R.sup.4, wherein R.sup.3 is a methyl group, 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 (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, 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 third monomer is preferably from about 3 mol % to about 30 mol %; and (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 (iii) providing a stabilizing agent comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers; and b) an absorber of UV light; and (iv) combining said one or more fluorocopolymers with said carrier and said light stabilizer 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.

(50) In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: (i) providing one or more fluorocopolymers by copolymerization of (1) first monomer consisting essentially 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 %, (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).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 B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—O—R.sup.4, wherein R.sup.3 is a methyl group and wherein R.sup.4 is selected from 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 (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, where R.sup.3 is either hydrogen or a methyl group, 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 third monomer is preferably from about 3 mol % to about 30 mol %; and (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 (iii) providing a stabilizing agent comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers; and b) an absorber of UV light; and (iv) combining said one or more fluorocopolymers with said carrier and said light stabilizer 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.

(51) In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: (i) providing one or more fluorocopolymers by copolymerization of (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 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 %, (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is a methyl group, 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 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 B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—O—R.sup.4, wherein R.sup.3 is a methyl group 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 (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, 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 third monomer is preferably from about 3 mol % to about 30 mol %; and (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 (iii) providing a stabilizing agent comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers; and b) an absorber of UV light; and (iv) combining said one or more fluorocopolymers with said carrier and said light stabilizer 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.

(52) In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: (i) providing one or more fluorocopolymers by copolymerization of (1) first monomer consisting essentially 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 %, (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is hydrogen, and wherein R.sup.2 is an unsubstituted branched-chain alkyl group having 6 to 8 carbon atoms including 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 %, more preferably from about 10 mol % to about 30 mol %, and even more preferably from about 10 mol % to about 20 mol %; and B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—O—R.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 branched-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 (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, where R.sup.3 is either hydrogen or a methyl group 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 %; and (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 (iii) providing a stabilizing agent comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers; and b) an absorber of UV light; and (iv) combining said one or more fluorocopolymers with said carrier and said light stabilizer 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.

(53) In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: (i) providing one or more fluorocopolymers by copolymerization of (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 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 %, (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is a methyl group, 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 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 B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—O—R.sup.4, wherein R.sup.3 is a methyl group, 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 (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, where R.sup.3 is methyl, and R.sup.5 is selected from the group consisting of an 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 %; and (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 (iii) providing a stabilizing agent comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers; and b) an absorber of UV light; and (iv) combining said one or more fluorocopolymers with said carrier and said light stabilizer 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.

(54) In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: (i) providing one or more fluorocopolymers by copolymerization of (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 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 %, (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is 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 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 B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—O—R.sup.4, wherein R.sup.3 is 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 (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, where R.sup.3 is hydrogen or methyl, 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 %; and (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 (iii) providing a stabilizing agent comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers; and b) an absorber of UV light; and (iv) combining said one or more fluorocopolymers with said carrier and said light stabilizer 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.

(55) In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: (i) providing one or more fluorocopolymers by copolymerization of (1) first monomer consisting essentially of trans-HFO-1234ze, preferably 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 %, (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is hydrogen or methyl, 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 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 B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—O—R.sup.4, wherein R.sup.3 is hydrogen or methyl, preferably hydrogen, and wherein R.sup.4 is straight chain alkyl group having 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 (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, where R.sup.3 is hydrogen or methyl, preferably hydrogen, and R5 is selected from the group consisting of an 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 %; and (ii) providing a carrier for said one or more fluorocopolymers, said carrier comprising at least about 50% by weight of C2-C5 alkyl acetate and even more preferably butyl acetate; and (iii) providing a stabilizing agent comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers, said hindered amine being selected from the group consisting of bis(1,2,2,6,6-pentamethyl-4-piperidinyl)-sebacate; 1-(methyl)-8-(1,2,2,6,6-pentamethyl-4-piperidinyl)-sebacate; bis (1-octyloxy-2,2,6-tetramethyl-4-piperidyl) sebacate and combinations of these; and b) an absorber of UV light comprising one or more compounds of hydroxyphenylbenzotriazole class. In certain preferred embodiments, the UV absorber comprises: beta-[3-(2-H-benzotriazole-2-yl)-4-hydroxy-5-tert-butylphenyl]-propionic acid poly(ethylene glycol) 300-ester; bis{b-[3-(2-H-benzotriazole-2-yl)-4-hydroxy-5-tert-butylphenyl]-propionic acid}-poly(ethylene glycol) 300-ester; and the combination of these; and (iv) combining said one or more fluorocopolymers with said carrier and said light stabilizer 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.

(56) In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: (i) providing one or more fluorocopolymers by copolymerization of (1) first monomer consisting essentially of trans-HFO-1234ze, preferably 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 %, (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is hydrogen or methyl, 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 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 B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—O—R.sup.4, wherein R.sup.3 is hydrogen or methyl, preferably hydrogen, and wherein R.sup.4 is straight chain alkyl group having 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 (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, where R.sup.3 is hydrogen or methyl, preferably hydrogen, and R.sup.5 is selected from the group consisting of an 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 %; and (ii) providing a carrier for said one or more fluorocopolymers, said carrier comprising at least about 50% by weight of C2-C5 alkyl acetate and even more preferably butyl acetate; and (iii) providing a stabilizing agent comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers, said hindered amine being selected from the group consisting of bis(1,2,2,6,6-pentamethyl-4-piperidinyl)-sebacate; 1-(methyl)-8-(1,2,2,6,6-pentamethyl-4-piperidinyl)-sebacate; bis (1-octyloxy-2,2,6-tetramethyl-4-piperidyl) sebacate and combinations of these; and b) an absorber of UV light comprising at least one compounds selected from the group of consisting of beta-[3-(2-H-benzotriazole-2-yl)-4-hydroxy-5-tert-butylphenyl]-propionic acid poly(ethylene glycol) 300-ester; bis{b-[3-(2-H-benzotriazole-2-yl)-4-hydroxy-5-tert-butylphenyl]-propionic acid}-poly(ethylene glycol) 300-ester; and the combination of these; and (iv) combining said one or more fluorocopolymers with said carrier and said light stabilizer 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.

(57) In preferred embodiments, the formation of fluorocopolymer coating compositions comprises, and preferably consists essentially of: (i) providing one or more fluorocopolymers by copolymerization of (1) first monomer consisting essentially of trans-HFO-1234ze, preferably 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 %, (2) second monomer(s) comprising: A) vinyl ester monomer represented by formula CH.sub.2═CR.sup.1—O(C═O).sub.xR.sup.2 wherein x is 1 and wherein R.sup.1 is 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 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 B) vinyl ether monomer(s), represented by formula CH.sub.2═CR.sup.3—O—R.sup.4, wherein R.sup.3 is hydrogen and R.sup.4 is selected from the group consisting of a substituted or unsubstituted branched-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 (3) third monomer(s) consisting of hydroxyalkyl vinyl ether represented by the formula CH.sub.2═CR.sup.3—O—R.sup.5—OH, where R.sup.3 is hydrogen, and R.sup.5 is a C4 unsubstituted straight-chain alkyl group, wherein the amount of said third monomer is preferably from about 3 mol % to about 30 mol %; and (ii) providing a carrier for said one or more fluorocopolymers, said carrier comprising at least about 50% by weight of C2-C5 alkyl acetate and even more preferably butyl acetate; and (iii) providing a stabilizing agent comprising: a) a radical scavenger, preferable a hindered amine capable of scavenging one or more of the radical intermediates produced in the photooxidation of said fluorocopolymers, said hindered amine being selected from the group consisting of bis(1,2,2,6,6-pentamethyl-4-piperidinyl)-sebacate; 1-(methyl)-8-(1,2,2,6,6-pentamethyl-4-piperidinyl)-sebacate; bis (1-octyloxy-2,2,6-tetramethyl-4-piperidyl) sebacate and combinations of these; and b) an absorber of UV light comprising at least one compounds selected from the group of consisting of beta-[3-(2-H-benzotriazole-2-yl)-4-hydroxy-5-tert-butylphenyl]-propionic acid poly(ethylene glycol) 300-ester; bis{b-[3-(2-H-benzotriazole-2-yl)-4-hydroxy-5-tert-butylphenyl]-propionic acid}-poly(ethylene glycol) 300-ester; and the combination of these; and (iv) combining said one or more fluorocopolymers with said carrier and said light stabilizer 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.

(58) According to preferred embodiments, the fluorocopolymer composition of the present invention, and in particular the fluorocopolymer formed as described in the preceding paragraphs [0049]-[0060], 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 and 50,000, more preferably from about 7000 to about 15,000 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 as 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.

(59) Coating Composition Formation Methods

(60) 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.

(61) 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% go 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 anyone of known methods, in preferred embodiment 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 μm.

EXAMPLES

(62) The present invention is further illustrated by the following non-limiting examples.

Example 1

(63) Fluoropolymer Preparation

(64) A solution polymerization operation is carried out by charging into a 5500 ml stainless steel autoclave equipped with a stirrer the components as indicated in the following Table 1A:

(65) TABLE-US-00001 TABLE lA TYPE COMPONENT NAME Weight, grams Solvent butyl acetate 61.4 Solvent methanol 30 First Monomer trans-1,3,3,3- 253 (fluoropolynner) tetrafluoropropene (trans-HFO-1234ze) Second VEOVA-10 157.3 Monomer (vinyl ester) Third Monomer ethyl vinyl ether 57.5 (vinyl ether) Third Monomer hydroxybutylvinyl 72 (alkylhydroxy ether ether) Initiator tertbutylperoxypivalate 6.5

(66) 61.4 g of butyl acetate, 57.5 g of ethyl vinyl ether, 157.3 g of VEOVA-10 (Momentive product), 72.0 g of hydroxyl butyl vinyl ether, 6.0 g zinc oxide were charged into a 1 L stainless steel autoclave equipped with a stirrer. The mixture was solidified with liquid nitrogen, and then the dissolved air was removed in vacuum. Then, 253.0 g of trans-HFO-1234ze was added into the autoclave. The mixture was gradually heated to 57° C. in the autoclave, and 1.5 g of tert-butyl peroxypivalate was charged into the autoclave and then the other 5 g of tert-butyl peroxypivalate was continuously fed into the autoclave within 24 hours with a constant flow velocity. When all the -butyl peroxypivalate (totally 6.5 g) have been fed into the autoclave, 30 g of methanol was added into the autoclave and the autoclave temperature was kept at 57° C. for 2 hrs. Then the autoclave was cooled to room temperature, the unreacted monomers were purged and the autoclave was opened. A crude copolymer solution was obtained.

(67) Post-Treatment of Crude Copolymer Solution

(68) Butyl acetate is added as a thinner into the crude copolymer solution according to the procedure described above to obtain a solution with a solid content of 30 wt % to about 40 wt %. The diluted solution is charged into a glass flask, and agitation at 250 rpm is initiated under vacuum on the flask until the vacuum reach about 100 Pa, with the temperature of the copolymer solution being maintained at 18±1° C. Distilled solution is collected in the cold trap and monitored by GC-MS until no unreacted monomers, including 1234ze, ethyl vinyl ether or methanol were detected. The vacuum pump, agitation and temperature controller are then stopped. Then ZnO was removed off by filtration. A transparent and colorless copolymer solution was obtained.

(69) Generally, the post-treatment of the solution will include heating the solution (e.g., 87° C.) for an extended period of time (e.g., 1 day), and as a result of such post-treatment residual initiator in the solution will become decomposed and some HF acid will tend to be formed. In order to counteract potential negative effects of the presence of the HF and other unwanted contaminants that may be present, we have added Al.sub.2O.sub.3 molecular sieve A2O2-HF, a UOP product (8.0 wt % of the total polymer weight) or molecular sieve P188, a UOP product (2.0 wt % of the total polymer weight) or Al.sub.2O.sub.3 powder (7% wt) into the clear copolymer solution and then conduct the post-treatment by heating the solution to 87±2° C. for 14-18 h with 250 rpm agitation. Then agitation was discontinued and the contents were cooled to room temperature, after which the Al.sub.2O.sub.3 molecular sieve was removed off by filtration. A clear solution was obtained, and then the solution was condensed to 50-80 wt % solid content having a yield of 90%, hydroxyl value=65 mg KOH/g, Mn=11453, Mw/Mn=2.5, F content=31.0 wt %.

(70) Standard Coating Formulation and Procedure

(71) TABLE-US-00002 Pigment Paste (Parts by Weight) white grey grey grey grey grey grey 1 1 2 3 4 5 6 Fluoro- FPVE 33.6 36.2 36.2 36.2 36.2 36.2 36.2 polymer (80% wt) Pigment 1 Ti-Pure 47.9 34 34 34 34 34 34 R-960{circle around (1)} Pigment 2 FW 200{circle around (2)} 0 5.5 5.5 5.5 5.5 5.5 5.5 Dispersant Solsperse 3 5.5 5.5 5.5 5.5 5.5 5.5 32500{circle around (3)} Solvent Butyl 15.5 18.8 18.8 18.8 18.8 18.8 18.8 acetate Total 100 100 100 100 100 100 100 {circle around (1)}DuPont {circle around (2)}Evonik {circle around (3)}Lubrizol
Let Down Formulation (Parts by Weight)

(72) TABLE-US-00003 white grey grey grey grey grey grey 1 1 2 3 4 5 6 Pigment As Above 73 55 55 55 55 55 55 Paste Fluoro- FPVE 19.3 29.6 29.6 29.6 29.6 29.6 29.6 polymer (80% wt) Light Tinuvin 0 0 2 0 0 0.7 stabilizers 292{circle around (4)} Tinuvin 0 0 0 2 0 0.7 123 Tinuvin 0 0 0 0 2 1.3 1.3 1130 Solvent Butyl 6.7 14.4 12.4 12.4 12.4 12.4 12.4 acetate Catalyst 50 ppm 1 1 1 1 1 1 1 DBTDL{circle around (5)} (Butyl acetate) Total 100 100 100 100 100 100 100 Basf {circle around (5)}DBTDL = Dibutyltin dilaurate
Coating Formulation

(73) TABLE-US-00004 white grey grey grey grey grey grey 1 1 2 3 4 5 6 Main Pack As Above 100 100 100 100 100 100 100 (Let Down Formulation) Solvent Butyl 5 15 15 15 15 15 15 acetate Hardener Desmodur 8.0 9.1 9.1 9.1 9.1 9.1 9.1 N339{circle around (6)} Bayer
Detailed Procedure
Pigment Paste Preparation

(74) In the lab, high-speed dispersion machine is used to reduce the pigment size and disperse the FPVE resin, the pigment and the dispersant throughout the mixture with glass beads. The dispersing condition is typically about 3000 RPM and continues several hours until the composition fineness is less than 20 μm. The dispersing time can be varied to accommodate the type of pigments used. For example, for sample White 1 (white color coating formulation), it takes about 2 hours to disperse, while for samples Grey 2-6 (grey color coating), and it takes about 3 hours to disperse. The mixture is then filtered to remove the glass beads.

(75) Let Down

(76) The paste is as produced above is then thinned to produce “Let Down” formulation by adding FPVE resin, solvent, and additives such as stabilizers as indicated above, and then the components are mixed by high-speed dispersion machine at 1500 RPM for 30 minute.

(77) Coating Formulation Preparation

(78) FPVE resin has hydroxyl group which can be cured with isocyanate compounds. In order to prepare the final coating formulation (see samples 1-6 above), Desmodur N3390 is chosen as curing agent and added to the Let Down formulation as indicated in the table above. The final coating formulation is prepared by mix all the components identified above by high-speed dispersion machine at 1500 RPM for 30 minute.

(79) Characteristics of Coating Formulation

(80) TABLE-US-00005 white 1 grey 1 grey 2 grey 3 grey 4 grey 5 grey 6 Solid content 68% 54% 54% 54% 54% 54% 54% Specific Gravity (at 1.24 1.18 1.18 1.18 1.18 1.18 1.18 25degC) Viscosity (Ford Cup 38 (sec) 47 (sec) 47 (sec) 47 (sec) 47 (sec) 47 (sec) 47 (sec) No. 4)

(81) In order to form a 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 applied, and 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. The outermost cured coating film layer usually has a layer thickness of 20-30 μm.

(82) After coated on the substrate, the film will be kept in the room temperature in 1 week to make sure completely cured. After that, it can be tested for mechanical properties and weather resistance, etc.

(83) Coating Mechanical Properties

(84) TABLE-US-00006 Cure Conditions: 1 week at 25 deg. C; Substrate: Tin Panels white 1 grey 1 grey 2 grey 3 grey 4 grey 5 grey 6 Film Thickness 35 35 34 35 34 36 35 (micrometer) Gloss (20 deg./60 deg.) 60/75 61/76 60/76 59/76 60/76 60/76 60/76 ISO 2813 Hardness (scratch H hardness) ASTM D3363 Flexibility ASTM D4145 1T Bend Adhesion (Cross-cut 5B Tape Test) ASTM D3359
Weathering of FPVE-P220

(85) FIG. 1 shows the gloss retention of the coating films. (QUV-B, 1,500 hours) UV/Condensation Cabinet Cycle: 24 hours UV at 60° C.

(86) Comparing to commercial available alternatives, based on same solid content, the viscosity of FPVE is much lower than competitor's; based on same viscosity; the solid content of FPVE is about 9-10% higher than competitor's. With the low viscosity benefit of FPVE, customer can make a coating formulation with VOC (volatile Organic Compound) level below 420 g/l, which is the threshold of VOC tax, in another words, customers do not need to pay VOC tax by using FPVE polymer in their formulation, while they cannot get the same benefit by using commercial available alternatives.