CA2234425C - Acrylic fluorocarbon polymer containing coatings - Google Patents

Acrylic fluorocarbon polymer containing coatings Download PDF

Info

Publication number
CA2234425C
CA2234425C CA002234425A CA2234425A CA2234425C CA 2234425 C CA2234425 C CA 2234425C CA 002234425 A CA002234425 A CA 002234425A CA 2234425 A CA2234425 A CA 2234425A CA 2234425 C CA2234425 C CA 2234425C
Authority
CA
Canada
Prior art keywords
weight
carbon atoms
alkyl
group
acrylic polymer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CA002234425A
Other languages
French (fr)
Other versions
CA2234425A1 (en
Inventor
Douglas Robert Anton
Michael J. Darmon
William Frank Graham
Richard Ronald Thomas
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of CA2234425A1 publication Critical patent/CA2234425A1/en
Application granted granted Critical
Publication of CA2234425C publication Critical patent/CA2234425C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/62Polymers of compounds having carbon-to-carbon double bonds
    • C08G18/6287Polymers of sulfur containing compounds having carbon-to-carbon double bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/62Polymers of compounds having carbon-to-carbon double bonds
    • C08G18/6275Polymers of halogen containing compounds having carbon-to-carbon double bonds; halogenated polymers of compounds having carbon-to-carbon double bonds
    • C08G18/6279Polymers of halogen containing compounds having carbon-to-carbon double bonds; halogenated polymers of compounds having carbon-to-carbon double bonds containing fluorine atoms

Abstract

A clear coating composition containing about 45-80 % by weight of a binder a nd 20-55 % by weight of an organic liquid; wherein the binder contains (A) about 40-90 % by weight, based on the weight of the binder, of an acrylic polymer containing polymerized hydroxyl containing monomers of the following group of hydroxy alkyl acrylate or methacrylates having 1-4 carbon atoms in the alkyl group, and polymerized alkyl acrylates and methacrylates having 1-18 carbon atoms in th e alkyl groups, or styrene or any mixtures of the above and 0.1 - 5.0 % by weight, based on the weight of the acrylic polymer, of polymerized fluoroalkyl containing monomer represented by formula (I), where R is hydrogen or an alkyl group having 1-2 carbon atoms, n is an integer of 1-11 and R f is a fluoroalkyl containing group having at least 4 carbon atoms and (B) about 10-60 % by weight, based on the weight of the binder, of an organic polyisocyanate cross-linking agent; and where a cured layer of the coating composition has a combination of a water advancing contact angle of at least 100.degree. and a hexadecane contact angle of at least 40.degree.. A process for making the acrylic fluorocarbon polymer and articles coated with the composition also are part of this invention.

Description

TITLE
ACRYLIC FLUOROCARBON POLYMER CONTAINING COATINGS
s BACKGROUND OF THE INVENTION
1. Field of the Invention i o This invention is directed to acrylic fluorocarbon polymer containing coatings that remain relatively clean under exterior use conditions and are easily cleaned for example by washing with water when soiled.
2. Description of the Prior Art i s Acrylic fluorocarbon polymer containing coating compositions that contain relatively small amounts of fluorocarbon having resistance to cratering are shown in Chang US Patent 4,371,657 issued February 1, 1983 and Chang US Patent 4,396,680 issued August 2, 1983.
Coating compositions of blends of acrylic polymers and acrylic polymer 2 o containing fluorocarbons that form antiicing coatings are well known.
Clear coats containing acrylic polymers having small amounts of fluorocarbon constituents that are applied over metallic base coats to provide auto finishes that have good weatherability, have high water and oil repellency and stain resistance are shown in Sugimura et al US Patent 2s 4,812,337 issued March 14, 1989. There is a need for a coating composition that provides for soil resistance, is easily cleaned, has a low content of fluorocarbon constituents which reduces the cost of the composition since fluorocarbon monomers are expensive, and gives a coating that is high in solids that can be applied with conventional so equipment and cures to a hard tough durable and weatherable finish without baking at eleva.ed temperatures.
SUMMARY OF THE INVENTION
A clear coating composition containing 45-80% by weight of 3s a binder and 20-55% by weight of an organic liquid; wherein the binder contains (A) 40-90% by weight, based on the weight of the binder, of an acrylic polymer containing 20-45% by weight, based on the weight of~the acrylic~pu~ymer, of .
polymerized hydroxyl containing monomers selected from the following group of hydroxy alkyl acrylate or methacrylates having 1-4. carbon atoms in the alkyl group, 50-79.9% by s weight, based on the weight of the acrylic polymer, of polymerized alkyl acrylates and methacrylates having 1-18 carbon atoms in the alkyl groups, or styrene or any mixtures of the above and 0.1 - 5.0% by weight, based on the weight of the acrylic polymer, of polymerized fluoroalkyl containing i o monomer represented by the formula O
C HZ=C R-~- O- ( C H2) ~-Rt where R is hydrogen or an alkyl group having 1-2 carbon atoms, n is an integer of 1-11 and R f is a fluoroalkyl containing group having at least 4 carbon atoms and the i5 acrylic polymer has a weight average molegular weight of 2,000-20,000 determined by gel permeation chromatography and (B) 10-60% by weight, based on the weight of the binder, of a o an organic polyisocyanate crosslinking agent; and where a cured layer of the coating composition has a combination of a water advancing contact angle of at least 100° and a hexadecane advancing contact angle of at least 40°.
A process for making the acrylic fluorocarbon polymer and 25 articles coated with the composition also are part of this invention.
DETAILED DESCRIPTION OF THE INVENTION
The coating composition of this invention primarily is used a clear coat over a pigmented base coat containing solid color pigments or s o metallic flake pigments or mixtures thereof. The coating composition can be applied with conventional spray equipment and cured at ambient temperatures or slightly elevated temperatures which decrease drying time.
The resulting clear finish has excellent dirt, water and oil repellency, is easily cleaned by washing with water or a water surfactant mixture or can s5 readily be wiped clean and has good stain resistance and good weatherability.
A;~'dlDLO S~~ET

r CA 02234425 1998-04-08 ..
The coating composition is a~clear coating composition; i.e.
containing no pigments or a small amount of transparent pigment. The composition has a relatively high solids content of 45-80% by weight of binder and 20-55% by weight of an organic carrier which can be a solvent s for the binder or a mixture of solvents and non solvent which would form a non aqueous dispersion. The composition has a low VOC (volatile organic content) and meets current pollution regulations.
The coating composition when applied to a substrate and fully cured has a water advancing contact angle of at least 100°, preferably io 120° and a hexadecane advancing contact angle of at least 40°, preferably 45-85° and more preferably 60-85°.
Contact angles are measured by the Sessile Drop Method which is fully described in A.W. Adamson, The Physical Chemistry of Surfaces, 5 ~ Ed., Wiley & Sons, New York, 1990, Chapter II.
i5 Briefly, in the Sessile Drop Method, a drop of liquid, either water or solvent, is placed on a surface and the tangent is precisely determined at the point of contact between the drop and the surface. An advancing angle is determined by increasing the size of the drop of liquid and a receding angle is determined by decreasing the size of the drop of 20 liquid. Additional information on the equipment and procedure needed to measure these contact angles are more fully described in R.H. Dettre, R.E.
Johnson Jr., Wettability, Ed. by J.C. Berg, Marcel Dekker, New York, 1993, Chapter 1.
The relationship between water and organic liquid contact a5 angles and cleanability and dirt retention is described in chapters XII and XIB of A.W. Adamson, above. In general, the higher the contact angle the more dirt or soil resistant the surface is and the easier the surface is to clean.
The acrylic polymer used in the coating composition is 3 o prepared by conventional polymerization techniques in which the monomers, except the ffuoroalkyl containing monomer, solvent, and polymerization initiator are charged over a 1-24 hour period of time, preferably in a 2-8 hour time period, into a conventional polymerization reactor in which the constituents are heated to 60-175°C, preferably 35 170°C. At any a time during the polymerization such as the beginning, end or middle, the polymerizable fluoroalkyl containing monomer usually blended with a solvent can be added at one time period to ~~~Np~.O

the reactor. The fluoroalkyl containing monomei is added~:n 0.01 10% of the total time of polymerization. Preferably, the fluoroalkyl containing monomer is added after at least some of the other monomers have been added and polymerized at least to some extent. The polymer formed has a s weight average molecular weight of 2,000 - 20,000, preferably 5,000 -10,000.
Molecular weight is determined by gel permeation chromatography using polystyrene as the standard.
Typical polymerization initiators that are used in the process io are azo type initiators such as azo-bis-isobutyronitrile, 1,1'-azo-bis(cyanocyclohexane), peroxy acetates such as t-butyl peracetate, peroxides such as di-t-butyl peroxide, benzoates such as t-butyl perbenzoate, octoates such as t-butyl peroctoate and the like.
Typical solvents that can be used in the process are ketones i5 such as methyl amyl ketone, methyl isobutyl ketone, methyl ethyl ketone, aromatic hydrocarbons such as toluene, xylene, alkylene carbonates such as propylene carbonate, n-methyl pyrrolidone, ethers, esters, acetates and mixtures of any of the above.
Typical polymerizable monomers that are used to form the zo acrylic-poly'rner--are-alky~(rne~h)acrylates, mPar,in_galk_y1_ a_c_ryl_ates _and alkyl methacrylates, having 1-18 carbon atoms in the alkyl group such as methyl methacryiate, ethyl acrylate, ethyl methacrylate, propyl acrylate, propyl methacrylate, isopropyl methacrylate, butyl acrylate, isobutyl methacrylate, butyl methacrylate, t-butyl methacrylate, pentyl acrylate, pentyl 25 methacrylate, hexyl acrylate, hexyl methacrylate, octyl acrylate, octyl methacrylate, nonyl acrylate, nonyl methacrylate, decyl acrylate, decyl methacrylate, lauryl acrylate, lauryl methacrylate, stearyl acrylate, stearyl methacrylate; other useful monomers are styrene, alpha methyl styrene or any mixtures of these monomers, and hydroxy alkyl (meth)acrylates s o meaning hydroxy alkyl acrylates and hydroxy alkyl methacrylates having 1-4 carbon atoms in the alkyl groups such as hydroxy methyl acrylate, hydroxy methyl methacrylate, hydroxy ethyl acrylate, hydroxy ethyl methacrylate, hydroxy propyl methacrylate, hydroxy propyl acrylate, hydroxy butyl acrylate, hydroxy butyl methacrylate and the like, s s acrylamide, methacrylamide, acrylonitrile, and hydroxy methacrylamide.

~~cc~~~~ ~~~

._ ._ . .
. : .. a , , The fluoroalkyl containing monomers ate us.c~ in ambu.~ts of 0.1-5.0% by weight, based on the weight of the acrylic polymer. Useful fluorocarbon monomers are represented by the formula O
CHZ=CR-~-O-(CH2) n-Rf where R is hydrogen or an alkyl group having 1-2 carbon atoms, n is an integer of 1-18 and Rfis a fluoroalkyl containing group having at least 4 ,carbon atoms and preferably a straight chain or branched chain ffuoroallcyl group having 4-20 carbon atoms which optionally can contain an oxygen atom.
i o Typically useful ffuoroalkyl containing monomers are perffuoro methyl ethyl methacrylate, perfluoro ethyl ethyl methacrylate, perfluoro butyl ethyl methacrylate, perfluoro pentyl ethyl methacrylate, perfluoro hexyl ethyl methacrylate, perfluoro octyl ethyl methacrylate, perfluoro decyl ethyl methacrylate, perfluoro lauryl ethyl methacrylate, i5 perffuoro stearyl ethyl methacrylate, perfluoro methyl ethyl acrylate, perfluoro ethyl ethyl acrylate, perfluoro butyl ethyl acrylate, perftuoro pentyl ethyl acrylate, perffuoro hexyl ethyl acrylate, perfluoro octyl ethyl acrylate, perffuoro decyl ethyl acrylate, and perfluoro lauryl ethyl acrylate, perfluoro stearyl ethyl acrylate. Preferred are perffuoro alkyl ethyl a o methacrylates wherein the perfluoroalkyl group contains 4-20 carbon atoms.
Other useful fluoroalkyl containing monomers are represented by the formula where RZ O
R~-SOZ-N-(CH2) n-O-~-CR=CH2 25 R is as defined above, R1 is a ffuoroalkyl group having 4-12 carbon atoms, R2 is an alkyl group having 1-4 carbon atoms and n is an integer of 1-4.
Typical of these monomers are the following:

CgF~7SO2N(CH2)2 O-O-CH=CH2 1.: L
AN'.ESt"~ ~ ET

. w , /O ~~~

CgF~7$02(V(CH2)2-O-C-C=CH2 iZHS O
CgF~7SO2N(CH2)2-O ~-CH=CHZ
~O C H3 C$F~7SO2N(CHZ)2-O ~ C-CH2 to C$F17S02N(CHz)2-O O CH=CHZ
Preferred acrylic polymers which form high quality coatings contain polymerized monomers of an alkyl methacrylate having 2-6 carbon i5 atoms in the alkyl group, an alkyl acrylate having 2-8 carbon atoms in the alkyl group, a hydroxy alkyl acrylate having 2-4 carbon atoms in the alkyl group, styrene and perfluoroalkyl ethyl methacrylate having 4-20 carbon atoms in the alkyl group. One particularly preferred polymer contains butyl methacrylate, butyl acrylate, styrene, hydroxy propyl acrylate and the above a o perfluoroalkyl containing monomer.
Another preferred acrylic polymer contains polymerized monomers of an alkyl methacrylate having 2-6 carbon atoms in the alkyl group, an alkyl acrylate having 2-8 carbon atoms in the alkyl group, styrene, an alkylene glycol methacrylate and a perfluoro allcyl ethyl methacrylate z5 having 4-20 carbon atoms in the alkyl group. One particularly preferred polymer contains butyl methacrylate, butyl acrylate, hydroxy propyl acrylate, ethylene triglycol methacrylate and the above perfluoro alkyl ethyl methacrylate monomer.
The coating composition contains an organic polyisocyanate 3o crosslinking agent. Any of the conventional aromatic, aliphatic, cycloaliphatic isocyanates, trifunctional isocyanates and isocyanate functional adducts of polyols and diisocyanates can be used. Typically ~~~=ynr..,r~
,, useful diisocyanates are 1,6-hexamethylene diisocyanate, isophorone diisocyanate, 4,4'-biphenylene diisocyanate, toluene diisocyanate, bis cyclohexyl diisocyanate, tetramethylene xylene diisocyanate, ethyl ethylene diisocyanate, 2,3-dimethyl ethylene diisocyanate, 1-methyltrimethylene s diisocyanate, 1,3-cyclopentylene diisocyanate, 1,4-cyclohexylene diisocyanate, 1,3-phenylene diisocyanate, 1,5-naphthalene diisocyanate, bis-(4-isocyanatocyclohexyl)-methane, and 4,4'-diisocyanatodiphenyl ether.
Typical trifunctional isocyanates that can be used are triphenylmethane triisocyanate, 1,3,5-benzene triisocyanate, 2,4,5-toluene i o triisocyanate and the like. Oligomers of diisocyanates also can be used such as the trimer of hexamethylene diisocyanate which is sold under the tradename "Desmodur" N-3390TM
Isocyanate functional adducts can be used that are formed' from an organic polyisocyanate and a polyol. Any of the aforementioned i s polyisocyanates can be used with a polyol to form an adduct. Polyols such as trimethylol alkanes like trimethylol propane or ethane can be used. One useful adduct is the reaction product of tetramethylxylidine diisocyanate and trimethylol propane and is sold under the tradename "Cythane" 3160.
To improve weatherability of the clear coating composition 20 0.1-10% by weight, based on the weight of the binder , of ultraviolet light stabilizers, screeners, quenchers and antioxidants usually are added.
Typical ultraviolet light screeners and stabilizers include the following:
Benzophenones such as hydroxy dodecyl oxy benzophenone, 2,4-dihydroxy benzophenone, hydroxy benzophenones containing sulfonic 2s acid groups.
Benzoates such as dibenzoate of diphenylol propane, tertiary butyl benzoate of diphenylol propane.
Triazines such as 3,5-dialkyl-4-hydroxy phenyl derivatives of triazine, sulfur containing derivatives of dialkyl-4-hydroxy phenyl triazine, so hydroxy phenyl-1,3,5-triazine.
Triazoles such as 2-phenyl-4-(2,2'-dihydroxybenzoyl)-triazole, substituted benzotriazoles such as hydroxy-phenyltriazole.
Hindered amines such as bis(1,2,2,6,6 pentamethyl-4-piperidinyl sebacate), di[4(2,2,6,6,tetramethyl piperidinyl)] sebacate and 3 s any mixtures of any of the above.
y ." ..
The coating composition contains a ,suffic;ient~amoi:ni o~ a catalyst to cure the composition at ambient temperatures. Generally, 0.01-2% by weight, based on the weight of the binder, of catalyst is used.
Typically useful catalysts are triethylene diamine and allcyl tin laurates such s as dibutyl tin dilaurate, dibutyl tin diacetate, and tertiary amine.
Preferred is dibutyl tin dilaurate.
Generally, flow control agents are used in the composition in amounts of 0.1-5% by weight, based on the weight of the binder, such as polyacrylic acid, polyalkylacrylates, polyether modified dimethyl io polysiloxane copolymers and polyester modified polydimethyl siloxane.
When the coating composition is used as a clear coating composition usually over a pigmented base coat, it may be desirable to use pigments in the coating composition which have the same refractive index as the dried coating. Typically useful pigments have a particle size of i5 0.015-50 micrometers and are used in a pigment to binder weight ratio of 1:100 to 10:100 and are inorganic siliceous pigments such as silica pigment having a refractive index of 1.4-1.6.
When the coating composition is used as a clear coating on a vehicle such as a car, truck, bus, train, or on construction equipment, a o industrial equipment, structures such as tanks, bridges, exterior or interior of buildings, a basecoating which may be either a solvent based or waterbased composition is first applied and then dried to at least remove solvent or water before the clear coating is applied usually by conventional means such as spraying or electrostatic spraying. The clear coating is dried a s and cures at ambient temperatures but moderately high temperatures of up to 90°C can be used to shorten drying time.
The coating composition with its ease of cleaning and soil resistance is an excellent anti graffiti coating and can be applied as a clear over conventional coatings that are used for the exterior and interior of 3 o buildings, subways, buses, trains and for any other structure or vehicle where graffiti is a problem. The composition has good adhesion to a variety of substrates and special treatments or primers are not required.
The following examples illustrate the invention. All parts and percentages are on a weight basis unless otherwise specified. Molecular 3s weight was determined by gel permeation chromatography using polystyrene as the standard.
AM~f~f7LD S~tEFT

~3 ~' 3 EXAMPLE 1 ~ a An acrylic polymer I solution was prepared in which the acrylic polymer has fluoroalkyl groups by charging the following constituents into a reactor equipped with a heat source, a thermometer and a s stirrer:
Portion 1 Parts By Wei t Methyl amyl ketone 699.20 Portion 2 Butyl methacrylate monomer (BMA) 583.80 Styrene monomer (S) 307.28 Butyl acrylate monomer (BA) 343.20 Hydroxy propyl acrylate monomer (HPA) 783.60 Methyl amyl ketone 4.72 Portion 3 Fluoro alkyl ethyl methacrylate monomer (FAMA) - 30.73 (fluoroalkyl group containing C-4 4%, C-6 30%, C-8 30%, C-10 20%, C-12 10% C-14 and above 5%) Methyl amyl ketone 30.00 Portion 4 T-butyl peroxy acetate 69.01 Methyl amyl ketone 114.59 Portion 5 Methyl amyl ketone 33.28 Total 2999.99 Portion 1 was charged into the reaction vessel and blanketed with nitrogen and Portion 2 was premixed and added over a 360 minute period while holding the resulting mixture at its reflux temperature of 150°
C. Portion 3 was premixed and then added at one time to the reaction io mixture 350 minutes after the start of the addition of Portion 2. Portion 4 was premixed and added at the same time as Portion 2 to the reaction mixture over a 375 minute period and then Portion 5 was added and the reaction mixture was held at its reffux temperature for an additional 60 minutes. The resulting polymer solution was cooled to room temperature.
i5 The resulting acrylic polymer solution I had a weight solids content of 70%, a polymer of BMA/SBA/I~A/FAMA in the following percentages 28.5%/15.0%/16.75%/38.25%/1.5% and the polymer had a weight average molecular weight of 7,000.
AAAENL~G S;~iEET

A clear acn~lic coating composition I was prepared as follows:
Parts by Weieht Portion 1 Methyl 'ethyl ketone 2.54 Toluene 2.67 Dibasic acid ester (ester mixture of adipic 1.79 acid, glutaric acid and succinic acid) Butyl CellosoIve AcetateTM 4.96 Portion 2 Acrylic polymer I solution (prepared above) 72.79 Portion 3 Resiflow STM (Acrylic polymer flow additive)0.35 "Tinuvin" 328TM - 2-(2-hydroxy-3,5-ditertiary5,5g amyl phenol) -2H-benzotriazole) "Tinuvin" 292TM - (1,2,2,6,6-pentamethyl-4-piperidinyl)0.87 sebacate Dibutyl tin dilaurate 0.92 PM acetate 7.3 100.00 Total The constituents of Portion 1 were charged into a mixing vessel in the order shown with continuous mixing. Portion 2 was added and mixed for 15 minutes. The constituents of Portion 3 were charged into the mixing vessel in the order shown with constant mixing. The resulting composition had a solids content of 53.5%. A clear coating composition was prepared by mixing the above composition with a polyisocyanate solution in a 3/1 volume ratio. The polyisocyanate solution contains 90%
i o by weight of the trimer of hexamethylene diisocyanate and 10% by weight solvent of n-butyl acetate/Aromatic 100 solvent in a 1:1 ratio.
Two phosphated cold rolled steel panels that had been coated with a cured electrocoating composition of a polyepoxy hydroxy ether resin crosslinked with a polyisocyanate were spray coated with a white is basecoat coating composition of an acrylic polymer containing an organic polyisocyanate crosslinking agent to a dry film thickness of 18-23 micrometers. The basecoat was allowed to stand for 10 minutes to allow solvent to evaporate and then the above prepared clear acrylic coating . ~, . , . , , .
composition I was spray applied. Two coats were applied with a solvent " ' evaporation time of 2 minutes between the application of each coat. The resulting filin was dried at 83°C for 30 minutes. The dry filin thickness of the clear coat was 44-56 micrometers. The resulting clear coat was smooth s and essentially free of craters and had an excellent appearance.
A second set of two panels was prepared. Phosphated cold rolled steel panel electrocoated with the same above described electrocoating composition were coated with a black basecoat coating composition identical to the white basecoat coating composition except i o black pigmentation was used instead of white pigment and coated with the clear acrylic coating composition I as above and dried and cured as above.
The resulting clear coat was smooth and essentially free of craters and had an excellent appearance. The following properties of the clear coated panel were measured and the results are shown in Table I: 20° Gloss, is Distinctness of Image (DOI), Hardness measured in Knoops, Color L, a and b values , advancing and receding water contact angles and advancing and receding hexadecane solvent contact angles.
Acrylic polymer II solution was prepared which is identical to the above acrylic polymer I solution except that fluoroalkyl ethyl 2 o methacrylate monomer was not added. The molecular weight of the polymer and the solids of the solution were the same. A clear acrylic coating composition II was prepared as above using the same polyisocyanate crosslinking agent except that acrylic polymer II solution was used in place of acrylic polymer I solution. Two panels of 25 phosphatized cold rolled steel coated with the same electrocoating composition and with the same white base coat were sprayed with the clear acrylic coating composition II and cured as above. Also, two panels of phosphatized cold rolled steel coated with the same electrocoating composition and with the same black base coat were sprayed with the clear 3 o acrylic coating composition II and cured as above. The same properties were measured for both sets of panels as above and the results are shown in Table 1.

AhIEPJDEO S#-fEET

*Cont. *Cont.
Clear Base 20 DOI Knoo L a b angle angle Coat Coat loss water hex.

I black89 88 2.2 2.08 -0.11 -0.20 108/68 65/49 I black87 86 4.10 2.21 0.02 -0.02 108/68 65/49 I white84 85 3.50 87.46-0.77 0.79 108/68 65/49 I white86 87 3.30 87.59-0.76 0.87 108/65 65/49 II black85 65 2.30 2.87 0.32 0.54 76/56 2/0 II black87 65 2.60 2.22 0.02 0.02 76/56 2/0 II white90 82 2.20 87.52-0.87 0.27 76/56 2/0 II white89 83 2.10 87.31-0.93 0.17 76/56 2/0 *Advancing/Receding contact angles for water and hexadecane Soil Resistance Test A soil substitute was prepared by blending 10 g of Nujol s (mineral oil), 20g of carbon black, 500 ml of heptane and 1 liter of "Surlyn" polymer beads (polymer of an acrylic ionomer). The resulting suspension was thoroughly mixed and then the heptane solvent was stripped off using a vacuum stripper.
A 2.54 cm length of 7.62 cm OD polyvinyl chloride pipe was to place on the surface of the test panel. Three grams of the above prepared soil substitute was poured into the pipe and gently rolled around on the surface of the test panel for a total of fifty rotations. The soil substitute was poured off and the pipe segment was removed. The test panel was then tapped sharply twice on the side of a trash can to remove lightly adhered 15 dirt. The amount of dirt remaining on the panel was measured in delta E
units with a color analyzer. The results of this test are as follows:
Clear coating composition of Acrylic Polymer I containing polymerized fluoroalkyl containing monomers - retained 5.4 delta E units of dirt.
2 o Clear coating composition of Acrylic Polymer II which did not contain fluoroalkyl monomers - retained 35.3 delta E units of dirt.
The data in Table I shows that clear coating compositions made from Acrylic Polymer I containing polymerized fluoroalkyl containing monomers have a higher contact angle for water and for 25 hexadecane which shown in the above Soil Resistance Test provides for a finish which is resistant to soiling and also is easily washed or wiped clean in comparison to the clear coating composition made from Acrylic Polymer ,_ >; i~~'R~ °. 3""t':'~~ '.4~'°gr~,~x;"'"',, 12 ., . . ,.., . v . ~ , ~ .., , II which did not contain the polymerized ffuoroalkyl containing'inoricimers~ ~
a which had low contact angles and exhibited poor soil resistance in the Soil Resistance Test and poor cleanability.
s EXAMPLE 2 An acrylic polymer solution III was prepared in which the acrylic polymer has ffuoro alkly groups by changing the following constituents into a reactor equipped with a heat source, a thermometer and a stirrer:
Portion 1 Parts B Wei t Methyl amyl ketone 699.92 Portion 2 Butyl methacrylate monomer (BMA) 583.80 Styrene monomer (S) 307.28 Butyl acrylate monomer (BA) 343.20 Hydroxy propyl acrylate monomer (HI'A) 783.46 Methyl amyl ketone 4.72 Portion 3 Fluoromethacrylate monomer [2-(N-ethyl 30.73 perfluorooctane sulfonamido) ethyl methacrylate monomer]
Methyl amyl ketone 30.00 Portion 4 T-butyl peroxy acetate 69.01 Methyl amyl ketone 114.59 Portion 5 Methyl amyl ketone 33.28 Total 2999.99 io Portion 1 was charged into the reaction vessel and blanketed with nitrogen and Portion 2 was premixed and added over a 360 minutes period while holding the resulting mixture at its reflex temperature of 150°
C. Portion 3 was premixed and then added at one time to the reaction mixture 350 minutes after the start of the addition of Portion 2. Portion 4 is was premixed and added at the same time as Portion 2 to the reaction mixture over a 375 minute period and then Portion 5 was added and the reaction mixture held at its reflex temperature for an additional 60 minutes.
The resulting polymer solution was cooled to room temperature.

Aw ~~,,is,cf~ C?'!~~' CA 02234425 1998-04-08 ,'"' ,.., ,_. l'~ ~ 3la The resulting acrylic polymer solution III had a weight'solids~
content of 70%, a polymer of BMA/SBABPA/Fluoromethacrylate in the following percentages 28.5/15/17/38/1.5 and the polymer had a weight average molecular weight of 6400 and a number average molecular weight s of 3200.
A clear acrylic coating composition III was prepare as in Example 1 using the same polyisocyanate crosslinking agent in the same ratio except the above prepared acrylic polymer solution III was used in the place of acrylic polymer solution I. Two panels of phosphatized cold rolled io steel coated with the same electrocoating composition and with the same white base coat as in Example 1 were sprayed with the clear acrylic coating composition III and cured as above. Also, two panels of phosphatized cold rolled steel coated with the same electrocoating composition and with the same black base coat as in Example 1 were sprayed with the clear coating is acrylic composition III and cured as above. The resulting cured coating had a smooth glossy finish which was essentially free of craters. The same properties were measured for both sets of panels as above and the results are shown in Table 2 below.

*Cont. *Cont Clear Base 20' angle angle Coat Coat loss DOI knoo L a b water hex.

L1T black 85 56 2.3 2.27 -0.14 -0.15101/61 60/44 III white 89 86 1.9 87.57 -0.90 0.30 107/65 61/42 z o *Advancing /Receding contact angles for water and hexadecane.
The above data shows that the clear coating composition made from acrylic polymer solution III containing polymerized fluoroalkyl containing monomers had a high contact angle for water and for solvents which provides for a finish which is resistant to soiling and is easily washed a s or wiped clean.

This is a comparative Example in which the following clear acrylic coating compositions IV - Vll were formulated by blending a non s o fluorinated acrylic polymer with an a highly fluorinated acrylic polymer in an attempt to achieve the same results as in Examples l and 2 where an acrylic polymer was used having a small percentage of polymerized fluoro alkyl ethyl methacrylate monomer.

CA 02234425 1998-04-08 ~ ~ ~ 3 ~/
: .. , . An acrylic polymer solution IV was prepared in which' the ~ °
acrylic polymer has perfluoro alkly groups by charging the following constituents into a reactor equipped with a heat source, a thermometer and a stirrer:
Portion 1 Parts By Weig~,ht Methyl amyl ketone 232.92 Portion 2 Hydroxy propyl acrylate monomer (HPA) 260.72 Fluoro alkly ethyl methacrylate monomer422.64 (FAMA) described in Example 1 Methyl amyl ketone 1.57 Portion 3 T-butyl peroxy acetate 22.97 Methyl amyl ketone 3 8.14 Portion 4 Methyl amyl ketone 21.06 Total 1000.02 Portion 1 was charged into the reaction vessel and blanketed with nitrogen and Portion 2 was premixed and added over a 240 minutes period while holding the resulting mixture at its reflux temperature of 150°
io C. Portion 3 was premixed and then added at the same time as Portion 2 over a 255 minute period of time. Portion 4 was added and the resulting polymer solution was cooled to room temperature.
The resulting acrylic polymer solution IV had a weight solids content of 70%, a polymer of HPA/FAMA in the following percentages i5 38/72 and the polymer had a weight average molecular weight of 7,600 and a number average molecular weight of 5,300.
A clear acrylic coating composition IV was prepared with the above prepared acrylic polymer solution IV as follows:
Parts by Wei t Portion 1 Methyl ethyl ketone 25.40 Toluene 26.70 Dibasic acid ester (ester mixture of adipic acid, glutaric 17.90 acid and succinic acid) ~wCwZj:G~ ~~~

CA 02234425 1998-04-08 /9 ~ 3,~
Butyl Cellosolve Acetate 49.60 Portion 2 Acrylic polymer solution IV (prepared above) 2.00 Portion 3 Acrylic polymer solution (70% solids of an acrylic 730.90 polymer of BMA/BA/S/HPA in a weight ratio of 30/17/15/38 in methyl amyl ketone) "Tinuvin" 328 - 2-(2-hydroxy-3,5-ditertiary amyl phenol) 55.80 -ZH-benzotriazole) "Tinuvin" 292 - (1,2,2,6,6-pentamethyl-4-piperidinyl) 8.70 sebecate Dibutyl tin dilaurate 9.20 PM acetate 73.80 1000.00 Total The constituents of Portion 1 were charged into a mixing vessel in the order shown with continuous mixing. Portion 2 was added and mixed for 15 minutes. The constituents of Portion 3 were charged into the j g ~1PCCP~ ;~ the ~r~P_r chnum__ uri_th_ ~n_n_ctan_t mixing, The reSUltlrig rJJV1 composition had a solids content of 53.5%. A clear coating composition was prepared by mixing the above composition with a polyisocyanate solution in a 3/1 volume ratio. The polyisocyanate solution contains 90%
by weight of the trimer of hexamethylene diisocyanate and 10% by weight io solvent of n-butyl acetate/Aromatic 100 solvent in a 1:1 ratio.
Clear acrylic coating compositions V, VI and VII were prepared using the same constituents as above except the fluorinated acrylic polymer content was increased to 5.00 parts by weight in composition V, to 10.00 parts by weight in composition VI and to 20.00 parts by weight in i5 composition VII with an equivalent reduction in the amount of acrylic polymer IV in each composition.
Four panels of phosphatized cold rolled steel coated with the same electrocoating composition and with the same black base coat as described in Example 1 were each sprayed respectively with one of the ao above prepared clear acrylic coating composition IV - VII and cured as in Example 1. Each of the panels had a finish with an unacceptable number of craters and the appearance was unacceptable. The properties of each of the panel was measured as in Example 1 and are shown in the table below.

AM~N~~~ ~' '~~

*Cont. *Cont Clear Base 20 DOI knoo L a b angle angle Coat Coat Ioss water hex.

IV black 76 42 6.5 2.29 -0.06 -0.26 108/60 67/63 V black 73 31 6.4 3.69 0.14 0.14 109/60 68/64 VI black 88 84 6.8 2.25_ -0.09 -0.09 109/60 70/64 VII black 87 73 6.0 2.43 -0.06 -0.28 110/63 71/65 ~ I ~ ~

*Advancing /Receding contact angles for water and hexadecane The water and solvent contact angles indicate that the clear acrylic coating compositions IV-VII would have good soil resistance and s good cleanability; however, the appearance of each of the compositions due to cratering of the coating make the compositions unacceptable for commercial use.
'Y °k j'~~~:'Y~~x.'t~~; ,~~.__ - 17

Claims (12)

1. A clear coating composition containing 45-80% by weight of a binder and 20-55% by weight of an organic liquid; wherein the binder comprises (A) 40-90% by weight, based on the weight of the binder, of an acrylic polymer consisting essentially of 20-45% by weight, based on the weight of the acrylic polymer, of polymerized hydroxyl containing monomers selected from the group consisting of hydroxy alkyl acrylate and hydroxy alkyl methacrylates having 1-4 carbon atoms in the alkyl groups, 50-79.9% by weight, based on the weight of the acrylic polymer, of polymerized monomers selected from the group consisting of alkyl acrylates and alkyl methacrylates having 1-18 carbon atoms in the alkyl groups, styrene, alpha methyl styrene or any textures of the above and 0.1-5.0% by weight, based on the weight of the acrylic polymer, of polymerized perfluoroalkyl containing monomer represented by the formula where R is selected from the group consisting of hydrogen or an alkyl group having 1-2 carbon atoms, n is an integer of 1-11 and R f a perfluoroalkyl containing group having at least 4 carbon atoms and the acrylic polymer having a weight average molecular weight of 2,000 - 20,000 determined by gel permeation chromatography, (B) 10-60% by weight, based on the weight of the binder, of an organic polyisocyanate crosslinking agent; and where a cured coating of the coating of the composition has a combination of advancing-water contact angle of at least 100° and a hexadecane advancing contact angle of at least 40° as measured by the Sessile Drop Method.
2. The coating composition of Claim 1 in which R f is a straight chain or branched chain perfluoroalkyl group having 4-20 carbon atoms.
3. The coating composition of claim 2 in which the acrylic polymer consists essentially of polymerized monomers of an alkyl methacrylate having 2-6 carbon atoms in the alkyl group, an alkyl acrylate having 2-8 carbon atoms in the alkyl group, a hydroxy alkyl acrylate having 2-4 carbon atoms in the alkyl group, styrene, alpha methyl styrene and a perfluoroalkyl containing monomer wherein R is CH3, n is 2 and R f is a perfluoroalkyl group having 4-20 carbon atoms and the polyisocyanate is an aliphatic or cycloaliphatic polyisocyanate and the polymer has an advancing water contact angle of 100-120° and a hexadecane advancing contact angle of 60-85°C.
4. The coating composition of claim 3 in which the acrylic polymer consists essentially of butyl methacrylate, butyl acrylate, styrene, hydroxy propyl acrylate and the perfluoroalkyl containing monomer.
5. The coating composition of claim 1 in which the perfluoroalkyl containing monomer is represented by the formula where R is as defined in claim 1, R1 is a perfluoroalkyl group having 4-12 carbon atoms, R2 is an alkyl group having 1-4 carbon atoms and n is an integer of 1-4.
6. The coating composition of claim 1 containing 0.1-10% by weight, based on the weight of the binder, of ultraviolet light stabilizer or an antioxidant or mixtures thereof.
7. A substrate coated with a dried and cured layer of the composition of claim 1.
8. A process for forming a fluoroalkyl acrylic polymer which comprises polymerizing the following monomers: hydroxyl containing monomers selected from the group consisting of hydroxy alkyl acrylates and hydroxyl alkyl methacrylates having 1-4 carbon atoms in the alkyl groups, and monomers selected from the group consisting of alkyl acrylates, alkyl methacrylates each having 1-18 carbon atoms in the alkyl group, styrene, alpha methyl styrene or any mixtures of the above and 0.1-5% by weight, based on the weight of the polymer, of a fluoroalkyl containing monomer represented by the formula where R is selected from the group consisting of hydrogen or an alkyl group having 1-2 carbon atoms, n is an integer of 1-11 and R f is a fluoroalkyl containing group having at least 4 carbon atoms and a polymerization catalyst and continuing polymerization to form a polymer having a weight average molecular weight of 2,000 - 20,000 determined by gel permeation chromatography;
wherein the fluoroalkyl containing monomer is added in the entire amount at any time during the polymerization in 0.01-10% of the total time of polymerization.
9. The process of claim 8 in which R f is a straight chain or branched chain fluoroalkyl group having 1-20 carbon atoms
10. The process of claim 8 in which the monomers consist essentially of an alkyl methacrylate having 2-6 carbon atoms in the alkyl group, an alkyl acrylate having 2-8 carbon atoms in the alkyl group, a hydroxy alkyl acrylate having 2-4 carbon atoms in the alkyl group, styrene, alpha methyl styrene and a fluoroalkyl containing monomer wherein R is CH3, n is 2 and R f is a fluoroalkyl group having 4-20 carbon atoms and the polymerization is run at 60-175°C.
11. The process of claim 10 in which the monomers consist essentially of styrene, butyl methacrylate, butyl acrylate, hydroxy propyl acrylate and the fluoroalkyl containing monomer.
12. The process of claim 8 in which the fluoroalkyl containing monomer is represented by the formula where R is as defined in claim 9, R1 is a fluoroalkyl group having 4-12 carbon atoms, R2 is an alkyl group having 1-4 carbon atoms and n is an integer of 1-4.
CA002234425A 1995-10-16 1996-10-11 Acrylic fluorocarbon polymer containing coatings Expired - Fee Related CA2234425C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US08/543,770 1995-10-16
US08/543,770 US5629372A (en) 1994-11-22 1995-10-16 Acrylic fluorocarbon polymer containing coating
PCT/US1996/016287 WO1997014732A1 (en) 1995-10-16 1996-10-11 Acrylic fluorocarbon polymer containing coatings

Publications (2)

Publication Number Publication Date
CA2234425A1 CA2234425A1 (en) 1997-04-24
CA2234425C true CA2234425C (en) 2005-05-10

Family

ID=24169499

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002234425A Expired - Fee Related CA2234425C (en) 1995-10-16 1996-10-11 Acrylic fluorocarbon polymer containing coatings

Country Status (9)

Country Link
US (1) US5629372A (en)
EP (1) EP0856020B1 (en)
JP (1) JPH11513734A (en)
AU (1) AU708759B2 (en)
BR (1) BR9611103A (en)
CA (1) CA2234425C (en)
DE (1) DE69617983T2 (en)
NZ (1) NZ321112A (en)
WO (1) WO1997014732A1 (en)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5629372A (en) * 1994-11-22 1997-05-13 E. I. Du Pont De Nemours And Company Acrylic fluorocarbon polymer containing coating
JPH09157578A (en) * 1995-12-08 1997-06-17 Daikin Ind Ltd Fluorine-containing material for coating material and method for coating object therewith
US7268179B2 (en) * 1997-02-03 2007-09-11 Cytonix Corporation Hydrophobic coating compositions, articles coated with said compositions, and processes for manufacturing same
US5914384A (en) * 1997-11-21 1999-06-22 E. I. Du Pont De Nemours And Company Coating compositions containing a highly fluorinated hydroxyl containing additive
US6413588B1 (en) * 1999-01-11 2002-07-02 E. I. Du Pont De Nemours And Company Method of producing durable layered coatings
US6583223B2 (en) 2001-09-27 2003-06-24 Ppg Industries Ohio, Inc. Coating compositions which contain a low surface tension (meth) acrylate containing block copolymer flow control agent
US6841641B2 (en) 2001-09-27 2005-01-11 Ppg Industries Ohio, Inc. Copolymers comprising low surface tension (meth) acrylates
US6586530B1 (en) 2001-09-27 2003-07-01 Ppg Industries Ohio, Inc. Low surface tension (meth) acrylate containing block copolymer prepared by controlled radical polymerization
US7348389B2 (en) * 2003-09-22 2008-03-25 E. I. Du Pont De Nemours And Company Method for achieving recoat adhesion over a fluorinated topcoat
US7288282B2 (en) * 2003-09-22 2007-10-30 E. I. Du Pont De Nemours And Company Coating compositions containing a fluorinated organosilane polymer
US6933005B2 (en) * 2003-09-22 2005-08-23 E. I. Du Pont De Nemours And Company Method for achieving recoat adhesion over a fluorinated topcoat
KR20080009760A (en) * 2004-01-30 2008-01-29 그레이트 레이크스 케미칼 코퍼레이션 Compositions and halogenated compositions
KR20070000462A (en) * 2004-01-30 2007-01-02 그레이트 레이크스 케미칼 코퍼레이션 Production processes and systems, compositions, surfactants, monomer units, metal complexes, phosphate esters, glycols, aqueous film forming foams, and foam stabilizers
JP2007526360A (en) * 2004-01-30 2007-09-13 グレート・レークス・ケミカル・コーポレーション Manufacturing method and system, composition, surfactant, monomer unit, metal complex, phosphate ester, glycol, aqueous film-forming foam, and foam stabilizer
WO2005074594A2 (en) 2004-01-30 2005-08-18 Great Lakes Chemical Corporation Production processes and systems, compositions, surfactants, monomer units, metal complexes, phosphate esters, glycols, aqueous film forming foams, and foam stabilizers
US7300976B2 (en) * 2004-06-10 2007-11-27 3M Innovative Properties Company Fluorochemical oligomeric polish composition
US20070027349A1 (en) * 2005-07-28 2007-02-01 Stephan Brandstadter Halogenated Compositions
US20090137773A1 (en) * 2005-07-28 2009-05-28 Andrew Jackson Production Processes and Systems, Compositions, Surfactants, Monomer Units, Metal Complexes, Phosphate Esters, Glycols, Aqueous Film Forming Foams, and Foam Stabilizers
JP2009545653A (en) * 2006-08-03 2009-12-24 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Telomer composition and method of manufacture
US8318656B2 (en) 2007-07-03 2012-11-27 E. I. Du Pont De Nemours And Company Production processes and systems, compositions, surfactants, monomer units, metal complexes, phosphate esters, glycols, aqueous film forming foams, and foam stabilizers
WO2009029512A2 (en) * 2007-08-24 2009-03-05 Rhodia, Inc. Two component waterborne polyurethane coatings for anti-graffiti application
EP2716680A1 (en) 2012-10-04 2014-04-09 Basf Se Fluorinated polymerizable compound
KR20150065775A (en) * 2012-10-04 2015-06-15 바스프 코팅스 게엠베하 Fluorine-containing non-aqueous coating composition, coating process, and the use of the coating composition
WO2015076314A1 (en) * 2013-11-20 2015-05-28 大阪有機化学工業株式会社 Clear coat composition
JP6157442B2 (en) * 2013-12-25 2017-07-05 大阪有機化学工業株式会社 Clear coat composition
CN107709477B (en) 2015-04-30 2021-10-29 科慕埃弗西有限公司 Durable architectural coatings comprising crosslinkable polymeric additives
DE202018102849U1 (en) 2018-05-22 2018-05-30 Zipps Skiwachse Gmbh Lubricant for use on sliding surfaces of winter sports equipment

Family Cites Families (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2803615A (en) * 1956-01-23 1957-08-20 Minnesota Mining & Mfg Fluorocarbon acrylate and methacrylate esters and polymers
CH1121365D (en) * 1964-08-14
US3318852A (en) * 1965-04-05 1967-05-09 Minnesota Mining & Mfg Fluorine-containing polymers
FR2476097A1 (en) * 1980-02-19 1981-08-21 Ugine Kuhlmann
US4396680A (en) * 1981-03-04 1983-08-02 E. I. Du Pont De Nemours And Co. Substrate coated with crater resistant acrylic enamel
US4371657A (en) * 1981-03-04 1983-02-01 E. I. Du Pont De Nemours And Company Crater resistant acrylic enamel
JPS5834866A (en) * 1981-08-27 1983-03-01 Dainippon Ink & Chem Inc Composition for urethane coating
FR2540131B1 (en) * 1983-01-28 1986-04-04 Atochem COMPOSITIONS AND METHOD FOR OLEOPHOBIC AND HYDROPHOBIC TREATMENT OF CONSTRUCTION MATERIALS
JPS60184513A (en) * 1984-03-02 1985-09-20 Showa Denko Kk Production of graft polymer
JPS6114267A (en) * 1984-06-29 1986-01-22 Showa Denko Kk Water-and oil-repellent paint
JPS6123656A (en) * 1984-07-11 1986-02-01 Kansai Paint Co Ltd Anti-icing organic coating composition
JPS6123657A (en) * 1984-07-11 1986-02-01 Kansai Paint Co Ltd Anti-icing organic resin coating composition
JPS6195078A (en) * 1984-10-15 1986-05-13 Kansai Paint Co Ltd Anti-icing organic resin coating composition
US5159017A (en) * 1986-01-17 1992-10-27 Nippon Paint Co., Ltd. Crosslinked polymer microparticles and coating composition containing the same
JPS62267376A (en) * 1986-05-15 1987-11-20 Atom Kagaku Toryo Kk Paint composition
US4812337A (en) * 1986-11-25 1989-03-14 Kansai Paint Company, Limited Metallic coating method
US4722545A (en) * 1987-05-04 1988-02-02 Ford Motor Company Method and apparatus for determining the center position of a vehicular steering system
JP2508760B2 (en) * 1987-10-20 1996-06-19 旭硝子株式会社 Water and oil repellent with dirt removability
US4791166A (en) * 1988-03-23 1988-12-13 Hoechst Celanese Corporation Fluorocarbon polymer compositions and methods
JPH02182712A (en) * 1989-01-10 1990-07-17 Nok Corp Novel isocyanate group-containing acrylic copolymer and composition of same copolymer
JPH0312269A (en) * 1989-06-12 1991-01-21 Mitsubishi Rayon Co Ltd Film forming method
DE3943127A1 (en) * 1989-12-28 1991-07-04 Hoechst Ag URETHANES AS ALIPHATIC FLUORO ALCOHOL, ISOCYANATES AND CARBONIC ACIDS, PROCESS FOR THEIR PREPARATION AND THEIR USE
US5206286A (en) * 1990-04-02 1993-04-27 Ppg Industries, Inc. Aqueous emulsion polymers prepared with crosslinkable non-ionic surfactants
DE4027594A1 (en) * 1990-08-31 1992-03-05 Herberts Gmbh WATER-DUMBABLE COPOLYMER, THEIR PRODUCTION AND USE, AND AQUEOUS COATING AGENTS
GB9026687D0 (en) * 1990-12-07 1991-01-23 Vascutek Ltd Process for providing a low-energy surface on a polymer
US5250698A (en) * 1992-08-05 1993-10-05 Ciba-Geigy Corporation 2-(2-hydroxy-3-perfluoroalkyl thiomethyl-5-alkylphenyl)2H-benzotriazoles and stabilized compositions thereof
US5629372A (en) * 1994-11-22 1997-05-13 E. I. Du Pont De Nemours And Company Acrylic fluorocarbon polymer containing coating

Also Published As

Publication number Publication date
EP0856020B1 (en) 2001-12-12
NZ321112A (en) 2000-01-28
AU708759B2 (en) 1999-08-12
US5629372A (en) 1997-05-13
AU7439096A (en) 1997-05-07
DE69617983D1 (en) 2002-01-24
CA2234425A1 (en) 1997-04-24
WO1997014732A1 (en) 1997-04-24
JPH11513734A (en) 1999-11-24
BR9611103A (en) 1999-07-13
DE69617983T2 (en) 2002-08-22
EP0856020A1 (en) 1998-08-05

Similar Documents

Publication Publication Date Title
CA2234425C (en) Acrylic fluorocarbon polymer containing coatings
AU743231B2 (en) Coating compositions containing a highly fluorinated polymeric additive
AU742687B2 (en) Coating compositions containing a highly fluorinated hydroxyl containing additive
CA2234421C (en) Coating compositions of an acrylic fluorocarbon polymer and a fluorinated polyisocyanate
CA2234370C (en) Coating compositions of an acrylic polymer and a fluorinated polyisocyanate
MXPA00004914A (en) Coating compositions containing a highly fluorinated hydroxyl containing additive
MXPA00004915A (en) Coating compositions containing a highly fluorinated polymeric additive
MXPA98002557A (en) Compositions of coating of an acrylic polymer and a fluor polyisocianate
MXPA98002958A (en) Compositions of coating of an acrylic defluorocarburo polymer and a fluor polyisocianate

Legal Events

Date Code Title Description
EEER Examination request
MKLA Lapsed