Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
  • C09D133/04—Homopolymers or copolymers of esters
  • C09D133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
  • C09D133/16—Homopolymers or copolymers of esters containing halogen atoms
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
• • G—PHYSICS
  • G11—INFORMATION STORAGE
  • G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
  • G11B5/00—Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
  • G11B5/62—Record carriers characterised by the selection of the material
• • G—PHYSICS
  • G11—INFORMATION STORAGE
  • G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
  • G11B5/00—Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
  • G11B5/74—Record carriers characterised by the form, e.g. sheet shaped to wrap around a drum
  • G11B5/82—Disk carriers
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/11—Magnetic recording head
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/11—Magnetic recording head
  • Y10T428/1164—Magnetic recording head with protective film
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
  • Y10T428/2852—Adhesive compositions
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
  • Y10T428/2852—Adhesive compositions
  • Y10T428/2878—Adhesive compositions including addition polymer from unsaturated monomer
  • Y10T428/2891—Adhesive compositions including addition polymer from unsaturated monomer including addition polymer from alpha-beta unsaturated carboxylic acid [e.g., acrylic acid, methacrylic acid, etc.] Or derivative thereof
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers

Definitions

• the present disclosure relates to high purity apparati, e.g., magnetic hard disk drives, and more specifically, to coatings for particle reduction in such apparati.
• Magnetic disk drives typically comprise a number of precisely dimensioned operating parts, e.g., spacers, disk clamps, e-blocks, cover plates, base plates, actuators, voice coils, voice coil plates, etc. These components can all be potential sources of particles.
• the head typically flies over the media at a spacing of about 100A. This spacing is decreasing with increasing areal density, making the reduction and prevention of particle generation ever more critical. Particles at the head disk interface can cause thermal asperities, high fly writes, and head crashes; any of these are detrimental to performance of a disk drive.
• Publ. No. 2003/0223154 discloses prevention of particle generation by encapsulation with a coating "made of a soft and tenacious material, such as gold, platinum, epoxy resin, etc.”
• U.S. Pat. Publ. No. 2002/0093766 discloses the use of adhesive -backed heat shrinkable conformal films to protect against particle generation.
• U.S. Pat. No. 6,671,132 discloses the use of metal or polymeric coatings.
• U.S. Pat. No. 7,035,055 discloses the use of resin coatings.
• Particles within hard drive assemblies can lead to friction and localized hot spots, which in turn can lead to failure of the hard drive and loss of the data magnetically encoded with it.
• One approach to this issue has been use of electroplated nickel as a particle suppression coating on the cover to the hard drive.
• nickel has tripled in price between about 2001 and about 2006.
• the requirement to electroplate the hard drive cover leads to more steps in assembly than coating and curing of a low surface energy coating onto the hard drive assemblies, the electroplating process entails use of potentially hazardous materials, and particles shed from such coated parts are very hard, i.e., nickel particles, that can readily cause significant damage to the media and read/write head(s).
• E-coats or electrophoretically-deposited coatings are also used as particle suppression coatings but it can be difficult to obtain uniform coatings (necessitating some post coating machining).
• outgassing related to uncured monomers or absorption of hydrocarbons into the coatings that later outgas into the drive is encountered.
• improved coatings for particle suppression from substrates with oxide surfaces such as metals, e.g., aluminum, copper, stainless steel, etc., plastics, glass, ceramics, silicon, etc.
• the provided coatings can be applied with simple techniques (e.g., dip coating and thermal cure), exhibit thermal stability, can be formed in substantially uniform thin (e.g., from about 0.1 to about 5.0 microns) layers over complex substrate topographies.
• the coatings are clean (i.e., low outgassing, low extractable ions), are resistant to typical cleaning processes (e.g., aqueous and solvent-based cleaning solutions with or without ultrasonic treatment), are environmentally benign (i.e., delivered with solvents such as segregated hydrofluoroethers), have a good safety profile, and provide relatively superior cost-to-benefit performance as compared to the current industry method of nickel coating.
• the provided coatings may also provide corrosion protection.
• the provided coatings comprise a thin polymer coating with reactive pendant groups having crosslinking functionality and superior ability to anchor to the substrate surface to suppress particle shedding from substrate surfaces. These particles can be from the substrate material or materials left over from processing and/or incomplete cleaning. This coating, in essence, forms a net over the surface of the substrate holding in particles, which otherwise could shed from the substrate.
• a substrate that includes a coating on at least a portion of said substrate wherein said coating comprises a fluorinated acrylate random copolymer having the following general formula: XA w B x C y D z T where X is the initiator residue or hydrogen, A represents units derived from one or more divalent fluorochemical acrylate monomers, B represents units derived from one or more divalent acrylate monomers with a functional group, C represents units derived from one or more non-fluorinated divalent acrylate monomers with a hydrocarbon group, D represents units derived from one or more curatives, T represents a functional terminal group or X defined as above, w is an integer from 1 up to about 200, x is an integer from 1 up to about 300, y is an integer from 1 up to about 100, and z is an integer from 0 up to about 30, and wherein C is selected from the group consisting of monomers whose homopolymer has a glass transition temperature of less than or equal to 2O
• a method of reducing particulate contamination includes providing at least one of a hard disk drive assembly, a MEMS device, a process equipment for electronics or a printed circuit card assembly, and applying a coating on at least a portion of the assembly of at least one of a hard disk drive assembly, a MEMS device, a process equipment for electronics or a printed circuit card assembly, wherein the coating comprises a fluorinated acrylate random copolymer having the following general formula:
• X is the initiator residue or hydrogen
• A represents units derived from one or more divalent fluorochemical acrylate monomers
• B represents units derived from one or more divalent acrylate monomers with a functional group
• C represents units derived from one or more non-fluorinated divalent acrylate monomers with a hydrocarbon group
• D represents units derived from one or more curatives
• a, b, c, d, and e are weight percentages of A, B, C, D, and T, respectively, and wherein C is selected from the group consisting of monomers whose homopolymer has a glass transition temperature of less than or equal to 2O 0 C.
• the provided substrates, coatings, and methods comprise the reaction product of specified fluorochemical monomers and hydrocarbon monomers wherein the coating is at least partially cured in situ on the substrate.
• the coating can provide surprisingly good performance as particle reduction coatings on substrates.
• Incorporation of hydrocarbon segments into the backbone of the copolymer has been surprisingly found to improve the particle suppression performance of the subject coatings and increase the resistance of resultant coatings to cleaning processes, particularly those processes used on electronics components such as ultrasonic cleaning processes.
• the provided coatings offer many advantages including but not limited to the ease of obtaining thin, uniform coating on complex surfaces, good safety and environmental properties, and resultant coatings that exhibit low surface energy.
• the provided coatings provides particle suppression coatings that are of relatively lower cost, provide improved resistance to cleaning, improved particle suppression performance. Improved handling and abrasion resistance has also been observed.
• acrylate can also be understood to mean “methacyrlate”; and “pendant” refers to end groups and side groups.
• a 174 is 3-trimethoxysilane propyl methacrylate; • AA is acrylic acid;
• BuMA is butyl methacrylate
• EHA 2-ethyl hexyl acrylate
• HFE hydrofluoroether
• HFPOMA hexafluoroproplyene oxide methacrylate which can be made by the procedure of Preparative Example 3 of US Patent No. 6,995,222 (Buckanin et al.); • IOA is iso-octyl acrylate;
• MMA is methylmethacrylate
• MPTS is 3-mercaptopropyl trimethoxysilane
• coatings of the invention comprise fluorinated acrylate copolymer compounds of the following general formula:
• X represents the residue of an initiator or hydrogen
• A represents units derived from one or more divalent fluorochemical acrylate monomers
• B represents units derived from one or more divalent acrylate monomers with a functional group
• C represents units derived from one or more non- fluorinated divalent acrylate monomers with a hydrocarbon group (preferably BA)
• D represents units derived from one or more curatives, e.g., acidic acrylate (preferably acrylic acid)
• T represents a functional terminal group or X as described above.
• the curative, D may be present in the copolymer or may be provided as an external catalyst.
• the copolymer can be random, i.e., the order of the A, B, C and D segments is random though it will be understood that some local portions may exhibit a more block copolymer structure.
• the number average molecular weight of the copolymer is from about 500 to about 50,000, preferably from about 1000 to about 10,000.
• w is an integer from 1 up to about 200
• x is an integer from 1 up to about 300
• y is an integer from 1 up to about 100
• z is an integer from 0 up to about 30 wherein the ratio of z : (x + 1) is from 0 up to less than about 0.3.
• the ratio of the sum of (w + y) : x is greater than about 1 and less than about 20, preferably greater than about 2 and less than about 8.
• the ratio of y : w is typically from 0 up to less than 7, preferably greater than about 0.2 and less than about 1.5. This ratio is also limited by solubility of the resultant copolymer.
• the resultant copolymer will no longer be sufficiently soluble in HFE making such embodiments more difficult to use.
• Co-solvents can help extend this ratio.
• the resultant coating may subject to increased tendency to absorb and later emit, e.g., outgas, organic contaminants.
• A can be derived from fluorinated acrylic monomers, preferably FBSEA, PFPHMA, and HFPOMA. Other suitable fluorinated monomers may be used instead or in addition to the preferred materials listed here if desired.
• B can derived from a functionalized divalent acrylate monomer, e.g., silane- containing propyl acrylate or ethyl acrylate, epoxy acrylate, or a divalent urethane acrylate.
• a preferred example is Al 74.
• B can serve to provide crosslinking between polymers as well as bonding to the substrate.
• the hydrocarbon segments, i.e., C in the formula above, impart improved softness to the resultant copolymer making the resultant particle suppression coating more resistant to thermal stresses and mechanical stresses.
• the C segment can be derived from monomers that are preferably those whose homopolymer has a low T g , i.e., less than or equal to about 2O 0 C.
• the C segment preferably does not contain a reactive group.
• the C segment also preferably exhibits effective solubility in fluorocarbon solvents which are used in the preparation process of the random acrylic copolymer before cross-linking.
• HFEs are preferred for this purpose as their use offers a number of processing and environmental advantages as well as allows for thin uniform coatings even on complex surfaces.
• blends of fluorocarbons solvents with organic solvents i.e. ethyl acetate, IPA, etc.
• organic solvents i.e. ethyl acetate, IPA, etc.
• the polymer precursor composition may optionally include one or more curatives, i.e., D in the formula.
• Illustrative examples include acidic acrylates, e.g., acrylic acid, methacrylic acid, carboxy propyl acrylate, carboxylic acids, and sulfonic acids, e.g., 2-acrylamido-2-methylpropane sulfonic acid.
• the curative may be fluorinated or not as desired. Use of a curative is generally preferred; because it is incorporated into the reaction product, there is typically no outgassing.
• the curing rate of the coating material may be enhanced as desired by addition of effective amounts of suitable catalyst depending upon the selection of reactive groups, parameters of the substrate, desired processing conditions, etc.
• suitable catalyst for coatings made using a perfluoropolyether silanes may be catalyzed using such agents as KRYTOX 157 FSL perfluoropolyalkylether carboxylic acid from DuPont.
• T can be a functionalized terminal group, e.g., a silane.
• T can be derived from a chain transfer agent.
• a preferred agent is MPTS.
• a free radical initiator is generally used to initiate the polymerization or oligomerization reaction.
• free-radical initiators can be used and examples thereof include azo compounds, such as azobisisobutyronitrile (AIBN), azo-2- cyanovaleric acid and the like, hydroperoxides such as cumene, t-butyl and t-amyl hydroperoxide, dialkyl peroxides such as di -t-butyl and dicumylperoxide, peroxyesters such as t-butyl peroctoate, t-butylperbenzoate and di-t-butylperoxy phthalate, diacylperoxides such as benzoyl peroxide and lauroyl peroxide.
• compounds that generate free radicals or acidic and radical species upon exposure to actinic radiation can also be used to initiate the polymerization reaction. Examples of such species include IRGACURE 651 and DAROCUR 1173 available from Ciba
• the substrate and coating are selected such that the coating can be anchored to the substrate surface via covalent bonding.
• the reactive pendant groups, i.e., silane groups, on the molecule can contribute to this desired bonding performance.
• the coating may provide superior corrosion protection as the silane groups react with bonds sites on the substrate that would otherwise be susceptible to corrosion reactions.
• the coating thickness may be on the order of or substantially smaller than the size of the particles being held on the substrate, e.g., coating thickness in the range of from about 0.01 to about 1.0 micron as compared to an average particle size in the range of from about 0.1 to more than 5 microns.
• alkoxy groups can react with the functional groups of the B and/or T unit to form a silanol group on the polymer.
• the silanol group can react with other silanol groups, thus crosslinking the polymer, and in the case of oxide surfaces (e.g., aluminum, copper, silicon, ceramic materials, etc.), covalently bonding the polymer to the surface.
• An illustrative method of coating substrates in accordance with the invention is as follows: a) mixing the precursor materials described above, i.e., initiator, acrylates, curative (if any), etc. in a suitable solvent, e.g., a hydrofluoroether and reacting the precursor materials to yield a coating composition containing the random copolymer; b) applying the coating composition to desired portions of a substrate (any suitable coating technique can be used); c) evaporating the solvent to leave the random copolymer on the substrate (an advantage of HFE solvents is that they will evaporate quickly); d) elevating the temperature, e.g., to from about 100 0 C to about 15O 0 C, to cause the coating to cross link and build adhesion to the substrate.
• a suitable solvent e.g., a hydrofluoroether
• step d) is divided into two steps.
• the coated substrate is cured so that the coating is tack-free, but has remaining reactive pendant groups.
• the coated substrate may then be run through additional processing. This may include addition of tapes, labels, epoxies or "form-in-place-gaskets".
• the coated substrate is completely cured. This two stage cure can improve the adhesion of tapes, labels, epoxies and "form- in-place-gaskets.
• the curing in each step is preferably done at elevated temperatures.
• a method of reducing particulate contamination includes providing at least one of a hard disk drive assembly, a MEMS device, a process equipment for electronics or a printed circuit card assembly; and applying a coating on at least a portion of the assembly of at least one of a hard disk drive assembly, a MEMS device, a process equipment for electronics or a printed circuit card assembly, wherein the coating comprises a fluorinated acrylate random copolymer having the following general formula:
• X is the initiator residue or hydrogen
• A represents units derived from one or more divalent fluorochemical acrylate monomers
• B represents units derived from one or more divalent acrylate monomers with a functional group
• C represents units derived from one or more non-fluorinated divalent acrylate monomers with a hydrocarbon group
• D represents units derived from one or more curatives
• the provided coatings can be of use in a variety of high purity applications such in hard disk drive assemblies including such components as spacers, disk clamps, e-blocks, cover plates, base plates, microactuators, sliders, voice coils, voice coil plates etc. These components are all potential sources of particles in finished disk drive systems. Coatings of the invention may also be used to reduce particle shedding for MEMS (Micro Electrical-Mechanical Systems), high purity processing (coating process equipment to reduce potential contamination), and semiconductor processing applications, e.g., surface mount components on a printed circuit card assembly.
• MEMS Micro Electrical-Mechanical Systems
• high purity processing coating process equipment to reduce potential contamination
• semiconductor processing applications e.g., surface mount components on a printed circuit card assembly.
• coatings of the invention have been observed to impart anti-smudge and easy clean performance to substrates to which they are applied.
• Objects and advantages of this invention are further illustrated by the following examples, but the particular materials and amounts thereof recited in these examples, as well as other conditions and details, should not be construed to unduly limit this invention.
• Test Substrates Aluminum (A15052 H32) and stainless steel (SS304) sheets were purchased from M. Vincent & Associates of Minneapolis, Minnesota and cut into test coupons approximately 51 mm x 25 mm x 1.6 mm in size for aluminum and 51 mm x 25 mm x 0.4 mm for stainless steel.
• Cleaning Method 1 Prior to applying the coating, the substrates were cleaned by wipe cleaning using isopropyl alcohol (from EMD Chemicals of Gibbstown, New Jersey, part number PX1835P-4) and VWR SPEC-WIPE 7 Wipers (from VWR International, LLC of West Chester, Pennsylvania).
• a two sump vapor degreaser model number LAB-KLEEN 612 Degreasing System, from Unique Equipment Corporation of Montrose, California was used to clean with an azeotrope of 89% (by weight) 3M NOVEC 7300 Engineered Fluid (from 3M Co. of St. Paul, MN) and 11% DOWANOL PM Propylene Glycol Methyl Ether (from Dow Chemical Company of Midland, Michigan) using the following parameters:
• Coating Method The coating was applied to the substrate by dip coating.
• LPC Liquid particle counter
• test apparatus consisted of a 600 mL beaker (from VWR International, LLC of West Chester, Pennsylvania) fixtured in an ultrasonic bath (from Crest Ultrasonics
• the ultrasonics to the tank was supplied by a generator (from Crest Ultrasonics Corporation of Trenton, New Jersey, part number 6HT- 1014-6W).
• the substrates to be tested were suspended in the beaker using a 28 gauge, solderable polyurethane stator wire (from MWS Wire Industries of Westlake Village, California, part number 28 SPN-155 RED) such that the neither the wire nor the substrate contact the beaker.
• the particle levels in the water were measured using an 8103 syringe sampling system (from Hach Ultra Analytics of Grants Pass, Oregon).
• a copolymer was prepared by charging 25 g HFPOMA, 1O g BA (from Aldrich Chemical Company of Milwaukee, Wisconsin), 10 g A 174 (from United Chemical Technologies of Bristol, New Jersey), 5 g MPTS (from United Chemical Technologies, Inc.) and 250 g of 3M NOVEC 7200 Engineering Fluid (ethoxy-nonafluorobutane
• A15052 H32 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above using a pull rate of 2.54 millimeters/second (6 inches/minute). A two step cure was used with the first cure done at 85 0 C for one hour and the second cure done at 15O 0 C for 1 hour. Solvent extraction testing showed 95% cure for coatings on the aluminum coupon. The LPC extraction results on for these coatings are presented in Table 1.
• a copolymer was prepared by charging 30 g HFPOMA, 5 g BA, 10 g A174, 5 g MPTS and 250 g of 3M NOVEC 7200 Engineering Fluid to a flask equipped with a mixer. The solution was purged with nitrogen for 5 minutes. Following this, 1 g of LUPEROX 26M50 initiator was charged to the flask. The solution was stirred under nitrogen and heated to 65 0 C for 18 hours. This solution was diluted to 10% polymer with 3M NOVEC 7200 Engineering Fluid. The polymer solution was catalyzed by adding KRYTOX 157 FSL at 2% of the polymer level, about 0.2% of the overall solution.
• A15052 H32 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above using a pull rate of 2.54 millimeters/second (6 inches/minute). A two step cure was used with the first cure done at 85 0 C for one hour and the second cure done at 15O 0 C for 1 hour. Solvent extraction testing showed 86% cure for coatings. The LPC extraction results on for these coatings are presented in Table 1.
• a copolymer was prepared by charging 35 g HFPOMA, 1O g Al 74, 5 g MPTS and 250 g of 3MTM NOVEC 7200 Engineering Fluid to a flask equipped with a mixer. The solution was purged with nitrogen for 5 minutes. Following this, 1 g of LUPEROX 26M50 initiator was charged to the flask. The solution was stirred under nitrogen and heated to 65 0 C for 18 hours. This solution was diluted to 10% polymer with 3M NOVEC 7200 Engineering Fluid. The polymer solution was catalyzed by adding KRYTOX 157 FSL at 2% of the polymer level, i.e., about 0.2% of the overall solution.
• A15052 H32 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above using a pull rate of 2.54 millimeters/second (6 inches/minute). A two step cure was used with the first cure done at 85 0 C for one hour and the second cure done at 15O 0 C for 1 hour. Solvent extraction testing showed 100% cure for coatings. The LPC extraction results for these coatings are presented in Table 1.
• Results are average of 5 samples ** Number of particles >0.3 ⁇ per cm 2 of substrate
• Example 1 and Example 2 were Analysis of the data in Table 1 showed Example 1 and Example 2 to have a statistically significant improvement in particle suppression over Comparative Example 1.
• a copolymer was prepared by charging 15 g FBSEA, 26 g BA, 4.5 g Al 74, 1.5 g
• A15052 H32 and SS304 test coupons were cleaned by Cleaning Method 2. These coupons were then coated with the polymer solution using the method described above using a pull rate of 2.54 millimeters/second (6 inches/minute). A two step cure was used with the first cure done at 85 0 C for one hour and the second cure done at 15O 0 C for 1 hour.
• a copolymer was prepared by charging 12 g FBSEA, 26 g BA, 4.5 g A174, 1.5 g MPTS, 6.0 g CN973J75, 100 g 3M NOVEC 7200 Engineering Fluid, and 100 g ethyl acetate to a flask equipped with a mixer. The solution was purged with nitrogen for 5 minutes. Following this, 0.5 g of VAZO 67 was charged to flask. The solution was stirred under nitrogen and was heated to 65 0 C for 16 hours. The solution was diluted to 10% polymer with a 50/50 blend by mass of 3MTM NOVEC 7200 Engineering Fluid and ethyl acetate.
• the polymer solution was catalyzed by adding KRYTOX 157 FSL at 3% of the polymer level, i.e., about 0.3% of the overall solution.
• A15052 H32 and SS304 test coupons were cleaned by Cleaning Method 2. These coupons were then coated with the polymer solution using the method described above using a pull rate of 2.54 millimeters/second (6 inches/minute).
• a two step cure was used with the first cure done at 85 0 C for one hour and the second cure done at 15O 0 C for 1 hour.
• Solvent extraction testing showed 78% cure on aluminum and 92% cure on stainless steel.
• the LPC extraction testing for this coating is presented in Table 2.
• a copolymer was prepared by charging 54 g PFPHMA, 20 g BA, 18 g Al 74, 6 g MPTS, 2 g AA (from Alfa Aesar of Heysham, Lancashire LA3 2XY United Kingdom), 1 g t-butyl peroctoate (LUPEROX 26, 100% active ingredient) (from Atofina of Philadelphia, Pennsylvania), and 500 g 3M NOVEC 7200 Engineering Fluid to a flask under positive nitrogen pressure. The solution was stirred under nitrogen and was heated to 7O 0 C for 18 hours. The solution was diluted to 10% polymer by mass with 3M NOVEC 7200 Engineering Fluid.
• A15052 H32 and SS304 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above using a pull rate of 4.66 millimeters/second (11 inches/minute). The cure was done at 12O 0 C for 1 hour. Solvent extraction testing showed 97% cure on aluminum and 100% cure on stainless steel. The LPC extraction testing for this coating is presented in Table 3.
• Example 6 A copolymer was prepared by charging 54 g PFPHMA, 20 g BA, 20 g Al 74, 4 g MPTS, 2 g mercaptoproprionic acid (from Aldrich of Milwaukee, Wisconsin), 1 g t-butyl peroctoate (100%) and 500 g 3M NOVEC 7200 Engineering Fluid to a flask under positive nitrogen pressure. The solution was stirred under nitrogen and was heated to 7O 0 C for 18 hours. The solution was diluted to 10% polymer by mass with 3M NOVEC
• A15052 H32 and SS304 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above using a pull rate of 4.66 millimeters/second (11 inches/minute). The cure was done at 12O 0 C for 1 hour. Solvent extraction testing showed 93% cure on aluminum and 95% cure on stainless steel. The LPC extraction testing for this coating is presented in Table 3.
• a copolymer was prepared by charging 54 g FBSEA, 20 g BA, 18 g Al 74, 6 g MPTS, 2 g AA, 1 g t-butyl peroctoate (LUPEROX 26), and 500 g 3M NOVEC 7200
• A15052 H32 and SS304 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above using a pull rate of 4.66 millimeters/second (11 inches/minute). The cure was done at 12O 0 C for 1 hour. Solvent extraction testing showed 95% cure on aluminum and 100% cure on stainless steel. The LPC extraction testing for this coating is presented in Table 3.
• a copolymer was prepared by charging 54 g FBSEMA, 20 g BA, 18 g Al 74, 6 g MPTS, 2 g AA, 1 g t-butyl peroctoate (LUPEROX 26), 450 g 3M NOVEC 7200 Engineering Fluid and 50 g of ethyl acetate to a flask under positive nitrogen pressure. The solution was stirred under nitrogen and was heated to 7O 0 C for 18 hours. The solution was diluted to 10% polymer by mass with 3M NOVEC 7200 Engineering Fluid.
• A15052 H32 and SS304 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above using a pull rate of 4.66 millimeters/second (11 inches/minute). The cure was done at 12O 0 C for 1 hour. Solvent extraction testing showed 100% cure on aluminum and 100% cure on stainless steel. The LPC extraction testing for this coating is presented in Table 3.
• a copolymer was prepared by charging 54 g PFPHMA, 20 g BA, 19 g Al 74, 6 g MPTS, 1 g AA, 1 g t-butyl peroctoate (LUPEROX 26), and 500 g 3M NOVEC 7200 Engineering Fluid to a flask under positive nitrogen pressure. The solution was stirred under nitrogen and was heated to 7O 0 C for 18 hours. The solution was diluted to 10% polymer by mass with 3M NOVEC 7200 Engineering Fluid.
• A15052 H32 and SS304 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above using a pull rate of 4.66 millimeters/second (11 inches/minute). The cure was done at 12O 0 C for 1 hour. Solvent extraction testing showed 90% cure on aluminum and 92% cure on stainless steel. The LPC extraction testing for this coating is presented in Table 3.
• a copolymer was prepared by charging 54 g PFPHMA, 20 g EHA (from Aldrich),
• A15052 H32 and SS304 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above using a pull rate of 4.66 millimeters/second (11 inches/minute). The cure was done at
• Example 11 A copolymer was prepared by charging 54 g PFPHMA, 20 g IOA (from Aldrich),
• A15052 H32 and SS304 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above using a pull rate of 4.66 millimeters/second (11 inches/minute). The cure was done at 12O 0 C for 1 hour. Solvent extraction testing showed 98% cure on aluminum and 100% cure on stainless steel. The LPC extraction testing for this coating is presented in Table 3.
• a copolymer was prepared by charging 54 g PFPHMA, 20 g MMA (from Rohm and Haas of Philadelphia, Pennsylvania), 19 g Al 74, 6 g MPTS, 1 g AA, 1 g t-butyl peroctoate (LUPEROX 26), and 500 g 3M NOVEC 7200 Engineering Fluid to a flask under positive nitrogen pressure. The solution was stirred under nitrogen and was heated to 7O 0 C for 18 hours. The solution was diluted to 10% polymer by mass with 3M NOVEC 7200 Engineering Fluid.
• A15052 H32 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above with using a pull rate of 4.66 millimeters/second (11 inches/minute). The cure was done at 12O 0 C for 1 hour. Solvent extraction testing showed 98% cure. The LPC extraction testing for this coating is presented in Table 4.
• Comparative Example 3 A copolymer was prepared by charging 54 g FBSEA, 20 g MMA, 19 g Al 74, 6 g
• a copolymer was prepared by charging 54 g PFPHMA, 20 g BA, 19 g Al 74, 6 g MPTS, 1 g AA, 1 g t-butyl peroctoate (LUPEROX 26), and 500 g 3M NOVEC 7200 Engineering Fluid to a flask under positive nitrogen pressure. The solution was stirred under nitrogen and was heated to 7O 0 C for 18 hours. The solution was diluted to 10% polymer by mass with 3M NOVEC 7200 Engineering Fluid.
• A15052 H32 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above with using a pull rate of 4.66 millimeters/second (11 inches/minute). The cure was done at 12O 0 C for 1 hour.
• Example 13 A copolymer was prepared by charging 54 g FBSEA, 20 g BuMA (from Lucite
• A15052 H32 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above with using a pull rate of 4.66 millimeters/second (11 inches/minute). The cure was done at 12O 0 C for 1 hour.
• a copolymer was prepared by charging 54 g PFPHMA, 20 g BuMA, 19 g Al 74, 6 g MPTS, 1 g AA, 1 g t-butyl peroctoate (LUPEROX 26), and 500 g 3M NOVEC 7200 Engineering Fluid to a flask under positive nitrogen pressure. The solution was stirred under nitrogen and was heated to 7O 0 C for 18 hours. The solution was diluted to 10% polymer by mass with 3MTM NOVEC 7200 Engineering Fluid.
• A15052 H32 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above with using a pull rate of 4.66 millimeters/second (11 inches/minute). The cure was done at 12O 0 C for 1 hour. Solvent extraction testing showed 89% cure. The LPC extraction testing for this coating is presented in Table 4.
• a copolymer was prepared by charging 54 g PFPHMA, 20 g BuMA, 19 g Al 74, 6 g MPTS, 1 g t-butyl peroctoate (LUPEROX 26), and 500 g 3M NOVEC 7200 Engineering Fluid to a flask under positive nitrogen pressure. The solution was stirred under nitrogen and was heated to 7O 0 C for 18 hours. The solution was diluted to 10% polymer by mass with 3MTM NOVEC 7200 Engineering Fluid.
• A15052 H32 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above with using a pull rate of 4.66 millimeters/second (11 inches/minute). The coated coupons were heated at 12O 0 C for 1 hour. Solvent extraction testing showed 0% cure.
• a copolymer was prepared by charging 54 g PFPHMA, 20 g BA, 19.5 g Al 74, 6 g
• A15052 H32 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above with using a pull rate of 4.66 millimeters/second (11 inches/minute). Three types of cures were run.
• a copolymer was prepared by charging 54 g PFPHMA, 20 g BA, 19.7 g Al 74, 6 g MPTS, 0.3 g AA, 1 g t-butyl peroctoate (LUPEROX 26), and 500 g 3M NOVEC 7200 Engineering Fluid to a flask under positive nitrogen pressure. The solution was stirred under nitrogen and was heated to 7O 0 C for 18 hours. The solution was diluted to 10% polymer by mass with 3MTM NOVEC 7200 Engineering Fluid.
• A15052 H32 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above with using a pull rate of 4.66 millimeters/second (11 inches/minute). Three types of cures were run. The solvent extraction data is presented in Table 5.
• a copolymer was prepared by charging 54 g PFPHMA, 20 g BA, 19.5 g Al 74, 6 g MPTS, 0.5 g AA, 0.22 g of polymerizable dye AD-4 (U. S. Pat. No. 6,894,105 (Parent et al), Column 9 and 22 line 44), 2 g t-butyl peroctoate (LUPEROX 26), and 500 g 3M NOVEC 7200 Engineering Fluid to a flask under positive nitrogen pressure. The solution was stirred under nitrogen and was heated to 7O 0 C for 18 hours. The solution was filtered through a 0.1 micron nylon filter and was diluted to 10% polymer by mass with 3MTM NOVEC 7200 Engineering Fluid.
• A15052 H32 test coupons were cleaned by Cleaning Method 1. These coupons were then coated with the polymer solution using the method described above with using a pull rate of 4.66 millimeters/second (11 inches/minute). The cure was done at 15O 0 C for 1 hour. Solvent extraction testing showed 92% cure. The LPC extraction testing for this coating is presented in Table 6.

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