Patent Application
20240279512
A silicone release coating dispersion can be dried and cured to form a silicone release coating with anti-static properties. Methods for preparation and use of the silicone release coating dispersion are provided.
Static charges generated during the delamination of adhesives from release liners must be dissipated to protect the adhesive films from electrical discharge and dust adsorption. The incumbent anti-static solution in the silicone pressure sensitive industry requires additional coating of anti-static primers on one or both sides of plastic substrates such as polyethylene terephthalate (PET). This method for fabricating a release liner may suffer from the drawbacks of multiple process steps, which can increase cost and limit productivity; and the anti-static primers may interfere with the curing reaction of the silicone release coating composition or compromise interfacial anchorage of the silicone release coating.
A silicone release coating dispersion comprises a continuous phase comprising a hydrosilylation reaction curable silicone release coating composition, a surfactant, and an aqueous discontinuous phase dispersed in the continuous phase. The aqueous phase comprises (A) an ionic liquid and (B) water.
The silicone release coating dispersion may be formed by a method comprising: (1) dissolving (A) the ionic liquid in (B) the water to form an aqueous solution; (2) dispersing the aqueous solution in a siloxane intermediate composition comprising (C) a branched polyorganosiloxane polymer and (D) a silicone polyether, thereby forming a dispersion intermediate; and (3) combining the dispersion intermediate and additional starting materials, where the additional starting materials comprise: (E) a polydiorganosiloxane having at least two aliphatically unsaturated groups per molecule, (F) a polyorganohydrogensiloxane having at least three silicon bonded hydrogen atoms per molecule, and (G) a hydrosilylation reaction catalyst.
A release liner may be prepared using the dispersion described above by a method comprising: optionally (I) treating a surface of a backing substrate, (II) coating the silicone release coating dispersion on the surface of the backing substrate, (III) drying the silicone release coating dispersion to form a film, and (IV) curing the film to form a silicone release coating on the surface of the backing substrate.
The silicone release coating dispersion (dispersion), introduced above, comprises:
Starting material (A), the ionic liquid, is an anti-static additive that imparts anti-static properties to the silicone release coating prepared from the dispersion. Ionic liquids suitable for use herein are salts, which may comprise a large cation and a charge-delocalized anion. The ionic liquid comprises a water soluble alkali metal salt, such as a lithium salt. The ionic liquid may be one alkali metal salt or a combination of two or more alkali metal salts. Examples of alkali metal salts include metal salts comprising a cation selected from a lithium ion, a sodium ion, and a potassium ion; and an anion selected from a chloride ion, a bromide ion, an iodide ion, a tetrachloroaluminum ion, a hexafluorophosphate ion, a tetrafluoroborate ion, a thiocyanate ion, a perchlorate ion, a p-toluene sulfonate ion, a trifluoromethanesulfonate ion, a pentafluoroethanesulfonate ion, a bis(trifluoromethanesulfonyl)imide, a dicyanamide ion, a tris(trifluoromethylsulfonyl)methide ion, an acetate ion, a trifluoroacetate ion, and a hexafluoroantimony ion. Alternatively, the alkali metal salt may be a lithium salt. The lithium salt may be, for example, (A1) lithium trifluoromethanesulfonate LiSO3CF3, (A2) lithium bis(trifluoromethylsulfonyl)imide LiN(SO2CF3)2, LiSO3C4F9, LiC(SO2CF3)3, (A3) LiBF4, (A4) LiClO4, (A5) LiPF6, (A6) LiAsF6, (A7) LiSbF6, and (A8) LiB(C6H5)4. These lithium salts may be used either alone, or in combinations of two or more of (A1) to (A8). Alternatively, the ionic liquid may comprise a mixture of (A1) lithium trifluoromethanesulfonate and (A2) lithium bis(trifluoromethylsulfonyl)imide. Lithium salts, such as lithium trifluoromethanesulfonate and lithium bis(trifluoromethylsulfonyl)imide, are commercially available, e.g., from Monils Chemical Engineering Science & Technology (Shanghai) Co., Ltd. The (A1) lithium trifluoromethanesulfonate and (A2) lithium bis(trifluoromethylsulfonyl)imide may be present in amounts such that (A) the ionic liquid comprises 90 weight %, based on combined weights of (A1) and (A2), of (A1) lithium trifluoromethylsulfonate, and 10 weight %, based on combined weights of (A1) and (A2). Starting material (A), the ionic liquid, and starting material (B), the water, may be present in a weight ratio (A):(B) of 2:1 to 1:2 in the aqueous discontinuous phase.
The water (B) is not generally limited, and may be utilized neat (i.e., absent any carrier vehicles/solvents), and/or pure (i.e., free from or substantially free from minerals and/or other impurities). For example, the water (B) may be processed or unprocessed prior to dissolving (A) the ionic liquid therein. Examples of processes that may be used for purifying the water include distilling, filtering, deionizing, and combinations of two or more thereof, such that (B) the water may be deionized, distilled, and/or filtered. Alternatively, (B) the water may be unprocessed (e.g. may be tap water, i.e., provided by a municipal water system or well water, used without further purification). Alternatively, (B) the water may be purified before dissolving (A) the ionic liquid therein. Alternatively, (B) the water may be utilized as a mixture (e.g. solution or suspension) comprising a carrier vehicle/solvent, such as any of those described below that can be used in the silicone release coating composition.
The hydrosilylation reaction curable silicone release coating composition comprises: (C) a branched polyorganosiloxane polymer, (E) a polydiorganosiloxane having at least two aliphatically unsaturated groups per molecule, (F) a polyorganohydrogensiloxane having at least three silicon bonded hydrogen atoms per molecule, and (G) a hydrosilylation reaction catalyst. The silicone release coating composition may optionally further comprise one or more additional starting materials. The one or more additional starting materials may be selected from the group consisting of (H) a solvent; (I) a hydrosilylation reaction inhibitor; and (J) an anchorage additive.
Starting material (C) is a branched polyorganosiloxane polymer. The branched polyorganosiloxane polymer may have unit formula (C1): (R31SiO1/2)a(R21R2SiO1/2)b(R1R2SiO2/2)c(R21SiO2/2)d(SiO4/2), where each R1 is an independently selected monovalent hydrocarbon group free of aliphatic unsaturation, each R2 is an independently selected aliphatically unsaturated monovalent hydrocarbon group; subscripts a and b represent average numbers of monofunctional units and subscripts c and represent average numbers of difunctional units, per molecule, where a, b, c, and d have average values such that 2≥a≥0, 4≥b≥0, (a+b)=4, 4≥c≥0, 995≥d≥4, and (a+b+c+d) has a value sufficient to impart a viscosity≥170 mPa·s measured by rotational viscometry at room temperature to the branched polyorganosiloxane polymer. Alternatively, viscosity may be ≥170 mPa·s to 1000 mPa-s, alternatively≥170 to 500 mPa-s, alternatively 180 mPa·s to 450 mPa·s, and alternatively 190 mPa·s to 420 mPa·s. Viscosity may be measured at RT at 0.1 rpm to 50 rpm on a Brookfield DV-III cone & plate viscometer with #CP-52 spindle. One skilled in the art would recognize that as viscosity increases, rotation rate decreases. Suitable branched polyorganosiloxane polymers are known in the art and can be made by known methods, exemplified by those disclosed in U.S. Pat. No. 6,806,339 to Cray, et al. and U.S. Patent Publication 2007/0289495 to Cray, et al.
Suitable alkyl groups for R1 may be linear, branched, cyclic, or combinations of two or more thereof. The alkyl groups are exemplified by methyl, ethyl, propyl (including n-propyl and/or isopropyl), butyl (including n-butyl, tert-butyl, sec-butyl, and/or isobutyl); pentyl, hexyl, heptyl, octyl, decyl, dodecyl, undecyl, and octadecyl (and branched isomers having 5 to 18 carbon atoms), and the alkyl groups are further exemplified by cycloalkyl groups such as cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl. Alternatively, the alkyl group for R1 may be selected from the group consisting of methyl, ethyl, propyl and butyl; alternatively methyl, ethyl, and propyl; alternatively methyl and ethyl. Alternatively, the alkyl group for R1 may be methyl.
Suitable aryl groups for R1 may be monocyclic or polycyclic and may have pendant hydrocarbyl groups. For example, the aryl groups for R1 include phenyl, tolyl, xylyl, and naphthyl and further include aralkyl groups such as benzyl, 1-phenylethyl and 2-phenylethyl. Alternatively, the aryl group for R1 may be monocyclic, such as phenyl, tolyl, or benzyl; alternatively the aryl group for R1 may be phenyl.
In the formulas above and below, R2 may be an alkenyl group. Suitable alkenyl groups may have terminal alkenyl functionality to facilitate hydrosilylation reaction, e.g., R2 may have formula 7 where
subscript y is 0 to 6 and * denotes a point of attachment (i.e., to a silicon atom). Alternatively, each R2 may be independently selected from the group consisting of vinyl, allyl, and hexenyl. Alternatively, each R2 may be independently selected from the group consisting of vinyl and allyl. Alternatively, each R2 may be vinyl. Alternatively, each R2 may be allyl.
Alternatively, (C) the branched polyorganosiloxane polymer may comprise formula (C2): [R2R1Si—(O—SiR21)x—O](4-w)—Si—[O—(R21SiO)vSiR31]w, where R1 and R2 are as described above; and subscripts v, w, and x have values such that 200≥v≥1, 2≥w≥0, and 200≥x≥1. Alternatively, in this formula (C2), each R1 may be independently selected from the group consisting of methyl and phenyl, and each R2 may be independently selected from the group consisting of vinyl, allyl, and hexenyl. Branched polyorganosiloxane suitable for starting material (C2) may be prepared by known methods such as heating a mixture comprising a polyorganosilicate resin, and a cyclic polydiorganosiloxane or a linear polydiorganosiloxane, in the presence of a catalyst, such as an acid or phosphazene base, and thereafter neutralizing the catalyst.
Alternatively, the branched polyorganosiloxane polymer for starting material (C) may comprise a silsesquioxane of unit formula (C3): (R31SiO1/2)aa(R2R21SiO1/2)bb(R21SiO2/2)cc(R2R1SiO2/2)ee(R1SiO3/2)aa, where R1 and R2 are as described above, subscript aa≥0, subscript bb≥0, subscript cc is 15 to 995, subscript dd≥0, and subscript ee≥0. Subscript aa may be 0 to 10. Alternatively, subscript aa may have a value such that: 12≥aa≥0; alternatively 10≥aa≥0; alternatively 7≥aa≥0; alternatively 5≥aa≥0; and alternatively 3≥aa≥0. Alternatively, subscript bb≥1. Alternatively, subscript bb≥3. Alternatively, subscript bb may have a value such that: 12≥bb≥0; alternatively 12≥bb≥3; alternatively 10≥bb≥0; alternatively 7≥bb≥1; alternatively 5≥bb≥2; and alternatively 7≥bb≥3. Alternatively, subscript cc may have a value such that: 800≥cc≥15; and alternatively 400≥cc≥15. Alternatively, subscript ee may have a value such that: 800≥ee≥0; 800≥ee≥15; and alternatively 400≥ee≥15. Alternatively, subscript ee may b 0. Alternatively, a quantity (cc+ee) may have a value such that 995≥(cc+ee)≥15. Alternatively, subscript dd≥1. Alternatively, subscript dd may be 1 to 10. Alternatively, subscript dd may have a value such that: 10≥dd≥0; alternatively 5≥dd≥0; and alternatively dd=1. Alternatively, subscript dd may be 1 to 10, alternatively subscript dd may be 1 or 2. Alternatively, when subscript dd=1, then subscript bb may be 3 and subscript cc may be 0. The values for subscript bb may be sufficient to provide the silsesquioxane with an alkenyl content of 0.1% to 1%, alternatively 0.2% to 0.6%, based on the weight of the silsesquioxane. Suitable silsesquioxanes for starting material (C3) are exemplified by those disclosed in U.S. Pat. No. 4,374,967 to Brown, et al; U.S. Pat. No. 6,001,943 to Enami, et al.; U.S. Pat. No. 8,546,508 to Nabeta, et al.; and U.S. Pat. No. 10,155,852 to Enami.
Starting material (E) in the silicone release coating composition is a polydiorganosiloxane having at least two aliphatically unsaturated groups per molecule. The polydiorganosiloxane may have unit formula (E1):(R2R21SiO1/2)2(R21SiO2/2)j, where R1 and R2 are as described above, subscript j represents average number of difunctional units per molecule, and 10,000≥j≥100.
Starting material (E) may comprise an alkenyl-functional polydiorganosiloxane such as (E1-1)bis-dimethylvinylsiloxy-terminated polydimethylsiloxane, (E1-2)bis-dimethylvinylsiloxy-terminated poly(dimethylsiloxane/methylphenylsiloxane), (E1-3)bis-dimethylvinylsiloxy-terminated poly(dimethylsiloxane/diphenylsiloxane), (E1-4)bis-phenyl,methyl,vinyl-siloxy-terminated polydimethylsiloxane, (E1-5)bis-dimethylhexenylsiloxy-terminated polydimethylsiloxane, (E1-6)bis-dimethylhexenyl-siloxy-terminated poly(dimethylsiloxane/methylphenylsiloxane), (E1-7)dimethylhexenyl-siloxy-terminated poly(dimethylsiloxane/diphenylsiloxane), and (E1-8) a combination of two or more of (E1-1) to (E1-7). Alternatively, starting material (E) may be selected from the group consisting of (E1-1)bis-dimethylvinylsiloxy-terminated polydimethylsiloxane, (E1-5)bis-dimethylhexenylsiloxy-terminated polydimethylsiloxane, or both.
Methods of preparing polydiorganosiloxanes as described above for starting material (E), such as hydrolysis and condensation of the corresponding organohalosilanes and oligomers or equilibration of cyclic polydiorganosiloxanes, are known in the art, see for example U.S. Pat. Nos. 3,284,406; 4,772,515; 5,169,920; 5,317,072; and 6,956,087, which disclose preparing linear polydiorganosiloxanes with alkenyl groups. Examples of linear polydiorganosiloxanes having alkenyl groups are commercially available from, e.g., Gelest Inc. of Morrisville, Pennsylvania, USA under the tradenames DMS-V00, DMS-V03, DMS-V05, DMS-V21, DMS-V22, DMS-V25, DMS-V-31, DMS-V33, DMS-V34, DMS-V35, DMS-V41, DMS-V42, DMS-V43, DMS-V46, DMS-V51, DMS-V52. Other linear polydiorganosiloxanes having alkenyl groups are commercially available from DSC.
Starting material (C) the branched polyorganosiloxane polymer and starting material (E) the polydiorganosiloxane having at least two aliphatically unsaturated groups per molecule are present in amounts that combined total 100 weight parts of the silicone release coating composition. Alternatively, the amount of starting material (C) may be 2 weight parts to 10 weight parts, alternatively 3 weight parts to 9 weight parts of the silicone release coating composition. Alternatively, the amount of starting material (E) may be 20 weight parts to 40 weight parts of the silicone release coating composition.
Starting material (F) in the silicone release coating composition is a polyorganohydrogensiloxane, which may function as a crosslinker to cure the silicone release coating composition. The polyorganohydrogensiloxane has at least three silicon bonded hydrogen atoms per molecule. The polyorganohydrogensiloxane may have unit formula (F1): (R21HSiO1/2)k(R31SiO1/2)m(R1HSiO2/2)n(R31SiO2/2)o, where R1 is as described above, subscripts k and m represent average numbers of monofunctional units per molecule, subscripts n and o represent average number of difunctional units per molecule, and subscripts k, m, n, and o have values such that 2≥k≥0, 1≥m≥0, (k+m)=2, n≥0, o≥0, (k+n)≥3, and 8≤(k+m+n+o)≤400.
Suitable polyorganohydrogensiloxanes for use herein are exemplified by:
Polyorganohydrogensiloxanes are also commercially available, such as those available from Gelest, Inc. of Morrisville, Pennsylvania, USA, for example, HMS-H271, HMS-071, HMS-993; HMS-301 and HMS-301 R, HMS-031, HMS-991, HMS-992, HMS-993, HMS-082, HMS-151, HMS-013, HMS-053, HAM-301, HPM-502, and HMS-HM271. Methods of preparing linear and branched polyorganohydrogensiloxanes suitable for use herein, such as hydrolysis and condensation of organohalosilanes, are well known in the art, as exemplified in: U.S. Pat. No. 2,823,218 to Speier, U.S. Pat. No. 3,957,713 to Jeram et al., and U.S. Pat. No. 4,329,273 to Hardman, et al.
The silicon-bonded hydrogen (Si—H) content of polyorganohydrogensiloxanes can be determined using quantitative infra-red analysis in accordance with ASTM E168. The silicon-bonded hydrogen to aliphatically unsaturated groups (e.g., alkenyl such as vinyl and/or alkynyl) ratio is important when relying on a hydrosilylation cure process. Generally, this is determined by calculating the total weight % of aliphatically unsaturated groups in the composition, e.g. vinyl [V] and the total weight % of silicon bonded hydrogen [H] in the composition and given the molecular weight of hydrogen is 1 and of vinyl is 27 the molar ratio of silicon bonded hydrogen to vinyl is 27[H]/[V]. The polyorganohydrogensiloxane is present in an amount sufficient to provide a molar ratio of silicon bonded hydrogen atoms to aliphatically unsaturated groups (SiH:Vi ratio) in the silicone release coating composition of ≥1:1 to 5:1.
Starting material (G) in the silicone release coating composition is a hydrosilylation reaction catalyst. This catalyst will promote a reaction between the aliphatically unsaturated groups in starting materials (C) and (E), and the silicon bonded hydrogen atoms in starting material (F). Said catalyst comprises a platinum group metal. The platinum group metal may be selected from the group consisting of platinum, rhodium, ruthenium, palladium, osmium, and iridium. Alternatively, the platinum group metal may be platinum.
For example, (G) the hydrosilylation reaction catalyst may be (G1) the platinum group metal, described above; (G2) a compound of such a metal, for example, chloridotris(triphenylphosphane)rhodium(I) (Wilkinson's Catalyst), a rhodium diphosphine chelate such as [1,2-bis(diphenylphosphino)ethane]dichlorodirhodium or [1,2-bis(diethylphospino)ethane]dichlorodirhodium, chloroplatinic acid (Speier's Catalyst), chloroplatinic acid hexahydrate, platinum dichloride, (G3) a complex of a compound, (G2), with an aliphatically unsaturated organopolysiloxane, or (G4) a platinum group metal compound microencapsulated in a matrix or coreshell type structure. Complexes of platinum with aliphatically unsaturated organopolysiloxanes include 1,3-diethenyl-1,1,3,3-tetramethyldisiloxane complexes with platinum (Karstedt's Catalyst) and Pt(0) complex in tetramethyltetravinylcyclotetrasiloxane (Ashby's Catalyst). Alternatively, the hydrosilylation reaction catalyst may be (G5) a compound or complex, as described above, microencapsulated in a resin matrix. Specific examples of suitable platinum-containing catalysts include chloroplatinic acid, either in hexahydrate form or anhydrous form, or a platinum-containing catalyst which is obtained by a method comprising reacting chloroplatinic acid with an aliphatically unsaturated organosilicon compound such as with a vinyl functional polydimethylsiloxane (e.g., divinyltetramethyldisiloxane), or alkene-platinum-silyl complexes as described in U.S. Pat. No. 6,605,734 to Roy. These alkene-platinum-silyl complexes may be prepared, for example by mixing 0.015 mole (COD)PtCl2 with 0.045 mole COD and 0.0612 moles HMeSiCl2, where COD represents cyclooctadienyl and Me represents methyl. Other exemplary hydrosilylation reaction catalysts are described in U.S. Pat. No. 2,823,218 to Speier; U.S. Pat. No. 3,159,601 to Ashby; U.S. Pat. No. 3,220,972 to Lamoreaux; U.S. Pat. No. 3,296,291 to Chalk, et al.; U.S. Pat. No. 3,419,593 to Willing; U.S. Pat. No. 3,516,946 to Modic; U.S. Pat. No. 3,715,334 to Karstedt; U.S. Pat. No. 3,814,730 to Karstedt; U.S. Pat. No. 3,928,629 to Chandra; U.S. Pat. No. 3,989,668 to Lee, et al.; U.S. Pat. No. 4,766,176 to Lee, et al.; U.S. Pat. No. 4,784,879 to Lee, et al.; U.S. Pat. No. 5,017,654 to Togashi; U.S. Pat. No. 5,036,117 to Chung, et al.; and 5,175,325 to Brown; and EP 0 347 895 A to Togashi, et al. Suitable hydrosilylation reaction catalysts for starting material (G) are commercially available, for example, SYL-OFF™ 4000 Catalyst and SYL-OFF™ 2700 are available from Dow Silicones Corporation of Midland, Michigan, USA.
Starting material (G) may be one hydrosilylation reaction catalyst or a combination of two or more of the hydrosilylation reaction catalysts described above. The amount of (G) the hydrosilylation reaction catalyst in the composition will depend on various factors including the selection of starting materials (C), (E), and (F), their respective contents of alkenyl groups and silicon bonded hydrogen atoms, and the amount of (I) hydrosilylation reaction inhibitor present in the silicone release coating composition, however, the amount of catalyst is sufficient to catalyze hydrosilylation reaction of SiH and alkenyl groups, alternatively the amount of catalyst is sufficient to provide at least 0.01 ppm, alternatively at least 0.05 ppm, alternatively at least 0.1 ppm, alternatively at least 0.5 ppm, alternatively at least 1 ppm, and alternatively at least 170 ppm by weight of the platinum group metal based on weight of the silicone release coating dispersion. At the same time, the amount of catalyst is sufficient to provide up to 800 ppm, alternatively up to 500 ppm, and alternatively up to 200 ppm by mass of the platinum group metal, on the same basis.
The continuous phase of the silicone release coating dispersion may optionally further comprise a solvent. The solvent may be added during preparation of the silicone release coating composition to facilitate flow of the composition and introduction of certain starting materials, such as the hydrosilylation reaction catalyst. Solvents that can be used herein are those that help fluidize the starting materials of the silicone release coating composition but essentially do not react with the starting materials. The solvent may be selected based on solubility the starting materials and volatility of the solvent. The solubility refers to the solvent being sufficient to dissolve and/or disperse a starting material. Volatility refers to vapor pressure of the solvent. If the solvent is too volatile (having too high vapor pressure) bubbles may form during hydrosilylation reaction, and the bubbles may cause cracks or otherwise weaken or detrimentally affect properties of the reaction product. However, if the solvent is not volatile enough (too low vapor pressure) the solvent may remain as a plasticizer in the silicone release coating prepared by curing the silicone release coating composition.
Suitable solvents include polyorganosiloxanes with suitable vapor pressures, such as hexamethyldisiloxane, octamethyltrisiloxane, hexamethylcyclotrisiloxane and other low molecular weight polyorganosiloxanes, such as 0.5 to 1.5 cSt DOWSIL™ 200 Fluids and DOWSIL™ OS FLUIDS, which are commercially available from DSC.
Alternatively, the solvent may comprise an organic solvent. The organic solvent can be an aromatic hydrocarbon such as benzene, toluene, ethylbenzene or xylene; an aliphatic hydrocarbon such as heptane, hexane, or octane; or a halogenated hydrocarbon such as dichloromethane, 1,1,1-trichloroethane or methylene chloride. Alternatively, the solvent may be selected from the group consisting of benzene, toluene, xylene, ethyl benzene, heptane, and a combination of two or more thereof.
The amount of solvent will depend on various factors including the type of solvent selected and the amount and type of other starting materials selected for the silicone release coating composition. However, the amount of solvent may range from 1% to 99%, alternatively 2% to 90%, based on the weight of all starting materials in the silicone release coating composition. Solvent can be added during preparation of the composition, for example, to aid mixing and delivery. All or a portion of the solvent may optionally be removed after the composition is prepared. Alternatively, the continuous phase of the silicone release coating dispersion may comprise up to 90 weight % of the solvent, with a balance to 100 weight % of the continuous phase being the silicone release coating composition.
Starting material (I) is a hydrosilylation reaction inhibitor (inhibitor) that may be used for altering the hydrosilylation reaction, as compared to a composition containing the same starting materials but with the inhibitor omitted. Starting material (I) may be selected from the group consisting of (I1) an acetylenic alcohol, (I2) a silylated acetylenic alcohol, (I3) an ene-yne compound, (I4) a triazole, (I5) a phosphine, (I6) a mercaptan, (I7) a hydrazine, (I8) an amine, (19) a fumarate, (110) a maleate, (I11) an ether, (112) carbon monoxide, (I13) an alkenyl-functional siloxane oligomer, and (114) a combination of two or more thereof. Alternatively, the hydrosilylation reaction inhibitor may be selected from the group consisting of (I1) an acetylenic alcohol, (I2) a silylated acetylenic alcohol, (19) a fumarate, (I10) a maleate, (I13) carbon monoxide, (114) a combination of two or more thereof. Alternatively, the inhibitor may comprise an acetylenic alcohol.
Acetylenic alcohols are exemplified by 3,5-dimethyl-1-hexyn-3-ol, 1-butyn-3-ol, 1-propyn-3-ol, methyl butynyls such as 2-methyl-3-butyn-2-ol and 3-methyl-1-butyn-3-ol, 3-methyl-1-pentyn-3-ol, 3-phenyl-1-butyn-3-ol, 4-ethyl-1-octyn-3-ol, 3,5-dimethyl-1-hexyn-3-ol, and ethynyl cyclohexanols such as 1-ethynyl-1-cyclohexanol, and a combination thereof. Acetylenic alcohols are known in the art and are commercially available from various sources, see for example, U.S. Pat. No. 3,445,420 to Kookootsedes et al. Alternatively, the inhibitor may be a silylated acetylenic compound. Without wishing to be bound by theory, it is thought that adding a silylated acetylenic compound reduces yellowing of the reaction product prepared from hydrosilylation reaction as compared to a reaction product from hydrosilylation of starting materials that do not include a silylated acetylenic compound or that include an organic acetylenic alcohol inhibitor, such as those described above. The silylated acetylenic compound is exemplified by (3-methyl-1-butyn-3-oxy)trimethylsilane, ((1,1-dimethyl-2-propynyl)oxy)trimethylsilane, bis(3-methyl-1-butyn-3-oxy)dimethylsilane, bis(3-methyl-1-butyn-3-oxy)silanemethylvinylsilane, bis((1,1-dimethyl-2-propynyl)oxy)dimethylsilane, methyl(tris(1,1-dimethyl-2-propynyloxy))silane, methyl(tris(3-methyl-1-butyn-3-oxy))silane, (3-methyl-1-butyn-3-oxy)dimethylphenylsilane, (3-methyl-1-butyn-3-oxy)dimethylhexenylsilane, (3-methyl-1-butyn-3-oxy)triethylsilane, bis(3-methyl-1-butyn-3-oxy)methyltrifluoropropylsilane, (3,5-dimethyl-1-hexyn-3-oxy)trimethylsilane, (3-phenyl-1-butyn-3-oxy)diphenylmethylsilane, (3-phenyl-1-butyn-3-oxy)dimethylphenylsilane, (3-phenyl-1-butyn-3-oxy)dimethylvinylsilane, (3-phenyl-1-butyn-3-oxy)dimethylhexenylsilane, (cyclohexyl-1-ethyn-1-oxy)dimethylhexenylsilane, (cyclohexyl-1-ethyn-1-oxy)dimethylvinylsilane, (cyclohexyl-1-ethyn-1-oxy)diphenylmethylsilane, (cyclohexyl-1-ethyn-1-oxy)trimethylsilane, and combinations thereof. The silylated acetylenic compound useful as the inhibitor herein may be prepared by methods known in the art, for example, U.S. Pat. No. 6,677,407 to Bilgrien, et al. discloses silylating an acetylenic alcohol described above by reacting it with a chlorosilane in the presence of an acid receptor.
Alternatively, the inhibitor may be an ene-yne compound such as 3-methyl-3-penten-1-yne, 3,5-dimethyl-3-hexen-1-yne; and a combination thereof. Alternatively, the inhibitor may comprise a triazole, exemplified by benzotriazole. Alternatively, the inhibitor may comprise a phosphine. Alternatively, the inhibitor may comprise a mercaptan. Alternatively, the inhibitor may comprise a hydrazine. Alternatively, the inhibitor may comprise an amine. Amines are exemplified by tetramethyl ethylenediamine, 3-dimethylamino-1-propyne, n-methylpropargylamine, propargylamine, 1-ethynylcyclohexylamine, or a combination thereof. Alternatively, the inhibitor may comprise a fumarate. Fumarates include dialkyl fumarates such as diethyl fumarate, dialkenyl fumarates such as diallyl fumarate, and dialkoxyalkyl fumarates such as bis-(methoxymethyl)ethyl fumarate. Alternatively, the inhibitor may comprise a maleate. Maleates include dialkyl maleates such as diethyl maleate, dialkenyl maleates such as diallyl maleate, and dialkoxyalkyl maleates such as bis-(methoxymethyl)ethyl maleate. Alternatively, the inhibitor may comprise an ether.
Alternatively, the inhibitor may comprise carbon monoxide. Alternatively, the inhibitor may comprise an alkenyl-functional siloxane oligomer, which may be cyclic or linear such as methylvinylcyclosiloxanes exemplified by 1,3,5,7-tetramethyl-1,3,5,7-tetravinylcyclotetrasiloxane, 1,3,5,7-tetramethyl-1,3,5,7-tetrahexenylcyclotetrasiloxane, 1,3-divinyl-1,3-diphenyl-1,3-dimethyldisiloxane; 1,3-divinyl-1,1,3,3-tetramethyldisiloxane; and a combination of two or more thereof. The compounds useful as inhibitors described above are commercially available, e.g., from Sigma-Aldrich Inc. or Gelest, Inc., and are known in the art, for example, see U.S. Pat. No. 3,989,667 to Lee, et al. Suitable inhibitors for use herein are exemplified by those described as stabilizer E in U.S. Patent Application Publication 2007/0099007 at paragraphs [0148] to [0165].
The amount of inhibitor will depend on various factors including the desired pot life, the particular inhibitor used, and the selection and amount of catalyst. However, when present, the amount of inhibitor may be 0% to 1%, alternatively 0% to 5%, alternatively 0.001% to 1%, alternatively 0.01% to 0.5%, and alternatively 0.0025% to 0.025%, based on the weight of all starting materials in the silicone release coating composition.
Starting material (J) is an optional anchorage additive. Without wishing to be bound by theory, it is thought that the anchorage additive will facilitate bonding to a backing substrate by a silicone release coating prepared from the silicone release coating dispersion described herein.
Suitable anchorage additives include silane coupling agents such as methyltrimethoxysilane, vinyltrimethoxysilane, allyltrimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-aminopropyltrimethoxysilane, N-(2-aminoethyl)-3-aminopropyltrimethoxysilane, bis(trimethoxysilyl)propane, and bis(trimethoxysilylhexane; and mixtures or reaction mixtures of said silane coupling agents. Alternatively, the anchorage additive may be tetramethoxysilane, tetraethoxysilane, dimethyldimethoxysilane, methylphenyldimethoxysilane, methylphenyldiethoxysilane, phenyltrimethoxysilane, methyltrimethoxysilane, methyltriethoxysilane, vinyltriethoxysilane, allyltriethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, or 3-methacryloxypropyl trimethoxysilane.
Exemplary anchorage additives are known in the art, such as in U.S. Patent Publication 2012/0328863 at paragraph [0091] and U.S. Patent Publication 2017/0233612 at paragraph [0041]. Anchorage additives are commercially available. For example, SYL-OFF™ 297, SYL-OFF™ SL 9176, and SYL-OFF™ SL 9250 are available from DSC. Other exemplary anchorage additives include (J-1) vinyltriacetoxysilane, (J-2)glycidoxypropyltrimethoxysilane, and (J-3) a combination of (J-1) and (J-2). This combination (J-3) may be a mixture and/or a reaction product.
The amount of anchorage additive depends on various factors including the type of substrate to which the composition will be applied. However, the amount of anchorage additive may be 1% to 5%, alternatively 1% to 3%, and alternatively 1.9% to 2.1%, based on combined weights of all starting materials in the composition.
The silicone release coating dispersion described above further comprises (II) a surfactant. The surfactant is capable of forming a dispersion of the aqueous discontinuous phase comprising the ionic liquid and water, described above, in the continuous phase comprising the silicone release coating composition, also described above. The surfactant comprise (D) a silicone polyether.
The silicone polyether has unit formula (D1):(R31SiO1/2)2(R21SiO2/2)e(R1R3SiO2/2)f, where R1 is as described above, each R3 is an independently selected polyether group, subscript e is 1 to 500, alternatively 1 to 200, alternatively 1 to 50, alternatively 40 to 50, and alternatively 10 to 45; and subscript f is 1 to 1000, alternatively 1 to 300, alternatively 1 to 40, alternatively 1 to 5, and alternatively 2 to 5. R3, the polyether group, has formula (D1)gO(D2O)hR4, where each D1 is an independently selected divalent hydrocarbon group of 2 to 4 carbon atoms, each D2 is an independently selected divalent hydrocarbon group of 2 to 4 carbon atoms, R4 is selected from the group consisting of H or an alkyl group of 1 to 10 carbon atoms, subscript g is 1 to 20, alternatively 1 to 3, and subscript h is 1 to 50, alternatively 4 to 50, and alternatively 8 to 40. Alternatively, D1 may have formula CpH2p, where subscript p is 3 to 12, alternatively 3 to 6. Alternatively, each D2 may be selected from the group consisting of C2H4 and C3H6. Alternatively, R4 may be H. Suitable (D) silicone polyethers are known in the art and may be made by known methods, such as those disclosed in U.S. Pat. No. 8,877,886 to Souda, et al. Suitable silicone polyethers for starting material (D) are commercially available, for example, DOWSIL™ ES-5612 is commercially available from DSC.
Starting material (II), the surfactant may optionally further comprise a cosurfactant. The cosurfactant may be a second silicone polyether that differs from (D1) in at least one respect, an organic polyether, or a combination thereof.
The second silicone polyether may have unit formula (D2): formula (R31SiO1/2)2(R21SiO2/2)e′(R1R5SiO2/2), where R1 and R2 are as described above, subscript e′ and subscript f′ represent average numbers of difunctional units per molecule and have values such that e is 0 to 500, alternatively 0 to 200, alternatively 0 to 50, and alternatively 0 to 45, with the proviso that e′<e; and subscript f′ is 1 to 1000, alternatively 1 to 300, alternatively 1 to 40, alternatively 1 to 5, and alternatively 1 to 2. Rs has formula—(D1)gO(D3O)iH, where each D3 is an independently selected divalent hydrocarbon group of 2 to 4 carbon atoms, subscript g is 1 to 20, alternatively 1 to 3, and subscript i is 1 to 50. Alternatively, each D3 may be selected from the group consisting of C2H4 and C3H6. Alternatively, subscript i may be 1 to 10, and alternatively 5 to 10. Alternatively, in unit formula (D2), subscript e′ may be 0, and subscript f′ may be 1. Silicone polyethers of formula (D2) are commercially available, for example, XIAMETER™ OFX-5211 is commercially available from DSC.
Alternatively, the silicone polyether cosurfactant may have a rake type structure wherein the polyoxyethylene or polyoxyethylene-polyoxypropylene copolymeric units are grafted onto the siloxane backbone, or the silicone polyether can have an ABA block copolymeric structure wherein A represents the polyether portion and B the siloxane portion of an ABA structure. Alternatively, the SPE may have a resinous structure, such as a polyorganosilicate resin having polyether groups bonded to silicon atoms therein. Suitable SPE's include DOWSIL™ OFX-5329 Fluid from DSC. Other silicone polyether surfactants are known in the art and are also commercially available, e.g., DOWSIL™ 502W and DOWSIL™ 67 Additive are commercially available from DSC.
Alternatively, the cosurfactant may comprise an organic polyether. Suitable organic polyethers are known in the art and are commercially available. For example, suitable organic polyethers include DOWFAX™ nonionic surfactants, e.g., linear EO/PO block copolymers, such as the DOWFAX™ N series, available from TDCC.
The amount of (II) the surfactant in the silicone release coating dispersion depends on various factors including the selection and amounts of (C) the branched polyorganosiloxane polymer and (E) the polydiorganosiloxane having at least two aliphatically unsaturated groups per molecule, however, the amount of (II) the surfactant may be 0.1 weight parts to 5 weight parts, based on combined weights of starting materials (C) and (E). Alternatively, the amount of (D1) the silicone polyether may be 0.1 weight parts to 5 weight parts, based on combined weights of starting materials (C) and (E). Alternatively, when the cosurfactant is present, the amount of (D1) the silicone polyether may be 0.1 weight parts to <5 weight parts, based on combined weights of starting materials (C) and (E).
Other optional starting materials may be present in the silicone release coating dispersion, including, for example, reactive diluents, fragrances, preservatives, colorants, dyes, pigments, anti-oxidants, heat stabilizers, flame retardants, flow control additives, biocides, fillers (including extending and reinforcing fillers), surfactants, thixotroping agents, and pH buffers. The composition may be in any form and may be incorporated into further compositions. Alternatively, the silicone release coating dispersion may be free of particulates or contains only a limited amount of particulate (e.g., filler and/or pigment), such as 0 to 30% by weight of the dispersion. Without wishing to be bound by theory, it is thought that particulates can agglomerate or otherwise stick to the coater equipment used to form the silicone release coating. In addition, particulates can hinder optical properties, for example transparency, of the silicone release coating and of the release liner formed therewith, if optical transparency is desired, and/or the particulates may be prejudicial to the adherence of an adherend.
The silicone release coating dispersion may be free from fluoroorganosilicone compounds. It is believed that, during the cure, a fluorocompound, because of its low surface tension, may rapidly migrate to the interface of the dispersion or the silicone release coating formed therewith and a substrate on which the dispersion is applied and the silicone release coating is formed, for example a dispersion/PET film interface. Such migration may detrimentally affect anchorage of the silicone release coating (prepared by curing) to the substrate by making a fluorine containing barrier. By making a barrier, the fluoroorganosilicone compounds may prevent any starting material of the silicone release coating dispersion from reacting at the interface, impacting curing and/or anti-static properties. Moreover, fluoroorganosilicone compounds are usually expensive.
The silicone release coating dispersion described above may be prepared by a method comprising:
Step (1) may be performed by any convenient means, such as mixing at RT or elevated temperature, in batch, semi-batch, or continuous equipment. Mixing in step (1) may occur, for example using, batch mixing equipment with medium/low shear such as change-can mixers, double-planetary mixers, conical-screw mixers, ribbon blenders, double-arm or sigma-blade mixers. Alternatively, batch equipment with high-shear and/or high-speed dispersers can be used in step (1), step (2), and/or step (3), and these include equipment such as that made by Charles Ross & Sons (NY), Hockmeyer Equipment Corp. (NJ); batch mixing equipment such as those sold under the tradename Speedmixer™; and batch equipment with high shear actions include Banbury-type (CW Brabender Instruments Inc., NJ) and Henschel type (Henschel mixers America, TX). Illustrative examples of continuous mixers/compounders include extruders single-screw, twin-screw, and multi-screw extruders, co-rotating extruders, such as those manufactured by Krupp Werner & Pfleiderer Corp (Ramsey, NJ), and Leistritz (NJ); extruders such as twin-screw counter-rotating extruders, two-stage extruders, twin-rotor continuous mixers, dynamic or static mixers or combinations of these equipment. Steps (2) and (3) may also be performed at RT.
The silicone release coating dispersion prepared as described above may be used to prepare a release liner. The release liner may be prepared by a method comprising: optionally (I) treating a surface of a backing substrate, (II) coating the silicone release coating dispersion as described above on the surface of the backing substrate, (III) drying the silicone release coating dispersion to form a film, and (IV) curing the film to form a silicone release coating on the surface of the backing substrate.
In step (I), the backing substrate (substrate) is not limited. The substrate may comprise a plastic, which maybe a thermosetting and/or thermoplastic. However, the substrate may alternatively be or comprise glass, metal, cellulose (e.g. paper), cardboard, paperboard, a polymeric material, or a combination thereof. Specific examples of suitable substrates include paper substrates such as Kraft paper, polyethylene coated Kraft paper (PEK coated paper), thermal paper, and regular papers; polymeric substrates such polyamides (PA); polyesters such as polyethylene terephthalates (PET), polybutylene terephthalates (PET), polytrimethylene terephthalates (PTT), polyethylene naphthalates (PEN), and liquid crystalline polyesters; polyolefins such as polyethylenes (PE), polypropylenes (PP), and polybutylenes; styrenic resins; polyoxymethylenes (POM); polycarbonates (PC); polymethylenemethacrylates (PMMA); polyvinyl chlorides (PVC); polyphenylene sulfides (PPS); polyphenylene ethers (PPE); polyimides (PI); polyamideimides (PAI); polyetherimides (PEI); polysulfones (PSU); polyethersulfones; polyketones (PK); polyetherketones; polyvinyl alcohols (PVA); polyetheretherketones (PEEK); polyetherketoneketones (PEKK); polyarylates (PAR); polyethernitriles (PEN); phenolic resins; phenoxy resins; celluloses such as triacetylcellulose, diacetylcellulose, and cellophane; fluorinated resins, such as polytetrafluoroethylenes; thermoplastic elastomers, such as polystyrene types, polyolefin types, polyurethane types, polyester types, polyamide types, polybutadiene types, polyisoprene types, and fluoro types; and copolymers, and combinations thereof.
In step (I), treating the surface of the substrate before applying the release coating dispersion may be performed by any convenient means such as a plasma treatment or a corona discharge treatment. Alternatively, the substrate may be treated by applying a primer. Step (I) is optional and may be absent.
The silicone release coating dispersion can, for example, be applied to the substrate by any convenient means such as spraying, doctor blade, dipping, screen printing or by a roll coater, e.g. an offset web coater, kiss coater or etched cylinder coater.
In step (II), the silicone release coating dispersion can be applied to any substrate, such as those described above. Alternatively, the silicone release coating composition may be applied to polymer film substrates, for example polyester, particularly polyethylene terephthalate (PET), polyethylene, polypropylene, polyester, or polystyrene films. The silicone release coating dispersion can alternatively be applied to a paper substrate, including plastic coated paper, for example paper coated with polyethylene, glassine, super calender paper, or clay coated kraft. The release coating composition can alternatively be applied to a metal foil substrate, for example aluminum foil.
Step (III) may be performed by any conventional means, such as heating at 50° C. to 100° C. for a time sufficient to remove all or a portion of (B) the water, and when present, (H) the solvent. The method may further comprise curing the silicone release coating composition to form the silicone release coating on the surface of the substrate. Curing may be performed by any conventional means such as heating at 100° C. to 200° C.
Under production coater conditions, cure can be effected in a residence time of 1 second to 6 seconds, alternatively 1.5 seconds to 3 seconds, at an air temperature of 120° C. to 150° C. Heating can be performed in an oven, e.g., an air circulation oven or tunnel furnace or by passing the coated substrate around heated cylinders.
The following examples are presented to illustrate the invention to one skilled in the art and are not to be construed to limit the scope of the invention set forth in the claims. Starting materials used in these examples are described in Table 1.
Starting materials branded DOWSIL™, SYL-OFF™, and XIAMETER™ are commercially available from DSC. The Lithium Salts were purchased from Monils Chemical Engineering Science & Technology (Shanghai) Co., Ltd. The toluene was obtained from Sinopharm Chemical Reagent Co. LTD. Anti-static Additives 2 and 3 were also purchased from Monils Chemical Engineering Science & Technology (Shanghai) Co., Ltd.
In this Reference Example 1, silicone release coating dispersions were prepared as follows:
In this Reference Example 2, the silicone release coating dispersions prepared according to Reference Example 1 were coated on a PET film ((210 cm×297 cm, 50 μm, corona-treated) with a Mayer rod (#6) at a speed of 10 cm s−1, which corresponded to a coating weight of 0.6-0.8 g m−2. The resulting films were then dried and cured by heating at 140° C. for 30 s and then cooled to room temperature, thereby forming release liners comprising silicone release coatings on the surface of the PET films.
In this Reference Example 3, surface resistance of each silicone release coating prepared as described in Reference Example 2 was measured by a digital surface resistance metre (TECMAN, TM385, measuring range: 103-1012Ω sq−1 accuracy: ±10%) at room temperature (20-25° C.). The measurement of surface resistance was performed in triplicate, at three different places on each silicone release coating. The coating weight (CW), i.e., the areal density of the silicone release coating, was determined by an X-Ray fluorescence spectrometer (XRF, Oxford Lab-X Supreme8000) with a bare PET film as the reference. The silicone release coatings were aged for either 7 days or 30 days before testing.
In this Reference Example 4, release force at room temperature (RF-RT) was evaluated using the 180 degree peeling test to measure release force from the release liner. A Tesa 7475 standard tape was laminated on a (cured) silicone release coating, a loaded weight of 20 g/cm2 was placed on the laminated sample and left under RT (room temperature of 25° C.) for 20 hours. After 20 hours, the loaded weight was removed, and the sample was allowed to rest for 30 minutes. The release force was then tested by a ChemInstruments AR-1500 using FINAT Test Method No. 10 (FINAT Technical Handbook 7th edition, 2005).
Release force after aging at 70° C. (RF-70° C. aging) was evaluated using the 180 degree peeling test to measure release force from the release liner. A Tesa 7475 standard tape was laminated on a (cured) silicone release coating, a loaded weight of 20 g/cm2 was placed on the laminated sample and left under 70 3C for 20 hours. After 20 hours, the loaded weight was removed and the sample allowed to rest for 30 minutes. Release force was then tested by ChemInstruments AR-1500 using FINAT Test Method No. 10 (FINAT Technical Handbook 7th edition, 2005).
Coat weight was evaluated as described above in Reference Example 3, and thereafter an Abrasion Tester (Elcometer 1720) was used to rub each sample 30 cycles at a speed of 30 cycles/minute. The coat weight after Rub off was evaluated as described above again to measure the relative anchorage performance. Anchorage was calculated as (CW after Rub-off)/(CW before Rub-off)×100%.
Comparative Examples 1 and 5 (CE1, CE5) showed that silicone release coatings prepared from silicone release coating compositions without an anti-static additive were insulating under the conditions tested, and thus unable to dissipate static charges, as shown by the Surface Resistance values≥1012Ω sq−1 in Table 2.
Comparative Examples 2 and 3 (CE2, CE3) showed that conventional anti-static additives ([BMIM][TFSI]) and ([MeBu3N][TFSI]) did not provide sufficient anti-static effects to a silicone release coating prepared from silicone release coating compositions containing these conventional anti-static additives. Under the conditions tested, the Surface Resistance values for both CE1 and CE2 were ≥1012Ω sq−1 as shown in Table 2. Without wishing to be bound by theory, it is thought that the poor anti-static effects were due to immiscibility of the conventional anti-static additives in silicone release coating compositions.
Comparative Example 4 (CE4) was prepared according to the method described in U.S. Patent Application Publication 2020/0048508A1, in which a lithium salt was directly blended into the silicone release coating composition. The resulting silicone release coating had poor resistance values, showing that the silicone release coating dispersion prepared as described herein (in the working examples) had superior performance under the conditions tested.
Working Examples 1 and 2 (IE1, IE2) contained 10% and 20%, respectively, of anti-static additive 1 and showed surface resistance decreased by several orders of magnitude after the films being left at room temperature for several days.
Working Example 3 (IE3) contained 30% of anti-static additive 1 and exhibited a surface resistance of 108 Ω sq−1 after 30 d. The large quantity of anti-static additive 1 may impact the appearance of the silicone release coating, thus making this silicone release coating composition more suitable for use in applications not requiring a transparent silicone release coating.
Working Example 4 (IE4) showed that adding surfactant XIAMETER™ OFX-5211 into the silicone release coating composition of IE2 still provided a silicone release coating with surface resistance ≤1011Ω sq−1, which was less than that in all of the comparative examples in Table 2.
IE5, IE6, IE7: The fraction of anti-static additive 1 in the water-in-silicone emulsion was reduced to 20% by decreasing concentration of the anti-static additive in the internal phase, compared with IE1-IE4 where the anti-static additive 1 accounted for 40%. of the aqueous phase. The quantity of anti-static additive 1 was reduced by half when the same amount of aqueous phase was combined with the other starting materials. As a result, a surface resistance of 109Ω sq−1 was recorded with 10% of anti-static additive 1 (IE5, IE6). The addition of cosurfactant (XIAMETER™ OFX-5211) did not alter the initial resistance, but did have an impact on the resistance after aging at room temperature, under the conditions tested. The surface resistance decreased to 108Ω sq−1 from seven days onwards with additional 2% of cosurfactant (IE6). Further reduction the content of anti-static additive 1 diminished the initial conductivity (IE7) under the conditions tested.
Ionic liquids, which comprise large ions with bulky substituents, particularly lithium salts, are useful as anti-static agents, but are poorly miscible with non-polar polyorganosiloxanes. Therefore, ionic liquids are prone to separate from polyorganosiloxane matrices, which may lead to structural defects and appearance flaws in silicone release coatings prepared from compositions containing polyorganosiloxane matrices and ionic liquids, such as those disclosed in U.S. Patent Application Publication 2020/0048508A1. In addition, the degree of dissociation and ionic mobility of the ionic liquid are limited in non-polar matrices, which results in limited ionic conductivity. Although lithium salts have been previously used as anti-static additives in silicone release coatings, these may achieve a surface resistance≥1012Ω sq−1, which is higher than desired for providing anti-static properties to a silicone release coating for some applications.
The present silicone release coating dispersion incorporates a water-soluble ionic liquid and a silicone release coating composition. As shown in the examples above, a film formed from the silicone release coating dispersion can be dried and cured to form a silicone release coating with a surface resistance≤10l Q sq−1 after 7 to 30 days under the conditions tested. One or more orders of magnitude improvement (i.e. reduction) in surface resistance can be achieved using the silicone release coating dispersion described herein to prepare a silicone release coating.
All amounts, ratios, and percentages are by weight unless otherwise indicated. The amounts of all starting materials in a composition total 100% by weight. The Summary and the Abstract are hereby incorporated by reference. The articles ‘a’, ‘an’, and ‘the’ each refer to one or more, unless otherwise indicated by the context of specification. The singular includes the plural unless otherwise indicated. The term “comprising” and derivatives thereof, such as “comprise” and “comprises” are used herein in their broadest sense to mean and encompass the notions of “including,” “include,” “consist(ing) essentially of,” and “consist(ing) of. The use of “for example,” “e.g.,” “such as,” and “including” to list illustrative examples does not limit to only the listed examples. Thus, “for example” or “such as” means “for example, but not limited to” or “such as, but not limited to” and encompasses other similar or equivalent examples.
It is to be understood that the appended claims are not limited to express and particular compounds, compositions, or methods described in the detailed description, which may vary between particular embodiments which fall within the scope of the appended claims. With respect to any Markush groups relied upon herein for describing particular features or aspects of various embodiments, different, special, and/or unexpected results may be obtained from each member of the respective Markush group independent from all other Markush members. Each member of a Markush group may be relied upon individually and or in combination and provides adequate support for specific embodiments within the scope of the appended claims.
Abbreviations used herein are defined in Table 4.
In a first embodiment, a method for making a silicone release coating dispersion comprises:
In a second embodiment, in the method of the first embodiment, the additional starting materials in step (III) further comprise a starting material selected from the group consisting of (H) a solvent, (I) a hydrosilylation reaction inhibitor, (J) an anchorage additive, or a combination of two or more of (H), (I), and (J).
In a third embodiment, the method of the first embodiment or the second embodiment further comprises adding a cosurfactant in step (II).
In a fourth embodiment, in the method of any one of the first to third embodiments, (A) the ionic liquid comprises:
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2021/115592 | 8/31/2021 | WO |
