Adhesive compositions comprising a silsesquioxane polymer crosslinker, articles and methods

Abstract
A pressure sensitive adhesive composition is described comprising at least one low Tg (meth)acrylic polymer, and at least one silsesquioxane polymer crosslinker comprising a plurality of ethylenically unsaturated groups. The low Tg (meth)acrylic polymer typically has a Tg no greater than 10° C. In some embodiments, the low Tg (meth)acrylic polymer comprises at least 50, 55, 60, 65, or 70 wt-% of polymerized units derived from low Tg ethylenically unsaturated monomer(s). The low Tg ethylenically unsaturated monomer(s) is typically an alkyl (meth)acrylate comprising 4 to 20 carbon atoms. Also described are pressure sensitive adhesive articles and methods of preparing such articles.
Description
SUMMARY

In one embodiment, a pressure sensitive adhesive composition is described comprising at least one low Tg (meth)acrylic polymer, and at least one silsesquioxane polymer crosslinker comprising a plurality of ethylenically unsaturated groups. The low Tg (meth)acrylic polymer typically has a Tg no greater than 10° C. In some embodiments, the low Tg (meth)acrylic polymer comprises at least 50, 55, 60, 65, or 70 wt-% of polymerized units derived from low Tg ethylenically unsaturated monomer(s). The low Tg ethylenically unsaturated monomer(s) is typically an alkyl (meth)acrylate comprising 4 to 20 carbon atoms.


The silsesquioxane polymer crosslinker typically comprises a three-dimensional branched network having the formula:




embedded image



wherein:


the oxygen atom at the * is bonded to another Si atom within the three-dimensional branched network;


R is an organic group comprising an ethylenically unsaturated group;


R2 is an organic group that is not an ethylenically unsaturated group; and


n is at least 2 and m is at least 1.


The silsesquioxane polymer crosslinker may comprise a core comprising a first silsesquioxane polymer and an outer layer comprising a second (different) silsesquioxane polymer bonded to the core wherein the silsesquioxane polymer of the core, outer layer, or a combination thereof comprises ethylenically unsaturated groups.


In some embodiments, the silsesquioxane polymer crosslinker comprises terminal groups having the formula —Si(R3)3 wherein R3 is independently selected from alkyl, aryl, aralkyl, or alkaryl; optionally further comprising substituents.


In favored embodiments, the ethylenically unsaturated groups of the silsesquioxane polymer are vinyl, vinyl ether, alkenyl or combinations thereof.


Also described are pressure sensitive adhesive articles and method of preparing adhesive articles.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is an illustrative schematic of a silsesquioxane polymer crosslinker.





DETAILED DESCRIPTION

The present disclosure describes adhesives that can be prepared from composition comprising a low Tg (meth)acrylic polymer, as well as articles. In some embodiments, the adhesive is a pressure sensitive adhesive (PSA), prior to crosslinking. In other embodiments, the crosslinked adhesive is a pressure sensitive adhesive (PSA). A PSA generally provides a suitable balance of tack, peel adhesion, and shear holding power. Further, the storage modulus of a PSA at the application temperature, typically room temperature (25° C.), is generally less than 3×106 dynes/cm2 (i.e. 3×105 Pa) at a frequency of 1 Hz. In some embodiments, the adhesive is a PSA at an application temperature that is greater than room temperature. For example, the application temperature may be 30, 35, 40, 45, 50, 55, or 65° C. In this embodiment, the storage modulus of the adhesive at room temperature (25° C.) can be greater than 3×106 dynes/cm2 at a frequency of 1 Hz.


The term “alkyl” includes straight-chained, branched, and cyclic alkyl groups and includes both unsubstituted and substituted alkyl groups. Unless otherwise indicated, the alkyl groups typically contains from 1 to 30 or 1-20 carbon atoms. Examples of “alkyl” as used herein include, but are not limited to, methyl, ethyl, n-propyl, n-butyl, n-pentyl, isobutyl, t-butyl, isopropyl, n-octyl, 2-octyl, n-heptyl, ethylhexyl, cyclopentyl, cyclohexyl, cycloheptyl, adamantyl, and norbornyl, and the like. Unless otherwise noted, alkyl groups may be mono- or polyvalent.


The term heteroalkyl refers to an alkyl group, as just defined, having at least one catenary carbon atom (i.e. in-chain) replaced by a catenary heteroatom such as O, S, or N.


The term “aryl” refers to a substituent derived from an aromatic ring and includes both unsubstituted and substituted aryl groups. Examples of “aryl” include phenyl, halogenated pheny, and the like.


The term “aralkyl” refers to a monovalent group that is an alkyl group substituted with an aryl group (e.g., as in a benzyl group). The term “alkaryl” refers to a monovalent group that is an aryl substituted with an alkyl group (e.g., as in a tolyl group). Unless otherwise indicated, for both groups, the alkyl portion often has 1 to 10 carbon atoms, 1 to 6 carbon atoms, or 1 to 4 carbon atoms and an aryl portion often has 6 to 20 carbon atoms, 6 to 18 carbon atoms, 6 to 16 carbon atoms, 6 to 12 carbon atoms, or 6 to 10 carbon atoms.


The term “alkylene” refers to a divalent group that is a radical of an alkane and includes groups that are linear, branched, cyclic, bicyclic, or a combination thereof. Unless otherwise indicated, the alkylene group typically has 1 to 30 carbon atoms. In some embodiments, the alkylene group has 1 to 20 carbon atoms, 1 to 10 carbon atoms, 1 to 6 carbon atoms, or 1 to 4 carbon atoms. Examples of alkylene groups include, but are not limited to, methylene, ethylene, 1,3-propylene, 1,2-propylene, 1,4-butylene, 1,4-cyclohexylene, and 1,4-cyclohexyldimethylene.


The term “arylene” refers to a divalent group that is aromatic and, optionally, carbocyclic. The arylene has at least one aromatic ring. Any additional rings can be unsaturated, partially saturated, or saturated. Optionally, an aromatic ring can have one or more additional carbocyclic rings that are fused to the aromatic ring. Unless otherwise indicated, arylene groups often have 6 to 20 carbon atoms, 6 to 18 carbon atoms, 6 to 16 carbon atoms, 6 to 12 carbon atoms, or 6 to 10 carbon atoms.


The term “aralkylene” refers to a divalent group that is an alkylene group substituted with an aryl group or an alkylene group attached to an arylene group. The term “alkarylene” refers to a divalent group that is an arylene group substituted with an alkyl group or an arylene group attached to an alkylene group. Unless otherwise indicated, for both groups, the alkyl or alkylene portion typically has from 1 to 20 carbon atoms, 1 to 10 carbon atoms, 1 to 6 carbon atoms, or 1 to 4 carbon atoms. Unless otherwise indicated, for both groups, the aryl or arylene portion typically has from 6 to 20 carbon atoms, 6 to 18 carbon atoms, 6 to 16 carbon atoms, 6 to 12 carbon atoms, or 6 to 10 carbon atoms.


The term “hydrolyzable group” refers to a group that can react with water having a pH of 1 to 10 under conditions of atmospheric pressure. The hydrolyzable group is often converted to a hydroxyl group when it reacts. The hydroxyl group often undergoes further reactions (e.g. condensation). Typical hydrolyzable groups include, but are not limited to, alkoxy, aryloxy, aralkyloxy, alkaryloxy, acyloxy, or halogen (directly boned to s silicon atom. As used herein, the term is often used in reference to one of more groups bonded to a silicon atom in a silyl group.


“Renewable resource” refers to a natural resource that can be replenished within a 100 year time frame. The resource may be replenished naturally or via agricultural techniques. The renewable resource is typically a plant (i.e. any of various photosynthetic organisms that includes all land plants, inclusive of trees), organisms of Protista such as seaweed and algae, animals, and fish. They may be naturally occurring, hybrids, or genetically engineered organisms. Natural resources such as crude oil, coal, and peat which take longer than 100 years to form are not considered to be renewable resources.


When a group is present more than once in a formula described herein, each group is “independently” selected unless specified otherwise.


Presently described are (e.g. pressure sensitive) adhesive compositions comprising at least one low Tg (meth)acrylic polymer and at least one silsesquioxane polymer crosslinker comprising a plurality of ethylenically unsaturated groups.


A silsesquioxane (SSQ) is an organosilicon compound with the empirical chemical formula R′SiO3/2 where Si is the element silicon, O is oxygen and R′ is either hydrogen or an aliphatic or aromatic organic group that optionally further comprises an ethylenically unsaturated group. Thus, silsesquioxanes polymers comprise silicon atoms bonded to three oxygen atoms. Silsesquioxanes polymers that have a random branched structure are typically liquids at room temperature. Silsesquioxanes polymers that have a non-randomstructure like cubes, hexagonal prisms, octagonal prisms, decagonal prisms, and dodecagonal prisms are typically solids as room temperature.


The SSQ polymer crosslinker comprises a plurality of ethylenically unsaturated groups. The ethylenically unsaturated groups of the SSQ polymer are typically free-radically polymerizable groups such as vinyl (H2C═CH—) including vinyl ethers (H2C═CHO—) and alkenyl (H2C═CH(CH2)n— wherein —(CH2)n— is alkylene as previously defined. The ethylenically unsaturated groups of the SSQ polymer may also be (meth)acryl such as (meth)acrylamide (H2C═CHCONH— and H2C═CH(CH3)CONH—) and (meth)acrylate(CH2═CHCOO— and CH2═C(CH3)COO—). The term “(meth)acrylate” includes both methacrylate and acrylate.


Silsesquioxane polymers comprising a plurality of ethylenically unsaturated groups can be made by hydrolysis and condensation of hydrolyzable silane reactants, such as alkoxy silanes, that further comprise an ethylenically unsaturated group, as known in the art. See for example U.S. Publication No. 2014/0178698, and Provisional Patent Application Nos. 61/913,568, filed Dec. 9, 2014; 62/014,735, filed Jun. 20, 2014; and 62/014,778, filed Jun. 20, 2014; incorporated herein by reference.


In some embodiments, the silsesquioxane polymer crosslinker can be a homopolymer, characterized as a three-dimensional branched network having the formula:




embedded image



wherein R is an organic group comprising an ethylenically unsaturated group and the oxygen atom at the * is bonded to another Si atom within the three-dimensional branched network. In some embodiments, R has the formula Y—Z, as can be derived from a reactant Z—Y—Si(R1)3, wherein R1 is a hydrolyzable group, Y is a covalent bond (as depicted in the formula) or a divalent organic linking group, and Z is an ethylenically unsaturated group, as previously described.


Examples of Z—Y—Si(R1)3 reactants include vinyltriethoxysilane, allyltriethoxysilane, allylphenylpropyltriethoxysilane, 3-butenyltriethoxysilane, docosenyltriethoxysilane, hexenyltriethoxysilane, and methacryloxylpropyltrimethoxyl silane.


In some embodiments, Y is a (e.g. C1-C20) alkylene group, a (e.g. C6-C12) arylene group, a (e.g. C6-C12)alk (e.g. C1-C20)arylene group, a (e.g. C6-C12)ar (e.g. C1-C20) alkylene group, or a combination thereof. Y may optionally further comprise (e.g. contiguous) oxygen, nitrogen, sulfur, silicon, or halogen substituents, and combinations thereof. In some embodiments, Y does not comprise oxygen or nitrogen substituents that can be less thermally stable.


The number of polymerized units, n, is at least 2, 3, 4, 5, 6, 7, 8, 9, or 10. In some embodiments, n is at least 15, 20, 25, 30, 35, 40, 45, or 50. In some embodiments, n is no greater than 500, 450, 400, 350, 300, 250 or 200.


In other embodiments, the silsesquioxane polymer crosslinker can be a copolymer, characterized as a three-dimensional branched network having the formula:




embedded image



wherein R is an organic group comprising an ethylenically unsaturated group as previously described, R2 is an organic group lacking an ethylenically unsaturated group, the oxygen atom at the * is bonded to another Si atom within the three-dimensional branched network, and n is at least 2 and m is at least 1. In some embodiments, R2 has the formula Y—X, as can be derived from a reactant X—Y—Si(R1)3, wherein R1 is a hydrolyzable group, Y is a covalent bond (as depicted in the formula) or a divalent organic linking group as previously described. X is hydrogen, a (monovalent) organic group such as alkyl, aryl, aralkyl, or alkaryl that may optionally comprise halogen or other substituents; or a reactive group that is not an ethylenically unsaturated group. X may optionally further comprise (e.g. contiguous) oxygen, nitrogen, sulfur, silicon, substituents. In some embodiments, X is an optionally halogenated (e.g. C1-C20) alkyl group such as (e.g. C4-C6) fluoroalkyl, a (e.g. C6-C12)aryl group such as phenyl, a (e.g. C6-C2)alk (e.g. C1-C20)aryl group, a (e.g. C6-C12)ar(e.g. C1-C20)alkyl group. In some embodiments, X comprises an epoxide ring.


Examples of X—Y—Si(R1)3 reactants include for example aromatic trialkoxysilanes such as phenyltrimethoxylsilane, (C1-C12) alkyl trialkoxysilanes such as methyltrimethoxylsilane, fluoroalkyl trialkoxysilanes such as nonafluorohexyltriethoxysilane, and trialkoxysilanes comprising a reactive group that is not an ethylenically unsaturated group such as glycidoxypropyltriethoxysilane; 3-glycidoxypropyltriethoxysilane 5,6-epoxyhexyltriethoxysilane; 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane 3-(diphenylphosphino)propyltriethoxysilane; mercaptopropyltriethoxysilane; s-(octanoyl)mercaptopropyltriethoxysilane; 3-isocyanatopropyltriethoxysilane; hydroxy(polyethyleneoxy)propyl]triethoxysilane; hydroxymethyltriethoxysilane; 3-cyanopropyltriethoxysilane; 2-cyanoethyltriethoxysilane; and 2-(4-pyridylethyl)triethoxysilane.


Other commercially available X—Y—Si(R1)3 reactants include for example trimethylsiloxytriethoxysilane; p-tolyltriethoxysilane; tetrahydrofurfuryloxypropyltriethoxysilane; n-propyltriethoxysilane; (4-perfluorooctylphenyl)triethoxysilane; pentafluorophenyltriethoxysilane; nonafluorohexyltriethoxysilane; 1-naphthyltriethoxysilane; 3,4-methylenedioxyphenyltriethoxysilane; p-methoxyphenyltriethoxysilane; 3-isooctyltriethoxysilane; isobutyltriethoxysilane; (heptadecafluoro-1,1,2,2-tetrahydrodecyl)triethoxysilane; 3,5-dimethoxyphenyltriethoxysilane; (n,n-diethylaminomethyl)triethoxysilane; n-cyclohexylaminomethyl)triethoxysilane; 11-chloroundecyltriethoxysilane; 3-chloropropyltriethoxysilane; p-chlorophenyltriethoxysilane; chlorophenyltriethoxysilane; butylpoly(dimethylsiloxanyl)ethyltriethoxysilane; n,n-bis(2-hydroxyethyl)-3-aminopropyltriethoxysilane; benzyltriethoxysilane; and 2-[(acetoxy(polyethyleneoxy)propyl]triethoxysilane.


The reactant X—Y—Si(R1)3 and/or Z—Y—Si(R1)3 comprises three R1 groups. In order to form a silsesquioxane polymer at least two of the R1 groups are independently a hydrolyzable group. In typical embodiments, based on commercially available reactants, each R1 group is independently a hydrolyzable group. In some embodiments of R1, the hydrolyzable group is selected from alkoxy, aryloxy, aralkoxy, alkaryloxy, acyloxy, and halo. In some embodiments, R1 is an alkoxy group.


SSQ copolymer crosslinkers can also be prepared from at least one X—Y—Si(R1)3 reactant and at least one Z—Y—Si(R1)3. For example, vinyltriethoxylsilane or allytriethoxysilane can be coreacted with an alkenylalkoxylsilane such as 3-butenyltriethoxysilane and hexenyltriethoxysilane. Representative copolymers include for example vinyl-co-nonafluorohexyl silsequioxane, vinyl-co-glycidoxylpropyl silsesquioxane, vinyl-co-phenyl silsesquioxane, vinyl-co-methyl silsesquioxane, vinyl-coethyl silsesquioxane, and vinyl-co-hydro silsesquioxane.


The inclusion of the silsesquioxane compound having an R2 group that is not an ethylenically unsaturated group can be used to enhance certain properties depending on the selection of the R2 group. For example, when R2 comprises an aromatic group such as phenyl, the thermal stability can be improved (relative to a homopolymer of vinyltrimethoxysilane). When R2 comprises a reactive group, such as an epoxy, improved hardness can be obtained (relative to a homopolymer of vinyltrimethoxysilane). Further, when R2 comprises a fluoroalkyl group, the hydrophobicity can be improved.


SSQ copolymer crosslinkers may comprise at least two different X groups (e.g. X′ and X″), yet the same Y groups. Alternatively, the silsesquioxane polymers may comprise at least two different Y groups (e.g. Y′ and Y″), yet the same X group. Further, the silsesquioxane polymers may comprise at least two reactants wherein both Y and X are different from each other. In such embodiment, R2 of the silsesquioxane polymer formula is independently an organic group lacking an ethylenically unsaturated group. Further, m represents the total number of repeat units independently lacking ethylenically unsaturated group.


SSQ copolymer crosslinkers can also be prepared from at least two Z—Y—Si(R1)3 reactants. For example, vinyltriethoxylsilane can be coreacted with allytriethoxysilane. In this embodiment, the silsesquioxane polymers may comprise at least two different Z groups (e.g. Z′ and Z″), yet the same Y groups. Alternatively, the silsesquioxane polymers may comprise at least two different Y groups (e.g. Y′ and Y″), yet the same Z group (e.g. vinyl). Further, the silsesquioxane polymers may comprise at least two reactants wherein both Y and Z are different from each other. In such embodiment, R is independently an organic group comprising an ethylenically unsaturated group (e.g. such as a vinyl group). Further, n represents the total number of repeat units independently comprising an ethylenically unsaturated group.


In yet other embodiments, the silsesquioxane polymer comprises a core comprising a first silsesquioxane polymer and an outer layer comprising a second silsesquioxane polymer bonded to the core wherein the silsesquioxane polymer of the core, outer layer, or a combination thereof comprises ethylenically unsaturated groups, as described in cofiled U.S. Provisional Patent Application Ser. No. 42/014,778. The SSQ polymer of the outer layer is bonded to the SSQ polymer of the core via silicon atoms bonded to three oxygen atoms. The core or outer layer may comprise the SSQ homopolymers and copolymers previously described. In some embodiments, the core has a higher concentration of ethylenically unsaturated groups than the outer layer. In other embodiments, the outer layer has a higher concentration of ethylenically unsaturated groups than the core. In some embodiments, the core is substantially free of ethylenically unsaturated groups. The core and outer layer each comprise a three-dimensional branched network of a different silsesquioxane polymer. The silsesquioxane polymers of the core and outer layer may be homopolymers or copolymers. One representative SSQ polymer crosslinker wherein the core is the reaction product of methyltrimethoxysilane and the outer layer is the reaction product of vinyltriethoxysilane is depicted in FIG. 1.


During hydrolysis, the hydrolyzable groups are converted to a hydrolyzed group, such as —OH. The Si—OH groups react with each other to form silicone-oxygen linkages such that the majority of silicon atoms are bonded to three oxygen atoms. After hydrolysis, remaining hydrolyzed (e.g. —OH) groups are preferably further reacted with end-capping agents to convert the hydrolyzed (e.g. —OH) groups to —OSi(R3)3. The silsesquioxane polymer crosslinker comprises terminal groups having the formula —Si(R3)3 after end-capping.


Due to the end-capping, the SSQ polymer crosslinker typically comprises little or no —OH groups. In some embodiments, the —OH groups are present in an amount of no greater than 5, 4, 3, 2, 1 or 0.5 wt-% of the SSQ polymer crosslinker. In some embodiments, the SSQ polymer crosslinker is free of —OH groups.


Various alkoxy silane end-capping agents are known. In some embodiments, the end-capping agent has the general structure R5OSi(R3)3 or O[Si(R3)3]2 wherein R5 is a hydrolyzable group, as previously described and R3 is independently a non-hydrolyzable group. Thus, in some embodiments R3 generally lacks an oxygen atom or a halogen directly bonded to a silicon atom. R3 is independently alkyl, aryl (e.g. phenyl), aralkyl, or alkaryl that optionally comprise halogen substituents (e.g. chloro, bromo, fluoro), aryl (e.g. phenyl), aralkyl, or alkaryl. The optionally substituted alkyl group may have a straight, branched, or cyclic structure. In some embodiments, R3 is C1-C12 or C1-C4 alkyl optionally comprising halogen substituents. R3 may optionally comprise (e.g. contiguous) oxygen, nitrogen, sulfur, or silicon substituents. In some embodiments, R3 does not comprise oxygen or nitrogen substituents that can be less thermally stable.


A non-limiting list of illustrative end-capping agents and the resulting R3 groups is as follows:













End-capping agent
R3







n-butyldimethylmethoxysilane
n-butyldimethyl


t-butyldiphenylmethoxysilane
t-butyldiphenyl


3-chloroisobutyldimethylmethoxysilane
3-chloroisobutyldimethyl


phenyldimethylethoxysilane
phenyldimethyl


n-propyldimethylmethoxysilane
n-propyldimethyl


triethylethoxysilane
triethyl


trimethylmethoxysilane
trimethyl


triphenylethoxysilane
triphenyl


n-octyldimethylmethoxysilane
n-octyldimethyl


Hexamethyldisiloxane
trimethyl


Hexaethyldisiloxane
triethyl


1,1,1,3,3,3-hexaphenyldisiloxane
triphenyl


1,1,1,3,3,3-hexakis(4-
tri-[4-(dimethylamino)phenyl]


(dimethylamino)phenyl)disiloxane


1,1,1,3,3,3-hexakis(3-
tri-(3-fluorobenzyl)


fluorobenzyl)disiloxane









When the silsesquioxane polymer is further reacted with an end-capping agent to convert the hydrolyzed group, e.g. —OH, to —OSi(R3)3 the silsesquioxane polymer crosslinker typically comprises a three-dimensional branched network having the formula:




embedded image



wherein:


the oxygen atom at the * is bonded to another Si atom within the three-dimensional branched network,


R is an organic group comprising an ethylenically unsaturated group,


R2 is an organic group that is not an ethylenically unsaturated group,


R3 is a non-hydrolyzable group (as previously described); and


n is at least 2 and m is at least 1.


In one naming convention, the R3 group derived the end-capping agent is included in the name of the SSQ polymer. For example poly(vinylsilsesquioxane) end-capped with ethoxytrimethylsilane or hexamethyldisiloxane may be named “trimethyl silyl poly(vinylsilsesquioxane)” and has the general formula:




embedded image



wherein the oxygen atom in the formula above at the * above is bonded to another Si atom within the three-dimensional branched network. Such three-dimensional branched network structure is depicted as follows:




embedded image


The SSQ polymer crosslinker comprises at least two ethylenically unsaturated groups. Thus, n is at least 2, 3, 4, 5, 6, 7, 8, 9, or 10. In the case of SSQ copolymer crosslinkers comprising n and m units, m is at least 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. In some embodiments, n, m, or n+m is at least 15, 20, 25, 30, 35, 40, 45, or 50. In some embodiments, n or m, or n+m is no greater than 500, 450, 400, 350, 300, 250 or 200. Thus n+m can range up to 1000. When the SSQ polymer is prepared from one or more SSQ reactants, wherein all the reactants comprise an ethylenically unsaturated group, all (i.e. 100%) of the repeat units comprise an ethylenically unsaturated group. In some embodiments, n and m are selected such the polymer comprises at least 25, 30, 35, 40, 45, or 50 mol % of repeat units comprising ethylenically unsaturated group(s) R. In some embodiments, n and m are selected such the polymer comprises no greater than 95, 90, 85, 80, 75, 70, 65, 60, or 55 mol % of repeat units comprising ethylenically unsaturated group(s) R.


The SSQ polymer crosslinker is generally combined with a low Tg (meth)acrylic polymer. The concentration of SSQ crosslinking polymer is typically at least 0.1, 0.2, 0.3, 0.4 or 0.5 wt-% and can range up to 15 or 20 wt-% of the (e.g. pressure sensitive) adhesive composition. However, as the concentration of such crosslinking polymer increases, the peel adhesion (180° to stainless steel) can decrease. Thus, in typically embodiments, the concentration of the SSQ crosslinking polymer is no greater than 10, 9, 8, 7, 6, or 5 wt-% and in some favored embodiments, no greater than 4, 3, 2, or 1 wt-%. When the SSQ polymer crosslinker comprises a relatively high number of repeat units that comprise ethylenically unsaturated groups, such as in the case of (trialkyl silyl) polyvinylsilsesquioxane homopolymer, small concentrations of SSQ polymer crosslinker can increase the shear holding power to 10,000+ minutes, However, when the SSQ polymer crosslinker comprises a lower number of repeat units that comprise ethylenically unsaturated groups, such as in the case of (trialkyl silyl) polyvinyl-co-ethyl-silsesquioxane copolymer, proportionately higher concentrations of SSQ copolymer crosslinker would be utilized to obtain comparable shear holding power.


The (e.g. pressure sensitive) adhesive composition may comprise a single SSQ polymer or a combination of two or more of such SSQ polymers. When the composition comprises a combination of SSQ polymers, the total concentration generally falls within the ranges just described.


The (meth)acrylic polymer and/or pressure sensitive adhesive comprising polymerized units derived from one or more (meth)acrylate ester monomers derived from a (e.g. non-tertiary) alcohol containing from 1 to 14 carbon atoms and preferably an average of from 4 to 12 carbon atoms. The (meth)acrylic polymer and/or pressure sensitive adhesive composition may also comprise polymerized units derived from one or more monomers (e.g. common to acrylic polymers and adhesives) such as a (meth)acrylic ester monomers (also referred to as (meth)acrylate acid ester monomers and alkyl(meth)acrylate monomers) optionally in combination with one or more other monomers such as acid-functional ethylenically unsaturated monomers, non-acid-functional polar monomers, and vinyl monomers.


Examples of monomers include the esters of either acrylic acid or methacrylic acid with non-tertiary alcohols such as ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, 1-pentanol, 2-pentanol, 3-pentanol, 2-methyl-1-butanol, 3-methyl-1-butanol, 1-hexanol, 2-hexanol, 2-methyl-1-pentanol, 3-methyl-1-pentanol, 2-ethyl-1-butanol, 3,5,5-trimethyl-1-hexanol, 3-heptanol, 1-octanol, 2-octanol, isoctylalcohol, 2-ethyl-1-hexanol, 1-decanol, 2-propyl-heptanol, 1-dodecanol, 1-tridecanol, 1-tetradecanol, and the like. In some embodiments, a preferred (meth)acrylate ester monomer is the ester of (meth)acrylic acid with isooctyl alcohol.


In some favored embodiments, the monomer is the ester of (meth)acrylic acid with an alcohol derived from a renewable source. A suitable technique for determining whether a material is derived from a renewable resource is through 14C analysis according to ASTM D6866-10, as described in US2012/0288692. The application of ASTM D6866-10 to derive a “bio-based content” is built on the same concepts as radiocarbon dating, but without use of the age equations. The analysis is performed by deriving a ratio of the amount of organic radiocarbon (14C) in an unknown sample to that of a modern reference standard. The ratio is reported as a percentage with the units “pMC” (percent modern carbon).


One suitable monomer derived from a renewable source is 2-octyl (meth)acrylate, as can be prepared by conventional techniques from 2-octanol and (meth)acryloyl derivatives such as esters, acids and acyl halides. The 2-octanol may be prepared by treatment of ricinoleic acid, derived from castor oil, (or ester or acyl halide thereof) with sodium hydroxide, followed by distillation from the co-product sebacic acid. Other (meth)acrylate ester monomers that can be renewable are those derived from ethanol, 2-methyl butanol and dihydrocitronellol.


In some embodiments, the (meth)acrylic polymer and/or pressure sensitive adhesive composition comprises a bio-based content of at least 25, 30, 35, 40, 45, or 50 wt. % using ASTM D6866-10, method B. In other embodiments, the (e.g. pressure sensitive) adhesive composition comprises a bio-based content of at least 55, 60, 65, 70, 75, or 80 wt. %. In yet other embodiments, the composition comprises a bio-based content of at least 85, 90, 95, 96, 97, 99 or 99 wt. %.


The (meth)acrylic polymer and/or pressure sensitive adhesive composition comprises one or more low Tg monomers, having a Tg no greater than 10° C. when the monomer is polymerized (i.e. independently) to form a homopolymer. In some embodiments, the low Tg monomers have a Tg no greater than 0° C., no greater than −5° C., or no greater than −10° C. when reacted to form a homopolymer. The Tg of these homopolymers is often greater than or equal to −80° C., greater than or equal to −70° C., greater than or equal to −60° C., or greater than or equal to −50° C. The Tg of these homopolymers can be, for example, in the range of −80° C. to 20° C., −70° C. to 10° C., −60° C. to 0° C., or −60° C. to −10° C.


The low Tg monomer may have the formula

H2C═CR1C(O)OR8

wherein R1 is H or methyl and R8 is an alkyl with 1 to 22 carbons or a heteroalkyl with 2 to 20 carbons and 1 to 6 heteroatoms selected from oxygen or sulfur. The alkyl or heteroalkyl group can be linear, branched, cyclic, or a combination thereof.


Exemplary low Tg monomers include for example ethyl acrylate, n-propyl acrylate, n-butyl acrylate, isobutyl acrylate, t-butyl acrylate, n-pentyl acrylate, isoamyl acrylate, n-hexyl acrylate, 2-methylbutyl acrylate, 2-ethylhexyl acrylate, 4-methyl-2-pentyl acrylate, n-octyl acrylate, 2-octyl acrylate, isooctyl acrylate, isononyl acrylate, decyl acrylate, isodecyl acrylate, lauryl acrylate, isotridecyl acrylate, octadecyl acrylate, and dodecyl acrylate.


Low Tg heteroalkyl acrylate monomers include, for example, 2-methoxyethyl acrylate and 2-ethoxyethyl acrylate.


In some embodiments, the (meth)acrylic polymer and/or pressure sensitive adhesive composition comprises polymerized units of at least one low Tg monomer having a non-cyclic alkyl (meth)acrylate monomer(s) having 4 to 20 carbon atoms. In some embodiments, the (meth)acrylic polymer and/or (e.g. pressure sensitive) adhesive comprises at least one low Tg monomer having a (e.g. branched) alkyl group with 6 to 20 carbon atoms. In some embodiments, the low Tg monomer has a (e.g. branched) alkyl group with 7 or 8 carbon atoms. Exemplary monomers include, but are not limited to, 2-ethylhexyl methacrylate, isooctyl methacrylate, n-octyl methacrylate, 2-octyl methacrylate, isodecyl methacrylate, and lauryl methacrylate.


In some embodiments, the (meth)acrylic polymer and/or pressure sensitive adhesive composition comprises polymerized units derived from a high Tg monomer, having a Tg greater than 10° C. and typically of at least 15° C., 20° C. or 25° C., and preferably at least 50° C. Suitable high Tg monomers include, for example, t-butyl acrylate, methyl methacrylate, ethyl methacrylate, isopropyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, s-butyl methacrylate, t-butyl methacrylate, stearyl methacrylate, phenyl methacrylate, cyclohexyl methacrylate, isobornyl acrylate, isobornyl methacrylate (110° C., according to Aldrich), norbornyl (meth)acrylate, benzyl methacrylate, 3,3,5 trimethylcyclohexyl acrylate, cyclohexyl acrylate, N-octyl acrylamide, and propyl methacrylate or combinations.


The (meth)acrylic polymer is a copolymer of at least one low Tg monomer, optionally other monomers, as described herein. The Tg of the copolymer may be estimated by use of the Fox equation, based on the Tgs of the constituent monomers and the weight percent thereof.


The alkyl (meth)acrylate monomer polymerized units are typically present in the (meth)acrylic polymer in an amount of at least 50, 55, 60, 65, or 75 wt. % of the composition. When the composition is free of non-polymerized components such as tackifier, plasticizer, and/or filler; the concentrations described herein are also equivalent to the concentration of such polymerized units in the (meth)acrylic polymer.


In some embodiments, the (meth)acrylic polymer and/or pressure sensitive adhesive composition comprises at least 50, 55, 60, 65, 70, 75, 80, 85, 90 or 95 wt. % or greater of polymerized units derived from low Tg (e.g. alkyl) (meth)acrylate monomer(s). When high Tg monomers are included in a pressure sensitive adhesive, the adhesive may include at least 5, 10, 15, 20, to 30 parts by weight of such high Tg (e.g. alkyl) (meth)acrylate monomer(s).


The (meth)acrylic polymer may alternatively comprise less low Tg alkyl (meth)acrylate monomer(s). For example, the (meth)acrylic polymer may comprise at least 25, 30, 35, 40, or 45 wt. % of low Tg alkyl (meth)acrylate monomer in combination with high Tg alkyl (meth)acrylate monomer(s) such that the total alkyl(meth)acrylate monomer is at least 50, 55, 60, 65, or 75 wt. %.


The (meth)acrylic polymer and/or pressure sensitive adhesive composition may optionally comprise polymerized units derived from an acid functional monomer (a subset of high Tg monomers), where the acid functional group may be an acid per se, such as a carboxylic acid, or a portion may be salt thereof, such as an alkali metal carboxylate. Useful acid functional monomers include, but are not limited to, those selected from ethylenically unsaturated carboxylic acids, ethylenically unsaturated sulfonic acids, ethylenically unsaturated phosphonic acids, and mixtures thereof. Examples of such compounds include those selected from acrylic acid, methacrylic acid, itaconic acid, fumaric acid, crotonic acid, citraconic acid, maleic acid, oleic acid, β-carboxyethyl (meth)acrylate, 2-sulfoethyl methacrylate, styrene sulfonic acid, 2-acrylamido-2-methylpropanesulfonic acid, vinylphosphonic acid, and mixtures thereof.


Due to their availability, acid functional monomers are generally selected from ethylenically unsaturated carboxylic acids, i.e. (meth)acrylic acids. When even stronger acids are desired, acidic monomers include the ethylenically unsaturated sulfonic acids and ethylenically unsaturated phosphonic acids. The acid functional monomer is generally used in amounts of 0.5 to 15 parts by weight, preferably 0.5 to 10 parts by weight, based on 100 parts by weight total monomer.


The (meth)acrylic polymer and/or pressure sensitive adhesive composition may optionally comprise polymerized units derived from other monomers such as a non-acid-functional polar monomer.


Representative examples of suitable polar monomers include but are not limited to 2-hydroxyethyl (meth)acrylate; N-vinylpyrrolidone; N-vinylcaprolactam; acrylamide; mono- or di-N-alkyl substituted acrylamide; t-butyl acrylamide; dimethylaminoethyl acrylamide; N-octyl acrylamide; poly(alkoxyalkyl) (meth)acrylates including 2-(2-ethoxyethoxy)ethyl (meth)acrylate, 2-ethoxyethyl (meth)acrylate, 2-methoxyethoxyethyl (meth)acrylate, 2-methoxyethyl methacrylate, polyethylene glycol mono(meth)acrylates; alkyl vinyl ethers, including vinyl methyl ether; and mixtures thereof. Preferred polar monomers include those selected from the group consisting of 2-hydroxyethyl (meth)acrylate and N-vinylpyrrolidinone. The non-acid-functional polar monomer may be present in amounts of 0 to 10 parts by weight, or 0.5 to 5 parts by weight, based on 100 parts by weight total monomer.


When used, vinyl monomers useful in the (meth)acrylic polymer include vinyl esters (e.g., vinyl acetate and vinyl propionate), styrene, substituted styrene (e.g., α-methyl styrene), vinyl halide, and mixtures thereof. As used herein vinyl monomers are exclusive of acid functional monomers, acrylate ester monomers and polar monomers. Such vinyl monomers are generally used at 0 to 5 parts by weight, preferably 1 to 5 parts by weight, based on 100 parts by weight total monomer.


Due to the inclusion of a sufficient amount of low Tg (e.g. alkyl (meth)acrylate) polymerized units and/or other additives such as plasticizer and tackifier, pressure sensitive compositions described herein typically have a glass transition temperature “Tg” of no greater than 25° C., or 20° C. In some embodiments, the compositions have a Tg no greater than 15° C., 10° C., 5° C., 0° C., or −0.5° C.


The (meth)acrylic polymer and/or (e.g. pressure sensitive) adhesive may optionally comprise at least one other crosslinker, in addition to the SSQ polymer crosslinker.


In some embodiments, the pressure sensitive adhesive comprises a multifunctional (meth)acrylate crosslinking monomer. Examples of useful multifunctional (meth)acrylate include, but are not limited to, di(meth)acrylates, tri(meth)acrylates, and tetra(meth)acrylates, such as 1,6-hexanediol di(meth)acrylate, poly(ethylene glycol) di(meth)acrylates, polybutadiene di(meth)acrylate, polyurethane di(meth)acrylates, and propoxylated glycerin tri(meth)acrylate, and mixtures thereof. When utilized, the multifunctional (meth)acrylate is typically used in an amount of at least 0.05, 0.10, 0.15, 0.20 up to 1, 2, 3, 4, or 5 parts by weight, relative to 100 parts by weight of the total monomer content.


In some embodiments, the pressure sensitive adhesive comprises predominantly (greater than 50%, 60%, 70%, 80%, or 90% of the total crosslinks) or exclusively crosslinks from the SSQ polymer crosslinker. In such embodiment, the composition may be free of other crosslinking monomers, particularly multi(meth)acrylate crosslinkers such as 1,6-hexane diol diacrylate (HDDA).


The pressure sensitive adhesive may optionally contain one or more conventional additives. Preferred additives include tackifiers, plasticizers, dyes, antioxidants, UV stabilizers, and (e.g. inorganic) fillers such as (e.g. fumed) silica and glass bubbles. In some embodiments no tackifier is used. When tackifiers are used, the concentration can range from 5 or 10, 15 or 20 wt. % or greater of the (e.g. cured) adhesive composition.


Various types of tackifiers include phenol modified terpenes and rosin esters such as glycerol esters of rosin and pentaerythritol esters of rosin that are available under the trade designations “Nuroz”, “Nutac” (Newport Industries), “Permalyn”, “Staybelite”, “Foral” (Eastman). Also available are hydrocarbon resin tackifiers that typically come from C5 and C9 monomers by products of naphtha cracking and are available under the trade names “Piccotac”, “Eastotac”, “Regalrez”, “Regalite” (Eastman), “Arkon” (Arakawa), “Norsolene”, “Wingtack” (Cray Valley), “Nevtack”, LX (Neville Chemical Co.), “Hikotac”, “Hikorez” (Kolon Chemical), “Novares” (Rutgers Nev.), “Quintone” (Zeon), “Escorez” (Exxonmobile Chemical), “Nures”, and “H-Rez” (Newport Industries). Of these, glycerol esters of rosin and pentaerythritol esters of rosin, such as available under the trade designations “Nuroz”, “Nutac”, and “Foral” are considered biobased materials.


The (meth)acrylic copolymers can be polymerized by various techniques including, but not limited to, solvent polymerization, dispersion polymerization, solventless bulk polymerization, and radiation polymerization, including processes using ultraviolet light, electron beam, and gamma radiation. The monomer mixture may comprise a polymerization initiator, especially a thermal initiator or a photoinitiator of a type and in an amount effective to polymerize the comonomers.


A typical solution polymerization method is carried out by adding the monomers, a suitable solvent, and an optional chain transfer agent to a reaction vessel, adding a free radical initiator, purging with nitrogen, and maintaining the reaction vessel at an elevated temperature (e.g. about 40 to 100° C.) until the reaction is complete, typically in about 1 to 20 hours, depending upon the batch size and temperature. Examples of typical solvents include methanol, tetrahydrofuran, ethanol, isopropanol, acetone, methyl ethyl ketone, methyl acetate, ethyl acetate, toluene, xylene, and an ethylene glycol alkyl ether. Those solvents can be used alone or as mixtures thereof.


Useful initiators include those that, on exposure to heat or light, generate free-radicals that initiate (co)polymerization of the monomer mixture. The initiators are typically employed at concentrations ranging from about 0.0001 to about 3.0 parts by weight, preferably from about 0.001 to about 1.0 parts by weight, and more preferably from about 0.005 to about 0.5 parts by weight of the total monomer or polymerized units.


Suitable initiators include but are not limited to those selected from the group consisting of azo compounds such as VAZO 64 (2,2′-azobis(isobutyronitrile)), VAZO 52 (2,2′-azobis(2,4-dimethylpentanenitrile)), and VAZO 67 (2,2′-azobis-(2-methylbutyronitrile)) available from E.I. du Pont de Nemours Co., peroxides such as benzoyl peroxide and lauroyl peroxide, and mixtures thereof. The preferred oil-soluble thermal initiator is (2,2′-azobis-(2-methylbutyronitrile)). When used, initiators may comprise from about 0.05 to about 1 part by weight, preferably about 0.1 to about 0.5 part by weight based on 100 parts by weight of monomer components in the (e.g. pressure sensitive) adhesive.


The exemplified (meth)acrylic polymer was prepared in a manner to insure that the (meth)acrylic polymer is free of ethylically unsaturated groups. Thus, in this embodiment, the SSQ polymer crosslinker is the sole component comprising ethylenically unsaturated free radically polymerizable groups. It is a surprising result that the SSQ polymer crosslinker can crosslink such (meth)acrylic polymer.


However, as evident by cofiled U.S. Provisional Patent Application Ser. No. 62/014,802, the SSQ polymer crosslinker can also crosslink (meth)acrylic polymers that comprise ethylenically unsaturated groups as well a composition that comprises a low Tg ethylenically unsaturated monomer. Thus, although the present invention does not necessitate the (meth)acrylic polymer or any other component of the pressure sensitive adhesive to comprise ethylenically unsaturated free radically polymerizable groups for the crosslinking to occur, the presence of ethylenically unsaturated groups does not detract from such crosslinking Thus, when the pressure sensitive adhesive composition comprises a sufficient concentration of ethylenically unsaturated groups, the ethylenically unsaturated groups of the SSQ polymer crosslinker are surmised to polymerize with the ethylenically unsaturated groups of the composition, as described in U.S. Provisional Patent Application Ser. No. 62/014,802, filed Jun. 20, 2014. However, when the pressure sensitive adhesive composition does not comprise a sufficient concentration of ethylenically unsaturated groups to obtain the desired degree of polymerization by the reaction of such ethylenically unsaturated groups with the SSQ polymer crosslinker, the (meth)acrylic polymer crosslinks by an alternative mechanism as exemplified herein.


The polymerization of the (meth)acrylic polymer by means of the SSQ polymer crosslinker is typically conducted in the presence of solvents such as ethyl acetate, toluene and tetrahydrofuran, which are non-reactive with the ethylenically unsaturated groups of the SSQ polymer


The pressure sensitive adhesive further comprises a free radical initiator. Free-radical generating photoinitiators include Norrish Type I type reactions, which are commonly referred to as alpha cleavage type initiators. The Norrish Type I reactions can be characterized as the photochemical cleavage of aldehydes and ketones. Various aryl ketone and aryl aldehyde groups that are capable of Norrish Type I type cleavage are known, some of which are described in U.S. Pat. No. 5,506,279 (Gaddam et al.).


Free-radical generating photoinitiators can also be Norrish Type II type reactions, which are commonly referred to as alpha cleavage type initiators. Various groups that are capable of Norrish Type II cleavage are also known, some of which are described in U.S. Pat. No. 5,773,485 (Gaddam et al.).


Useful photoinitiators include benzoin ethers such as benzoin methyl ether and benzoin isopropyl ether; substituted acetophenones such as 2,2-dimethoxy-2-phenylacetophenone photoinitiator, available the trade name IRGACURE 651 or ESACURE KB-1 photoinitiator (Sartomer Co., West Chester, Pa.), and dimethylhydroxyacetophenone; substituted α-ketols such as 2-methyl-2-hydroxy propiophenone; aromatic sulfonyl chlorides such as 2-naphthalene-sulfonyl chloride; and photoactive oximes such as 1-phenyl-1,2-propanedione-2-(O-ethoxy-carbonyl)oxime. Particularly preferred among these are the substituted acetophenones.


Polymerizable photoinitiators may also be utilized such as those described in previously cited U.S. Pat. Nos. 5,506,279 and 5,773,485.


A single photoinitiator or a combination of photoinitiators may be utilized. The photoinitiator(s) are typically present in an amount of from 0.1 to 1.0 part by weight, relative to 100 parts by weight of the total (meth)acrylic polymer.


The composition and the photoinitiator may be irradiated with activating UV radiation to crosslink the (meth)acrylic polymer. UV light are typically relatively high light intensity sources such as medium pressure mercury lamps which provide intensities generally greater than 10 mW/cm2, preferably 15 to 450 mW/cm2. For efficient processing, high intensities and short exposure times are preferred. For example, an intensity of 600 mW/cm2 and an exposure time of about 1 second may be used successfully. Intensities can range from 0.1 to 150 mW/cm2, preferably from 0.5 to 100 mW/cm2, and more preferably from 0.5 to 50 mW/cm2.


The change in 180° peel adhesion to stainless steel and gel content can be indicative of the extent of crosslinking. For example, a reduction is peel adhesion by about 10-20% of the average value can be indicative of low levels of crosslinking A gel content ranging from about 20 to 50% can be indicative of moderate levels of crosslinking Gel contents ranging from greater than 50% (e.g. 55 or 60%) to about 80% can be indicative of high levels of crosslinking, accompanied by shear holding power in excess of 10,000 minutes.


In some embodiments, the pressure sensitive adhesive comprises fumed silica. Fumed silica, also known as pyrogenic silica, is made from flame pyrolysis of silicon tetrachloride or from quartz sand vaporized in a 3000° C. electric arc. Fumed silica consists of microscopic droplets of amorphous silica fused into (e.g. branched) three-dimensional primary particles that aggregate into larger particles. Since the aggregates do not typically break down, the average particle size of fumed silica is the average particle size of the aggregates. Fumed silica is commercially available from various global producers including Evonik, under the trade designation “Aerosil”; Cabot under the trade designation “Cab-O-Sil”, and Wacker Chemie-Dow Corning. The BET surface area of suitable fumed silica is typically at least 50 m2/g, or 75 m2/g, or 100 m2/g. In some embodiments, the BET surface area of the fumed silica is no greater than 400 m2/g, or 350 m2/g, or 300 m2/g, or 275 m2/g, or 250 m2/g. The fumed silica aggregates preferably comprise silica having a primary particle size no greater than 20 nm or 15 nm. The aggregate particle size is substantially larger than the primary particle size and is typically at least 100 nm or greater.


The concentration of (e.g. fumed) silica can vary. In some embodiments, the (e.g. pressure sensitive) adhesive comprises at least 0.5, 1. 0, 1.1, 1.2, 1.3, 1.4, or 1.5 wt-% of (e.g. fumed) silica and in some embodiments no greater than 5, 4, 3, or 2 wt-%. In other embodiments, the adhesive comprises at least 5, 6, 7, 8, 9, or 10 wt-% of (e.g. fumed) silica and typically no greater than 20, 19, 18, 17, 16, or 15 wt-% of (e.g. fumed) silica.


In some embodiments, the pressure sensitive adhesive comprises glass bubbles. Suitable glass bubbles generally have a density ranging from about 0.125 to about 0.35 g/cc. In some embodiments, the glass bubbles have a density less than 0.30, 0.25, or 0.20 g/cc. Glass bubbles generally have a distribution of particles sizes. In typical embodiments, 90% of the glass bubbles have a particle size (by volume) of at least 75 microns and no greater than 115 microns. In some embodiments, 90% of the glass bubbles have a particle size (by volume) of at least 80, 85, 90, or 95 microns. In some embodiments, the glass bubbles have a crush strength of at least 250 psi and no greater than 1000, 750, or 500 psi. Glass bubbles are commercially available from various sources including 3M, St. Paul, Minn.


The concentration of glass bubbles can vary. In some embodiments, the adhesive comprises at least 1, 2, 3, 4 or 5 wt-% of glass bubbles and typically no greater than 20, 15, or 10 wt-% of glass bubbles.


The inclusion of glass bubbles can reduce the density of the adhesive. Another way of reducing the density of the adhesive is by incorporation of air or other gasses into the adhesive composition. For example the adhesive composition can be transferred to a frother as described for examples in U.S. Pat. No. 4,415,615; incorporated herein by reference. While feeding nitrogen gas into the frother, the frothed composition can be delivered to the nip of a roll coater between a pair of transparent, (e.g. biaxially-oriented polyethylene terephthalate) films. A silicone or fluorochemical surfactant is typically included in the froathed composition. Various surfactants are known including copolymer surfactants described in U.S. Pat. No. 6,852,781.


In some embodiments no tackifier is used. When tackifiers are used, the concentration can range from 5 or 10 wt-% to 40, 45, 50, 55, or 60 wt-% of the (e.g. cured) adhesive composition.


Various types of tackifiers include phenol modified terpenes and rosin esters such as glycerol esters of rosin and pentaerythritol esters of rosin that are available under the trade designations “Nuroz”, “Nutac” (Newport Industries), “Permalyn”, “Staybelite”, “Foral” (Eastman). Also available are hydrocarbon resin tackifiers that typically come from C5 and C9 monomers by products of naphtha cracking and are available under the trade names “Piccotac”, “Eastotac”, “Regalrez”, “Regalite” (Eastman), “Arkon” (Arakawa), “Norsolene”, “Wingtack” (Cray Valley), “Nevtack”, LX (Neville Chemical Co.), “Hikotac”, “Hikorez” (Kolon Chemical), “Novares” (Rutgers Nev.), “Quintone” (Zeon), “Escorez” (Exxonmobile Chemical), “Nures”, and “H-Rez” (Newport Industries). Of these, glycerol esters of rosin and pentaerythritol esters of rosin, such as available under the trade designations “Nuroz”, “Nutac”, and “Foral” are considered biobased materials.


Depending on the kinds and amount of components, the pressure sensitive adhesive can be formulated to have a wide variety of properties for various end uses. In some embodiments, the adhesive is cleanly removable from stainless steel and the 180° peel adhesion (according to test method described in the forthcoming examples) is at least 10, 25, 50, 75 or 100 N/dm and can range up to 200 N/dm or greater. In some embodiments, the shear holding power is greater than 10,000 minutes (according to test method described in the forthcoming examples)


The adhesives may be coated upon a variety of flexible and inflexible backing materials using conventional coating techniques to produce adhesive-coated materials. Flexible substrates are defined herein as any material which is conventionally utilized as a tape backing or may be of any other flexible material. Examples include, but are not limited to plastic films such as polypropylene, polyethylene, polyvinyl chloride, polyester (polyethylene terephthalate), polycarbonate, polymethyl(meth)acrylate (PMMA), cellulose acetate, cellulose triacetate, and ethyl cellulose. In some embodiments, the backing is comprised of a bio-based material such as polylactic acid (PLA). Foam backings may be used. Foams are commercially available from various suppliers such as 3M Co., Voltek, Sekisui, and others. The foam may be formed as a coextruded sheet with the adhesive on one or both sides of the foam, or the adhesive may be laminated to it. When the adhesive is laminated to a foam, it may be desirable to treat the surface to improve the adhesion of the adhesive to the foam or to any of the other types of backings Such treatments are typically selected based on the nature of the materials of the adhesive and of the foam or backing and include primers and surface modifications (e.g., corona treatment, surface abrasion).


Backings may also be prepared of fabric such as woven fabric formed of threads of synthetic or natural materials such as cotton, nylon, rayon, glass, ceramic materials, and the like or nonwoven fabric such as air laid webs of natural or synthetic fibers or blends of these. The backing may also be formed of metal, metalized polymer films, or ceramic sheet materials may take the form of any article conventionally known to be utilized with (e.g. pressure sensitive) adhesive compositions such as labels, tapes, signs, covers, marking indicia, and the like.


In some embodiments, the backing material is a transparent film having a transmission of visible light of at least 90 percent. The transparent film may further comprise a graphic. In this embodiment, the adhesive may also be transparent.


The above-described compositions can be coated on a substrate using conventional coating techniques modified as appropriate to the particular substrate. For example, these compositions can be applied to a variety of solid substrates by methods such as roller coating, flow coating, dip coating, spin coating, spray coating knife coating, and die coating. These various methods of coating allow the compositions to be placed on the substrate at variable thicknesses thus allowing a wider range of use of the compositions. Coating thicknesses may vary as previously described. The composition may be of any desirable concentration for subsequent coating, but is typically 5 to 20 wt-% polymer solids in monomer. The desired concentration may be achieved by further dilution of the coating composition, or by partial drying. Coating thicknesses may vary from about 25 to 1500 microns (dry thickness). In typical embodiments, the coating thickness ranges from about 50 to 250 microns.


The adhesive can also be provided in the form of a (e.g. pressure sensitive) adhesive transfer tape in which at least one layer of the adhesive is disposed on a release liner for application to a permanent substrate at a later time. The adhesive can also be provided as a single coated or double coated tape in which the adhesive is disposed on a permanent backing.


For a single-sided tape, the side of the backing surface opposite that where the adhesive is disposed is typically coated with a suitable release material. Release materials are known and include materials such as, for example, silicone, polyethylene, polycarbamate, polyacrylics, and the like. For double coated tapes, another layer of adhesive is disposed on the backing surface opposite that where the adhesive of the invention is disposed. The other layer of adhesive can be different from the adhesive of the invention, e.g., a conventional acrylic PSA, or it can be the same adhesive as the invention, with the same or a different formulation. Double coated tapes are typically carried on a release liner. Additional tape constructions include those described in U.S. Pat. No. 5,602,221 (Bennett et al.), incorporated herein by reference.


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. These examples are merely for illustrative purposes only and are not meant to be limiting on the scope of the appended claims.









TABLE 1







Materials








Designa-



tion
Description and Source





IOA
Isooctyl acrylate, available from 3M Company, St. Paul, MN


AA
Acrylic acid, available from Alfa Aesar, Ward Hill, MA


IRG651
2,2-Dimethoxy-1,2-diphenylethan-1-one, an initiator available



from BASF Corporation, Florham Park, NJ, under the trade



designation “IRGACURE 651”


KB1
2,2-dimethoxy-1,2-di(phenyl)ethanone, available from



Lamberti USA, Inc., Conshohocken, PA, under the trade



designation “ESACURE KB1”


VAZO-67
An initiator available from DuPont, Wilmington, DE, under



the trade designation “VAZO-67”










180° Peel Adhesion Test


Peel adhesion strength was measured at a 180° angle using an IMASS SP-200 slip/peel tester (available from IMASS, Inc., Accord Mass.) at a peel rate of 305 mm/minute (12 inches/minute). Stainless steel test panels were cleaned by wiping the substrate panels with a tissue wetted with isopropanol using heavy hand pressure to wipe the test panel 8 to 10 times. This procedure was repeated two more times with clean tissues wetted with solvent. The cleaned panel was allowed to air dry for 30 minutes. The adhesive tape was cut into strips measuring 1.27 cm×20 cm (½ in.×8 in.) and the strips were rolled down onto the cleaned panel with a 2.0 kg (4.5 lb.) rubber roller using 2 passes. The prepared samples were stored at 23° C./50% relative humidity for different periods of aging times, typically 1 h, before testing. The peel strengths reported were the average result of 3-5 repeated experiments.


Shear Holding Power Test


Shear holding power (i.e., static shear strength) was evaluated at 23° C./50% relative humidity using 1 Kg load. Tape test samples measuring 1.27 cm by 15.24 cm (½ in. by 6 in.) were adhered to 1.5 inch by 2 inch (˜3.8 by 5.1 cm) stainless steel (SS) panels using the method to clean the panel and attach the tape described in the peel adhesion test. The tape overlapped the panel by 1.27 cm by 2.54 cm (½ in. by 1 in.), and the strip was folded over itself on the adhesive side, and then folded again. A hook was hung in the second fold and secured by stapling the tape above the hook. The weight was attached to the hook and the panels were hung in a 23° C./50% RH room. The time to failure in minutes was recorded. If no failure was observed after 10,000 minutes, the test was stopped and a value of 10,000+ minutes was recorded. The modes of failure were recorded. If there were adhesive residue on the SS test panel as well as on the backing, then a “cohesive” failure was recorded. If the adhesive remained attached on the backing, then the failure was recorded as an “adhesive” failure.


Gel Content Test Method


Percent get (gel content) was determined in generally similar manner as described in ASTM D3616-.95 (as specified in 2009), with the following modifications, A test specimen measuring 63/64 inch (2.50 cm) in diameter was die-cut from a tape coated with crosslinked pressure-sensitive adhesive. The specimen was placed in a mesh basket measuring 1.5 inch (˜3.8 cm) by 1.5 inch (˜3.8 cm). The basket with the specimen was weighed to the nearest 0.1 mg and placed in a capped jar containing sufficient amount of ethyl acetate to cover the sample. After 24 hours the basket (containing the specimen) was removed, drained and placed in an oven at 120° C. for 30 minutes. The percent gel was determined by calculating the ratio of (a) the weight of the remaining unextracted portion of the adhesive sample to (b) the weight of the adhesive sample before extraction. To correct for the weight of the tape backing, a disc of the uncoated backing material of the same size as the test specimen was die-cut and weighed. The formula used for percent gel determination was as shown immediately below:







Percent






Gel


(

percent





by





weight

)



=

100
×


(


unextracted





sample






wt
.




after






extraction

-

backing






wt
.



)


(

original





sample






wt
.





-




backing








wt
.


)







Preparatory Example 1 (PE-1): Trimethyl Silyl Polyvinylsilsesquioxane (“PVSSQ”)

VinylTEOS (100 g), deionized (DI) water (50 g), and oxalic acid (0.5 g) were mixed together at room temperature in a 500 mL round bottom flask equipped with a condenser. Ethoxytrimethylsilane (20 g) was then added, and the resulting mixture was stirred at room temperature for 6-8 hours followed by the evaporation of the solvents (water/ethanol mixture). The resulting liquid was dissolved in methyl ethyl ketone (“MEK”, 100 mL) and washed three-times with DI water (100 mL). After washing, the MEK was evaporated under reduced pressure to yield polymer product polyvinylsilsesquioxane as a viscous liquid.


Preparatory Example 2 (PE-2): Preparation of 95:5 (w/w) poly(IOA:AA)

An 87 g portion of IOA, 4.6 g of AA, 0.045 g of VAZO-67, and 214 g of ethyl acetate were combined in a transparent glass jar. Nitrogen gas was purged through the mixture for 10 minutes. The jar was then tightly capped and placed inside a Launderometer filled with water maintained at a temperature of 60° C. After 24 hours, the glass jar was removed from the Launderometer and the cap was opened, resulting in termination of the polymerization reaction. The concentration of the PE-2 material (i.e., 95:5 (w/w) poly(IOA:AA)) as a polymer solution in ethyl acetate was estimated to be 27.3% solids by weight.


Example 1 (EX-1)

An adhesive tape EX-1 was prepared as follows. A sample of the polymer solution of PE-2 in ethyl acetate (est. 27.3 wt. % solids) was combined with the relative amounts of KB-1 and PVSSQ (PE-1) indicated in Table 2 (“pbw” is parts by weight of solids) to form a coating mixture. The coating mixture was coated onto a PET backing (Mitsubishi 3SAB) using a notch bar coater with a knife gap of 15 mils (˜380 micrometers). The wet coating was then dried in an oven at 70° C. for 15 minutes, resulting in a dried PSA coating thickness of 2.7 mils (˜69 micrometers). The dried coating was cooled back to room temperature and then irradiated with UV radiation. A high intensity UV light with a D-bulb was used, at a dose of 1000 mJ/cm2 of UVB.


Examples 2 to 10 (EX-2 to EX-10)

Adhesive tapes EX-2 to EX-10 were prepared according to the procedure described for EX-1, except using the amounts summarized in Table 2.









TABLE 2







Composition and process conditions for PSA tapes
















PSA




PE-2 (IOA:AA,


Thickness
UV dose



95:5 w/w)
KB1
PVSSQ
Mils
mJ/cm2,


Sample
pbw
pbw
pbw
(micrometers)
UVB















Comp
100
0
0.00
2.7 (69)
1000


EX-1


Comp
100
0.3
0.00
2.5 (64)
1000


EX-2


EX-3
100
0.3
0.15
2.5 (64)
1000


EX-4
100
0.3
0.30
2.5 (64)
1000


EX-5
100
1
0.50
2.1 (53)
1000


EX-6
100
1
0.75
2.1 (53)
1000


EX-7
100
1
1.00
2.1 (53)
1000


EX-8
100
1
1.65
2.0 (51)
1000


EX-9
100
1
2.50
2.0 (51)
1000


EX-10
100
1
4.00
1.8 (46)
1000









The “180° Peel Adhesion Test”, “Shear Holding Power Test”, and “Gel Content Test” was performed on the adhesive tapes of EX-1 to EX-10, using samples aged for 1 week, and with results as summarized in Table 3 (“coh” designated a “cohesive” failure mode; “NA” designated “not applicable”; and “ND” designated “not determined”).













TABLE 3









180° Peel Adhesion,
Shear Holding




samples aged
Power, samples



for 1 week
aged for 1 week














failure

failure
Gel Content


Sample
oz/in (N/dm)
mode
minutes
mode
% by weight





Comp
118 (129)
coh
4
coh
ND


EX-1


Comp
118 (129)
coh
5
coh
ND


EX-2


EX-3
 94 (103)
coh
5
coh
ND


EX-4
80 (88)
coh
5
coh
ND


EX-5
34 (37)
clean
31 
coh
32


EX-6
31 (34)
clean
119 
coh
56


EX-7
31 (34)
clean
10,000+   
NA
67


EX-8
23 (25)
clean
10,000+   
NA
70


EX-9
22 (24)
clean
10,000+   
NA
75


EX-10
10 (11)
clean
10,000+   
NA
79








Claims
  • 1. A pressure sensitive adhesive composition comprising: at least one low glass transition temperature (Tg) (meth)acrylic polymer having a Tg no greater than 10° C.,a free-radical initiator; andat least one silsesquioxane (SSQ) polymer crosslinker comprising a plurality of ethylenically unsaturated groups independently selected from vinyl ether and alkenyl.
  • 2. The pressure sensitive adhesive composition of claim 1 wherein the low Tg (meth)acrylic polymer comprises at least 50 wt-% of polymerized units derived from one or more low Tg ethylenically unsaturated monomer.
  • 3. The pressure sensitive adhesive composition of claim 2 wherein the one or more low Tg ethylenically unsaturated monomer is an alkyl (meth)acrylate comprising 4 to 20 carbon atoms.
  • 4. The pressure sensitive adhesive composition of claim 1 wherein the low Tg (meth)acrylic polymer further comprises polymerized units derived from at least one monomer selected from acid-functional monomers, non-acid functional polar monomers, vinyl monomers, and combinations thereof.
  • 5. The pressure sensitive adhesive composition of claim 1 wherein the low Tg (meth)acrylic polymer comprises ethylenically unsaturated groups and/or the pressure sensitive adhesive further comprises a component comprising an ethylenically unsaturated group.
  • 6. The pressure sensitive adhesive composition of claim 1 wherein the free-radical initiator is an alpha cleavage photoinitiator.
  • 7. The pressure sensitive adhesive composition of claim 1 wherein the composition comprises 0.1 to 20 wt. % of the silsesquioxane polymer crosslinker.
  • 8. The pressure sensitive adhesive composition of claim 1 wherein the silsesquioxane polymer crosslinker comprises a three-dimensional branched network having the formula:
  • 9. The pressure sensitive adhesive composition of claim 8 wherein R has the formula Y—Z or Z, wherein Y is the depicted covalent bond or Y is a divalent organic linking group, and Z is the ethylenically unsaturated group selected from vinyl ether and alkenyl.
  • 10. The pressure sensitive adhesive composition of claim 8 wherein R2 has the formula Y—X, wherein Y is the depicted covalent bond or Y is a divalent organic linking group, and X is hydrogen; alkyl, aryl, alkaryl, aralkyl that optionally comprise substituents; or a reactive group that is not an ethylenically unsaturated group.
  • 11. The pressure sensitive adhesive composition of claim 8 wherein n and m are no greater than 500.
  • 12. The pressure sensitive adhesive composition of claim 1 wherein the silsesquioxane polymer crosslinker comprises a core comprising a first silsesquioxane polymer and an outer layer comprising a second silsesquioxane polymer bonded to the core, wherein the core, outer layer, or a combination thereof, comprises the ethylenically unsaturated groups selected from vinyl ether and alkenyl.
  • 13. The pressure sensitive adhesive composition of claim 12 wherein the outer layer is bonded to the core via silicon atoms boned to three oxygen atoms.
  • 14. The pressure sensitive adhesive composition of claim 1 wherein the silsesquioxane polymer crosslinker comprises terminal groups having the formula —Si(R3)3 wherein R3 is independently selected from alkyl, aryl, aralkyl, or alkaryl that optionally comprise substituents.
  • 15. The pressure sensitive adhesive composition of claim 1 wherein the silsesquioxane polymer crosslinker comprise —OH groups present in an amount of no greater than 5 wt-% of the silsesquioxane polymer.
  • 16. A crosslinked composition comprising the pressure sensitive adhesive composition of claim 1; wherein the composition is free-radically cured.
  • 17. A pressure sensitive adhesive article comprising the pressure sensitive adhesive composition of claim 1 on a substrate; wherein the composition is free-radically cured.
  • 18. The pressure sensitive adhesive article of claim 17 wherein the substrate is a backing or a release liner.
  • 19. A method of preparing an article comprising: a) providing a composition according to claim 1;b) applying the composition to a substrate; andc) irradiating the applied composition thereby crosslinking the (meth)acrylic polymer.
CROSS REFERENCE TO RELATED APPLICATIONS

This application is a national stage filing under 35 U.S.C. 371 of PCT/US2015/034325, filed Jun. 5, 2015, which claims the benefit of U.S. Provisional Application No. 62/014,847, filed Jun. 20, 2014, the disclosure of which is incorporated by reference in its/their entirety herein.

PCT Information
Filing Document Filing Date Country Kind
PCT/US2015/034325 6/5/2015 WO 00
Publishing Document Publishing Date Country Kind
WO2015/195355 12/23/2015 WO A
US Referenced Citations (95)
Number Name Date Kind
3775452 Karstedt Nov 1973 A
4351875 Arkens Sep 1982 A
4415615 Esmay Nov 1983 A
4510094 Drahnak Apr 1985 A
4530879 Drahnak Jul 1985 A
4535485 Ashman Aug 1985 A
4600484 Drahnak Jul 1986 A
4723978 Clodgo Feb 1988 A
4732934 Hathaway Mar 1988 A
4761358 Hosoi Aug 1988 A
4788252 De Boer Nov 1988 A
4879362 Morgan Nov 1989 A
4885209 Lindner Dec 1989 A
4889901 Shama Dec 1989 A
4948837 Wittmann Aug 1990 A
4963619 Wittmann Oct 1990 A
4997260 Honjo Mar 1991 A
5030699 Motoyama Jul 1991 A
5057577 Matsuo Oct 1991 A
5073595 Almer Dec 1991 A
5145886 Oxman Sep 1992 A
5178947 Charmot Jan 1993 A
5188899 Matsumoto Feb 1993 A
5212237 Siol May 1993 A
5219931 Siol Jun 1993 A
5223586 Mautner Jun 1993 A
5278451 Adachi Jan 1994 A
5360878 Shen Nov 1994 A
5506279 Babu Apr 1996 A
5602221 Bennett Feb 1997 A
5609925 Camilletti Mar 1997 A
5695678 Edamura Dec 1997 A
5773485 Bennett Jun 1998 A
5814685 Satake Sep 1998 A
5902836 Bennett May 1999 A
6376078 Inokuchi Apr 2002 B1
6624214 Zimmer Sep 2003 B2
6627314 Matyjaszewski Sep 2003 B2
6743510 Ochiai Jun 2004 B2
6852781 Savu Feb 2005 B2
6927301 Laine Aug 2005 B2
7056840 Miller Jun 2006 B2
7081295 James Jul 2006 B2
7241437 Davidson Jul 2007 B2
7385020 Anderson Jun 2008 B2
7488539 Kozakai Feb 2009 B2
7723438 Hedrick May 2010 B2
7976585 Cremer Jul 2011 B2
7985523 Zhou Jul 2011 B2
8012583 Wu Sep 2011 B2
8071132 Adair Dec 2011 B2
8084177 Zhou Dec 2011 B2
8168357 Wu May 2012 B2
8173342 Wu May 2012 B2
8323803 Wu Dec 2012 B2
8329301 Wu Dec 2012 B2
8431220 Wu Apr 2013 B2
8758854 Ishii Jun 2014 B2
20040166077 Toumi Aug 2004 A1
20040247549 Lu Dec 2004 A1
20050025820 Kester Feb 2005 A1
20050215807 Morimoto Sep 2005 A1
20070073024 Wariishi Mar 2007 A1
20070167552 Stoeppelmann Jul 2007 A1
20070213474 Ebenhoch Sep 2007 A1
20080045631 Henn Feb 2008 A1
20080051487 Kumon Feb 2008 A1
20080057431 Lai Mar 2008 A1
20080119120 Zuniga May 2008 A1
20080254077 Prigent Oct 2008 A1
20080279901 Prigent Nov 2008 A1
20080286467 Allen Nov 2008 A1
20090162650 Hong Jun 2009 A1
20090197071 Cramail Aug 2009 A1
20090215927 Mohite Aug 2009 A1
20090312457 Tokumitsu Dec 2009 A1
20100280151 Nguyen Nov 2010 A1
20110045387 Allen Feb 2011 A1
20110054074 Jonschker Mar 2011 A1
20110083887 Brock Apr 2011 A1
20110117145 Inokuchi May 2011 A1
20110223404 Wu Sep 2011 A1
20120132108 Ishihara May 2012 A1
20120205315 Liu Aug 2012 A1
20120288692 Broyles Nov 2012 A1
20120298574 Kang Nov 2012 A1
20130101934 Chiba Apr 2013 A1
20130102733 Chen Apr 2013 A1
20130139963 Lee Jun 2013 A1
20130318863 Chang Dec 2013 A1
20130343969 Bromberg Dec 2013 A1
20140023855 Masuda Jan 2014 A1
20140030441 Nagai Jan 2014 A1
20140135413 Yoo May 2014 A1
20140178698 Rathore Jun 2014 A1
Foreign Referenced Citations (131)
Number Date Country
1827668 Sep 2006 CN
1887921 Jan 2007 CN
101376812 Mar 2009 CN
101550217 Oct 2009 CN
101717565 Jun 2010 CN
101724394 Jun 2010 CN
101781390 Jul 2010 CN
102432920 May 2012 CN
102532554 Jul 2012 CN
102585073 Jul 2012 CN
102718930 Oct 2012 CN
103012689 Apr 2013 CN
103030752 Apr 2013 CN
103113812 May 2013 CN
103173041 Jun 2013 CN
103275273 Sep 2013 CN
103289021 Sep 2013 CN
0254418 Jan 1988 EP
0315226 May 1989 EP
0373941 Jun 1990 EP
0398701 Nov 1990 EP
0420155 Apr 1991 EP
0420585 Apr 1991 EP
0459257 Dec 1991 EP
0556953 Aug 1993 EP
0958805 Nov 1999 EP
2155761 Feb 2010 EP
S55-111148 Aug 1980 JP
S62-124159 Jun 1987 JP
S62-130807 Jun 1987 JP
S62-255957 Nov 1987 JP
S63-291962 Nov 1988 JP
2541566 Jan 1989 JP
01090201 Apr 1989 JP
H01-096265 Apr 1989 JP
H01-195458 Aug 1989 JP
H02-233537 Sep 1990 JP
H03-002808 Jan 1991 JP
H03-154007 Jul 1991 JP
H04-050243 Feb 1992 JP
H04-110351 Apr 1992 JP
04178411 Jun 1992 JP
H04-173863 Jun 1992 JP
H04-175370 Jun 1992 JP
H04-178411 Jun 1992 JP
H05-271362 Oct 1993 JP
H08-134308 May 1996 JP
H11-060931 Mar 1999 JP
H11-116681 Apr 1999 JP
2000-063674 Feb 2000 JP
2000-157928 Jun 2000 JP
2000-169591 Jun 2000 JP
2001-106925 Apr 2001 JP
2002-121536 Apr 2002 JP
2002-327030 Nov 2002 JP
2003-055459 Feb 2003 JP
2003-226835 Aug 2003 JP
3817192 Sep 2003 JP
2004-292541 Oct 2004 JP
2005-014293 Jan 2005 JP
2006-160880 Jun 2006 JP
2006-335978 Dec 2006 JP
2007-090865 Apr 2007 JP
2007-146148 Jun 2007 JP
2007-146150 Jun 2007 JP
2008-056751 Mar 2008 JP
2008-115302 May 2008 JP
2008-127405 Jun 2008 JP
2008-144053 Jun 2008 JP
2008-201908 Sep 2008 JP
2008-303358 Dec 2008 JP
2009-009045 Jan 2009 JP
2009-024077 Feb 2009 JP
2009-029893 Feb 2009 JP
2009-051934 Mar 2009 JP
2009-091466 Apr 2009 JP
2009-155496 Jul 2009 JP
2009-191120 Aug 2009 JP
2009-253203 Oct 2009 JP
2009-280706 Dec 2009 JP
2010-005613 Jan 2010 JP
2010-095619 Apr 2010 JP
2010-116442 May 2010 JP
2010-128080 Jun 2010 JP
2010-144153 Jul 2010 JP
2010-175798 Aug 2010 JP
2010-229303 Oct 2010 JP
2010-260881 Nov 2010 JP
2010-265410 Nov 2010 JP
2010-275521 Dec 2010 JP
2011-063482 Mar 2011 JP
2011-081123 Apr 2011 JP
2011-099074 May 2011 JP
2011-115755 Jun 2011 JP
2011-132087 Jul 2011 JP
2012-036335 Feb 2012 JP
2012-036336 Feb 2012 JP
2012-144661 Aug 2012 JP
2013-010843 Jan 2013 JP
2013-022791 Feb 2013 JP
2013-076075 Apr 2013 JP
2013-249371 Dec 2013 JP
2013-251103 Dec 2013 JP
2014-005363 Jan 2014 JP
2014-007058 Jan 2014 JP
2006-017891 Feb 2006 KR
2009-067315 Jun 2009 KR
2010-075235 Jul 2010 KR
2011-038471 Apr 2011 KR
2012-021926 Mar 2012 KR
2013-026991 Mar 2013 KR
2013-067401 Jun 2013 KR
2005-100426 Oct 2005 WO
2007-103654 Sep 2007 WO
2008-124080 Oct 2008 WO
2008-147072 Dec 2008 WO
WO 2009-002660 Dec 2008 WO
WO 2009-005880 Jan 2009 WO
WO 2009-008452 Jan 2009 WO
WO 2009-085926 Jul 2009 WO
WO 2009-128441 Oct 2009 WO
WO 2010-055632 May 2010 WO
WO 2013-015469 Jan 2013 WO
WO 2013-087365 Jun 2013 WO
WO 2013-087366 Jun 2013 WO
WO 2013-087368 Jun 2013 WO
WO 2014-024379 Feb 2014 WO
WO 2014-099699 Jun 2014 WO
WO 2015-088932 Jun 2015 WO
WO 2015-195268 Dec 2015 WO
WO 2015-195391 Dec 2015 WO
Non-Patent Literature Citations (11)
Entry
Human translation of JP 04178411 A (Year: 1992).
“Norrish Reaction”, Wikipedia, [Retrieved from the Internet on Jun. 12, 2014], URL <http://en.wikipedia.org/wiki/Norrish_reaction>, pp. 4.
Boardman, “(η5-Cyclopentadienyl) Trialkylplatinum Photohydrosilylation Catalysts. Mechanism of Active Catalyst Formation and Preparation of a Novel Bis (Sily1) Platinum Hydride,” Organometallics, 1992, vol. 11, No. 12, pp. 4194-4201.
Burget, “Kinetic Study of the Photoactivated Hydrosilylation of Some β-Dicarbonyl Complexes of Trialkylplatinum (IV)”, Journal of Photochemistry and Photobiology A: Chemistry, 1996, vol. 97, pp. 163-170.
Ciba, “Coating Effects Segment IRGACURE 651”, 2001, 2pgs.
Dow, “Dow Corning (R) 2-7466 Resin”, Material Data Sheet, 2013, 2pgs.
Jakuczek, “Well-defined core-shell structures based on silsesquioxane microgels: Grafting of polystyrene via ATRP and product characterization”, Polymer, 2008, vol. 49, pp. 843-856.
Lewis, “Platinum(II) Bis(β-Diketones) as Photoactivated Hydrosilation Catalysts”, Inorganic Chemistry, 1995, vol. 34, No. 12, pp. 3182-3189.
Su, “New Photocurable Acrylic/Silsesquioxane Hybrid Optical Materials: Synthesis, Properties, and Patterning”, Macromolecular Materials and Engineering, 2007, vol. 292, pp. 666-673.
Wang, “Photoactivated Hydrosilylation Reaction of Alkynes,” Journal of Organometallic Chemistry, 2003, vol. 665, pp. 1-6.
International Search Report for PCT International Application No. PCT/US2015/034325, dated Jul. 17, 2015, 3pgs.
Related Publications (1)
Number Date Country
20170088756 A1 Mar 2017 US
Provisional Applications (1)
Number Date Country
62014847 Jun 2014 US