Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F287/00—Macromolecular compounds obtained by polymerising monomers on to block polymers
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
  • C09J4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09J159/00 - C09J187/00

Definitions

• the present invention relates to controllably curable adhesive compositions which depending upon the particular formulation can upon cure provide polymers exhibiting pressure-sensitive adhesive properties, and optionally vibration damping properties, and optionally structural adhesive properties.
• Acrylate pressure-sensitive adhesives are well known in the art. Ulrich (U.S. Reissue No. 24,906) describes alkyl acrylate copolymers comprising a predominant amount of C 4 - to C ⁇ alkyl esters of acrylic acid and a minor amount of a copolymerizable polar monomer such as acrylic acid. Such adhesives are widely popular due to their availability, low cost, and ability to provide the requisite fourfold balance of adhesion, cohesion, stretchiness, and elasticity known to be required for an effective pressure-sensitive adhesive. Subsequent references suggest various modifications in the basic acrylic polymer to enhance various physical properties in the PSA composition. For example, Martens et al. (U.S. Patent No.
• Harlan U.S. Patent No. 3,239,4708 discloses the preparation of block or segmented copolymers to provide PSA compositions which have improved strength and overall PSA properties because of phase separation of soft butadiene or butadiene-isoprene polymer blocks and hard polystyrene blocks of the block copolymer.
• Another well-known method of modifying acrylic pressure-sensitive adhesives is to form a syrup comprising a pre-formed acrylic polymer or oligomer and an acrylic monomer. The pre-formed polymer can be inert or reactive under subsequent polymerization or crosslinking reactions. Japanese Patent No.
• Photoiniferter technology is a recently developed technology which allows for the polymerization of block copolymers from various monomers.
• the control of the polymerization provided by the photoiniferter technology permits "tailoring" of the block copolymers formed thereby so that polymers having a wide spectrum of physical properties can be prepared.
• Such high precision tailoring is not possible with previously known polymerization methods such as thermal polymerization.
• photoiniferter refers to a chemical compound that has a combined function of being a free-radical initiator, transfer agent, and terminator, the term “iniferter” being a word formed by the underlined portions of the terms identifying these functions.
• the "photo” portion of the term indicates that the polymerization is photolytically induced.
• This term and its use in the production of block copolymers is well known, particularly because of the work of Takayuki Otsu of the Department of Applied Chemistry, Osaka City University, Osaka, Japan. This work is discussed, for example, in an article by Otsu et. al.
• European Patent Application 0,286,376, published October 12, 1988 provides ABA-type block copolymers made using photoiniferter technology, in which the constituent B-block (soft) monomers are acrylic acid esters and the A-block (hard) monomers are methacrylic esters, maleimido or aromatic vinyl derivatives.
• the resultant polymers are claimed to be in the form of an elastomer, sealant, packing, adhesive material, vibration-proof material, sound absorbing material, soiling material or hose. These polymers are specifically limited to ABA blocks of the monomers listed above. No added photoinitiator is present, and no post-coating ultraviolet radiation (UN) cure is taught or suggested.
• Japanese Patent Application (Kokai) 64-29410 laid open January 31, 1989, discloses a UN-curable pressure-sensitive adhesive prepared using photoiniferter technology.
• a vinyl monomer or vinyl monomer mixture is photopolymerized in the presence of a dithiocarbamate to make a polymeric photoiniferter.
• the dithiocarbamate-terminated polymer is then mixed with one or more monomers, at least one of which must be a multifunctional (i.e., two or more vinyl groups) monomer such as HDDA, and a photoinitiator.
• the mixture is coated and cured with UN light. No attempt was made to optimize the resulting polymer for vibration-damping use, and such use is not taught or suggested.
• 3,986,581 discloses an acrylate copolymer produced by conventional photopolymerization processes which possesses vibration-damping properties, but the polymer is not an adhesive, so a separate adhesive is required for application of the polymer to a substrate.
• European Patent Application 390,207 published October 3, 1990, discloses a pseudo-JPN comprising a vinylidene fluoride/hexafluoroproplyene copolymer dissolved in an acrylate monomer which is subsequently polymerized thermally or photochemically, then coated and crosslinked. Crosslinking occurs in the fluoroelastomer or the acrylate or both. No PSA properties are taught or claimed for this fluoroelastomer/acrylate system.
• a need thus exists for a pressure-sensitive adhesive composition which can be controllably cured by exposure to ultraviolet radiation and which depending on the formulation can upon cure provide pressure-sensitive adhesive properties, optionally vibration damping properties, and optionally structural adhesive properties.
• a pressure-sensitive adhesive composition which can be controllably cured by exposure to ultraviolet radiation and which depending on the formulation can upon cure provide pressure-sensitive adhesive properties, optionally vibration damping properties, and optionally structural adhesive properties.
• the present invention relates to radiation curable acrylate compositions each comprising a single phase blend of photopolymerizable vinyl-group containing monomers, a radiation activatable crosslinking agent, a photoinitiator, and a photoiniferter polymer having one or more reactive end groups, wherein the single phase blends can be coated onto a substrate as a syrup and subsequently subjected to sufficient radiant energy to effect crosslinking.
• the crosslinked polymer systems thus obtained possess excellent properties for use as pressure-sensitive adhesives, optionally vibration-dampers, and optionally structural adhesives.
• the present invention relates to a radiation curable pressure-sensitive adhesive composition
• a radiation curable pressure-sensitive adhesive composition comprising:
• B comprises a polymer block having a T g of between about -70°C and about 0°C wherein the polymer block B comprises polymerizable monoethylenically-unsaturated monomer(s);
• A comprises a polymer block having a T g of between about +30°C and about +160°C wherein the polymer block A comprises polymerizable monoethylenically-unsaturated monomer(s);
• I represents a free-radical initiator portion of an iniferter of the formula I(T) n , wherein T represents the terminator portion of said iniferter;
• I(T) ⁇ is capable upon being subjected to an appropriate energy source of forming free radicals I( -) n and n T « wherein I - is a highly reactive free radical capable of initiating free radical polymerization, and T • is a less reactive free radical which is generally much less capable of initiating free radical polymerization than I- but will rejoin with I(- ⁇ upon te-- ⁇ nination of said energy source;
• the present invention also relates to a vibration damping composition
• a vibration damping composition comprising:
• n is an integer of 1 to 2;
• B comprises a polymer block having a T s of between about -70°C and about -15°C, and a number average molecular weight ranging from about 20,000 to about 50,000, wherein polymer block B comprises polymerizable monoethylenically-unsaturated monomer(s);
• I represents a free-radical initiator portion of an iniferter of the formula l(T) a , wherein
• T represents the terminator portion of the iniferter; and ICr) a is capable upon being subjected to an appropriate energy source of forming free radicals I(-) n and nT « wherein I- is a highly reactive free radical capable of initiating free radical polymerization, and T- is a less reactive free radical which is generally much less capable of initiating free radical polymerization than I- but will rejoin with I(-) ⁇ upon termination of the energy source;
• the present invention also relates to a structural pressure-sensitive adhesive composition
• a structural pressure-sensitive adhesive composition comprising: (a) 100 parts by weight of free radically (co)polymerizable monomer comprising:
• n is an integer of 2;
• B comprises a polymer block having a T g of between about 0°C and about -70°C, wherein polymer block B comprises polymerizable monoethylenically-unsaturated monomer(s);
• polymer block A comprises a polymer block having a T 8 of about 30 °C to about 160°C wherein polymer block A comprises polymerizable monoethylenically-unsaturated monomer(s) ;
• I represents a free-radical initiator portion of an iniferter of the formula I(T) n , wherein
• T represents the terminator portion of said iniferter; and I(T) n is capable upon being subjected to an appropriate energy source of forming free radicals I( «) protest and nT « wherein I* is a highly reactive free radical capable of initiating free radical polymerization, and T • is a less reactive free radical which is generally much less capable of initiating free radical polymerization than I - but will rejoin with !(•)__ upon termination of said energy source;
• compositions of the invention are the unique morphology and excellent balance of properties of the crosslinked polymer systems prepared therefrom and the minimization of phase separation due to incorporation of the photoiniferter polymer through its reactive end group(s).
• Another advantage of the compositions of the invention is that the photoiniferter technology employed allows precise tailoring of the resultant crosslinked polymer system to maximize the effectiveness of the resultant material.
• compositions of the invention may comprise photoiniferter polymer selected from the group consisting of I(BT) n , I(BAT) n , and mixtures thereof, depending upon the particular composition.
• Photoiniferter polymer I(BT) n is made by reaction of a photoiniferter and an acrylic monomer.
• photoiniferter and iniferter are used interchangeably herein.
• An iniferter represented by the general formula I(T) n , is capable, upon being subjected to an appropriate energy source, of forming free radicals I(-) n and nT « wherein n is an integer of 1 to 2, I- is a highly reactive free radical capable of initiating free-radical polymerization, and T • is a less-reactive free-radical which is generally much less capable of initiating free-radical polymerization than I- but will rejoin with !(-),__ or a free-radical polymer segment which is free-radically polymerized with I( • ) n upon termination of the energy source.
• Such an iniferter is mixed with a first monomer charge comprising acrylic monomer(s) which are free-radically polymerizable in the presence of I(*) n to form an acrylic polymer block which may be a homopolymer or a random copolymer.
• the mixture is exposed to an energy source capable of forming free radicals l(-) n and nT « arising from the iniferter.
• the exposure is maintained until the first monomer charge polymerizes with I(-) n to form a free-radical polymer segment represented by the formula I(B -) n - wherein B represents a homopolymer or random copolymer block.
• I(B «) n nd nT « combine to form a polymer represented by the formula I(BT) n . It is theorized that iniferters wherein n is an integer of 3 or 4 would also be useful according to the invention.
• I(BT) n is mixed with a second monomer charge comprising monomer(s) which are free-radically polymerizable in the presence of I(B -) n to form a thermoplastic reinforcing polymer block A.
• the monomer(s) from which block A is formed thus are not the exact same monomer(s) from which block B is formed.
• I(BT) n is exposed to an energy source capable of producing free radicals I(B *) n and nT « .
• the exposure is maintained until the second monomer charge polymerizes with I(B-) n to form a free-radical block copolymer segment represented by the formula I(BA-) n wherein A represents a relatively hard polymer block formed of the second monomer charge.
• l(BA-) a znd nT- combine to form a block copolymer represented by the formula I(BAT) n .
• the photoiniferter polymer typically has a number average molecular weight in the range of about 15,000 to about 500,000 depending upon the intended application of the final cured polymer system, as will be explained below in more detail.
• the compositions of the invention comprise about 20 to about 30 parts by weight photoiniferter polymer in order to provide superior adhesive properties.
• the polymer block B of the I(BT) n or I(BAT) n photoiniferter polymer can comprise a homopolymer or a random copolymer of two or more free-radically (co)polymerizable monomers.
• Examples of monomers which polymer block B can comprise include but are not limited to those selected from the group consisting of nonpolar vinyl monomers such as styrene, t-butyl styrene, methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, methyl acrylate, butyl acrylate, isooctyl acrylate, 2-ethylhexyl acrylate, isobornyl acrylate, and mixtures thereof.
• nonpolar vinyl monomers such as styrene, t-butyl styrene, methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, methyl acrylate, butyl acrylate, isooctyl acrylate, 2-ethylhexyl acrylate, isobornyl acrylate, and mixtures thereof.
• nonpolar monomer as defined herein includes both nonpolar and
• Another type of monomer which the polymer block B can comprise is a polar monoethylenically-unsaturated monomer that is copolymerizable with the aforementioned nonpolar monomers.
• useful polar monomers include but are not limited to those selected from the group consisting of acrylic acid, methacrylic acid, itaconic acid, acrylamide, acrylonitrile, methacrylonitrile, N-vinylpyrrolidone, polyethylene oxide acrylate, and mixtures thereof.
• Examples of the polar groups which the monomers may contain include but are not limited to those selected from the group consisting of carboxylic acid, amine, hydroxy, nitrile, and amide groups.
• the preferred polar monomers are acrylic acid and methacrylic acid, for reasons of enhanced intermolecular interactions of the resulting polymer.
• polymer block B is a random copolymer comprising a nonpolar monomer selected from the group consisting of butyl acrylate, isooctyl acrylate, 2-ethylhexyl acrylate, and mixtures thereof, and a polar monomer selected from the group consisting of acrylic acid, N-vinylpyrrolidone, methacrylic acid, and mixtures thereof.
• the photoiniferter polymer can also comprise an AB-type diblock copolymer or an ABA-type triblock copolymer. I-n these cases, the B-block, as described above, comprises a softer, elastomeric block having a glass transition temperature below about 0°C, as will be noted in further detail below.
• the A-block of the AB or ABA block copolymers preferably comprises a homopolymer or copolymer formed from free-radically (co)polymerizable monomers selected from the group consisting of methyl methacrylate, poly(styrylethyl) methacrylate, acrylonitrile, isobornyl acrylate, isobornyl methacrylate, N-vinylpyrrolidone, glycidyl methacrylate, and mixtures thereof. These monomers are generally considered to provide "hard" thermoplastic polymers having glass transition temperatures above about 30°C. Most preferably the A-block is prepared from monomers selected from the group consisting of methyl methacrylate, isobornyl methacrylate, isobornyl acrylate, and mixtures thereof, for reasons of performance and availability.
• Photoiniferters useful for producing the I(BT) n and ICBAT) n polymers according to the present invention include but are not limited to those photoiniferters selected from the group consisting of dithiocarbamates, disulfides, and mixtures thereof.
• Examples of specific useful iniferters include but are not limited to those selected from the group consisting of n-butyl-N,N-dimethyldithiocarbamate; benzyldithiocarbamate; benzyl N-methyldithiocarbamate; benzyl N,N-dimethyldithiocarbamate; benzyl N-ethyldithiocarbamate; benzyl N,N-diethyldithiocarbamate; p-xylylene bis(dithiocarbamate); p-xylylene bis(N-methyldithiocarbamate; p-xylylene bis(N,N-dimethyldithiocarbamate); p-xylylene bis(N-ethyldithiocarbamate; p-xylylene bis(N,N-diethyldithiocarbamate); 1 ,2-bis(N,N-dimethyldithio
• N,N-diethyldithiocarbamate N,N-diethyldithiocarbamate, p-xylylene bis(N,N-diethyldithiocarbamate), and mixtures thereof.
• the photoiniferter concentration is chosen so as to optimize the molecular weight of the photoiniferter polymer (i.e., the higher the concentration of photoiniferter, the lower the molecular weight of the photoiniferter polymer).
• the polymerization of the monomer(s) to produce the polymer block of the photoiniferter polymer is by step- wise free radical polymerization.
• the monomer is dissolved in a suitable inert solvent, if needed, and polymerized by a first free radical polymerization utilizing a suitable iniferter as a free radical initiator source.
• a suitable iniferter as a free radical initiator source.
• from about 0.01 to about 5 percent by weight of iniferter based upon the total weight of polymerizable composition (i.e. , the total weight of monomers) is used.
• the iniferter is caused to dissociate to form free radicals by exposure to an appropriate energy source.
• the preferred iniferter is one which will dissociate upon exposure to a radiant energy source, most preferably an ultraviolet radiant energy source.
• the iniferter Upon exposure to the energy source, the iniferter dissociates to form free radicals which promote free radical polymerization. Upon completion of the free radical polymerization of the monomer the energy source is discontinued to permit the free radically polymerized segments to recombine with the terminator portion of the iniferter to form polymer segments. The second monomer charge, if desired, is then introduced, and the new mixture is exposed to the energy source to cause dissociation of the terminator radical and free radical polymerization of the second monomer charge onto the first polymer segment, which now becomes the initiator of the second free radical polymerization.
• the energy source Upon completion of polymerization of the second monomer charge, the energy source is terminated and the terminator portion of the iniferter recombines with the reinforcing thermoplastic polymer block to provide a block copolymer.
• the particular energy source and its intensity are selected to result in dissociation of the iniferter to free radicals.
• an ultraviolet light source is utilized. The intensity and rate of radiation are chosen to advance the polymerization at a reasonable rate without deleteriously affecting the polymer segment being produced.
• An ultraviolet light source having a wave length on the order of about 300 to about 400 nm spaced approximately 10 cm from the reactants to provide an exposure of 2 milliwatts per square centimeter has been found to produce suitable results.
• Reaction times on the order of about 2 to about 50 hours have been found to be typical, depending upon the intensity of the radiation, with faster reaction times being observed at greater intensities.
• the reactants and any solvent employed are charged into an energy source-transparent vessel and therein subjected to the energy source.
• the energy source is ultraviolet light radiation
• a suitable ultraviolet light- transparent vessel is utilized.
• the reaction is preferably conducted in a vessel with agitation to permit uniform exposure of the reactants to the energy source. While most of the reactions have been conducted by employing a batch process, it is possible to utilize the same technology in a continuous polymerization operation.
• the reaction mixture may include a suitable inert solvent but it is not necessary since some of the monomeric materials are liquid themselves and may thus be charged into the reaction vessel without utilization of a solvent.
• the solvent if utilized in the free radical polymerization, may be any substance which is liquid in a temperature range of about -10°C to about 50°C, is substantially transparent to the energy source employed to permit dissociation of the iniferter to form free radicals, is essentially inert to the reactants and products, and will not otherwise adversely affect the reaction.
• Suitable solvents include but are not limited to those selected from the group consisting of water, alkyl acetates such as ethyl acetate, alkanes such as hexane or heptane, alcohols such as methyl alcohol, ethanol, isopropyl alcohol, and mixtures thereof.
• the amount of solvent is generally about 30 to about 80 percent by weight based on the total weight of the reactants and solvent.
• the copolymerization may be carried out by other well known techniques such as suspension, emulsion, and bulk polymerization.
• the pressure sensitive adhesives, vibration damping materials, and structural materials of the present invention arise from the photopolymerization of a mixture of a photoiniferter polymer, compatible free-radically (co)polymerizable monomer(s), radiation-activatable crosslinking agent, and photoinitiator.
• the compatible free-radically (co)polymerizable monomers are preferably identical to the monomers which comprise polymer segment B of the I(BT) n and/or I(BAT) n photoiniferter polymer.
• the photoiniferter polymer consists entirely of 2-ethylhexyl acrylate homopolymer
• the photoiniferter polymer is preferably dissolved at the desired concentration in 2-ethylhexyl acrylate monomer (e.g. , the free-radically
• the free-radically (co)polymerizable monomer in which it is dissolved for further polymerization is preferably a mixture of N-vinylpyrrolidone and 2-ethylhexyl acrylate, in preferably approximately the ratios represented in the photoiniferter random copolymer, most preferably the exact same ratios.
• the photoiniferter if the B block of the photoiniferter polymer is a random copolymer of 2-ethylhexyl acrylate and N-vinylpyrrolidone, the free-radically (co)polymerizable monomer in which it is dissolved for further polymerization is preferably a mixture of N-vinylpyrrolidone and 2-ethylhexyl acrylate, in preferably approximately the ratios represented in the photoiniferter random copolymer, most preferably the exact same ratios.
• the photoiniferter if the B block of the photoiniferter polymer is a random cop
• the polymer can be dissolved in the free-radically (co)polymerizable monomer by at least two different methods.
• the first method which is preferred, involves forming the photoiniferter polymer by adding an iniferter to free-radically (co)polymerizable monomer(s) and not polymerizing to completion.
• UI Photoinitiators
• the mixture of the free-radically (co)polymerizable monomer(s), radiation activatable crosslinking agent, and the photoiniferter polymer also contains a photoinitiator to induce polymerization of the free-radically (co)polymerizable monomers.
• photoinitiators which are useful include but are not limited to those selected from the group consisting of the benzoin ethers such as benzoin methyl ether, benzoin isopropyl ether, benzoin methyl ether, benzoin n-butyl ether, and methyl-o-benzoylbenzoates; substituted benzoin ethers such as anisole methyl ether; substituted acetophenones such as 2,2'-diethoxyacetophenone, 2,2 diethoxymethyl acetophenone, l-phenyl-2-hydroxy-2 methyl-propane-l-one, hydroxy-cyclohexyl-phenyl-ketone, and 2,2'-dimethoxy-2-phenylacetophenone; substituted alpha-ketols such as 2-methyI-2-hydroxypropiophenone; aromatic sulfonyl chlorides such as 2-naphthalene sulfonyl chloride; photoactive oximes such as l
• the preferred photoinitiators are the substituted acetophenones.
• the photoinitiator is present in an amount of about 0.01 to about 5 parts by weight, preferably about 0.01 to about 0.5 parts by weight, based on the total weight of the free-radically (co)polymerizable monomer(s).
• the mixture of the photoiniferter polymer, free-radically (co)polymerizable monomers, and photoinitator must also contain a radiation activatable crosslinking agent (i.e. a photocrosslinking agent).
• a radiation activatable crosslinking agent i.e. a photocrosslinking agent.
• Preferred radiation activatable crosslinking agents include but are not limited to those selected from the group consisting of multifunctional acrylates such as 1,6-hexanediol diacrylate, 1,4-butanediol di(meth)acrylate, hexamethylenediol di(meth)acrylate, as well as those disclosed in U.S. Patent No.
• 4,379,201 Heilmann et al.
• trimethylolpropane triacrylate such as trimethylolpropane triacrylate, pentaerythritol tetracrylate, ethylenediol di(meth)acrylate, and 1,12-dodecanediol diacrylate.
• Preferred multifunctional acrylates are those selected from the group consisting of 1,6-hexanediol diacrylate, 1,2-ethylene glycol diacrylate, 1,4-butanediol (meth)acrylate, and mixtures thereof.
• Other useful crosslinking agents include but are not limited to those selected from the group consisting of the chromophore-substituted triazines, such as those disclosed in U.S. Patent Nos.
• Patent No. 4,181,752 (Martens), e.g., 2,4-bis(trichloromethyl)-6-(4-methoxystyryl)-s- triazine.
• the preferred triazine is 2,4-bis(trichloromethyl)-6-p-methoxystyrene- 5-triazine.
• the crosslinking agent is present in an amount of from about 0.01 to about 5 parts, preferably about 0.05 to about 2 parts by weight, and most preferably about 0.1 to about 0.5 parts by weight, based upon the total weight of the free-radically (co)polymerizable monomer(s) plus photoiniferter polymer.
• compositions of this invention include, but are not limited to, those additives selected from the group consisting of fillers, pigments, plasticizers, tackifiers, chain transfer agents, fibrous reinforcing agents, woven and nonwoven fabrics, foaming agents, antioxidants, stabilizers, fire retardants, viscosity adjusting agents, and mixtures thereof.
• An especially useful filler material is hydrophobic silica as disclosed in U.S. Patent Nos. 4,710,536 and 4,749,590, (Klingen, et al.).
• the pressure-sensitive adhesive layer further comprises from about 2 to about 15 parts by weight of a hydrophobic silica having a surface area of at least 10 m 2 /g based upon the weight of the composition.
• the surface area of the hydrophobic silica is from 50 to 400 m 2 /g.
• the monomer mixture in which the photoiniferter polymer is dissolved preferably comprises about 80 to about 100 percent by weight nonpolar monomer and about 0 to about 20 percent by weight polar monomer, preferably about 85 to about 99 percent by weight nonpolar monomer and about 1 to about 15 percent by weight polar monomer, and most preferably about 90 to about 99 percent by weight polar monomer and about 1 to about 10 percent by weight polar monomer, based upon the total weight of nonpolar plus polar monomer.
• Useful polar monomers which I(BT) n can comprise include but are not limited to those selected from the group consisting of acrylic acid, methacrylic acid, itaconic acid, acrylamide, acrylonitrile, methacrylonitrile, N- vinylpyrrolidone, poly(ethylene oxide) acrylate, and mixtures thereof.
• Preferred polar monomers include those selected from the group consisting of acrylic acid, methacrylic acid, acrylamide, N-vinylpyrrolidone, and mixtures thereof.
• Most preferred polar monomers include those selected from the group consisting of acrylic acid, methacrylic acid, and mixtures thereof.
• Typical number average molecular weights of the B block of the I(BT) n random copolymer or homopolymer range from about 15,000 to about . 500,000; preferably about 25,000 to about 250,000; and most preferably about 50,000 to about 200,000.
• the glass transition temperature (T g ) of the B block of the random copolymer or homopolymer should be in the range of about -70°C to about 0°C, preferably about -60°C to about -10°C, and most preferably about -50°C to about -20°C, for reasons of processability and in order to achieve the requisite fourfold balance of desired PSA properties. Any combination of monomers which achieves the above parameters of molecular weight and T s will be useful. Ir ⁇ AT).
• the B-block is characterized essentially as above, except that the number average molecular weight ranges sought for the B-block typically range from about 15,000 to about 500,000; preferably about 25,000 to about 500,000; and most preferably about 35,000 to about 250,000. The higher ranges are employed when PSAs having higher shear values are required.
• Thermoplastic A-block monomers useful for preparing AB type block copolymers include but are not limited to those selected from the group consisting of methyl methacrylate, acrylonitrile, isobornyl acrylate, N-vinylpyrrlidone, glycidyl methacrylate, isobornyl methacrylate, isobutyl methacrylate and poly(styryl)methacrylate, and mixtures thereof.
• Preferred A-block monomers include those selected from the group consisting of methyl methacrylate, isobornyl acrylate, isobornyl methacrylate, and mixtures thereof.
• the preferred A-block monomer comprises methyl methacrylate.
• the glass transition temperature of the A block of the copolymer should be in the range of about 30°C to about 160°C, preferably about 50°C to about 150°C, and most preferably about 70°C to about 120°C.
• Typical number average molecular weights of the A block range from about 5,000 to about 100,000; preferably about 5,000 to about 50,000; and most preferably about 8,000 to about 30,000.
• the A-block can comprise either a homopolymer or a random copolymer, as long as the resultant AB-type block copolymer exhibits molecular weight and T g values within the ranges prescribed.
• the A-block typically comprises about 2 percent to about 30 percent of the copolymer, preferably about 5 percent to about 25 percent, and most preferably about 10 percent to about 20 percent by weight of the diblock copolymer. These parameters provide a suitable balance of processability, cost, and desired PSA properties.
• the B-block typically comprises about 70 percent to about 98 percent, preferably about 75 percent to about 95 percent, and most preferably about 80 percent to about 90 percent by weight based upon the weight of the block copolymer.
• the PSA composition comprises about 10 to about 100 parts by weight photoiniferter polymer, preferably about 15 to about 60 parts by weight, most preferably about 15 to about 50 parts by weight.
• the adhesive composition prepared in accordance with the present invention is easily coated upon suitable flexible or inflexible backing materials by conventional coating techniques to produce adhesive coated sheet materials in accordance with the present invention.
• the flexible backing material may be any material conventionally utilized as a tape backing or any other flexible material.
• Typical examples of flexible backing materials employed as conventional tape backings which may be useful for the adhesive compositions of the present invention include but are not limited to those selected from the group consisting of paper, plastic films such as polypropylene, polyethylene, polyvinyl chloride, polyester (e.g., polyethylene terephthalate), cellulose acetate and ethyl cellulose, as well as woven and nonwoven materials made from material and synthetic fibers.
• plastic films such as polypropylene, polyethylene, polyvinyl chloride, polyester (e.g., polyethylene terephthalate), cellulose acetate and ethyl cellulose, as well as woven and nonwoven materials made from material and synthetic fibers.
• Preferred tapes are made by coating adhesive on a backing or a core layer.
• the core layer may consist of a material including but not limited to those selected from the group consisting of acrylates, polyethylenes, polypropylenes, neoprenes, polyolefins, polyurethanes, silicones, etc.
• the core layer comprises an ultraviolet-radiation polymerized acrylic copolymer which may incorporate similar or dissimilar acrylic monomers in like or unlike thicknesses, having similar or different additives from those acrylic copolymers contained in the adhesive layer.
• the core layers preferably comprise about 90 parts, most preferably at least about 95 parts of an alkyl acrylate polymer, and correspondingly, up to about 10 parts, most preferably up to about 5 parts of a strongly polar copolymerizable monomer.
• Such core layer may be a foam-like layer, e.g., a monomer blend comprising microspheres maybe used.
• the microspheres may be glass or polymeric.
• the microspheres should have an average diameter of about 10 to about 200 micrometers, and comprise from about 5 to about 65 volume percent of the core layer.
• the thickness of foam-like layers in preferred tapes of the invention range from about 0.3 mm to about 4.0 mm in thickness.
• microspheres are polymeric microspheres, such as those described in U.S. Patent Nos. 3,615,972; 4,075,238; and 4,287,308.
• the microspheres are available from the Pierce & Stevens Company under the trade name "Microlite” in unexpanded form and "Miralit” in expanded forni. Similar microspheres are available from Kema Nord
• the microspheres In expanded form, the microspheres have a specific density of approximately 0.02 to 0.036 g/cc. It is possible to include the unexpanded microspheres in the core layer and subsequently heat them to cause expansion, but it is generally preferred to mix in the expanded microspheres. This process ensures that the hollow microspheres in the final core layer are substantially surrounded by at least a thin layer of adhesive.
• Preferred glass microspheres have average diameters of about 80 micrometers.
• the pressure-sensitive adhesive layer should be at least 3 times as thick as their diameter, preferably at least 7 times.
• the thickness of layers containing such glass microspheres should be at least six times, preferably at least twenty times that of each microsphere-free layer.
• Useful polar monomers which B can comprise for this application include but are not limited to those selected from the group consisting of acrylic acid, methacrylic acid, itaconic acid, acrylamide, acrylonitrile, methacrylonitrile, ⁇ -vinylpyrrolidone, poly(ethylene oxide)acrylate, and mixtures thereof.
• Preferred polar monomers include those selected from the group consisting of acrylic acid, methacrylic acid, acrylamide, ⁇ -vinylpyrrolidone, and mixtures thereof.
• Most preferred polar monomers include those selected from the group consisting of acrylic acid, methacrylic acid, and mixtures thereof.
• nonpolar monomers which B can comprise for this application include but are not limited to those selected from the group consisting of methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, methyl acrylate, isooctyl acrylate, n-butyl acrylate, iso-butyl acrylate, and mixtures thereof.
• Preferred nonpolar monomers include those selected from the group consisting of methyl methacrylate, n-butyl acrylate, isooctyl acrylate, and mixtures thereof.
• Most preferred nonpolar monomers include those selected from the group consisting of n-butyl acrylate, isooctyl acrylate, and mixtures thereof.
• the free-radically (co)polymerizable monomer which the B block comprises (and in which the photoiniferter polymer may be dissolved) preferably comprises about 80 to about 100 percent by weight nonpolar monomer and about 0 to about 20 percent by weight polar monomer, more preferably about 90 to about 100 percent by weight nonpolar monomer and about 0 to about 10 percent by weight polar monomer, and most preferably about 95 to about 100 percent by weight nonpolar monomer and about 0 to about 5 percent by weight polar monomer.
• Glass transition temperature ranges of the B block of the I(BT) n random copolymer for this application range from about -70°C to about -15 °C, preferably about -60°C to about -30°C, and most preferably about -50°C to about -30°C in order to obtain the best vibration damping properties.
• B blocks of the I ⁇ BT),- random copolymers have number average molecular weights in the range of about 20,000 to about 50,000; preferably about 20,000 to about 40,000; and most preferably about 25,000 to about 40,000 in order to obtain the best vibration damping properties.
• the vibration damping composition comprises about 10 to about
• photoiniferter polymer 100 parts by weight photoiniferter polymer, preferably about 10 to about 50 parts by weight, and most preferably about 20 to about 30 parts by weight. If the concentration of the free-radically (co)polymerizable monomer(s) is too high, the photo-curing rate becomes too fast. If the concentration of free-radically (co)polymerizable monomer is too low, the viscosity of the composition becomes too high and the composition cannot be coated.
• the high temperature-resistant vibration damping material of the invention is useful for applications in the automotive and computer industries, and possesses a loss tangent, tan-delta, above about 0.5, preferably above about 0.7, and a storage modulus above about lxlO 7 dynes/cm 2 , preferably between about lxlO 7 and about 5xl0 8 dynes/cm 2 or higher at temperatures above about 50°C, preferably above about 75°C, and most preferably in the range of about 100° to about 150°C.
• the vibration damping material of the invention is stable against change of these characteristics following exposure of the vibration damping material to air at about 100°C for at least 1000 hours.
• the preferred iniferter for synthesis of ABA-type triblock copolymers is p-xylylene bis(N,N-diethyldithiocarbamate) because of its enhanced reactivity.
• the elastomeric central B-block has been described above with reference to AB-type diblock polymers useful in the pressure-sensitive adhesive compositions of the invention.
• nonpolar B-block monomers for this application include but are not limited to those selected from the group consisting of methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, methyl acrylate, n-butyl acrylate, isobutyl acrylate, isobutyl methacrylate, isooctyl acrylate, and mixtures thereof.
• Preferred nonpolar B block monomers include those selected from the group consisting of n-butyl acrylate, n-butyl methacrylate, isooctyl acrylate, and mixtures thereof.
• nonpolar B block monomers include those selected from the group consisting of n-butyl acrylate, isooctyl acrylate, and mixtures thereof.
• Useful polar B block monomers for this application include but are not limited to those selected from the group consisting of acrylic acid, methacrylic acid, itaconic acid, acrylamide, acrylonitrile, methacrylonitrile, N-vinylpyrrolidone, poly(ethylene oxide)acrylate, and mixtures thereof.
• Preferred polar B block monomers include those selected from the group consisting of acrylic acid, methacrylic acid, acrylamide, N-vinylpyrrolidone, and mixtures thereof.
• Most preferred polar B block monomers include those selected from the group consisting of acrylic acid, methacrylic acid, and mixtures thereof.
• Typical number average molecular weights of the B block for this application range from about 15,000 to about 500,000; preferably about 25,000 to about 250,000; and most preferably about 50,000 to about 200,000.
• a block monomers for this application include but are not limited to those selected from the group consisting of methyl methacrylate, acrylonitrile, isobornyl acrylate, N-vinylpyrrlidone, glycidyl methacrylate, isobornyl methacrylate, isobutyl methacrylate and poly(styryl)methacrylate, and mixtures thereof.
• Preferred A-block monomers include those selected from the group consisting of methyl methacrylate, isobornyl acrylate, isobornyl methacrylate, and mixtures thereof.
• the preferred A-block monomer comprises methyl methacrylate.
• Typical number average molecular weights of the A block for this application range from about 5,000 to about 100,000; preferably about 5,000 to about 50,000; and most preferably about 8,000 to about 30,000.
• the polar monomer if used, preferably constitutes a smaller percentage of the B block of the ABA copolymer.
• the free-radically (co)polymerizable monomer which the B block comprises (and in which the photoiniferter polymer may be dissolved) preferably comprises about 80 to about 100 percent by weight nonpolar monomer and about 0 to about 20 percent by weight polar monomer, more preferably about 90 to about 100 percent by weight nonpolar monomer and about 0 to about 10 percent by weight polar monomer, and most preferably about 95 to about 100 percent by weight nonpolar monomer and about 0 to about 5 percent by weight polar monomer.
• the A blocks preferably comprise a relative proportion of about 3 to about 30 percent by weight, preferably about 4 to about 20 percent by weight, and most preferably about 4 to about 8 percent by weight, relative to the total weight of the ABA copolymer.
• concentration of ABA copolymer relative to the free radically (co)polymerizable monomer in the composition prior to photopolymerization is the same as stated for AB-type diblock PSAs discussed above.
• the B block of I(BAT) n must have a T g of about -70°C to about 0°C, preferably about -60°C to about -10°C, and most preferably about -50°C to about -20°C, in order to obtain the best properties for structural adhesive applications.
• the A block of I(BAT) n must have a T g of about 30°C to about 160°C, preferably about 50°C to about 150°C, and most preferably about 70°C to about 120°C, in order to obtain the best properties for structural adhesive applications.
• compositions of the present invention are preferably prepared by dissolving or dispersing the photoiniferter (co)polymer into the corresponding free-radically (co)polymerizable monomer or monomer mixture, then adding a photoinitiator, a crosslinking agent, and any additives.
• the composition is coated onto a flexible carrier web and polymerized in an inert, i.e., oxygen free, atmosphere, e.g., a nitrogen atmosphere.
• a sufficiently inert atmosphere can be achieved by covering a layer of the photoactive coating with a plastic film which is substantially transparent to ultraviolet radiation, and irradiating through that film in air using fluorescent-type ultraviolet lamps.
• the permissible oxygen content of the inert atmosphere can be increased by mixing into the polymerizable monomer an oxidizable tin compound as taught in U.S. Patent No. 4,303,485 (Levens), which also teaches that such procedures will allow thick coatings to be polymerized in air.
• Useful oxidizable tin salts which are preferred because they readily dissolve in the above-described monomer or monomer mixture at room temperature include but are not limited to those chosen from the group consisting of stannous octoate, stannous chloride, stannous oleate, stannous naphthenate, stannous trifiuoromethane sulfonate and tributyltin hydride. When an oxidizable tin salt is used, stannous octoate is preferred.
• the present invention provides a crosslinked network of polymers via polymerization of one or more monomers in which the photoiniferter polymer is dissolved or dispersed.
• the blending of two or more structurally dissimilar polymers provides a convenient route for the modification of polymer properties to meet specific needs.
• Such polymer blends may exhibit increased flexibility, tensile strength, chemical resistance, ease of processing, and/or other improved physical and/or chemical properties.
• phase separation occurs on a microscale, however, positive effects, as noted above, result.
• the process of polymerizing free-radically (co)polymerizable monomer in which a polymer (i.e., the photoiniferter polymer) has been dissolved or dispersed minimizes the possibility of large-scale phase separation.
• a polymer i.e., the photoiniferter polymer
• existing chains of the photoiniferter polymer are also randomly incorporated, due to the reactive end groups of the photoiniferter polymer.
• the resultant polymer has properties of a polymer network and a polymer blend.
• the two polymers of the final polymer network are very compatible, since their monomeric make-up may be identical (in the case of an I(BT) n polymer dissolved in monomer from which B is formed) or may be partially identical (in the case of an I(BAT) n polymer dissolved in monomer from which B is formed). That is, some or all of the monomers which comprise the photoiniferter polymer may be the same monomers in which that polymer is dissolved for further radiation curing, and preferably are the same monomers which the B block comprises.
• MJ number-average molecular weight
• M w weight-average molecular weight
• MMA-b-IOA-b-MMA refers to a photoiniferter copolymer having blocks ("b") of polymerized methyl methacrylate (“MMA”) and a block of polymerized isooctyl acrylate (“IOA").
• Numbers appearing beneath each block refer to the portion of the weight percent of the total copolymer weight represented by the particular block. For example,
• MMA-b-IOA-b-MMA 4.7 90.6 4.7 refers to an ABA block copolymer having two A (polymethyl methacrylate) blocks of 4.7 weight percent each and a single B midblock (polyisooctyl acrylate) of 90.6 weight percent.
• A polymethyl methacrylate
• B midblock polyisooctyl acrylate
• test methods used to evaluate the adhesives of the examples are industry standard tests.
• the test methods which characterize the polymers of this invention are those which demonstrate its molecular architecture.
• GPC gel permeation chromatography
• inherent viscosity measurement results have been obtained.
• the performance of the acrylic polymers of the invention as PSA compositions has been measured in tape form with the adhesives coated by standard methods onto conventional film backings.
• the standard tests are described in detail in various publications of the American Society for Testing and Materials (ASTM), Philadelphia, PA, and the Pressure Sensitive Tape Council (PSTC), Glenview, IL.
• the standard test methods are described in detail below.
• the reference source of each of the standard test methods is also given.
• the shear strength is a measure of cohesiveness or internal strength of an adhesive. It is based upon the amount of force required to pull an adhesive strip from a standard flat surface in a direction parallel to the surface to which it has been affixed with a definite pressure. It is measured in terms of time (in minutes) required to pull a standard area of adhesive coated sheet material from a stainless steel test panel under stress of a constant, standard load.
• a strip of anodized aluminum 19 mm x 200 mm x 0.125 mm was positioned on one adhesive face of the tape sample. Pressure was applied to the aluminum by rolling with a 2 kg roller. The opposite face of the sample was then firmly bonded to a rigid substrate. After the specified dwell time, the sample was removed by pulling the aluminum strip at 90° to the adhesive surface at a speed of 30.5 cm/minute, noting the average adhesion in N/dm width, and the failure mode.
• Foam split (FS) is the most desired failure mode as it would indicate that adhesion to the substrate is stronger than the internal strength of the core layer.
• Peel adhesion is the force required to remove a coated flexible sheet material from a test panel measured at a specific angle and rate of removal. In the examples, this force is expressed in Newtons per 100 mm (N/100 mm) width of coated sheet. The procedure followed is:
• a 12.5 mm width of the coated sheet is applied to the horizontal surface of a clean glass test plate with at least 12.7 lineal cm in firm contact.
• a hard rubber roller is used to apply the strip.
• the free end of the coated strip is doubled back nearly touching itself so the angle of removal will be 90°.
• the free end is attached to the adhesion tester scale.
• the glass test plate is clamped ' in the jaws of a tensile testing machine which is capable of moving the plate away from the scale at a constant rate of 2.3 meters per minute. 4.
• the scale reading in Newtons is recorded as the tape is peeled from the glass surface. The data is reported as the range of numbers observed during the test.
• the shear holding power and peel adhesion are relative values which are influenced by how the samples to be tested are prepared and how they are coated. All of the examples reported in Tables I and ⁇ below were prepared by coating the composition to a dried thickness of 25 micrometers onto a primed 37 micrometer thick polyester film. The tapes were conditioned for 12 hours in a constant temperature testing room at 22°C and 50% relative humidity. Tensile/Elongation
• This test method describes the determination of tensile and elongation of a sample, using an Instron Tensile Tests, Model 1122.
• An Instron Tester "English” scale, equipped with clamp-type jaws and an “English” scale load cell was used. The jaw faces were coated with rubber or some other type of non-slip surface.
• the strip of material to be tested was 1 mm thick and approximately 10.2 cm longer than the initial jaw separation and 2.5 cm or less in width. Where applicable, the test material was cut in the machine direction. The equipment was set up as follows:
• the load range was selected so that the point of maximum force will range from between 30 to 90 percent of full scale.
• the test sample was aligned and clamped into the upper and lower jaws.
• the pen and chart were started in motion, and the tensile tester was started.
• Tensile strength is the maximum force applied to the test sample to obtain the tensile value. This was determined by counting the number of small divisions reached by the pen in its maximum travel to the right across the chart during the test. The maximum tensile value point and the point of rupture may or may not coincide. Maximum force was calculated in pounds by use of the following equation:
• Elongation is the maximum percent of stretch reached by the test specimen. To obtain the percent of elongation, the number of horizontal small divisions reached in the vertical chart dimension from the start to the point of specimen rupture was counted. This number is used to calculate the percent elongation by use of the following equation:
• Samples for testing were prepared by coating a 10 mm thick layer between release liners, then curing via UV radiation. The cured polymer was cut into 25 cm circles, the liner was removed, and a laminate of 10 circular samples, equal to 100 mm, was placed in the rheometer for testing.
• a layer of viscoelastic composition having a thickness of at least about 0.01 mm up to about 100 mm, preferably about 0.025 to about 100 mm, and most preferably about 0.05 to about 100 mm, is coated onto a suitable substrate by any of the techniques known in the art such as by spray, dip, or knife coating.
• BDC was dissolved in an IOA/AA mixture in a pyrex bottle (see Table I for concentrations). The bottle was thoroughly purged with nitrogen, then sealed and irradiated with a bank of six General Electric 15-watt cylindrical black light bulbs while on a roller mill. Irradiation continued until the reaction mixture reached a viscosity sufficient for coating (i.e., about 20- 30% conversion for this example although 5-30% conversion would be useful).
• Adhesive compositions were prepared from various amounts of photoiniferter polymer composition, crosslinker (HDD A), and 0.14% of photoinitiator 2,2- dimethoxy-2-phenyl acetophenone, which is available from Ciba Geigy under the tradename IrgacureTM 651.
• Adhesive films were prepared by knife coating the syrup onto the release coated surface of a 50 micrometer biaxially oriented poly(ethyleneterephthalate) (PET) film to provide a coating thickness of about 125 micrometers. The coated surface was then covered with a 50 micrometer release coated PET film.
• PET poly(ethyleneterephthalate)
• the "sandwich construction" emerging from the knife coater was cured by exposure to 580 to 600 mJ/cm 2 of UV radiation from a bank of fluorescent lamps. The film was cooled by blowing air against the bottom layer during irradiation to keep the temperature of the film below 85°C to avoid wrinkling.
• UV radiation was between 300 nm and 400 nm with a maximum at 351 nm as measured by an ETT model UR365CH1 Radiometer that was spectrally responsive between 300 and 400 nm.
• Table I shows peel adhesion and shear properties thus obtained. As can be seen, increases in crosslinker concentration afforded increased crosslinking density, hence generally increased shear but decreased peel adhesion.
• the active dithiocarbamate end groups can participate in chain transfer or chain termination reactions, and thus are chemically linked into the growing network. Further, the short-chain BDC-terminated random copolymers are incorporated into the growing IOA/AA chains from the
• Example 2 An isooctyl acrylate/acrylic acid random copolymer and vibration-damping compositions were made following the procedure of Example 1.
• the amount of BDC was varied as indicated in Table ⁇ . 0.2% amount of HDDA was used based upon the weight of the copolymer plus IOA/AA monomers.
• the cured compositions were tested for vibration damping characteristics as described above. Results are reported in Table ⁇ . Table ⁇ shows that cured compositions containing random IOA/AA copolymers made with increasing amounts of BDC exhibited improved vibration damping.
• a solution of BDC in methyl methacrylate (MMA) was charged into a reaction bottle.
• the bottle was purged with nitrogen, sealed, then placed on a roller mill and irradiated with a bank of six GE 15 watt cylindrical black light bulbs. All of the MMA was allowed to polymerize in bulk.
• the resulting solid polymer was dissolved in ethyl acetate and IOA to yield a solution of 60% solids.
• the bottle was again purged with nitrogen, sealed, and irradiated.
• MMA-b-IOA block copolymer having a reactive dithiocarbamate group at the end of the IOA block.
• 50 g of MMA and 100 g of IOA were used, yielding a copolymer that was 67 weight percent IOA and 33 weight percent MMA.
• the above MMA-b-IOA copolymer was dissolved in a mixture of IOA and AA following which photocrosslinker and photoinitiator were added to prepare a coatable syrup.
• the ratio of IOA to AA to diblock copolymer and the photocrosslinker (HDDA) concentration are shown in Table III.
• the IrgacureTM 651 photoinitiator (2,2-dimethoxy-2-phenyl acetophenone) was added at 0.14 percent by weight based on the total weight of the MMA-b- IOA copolymer plus IOA and AA monomers.
• the syrup was coated at 5 mil thickness between liners, then cured by exposure to UV radiation (400 mj/cm 2 ).
• Table HI shows the shear and peel adhesion values obtained for the adhesive. Again, the effect of higher crosslink density (increasing concentration of HDDA) was demonstrated. Peel adhesions decreased while shear values increased.
• MMA-b-IOA is a photoiniferter polymer
• A. Preparation of an MMA-b-QOA/AAVb-MMA Triblock Copolymer A solution of IOA, AA and XDC in ethyl acetate was charged into a reaction bottle following which the bottle was purged with nitrogen. The bottle was sealed and placed on a roller mill and subjected to irradiation from six GE 15-watt cylindrical black light bulbs until conversion was complete, as monitored by NMR. To this reaction mixture was added MMA, after which the bottle was again purged with nitrogen, sealed, and placed on the roller mill for further irradiation. The component amounts are set forth in Table IV. Conversion was again monitored by NMR. When the reaction was complete, the resulting triblock copolymer was used as indicated below. B. Preparation of Structural Pressure Sensitive
• the triblock copolymer of Example 4A was thoroughly mixed into a 9: 1 ratio mixture of IOA and AA, along with IrgacureTM 651 2,2-dimethoxy-2-phenyl acetophenone photoinitiator, and HDDA crosslinker.
• the component amounts are set forth in Table IV.
• the mixture was degassed in a vacuum desiccator, then knife-coated onto release-coated PET film, covered with a second release-coated PET film, and then cured by exposure to UV radiation. The cured polymer was removed from the liners.
• the adhesive properties of the cured polymer were evaluated and are reported in Table IV.
• All structural PSA composition formulations include 0.3% HDDA and 0.14% KB-1 photoinitiator, each ba ⁇ ed upon the total weight of triblock copolymer plus IOA/AA syrup.
• the PSA composition formulations each comprise a mixture of 10% by weight triblock copolymer and 90% by weight of an IOA/AA syrup that is 90% IOA and 10% AA.
• the triblock copolymer for each formulation was as follows:

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