Abstract: A laminating adhesive comprising an adhesive composition which comprises(a) An epoxidized block copolymer of the formula(A-B-A.sub.p).sub.n -Y.sub.r -(A.sub.q -B).sub.mwherein Y is a coupling agent or coupling monomers, andwherein A and B are polymer blocks which may be homopolymer blocks of conjugated diolefin monomers, copolymer blocks of conjugated diolefin monomers or copolymer blocks of conjugated diolefin monomers and monoalkenyl aromatic hydrocarbon monomers, andwherein the A blocks have a higher number of aliphatic double bonds between a tertiary carbon atom and either a primary, secondary, or tertiary carbon atom per unit of block mass than do the B blocks, andwherein the A blocks have a molecular weight from about 100 to about 3000 and the B blocks have a molecular weight from about 1000 to about 15,000, and wherein p and q are 0 or 1 and n>0, r is 0 or 1, m.gtoreq.

Abstract: A laminating adhesive comprising an adhesive composition which comprises(a) An epoxidized block copolymer of the formula(A--B--A.sub.p).sub.n --Y.sub.r --(A.sub.q --B).sub.mwherein Y is a coupling agent or coupling monomers, and wherein A and B are polymer blocks which may be homopolymer blocks of conjugated diolefin monomers, copolymer blocks of conjugated diolefin monomers or copolymer blocks of conjugated diolefin monomers and monoalkenyl aromatic hydrocarbon monomers, and wherein the A blocks have a higher number of aliphatic double bonds between a tertiary carbon atom and either a primary, secondary, or tertiary carbon atom per unit of block mass than do the B blocks, and wherein the A blocks have a molecular weight from about 100 to about 3000 and the B blocks have a molecular weight from about 1000 to about 15,000, and wherein p and q are 0 or 1 and n>0, r is 0 or 1, m.gtoreq.

Abstract: Acrylic hot melt pressure sensitive adhesive compositions having a good balance of tack, peel and creep resistance at ambient temperature combined with optical clarity and desirable melt viscosity at elevated temperatures are prepared by copolymerizing acrylic and methacrylic alkyl esters of a non-tertiary alcohol or optionally acids with polymerizable poly methacrylate based macromonomers. The resulting acrylic copolymer has a graft or comb structure in which the acrylic backbone has a low Tg and the pendant macromonomer side chains have a Tg above room temperature. Compounding those acrylic copolymers with tackifiers and plasticizers dramatically improves the balance of pressure sensitive adhesive properties while lowering melt viscosity into a desirable range. The invention provides significant property enhancements even for acrylic copolymers having poor initial peel and shear adhesive properties.

Abstract: Acrylic hot melt pressure sensitive adhesive compositions having a good balance of tack, peel and creep resistance at ambient temperature combined with optical clarity and desirable melt viscosity at elevated temperatures are prepared by copolymerizing acrylic and methacrylic alkyl esters of a non-tertiary alcohol or optionally acids with polymerizable poly methacrylate based macromonomers. The resulting acrylic copolymer has a graft or comb structure in which the acrylic backbone has a low Tg and the pendant macromonomer side chains have a Tg above room temperature.Compounding these acrylic copolymers with tackifiers and plasticizers dramatically improves the balance of pressure sensitive adhesive properties while lowering melt viscosity into a desirable range. The invention provides significant property enhancements even for acrylic copolymers having poor initial peel and shear adhesive properties.

Abstract: An alternate procedure for preparing multilithium initiators using DVB has been developed in order to achieve better control over the specific number of anionic sites per initiator molecule and to prepare star-block copolymers having a pre-determined number of branches. The process consists of 3 distinct steps; oligomerization, activation and polymer growth. The initial step involves the oligomerization of DVB yielding a mini-block having a predetermined number of pendant vinyl groups using a monofunctional initiator such as polystyryllithium. This is quickly followed by activation of the pendant vinyl groups using s-butyllithium prior to polymer growth.

Abstract: A new coupling agent has been disclosed which is acryloyl chloride. This coupling agent undergoes anionic polymerization through the acrylate unsaturation rather than anionic attack at the acid chloride.

Abstract: The alkyllithium initiated preparation of terminally functional polymers in high yield is accomplished by first capping a macromolecular polymer with an alkylene sulfide prior to terminating the molecule with a halogenated compound containing a polymerizable moiety. The resulting macromolecular monomers are useful in the preparation of graft copolymers by copolymerizing the macromolecular monomers with monomers copolymerizable therewith.

Abstract: The alkyllithium initiated preparation of terminally functional polymers in high yield is accomplished by first capping a macromolecular polymer with an alkylene sulfide prior to terminating the molecule with a halogenated compound containing a polymerizable moiety. The resulting macromolecular monomers are useful in the preparation of graft copolymers by copolymerizing the macromolecular monomers with monomers copolymerizable therewith.

Abstract: The alkyllithium initiated preparation of terminally functional polymers in high yield is accomplished by first capping a macromolecular polymer with an alkylene sulfide prior to terminating the molecule with a halogenated compound containing a polymerizable moiety.

Abstract: A new class of multi-ester coupling agents has been disclosed which have the general formula, (CH.sub.2 .dbd.CH-CO.sub.2).sub.n X, where X is a radical from a polyhydroxy compound having 2 to 6 hydroxyl groups, and n is an integer equal to the number of hydroxy groups in the polyhydroxy compound. These coupling agents undergo anionic polymerization through the acrylate unsaturation rather than anionic attack at the ester linkage.