This invention relates to a method for increasing wetting capability of a biomimetic polymer adhesive comprising the step of introducing plurality of phosphate moieties into said biomimetic polymer adhesive. In particular, the present disclosure relates a method to manufacture a biomimetic polymer adhesive with an increased wetting capability by inducing plurality of phosphate moieties by copolymerization of phosphate-containing monomer, such as monoacryloxyethyl phosphate (MAEP), together with other monomers, or by way of post-polymerization chemical derivertizations. The process and the product thereof are within the scope of this disclosure.

This invention relates to a method for increasing wetting capability of a biomimetic polymer adhesive comprising the step of introducing plurality of phosphate moieties into said biomimetic polymer adhesive. In particular, the present disclosure relates a method to manufacture a biomimetic polymer adhesive with an increased wetting capability by inducing plurality of phosphate moieties by copolymerization of phosphate-containing monomer, such as monoacryloxyethyl phosphate (MAEP), together with other monomers, or by way of post-polymerization chemical derivertizations. The process and the product thereof are within the scope of this disclosure.

A composition including a polymerizable monomer with a phosphate or phosphonate function on the one hand and a methacrylate, acrylate, acrylamide or methacrylamide function on the other hand at a concentration of between 5 and 40% by weight relative to the total weight of the composition,—a photoinitiator at a concentration of between 0.5 and 2% by weight, and a photopolymerizable resin.

A resin composition includes a urethane (meth)acrylate oligomer. When the resin composition is cured with an ultraviolet light and loaded a shear force of about 2,000 Pa, the difference between the shear strain of the cured resin composition about 5 seconds after the loading and a shear strain of the cured resin composition about 300 seconds after the loading is less than about 5% A shear strain of the cured resin composition about 30 seconds after the shear force is removed from the cured resin composition is less than about 2%.

A resin composition includes a urethane (meth)acrylate oligomer. When the resin composition is cured with an ultraviolet light and loaded a shear force of about 2,000 Pa, the difference between the shear strain of the cured resin composition about 5 seconds after the loading and a shear strain of the cured resin composition about 300 seconds after the loading is less than about 5% A shear strain of the cured resin composition about 30 seconds after the shear force is removed from the cured resin composition is less than about 2%.

An object of the present invention is to provide a two-part composition containing a first agent and a second agent: the first agent comprising (1) (meth)acrylate and (2) organoboron compound, and having an oxygen content of 5 ppm or less, and the second agent comprising (3) phosphate ester.

A composition having excellent adhesiveness to poorly adhesive materials such as polyolefins is provided. The solution is a composition comprising the following (1) to (2): (1) (meth)acrylates containing the following (1-1) to (1-3): (1-1) a (meth)acrylate having a hydroxyl group, (1-2) an alkyl (meth)acrylate, and (1-3) a (meth)acrylate having a cyclic ether skeleton, and (2) an organoboron compound. The content ratio of (1-1), (1-2), and (1-3) is (1-1):(1-2):(1-3)=(10 to 90):(5 to 80):(5 to 80) in mass ratio in 100 parts by mass of (1) (meth)acrylates.

A composition having excellent adhesiveness to poorly adhesive materials such as polyolefins is provided. The solution is a composition comprising the following (1) to (2): (1) (meth)acrylates containing the following (1-1) to (1-3): (1-1) a (meth)acrylate having a hydroxyl group, (1-2) an alkyl (meth)acrylate, and (1-3) a (meth)acrylate having a cyclic ether skeleton, and (2) an organoboron compound. The content ratio of (1-1), (1-2), and (1-3) is (1-1):(1-2):(1-3)=(10 to 90):(5 to 80):(5 to 80) in mass ratio in 100 parts by mass of (1) (meth)acrylates.

A copolymer includes a repeating unit represented by Formula (I); and a repeating unit represented by Formula (II), in Formula (I), R.sup.1 represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms; R.sup.2 represents an alkyl group having 1 to 20 carbon atoms and having at least one fluorine atom as a substituent, or a group including Si(R.sup.a3)(R.sup.a4)O; L represents a divalent linking group as defined herein; and R.sup.a3 and R.sup.a4 each independently represent an alkyl group as defined herein, in Formula (II), R.sup.10 represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms; R.sup.11 and R.sup.12 each independently represent a hydrogen atom, a substituted or unsubstituted aliphatic hydrocarbon group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heteroaryl group; R.sup.11 and R.sup.12 may be linked to each other; and X.sup.1 represents a divalent linking group.

A copolymer includes a repeating unit represented by Formula (I); and a repeating unit represented by Formula (II), in Formula (I), R.sup.1 represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms; R.sup.2 represents an alkyl group having 1 to 20 carbon atoms and having at least one fluorine atom as a substituent, or a group including Si(R.sup.a3)(R.sup.a4)O; L represents a divalent linking group as defined herein; and R.sup.a3 and R.sup.a4 each independently represent an alkyl group as defined herein, in Formula (II), R.sup.10 represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms; R.sup.11 and R.sup.12 each independently represent a hydrogen atom, a substituted or unsubstituted aliphatic hydrocarbon group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heteroaryl group; R.sup.11 and R.sup.12 may be linked to each other; and X.sup.1 represents a divalent linking group.