An adhesive film and a display member, the adhesive film being formed of an adhesive composition that includes a monomer mixture comprising a hydroxyl group-containing (meth)acrylate and a comonomer, wherein the adhesive film has a recovery rate of about 40% to about 99%, the recovery rate being determined according to Method A as described herein, and wherein the adhesive film has a bubble generation area of about 0%, the bubble generation area being determined according to Method B as described herein.

An adhesive film and a display member, the adhesive film being formed of an adhesive composition that includes a monomer mixture comprising a hydroxyl group-containing (meth)acrylate and a comonomer, wherein the adhesive film has a recovery rate of about 40% to about 99%, the recovery rate being determined according to Method A as described herein, and wherein the adhesive film has a bubble generation area of about 0%, the bubble generation area being determined according to Method B as described herein.

Provided are a photocurable composition which has excellent storage stability and is cured rapidly in bonding an opaque material, and a product. The photocurable composition contains (A) a compound having an unsaturated double bond, (B) at least one compound selected from the group consisting of compounds represented by the general formulae (1), (2), and (3), and (C) a sensitizer. In the general formulae (1), (2), and (3), R.sup.1 to R.sup.3 are each independently a substituent containing at least one group selected from the group consisting of a nitro group, a cyano group, a hydroxy group, an acetyl group, a carbonyl group, a substituted or unsubstituted allyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group, an unsubstituted or substituted aryl group, an unsubstituted or substituted aryloxy group, a heterocyclic ring structure-containing group, and a group having a plurality of rings. At least two groups selected from the group consisting of R.sup.1 to R.sup.3 may be bonded to each other to form a cyclic structure with carbon atoms to which the groups are bonded.

Provided are a photocurable composition which has excellent storage stability and is cured rapidly in bonding an opaque material, and a product. The photocurable composition contains (A) a compound having an unsaturated double bond, (B) at least one compound selected from the group consisting of compounds represented by the general formulae (1), (2), and (3), and (C) a sensitizer. In the general formulae (1), (2), and (3), R.sup.1 to R.sup.3 are each independently a substituent containing at least one group selected from the group consisting of a nitro group, a cyano group, a hydroxy group, an acetyl group, a carbonyl group, a substituted or unsubstituted allyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group, an unsubstituted or substituted aryl group, an unsubstituted or substituted aryloxy group, a heterocyclic ring structure-containing group, and a group having a plurality of rings. At least two groups selected from the group consisting of R.sup.1 to R.sup.3 may be bonded to each other to form a cyclic structure with carbon atoms to which the groups are bonded.

Provided are a photocurable composition which has excellent storage stability and is cured rapidly in bonding an opaque material, and a product. The photocurable composition contains (A) a compound having an unsaturated double bond, (B) at least one compound selected from the group consisting of compounds represented by the general formulae (1), (2), and (3), and (C) a sensitizer. In the general formulae (1), (2), and (3), R.sup.1 to R.sup.3 are each independently a substituent containing at least one group selected from the group consisting of a nitro group, a cyano group, a hydroxy group, an acetyl group, a carbonyl group, a substituted or unsubstituted allyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group, an unsubstituted or substituted aryl group, an unsubstituted or substituted aryloxy group, a heterocyclic ring structure-containing group, and a group having a plurality of rings. At least two groups selected from the group consisting of R.sup.1 to R.sup.3 may be bonded to each other to form a cyclic structure with carbon atoms to which the groups are bonded.

The present disclosure relates to a process of manufacturing curable precursor of a structural adhesive composition. According to another aspect, the present disclosure is directed to method of bonding two parts.

The present invention concerns a two-part curable composition comprising: •a first part (component A) comprising: —at least 51% by weight based on the total weight of the first part, of one or more cyanoacrylate monomer(s); —a transition metal complex; and—an antioxidant; •a second part (component B) comprising: —a per-compound; —at least one Michael acceptor M selected from the group consisting of (meth)acrylic monomers, (meth)acrylic functionalized oligomers, (meth)acrylic functionalized resins, and mixtures thereof; provided that the composition comprises (in the first part and/or in the second part) at least one compound C comprising a radical -EWG.sub.1-CH.sub.2-EWG.sub.2- wherein EWG.sub.2 and EWG.sub.1 are independently of each other an electron withdrawing group.

An optically transparent adhesive resin composition includes an ester polymer which contains an ester bond within a repeating unit, a (meth)acrylic ester polymer which contains a (meth)acrylic ester bond within the repeating unit, a rubber polymer, and a crystalline polymer.

An optically transparent adhesive resin composition includes an ester polymer which contains an ester bond within a repeating unit, a (meth)acrylic ester polymer which contains a (meth)acrylic ester bond within the repeating unit, a rubber polymer, and a crystalline polymer.

Disclosed pressure sensitive adhesive compositions, having enhanced heat resistance, obtained by the emulsion polymerization of (a) one or more acrylic acid ester or (meth)acrylate acid ester(s), (b) one or more hydroxyl functional (meth)acrylic monomer and (c) one or more ureido substituted (meth)acrylate monomers(s).