A rubber composition for golf balls includes (A) a base rubber, (B) an acrylate ester or methacrylate ester containing an isocyanate group or a blocked isocyanate group, (C) diacrylic acid, dimethacrylic acid or a metal salt thereof, and (D) an organic peroxide. In a golf ball having a core formed of the rubber composition and a cover of one or more layers which encases the core, the rubber composition exhibits a spin rate-lowering effect on shots and can thus improve the flight performance of the ball.

A latex of an acid-modified conjugated diene polymer including the acid-modified conjugated diene polymer obtained by modifying a conjugated diene polymer with an acid group-containing compound, in which a content of a structural unit derived from the acid group-containing compound is 0.2 to 0.7 parts by weight with respect to 100 parts by weight of the acid-modified conjugated diene polymer; a content of a water-soluble polymer in the latex is 2 parts by weight or less with respect to 100 parts by weight of the acid-modified conjugated diene polymer; when a solids content of the latex is adjusted to 60 wt %, a viscosity at 25° C. is 800 mPa.Math.s or less; and when the solids content of the latex is adjusted to 50 wt %, the viscosity at 25° C. is 300 mPa.Math.s or less.

A latex of an acid-modified conjugated diene polymer including the acid-modified conjugated diene polymer obtained by modifying a conjugated diene polymer with an acid group-containing compound, in which a content of a structural unit derived from the acid group-containing compound is 0.2 to 0.7 parts by weight with respect to 100 parts by weight of the acid-modified conjugated diene polymer; a content of a water-soluble polymer in the latex is 2 parts by weight or less with respect to 100 parts by weight of the acid-modified conjugated diene polymer; when a solids content of the latex is adjusted to 60 wt %, a viscosity at 25° C. is 800 mPa.Math.s or less; and when the solids content of the latex is adjusted to 50 wt %, the viscosity at 25° C. is 300 mPa.Math.s or less.

What are described are copolymers containing cationic structural units and macromonomeric structural units. The copolymers are, for example, advantageously suitable for use in detergent compositions and lead to advantageous shine results, for example, after application on hard surfaces.

What are described are copolymers containing cationic structural units and macromonomeric structural units. The copolymers are, for example, advantageously suitable for use in detergent compositions and lead to advantageous shine results, for example, after application on hard surfaces.

First embodiment of a (meth)acrylic copolymer in the present invention includes following: a (meth)acrylic copolymer having at least one kind of constitutional unit selected from the group consisting of a constitutional unit (A1) having at least one kind of structure (I) selected from the group consisting of structures represented by the following formula (1), formula (2), or formula (3) and a constitutional unit (A2) having a triorganosilyloxycarbonyl group and a constitutional unit (B) derived from a macromonomer (b): ##STR00001## (where, X represents —O—, —S—, or —NR.sup.14—, R.sup.14 represents a hydrogen atom or an alkyl group, R.sup.1 and R.sup.2 each represent a hydrogen atom or an alkyl group having from 1 to 10 carbon atoms, R.sup.3 and R.sup.5 each represent an alkyl group having from 1 to 20 carbon atoms, a cycloalkyl group, or an aryl group, and R.sup.4 and R.sup.6 each represent an alkylene group having from 1 to 10 carbon atoms).

First embodiment of a (meth)acrylic copolymer in the present invention includes following: a (meth)acrylic copolymer having at least one kind of constitutional unit selected from the group consisting of a constitutional unit (A1) having at least one kind of structure (I) selected from the group consisting of structures represented by the following formula (1), formula (2), or formula (3) and a constitutional unit (A2) having a triorganosilyloxycarbonyl group and a constitutional unit (B) derived from a macromonomer (b): ##STR00001## (where, X represents —O—, —S—, or —NR.sup.14—, R.sup.14 represents a hydrogen atom or an alkyl group, R.sup.1 and R.sup.2 each represent a hydrogen atom or an alkyl group having from 1 to 10 carbon atoms, R.sup.3 and R.sup.5 each represent an alkyl group having from 1 to 20 carbon atoms, a cycloalkyl group, or an aryl group, and R.sup.4 and R.sup.6 each represent an alkylene group having from 1 to 10 carbon atoms).

A high melt strength resin composition includes at least a) non-functionalized polypropylene, b) at least one acrylate such as zinc diacrylate, calcium diacrylate or aluminum triacrylate in a total amount of from 0.1 to 5% by weight based on the weight of non-functionalized polypropylene, and c) at least one acid neutralizer in a total amount of from 0.005 to 5% by weight based on the total weight of the at least one acrylate. The resin composition is compounded at a processing temperature between 185° C. and 260° C. to obtain the high melt strength polypropylene.

A high melt strength resin composition includes at least a) non-functionalized polypropylene, b) at least one acrylate such as zinc diacrylate, calcium diacrylate or aluminum triacrylate in a total amount of from 0.1 to 5% by weight based on the weight of non-functionalized polypropylene, and c) at least one acid neutralizer in a total amount of from 0.005 to 5% by weight based on the total weight of the at least one acrylate. The resin composition is compounded at a processing temperature between 185° C. and 260° C. to obtain the high melt strength polypropylene.

A high melt strength resin composition includes at least a) non-functionalized polypropylene, b) at least one acrylate such as zinc diacrylate, calcium diacrylate or aluminum triacrylate in a total amount of from 0.1 to 5% by weight based on the weight of non-functionalized polypropylene, and c) at least one acid neutralizer in a total amount of from 0.005 to 5% by weight based on the total weight of the at least one acrylate. The resin composition is compounded at a processing temperature between 185° C. and 260° C. to obtain the high melt strength polypropylene.