An aerosol coating composition contains at least one film-forming resin, trans-1-chloro-3,3,3-trifluoropropene and at least one propellant such as CO.sub.2. The aerosol coating composition is non-flammable and compatible with polyethylene terephthalate. The film-forming resin may be acrylic resins, alkyd resins or mixtures thereof. A glycol ether solvent may be present. The coating composition may have low toxicity, be non-ozone depleting, have low or no VOC, be low in maximum incremental reactivity and/or be low in global warming potential. A method of coating a substrate with the aerosol coating composition comprises providing at least one film-forming resin selected from the group consisting of acrylic resins, alkyd resins, and mixtures thereof and trans-1-chloro-trifluoropropene in a container comprising polyethylene terephthalate, which is charged with a propellant comprising carbon dioxide. The aerosol coating composition is non-flammable. The composition is applied to a substrate and allowed to dry.

An aerosol coating composition contains at least one film-forming resin, trans-1-chloro-3,3,3-trifluoropropene and at least one propellant such as CO.sub.2. The aerosol coating composition is non-flammable and compatible with polyethylene terephthalate. The film-forming resin may be acrylic resins, alkyd resins or mixtures thereof. A glycol ether solvent may be present. The coating composition may have low toxicity, be non-ozone depleting, have low or no VOC, be low in maximum incremental reactivity and/or be low in global warming potential. A method of coating a substrate with the aerosol coating composition comprises providing at least one film-forming resin selected from the group consisting of acrylic resins, alkyd resins, and mixtures thereof and trans-1-chloro-trifluoropropene in a container comprising polyethylene terephthalate, which is charged with a propellant comprising carbon dioxide. The aerosol coating composition is non-flammable. The composition is applied to a substrate and allowed to dry.

The present invention aims to provide a method for improving the fluidity of a crystal nucleating agent for polyolefin resins without impairing other properties, and a polyolefin resin composition containing the crystal nucleating agent with improved fluidity and having excellent properties including transparency, and a molded article thereof. Adjustment to specific characteristics can improve the fluidity of a crystal nucleating agent for polyolefin resins, and the use of such a crystal nucleating agent having specific characteristics remarkably improves the workability during molding processing and provides a polyolefin resin composition excellent in properties such as transparency, and a molded article thereof.

A rubber composition is prepared by mixing a specific hydrazide compound at a ratio of 0.5 to 3.0 parts by mass, zinc oxide at a ratio of 1 to 5 parts by mass, and carbon black having N.sub.2SA of 60 to 150 m.sup.2/g at a ratio of 30 to 60 parts by mass per 100 parts by mass of diene rubber containing 80 parts by mass or more of natural rubber. The rubber composition is prepared through (a) mixing the hydrazide compound and the carbon black to obtain a mixture, and (b) mixing the zinc oxide with the mixture obtained in step (a) to obtain a mixture. A maximum ultimate temperature during the mixture in step (a) is from 140 to 170° C. A storage modulus and elongation at break have a specific relationship.

A rubber composition is prepared by mixing a specific hydrazide compound at a ratio of 0.5 to 3.0 parts by mass, zinc oxide at a ratio of 1 to 5 parts by mass, and carbon black having N.sub.2SA of 60 to 150 m.sup.2/g at a ratio of 30 to 60 parts by mass per 100 parts by mass of diene rubber containing 80 parts by mass or more of natural rubber. The rubber composition is prepared through (a) mixing the hydrazide compound and the carbon black to obtain a mixture, and (b) mixing the zinc oxide with the mixture obtained in step (a) to obtain a mixture. A maximum ultimate temperature during the mixture in step (a) is from 140 to 170° C. A storage modulus and elongation at break have a specific relationship.

Provided is a polyacetal resin composition in which at least one dihydrazone compound (B) selected from the group of two kinds of dihydrazone compounds is blended in 0.02 to 5 parts by mass with respect to 100 parts by mass of a polyacetal resin (A).

Provided is a polyacetal resin composition in which at least one dihydrazone compound (B) selected from the group of two kinds of dihydrazone compounds is blended in 0.02 to 5 parts by mass with respect to 100 parts by mass of a polyacetal resin (A).

Provided is a polyacetal resin composition in which at least one dihydrazone compound (B) selected from the group of two kinds of dihydrazone compounds is blended in 0.02 to 5 parts by mass with respect to 100 parts by mass of a polyacetal resin (A).

Water-borne cross-linking polymeric compositions and related embodiments, such as methods of making and using the compositions, as well as products formed with said compositions are described. For example, the water-borne composition may comprise polymers incorporating cross-linking functionality such as, but not limited to, carbonyl or epoxy functionality, and a blocked cross-linking agent, for example, a hydrazone. The cross-linking functionality does not react with the blocked cross-linking agent; however, the blocked cross-linking agent is capable of reacting with the alternative form cross-linking agent such as, but not limited to, a hydrazide, to yield a cross-linked polymer. The alternative form cross-linking agent may be formed in an equilibrium reaction including the blocked cross-linking agent.

Water-borne cross-linking polymeric compositions and related embodiments, such as methods of making and using the compositions, as well as products formed with said compositions are described. For example, the water-borne composition may comprise polymers incorporating cross-linking functionality such as, but not limited to, carbonyl or epoxy functionality, and a blocked cross-linking agent, for example, a hydrazone. The cross-linking functionality does not react with the blocked cross-linking agent; however, the blocked cross-linking agent is capable of reacting with the alternative form cross-linking agent such as, but not limited to, a hydrazide, to yield a cross-linked polymer. The alternative form cross-linking agent may be formed in an equilibrium reaction including the blocked cross-linking agent.