The present invention relates to curable photochromic compositions which include an at least di-functional oxazoline functional material, an at least di-functional first carboxylic acid functional material, an optional second carboxylic acid functional material having at least three carboxylic acid groups, which optionally includes a carboxylic acid functional polymer, and a photochromic compound. The curable photochromic compositions have an equivalents ratio of oxazoline equivalents of the oxazoline functional material to a total carboxylic acid equivalents of the first and optional second carboxylic acid functional materials of from 0.5:1 to 10:1 when the second carboxylic acid functional material is not present, and from 0.5:1 to 3:1 when the second carboxylic acid functional material is present. The present invention, more particularly, relates to curable photochromic adhesive compositions, and curable photochromic coating compositions.

The present invention relates to curable photochromic compositions which include an at least di-functional oxazoline functional material, an at least di-functional first carboxylic acid functional material, an optional second carboxylic acid functional material having at least three carboxylic acid groups, which optionally includes a carboxylic acid functional polymer, and a photochromic compound. The curable photochromic compositions have an equivalents ratio of oxazoline equivalents of the oxazoline functional material to a total carboxylic acid equivalents of the first and optional second carboxylic acid functional materials of from 0.5:1 to 10:1 when the second carboxylic acid functional material is not present, and from 0.5:1 to 3:1 when the second carboxylic acid functional material is present. The present invention, more particularly, relates to curable photochromic adhesive compositions, and curable photochromic coating compositions.

The present invention relates to curable photochromic compositions which include an at least di-functional oxazoline functional material, an at least di-functional first carboxylic acid functional material, an optional second carboxylic acid functional material having at least three carboxylic acid groups, which optionally includes a carboxylic acid functional polymer, and a photochromic compound. The curable photochromic compositions have an equivalents ratio of oxazoline equivalents of the oxazoline functional material to a total carboxylic acid equivalents of the first and optional second carboxylic acid functional materials of from 0.5:1 to 10:1 when the second carboxylic acid functional material is not present, and from 0.5:1 to 3:1 when the second carboxylic acid functional material is present. The present invention, more particularly, relates to curable photochromic adhesive compositions, and curable photochromic coating compositions.

The present invention provides an aromatic polyester having several operative functional groups and a method for producing same. An aromatic polyester comprising a polycarboxylic acid component and a polyhydric alcohol component as a copolymerization component, wherein the aromatic polyester comprises a polycarboxylic acid component having an operative functional group by 50 mol % or more when a total amount of the polycarboxylic acid component is taken as 100 mol %, and the aromatic polyester comprises an aromatic polyhydric alcohol component by 50 mol % or more when a total amount of the polyhydric alcohol component is taken as 100 mol %.

The present invention provides an aromatic polyester having several operative functional groups and a method for producing same. An aromatic polyester comprising a polycarboxylic acid component and a polyhydric alcohol component as a copolymerization component, wherein the aromatic polyester comprises a polycarboxylic acid component having an operative functional group by 50 mol % or more when a total amount of the polycarboxylic acid component is taken as 100 mol %, and the aromatic polyester comprises an aromatic polyhydric alcohol component by 50 mol % or more when a total amount of the polyhydric alcohol component is taken as 100 mol %.

Disclosed are processes for making polymeric composite materials and composite materials made from those processes, the process comprising: providing a mixture, comprising: a liquid, a polymer precursor, and a dispersed-phase precursor; and subjecting the mixture to reaction conditions sufficient: to effect polymerization of the polymer precursor to produce a polymer and a reaction product; and to remove substantially all the liquid and reaction product from the mixture; wherein said reaction conditions comprise: pressure between about 10 millitorr and about 300 torr; and temperature: greater than or equal to the highest boiling point of the liquid and reaction product; less than the decomposition temperature of the polymer; and less than the decomposition temperature of the dispersed-phase precursor.

Disclosed are processes for making polymeric composite materials and composite materials made from those processes, the process comprising: providing a mixture, comprising: a liquid, a polymer precursor, and a dispersed-phase precursor; and subjecting the mixture to reaction conditions sufficient: to effect polymerization of the polymer precursor to produce a polymer and a reaction product; and to remove substantially all the liquid and reaction product from the mixture; wherein said reaction conditions comprise: pressure between about 10 millitorr and about 300 torr; and temperature: greater than or equal to the highest boiling point of the liquid and reaction product; less than the decomposition temperature of the polymer; and less than the decomposition temperature of the dispersed-phase precursor.

A food or beverage container, or portion thereof, including a metal substrate and a coating on at least a portion of the metal substrate, the coating formed being from a coating composition comprising a polymer having one or more substituted or unsubstituted spirocyclic segments such as substituted or unsubstituted segments of 2,4,8,10-tetraoxaspiro [5.5] undecane.

A food or beverage container, or portion thereof, including a metal substrate and a coating on at least a portion of the metal substrate, the coating formed being from a coating composition comprising a polymer having one or more substituted or unsubstituted spirocyclic segments such as substituted or unsubstituted segments of 2,4,8,10-tetraoxaspiro [5.5] undecane.

An object of an embodiment of the present invention is to provide a biodegradable polyester solution that exhibits good solubility in a halogen-free organic solvent and that has sufficient adhesive strength even when aged for a short time. The object is achieved by providing a biodegradable polyester solution containing a poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) copolymer and a solvent, the poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) copolymer having an average content of 16 mol % or more 3-hydroxyhexanoate.