A resin composition contains: a resin containing a constituent unit (A) represented by general formula (1); and a resin containing a constituent unit (B) represented by formula (2) and/or a constituent unit (C) represented by formula (3). (R.sub.1 represents a methyl group or an ethyl group, R.sub.2 and R.sub.3 represent a hydrogen atom or a methyl group, and n represents 0 or 1.) (R.sub.a and R.sub.b represent a hydrogen atom, etc., R.sub.h represents an aryl group of 6-20 carbons, X represents a single bond or a fluorene group, A and B represent an alkylene group of 1-4 carbons, m and n represent integers 0-6, and a and b represent integers 0-10.) (R.sub.c and R.sub.d represent a hydrogen atom, etc., Y represents a fluorene group, A and B represent an alkylene group of 1-4 carbons, p and q represent integers 0-4, and a and b represent integers 0-10.)

##STR00001##

A resin composition contains: a resin containing a constituent unit (A) represented by general formula (1); and a resin containing a constituent unit (B) represented by formula (2) and/or a constituent unit (C) represented by formula (3). (R.sub.1 represents a methyl group or an ethyl group, R.sub.2 and R.sub.3 represent a hydrogen atom or a methyl group, and n represents 0 or 1.) (R.sub.a and R.sub.b represent a hydrogen atom, etc., R.sub.h represents an aryl group of 6-20 carbons, X represents a single bond or a fluorene group, A and B represent an alkylene group of 1-4 carbons, m and n represent integers 0-6, and a and b represent integers 0-10.) (R.sub.c and R.sub.d represent a hydrogen atom, etc., Y represents a fluorene group, A and B represent an alkylene group of 1-4 carbons, p and q represent integers 0-4, and a and b represent integers 0-10.)

##STR00001##

A liquid crystal polyester comprising a structural unit derived from 6-hydroxy-2-naphthoic acid, wherein in thermal extraction GC-MS analysis of the liquid crystal polyester under the following measuring conditions, the relative content of the following impurity component determined from the GC peak area in the total ion chromatogram using methyl 6-hydroxy-2-naphthoate as a standard sample is 50 ppm or less based on the mass of the liquid crystal polyester, and the impurity component has main peaks at m/z=228, 186, 171, and 143 in the MS spectrum chart and a retention time detected in the range of 11.5 to 12.5 min in the total ion chromatogram.

A liquid crystal polyester comprising a structural unit derived from 6-hydroxy-2-naphthoic acid, wherein in thermal extraction GC-MS analysis of the liquid crystal polyester under the following measuring conditions, the relative content of the following impurity component determined from the GC peak area in the total ion chromatogram using methyl 6-hydroxy-2-naphthoate as a standard sample is 50 ppm or less based on the mass of the liquid crystal polyester, and the impurity component has main peaks at m/z=228, 186, 171, and 143 in the MS spectrum chart and a retention time detected in the range of 11.5 to 12.5 min in the total ion chromatogram.

Provided is a copolymer comprising an irregularly arranged structure of a repeating unit of the following Chemical Formula 1 and a repeating unit of the following Chemical Formula 2, and a repeating unit of the following Chemical Formula 3 present at least at one end of the structure:

##STR00001##

and is characterized by having an improved elongation and also having a high weight average molecular weight while maintaining intrinsic properties of a polylactic acid. Also provided are methods of preparing the copolymer.

Provided is a copolymer comprising an irregularly arranged structure of a repeating unit of the following Chemical Formula 1 and a repeating unit of the following Chemical Formula 2, and a repeating unit of the following Chemical Formula 3 present at least at one end of the structure:

##STR00001##

and is characterized by having an improved elongation and also having a high weight average molecular weight while maintaining intrinsic properties of a polylactic acid. Also provided are methods of preparing the copolymer.

Disclosed is a copolymer comprising a hydroxyacid, wherein the copolymer is biodegradable with a decomposition temperature is substantially higher than its melting temperature. Also disclosed is a method of synthesis of a poly(pivalolactone-co-caprolactone) copolymer.

Disclosed is a copolymer comprising a hydroxyacid, wherein the copolymer is biodegradable with a decomposition temperature is substantially higher than its melting temperature. Also disclosed is a method of synthesis of a poly(pivalolactone-co-caprolactone) copolymer.

Several embodiments of the invention relate generally to a system and methods for the treatment of gaseous emissions comprising methane and one or more non-methane compounds that can influence the metabolism of methane-oxidizing microorganisms. In several embodiments, there is provided a system and methods for the treatment of methane emissions through the use of methanotrophic microorganisms to generate functionally consistent and harvestable products. Certain embodiments of the invention are particularly advantageous because they reduce environmentally-destructive methane emissions and produce harvestable end-products.

Several embodiments of the invention relate generally to a system and methods for the treatment of gaseous emissions comprising methane and one or more non-methane compounds that can influence the metabolism of methane-oxidizing microorganisms. In several embodiments, there is provided a system and methods for the treatment of methane emissions through the use of methanotrophic microorganisms to generate functionally consistent and harvestable products. Certain embodiments of the invention are particularly advantageous because they reduce environmentally-destructive methane emissions and produce harvestable end-products.