Disclosed herein is an acetylated lactide oligomer-based plasticizer and a method of preparing the same having improved thermal stability, enhanced plasticity and excellent compatibility with a resin, the method, including: (a) synthesizing a lactide oligomer through ring-opening polymerization (ROP) of an initiator and lactide; (b) putting acetic anhydride into the lactide oligomer and performing acetylation; and (c) removing acetic acid generated in step (b) and unreacted acetic anhydride.

Disclosed herein is an acetylated lactide oligomer-based plasticizer and a method of preparing the same having improved thermal stability, enhanced plasticity and excellent compatibility with a resin, the method, including: (a) synthesizing a lactide oligomer through ring-opening polymerization (ROP) of an initiator and lactide; (b) putting acetic anhydride into the lactide oligomer and performing acetylation; and (c) removing acetic acid generated in step (b) and unreacted acetic anhydride.

A quaternary ammonium compound of formula (I): wherein R.sup.0, R.sup.1, R.sup.2 and R.sup.3 is each independently an optionally substituted hydrocarbyl group, X is a linking group, R.sup.4 is an optionally substituted alkylene group, R.sup.5 is hydrogen or an optionally substituted alkyl, alkenyl or aryl group, and n is 0 or a positive integer, provided that n is not 0 when R.sup.5 is hydrogen. ##STR00001##

An electrolyte is provided, which includes organic solvent; and (1) a compound and an ammonium salt thereof, (2) a diacid and an ammonium salt thereof, or (3) a combination thereof. The compound has a chemical structure of

##STR00001##

wherein R.sup.1 is C.sub.1-8 alkyl group, C alkenyl group, C.sub.1-8 alkynyl group, or aromatic group; and R.sup.2 is —(C.sub.nH.sub.2n)—OH, and n is an integer from 2 to 8. The diacid has a chemical structure of

##STR00002##

wherein R.sup.3 is C.sub.1-8 alkyl group, C.sub.1-8 alkenyl group, C.sub.1-8 alkynyl group, or aromatic group.

An electrolyte is provided, which includes organic solvent; and (1) a compound and an ammonium salt thereof, (2) a diacid and an ammonium salt thereof, or (3) a combination thereof. The compound has a chemical structure of

##STR00001##

wherein R.sup.1 is C.sub.1-8 alkyl group, C alkenyl group, C.sub.1-8 alkynyl group, or aromatic group; and R.sup.2 is —(C.sub.nH.sub.2n)—OH, and n is an integer from 2 to 8. The diacid has a chemical structure of

##STR00002##

wherein R.sup.3 is C.sub.1-8 alkyl group, C.sub.1-8 alkenyl group, C.sub.1-8 alkynyl group, or aromatic group.

Disclosed are methods or processes of synthesizing building blocks and feedstocks for producing a broader range of polymers, including renewable polymers, from renewable resources such as CO.sub.2. In a process of manufacturing a renewable feedstock for polymer production, a CO.sub.2 derived lactone is prepared and processed to form the renewable feedstock. The process may include alkoxycarbonylation of the CO.sub.2 derived lactone to form a diester and hydrogenation of the diester.

Disclosed are methods or processes of synthesizing building blocks and feedstocks for producing a broader range of polymers, including renewable polymers, from renewable resources such as CO.sub.2. In a process of manufacturing a renewable feedstock for polymer production, a CO.sub.2 derived lactone is prepared and processed to form the renewable feedstock. The process may include alkoxycarbonylation of the CO.sub.2 derived lactone to form a diester and hydrogenation of the diester.

This invention relates to the field of contaminated plastic waste decomposition. More specifically, the invention comprises methods and systems to decompose contaminated plastic waste and transform it into value-added products.

This invention relates to the field of contaminated plastic waste decomposition. More specifically, the invention comprises methods and systems to decompose contaminated plastic waste and transform it into value-added products.

A quaternary ammonium compound of formula (I): (I) wherein R.sup.0, R.sup.1, R.sup.2 and R.sup.3 is each independently an optionally substituted hydrocarbyl group, X is a linking group, R.sup.4 is an optionally substituted alkylene group, R5 is hydrogen or an optionally substituted alkyl, alkenyl or aryl group, and n is 0 or a positive integer, provided that n is not 0 when R5 is hydrogen. ##STR00001##