A biodegradable polymer usable in fishing gear and that biodegrades in aquatic environments. The polymer includes a polymer backbone that has monomeric units that are susceptible to hydrolytic degradation, and a plurality of pH responsive moieties. Each pH responsive moiety is grafted to a respective one of the monomeric units. The pH responsive moieties are relatively hydrophilic when exposed to an aqueous solution of a pro-biodegradation pH range to facilitate hydrolytic degradation of the monomeric units, and are relatively hydrophobic when removed from the aqueous solution of the pro-biodegradation pH range, to protect the monomeric units from hydrolytic degradation.

A hyperbranched polymer includes a hyperbranched, hydrophobic molecular core, respective low molecular weight polyethyleneimine chains attached to at least three branches of the hyperbranched, hydrophobic molecular core, and respective polyethylene glycol chains attached to at least two other branches of the hyperbranched, hydrophobic molecular core. Examples of the hyperbranched polymer may be used to form hyperbranched polyplexes, and may be included in DNA or RNA delivery systems.

A biodegradable aliphatic-aromatic polyester for the production of packaging films, having a Poisson's ratio (RVE) between 800 and 1700, comprising units of at least one dicarboxylic acid and at least one diol, in which Mn≥40000 and Mw/q≤90000, in which q is the percentage by weight of polyester oligomers having a molecular weight≤10000.

A chemical composition for a degradable polymeric material includes an isocyanate terminated polyester prepolymer, including prepolymer units as a main chain with a plurality of isocyanates at ends of the main chain, and a cross-linking agent. The isocyanate terminated polyester prepolymer has a structural formula as follows: ONC—R″—NH—[—CO—R—R′″-]n-NH—R″—CNO, wherein R′″ is selected from a group consisting of —O— and —CO—O—R′—O—, ##STR00001##
wherein R, R′ and R″ are an aryl group or alkyl group and wherein n is a number of prepolymer units corresponding to length of the main chain. The composition degrades at a rate and at a delay depending on temperature and the composition for a component of a downhole tool. The composition has strength and elasticity for a component of a downhole tool.

Disclosed in the present invention is poly(ester amide)s and method for preparing thermoplastic poly(ester amide)s therefor. The poly(ester amide)s are prepared using diamine or alkamine as initiator, with diacid and dialcohol-based cyclicester as the monomer, in the catalyst, and by cascade polycondensation-coupling ring-opening polymerization. The obtained poly(ester amide)s have good mechanical properties, solvent resistance and thermal stability. It effectively solves the deficiencies in the current poly(ester amide)s, such as low crystallization temperature and poor heat resistance of polyester parts, and low modulus and rigidity from polyamides part. For aliphatic poly(ester amide)s, they are biodegradable. By means of altering such factors as the ratio of ester bonds and amide bonds and polymer molecular weight and distribution, the performance of the poly(ester amide)s material can be adjusted, causing the invention to have broad application in such fields as engineering plastics, thermoplastic elastomers, tissue engineering, and controlled release.

The present invention relates to polyphosphazenes, polyurethanes based on these polyphosphazenes, methods for their manufacture and hydrogels based on the polyurethanes. The invention further relates to the use of the hydrogels in medical, veterinary and agricultural applications. The terminal ends of the polyphosphazenes bear NCO-reactive hydrogen atoms for reaction with polyisocyanates.

The present invention relates to a pressure-sensitive adhesive composition containing at least one polymer and at least one polyester polyol based on betulin. The invention also relates to the use of the pressure-sensitive adhesive composition according to the invention, to a method for preparing the pressure-sensitive adhesive composition, and to a method for bonding at least two substrates. Finally, the invention relates to an article comprising the pressure-sensitive adhesive composition according to the invention.

A foamed body includes a polylactic acid resin. An amount of the polylactic acid resin is 99.5% by mass or greater relative to a total amount of organic matter in the foamed body. A gel fraction of the foamed body is 0.1% or less. An expansion ratio of the foamed body is 5 times or greater.

A biodegradable aqueous mixture for coating substrates is disclosed, which includes from about 35 to about 75 weight percent water and from about 25 to about 65 weight percent solids. The solids in turn are made up of from about 40 to about 99 weight percent polyhydroxyalkanoates based on the total dry weight of the solids. Moreover, the polyhydroxyalkanoates are in the form of polyhydroxyalkanoate particles having a moisture content of no less than about 1% by weight prior to mixing with the water and a Dv (90) particle size of no more than about 10 microns, as determined using ISO 8130-13:2019.

Disclosed herein are processes of making furan-based polyamides using solvent-free melt condensation of a diamine and an ester derivative of 2,5-furandicarboxylic acid with a C.sub.2 to C.sub.12 aliphatic diol or a polyol. The processes comprise a) forming a reaction mixture by mixing one or more diamines, a diester comprising an ester derivative of 2,5-furandicarboxylic acid with a C.sub.2 to C.sub.12 aliphatic diol or a polyol, and a catalyst, such that the diamine is present in an excess amount of at least 1 mol % with respect to the diester amount; and b) melt polycondensing the reaction mixture in the absence of a solvent at a temperature in the range of 60° C. to a maximum temperature of 250° C. under an inert atmosphere, while removing alkyl alcohol to form a furan-based polyamide, wherein the one or more diamines comprises an aliphatic diamine, an aromatic diamine, or an alkylaromatic diamine.