C08G63/78

Method for preparing high molecular weight poly-L-lactic acid

A method for preparing high molecular weight poly(L-lactic acid) with high performance, including: a) providing a biogenic guanidine (BG) as a catalyst, and a nontoxic acid salt of an essential metal trace element as an activator (Act), and adding the catalyst, the activator, and L-lactide monomer to a polymerization reactor; b) evacuating under vacuum and charging the polymerization reactor with nitrogen for three consecutive times to remove air, and allowing the L-lactide monomer to undergo bulk polymerization under vacuum. The bulk polymerization includes a first reaction stage and a second reaction stage, which are separately carried out at different temperatures, pressures, and reaction times.

Method for preparing high molecular weight poly-L-lactic acid

A method for preparing high molecular weight poly(L-lactic acid) with high performance, including: a) providing a biogenic guanidine (BG) as a catalyst, and a nontoxic acid salt of an essential metal trace element as an activator (Act), and adding the catalyst, the activator, and L-lactide monomer to a polymerization reactor; b) evacuating under vacuum and charging the polymerization reactor with nitrogen for three consecutive times to remove air, and allowing the L-lactide monomer to undergo bulk polymerization under vacuum. The bulk polymerization includes a first reaction stage and a second reaction stage, which are separately carried out at different temperatures, pressures, and reaction times.

POLYESTERS PREPARED FROM 1,1-DIESTER-1-ALKENES CONTAINING A STRONG ACID AND STABILIZER

Disclosed are compositions comprising polyesters containing a chain of residue of: diols and diesters along the chain, wherein at least a portion of the diesters are 1, 1-diester-1-alkenes, and the chains have alkene groups incorporated into the chains; the composition comprising one or more of the following: i ether groups derived from alcohols, diols, polyols, or a combination thereof obtained via Michael addition to the alkene groups and a residue of the alkene groups remaining after Michael addition; ii the formed polyesters contain one percent or less of residual 1, 1-diester-1-alkene which are unreacted; iii one or more free radical inhibitors; and iv a stabilizer comprising one or more of: oxo acids phosphorous or esters thereof, aluminum sulfate, stannous pyrophosphate, stannous sulfate, aluminum dihydrogenphosphate or decomposition products thereof. The stabilizer is present in an amount sufficient to enhance stability of the polyester without lowering reactivity of the polyester.

POLYESTER RESIN, METHOD FOR PREPARING SAME, AND RESIN MOLDED PRODUCT FORMED THEREFROM
20220380529 · 2022-12-01 ·

The present invention relates to a polyester resin. The polyester resin contains a particular content of diol moieties, derived from isosorbide and diethylene glycol, and thus can provide a resin molded product exhibiting high transparency in spite of a large wall thickness thereof.

POLYESTER RESIN, METHOD FOR PREPARING SAME, AND RESIN MOLDED PRODUCT FORMED THEREFROM
20220380529 · 2022-12-01 ·

The present invention relates to a polyester resin. The polyester resin contains a particular content of diol moieties, derived from isosorbide and diethylene glycol, and thus can provide a resin molded product exhibiting high transparency in spite of a large wall thickness thereof.

WELL-DEFINED DEGRADABLE POLY(PROPYLENE FUMARATE) POLYMERS AND SCALABLE METHODS FOR THE SYNTHESIS THEREOF

The present invention provides a low molecular mass PPF polymer (and related methods) that is suitable for 3D printing and other polymer device fabrication modalities and can be made inexpensively in commercially reasonable quantities. These novel low molecular mass PPF polymers have a low molecular mass distribution (custom-character.sub.m) and a wide variety of potential uses, particularly as a component in resins for 3D printing of medical devices. The ability to produce low custom-character.sub.m PPF creates a new opportunity for reliable GMP production of PPF. It provides low cost synthesis and scalability of synthesis, blending of well-defined mass and viscosity PPF, and reduced reliance on solvents or heat to (a) achieve mixing of 3D printable resins or (b) and flowability during 3D printing. These PPF polymers are non-toxic, degradable, and resorbable and can be used in tissue scaffolds and medical devices that are implanted within a living organism.

WELL-DEFINED DEGRADABLE POLY(PROPYLENE FUMARATE) POLYMERS AND SCALABLE METHODS FOR THE SYNTHESIS THEREOF

The present invention provides a low molecular mass PPF polymer (and related methods) that is suitable for 3D printing and other polymer device fabrication modalities and can be made inexpensively in commercially reasonable quantities. These novel low molecular mass PPF polymers have a low molecular mass distribution (custom-character.sub.m) and a wide variety of potential uses, particularly as a component in resins for 3D printing of medical devices. The ability to produce low custom-character.sub.m PPF creates a new opportunity for reliable GMP production of PPF. It provides low cost synthesis and scalability of synthesis, blending of well-defined mass and viscosity PPF, and reduced reliance on solvents or heat to (a) achieve mixing of 3D printable resins or (b) and flowability during 3D printing. These PPF polymers are non-toxic, degradable, and resorbable and can be used in tissue scaffolds and medical devices that are implanted within a living organism.

Sustainable PBT Compositions with Improved Color Capability Using the Purified Terephthalic Acid Process

Thermoplastic compositions include from about 15 wt % to about 99 wt % of a polybutylene terephthalate (PBT) component; and from 0.01 wt % to about 85 wt % of at least one additional component, wherein: the PBT component comprises PBT derived from a post-consumer or post-industrial recycled (PCR) polyethylene terephthalate (PET) depolymerized to a high purity purified terephthalic acid (PTA) monomer and the thermoplastic composition exhibits an L* color value of at least about 74.

Soil Release Polyesters For Use In Detergent Compositions

Soil release polyesters for use in detergent compositions Polyesters are described comprising one or more structural units of the formula (I)

##STR00001##

and one or more structural units of the formula (II)

##STR00002##

and one or more terminal groups of the formula (III-a) or mixtures thereof

##STR00003##

wherein R.sup.1 is a linear or branched alkyl group comprising from 7 to 30 carbon atoms or a linear or branched alkenyl group comprising one or more double bonds and from 7 to 30 carbon atoms or mixtures thereof, a is, based on a molar average, a number from 1 to 200, and R.sup.2 is a linear or branched alkylene group (C.sub.mH.sub.2m) with m being a number from 2 to 10 or mixtures thereof.

The polyesters are particularly suited to be used as soil release agents.

ALIPHATIC POLYESTER COMPOSITION
20230183420 · 2023-06-15 ·

Provided is an aliphatic polyester composition. The aliphatic polyester composition comprises a polybutylene succinate, wherein the proton nuclear magnetic resonance of the aliphatic polyester composition has a first characteristic peak and a second characteristic peak. The first characteristic peak is located between 3.84 ppm and 4.32 ppm, and the second characteristic peak is located between 5.65 ppm and 5.85 ppm. The integral value of the first characteristic peak is set to be 100 and the integral value of the second characteristic peak is less than 0.10. By controlling the integral value of the second characteristic peak in H.sup.1-NMR of the aliphatic polyester composition, the aliphatic polyester composition has good appearance and low concentration of carboxylic acid end group and thereby the product value thereof is increased.