Patent classifications
C08F289/00
HETEROCYCLIC-DITHIOL CLICK CHEMISTRY
Disclosed are polymers, methods of making polymers, and compositions, focused on cross-linking heterocycles comprising a moiety of Formula I with thiols and thiolates.
COMPOSITION COMPRISING THERMOASSOCIATIVE AND EXCHANGEABLE COPOLYMERS
Compositions resulting from the mixing of at least: a comb polydiol copolymer A1 and a compound A2 including at least two boronic ester functional groups, the comb polydiol copolymer A1 including a main chain and side chains, at least a portion of the side chains of the copolymer A1 being composed of oligomers. They exhibit very varied rheological properties depending on the proportion of the compounds A1 and A2 used. Composition resulting from the mixing of at least one lubricating oil with such a composition of associative and exchangeable polymers and use of this composition for lubricating a mechanical part.
Halogenated wax grafted to low molecular weight polymer
A wax-polymer compound includes (a) a polymer component that is a polymerized unsaturated monomer, optionally copolymerized with a vinyl-aromatic monomer, and (b) a halogenated hydrocarbon wax component. The polymer component is grafted to the halogenated hydrocarbon wax component, and the wax-polymer compound has a number average molecular weight of about 1,000 to about 100,000. A method of making the wax-polymer compound and a coated silica particle are also disclosed.
Halogenated wax grafted to low molecular weight polymer
A wax-polymer compound includes (a) a polymer component that is a polymerized unsaturated monomer, optionally copolymerized with a vinyl-aromatic monomer, and (b) a halogenated hydrocarbon wax component. The polymer component is grafted to the halogenated hydrocarbon wax component, and the wax-polymer compound has a number average molecular weight of about 1,000 to about 100,000. A method of making the wax-polymer compound and a coated silica particle are also disclosed.
DELIMINING COMPOSITION AND METHOD FOR DELIMING HIDES
A deliming composition and a deliming method using graft polymers from polysaccharides and/or polypeptides or the corresponding derivatives, obtainable by radical polymerization of a monomer, selected at least from, or a monomer mixture of, acrylic acid or methacrylic acid or the mixtures thereof.
DELIMINING COMPOSITION AND METHOD FOR DELIMING HIDES
A deliming composition and a deliming method using graft polymers from polysaccharides and/or polypeptides or the corresponding derivatives, obtainable by radical polymerization of a monomer, selected at least from, or a monomer mixture of, acrylic acid or methacrylic acid or the mixtures thereof.
Method for preparing thinning ceramic additive using landfill leachate
A method for preparing a thinning ceramic additive using a landfill leachate, comprising the following steps: filtering the landfill leachate; adding aqueous alkali and regulating pH to 7.5-9; adding a coagulant, then stirring and mixing with a blender; taking precipitates to mix with water to prepare a solution, adding a sodium hydroxide solution for alkalization, and regulating the pH to 7-8.5; adding a sulfonating agent, and reacting under an environment of 80-100 C. for 2-4 h; adding acrylic acid and N,N-methylene bisacrylamide to the solution, then slowly adding the initiator, stirring under the condition of 80-90 C. to react for 1-3.5 h, and after the reaction is completed, drying the solution to obtain a solid matter; crushing the solid matter, and screening through a screen of 16-24 meshes; and uniformly mixing the above screened particulate matter with the montmorillonite and an additive to prepare the thinning ceramic additive.
Method for preparing thinning ceramic additive using landfill leachate
A method for preparing a thinning ceramic additive using a landfill leachate, comprising the following steps: filtering the landfill leachate; adding aqueous alkali and regulating pH to 7.5-9; adding a coagulant, then stirring and mixing with a blender; taking precipitates to mix with water to prepare a solution, adding a sodium hydroxide solution for alkalization, and regulating the pH to 7-8.5; adding a sulfonating agent, and reacting under an environment of 80-100 C. for 2-4 h; adding acrylic acid and N,N-methylene bisacrylamide to the solution, then slowly adding the initiator, stirring under the condition of 80-90 C. to react for 1-3.5 h, and after the reaction is completed, drying the solution to obtain a solid matter; crushing the solid matter, and screening through a screen of 16-24 meshes; and uniformly mixing the above screened particulate matter with the montmorillonite and an additive to prepare the thinning ceramic additive.
PHOTO-CURABLE BIOINK TO FABRICATE ULTRA-STRONG, ELECTROCONDUCTIVE, AND BIOCOMPATIBLE HYDROGEL FOR REGENERATIVE MEDICINE
The present disclosure relates to the composition and process for the production of an ultra-strong, biocompatible, electroconductive, and stretchable hydrogel, which comprises: a step (a) of physical or chemical modification of natural polymers e.g., preparation of silk nanofiber and double methacrylation of gelatin; a step (b) of graphene oxide (GO) carboxylation; a step (c) of carbodiimidation between methacrylated natural polymers of step (a) and carboxylated GO of step (b); and a step (d) of three dimensional (3D) bioprinting of step (c) with/without silk nanofiber. It was found that these steps in this disclosure give rise to a biocompatible hydrogel with high mechanical strength in the range of load-bearing soft tissue such as tendon and heart as opposed to conventional hydrogels.
PHOTO-CURABLE BIOINK TO FABRICATE ULTRA-STRONG, ELECTROCONDUCTIVE, AND BIOCOMPATIBLE HYDROGEL FOR REGENERATIVE MEDICINE
The present disclosure relates to the composition and process for the production of an ultra-strong, biocompatible, electroconductive, and stretchable hydrogel, which comprises: a step (a) of physical or chemical modification of natural polymers e.g., preparation of silk nanofiber and double methacrylation of gelatin; a step (b) of graphene oxide (GO) carboxylation; a step (c) of carbodiimidation between methacrylated natural polymers of step (a) and carboxylated GO of step (b); and a step (d) of three dimensional (3D) bioprinting of step (c) with/without silk nanofiber. It was found that these steps in this disclosure give rise to a biocompatible hydrogel with high mechanical strength in the range of load-bearing soft tissue such as tendon and heart as opposed to conventional hydrogels.