A rapid, scalable methodology for graphene dispersion with a polymer-organic solvent solution and subsequent solvent exchange, as can be utilized without centrifugation, to enhance graphene concentration.

A rapid, scalable methodology for graphene dispersion with a polymer-organic solvent solution and subsequent solvent exchange, as can be utilized without centrifugation, to enhance graphene concentration.

A rapid, scalable methodology for graphene dispersion with a polymer-organic solvent solution and subsequent solvent exchange, as can be utilized without centrifugation, to enhance graphene concentration.

Described herein are methods of syntheses and therapeutic uses of covalently modified peptides and/or proteins. The covalently modified peptides and/or proteins allow for improved pharmaceutical properties of peptide and protein-based therapeutics.

The present invention concerns a process for the covalent attachment of lignin to cellulose in aqueous solutions, which process is characterized by preparing an aqueous mixture of lignin particles modified with tall oil fatty acids (TOFA), and reacting these TOFA-modified lignin particles with cellulose particles. The obtained modified cellulose particles are biodegradable, and have antimicrobial properties, whereby they are suitable for use in antibacterial textile surfaces (sportswear, medical textiles), tissue adhesives and as porous carriers in drug delivery. Further, the material is useful in high-volume products, such as adhesives and dispersants.

The instant invention relates to primary coating compositions that comprises a cationic polysaccharide, to be applied on a hydrophobic surface before a subsequent application of a polar or water based coating composition, such a as a paint or an adhesive.

This invention relates to a process for preparing color dispersions comprising a first step of contacting water, a first colorant, and a polysaccharide selected from methylcellulose, hydropropylmethylcellulose, hydroxyethylmethylcellulose, hydroxybutylmethylcellulose, hydroxyethylethylcellulose, and the mixture thereof, to form a first colorant dispersion; a second step of contacting the first colorant dispersion with a protective composition comprising an aqueous dispersion of polymer particles, clay, and a peptizing agent to form a dispersion of protected first colorant particles; an optional third step of repeating the first step and the second step with a second colorant that is different from the first colorant to form a dispersion of protected second colorant particles; and an optional fourth step of mixing the dispersions of protected first and second colorant particles to form a multi-color dispersion. This invention also relates to a color dispersion comprising the first colorant dispersion, and a color coating comprising the color dispersion.

This invention relates to a process for preparing color dispersions comprising a first step of contacting water, a first colorant, and a polysaccharide selected from methylcellulose, hydropropylmethylcellulose, hydroxyethylmethylcellulose, hydroxybutylmethylcellulose, hydroxyethylethylcellulose, and the mixture thereof, to form a first colorant dispersion; a second step of contacting the first colorant dispersion with a protective composition comprising an aqueous dispersion of polymer particles, clay, and a peptizing agent to form a dispersion of protected first colorant particles; an optional third step of repeating the first step and the second step with a second colorant that is different from the first colorant to form a dispersion of protected second colorant particles; and an optional fourth step of mixing the dispersions of protected first and second colorant particles to form a multi-color dispersion. This invention also relates to a color dispersion comprising the first colorant dispersion, and a color coating comprising the color dispersion.

Described herein are methods of syntheses and therapeutic uses of covalently modified peptides and/or proteins. The covalently modified peptides and/or proteins allow for improved pharmaceutical properties of peptide and protein-based therapeutics.

The present invention relates to an efficient waterborne nano-silicon rubber sealing waterproof agent, comprising following components in parts by weight: 1090 parts of nano-silica gel, 10100 parts of nano-diatomaceous earth, 5150 parts of nano polyurethane, 15200 parts of nano inorganic dry powder, 10100 parts of nano methyl cellulose, 10150 parts of a chelating agent, 15200 parts of an expansion agent, 10250 parts of a strengthening agent, 5100 parts of an antifreezing agent, 2150 parts of a heat-resistant agent and 10100 parts of an acid and alkali-resistant agent. The efficient waterborne nano-silicon rubber sealing waterproof agent has good waterproofness, permeability, film forming property, elasticity, adhesion, water resistance and heat, humid and high temperature resistance, is suitable for being used for waterproof, anti-seepage and anti-leakage repair projects of underground engineering and roofing, and is an excellent vapor barrier material in a refrigerating chamber.