The present disclosure describes protein-based resin compositions. In particular, the compositions employ methacrylated or acrylated protein, a strengthening agent, a plasticizer, and an initiator. The protein-based resin compositions may be used for making solid articles that are biodegradable and possess a high degree of tensile strength and water resistance. Methods of preparing the biodegradable protein-based plastic articles are also disclosed.

There are provided a solvent composition which is excellent in solubility of various organic substances and excellent in detergency and a drying property, and has no adverse effect on a global environment and is excellent in stability; a cleaning method using the solvent composition; a method of forming a coating film; a heat transfer fluid including the solvent composition; and a heat cycle system using the heat transfer fluid. A solvent composition including 1-chloro-2,3,3-trifluoro-1-propene and 1-chloro-3,3-difluoro-1-propyne, a cleaning method of bringing the solvent composition and an article into contact with each other, a method of dissolving a nonvolatile organic compound in the solvent composition to produce a coating film-forming composition and evaporating the solvent composition after applying the coating film-forming composition on an article to be coated, to form a coating film, a heat transfer fluid including the solvent composition, and a heat cycle system using the heat transfer fluid.

There are provided a solvent composition which is excellent in solubility of various organic substances and excellent in detergency and a drying property, and has no adverse effect on a global environment and is excellent in stability; a cleaning method using the solvent composition; a method of forming a coating film; a heat transfer fluid including the solvent composition; and a heat cycle system using the heat transfer fluid. A solvent composition including 1-chloro-2,3,3-trifluoro-1-propene and 1-chloro-3,3-difluoro-1-propyne, a cleaning method of bringing the solvent composition and an article into contact with each other, a method of dissolving a nonvolatile organic compound in the solvent composition to produce a coating film-forming composition and evaporating the solvent composition after applying the coating film-forming composition on an article to be coated, to form a coating film, a heat transfer fluid including the solvent composition, and a heat cycle system using the heat transfer fluid.

[Problem] To provide an oil thickener which has high viscosity increasing effect on an oily ingredient such as silicone oil, a non-polar organic compound, a low-polarity organic compound or the like and which has good handlability

[Means to Solve the Problem] Surface-hydrophobized cellulose nanofibers for an oil thickener which are cellulose nanofibers having an average thickness of 3 to 200 nm and an average length of 0.1 μm or larger, and a 1 wt. % aqueous dispersion of which has a viscosity of 700 to 2100 mPa.Math.s, and hydroxyl groups in cellobiose units of which are substituted by vinyl esters and/or organic acid vinyl esters in a substitution degree of 0.2 to 0.8.

A process for producing dried, vinyl carboxylate surface-modified microfibrillated cellulose having improved mechanical properties and a microfibril structure and a process for producing a vinyl carboxylate, surface-modified microfibrillated cellulose—thermoplastic polyester or thermoplastic polyolefin composite material having improved mechanical strength properties utilizing dried, vinyl carboxylate surface-modified microfibrillated cellulose.

A process for producing dried, vinyl carboxylate surface-modified microfibrillated cellulose having improved mechanical properties and a microfibril structure and a process for producing a vinyl carboxylate, surface-modified microfibrillated cellulose—thermoplastic polyester or thermoplastic polyolefin composite material having improved mechanical strength properties utilizing dried, vinyl carboxylate surface-modified microfibrillated cellulose.

The present disclosure provides a process for the synthesis of bio-based formaldehyde-free wood adhesive with lignin and cellulose derived bio-oil which can be generated from the fractionation/liquefaction of lignocellulose biomass such as agricultural and forestry wastes. Curable groups are introduced onto the bio oil through functionalization reaction with cyclic anhydrides such as maleic anhydride, citric anhydride, phthalic anhydride, succinic anhydride, methyl succinic anhydride. Wood adhesives are formulated with the functionalized bio oil by addition of water and curing agents. Two-ply plywood samples were prepared following the ASTM International Standard 2017, D2339-98 and cured on a hot press between 190-200° C. for 3-4 min under 3 MPa pressure. The plywood samples have dry and wet strengths in the range of up to 3.5 MPa with over 80% wood failure.

The present application discloses regioselectively substituted cellulose esters, films made from the regioselectively substituted cellulose esters and methods for making the same. The regioselectively substituted cellulose esters are synthesized using trifluoroacetic anhydride and cellulose with various acyl donors or acyl donor precursors.

The present application discloses regioselectively substituted cellulose esters, films made from the regioselectively substituted cellulose esters and methods for making the same. The regioselectively substituted cellulose esters are synthesized using trifluoroacetic anhydride and cellulose with various acyl donors or acyl donor precursors.

Grafted, crosslinked cellulosic materials include cellulose fibers and polymer chains composed of at least one monoethylenically unsaturated acid group-containing monomer (such as acrylic acid) grafted thereto, in which one or more of said cellulose fibers and said polymer chains are crosslinked (such as by intra-fiber chain-to-chain crosslinks). Some of such materials are characterized by a wet bulk of about 10.0-17.0 cm3/g, an IPRP value of about 1000 to 7700 cm2/MPa.Math.sec, and/or a MAP value of about 7.0 to 38 cm H2O. Methods for producing such materials may include grafting polymer chains from a cellulosic substrate, followed by treating the grafted material with a crosslinking agent adapted to effect crosslinking of one or more of the cellulosic substrate or the polymer chains. Example crosslinking mechanisms include esterfication reactions, ionic reactions, and radical reactions, and example crosslinking agents include pentaerythritol, homopolymers of the graft species monomer, and hyperbranched polymers.