Processes for producing polymer microcapsules using vicinal functional oligomers are also described. The vicinal functional oligomers can be made by polymerizing an acrylate monomer, a styrene monomer, or both in the presence of a chain transfer agent. The vicinal functional oligomers can be reacted with epichlorohydrin to form vicinal epoxies. The vicinal epoxies can be reacted with polyamines to form epoxy polymer microspheres. The vicinal epoxies can be reacted with carbon dioxide in the presence of a catalyst to form vicinal cyclic carbonates. The vicinal cyclic carbonates can be reacted with polyamines to form isocyanate-free polymer microspheres. Polymer microspheres made by the processes are also described.

Disclosed herein are a cannabidiol (CBD)-containing bio-based polyurethane composite material and a preparation thereof. The composite material is prepared from a component A and a component B in a weight ratio of 100:(20-50), where the component A includes 40-60 parts by weight of a vegetable oil-based polyol, 35-50 parts by weight of polyether polyol I, 0-10 parts by weight of polyether polyol II, 0.5-5 parts by weight of CBD, 0-5 parts by weight of a natural pigment, 0.5-3 parts by weight of silicon oil, 0-5 parts by weight of a cross-linking agent, 0.2-1 part by weight of a catalyst and 0.8-4 parts by weight of water, and the component B includes 20-50 parts by weight of modified methylene diphenyl diisocyanate (MDI).

Disclosed herein are a cannabidiol (CBD)-containing bio-based polyurethane composite material and a preparation thereof. The composite material is prepared from a component A and a component B in a weight ratio of 100:(20-50), where the component A includes 40-60 parts by weight of a vegetable oil-based polyol, 35-50 parts by weight of polyether polyol I, 0-10 parts by weight of polyether polyol II, 0.5-5 parts by weight of CBD, 0-5 parts by weight of a natural pigment, 0.5-3 parts by weight of silicon oil, 0-5 parts by weight of a cross-linking agent, 0.2-1 part by weight of a catalyst and 0.8-4 parts by weight of water, and the component B includes 20-50 parts by weight of modified methylene diphenyl diisocyanate (MDI).

Provided are a two-component curable adhesive which can be aged at room temperature and has favorable adhesiveness to various base materials, a laminate in which the adhesiveness between a base material and an adhesive is excellent even when aged at room temperature, and a packaging material including the laminate. The two-component curable adhesive includes a polyisocyanate composition (X) including a polyisocyanate compound (A) and a polyol composition (Y) including a polyol (B), in which a viscosity of the polyol composition at 50° C. is 20 mPa.Math.s or more and 180 mPa.Math.s or less.

Provided are a two-component curable adhesive which can be aged at room temperature and has favorable adhesiveness to various base materials, a laminate in which the adhesiveness between a base material and an adhesive is excellent even when aged at room temperature, and a packaging material including the laminate. The two-component curable adhesive includes a polyisocyanate composition (X) including a polyisocyanate compound (A) and a polyol composition (Y) including a polyol (B), in which a viscosity of the polyol composition at 50° C. is 20 mPa.Math.s or more and 180 mPa.Math.s or less.

Described herein are anti-microbial and UV-protective biological devices and extracts produced therefrom. The biological devices include microbial cells transformed with a DNA construct containing genes for producing proteins such as, for example, zinc-related protein/oxidase, silicatein, silaffin, and alcohol dehydrogenase. In some instances, the biological devices also include a gene for lipase. Methods for producing and using the devices are also described herein. Finally, compositions and methods for using the devices and extracts to kill microbial species or prevent microbial growth and to reduce or prevent UV-induced damage or exposure to materials, items, plants, and human and animal subjects are described herein. Also disclosed are biological devices producing polyactive carbohydrates and carbo sugars, as well as compositions and articles incorporating both extracts from these devices and the anti-microbial and UV-protective extracts.

Isocyanate-reactive composition that include a polyol blend, a blowing agent composition, and a catalyst. The polyol blend includes a polyether polyol having a functionality of 2 to 6 and an OH number of 20 to 50 mg KOH/g, which is present in an amount of at least 30% by weight, based on total weight of the isocyanate-reactive composition, and an aromatic polyester polyol having a functionality of 1.5 to 3 and an OH number of 150 to 450 mg KOH/g, which is present in an amount of at least 40% by weight, based on total weight of the isocyanate-reactive composition. The blowing agent composition includes water, the water being present in an amount of 1 to 20% by weight, based on total weight of the isocyanate-reactive composition and in an amount of at least 90% by weight, based on total weight of the blowing agent composition. The isocyanate-reaction composition has a green content of at least 30% by weight, based on total weight of the isocyanate-reactive composition. Polyurethane foam-forming reaction mixtures, polyurethane foams, multi-layer composite articles and methods for their production are also described.

The invention relates to new oil gelling polyurethanes useful for preparing clear gels in organic media (oils, solvents) and to a process for their preparation. The invention also relates to the gels formed from these gelling polyurethanes and to compositions containing them, in particular cosmetic compositions.

The invention relates to new oil gelling polyurethanes useful for preparing clear gels in organic media (oils, solvents) and to a process for their preparation. The invention also relates to the gels formed from these gelling polyurethanes and to compositions containing them, in particular cosmetic compositions.

A method for preparing a polyol comprises the following steps of: (1) dissolving 2,3 -epoxybutane and an acid catalyst in an inert solvent to obtain a solution A; dissolving triethylene glycol in an inert solvent to obtain a solution B; and dissolving epoxy vegetable oil in an inert solvent to obtain a solution C; (2) respectively and simultaneously pumping the solutions A and B into a first micromixer for mixing; (3) pumping the solution C and an effluent of the first microreactor into a second micromixer for mixing while carrying out step (2); and (4) dissolving the vegetable oil polyol in an inert solvent to obtain a solution D; dissolving epoxypropane and an alkaline catalyst in an inert solvent to obtain a solution E; and pumping the solution D and the solution E into a tank reactor for reaction, thereby obtaining the polyol.