A method of making polyesters and polyurethanes from biomass-derived polyols. The polyol is biomass-derived and has the structure:

##STR00001##

wherein dashed bonds are single or double bonds and R is selected from the group consisting of —OH and ═O. Polyurethanes are made by reacting the polyol with a diisocyanate. Polyesters are made by reacting the polyol with a dicarboxylic acid.

The present invention relates to a process for preparing polyurethanes by mixing a) polyisocyanate, b) a mixture obtainable by introducing an alkali metal or alkaline earth metal salt into a compound comprising urethane groups, c) compounds comprising one or more epoxide groups, and, optionally, d) polyol, e) chain extenders, and f) fillers and further additives to form a reaction mixture and fully reacting the mixture to give the polyurethane, where the amount of alkali metal or alkaline earth metal ions per equivalent urethane groups in the compound (b) is 0.0001 to 3.5. The present invention further relates to a polyurethane obtainable by such a process, and to the use of such a polyurethane for producing bodywork components for vehicles.

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).

A crosslinkable composition is useful for preparing a skin contact adhesive or a coating on a substrate. The crosslinkable composition includes (A) a polyurethane-polyorganosiloxane copolymer and (B) a curing catalyst. The skin contact adhesive prepared by crosslinking the crosslinkable composition is useful in applications such as adhesives for medical tapes, adhesives for wound dressings, adhesives for prosthetics, ostomy appliance adhesives, adhesives for medical monitoring appliances, adhesives for scar therapy treatments, adhesives for cosmetic patches, and transdermal drug delivery systems.

A modification method of a polyurethane, including the steps of: preparing a polyurethane having an ethylenically unsaturated bond; and treating the polyurethane with a liquid containing a compound having a conjugated double bond, or a modification method of a polyurethane, including the steps of: preparing a polyurethane having a conjugated double bond; and treating the polyurethane with a liquid containing a compound having an ethylenically unsaturated bond is used.

The present application relates to polyurethane polymers produced by polymerizing a reactant mixture comprising triglycerides of Physaria fendleri, one or more polyisocyanates, and one or more polyols, wherein the triglycerides of Physaria fendleri have a hydroxyl value ranging from 90 milligrams of potassium hydroxide per gram of the triglycerides of Physaria fendleri to 250 milligrams of potassium hydroxide per gram of the triglycerides of Physaria fendleri. The present application also relates to polyester polymers produced by polymerizing a reactant mixture comprising triglycerides of Euphorbia Lagascae, and one or more dicarboxylic acids. Also disclosed are the methods of formation of the polyurethane and polyester polymers, and their use as adhesives.

Aqueous dispersions including multistage-prepared polymers of mixtures of olefinically unsaturated compounds are disclosed. The aqueous dispersions include at least one polyurethane containing olefinically unsaturated groups. Production and use of the aqueous dispersions, particularly in the field of automotive finishing, is disclosed. The disclosure further relates to an aqueous basecoat material including the multistage-prepared polymers, and also to a method for producing a multicoat paint system using the aqueous basecoat material.

Aqueous dispersions including multistage-prepared polymers of mixtures of olefinically unsaturated compounds are disclosed. The aqueous dispersions include at least one polyurethane containing olefinically unsaturated groups. Production and use of the aqueous dispersions, particularly in the field of automotive finishing, is disclosed. The disclosure further relates to an aqueous basecoat material including the multistage-prepared polymers, and also to a method for producing a multicoat paint system using the aqueous basecoat material.

Epoxy adhesives include a latent curing agent, a reactive toughener having capped isocyanate groups, and certain urea compounds. The toughener is made by chain extending and capping a mixture of isocyanate-terminated prepolymers. The prepolymers include an isocyanate-terminated polyether and an isocyanate-terminated diene polymer. The adhesives have excellent wash-off resistance and excellent ability to adhere to oily substrates.

A waterborne alternative polyurethane composition is provided which comprises a reaction product of: an azidated polyol; and a waterborne poly(alkynyl carbamate) prepolymer comprising a reaction product of a polyisocyanate and from 1 wt. % to 20 wt. % of an alkynol-polyether having a formula (I),

R.sub.1—R.sub.2—O—R.sub.3—OH  (I),

wherein, R.sub.1=a monovalent group selected from either HC≡C— or HC≡C—CO—, R.sub.2=a divalent alkylene group from 1 to 8 carbon atoms, and may be straight chain or branched and may contain cyclic moieties, and R.sub.3=a polyethylene glycol with number average molecular weight from 300-1,200 g/mol,
wherein the wt. % is based on the weight of the prepolymer, wherein reaction of the azidated polyol and the waterborne poly(alkynyl carbamate) occurs at a temperature of from 20° C. to 200° C. and optionally in the presence of a catalyst. The inclusion of an alkynol-polyether does not materially alter the performance properties and reactivity of the waterborne polyurethane composition relative to a solventborne polyurethane control composition. Inclusion of the alkynol-polyether reduces the need for organic solvents by allowing for the use of water as a carrier. The inventive waterborne alternative polyurethane compositions may find use in or as coatings, adhesives, sealants, films, elastomers, castings, foams, and composites.