A foamable polyurethane resin composition includes a polyisocyanate material, a polyol material, water, and a catalyst. The polyisocyanate material contains 1,4-H.sub.6XDI; the polyol material contains crystalline PTMEG and noncrystalline PTMEG and/or PPG; the total amount of the crystalline PTMEG, the noncrystalline PTMEG, and PPG is 90% by mass or more with respect to the total amount of the polyol material; and a ratio of the crystalline PTMEG is 60% by mass or more and 90% by mass or less with respect to the total amount of the crystalline PTMEG, the noncrystalline PTMEG, and PPG.

The present invention relates to a polyurethane composition with antimicrobial properties, a polyurethane foam or coating comprising said polyurethane composition, an article prepared from said composition, foam or coating, a process for the preparation of said composition, the use of a complexing agent and an antimicrobial agent for the preparation of said composition or for imparting antimicrobial properties to a polyurethane composition, and a kit of components for preparing said composition. A cooperative effect is observed when specific complexing agents are combined with specific organic antimicrobially active components within the polyurethane composition.

Disclosed are a polyol composition using carbon dioxide, a method for preparing a polyurethane foam using the polyol composition, and a polyurethane foam prepared using the method. A method for preparing a polyurethane foam includes reacting isocyanate with a polyol composition containing a polyol compound having a synthetic polyol containing carbon dioxide, a chain extender, and a foaming agent.

The present invention provides new impact protection materials and the method of making the same. More specifically, the impact protection materials are polymer-based shear-thickening composite comprising a non-shear-thickening polymer matrix material and one or more shear-thickening materials. Preferably, the non-shear-thickening polymer matrix material is in an amount from approximately 5 weight percent to approximately 90 weight percent with the balance being one or more shear-thickening materials. The first type of the one or more shear-thickening materials is sol-gel based shear-thickening material in which small inorganic particles are connected in a gel network; the second type is polymer-based shear-thickening material in which polymer chains form network. Compared to the existing shear-thickening materials, the present shear-thickening materials have different molecular structure and formulation and possess properties of good impact protection and good stability.

The invention is directed to biomedical polyurethanes. The invention is particularly directed to biomedical polyurethanes with improved biodegradability and to an improved preparation of the biomedical polyurethanes. In particular the present invention provides a biomedical polyurethane having the formula (A-B-C-B).sub.n, wherein A denotes a polyol, B denotes a diisocyanate moiety, C denotes a diol component and n denotes the number of recurring units, and wherein the B-C-B segment is bioresorbable.

A polymer having a hydrophobic polymer chain derived from monomers of farnesene and other optional monomers, such as dienes and vinyl aromatics. The polymer also includes one or more terminal functional groups, such as an amino group, a glycidyl group, a carboxylic acid group, a (meth)acrylate group, a silane group, an isocyanate group, an acetoacetate group, a phenolic group, and a hydroxyl group. Functional groups, such as carboxylic acids, may also be grafted along the hydrophobic polymer chain. The polymer may be incorporated in curable compositions that optionally include one or more polymer resins having similar functional groups. Methods for preparing the curable polymer compositions are also provided. The curable or cured form of the polymer composition may be used in various products, such as a sealant, a coating, a caulk, an electric potting compound, a membrane, a sponge, a foam, an adhesive, or a propellant binder.

An embodiment includes a polymer composition comprising a thermoplastic polymer that: (a) is bonded to iodine, (b) includes a vinyl group, and (c) includes urethane linkages. Other embodiments are described herein.

Foam composites and methods of preparation thereof are discussed. For example, the foam composite may include a polymeric material and a particulate filler, wherein the compressive strength of the foam composite is equal to or greater than 20 psi, the density is 4 pcf to 40 pcf, and wherein the thermal conductivity is equal to or less than 0.050 W/m K. the particulate filler may include fly ash, e.g., in an amount of about of 45% to about 75% by weight with respect to the total weight of the foam composite. The foam composite may be prepared from a mixture of a polyol, an isocyanate, the particulate filler, and a liquid blowing agent having a boiling point equal to or greater than 25° C. or 30° C.

A substantially biobased prepolymer mixture including 31.80 to 67.95 percent biogenic carbon content by weight, wherein the mixture is a combination of: an isocyanate; and a cleaned biobased polyoxyalkylene glycol polyol, wherein the cleaned biobased polyoxyalkylene glycol polyol is completely primary hydroxyl-tipped or primary hydroxyl end-grouped, further wherein said cleaned biobased polyoxyalkylene glycol polyol is polymerized from 100% biobased ethylene oxide, further wherein the cleaned biobased polyoxyalkylene glycol polyol comprises less than 15 ppm sodium and potassium metals, and further wherein the cleaned biobased polyoxyalkylene glycol polyol comprises less than 0.5% water by weight.

An on-orbit recycling method for a buffer foam of a cargo spacecraft includes the following steps: mechanically cutting a shaped PU foam into foam micro-blocks, and putting the foam micro-blocks into a packaging bag for packaging, where the packaging bag is filled with a foaming adhesive; the foaming adhesive includes a component A and a component B, which are independently packaged in a two-component packaging bag; and the component A and the component B are separated by a film; and squeezing the film between the component A and the component B, such that the two components are fully mixed, foamed and expanded to finally burst the two-component packaging bag, where after the packaging bag is burst, the foaming adhesive expands into gaps of the foam micro-blocks; and in a microgravity state of space, the foaming adhesive expands and fills uniformly in all directions and fully infiltrates the foam micro-blocks.