Clickable waterborne polymers, click crosslinking of waterborne polymers, click crosslinked waterborne polymers, clickable functional compounds, and click functionalized waterborne polymers are presented. For example, the waterborne polymers have pendant groups bearing alkyne and/or azide groups and alkyne. For example, the functionalized azide-containing functional compounds such as antimicrobial or infrared-refractive compounds. The click crosslinking of clickable waterborne polymers or polymer mixtures, and the click conjugation of clickable waterborne polymers with clickable functional compounds such as clickable antimicrobial or infrared-refractive compounds, which resulted in functional waterborne polymers with antimicrobial or infrared-refractive functions, are presented. The presented polymers, including clickable waterborne polymers, click-crosslinked waterborne polymers, and functional waterborne polymers with, for example, antimicrobial or infrared-refractive functions, can be used in applications such as coating and adhesive compositions. The aqueous suspensions of waterborne polymers can also be used directly as drug delivery systems, or can be crosslinked into hydrogels or composites for biomedical applications such as drug/cell delivery, tissue engineering, and other medical device.

The present invention relates to a process for the production of polyurethanes where (a) polyisocyanate, (b) polymeric compounds having groups reactive toward isocyanates, (c) catalysts, (d) polymer P formed from ethylenically unsaturated monomers and having an average of more than 2 functional groups of the formula ONH.sub.2 and optionally (e) blowing agent, (f) chain extender and/or crosslinking agent, and (g) auxiliaries and/or additives are mixed to give a reaction mixture, and the reaction mixture is allowed to complete a reaction to give the polyurethane. The present invention further relates to polyurethanes produced by this process and to the use of these polyurethanes in the interior of means of transport.

An ionic diol has formula wherein R.sup.1 represents an alkyl group having from 6 to 18 carbon atoms; R.sup.2 and R.sup.3 independently represent alkyl groups having from 1 to 4 carbon atoms; R.sup.4 represents an alkylene group having from 2 to 8 carbon atoms; and R.sup.5 represents an alkylene group having from 1 to 8 carbon atoms. Antistatic polymers are formed by copolymerization of monomers including a diisocyanate, an ionic diol, a polyether diol, and at least one non-ionic diols. Methods of making the antistatic polyurethanes are also disclosed. ##STR00001##

Provided is a photo-curable composition capable of creating a three-dimensional object excellent in both of: stiffness and strength; and toughness. Specifically, provided is a photo-curable composition including: a blocked isocyanate represented by the general formula (1); a chain extender; and a photo-radical generator:

##STR00001## in the general formula (1), A.sub.1 to A.sub.4 each independently represent a structure represented by the following general formula (2), and B represents a structure represented by the following general formula (3).

##STR00002##

The present invention relates to a hybrid polyurethane-polyhydroxyurethane (PU-PHU) composition obtained by a process comprising the following steps: (i) Reacting at least one isocyanate containing compound, in stoichiometric excess, with at least one isocyanate-reactive compound, resulting in the formation of at least one prepolymer, (ii) Reacting said at least one prepolymer with at least one cyclic carbonate functional group containing compound, leading to the formation of a cyclic carbonate-terminated prepolymer, (iii) Ring-opening reaction of said cyclic carbonate-terminated prepolymer with at least one amine functional group containing compound resulting in said hybrid PU-PHU composition,
characterised in that said ring-opening reaction step is carried out above room temperature, preferably above 20? C., more preferably above 25? C.

Provided is a cover window including a film portion on the substrate. The cover window may include a substrate, and a film portion on the substrate. The film portion includes polyurea, wherein the polyurea may be a polymer formed through a urea bond between an aliphatic polyisocyanate and an aliphatic polyamine.

Suggested is a urea urethane with improved rheological properties, obtainable or obtained according to a process encompassing or consisting of the following steps: (a) providing a monohydroxyl compound; (b) providing a diisocyanate compound; (c) reacting said monohydroxyl compound and said diisocyanate compound to form a pre-polymer; (d) reacting said pre-polymer with a diamine compound,
Wherein said pre-polymer and said diamine are reacted in the presence of a surfactant.

One purpose of the present invention is to provide a liquid-crystal compound which exhibits liquid crystallinity at low temperatures. Another purpose of the present invention is to provide a thermally responsive material which exhibits liquid crystallinity and rubber elasticity at low temperatures (around room temperature) ever, though a large amount of a liquid-crystal compound is contained therein, and a method for producing this thermally responsive material. A liquid-crystal compound according to the present invention is obtained by adding an alkylene oxide and/or styrene oxide to a mesogenic group-containing compound that has an active hydrogen group.

The present invention relates to a process for preparing a porous material, at least providing a mixture (I) comprising a composition (A) comprising components suitable to form an organic gel and a solvent(B), reacting the components in the composition (A) in the presence of the solvent (B) to form a gel, and drying of the gel obtained in step b), wherein the composition (A) comprises a catalyst (C) selected from the group consisting of alkali metal and earth alkali metal salts of a saturated or unsaturated monocarboxylic acid with 4 to 8 carbon atoms. The invention further relates to the porous materials which can be obtained in this way and the use of the porous materials as thermal insulation material and in vacuum insulation panels, in particular in interior or exterior thermal insulation systems.

A shape-memory self-healing polymeric network (SMSHP) is useful as a molded part, a coating, or as a matrix for a composite that can be repaired by heating to a controlled temperature. The SMSHP has thermally reversible repeating units where a thermally reversible adduct is situated between two common linking units formed during a polymerization process between thermally reversible monomers and cross-linking monomers. Optionally, other repeating units can be present from other monomers. Shape-memory results when the SMSHP is warmed to a temperature in excess of its glass transition temperature and self-healing then proceeds when a higher temperature is achieved where thermally reversible adducts dissociates to complementary groups that subsequently reform the adduct without distortion of the memorized shape. The thermally reversible adducts can be Diels-Alder (DA) adducts in a polyurethane, poly urea, or amine epoxy SMSHP network.