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.

A flexibilizing capped prepolymer can include a reaction product of reaction mixture including a polyisocyanate and an isocyanate-reactive component at an equivalent ratio of polyisocyanate equivalents to isocyanate-reactive component equivalents of from 1.4:1 to 2.1:1. The isocyanate-reactive component can include a polyol component and a branching agent component. The branching agent component can include a monoglyceride, a diglyceride, a triglyceride, or a combination thereof having a number average functionality of from 3 to 6 NCO-reactive functional groups. The reaction product is terminated with a capping agent to form the flexibilizing capped prepolymer.

A double coating, curing method, cured coating, and kit are provided. A first layer of the double coating can be a first cure coating composition, which has a first hydroxy-functional resin, a first crosslinking agent, and a first catalyst. A second layer of a second cure coating composition can have a low hydrophilicity acrylic resin as a second hydroxy-functional resin, a second crosslinking agent, and a second catalyst. The first catalyst catalyzes crosslinking between the second hydroxy-functional resin and crosslinking agent, and not between the first hydroxy-functional resin and crosslinking agent. The second catalyst catalyzes crosslinking between the first hydroxy-functional resin and crosslinking agent, and not between the second hydroxy-functional resin and crosslinking agent. The first and/or second hydroxy functional resins can facilitate catalyst migration from one layer to the other. The separate compositions can be shelf-stable and/or the curing can occur at low temperature.

To provide a polycarbodiimide copolymer and a modified polycarbodiimide copolymer each suitable for a curing agent that can allow a cured product of a carboxy group-containing resin composition to be improved in flexibility without any loss of water resistance, as well as a curing agent of a carboxy group-containing resin composition, and a carboxy group-containing resin composition. The present invention enables a cured product to be enhanced in water resistance due to introduction of a predetermined soft segment into a polycarbodiimide molecule, in use for a curing agent, and also enables a carboxy group-containing resin composition to be enhanced in storage stability due to modification with an aliphatic amine or an aromatic heterocyclic amine.

Described herein is a method for producing a PU foam insole, including the following steps of: (1) pouring the raw materials used to form a PU foam into a mould, reacting to obtain a PU sheet, where the height of the mould cavity is from about 1.0 to about 1.6 times of the total thickness of two finished insoles; (2) splitting the PU sheet into two halves in the horizontal direction to obtain two pieces of PU insole material, where one surface of the material has open pores, and the other surface of the material has a skin; and (3) attaching a piece of fabric onto the surface having open pores of the material obtained in step (2). Also described herein is a PU foam insole produced by the method.

A method of preparing an elastomer membrane with high water pressure resistance includes the following steps: preparing a dry material by subjecting first thermoplastic polyurethane (TPU) powder/particles to a drying treatment; preparing a first mixture by mixing the dry material thoroughly with one or a mixture of at least two of diethylenetriamine, diethylaminopropylamine, and diaminodiphenylmethane; preparing a second mixture by mixing an initiator thoroughly with the first mixture; preparing a first membrane layer from the second mixture; and preparing a second membrane layer and a third membrane layer through the above steps such that the second membrane layer and the third membrane layer are sequentially formed on the first membrane layer.

A resin composition for golf balls is made of (A) polyurethane or polyurea and (B) a styrene resin material, component (B) being included in an amount of 0.5 to 50 parts by weight per 100 parts by weight of component (A). In a golf ball having a core and a cover of one or more layer encasing the core, at least one cover layer is formed of this resin composition. The resin composition is especially useful as a golf ball cover material because the ball does not fly too far and is easier to control on approach shots, yet does not sacrifice distance on shots with a driver.

In a preferred embodiment, there is provided a self-healing polymer composition preferably for use in manufacturing a dielectric layer of a capacitive pressure sensor, and which comprises a central atom and a polymer having a main chain and one or more terminal moieties coupled to the main chain, wherein said one or more terminal moieties are selected to operate as ligands to form a coordination complex with the central atom, and preferably, the ligands and the central atom are selected to form the coordination complex after being subject to an external force sufficient to remove coordinate covalent bonds therebetween.

The present technology relates to antimicrobial cleaning compositions comprising a polyurethane having at least one acid group salted with a biguanide (e.g., bis-biguanide) free base compound. More specifically, the present technology relates to an antimicrobial cleaning composition comprising a) a polyurethane with at least one free acid group salted with a biguanide free base; b) at least one surfactant; and c) a diluent. Surfaces treated with the antimicrobial compositions of the disclosed technology are provided with residual inhibition against the proliferation of microbe growth.

A polymeric material includes a polyisobutylene-polyurethane block copolymer. The polyisobutylene-polyurethane block copolymer includes soft segments, hard segments, and end groups. The soft segments include a polyisobutylene diol residue. The hard segments include a diisocyanate residue. The end groups are bonded by urea bonds to a portion of the diisocyanate residue. The end groups include a residue of a mono-functional amine.