An epoxy compound having an aromatic ring represented by Formula 1 or Formula 2, a composition prepared from the epoxy compound, a semiconductor device prepared from the epoxy compound, an electronic device prepared from the epoxy compound, an article prepared from the epoxy compound, and a method of preparing the epoxy compound:

E1-(M1).sub.a1-(L1).sub.b1-(M2).sub.a2-L2-A1-L3-(M3).sub.a3-(L4).sub.b2-(M4).sub.a4-E2  Formula 1

E3-(A2).sub.c1-(L5).sub.b3-(M5).sub.a5-L6-(M6).sub.a6-L7-(M7).sub.a7-(L8).sub.b4-(A3).sub.c2-E4  Formula 2

In Formulae 1 and 2, M1, M2, M3, M4, M5, M6, M7, A1, A2, A3, L1, L2, L3, L4, L5, L6, L7, L8, E1, E2, E3, E4, a1, a2, a3, a4, a5, a6, a7, b1, b2, b3, b4, c1, and c2 are the same as defined in the detailed description.

A joint member having a thermoplastic elastomer composition including components (A), (B), and (C). Component (A): a hydrogenated product of a block copolymer including at least two polymer blocks composed primarily of a vinyl aromatic compound and at least one polymer block including butadiene, wherein, in the hydrogenated product of the block copolymer, a proportion of a hydrogenated product (A1) of a block copolymer having a weight-average molecular weight of 300,000 or more is 30% to 100% by mass, Component (B): a hydrocarbon rubber softener, Component (C): a polypropylene resin, Component (D): a crosslinking agent.

1) Two-component polyurethane-based adhesive composition comprising an —NCO component and an —OH component, such that: the —NCO component is obtained by polyaddition between MDI and a composition of polyols comprising a polyether diol and a polyether triol, in an —NCO/—OH molar equivalent ratio of between 2.5 and 6.5; the —OH component is obtained by polyaddition between MDI and a composition of polyols with a functionality of 2 comprising an aliphatic polyester diol, a partially aromatic polyester diol and an aliphatic polyether diol, in an —NCO/—OH molar equivalent ratio of between 0.05 0.50; the amounts of the —NCO and —OH components being such that the —NCO/—OH molar equivalent ratio is within a range extending from 1.5 to 1.7. 2) Multilayer film comprising 2 thin layers of material linked to one another by a continuous layer constituted by said crosslinked adhesive composition. 3) Process for preparing said film and use thereof in the manufacture of flexible packagings.

Applicant discloses a two part polymer mix for use in the aircraft industry that is applied with pneumatic mix and spray gun. A two part cartridge is used in the mix and spray gun so the mix is applied immediately upon mixing, but the two components are kept separated unless the gun is applying the mix. The mix cures to form a clear sealant that allows for inspection of cracks and corrosion beneath the sealant. It cures quickly so that the coated part may be further processed, for example in the assembly line during aircraft build.

The present invention relates to a 2-component system containing at least one specific N-, S-, O- and Si-containing compound. The invention further relates to a process for preparing silicon-containing polyurethanes, comprising reacting the first component with the second component of the 2-component system according to the present invention, and to the silicon-containing polyurethanes obtained therefrom. In addition, the invention relates to the use of the 2-component system according to the present invention for the production of coating, sealants or adhesives.

The present invention relates to a selective process for the preparation of NCO-functionalized polyols, to their use in the preparation of silylated polyurethanes, to processes for preparing silylated polyurethanes and to silylated polyurethanes obtainable by a reaction of NCO-functionalized polyol with amino silane and to their use in CASE applications (coatings, adhesives, sealants and elastomers).

A process for end-capping a dimethylsilanol terminated polydiorganosiloxane with one or more di, tri and/or tetra alkoxysilanes in the presence of an end-capping catalyst starting material is provided. The end-capping catalyst starting material comprises one or more linear, branched or cyclic molecules comprising at least one amidine group, guanidine group, or derivatives of the amidine group and/or guanidine group or a mixture thereof. The resulting capped polymeric material may be utilized as a polymer in, e.g., a polydiorganosiloxane elastomer composition.

Polymers include a monomer with a polyurethane, a supramolecular moiety, an elastomer moiety and a functional group that includes a —C═N— link. The polymers can be prepared and incorporated into a composition. The polymers can be double dynamic polymers, which present adhesive and self-healing properties. The polymers can also be recyclable.

Described herein is a process for preparing a polyurethane elastomer including the steps of (A) preparing an isocyanate prepolymer (a), where the isocyanate prepolymer has an isocyanate content in the range of ≥1 wt.-% to ≤9 wt.-%, and (B) preparing a reaction mixture by mixing at least one epoxy compound (b) with the isocyanate prepolymer (a) in presence of at least one catalyst (c), and where the amount of the alkali metal or alkaline earth metal salt is 0.00001 to 0.1 mol per kg of the total weight of the isocyanate prepolymer (a), the epoxy compound (b) and the catalyst (c), and heating the mixture to at least 80° C. to obtain the polyurethane elastomer. Also described herein are a polyurethane elastomer obtained by process and a method of using the polyurethane elastomer as part of a roller or as a sealant.

This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure. The disclosure provides aromatic polyester polyether polyols and compositions comprising such polyols. The disclosed aromatic polyester polyether polyols and compositions including same are the products of the transesterification reaction of polyethylene terephthalate (“PET”) and an ethoxylated triol, namely glycerin or trimethylolpropane, wherein the degree of ethoxylation is from 1 to 9 moles. At least some of the PET used to generate the aromatic polyester polyether polyols is derived from recycled PET. The disclosed aromatic polyester polyether polyols have utility in preparing polyurethane materials, for example.