1) A heat-crosslinkable adhesive composition, comprising: at least one polymer (A) comprising a hydrolyzable alkoxysilane group; at least one tackifying resin (B); at least one silsesquioxane resin (C); and at least one crosslinking catalyst (D).

2) A self-adhesive article comprising a support layer coated with a self-adhesive layer consisting of the adhesive composition in the crosslinked state.

A modified polymer includes a diene-based polymeric chain and at least one end terminated with a blocked isocyanate group. The blocked isocyanate group may be the reaction product of an isocyanate and a blocking agent, and the blocking agent is selected, such that the modified polymer deblocks at temperatures of at least 100 C. An aqueous emulsion of the modified polymer may be provided that may be surfactant-free. The emulsion may be combined with one or more latexes to provide a treatment solution for a fabric or fiber that does not require the use of resorcinol and formaldehyde. Once treated and dried, the fabric or fiber may be used to impart tensile strength to rubber products, such as tires, air springs, flexible couplings, power transmission belts, conveyor belts, and fluid routing hoses.

A two-part curable adhesive composition includes a main agent (A) containing a urethane prepolymer (a1) and a remaining polyisocyanate (a2), and a curing agent (B) containing a non-crystalline polyol compound (b1) and a polyamine compound (b2). An equivalent ratio of an isocyanate group in a raw polyisocyanate to a hydroxyl group in the polyol compound is from 2.05 to 12. The equivalent ratio of the isocyanate group in the main agent (A) to an amino group in the polyamine compound (b2) is from 1.2 to 6. The equivalent ratio of the isocyanate group in the main agent (A) to the hydroxyl group in the non-crystalline polyol compound (b1) is from 2 to 12.

Provided is an electrophotographic member that is excellent in charge-imparting performance for a toner, and that hardly causes tackiness on its surface even when placed under a high-temperature and high-humidity environment over a long time period. The electrophotographic member includes a substrate and a surface layer, in which the surface layer satisfies the following requirements (A) and (B): (A) the surface layer contains, in a region from its surface to a depth of up to 0.1 μm, a copolymer containing a constituent unit represented by the following structural formula (1), and at least one selected from the group consisting of a constituent unit represented by the following structural formula (2) and a constituent unit represented by the following structural formula (3); and (B) the concentration of a nitrogen atom derived from a nitrogen-containing aromatic heterocyclic amine structure in the copolymer is from 6.0 mass % to 30.0 mass %.

##STR00001##

A photocurable resin of the present technology contains: a main backbone chain having repeating units represented by Formulas (Ia) and (Ib), and a (meth)acryloyl group and a non-photoreactive group at terminals; the non-photoreactive group being at least one type selected from the group consisting of saturated hydrocarbon groups and aromatic hydrocarbon groups which optionally have a heteroatom; a hydroxy group, an amino group, —CH═NH, a carboxy group, or a mercapto group being not bonded to an end of the non-photoreactive group; a content of the repeating unit represented by Formula (Ia) being greater than 15 mol % of an amount of the main backbone chain; and contents of the (meth)acryloyl group and the non-photoreactive group each being 5 mol % or greater of an amount of the ends. ##STR00001##

A photocurable resin of the present technology contains: a main backbone chain having repeating units represented by Formulas (Ia) and (Ib), and a (meth)acryloyl group and a non-photoreactive group at terminals; the non-photoreactive group being at least one type selected from the group consisting of saturated hydrocarbon groups and aromatic hydrocarbon groups which optionally have a heteroatom; a hydroxy group, an amino group, —CH═NH, a carboxy group, or a mercapto group being not bonded to an end of the non-photoreactive group; a content of the repeating unit represented by Formula (Ia) being greater than 15 mol % of an amount of the main backbone chain; and contents of the (meth)acryloyl group and the non-photoreactive group each being 5 mol % or greater of an amount of the ends. ##STR00001##

An adhesive for laminated sheets, which is excellent in adhesive strength to a film after curing and long-term hydrolysis resistance at high temperature and high humidity when a laminated sheet is produced, and is also excellent in adhesive property at low temperature. Disclosed is an adhesive for laminated sheets, which comprises a urethane resin obtainable by mixing an acrylic polyol with an isocyanate compound, and also has a chemical structure derived from a diene polymer, wherein the diene polymer has a glass transition temperature of −40° C. or lower. The adhesive for laminated sheets is excellent in adhesive strength to a film after curing and long-term hydrolysis resistance at high temperature and high humidity when a laminated sheet is, produced, and is also excellent in adhesive property at low temperature.

An adhesive for laminated sheets, which is excellent in adhesive strength to a film after curing and long-term hydrolysis resistance at high temperature and high humidity when a laminated sheet is produced, and is also excellent in adhesive property at low temperature. Disclosed is an adhesive for laminated sheets, which comprises a urethane resin obtainable by mixing an acrylic polyol with an isocyanate compound, and also has a chemical structure derived from a diene polymer, wherein the diene polymer has a glass transition temperature of −40° C. or lower. The adhesive for laminated sheets is excellent in adhesive strength to a film after curing and long-term hydrolysis resistance at high temperature and high humidity when a laminated sheet is, produced, and is also excellent in adhesive property at low temperature.

The present invention relates to a polyurethane laminating adhesives, methods for producing a multilayer laminate by laminating at least two films with a polyurethane laminating adhesive, and multilayer laminates obtainable by these methods wherein the polyurethane laminating adhesive comprises an NCO-terminated polyurethane prepolymer obtainable by reacting a polyol mixture comprising: 0.1 to 20.0 wt % relative to the total weight of the polyol mixture of at least one polybutadiene polyol; and 5.0 to 99.9 wt % relative to the total weight of the polyol mixture of at least one polyether polyol, wherein the at least one polyether polyol comprises at least one polyether polyol with a number average molecular weight M.sub.n in the range of >1000 g/mol to 10000 g/mol; with at least one polyisocyanate, wherein the at least one polyisocyanate is used in an amount such that the isocyanate groups are present in molar excess relative to the hydroxyl groups of the polyol mixture. Also encompassed are the use of the described adhesives for laminating two or more films, and the multilayer laminates obtainable by the described methods.

An adhesive composition suitable for reverse osmosis modules, the adhesive composition includes (I) a polyurethane composition that includes (A) an isocyanate group-containing pre-polymer comprising a reaction product of (i) castor oil or a derivative thereof; and (ii) a polyisocyanate; and (iii) optionally a second polyol; and (B) an isocyanate-reactive polyol mixture comprising: (i) a polybutadiene polyol; and (ii) a urethane catalyst; and (iii) optionally the second polyol; and (II) a plasticizer wherein the adhesive composition is essentially free from diluent oils and solvents.