C09J175/00

Adhesive
10947425 · 2021-03-16 · ·

Provided is an adhesive as follows. The adhesive can bond/secure an adherend to a support with maintaining high adhesiveness during the existence of the need for securing of the adherend to the support, even in a high-temperature environment or in an environment with abrupt temperature change. The adhesive enables debonding of the adherend from the support without breakage of the adherend when the securing becomes unnecessary. The adhesive can be easily removed when remained on the adherend after debonding. The adhesive according to the present invention contains (A) a multivalent vinyl ether compound, (B) a compound including two or more of a constitutional unit represented by Formula (b), and (C) a thermoplastic resin. In the formula, X is selected from hydroxy and carboxy. ##STR00001##

Adhesive
10947425 · 2021-03-16 · ·

Provided is an adhesive as follows. The adhesive can bond/secure an adherend to a support with maintaining high adhesiveness during the existence of the need for securing of the adherend to the support, even in a high-temperature environment or in an environment with abrupt temperature change. The adhesive enables debonding of the adherend from the support without breakage of the adherend when the securing becomes unnecessary. The adhesive can be easily removed when remained on the adherend after debonding. The adhesive according to the present invention contains (A) a multivalent vinyl ether compound, (B) a compound including two or more of a constitutional unit represented by Formula (b), and (C) a thermoplastic resin. In the formula, X is selected from hydroxy and carboxy. ##STR00001##

FLEXIBILIZED POLYURETHANES FOR FLEXIBLE PACKAGING ADHESIVE WITHOUT AROMATIC AMINE MIGRATION
20210039359 · 2021-02-11 ·

Provided is an adhesive comprising a reaction product of (A1) an aliphatic isocyanate having an NCO group content of 18 to 64 and (A2) a polyol or polyamine having a molecular weight of from 400 to 4000; and (B) a polyaspartate compound, wherein viscosity of the adhesive, as measured @ 23 C. according to ASTM D4212-16, remains below 60 seconds for after four hours, and wherein the adhesive develops an acceptable bond strength to a substrate, defined as having a minimum of 150 g/in. measured @ 23 C. according to ASTM D 1876-01 or substrate tear, in less than or equal to five days after the substrate is laminated with the adhesive. The adhesives are free of aromatic amines and may find use in multi-layered laminated films for the production of flexible packaging useful in a variety of industries, including the food processing, cosmetics, and detergents industries.

Dipping bath compositions for treating reinforcing inserts
11059950 · 2021-07-13 · ·

The present invention relates to an aqueous, solids-containing dipping bath composition for treating reinforcing inserts for rubber products comprising the following components or consisting of these components, (A) at least one blocked MDI mixture, the MDI mixture comprising MDI oligomers of formula (I), n being a whole number from 1 to 8, and MDI monomers; (B) at least one resorcinol-formaldehyde latex; and (C) possibly at least one additive, wherein the dipping bath composition is essentially free of epoxides. ##STR00001##

Dipping bath compositions for treating reinforcing inserts
11059950 · 2021-07-13 · ·

The present invention relates to an aqueous, solids-containing dipping bath composition for treating reinforcing inserts for rubber products comprising the following components or consisting of these components, (A) at least one blocked MDI mixture, the MDI mixture comprising MDI oligomers of formula (I), n being a whole number from 1 to 8, and MDI monomers; (B) at least one resorcinol-formaldehyde latex; and (C) possibly at least one additive, wherein the dipping bath composition is essentially free of epoxides. ##STR00001##

COMPOSITIONS, METHOD OF BONDING, AND ASSEMBLY

A two-part curable composition comprises a Part A and a Part B. The Part A composition includes polyuretdione having an average uretdione ring functionality of at least 1.2. Part B composition includes polythiol having an average sulfhydryl group functionality of at least 1.2. At least one of the Part A composition and the Part B composition may further comprise accelerator for addition of the polythiol to the polyuretdione. The accelerator comprises a basic salt having the formula M+Zbx y wherein M+ is a cation having a single positive charge a, wherein a is 1, 2, or 3; Zb is an oxide anion having a negative charge b, wherein b is 1 or 2; and x and y are positive integers, wherein x equals y times b. Cured compositions, methods of making them and articles including them are also disclosed.

COMPOSITIONS, METHOD OF BONDING, AND BONDED ASSEMBLY

A two-part curable composition comprises a Part A and a Part B. Part A composition includes uretdione-containing compound having an average uretdione ring functionality of at least 1.2. Part B composition includes polythiol having an average sulfhydryl group functionality of at least 2. At least one of the Part A composition and the Part B composition may further comprise accelerator for addition of the polythiol to the uretdione-containing compound. The accelerator comprises a nonacidic amine curative. The amine curative does not comprise a substituted or unsubstituted amidine group. Cured compositions, methods of making them and articles including them are also disclosed. A two-part composition without accelerator is disclosed wherein the uretdione-containing compound has at least one pendant CH.sub.2NR.sup.4.sub.2 groups, wherein each R.sup.4 independently represents an alkyl group having from 1 to 8 carbon atoms, or two R.sup.4 groups taken together form an alkylene group having from 2 to 8 carbon atoms.

Improved assembly method in making shoe, and applied correction solution
20210015214 · 2021-01-21 ·

An improved assembly method in making a shoe, and an applied correction solution. In the method, according to the porosity or the density of a material to be bonded, correction solutions of different concentrations are added to a TPU binder of a single viscosity, so as achieve the viscosity of the TPU binder, and to overcome the problem of storage and management of various types of binders, and the assembly steps can be simplified.

Polyurethane catalyst and application thereof
10889681 · 2021-01-12 ·

A polyurethane catalyst comprises a sodium compound, the sodium compound being 1 to 60 wt % of the polyurethane catalyst by the mass percent, and further comprises a tertiary amine and/or pyridine compound. The sodium compound and the tertiary amine and/or pyridine compound achieve a synergistic effect; during the catalysis of the polymerization of isocyanate and polyalcohol, the speed of the polymerization reaction is increased; and the prepared polyurethane material has excellent physical properties, does not contain any heavy metal element at all, is an environment-friendly catalyst, solves the technical problem of ensuring environmental protection, safety and the catalytic efficiency of the polyurethane catalyst, and is particularly applicable to the preparation of polyurethane synthetic leather resin slurry, a polyurethane elastomer (prepolymer), a polyurethane coating, a polyurethane adhesive, a polyurethane composite material, flexible polyurethane foam, and a rigid polyurethane material.

Polyurethane catalyst and application thereof
10889681 · 2021-01-12 ·

A polyurethane catalyst comprises a sodium compound, the sodium compound being 1 to 60 wt % of the polyurethane catalyst by the mass percent, and further comprises a tertiary amine and/or pyridine compound. The sodium compound and the tertiary amine and/or pyridine compound achieve a synergistic effect; during the catalysis of the polymerization of isocyanate and polyalcohol, the speed of the polymerization reaction is increased; and the prepared polyurethane material has excellent physical properties, does not contain any heavy metal element at all, is an environment-friendly catalyst, solves the technical problem of ensuring environmental protection, safety and the catalytic efficiency of the polyurethane catalyst, and is particularly applicable to the preparation of polyurethane synthetic leather resin slurry, a polyurethane elastomer (prepolymer), a polyurethane coating, a polyurethane adhesive, a polyurethane composite material, flexible polyurethane foam, and a rigid polyurethane material.