C08G18/289

BLOCKING AGENT FOR AN ISOCYANATE GROUP AND ISOCYANATE PROTECTED BY SAID BLOCKING AGENT
20230062457 · 2023-03-02 ·

One of the purposes of the present invention is to provide a blocking agent for blocking an isocyanate group to thereby prepare an isocyanate compound which has excellent water resistance and is react with another polymerizable compound to be cured at a relatively low temperature; and another purpose is to provide a blocked isocyanate having an isocyanate group blocked with the blocking agent. The present invention provides a blocking agent for blocking an isocyanate group, wherein the blocking agent is an organic silicon alcohol having an organic group bonded to a silicon atom and said organic group is capable of forming a β-silyl cation together with the silicon atom. In a preferred embodiment, the present invention provides a blocking agent which is an organic silicon alcohol represented by the general formula (1). In the formula (1), R.sup.1 is an alkylene group having 3 to 5 carbon atoms and may have a substituent, provided that the number of carbon atoms of the substituent is not included in the number of the carbon atoms of the alkylene group, R.sup.2 is an alkyl group having 1 to 10 carbon atoms, Z is an organic group capable of forming a β-silyl cation together with the silicon atom to which Z bonds, and n is an integer of 1 to 3. The present invention further provides a blocked isocyanate having a structure in which the isocyanate group is blocked with the aforesaid blocking agent and a thermosetting composition comprising the blocked isocyanate.

Vegetable oil-modified, hydrophobic polyurethane dispersions
11629217 · 2023-04-18 · ·

Aqueous hydrophobic polyurethane dispersions are made from urethane prepolymers derived from reacting constituents including at least one polyisocyanate, vegetable oil based saturated monoglycerides, non-isocyanate based urethane polyols prepared from polyamines and cyclic carbonates, at least one long-chain polymeric polyol or long-chain polyol from biorenewable resources, polyols with hydrophilic groups, optional polydimethysiloxane based polyols with hydroxyl functional groups terminated in one end and alkyl groups terminated in another end.

POLYMERIC MATERIALS WITH IMPROVED ENVIRONMENTAL DURABILITY

Polymer composite materials and methods of preparation are discussed. The composite material may comprise a polyurethane foam and a plurality of inorganic particles dispersed in the polyurethane foam. The composite material may have moisture movement properties, such that (a) a sample of the composite material having a length of 48 inches has a moisture movement of less than 0.15% along the length, and/or (b) a sample having a length of 6 inches has a moisture movement of less than 0.8% along the length, when submerged in 45° C. distilled water for 14 days.

SELF-LUBRICATING MEDICAL ARTICLES
20230159843 · 2023-05-25 · ·

Medical articles formed from a polyurethane-based resin including a modifying oligomer provide enhanced properties. A modifying oligomer incorporated into a backbone, as a side chain, or both of the polyurethane-based resin formed by a diisocyanate, a polyglycol, and a diol chain extender has at least one, preferably two, alcohol moieties (C—OH) and a functional moiety. Exemplary modifying oligomers are: a diol-containing perfluoropolyether incorporated into the backbone, a monofunctional polysiloxane (e.g., monodialcohol-terminated polydimethylsiloxane) incorporated as the side chain, and combinations thereof. Medical articles herein are self-lubricating and/or anti-fouling.

SILYLATED ORGANOMODIFIED COMPOUNDS
20230159571 · 2023-05-25 ·

There is provided herein a silylated organo-modified compound which comprises: at least one moiety having the formula (A):

##STR00001##

wherein the subscript a is 1 or 2, each D is independently NH or O, each of X, Y and Z are independently an unsubstituted or substituted C or N, the dashed lines between X, Y, and Z indicate an optional double bond between either X and Y or Y and Z, with the proviso that when any of X, Y, or Z is a substituted N atom, such substituted N atom does not participate in a double bond, and each Q is independently O or S; and, at least two moieties having the formula (B):

##STR00002##

ISOCYANATE-AMINE-BASED CHEMICAL ANCHOR WITH IMPROVED PERFORMANCE, AND USE THEREOF

A multi-component resin system can be used for producing a mortar composition based on isocyanate amine adducts for the chemical fastening of construction elements. A mortar composition based on isocyanate amine adducts can be produced from the multi-component resin system. A method can be used for the chemical fastening of construction elements in mineral substrates with the mortar composition based on the isocyanate amine adducts.

POLYMER CONTAINING SILANE GROUPS

A silane group-containing polymer obtained from reacting (i) an isocyanate group-containing polymer having an NCO content in the range of 0.3 to 4% by weight and a monomeric diisocyanate content of at most 0.3 wt. % obtained from the reaction of at least one monomeric diisocyanate with at least one polyether polyol in a molar NCO/OH ratio of at least 3/1 and subsequent removal of a major part of the unreacted monomeric diisocyanates by means of a suitable separation process, (ii) with at least one amino-, mercapto- or hydroxysilane in a stoichiometric ratio of at least 1 mole of amino-, mercapto- or hydroxysilane per mole equivalent of isocyanate groups.

POLYMER CONTAINING SILANE GROUPS

A silane group-containing polymer obtained from reacting (i) an isocyanate group-containing polymer having an NCO content in the range of 0.3 to 4% by weight and a monomeric diisocyanate content of at most 0.3 wt. % obtained from the reaction of at least one monomeric diisocyanate with at least one polyether polyol in a molar NCO/OH ratio of at least 3/1 and subsequent removal of a major part of the unreacted monomeric diisocyanates by means of a suitable separation process, (ii) with at least one amino-, mercapto- or hydroxysilane in a stoichiometric ratio of at least 1 mole of amino-, mercapto- or hydroxysilane per mole equivalent of isocyanate groups.

Environmentally biodegradable microcapsules
11465117 · 2022-10-11 · ·

Disclosed is a composition including controlled release particles, wherein each of the controlled release particles includes: (a) a core including at least one hydrophobic active ingredient; and (b) a wall at least partially surrounding the core and including the reaction products of: (i) an organofunctional silane; (ii) an epoxy; (iii) an amine; (iv) an isocyanate; (v) an epoxide curing agent; wherein the controlled release particles are effective to retain the at least one hydrophobic active ingredient upon exposure to water and effective to release the at least one hydrophobic active ingredient in response to friction. A method for preparing the composition is also disclosed.

SUSTAINABLE REACTIVE HOT MELT ADHESIVE COMPOSITIONS
20230151248 · 2023-05-18 ·

The invention features a reactive hot melt adhesive composition comprising the reaction product of from 5% by weight to 40% by weight of a first polyester polyol comprising the reaction product of a dicarboxylic acid monomer, a tetra alkyl cyclobutane diol and optionally one or more additional monomers, from 10% by weight to 80% by weight of a sustainable polyol, and a diisocyanate.