Dow Global Technolgoies LLC

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The Dow Chemical Company

Blue Cube IP LLC

Dwight D Latham

Kaoru Aou

William Aaron Koonce

Stephen W King

Xue Chen

Phillip S Athey

Juan Carlos Medina

Debkumar Bhattacharjee

Nathan Wilmot

Harshad M Shah

Rajesh P Paradkar

Muhammad A Shafi

Huifeng Qian

Luigi Pellacani

Nicole Knight

Sara Arshad

William L Heaner, Iv

Mark F Sonnenschein

Maurice J Marks

Rajat Duggal

Michael T Malanga

Qiuyun Xu

Xin Jin

Steven P Crain

Hector Antonio Perez

Bindu Krishnan

Jorge Jimenez

Pankaj Gupta

Ling Zhang

Venkat S Minnikanti

Woo-Sung Bae

Kamesh R Vyakaranam

Allen S Bulick

Bedri Erdem

Liangkai Ma

Laura A Grier

Jeffery D Zawisza

Friederike Stollmaier

Hongming Ma

Jeffrey D Wenzel

Matthias Schaefer

Avery L Watkins

Kwanho Chang

Steven Crain

Jie Feng

Rujul M Mehta

Paul D Ries

Bindushree Radhakrishnan

Kameswara Vyakaranam

Michelle Tipps-Thomas

Ragat Duggal

Kameswara R Vyakaranam

Michael J Elwell

Gilbert L Nelson

Emanuele Maiocchi

William L Heaner Iv

Mark W Brown

Hector Perez

Phillip S c/o The Dow Chemical Company Intellectual Property Law Athey

Kamesh Vyakaranam

A curable resin composition comprising: (1) a urethane (meth)acrylate; (2) a reactive diluent selected from the group consisting of i) a hydroxyl alkyl (meth)acrylate monomer where the acrylate group, which is attached to the carbonyl group, is attached to a hydrogen or a methyl group and the carbonyl group is attached to the hydroxyl group thru an R2 alkylene group containing 2 to 18 carbon atoms per molecule.

Styrene-free reactive diluents for urethane acrylate resin compositions

A process for making a curable resin composition comprising the steps of: (1) reacting a) an isocyanate; and b) a polyol mixture with a bimodal distribution of i) a first polyol mixture comprising polyols having an average equivalent weight of from 50 to 400; and ii) a second polyol mixture comprising polyols having an average equivalent weight of from 1000 to 5000 to form a urethane prepolymer; and (2) adding a capping agent to the urethane prepolymer to form the curable resin composition.

Process for making urethane acrylates

A method for exposing a substrate to water under superatmospheric pressure at a temperature of at least 70&#xb0; C. includes (a) applying a reaction mixture to a substrate, which reaction mixture has an isocyanate index of at least 10 and includes an aromatic polyisocyanate component, a polyol component having a polyol with a hydroxyl equivalent weight of at least 500, and a catalyst component having an isocyanate trimerization catalyst, and at least partially curing the reaction mixture to form a polyisocyanurate or polyurethane-isocyanurate polymer having a glass transition temperature of at least 80&#xb0; C., and (b) exposing the substrate and the polyisocyanurate or polyurethane-isocyanurate polymer to water under superatmospheric pressure at a temperature of at least 70&#xb0; C.

Process for making urethane-isocyanurates

Solid compositions made from or coated with a non-melting organic polymer having a main glass transition temperature of at least 65&#xb0; C., few if any isocyanate groups and a wet aged glass transition temperature of up to 60&#xb0; C. are self-bonding materials that are useful in a variety of adhesive and molding operations. Under conditions of heat and moisture, these compositions will self-bond. The compositions can be used as adhesive coatings, which are solid and non-tacky and thus can be transported and stored easily under ambient conditions. These compositions are especially useful in applications in which, due to the location and/or orientation of the substrates, liquid or melting materials cannot be applied easily or will run off the substrates.

Solid, self-bondable organic polymers and methods for using same

A method for making joints in an electrical cable is disclosed. A first cable having polymeric insulation and a first bare conductor end and a second cable having polymeric insulation and a second bare conductor end are provided and joined create a conductor joint. A curable reaction mixture is applied over the conductor joint and cured to form a polymeric insulating sheath over the conductor joint and bonded to the polymeric insulation of each of the first and second cables. The reaction mixture includes a carbon-Michael acceptor compound, a carbon-Michael donor compound and a carbon-Michael reaction catalyst.

Method for making an electrical cable joint

Solid, non-melting polyurethanes having a glass transition temperature of at least 40&#xb0; C. and free isocyanate groups are self-bonding materials that are useful in a variety of adhesive and molding operations. Under conditions of heat and moisture, these polyurethanes will self-bond. The polyurethanes can be used as adhesive coatings, which are solid and non-tacky and thus can be transported and stored easily under ambient conditions. These polyurethane adhesives are especially useful in applications in which, due to the location and/or orientation of the substrates, liquid or melting materials cannot be applied easily or will run off the substrates.

Solid, self-bondable isocyanate-containing organic polymers and methods for using same

Polyisocyanurate or polyurethane-isocyanurate polymers are made by curing an aromatic polyisocyanate or a mixture of at least one aromatic polyisocyanate and at least one polyol having a hydroxyl equivalent weight of up to 200 in which the isocyanate index is at least 2.00, in the presence of at least one isocyanate trimerization catalyst, to form a polyisocyanurate or polyurethane-isocyanurate polymer having a glass transition temperature of at least 100&#xb0; C., and then exposing the polyisocyanurate or polyurethane-isocyanurate polymer formed step a) to water under superatmospheric pressure at a temperature of at least 70&#xb0; C.

Process for making urethane-isocyanates

Embodiments of the present disclosure are directed towards using a carbon-Michael compound. As an example, a method of using a carbon-Michael compound to reduce heat transfer can include locating the carbon-Michael compound between a heat provider and a heat receptor, where the carbon-Michael compound is a reaction product of a multifunctional acrylate compound with a multifunctional Michael donor, and the heat provider has a temperature from 100 C to 290 C.

Method of using a carbon-michael compound

Elastomers are formed by curing a reaction mixture that includes an polyepoxide-terminated polyether having a linear or branched polyether chain that has a molecular weight of at least 2000, at least two epoxide groups that has an epoxide equivalent weight of at least 400 2) a curing agent containing at least one polythiol compound having at least two thiol groups and an equivalent weight per thiol group of up to 500, and 3) at least one base catalyst.

Thiol-cured elastomeric epoxy resins

The present invention describes cyclic amine compounds useful for catalysts for polyurethane form-forming compositions. The cyclic amine compounds of the invention provide distinct benefits for reaction compositions, methods, and polyurethane foams based on their desirable physical and catalytic properties.

Cyclic amine compounds, compositions, and polyurethane foams made therefrom

A cyclic carbonate monomer including the reaction product of (a) a divinylarene dioxide, and (b) carbon dioxide; a process for making the cyclic carbonate monomer; and a polymer such as a poly(hydroxyurethane) composition made therefrom. The poly(hydroxyurethane) composition made from the above cyclic carbonate monomer forms a reactive intermediate that can be used for making, for example, a poly(hydroxyurethane) foam product.

Cyclic carbonate monomers and polymers prepared therefrom

Embodiments of the invention provide for polyurethane-based sealants. The sealants include a reaction product of a reaction system which includes at least one isocyanate, and at least one polyester polyol. The polyester polyol includes a reaction product of a polyester reaction mixture which includes one or more hydrophobic monomers, one or more organic diacids or methyl esters thereof, and one or more diols.

Polyurethane based insulated glass sealant

Moisture curable compositions including silylated polymers and methods for producing the same are provided. A two component moisture curable system for producing a cured or cross-linked silylated polymer having improved compression set properties is provided. The two component system comprises a first formulation and a second formulation. The first formulation comprises a silylated polymer, water, and filler and the second formulation comprises the silylated polymer, a curing catalyst comprising at least one Br&#xf8;nsted acid, and a moisture scavenger. The final cured formulation may have a compression set, determined by ASTM D395 or ISO 815-1, of less than 100%, and in some examples less than 50% and in some examples less than 15%. This demonstrated improvement in compression set not only allows the silylated polymers to be used in applications where cyclic loads are applied but also enhances product durability.

Compression set property in silylated polymers

Methods of forming olyurethane foams that are the reaction product of at least one polyisocyanate and a polyol composition are provided. The polyol composition includes at least one natural oil based polyol and at least one poly(propylene oxide) polyol and is desirably free of non-natural oil based polyols made from alkylene oxide units, other than propylene oxide units. The natural oil based polyol is present in a quantity sufficient to increase the processing window for the foam relative to a foam made using the same process and the same components, absent the natural oil based polyol. As a result, the present foams can provide very open-cellular structures with the superior performance properties of a poly(propylene oxide) polyol-based foam.

Process to prepare open cell foams made with natural oil based polyols and poly(propylene oxide) polyols

Embodiments of the invention provide for compositions including a crosslinkable silane-terminated polymer having at least one crosslinkable silyl group in each molecule. The crosslinkable silane-terminated polymer comprises a reaction product of at least a isocyanate capped hydrosilylated polymer and a polyol having a nominal functionality of at least 2 which is at least one of a polycarbonate polyol, a natural oil based polyol, a polyoxyalkyleneamine, a difunctional aromatic amine, a polybutyloxide polyether polyol, and a polytetramethylene glycol.

Silyl-terminated polymers

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Clute, TX, United States of America

Dwight D Latham