In this invention, a portion of the products from a pyrolysis reactor are reacted in a process to form one or more chemical intermediates.

In this invention, a portion of the products from a pyrolysis reactor are reacted in a process to form one or more chemical intermediates.

An anode for oxygen evolution that operates at a small overpotential and in a stable manner, and can be used favorably in an organic chemical hydride electrolytic synthesis apparatus.

An anode 10 for oxygen evolution that evolves oxygen in a sulfuric acid aqueous solution containing a substance to be hydrogenated dissolved at a concentration higher than 1 mg/L, wherein an anode substrate 10a is composed of a valve metal, and an anode catalyst layer 10b containing at least one oxide, nitride or carbide of iridium, and at least one oxide, nitride or carbide of at least one metal selected from the group consisting of elements belonging to groups 4, 5 and 13 of the periodic table is formed on the surface of the anode substrate 10a.

An anode for oxygen evolution that operates at a small overpotential and in a stable manner, and can be used favorably in an organic chemical hydride electrolytic synthesis apparatus.

An anode 10 for oxygen evolution that evolves oxygen in a sulfuric acid aqueous solution containing a substance to be hydrogenated dissolved at a concentration higher than 1 mg/L, wherein an anode substrate 10a is composed of a valve metal, and an anode catalyst layer 10b containing at least one oxide, nitride or carbide of iridium, and at least one oxide, nitride or carbide of at least one metal selected from the group consisting of elements belonging to groups 4, 5 and 13 of the periodic table is formed on the surface of the anode substrate 10a.

The present invention describes novel Cashew Nut Shell Liquid derived cycloaliphatic functional compounds and methods for making the same. The invention also provide methods to use these derivatives in antimicrobials, antioxidants, adhesives, coatings, corrosion retardants composites, cosmetics, detergents, soaps, de-icing products, elastomers, food, flavors, inks, lubricants, oil field chemicals, tackifiers, prepolymer chain-extenders, rheology modifiers, electrical and electronic components (potting, castings, encapsulants), personal care products, polymers, structural polymers, engineered plastics, 3D printable polymers, 3D printable polymers, UV/E-beam/cationic curable polymers, techno-polymers, rubbers, sealants, solvents, surfactants and varnishes, transformer oil, lubricants.

The present invention describes novel Cashew Nut Shell Liquid derived cycloaliphatic functional compounds and methods for making the same. The invention also provide methods to use these derivatives in antimicrobials, antioxidants, adhesives, coatings, corrosion retardants composites, cosmetics, detergents, soaps, de-icing products, elastomers, food, flavors, inks, lubricants, oil field chemicals, tackifiers, prepolymer chain-extenders, rheology modifiers, electrical and electronic components (potting, castings, encapsulants), personal care products, polymers, structural polymers, engineered plastics, 3D printable polymers, 3D printable polymers, UV/E-beam/cationic curable polymers, techno-polymers, rubbers, sealants, solvents, surfactants and varnishes, transformer oil, lubricants.

The present invention describes novel Cashew Nut Shell Liquid derived cycloaliphatic functional compounds and methods for making the same. The invention also provide methods to use these derivatives in antimicrobials, antioxidants, adhesives, coatings, corrosion retardants composites, cosmetics, detergents, soaps, de-icing products, elastomers, food, flavors, inks, lubricants, oil field chemicals, tackifiers, prepolymer chain-extenders, rheology modifiers, electrical and electronic components (potting, castings, encapsulants), personal care products, polymers, structural polymers, engineered plastics, 3D printable polymers, 3D printable polymers, UV/E-beam/cationic curable polymers, techno-polymers, rubbers, sealants, solvents, surfactants and varnishes, transformer oil, lubricants.

A method for manufacturing nonylcyclohexanol is provided. The method includes steps as follows: adding a liquid phase reactant into a reactor, and the liquid phase reactant includes a molten nonylphenol and a catalyst; introducing a gas phase reactant to maintain a pressure of the gas phase reactant to be from 36.5 bar to 70 bar, and the gas phase reactant consists of hydrogen; rotating a hollow stirring shaft of the reactor at a temperature of from 100° C. to 130° C. so that the gas phase reactant is transported through a channel formed in the hollow stirring shaft into the liquid phase reactant for carrying out a reaction; obtaining a product that contains nonylcyclohexanol. A conversion rate of the nonylcyclohexanol is higher than or equal to 99.0%.

A method for manufacturing nonylcyclohexanol is provided. The method includes steps as follows: adding a liquid phase reactant into a reactor, and the liquid phase reactant includes a molten nonylphenol and a catalyst; introducing a gas phase reactant to maintain a pressure of the gas phase reactant to be from 36.5 bar to 70 bar, and the gas phase reactant consists of hydrogen; rotating a hollow stirring shaft of the reactor at a temperature of from 100° C. to 130° C. so that the gas phase reactant is transported through a channel formed in the hollow stirring shaft into the liquid phase reactant for carrying out a reaction; obtaining a product that contains nonylcyclohexanol. A conversion rate of the nonylcyclohexanol is higher than or equal to 99.0%.

A method for manufacturing nonylcyclohexanol is provided. The method includes steps as follows: adding a liquid phase reactant into a reactor, and the liquid phase reactant includes a molten nonylphenol and a catalyst; introducing a gas phase reactant to maintain a pressure of the gas phase reactant to be from 36.5 bar to 70 bar, and the gas phase reactant consists of hydrogen; rotating a hollow stirring shaft of the reactor at a temperature of from 100° C. to 130° C. so that the gas phase reactant is transported through a channel formed in the hollow stirring shaft into the liquid phase reactant for carrying out a reaction; obtaining a product that contains nonylcyclohexanol. A conversion rate of the nonylcyclohexanol is higher than or equal to 99.0%.