Patent classifications
C07C31/36
Electrochemical, chlorination, and oxychlorination systems and methods to form propylene oxide or ethylene oxide
Disclosed herein are methods and systems that relate to various configurations of electrochemical oxidation, chlorine oxidation, oxychlorination, chlorination, and epoxidation reactions to form propylene oxide or ethylene oxide.
Electrochemical, chlorination, and oxychlorination systems and methods to form propylene oxide or ethylene oxide
Disclosed herein are methods and systems that relate to various configurations of electrochemical oxidation, chlorine oxidation, oxychlorination, chlorination, and epoxidation reactions to form propylene oxide or ethylene oxide.
Methods and systems to form propylene chlorohydrin from dichloropropane using Lewis acid
There are provided methods and systems to form propylene chlorohydrin by hydrolysis of dichloropropane in presence of Lewis acid and to further form propylene oxide from the propylene chlorohydrin.
Methods and systems to form propylene chlorohydrin from dichloropropane using Lewis acid
There are provided methods and systems to form propylene chlorohydrin by hydrolysis of dichloropropane in presence of Lewis acid and to further form propylene oxide from the propylene chlorohydrin.
METHOD FOR STABILIZING HIGH-PURITY ETHYLENE CARBONATE-CONTAINING COMPOSITION
To provide a novel stabilization method for suppressing over-time denaturation of a high-purity ethylene carbonate-containing composition, a stabilized high-purity ethylene carbonate-containing composition, and the like. A method for stabilizing a high-purity ethylene carbonate-containing composition includes adjustment of content of the total of formic acid and a formic acid salt, or 2-chloroethanol to 500 ppm by mass or less in the high-purity ethylene carbonate-containing composition including 90% by mass or more ethylene carbonate.
METHOD FOR STABILIZING HIGH-PURITY ETHYLENE CARBONATE-CONTAINING COMPOSITION
To provide a novel stabilization method for suppressing over-time denaturation of a high-purity ethylene carbonate-containing composition, a stabilized high-purity ethylene carbonate-containing composition, and the like. A method for stabilizing a high-purity ethylene carbonate-containing composition includes adjustment of content of the total of formic acid and a formic acid salt, or 2-chloroethanol to 500 ppm by mass or less in the high-purity ethylene carbonate-containing composition including 90% by mass or more ethylene carbonate.
METHODS AND SYSTEMS TO FORM PROPYLENE CHLOROHYDRIN FROM DICHLOROPROPANE USING LEWIS ACID
There are provided methods and systems to form propylene chlorohydrin by hydrolysis of dichloropropane in presence of Lewis acid and to further form propylene oxide from the propylene chlorohydrin.
METHODS AND SYSTEMS TO FORM PROPYLENE CHLOROHYDRIN FROM DICHLOROPROPANE USING LEWIS ACID
There are provided methods and systems to form propylene chlorohydrin by hydrolysis of dichloropropane in presence of Lewis acid and to further form propylene oxide from the propylene chlorohydrin.
Use of metal-accumulating plants for the preparation of catalysts that can be used in chemical reactions
A method of implementing organic synthesis reactions uses a composition containing a metal catalyst originating from a calcined plant. The plants can be from the Brassicaceae, Sapotaceae and Convolvulaceae family, and the metal catalyst contains metal in the M(II) form such as zinc, nickel, manganese, lead, cadmium, calcium, magnesium or copper. Examples of the organic synthesis reactions include halogenations, electrophilic reactions, cycloadditions, transesterification reactions and coupling reactions, among others.
Use of metal-accumulating plants for the preparation of catalysts that can be used in chemical reactions
A method of implementing organic synthesis reactions uses a composition containing a metal catalyst originating from a calcined plant. The plants can be from the Brassicaceae, Sapotaceae and Convolvulaceae family, and the metal catalyst contains metal in the M(II) form such as zinc, nickel, manganese, lead, cadmium, calcium, magnesium or copper. Examples of the organic synthesis reactions include halogenations, electrophilic reactions, cycloadditions, transesterification reactions and coupling reactions, among others.