A process for producing acetic acid includes: (a) reacting, via a catalytic partial oxidation (CPO) reaction, a CPO reactant mixture in a CPO reactor to produce a hydrogen-lean syngas; wherein the hydrocarbons include equal to or greater than about 3 mol % C2+ alkanes; wherein the hydrogen-lean syngas includes hydrogen, carbon monoxide, carbon dioxide, and unreacted hydrocarbons; and wherein the hydrogen-lean syngas is characterized by a hydrogen to carbon monoxide (H2/CO) molar ratio of from about 0.7 to about 1.3. Also included is (b) feeding at least a portion of the hydrogen-lean syngas and dimethyl ether (DME) to a DME carbonylation unit to produce methyl acetate and a hydrogen-enriched syngas characterized by a H2/CO molar ratio of from about 1.8 to about 2.2; and (c) feeding at least a portion of the methyl acetate and water to a methyl acetate hydrolysis reaction zone to produce acetic acid and a methanol stream.

A process for producing acetic acid includes: (a) reacting, via a catalytic partial oxidation (CPO) reaction, a CPO reactant mixture in a CPO reactor to produce a hydrogen-lean syngas; wherein the hydrocarbons include equal to or greater than about 3 mol % C2+ alkanes; wherein the hydrogen-lean syngas includes hydrogen, carbon monoxide, carbon dioxide, and unreacted hydrocarbons; and wherein the hydrogen-lean syngas is characterized by a hydrogen to carbon monoxide (H2/CO) molar ratio of from about 0.7 to about 1.3. Also included is (b) feeding at least a portion of the hydrogen-lean syngas and dimethyl ether (DME) to a DME carbonylation unit to produce methyl acetate and a hydrogen-enriched syngas characterized by a H2/CO molar ratio of from about 1.8 to about 2.2; and (c) feeding at least a portion of the methyl acetate and water to a methyl acetate hydrolysis reaction zone to produce acetic acid and a methanol stream.

A process for producing acetic acid includes: (a) reacting, via a catalytic partial oxidation (CPO) reaction, a CPO reactant mixture in a CPO reactor to produce a hydrogen-lean syngas; wherein the hydrocarbons include equal to or greater than about 3 mol % C2+ alkanes; wherein the hydrogen-lean syngas includes hydrogen, carbon monoxide, carbon dioxide, and unreacted hydrocarbons; and wherein the hydrogen-lean syngas is characterized by a hydrogen to carbon monoxide (H2/CO) molar ratio of from about 0.7 to about 1.3. Also included is (b) feeding at least a portion of the hydrogen-lean syngas and dimethyl ether (DME) to a DME carbonylation unit to produce methyl acetate and a hydrogen-enriched syngas characterized by a H2/CO molar ratio of from about 1.8 to about 2.2; and (c) feeding at least a portion of the methyl acetate and water to a methyl acetate hydrolysis reaction zone to produce acetic acid and a methanol stream.

A process for preparing methyl methacrylate by direct oxidative esterification of methacrolein has elevated yields compared to known processes. Methyl methacrylate (MMA) is used in large amounts for preparing polymers and copolymers with other polymerizable compounds. In addition, methyl methacrylate is an important synthesis unit for a variety of specialty esters based on methacrylic acid (MAA), which can be produced by transesterification with the appropriate alcohol. There is consequently a great interest in very simple, economic, and environmentally friendly processes for preparing methyl methacrylate. A superior workup of the reactor output from the oxidative esterification of methacrolein allows specific by-products to be isolated and then additionally converted to alkyl methacrylates, especially to MMA.

A process for preparing methyl methacrylate by direct oxidative esterification of methacrolein has elevated yields compared to known processes. Methyl methacrylate (MMA) is used in large amounts for preparing polymers and copolymers with other polymerizable compounds. In addition, methyl methacrylate is an important synthesis unit for a variety of specialty esters based on methacrylic acid (MAA), which can be produced by transesterification with the appropriate alcohol. There is consequently a great interest in very simple, economic, and environmentally friendly processes for preparing methyl methacrylate. A superior workup of the reactor output from the oxidative esterification of methacrolein allows specific by-products to be isolated and then additionally converted to alkyl methacrylates, especially to MMA.

A process for preparing methyl methacrylate by direct oxidative esterification of methacrolein has elevated yields compared to known processes. Methyl methacrylate (MMA) is used in large amounts for preparing polymers and copolymers with other polymerizable compounds. In addition, methyl methacrylate is an important synthesis unit for a variety of specialty esters based on methacrylic acid (MAA), which can be produced by transesterification with the appropriate alcohol. There is consequently a great interest in very simple, economic, and environmentally friendly processes for preparing methyl methacrylate. A superior workup of the reactor output from the oxidative esterification of methacrolein allows specific by-products to be isolated and then additionally converted to alkyl methacrylates, especially to MMA.

The present disclosure relates to a method for preparing an esterified alkane. The method includes mixing a gaseous alkane with oxygen or air to obtain a mixed gas; adding a chlorine-containing catalyst and/or a nitrogen-containing catalyst to a light-transmission reaction vessel; then adding the mixed gas, an acid and a solvent in sequence to carry out a reaction under ambient pressure and an illumination condition; and then conducting analysis to obtain an NMR yield, followed by extraction, drying, filtration, distillation under reduced pressure and separation by column chromatography to obtain an esterified alkane. The present disclosure has the advantages that the reaction can be carried out under the conditions of ambient temperature and pressure with a cheap and safe chlorine-containing compound and a nitrogen-containing compound as a catalyst and air as an oxidant, and the method has energy-saving and economic effects, convenient and safe operation and environmental friendliness.

The present disclosure relates to a method for preparing an esterified alkane. The method includes mixing a gaseous alkane with oxygen or air to obtain a mixed gas; adding a chlorine-containing catalyst and/or a nitrogen-containing catalyst to a light-transmission reaction vessel; then adding the mixed gas, an acid and a solvent in sequence to carry out a reaction under ambient pressure and an illumination condition; and then conducting analysis to obtain an NMR yield, followed by extraction, drying, filtration, distillation under reduced pressure and separation by column chromatography to obtain an esterified alkane. The present disclosure has the advantages that the reaction can be carried out under the conditions of ambient temperature and pressure with a cheap and safe chlorine-containing compound and a nitrogen-containing compound as a catalyst and air as an oxidant, and the method has energy-saving and economic effects, convenient and safe operation and environmental friendliness.

Methacrylic acid or alkyl methacrylate are produced starting from acrolein, which is available from glycerol or propane.

Methacrylic acid or alkyl methacrylate are produced starting from acrolein, which is available from glycerol or propane.