C07C29/94

A METHOD OF PURIFYING RAW METHANOL
20230265031 · 2023-08-24 ·

A method of purifying raw methanol obtained in chemical pulping, wherein heavy oil is admixed with the raw methanol to prevent precipitation, and the methanol mixture is distilled or evaporated to recover the methanol. The heavy oil is formed by mixing and heating raw methanol obtained from a side stream of chemical hardwood pulping with an acidic aqueous solution to vaporize low boiling point sulfurous compounds and provide acidified raw methanol. The acidified raw methanol is separated into a liquid top phase, a liquid aqueous middle phase, and a liquid bottom phase. The liquid bottom phase is extracted to obtain the heavy oil.

A METHOD OF PURIFYING RAW METHANOL
20230265031 · 2023-08-24 ·

A method of purifying raw methanol obtained in chemical pulping, wherein heavy oil is admixed with the raw methanol to prevent precipitation, and the methanol mixture is distilled or evaporated to recover the methanol. The heavy oil is formed by mixing and heating raw methanol obtained from a side stream of chemical hardwood pulping with an acidic aqueous solution to vaporize low boiling point sulfurous compounds and provide acidified raw methanol. The acidified raw methanol is separated into a liquid top phase, a liquid aqueous middle phase, and a liquid bottom phase. The liquid bottom phase is extracted to obtain the heavy oil.

A METHOD OF PURIFYING RAW METHANOL
20230265031 · 2023-08-24 ·

A method of purifying raw methanol obtained in chemical pulping, wherein heavy oil is admixed with the raw methanol to prevent precipitation, and the methanol mixture is distilled or evaporated to recover the methanol. The heavy oil is formed by mixing and heating raw methanol obtained from a side stream of chemical hardwood pulping with an acidic aqueous solution to vaporize low boiling point sulfurous compounds and provide acidified raw methanol. The acidified raw methanol is separated into a liquid top phase, a liquid aqueous middle phase, and a liquid bottom phase. The liquid bottom phase is extracted to obtain the heavy oil.

ACTIVATION OF ALKYL SUBSTRATES IN CONDENSED PHASE WITH OZONE
20230339830 · 2023-10-26 ·

A process for oxidizing an alkyl substrate may comprise combining an alkyl substrate (e.g., propane, n-butane) and ozone in a liquid phase medium comprising a branched alkane activator (e.g., isobutane) and a protic additive (e.g., water) under conditions sufficient to oxidize the alkyl substrate to products. The alkyl substrate may be selected from linear and cyclic alkanes.

ACTIVATION OF ALKYL SUBSTRATES IN CONDENSED PHASE WITH OZONE
20230339830 · 2023-10-26 ·

A process for oxidizing an alkyl substrate may comprise combining an alkyl substrate (e.g., propane, n-butane) and ozone in a liquid phase medium comprising a branched alkane activator (e.g., isobutane) and a protic additive (e.g., water) under conditions sufficient to oxidize the alkyl substrate to products. The alkyl substrate may be selected from linear and cyclic alkanes.

METHOD OF STORING AND/OR TRANSPORTING OXO ALCOHOL

A method of storing and/or transporting oxo alcohol, comprises: combining an oxo alcohol having an initial aldehyde content X and an initial peroxide content Y with 5 ppm to 100 ppm of a phenolic antioxidant, preferably a phenolic antioxidant without ester linkage groups; and storing and/or transporting the oxo alcohol. The oxo alcohol can be used to produce a plasticizer, e.g., without adversely affecting color.

METHOD OF STORING AND/OR TRANSPORTING OXO ALCOHOL

A method of storing and/or transporting oxo alcohol, comprises: combining an oxo alcohol having an initial aldehyde content X and an initial peroxide content Y with 5 ppm to 100 ppm of a phenolic antioxidant, preferably a phenolic antioxidant without ester linkage groups; and storing and/or transporting the oxo alcohol. The oxo alcohol can be used to produce a plasticizer, e.g., without adversely affecting color.

METHOD OF STORING AND/OR TRANSPORTING OXO ALCOHOL

A method of storing and/or transporting oxo alcohol, comprises: combining an oxo alcohol having an initial aldehyde content X and an initial peroxide content Y with 5 ppm to 100 ppm of a phenolic antioxidant, preferably a phenolic antioxidant without ester linkage groups; and storing and/or transporting the oxo alcohol. The oxo alcohol can be used to produce a plasticizer, e.g., without adversely affecting color.

Mixture for Use as a Liquid Sorption Agent in Methanol Synthesis and Methanol Synthesis Process Using Said Mixture

Some embodiments include a mixture for use as liquid sorbent for methanol or methanol and water in methanol synthesis using carbon monoxide and hydrogen, carbon dioxide and hydrogen or a mixture of hydrogen, carbon monoxide and carbon dioxide as synthesis reactants. The mixture comprises I) a component A) in the form of at least one salt and at least one component B) selected from the group consisting of: B1) a salt of an anion and one, two, or three of the cations of salt A), wherein the number of cations corresponds to an absolute value of a charge number of the respective anion; B2) a salt comprising one or more bis(trifluoromethylsulfonyl)imide anions and another component, wherein a number of bis(trifluoromethylsulfonyl)imide anions corresponds to an absolute value of a charge number of the respective metal cation; and B3) a zwitterionic compound.

Mixture for Use as a Liquid Sorption Agent in Methanol Synthesis and Methanol Synthesis Process Using Said Mixture

Some embodiments include a mixture for use as liquid sorbent for methanol or methanol and water in methanol synthesis using carbon monoxide and hydrogen, carbon dioxide and hydrogen or a mixture of hydrogen, carbon monoxide and carbon dioxide as synthesis reactants. The mixture comprises I) a component A) in the form of at least one salt and at least one component B) selected from the group consisting of: B1) a salt of an anion and one, two, or three of the cations of salt A), wherein the number of cations corresponds to an absolute value of a charge number of the respective anion; B2) a salt comprising one or more bis(trifluoromethylsulfonyl)imide anions and another component, wherein a number of bis(trifluoromethylsulfonyl)imide anions corresponds to an absolute value of a charge number of the respective metal cation; and B3) a zwitterionic compound.