Patent classifications
C07C45/83
Methods for separation of azeotrope or azeotrope-like compositions of trifluoroiodomethane (CF.SUB.3.I) and trifluoroacetyl chloride (CF.SUB.3.COCI)
The present disclosure provides azeotrope or azeotrope-like compositions including trifluoroiodomethane (CF.sub.3I) and trifluoroacetyl chloride (CF.sub.3COCl), methods of forming same, and methods of separating, or breaking, the azeotrope or azeotrope-like compositions of trifluoroiodomethane (CF.sub.3I) and trifluoroacetyl chloride (CF.sub.3COCl).
Methods for separation of azeotrope or azeotrope-like compositions of trifluoroiodomethane (CF.SUB.3.I) and trifluoroacetyl chloride (CF.SUB.3.COCI)
The present disclosure provides azeotrope or azeotrope-like compositions including trifluoroiodomethane (CF.sub.3I) and trifluoroacetyl chloride (CF.sub.3COCl), methods of forming same, and methods of separating, or breaking, the azeotrope or azeotrope-like compositions of trifluoroiodomethane (CF.sub.3I) and trifluoroacetyl chloride (CF.sub.3COCl).
PROCESS FOR PRODUCING METHACRYLIC ACID OR METHACRYLIC ACID ESTERS
Methacrylic acid or alkyl methacrylate are produced starting from acrolein, which is available from glycerol or propane.
PROCESS FOR PRODUCING METHACRYLIC ACID OR METHACRYLIC ACID ESTERS
Methacrylic acid or alkyl methacrylate are produced starting from acrolein, which is available from glycerol or propane.
Method for selectively separating impurities present in a hydro-alcoholic cut by recycling through a liquid-liquid extraction column
Liquid-liquid extraction and distillation of a liquid feedstock of at least ethanol, water, acetaldehyde and at least one hydrocarbon-based impurity with a boiling point of between 20° C. and 100° C. at atmospheric pressure, or which generates, with at least one of the compounds of the liquid feedstock and/or with the organic extraction solvent and/or with the aqueous back-washing solvent, an azeotrope and a partition coefficient of between 0.1 and 5 at any point in a back-washing (BW) column of the extraction section, by (a) a liquid-liquid extraction step a washing (W) column, a back-washing (BW) column and at least one injection (F2) of a cut withdrawn in step b), located in the top half of the back-washing column, (b) distillation of an aldehyde and ethanol separation producing at least one aldehyde-rich effluent, one ethanol-rich effluent and one water-rich effluent.
Method for selectively separating impurities present in a hydro-alcoholic cut by recycling through a liquid-liquid extraction column
Liquid-liquid extraction and distillation of a liquid feedstock of at least ethanol, water, acetaldehyde and at least one hydrocarbon-based impurity with a boiling point of between 20° C. and 100° C. at atmospheric pressure, or which generates, with at least one of the compounds of the liquid feedstock and/or with the organic extraction solvent and/or with the aqueous back-washing solvent, an azeotrope and a partition coefficient of between 0.1 and 5 at any point in a back-washing (BW) column of the extraction section, by (a) a liquid-liquid extraction step a washing (W) column, a back-washing (BW) column and at least one injection (F2) of a cut withdrawn in step b), located in the top half of the back-washing column, (b) distillation of an aldehyde and ethanol separation producing at least one aldehyde-rich effluent, one ethanol-rich effluent and one water-rich effluent.
Method for selectively separating impurities present in a hydro-alcoholic cut by recycling through a liquid-liquid extraction column
Liquid-liquid extraction and distillation of a liquid feedstock of at least ethanol, water, acetaldehyde and at least one hydrocarbon-based impurity with a boiling point of between 20° C. and 100° C. at atmospheric pressure, or which generates, with at least one of the compounds of the liquid feedstock and/or with the organic extraction solvent and/or with the aqueous back-washing solvent, an azeotrope and a partition coefficient of between 0.1 and 5 at any point in a back-washing (BW) column of the extraction section, by (a) a liquid-liquid extraction step a washing (W) column, a back-washing (BW) column and at least one injection (F2) of a cut withdrawn in step b), located in the top half of the back-washing column, (b) distillation of an aldehyde and ethanol separation producing at least one aldehyde-rich effluent, one ethanol-rich effluent and one water-rich effluent.
Process for preparing C.SUB.5 .aldehydes
A process for preparing C.sub.5 aldehydes involves hydroformylation of butenes with synthesis gas in the presence of a homogeneous catalyst system and a solvent. It is a feature of the process that the aldehyde concentration in the reaction mixture is limited.
Process for preparing C.SUB.5 .aldehydes
A process for preparing C.sub.5 aldehydes involves hydroformylation of butenes with synthesis gas in the presence of a homogeneous catalyst system and a solvent. It is a feature of the process that the aldehyde concentration in the reaction mixture is limited.
Process for the separation of formaldehyde from crude acrylic acid
A process for purification of a crude product stream recovered from the production of acrylic acid by an aldolisation reaction is disclosed. The product stream comprises acrylic acid, formaldehyde, water, non-condensable vapours and optionally heavy by-products. The process comprises: providing the crude product stream in the vapour phase to a first separation column operated at a temperature and pressure to form an intermediate overhead stream comprising water, formaldehyde and methanol; and passing said intermediate overhead stream to a formaldehyde separation column operated at a temperature and pressure to enable a stream having a higher formaldehyde concentration than the formaldehyde concentration in the intermediate overhead stream to be formed and recovered from at or near the bottom of the formaldehyde separation column as a formaldehyde enriched stream.