The invention provides a process for the separation of MEG and 1,2-BDO from a first mixture comprising MEG and 1,2-BDO in a first solvent by the steps of: (i) combining said first mixture with a second solvent stream comprising a second solvent in a first extraction column; (ii) recovering (a) a second mixture of MEG and 1,2-BDO in the second solvent, wherein the molar ratio of MEG:1,2-BDO is lower in the second mixture than in the first mixture; and (b) a solution comprising MEG in the first solvent; (iii) combining said second mixture with a first washing stream, said first washing stream also comprising the first solvent in a second extraction column; (iv) recovering (c) a first extract stream comprising the second solvent and 1,2-BDO and (d) a third mixture comprising MEG and, optionally, 1,2-BDO in the first solvent.

The invention provides a process for the separation of MEG and 1,2-BDO from a first mixture comprising MEG and 1,2-BDO in a first solvent by the steps of: (i) combining said first mixture with a second solvent stream comprising a second solvent in a first extraction column; (ii) recovering (a) a second mixture of MEG and 1,2-BDO in the second solvent, wherein the molar ratio of MEG:1,2-BDO is lower in the second mixture than in the first mixture; and (b) a solution comprising MEG in the first solvent; (iii) combining said second mixture with a first washing stream, said first washing stream also comprising the first solvent in a second extraction column; (iv) recovering (c) a first extract stream comprising the second solvent and 1,2-BDO and (d) a third mixture comprising MEG and, optionally, 1,2-BDO in the first solvent.

The invention provides a process for the separation of MEG and 1,2-BDO from a first mixture comprising MEG and 1,2-BDO in a first solvent by the steps of: (i) combining said first mixture with a second solvent stream comprising a second solvent in a first extraction column; (ii) recovering (a) a second mixture of MEG and 1,2-BDO in the second solvent, wherein the molar ratio of MEG:1,2-BDO is lower in the second mixture than in the first mixture; and (b) a solution comprising MEG in the first solvent; (iii) combining said second mixture with a first washing stream, said first washing stream also comprising the first solvent in a second extraction column; (iv) recovering (c) a first extract stream comprising the second solvent and 1,2-BDO and (d) a third mixture comprising MEG and, optionally, 1,2-BDO in the first solvent.

The present invention relates to synthetic membranes and use of these synthetic membranes for isolation of volatile organic compounds and purification of water. The synthetic membrane includes a hydrophobic polymer layer located on a polymeric membrane support layer. The invention includes a method of isolating volatile organic compounds with the synthetic membrane by contacting a volatile organic mixture with the hydrophobic polymer layer of the synthetic membrane and removing volatile organic compounds from the polymeric membrane support layer of the synthetic membrane by a process of pervaporation. The invention also includes a method of purifying water with the synthetic membrane by contacting an ionic solution with the hydrophobic polymer layer of the synthetic membrane and removing water from the polymeric membrane support layer of the synthetic membrane by a process of reverse osmosis. The invention also relates to methods of isolating non-polar gases by gas fractionation.

The present invention relates to synthetic membranes and use of these synthetic membranes for isolation of volatile organic compounds and purification of water. The synthetic membrane includes a hydrophobic polymer layer located on a polymeric membrane support layer. The invention includes a method of isolating volatile organic compounds with the synthetic membrane by contacting a volatile organic mixture with the hydrophobic polymer layer of the synthetic membrane and removing volatile organic compounds from the polymeric membrane support layer of the synthetic membrane by a process of pervaporation. The invention also includes a method of purifying water with the synthetic membrane by contacting an ionic solution with the hydrophobic polymer layer of the synthetic membrane and removing water from the polymeric membrane support layer of the synthetic membrane by a process of reverse osmosis. The invention also relates to methods of isolating non-polar gases by gas fractionation.

A method of recovering an alcohol from an aqueous stream comprising: providing an aqueous stream comprising an alcohol; extracting at least a portion of the alcohol from the aqueous stream with a solvent to form an extracted solvent stream; extracting at least a portion of the solvent from the extracted solvent stream to form an extracted aqueous stream; and recovering at least a portion of the alcohol from the extracted aqueous stream.

A method of recovering an alcohol from an aqueous stream comprising: providing an aqueous stream comprising an alcohol; extracting at least a portion of the alcohol from the aqueous stream with a solvent to form an extracted solvent stream; extracting at least a portion of the solvent from the extracted solvent stream to form an extracted aqueous stream; and recovering at least a portion of the alcohol from the extracted aqueous stream.

A method of recovering an alcohol from an aqueous stream comprising: providing an aqueous stream comprising an alcohol; extracting at least a portion of the alcohol from the aqueous stream with a solvent to form an extracted solvent stream; extracting at least a portion of the solvent from the extracted solvent stream to form an extracted aqueous stream; and recovering at least a portion of the alcohol from the extracted aqueous stream.

A process can be used to prepare alkenes by catalytic conversion of synthesis gas to a first mixture comprising alkenes and alcohols. The alcohols present in the first mixture are converted to the corresponding alkenes by dehydration in a subsequent step. At least one alkene having two to four carbon atoms is obtained as isolated product from a product mixture by processing thereof and/or separation steps. In the catalytic conversion, a catalyst is preferably used that comprises grains of non-graphitic carbon having cobalt nanoparticles dispersed therein. The cobalt nanoparticles have an average diameter d.sub.p of 1-20 nm. An average distance D between individual cobalt nanoparticles in the grains is 2-150 nm. A combined total mass fraction ω of metal in the grains is from 30%-70% by weight of a total mass of the grains such that 4.5 dp/ω>D≥0.25 dp/ω.

A process can be used to prepare alkenes by catalytic conversion of synthesis gas to a first mixture comprising alkenes and alcohols. The alcohols present in the first mixture are converted to the corresponding alkenes by dehydration in a subsequent step. At least one alkene having two to four carbon atoms is obtained as isolated product from a product mixture by processing thereof and/or separation steps. In the catalytic conversion, a catalyst is preferably used that comprises grains of non-graphitic carbon having cobalt nanoparticles dispersed therein. The cobalt nanoparticles have an average diameter d.sub.p of 1-20 nm. An average distance D between individual cobalt nanoparticles in the grains is 2-150 nm. A combined total mass fraction ω of metal in the grains is from 30%-70% by weight of a total mass of the grains such that 4.5 dp/ω>D≥0.25 dp/ω.