Patent classifications
C07C17/386
Integrated process to produce 2,3,3,3-tetrafluoropropene
The invention relates to a separation process whereby 2-chloro-3,3,3-trifluoropropene (1233xf) is separated from a mixture containing other fluorinated organics and high boiling materials such as dimers using azeotropes of HF formed by adding appropriate amounts to the mixture which facilitate separation by, e.g. distillation.
Integrated process to produce 2,3,3,3-tetrafluoropropene
The invention relates to a separation process whereby 2-chloro-3,3,3-trifluoropropene (1233xf) is separated from a mixture containing other fluorinated organics and high boiling materials such as dimers using azeotropes of HF formed by adding appropriate amounts to the mixture which facilitate separation by, e.g. distillation.
Integrated process to produce 2,3,3,3-tetrafluoropropene
The invention relates to a separation process whereby 2-chloro-3,3,3-trifluoropropene (1233xf) is separated from a mixture containing other fluorinated organics and high boiling materials such as dimers using azeotropes of HF formed by adding appropriate amounts to the mixture which facilitate separation by, e.g. distillation.
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), and a method of forming an azeotrope or azeotrope-like composition comprising the step of combining trifluoroacetyl chloride (CF.sub.3COCl) and trifluoroiodomethane (CF.sub.3I) to form an azeotrope or azeotrope-like composition.
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), and a method of forming an azeotrope or azeotrope-like composition comprising the step of combining trifluoroacetyl chloride (CF.sub.3COCl) and trifluoroiodomethane (CF.sub.3I) to form an azeotrope or azeotrope-like composition.
METHODS FOR SEPARATION OF AZEOTROPE OR AZEOTROPE-LIKE COMPOSITIONS OF TRIFLUOROIODOMETHANE (CF3I) AND TRIFLUOROACETYL CHLORIDE (CF3COCI)
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 (CF3I) AND TRIFLUOROACETYL CHLORIDE (CF3COCI)
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).
Method for preparing 2-methylallyl chloride from 1,2-dichloroisobutane
The present invention relates to a method for preparing 2-methylallyl chloride from 1,2-dichloroisobutane. The method is characterized in that 1,2-dichloroisobutane and a sodium hydroxide aqueous solution are used as raw materials; reactive rectification is performed in a combined rectifying tower to eliminate hydrogen chloride so as to obtain 2-methylallyl chloride. A plate tower is provided at the lower part of the combined rectifying tower; a packing tower is provided at the upper part of the combined rectifying tower; an inner reflux condenser is provided at the top of the combined rectifying tower. The sodium hydroxide aqueous solution is added from a first plate of the plate tower; and 1,2-dichloroisobutane is added from the middle part of the plate tower. The method has the advantages that the raw material 1 and 1,2-dichloroisobutane is fully converted; the selectivity of the 2-methylallyl chloride is high.
Method for preparing 2-methylallyl chloride from 1,2-dichloroisobutane
The present invention relates to a method for preparing 2-methylallyl chloride from 1,2-dichloroisobutane. The method is characterized in that 1,2-dichloroisobutane and a sodium hydroxide aqueous solution are used as raw materials; reactive rectification is performed in a combined rectifying tower to eliminate hydrogen chloride so as to obtain 2-methylallyl chloride. A plate tower is provided at the lower part of the combined rectifying tower; a packing tower is provided at the upper part of the combined rectifying tower; an inner reflux condenser is provided at the top of the combined rectifying tower. The sodium hydroxide aqueous solution is added from a first plate of the plate tower; and 1,2-dichloroisobutane is added from the middle part of the plate tower. The method has the advantages that the raw material 1 and 1,2-dichloroisobutane is fully converted; the selectivity of the 2-methylallyl chloride is high.
Method for preparing 2-methylallyl chloride from 1,2-dichloroisobutane
The present invention relates to a method for preparing 2-methylallyl chloride from 1,2-dichloroisobutane. The method is characterized in that 1,2-dichloroisobutane and a sodium hydroxide aqueous solution are used as raw materials; reactive rectification is performed in a combined rectifying tower to eliminate hydrogen chloride so as to obtain 2-methylallyl chloride. A plate tower is provided at the lower part of the combined rectifying tower; a packing tower is provided at the upper part of the combined rectifying tower; an inner reflux condenser is provided at the top of the combined rectifying tower. The sodium hydroxide aqueous solution is added from a first plate of the plate tower; and 1,2-dichloroisobutane is added from the middle part of the plate tower. The method has the advantages that the raw material 1 and 1,2-dichloroisobutane is fully converted; the selectivity of the 2-methylallyl chloride is high.