Methods for purification of a fluorocarbon or hydrofluorocarbon containing at least one undesired halocarbon impurities comprise flowing the fluorocarbon or hydrofluorocarbon through at least one adsorbent beds to selectively adsorb the at least one undesired halocarbon impurities through physical adsorption and/or chemical adsorption, wherein the at least one adsorbent beds contain a metal oxide supported on an adsorbent in an inert atmosphere.

Disclosed is a method of purifying a stream of crude hydrochlorofluoroolefin refrigerant produced by the reaction of 1,1,3,3 tetrachloropropene (R1230za) or 1,1,1,3,3-pentachloropropane (R240fa) with HF. The process includes a step of removing the cis-(Z) isomer by distillation of the crude refrigerant stream prior to a step of reacting the crude refrigerant stream with a base. The reaction with the base is a necessary step in production of the refrigerant and is done to remove HF and residual HCl from the crude refrigerant stream. Removal of the cis-(Z) isomer before the reaction with the base reduces the amount of toxic flammable trifluoropropyne (TFP) that is produced as a side-reaction during the reaction with the base. In addition, temperature control during the reaction with the base is less critical to minimizing the TFP production if the cis-(Z) isomer is first removed.

Heterogeneous azeotrope or azeotrope-like compositions comprising trifluoroiodomethane (CF.sub.3I) and water which may include from about 47.7 wt. % to about 99.0 wt. % trifluoroiodomethane (CF.sub.3I) and from about 1.0 wt. % to about 52.3 wt. % water and having a boiling point between about 18.0° C. and about 19.0° C. at a pressure of between about 58.0 psia and about 60.0 psia. The azeotrope or azeotrope-like compositions may be used to separate impurities from trifluoroiodomethane (CF.sub.3I).

Heterogeneous azeotrope or azeotrope-like compositions comprising trifluoroiodomethane (CF.sub.3I) and water which may include from about 47.7 wt. % to about 99.0 wt. % trifluoroiodomethane (CF.sub.3I) and from about 1.0 wt. % to about 52.3 wt. % water and having a boiling point between about 18.0° C. and about 19.0° C. at a pressure of between about 58.0 psia and about 60.0 psia. The azeotrope or azeotrope-like compositions may be used to separate impurities from trifluoroiodomethane (CF.sub.3I).

Impurities such as sulfur dioxide (SO.sub.2) are removed from trifluoroacetyl chloride (TFAC) through distillation, adsorption, or a combination thereof, and/or including the formation of an azeotrope or azeotrope-like composition including effective amounts of sulfur dioxide (SO.sub.2) and trifluoroacetyl chloride (TFAC). The trifluoroacetyl chloride (TFAC) thus purified may then be used in the manufacture of trifluoroiodomethane (CF.sub.3I). Also disclosed are azeotropes and azeotrope like compositions of sulfur dioxide (SO.sub.2) and trifluoroacetyl chloride (TFAC).

Impurities such as sulfur dioxide (SO.sub.2) are removed from trifluoroacetyl chloride (TFAC) through distillation, adsorption, or a combination thereof, and/or including the formation of an azeotrope or azeotrope-like composition including effective amounts of sulfur dioxide (SO.sub.2) and trifluoroacetyl chloride (TFAC). The trifluoroacetyl chloride (TFAC) thus purified may then be used in the manufacture of trifluoroiodomethane (CF.sub.3I). Also disclosed are azeotropes and azeotrope like compositions of sulfur dioxide (SO.sub.2) and trifluoroacetyl chloride (TFAC).

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.

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.

The present invention relates to the production of light (meth)acrylic esters by direct esterification of acrylic acid by methanol or ethanol. The invention more particularly relates to a process for the recovery/purification of C1-C2 alkyl acrylate comprising the azeotropic distillation of the crude reaction mixture using a distillation column comprising a sidestream drawing off of a fraction rich in alkyl alkoxypropionate byproduct, the boiling point of which is close to that of acrylic acid, and therefore problematic in the purification process.

A method for producing a terpene-enhanced cannabinoid concentrate and for removing contaminants such as pesticides and fungicides from cannabinoid extracts. Cannabinoid extracts containing contaminants may be dissolved in a water and ethanol solution, and then cooled to allow water-soluble contaminants to settle out of the mixture. The water and ethanol may then be removed via evaporation or distillation, leaving purified cannabinoids without contaminants. Contaminant removal may be incorporated into a method for producing a blended extract of cannabinoids and terpenes, which extracts terpenes using supercritical CO2, and extracts a cannabinoid concentrate from the residual material using a cold ethanol flush followed by distillation and then by contaminant removal; the CO2-extracted terpenes are then added back to the purified cannabinoid concentrate in a final blending step. Blending terpenes at the end of extraction may enhance the flavor and effectiveness of the purified cannabinoid concentrate.