Abstract:
To address the problem of insufficient biodegradability of perfluorinated surfactants, the present invention provides biodegradable fluorosurfactants derived from olefins having —CHR, —CHRf, —CHF, and/or —CH2 groups, where R is an alkyl group and Rf is a perfluoro or fluroroalkyl group. Preferably, the —CHR, —CHRf, —CHF, and/or —CH2 groups are contained within partially fluorinated alkenes.
Abstract:
To address the problem of insufficient biodegradability of perfluorinated surfactants, the present invention provides biodegradable fluorosurfactants derived from olefins having —CHR, —CHRf, —CHF, and/or —CH2 groups, where R is an alkyl group and Rf is a perfluoro or fluroroalkyl group. Preferably, the —CHR, —CHRf, —CHF, and/or —CH2 groups are contained within partially fluorinated alkenes.
Abstract:
Aspects of the present invention are directed to working fluids and their use in processes wherein the working fluids comprise compounds having the structure of formula (I): wherein R1, R2, R3, and R4 are each independently selected from the group consisting of: H, F, Cl, Br, and C1-C6 alkyl, at least C6 aryl, at least C3 cycloalkyl, and C6-C15 alkylaryl optionally substituted with at least one F, Cl, or Br, wherein formula (I) contains at least one F and at least one Cl or Br, provided that if any R is Br, then the compound does not have hydrogen. The working fluids are useful in Rankine cycle systems for efficiently converting waste heat generated from industrial processes, such as electric power generation from fuel cells, into mechanical energy or further to electric power. The working fluids of the invention are also useful in equipment employing other thermal energy conversion processes and cycles.
Abstract:
The present invention describes a process for making CF3CH═CHF (HFO-1234ze). The process involves the addition of carbon tetrachloride (CCl4) to 1,2-dichloroethylene to form CCl3CHClCHCl2. The compound CCl3CHClCHCl2 thus can then either be treated with HF to produce CF3CHClCHClF as the main product, or it can be converted to CCl2═CHCHCl2 (1230za) by dechlorination. CCl2═CHCHCl2 can be treated with HF such that the main product obtained is CF3CHClCHClF. CF3CH═CHCl may be produced as a by-product, but upon treatment with HF, it affords the compound CF3CHClCHClF. The desired compound, CF3CH═CHF (HFO-1234ze), is obtained as a trans/cis mixture by dehydrochlorination of CF3CH2CHClF or by dechlorination of CF3CHClCHClF.
Abstract:
A process for producing phosphorus pentafluoride by the reaction of elemental phosphorus and elemental fluorine gas, comprising supplying to the reaction non-stoichiometric amounts of elemental phosphorus and elemental fluorine gas.
Abstract:
The present disclosure provides a method of removing iodine (I2) and iodine-containing species from processes for producing trifluoroiodomethane (CF3I). The present disclosure further provides another method of removing iodine and iodine-containing species from trifluoroacetyl iodide (TFAI).
Abstract:
The present disclosure provides a process for producing trifluoroiodomethane, the process comprising providing a reactant stream comprising hydrogen iodide and at least one trifluoroacetyl halide selected from the group consisting of trifluoroacetyl chloride, trifluoroacetyl fluoride, trifluoroacetyl bromide, and combinations thereof, reacting the reactant stream in the presence of a first catalyst at a first reaction temperature from about 25° C. to about 400° C. to produce an intermediate product stream comprising trifluoroacetyl iodide, and reacting the intermediate product stream in the presence of a second catalyst at a second reaction temperature from about 200° C. to about 600° C. to produce a final product stream comprising the trifluoroiodomethane.
Abstract:
The present disclosure provides azeotrope or azeotrope-like compositions including trifluoroiodomethane (CF3I) and trifluoroacetyl chloride (CF3COCl), and a method of forming an azeotrope or azeotrope-like composition comprising the step of combining trifluoroacetyl chloride (CF3COCl) and trifluoroiodomethane (CF3I) to form an azeotrope or azeotrope-like composition.
Abstract:
The present disclosure provides a process for producing trifluoroiodomethane, the process comprising providing a reactant stream comprising hydrogen iodide and at least one trifluoroacetyl halide selected from the group consisting of trifluoroacetyl chloride, trifluoroacetyl fluoride, trifluoroacetyl bromide, and combinations thereof, reacting the reactant stream in the presence of a first catalyst at a first reaction temperature from about 25° C. to about 400° C. to produce an intermediate product stream comprising trifluoroacetyl iodide, and reacting the intermediate product stream in the presence of a second catalyst at a second reaction temperature from about 200° C. to about 600° C. to produce a final product stream comprising the trifluoroiodomethane.
Abstract:
Compositions and methods comprising one or more compounds according to Formula I: where R1, R2 and R3 are each independently CxR′(2x+1)−yHy; each R′ is independently selected from F or Cl and wherein the value of (2x+1)−y is the total number of R′ substituents on the indicated carbon atom(s); each x is independently equal to or greater than 1 and equal to or less than 6; and y is equal to or greater than 0 and less than or equal to 2x+1, provided that the total number of R′ present in the compound is 6 or greater, and that the compound has from zero up to two (2) Cl substituents.