CROSS-REFERENCE TO RELATED APPLICATION This application is a continuation-in-part of U.S. application Serial No. 07/418,832 filed October 10, 1989. BACKGROUND OF THE INVENTION

This invention relates to a process for the hydrogenolysis of halocarbons.

At this time there is a desire to produce halocarbons of reduced chlorine content. Hydrogenolysis is a known method for doing this. For example, see U.K. Patent 1,578,933 which discloses a process for the hydrogenolysis of CF3CFHCI to CF ₃ CH ₂ F using a hydrogenation catalyst, e.g., palladium supported on alumina or carbon. Hydrogenolysis of fluorochlorocarbons by passage through empty tubes made of various materials is also known, e.g., U.S. 2,615,926 discloses platinum tubes, U.S. 2,704,775 discloses nickel or stainless steel tubes and U.S. 3,042,727 discloses a Vycor® tube. It is desired to provide a process for converting a halocarbon to a more hydrogenated form with high selectivity and particularly to provide such a process wherein formation of solids and plugging of reaction vessels is minimized. SUMMARY OF THE INVENTION

We have discovered an improved hydrogenolysis process for reducing the chlorine and/or bromine content of halocarbons. The process may be used for producing saturated halocarbon products such that the yield loss to olefins, coupled by-products.

hydrocarbons or fragmented products is less than 10%. The process involves contacting a halocarbon of the formula: ^c n ^H m ^F ρ ^x q wherein X is Cl or Br, n is 1 to 10, m is 0 to 20, p is 0 to 21, q is 1 to 22, provided that m+p+q equals 2n+2 when the compound is acyclic and equals 2n when the compound is cyclic, and provided that when n is 1, q is at least 2, with at least 0.1 mole of hydrogen per mole of halocarbon at a temperature of 350° to 700°C, and a pressure of 0 to 1000 psig, in a reaction vessel (e.g., a tube) of aluminum, molybdenum, titanium, nickel, iron, cobalt, or their alloys, or of silicon carbide, optionally packed with aluminum, molybdenum, titanium, nickel, iron, cobalt or their alloys, or an inert material (e.g., silicon carbide) for a time sufficient to produce a product wherein at least one of X has been replaced by a hydrogen atom. Preferred alloys consist essentially of one or more metals selected from aluminum, molybdenum, titanium, nickel, iron and cobalt, optionally together with chromium and/or tungsten.

The process of the invention provides improved conversions and selectivity and has the further advantage that it does not produce olefins as the major product. Furthermore, the process minimizes the formation of solids in the reaction vessel, thus permitting long-term operation with less plugging. DESCRIPTION OF THE INVENTION An important aspect of the present invention is conducting the hydrogenolysis of halocarbons in the

presence of silicon carbide and/or at least one metal selected from aluminum, molybdenum, titanium, nickel, iron, cobalt or their alloys. The metals may be coated on the inside surface of a reaction vessel (e.g., by plating or sputtering the metals or their alloys onto the inside surface) . Such coating can help to minimize corrosion of the reaction vessel well. A reaction vessel of these materials (e.g., a metal tube) optionally packed with the metal in suitable form or an inert material such as silica, silicon carbide or low surface area carbon (e.g., shot coke) may also be used. When reference is made to alloys, it is meant a nickel alloy containing from 1 to 99.9% (by weight) nickel, a cobalt alloy containing 1 to 99.9% (by weight) cobalt, an iron alloy containing 0.2 to 99.9% (by weight) iron, a molybdenum alloy containing 70 to 99.9% (by weight) molybdenum, an aluminum alloy containing 80 to 99.9% (by weight) aluminum and a titanium alloy containing 72 to 99.8% (by weight) titanium. Preferably the remainder of these alloys is selected such that the alloy consists essentially of (i) one or more metals selected from aluminum, molybdenum, titanium, nickel, iron and cobalt, and optionally (ii) chromium and/or tungsten.

Most preferred for the practice of this invention are nickel or alloys of nickel such as those containing 52% to 80% nickel, e.g., Inconel® 600 nickel alloy or Hastelloy® C276 alloy.

When used for packing, the metal, alloys or inert material may be particles or formed shapes such as, for example, perforated plates, saddles, rings (e.g.. Pall® rings), wire, screen, chips, pipe, shot, gauze and wool. Although an empty reaction vessel

(e.g., an empty tube) may be used, the use of this type of packing material can provide the advantage of minimizing backmixing. These types of packing material can also serve as heat transfer materials. In many embodiments, perforated plates, saddles and rings can be especially useful.

The invention is applicable to the hydro- genolysis of halocarbons. The halocarbons can contain 1 to 10 carbon atoms, preferably 1 to 4 carbon atoms, most preferably 1 to 3 carbon atoms. The halocarbons include cyclic as well as acyclic compounds and can be generically represented by the empirical formula C _n H _m F _p Xq, where X is Cl and/or Br, preferably Cl, and n is an integer from 1 to 10, m is an integer from 0 to 20, p is an integer from 0 to 21, and q is an integer from 1 to 22, provided that m+p+q ■ 2n+2 when the compound is acyclic and equals 2n when the compound is cyclic. For single carbon compounds (i.e., n is 1) the invention is particularly applicable when q is at least 2.

In a preferred embodiment the halocarbons are represented by the above empirical formula where n * 1 to 4, m is 0 to 8, p is 0 to 9, and q is 1 to 9. Preferably, when n is 2 or more, p is at least 1.

The above halocarbons are either commercially available or can be prepared by known methods or adaptation of known methods. As previously indicated these starting materials when subjected to the process of the invention will result in products wherein one or more X (e.g., chlorine) has been replaced by hydrogen. Thus the products of the hydrogenolysis reactions of the C halocarbons will contain one or two hydrogen atoms, preferably one, and those from C ₂ compounds

from one to three hydrogen atoms, preferably one to two. The C ₃ halocarbons hydrogenolysis products will contain one to five hydrogen atoms with those containing one to four being preferred. In a similar manner the C ₄ to C^ _Q halocarbon products will contain one or more hydrogen atoms. The preferred process of this invention does not produce olefins as the major product. Instead, the major product of the conversion is a hydrogenolysis product wherein at least one X of the halocarbon starting material has been replaced by a hydrogen atom. This is particularly important for the hydrogenolysis of halocarbons where n is 2 to 10 (i.e., multicarbon halocarbons) _a where such factors as olefin production can be of concern at temperatures of 350°C or more. For example, CF CCI2F can be converted with high selectivity to a hydrogenolysis product consisting primarily of CF3CHCIF and CF ₃ CH F with very little olefin formulation. In a preferred embodiment of this invention using halocarbons containing fluorine and chlorine, at least 90% of the hydrogenolysis products contain the same number of fluorines as the original halocarbon. Furthermore the yield loss to olefins, coupled by-products, hydrocarbons, fragmentation products or carbon is less than 10%.

Examples of olefins are products such as CC1F»CCF ₂ or CF ₂ =CF the former of which can be obtained from hydrogenolysis of CC1 ₂ FCC1F2 and the latter from hydrogenolysis of CC1F ₂ CC1F2. An example of a coupled by-product is CF3CF-CFCF3 which can be obtained by the hydrogenolysis of CC1F ₂ CC1F ₂ • Examples of hydrocarbon products are CH , C ₂ H ₆ and C ₃ H ₈ which can be obtained by the hydrogenolysis of CC1 ₂ F ₂ , CC1 ₂ FCC1F ₂ and CF3CCIFCF3 respectively.

Examples of fragmentation products are CF ₃ H and CH ₂ F which can be obtained by the hydrogenolysis of CF ₃ CC1 ₂ F and its isomer.

The reaction temperature can range from 350°C to 700°C. Preferably the reaction temperature is at least about 400°C.

The amount of hydrogen contained in the gas stream contacted with the gaseous halocarbon should be at least 0.1 mole per mole of halocarbon. Hydrogen amounts ranging from 0.2 to 5 moles per mole of halocarbon are used for some embodiments. In general, the amount of hydrogen preferably ranges from 0.2 to 60 moles per mole of halocarbon and more preferably ranges from 0.4 to 40 moles per mole of halocarbon. The hydrogen can be fed either in the pure state or diluted with an inert gas, e.g., nitrogen, helium, or argon. The process pressure is operable over a broad range of pressures. Generally atmospheric (i.e., 0 psig) or superatmospheric pressures of up to 1000 psig are employed. Preferably the pressure is at least about 25 psig. The extent of the replacement of halogen by hydrogen increases with reaction time. Reaction times between 0.1 minutes and 25 minutes are preferred. Most preferred are reaction times between 0.2 and 8 minutes. An important feature of the process of the invention is that through selection of the appropriate metal and process conditions, a desired halocarbon hydrogenolysis product can be obtained as the major product with high selectivity and minimal formation of unwanted by-products. Preferably the reaction time and temperature are selected to obtain

long term (>1000 hours) plug free operation and to provide as the major product of the conversion hydrogenolysis product which retains the fluorine content of the starting halocarbon while at least one X is replaced by hydrogen. In many embodiments the reaction time and temperature are controlled so that at least about 90% of halocarbon converted has the same number of fluorine atoms as the halocarbon starting material. Also, in many embodiments the combined yield losses to olefins, coupled by-products, hydrocarbons, or fragmentation products is less than 10%. An additional desirable feature is that through a selection of an appropriate reaction vessel and packing (e.g., metals, alloys, or inert materials) and process conditions, the products of the hydrogenolysis can contain in high selectivity just one less chlorine or bromine than was present in the starting material. This is particularly useful when q is 2 or more, and it is desired to obtain a major product of the conversion, hydrogenolysis product which contains chlorine and/or bromine. For example, starting with a one-carbon compound containing two or more chlorine or bromine atoms, products containing just one less chlorine or bromine can be obtained in high selectivity.

Although substantial conversions can be achieved in a once-through system, recycle of unreacted halocarbons or intermediates can be employed in a conventional manner. The processes of this invention are considered to be characterized by relativity high activation energies when compared to catalytic hydrogenolysis over conventional Pd/C catalyst. For example, the activation energy for the

hydrogenolysis of CF ₃ CC1 ₂ F over a 0.5% Pd/C catalyst at 167°C to 200°C was found to be 14-17 Kcal/mole. The activation energy for the hydrogenolysis of CF3CHCIF over a 0.5% Pd/C catalyst at 249°C to 288°C was found to be 22-28 Kcal/mole. In contrast, the activation energies for the hydrogenolysis reactions of these compounds conducted in the reaction vessels of this invention, either empty or packed, were found to be considerably larger as exemplified in Table A.

TABLE A

Activation Energy Data

Hiσh Temperature Hydrogenolysis

Temp.

______ Range

F114 ₃ ¹ 450-550°C

F114, 440-600°C

F124 ^: 510-600°C

F114, 400-570°C

F114, 400-500°C

F124 510-570°C

F124 520-580°C

^114 ₃ « CF ₃ CC1 ₂ F F114 _χ ■ Du Pont commercial CC1F ₂ CC1F ₂ containing some CF ₃ CC1 ₂ F

³ F124 - CF CHClF

The products of the reaction can be separated and purified by conventional means. The products can be used as solvents, blowing agents, refrigerants and propellents.

Practice of the invention will become further apparent from the following non-limiting examples. In the following Examples the following general procedure was employed, unless otherwise indicated.

General Procedure - A flow reactor under microprocessor control was used. The reactor, unless otherwise indicated, was a 15" x 1/4" o.d. or 3/8" o.d. Inconel® 600 nickel alloy tube or a 15" x 3/8"

Hastelloy® C276 nickel alloy tube bent into a U shape and immersed in a heated fluidized sand bath for temperature control. Inconel® 600 is a commercial alloy containing 76% nickel, 15.5% chromium and 8% iron. Hastelloy® C-276 is a commercial alloy containing 59% nickel, 15.5% chromium, 16% molybdenum and 3.75% tungsten.

The reactor was used either empty or filled with various packing materials as described in the Examples. Hydrogen gas was metered into the system through mass flow controllers. Liquid halocarbons were fed from a syringe pump and vaporized before entering the reactor. Conversions and yields were measured by taking gas stream samples into a gas chromatograph. Product identification was by gc retention times with confirmation by gc-mass spectrometer analysis of samples.

EXAMPLE 1 CF ₃ CC1 ₂ F + H ₂ > CF3CHCIF + CF ₃ CH ₂ F 2,2-Dichloro-l,l,l,2-tetrafluoroethane

(1.47 g/hr) and hydrogen (molar ratio of H ₂ /CF ₃ CC1 ₂ F 1.9) were fed into the 1/4" empty Inconel® nickel alloy reactor for 38 hours at 450°-550°C and 250 psig. A sample taken after 14 hours at 550°C showed an 89% conversion of CF ₃ CC1 ₂ F with a 65% selectivity to CF3CHCIF and a 32% selectivity to CF ₃ CH ₂ F. Overall selectivity to the two products was 97%.

EXAMPLE 2

CF ₃ CC1 ₂ F + H ₂ > CF3CHCIF + CF ₃ CH ₂ F 2,2-Dichloro-l,1,1,2-tetrafluoroethane

(1.47 g/hr) and hydrogen (molar ratio of H ₂ /CF ₃ CC1 ₂ F « 1.9) were fed into the 1/4" empty Inconel® nickel alloy reactor for 132 hours at 350°-550°C and 250 psig. At 350°C a 2.3% conversion of CF ₃ CC1 ₂ F with a 76% selectivity to CF3CHCIF and CF ₃ CH ₂ F was observed. A sample taken after 20 hours at 500°C showed an 83% conversion of CF ₃ CC1 ₂ F with a 98% selectivity to CF3CHCIF and CF ₃ CH ₂ F.

EXAMPLE 3 CF3CHCIF + H ₂ > CF ₃ CH ₂ F

2-Chloro-l,l,1,2-tetrafluoroethane (1.0 g/hr) and hydrogen (molar ratio of H ₂ /CF ₃ CC1 ₂ F = 4.9) were fed into the 1/4" empty Inconel® nickel alloy reactor for 7 hours at 550°C and 250 psig with average CF3CHCIF conversions of 86% with 98% selectivity to CF ₃ CH ₂ F and 0.4% selectivity to CF3CH3.

EXAMPLE 4

CF ₂ C1 ₂ + H ₂ > CF ₂ HC1

Dichlorodifluoromethane (9.0 g/hr) and hydrogen (molar ratio of H ₂ /CF ₂ C1 ₂ » 1.0) were fed into the

1/4" empty Inconel® nickel alloy reactor as described above for 89 hours at 300 psig, including 79 hours at 500-550°C. For 12 hours at 500°C during this run, at a mean age of 64 synthesis hours, the average conversion of CF ₂ C1 ₂ was 26% with a 97% selectivity to CF HC1 and a 3% selectivity to CH ₂ F .

EXAMPLE 5

CF3CCIFCF3 + H ₂ > CF3CHFCF3

2-Chloroheptafluoropropane (1.5 g/hr) and hydrogen (22 cc/min) were fed into the 1/4" empty

Inconel® nickel alloy reactor for 3 hours at 450°C and 250 psig with 30-40% conversion and a 98% selectivity to CF3CHFCF3.

EXAMPLE 6

CF3CCIFCF3 + H ₂ > CF3CHFCF3

2-Chloroheptafluoropropane (1.38 g/hr) and hydrogen (22 cc/min) were fed into the 1/4" Inconel® nickel alloy reactor filled with Inconel® nickel alloy chips (10 g) . Operation at 500°C and 250 psig for 33.3 hours gave an average of 91.3% conversion with 99.4% selectivity to CF3CHFCF3.

EXAMPLE 7 CF ₃ CC1 ₂ F + H ₂ > CF3CHCIF + CF ₃ CH ₂ F

2,2-Dichloro-l,l,1,2-tetrafluoroethane (2.9 or 5.9 g/hr) and hydrogen (molar ratio of H ₂ /CF ₃ CC1 F - 2.2 or 4.3) were fed into the 3/8" Inconel® nickel alloy reactor filled with Inconel® nickel alloy wool (7.96 g) for 106 hours at 400-500°C and 250 psig. The average conversion of CF3CCI2F over the whole period was 99.9%. For a 12-hour period at 450°C with a CF ₃ CC1 ₂ F feed rate of 5.9 g/hr (molar ratio H ₂ /CF ₃ CC1 ₂ F - 4.3) the following average selectivities were observed: 69% CF3CHCIF and 26%

EXAMPLE 8

CF3CHCIF + H ₂ > CF ₃ CH ₂ F

2-Chloro-l,l,1,2-tetrafluoroethane (5.5 g/hr) and hydrogen (molar ratio of H ₂ /CF ₃ CHC1F ■ 1.1) were fed into the 3/8" Inconel® nickel alloy reactor filled with a pure nickel screen (8.77 g), operated at various feed rates and a pressure of 300 psig. With a CF3CHCIF feed rate of 5.48 g/hr and hydrogen (molar ratio of H /CF ₃ CHC1F ■ 1.1) conversion at 525°C and an average synthesis time of 82 hours

averaged 47% with 98% selectivity to CF ₃ CH ₂ F for 12 hours. At an average synthesis time of 644 hours conversion averaged 39% with 97% selectivity to CF ₃ CH ₂ F. At 1181 synthesis hours the operating pressure was increased to 500 psig. Conversion of CF3CHCIF averaged 68% for 14 hours with a selectivity to CF ₃ CH ₂ F of 98%. EXAMPLE 9

CF3CHCIF + H ₂ > CF ₃ CH ₂ F

2-Chloro-l,l,l,2-tetrafluoroethane (2.7 or 5.5 g/hr) and hydrogen (molar ratio of H ₂ /CF ₃ CHC1F = 1.9) were fed into the 3/8" Inconel® nickel alloy reactor filled with Inconel® nickel alloy wool

(7.96 g) for 23 hours at 400-500°C and 250 psig. Between 18 and 23 hours, at 400°C with a CF3CHCIF feed rate of 2.7 g/hr, the average conversion was 23% and the selectivity to CF ₃ CH ₂ F was 82%. EXAMPLE 10

CF ₂ C1 ₂ + H ₂ > CF ₂ HC1

Dichlorodifluoromethane (4.5 or 33.0 g/hr) and hydrogen (molar ratio of H ₂ /CF ₂ C1 ₂ « 1 or 0.5) were fed into the 3/8" Inconel® nickel alloy reactor filled with pure nickel screen (17.5 g) for 135 hours at 300 psig. For 12 hours at 450° during this run, at a mean synthesis time of 78 hours, with a CF ₂ C1 ₂ feed rate of 4.5 g/hr (molar ratio H /CF C1 ₂ = 1.0), the average conversion of CF ₂ C1 ₂ was 34% with the following average selectivities: 95% CF ₂ HC1 and 2.9%

^CF 2 ^H 2*

EXAMPLE 11

CF ₃ CC1F ₂ + H ₂ > CF ₃ CHF ₂

Chloropentafluoroethane vapor (6 cc/min) and hydrogen (5 cc/min) were fed into a Hastelloy® nickel alloy reactor (6" x 1/2" O.D.) filled with pure

nickel screen (39.68 g) at 550°C and atmospheric pressure. The reaction products were analyzed with the following results: 59% conversion of CF ₃ CC1F ₂ with a 97% selectivity to CF ₃ CHF ₂ .

EXAMPLE 12

CF ₃ CC1F ₂ + H ₂ > CF ₃ CHF ₂

Chloropentafluoroethane vapor (5 cc/min) and hydrogen (6 cc/min) were fed into an Inconel® nickel alloy reactor (6" x 1/2" O.D.) filled with pure nickel screen (51.98 g) at 550°C and atmospheric pressure. The reaction products were analyzed with the following results: 65% conversion of CF ₃ CC1F ₂ with a 95% selectivity to CF ₃ CHF ₂ .

The reaction was run under the same conditions as described above, except that the feed rates were changed to CF ₃ CC1F ₂ (5 cc/min) and H ₂ (12 cc/min). The reaction products were analyzed with the following results: 62% conversion of CF ₃ CC1F ₂ with an 86% selectivity to CF ₃ CHF ₂ .

EXAMPLE 13

CC1F ₂ CC1F ₂ /CF ₃ CC1 ₂ F + H ₂

CHF ₂ CC1F ₂ /CF ₃ CHC1F + CHF ₂ CHF ₂ /CF ₃ CH ₂ F A vapor mixture of CC1F ₂ CC1F ₂ (9)/CF ₃ CC1 ₂ F(1) (5 cc/min) and hydrogen (6 cc/min) was fed into a Hastelloy® nickel alloy reactor (6" x 1/2" O.D.) filled with pure nickel screen (39.68 g) at 550°C and atmospheric pressure. The reaction products were analyzed with the following results: 61% conversion of CC1F ₂ CC1F ₂ /CF ₃ CC1 ₂ F with a 46% selectivity to CHF ₂ CC1F ₂ /CF ₃ CHC1F and a 34% selectivity to CHF ₂ CHF ₂ /CF ₃ CH ₂ F.

EXAMPLE 14

CF ₃ CC1 ₂ F + H ₂ > CF3CHCIF + CF ₃ CH ₂ F 2,2-Dichlorotetrafluoroethane vapor (5 cc/min) and hydrogen (6 cc/min) were fed into an Inconel® nickel alloy reactor (6" x 1/2" O.D.) filled with pure nickel screen (51.98 g) at 550°C and atmospheric pressure. The reaction products were analyzed with the following results: 83% conversion of CF ₃ CC1 F with a 5% selectivity to CF3CHCIF and a 66% selectivity to CF ₃ CH ₂ F.

EXAMPLE 15

CF3CHCIF + H ₂ > CF ₃ CH ₂ F 2-Chloro-l,l,1,2-tetrafluoroethane vapor (5 cc/min) and hydrogen (6 cc/min) were fed into an Inconel® nickel alloy reactor (6" x 1/2" O.D.) filled with pure nickel screen (51.98 g) at 550°C and atmospheric pressure. The reaction products were analyzed with the following results: 58% conversion of CF3CHCIF with an 85% selectivity to CF ₃ CH ₂ F.

EXAMPLE 16

CC1F ₂ CC1 ₂ F + H ₂ > CHC1FCC1F ₂ + CHC1FCHF ₂

1,1,2-Trichloro-l,2,2-trifluoroethane (3.13 g/hr) and hydrogen (molar ratio = 4.75) were fed into the 3/8" Inconel® nickel alloy U-tube reactor as described in the general procedure, with the exit leg filled with pure nickel screen (8 g) , at 450°C and 500 psig. Over a 6-hour period the reaction products were analyzed with the following results: 81% conversion of CC1 ₂ FCC1F ₂ with 96% combined selectivity to C ₂ H ₃ F ₃ , C ₂ H ₂ C1F ₃ , and C ₂ HC1 ₂ F ₃ . Selectivity to CC1F » CF ₂ was 2%. When the temperature was raised to 475°C for 7 hours, the average conversion of CC1 ₂ FCC1F ₂ was 97% with 95% combined selectivity to C ₂ H ₃ F ₃ , C ₂ H ₂ C1F ₃ , and C ₂ HC1 ₂ F ₃ . Selectivity to CC1F « CF ₂ was 1%.

EXAMPLE 17

CF3CHCIF + H ₂ > CF ₃ CH ₂ F 2-Chloro-l,l,1,2-tetrafluoroethane (2.7 g/hr) and hydrogen (molar ratio of H2/CF3CHCIF ■ 0.2) were fed into an empty 6" x 1/2" O.D. Hastelloy® C276 nickel alloy reactor for 8 hours at 535°C and 300 psig. The average conversion of CF3CHCIF was 22% with an average 97% CF ₃ CH ₂ F selectivity.

EXAMPLE 18

CF3CHCIF + H ₂ > CF ₃ CH ₂ F

2-Chloro-l,l,1,2-tetrafluoroethane (2.7 g/hr) and hydrogen (molar ratio of H /CF ₃ CHC1F - 1.5) were fed into 6" x 1/2" O.D. Hastelloy® C276 nickel alloy reactor containing 14/20 mesh acid-washed SiC (6.5 g) for 60 hours at 535°C and 300 psig. The average conversion of CF3CHCIF was 75% with an average 97% CF ₃ CH ₂ F selectivity. EXAMPLE 19

CF3CHCIF + H ₂ > CF ₃ CH ₂ F

2-Chloro-l,l,1,2-tetrafluoroethane and hydrogen were fed at various rates over 113 hours into the 3/8" Hastelloy® C276 nickel alloy tube operated at 300 psig and containing Conoco Shot coke (9.2 grams, 10 cc) , a highly fused petroleum coke with a surface area of 0.5 sq m/g. For an 8-hour period at 560°C and an average time in synthesis of 102 hours, with a CF3CHCIF feed rate of 11.0 g/hr and a hydrogen feed rate of 32 cc/min (molar ratio of H ₂ /CF ₃ CHC1F - 1) the average conversion of CF3CHCIF was 13% with an average selectivity to CF ₃ CH ₂ F of 99%.

EXAMPLE 20

CC1F ₂ CC1F ₂ + H ₂ > CHF ₂ CC1F ₂ + CHF ₂ CHF ₂ Commercial 1,2-dichloro-l,l,2,2-tetrafluoro¬ ethane, containing 9% (molar) l,l-dichloro-l,2,2,2-

tetrafluoroethane, and hydrogen were fed at various rates over 150 hours into the 3/8" Inconel® nickel alloy tube operated at 300 psig and containing Conoco Shot coke (9.2 grams, 10 cc), a highly fused petroleum coke with a surface area of 0.5 sq. m/g. For a 16-hour period at 550°C and an average time in synthesis of 59 hours, with a CC1F ₂ CC1F ₂ feed rate of 5.9 g/hr and a hydrogen feed rate of 28 cc/min (molar ratio of H ₂ /CC1F CC1F ₂ = 2) the average conversion of the C ₂ C1 ₂ F ₄ isomers was 84% with an average selectivityto CHF ₂ CC1F ₂ and its isomer of 49%, and an average selectivity to CHF ₂ CHF ₂ and its isomer of 47%.

EXAMPLE 21

CF ₃ CC1 ₂ F + H ₂ > CF3CHCIF + CF ₃ CH ₂ F

2,2-Dichloro-l,1,1,2-tetrafluoroethane (2 mL/h), which was vaporized before being mixed with hydrogen (13 cc/min), was fed into a Hastelloy® C nickel alloy reactor (6" x 1/2" O.D.) as described above, containing Conoco Shot coke (14.0 grams, 10 mesh) , a highly fused petroleum coke with a surface area of 0.5 sq m/g at 550°C and 100 psig. After 28 hours of operation, product analysis indicated that CF3CC1 ₂ F conversion was quantitative and selectivity to CF3CHCIF and CF ₃ CH ₂ F was 64.7% and 33.3% respectively.

EXAMPLE 22 CF ₃ CC1F ₂ + H ₂ > CF ₃ CHF ₂

Chloropentafluoroethane vapor (10 cc/min) and hydrogen (10 cc/min) were fed into a Hastelloy® C nickel alloy reactor (6" x 1/2" O.D.) as described above, charged with Conoco Shot coke (14.0 grams, 10 mesh), a highly fused petroleum coke with a surface area of 0.5 sq m/g at 550°C. After 10 hours of

operation, product analysis indicated that CF3CC1F ₂ conversion was 7.5% and selectivity to CF ₃ CHF ₂ was 94.7%.

This experiment was substantially repeated except that the CF ₃ CC1F ₂ flow was 5 cc/min and the hydrogen flow was 6 cc/min. Product analysis indicated that CF ₃ CC1F ₂ conversion was 13.3% and selectivity to CF ₃ CHF ₂ was 89.6%.

EXAMPLE 23

CC1F ₂ CC1F ₂ + H ₂ > CHF ₂ CC1F ₂ + CHF ₂ CHF ₂

Commercial l,2-dichloro-l,l,2,2-tetrafluoro- ethane, containing 9% (molar) 1,1-dichloro-l,2,2,2- tetrafluoroethane, and hydrogen were fed at various rates for 172 hours into an empty 15" x 3/8" O.D. Hastelloy® C276 nickel alloy tube, as described above, operated at 500 psig. For a 13 hour period at 500°C and an average time in synthesis of 66 hours, with a CC1F ₂ CC1F ₂ feed rate of 5.9 g/hr and hydrogen feed rate of 10 cc/min (molar ratio of H ₂ /CC1F ₂ CC1F ₂ = 0.7) the average conversion of C ₂ C1 ₂ F ₄ isomers was 58% with an average selectivity to CHF CC1F ₂ and its isomer of 75% and an average selectivity to CHF ₂ CHF ₂ and its isomer of 24%. For a 9 hour period at 500°C and an average time in synthesis of 148 hours, with a CC1F ₂ CC1F ₂ feed rate of 1.47 g/hr and a molar feed ratio of H /CC1F CC1F ₂ of 1.5 the average conversion of C ₂ C1 ₂ F ₄ isomers was 88% with an average selectivity of CHF ₂ CC1F ₂ and its isomer of 45% and an average selectivity to CHF ₂ CHF ₂ and its isomer of 54%.

EXAMPLE 24

CC1F ₂ CC1F ₂ + H ₂ > CHF ₂ CC1F ₂ + CHF ₂ CHF ₂ Commercial 1,2-dichloro-l,l,2,2-tetrafluoro¬ ethane, containing 9% (molar) l,l-dichloro-l,2,2,2- tetrafluoroethane, and hydrogen were fed at various rates for 192 hours into a 15" x 3/8" O.D. Inconel® 600 nickel alloy tube, as described above, containing 8.0 g of 24 x 100 mesh nickel screen and operated at 500 psig. For a 10 hour period at 400°C and a CC1F ₂ CC1F ₂ feed rate of 0.7 g/hr and hydrogen feed rate of 1.7 cc/min (molar ratio of H ₂ /CC1F CC1F - 1); the average conversion of C ₂ C1 ₂ F ₄ isomers was 61% with an average selectivity to CHF CC1F ₂ and its isomer of 77.0% and an average selectivity to CHF ₂ CHF ₂ and its isomer of 22.7%.

EXAMPLE 25 CF ₃ CC1 ₂ F + H ₂ > CF3CHCIF + CF ₃ CH ₂ F

2,2-Dichloro-l,1,1,2-tetrafluoroethane and hydrogen were fed at various rates for 68 hours to an empty Hastelloy® C276 nickel alloy tube, as described above, operated at 500 psig. For a five hour period at 500°C and an average time in synthesis of 41 hours, with a CF ₃ CC1 ₂ F feed rate of 5.9 g/hr and a hydrogen rate of 14 cc/min (molar ratio of H ₂ /CF CC1 ₂ F = 1), the average conversion was 64% with an average selectivity to CF3CHCIF of 83.6 and an average selectivity of CF ₃ CH ₂ F of 15.6%.

EXAMPLE 26

CC1F ₂ CC1F ₂ + H ₂ > CHF ₂ CC1F ₂ + CHF ₂ CHF ₂

Chrome-Plated Reactor Commercial 1,2-dichloro-l,1,2,2 tetrafluoro¬ ethane, containing 9% (molar) l,l-dichloro-l,2,2,2

tetrafluoroethane, and hydrogen were fed at various rates over 55 hours into a 15" x 1/4" o.d. empty chrome-plated U-tube reactor, as described above, operated at 300 psig. For a 20-hour period at 500°C and an average time in synthesis of 16 hours, with a CC1F ₂ CC1F ₂ feed rate of 2.9 g/hr and a hydrogen feed rate of 13.3 cc/min (molar ratio H ₂ /CC1F ₂ CC1F ₂ = 2); the average conversion of the CC1F ₂ CC1F ₂ isomers was 56% with an average selectivity to CHF ₂ CC1F ₂ and its isomer of 21%, and an average selectivity to CHF ₂ CHF ₂ and its isomer of 76%.

EXAMPLE 27

CC1F ₂ CC1F ₂ + H ₂ > CHF ₂ CC1F ₂ + CHF ₂ CHF ₂

Aluminum Reactor Commercial 1,2-dichloro-l,1,2,2 tetrafluoro¬ ethane, containing 9% (molar) 1,l-dichloro-1,2,2,2 tetrafluoroethane, and hydrogen were fed at various rates over 31 hours into an empty 15" x 1/4" o.d. aluminum U-tube reactor, as described above, operated at 50 psig. For a 3-hour period at 500°C and an average time in synthesis of 28 hours, with a CC1F ₂ CC1F ₂ feed rate of 1.47 g/hr and a hydrogen feed rate of 7.0 cc/min (molar ratio H ₂ /CC1F ₂ CC1F ₂ ■ 2); the average conversion of the CC1F ₂ CC1F ₂ isomers was 5% with an average selectivity to CHF ₂ CC1F ₂ and its isomer of 49%, and an average selectivity to CHF ₂ CHF ₂ and its isomers of 33%.

EXAMPLE 28

CC1F ₂ CC1F ₂ + H ₂ > CHF ₂ CC1F ₂ + CHF ₂ CHF ₂

Titanium Reactor Commercial 1,2-dichloro-l,1,2,2 tetrafluoro¬ ethane, containing 9% (molar) 1,l-dichloro-1,2,2,2-

tetrafluoroethane, and hydrogen were fed at various rates over 42 hours into a 15" x 1/4" o.d. empty titanium U-tube reactor, as described above, operated at 50 psig. For a 17-hour period at 500°C and an average time in synthesis of 9.5 hours, with a CC1F CC1F ₂ feed rate of 2.9 g/hr and a hydrogen feed rate of 13.9 cc/min (molar ratio H ₂ /CC1F ₂ CC1F ₂ - 2) the average conversion of the CC1F ₂ CC1F ₂ isomers was 14.2% with an average selectivity to CHF ₂ CC1F ₂ and its isomer of 57%, and an average selectivity to CHF ₂ CHF and its isomer of 24.4%.

EXAMPLE 29

CF3CHCIF + H ₂ > CF ₃ CH ₂ F

Silicon Carbide Reactor 2-Chloro-l,1,1,2 tetrafluoroethane and hydrogen were fed at various rates over 47 hours into a 15" x 1/4" o.d. empty silicon carbide straight tube reactor, as described above, operated at 0 psig. For a 12-hour period at 600°C and an average time in synthesis of 29 hours, with a CF3CHCIF. feed rate of 2.74 g/hr and a hydrogen feed rate of 8.2 cc/min (molar ratio H ₂ /CF ₃ CHC1F « 1); the average conversion of the CF3CHCIF was 4.3%, with an average selectivity to CF ₃ CH ₂ F of 89.7%.

EXAMPLE 3Q CF ₃ CC1 ₂ F + H ₂ > CF3CHCIF + CF ₃ CH ₂ F

Silicon Carbide Reactor 2,2-Dichloro-l,1,1,2-tetrafluoroethane 2.94 g/hr were fed into a silicon carbide straight tube reactor, as described above, with 6.4 cc/min of hydrogen (molar ratio H ₂ /CF CC1 ₂ F = 1) operated at 0 psig for 41 hours. Over a 15-hour period at 500°C

and an average time in synthesis of 27 hours; the average conversion of CF CC1 ₂ F was 23% with an average selectivity to CF3CHCIF of 54% and an average selectivity to CF ₃ CH ₂ F of 0.6%.

EXAMPLE 31 CC1F ₂ CC1F ₂ + H ₂ > CHF ₂ CC1F ₂ + CHF ₂ CHF ₂ Silicon Carbide Reactor

Commercial l,2-dichloro-l,l,2,2 tetrafluoro- ethane, containing 9% (molar) 1,l-dichloro-1,2,2,2 tetrafluoroethane, and hydrogen were fed at various feed rates over 38 hours into a straight tube silicon carbide reactor tube, as described above, operated at 0 psig. For a 12-hour period at 575°C and at an average time in synthesis of 14 hours, with a feed rate of 13.9 cc/min of hydrogen and 2 grams/hr of CC1F ₂ CC1F ₂ (molar ratio H ₂ /CC1F ₂ CC1F ₂ - 2); the average conversion of the CC1F ₂ CC1F ₂ isomers was

35.6% with an average selectivity to CHF ₂ CC1F ₂ and its isomers of 28% and an average selectivity to CHF CHF ₂ and its isomers of 27%.

EXAMPLE 32

CF ₂ C1 ₂ + H ₂ > CF ₂ HC1 + CH ₂ F ₂

Silicon Carbide Reactor Dichlorodifluoromethane (2.6 g/hr) and hydrogen (molar ratio H2/CF2CI2 ■ 1.0) were fed into an empty 1/2" x 15" silicon carbide straight tube reactor, as described above, over a 28-hour period. For four hours at 575°C during this run, at an average synthesis time of 26 hours; the average conversion of CF ₂ C1 ₂ was 35.6% with an 82% selectivity to CF ₂ HC1 and a 2% selectivity to CH ₂ F ₂ .

EXAMPLE 33

CF ₃ CC1 ₃ + H ₂ > CF ₃ CHC1 ₂ + CF ₃ CH ₂ C1 Hastelloy® Nickel Alloy Reactor

1,1,l-Trichloro-2,2,2-trifluoroethane and hydrogen were fed into an empty 15" x 3/8" Hastelloy® C276 nickel alloy U-tube reactor, as described above, at 300 psig for a period of 28 hours. Over a 6-hour period at 425°C and 300 psig, at an average time in synthesis of 17 hours, with a feed rate of CF3CCI3 of 6.25 g/hr and a hydrogen feed rate of 14.0 seem (molar ratio H ₂ /CF ₃ CC1 ₃ » 1.0); the average conversion of CF3CCI3 was 33% with a selectivity to CF ₃ CHC1 ₂ of 95% and a selectivity to CF ₃ CH ₂ C1 of 5%.

EXAMPLE 34

Inconel® Nickel Alloy Reactor Carbon tetrachloride (6.57 g/hr) and hydrogen

(200 seem) were fed into an empty 15" x 1/4" Inconel® 600 nickel alloy U-tube reactor, as described above, operated at pressures between 0 psig and 300 psig for 149 hours. For a 10-hour period at 457°C and 300 psig and an average time in synthesis of 136 hours, with a CC1 ₄ feed rate of 6.57 g/hr and a hydrogen feed rate of 200 seem (molar ratio H ₂ /CC1 ₄ *» 12); the average conversion of CC1 ₄ was 45% with an average selectivity to CHCI3 of 59% and an average selectivity to CH ₂ C1 ₂ of 2.8%.

EXAMPLE 35

CF3CHCIF + H ₂ > CF ₃ CH ₂ F

High Hydrogen Ratio 2-Chloro-l,l,1,2-tetrafluoroethane and hydrogen were fed at varying rates for over 48 hours to a 56"

x 1/4" Inconel® 600 nickel alloy coil reactor at 300 psig and temperatures between 550 and 600°C. For 4 hours at 600°C, at an average time in synthesis of 39 hours, with a CF ₃ CHC1F feed rate of 1.6 mL/hr and a H ₂ feed rate of 130 seem (H ₂ /CF ₃ CHC1F mol ratio = 20) the average conversion of CF3CHCIF was 83% and the selectivity to CF ₃ CH ₂ F was 94%. At a lower H ₂ flow of 65 seem and the same CF ₃ CHCIF feed rate and temperature (H ₂ /CF ₃ CHC1F mol ratio ■ 10) the average conversion of CF3CHCIF over a 5-hour period was 90% with a 94% selectivity to CF ₃ CH ₂ F.

EXAMPLE 36

CF3CHCIF + H ₂ > CF ₃ CH ₂ F

High Hydrogen Ratio 2-Chloro-l,l,1,2-tetrafluoroethane and hydrogen were fed at various rates for 1207 hours into a 15" x 3/8" Inconel® 600 nickel alloy U-tube, packed with 8.77 g 150 mesh nickel screen, and operated at various temperatures at 300 psig. For a 23-hour period at 550°C and an average time in synthesis of 755 hours with a CF3CHCIF feed rate of 0.4 ml/hour and a hydrogen feed rate of 18 sccm/min (molar ratio H ₂ /CF ₃ CHC1F » 11), the average conversion of CF3CHCI was 99.6% with a selectivity to CF ₃ CH ₂ F of 93%.

E-XAMPLE 37 CC1 ₂ FCF ₃ + H ₂ > CHCIFCF3 + CH ₂ FCF ₃

High Hydrogen Ratio 1,1-Dichloro-l,2,2,2-tetrafluoroethane and hydrogen were fed at various rates for 237 hours into a 15" x 3/8" Hastelloy® C nickel alloy U-tube packed with 9.29 g of Conoco shot coke and operated at various temperatures at 300 psig. For a 5-hour

period at 575°C and an average time in synthesis of 227 hours with a CC1 ₂ FCF ₃ feed rate of 36 mL/hr and a hydrogen feed rate of 50 sccm/min (molar ratio

H ₂ /CC1 ₂ FCF ₃ ■ 40), the average conversion of CC1 ₂ FCF ₃ was 100%. The selectivity to CHC1FCF ₃ was 32% and the selectivity to CH ₂ FCF ₃ was 59%.

EXAMPLE 38

CF ₃ CC1F ₂ + H ₂ > CF ₃ CHF ₂

2-Chloro-l,1,1,2,2-pentafluoroethane and hydrogen were fed at various rates to 15" x 3/8" Hastelloy® C276 nickel alloy U-tube operated at 300 psig and various temperatures for 136 hours. For 10 hours, at an average time in synthesis of 58 hours and a temperature of 575°C, with a CF ₃ CC1F ₂ feed rate of 2.1 g/hr and a hydrogen feed rate of 14.0 seem (molar ratio H ₂ /CF ₃ CC1F ₂ » 2.5), the conversion of CF ₃ CC1F ₂ was 89.5% and the selectivity to CF ₃ CHF ₂ was 99.9%.

For an 8-hour period at an average time in synthesis of 131 hours and a temperature of 575°C, with a feed rate of CF3CC1F ₂ of 4.15 g/hr and a hydrogen feed rate of 329 seem (molar ratio

H ₂ /CF ₃ CC1F ₂ ■ 30), the average conversion of CF ₃ CC1F ₂ was 39% with a selectivity to CF ₃ CHF ₂ was 99.6%.

Particular embodiments of the invention are included in the examples. Other embodiments will become apparent to those skilled in the art from a consideration of the specification or practice of the invention disclosed herein. It is understood that modifications and variations may be practiced without departing from the spirit and scope of the novel concepts of this invention. It is further understood

that the invention is not confined to the particular formulations and examples herein illustrated, but it embraces such modified forms thereof as come within the scope of the following claims.