TEBBE FREDERICK NYE (US)
| WO1989011467A1 | 1989-11-30 |
| EP0056548A1 | 1982-07-28 |
| 1. | A process for preparing 1,1dichloro 1,2,2,2tetrafluoroethane by chlorofluorination comprising the step of contacting a gaseous mixture comprising at least one tetrahaloethyiene having the formula C Cl4_xFχ, wherein x is an integer from zero to 3, and both Cl2 and HF with a catalyst composition at a temperature within the range of about 300°C to 450°C, said catalyst composition consisting essentially of an aluminum fluoride prepared by the reaction of aluminum hydroxide and HF. |
| 2. | The process of Claim 1 wherein the at least one tetrahaloethyiene is. |
| 3. | The process of Claim 1 wherein byproducts having less than five fluorine atoms per molecule are recycled. |
| 4. | The process of Claim 1 wherein the molar ratio of said HF to said tetrahaloethyiene is within the range of about 1:1 to 20:1; and wherein the molar ratio of said Cl2 to said tetrahaloethyiene is within the range of about 1:1 to 2:1. |
| 5. | The process of Claim 1 wherein the contact times are within the range of about 5 to 100 seconds. |
| 6. | The process of Claim 1 wherein before the catalyst is contacted by said at least one tetrahaloethyiene it is pretreated with HF gas. |
| 7. | An improved process for producing 2chlorol,1,1,2tetrafluoroethane and/or 1,1,1,2tetrafluoroethane by hydrodechlorinating 1,1dichlorol,2,2,2tetrafluoroethane, the improvement comprising the step of preparing said l,ldichlorol,2,2,2tetrafluoroethane by contacting a gaseous mixture comprising at least one tetrahaloethyiene having the formula c2c4χF ' wherein x is an integer from zero to 3, and both Cl2 and HF with a catalyst composition at a temperature within the range of about 300°C to 450°C, said catalyst composition consisting essentially of an aluminum fluoride prepared by the reaction of aluminum hydroxide and HF. |
| 8. | A catalyst composition consisting essentially of an aluminum fluoride prepared by the reaction of aluminum hydroxide with HF. |
| 9. | The catalyst composition of Claim 8 prepraed by dissolving aluminum hydroxide in aqueous HF; evaporating the resulting solution to obtain a residue of an aluminum fluoride; and heating said residue to produce a dried solid. |
| 10. | The catalyst composition of Claim 8 wherein said aluminum hydroxide is prepared by the hydrolysis of A1R3 or the hydrolysis of Al(OR)3 where each R is independently selected from C_ to C6 alkyl groups. |
FOR PREPARING 1,1-DICHLORO-l,2,2,2-TETRAFLUOROETHANE
FIELD OF THE INVENTION This invention relates to catalysts and their use for the manufacture of 1,l-dichloro-l,2,2,2-tetra- fluoroethane (i.e. "CFC-114a"), and more particularly to aluminum fluoride catalysts and use thereof for preparing CFC-114a.
BACKGROUND OF THE INVENTION Fluorinated aluminas are well known as fluorination or chlorofluorination catalysts. For example the use of both aluminum fluoride and aluminum fluoride containing iron, chromium and nickel for fluorination or chlorofluorination reactions ' is described in U.S. Patent No. 3,650,987. The fluorided alumina is often prepared by the addition of HF to A1 2 0 3 . The products from these reactions contain large amounts of the symmetrical isomers of various chlorofluorocarbons. The addition of metal dopants increases the amount of symmetrical isomers.
German (DDR) Patent Specification 117,580 discloses a process for the preparation of asymmetrical fluorochlorocarbon compounds of the C 2 series (e.g. CFC-114a) by the reaction of tetrachloroethylene, chlorine and hydrogen fluoride over a metal doped aluminum fluoride catalyst. In the example of this patent with the highest amount of asymmetrical products, the 1,1-dichloro-l,2,2,2- tetrafluoroethane (CFC-114a)/l,2-dichloro-l,1,2,2- tetra-fluoroethane (CFC-114) ratio is about 11.5; and
the 1,1,l-trichloro-2,2,2-trifluoroethane (CFC-113a)/l,l,2-trichloro-l, 2 ,2-trifluoroethane (CFC-113) ratio is about 8.0. However 57.4% of the product is chloropentafluoroethane (CFC-115), which is generally considered an undesirable byproduct in CFC-114a manufacturing processes. In another example where 6.1% of the product is CFC-115, the ratios of CFC-114a/CFC-114 and CFC-113a/CFC-113 are 7.3 and 3.8 respectively.
European Patent Application 317,981 discloses a process for isomerizing CFC-113 to CFC-113a followed by fluorination with HF to produce CFC-114a. In the example of this patent with the highest ratio of
CFC-114a/CFC-114 (52.7) the ratio of CFC-113a/CFC-113 is 1.1. In other examples the CFC-114a/CFC-114 ratio varied from 45.3 to 5.5 and the CFC-113a/CFC-113 ratio from 6.2 to 1.1. Japanese Kokai 1-172347 discloses a process for the preparation of CFC-114a by first dispropor- tionating CFC-114 to CFC-113a followed by reaction with HF. In the examples the CFC-114a/CFC-114 ratios vary from 9.0 to 16.7 and the CFC-113a/CFC-113 ratios from 0.1 to >36. In the high 113a/113 ratio example the yield of 114a is only 15.0%. In the other examples the yields of 114a varied from 43.0% to 51.0%.
It is also known in the art (GB 1,578,933) that both CC1F 2 CC1F 2 (CFC-114) and CF 3 CC1 2 F (CFC-114a) may be hydrogenated over a Pd catalyst to CHF 2 CHF 2 (HFC-134) and CF 3 CH 2 F (HFC-134a) respectively. The latter compound (HFC-134a) is considered a refrigerant suitable for replacing CC1 2 F 2 since it does not significantly contribute to stratospheric ozone depletion while CC1 2 F 2 is suspected of being a major contributor.
Accordingly, there is continued interest in developing economic and efficient processes for preparing 1,l-dichloro-l,2,2,2-tetrafluoroethane.
SUMMARY OF THE INVENTION
In accordance with this invention, a process is provided for preparing 1,l-dichloro-l,2,2,2-tetra- fluoroethane by chlorofluorination. The process comprises the step of contacting a gaseous mixture comprising at least one tetrahaloethyiene having the formula C 2 CCl 4 _ χ F χ , wherein x is an integer from zero to 3, and both Cl 2 and HF with a catalyst composition at an elevated temperature, said catalyst composition consisting essentially of an aluminum fluoride prepared by the reaction of aluminum hydroxide and HF. The l,l-dichloro-l,2,2,2-tetrafluoroethane prepared by the process may be hydrodechlorinated to produce 2-chloro-l,l,l,2-tetrafluoroethane and/or tetrafluoroethane. A catalyst composition is also provided in accordance with this invention which consists essentially of an aluminum fluoride prepared by the reaction of aluminum hydroxide with HF. DETAILED DESCRIPTION OF THE INVENTION A process for preparing 1,l-dichloro-1,2,2,2- tetrafluoroethane by chlorofluorination is provided in accordance with this invention and comprises the step of contacting a gaseous mixture comprising at least one tetrahaloethyiene and both Cl 2 and HF with a catalyst composition at an elevated temperature, said catalyst composition consisting essentially of an aluminum fluoride prepared by the reaction of aluminum hydroxide and HF. Tetrahaloethylenes useful in this invention include those having the formula c 2 cl 4-x F x' wh erein x is an integer from zero to 3. Examples of tetrahaloethylenes useful for this
process include CC1 2 =CC1 2 , CC1F=CC1 2 , CC1F=CC1F, and mixtures of these. Tetrachloroethylene is preferred.
The reaction of the tetrahaloethyiene with HF and Cl 2 in the presence of the catalyst composition of the instant invention is conducted at an elevated temperature. Suitable temperatures are generally within the range of about 300°C to 450°C. Preferably the temperature is within the range of about 300°C to 400°C, and most preferably is within the range of about 350°C to 375°C. Contact times can influence the yield of the reaction to some extent. Preferably the temperature and contact time are balanced to achieve a yield of at least about 95% total of CFC-114a and recyclable by-products (i.e. by-products having less than 5 fluorine atoms per molecule); and preferably the aluminum fluoride purity of the catalyst composition is sufficient to provide a molar ratio of 1,1-dichloro-l,2,2,2-tetrafluoroethane to l,2-dichloro-l,l,2,2-tetrafluoroethanes (i.e. of CFC-114a to CFC-114) of at least about 45 and most preferably sufficient to provide a molar ratio of CFC-114a to CFC-114 of at least about 47.5. A contact time within the range of about 5 to 100 seconds is typical. Preferably the contact time is within the range of about 10 to 90 seconds, and most preferably is within the range of about 15 to 60 seconds.
The HF in the gaseous mixture is preferably at least the stoichiometric amount needed to produce CFC-114a. The molar ratio of the HF to the tetrahaloethyiene is typically within the range of about 1:1 to 20:1. Preferably the ratio of HF to the tetrahaloethyiene is within the range of about 3:1 to 10:1, and most preferably is within the range of about 4:1 to 7:1.
Preferably Cl 2 is provided in the gaseous mixture in at least the amount needed to produce CFC-114a. The molar ratio of Cl 2 to the tetrahaloethyiene is preferably within the range of about 1:1 to 2:1, and most preferably is about 1:1. The desired product of the present invention can be separated by a usual method such as fractional distillation. By-products having less than five fluorine atoms per molecule such as C 2 Cl5F, C 2 Cl F 2 , C 2 F 3 C1 3 , and CC1F 2 CC1F 2 are considered recyclable, and may advantageously be further contacted with the catalyst composition used in this invention. The reaction of the tetrahaloethyiene with HF and chlorine may be conducted in any suitable reactor, including fixed and fluidized bed reactors which are charged with the catalyst compositions. The reaction vessel should be constructed from materials which are resistant to the corrosive effects of HF and Cl 2 such as Hastelloy® nickel alloy and Inconel® nickel alloy. Optionally, before the catalyst is contacted by the tetrahaloethylenes, it may be pretreated with gaseous HF. Pressure is not critical. Atmospheric and superatmospheric pressures are the most convenient and are therefore preferred.
1,1-dichloro-l,2,2,2-tetrafluoroethane produced by this invention has utility as a solvent and as an intermediate for the preparation of 2-chloro-l,1,1,2- tetrafluoroethane and/or 1,1,1,2-tetrafluoroethane. Indeed an improved process for producing 1,1,1,2-tetrafluoroethane and/or 2-chloro- 1,1,2,2-tetrafluoroethane by hydrodechlorinating 1,1-dichloro-l,2,2,2-tetrafluoroethane is provided in accordance with this invention. The improvement comprises the step of preparing CFC-114a by
chlorofluorination using tetrahaloethylenes and the catalyst compositions of this invention as described above.
Catalyst compositions are provided in accordance with this invention which consist essentially of an aluminum fluoride prepared by the reaction of aluminum hydroxide with HF. The catalyst composition of this invention may be suitably prepared by reacting aqueous HF (e.g. 48% solution) with aluminum hydroxide. Suitable aluminum hydroxide may be prepared by the hydrolysis of A1R 3 , where each R is independently selected from C-^ to C 6 alkyl groups. For example, a preparation of high purity Al(OH) 3 prepared by the hydrolysis of A1(CH 2 CH 3 ) 3 is described by F. N. Tebbe et al., J. Am. Ceram. Soc.. 71 [4] , C-204 - C-206, (1988). Suitable aluminum hydroxide may also be prepared by hydrolysis of Al(OR) 3 , where each R is independently selected from C^ to C 6 alkyl groups. For example, high purity Al(OH) 3 may be prepared by the hydrolysis of Al(OCH(CH 3 )CH 2 CH 3 ) 3 .
A particularly useful catalyst composition consisting essentially of an aluminum fluoride is prepared by dissolving aluminum hydroxide in aqueous HF; evaporating the resulting solution to obtain a residue of an aluminum fluoride; and heating said residue to produce a dried solid. The catalyst compositions of this invention are also useful for catalyzing other reactions such as the chlorofluorination of CF 3 CC1 3 , CF 3 CHC1F and/or CF 3 CH 3 to CFC-114a, isomerization of CC1F 2 -CC1F 2 to CC1 2 F-CF 3 , isomerization of CHF 2 -CHF 2 to CH 2 F-CF 3 , fluorination of CF 3 -CHC1 2 to CF 3 -CHC1F and fluorination of CHC1=CC1 2 to CC1F 2 CH 2 C1 and CF 3 CH 2 C1.
Practice of the invention will become further apparent from the following non-limiting examples. EXAMPLE I
Aluminum sec-butoxide (Alfa, 95%), about 300 g, was placed in an open dish and allowed to hydrolyze in air over two days. The aluminum hydroxide produced was a powder and clusters of powdery solids. In a polyethylene tray a portion of the aluminum hydroxide (39 g) was dissolved in 48% aqueous hydrofluoric acid (100 mL) . The volatiles were evaporated at ambient temperature over three days in a fume hood. The resulting white residue was dried at 110°C for 48 hours. The solid was then heated in air at a rate of 5°C/min to 500°C, and held at this temperature for three hours. After cooling, the solid (30.3 g) was crushed and passed through a sieve to yield fines (12.8 g) and a fraction of granules 12x20 mesh in size (17.5 g) . Analysis showed 31.5% Al and 227 ppm (0.0227%) of metal ion impurities.
EXAMPLE II A reactor (a 0.5 inch ID, 12 inch long Inconel® nickel alloy pipe) was charged with the aluminum fluoride catalyst composition (15.7 g, 25 mL) prepared as described in Example I above. The charged reactor was placed in a sand bath. The bath was gradually heated to 250°C while nitrogen gas at a flow rate of 50cc/minute was passed through the reactor to remove traces of water. HF and nitrogen gas (1:4 molar ratio) were then passed through the reactor. An exotherm of about 10°C, which travelled down the reactor, was observed. The temperature was gradually raised to 450°C, the nitrogen flow decreased with time until neat HF was passed through
the reactor. The HF flow was stopped after no further exotherm was recorded. HF/CC1 2 =CC1 2 /C1 2 in a 5/1/1 molar ratio was then passed over the catalyst at 375°C and a 30 second contact time. The reactor effluent was sampled on-line with a Hewlett-Packard 5890 gas chromatograph using a 20 foot long, 1/8" diameter, column containing Krytox® perfluorinated polyether on an inert support and a helium flow of 35 cc/minute. Gas chromatographic conditions were 70°C for 3 minutes followed by temperature programming to 180°C at a rate of 6°C/minute. Analysis showed the following to be present (area percent): 25.4% CC1 2 =CC1 2 , 0.2% CC1 3 CC1 2 F, 0.5% CC1 2 FCC1 2 F/CC1F 2 CC1 3 , 1.6% CC1 2 FCC1F 2 (CFC-113), 9.4% CF 3 CC1 3 (CFC-113a), 1.2% CC1F 2 CC1F 2 (CFC-114), 58.8% CF 3 CC1 2 F (CFC-114a) , 1.0% CC1F 2 CF 3 (CFC-115), 0.1% CC1F 2 CHC1 2 , and 0.2% CC1 2 =CC1F. The yield to useful products including both
CFC-114a and recyclable by-products, is greater than 98% and the molar ratio of CFC-114a/CFC-114 is 49.
Particular embodiments of the invention are described 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.
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