Process for producing 2,3,3,3-tetrafluoropropene

Abstract

The present invention discloses a manufacturing process to produce high purity 1234yf from 245eb, which preferably includes the removal of impurities present in 245eb raw material, the dehydrofluorination of 245eb, and the removal of impurities present in final crude product. The disclosed manufacturing process allows the production of a 1234yf product with lower the levels of 1225ye and/or trifluoropropene, preferably in amounts of less than about 500, and 50 ppm, respectively.

Claims

1. A composition comprising (i) at least 50% by weight 1,1,1,2,3-pentafluoropropane (245eb), (ii) 1,1,1,2,3,3-hexafluoropropane (236ea) and (iii) 1,2,3,3,3-pentafluoropropene (1225ye), wherein the composition comprises less than 2% by weight each of 1,1,1,2,3,3-hexafluoropropane (236ea) and 1,2,3,3,3-pentafluoropropene (1225ye).

2. The composition of claim 1, having a concentration of 1,1,1,2,3-pentafluoropropane (245eb) of at least 99.9%.

3. The composition of claim 1, including less than 1% by weight of 1,1,1,2,3,3-hexafluoropropane (236ea).

4. The composition of claim 1, including less than 1% by weight of 1,2,3,3,3-pentafluoropropene (1225ye).

5. The composition of claim 1, including less than 0.5% by weight of 1,1,1,2,3,3-hexafluoropropane (236ea).

6. The composition of claim 1, including less than 0.5% by weight of 1,2,3,3,3-pentafluoropropene (1225ye).

Description

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS OF THE INVENTION

(1) The present invention can be generally described as a process for manufacturing high purity 1234yf from 245eb. As mentioned above, a critical step according to one aspect of certain embodiments of the invention comprises ensuring that the feed to the reactor in such a process contains not more than about 2% by weight of any one of the compounds 1,1,1,2,3,3-hexafluoropropane (236ea) and 1,2,3,3,3,-penatfluoropropene (1225ye), based on the total weight of 245eb in the reactor feed stream(s). Applicants contemplate that in many embodiments the ensuring step will involve treating a raw feedstock having an amount of one or more of these materials that is greater than the specified amount. However, it is also contemplated that in certain embodiments the ensuring step may comprise simply obtaining, for example from outside sources, a 245eb feedstock having less than the specified amount of the indicated materials.

(2) According to certain preferred embodiments, the methods comprise the steps of:

(3) (A) removal of impurities from the 245eb raw material (or raw feed stock) which, optionally but preferably, involves photochlorinating the unsaturates, such as 1225ye, present in the 245eb raw feed stock, preferably into 2,3-dichloro-1,1,1,2,3-pentafluoropropane, and/or involves distilling the 245eb feed to remove impurities such as 236 ea, 1225ye, 2,3-dichloro-1,1,1,2,3-pentafluoropropane, etc. to obtain a high purity 245eb feed,

(4) (B) dehydrofluorinating the high purity 245eb feed, preferably in the presence of a caustic solution in liquid phase or a catalyst in vapor phase into 1234yf, and

(5) (C) optionally but preferably distilling the 1234yf reaction product to have a final product concentration of 1225ye that is below 500 ppm, preferably below 200 ppm, and more preferably below 100 ppm, and a final product concentration of trifluoropropyne that is below 50 pp.

(6) A. The Removal of Impurities Included in 245eb Raw Material

(7) In certain preferred embodiments, the unsaturated impurities such as 1225ye are converted, prior to entering the 245eb dehydrofluorination reactor, into corresponding saturated halogenated hydrocarbons having increased chlorine content, preferably via photochlorination in which chlorine (Cl.sub.2) reacts with the unsaturated impurities in the presence of an ultraviolet light source. In one preferred photochlorination process, electromagnetic radiation, preferably light, from a suitable source is directed through a reactor wall to interact with the reactants therein. The source of light may be, for example, any one of a number of arc or filament lamps known in the art. Quartz or borosilicate glass such as Pyrex glass may be employed as transparent material to construct the portion of the reactor wall through which the light passes and enters the reactor. The photochlorination may be continuously carried out in the gas phase, in which starting materials are vaporized and contacted with chlorine vapor in a reaction zone. Although a wide range of chlorination reaction conditions are believed to be suitable, in certain preferred embodiments the reaction temperature is from about room temperature to about 50 C. Alternatively or additionally, the chlorination may be carried out in the liquid phase by feeding chlorine to a reactor containing starting materials, with it generally being preferred to control the reaction temperature below the boiling points of the starting materials and products.

(8) The content of impurities such as 1225ye, 236ea, 254eb, and 2,3-dichloro-1,1,1,2,3-pentafluoropropane in the 245eb raw feed may be reduced by any means known in the art, such as extraction and preferably distillation. Although it is contemplated that a wide range of separation conditions can be used in accordance with the present invention, it is preferred in certain embodiments that the 245eb raw materials are distilled by passing at least a portion thereof through a standard distillation column and/or packed tower, or the like at atmospheric pressure, super-atmospheric pressure or a vacuum. Preferably the pressure is less than about 300 psig, more preferably less than about 150 psig and most preferably less than 100 psig. The pressure of the distillation column inherently determines the distillation operating temperature for a given degree of separation. The 245eb may be recovered as distillate by operating the distillation column at from about 10 C. to about 90 C., preferably from about 0 C. to about 80 C. Single or multiple distillation columns may be used. In certain preferred embodiments, the purity of 245eb after distillation is at least about 99.9% by weight.

(9) B. The Dehydrofluorination of 245eb

(10) The dehydrofluorination step can be carried out in a liquid phase in the presence of a caustic solution or in a gas phase in the presence of a dehydrofluorination catalyst. It is contemplated that the reaction can be carried out batch wise, continuous, or a combination of these.

(11) One preferred converting step involves a reaction in which 245eb is contacted with a dehydrohalogenating agent, such as potassium hydroxide (KOH), sodium hydroxide (NaOH), Ca(OH).sub.2, CaO, and combinations of these and/or other catalysts, to form a reaction product comprising 2,3,3,3-tetrafluoropropene. This reaction may be described, by way of illustration but not necessarily by way of limitation, by the following reaction equation:
CF.sub.3CHFCH.sub.2F+KOH.fwdarw.CF.sub.3CF=CH.sub.2+KF+H.sub.2O

(12) In preferred aspects of such embodiments, the dehydrohalogenating agent comprises, and in certain embodiments consists essentially of, caustic material, such as KOH, and is preferably provided as an aqueous solution comprising from about 2% to about 100%, more preferably from about 5% to about 90%, and even more preferably from about 10% to about 80% by weight of the caustic material, preferably comprising or consisting essentially of KOH.

(13) In certain preferred embodiments, the caustic solution, and preferably the KOH solution, is brought to a temperature of from about 20 C. to about 100 C., more preferably from about 30 C. to about 90 C., and most preferably from about 40 C. to about 80 C. The reaction pressure in such embodiments may vary, depending on particular processing parameters of each application. In certain embodiments, the reaction pressure ranges from atmospheric pressure, super-atmospheric pressure or under vacuum. The vacuum pressure, when used, preferably in certain embodiments ranges from about 5 torr to about 760 torr.

(14) Another preferred converting step involves a reaction in which 245eb is contacted with a dehydrohalogenating catalyst, under conditions effective to form a reaction product comprising of 2,3,3,3-tetrafluoropropene and hydrogen fluoride. The dehydrofluorination reaction may be conducted in any suitable reaction vessel or reactor, but it should preferably be constructed from materials which are resistant to the corrosive effects of hydrogen fluoride such as nickel and its alloys, including Hastelloy, Inconel, Incoloy, and Monel. These may be single or multiple tubes packed with a dehydrofluorinating catalyst which may be one or more of halogenated metal oxides in bulk form or supported, metal halides in bulk form or supported, and carbon supported transition metals, metal oxides and halides. Suitable catalysts non-exclusively include fluorinated chromia (Cr.sub.2O.sub.3), fluorinated alumina (Al.sub.2O.sub.3), metal fluorides (e.g., CrF.sub.3 and AlF.sub.3) and carbon supported transition metals (zero oxidation state) such as Fe/C, Co/C, Ni/C, Pd/C or transition metals halides. In a preferred embodiment of the invention, the 245eb is pre-vaporized or preheated prior to entering the reactor. Alternatively, the 245eb is vaporized inside the reactor. Useful reaction temperatures may range from about 100 C. to about 600 C. Preferred temperatures may range from about 150 C. to about 450 C., and more preferred temperatures may range from about 250 C. to about 350 C. The reaction may be conducted at atmospheric pressure, super-atmospheric pressure or under vacuum. The vacuum pressure can be from about 5 ton to about 760 torr. Contact time of the 245eb with the catalyst may range from about 0.5 seconds to about 120 seconds, however, longer or shorter times can be used.

(15) C. The Removal of Impurities Included in 1234yf Crude Product

(16) 2,3,3,3-tetrafluoropropene may be recovered from the reaction product mixture comprised of unconverted starting materials, product, and by-products including some or all of HF, 1234ze, 1225ye, and trifluoropropyne by any means known in the art, such as extraction and preferably distillation. In certain preferred embodiments, HF is removed or preferably recovered from the mixture of hydrogen fluoride and fluorocarbons prior to distillation. The removal of hydrogen fluoride may be realized via acid-base neutralization in a caustic solution scrubber. This may be conducted by running the product stream containing hydrogen fluoride and fluorocarbons through a caustic solution scrubber followed by a drying column. The recovering of hydrogen fluoride may be conducted in a gaseous phase by a continuous process of introducing a stream of sulfuric acid to a stream of fluorocarbon and hydrogen fluoride. This may be conducted in a standard scrubbing tower by flowing a stream of sulfuric acid countercurrent to a stream of fluorocarbon and hydrogen fluoride. Sulfuric acid extraction is described, for example in U.S. Pat. No. 5,895,639, which is incorporated herein by reference. The mixture of 2,3,3,3-tetrafluoropropene, unconverted 245eb and any other by-products are then passed through a distillation column. For example, the distillation may be preferably conducted in a standard distillation column at atmospheric pressure, super-atmospheric pressure or a vacuum. Preferably the pressure is less than about 300 psig, more preferably less than about 150 psig and most preferably less than 100 psig. The pressure of the distillation column inherently determines the distillation operating temperature. 2,3,3,3-tetrafluoropropene may be recovered as distillate by operating the distillation column at from about 10 C. to about 90 C., preferably from about 0 C. to about 80 C. Single or multiple distillation columns may be used. In certain preferred embodiments, the levels of undesired 1225ye and trifluoropropyne in the final 1234yf product may be below 500, and 50 ppm, respectively.

EXAMPLES

(17) The following examples serve to demonstrate that high purity 1234yf can be produced through the process disclosed in the present invention.

Example 1

Purification of 245eb

(18) A glassware set-up was used for purifying 245eb. The distillation flask was cooled with wet ice and was then charged with 3.00 kg of 88.1% 245eb crude feed. A couple of boiling chips were added into the flask to aid boiling. After reattaching the flask, the liquid was heated to cause distillation. The progress of the distillation was followed by measuring the temperature of the vapor at the top of fractionation column and by analyzing the compositions of periodically collected distillates. 245eb was collected during the period when its 245eb concentration was 99.9%. In the end, 1.73 kg of purified feed was obtained.

Example 2

245eb Dehydrofluorination in Caustic Solution

(19) To a 50 gallon agitated reactor about 300 pounds of 245eb is charged into this vessel that contains a 20% molar excess of 25% KOH. A packed column with a condenser is also installed on top of the reactor, which is used to reflux the unreacted 245eb and relatively pure 1234yf is taken off at the exit of the condenser. The reaction is conducted at a temperature of 60 C. and the pressure is allowed to increase to about 190 psig and the product is taken off overhead as the reaction proceeds. Analysis of the product shows a 95.0% conversion of the 245eb and a selectivity of 96.9% to 1234yf.

Example 3

245eb Dehydrofluorination in the Presence of a Catalyst

(20) A Monel tube reactor (0.75 OD0.625 ID23.0 L) was charged with 20 cc of catalyst pellets. The reactor was heated by a 12 split tube furnace. A multi-point thermocouple, inserted through catalyst bed, was used to measure the temperatures at the bottom of catalyst bed and at the top of catalyst bed. A purified 245eb feed (>99.9%) was passed through catalyst bed at a rate of 6 g/h (grams/hour). The effluent was analyzed by an on-line GC to determine 245eb conversion and 1234yf selectivity.

(21) As shown in Table 1, the fluorinated Cr.sub.2O.sub.3 provided a 245eb conversion of about 99% and a selectivity of about 97% to 1234yf at 240-320 C., and the fluorinated MgO provided a 245eb conversion of about 98% and a selectivity of about 99% to 1234yf at 300-410 C.

(22) TABLE-US-00001 TABLE 1 245eb dehydrofluorination over fluorinated metal oxide catalysts Temp. Conversion Selectivity Selectivity, Bottom-Top 245eb 1234yf others Catalyst () (%) (%) (%) Fluorinated Cr.sub.2O.sub.3 240-320 98.9 96.9 3.1 Fluorinated MgO 300-410 97.8 98.8 1.2

Example 4

Purification of 1234yf

(23) Approximately 100.0 lbs of 1234yf crude product is charged into a distillation still, which consists of a 10 gallon reboiler, 2 inch ID by 10 feet propack column, and a shell and tube condenser. The column has about 30 theoretical plates. The distillation still is equipped with temperature, pressure, and differential pressure transmitters. The distillation is run at a pressure of about 85 psig. The distillate is sampled and analyzed by GC at regular intervals. 1234yf is collected during the period when its 1234yf purity is 99.9%. In the end, 75.5 lbs of purified product is obtained. GC analysis of the final product indicates it contains 100 ppm of 1225ye and 10 ppm of trifluoropropyne.