CA2185328C - Process for the purification of pentafluoroethane - Google Patents
Process for the purification of pentafluoroethane Download PDFInfo
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Abstract
A process for the purification of pentafluoroethane by removing chloropentafluoroethane therefrom which comprises adding to the impure pentafluoroethane a component which undergoes a non-ideal interaction with chloropentafluoroethane and/or with the azeotrope of chloropentafluoroethane and pentafluoroethane such that the volatility of chloropentafluoroethane and/or the azeotrope of chloropentafluoroethane and pentafluoroethane relative to bulk pentafluoroethane is increased and distilling the mixture.
Description
WO 95127689 ~ ~ PCTIGB95100672 PROCESS FOR THE PURIFICATION OF PENTAFLUOROETHANE
This invention relates to a process for the purification of pentafluoroethane (HFA 125) and particularly to a process for removing the impurity chloropentafluoroethane (CFC 115) from pentafluoroethane.
Recently, processes have been proposed for the production of pentafluoroethane which has been proposed, together with other hydrofluoroalkanes such as 1,1,1,2-tetrafluoroethane, difluoromethaneand 1,1,1-trifluoroethane, and blends thereof, as a suitable replacement for chlorofluorocarbons and hydrochlorofluorocarbons due to the zero ozone depleting potential of hydrofluoroalkanes.
Thus it has been proposed in Japanese Patent Application Nos Kokai 3099026, and 4029941 to produce pentafluoroethane by contacting pentafluorochloroethane with hydrogen in the presence of a hydrogenation catalyst. Suitable conditions of temperature and pressure and suitable catalysts are described in the aforementioned Japanese patent applications.
It has also been proposed to manufacture HFA 125 by the fluorination of perchloroethylene, chlorotetrafluoroethane and/or dichlorotrifluoroethane by reacting perchloroethylene, chlorotetrafluoroethane and/or dichlorotrifluoroethane with hydrogen fluoride in the vapour phase at a temperature in the range of about 200°C to 500° in the presence of a fluorination catalyst such as alumina, aluminium fluoride, aluminium oxyfluoride, chromic, halogenated chromia or chromium oxyhalide. The fluorination catalyst may also comprise one or more metals other than chromium or aluminium, for example zinc and/or nickel in combination with alumina and/or chromic.
However, these and other processes for the production of pentafluoroethane result in a product comprising pentafluoroethane together with impurities, in particular the chlorofluorocarbon impurity chloropentafluoroethane (CFC I 15).
The removal of CFC 115 from HFA 125 by distillation is possible in theory but is impractical ; the boiling points of the components are -38.7°C and -48°C respectively at atmospheric pressure and of the azeotrope thereof is -55°C at atmospheric pressure. To obtain pure 125 requires iarge stills with very low condenser temperatures.
Moreover, the azeotropic composition is rich in 125 (around 90 wt% HFA 125) and hence azeotropic distillation is wasteful of HFA 125. The separation is even more difficult at 2185328 ,~
superatmospheric pressure, where the relative volatility of HFA 125 versus CFC
115 is close to L0 as HF'A 125 purity of 100% is approached.
We have now found that CFC I IS can be effectively removed from HFA 125 by a technique herein termed third component distillation.
According to the present invention there is provided a process for the purification of pentafluoroethane by removing chloropentafluoroethane therefrom which comprises adding to the impure pentafluoroethane a component which undergoes a non-ideal interaction with chloropentafluoroethane and/or with the azeotrope of chloropentafluoroethane and pentaffuoroethane such that the volatility of chloropentafluoroethane and/or the azeotrope of chloropentafluoroethane and pentafluoroethane relative to bulk pentafluoroethane is increased and distilling the mixture.
The component added to the impure HFA 125 to increase the relative volatility of the CFC 115 is referred to hereinafter for convenience as "the third component"
although it is to be understood that the invention is not limited to treatment of compositions containing only the two components HFA 125 and CFC 1 I 5.
The third component may be any compound which undergoes a non-ideal interaction with CFC I 15 and/or the azeotrope of CFC 115 and HFA 125 whereby to increase the volatility of the CFC I 15 relative to bulk HFA 125 and thereby enable removal of the CFC
115 from the HFA 125 by simple distillation. In general, the compound preferably will be polar and will have a boiiing point below that of HFA 125 so that its effect is to increase the volatility of CFC 115 relative to bulk HFA 125 thereby enabling its removal as a top product from a distillation column or still whilst the HFA 125 is collected as a bottoms product from the column or still. Typically, in this case, the third component will have a boiling point less than -50°C. We especially prefer to employ a third component having a boiling point in the range of about -50°C to -100°C at atmospheric pressure.
A wide variety of compounds may be employed as the third component which may be an organic or inorganic compound. Examples of suitable inorganic compounds include hydrogen chloride (as well as mixtures thereof, for example with hydrogen fluoride) and carbon dioxide. Where an organic compound is employed, the organic compound may contain one or more carbon atoms. Where it contains two or more carbon atoms, the compound may be ethylerucally unsaturated or saturated. Mixtures of third components may be employed, if desired. The identification and selection of the third component is a matter _2_ WO 95!27689 218 5 3 2 $ . p~~Gg95/00672 of simple routine experiment on a trial and error basis. We prefer that the third component is selected from the group consisting of hydrogen chloride, carbon dioxide or a compound of formula CF2HX where X is Cl or H. We especially prefer to employ difluoromethane (I~'C 32) as the third component.
A factor which may affect the selection of the optimum third component is the subsequent treatment of the interaction product containing CFC I 15 which is removed from the distillation column or still; if this interaction product is disposed of by destruction, for example by thermal oxidation, then the amount of the third component not readily separable from CFC 115 should be minimised.
The selection of the optimum third component is often a compromise between high efficiency of CFC 115 removal, undesirable interaction with HFA 125 and subsequent separation and/or disposal of the CFC 115/third component interaction product.
We have found, though, that a particularly usefizl third component is difluoromethane.
The amount of third component added to the mixture will depend to a large extent upon the particular compound employed and the amount of the CFC 115 to be removed from the HFA 125. In general, however, and as a guide, the amount by weight ratio of the third component to CFC 1 I S in the mixture to be treated will be in the range from 1:2 to 200:1.
More particularly where the third component is a compound of formula CF2HX
where X is Cl or H, the weight ratio will be in the range from 1:2 to 10:1 and the amount by weight of the third component will usually be about equal to the amount by weight of CFC
115 to be removed. Where the third component is hydrogen chloride, the weight ratio is preferably in the range from 50:1 to 200:1.
The third component may be generated in situ. Thus, where the 115/125 mixture is produced by hydrogenation of 115, a compound may be co-fed to the hydrogenation process which, under the hydrogenation conditions is converted to the third component, or where the 1 IS/125 mixture is produced by hydrofluorination, then a compound may be co-fed to the hydrofluorination reaction which the under the hydrofluorination conditions is converted to the third component. Thus for example, where the third component is diffuoromethane, 12122 may be fed to the hydrogenation reaction together with 115 and methylene chloride may be feed to the hydrofluorination reaction.
Alternatively, where the third component employed is hydrogen chloride, the hydrogen chloride may be generated as a by-product of the HFA 125 production process, for example the hydrofluorination of
This invention relates to a process for the purification of pentafluoroethane (HFA 125) and particularly to a process for removing the impurity chloropentafluoroethane (CFC 115) from pentafluoroethane.
Recently, processes have been proposed for the production of pentafluoroethane which has been proposed, together with other hydrofluoroalkanes such as 1,1,1,2-tetrafluoroethane, difluoromethaneand 1,1,1-trifluoroethane, and blends thereof, as a suitable replacement for chlorofluorocarbons and hydrochlorofluorocarbons due to the zero ozone depleting potential of hydrofluoroalkanes.
Thus it has been proposed in Japanese Patent Application Nos Kokai 3099026, and 4029941 to produce pentafluoroethane by contacting pentafluorochloroethane with hydrogen in the presence of a hydrogenation catalyst. Suitable conditions of temperature and pressure and suitable catalysts are described in the aforementioned Japanese patent applications.
It has also been proposed to manufacture HFA 125 by the fluorination of perchloroethylene, chlorotetrafluoroethane and/or dichlorotrifluoroethane by reacting perchloroethylene, chlorotetrafluoroethane and/or dichlorotrifluoroethane with hydrogen fluoride in the vapour phase at a temperature in the range of about 200°C to 500° in the presence of a fluorination catalyst such as alumina, aluminium fluoride, aluminium oxyfluoride, chromic, halogenated chromia or chromium oxyhalide. The fluorination catalyst may also comprise one or more metals other than chromium or aluminium, for example zinc and/or nickel in combination with alumina and/or chromic.
However, these and other processes for the production of pentafluoroethane result in a product comprising pentafluoroethane together with impurities, in particular the chlorofluorocarbon impurity chloropentafluoroethane (CFC I 15).
The removal of CFC 115 from HFA 125 by distillation is possible in theory but is impractical ; the boiling points of the components are -38.7°C and -48°C respectively at atmospheric pressure and of the azeotrope thereof is -55°C at atmospheric pressure. To obtain pure 125 requires iarge stills with very low condenser temperatures.
Moreover, the azeotropic composition is rich in 125 (around 90 wt% HFA 125) and hence azeotropic distillation is wasteful of HFA 125. The separation is even more difficult at 2185328 ,~
superatmospheric pressure, where the relative volatility of HFA 125 versus CFC
115 is close to L0 as HF'A 125 purity of 100% is approached.
We have now found that CFC I IS can be effectively removed from HFA 125 by a technique herein termed third component distillation.
According to the present invention there is provided a process for the purification of pentafluoroethane by removing chloropentafluoroethane therefrom which comprises adding to the impure pentafluoroethane a component which undergoes a non-ideal interaction with chloropentafluoroethane and/or with the azeotrope of chloropentafluoroethane and pentaffuoroethane such that the volatility of chloropentafluoroethane and/or the azeotrope of chloropentafluoroethane and pentafluoroethane relative to bulk pentafluoroethane is increased and distilling the mixture.
The component added to the impure HFA 125 to increase the relative volatility of the CFC 115 is referred to hereinafter for convenience as "the third component"
although it is to be understood that the invention is not limited to treatment of compositions containing only the two components HFA 125 and CFC 1 I 5.
The third component may be any compound which undergoes a non-ideal interaction with CFC I 15 and/or the azeotrope of CFC 115 and HFA 125 whereby to increase the volatility of the CFC I 15 relative to bulk HFA 125 and thereby enable removal of the CFC
115 from the HFA 125 by simple distillation. In general, the compound preferably will be polar and will have a boiiing point below that of HFA 125 so that its effect is to increase the volatility of CFC 115 relative to bulk HFA 125 thereby enabling its removal as a top product from a distillation column or still whilst the HFA 125 is collected as a bottoms product from the column or still. Typically, in this case, the third component will have a boiling point less than -50°C. We especially prefer to employ a third component having a boiling point in the range of about -50°C to -100°C at atmospheric pressure.
A wide variety of compounds may be employed as the third component which may be an organic or inorganic compound. Examples of suitable inorganic compounds include hydrogen chloride (as well as mixtures thereof, for example with hydrogen fluoride) and carbon dioxide. Where an organic compound is employed, the organic compound may contain one or more carbon atoms. Where it contains two or more carbon atoms, the compound may be ethylerucally unsaturated or saturated. Mixtures of third components may be employed, if desired. The identification and selection of the third component is a matter _2_ WO 95!27689 218 5 3 2 $ . p~~Gg95/00672 of simple routine experiment on a trial and error basis. We prefer that the third component is selected from the group consisting of hydrogen chloride, carbon dioxide or a compound of formula CF2HX where X is Cl or H. We especially prefer to employ difluoromethane (I~'C 32) as the third component.
A factor which may affect the selection of the optimum third component is the subsequent treatment of the interaction product containing CFC I 15 which is removed from the distillation column or still; if this interaction product is disposed of by destruction, for example by thermal oxidation, then the amount of the third component not readily separable from CFC 115 should be minimised.
The selection of the optimum third component is often a compromise between high efficiency of CFC 115 removal, undesirable interaction with HFA 125 and subsequent separation and/or disposal of the CFC 115/third component interaction product.
We have found, though, that a particularly usefizl third component is difluoromethane.
The amount of third component added to the mixture will depend to a large extent upon the particular compound employed and the amount of the CFC 115 to be removed from the HFA 125. In general, however, and as a guide, the amount by weight ratio of the third component to CFC 1 I S in the mixture to be treated will be in the range from 1:2 to 200:1.
More particularly where the third component is a compound of formula CF2HX
where X is Cl or H, the weight ratio will be in the range from 1:2 to 10:1 and the amount by weight of the third component will usually be about equal to the amount by weight of CFC
115 to be removed. Where the third component is hydrogen chloride, the weight ratio is preferably in the range from 50:1 to 200:1.
The third component may be generated in situ. Thus, where the 115/125 mixture is produced by hydrogenation of 115, a compound may be co-fed to the hydrogenation process which, under the hydrogenation conditions is converted to the third component, or where the 1 IS/125 mixture is produced by hydrofluorination, then a compound may be co-fed to the hydrofluorination reaction which the under the hydrofluorination conditions is converted to the third component. Thus for example, where the third component is diffuoromethane, 12122 may be fed to the hydrogenation reaction together with 115 and methylene chloride may be feed to the hydrofluorination reaction.
Alternatively, where the third component employed is hydrogen chloride, the hydrogen chloride may be generated as a by-product of the HFA 125 production process, for example the hydrofluorination of
2 ~ g ~ 3 2 g PCTIGB95/00672 perchloroethylene/dichlorotrifluoroethane and the hydrogenation of chloropentafluoroethane.
Distillation of the mixture may be carried out at atmospheric, superatmospheric or subatmospheric pressure, superatmospheric pressure of from about 2 bar to about 15 bar, especially from about 2 bar to about 10 bar, being preferred. The temperature profile within the distillation column or still will usually be such that distillation occurs under conditions of partial reflux, for example a bottoms (I-IF'A 125) fraction temperature of about 10°C to 30°C at about 10 bar pressure.
The process is useful for the treatment of HFA 125 containing a wide range of amounts of CFC 115 impurity, for example as little as 0.1% CFC 115 or as much as 20%
(or even more) CFC 115. Where the amount of the impurity is low a single pass through the distillation column or still will usually be sufficient to reduce the impurity level in the HFA
125 to an acceptable level, eg below 10 ppm, whilst where the initial impurity level is high it may be desirable to pass the HFA 125 through the column or still more than once to employ more than one column or still to excessively reduce the level of the impurity.
The products of the separation are a bottoms fraction comprising purified HFA
125 and an overheads fraction comprising CFC 115 and the third component. The overheads fraction may be disposed of, for instance by thermal oxidation, but if desired it may be separated, for example by further reaction of the CFC 115 content eg by hydrogenation or reaction with LiAlH4. The third component thus obtained may be recycled to the purification stage.
It is possible, by carefitl control of the operating conditions, to obtain a bottoms fraction (HF'A 125) essentially free from CFC 1 I5 and an overheads fraction essentially free from HFA 125 in a single separation stage. However it may be preferable in practice to effect the separation in two stages. In one embodiment of the two stage process, the overheads fi~action from the first stage contains some HFA 125 and comprises the third component, CFC 115 and HFA 125 and the bottoms fraction comprises HFA 125. The overheads fraction is then separated in a second stage to obtain a second-stage overheads fraction comprising the third component and CFC 115 and a second-stage bottoms fraction comprising the third component and HFA 125. Where the third component is difluoromethane, the second-stage bottoms fraction may be collected far use as or as a 2?85328 component of refrigerant compositions (blends) or it may be recycled to the first-stage separation column or still.
In another embodiment of the two stage process the overheads fraction from the first stage comprises the third component, CFC 115 and possibly a small amount of HFA 125 and the bottoms fraction comprises the third component and I-IFA 125.
The first-stage bottoms fraction is passed together with additional third component to a second stage column or still from which are withdrawn a second-stage bottoms fraction comprising essentially pure HFA 125 and a second-stage overheads fraction comprising the third component and a small amount of HEA 125. The second-stage overheads fraction is fed together with impure HF'A 125 (containing CFC 115) to the first-stage column or still.
Two-stage embodiments of the process will now be described with reference to the accompanying drawings which show schematic representations of alternative embodiments of the process employing two distillation columns or stills.
With reference to Figure 1 of the drawings, impure HFA 125 such as the product of a HF'A 125 production process is fed to a distillation column 1 via feed line 2 and a liquid third component (hereinafter HFA-32 for convenience) is fed to column 1 via feed line 3. A
bottoms fraction comprising HFA 125 essentially free from CFC 115 is withdrawn via outlet 4 and an overheads fraction comprising I->F'A 32, CFC 115 and IdF'A 125 is withdrawn via outlet 5. The overheads fraction is fed to a second distillation column 6. A
second-stage overheads fraction comprising FJF'A 32 and CFC 115 is withdrawn from column 6 via outlet 7 whilst a second-stage bottoms fraction comprising I-3F'A
32 and HFA
125 is withdrawn from column 6 via outlet 8.
The second-stage bottoms fraction withdrawn via outlet 8 may be collected via product line 9 or recycled via recycle line 10 to the first-stage distillation column 1. The second-stage overheads fraction withdrawn via outlet 7 may be passed to disposal or treated to recover HFA 32, in which case the HFA 32 may be recycled to the first-stage distillation column 1 or the second-stage distillation column 2.
With reference to Figure 2 of the drawings, impure HFA 125 (containing CFC
115) is fed to a first distillation column 103 via feed line 101 and HFA 32 is fed to the column 103 via feed line 102. The overheads fraction from a second column 106, comprising w0 95/27689 PCTIGB95100672 and HFA 125, is fed via Gne 108 to the first column 103 and essentially pure HFA 125 is withdrawn as a bottoms fraction via line 107. An overheads fraction comprising HFA 32, CFC 115 and probably a little HFA 125 is withdrawn from the first column 103 via line 104 and a bottoms fraction comprising HFA 32 and HFA 125 is withdrawn via line 105 and fed to the second column 106.
The invention is illustrated but in no way limited by the following examples.
Example 1 All compositions are quoted as mole percentages.
A still comprising a 250 ml flask, a 5 stage vacuum jacketed packed column (2.5 cm diameter), condenser and take-off controller was charged at -80°C with 155.4g of a mixture of 88.5% HFA 125, 1.6% CFC 115 and 9.9% HFA 32. The column was stabilised under I S total reflux (still bottom temperature -52°C) at atmospheric pressure. Following equilibration, a vapour sample was removed from the column top and was shown by GC
analysis to have the composition:
HFA 125-80.3% HFA 32-16.5% CFC 115-2.6%
Distillation was commenced at a reflux ratio of 5:1 and after approximately half the charge was removed, the distillate composition was:
HFA 125-90.9% HFA 32-7.8% CFC I 15-0.9%
Comparative Example The above experiment was repeated using 150g of a mixture of IiFA 125-98.2%
and CFC
115-1.8%. After equilibration under total reflux a vapour sample was taken and analysed as:
HFA 125-98.0% CFC 115-2.0%
After distillation of about half the charge at a reflux ratio of 5:1, the distillate composition was:
HFA 125-98.3% CFC 115-1.7%
Examples 2-4 These examples demonstrate the removal of CFC 115 from impure HFA 125 by selective entrainment in HFA 32 during third-component distillation.
The distillations were performed in a Hastelloy C still equipped with a 3.5 cm internal diameter column having 6 theoretical stages. The still was charged with material, left to equilibrate under total reflux and sampled at 6 points. Column profile compositions were obtained by GC analysis and are recorded as mole percentages.
Comparative Example HFA 125 and CFC 115 distillation with no HFA 32 Charge:
HFA 125 = 13328 Still Pressure = 5.9 Bar Still Profile Sample Position Temp °C HFA 125 CFC 115 Condenser -5 98.72 1.28 Top -2.8 98.77 1.23 Upper -3.6 98.92 1.07 Lower -3.1 99 0.99 Bottom -1:5 98.92 1.08 Reboiler I 99.11 0.89 _'7_ WO 95127689 ~ ~ ~ ~ ~ PCTIGB95/00672 These results show little change in the relative amounts of 115 and 125 throughout the column.
Example 2 HFA 125 CFC 115 Separation with HFA 32. [32:115 Molar Feed Ratio = 4.5:1 ]
Charge: ' HFA 125 773g:
CFC 115 37.6g:
HFA 32 57g: 6.6 Still Pressure = 6.6 bar Sample Position Temp °C CFC 115 HFA 32 HFA 125 Condenser - 4.39 17.49 78.11 IS Top -4.5 1.35 9.76 88.87 Upper -1.4 0.33 0.9 98.76 Lower -1.2 0.33 0.58 99.08 Bottom 0 0.37 0.46 99.16 Reboiler 1.8 0.45 0.5 99.03 This example shows that the concentration of CFC 115 alters significantly across the column in the presence of HFA 32, with higher CFC 115 concentrations at the top of the column.
Example 3 HFA 125 CFC 115 Separation With HFA 32.[32:115 Molar Feed Ratio = 11.1]
Charge HFA 125 = 877g CFC 115 = 17g HFA 32 = 1688 Still Pressure = 6.6 Bar r _g_ Sample Position Temp °C FiFA 125 CFC I15 HFA 32 Condenser - 41.5 9.6 48.8 Top -7 43.9 5 51.1 Upper -5 55.6 0.9 43.5 Lower -4 87.2 0.1 12.7 Bottom 2 - - -Reboiler 3 98 0.5 1.5 This example, when compared with Example 2, demonstrates that the concentration of CFC
115 at the top of the still is increased with increasing HFA 32 concentration in the feed.
Example 4 HFA 125/CFC 115 Separation With HFA 32.[32: 115 Molar Feed Ratio = 11:1]
Charge HFA 125 = 877g, CFC I 15 = 17g, F1FA 32 = 168g:
Still Pressure = 12.8 Bar Sample Position Temp °C 125 115 32 Condenser 14 55.2 4.1 40.7 Top 15 56.2 3.8 40 Upper 17 78.3 1.4 20.2 Lower 20 99.3 0.2 0.5 Bottom 23 99.3 0.2 0.5 Reboiler 43 99.2 0.2 0.7 Example 5.
The use of hydrogen chloride (HCl) as the entrainer in the separation of 8125 from Rl 15 in a nuxture containing 1 mol% RI 15 has been modelled using the'RADFRAC' [Aspen Technology Ltd] calculation package and measured physical properties data which is both publicly and freely available.
The calculations were carried out considering a distillation column with 39 theoretical stages and having a single column feed point at the 14th stage (counting from the top of the column). A 4.67 :1.00:0.01 molar ratio of HCIIR125/CFC 115 liquid feed is admitted to a column operating at a pressure of I O Bara. The column has a total condenser operating at a refiux ratio of 3. A tops fraction of RI15IHC1 is produced and a bottoms fraction of 8125 with minor impurities of RI 15 and HCI. The 8125 product purity achieved is 99.87 mol%.
1 S The column must be controlled such that the HCl composition profile has a significant mole fraction in stages I S-25 where the majority of the R125/R115 separation is to occur. A
calculated mass balance for the column is given below in which "lights" is the tops fraction from the column and "product" is the bottoms fraction from the column..
COLUMN
MASS
MOLAR MOLE FRACTION
FLOW
STREAM TEMP HCl 8125 8115 HCl 8125 8115 deg C
FEED -35 19.45 4.17 0.04 0.82 0.18 0 LIGHTS -31.9 19.45 0.1 0.04 0.99 0.01 0 PRODUCT I 13.2 0 I 4.07 I 0.01 I 0 ~ 1 I
BALANCE
Distillation of the mixture may be carried out at atmospheric, superatmospheric or subatmospheric pressure, superatmospheric pressure of from about 2 bar to about 15 bar, especially from about 2 bar to about 10 bar, being preferred. The temperature profile within the distillation column or still will usually be such that distillation occurs under conditions of partial reflux, for example a bottoms (I-IF'A 125) fraction temperature of about 10°C to 30°C at about 10 bar pressure.
The process is useful for the treatment of HFA 125 containing a wide range of amounts of CFC 115 impurity, for example as little as 0.1% CFC 115 or as much as 20%
(or even more) CFC 115. Where the amount of the impurity is low a single pass through the distillation column or still will usually be sufficient to reduce the impurity level in the HFA
125 to an acceptable level, eg below 10 ppm, whilst where the initial impurity level is high it may be desirable to pass the HFA 125 through the column or still more than once to employ more than one column or still to excessively reduce the level of the impurity.
The products of the separation are a bottoms fraction comprising purified HFA
125 and an overheads fraction comprising CFC 115 and the third component. The overheads fraction may be disposed of, for instance by thermal oxidation, but if desired it may be separated, for example by further reaction of the CFC 115 content eg by hydrogenation or reaction with LiAlH4. The third component thus obtained may be recycled to the purification stage.
It is possible, by carefitl control of the operating conditions, to obtain a bottoms fraction (HF'A 125) essentially free from CFC 1 I5 and an overheads fraction essentially free from HFA 125 in a single separation stage. However it may be preferable in practice to effect the separation in two stages. In one embodiment of the two stage process, the overheads fi~action from the first stage contains some HFA 125 and comprises the third component, CFC 115 and HFA 125 and the bottoms fraction comprises HFA 125. The overheads fraction is then separated in a second stage to obtain a second-stage overheads fraction comprising the third component and CFC 115 and a second-stage bottoms fraction comprising the third component and HFA 125. Where the third component is difluoromethane, the second-stage bottoms fraction may be collected far use as or as a 2?85328 component of refrigerant compositions (blends) or it may be recycled to the first-stage separation column or still.
In another embodiment of the two stage process the overheads fraction from the first stage comprises the third component, CFC 115 and possibly a small amount of HFA 125 and the bottoms fraction comprises the third component and I-IFA 125.
The first-stage bottoms fraction is passed together with additional third component to a second stage column or still from which are withdrawn a second-stage bottoms fraction comprising essentially pure HFA 125 and a second-stage overheads fraction comprising the third component and a small amount of HEA 125. The second-stage overheads fraction is fed together with impure HF'A 125 (containing CFC 115) to the first-stage column or still.
Two-stage embodiments of the process will now be described with reference to the accompanying drawings which show schematic representations of alternative embodiments of the process employing two distillation columns or stills.
With reference to Figure 1 of the drawings, impure HFA 125 such as the product of a HF'A 125 production process is fed to a distillation column 1 via feed line 2 and a liquid third component (hereinafter HFA-32 for convenience) is fed to column 1 via feed line 3. A
bottoms fraction comprising HFA 125 essentially free from CFC 115 is withdrawn via outlet 4 and an overheads fraction comprising I->F'A 32, CFC 115 and IdF'A 125 is withdrawn via outlet 5. The overheads fraction is fed to a second distillation column 6. A
second-stage overheads fraction comprising FJF'A 32 and CFC 115 is withdrawn from column 6 via outlet 7 whilst a second-stage bottoms fraction comprising I-3F'A
32 and HFA
125 is withdrawn from column 6 via outlet 8.
The second-stage bottoms fraction withdrawn via outlet 8 may be collected via product line 9 or recycled via recycle line 10 to the first-stage distillation column 1. The second-stage overheads fraction withdrawn via outlet 7 may be passed to disposal or treated to recover HFA 32, in which case the HFA 32 may be recycled to the first-stage distillation column 1 or the second-stage distillation column 2.
With reference to Figure 2 of the drawings, impure HFA 125 (containing CFC
115) is fed to a first distillation column 103 via feed line 101 and HFA 32 is fed to the column 103 via feed line 102. The overheads fraction from a second column 106, comprising w0 95/27689 PCTIGB95100672 and HFA 125, is fed via Gne 108 to the first column 103 and essentially pure HFA 125 is withdrawn as a bottoms fraction via line 107. An overheads fraction comprising HFA 32, CFC 115 and probably a little HFA 125 is withdrawn from the first column 103 via line 104 and a bottoms fraction comprising HFA 32 and HFA 125 is withdrawn via line 105 and fed to the second column 106.
The invention is illustrated but in no way limited by the following examples.
Example 1 All compositions are quoted as mole percentages.
A still comprising a 250 ml flask, a 5 stage vacuum jacketed packed column (2.5 cm diameter), condenser and take-off controller was charged at -80°C with 155.4g of a mixture of 88.5% HFA 125, 1.6% CFC 115 and 9.9% HFA 32. The column was stabilised under I S total reflux (still bottom temperature -52°C) at atmospheric pressure. Following equilibration, a vapour sample was removed from the column top and was shown by GC
analysis to have the composition:
HFA 125-80.3% HFA 32-16.5% CFC 115-2.6%
Distillation was commenced at a reflux ratio of 5:1 and after approximately half the charge was removed, the distillate composition was:
HFA 125-90.9% HFA 32-7.8% CFC I 15-0.9%
Comparative Example The above experiment was repeated using 150g of a mixture of IiFA 125-98.2%
and CFC
115-1.8%. After equilibration under total reflux a vapour sample was taken and analysed as:
HFA 125-98.0% CFC 115-2.0%
After distillation of about half the charge at a reflux ratio of 5:1, the distillate composition was:
HFA 125-98.3% CFC 115-1.7%
Examples 2-4 These examples demonstrate the removal of CFC 115 from impure HFA 125 by selective entrainment in HFA 32 during third-component distillation.
The distillations were performed in a Hastelloy C still equipped with a 3.5 cm internal diameter column having 6 theoretical stages. The still was charged with material, left to equilibrate under total reflux and sampled at 6 points. Column profile compositions were obtained by GC analysis and are recorded as mole percentages.
Comparative Example HFA 125 and CFC 115 distillation with no HFA 32 Charge:
HFA 125 = 13328 Still Pressure = 5.9 Bar Still Profile Sample Position Temp °C HFA 125 CFC 115 Condenser -5 98.72 1.28 Top -2.8 98.77 1.23 Upper -3.6 98.92 1.07 Lower -3.1 99 0.99 Bottom -1:5 98.92 1.08 Reboiler I 99.11 0.89 _'7_ WO 95127689 ~ ~ ~ ~ ~ PCTIGB95/00672 These results show little change in the relative amounts of 115 and 125 throughout the column.
Example 2 HFA 125 CFC 115 Separation with HFA 32. [32:115 Molar Feed Ratio = 4.5:1 ]
Charge: ' HFA 125 773g:
CFC 115 37.6g:
HFA 32 57g: 6.6 Still Pressure = 6.6 bar Sample Position Temp °C CFC 115 HFA 32 HFA 125 Condenser - 4.39 17.49 78.11 IS Top -4.5 1.35 9.76 88.87 Upper -1.4 0.33 0.9 98.76 Lower -1.2 0.33 0.58 99.08 Bottom 0 0.37 0.46 99.16 Reboiler 1.8 0.45 0.5 99.03 This example shows that the concentration of CFC 115 alters significantly across the column in the presence of HFA 32, with higher CFC 115 concentrations at the top of the column.
Example 3 HFA 125 CFC 115 Separation With HFA 32.[32:115 Molar Feed Ratio = 11.1]
Charge HFA 125 = 877g CFC 115 = 17g HFA 32 = 1688 Still Pressure = 6.6 Bar r _g_ Sample Position Temp °C FiFA 125 CFC I15 HFA 32 Condenser - 41.5 9.6 48.8 Top -7 43.9 5 51.1 Upper -5 55.6 0.9 43.5 Lower -4 87.2 0.1 12.7 Bottom 2 - - -Reboiler 3 98 0.5 1.5 This example, when compared with Example 2, demonstrates that the concentration of CFC
115 at the top of the still is increased with increasing HFA 32 concentration in the feed.
Example 4 HFA 125/CFC 115 Separation With HFA 32.[32: 115 Molar Feed Ratio = 11:1]
Charge HFA 125 = 877g, CFC I 15 = 17g, F1FA 32 = 168g:
Still Pressure = 12.8 Bar Sample Position Temp °C 125 115 32 Condenser 14 55.2 4.1 40.7 Top 15 56.2 3.8 40 Upper 17 78.3 1.4 20.2 Lower 20 99.3 0.2 0.5 Bottom 23 99.3 0.2 0.5 Reboiler 43 99.2 0.2 0.7 Example 5.
The use of hydrogen chloride (HCl) as the entrainer in the separation of 8125 from Rl 15 in a nuxture containing 1 mol% RI 15 has been modelled using the'RADFRAC' [Aspen Technology Ltd] calculation package and measured physical properties data which is both publicly and freely available.
The calculations were carried out considering a distillation column with 39 theoretical stages and having a single column feed point at the 14th stage (counting from the top of the column). A 4.67 :1.00:0.01 molar ratio of HCIIR125/CFC 115 liquid feed is admitted to a column operating at a pressure of I O Bara. The column has a total condenser operating at a refiux ratio of 3. A tops fraction of RI15IHC1 is produced and a bottoms fraction of 8125 with minor impurities of RI 15 and HCI. The 8125 product purity achieved is 99.87 mol%.
1 S The column must be controlled such that the HCl composition profile has a significant mole fraction in stages I S-25 where the majority of the R125/R115 separation is to occur. A
calculated mass balance for the column is given below in which "lights" is the tops fraction from the column and "product" is the bottoms fraction from the column..
COLUMN
MASS
MOLAR MOLE FRACTION
FLOW
STREAM TEMP HCl 8125 8115 HCl 8125 8115 deg C
FEED -35 19.45 4.17 0.04 0.82 0.18 0 LIGHTS -31.9 19.45 0.1 0.04 0.99 0.01 0 PRODUCT I 13.2 0 I 4.07 I 0.01 I 0 ~ 1 I
BALANCE
Claims (11)
1. A process for the purification of pentafluoroethane by removing chloropentafluoroethane therefrom which comprises adding to the impure pentafluoroethane a component which undergoes a non-ideal interaction with chloropentafluoroethane and/or with the azeotrope of chloropentafluoroethane and pentafluoroethane such that the volatility of chloropentafluoroethane and/or the azeotrope of chloropentafluoroethane and pentafluoroethane relative to bulk pentafluoroethane is increased and distilling the mixture.
2. A process as claimed in claim 1 in which the component is polar and has a boiling point below that of HFA 125 whereby to increase the volatility of CFC 115 relative to bulk HFA
125 thereby enabling the removal of CFC 115 as a top product from a distillation column or still whilst the HFA 125 is collected as a bottoms product from the column or still.
125 thereby enabling the removal of CFC 115 as a top product from a distillation column or still whilst the HFA 125 is collected as a bottoms product from the column or still.
3. A process as claimed in claim 1 or claim 2 in which the component has a boiling point less than -50°C.
4. A process as claimed in claim 1 to claim 3 in which the component has a boiling point in the range of about -50°C to -100°C at atmospheric pressure.
5. A process as claimed in any one of claims 1 to 4 in which the component is selected from hydrogen chloride or a compound of formula CF2HX in which X is H or Cl.
6. A process as claimed in claim 5 in which the component is difluoromethane.
7. A process as claimed in any one of claims 1 to 6 in which the amount of the component added is such that the weight ratio of chloropentafluoroethane to component is in the range from about 10:1 to about 1:10.
8. A process as claimed in any one of claims 1 to 7 in which the distillation is effected at a pressure in the range from about 2 barg to about 15 barg.
9. A process as claimed in any one of claims 1 to 8 in which the distillation is effected at a temperature such that the distillation occurs under conditions of partial reflux.
10. A process as claimed in claim 2 in which the tops fraction from the distillation column or still comprising chloropentafluoroethane and the component is then treated to separate the component from CFC 115 and the component is recycled to the distillation column or still.
11. A process as claimed in claim 2 in which the tops fraction comprising pentafluoroethane chloropentafluoroethane and the component is passed to a second distillation column or still from which a tops fraction comprising the component and 115 and a bottoms fraction comprising 125 and the component are recovered.
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9406961.4 | 1994-04-08 | ||
| GB9406961A GB9406961D0 (en) | 1994-04-08 | 1994-04-08 | Process for the purification of pentafluoroethane |
| GB9417868A GB9417868D0 (en) | 1994-09-06 | 1994-09-06 | Process for the purification of pentafluoroethane |
| GB9417868.8 | 1994-09-06 | ||
| GB9420510.1 | 1994-10-11 | ||
| GB9420510A GB9420510D0 (en) | 1994-10-11 | 1994-10-11 | Process for the purification of pentafluoroethane |
| PCT/GB1995/000672 WO1995027689A1 (en) | 1994-04-08 | 1995-03-27 | Process for the purification of pentafluoroethane |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2185328A1 CA2185328A1 (en) | 1995-10-19 |
| CA2185328C true CA2185328C (en) | 2006-02-07 |
Family
ID=35891039
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002185328A Expired - Fee Related CA2185328C (en) | 1994-04-08 | 1995-03-27 | Process for the purification of pentafluoroethane |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2185328C (en) |
-
1995
- 1995-03-27 CA CA002185328A patent/CA2185328C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2185328A1 (en) | 1995-10-19 |
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