Classifications

• • C—CHEMISTRY; METALLURGY
  • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
  • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
  • C25B3/00—Electrolytic production of organic compounds
  • C25B3/20—Processes
  • C25B3/27—Halogenation
  • C25B3/28—Fluorination

Definitions

• the present invention relates to a process for the electrochemical fluorination ofalkanes.
• Fluorinated alkanes are commercially valuable and useful chemical materials. Fluorinated alkanes can exhibit various useful properties, e.g., they may be inert, nonpolar, hydrophobic, oleophobic, etc. As such, these fluorochemicals can be useful in a wide variety of applications, such as for inert fluids, solvents, cleaning fluids, heat transfer fluids, foam blowing agents, oxygen carriers in artificial blood, etc. Due to the versatility of fluorinated alkanes, and a consequent strong demand for these materials, there is a continuing need for new and improved methods of preparing fluorinated alkanes.
• the Simons process of electrochemical fluorination although commercially useful, includes aspects that might desirably be improved upon.
• the Simons process requires a significant amount of electrical energy passing through the electrolyte solution.
• Much electrical energy is effectively used to fluorinate the substrate, but a certain amount of this electrical energy converts to heat energy that must necessarily be carried away from the electrochemical fluorination cell as wasted energy, and adds to the overall cost of operating the process. It would be desirable to reduce the amount of electrical energy that is wasted as dissipated heat energy in the Simons process, and thereby reduce the overall cost of electricity needed to operate this process.
• the conventional Simons process often includes the use of conductivity additives to allow the passage of current through the electrolyte solution. See for example J. Burdon and J.C. Tatlow, The Electrochemical Process for the Synthesis of Fluoro-Organic Compounds, Advances in Fluorine Chemistry, edited by M. Stacey et al., volume 1 p. 129 (1960).
• Conductivity additives can cause undesired results when used in the Simons process.
• Conductivity additives for example, can interfere with the fluorination of the substrate, either by causing increased corrosion of the anode, or by themselves being consumed or fluorinated in the fluorination reaction. This can reduce the overall yield of the desired fluorinated product, and in many ways can increase the costs of the fluorination operation. Therefore, it would be desirable to reduce or even substantially eliminate the need for conductivity additives.
• the Simons process can be difficult to maintain at steady state for extended periods of time because high resistance by-product films and tars can tend to accumulate on electrodes of the fluorination cell, specifically, at the anode.
• the accumulation of films and tars on the anode causes increased resistance of the electrochemical cell, and an upward drift in cell voltage.
• the problem can become more serious and lead to the condition referred to as "current blocking,” which is manifested as a permanent increase of resistance and loss of conductivity within the cell.
• To correct current blocking often requires shut-down of the apparatus for cleaning. It would therefore be desirable to prevent increases in the resistance of a fluorination cell that can lead to loss of conductivity within the cell, and the permanent condition of current blocking.
• Simons electrochemical fluorination is not considered to be especially useful in fluorinating hydrocarbon alkanes to produce fluorinated alkanes.
• the substrate To fluorinate a substrate using the Simons process, the substrate must be dissolved in the reaction solution.
• functional compounds such as hydrocarbon carbonyl fluorides and hydrocarbon sulfonyl fluorides can often be soluble in anhydrous hydrogen fluoride and can thus be relatively easily fluorinated by the Simons process, hydrocarbons and halohydrocarbons are less soluble in hydrogen fluoride, and are therefore somewhat difficult to fluorinate using the Simons process.
• U.S. Pat. No. 3,950,235 (Benninger) notes the difficulty of preparing perfluoroalkanes by the Simons electrochemical fluorination of aliphatic hydrocarbons (due to the "insolubility" of the hydrocarbons in hydrogen fluoride) or by the Simons electrochemical fluorination of olefinic hydrocarbons (because of the quick anode blocking resulting from the formation of polymer products on the anode surface) and describes an alternative process wherein branched perfluoroolefins are electrochemically fluorinated to produce the corresponding branched perfluoroalkanes.
• JP 4-12243 (Daikin Kogyo KK.) describes a process for preparing octafluoropropane by electrochemically fluorinating hexafluoropropene using an alkyl amine as a conductivity additive. This additive is said to function without seriously corroding the anode, and, if propyl amine or dipropyl amine is chosen, is said to be converted to additional octafluoropropane during the fluorination process.
• U.S. Pat. No. 3,957,596 (Seto) discloses an improved process for the electrochemical fluorination of hydrocarbons, wherein the electrochemical fluorination cell is maintained at superatmospheric pressure, conductivity additives are omitted, and the electrode gap, turbulence, and electrical energy input are controlled to provide improved yield and current efficiency.
• the present invention relates to a process for the electrochemical fluorination of alkane hydrocarbons.
• a reaction solution is provided that comprises an alkane substrate and hydrogen fluoride.
• An electric potential (voltage) is established across the reaction solution causing an electric current to pass through the reaction solution, and thereby causing fluorination of the alkane substrate.
• the electric current is periodically and regularly interrupted, i.e., the current flows at a first current level, identified as an elevated current level, and is periodically interrupted to flow at a reduced current level.
• the current is interrupted in such a manner that the resistance of the electrochemical fluorination cell operated under the conditions of the present invention is lower than the resistance of the cell operated without interruption of the current.
• the current can be interrupted in such a manner that the resistance of the fluorination cell will be reduced compared to the resistance of the same fluorination cell operating with uninterrupted current.
• the reduced cell resistance resulting from interrupted current in turn results in a lower cell voltage being required to achieve fluorination at constant current; i.e., the voltage between the anode and the cathode with interrupted electric current can be lower relative to the voltage of the same cell, operated with the same amount of current, wherein the current is interrupted.
• the cell resistance is comparatively lower, the amount of wasted heat energy created during the fluorination process is also reduced, reducing or eliminating the need to remove wasted heat energy from the fluorination cell.
• the achievement of a lower operating voltage allows stable cell operation at higher current densities, which in turn allows more product to be produced in a given time period, and extended production runs (e.g., days, weeks, etc.) without significant interruptions.
• reduced cell voltage, cell resistance, and increased current result in a more efficient process with higher production rates of a fluorinated product, often at a lower cost.
• interrupted current can reduce or eliminate the need for conductivity additives in an electrochemical fluorination process.
• An aspect of the present invention relates to a process for fluorinating an alkane substrate using an electrochemical fluorination cell.
• the process includes the steps of: (1) providing an alkane substrate comprising at least one carbon-bonded hydrogen; (2) preparing a reaction solution comprising the alkane substrate and hydrogen fluoride; (3) passing electric current through the reaction solution sufficient to cause replacement of one or more hydrogens of the alkane substrate with fluorine.
• the electric current is interrupted through a cycle defined by current levels comprising an elevated current and a reduced current, and in such a manner that the resistance of the cell operated with interrupted current is lower than the resistance of the cell operated with uninterrupted current.
• Another aspect of the present invention relates to a method for perfluorinating an alkane substrate according to the above method.
• Yet another aspect of the invention relates to a process for electrochemical fluorination including the steps of: providing a substrate having at least one carbon- bonded hydrogen; providing a fluorochemical in which the substrate is soluble; providing an electrochemical fluorination cell; providing hydrogen fluoride; introducing the substrate to the fluorochemical so that the substrate dissolves into the fluorochemical; introducing the hydrogen fluoride to the electrochemical fluorination cell; introducing the fluorochemical with substrate dissolved therein, to the fluorochemical cell, at a temperature that is below the temperature of the hydrogen fluoride; and passing electric current through the cell sufficient to cause replacement of one or more hydrogens of the substrate with fluorine.
• Fluorinated refers to chemical compounds having at least one carbon- bonded hydrogen replaced by a fluorine, and specifically includes perfluorinated compounds.
• Perfluorinated compounds refers to chemical compounds in which essentially all carbon-bonded hydrogens have been replaced by fluorines, although typically some residual hydride will be present in a perfluorinated composition; e.g., preferably less than 1 milligram hydride per gram perfluorinated product.
• Uninterrupted current refers to the electric current flowing through an electrochemical fluorination cell, wherein the current is substantially constant; i.e., not substantially varied, and specifically, not periodically interrupted as described in the following description.
• Figures 1 and 2 are graphs of current versus process time; the current is interrupted according to the present invention.
• Figures 3 and 4 are graphs of voltage versus process time, with voltage varying according to the present invention.
• Figure 5 is a graph of electric power versus process time, with power varying according to the present invention.
• Figure 6 is a graph of current versus time with current being interrupted (varying) in a sinusoidal manner according to the present invention.
• Figure 7 is a graph of current versus terminal voltage of an electrochemical fluorination cell during a fluorination process.
• Figure 8 schematically illustrates an embodiment of the invention wherein the fluorinated product (fluorochemical phase) is recirculated and combined with the alkane substrate feed in a decanter, and the substrate is fed to the cell as a solute within the fluorochemical phase.
• the present invention relates to methods of fluorinating a substrate to produce a fluorinated product.
• the methods can be practiced according to methods similar to electrochemical fluorination methods generally known as "Simons” electrochemical fluorination.
• the "Simons process” or the “Simons electrochemical fluorination process” is a commercial process for fluorinating a substrate dissolved or dispersed in liquid, anhydrous, hydrogen fluoride (HF). Simons electrochemical fluorination can be carried out essentially as follows.
• a substrate and an optional conductivity additive are dispersed or dissolved in anhydrous hydrogen fluoride to form an electrolytic "reaction solution.”
• One or more anodes and one or more cathodes are placed in the reaction solution and an electric potential (voltage) is established between the anode(s) and cathode(s), causing electric current to flow between the cathode and anode, through the reaction solution, and resulting in an oxidation reaction (primarily fluorination, i.e., replacement of one or more carbon-bonded hydrogens with carbon-bonded fluorines) at the anode, and a reduction reaction (primarily hydrogen evolution) at the cathode.
• an oxidation reaction primarily fluorination, i.e., replacement of one or more carbon-bonded hydrogens with carbon-bonded fluorines
• electrical current refers to electric current in the conventional meaning of the phrase, the flow of electrons, and also refers to the flow of positively or negatively charged chemical species (ions); while wishing not to be bound by theory, it is believed that the current flowing through the reaction solution in the process is significantly a flow of such ionic chemical species through the reaction solution.
• the Simons process is well-known, and the subject of numerous technical publications. An early patent describing the Simons process is U.S. Patent No. 2,519,983 (Simons), which contains a drawing of a Simons cell and its appurtenances. A description and photograph of laboratory and pilot plant-scale electrochemical fluorination cells suitable for practicing the Simons process appear at pages 416-418 of Vol.
• a reaction solution which comprises hydrogen fluoride and a substrate.
• the hydrogen fluoride is preferably anhydrous hydrogen fluoride, meaning that it contains at most only a minor amount of water, e.g., less than about 1 weight percent (wt%) water, preferably less than about 0.1 weight percent water.
• wt% weight percent
• Such a minor amount of water present in the hydrogen fluoride is not unacceptable because this water is typically oxidized upon application of a voltage between the cathode and the anode.
• the substrate can be any compound that comprises a carbon-bonded hydrogen, and that can be combined with hydrogen fluoride (optionally in the presence of a conductivity additive) to prepare a reaction solution through which electric current can be passed to cause fluorination of the substrate.
• preferred organic substrates include hexane and octane.
• the reaction solution within the ECF cell includes an electrolyte phase comprising HF and an amount of substrate dissolved therein.
• the substrate is preferably to some degree soluble or dispersible in liquid hydrogen fluoride.
• the substrate can be in the form of a liquid, solid, or gaseous vapor, and can be introduced to the hydrogen fluoride as appropriate for its physical state. Specifically, gaseous substrates can be bubbled through the hydrogen fluoride to prepare the reaction solution, or charged to the cell under pressure. Solid or liquid substrates can be dissolved or dispersed in the hydrogen fluoride.
• the substrate can be introduced to the cell as a solute dissolved in a fluorochemical fluid, as described below.
• Some substrates e.g., alkanes
• these relatively insoluble substrates are considered to be difficult to fluorinate by Simons electrochemical fluorination methods.
• a separate substrate phase, such as an alkane phase within the cell is to be avoided because if present, a substrate phase can cause significant problems during the electrochemical fluorination process.
• the alkane substrate within this alkane phase can be polymerized to form a high molecular weight, polymerized, partially fluorinated tar which can accumulate within the electrolyte and which can build up as a coating on the electrodes and thereby deactivate the electrodes.
• the tar must be removed from the electrolyte and the electrodes, which involves significant time and expense.
• the substrate is sufficiently soluble in the electrolyte phase there is little possibility that a separate substrate phase will develop in the cell. If, however, the substrate is relatively less soluble in the electrolyte (HF), then the possibility is greater that a separate substrate phase will develop in the cell. This can be the case with many alkane substrates, and therefore a separate fluorochemical phase within the reaction solution within the electrochemical fluorination cell can be beneficial when the substrate is an alkane such as hexane, heptane, octane, etc.
• HF electrolyte
• the formation of a substrate phase when fluorinating alkane substrates that are relatively less soluble in HF can be prevented by ensuring the presence of a separate fluorochemical phase within the ECF cell, where the substrate is sufficiently soluble in the fluorochemical phase so that a separate substrate phase will not develop.
• a separate fluorochemical phase in electrochemical fluorination is described, for example, in United States Patent No. 5,387,323.
• a fluorochemical phase is believed to act as a "reservoir" for a substrate which has relatively poor solubility in the anhydrous hydrogen fluoride electrolyte, but much higher solubility in the fluorochemical phase. Amounts of substrate beyond that which can be dissolved in the hydrogen fluoride phase will be dissolved by the fluorochemical phase, thus preventing the substrate from accumulating separately in the cell and forming a substrate phase.
• a fluorochemical phase can be desired, and can facilitate the fluorination process, because the increased solubility of the alkane in the fluorochemical phase gives a wider window of operation between starvation of the fluorination process (e.g., by lack of substrate in the electrolyte) and formation of either a separate substrate phase or a single substrate/fluorocarbon phase containing so much substrate that the phase floats on the electrolyte phase instead of sinking beneath it.
• the use of a fluorocarbon phase (particularly at a reduced temperature, as described below) to feed the substrate, provides an improved method of feeding a reliable, controlled, amount of the substrate into the cell.
• the fluorochemical phase can comprise any fluorochemical material that allows relatively higher solubility of the substrate than does the electrolyte phase (HF), thus dissolving substrate that is not able to be dissolved by the HF phase, and thereby preventing the formation of a separate substrate phase.
• the fluorochemical phase can comprise the electrochemical fluorination product.
• fluorochemical compounds suitable for use as the fluorochemical phase include perfluorochemicals such as perfluoroalkanes, pentafluorosulfanyl-substituted perfluoroalkanes, perfluorocycloalkanes, perfluoroamines, perfluoroethers, perfluoropolyethers, perfluoroaminoethers, perfluoroalkanesulfonyl fluorides, perfluorocarboxylic acid fluorides, and mixtures thereof.
• perfluorochemicals such as perfluoroalkanes, pentafluorosulfanyl-substituted perfluoroalkanes, perfluorocycloalkanes, perfluoroamines, perfluoroethers, perfluoropolyethers, perfluoroaminoethers, perfluoroalkanesulfonyl fluorides, perfluorocarboxylic acid fluorides
• Such compounds include perfluorobutane, perfluoroisobutane, perfluoropentane, perfluoroisopentane, perfluorohexane, perfluoromethylpentane, perfluoroheptane, perfluoromethylhexane, perfluorodimethylpentane, perfluorooctane, perfluoroisooctane, perfluorononane, perfluorodecane, 1- pentafluorosulfanylperfluorobutane, 1-pentafluorosulfanylperfluoropentane, 1 pentafluorosulfanylperfluorohexane, perfluorocyclobutane, perfluoro( 1 ,2dimethylcyclobutane), perfluorocyclopentane, perfluorocyclohexane, perfluorotrimethylamine, perfluorotriethylamine, perfluoro
• the fluorochemical phase can comprise the fluorinated product of the substrate.
• the fluorochemical phase can be introduced to the ECF cell as a separate charge, can be introduced as a continuous feed, or, if chosen to be the electrochemical fluorination reaction product, can be allowed to build up within the cell.
• a combination of these techniques can also be used to provide the fluorochemical phase within the cell.
• the fluorochemical phase can be introduced to the cell as an initial charge prior to the start of the ECF process, and, the substrate can be dissolved in a fluorochemical phase with the fluorochemical phase then being continuously fed into and/or recirculated (with substrate dissolved therein) back to the ECF cell to simultaneously provide both the fluorochemical phase and the alkane substrate.
• the amount of the fluorochemical phase can be any useful amount. The amount will generally be sufficient to create a separate fluorochemical phase within the electrochemical fluorination cell, but should not be so much as to interfere with the electrochemical fluorination process, which is generally thought to occur within the conductive electrolytic (HF) phase.
• the reaction solution can contain any relative amounts of hydrogen fluoride, substrate, and fluorochemical phase that will allow effective fluorination of the substrate, and that will preferably avoid the existence of a substrate phase within the ECF cell.
• a useful mass ratio of hydrogen fluoride to alkane substrate will depend on the identity of the alkane substrate and its solubility in HF.
• the amount of alkane should be sufficiently low to prevent the formation of a significant alkane phase within the reaction solution.
• useful amounts of HF versus substrate can be, for example, in the range from about 1:1 to 99:1 (hydrogen fluoride:alkane substrate), preferably from about 75:25 to 99:1 hydrogen fluoride: alkane substrate, and more preferably from about 9:1 to 99:1 hydrogen fluoride: alkane substrate.
• the reaction solution should be sufficiently electrically conductive to allow electric current to pass through the reaction solution in an amount sufficient to result in fluorination of the substrate.
• Pure liquid anhydrous hydrogen fluoride is substantially nonconductive. Therefore, to be conductive the reaction solution must contain an electrolytic component that allows passage of electric current through the reaction solution.
• a wide variety of organic substrates, particularly those containing functional groups, are both soluble in hydrogen fluoride and sufficiently electrolytic to allow passage of an effective amount of electrolyzing current. Thus, in some instances the organic substrate can function as the electrolytic component of the reaction solution. If, however, the organic substrate does not impart sufficient electrical conductivity to the hydrogen fluoride, the reaction solution can be made sufficiently electrically conductive by the addition of a conductivity additive.
• a conductivity additive can be any usefully conductive material or compound, and can be either organically or ionically conductive.
• a short list of examples includes mercaptans such as butyl mercaptan and methyl mercaptan, esters, anhydrides, dimethyl disulfide (DMDS), and ionic salts such as potassium fluoride and lithium fluoride, just to name a few.
• mercaptans such as butyl mercaptan and methyl mercaptan
• esters such as butyl mercaptan and methyl mercaptan
• DMDS dimethyl disulfide
• ionic salts such as potassium fluoride and lithium fluoride
• the conductivity additive can be included at any amount that will result in a reaction solution sufficiently conductive to allow fluorination of the substrate. It can be preferred to use the minimum amount of conductivity additive necessary to maintain a useful amount of electric conductivity of the reaction solution, because a minimal amount of conductivity additive can allow steady operation of a fluorination cell while maximizing efficient use of electricity, and may also reduce or minimize the amount of unwanted by-products caused by undesired fluorination of the conductivity additive. Most preferably, no conductivity additive is used unless necessary for stable cell operation.
• improved conductivity of the fluorination cell can be achieved by using interrupted current, without the use of conductivity additives, or, with the use of a reduced amount of conductivity additive.
• the reduced amount of conductivity additive needed in the reaction solution allows increased yields of fluorinated product by reducing the amount of by-product created by the conductivity additives (e.g., when organic conductivity additives are used), and by reducing the amount of current wasted in causing the fluorination of such undesired by-products.
• the conductivity additive when required, can be present in an amount of less than 20 weight percent conductivity additive, based on the amount of substrate; e.g., less than about 10 weight percent, or 5 weight percent, based on the amount of substrate.
• reaction solution can be exposed to reaction conditions (e.g., reaction temperature, reaction pressure, and electric voltage, current, and power) sufficient to cause fluorination of the substrate.
• reaction conditions can be any that are found to facilitate the production of a desired fluorinated product.
• Reaction conditions chosen for a particular fluorination process can be chosen depending on factors such as the size and construction of the electrochemical fluorination cell; the composition (i.e., identity and relative amounts) of each component of the reaction solution and the presence or absence of a conductivity additive; in a continuous reaction process, the flow rates of each component; the desired fluorinated product, etc.
• the reaction temperature that the electrochemical fluorination cell is operated at can be any temperature that allows a useful degree of fluorination of the substrate.
• the reaction temperature can be chosen and controlled depending on the various factors identified above, as well as others. For instance, the reaction temperature can be chosen depending on the solubility of the substrate, the physical state of either the substrate or the fluorinated product (e.g., whether one or the other is desired to be in a liquid or a gaseous state), and also depending on other reaction conditions such as the reaction pressure.
• the reaction (operating) temperature can be chosen to be above the boiling point of the fluorinated product, in which case it can be beneficial to operate the cell in a pressure vessel under autogenous pressures.
• Operating temperatures in the range from about -20°C to 80°C have been found to be useful. Operating temperatures in the range from about 20 to 65°C can be preferred. Useful reaction pressures have been found to be in the range from about ambient (atmospheric) pressure to about 65 psig (4.48x10 5 Pa), and can preferably be in the range from about 5 to 45 psig (0.34xl0 5 to 3.10xl0 5 Pa). Still, operating pressures outside of these ranges can also be used.
• the electricity passed through the reaction solution can be any amount, as described by parameters including the current, voltage, and power of the electricity, that will result in fluorination of the substrate.
• the electric current is interrupted.
• the term "interrupted" when used with respect to an electrical parameter e.g., current, current density, voltage, power, etc.
• cycle as in current cycle, voltage cycle, or power cycle, etc., refers to a single, complete execution through the different levels through which the parameter varies.
• a current cycle describes a single execution through various levels of current that pass through a fluorination cell, beginning at a starting current level (taken as any arbitrarily chosen point of the cycle), continuing through operation at one or more other current levels, and returning to the starting point at the initial current level.
• An example of a current cycle is illustrated in Figure 1, showing a graph of electric current versus process time.
• the electric current varies through a regular, periodic cycle (identified as the darkened portion of the cycle, labeled C), having a period P, an elevated current level I ⁇ , and a reduced current level I r .
• Period (P) is defined herein as the time taken for the execution of a single cycle. Examples of a voltage cycle and a power cycle are provided, respectively, in Figures 3 and 5, respectively, and are identified as C 3 and C 5 .
• a cycle e.g., a current cycle
• the cycle can take any useful form, and can be described as a waveform.
• the cycle can be, for example, a square wave (see Figures 1 and 3), a substantially square wave, a sinusoidal wave (see Figure 6), or any other periodic cycle.
• An idealized wave form is the square wave cycle illustrated in Figures 1, 3, and 5, relating to electric current, voltage, and power.
• Figure 3 illustrates variation (i.e., interruption) of cell voltage as follows: from a starting point at the beginning of the cycle C 3 , and at a reduced voltage V r , voltage increases to elevated voltage V e , where it is maintained for a period T e ; voltage then decreases to a reduced voltage V r , where it is maintained for a period of T r to complete a single cycle. This cycle repeats regularly throughout the fluorination process.
• the elevated current level is illustrated as constant within each cycle. In practice, however, neither the elevated nor the reduced current level need to be constant, and can vary throughout a cycle. This is shown in Figure 2, which illustrates a plot of electric current versus process time wherein current (e.g., elevated current) is shown to slowly increase (while cell voltage is held constant). Furthermore, the elevated and reduced current levels can, if desired, be only the extremes of a cycle, wherein other portions of the cycle include intermediate current levels, such as is exemplified in Figure 6, showing a sinusoidal waveform for a current cycle.
• the current flowing through the reaction solution can be any amount of current that will result in fluorination of the substrate.
• Current can be limited by the inherent properties of the electrochemical fluorination cell.
• the current is preferably insufficient to cause excessive fragmentation of the substrate, or to cause the liberation of fluorine gas during fluorination.
• electric current measurements can be described in terms of current density, which is the current in amps passing through the reaction solution measured at an active site of the anode or anodes, divided by the area of the anode or anodes.
• elevated current densities can be, for example, in a range from about 10 to 400 mA cm 2 (milliamps per square centimeter), e.g., 50 to 200 or 300 milliamps, and are preferably in the range from about 20 to 160 mA/cm 2 .
• Reduced current densities can be preferably substantially zero, e.g., in the range from about 0 to 2 mA/cm 2 .
• a periodic current cycle can be effected by any known and useful method of controlling electricity in an electrochemical fluorination cell. Because cell resistance in an electrochemical fluorination cell is relatively constant, current can be periodically cycled by controlling any one of the electric voltage across the reaction solution, the power flowing through the reaction solution, or the current flowing through the reaction solution, whichever is most convenient. Generally, the electrical parameter that is easiest to control is the voltage applied across a fluorination cell.
• the voltage applied across the reaction solution can be varied to result in a current cycle of the type described above.
• the voltage can be varied through a regular, repeating, periodic cycle, wherein the cycle is defined by voltage levels comprising an elevated voltage and a reduced voltage.
• Such a voltage cycle will have a period and a waveform similar to the period and waveform described above for the periodically interrupted electric current.
• An example of a voltage cycle is illustrated in Figure 3, showing a graph of cell voltage versus process time.
• voltage varies through a regular, periodic cycle C 3 , having a period P 3 , an elevated voltage V ⁇ , and a reduced voltage V r .
• Figure 3 also identifies a zero current intercept voltage, V 0 , defined for purposes of the present description as the minimum voltage required to result in fluorination of a particular substrate.
• the zero current intercept voltage V render can be empirically determined for a given fluorination reaction by plotting the current vs. voltage of electricity passing through a given reaction solution, and extrapolating the linear portion of the curve to the zero current intercept (see Figure 7).
• the value of the zero current intercept voltage V 0 will be a function of a particular fluorination reaction, but, for purposes of the present description, will be approximated for the fluorination of an organic substrate as to be 4.2 volts.
• the elevated voltage can be any voltage that results in fluorination of the substrate, e.g., a voltage that will cause current to flow through the reaction solution.
• the elevated voltage should be at least equal to or greater than the zero current intercept voltage V trim of the fluorination reaction, and for many fluorination reactions of organic substrates, can preferably be in a range from about 4.2 to about 9 volts (V), more preferably from about 4.5 to 6 V.
• the reduced voltage can be any voltage that will result in a reduced cell resistance relative to cell resistance when operated with uninterrupted current.
• the reduced voltage is of a value that will result in substantially no current flowing through the reaction solution (e.g., I r will be substantially zero). This can preferably be accomplished by providing a reduced voltage that is below the zero current intercept voltage V 0 .
• Figures 3 and 4 each show a reduced voltage of the same polarity as the elevated voltage, and although the reduced voltage can often be positive, this is not a requirement of the present invention as it would be possible, if desired, to use a reduced voltage having a negative polarity compared to the elevated voltage; e.g., a voltage that would be shown as a negative voltage on either of Figures 3 or 4.
• Voltage in terms of cell voltage, reduced voltage, elevated voltage, etc., refers to voltage measured between cathode and anode.
• the elevated voltage (V e ) is shown to be a constant value. In practice, however, neither the elevated voltage nor the reduced voltage are required to be completely or substantially constant, and either or both can vary throughout a pulse cycle.
• Figure 4 illustrates voltage cycle C wherein the elevated voltage is not constant through the pulse cycle.
• the cell voltage is shown to increase from the reduced voltage to an elevated voltage greater than the zero current intercept voltage V 0 . The elevated voltage then gradually increases before falling back to the reduced voltage level V r .
• the value of the electric power, in watts or joules/sec, passing through the reaction solution can also vary as described above for electric current and voltage.
• the power can vary through a regular, repeating, periodic cycle, wherein the power varies between elevated and reduced power levels.
• Such a cycle will have a period and a waveform analogous to that described above for varying electric current and voltage.
• An example of a power cycle is illustrated in Figure 5, showing a graph of power versus process time.
• the power varies through a regular, periodic cycle C 5 , having a period P 5 , an elevated power level P e , and a reduced power level P r .
• the amount of electric current passing through the reaction solution in terms of electric power, can be any amount of current that in combination with the other reaction conditions of the fluorination process will result in fluorination of the organic substrate.
• Electric power is defined as voltage times current (Vxl), and therefore, the amount of electric power used in the fluorination process is dependent on the current and voltage used, and on the size of the fluorination cell.
• the electric current flowing through the fluorination cell can be controlled by any control means useful to provide a periodically interrupted electric current through the reaction solution. Many such control means will be understood by those skilled in the art of electricity and electrochemical fluorination.
• the electric voltage applied across the reaction solution can be periodically interrupted (i.e., reduced) by connecting the anode and cathode to a power supply having a cycle timer with two predetermined voltage set points, one set point corresponding to an elevated voltage and another set point corresponding to a reduced voltage.
• the timer can cycle between these two set points at preselected timing intervals.
• PLC programmable logic controller
• V lvg is the average voltage of the cell (when current is interrupted the average elevated voltage (V e ) can be used), V 0 is defined above.
• the normalized resistance has dimensions of resistance times area, and units, e.g., of ohm-ft 2 , or ohm-dm 2 .
• the use of a normalized resistance is convenient for purposes of this description because normalized resistance can be considered to be relatively constant for a given fluorination cell and fluorination process. Therefore, normalized resistance is a convenient measure of improvement between operation with interrupted current and operation with uninterrupted current.
• the normalized resistance of an electrochemical cell operating according to the present invention can vary, but as an exemplary range Ro can be in the range from about 0.001 to 0.05 ohm-ft 2 .
• a result of the reduced resistance within the electrochemical fluorination cell of the present invention is that the cell can operate at an elevated voltage (V e ) that is relatively lower than the voltage that the cell would otherwise operate at with uninterrupted current.
• V e elevated voltage
• This effect is illustrated in Figure 3, showing the voltage that the fluorination cell would operate at under conditions of uninterrupted current V render, compared to the voltage when operated with interrupted current (elevated voltage) V e . Described differently, with cell voltage remaining the same, the reduced resistance results in an increased amount of current flowing through the electrochemical fluorination cell, as compared to a system with uninterrupted current.
• the cycle period P can be any period that is sufficient to cause the advantage of reducing the resistance of the electrochemical fluorination cell compared to resistance during operation with uninterrupted current. Cycle periods as low as 0.4 seconds have been found to be useful as well as cycle periods of 1.5, 3, 10, 30, 150, 300 seconds.
• the portion of the cycle period wherein the current is at elevated current and elevated voltage (identified herein as T e ), and the portion of the cycle period at reduced current and reduced voltage (identified herein as T r ) can be any amounts of time that will be effective in the fluorination process to produce a fluorinated product, and sufficient to cause a relatively reduced cell resistance. It can be preferable to minimize the reduced current time period (T r ), both in absolute terms and in terms relative to the elevated period, because the reduced current time period is non-productive. That is, fluorination of the substrate occurs as a result of operation at elevated current, e.g., at a rate proportional to the ratio of elevated current (T e ) to cycle time or cycle period (P).
• the percentage of the current cycle at elevated current (T e ) is desirably maximized, and the amount of time at reduced current (T r ) is desirably minimized.
• Preferred reduced voltage periods (T r ) can be less than 50% of the total period P, and are even more preferably less than about 20%, 10%, or less, of the total period P.
• the reduced period T r can preferably be in the range from about 1 to 5, e.g., 3 seconds, with the elevated period T e being preferably 150, 200, or 300 seconds.
• the elevated period T e being preferably 150, 200, or 300 seconds.
• the types of compounds (“electrochemical fluorinated product,” or “fluorinated product”) that can be prepared according to the present invention are various, and will depend primarily on the chemical identity of the substrate.
• the desired fluorinated product will be a fluorinated or perfluorinated analog of the substrate; i.e., the fluorinated product will have a carbon backbone of a length similar to the length of the substrate, but will have one or more of the carbon-bonded hydrogens replaced with fluorine.
• the fluorinated product will be substantially perfluorinated.
• Electrochemical fluorination cells in which the process of the present invention can be performed may be any conventional electrochemical fluorination cell known in the art of electrochemical fluorination.
• a suitable fluorination cell can be constructed of components including a cell body comprising a reaction vessel capable of containing the reaction solution, and electrodes that may be submerged into the reaction solution for the passage of current through the reaction solution.
• cells useful in the practice of the invention can comprise a cell body constructed typically of carbon steel in which is suspended an electrode pack comprising a series of alternating and closely-spaced cathode plates (typically but not necessarily made of iron, nickel, or nickel alloy) and anode plates (typically but not necessarily made of nickel).
• the plates are immersed in the reaction solution, a voltage is applied to the electrodes, and current passes through the reaction solution.
• Electrochemical fluorination cells that can be useful in the practice of the present invention are described, for example, in U.S. 2,519,983, GB 741,399 and 785,492.
• Other useful electrochemical fluorination cells include the type generally known in the electrochemical fluorination art as flow cells.
• Flow cells comprise a set (one of each), stack, or series of anodes and cathodes, where reaction solution is caused to flow over the surfaces of the anodes and cathodes using forced circulation.
• bipolar flow cells having a series of anodes and cathodes. Bipolar flow cells are described, for example, in United States Patent No. U.S. 5,474,657.
• the process of the invention can be carried out by introducing an alkane substrate into an electrochemical fluorination cell (e.g., a Simons cell or a flow cell) containing anhydrous hydrogen fluoride, or to which anhydrous hydrogen fluoride is simultaneously or subsequently added.
• an electrochemical fluorination cell e.g., a Simons cell or a flow cell
• the reaction solution comprises a fluorochemical phase and a hydrogen fluoride phase
• the alkane substrate can be introduced to the cell as a solute dissolved in the fluorochemical phase, with the fluorochemical phase being continuously fed and/or recirculated into the cell.
• a separate feed decanter can contain a reservoir of an alkane substrate dissolved in the fluorochemical phase (feed stream), which is then fed into the cell.
• a decanter allows control of the temperature of the feed stream, and thereby allows control of the concentration of the substrate (e.g., alkane) within the feed stream.
• the substrate and the fluorochemical can both be contained and mixed within the decanter, with the amount of substrate being dissolved in the fluorochemical phase being such that the fluorochemical phase is saturated with the substrate.
• This can be easily accomplished by charging an excess of the substrate to the decanter so that a separate substrate phase exists above the fluorocarbon phase.
• the amount of substrate flowing into the cell will depend on the amount of substrate dissolved in the fluorochemical phase, which will depend on the temperature of the fluorochemical phase, because solubility of the substrate in the fluorochemical phase will be dependent on temperature.
• the temperature of the feed stream is preferably below the operating temperature of the cell, and is preferably at least about 5°C below the operating temperature of the cell, more preferably at least about 10°C below, e.g., 15 or 20°C below the operating temperature of the cell.
• Feeding the fluorochemical phase at a relatively reduced temperature ensures that the amount of the alkane substrate within the feed stream, and therefore the fluorochemical phase of the reaction solution, does not exceed the solubility limits of either the fluorochemical phase or the hydrogen fluoride phase at operating temperature within the cell, thus preventing the formation of a separate phase of the alkane substrate.
• This procedure has been found to prevent overfeeding (the addition of substrate to the cell in excess of the rate at which the substrate is fluorinated and removed as a product) and significantly reduces the formation of tars, current blocking, and fouling of the electrodes.
• FIG. 8 An illustration of this embodiment of the process is shown in Figure 8.
• a solution of fluorochemical phase 2, saturated with alkane substrate 6, is held in feed decanter 4.
• the decanter also contains alkane phase 6, which is the organic feed.
• Fluorochemical phase 2 is fed to electrochemical fluorination cell 8 containing anhydrous hydrogen fluoride (electrolyte phase 10) and optionally an initial amount of fluorochemical phase 12.
• the cell is optionally and preferably equipped with sight glass tubes 14 to monitor the levels of the fluorochemical phase 12 and the hydrogen fluoride electrolyte phase 10.
• the electrochemical cell can contain a drain valve (not shown) for removal of fluorinated product, and for optional connection to a circulation pump 16 which permits a portion of the fluorochemical phase (preferably containing fluorinated product) to be recycled back to the decanter.
• the circulation pump has been found to improve cell performance by enhancing the mixing process that transfers the alkane substrate to the fluorochemical compound phase, and then to the electrolyte phase, and by increasing mass transfer of the alkane substrate to and from the electrodes.
• the cell can optionally be fitted with refrigerated condensers 18 for condensing vapor comprising hydrogen fluoride, alkane substrate, and fluorochemicals of the fluorochemical phase and/or fluorochemical product, which can be sent back to the cell.
• the embodiment of the invention illustrated in Figure 8 wherein substrate feed is fed into the cell as a solute in a fluorochemical phase, can be useful with different types of ECF setups including flow cell applications, bipolar flow cell applications, and conventional Simons cell applications, can be useful with pulsed, interrupted, or continuous current, and, can be useful with any type of substrate.
• this embodiment is useful for any substrate, it can be especially useful with substrates that are relatively insoluble in hydrogen fluoride and therefore tend to form a separate phase within the electrochemical fluorination cell, such as alkanes and especially higher alkanes such as octane.
• Example 1 Example 1
• the current was increased to 100 A/ft 2 (10.8 amps/dm 2 ).
• the average elevated cell voltage V e (the voltage during T e ) was initially about 6.2 volts and gradually fell to about 5.4 volts over a period of several days.
• the current was increased to 150 A/ft 2 (16.1 A/dm 2 ) and V e remained between 5 and 6 volts for the rest of the run, which was continued at steady-state conditions for an additional 500 hours.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Electrochemistry (AREA)
• Materials Engineering (AREA)
• Metallurgy (AREA)
• Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)

Applications Claiming Priority (3)

Publications (1)

Family

ID=22121925

Family Applications (1)

Country Status (3)

Cited By (1)

Families Citing this family (1)

Family Cites Families (3)

• 1999
  • 1999-03-29 EP EP99914240A patent/EP1080251A1/de not_active Withdrawn
  • 1999-03-29 WO PCT/US1999/006789 patent/WO1999058745A1/en not_active Application Discontinuation
  • 1999-03-29 JP JP2000548532A patent/JP2002514688A/ja active Pending

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events