US3729395A - Process for the production of fluorine - Google Patents

Process for the production of fluorine Download PDF

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Publication number
US3729395A
US3729395A US00124530A US3729395DA US3729395A US 3729395 A US3729395 A US 3729395A US 00124530 A US00124530 A US 00124530A US 3729395D A US3729395D A US 3729395DA US 3729395 A US3729395 A US 3729395A
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United States
Prior art keywords
bath
fluorine
electrolysis
cell
temperature
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Expired - Lifetime
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US00124530A
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English (en)
Inventor
M Caron
C Coquet
P Coste
M Rey
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PIERRELATTE USINES CHIM
SOC USINES CHIMIQUES DE PIERRELATTE FR
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PIERRELATTE USINES CHIM
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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00Electrolytic production of inorganic compounds or non-metals
    • C25B1/01Products
    • C25B1/24Halogens or compounds thereof
    • C25B1/245Fluorine; Compounds thereof

Definitions

  • Fluorine is usually obtained on an industrial scale by the electrolytic decomposition, in the absence of air, of a bath of anhydrous HF added to an alkaline fluoride salt such as KF in order to ionize the bath.
  • the molar composition of this bath is approximately 1 mole KF to 2 moles HF and the temperature at which electrolysis is carried out is not lower than 80 C.
  • Fluorine is recovered at the anode which contains at least 6% HF vapor.
  • the anodic current density does not exceed 15 a./dm. at an average total voltage of volts at the terminals of the electrolytic apparatus.
  • the electrolytic cells and the cathodes are ordinarily made from mild steel.
  • the anodes are made from carbon.
  • the temperature of the electrolytic bath is maintained by circulation of cold water through a jacket surrounding the cell and a centrally positioned coil. The lifespan of the cells is limited to the duration of the anodes which eventually crack from localized heating and chemical corrosion.
  • Applicants have unexpectedly found in view of the teaching of the prior art that electrolysis of an anhydrous mixture of NH F and HF under certain advantageous conditions will produce fluorine containing less than 6%, and often less than 3% by volume HF in addition to trace amounts of other products.
  • the fluorine which is produced by the process of this invention is at least equal in quality to the fluorine produced by the known process of electrolysis of baths containing KF and HF and under conditions which are more favorable than hereinbefore possible.
  • This invention relates to a process for the production of fluorine containing less than 6% HF by volume which comprises subjecting to electrolysis in a conventional electrolytic cell in the absence of air at a voltage of at least 6 volts and within a temperature range of from 0 to 50 C., an anhydrous mixture of NH F and HF characterized by the fact that the content of NH in the bath as calculated from NH F is held substantially between 17.5 and 20% by weight.
  • the process of this invention comprises electrolyzing in the absence of air at a temperature between 0 and 50 C., at at least 6 volts in a steel or Monel metal cell with a steel cathode and a carbon anode, an anhydrous mixture of NH HF and HF continuously or intermittently fed with HF at regular intervals, the mixture characterized in that it contains between 17.5 and 20.5% by weight, and advantageously, about 19% by weight of NH, calculated from NH F, and advantageously, a molar ratio of NH F to HF between 1:3 and 1:2.3. A molar ratio of NH F to HF of 1:2.6 has been found to provide especial- 1y advantageous results.
  • This process utilizes the unusual and unobvious properties which characterize the above range of concentration of bath components which properties were not known hereinbefore.
  • the NH F component of the bath can be partially replaced with up to about 25% of the molar fraction of an alkaline fluoride.
  • a portion of the NH F can be replaced with an alkaline fluoride salt such as KF to provide a bath having the composition: 0.25 mole KF, 0.75 mole NH F and 2.6 moles HF.
  • the weight concentration of NH does not remain between 17.5 and 20%.
  • the combined molar concentration of NH F and alkaline fluoride remain within the ratio indicated for the molar concentration of NH F and HF when the latter is used alone.
  • the apparatus which is conventionally employed for the electrolysis of fluorine may be advantageously employed for the process of this invention, i.e., a watercooled cell made of steel or Monel metal and cathodes of steel and anodes of carbon.
  • the anodic voltage of the instant process is lower by at least 0.5 to 1.0 volts over that of known processes at the same current density.
  • the apparent resistance of the bath employed in the process of this invention is significantly lower than that of the baths of known processes.
  • the efiiciency of the cell is improved. For example, when one carries out the process of this invention at 30 C. at a current density of 15 a./dm. an energy saving of about 25% is realized compared to the known process carried out at 90 C. and at a current density of 15 a./dm. 7 to 8 volts are required in the instant process compared to 9 to 10 volts in the prior art process.
  • Another advantage of this invention is to be found in the reduction of heat given off by the anodes which reduction is brought about by a lowering of the voltage and reduced resistance of the bath.
  • one can increase current density without abnormal wear of the anode.
  • At a voltage level of from 9 to 10 volts one can carry out the process of this invention at a temperature of 30 C. and a current density of 35 a./dm.
  • the instant process results in substantial economies upon deterioration of the cell.
  • Another advantage of this invention is that at a process temperature as low as to 35 C., the amount of HF vapor in the bath is low thus permitting the recovery of fluorine containing very little HF. Furthermore, in this temperature range, one avoids undesirable secondary chemical reactions between NH and the fluorine being evolved which reactions mainly give rise to N1 Accordingly, one recovers fluorine which does not contain explosive compounds of fluorine and nitrogen such as the fluoroamines. Thus the process of this invention results not only in fluorine having a high degree of purity, but at the same time, avoids the danger of an explosion.
  • Another advantage of the process of this invention is that the lifespan of the anodes is increased.
  • corrosion due to fluorine is reduced and a plastic material, such as polypropylene, methylpolyrnetacrylate can be used for the cell tank.
  • a plastic material such as polypropylene, methylpolyrnetacrylate can be used for the cell tank.
  • heating of the anodes is reduced and the temperature of the anodes does not exceed the temperature of the bath by more than 10 C. while the temperature of the anodes may exceed the temperature of the bath in a known process by more than 30 C.
  • the lower amount of heat and the better thermal conductivity of the bath reduce the thermal gradient within the interior of the anodes and therefore reduce the risk of cracking and deteriorating the contacts with the bars introducing the electric current.
  • the baths utilized in the process of this invention have melting points between 7 C. to 23 C. while the baths consisting of 1 mole KF22 moles HF do not melt below 72 C. This fact, combined with the better thermal conductivity of the baths of this invention result in easier maintenance of the temperature of the cells which are effectively cooled by circulation of water. The cell walls are not covered with crystals. Slowing or stopping electrolysis generally does not lead to solidification of the bath and restarting electrolysis no longer requires the great inconvenience of melting the contents of the cell which are more easily managed in this invention.
  • This invention provides a process having greater econonly, reliability and productivity and one which is more easily managed.
  • the process of this invention provides numerous advantages. In the first place, there is less HP in the baths of the instant invention thereby resulting in a considerable reduction in the corrosion of the metallic surfaces and the carbon anodes. Furthermore, the vapor pressure of the baths of the process of this invention is much lower. Electrolysis of a bath containing less than 10% NH at the usual temperature range produces a vapor pressure over 100 torr whereas our bath which contains 19% NH produces a vapor pressure of only 15 torr.
  • the fluorine produced by the process of this invention is purer and therefore economies are realized in the purification apparatus. And in contrast to the 20 C. working temperature reported by Spears and hackermann, the process of this invention may be carried out at ambient temperature.
  • Example 1 An electrolytic cell having a single anode was operated.
  • the centrally positioned carbon anode had a useful surface area of 7 dm.
  • the steel cell was electrically connected to two steel cathodes situated on both sides of thecarbon anode plate.
  • a flat electrically insulated diaphragm comprising a grating of Monel metal threads was situated in the middle of the distance (40 mm.) which separated the anode and cathodes. Cooling was accomplished by the circulation of water through a jacket surrounding the cell.
  • the bath used in the above cell contained a mixture of anhydrous NH F and HP in which the concentration of NH in the bath was maintained at about 19.1% by weight by constant feeding of HF and the temperature was held at about 28 C. during the electrolysis.
  • the voltage of the terminals was 7.8 volts at amp. and the concentration of HF in the fluorine produced at the anode was 2.9% by volume.
  • Example 2 An electrolytic cell having 32 anodes was operated at a current density of 15 a./dm. for 800 hours.
  • the 32 anodes of this cell were rectangular carbon plates providing a useful surface area of 270 dm.
  • the steel cell was electrically connected to the steel cathodes of which the useful surface was 560 dm.
  • the space between the anodes and cathodes was 40 mm.
  • the electrically insulated Monel metal diaphragm was situated 20 mm. away from the anodes. Cooling was accomplished by the circulation of water through a jacket surrounding the cell and a centrally positioned coil.
  • the bath used in the above cell contained anhydrous NH F in which the concentration of NH in the bath was maintained at about 19% by weight of constant feeding of HF and the temperature was held at about 30 C. during the electrolysis.
  • the voltage of the terminals was 7.8 volts at 4050 amp. and the concentration of HP in the fluorine produced at the anode 2.9% by volume.
  • Example 3 The cell employed in Example 2 was operated at a current density of 22 a./dm. for 1000 hours.
  • the bath used in the above cell contained a mixture of anhydrous NH F and HF in which the concentration of NH in the bath varied between 18 and 20% by weight.
  • the cooling means provided for the cell was the same as that provided in Example 2.
  • the temperature of the bath was held at about 32 C. during the electrolysis and the voltage of the terminals was 8.9 v. at 6000 amps.
  • the concentration of HP in the anodic fluorine was 3.1% by volume.
  • Example 4 The cell employed in Example 1 was operated at a current density of 28 a./dm. for 2460 hours.
  • the bath used in the above cell contained a mixture of anhydrous NH F and HF in which the concentration of NH was maintained at 19.2% by weight and the temperature was held to about 32 C. during the electrolysis.
  • the voltage of the terminals constantly remained at 9.3 v.
  • a volumetric analysis of the gas produced at the anode gave the following results:
  • Example An electrolytic cell having four anodes was operated at a current density of 34 a./dm. for 960 hours.
  • the four carbon anodes of this cell had a useful surface area of 35 dm.
  • the cell was made of steel and the cathodes which were made of steel were electrically connected to the cell.
  • An electrically insulated diaphragm made of Monel metal was provided as in the apparatus of the preceding examples.
  • the distance between the cathode and anodes was about 40 mm. and cooling was accomplished by circulation of water through a jacket surrounding the cell.
  • the bath contained 14% NH by weight, 15% KF by weight and anhydrous HF was fed into the bath at regular intervals to maintain the combined concentrations of NH F and KP to HF between 1:3 and 1:2.3.
  • the voltage at the terminals which carried at 1200 amps. was 910.1 volts and the temperature was held at about 45 C.
  • the gas recovered at the anode had the following volumetric composition:
  • a process for the production of fluorine containing less than about 6% HF by volume which comprises subjecting to electrolysis in the absence of air at a voltage of at least 6 volts and within a temperature range of 6 from about 0 to 50 C., a bath of an anhydrous mixture of NH F and HF, adding HP to the bath during the electrolysis and maintaining the content of NH in the bath as calculated from NH F substantially between about 17.5 and 20.5% by weight, and recovering said fluorine.
  • a process for the production of fluorine containing less than about 6% HF by volume which comprises subjecting to electrolysis in the absence of air at a voltage of at least 6 volts and within a temperature range of from about 0 to 50 C., a bath of an anhydrous mixture of NH F and HF with a portion of NH F not exceeding 25 of its molar proportion replaced mole for mole with at least one alkaline fluoride and the ratio of the combined molar concentration of NH F and KF to HF is substantially maintained during the electrolysis within the range from about 1:3 to 1:2.3, and recovering said fluorine.

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
US00124530A 1970-03-12 1971-03-15 Process for the production of fluorine Expired - Lifetime US3729395A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7008897A FR2082366A5 (enrdf_load_stackoverflow) 1970-03-12 1970-03-12

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US3729395A true US3729395A (en) 1973-04-24

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US (1) US3729395A (enrdf_load_stackoverflow)
BE (1) BE763640A (enrdf_load_stackoverflow)
DE (1) DE2108277C3 (enrdf_load_stackoverflow)
FR (1) FR2082366A5 (enrdf_load_stackoverflow)
GB (1) GB1303389A (enrdf_load_stackoverflow)
LU (1) LU62771A1 (enrdf_load_stackoverflow)
NL (1) NL7103262A (enrdf_load_stackoverflow)
SE (1) SE359280B (enrdf_load_stackoverflow)
ZA (1) ZA711521B (enrdf_load_stackoverflow)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5580437A (en) * 1993-11-22 1996-12-03 E. I. Du Pont De Nemours And Company Anode useful for electrochemical conversion of anhydrous hydrogen halide to halogen gas
US5824199A (en) * 1993-11-22 1998-10-20 E. I. Du Pont De Nemours And Company Electrochemical cell having an inflatable member
US5855759A (en) * 1993-11-22 1999-01-05 E. I. Du Pont De Nemours And Company Electrochemical cell and process for splitting a sulfate solution and producing a hyroxide solution sulfuric acid and a halogen gas
US5855748A (en) * 1993-11-22 1999-01-05 E. I. Du Pont De Nemours And Company Electrochemical cell having a mass flow field made of glassy carbon
US5863395A (en) * 1993-11-22 1999-01-26 E. I. Du Pont De Nemours And Company Electrochemical cell having a self-regulating gas diffusion layer
US5868912A (en) * 1993-11-22 1999-02-09 E. I. Du Pont De Nemours And Company Electrochemical cell having an oxide growth resistant current distributor
US5961795A (en) * 1993-11-22 1999-10-05 E. I. Du Pont De Nemours And Company Electrochemical cell having a resilient flow field
US5976346A (en) * 1993-11-22 1999-11-02 E. I. Du Pont De Nemours And Company Membrane hydration in electrochemical conversion of anhydrous hydrogen halide to halogen gas
US6042702A (en) * 1993-11-22 2000-03-28 E.I. Du Pont De Nemours And Company Electrochemical cell having a current distributor comprising a conductive polymer composite material
US20080085604A1 (en) * 2004-07-07 2008-04-10 Showa Denko K.K. Plasma Treatment Method and Plasma Etching Method

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8727188D0 (en) * 1987-11-20 1987-12-23 British Nuclear Fuels Plc Fluorine-generating electrolytic cells
US20030121796A1 (en) * 2001-11-26 2003-07-03 Siegele Stephen H Generation and distribution of molecular fluorine within a fabrication facility

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5580437A (en) * 1993-11-22 1996-12-03 E. I. Du Pont De Nemours And Company Anode useful for electrochemical conversion of anhydrous hydrogen halide to halogen gas
US5824199A (en) * 1993-11-22 1998-10-20 E. I. Du Pont De Nemours And Company Electrochemical cell having an inflatable member
US5855759A (en) * 1993-11-22 1999-01-05 E. I. Du Pont De Nemours And Company Electrochemical cell and process for splitting a sulfate solution and producing a hyroxide solution sulfuric acid and a halogen gas
US5855748A (en) * 1993-11-22 1999-01-05 E. I. Du Pont De Nemours And Company Electrochemical cell having a mass flow field made of glassy carbon
US5863395A (en) * 1993-11-22 1999-01-26 E. I. Du Pont De Nemours And Company Electrochemical cell having a self-regulating gas diffusion layer
US5868912A (en) * 1993-11-22 1999-02-09 E. I. Du Pont De Nemours And Company Electrochemical cell having an oxide growth resistant current distributor
US5961795A (en) * 1993-11-22 1999-10-05 E. I. Du Pont De Nemours And Company Electrochemical cell having a resilient flow field
US5976346A (en) * 1993-11-22 1999-11-02 E. I. Du Pont De Nemours And Company Membrane hydration in electrochemical conversion of anhydrous hydrogen halide to halogen gas
US6042702A (en) * 1993-11-22 2000-03-28 E.I. Du Pont De Nemours And Company Electrochemical cell having a current distributor comprising a conductive polymer composite material
USRE36985E (en) * 1993-11-22 2000-12-12 E. I. Du Pont De Nemours And Company Anode useful for electrochemical conversion of anhydrous hydrogen halide to halogen gas
US20080085604A1 (en) * 2004-07-07 2008-04-10 Showa Denko K.K. Plasma Treatment Method and Plasma Etching Method
TWI392014B (zh) * 2004-07-07 2013-04-01 Showa Denko Kk Plasma processing method and plasma etching method

Also Published As

Publication number Publication date
GB1303389A (enrdf_load_stackoverflow) 1973-01-17
FR2082366A5 (enrdf_load_stackoverflow) 1971-12-10
DE2108277C3 (de) 1973-10-04
BE763640A (fr) 1971-08-02
LU62771A1 (enrdf_load_stackoverflow) 1971-08-23
NL7103262A (enrdf_load_stackoverflow) 1971-09-14
DE2108277A1 (de) 1971-10-14
ZA711521B (en) 1971-12-29
DE2108277B2 (de) 1973-03-08
SE359280B (enrdf_load_stackoverflow) 1973-08-27

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