US3729395A - Process for the production of fluorine - Google Patents
Process for the production of fluorine Download PDFInfo
- 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
- Authority
- US
- United States
- Prior art keywords
- bath
- fluorine
- electrolysis
- cell
- temperature
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title abstract description 51
- 229910052731 fluorine Inorganic materials 0.000 title abstract description 42
- 239000011737 fluorine Substances 0.000 title abstract description 33
- 238000004519 manufacturing process Methods 0.000 title abstract description 6
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 title abstract 2
- 238000005868 electrolysis reaction Methods 0.000 abstract description 27
- 239000000203 mixture Substances 0.000 abstract description 18
- LDDQLRUQCUTJBB-UHFFFAOYSA-N ammonium fluoride Chemical compound [NH4+].[F-] LDDQLRUQCUTJBB-UHFFFAOYSA-N 0.000 abstract 1
- 210000004027 cell Anatomy 0.000 description 32
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 31
- 229910000831 Steel Inorganic materials 0.000 description 10
- 239000011698 potassium fluoride Substances 0.000 description 10
- 239000010959 steel Substances 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 229910052799 carbon Inorganic materials 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 6
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 5
- 229910000792 Monel Inorganic materials 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000001816 cooling Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 150000004673 fluoride salts Chemical class 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical group [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 2
- DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 description 1
- MIMUSZHMZBJBPO-UHFFFAOYSA-N 6-methoxy-8-nitroquinoline Chemical compound N1=CC=CC2=CC(OC)=CC([N+]([O-])=O)=C21 MIMUSZHMZBJBPO-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
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
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/24—Halogens or compounds thereof
- C25B1/245—Fluorine; 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.
Landscapes
- 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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7008897A FR2082366A5 (enrdf_load_stackoverflow) | 1970-03-12 | 1970-03-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3729395A true US3729395A (en) | 1973-04-24 |
Family
ID=9052157
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00124530A Expired - Lifetime US3729395A (en) | 1970-03-12 | 1971-03-15 | Process for the production of fluorine |
Country Status (9)
| Country | Link |
|---|---|
| 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)
| 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)
| 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 |
-
1970
- 1970-03-12 FR FR7008897A patent/FR2082366A5/fr not_active Expired
-
1971
- 1971-02-20 DE DE2108277A patent/DE2108277C3/de not_active Expired
- 1971-03-02 BE BE763640A patent/BE763640A/xx unknown
- 1971-03-05 SE SE02872/71A patent/SE359280B/xx unknown
- 1971-03-09 ZA ZA711521A patent/ZA711521B/xx unknown
- 1971-03-10 LU LU62771D patent/LU62771A1/xx unknown
- 1971-03-11 NL NL7103262A patent/NL7103262A/xx unknown
- 1971-03-15 US US00124530A patent/US3729395A/en not_active Expired - Lifetime
- 1971-04-19 GB GB2351371*A patent/GB1303389A/en not_active Expired
Cited By (12)
| 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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