US3306836A - Process for the electrolytic production of magnesium dialkyls and aluminium trialkyls - Google Patents

Process for the electrolytic production of magnesium dialkyls and aluminium trialkyls Download PDF

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US3306836A
US3306836A US258102A US25810263A US3306836A US 3306836 A US3306836 A US 3306836A US 258102 A US258102 A US 258102A US 25810263 A US25810263 A US 25810263A US 3306836 A US3306836 A US 3306836A
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aluminium
sodium
cathode
electrolyte
electrolysis
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US258102A
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Ziegler Karl
Lehmkuhl Herbert
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ZIEGLER AG
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ZIEGLER AG
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    • 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
    • C25B3/01—Products
    • C25B3/13—Organo-metallic compounds

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  • This invention relates to a process for the electrolytic production of magnesium dialkyls and aluminium trialkyls.
  • the electrolyte used is an aluminium alkoxy or aroxy complex compound or a mixture of these complex compounds with compounds of the general formula MeAlR4. ln the process of our co-pending patent application 792,467 the electrolysis is rst carried out with a compound of the general formula MeAlR4. The resultant reaction product is reacted with an aluminium alkoxy or aroxy complex compound.
  • This invention relates to a new process for the production of these two metal alkyls, which process offers considerable simplifications and improved economy over the prior art processes.
  • sodium is deposited at the cathode in accordance with the invention. It is particularly preferred to maintain the content of -free aluminium trialkyl in the electrolyte in the neigh'borhood of the cathode below 1%.
  • Suitable cathode materials are all good conductors of electric current, which do not form alloys ⁇ with the sodium deposited at the cathode under the reaction conditions.
  • the metal alkyl forming from the anode metal and free aluminium trialkyl as a decomposition product of the electrolyte are formed at the anode during the electrolysis.
  • a diaphragm which may be made of, for example, asbestos, glass wool, quartz wool and preferably of porous cellulose products, eg., lter paper. Suitable diaphragm materials and electrolytic cells equipped with such diaphragms are described in the earlier tiled .patent specifications mentioned above.
  • the diaphragm prevents the anodically formed and uncomplexed aluminium trialkyl or the resulting magnesium dialkyl from mixing with the electrolyte liquid in the neighborhood of the cathode, which mixing would interfere in an undesirable manner with the deposition of sodium and the anodic formation of metal alkyl.
  • the anodically formed aluminium trialkyl is distilled out of the electrolyte immediately after its formation. It is advantageous, however, to use as high a vacuum as is possible. Thus, for example, final pressures of below 1 mm. Hg may be used.
  • the free aluminium trialkyl will then have no opportunity oi' proceeding into the neighborhood of the cathode but will leave the electrolyte prior to proceeding close to the cathode.
  • Another possibility is the use of liquid extracting agents which do not mix with the electrolyte. In this embodiment of the process of the invention, the electrolyte is constantly flushed with the extracting agent during the electrolysis.
  • the extracting agent absorbs the organometallic compounds anodically formed and thereby excludes them from the undesirable reaction with the sodium deposited at the cathode.
  • the extraction liquid which, for example, collects on top of the electrolyte may be withdrawn from the electrolytic cell intermittently or continuously and then separated into extracting agent and organometallic compound.
  • extracting agents there may be used saturated hydrocarbons and preferably aliphatic and hydroaromatic hydrocarbons which are immiscible with the electrolyte.
  • the operation of the process of the invention is extremely simple.
  • the uncomplexe'd metal alkyl compounds formed during the electrolysis do not commingle with the complex electrolyte. Instead, they separate as the lighter liquid phase on the electrolyte and may thence be withdrawn intermittently or continuously from the electrolyzer.
  • the resultant mixture of magnesium dialkyl and aluminium trialkyl which is present in the form of a loose complex compound is easily separated, e.g., by distillation. In doing so, the volatile aluminium trialkyl distils while the magnesium dialkyl is left as the residue.
  • the distillation is preferably effected under a slight vacuum.
  • aluminium anodes only aluminium trialkyl is formed. Three equivalents of aluminium trialkyl are simultaneously formed from the decomposition of the electrolyte per equivalent of the aluminium trialkyl formed from the anode metal. Thus, a total of four equivalents of aluminium trialkyl is obtained.
  • the sodium deposited cathodically in the electrolysis may be used to advantage.
  • a complex compound of the general formula MeAlR4 mentioned above is electrolyzed while maintaining the content of uncomplexed aluminium trialkyl i-n the electrolyte low in the neighborhood of the cathode by the method described above.
  • the organometallic compounds formed at the anode and comprising a mixture of magnesium dialkyl and aluminium trialkyl or only aluminium trialkyl are separated from the electrolyte and separated into aluminium trialkyl derived from the decomposition of the electrolyte and metal alkyl formed from the anode metal.
  • the aluminium trialkyl formed by decomposition of the electrolyte, together with the sodium deposited at the cathode, is then treated with hydrogen and the appropriate olefin outside of the electrolytic cell to be reconverted into the complex compound of the general formula MeAlR4.
  • the latter is subsequently introduced intermittently or preferably continuously into the electrolytic cell.
  • the only starting materials constantly used in this embodiment of the process are the anode metal, hydrogen and olefin.
  • temperatures in excess of about 100 C. are preferred in accordance with the invention. Particularly preferred is the temperature range from about 100 to about 140 C.
  • the process may be operated at relatively W voltages. Suitable voltages are, for example, in the range from about 0.5 to about 5 volts and preferably from 1.5 to 3 volts. lt is preferred for economic utilization of the process to operate at higher current densities, particularly preferred being current densities up to about 80 a./dm.2. However, higher current densities may be used. Furthermore, it is preferred to operate with current densities of at leas-t about 2 to about 5 a./drn.2. Particularly suited is a range from about 30 to about 50 a./dm.2. Of the complex compounds of the general formula MeAlR4, the potassium compounds are better conductors of current than the sodium compounds.
  • the electrolytic cell shown comprises an opening 1 through which the electrolyte which is preferably in molten state may be introduced.
  • the metal whose metal alkyls are to Ibe produced may be introduced through the opening 2 in the form of, for example, small spheres or granules.
  • the sodium is deposited at the cylindrical cathode S of, for example, copper in the center of the electrolysis vessel. 1t flows to the bottom and may thence be withdrawn from the electrolyte cell through the opening 3.
  • the cathode space is separated from the anode space by a perforated cylinder of insulating material 7 With a superimposed diaphragm. This may, for example, consist of hardened filter paper or a ne cloth or glass filter cloth.
  • a perforated cylinder of insulating material 7 With a superimposed diaphragm. This may, for example, consist of hardened filter paper or a ne cloth or glass filter cloth.
  • the anode space which is filled with the small metal spheres 11 and may continuously be supplied with fresh metal .at the rate at which the metal dissolved in the electrolysis.
  • the anode space is provided with two outlet openings (4 and 6).
  • the metal alkyl (aluminium trialkyl or a mixture of aluminium trialkyl and magnesium dialkyl) formed during the electrolysis rises in upward direction in the anode space and may be withdrawn through the opening 6.
  • the catholyte Disposed in the inner space of the perforated cylinder 7 is the catholyte which, for example, may be withdrawn from the apparatus through the overflow 5.
  • the cathode cylinder 8 may be filled in its interior with a heating or cooling liquid the temperature of which is controlled Iby the heating element 9. It is possible in this manner to adjust the temperature of the catholyte as desired while the temperature of the anolyte is adjustable by the heating element 10 which, in this case, is operated by recirculating liquid.
  • Example 1 Sodium-aluminium tetraethyl which is preferably in molten state -is introduced into an electrolyzer as shown in the appended drawing.
  • the cathode is constituted by a copper cylinder.
  • a perforated cylinder of porcelain or a plastic composition eg., Bakelite reinforced by a fabric.
  • Tightened round the cylinder is a diaphragm of hardened filter paper or a line cloth or glass lter fabric. Behind the diaphragm is the anode space which is filled with aluminium granules and may be supplied continuously with aluminium granules at the rate at which aluminium is dissolved in the electrolysis.
  • Heating of the electrolyte or removal of the Joulean heat formed during the electrolysis is effected yby recirculating a liquid of C. in the interior of the closed cathode cylinder.
  • the current is adjusted to l5 amperes with a terminal voltage of 3 volts. With the present dimensioning of the apparatus, this corresponds to an anodic current density of 14 a./dm.2 and a cathodic current density of 10 a./dm.2.
  • the cathodically formed sodium flows as a thin film down at the surface lof the cathode into the lower cathode space where it is intermittently withdrawn in m-olten state.
  • the Ianodically formed aluminium triethyl is sparingly soluble in the electrolyte and rises as droplets to the electrolyte surface where it forms a second liquid phase in the anode space, which is intermittently withdrawn.
  • the influx of NaA1(C2H5).,A linto the vcathode ⁇ space should be adjusted such that the liquid level in the cathode space is by 4 to 5 cm. higher than in the anode space.
  • the yields of newly formed aluminium triethyl is 1.4 gms. per ampere hour (corresponding to 99% of the theoretical yield).
  • a total of 5.7 gms. of A1(C2H5)3 is separated in the anode space per ampere hou-r. Threequarters of this amount are derived from the electrolyte and are reacted with NaH and ethylene at C. and an ethylene pressure of 10 atmospheres to be reconverted into sodium-aluminium tetraethyl.
  • Example 2 The sodium-aluminium tetrapropyl obtained in accordance with Example 4 of our Patent 2,826,598 is introduced into the electrolyzer as shown in the appended drawing while being preferably in molten state.
  • the temperature during the electrolysis is maintained at the preferred level of about 100 C.
  • the current is adjusted to 15 amperes at a terminal voltage Iof 8 volts, which corresponds to an anodic current density of 4 a./dm.2 and a cathodic current density of 10 a./dm.2.
  • the sodium deposited at the cathode flown downwardly as a thin film on the surface of the cathode and into the lower cathode space from where it is intermittently w-ithdrawn in molten state.
  • the effluent from the anode space is adjusted such that a reaction mixture containing about 20% of aluminium tripropyl ows off, which will be the case if a total of about 550 ml. of liquid per hour is withdrawn from the anode space.
  • the influx of molten sodium-aluminium tetrapropyl into the cathode space should be adjusted such that the liqu-id level in the cathode space is by 4 to 5 centimeters higher than that in the anode space.
  • Aluminium tripropyl is separated from sodium-aluminium tetrapropyl in a lilm evaporator (at 100 C. and l mm. Hg). One-fourth ofthe distillate obtained is newly formed aluminium tripropyl and is removed from the cycle. The-remaining 3A of the quantity obtained are reacted with sodium hydride and propylene according to the process of our Patent 2,826,598 to form sodiumaluminium tetrapropyl which is returned into the cycle. Aluminium tripropyl ⁇ in amount of 1.8 gms. per ampere hour (corresponding to 94% of the theoretical yield) is newly formed.
  • Example 3 The procedure is the same as in Example 2 except that sodium-aluminium tetrabutyl is used as the electrolyte and a mixture of 30% of aluminium tributyl and sodiumaluminium tetrabutyl is withdrawn from the -anode space. Pure aluminium tributyl (B P., 100 C./0.5 mm. Hg) is obtained after appropriate processing.
  • Example 4 The procedure and the apparatus are the same as in Example 1, except that NaAl(C2H5)4 is electrolyzed with the use of magnesium granules as the anode material.
  • the electrolysis temperature is 120 C.
  • the current intensity is adjusted to 15 amperes with a terminal voltage of 4 volts.
  • the anodically formed compound of the composition Mg(C2H5)22Al(C2H5)3 dissolves only sparingly in the sodium aluminium tetraalkyl (about 10%), rises in droplets to the surface where it forms a second liquid phase which may be Withdrawn from time to time.
  • the obtained compound Mg(C2H5)2-2Al(C2H5)3 is heated at 100 C. under high vacuum. In doing so, the aluminium trialkyl distils oli' completely.
  • the residue is pure magnesium diethyl.
  • the yield of Mg(C2H5)2 is 39 gms. per 26.8 amps. hrs. corresponding to 95% of the theoretical yield.
  • Example Use is made of an electrolytic cell which simply consists of ya vacuum-resistant steel kettle which has arranged in the center a cathode of sheet copper and, on both sides at a distance of about 1 to 2 cm. therefrom, anodes of t'hick aluminium plates. The anodes are led in with insulation. The cathode is connected with the steel shell of the kettle with metallic conduction.
  • the cathode is suiciently long to touch with its lower end the bottom of the kettle while a free space of about 20 cm. is left between the kettle and the lower end of the anode.
  • An electrolyte comprising 80% of potassiumaluminium tetraethyl and 20% of sodium-aluminium tetraethyl is introduced int-o the kettle under a nitrogen atmosphere.
  • the kettle is connected with a cooled receiver and a vacuum pump via a descending condenser.
  • the kettle is heated to 130-140 C. and evacuated 0.1 mm. Hg and preferably less.
  • the current is then switched on and molten sodium-aluminium tetraethyl at a rate equivalent to the amount of current passed through is allowed to flow in through a separate line arranged at the kettle.
  • the current is adjusted to a current density of to 30 a./dm.2 and 166 gms. of sodium-aluminium tetraethyl are allowed to ow in per 26.8 amps. hrs.
  • the anodically formed aluminium triethyl continuously distils oit at a rate of 150 gms. per 26.8 amps. hrs. of which 38 gms. are newly formed (corresponding to 100% of the theoretical yield).
  • the electrolyte containing complex potassium and sodium remains practically unchanged in the kettle and only the inowing sodium-alum-inium tetraethyl is decomposed.
  • the molten sodium collects at the correct rate, i.e., 23 grams per 26.8 amps. hrs., at the bottom of the kettle.
  • the electrolysis may be run until the sodium level in the kettle is high enough that short-circuit with the aluminium anodes would occur.
  • the sodium may, of course, be withdrawn in molten form from the lapparatus, perhaps after having temporarily interrupted the vacuum and switched off the current. One-fourth of the amount of distillate is put aside as newly recovered aluminium triethyl. The balance is reacted with NaH and ethylene as described in EX- ample 1 to form sodium-aluminium tetraethyl which may be returned into the electrolysis.
  • R in said general formula represents an alkyl radical containing from 2 to 6 carbon atoms.
  • Improvement according to claim 1 which includes separating the anode space from the cathode space by a diaphragm.
  • Process according to claim 1 which includes continuously extracting the alkyl compound formed from the electrolyte with a saturated hydrocarbon immiscible therewith.
  • Improvement according to claim 1 which includes continuously extracting the alkyl compound formed from the electrolyte with a hydrocarbon immiscible therewith and selected from the group consisting of aliphatic and hydroaromatic hydrocarbons.
  • Me in said general formula is a mixture of sodium and potasslum having a potassium content of up to 80%.
  • Improvement according to claim 1 which includes separating the anodically formed organometal compounds from the electrolyte, separating from the latter the aluminium alkyls formed by decomposition of the electrolyte, recovering the sodium deposited at the cathode, reacting a portion of the separated aluminium alkyls with the sodium, hydrogen, and an olen to form the compound of the general formula MSAIR., and recycling said compound to the electrolysis.

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  • 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 Metals (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
US258102A 1959-05-06 1963-02-04 Process for the electrolytic production of magnesium dialkyls and aluminium trialkyls Expired - Lifetime US3306836A (en)

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DEZ7316A DE1150078B (de) 1959-05-06 1959-05-06 Verfahren zur elektrolytischen Herstellung von Magnesiumdialkylen und Aluminiumtrialkylen

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3479274A (en) * 1967-03-27 1969-11-18 Nalco Chemical Co Electrochemical cell having ceramic-lined tubular cathodes

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2849349A (en) * 1955-06-13 1958-08-26 Ziegler Process for the electrolytic deposition of aluminium
US2985568A (en) * 1954-11-26 1961-05-23 Ziegler Electrolytic process for the production of metal alkyls
US3028322A (en) * 1962-04-03 Malmei
US3088885A (en) * 1959-12-24 1963-05-07 Ethyl Corp Manufacture of lead organometallic compounds

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE14891C (de) * A. MONCHABLON in Paris Maschine zur Herstellung gefilzter Garne

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3028322A (en) * 1962-04-03 Malmei
US2985568A (en) * 1954-11-26 1961-05-23 Ziegler Electrolytic process for the production of metal alkyls
US2849349A (en) * 1955-06-13 1958-08-26 Ziegler Process for the electrolytic deposition of aluminium
US3088885A (en) * 1959-12-24 1963-05-07 Ethyl Corp Manufacture of lead organometallic compounds

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3479274A (en) * 1967-03-27 1969-11-18 Nalco Chemical Co Electrochemical cell having ceramic-lined tubular cathodes

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DE1150078B (de) 1963-06-12

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