US589415A - Guillaume de chalmot - Google Patents

Guillaume de chalmot Download PDF

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US589415A
US589415A US589415DA US589415A US 589415 A US589415 A US 589415A US 589415D A US589415D A US 589415DA US 589415 A US589415 A US 589415A
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silicon
silicid
silicids
metal
metallic
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C28/00Alloys based on a metal not provided for in groups C22C5/00 - C22C27/00

Definitions

  • My invention relates to the production of alloys of silicids of metals with crystalline silicon.
  • a metallic-looking mass which consists of an alloy of crystalline silicon with a high-grade silicid of the 0 metal or metals whose oXids have been used.
  • the alloy can readily obtain the silicon in pure condition by dissolving out the metallic silicids by use of any solvent thereof.
  • the alloy is preferably boiled 5 with hydrochloric or sulfuric acid or other strong acids and then treated with hydrofluoric acid and washed, whereby the silicids are dissolved out and the crystalline silicon remains. In this way pure crystalline sili- .10 con can be obtained at very moderate cost.
  • Crystalline silicon such as is produced by myprocess is useful as a reducing agent and for other purposes. Some metals are improved by the introduction of a small amount of silicon, which may be effected by melting the metal with the silicon. In many instances it will not be necessary to obtain the pure silicon if it is to be used to reduce a metal, or to be added to a metal, as for such purpose it will usually answer quite as well to use a high-grade silicid of the metal in question alloyed with crystalline silicon, such as can be easily and cheaply made by my process, whereby the expense of the subsequent dissolving out of the silicid is avoided.
  • the high-grade crystalline silicids of metals which are produced by my process have usually the formula MeSi as, for example, OaSi calcium silicid; FeSi iron silicid; MnSi manganese silicid. ⁇ Vith these silicids there is alloyed in the product a greater or less proportion of free ununited silicon.
  • the silicic acid which is formed when the silicids are treated with hydrochloric or sulfuric acid can in some cases (for example, in the case of calcium silicid) be separated from the silicon by 5 running water, since owing to the less specific gravity of the silicic acid it can be Washed away, or it may be dissolved in alkali solutions.
  • the described new product consisting of an alloy of silicon with a metallic silicid.

Description

UNITED STATES PATENT OFFICE GUILLAUME DE OHALl VIOT, OF LEAKSVILLE, NORTH CAROLINA, ASSIGNOR TO THE \VILLSON LABORATORY COMPANY, OF NElV YORK, N. Y.
SILICON ALLOY.
SPECIFICATION forming part of Letters Patent No. 589,415, dated September '7, 1897.
Application filed May 14,1896. Serial No. 591,514. (Specimens) To aZZ whom it may concern.-
Be it known that I, GUILLAUME DE CHAL- MOT, a subject of the Queen of the Netherlands, who have declared my intention of becoming a citizen of the United States, residing in Leaksville, in the county of Rockingham and State of North Carolina, have invented certain new and useful Improvements in Silicon Alloys and their Manufacture, of
IO which the following is a specification.
My invention relates to the production of alloys of silicids of metals with crystalline silicon.
I take a silicon compound, such as silica or a silicate, a metal or metallic compound, such as a metallic oxid or salt, (or a mixture of metals or their compounds,) and a carbonaceous reducing agent, and 1 heat them in an electric furnace with a direct current of high amperage and sufficient voltage, preferably, to maintain only a small arc. It is often well to start with a higher voltage and maintain a strong arc until some of the mixture has become molten, when the voltage can be de- 2 5 creased and the amperage maybe increased. At the end of the operation the cathode will be found covered with a metallic-looking mass, which consists of an alloy of crystalline silicon with a high-grade silicid of the 0 metal or metals whose oXids have been used.
From this alloy I can readily obtain the silicon in pure condition by dissolving out the metallic silicids by use of any solvent thereof. To do this, the alloy is preferably boiled 5 with hydrochloric or sulfuric acid or other strong acids and then treated with hydrofluoric acid and washed, whereby the silicids are dissolved out and the crystalline silicon remains. In this way pure crystalline sili- .10 con can be obtained at very moderate cost.
In working myprocess I have obtained silicon from an alloy of calcium silicid and silicon and from an alloy of manganese silicid and silicon. I have also with the same elec- 4 5 trio-furnace process prepared high-grade silicids or alloys thereof of the following composition: calcium silicid containing eightyone per cent. silicon, manganese silicid containing seventy-one per cent. silicon, and iron silicid containing sixty-nine per cent. silicon. I have also produced silicon alloys of tungsten and silver containing free crystalline silicon.
Crystalline silicon such as is produced by myprocess is useful as a reducing agent and for other purposes. Some metals are improved by the introduction of a small amount of silicon, which may be effected by melting the metal with the silicon. In many instances it will not be necessary to obtain the pure silicon if it is to be used to reduce a metal, or to be added to a metal, as for such purpose it will usually answer quite as well to use a high-grade silicid of the metal in question alloyed with crystalline silicon, such as can be easily and cheaply made by my process, whereby the expense of the subsequent dissolving out of the silicid is avoided.
I have found that when a mixture of silica, a metallic oxid, and carbon is subjected to the smelting action of an electric-arc furnace fed by an alternating current the product becomes largely a carbid of the metal. This is especially true in case the metallic oXid is lime, in which case the reduced calcium is almost Wholly converted into calcium carbid; but with a direct current the same mixtures yield the silicids and silicon in preference to the carbids. This fact indicates that in produc- 8o ing high-grade silicids and silicon some part is played by electrolytic action.
The high-grade crystalline silicids of metals which are produced by my process have usually the formula MeSi as, for example, OaSi calcium silicid; FeSi iron silicid; MnSi manganese silicid. \Vith these silicids there is alloyed in the product a greater or less proportion of free ununited silicon.
For separating the silicids from the silicon 0 instead of using hydrofluoric acid the silicic acid which is formed when the silicids are treated with hydrochloric or sulfuric acid can in some cases (for example, in the case of calcium silicid) be separated from the silicon by 5 running water, since owing to the less specific gravity of the silicic acid it can be Washed away, or it may be dissolved in alkali solutions.
The references herein to metallic silicids or compounds and to metals are on the usual assumption that silicon is not a metallic element. If, however, silicon is held to be a metal, these expressions are to be understood as meaning" that the metal referred to is a metal other than silicon.
I claim as my invention the following defined novel features, substantially as hereinbefore specified, namely:
1. The described new product consisting of an alloy of silicon with a metallic silicid.
2. The described process consisting in subjecting, a material or materials containing a metal and silicon, with carbonaceous matter,- to the action of an electric furnace with a direct current, until the carbonaceous matter is eliminated by the reduction of said mate- G. DE OIIALMOT.
Vitn esses: W. 'l. COLEMAN, J. E. WILLIAMs.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2803521A (en) * 1952-03-05 1957-08-20 Wacker Chemie Gmbh Method of treating spent metallic reaction masses from the direct process production of organohalosilanes
US2908553A (en) * 1955-01-14 1959-10-13 Frank Hubert Process for the production of silicon carbide
US3097068A (en) * 1959-05-29 1963-07-09 Union Carbide Corp Crystallization of pure silicon platelets
US3139363A (en) * 1960-01-04 1964-06-30 Texas Instruments Inc Method of making a silicon article by use of a removable core of tantalum

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2803521A (en) * 1952-03-05 1957-08-20 Wacker Chemie Gmbh Method of treating spent metallic reaction masses from the direct process production of organohalosilanes
US2908553A (en) * 1955-01-14 1959-10-13 Frank Hubert Process for the production of silicon carbide
US3097068A (en) * 1959-05-29 1963-07-09 Union Carbide Corp Crystallization of pure silicon platelets
US3139363A (en) * 1960-01-04 1964-06-30 Texas Instruments Inc Method of making a silicon article by use of a removable core of tantalum

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