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    • 42. 发明专利
    • Improvements in and relating to the treatment of materials containing silica
    • GB366015A
    • 1932-01-22
    • GB3178330
    • 1930-10-22
    • ERNST JUSTUS KOHLMEYER
    • C01F7/40
    • Ores and other materials containing silica and/or silicates and oxides of light metals such as aluminium, beryllium and magnesium or high melting heavy metals such as zirconium, chromium and vanadium are mixed with metal sulphides and carbon and the mixture is heated to such temperatures that, without melting, the silicon is driven as a volatile product comprising silicon and sulphur in the atomic ratio Si : S. A temperature of 1350-1400 DEG C. is suitable. If zinc sulphide is the sulphide employed a zinc-silicon-sulphur vapour is given off which is thought to contain the compound Zn-Si-S which has been formed from an intermediately formed compound Zn-C-S. Other sulphides with the exception of aluminium sulphide may also be employed, for example ferrous sulphide, silicon sulphide (Si-S) vapour being produced. The reaction mixture may be agglomerated by briquetting, pressing or sintering. According to an example bauxite is mixed with zinc blend and carbon and the mixture is heated to 1350-1400 DEG C. The highly combustible gases evolved are burnt to produce zinc oxide and silica. The zinc oxide may be removed by lixiviation with acids or alkalis. By controlling the temperature of the combustion the silica may either be obtained as insoluble silicic acid or a colloidal silicic acid which may be converted into silica gel. The materials may be treated to remove a greater part of their silica content by flotation before applying the process. Specifications 232,549, [Class 1 (iii), Oxides &c., Metallic], and 341,160 are referred to.
    • 46. 发明专利
    • A process for the treatment of raw materials containing highly refractory oxide
    • GB232549A
    • 1925-11-26
    • GB2903524
    • 1924-12-03
    • TURE ROBERT HAGLUND
    • C01F7/40C22B4/00
    • Refractory oxides such as alumina, magnesia, chromium oxide or zirconium oxide are obtained from crude materials which in the case of alumina may be bauxite, clay, alundum, feldspar, shale, carboniferous clay, coal dross &c. by fusing the raw material mixed with a carbonaceous reducing agent such as coke, anthracite charcoal or calcium carbide and a sulphur-bearing body such as a sulphide of a heavy metal (pyrites, galena, copper pyrites, copper matte), a sulphide of aluminium, calcium barium, magnesium or sodium, or a mixture of a sulphate such as calcium or barium sulphate and a sulphide. The fusion is effected in an electric arc furnace, the arc being covered by the charge. When there is much sulphur in the charge, metallic iron may be added. The reducible metals and the silicon form an alloy which is easily separable from the sulphide slag in which the refractory oxide is dissolved. In the case of bauxite, the alloy consists of iron, titanium and silicon. The slag is cooled (causing the crystallization of the dissolved oxide) and is treated with water, acid, alkali, or steam to dissolve or decompose the sulphide and leave the oxide. When aluminium sulphide occurs in the slag the treatment with water produces aluminium hydroxide which is separated from the crystalline alumina by mechanical means and may be employed in the next charge. The materials for the fusion may be briquetted. The crystalline product may be purified from magnetic materials by electrostatic or electromagnetic separation and from any remaining sulphide by treatment with acid, or from other impurities by treatment with alkali. The Specification as open to inspection under Sect. 91 (3) (a) mentions as aluminous raw materials firebrick, alum, and "leptite." This subject-matter does not appear in the Specification as accepted.