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    • 4. 发明授权
    • Recovery of cobalt and chromium
    • 回收钴和铬
    • US4608084A
    • 1986-08-26
    • US718257
    • 1985-04-01
    • Richard A. ScheithauerMichael J. MillerClarence D. VanderpoolMartin B. MacInnis
    • Richard A. ScheithauerMichael J. MillerClarence D. VanderpoolMartin B. MacInnis
    • C22B23/00C22B3/32C22B7/00C22B34/32C22B23/04
    • C22B23/0484C22B23/0423C22B3/0025C22B34/32C22B7/007Y02P10/234
    • A process is disclosed for recovering cobalt and chromium from a cobalt and chromium containing alloy. The process involves first digesting the alloy in concentrated hydrochloric acid at a sufficient temperature for a sufficient time to form a first solution containing the major portion of the cobalt, chromium, and any iron and nickel present in the alloy and a first solid and separating the first solution from the first solid. Oxalic acid is then added to the first solution in an amount sufficient to subsequently precipitate the major portion of the cobalt and any iron and nickel contained in the first solution followed by adjustment of the ph to from about 1 to about 2 with a base and maintaining the temperature below about 20.degree. for a sufficient time to form a second solid containing the major portion of the cobalt and the major portion of any iron and nickel which is present in the first solution and a second solution containing the major portion of the chromium which is present in the first solution and separation of the second solid from the second solution. The second solid is then washed with sufficient water to remove any water soluble impurities and separated from the resulting wash water. The resulting washed second solid is then contacted with a calcium chloride solution of sufficient calcium chloride concentration, at a sufficient temperature, for a sufficient time to form a third solution containing the major portion of the cobalt which was present in the second solid, and a third solid. The third solution is then separated from the third solid.
    • 公开了从含钴和铬的合金中回收钴和铬的方法。 该方法包括首先在足够的温度下将浓缩的合金中的合金消化足够的时间以形成含有合金中存在的钴,铬和任何铁和镍的主要部分的第一溶液和第一固体, 从第一个固体的第一个解决方案。 然后将草酸以足以随后沉淀出主要部分的钴和第一溶液中所含的任何铁和镍的量,然后用碱将ph调节至约1至约2,并保持 温度低于约20°足够的时间以形成第二固体,其含有钴的主要部分和存在于第一溶液中的任何铁和镍的主要部分和含有主要部分铬的第二溶液, 存在于第一溶液中并且将第二固体与第二溶液分离。 然后用足够的水洗涤第二固体以除去任何水溶性杂质并从得到的洗涤水中分离。 然后将所得洗涤后的第二固体在足够的温度下与足够氯化钙浓度的氯化钙溶液接触足够的时间以形成含有存在于第二固体中的钴的主要部分的第三溶液, 第三个固体。 然后将第三溶液与第三固体分离。
    • 9. 发明授权
    • Method for producing ammonium paratungstate
    • 生产仲钨酸铵的方法
    • US4623534A
    • 1986-11-18
    • US714327
    • 1985-03-21
    • Richard A. ScheithauerClarence D. VanderpoolMichael J. Miller
    • Richard A. ScheithauerClarence D. VanderpoolMichael J. Miller
    • C01G41/00C22B3/28
    • C22B3/0012C01G41/00C01G41/003Y02P10/234
    • A method is disclosed for producing relatively pure ammonium paratungstate from an impure tungsten solution. The method involves first adding hexamethylenetetramine to the tungsten solution and adjusting the pH to from about 1.0 to about 2.0 with a mineral acid to form a first precipitate of a tungsten hexamethylenetetramine product, which is then separated from its mother liquor. The precipitate is then slurried in water and the pH adjusted to from about 7.0 to about 8.5 with ammonia to dissolve the precipitate. The resulting solution is then adjusted to from about 1.0 to about 2.0 with a mineral acid to form a second precipitate of the tungsten hexamethylenetetramine product which is then separated from its mother liquor. The second precipitate is then slurried in a solution of water and sufficient ammonia to form ammonium paratungstate which crystallizes out on evaporation of the slurry. The ammonium paratungstate is then separated from its mother liquor.
    • 公开了从不纯的钨溶液中生产相对纯的仲钨酸铵的方法。 该方法包括首先将六亚甲基四胺加入到钨溶液中,并用无机酸将pH调节至约1.0至约2.0,以形成六亚甲基四胺产物的第一沉淀,然后将其从母液中分离出来。 然后将沉淀物在水中浆化并用氨将pH调节至约7.0至约8.5以溶解沉淀物。 然后将所得溶液用无机酸调节至约1.0至约2.0,以形成六亚甲基四胺产物的第二沉淀物,然后从其母液中分离。 然后将第二沉淀物在水和足够的氨的溶液中浆化以形成仲钨酸铵,其在浆料蒸发时结晶出来。 然后将仲钨酸铵与母液分离。