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    • 13. 发明授权
    • Co-precipitation synthesis of precursors to bismuth-containing
superconductors
    • 含铋超导体的前体的共沉淀合成
    • US5077265A
    • 1991-12-31
    • US622155
    • 1990-11-30
    • Joseph J. Ritter
    • Joseph J. Ritter
    • C01B13/18C01G29/00C04B35/45
    • C01G29/006C01B13/185C04B35/45C01P2006/32C01P2006/40C01P2006/42C01P2006/60Y10S505/738
    • A co-precipitation synthesis of precursors to bismuth-containing ceramic superconducting materials is disclosed in which bismuth and at least one other approrpiate metal are dissolved in a non-aqueous acidic solvent, which are then recovered as a homogeneous dry powder. The mixed metal salts are co-precipitated from aqueous solution in the form of the corresponding homogeneous hydroxycarbonate precursor mixture by reaction with either sodium carbonate or potassium carbonate. The homogeneous precursor may be then converted to the BiCuSrCuO.sub.x ceramic by calcining the mixed hydroxycarbonate to a powder, compressing said powder into a green compact, sintering said green compact at a temperature of at least 750.degree. C., and cooling the ceramic material so produced at a controlled rate, preferably about 50.degree. C./minute.
    • 公开了含铋陶瓷超导材料的前体的共沉淀合成法,其中将铋和至少一种其它邻接金属溶解在非水性酸性溶剂中,然后将其作为均匀的干燥粉末回收。 通过与碳酸钠或碳酸钾反应,将混合的金属盐以相应的均匀羟基碳酸酯前体混合物的形式从水溶液中共沉淀。 然后将均匀前体转化成BiCuSrCuOx陶瓷,通过将混合的羟基碳酸酯煅烧成粉末,将所述粉末压制成生坯,在至少750℃的温度下烧结所述生坯,并冷却如此生产的陶瓷材料 优选约50℃/分钟。
    • 14. 发明授权
    • Process for making superconductors using barium hydroxide
    • 使用氢氧化钡制造超导体的工艺
    • US5061683A
    • 1991-10-29
    • US197961
    • 1988-05-31
    • Harold S. Horowitz
    • Harold S. Horowitz
    • C04B35/00C01F1/00C01G1/00C01G1/02C01G3/00C01G3/02C04B35/45C04B35/50H01B12/00H01B13/00H01L39/00H01L39/12H01L39/24
    • H01L39/2419C01G3/006C04B35/4504C04B35/4512C04B35/4521C01P2002/72C01P2002/76C01P2004/61C01P2004/62Y10S505/734Y10S505/737Y10S505/738
    • There is disclosed an improved process for preparing a superconducting composition having the formula M.sub.w A.sub.z Cu.sub.v O.sub.x wherein M is selected from the group consisting if Bi, Tl, Y, Nd, Sm, Eu, Gd, Dy, Ho, Er, Tm Yb and Lu; A is at least one alkaline earth metal selected from the group consisting of Ba, Ca and Sr; x is at least 6; w is at least 1; z is at least 2 and v is at least 1; said composition having a superconducting transition temperature of above 77 K, preferably above about 90 K; said process consisting essentially of (a) forming a suspension having an M:A:Cu atomic ratio of w:z:v by mixing A(OH).sub.2, AO or AO.sub.2 and M.sub.2 O.sub.3 with an aqueous solution of cupric carboxylate or cupric nitrate at a temperature from about 50.degree. C. to about 100.degree. C., or mixing A(OH).sub.2 with an aqueous solution of Cu carboxylate, nitrate or a mixture thereof and M carboxylate, nitrate or a mixture thereof at a temperature from about 50.degree. C. to about 100.degree. C.; (b) drying the suspension formed in step (a) to obtain a precursor powder; and (c) heating and cooling the powder under specified conditions to form the desired superconducting composition. Shaped articles thereof are also disclosed.
    • 公开了一种制备具有式MwAzCuvOx的超导组合物的改进方法,其中M选自Bi,Tl,Y,Nd,Sm,Eu,Gd,Dy,Ho,Er,Tm Yb和Lu中的一种; A是选自Ba,Ca和Sr中的至少一种碱土金属; x至少为6; w至少为1; z至少为2,v为至少1; 所述组合物的超导转变温度高于77K,优选高于约90K; 所述方法基本上由(a)通过将A(OH)2,AO或AO 2和M 2 O 3与羧酸铜或硝酸铜的水溶液混合在一起而形成具有M:A:Cu原子比为w:z:v的悬浮液。 温度为约50℃至约100℃,或在约50℃的温度下将A(OH)2与Cu羧酸盐,硝酸盐或其混合物的水溶液和M羧酸盐,硝酸盐或其混合物混合 C.至约100℃。 (b)干燥步骤(a)中形成的悬浮液以获得前体粉末; 和(c)在特定条件下加热和冷却粉末以形成所需的超导组合物。 其形状也被公开。