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    • 53. 发明授权
    • Flux method for producing crystals of superconducting YBa.sub.2 Cu.sub.3
O.sub.7
    • 用于生产超导YBa2Cu3O7晶体的通量法
    • US4996186A
    • 1991-02-26
    • US228979
    • 1988-08-05
    • Zhao Z. WangNai-Phuan Ong
    • Zhao Z. WangNai-Phuan Ong
    • C30B9/00
    • C30B29/225C30B9/00Y10S420/901Y10S505/729
    • Method for producing single crystals of YBa.sub.2 Cu.sub.3 O.sub.7 which undergo a transition to the superconducting state above 90K, comprising:(a) preparing a flux composition by mixing BaO.sub.2 and CuO powders in the molecular weight ratio of approximately 1:1, layering on top of the mixture powdered YBa.sub.2 Cu.sub.3 O.sub.7 in an amount up to approximately 20% of the total weight of the BaO.sub.2 --CuO mixture, firing the mixture in air at approximately 930.degree. C.-950.degree. C. for approximately 24 hours, and thereafter raising the temperature from 930.degree. C.-950.degree. C. to approximately 1025.degree.-1030.degree. C. within 1/2 hour and maintaining the temperature at approximately 1025.degree. C.-1030.degree. C. for approximately one hour to one and one-half hours;(b) cooling thereafter the flux to approximately 1020.degree. C.-980.degree.;(c) providing an oxygen gas flow to the flux when the temperature is approximately 1020.degree. C.-980.degree. C.;(d) maintaining the flux in an oxygen gas flow at approximately 980.degree. C. for approximately 30 minutes or longer;(e) cooling thereafter the flux in oxygen gas flow from approximately 980.degree. C. to 960.degree. C. at a rate of no more than 2.degree. to 20.degree. C./hour; and(f) cooling thereafter the flux slowly to room temperature in an oxygen gas flow.
    • 生产YBa2Cu3O7单晶的方法,该YBa2Cu3O7过渡到超过90K的超导状态,包括:(a)通过将BaO 2和CuO粉末以大约1:1的分子量比混合来制备助熔剂组合物,分层在混合物的顶部 粉末YBa2Cu3O7的量高达BaO 2-CuO混合物总重量的约20%,在空气中将混合物在约930℃-95℃下焙烧约24小时,然后升温至930℃ 在1/2小时内,在-95℃至约1025℃-1030℃,并将温度保持在约1025℃-1030℃约1小时至1.5小时; (b)然后将助熔剂冷却至约1020℃-980℃; (c)当温度约为1020℃-980℃时,向焊剂提供氧气流。 (d)将氧气流中的助熔剂维持在约980℃约30分钟或更长时间; (e)此后,其中氧气中的助熔剂以不超过2℃至20℃/小时的速率从约980℃流动至960℃; 和(f)之后将助熔剂在氧气流中缓慢地冷却至室温。
    • 59. 发明授权
    • Method for growing boron nitride crystals of cubic system
    • 用于生长立方体系的氮化硼晶体的方法
    • US4551195A
    • 1985-11-05
    • US654293
    • 1984-09-25
    • Eiichi IizukaTomoji SandoShinji KashimaMasakazu Maki
    • Eiichi IizukaTomoji SandoShinji KashimaMasakazu Maki
    • C30B9/00C30B29/38
    • C30B9/00C30B29/38
    • Cubic boron nitride crystals are grown by subjecting reaction materials of low pressure phase boron nitride, a solvent material, and cubic boron nitride seeds to pressure and temperature conditions in the cubic boron nitride-stable region. The reaction materials are in the form of a pair of a superimposed solvent material plate and a low pressure phase boron nitride plate or a pile made of a plurality of the pairs of the superimposed solvent material plate and low pressure phase boron nitride plate, and a plurality of the seeds are disposed on either one or each of the confronting surfaces of the pair of the superimposed solvent material plate and low pressure phase boron nitride plate. Alternatively, the reaction materials are in the form of a plate made of a mixture of the solvent material and the low pressure phase boron nitride or a pile made of a plurality of the mixture plates, and a plurality of the seeds are disposed on a surface of each plate. The seeds have a particle size of not larger than 150 .mu.m and are regularly disposed in such a manner that the seeds are located at a substantially equal distance and the distance between the peripheries of every two adjacent grown cubic boron nitride crystal particles is from 20 to 200 .mu.m. The cubic boron nitride crystals are allowed to grow until their sizes reach at least 1.5 times the size of the seeds.
    • 通过将低压相氮化硼,溶剂材料和立方氮化硼种子的反应材料经受立方氮化硼稳定区域的压力和温度条件来生长立方氮化硼晶体。 反应材料是一对叠加的溶剂材料板和低压相氮化硼板或由多对叠加的溶剂材料板和低压相氮化硼板组成的桩的形式,以及 多个种子配置在一对叠加的溶剂材料板和低压相氮化硼板的相对表面的一个或每个上。 或者,反应材料为由溶剂材料和低压相氮化硼的混合物制成的板或由多个混合板制成的桩,并且多个种子设置在表面上 的每个板。 种子具有不大于150μm的粒径,并且以这样的方式规则地设置种子位于基本上相等的距离处,并且每两个相邻生长的立方氮化硼晶体颗粒的周边之间的距离为20 至200亩。 允许立方氮化硼晶体生长直到其尺寸达到种子大小的至少1.5倍。
    • 60. 发明授权
    • Diamond single crystals, a process of manufacturing and tools for using
same
    • 钻石单晶,制造工艺及其使用工具
    • US4544540A
    • 1985-10-01
    • US506935
    • 1983-06-22
    • Kazuo Tsuji
    • Kazuo Tsuji
    • B01J3/06C30B9/00C30B13/02C01B31/06
    • C30B13/02B01J3/062C30B29/04C30B9/00B01J2203/061B01J2203/062B01J2203/0625B01J2203/0655B01J2203/068
    • An artificial diamond single crystal, a process for producing it, and tools for utilizing it are disclosed. The artificial diamond crystal has at least one surface which has a rough surface formed by suppressed crystal growth at that surface. The single crystal is produced by providing a diamond synthesis reaction system comprised of a reaction chamber, a carbon source and a solvent metal arranged in contact with the carbon source. A seed crystal is provided in the reaction chamber under elevated pressures and temperatures which permit diamond to be maintained thermodynamically stable. The reaction system is heated to provide a temperature gradient in such a way that a portion of the solvent metal in contact with the carbon source is higher in temperature than a portion of the solvent metal in contact with the seed crystal. This temperature gradient causes a migration of the carbon from the higher temperature portion to the lower temperature portion using the solvent metal as a medium. This allows the carbon to precipitate and grow as diamond on the seed crystal due to the difference in solubility caused by the temperature gradient. The conditions in the reaction chamber housing are maintained so as to suppress crystal growth in at least one direction perpendicular to the direction of the temperature gradient, at the end of the solvent metal. The suppressed crystal growth provides the rough surface of the single crystal which can be connected to a tool and thus provides good adherence between the crystal and the tool.
    • 公开了一种人造金刚石单晶,其制造方法及其利用工具。 人造金刚石晶体具有至少一个表面,其具有通过在该表面处抑制晶体生长而形成的粗糙表面。 通过提供由反应室,碳源和布置成与碳源接触的溶剂金属组成的金刚石合成反应系统来生产单晶。 在升高的压力和温度下在反应室中提供晶种,这允许金刚石在热力学上保持稳定。 将反应体系加热以提供温度梯度,使得与碳源接触的溶剂金属的一部分温度高于与晶种接触的溶剂金属的一部分。 该温度梯度使用溶剂金属作为介质使碳从较高温度部分迁移到较低温度部分。 这允许碳由于温度梯度引起的溶解度的差异而在晶种上沉淀和生长为金刚石。 保持反应室壳体中的条件,以便在溶剂金属末端的至少一个垂直于温度梯度方向的方向上抑制晶体生长。 抑制的晶体生长提供可以连接到工具的单晶的粗糙表面,从而在晶体和工具之间提供良好的粘附。