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    • 4. 发明授权
    • Method for concurrent production of copper powder and a metal chloride
    • 同时生产铜粉和金属氯化物的方法
    • US5279641A
    • 1994-01-18
    • US5980
    • 1993-01-19
    • Toshio NarisawaRyohei KatoMasanori NakamuraHitoyoshi Yamaguchi
    • Toshio NarisawaRyohei KatoMasanori NakamuraHitoyoshi Yamaguchi
    • B22F9/24C01G1/06C22B15/00C23F1/46
    • C22B15/0089B22F9/24C01G1/06Y02P10/236
    • A novel method is proposed for concurrently producing a metallic copper powder and a valuable chloride of a metal other than copper, e.g., manganese, zinc, cobalt, nickel and tin, from a depleted aqueous etching solution containing copper (II) chloride as discharged from the etching process in the manufacture of copper-foiled printed circuit boards. The inventive method also contributes to solve the problem for the disposal of such a waste solution without causing the troubles in connection with environmental pollution. The inventive method comprises the steps of: treating the waste solution with an active carbon so as to remove organic impurities; admixing the solution with a powder, granules or flakes of the above mentioned metal so as to precipitate the copper value in the metallic form, instead, giving an aqueous solution of the chloride of the added metal; and separating the copper metal powder and the chloride solution.
    • 提出了一种新颖的方法,用于从含有氯化铜(II)的贫化水溶液中同时制备金属铜粉末和铜以外的金属(例如锰,锌,钴,镍和锡)的有价值氯化物, 在铜箔印刷电路板的制造中的蚀刻工艺。 本发明的方法还有助于解决这种废溶液的处理问题,而不会引起与环境污染有关的麻烦。 本发明的方法包括以下步骤:用活性炭处理废溶液以去除有机杂质; 将溶液与上述金属的粉末,颗粒或薄片混合,以沉淀金属形式的铜值,而不是给出添加的金属的氯化物的水溶液; 并分离铜金属粉末和氯化物溶液。
    • 7. 发明授权
    • Multiple mode microprogram controller
    • 多模式微程序控制器
    • US4920482A
    • 1990-04-24
    • US932277
    • 1986-11-19
    • Atsushi HasebeRyohei Kato
    • Atsushi HasebeRyohei Kato
    • G06F15/177G06F9/22G06F9/24G06F9/445G06F15/16
    • G06F9/24
    • An information processing apparatus comprising a program supplying portion, write signal generator, and a data processor, which includes a microprogram controller, microprogram memory, arithmetic unit, and a selector for selecting in an alternative way an address from the microprogram controller and an address from the program supplying portion and supplying the same to the microprogram memory. In the apparatus, it is adapted such that, in a first (program execution) mode, the address from the microprogram controller is supplied through the selector to the microprogram memory, in a second (reset, or stop) mode, the microprogram controller is supplied with a signal, whereby the same is caused to continuously generate program start addresses, and in a third (program transfer) mode, the address from the program supplying portion is supplied through the selector means to the microprogram memory and, according to a write signal from the write signal generator, the program from the program supplying portion is written in the microprogram memory.When supplying a plurality of different programs from the program supplying portion to the processors operating under the program, such a method can be used to treat the whole of the plurality of different programs as one program and supply this program to the processors at one time of transfer and separately supply an execution start address of one program out of the plurality of different programs to each of said processors.
    • 一种包括程序提供部分,写入信号发生器和数据处理器的信息处理装置,其包括微程序控制器,微程序存储器,运算单元和用于以替代方式从微程序控制器选择地址的选择器, 程序提供部分并将其提供给微程序存储器。 在该装置中,适于使得在第一(程序执行)模式中,来自微程序控制器的地址在第二(复位或停止)模式中通过选择器提供给微程序存储器,微程序控制器是 提供一个信号,从而使其连续地产生程序开始地址,并且在第三(程序传送)模式中,来自程序提供部分的地址通过选择器提供给微程序存储器,并且根据写入 来自写入信号发生器的信号,来自程序提供部分的程序被写入微程序存储器。 当将多个不同的程序从程序提供部分提供给在程序下运行的处理器时,可以使用这种方法来将整个多个不同的程序视为一个程序,并将该程序提供给处理器一次 将各个不同的节目中的一个节目的执行开始地址分别提供给各处理器。
    • 8. 发明授权
    • Methods of preparing novel dipeptide compounds or pharmaceutically acceptable salts thereof
    • 制备新型二肽化合物或其药学上可接受的盐的方法
    • US06222043B1
    • 2001-04-24
    • US09228009
    • 1999-01-08
    • Ryohei KatoTsutomu MimotoTominaga FukazawaNaoko MorohashiYoshiaki Kiso
    • Ryohei KatoTsutomu MimotoTominaga FukazawaNaoko MorohashiYoshiaki Kiso
    • C07D27706
    • C07D263/06C07D207/16C07D277/06
    • The present invention provides synthetic methodology to produce novel dipeptide compounds and pharmaceutically acceptable salts thereof which exhibit excellent HIV protease inhibitory activity and excellent bioavailability from digestive tracts. Methods of using the dipeptide compounds and pharmaceutically acceptable salts thereof also are provided. A non-limiting example of a dipeptide compound of the invention has the general formula (IA): where R1 represents a 5-membered or 6-membered monocyclic hydrocarbon group or heterocyclic group wherein 3 or fewer substituents other than hydrogen are present on the cyclic group; R21 and R22 each represents a hydrogen atom or a linear or branched aliphatic hydrocarbon group having 1-6 carbon atoms; and R3 represents a linear or branched aliphatic hydrocarbon group having 1-6 carbon atoms or a monovalent group comprising an aromatic monocyclic hydrocarbon group having 12 or fewer carbon atoms in total, wherein a halogen atom can be substituted on the aromatic ring of the aromatic monocyclic hydrocarbon group.
    • 本发明提供合成方法以产生新的二肽化合物及其药学上可接受的盐,其表现出优异的HIV蛋白酶抑制活性和从消化道获得优异的生物利用度。 还提供了使用二肽化合物及其药学上可接受的盐的方法。 本发明的二肽化合物的非限制性实例具有通式(IA):其中R 1表示5元或6元单环烃基或杂环基,其中3个或更少个除氢以外的取代基存在于环状 组; R 21和R 22各自表示氢原子或具有1-6个碳原子的直链或支链脂族烃基; R3表示具有1-6个碳原子的直链或支链脂族烃基或包含总共具有12个或更少碳原子的芳族单环烃基的一价基团,其中卤素原子可以在芳族单环的芳环上被取代 烃基。