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    • 41. 发明专利
    • METHOD AND APPARATUS FOR DECOMPOSING SAMPLE
    • JPH06160256A
    • 1994-06-07
    • JP20366592
    • 1992-07-30
    • TOSHIBA CORP
    • TAKENAKA MIYUKIHAYASHI MASARUMATSUNAGA HIDEKIKOZUKA SHOJIYABUKI MOTOO
    • G01N1/28G01N30/02G01N30/06
    • PURPOSE:To decompose a sample efficiently by cooling gas produced by heating solvent for decomposing the sample in an enclosed vessel and absorbing the gas into pure water contained while being spaced apart therefrom thereby decomposing the sample immersed in the pure water by means of the solvent absorbed into the pure water. CONSTITUTION:Cover 1a of an enclosed vessel 1 is removed and an acid liquid A is injected therein. A container 3 is then set above the vessel 1 and pure water is filled in the container 3. A sample is then immersed in the pure water and the cover 1a is applied onto the container 3 thus closing the container tightly. Botton part of the vessel 1 is then heated by heating means 7 thus heating the acid liquid A. Consequently, the acid liquid A evaporates and intrudes through a vent 3a into the container 3. Since the interior of the container 3 is cooled forcibly by means of a cooling pipe 5, the acid vapor is absorbed into the pure water in the container 3 thus recovering a high purity acid liquid A. In this regard, impurities in the acid liquid A do not evaporate because of the atmospheric pressure and thereby extremely high purity acid vapor is obtained. The sample is decomposed by the high purity acid liquid A to produce a solution causing no external contamination.
    • 43. 发明专利
    • METHOD FOR ANALYZING SINTERED BODY OF ALUMINUM NITRIDE
    • JPH02262056A
    • 1990-10-24
    • JP8359489
    • 1989-03-31
    • TOSHIBA CORP
    • HAYASHI MASARUYABUKI MOTOHISAHASHIMOTO YOSHIMI
    • G01N31/00G01N33/38
    • PURPOSE:To determine the crystal grain and the grain boundary phase of AlN by analyzing a sample liquid wherein the sintered body of AlN is treated with alkali solution and the crystal grains are dissolved, and a sample liquid wherein the grain boundary phase which is not dissolved is vitrified and the glass is dissolved with inorganic acid. CONSTITUTION:A specified amount of powder 5 of the sintered body of AlN is inputted in a round flask 2, and 2N-NaOH solution 6 is added. The material is heated on a magnetic stirrer 1. After cooling, 6N-HC is slowly added into the solution in the flask 2 through a cooler 4, and the reacted solution is filtered. The filtered liquid is diluted with distilled water. The first sample solution wherein crystal grains are dissolved is prepared. Then, undissolved grain boundary phase is inputted into a platinum crucible and ashed with a burner. Thereafter the material is fused with Na2CO3 powder and vitrified. The material is dissolved with HCl and diluted with distilled water. Thus, the second sample solution wherein the grain boundary phase is dissolved is prepared. The sample liquid is analyzed with the solutions.
    • 48. 发明专利
    • CONCENTRATING DEVICE FOR MOLYBDENUM OR TUNGSTEN SOLUTION
    • JPS61209918A
    • 1986-09-18
    • JP4925785
    • 1985-03-14
    • TOSHIBA CORP
    • ENDO HIROSHIIIRI SHIGEOHAYASHI MASARUYAMASHITA TSUTOMU
    • C01G39/00C01G41/00
    • PURPOSE:To obtain a concentrating device capable of prepg. high purity powder of Mo or W by providing a closed vessel for heating and concentrating solution of Mo or W capable of performing evaporation of the soln. under reduced pressure. CONSTITUTION:A concentration device is provided with a closed vessel 1, a heating means 3 provided to the external periphery of the vessel 1, and an evacuating means 4 connected to the vessel 1. For example, a vessel 2a contg. Mo soln. 2 to be concentrated is laid in the bottom of a box 1a and an upper cover 1b is set to the box 1a air-tightly. A means 4 is then operated to evacuate the inside of the vessel 1, and a means 3 is also operated. Thus, heating and concentration is performed under specified reduced pressure and temp. When the water in the soln. 2 is removed by evaporation, the operation of the means 3, 4 are stopped and cocks 4a, 5a are changed over. Clean air through an air filter 5 is introduced into the vessel 1 to return the pressure to the normal pressure, then the cover 1b is removed and concentrated solid product is taken out. When the product is reduced with H2, Mo powder having high purity is obtd.
    • 50. 发明专利
    • Preparation of manganese ferrite
    • 锰铁矿的制备
    • JPS6136122A
    • 1986-02-20
    • JP15757484
    • 1984-07-30
    • Toshiba Corp
    • ENDO HIROSHINAKAMURA SHINICHIIIRI SHIGEOHAYASHI MASARUYAMASHINA YASUYUKIYAMASHITA TSUTOMU
    • C01G28/00B01J20/02B01J20/06C01G49/00
    • PURPOSE: To produce manganese ferrite having high adsorptivity of Fe ion, Cr ion, etc., by forming a specific manganese ferrite precursor, and calcining the product.
      CONSTITUTION: An aqueous solution containing ferrous ion, ferric ion and manganese ion at a stoichiometric ratio corresponding to the manganese ferrite composition of formula [M is Mn(II) or Fe(II); the molar ratio of Fe(III) is 0.01W0.2] and having a pH of ≥12 is left to stand at about 70W150°C for about 20minW1hr to precipitate the crystal of manganese ferrite precursor. The precursor crystal is washed with water, dried, and granulated optionally using a binder such as polyvinyl alcohol, and calcined in a nonoxidizing atmosphere at ≥600°C to obtain the objective manganese ferrite. The manganese ferrite is suitable as an inorganic ion adsorbent to be used in the feed water piping of a steam power plant, etc.
      COPYRIGHT: (C)1986,JPO&Japio
    • 目的:通过形成特定的锰铁氧体前体来制备Fe离子,Cr离子等吸附性高的锰铁氧体,并煅烧该产物。 构成:含有铁离子,铁离子和锰离子的水溶液,其化学计量比对应于式[M的锰铁氧体组成为Mn(II)或Fe(II)); Fe(III)的摩尔比为0.01-0.2],并且将pH> = 12的摩尔比在约70-150℃下放置约20分钟-1小时以沉淀锰铁氧体前体的晶体。 前体晶体用水洗涤,干燥,任选地使用粘合剂如聚乙烯醇造粒,并在> 600℃的非氧化气氛中煅烧,得到目标锰铁氧体。 锰铁氧体适合用作蒸汽发电厂等的给水管道中的无机离子吸附剂。