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    • 3. 发明申请
    • Flaky Copper Powder, Method For Producing The Same, And Conductive Paste
    • 片状铜粉,生产方法和导电膏
    • US20070209475A1
    • 2007-09-13
    • US11587976
    • 2005-04-26
    • Takahiko SakaueKatsuhiko YoshimaruYoshinobu NakamuraHiroyuki Shimamura
    • Takahiko SakaueKatsuhiko YoshimaruYoshinobu NakamuraHiroyuki Shimamura
    • B22F9/24
    • B22F1/0014B22F1/0044B22F1/0055B22F1/0062B22F9/24B22F2001/0033H01B1/22H05K1/095
    • It is an object of the present invention to provide a flaky copper powder composed of fine particles having a sharp distribution particle size, a large crystallite diameter and high oxidation resistance. The flaky copper powder of the present invention contains P and has a crystallite diameter/D1A ratio of 0.01 or more to achieve the object. The method for producing the flaky copper powder comprises four steps: a first step of preparing an aqueous solution containing a copper salt and complexing agent; a second step of adding an alkali hydroxide to the aqueous solution to prepare a first slurry containing cupric oxide; a third step of adding a first reducing agent which can reduce the cupric oxide into cuprous oxide to the first slurry to prepare a second slurry containing cuprous oxide; and a fourth step of adding a second reducing agent which can reduce the cuprous oxide into copper to the second slurry to provide a flaky copper powder, wherein phosphoric acid and its salt are added in at least one of the first to third steps and/or in the second slurry in the fourth step.
    • 本发明的目的是提供一种由具有尖锐分布粒度,大晶粒直径和高抗氧化性的细颗粒组成的片状铜粉末。 本发明的片状铜粉含有P,并且具有0.01以上的微晶直径/ D 1A%比以达到目的。 片状铜粉的制造方法包括四个步骤:制备含有铜盐和络合剂的水溶液的第一步骤; 向该水溶液中添加碱性氢氧化物以制备含有氧化铜的第一浆料的第二步骤; 第三步骤,将第一还原剂加入到第一浆料中以制备含有氧化亚铜的第二浆料; 以及第四步骤,添加第二还原剂,其可以将氧化亚铜还原成铜到第二浆料中以提供片状铜粉末,其中在第一至第三步骤中的至少一个中加入磷酸及其盐,和/或 在第四步中的第二浆料中。
    • 4. 发明申请
    • HIGHLY CRYSTALLINE SILVER POWDER AND METHOD FOR PRODUCING THE SAME
    • 高晶体银粉及其制造方法
    • US20090023007A1
    • 2009-01-22
    • US10588970
    • 2005-02-04
    • Taku FujimotoTakuya SasakiKatsuhiko YoshimaruHiroyuki Shimamura
    • Taku FujimotoTakuya SasakiKatsuhiko YoshimaruHiroyuki Shimamura
    • C22C5/06B22F9/24
    • B22F1/0044B22F9/24Y10T428/12014
    • An object of the present invention is to provide highly crystalline silver powder which is characterized in fine particles, showing high dispersibility, it's particle size distribution is not excessively sharp but relatively broad and crystallites are large; and a method for producing the same. In order to achieve the object, a method for producing highly crystalline silver powder is characterized in that mixing a first aqueous solution and a second aqueous solution, wherein the first aqueous solution contains silver nitrate, a dispersing agent and nitric acid, and the second solution contains ascorbic acid. For dispersing agent, polyvinylpyrrolidone or gelatin is preferred. Highly crystalline silver powder produced by the above-described method is preferred to be a crystallite diameter of 300 Å or more, an average particle diameter D50 in the range from 0.5 μm to 10 μm, and a thermal shrinkage rate for the length direction after heating at 700° C. in the range from −3% to 3%. For ratio D90/D10 of the silver powder is preferred to be in the range from 2.1 to 5.0.
    • 本发明的目的是提供高分散性的高结晶性银粉末,其特征在于细颗粒,显示出高分散性,其粒度分布不过分锐利但相对宽且微晶大; 及其制造方法。 为了达到上述目的,制造高结晶度银粉的方法的特征在于,将第一水溶液和第二水溶液混合,其中第一水溶液含有硝酸银,分散剂和硝酸,第二溶液 含有抗坏血酸。 对于分散剂,优选聚乙烯吡咯烷酮或明胶。 通过上述方法制造的高结晶度银粉末优选为微晶直径为300以上,平均粒径D50为0.5μm〜10μm,加热后的长度方向的热收缩率 在700℃,在-3%至3%的范围内。 对于银粉的D90 / D10比优选为2.1〜5.0。
    • 8. 发明授权
    • Copper fine powder and method for preparing the same
    • 铜精细粉及其制备方法
    • US06391087B1
    • 2002-05-21
    • US09714198
    • 2000-11-17
    • Takao HayashiYoshinobu NakamuraHiroyuki Shimamura
    • Takao HayashiYoshinobu NakamuraHiroyuki Shimamura
    • B22F924
    • B22F9/24B22F1/0011H05K1/095
    • Copper fine powder has an electrical resistance in its powdery state of not more than 1×10−3 &OHgr;·cm; a BET specific surface area ranging from 0.15 to 0.3 m2/g; a tap density of not less than 4.5 g/cc; a product of the tap density and the particle size, of not less than 13, the particle size being calculated from the specific surface area and; a particle size distribution observed in the microtrack measurement as expressed in terms of D50 and D90 ranging from 4 to 7 &mgr;m and 9 to 11 &mgr;m, respectively; and a weight loss through hydrogen-reduction of not more than 0.30%. The copper fine powder is prepared by adding an alkali hydroxide to an aqueous copper salt solution containing divalent copper ions maintained at not less than 55° C. in an amount of not less than the chemical equivalent to form cupric oxide; then gradually adding a reducing sugar to the reaction system while maintaining the temperature of the system to not less than 55° C. to reduce the cupric oxide to cuprous oxide; followed by filtration and washing, re-suspension to form a slurry, gradual addition of a hydrazine reducing agent to the slurry in the presence of a pH buffer capable of maintaining the pH to 5.5 to 8.5 to thus reduce the cuprous oxide to metal copper.
    • 铜精细粉末的电阻在其粉末状态不超过1×10-3欧米加•厘米; BET比表面积为0.15〜0.3m2 / g; 振实密度不小于4.5g / cc; 振实密度和粒径的乘积不小于13,粒径由比表面积计算; 在微轨迹测量中观察到的粒度分布如D50和D90所示,分别为4至7μm和9至11μm; 并且通过氢还原的重量减少不大于0.30%。 通过向不低于55℃的含有二价铜离子的铜盐水溶液中加入碱金属氢氧化物,其量不小于形成氧化铜的化学当量; 然后逐渐向反应体系中加入还原糖,同时将体系温度保持在不低于55℃,将氧化铜还原为氧化亚铜; 然后过滤和洗涤,再悬浮以形成浆料,在能够将pH维持在5.5至8.5的pH缓冲剂存在下,向该浆液中逐渐加入肼还原剂,从而将氧化亚铜还原成金属铜。
    • 9. 发明授权
    • Method for preparing nickel fine powder
    • 镍微粉制备方法
    • US6120576A
    • 2000-09-19
    • US112361
    • 1998-07-09
    • Yoshiharu ToshimaTakayuki ArakiTakao HayashiHiroyuki Shimamura
    • Yoshiharu ToshimaTakayuki ArakiTakao HayashiHiroyuki Shimamura
    • B22F1/00B22F9/24
    • C22B23/0453B22F1/0014B22F9/24B22F2998/00
    • A method for preparing nickel fine powder is herein disclosed, which comprises the steps of mixing an aqueous sodium hydroxide solution comprising, on the basis of the total weight of the sodium hydroxide present in the aqueous solution, 75 to 85% by weight of liquid caustic soda as specified in JIS K 1203 and 25 to 15% by weight, in total, of at least one of sodium hydroxide as specified in JIS K 8576 and solid caustic soda as specified in JIS K 1202, with an aqueous solution of nickel sulfate to form nickel hydroxide, then reducing the resulting nickel hydroxide with hydrazine and recovering nickel fine powder produced. The nickel fine powder prepared by the method has an average particle size of the primary particles ranging from 0.1 to 0.9 .mu.m, a D.sub.90 value of not more than 2.1 .mu.m and a tap density of not less than 3.5 g/cc. The nickel fine powder has a low degree of aggregation, a narrow particle size distribution and a high tap density and therefore, the powder is quite suitably used as a material for producing an internal electrode for a laminated ceramic condenser.
    • 本文公开了一种制备镍微粉的方法,其包括以下步骤:将氢氧化钠水溶液混合,所述氢氧化钠水溶液基于存在于水溶液中的氢氧化钠的总重量为75至85重量%的液体苛性碱 按照JIS K 1203中规定的苏打水,以及JIS-8576中规定的氢氧化钠中的至少一种和JIS K 1202中规定的固体苛性钠中的至少一种的25〜15重量%的硫酸镍水溶液 形成氢氧化镍,然后用肼还原所得的氢氧化镍并回收生产的镍细粉。 通过该方法制备的镍微粉末,其一次粒子的平均粒径为0.1〜0.9μm,D90值不大于2.1μm,振实密度为3.5g / cc以上。 镍微粉末具有低聚集度,窄粒度分布和高振实密度,因此该粉末非常适合用作制备用于层压陶瓷冷凝器的内部电极的材料。