会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 3. 发明专利
    • FUEL CELL
    • JPS58155663A
    • 1983-09-16
    • JP3797082
    • 1982-03-12
    • HITACHI LTD
    • OKADA HIDEOTAKEUCHI MASAHITOOKABE SHIGERUHIDA HIROSHITONAMI MUNEHIKO
    • H01M4/86
    • PURPOSE:To provide a fuel cell which has an excellent electrode which can generate electricity efficiently by preventing any excessive or deficient wetting by electrolyte by providing both a minute-grain layer with small hole diameters and a coarse-grain layer with large hole diameters in the electrode. CONSTITUTION:When the micro-granular layer 3 of an electrode 2 touches an electrolyte body 1, since electrolyte permeates into the minute-grain layer 3 of the electrode 2 due to capillary action, a three-phase interface is formed around the interface between the minute-grain layer 3 and a coarse-grain layer 4, and electrochemical reaction proceeds. In the electrode 2 consisting of the minute- grain layer 3 and the coarse-grain layer 4, the grain diameters of the minute- grain layer 3 are preferred to be below 5mum, and the grain diameters of the coarse-grain layer 4 are preferred to be 10mum-100mum. In addition, the porosities of the micro-granular layer 3 and the coarse-grain layer 4 are preferred to be 35-55vol% and 50-70vol% respectively.
    • 6. 发明专利
    • FUSED SALT TYPE FUEL CELL
    • JPS58129781A
    • 1983-08-02
    • JP1151582
    • 1982-01-29
    • HITACHI LTD
    • OKABE SHIGERUTAKEUCHI MASAHITOOKADA HIDEOHIDA HIROSHITONAMI MUNEHIKO
    • H01M8/02
    • PURPOSE:To secure such an electrolytic plate that is large in mechanical strength and bears strong electrolyte holding power, by using more than two types of electrolytic materials different in a mean grain diameter. CONSTITUTION:alpha-Alumina 102g and lithium hydroxide 92.4g in a mean grain diameter of 0.5mum are mixed with a stirrer. This material powder is processed in thermomechanical treatment for six hours constant at a temperature of 55 deg.C while lithium aluminate is synthesized. With this thermomechanical treatment carried out, alpha-alumina and lithium hydroxide react on each other whereby grain growth takes place up to 5mum or so in maximum from 1mum. This size fraction is pulverized into fines and thereby powder 70wt% of less than the mean grain diamter of 1mum and powder 30wt% having the mean grain diameter ranging from 3-5mum that still remains unpulverized are mixed by a V-type mixer so as not to alter the grain form. Then, after an aqueous solution of carboxymethylcellulose is mixed with 8pts.wt. added, the fines are pressurized and press-molded, kilning them in an electric furnace at a temperature of 1,200 deg.C after being heated and dried up for five hours long at 50-60 deg.C, through which a porous sintered body is obtained. Water absorption of the said porous sintered body is in a range of 50-60%.
    • 7. 发明专利
    • FUEL BATTERY
    • JPS58129775A
    • 1983-08-02
    • JP1151482
    • 1982-01-29
    • HITACHI LTD
    • TAKEUCHI MASAHITOOKADA HIDEOOKABE SHIGERUHIDA HIROSHITONAMI MUNEHIKO
    • H01M8/02
    • PURPOSE:To obtain an electrolytic body higher in its ability to support an electrolyte and excellent in its mechanical strength by providing an electrolyte supporting layer, on at least one face of the electrolytic body, differing in its pore properties. CONSTITUTION:A multilayer electrolytic body obtained by providing an electrolyte supporting layer comprising nonconducting impalpable powder differing in its pore properties on the at least one face, preferably on the both faces of an electrolytic body constructed by supporting an electrolyte on a long fiber structural body having a self supporting property or a porous sintered body, and supporting an electrolyte on said electrolyte supporting layer. For the particle diameter of the nonconducting impalpable powder used for said electrolytic body, particles fine to the utmost, less than at least 1mum, are preferred in order to raise the electrolyte supporting property thereof. Further, for the electrolyte supporting layer formed by said palpable powder either will do between a paste type electrolyte structure and a matrix type electrolytic body structure. Moreover, it is also proper to form the electrolyte layer in a state where the electrolyte is previously mixed with the nonconducting palpable powder, or to form the same by allowing the former to soak into the latter.