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溶剂热制备条件对镍晶体结构的影响
引用本文:米远祝,刘应亮,肖勇,袁定胜,张静娴. 溶剂热制备条件对镍晶体结构的影响[J]. 无机化学学报, 2005, 21(4): 603-606
作者姓名:米远祝  刘应亮  肖勇  袁定胜  张静娴
作者单位:1. 暨南大学化学系,广州,510632;湖北民族学院化学与环境工程学院,恩施,445000
2. 暨南大学化学系,广州,510632
基金项目:广东省教育厅“千百十人才工程”资助项目(No.Q02059),广东省科技计划资助项目(No.2KM02304G)。
摘    要:Nickel powders were obtained after chemical reduction of nickel chloride by KBH4 using absolute ethylenediamine as solvent in a stainless autoclave. The product was characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). XRD results show that the as-prepared sample have different crystal structures at different reaction temperatures. It was face-centered cubic (fcc) nickel under 200 ℃, and there was only hexagonal close-packed (hcp) Ni above 300 ℃. At 250 ℃, the patterns indicate that both fcc and hcp phases of Ni coexist in the as-prepared sample. When the ethylenediamine was respectively substituted by benzene and toluene, only fcc phase nickel was obtained. SEM and TEM indicate that the fcc Ni is nano-particles with about 100 nm in diameter, and hcp nickel is nano-crystalline clusters.

关 键 词:有机溶剂; 镍; 晶体结构
文章编号:1001-4861(2005)04-0603-04
收稿时间:2004-09-20
修稿时间:2004-09-20

Effect of Solvothermal Reduction Process on Crystal Phase of Nickel
MI Yuan-Zhu,LIU Ying-Liang,XIAO Yong,YUAN Ding-Sheng and ZHANG Jing-Xian. Effect of Solvothermal Reduction Process on Crystal Phase of Nickel[J]. Chinese Journal of Inorganic Chemistry, 2005, 21(4): 603-606
Authors:MI Yuan-Zhu  LIU Ying-Liang  XIAO Yong  YUAN Ding-Sheng  ZHANG Jing-Xian
Affiliation:Department of Chemistry, Jinan University, Guangzhou 510632;School of Chemistry & Environmental Engineering , Hubei Institute For Nationalities, Enshi 445000,Department of Chemistry, Jinan University, Guangzhou 510632,Department of Chemistry, Jinan University, Guangzhou 510632,Department of Chemistry, Jinan University, Guangzhou 510632 and Department of Chemistry, Jinan University, Guangzhou 510632
Abstract:
Keywords:organic solvent   nickel   crystal phase
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