期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
滇西南墨江金厂金镍矿床金、镍赋存状态及成矿过程探讨 被引量:17
1
作者 熊伊曲 杨立强 +4 位作者 邵拥军 赵凯 李坡 卢宜冠 杜达洋 《岩石学报》 SCIE EI CAS CSCD 北大核心 2015年第11期3309-3330,共22页
墨江金厂金镍矿床位于滇西南哀牢山造山带中段,是西南三江地区一个独特的金镍共生矿床。笔者通过野外地矿物主要为针镍矿、辉砷镍矿、锑硫镍矿、黄铁矿等。依据矿(化)脉切割关系、矿石结构构造及矿物共生组合,墨江金厂金镍矿床成岩-... 墨江金厂金镍矿床位于滇西南哀牢山造山带中段,是西南三江地区一个独特的金镍共生矿床。笔者通过野外地矿物主要为针镍矿、辉砷镍矿、锑硫镍矿、黄铁矿等。依据矿(化)脉切割关系、矿石结构构造及矿物共生组合,墨江金厂金镍矿床成岩-成矿期共发育4个世代黄铁矿。沉积变质期以草莓状黄铁矿和胶状黄铁矿为主,热液成矿期可划分为:早阶段石英-针镍矿-辉砷镍矿-锑硫镍矿-黄铁矿;主阶段石英-黄铁矿-毒砂-硫锑铜银矿-自然金;晚阶段方解石-石英-黄铁矿。对矿区赋金镍贯通性矿物黄铁矿进行详细的电子探针分析,结果显示4个世代黄铁矿微量元素有所差异。其中热液主阶段黄铁矿中含有Au、As、Sb、Pb、Zn、Cu、Co、Ni和Te,显示其流体成分复杂。不同阶段黄铁矿Ni含量不同,沉积变质期黄铁矿中Ni含量较低,为0.00%~0.82%,平均0.26%;热液早阶段黄铁矿中Ni含量最高,为0.43%~3.15%,平均1.38%;热液主阶段黄铁矿中Ni含量降低,为0.00%~0.99%,平均0.22%;热液晚阶段黄铁矿中Ni含量最低,为0.00%~0.09%,平均0.03%。研究结果表明墨江金厂金镍矿床中主要含金矿物和含镍矿物形成于热液期,含金矿物形成晚于含镍矿物。Ni在热液流体中的迁移能力与流体温度正相关,温度越高,Ni进入黄铁矿晶格的能力越强。基于上述金、镍成矿过程研究成果,并对比国内外热液镍矿床的地质-地球化学特征,推断墨江金厂金镍矿床是一个受岩浆热液改造的中-低温热液金镍矿床。 展开更多
关键词 金镍矿物 微量元素 成矿过程 墨江 滇西南
下载PDF
Leaching of nickel-molybdenum sulfide ore in membrane biological reactor 被引量:1
2
作者 陈家武 高从堦 +2 位作者 张启修 肖连生 张贵清 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2011年第6期1395-1401,共7页
The bioleaching of molybdenum from its sulfide ore using a Mo-resistant thermophilic bacterium sulfolobus metallics combined with a membrane biological reactor(MBR) was studied.The experimental results showed that t... The bioleaching of molybdenum from its sulfide ore using a Mo-resistant thermophilic bacterium sulfolobus metallics combined with a membrane biological reactor(MBR) was studied.The experimental results showed that the concentration of Mo can be controlled by filter of the membrane in MBR and the toxicity of Mo to microorganism is decreased in the process of bioleaching.It was also evidenced that there were different leaching rates of Ni and Mo when the concentration of Mo was different.After leaching for 20 d in the MBR at Mo concentration of 395 mg/L,the leaching rates of Ni and Mo reached the maximum of 79.57% and 56.23% respectively under the conditions of 100 g/L of mineral density,65 ℃,pH=2 and 1.0 L/min of the aeration rate.While 75.59% Ni and 54.33% Mo were leached out in column without membrane under the same conditions. 展开更多
关键词 membrance biological reactor nickel-molybdenum sulfide ore sulfolobus metallics BIOLEACHING molybdenum toxicity
下载PDF
Fe/Co and Ni/Co-pentlandite type electrocatalysts for the hydrogen evolution reaction 被引量:2
3
作者 Mathias Smialkowski David Tetzlaff +2 位作者 Lars Hensgen Daniel Siegmund Ulf-Peter Apfel 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 2021年第8期1360-1369,共10页
Metal-rich transition metal sulfides recently gained increasing attention as electrocatalysts for the hydrogen evolution reaction(HER),as they are capable to overcome major challenges faced by sulfide-rich metal catal... Metal-rich transition metal sulfides recently gained increasing attention as electrocatalysts for the hydrogen evolution reaction(HER),as they are capable to overcome major challenges faced by sulfide-rich metal catalysts such as limited conductivity and the necessity of nanostructuring.Herein,we present the synthesis,characterization and electrocatalytic investigation of ternary metal-rich sulfide composites FexCo9-xS8 as well as Ni_(y)Co_(9-y)S_(8)(x=y=0-4.5),which possess pentlandite-type structures.In this study,we show a stepwise alteration of the binary cobalt pentlandite Co9S8 and report on the replacement of cobalt with up to 4.5 equivalents of either iron or nickel.These altered pentlandite composites facilitate the proton reduction in acidic media at different temperatures.We furthermore show that the stoichiometric variation has a decisive influence on the electrochemical activation/deactivation behavior of the catalysts under reductive electrocatalytic conditions.Here,Co-deficient composites display an improved HER performance in contrast to Co_(9)S_(8).Notably,Ni/Co compounds generally tend to show higher catalytic activities towards HER than their respective Fe/Co compounds. 展开更多
关键词 Hydrogen PENTLANDITE Metal sulfides Transition metals ELECTROCATALYSIS
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部