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作 者:刘崇峻 吴桂叶 马艳红 卢通 刘慧南 赵志强 朱阳戈 钟在定[2] 安耿[2] 陈丽娟[2] LIU Chongjun;WU Guiye;Ma Yanhong;LU Tong;LIU Huinan;ZHAO Zhiqiang;ZHU Yangge;ZHONG Zaiding;AN Geng;CHEN Lijuan(State Key Laboratory of Mineral Processing Science and Technology, Beijing General Research Institute of Mining and Metallurgy, Beijing 100160, China;Jinduicheng Molybdenum Co., Ltd., Xi' an 710077, China)
机构地区:[1]矿冶科技集团有限公司矿物加工科学与技术国家重点实验室,北京100160 [2]金堆城钼业股份有限公司,陕西西安710077
出 处:《矿产保护与利用》2022年第1期75-81,共7页Conservation and Utilization of Mineral Resources
基 金:矿冶科技集团有限公司院基金(02-2010);国家自然科学基金(U20A20269)。
摘 要:传统钼铅分离过程中使用磷诺克斯作为抑制剂,存在毒性大、污染严重等问题。为了降低金堆城钼精矿中铅的含量,对比了毒性较弱的巯基丙醇、L-半胱氨酸、1,3-氧硫杂戊环-羧酸、硫普罗宁的铅抑制效果,并对抑制剂用量进行了考察,经过比较选取1,3-氧硫杂戊环-羧酸作为金堆城钼铅混合精矿的抑制剂。经过条件试验,最终确定在再磨细度-38μm占80%时,经过一次粗选、五次精选,可以获得钼品位52.20%、回收率85.01%、含铅0.010%的钼精矿产品,其效果与磷诺克斯相当。采用配位化学以及密度泛函理论计算了方铅矿和辉钼矿的前线轨道特征,并通过对方铅矿和辉钼矿中金属位点的前线轨道特征进行分析指出,钼铅分离抑制剂的前线轨道对称性是影响抑制剂选择性的关键。In the traditional separation of molybdenum and lead,phosphorus nox is used as an inhibitor,which has serious toxicity and pollution.In order to reduce the content of lead in molybdenum concentrate from Jinduicheng,the lead inhibition effects of mercaptopropanol,L-cysteine,1,3-oxythiopentane carboxylic acid and tiopronin with weak toxicity were compared,and the amount of inhibitor were investigated.After comparison,1,3-oxythiopentane carboxylic acid was selected as the inhibitor of molybdenum-lead-bearing concentrate in Jinduicheng.After condition test,molybdenum concentrate can be obtained with molybdenum grade of 52.20%,recovery rate of 85.01%and lead content of 0.010%through one roughings and five cleanings when the regrinding fineness of-38μm was 80%.The effect of 1,3-oxythiopentane carboxylic acid is equivalent to that of phosphorus Knox.The characteristics of frontier orbits of galena and molybdenite were calculated by means of coordination chemistry and density functional theory,and the characteristics of frontier orbits of metal sites in galena and molybdenite were analyzed.It is pointed out that the symmetry of frontier orbits of the inhibitors is the key to affect the selectivity of inhibitors.
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