Direct reduction is an emerging technology for ferric bauxite utilization. However, because of sodium volatilization, its sodium carbonate consumption is considerably higher than that in ordinary bauxite processing te...Direct reduction is an emerging technology for ferric bauxite utilization. However, because of sodium volatilization, its sodium carbonate consumption is considerably higher than that in ordinary bauxite processing technology. TG-DSC and XRD were applied to detecting phase transformation and mass loss in direct reduction to reveal the mechanism on sodium volatilization. The results show that the most significant influence factor of ferric bauxite on sodium volatilization in direct reduction system is its iron content. Sodium volatilization is probably ascribed to the instability of amorphous substances structure. Amorphous substances are the intermediate-products of the reaction, and the volatilization rate of sodium increases with its generating rate. These amorphous substances are volatile, thus, more sodium is volatilized with its generation. A small amount of amorphous substances are generated in the reaction between Na2CO3 and Al2O3; thus, only 3.15% of sodium is volatilized. Similarly, the volatilization rate is 1.87% in the reaction between Na2CO3 and SiO2. However, the volatilization rate reaches 7.64% in the reaction between Na2CO3 and Fe2O3 because of the generation of a large amount of amorphous substances.展开更多
Malachite,being highly hydrophilic and difficult to be floated conventionally,is usually beneficiated by sulfidation flotation in industry.However,the complex crystal structure of malachite leads to the formation of v...Malachite,being highly hydrophilic and difficult to be floated conventionally,is usually beneficiated by sulfidation flotation in industry.However,the complex crystal structure of malachite leads to the formation of various fracture surfaces with distinct properties during crushing and grinding,resulting in surface anisotropy.In this study,we explored the surface anisotropy of malachite and further investigated its sulfidation mechanism from the coordination chemistry perspective,considering the influence of the Jahn-Teller effect on malachite sulfidation.Computational results reveal that the penta-coordinated Cu ions on the malachite(201)and(010)surfaces exhibit stronger activity compared to those on the malachite(201)surface.Additionally,the tetra-coordinated structure formed by HS^(−)adsorption on the malachite(010)and(201)surfaces is more stable,with more negative adsorption energy,compared to the hexa coordinated structure formed by HS−adsorption on the(201)surface.The sulfidized malachite surface has an additional pair ofπelectron and smaller HOMO(highest occupied molecular orbital)-LUMO(lowest unoccupied molecular orbital)gap with xanthate molecules,causing strongerπbackbonding with xanthate.This study provides new insights into the surface sulfidation mechanism of malachite and offers a theoretical reference for the design of targeted flotation reagents.展开更多
基金Project(51304012)supported by the National Natural Science Foundation of ChinaProject(2014M550845)supported by China Postdoctoral Science FoundationProject(KF13-05)supported by Open Foundation of the State Key Laboratory of Advanced Metallurgy(USTB),China
文摘Direct reduction is an emerging technology for ferric bauxite utilization. However, because of sodium volatilization, its sodium carbonate consumption is considerably higher than that in ordinary bauxite processing technology. TG-DSC and XRD were applied to detecting phase transformation and mass loss in direct reduction to reveal the mechanism on sodium volatilization. The results show that the most significant influence factor of ferric bauxite on sodium volatilization in direct reduction system is its iron content. Sodium volatilization is probably ascribed to the instability of amorphous substances structure. Amorphous substances are the intermediate-products of the reaction, and the volatilization rate of sodium increases with its generating rate. These amorphous substances are volatile, thus, more sodium is volatilized with its generation. A small amount of amorphous substances are generated in the reaction between Na2CO3 and Al2O3; thus, only 3.15% of sodium is volatilized. Similarly, the volatilization rate is 1.87% in the reaction between Na2CO3 and SiO2. However, the volatilization rate reaches 7.64% in the reaction between Na2CO3 and Fe2O3 because of the generation of a large amount of amorphous substances.
基金Projects(52074356,U22A20170)supported by the National Natural Science Foundation of ChinaProject(2022YFC2904503)supported by the National Key R&D Program of China+4 种基金Project(2023SK2061)supported by the Special Fund for the Construction of Hunan Innovative Province,ChinaProject(2023CXQD002)supported by the Innovation-driven Project of Central South University,ChinaProject(2022RC1183)supported by the Science and Technology Innovation Program of Hunan Province,ChinaProject(kq2009005)supported by the Changsha Science and Technology Project(Changsha Outstanding Innovative Youth Training Program),ChinaProject supported by the High-performance Computing Centers of Central South University,China。
文摘Malachite,being highly hydrophilic and difficult to be floated conventionally,is usually beneficiated by sulfidation flotation in industry.However,the complex crystal structure of malachite leads to the formation of various fracture surfaces with distinct properties during crushing and grinding,resulting in surface anisotropy.In this study,we explored the surface anisotropy of malachite and further investigated its sulfidation mechanism from the coordination chemistry perspective,considering the influence of the Jahn-Teller effect on malachite sulfidation.Computational results reveal that the penta-coordinated Cu ions on the malachite(201)and(010)surfaces exhibit stronger activity compared to those on the malachite(201)surface.Additionally,the tetra-coordinated structure formed by HS^(−)adsorption on the malachite(010)and(201)surfaces is more stable,with more negative adsorption energy,compared to the hexa coordinated structure formed by HS−adsorption on the(201)surface.The sulfidized malachite surface has an additional pair ofπelectron and smaller HOMO(highest occupied molecular orbital)-LUMO(lowest unoccupied molecular orbital)gap with xanthate molecules,causing strongerπbackbonding with xanthate.This study provides new insights into the surface sulfidation mechanism of malachite and offers a theoretical reference for the design of targeted flotation reagents.
