留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码
Volume 24 Issue 4
Apr.  2017
数据统计

分享

计量
  • 文章访问数:  534
  • HTML全文浏览量:  90
  • PDF下载量:  30
  • 被引次数: 0
Ri-jin Cheng, Hong-wei Ni, Hua Zhang, Xiao-kun Zhang, and Si-cheng Bai, Mechanism research on arsenic removal from arsenopyrite ore during a sintering process, Int. J. Miner. Metall. Mater., 24(2017), No. 4, pp. 353-359. https://doi.org/10.1007/s12613-017-1414-5
Cite this article as:
Ri-jin Cheng, Hong-wei Ni, Hua Zhang, Xiao-kun Zhang, and Si-cheng Bai, Mechanism research on arsenic removal from arsenopyrite ore during a sintering process, Int. J. Miner. Metall. Mater., 24(2017), No. 4, pp. 353-359. https://doi.org/10.1007/s12613-017-1414-5
引用本文 PDF XML SpringerLink
研究论文

Mechanism research on arsenic removal from arsenopyrite ore during a sintering process

  • The mechanism of arsenic removal during a sintering process was investigated through experiments with a sintering pot and arsenic-bearing iron ore containing arsenopyrite; the corresponding chemical properties of the sinter were determined by inductively coupled plasma atomic emission spectrometry (ICP-AES), X-ray diffraction (XRD), and scanning electron microscopy (SEM) coupled with energy-dispersive X-ray spectroscopy (EDS). The experimental results revealed that the reaction of arsenic removal is mainly related to the oxygen atmosphere and temperature. During the sintering process, arsenic could be removed in the ignition layer, the sinter layer, and the combustion zone. A portion of FeAsS reacted with excess oxygen to generate FeAsO4, and the rest of the FeAsS reacted with oxygen to generate As2O3(g) and SO2(g). A portion of As2O3(g) mixed with Al2O3 or CaO, which resulted in the formation of arsenates such as AlAsO4 and Ca3(AsO4)2, leading to arsenic residues in sintering products. The FeAsS component in the blending ore was difficult to decompose in the preliminary heating zone, the dry zone, or the bottom layer because of the relatively low temperatures; however, As2O3(g) that originated from the high-temperature zone could react with metal oxides, resulting in the formation of arsenate residues.
  • Research Article

    Mechanism research on arsenic removal from arsenopyrite ore during a sintering process

    + Author Affiliations
    • The mechanism of arsenic removal during a sintering process was investigated through experiments with a sintering pot and arsenic-bearing iron ore containing arsenopyrite; the corresponding chemical properties of the sinter were determined by inductively coupled plasma atomic emission spectrometry (ICP-AES), X-ray diffraction (XRD), and scanning electron microscopy (SEM) coupled with energy-dispersive X-ray spectroscopy (EDS). The experimental results revealed that the reaction of arsenic removal is mainly related to the oxygen atmosphere and temperature. During the sintering process, arsenic could be removed in the ignition layer, the sinter layer, and the combustion zone. A portion of FeAsS reacted with excess oxygen to generate FeAsO4, and the rest of the FeAsS reacted with oxygen to generate As2O3(g) and SO2(g). A portion of As2O3(g) mixed with Al2O3 or CaO, which resulted in the formation of arsenates such as AlAsO4 and Ca3(AsO4)2, leading to arsenic residues in sintering products. The FeAsS component in the blending ore was difficult to decompose in the preliminary heating zone, the dry zone, or the bottom layer because of the relatively low temperatures; however, As2O3(g) that originated from the high-temperature zone could react with metal oxides, resulting in the formation of arsenate residues.
    • loading
    • [1]
      P. A. Riveros, J. E. Dutrizac, and P. Spencer, Arsenic disposal practices in the metallurgical industry, Can. Metall. Q., 40(2001), No. 4, p. 395.
      [2]
      Y. S. Liang, The possibility of oxidation of arsenic in the steelmaking process:a thermodynamic calculation and practice, Iron Steel, 14(1979), No. 6, p. 35.
      [3]
      J. J. Wang, L. G. Luo, H. Kong, and L. Zhou, The arsenic removal from molten steel, High Temp. Mater. Processes, 30(2011), No. 1-2, p. 171.
      [4]
      H. Z. Zhuang, S. Y. Deng, and J. H. Yuan, The influence of arsenic on the performance of reinforced bar made of carbon structural steel and low alloy steel, Steelmaking, 12(1996), No. 6, p. 35.
      [5]
      Y. S. Liang, The influence of arsenic (As) on the physical properties of carbon steel, Iron Steel, 18(1983), No. 7, p. 55.
      [6]
      W. B. Xin, B. Song, Z. B. Yang, Y. H. Yang, and L. F. Li, Effect of arsenic and copper+arsenic on high temperature oxidation and hot shortness behavior of C-Mn Steel, ISIJ Int., 56(2016), No. 7, p. 1232.
      [7]
      W. B. Xin, B. Song, C. G. Huang, M. M. Song, and G. Y. Song, Effect of arsenic content and quenching temperature on solidification microstructure and arsenic distribution in iron-arsenic alloys, Int. J. Miner. Metall. Mater., 22(2015), No. 7, p. 704.
      [8]
      F. Y. Liu, Surface enrichment of residual elements and oxidation of the austenite grain boundaries, Acta Metall. Sin., 14(1978), No. 3, p. 310.
      [9]
      L. Yin and S. Sridhar, Effects of residual elements arsenic, antimony, and tin on surface hot shortness, Metall. Mater. Trans. B, 42(2011), No. 5, p. 1031.
      [10]
      X. W. Chen, Effect of trace detrimental elements on surface cracking of ingot during forging, Iron Steel, 20(1985), No. 2, p. 31.
      [11]
      Y. H. Ju, J. L. Zhang, and H. Guo, Research on arsenic removal in sintering process in Nansteel, Sintering Pelletizing, 34(2009), No. 5, p. 1.
      [12]
      Y. Z. Zhu, J. C. Li, D. M. Liang, and P. Liu, Distribution of arsenic on micro-interfaces in a kind of Cr, Nb and Ti microalloyed low carbon steel produced by a compact strip production process, Mater. Chem. Phys., 130(2011), No. 1-2, p. 524.
      [13]
      Y. Z. Zhu, Z. Zhu, and J. P. Xu, Grain boundary segregation of minor arsenic and nitrogen at elevated temperatures in a microalloyed steel, Int. J. Miner. Metall. Mater., 19(2012), No. 5, p. 399.
      [14]
      Z. L. Yin, W. H. Lu, and H. Xiao, Arsenic removal from copper-silver ore by roasting in vacuum, Vacuum, 101(2014), No. 3, p. 350.
      [15]
      W. H. Lu and Z. L. Yin, Study on thermal decomposition and arsenic removal of a silver bearing copper ore, Int. J. Miner. Process., 153(2016), p. 1.
      [16]
      N. Chakraborti and D. C. Lynch, Thermodynamics of roasting arsenopyrite, Metall. Trans. B, 14(1983), No. 2, p. 239.
      [17]
      Q. Lu, S. H. Zhang, and X. Hu, Experimental study on removal arsenic in iron ore with arsenic sintering process, Iron Steel, 45(2010), No. 6, p. 7.
      [18]
      Y. T. Li, X. M. Huang, and Z. Y. Duan, Experimental study on arsenic removal in Guangxi Luocheng limonite, Ironmaking, 8(1989), No. 5, p. 59.
      [19]
      D. J. Yang, Y. Z. Zuo, J. R. Peng, L. X. Yang, and R. Z. Xu, Experimental study on arsenic removal of high arsenic laterite ore by roasting, Nonferrous Met. Extract. Metall., 39(2001), No. 3, p. 5.
      [20]
      T. Jiang, Y. F. Huang, Y. B. Zhang, G. H. Han, G. H. Li, and Y. F. Guo, Behavior of arsenic in arsenic-bearing iron concentrate pellets by preoxidizing-weak reduction roasting process, J. Cent. South Univ. Sci. Technol., 41(2010), No. 1, p. 1.
      [21]
      R. J. Cheng, H. W. Ni, H. Zhang, H. Y. He, H. H. Yang, and S. Xiong, Experimental study on arsenic removal from low arsenic-bearing iron ore with sintering process, Sintering Pelletizing, 41(2016), No. 3, p. 13.
      [22]
      N. Chakraborti and D. C. Lynch, Thermodynamic analysis of the As-S-O vapor system, Can. Metall. Q., 24(1985), No. 1, p. 39.
      [23]
      M. L. Contreras, J. M. Arostegui, and L. Armesto, Arsenic interactions during co-combustion processes based on thermodynamic equilibrium calculations, Fuel, 88(2009), No. 3, p. 539.
      [24]
      Y. Q. Hu, Q. Yu, C. H. Zhou, and G. X. Li, Oxidative thermal analysis for arsenopyrite and gold-bearing concentrate, Nonferrous Met., 49(1997), No. 2, p. 72.
      [25]
      S. H. Zhang, Q. Lü, and X. Hu, Thermodynamics of arsenic removal from arsenic-bearing iron ores, Chin. J. Nonferrous Met., 21(2011), No. 7, p. 1705.
      [26]
      P. G. Coombs and Z. A. Munir, The mechanism of oxidation of ferrous sulfide (FeS) powders in the range of 648 to 923 K, Metall. Trans. B, 20(1989), No. 5, p. 661.

    Catalog


    • /

      返回文章
      返回