• 中国出版政府奖提名奖

    中国百强科技报刊

    湖北出版政府奖

    中国高校百佳科技期刊

    中国最美期刊

    Volume 25 Issue 5
    Sep.  2000
    Turn off MathJax
    Article Contents
    LI Yilian, WANG Yanxin, ZHANG Jianghua, GAO Hongbo, 2000. GEOCHEMICAL MODELING OF SULFATE POLLUTION IN KARST WATER OF NIANGZIGUAN REGION, SHANXI PROVINCE, CHINA. Earth Science, 25(5): 467-471.
    Citation: LI Yilian, WANG Yanxin, ZHANG Jianghua, GAO Hongbo, 2000. GEOCHEMICAL MODELING OF SULFATE POLLUTION IN KARST WATER OF NIANGZIGUAN REGION, SHANXI PROVINCE, CHINA. Earth Science, 25(5): 467-471.

    GEOCHEMICAL MODELING OF SULFATE POLLUTION IN KARST WATER OF NIANGZIGUAN REGION, SHANXI PROVINCE, CHINA

    • Received Date: 2000-05-29
    • Publish Date: 2000-09-25
    • The hydro geochemical research into the karst water of Niangziguan spring area indicates the gradual decrease both in the concentration of sulfate and in the mineralization degree, but the gradual increase in the ratios between Ca2+, Mg2+ and SO42- along the flow path. The hydro geochemical modeling shows that the widely dissolving of gypsum causes the high concentration of gypsum from recharge area to discharge area, and even at the shallow aquifer. In addition, the mixing with deep water and sidewise water from the runoff to the discharge area reduces the concentration of sulfate in the water. The extraordinarily high concentration of sulfate was initiated by the pollution by the seepage from the Carboniferous-Permian where the oxidation of sulfide produced much higher sulfate in the Middle Ordovician aquifer. The water from the Lower Ordovician aquifer would be much better.

       

    • loading
    • [1]
      李义连. 山西娘子关岩溶水系统地球化学演化及模拟[D]. 武汉: 中国地质大学, 2000.
      [2]
      Parkhurst D L. Geochemical mole-balance modeling with uncertain data[J]. Water Resources Research, 1997, 33 (8): 1957~1970. doi: 10.1029/97WR01125
      [3]
      Plummer L N, Busby J F, Lee R W, et al. Geochemical modeling of the madison aquifer in parts of Montana, Wyoming, and South Dokota[J]. Water Resource Research, 1990, 26(9): 1981~2014. doi: 10.1029/WR026i009p01981
      [4]
      Plummer L N, Wigley T M L, Parkhurst D L. The kinetics of calcite dissolution in CO2-water system at 5-60 ℃ and 0.0-1.0 atm CO2[J]. Am J Sci, 1978, 278: 179~ 216. doi: 10.2475/ajs.278.2.179
      [5]
      Plummer L N, Busenberg E. The solubilities of calcite, aragonite, and vaterite in CO2-H2O solutions between 0 and 90℃, and an evaluation of the aqueous model for the system CaCO3-CO2-H2O[J]. Geochim Cosmochim Acta, 1982, 46: 1011~1040. doi: 10.1016/0016-7037(82)90056-4
      [6]
      Busenberg E, Plummer L N. Kinetic and thermodynamic factors controlling the distribution of SO42- and Na+ in calcites and selected aragonites[J]. Geochim Cosmochim Acta, 1985, 49: 713~725. doi: 10.1016/0016-7037(85)90166-8
      [7]
      Harvie C E, Weare J H. The predication of mineral solubilities in natural water— the Na-K-Mg-Ca-Cl-SO4-H2O system from zero to higher concentrations at 25 ℃[J]. Geochim Cosmochim Acta, 1980, 44: 981~997. doi: 10.1016/0016-7037(80)90287-2
      [8]
      Plummer L N, Back W. The mass balance approach: applications to interpreting the chemical evolution of hydrologic system[J]. Am J Sci, 1980, 280: 130~142. doi: 10.2475/ajs.280.2.130
      [9]
      Plummer L N, Parkhurst D L, Thorstenson D C. Development of reaction models for ground water systems[J]. Geochim Cosmochim Acta, 1983, 47: 665~685. doi: 10.1016/0016-7037(83)90102-3
    • 加载中

    Catalog

      通讯作者: 陈斌, bchen63@163.com
      • 1. 

        沈阳化工大学材料科学与工程学院 沈阳 110142

      1. 本站搜索
      2. 百度学术搜索
      3. 万方数据库搜索
      4. CNKI搜索

      Figures(1)  / Tables(4)

      Article views (4051) PDF downloads(14) Cited by()
      Proportional views

      /

      DownLoad:  Full-Size Img  PowerPoint
      Return
      Return