4.8 Article

Sorption of Non-ionic Aromatic Organics to Mineral Micropores: Interactive Effect of Cation Hydration and Mineral Charge Density

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 53, Issue 6, Pages 3067-3077

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.9b00145

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Funding

  1. National Natural Science Foundation of China [21607131, 41877357]
  2. Natural Science Foundation of Zhejiang Province [LR16E080003]

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The influence of K+ and Ca2+ on the sorption of non-ionic aromatic contaminants (1,4-dinitrobenzene and p-xylene) on a series of microporous zeolite minerals (HZSM-5) with various surface charge densities was investigated. For zeolites with high or low charge density (>1.78 or <0.16 sites/nm(2)), K+ and Ca2+ had negligible influence on the sorption of organics, which mainly occurred at the hydrophobic nanosites. For zeolites with charge density in the moderate range (0.16-1.78 sites/nm(2)), the sorption of organics was strongly dependent upon the cation hydration effect. K+ with a lower hydration free energy greatly favored sorption of organics to the micropores compared to Ca2+. Differential scanning calorimetry and X-ray photoelectron spectroscopy results indicated that K+ can reduce the water affinity and promote specific sorption of organics in the zeolites with moderate charge density. The above mechanisms were successfully applied to explain the retention of 1,4-dinitrobenzene and p-xylene on four natural minerals (smectite, illite, kaolinite, and mordenite). This study shed new insights on how cation hydration influences sorption interactions of non-ionic aromatic contaminants at mineral water interfaces as a function of the mineral charge density.

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