4.5 Article

The adsorption and reduction mechanism of Cr(VI) by kerogen with different degrees of geochemical alteration using a thermal simulation method

期刊

APPLIED GEOCHEMISTRY
卷 140, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.apgeochem.2022.105261

关键词

Adsorption; Reduction; Hexavalent chromium; Kerogen; Thermal simulation

资金

  1. National Natural Science Foundation of China [42107075, 41977172]
  2. National Key Research and Development Program of China [2020YFC1807000]
  3. Fundamental Research Funds for the Central Universities [2652019019]

向作者/读者索取更多资源

This study emphasizes that the organic matter in soils and sediments, known as kerogen, plays a crucial role in the adsorption, reduction, and complexation of Cr(VI) within the subsurface environment. The geochemical processes of kerogen can vary at different temperature stages, affecting its interaction with Cr(VI) and ultimately influencing the fate of this contaminant. It is important to consider the complexities of kerogen, characterized by its heterogeneity, functionalities, aliphaticity, and aromaticity, rather than treating it as a uniform organic phase.
Any analysis that fails to consider the existence of kemgen materials in soils and sediments within the subsurface environment may result in serious deviations in quantifying and characterizing the fate of Cr(VI), especially considering that kemgen may be of different degrees of geochemical alteration, and the effect is still unclear. An anaerobic thermal simulation technique was utilized to simulate the diagenesis (T <= 350 degrees C), catagenesis (350 degrees C < T <= 500 degrees C) and metagenesis (500 degrees C < T <= 700 degrees C) geochemical processes of kerogen using a typical lignite. The molecular characteristics transition of kerogen from aliphatic to aromatic and aromatic to aliphatic were recorded at 300 and 600 degrees C respectively with temperature increasing. The adsorption capacity increased as a function of temperature, and Cr(VI) adsorption mechanism by kerogen was controlled by the carboxylic group driven by different forces at diagenesis, catagenesis, and metagenesis stages. Cr(VI) reduction capacities decreased with temperature increasing due to the decreasing of phenolic moieties and hydroxyl groups, which were the main electron donors for Cr(VI) reduction. The complexation mechanism of Cr(III), which is mainly related to the process of Cr(VI) reduction by phenol, was consequently complexed by the oxidized phenol sites, rather than to be released into aqueous phase and then be complexed by carboxylic groups. This study highlighted that within the subsurface environment, the highly physicochemically heterogeneous kerogen have varied functionalities, aliphaticity and aromaticity, which could play various roles in Cr(VI) adsorption, reduction and complexation, and hence should not be considered as a single organic phase.

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