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Re-biodegradation of all alkanes after chemical oxidation in soils

机译:在土壤中化学氧化后重新生物降解所有烷烃

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摘要

Purpose This study aimed to investigate the rapid restoration of indigenous hydrocarbon degraders after chemical oxidation, in order to enhance the subsequent biodegradation of crude oil in soils.Materials and methods The Fe-SOM (2231 mg kg(-1)) and H2O2 were added into the oil-contaminated soil (total petroleum hydrocarbon (TPH): 16064 mg kg(-1)) for chemical oxidation. Then, the all and partial alkane re-biodegradation reagents were added for re-biodegradation experiments. Calculated and analyzed C-source (DOC and TPH) and N-source (NH4+-N, NO3--N, NO2--N) consumption and the population of hydrocarbon degraders in each period.Results and discussion After chemical oxidation, the total biodegradation of all alkanes (re-biodegradation degree: 100%) with reagent for all alkane re-biodegradation in the late stage was higher than that in the early stage. Further study found that DOC was the main C-source and NH4+-N was the main N-source in the early stage, while TPH and nitrate were the main C&N-sources in the late stage of re-biodegradation. In other words, the C&N-sources changed over to TPH and nitrate in the late stage. After re-biodegradation stage, increasing biodegradation (from 644 mg kg(-1) in the 1st stage to 842 mg kg(-1) in the 3rd stage) was observed.Conclusions The results showed that re-biodegradation of all alkanes could recover growth of indigenous hydrocarbon degraders and continuously increase biodegradation of all alkanes after chemical oxidation. The C&N-sources changed from DOC and NH4+-N to all alkanes and NO3--N during re-biodegradation stage was the key factor.
机译:目的本研究旨在研究化学氧化后的土着烃降解剂的快速恢复,以提高土壤中原油的后续生物降解。添加Fe-SOM(2231mg kg(-1))和H2O2进入油污污染土壤(总石油烃(TPH):16064mg kg(-1))用于化学氧化。然后,加入全部和部分烷烃的再生物降解试剂以进行再生物降解实验。计算和分析的C源(DOC和TPH)和N-源(NH4 + -N,NO3 - N,NO2-N)的消耗和烃源的群体在每个期间。结果和讨论后化学氧化,总计在晚期后阶段的所有烷烃再生物降解的试剂的所有烷烃(重新生物降解程度:100%)的生物降解均高于早期阶段的试剂。进一步的研究发现,DOC是主要的C源,NH4 + -N是早期阶段的主要n-源,而TPH和硝酸盐是重新生物降解后期的主要C&N-源。换句话说,C&N-源在晚期的TPH中变为TPH和硝酸盐。在再生物降解阶段之后,观察到在第3阶段的第1阶段中的生物降解(从644mg kg(-1)增加至842mg kg(-1))。结论结果表明所有烷烃的再生物降解可以恢复本土烃降解剂的生长并连续增加化学氧化后所有烷烃的生物降解。在重新生物降解阶段,从DOC和NH4 + -N变为所有烷烃和NO3 - N的C&N-源是关键因素。

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  • 来源
    《Journal of soils & sediments》 |2021年第3期|1348-1359|共12页
  • 作者单位

    Xian Univ Architecture & Technol Sch Environm & Municipal Engn Xian 710055 Shaanxi Peoples R China|MOE Key Lab Northwest Water Resources Environm & Ecol Xian Peoples R China|Key Lab Environm Engn Xian Shaanxi Peoples R China;

    Xian Univ Architecture & Technol Sch Environm & Municipal Engn Xian 710055 Shaanxi Peoples R China|MOE Key Lab Northwest Water Resources Environm & Ecol Xian Peoples R China|Key Lab Environm Engn Xian Shaanxi Peoples R China;

    Xian Univ Architecture & Technol Sch Environm & Municipal Engn Xian 710055 Shaanxi Peoples R China|MOE Key Lab Northwest Water Resources Environm & Ecol Xian Peoples R China|Key Lab Environm Engn Xian Shaanxi Peoples R China;

    Xian Univ Architecture & Technol Sch Environm & Municipal Engn Xian 710055 Shaanxi Peoples R China|MOE Key Lab Northwest Water Resources Environm & Ecol Xian Peoples R China|Key Lab Environm Engn Xian Shaanxi Peoples R China;

    Xian Univ Architecture & Technol Sch Environm & Municipal Engn Xian 710055 Shaanxi Peoples R China|MOE Key Lab Northwest Water Resources Environm & Ecol Xian Peoples R China|Key Lab Environm Engn Xian Shaanxi Peoples R China;

    Xian Univ Architecture & Technol Sch Environm & Municipal Engn Xian 710055 Shaanxi Peoples R China|MOE Key Lab Northwest Water Resources Environm & Ecol Xian Peoples R China|Key Lab Environm Engn Xian Shaanxi Peoples R China;

    Xian Univ Architecture & Technol Sch Environm & Municipal Engn Xian 710055 Shaanxi Peoples R China|MOE Key Lab Northwest Water Resources Environm & Ecol Xian Peoples R China|Key Lab Environm Engn Xian Shaanxi Peoples R China;

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  • 正文语种 eng
  • 中图分类
  • 关键词

    Re-biodegradation; Hydrocarbon degrader; Oil-contaminated soil; Nutrients;

    机译:重新生物降解;碳氢化合物降解剂;油污土;营养素;
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