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Sequential Electrolytic Oxidation and Reduction of Aqueous Phase Energetic Compounds

机译:顺序电解氧化和还原水相高能化合物

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摘要

Contamination of soils and groundwater with energetic compounds has been documented atmanyformer ammunition manufacturing plants and ranges.Recent research at Colorado State University(CSU)has demonstrated the potential utility of electrolytic degradation of organic compounds using an electrolytic permeable reactive barrier(e~-barrier).In principle,an electrolytic approach to degrade aqueous energetic compounds such as hexahydro-1,3,5-trinitro-1,3,5-triazine(RDX)or 2,4,6-trinitrotoluene(TNT)can overcome limitations of management strategies that involve solely oxidation or reduction,through sequential oxidation-reduction or reduction-oxidation.The objective of this proof-of-concept research was to evaluate transformation of aqueous phase RDX and TNT in flow-through electrolytic reactors.Laboratory experiments were conducted using six identical column reactors containing porous media and expanded titanium-mixed-metal-oxide electrodes.Three columns tested TNT transformation and three tested RDX transformation.Electrode sequence was varied between columns and one column for each contaminant acted as a no-voltage control.Over 97% of TNT and 93% of RDX was transformed in the reactors under sequential oxidation-reduction.Significant accumulation of known degradation intermediates was notobserved undersequential oxidation-reduction.Removal of approximately 90% of TNT and 40% of RDX was observed under sequential reduction-oxidation.Power requirements on the order of 3 W/m~2 were measured during the experiment.This suggests that an in-situ electrolytic approach may be cost-practical for managing groundwater contaminated with explosive compounds.
机译:在许多前身的弹药制造厂和范围内,有文件记录了高能化合物对土壤和地下水的污染。科罗拉多州立大学(CSU)的最新研究表明,利用电解可渗透反应性势垒(e〜-barrier)可以电解降解有机化合物。原则上,电解方法可以降解含水高能化合物,例如六氢-1,3,5-三硝基-1,3,5-三嗪(RDX)或2,4,6-三硝基甲苯(TNT),可以克服管理上的限制该概念验证研究的目的是评估流通式电解反应器中水相RDX和TNT的转化。概念验证研究的目的是评估流式电解反应器中水相RDX和TNT的转化。六个相同的装有多孔介质和膨胀的钛混合金属氧化物电极的柱式反应器。三个柱子测试了TNT的转化,三个柱子测试了ed RDX转化。电极顺序在各列之间变化,每种污染物充当无电压控制。在连续氧化还原反应器中,超过97%的TNT和93%的RDX在反应器中转化。已知降解的大量积累在连续的氧化还原条件下未观察到中间体,在连续的还原氧化条件下观察到约90%的TNT和40%的RDX被去除,在实验过程中测得的功率需求约为3 W / m〜2。原位电解方法对于管理被爆炸性化合物污染的地下水可能具有成本效益。

著录项

  • 来源
    《Environmental Science & Technology》 |2005年第23期|p.9270-9277|共8页
  • 作者

    DAVID M.GILBERT; TOM C.SALE;

  • 作者单位

    Department of Civil Engineering,Colorado State University,1320 Campus Delivery,Fort Collins,Colorado 80523;

    Department of Civil Engineering,Colorado State University,1320 Campus Delivery,Fort Collins,Colorado 80523;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 环境化学;
  • 关键词

  • 入库时间 2022-08-17 14:08:12

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