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Activated persulfate and catalyzed hydrogen peroxide propagation system reactivity and stability during in situ chemical oxidation.

机译:活化的过硫酸盐和催化的过氧化氢传播系统在原位化学氧化过程中的反应性和稳定性。

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摘要

The types of activators and kinetics for persulfate activation are still being researched, as well as stabilization methods to prolong CHP reactions. The objective of this research was to investigate the activation of persulfate by surfactants, study persulfate activation during exertion of total oxidant demand (TOD), and compare CHP stabilization by phosphate, phytate, and citrate. The first chapter presents an introduction to the theory and purpose of the research. The second chapter examines activation of persulfate at acidic and basic pH by anionic, nonionic, and cationic surfactants, and the reactive oxygen species generated by persulfate in the presence the surfactants. The results of this research demonstrate that surfactants added to ISCO systems often activate persulfate to generate reductants at both acidic and basic pH, and hydroxyl radical at basic pH. These findings provide a new paradigm for persulfate activation in SISCO systems; pH regimes >11 may not be necessary for persulfate activation resulting in cost savings and potentially more effective activation of persulfate.;The third chapter investigates the generation of reactive oxygen species and the destruction of a common groundwater contaminant, trichloroethylene (TCE), during TOD exertion in low (0.5%), medium (1.3%), and high (2.4%) SOM soils. The results from this research demonstrate that persulfate activation occurred as TOD was exerted. The activation was specific to the generation of reductants + nucleophiles, but not hydroxyl radical. In addition, TCE degradation occurred in proportion to the TOD exerted. The findings of this research document that, unlike permanganate TOD, the TOD exerted during persulfate ISCO applications can activate persulfate to generate reductants + nucleophiles that can potentially degrade contaminants during persulfate ISCO applications.;The forth chapter explores the use of lower concentrations of stabilizers in catalyzed hydrogen peroxide propagations and their effect on hydrogen peroxide decomposition and the reactive oxygen species generated. The findings of this research demonstrate that lower concentrations of effective stabilizers such as phytate and phosphate can increase hydrogen peroxide longevity in CHP ISCO while maintaining the generation of reactive oxygen species, thus reducing overall treatment costs and providing more effective process conditions.
机译:仍在研究过硫酸盐活化的活化剂类型和动力学以及延长CHP反应的稳定化方法。这项研究的目的是研究表面活性剂对过硫酸盐的活化作用,研究在施加总氧化剂需求(TOD)期间过硫酸盐的活化作用,并比较磷酸盐,植酸盐和柠檬酸盐对CHP的稳定性。第一章介绍了研究的理论和目的。第二章研究了阴离子,非离子和阳离子表面活性剂在酸性和碱性pH下对过硫酸盐的活化,以及在表面活性剂存在下过硫酸盐产生的活性氧种类。这项研究的结果表明,添加到ISCO系统中的表面活性剂通常会在酸性和碱性pH值下活化过硫酸盐生成还原剂,在碱性pH值下生成羟基自由基。这些发现为SISCO系统中的过硫酸盐活化提供了新的范例。 pH值大于11的溶液对于过硫酸盐的活化可能不是必需的,这样可以节省成本并可能更有效地活化过硫酸盐。第三章研究了TOD期间活性氧的产生和常见地下水污染物三氯乙烯(TCE)的破坏。在低(0.5%),中(1.3%)和高(2.4%)SOM土壤中发挥作用。这项研究的结果表明,过硫酸盐活化发生在施加TOD时。活化是特定于还原剂+亲核试剂的生成,而不是羟基自由基的生成。另外,TCE降解与所施加的TOD成正比。该研究文件的发现表明,与高锰酸盐TOD不同,在过硫酸盐ISCO施用期间施加的TOD可以活化过硫酸盐以生成还原剂+亲核试剂,这些物质可能会在过硫酸盐ISCO施用期间潜在地降解污染物。;第四章探讨了在低硫酸盐ISCO施用中使用较低浓度的稳定剂。催化过氧化氢的传播及其对过氧化氢分解和产生的活性氧的影响。这项研究的结果表明,较低浓度的有效稳定剂(例如肌醇六磷酸和磷酸盐)可以提高CHP ISCO中的过氧化氢寿命,同时保持活性氧的生成,从而降低了总体处理成本并提供了更有效的工艺条件。

著录项

  • 作者

    Elloy, Farah Catherine.;

  • 作者单位

    Washington State University.;

  • 授予单位 Washington State University.;
  • 学科 Environmental engineering.;Environmental science.
  • 学位 Ph.D.
  • 年度 2014
  • 页码 112 p.
  • 总页数 112
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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