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Compatibility Of Polymers And Chemical Oxidants For Enhanced Groundwater Remediation

机译:聚合物和化学氧化剂的相容性,可增强地下水的修复能力

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Polymer floods provide a promising method to more effectively deliver conventional groundwater treatment agents to organic contaminants distributed within heterogeneous aquifer systems. Combinations of nontoxic polymers (xanthan and hydrolyzed polyacrylamide) and common chemical oxidants (potassium permanganate and sodium persulfate) were investigated to determine the suitability of these mixtures for polymer-enhanced in situ chemical oxidation applications. Oxidant demand and solution viscosity were utilized as initial measures of chemical compatibility. After 72 h of reaction with both test oxidants, solution viscosities in mixtures containing hydrolyzed polyacrylamide were decreased by more than 90% (final viscosities ~2 cP), similar to the 95% viscosity loss (final viscosities ~1 cP, near that of water) observed in xanthan/ persulfate experiments. In contrast, xanthan solutions exposed to potassium permanganate preserved 60-95% of initial viscosity after 72 h. Permanganate depletion in xanthan-containing experiments ranged from 2% to 24% over the same test period. Although oxidant consumption in xanthan/ permanganate solutions appeared to be correlated with increasing xanthan concentrations, solutions of up to 2000 mg/L xanthan did not inhibit permanganate from oxidizing a dissolved-phase test contaminant (tetrachloroethene, PCE) in xanthan solution. These advantageous characteristics (high viscosity retention, moderate oxidant demand, and lack of competitive effects on PCE oxidation rate) render xanthan/ permanganate the most compatible polymer/oxidant combination of those tested for remediation by polymer-enhanced chemical oxidation.
机译:聚合物驱提供了一种有前途的方法,可以更有效地将常规地下水处理剂输送到分布在非均质含水层系统中的有机污染物。研究了无毒聚合物(黄原胶和水解聚丙烯酰胺)与常见化学氧化剂(高锰酸钾和过硫酸钠)的组合,以确定这些混合物对聚合物增强的原位化学氧化应用的适用性。氧化剂需求量和溶液粘度被用作化学相容性的初始量度。与两种测试氧化剂反应72小时后,含水解聚丙烯酰胺的混合物中的溶液粘度降低了90%以上(最终粘度〜2 cP),类似于95%的粘度损失(最终粘度〜1 cP,接近水)。 )在黄原胶/过硫酸盐实验中观察到。相反,暴露于高锰酸钾中的黄原胶溶液在72小时后保留了初始粘度的60-95%。在相同的测试期间,含黄原胶的实验中高锰酸盐的消耗范围为2%至24%。尽管黄原胶/高锰酸盐溶液中的氧化剂消耗量似乎与黄原胶浓度的增加有关,但高达2000 mg / L的黄原胶溶液并不能抑制高锰酸盐氧化黄原胶溶液中的溶解相测试污染物(四氯乙烯,PCE)。这些有利的特性(高粘度保持性,适度的氧化剂需求以及对PCE氧化速率缺乏竞争性影响)使黄原酸/高锰酸盐成为测试通过聚合物增强的化学氧化修复的那些中最相容的聚合物/氧化剂组合。

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