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Mechanistic study of fouling and regeneration of palladium-based bimetallic catalysts used for the removal of pollutants from drinking water.

机译:用于从饮用水中去除污染物的钯基双金属催化剂的结垢和再生机理研究。

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Nitrate is one of the world's most widespread pollutants in both surface and groundwater and is caused by the over application of fertilizers and leaking septic tanks. The consumption of drinking water containing high levels of nitrate has been directly linked to adverse health effects in humans. Palladium-based bimetallic catalysts hold promise as a potential technology for the removal of nitrate from drinking water. The success of catalytic nitrate reduction however is dependent on the longevity of the catalyst. The primary goals of this work were to assess the effects of non-target water constituents on catalytic nitrate reduction, determine regeneration strategies for fouled-catalysts, and gain insight into the fouling and regeneration mechanisms associated with Pd-based catalysts. A series of batch experiments with Pd-Cu/gamma-Al 2O3 and Pd-In/gamma-Al2O3 catalysts showed that sulfide was the most severe foulant, decreasing the nitrate reduction rate by over two orders of magnitude. Sodium hypochlorite and heated air were effective regenerants for sulfide-fouled catalysts, restoring nitrate reduction rates for a Pd-In/gamma-Al2O3 catalyst from 20% to between 39 and 60% of original levels. Results from ICP-MS revealed that sodium hypochlorite caused dissolution of Cu from the Pd-Cu catalyst but that the Pd-In catalyst was chemically stable during oxidative regenerative conditions. These results indicate that Pd-In catalysts show promise for being robust under fouling and regeneration conditions that may occur when treating natural waters. A subsequent study tested Pd-In/gamma-Al2O3 catalysts for nitrate reduction with hydrogen in a continuous-flow packed-bed reactor. Results showed that the main products of nitrate reduction were ammonia and nitrogen, and the distribution was sensitive to solution conditions. Increases in solution pH, H2, and sulfide concentrations resulted in increases in ammonia production. Regeneration of the sulfide-fouled catalyst bed was able to restore nitrate reduction to near its pre-fouled level, but high ammonia production and low levels of nitrous oxide were observed. Ammonia production from the fresh and regenerated sulfide-fouled catalyst was 32.1+/-0.5 and 82.3+/-1.9% of nitrate reduced, respectively. These results emphasize the need for the removal of reduced sulfur species from nitrate-contaminated source water before they come in contact with Pd-In catalysts.
机译:硝酸盐是地表和地下水中世界上最广泛的污染物之一,其原因是化肥施用过多和化粪池泄漏。饮用含高浓度硝酸盐的饮用水已与人类的不良健康影响直接相关。钯基双金属催化剂有望作为一种从饮用水中去除硝酸盐的潜在技术。然而,催化硝酸盐还原的成功取决于催化剂的寿命。这项工作的主要目标是评估非目标水成分对催化硝酸盐还原的影响,确定结垢催化剂的再生策略,并深入了解与Pd基催化剂相关的结垢和再生机理。使用Pd-Cu /γ-Al2O3和Pd-In /γ-Al2O3催化剂进行的一系列分批实验表明,硫化物是最严重的污垢,使硝酸盐的还原速率降低了两个数量级。次氯酸钠和热空气是硫化物污染催化剂的有效再生剂,将Pd-In /γ-Al2O3催化剂的硝酸盐还原率从原来的20%恢复到39%至60%。 ICP-MS的结果表明,次氯酸钠可导致Cu从Pd-Cu催化剂中溶解,但Pd-In催化剂在氧化再生条件下化学稳定。这些结果表明,Pd-In催化剂有望在处理天然水时可能发生的结垢和再生条件下保持坚固。随后的研究测试了Pd-In /γ-Al2O3催化剂在连续流动填充床反应器中用氢还原硝酸盐的能力。结果表明,硝酸盐还原的主要产物为氨和氮,其分布对溶液条件敏感。溶液pH,H2和硫化物浓度的增加导致氨产量的增加。硫化物污染的催化剂床的再生能够将硝酸盐还原恢复到接近污染前的水平,但是观察到氨的高产量和一氧化二氮的低水平。由新鲜的和再生的硫化物结垢的催化剂生产的氨分别减少了32.1 +/- 0.5%和82.3 +/- 1.9%的硝酸盐还原。这些结果强调了在与Pd-In催化剂接触之前,需要从硝酸盐污染的原水中去除还原的硫。

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