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Influence of velocity gradient and rapid mixing time on floes formed by polysilica iron (PSI) and polyaluminum chloride (PAC1)

机译:速度梯度和快速混合时间对聚硅铁(PSI)和聚氯化铝(PAC1)形成的絮凝物的影响

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The aim of this investigation was to evaluate the effect of different velocity gradient and rapid mixing time on coagulation and floe properties, using polysilica iron (PSI) and polyaluminum chloride (PAC1) with different rapid mixing speeds and times. The growth, breakage, and re-growth of floes were monitored by a particle-size analyzer during the rapid mixing, in order to determine the underlying mechanisms. For PSI and PAC1, three different zones were found to depending on the G value in the coagulation process. At low G values (G<546s~(-1) for PSI floes and G<390 s~(-1) for PAC1 floes), the aggregation dominated over breakup. At mean G values (G = 546 s~(-1) for PSI floes and G = 390s~(-1) for PAC1 floes), floe formation was maximized with the largest floes produced at the lowest residual turbidity. For large G values (G>546s~(-1) for PSI floes and G>390s~(-1) for PAC1 floes), breakup dominated over floe formation. Broken floes did not fully re-grow after breakage, probably as a result of a change in the floe surface properties arising from the rupture of bonds within the hydroxide precipitate. A rapid mixing time of 60s led to maximum floe formation. In addition, PSI floes were more durable to high than PAC1.
机译:这项研究的目的是使用不同快速混合速度和时间的聚乙烯铁(PSI)和聚氯化铝(PAC1)评估不同的速度梯度和快速混合时间对混凝和絮凝性能的影响。在快速混合过程中,通过粒度分析仪监测絮凝物的生长,破损和再生长,以确定潜在的机理。对于PSI和PAC1,发现了三个不同的区域,取决于凝血过程中的G值。在低G值下(PSI絮凝剂的G <546s〜(-1),PAC1絮凝剂的G <390 s〜(-1)),聚​​集作用主要取决于分解。在平均G值下(PSI絮凝剂的G = 546 s〜(-1),PAC1絮凝剂的G = 390 s〜(-1)),絮凝剂形成最大化,最大的絮凝剂产生,残留浊度最低。对于较大的G值(PSI絮凝剂的G> 546s〜(-1),PAC1絮凝剂的G> 390s〜(-1)),在絮凝物形成过程中分解占主导地位。破损后的絮凝物在断裂后并未完全重新长大,这可能是由于氢氧化物沉淀中的键断裂而导致的絮凝物表面特性发生了变化。 60s的快速混合时间导致形成最大的絮凝物。另外,PSI絮凝物比PAC1更耐久。

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