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Effects of current density, bicarbonate and humic acid on electrochemical induced calcium phosphate precipitation

机译:电流密度,碳酸氢盐和腐殖酸对电化学诱导磷酸钙沉淀的影响

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Phosphorus (P) removal and recovery from sewage as calcium phosphate (CaP) by chemical precipitation is a widely used method. To avoid the addition of chemicals to increase the pH of the bulk solution and the need for a further separation step in conventional chemical precipitation process, we developed an electrochemical method, which can locally increase the pH near a Ti cathode. The separation of product and liquid then happens simultaneously by accumulating CaP at the electrode surface. The current density plays a crucial role in this system. A current density of 19 A/m(2) results in the formation of crystalline CaP rather than amorphous CaP, but it does not enhance the removal of P in 24 h. Moreover, the current efficiency decreases with increasing current density. Furthermore, the increased H-2 production at high current density may push the precipitated CaP back to the bulk solution, resulting in its dissolution. In the presence of bicarbonate (1-5 mM) or humic acid (1-20 mg/L), the removal of P was higher. This is probably due to the inhibited CaP precipitation in the bulk solution which in turn leaves more Ca and P ions available for the local precipitation on the cathode. However, bicarbonate at high concentration (10 mM) dropped P removal from 52 to 25%. This is caused by competition of carbonate and phosphate with the free Ca2+ ions and also by buffering the producted hydroxide ions at the cathode. The study shows that P can be removed as CaP by electrochemical precipitation at low current densities at common concentrations of bicarbonate and humic acid.
机译:通过化学沉淀的磷酸钙(帽)从污水中除去和恢复磷(P)是一种广泛使用的方法。为避免添加化学物质以增加本体溶液的pH,并且需要在常规化学沉淀过程中进一步分离步骤,我们开发了一种电化学方法,其可以在Ti阴极附近局部增加pH。然后,通过在电极表面累积帽,将产品和液体的分离同时发生。目前的密度在该系统中起着至关重要的作用。电流密度为19A / m(2)导致结晶帽而不是无定形帽的形成,但它不会增强24小时的去除。此外,电流效率随着电流密度的增加而降低。此外,高电流密度的H-2增加可以将沉淀的帽推​​回散装溶液,导致其溶解。在碳酸氢盐(1-5mm)或腐殖酸(1-20mg / L)的存在下,去除p较高。这可能是由于批量溶液中的抑制帽沉淀,其又留下了在阴极上可用于局部沉淀的Ca和P离子。然而,高浓度(10mm)的碳酸氢盐下降,P除去52%至25%。这是由碳酸酯和磷酸盐与游离Ca2 +离子的竞争引起的,并且还通过缓冲在阴极处的产物氢氧化物离子。该研究表明,P可以通过在碳酸氢盐和腐殖酸的常见浓度下通过电化学沉淀除去作为帽。

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