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使用羟基磷灰石从单金属和双金属溶液中去除铜和锌

Copper and zinc decontamination from single- and binary-metal solutions using hydroxyapatite.

作者信息

Corami Alessia, Mignardi Silvano, Ferrini Vincenzo

机构信息

Department of Earth Sciences, University of Rome La Sapienza, P.le Aldo Moro 5, 00185 Rome, Italy.

出版信息

J Hazard Mater. 2007 Jul 19;146(1-2):164-70. doi: 10.1016/j.jhazmat.2006.12.003. Epub 2006 Dec 15.

Abstract

Toxic metals contamination of waters, soils and sediments can seriously affect plants, animals and human being. The bioavailability of metal ions can be reduced trapping them in minerals with low solubilities. This study investigated the sorption of aqueous Cu and Zn onto hydroxyapatite surfaces. Batch experiments were carried out using synthetic hydroxyapatite. The metals were applied as single or binary species, in a range of metal concentrations ranging from 0 to 8 mmol/L at 25+/-2 degrees C. The removal capacity of hydroxyapatite was 0.016-0.764 mmol of Cu/g and 0.015-0.725 mmol of Zn/g. In the Cu-Zn binary system, competitive metal sorption occurred with reduction of the removal capacity by 13-76% and 10-63% for Cu and Zn, respectively, compared to the single-metal systems. The sorption of Cu and Zn was well characterized by the Langmuir model. Heavy metal immobilization was attributed to a two-step mechanism: first rapid surface complexation and secondly partial dissolution of hydroxyapatite and ion exchange with Ca followed by the precipitation of a heavy metal-containing hydroxyapatite.

摘要

水、土壤和沉积物中的有毒金属污染会严重影响植物、动物和人类。金属离子的生物有效性会因将它们捕获在低溶解度的矿物质中而降低。本研究调查了水溶液中的铜和锌在羟基磷灰石表面的吸附情况。使用合成羟基磷灰石进行了批量实验。金属以单一或二元形式存在,在25±2℃下金属浓度范围为0至8 mmol/L。羟基磷灰石对铜的去除能力为0.016 - 0.764 mmol/g,对锌的去除能力为0.015 - 0.725 mmol/g。在铜 - 锌二元体系中,与单一金属体系相比,发生了竞争性金属吸附,铜和锌的去除能力分别降低了13 - 76%和10 - 63%。铜和锌的吸附用朗缪尔模型很好地进行了表征。重金属固定归因于两步机制:首先是快速的表面络合,其次是羟基磷灰石的部分溶解以及与钙的离子交换,随后是含重金属的羟基磷灰石沉淀。

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