Phosphate removal from synthetic and real wastewater using steel slags produced in Europe

被引:255
|
作者
Barca, Cristian [1 ,2 ]
Gerente, Claire [1 ]
Meyer, Daniel [1 ,2 ]
Cliazarenc, Florent [1 ]
Andres, Yves [1 ]
机构
[1] LUNAM Univ, Ecole Mines Nantes, CNRS, GEPEA,UMR 6144, F-44307 Nantes 3, France
[2] ZAC Balarucs, Epur Nat SAS, F-84510 Caumont Sur Durance, France
关键词
Phosphate removal; Steel slag; Hydroxyapatite; Batch experiment; BASIC OXYGEN FURNACE; PHOSPHORUS REMOVAL; BLAST-FURNACE; CONVERTER SLAG; CRYSTALLIZATION; MECHANISMS; ADSORPTION; RECOVERY;
D O I
10.1016/j.watres.2012.02.012
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Electric arc furnace steel slags (EAF-slags) and basic oxygen furnace steel slags (BOF-slags) were used to remove phosphate from synthetic solutions and real wastewater. The main objective of this study was to establish an overview of the phosphate removal capacities of steel slags produced in Europe. The influences of parameters, including pH, and initial phosphate and calcium concentrations, on phosphate removal were studied in a series of batch experiments. Phosphate removal mechanisms were also investigated via an in-depth study. The maximum capacities of phosphate removal from synthetic solutions ranged from 0.13 to 0.28 mg P/g using EAF-slags and from 1.14 to 2.49 mg P/g using BOF-slags. Phosphate removal occurred predominantly via the precipitation of Ca-phosphate complexes (most probably hydroxyapatite) according to two consecutive reactive phases: first, dissolution of CaO-slag produced an increase in Ca2+ and OH- ion concentrations; then the Ca2+ and OH- ions reacted with the phosphates to form hydroxyapatite. It was found that the release of Ca2+ from slag was not always enough to enable hydroxyapatite precipitation. However, our results indicated that the Ca2+ content of wastewater represented a further source of Ca2+ ions that were available for hydroxyapatite precipitation, thus leading to an increase in phosphate removal efficiencies. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2376 / 2384
页数:9
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