摘要
The coexistence with other similar valence counterparts greatly hinders the selective recovery of metals, resulting in serious resource waste and environmental pollution. Herein, biochar with numerous surface –NO 2 and –COOH groups was prepared, and in-situ ammonization reaction was catalyzed by electricity to transform those attached –NO 2 into –NH 2 . The as-obtained biochar with stable ligand of –NH 2 (BC-NH 2 ) exhibited an excellent selective adsorption efficiency for copper. Among six bi-valence ions of copper, lead, cadmium, zinc, magnesium and calcium, the above adsorbent could selective recollect 88.76 % and 73.61 % of copper from aqueous and soil respectively. More importantly, the other existent bi-valence ions can be effectively substituted by Cu(II) with a high efficiency up to 91.92 %, even they were saturated on the BC-NH 2 . The Linear sweep voltammetry curves (LSV) and density functional theory (DFT) demonstrate the strongest affinity between Cu(II) and BC-NH 2 than that of other heavy metals, indicating the keynote of the selective mechanism should be the formation of ultra-stable complex between –NH 2 and copper ions. Besides, –COOH group participate the pathway for the transformation from –NO 2 to –NH 2 . This study provides a new concept, and an ideal material as well as novel preparing stratagem, for selective recollecting copper through chelating.
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