共 68 条
A structurally engineered flower shaped magnetic hierarchical sorbent for rapid and selective uptake of Pb2+ ions from water samples
被引:2
作者:

Solanki, Kanika
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Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India
Univ Delhi, Shyamlal Coll, Dept Chem, New Delhi 110032, India Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India

Sharma, Shivani
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Univ Delhi, Ramjas Coll, Dept Chem, New Delhi 110007, India Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India

Rana, Pooja
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Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India

Kaushik, Bhawna
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Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India

Yadav, Sneha
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Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India
Univ Delhi, Inst Home Econ, Dept Chem, Delhi 110016, India Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India

Dixit, Ranjana
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Univ Delhi, Ramjas Coll, Dept Chem, New Delhi 110007, India Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India

Birdar, Ankush V.
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CSIR, CSMCRI, Bhavnagar 364002, Gujrat, India Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India

Gupta, Ashu
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Univ Delhi, Shyamlal Coll, Dept Chem, New Delhi 110032, India Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India

Sharma, R. K.
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h-index: 0
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Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India
机构:
[1] Univ Delhi, Green Chem Network Ctr, Dept Chem, New Delhi 110007, India
[2] Univ Delhi, Shyamlal Coll, Dept Chem, New Delhi 110032, India
[3] Univ Delhi, Ramjas Coll, Dept Chem, New Delhi 110007, India
[4] CSIR, CSMCRI, Bhavnagar 364002, Gujrat, India
[5] Univ Delhi, Inst Home Econ, Dept Chem, Delhi 110016, India
关键词:
ONE-POT SYNTHESIS;
IRON-OXIDE NANOSTRUCTURES;
SCHIFF-BASE COMPLEXES;
EFFICIENT REMOVAL;
HIGHLY EFFICIENT;
AQUEOUS-SOLUTION;
LEAD IONS;
CHROMIUM VI;
PB(II);
ADSORPTION;
D O I:
10.1039/d3qm00264k
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Considering the noxious effects of Pb2+ ions on living organisms as well as the environment, we focus our attention to achieve rapid and selective uptake of Pb2+ ions from aqueous solutions. In this direction, our current work describes an efficient synthetic protocol for the development of economically viable, three-dimensional (3D) ferrite-based hierarchical structures to eradicate Pb2+ ions from wastewater. These magnetic architectures exhibited high BET surface area of 39.5312 m(2) g(-1), good thermal stability up to 400 & DEG;C and flower shaped morphology. The synthesized iron oxide-based materials were systematically characterized through XRD, SEM, VSM, TEM, FT-IR, EDS, XPS, and ED-XRF to elucidate their physio-chemical properties. The designed SALDETA@CPTMS@Fe3O4 adsorbent displayed excellent performance, faster kinetics, rapid separation, high selectivity, and good recyclability for the sorption of Pb2+ ions. Adsorption equilibrium results were justified by the Langmuir model, which indicated the maximum adsorption capacity of 415.5 mg g(-1) and conformed to pseudo second order kinetics. Sorption investigations disclosed that the functionalities available on the surface of the developed sorbent and its hierarchical structure played an active role in the uptake of metal ions and readily removed (within 8 min) Pb2+ ions from solution. Different variables such as pH, amount of sorbent, contact time, eluting agent, effect of interfering ions, etc. were optimized to achieve the best results. This 3D magnetic adsorbent was successfully employed for the elimination of Pb2+ ions in real water samples with good selectivity and efficiency. Furthermore, experimental exploration also indicated that the fabricated material could be advantageous for industrial applications due to its high stability, good regeneration ability (5 runs) and fast sorption-desorption cycle.
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收藏
页码:4482 / 4496
页数:16
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