Publication Type Journal Article
Title Synthesis of magnetic orderly mesoporous alpha-Fe2O3 nanocluster derived from MIL-100(Fe) for rapid and efficient arsenic(III,V) removal
Authors Zhongmin Liu Jitao Chen Yongchuan Wu Yaru Li Jingyu Zhao Ping Na Samuel Williams Brittany Chandler
Groups G2 G4
Journal JOURNAL OF HAZARDOUS MATERIALS
Year 2018
Month February
Volume 343
Number
Pages 304-314
Abstract A calcination time regulation method has been unprecedentedly used to adjust the orderly mesostructure of novel alpha-Fe2O3 nanoclusters derived from MIL-100(Fe) (MIL: Materials of Institute Lavoisier). The as-synthesized magnetic orderly mesoporous alpha-Fe2O3 nanoclusters were characterized by XRD, SEM, TEM, TGA, N-2 adsorption-desorption isotherms, VSM, Zeta potential, FTIR and XPS. The 6 h calcinated alpha-Fe2O3 nanocluster exhibited the optimal properties, including the high specific surface area and the orderly mesoporous properties, which facilitate the arsenic(III,V) adsorption capacity. The maximum adsorption capacities of As(III) and As(V) were 109.89 and 181.82 mg g(-1), respectively, and adsorption equilibrium can be reached just within 30 min. The kinetics intra-particle diffusion model and adsorption isotherms reveal that the adsorption rate is controlled by pore diffusion and the adsorption process belongs to Langmuir monolayer adsorption. These results indicate that the orderly mesoporous structure of alpha-Fe2O3 nanoclusters plays a key role in rapid and efficient adsorption for arsenic(III,V). Meanwhile, adsorption mechanism verifies that arsenic can react with active sites (Fe-OH) to form complexes by Fe-O-As bond. Moreover, alpha-Fe2O3 nanocluster can be separated easily due to its excellent magnetism. Above all, the magnetism orderly mesoporous alpha-Fe2O3 nanocluster is a promising adsorbent for emergent treatment of arsenic in practice. (C) 2017 Elsevier B.V. All rights reserved.
DOI http://dx.doi.org/10.1016/j.jhazmat.2017.09.047
ISBN
Publisher
Book Title
ISSN 0304-3894
EISSN 1873-3336
Conference Name
Bibtex ID ISI:000414106700034
Observations
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