Simultaneous adsorption and oxidative degradation of Bisphenol A by zero-valent iron/iron carbide nanoparticles encapsulated in N-doped carbon matrix
Creators
- 1. College of Environmental Science and Engineering, North China Electric Power University, Beijing, 102206, PR (China)
- 2. NAAM Research Group, Faculty of Science, King Abdulaziz University, Jeddah, 21589 (Saudi Arabia)
- 3. Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, School for Radiological and Interdisciplinary Sciences, Soochow University, Suzhou, 215123, PR (China)
Description
Highlights: • The materials with graphitized shell and dispersed active kernel were fabricated. • The N-doped Fe0/Fe3C@C microcubes have high sorption ability for Bisphenol A (BPA). • The SO4- and OH radicals were responsible for the superior degradation of BPA. • This work affords a feasibly perspective to eliminate organic pollutants. The increased release and accumulation of Bisphenol A (BPA) in contaminated wastewater has resulted in the world wide concerns because of its potential negative effects on human health and aquatic ecosystems. Starting with metal-organic frameworks, we present a simple method to synthesize magnetic porous microcubes (N-doped Fe0/Fe3C@C) with graphitized shell and highly dispersed active kernel via the pyrolysis process under N2 atmosphere. Batch adsorption experimental results showed that N-doped Fe0/Fe3C@C had high adsorption capacity for BPA (∼138 mg g−1 at pH = 7 and 298 K). Degradation of BPA adsorbed on N-doped Fe0/Fe3C@C was further investigated as a function of BPA concentration, persulfate amount, temperature and solution pH. It was found that potassium peroxodisulfate could be activated by N-doped Fe0/Fe3C@C, and a large number of free radicals were generated which was crucial for the degradation of BPA. The concentration of BPA was barely changed in the individual persulfate system. BPA (10 mg L−1) was almost completely degraded within 60 min in the presence of N-doped Fe0/Fe3C@C (∼0.2 g L−1). When the BPA content increased to 25 mg L−1, the removal efficiency of BPA achieved to 98.4% after 150 min. From the XRD, Raman, and XPS analysis, the main adsorption mechanism of BPA was π-π interactions between the π orbital on the carbon basal planes and the electronic density in the BPA aromatic rings. While the superior degradation was attributed to the radical generation and evolution in phenol oxidation. This work not only proved the potential application of N-doped Fe0/Fe3C@C in the adsorption and degradation of BPA, but also opened the new possibilities to eliminate organic pollutants using this kind of magnetic materials in organic pollutants' cleanup.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.envpol.2018.08.061Additional details
Identifiers
- DOI
- 10.1016/j.envpol.2018.08.061;
- PII
- S0269749118314866;
Publishing Information
- Journal Title
- Environmental Pollution (1987)
- Journal Volume
- 243
- Journal Page Range
- p. 218-227
- ISSN
- 0269-7491
- CODEN
- ENPOEK
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 53006190
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- AQUATIC ECOSYSTEMS; CONTROLLED ATMOSPHERES; DOPED MATERIALS; HYDROXYL RADICALS; IRON CARBIDES; MAGNETIC MATERIALS; NANOPARTICLES; NITROGEN; ORGANOMETALLIC COMPOUNDS; OXIDATION; PERSULFATES; PHENOL; POLLUTANTS; POROUS MATERIALS; PUBLIC HEALTH; PYROLYSIS; TEMPERATURE RANGE 0273-0400 K; WASTE WATER; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- AROMATICS; ATMOSPHERES; CARBIDES; CARBON COMPOUNDS; CHEMICAL REACTIONS; COHERENT SCATTERING; DECOMPOSITION; DIFFRACTION; ECOSYSTEMS; ELECTRON SPECTROSCOPY; ELEMENTS; HYDROCARBONS; HYDROGEN COMPOUNDS; HYDROXY COMPOUNDS; IRON COMPOUNDS; LIQUID WASTES; MATERIALS; NONMETALS; ORGANIC COMPOUNDS; OXYGEN COMPOUNDS; PARTICLES; PHENOLS; PHOTOELECTRON SPECTROSCOPY; RADICALS; SCATTERING; SPECTROSCOPY; SULFUR COMPOUNDS; TEMPERATURE RANGE; THERMOCHEMICAL PROCESSES; TRANSITION ELEMENT COMPOUNDS; WASTES; WATER
Optional Information
- Copyright
- Copyright (c) 2018 Published by Elsevier Ltd.