Unveiling the catalytic ability of carbonaceous materials in Fenton-like reaction by controlled-release CaO2 nanoparticles for trichloroethylene degradation
- 1. Department of Chemical Engineering, Muhammad Nawaz Sharif University of Engineering and Technology, Multan 60000 (Pakistan)
- 2. State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, Shanghai 200237 (China)
- 3. Institute of Nano-tech and Nano-bionics, Chinese Academy of Sciences (CAS), Suzhou 215123 (China)
- 4. Shanghai Urban Construction Design & Research Institute (Group) Co., Ltd, 3447 Dongfang Road, Shanghai 200125 (China)
Description
Highlights: • Various CMs as catalysts were investigated in Fe(III) activated PVA@nCP reaction for TCE removal. • Besides adsorption, BC and AC degraded 66.2% and 65.2% TCE by catalytic mechanism. • Fe(II) generation on CMs-surface contributed to TCE degradation via active radicals. • XPS, FTIR, and quenching tests unveiled the catalytic-degradation routes of TCE. • The suggested techniques anticipated a new direction towards green environmental remediation for prolonged benefits. Carbonaceous materials (CMs) have been applied extensively for enhancing the catalytic performance of environmental catalysts, however, the self-catalytic mechanism of CMs for groundwater remediation is rarely investigated. Herein, we unveiled the catalytic ability of various CMs via Fe(III) reduction through polyvinyl alcohol-coated calcium peroxide nanoparticles (PVA@nCP) for trichloroethylene (TCE) removal. Among selected CMs (graphite (G), biochar (BC) and activated carbon (AC)), BC and AC showed enhancement of TCE removal of 89% and 98% via both adsorption and catalytic degradation. BET and SEM analyses showed a higher adsorption capacity of AC (27.8%) than others. The generation of solution-Fe(II) and surface-Fe(II) revealed the reduction of Fe(III) on CMs-surface. The role of O-containing groups was investigated by the FTIR technique and XPS quantified the 52% and 57% surface-Fe(II) in BC and AC systems, respectively. EPR and quenching tests confirmed that both solution and surface-bound species (HO• , O2−• and 1O2) contributed to TCE degradation. Acidic pH condition encouraged TCE removal and the presence of HCO3− negatively affected TCE removal than other inorganic ions. Both schemes (PVA@nCP/Fe(III)/BC and PVA@nCP/Fe(III)/AC) exhibited promising results in the actual groundwater, surfactant-amended solution, and removal of other chlorinated-pollutants, opening a new direction towards green environmental remediation for prolonged benefits.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jhazmat.2021.125935Additional details
Identifiers
- DOI
- 10.1016/j.jhazmat.2021.125935;
- PII
- S0304389421008992;
Publishing Information
- Journal Title
- Journal of Hazardous Materials
- Journal Volume
- 416
- Journal Page Range
- vp.
- ISSN
- 0304-3894
- CODEN
- JHMAD9
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54027645
- Subject category
- S36: MATERIALS SCIENCE; S46: INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND TECHNOLOGY;
- Descriptors DEI
- AC SYSTEMS; ACID CARBONATES; ACTIVATED CARBON; ADSORPTION; CALCIUM; CARBONACEOUS MATERIALS; FOURIER TRANSFORM SPECTROMETERS; GRAPHITE; GROUND WATER; INFRARED SPECTRA; NANOPARTICLES; PEROXIDES; PH VALUE; POLLUTANTS; PVA; REMEDIAL ACTION; SCANNING ELECTRON MICROSCOPY; SURFACES; SURFACTANTS; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- ADSORBENTS; ALCOHOLS; ALKALINE EARTH METALS; CARBON; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; ELEMENTS; ENERGY SYSTEMS; HYDROGEN COMPOUNDS; HYDROXY COMPOUNDS; MATERIALS; MEASURING INSTRUMENTS; METALS; MICROSCOPY; MINERALS; NONMETALS; ORGANIC COMPOUNDS; ORGANIC POLYMERS; OXYGEN COMPOUNDS; PARTICLES; PHOTOELECTRON SPECTROSCOPY; POLYMERS; POLYVINYLS; POWER SYSTEMS; SORPTION; SPECTRA; SPECTROMETERS; SPECTROSCOPY; WATER
Optional Information
- Copyright
- Copyright (c) 2021 Elsevier B.V. All rights reserved.