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Degradation of carbon tetrachloride using ultrasound‐assisted nanoscaled zero‐valent iron particles@sulfur/nitrogen dual‐doped reduced graphene oxide composite: Kinetics, activation energy, effects of reaction conditions and degradation mechanism
Author(s) -
Meng Fansheng,
Ma Yiyang,
Wang Yeyao
Publication year - 2019
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.5014
Subject(s) - chemistry , graphene , oxide , inorganic chemistry , x ray photoelectron spectroscopy , activation energy , reaction mechanism , sulfur , catalysis , chemical engineering , organic chemistry , engineering
We report a study of the synthesis of nanoscale zero‐valent iron particles stabilized by sulfur/nitrogen dual‐doped reduced graphene oxide (i.e. nZVI@SN‐rGO) and their applications as major reactants for the dechlorination of carbon tetrachloride (CT) by combining sonolysis with consideration of several operation parameters such as pH, temperature, catalyst dosage, as well as in the presence of common inorganic anions. The experimental results showed that the modified technology could remain effective for up to 180 min of reaction time under optimal conditions. Especially, there was no significant reduction in the removal efficiency toward CT even after five cycles, which was indicative of good stability. A study of the effects of common inorganic anions revealed that the presence of Clˉ and HCO 3 ˉ exhibited different positive effects in the following order: Clˉ > HCO 3 ˉ; NO 3 ˉ and SO 4 2 ˉ showed inhibition effects on CT removal. The structure and properties of nZVI@SN‐rGO were characterized using X‐ray diffraction, scanning electron microscopy, surface area analysis, Raman spectroscopy and X‐ray photoelectron spectroscopy. Additionally, the corresponding activation energy was approximately 31.04 kJ mol −1 , suggesting that the surface chemical reaction rather than diffusion was the rate‐limiting step in the CT decomposition process. More importantly, the possible reaction mechanism and dechlorination pathway of CT using the ultrasound‐assisted nZVI@SN‐rGO system were also investigated.