Santhanaraj D, Joseph N Ricky, Ramkumar V, Selvamani A, Bincy I P, Rajakumar K
Department of Chemistry, Loyola College Chennai 600 034 Tamilnadu India
Department of Polymer Science and Technology, Council of Scientific and Industrial Research (CSIR) - Central Research Laboratory Adyar Chennai 600020 Tamilnadu India.
RSC Adv. 2020 Oct 26;10(64):39146-39159. doi: 10.1039/d0ra07866b. eCollection 2020 Oct 21.
In this study, 8, 25 and 50 wt% FeO@activated carbon (AC) catalysts were prepared by simple coprecipitation method. The efficiency of the catalysts for the advanced Fenton's oxidation process using methylene blue (MB) as a model substrate was tested. Both modified and unmodified activated carbon catalysts exhibited similar activity towards the Fenton's oxidation process. Therefore, it is difficult to identify the role of the catalyst in this dye removal process. Hence, we proposed a new methodology to remove the MB by adopting the adsorption process initially, followed by the Fenton's oxidation process. The proposed process significantly improved the methylene blue decomposition reaction over the 25 wt% FeO@AC catalyst. However, this trend was not seen in pure activated carbon and FeO@AC (8 and 50 wt%) catalysts due to the instability of the material in the oxidizing medium. The possible reason for the deactivation of the catalysts was evaluated from lattice strain calculations, as derived from the modified W-H models (Uniform Deformational Model (UDM), Uniform Stress Deformation Model (USDM) and Uniform Deformation Energy Density Model (UDEDM)). These results provided a quantitative relationship between the experimentally calculated lattice strain values and Fenton's catalytic activity. Furthermore, the optimized strain value and crystalite size of FeO on the activated carbon matrix are responsible for the high catalytic activity.
在本研究中,通过简单的共沉淀法制备了8 wt%、25 wt%和50 wt%的FeO@活性炭(AC)催化剂。以亚甲基蓝(MB)为模型底物,测试了这些催化剂在高级芬顿氧化过程中的效率。改性和未改性的活性炭催化剂在芬顿氧化过程中均表现出相似的活性。因此,很难确定催化剂在该染料去除过程中的作用。因此,我们提出了一种新方法,即先采用吸附过程,然后进行芬顿氧化过程来去除MB。所提出的过程显著提高了25 wt% FeO@AC催化剂上的亚甲基蓝分解反应。然而,由于材料在氧化介质中的不稳定性,在纯活性炭和FeO@AC(8 wt%和50 wt%)催化剂中未观察到这种趋势。从基于修正的W-H模型(均匀变形模型(UDM)、均匀应力变形模型(USDM)和均匀变形能量密度模型(UDEDM))得出的晶格应变计算中评估了催化剂失活的可能原因。这些结果提供了实验计算的晶格应变值与芬顿催化活性之间的定量关系。此外,活性炭基体上FeO的优化应变值和微晶尺寸是高催化活性的原因。