scholarly journals Application of Mineral Iron-Based Natural Catalysts in Electro-Fenton Process: A Comparative Study

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 57
Author(s):  
Zahra Heidari ◽  
Rasool Pelalak ◽  
Reza Alizadeh ◽  
Nihal Oturan ◽  
Saeed Shirazian ◽  
...  

The potential use of novel iron based mineral catalysts as an effective and available material for electrocatalytic oxidation of refractory contaminants by heterogeneous electro-Fenton (HEF) process was studied for the first time. For this purpose, four natural catalysts, namely ilmenite (FeTiO3), pyrite (FeS2), chromite (FeCr2O4), and chalcopyrite (CuFeS2) were selected as the source of ferrous iron (Fe2+) ions. The catalyst samples were appropriately characterized by X-ray diffraction (XRD) and RAMAN analysis. The degradation kinetics and mineralization rate of 0.2 mM antibiotic cefazolin (CFZ), as a contaminant of emerging concern, were comparatively investigated by HEF using the catalysts mentioned above. The effect of important experimental parameters such as catalysts loading and current on the process efficiency was investigated. Moreover, the performance of these new mineral catalysts was compared in term of CFZ degradation kinetics, mineralization power, mineralization current efficiency and electrical energy consumption. A greater enhancement in degradation/mineralization of CFZ was obtained when using chalcopyrite as the catalyst in HEF. The stability and reusability experiments demonstrated negligible decrease in catalytic activity of chalcopyrite after five consecutive runs. Besides, the rate constant for CFZ oxidation by hydroxyl radicals was estimated according the pseudo-first-order reaction kinetics. The empirical assessment, in addition to economic evaluation, confirmed that iron based mineral catalysts and specifically chalcopyrite could be an appropriate and cost-effective alternative catalyst for HEF due to its high catalytic activity, availability, eco-friendly nature and low energy consumption compared to other synthesized catalysts.

2014 ◽  
Vol 53 (47) ◽  
pp. 12855-12859 ◽  
Author(s):  
Ping Jiang ◽  
Qian Liu ◽  
Yanhui Liang ◽  
Jingqi Tian ◽  
Abdullah M. Asiri ◽  
...  

2014 ◽  
Vol 70 (9) ◽  
pp. 1548-1554 ◽  
Author(s):  
Deli Wu ◽  
Yanxia Liu ◽  
Dong Duan ◽  
Luming Ma

Pyrite cinder (PyC) was employed as a heterogeneous Fenton-like catalyst, and its catalytic activity was evaluated in view of the effects of catalyst dosage, pH and leaching metal ions. PyC showed significant reactivity, and the pseudo-first-order kinetic rate constant for decomposition of H2O2 and degradation of Acid Red B (ARB) were 3.4 and 14.89 (10−3 min−1) respectively when pH = 5. When 20 g/L PyC was added into 10 mM H2O2 solution in neutral pH, H2O2 could be completely degraded within 4 h, and more than 90% ARB was removed. Leaching metal ions from PyC were found to have little effect on decomposition of H2O2 or on degradation of ARB. PyC still had high catalytic activity after five successive runs. The decomposition mechanism of H2O2 was analyzed and the Haber–Weiss mechanism was employed in this paper. The electron spin resonance image showed •OH was produced and increased between 3 and 5 min in the PyC catalyzing H2O2 reaction, which demonstrated that PyC had a durable ability to produce •OH.


Catalysts ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 484 ◽  
Author(s):  
Alena Kulakova ◽  
Alexey Bilyachenko ◽  
Victor Khrustalev ◽  
Yan Zubavichus ◽  
Pavel Dorovatovskii ◽  
...  

Unprecedented germanium-based sesquioxane exhibits an extremely high nuclearity (Cu42Ge24Na4) and unusual encapsulation features. The compound demonstrated a high catalytic activity in the oxidative amidation of alcohols, with cost-effective catalyst loading down to 400 ppm of copper, and in the oxidation of cyclohexane and other alkanes with H2O2 in acetonitrile in the presence of nitric acid. Selectivity parameters and the mode of dependence of initial cyclohexane oxidation rate on initial concentration of the hydrocarbon indicate that the reaction occurs with the participation of hydroxyl radicals and alkyl hydroperoxides are formed as the main primary product. Alcohols have been transformed into the corresponding ketones by the catalytic oxidation with tert-butyl hydroperoxide.


ACS Catalysis ◽  
2014 ◽  
Vol 4 (11) ◽  
pp. 4065-4069 ◽  
Author(s):  
Yanhui Liang ◽  
Qian Liu ◽  
Abdullah M. Asiri ◽  
Xuping Sun ◽  
Yonglan Luo

2018 ◽  
Vol 42 (11) ◽  
pp. 9324-9331 ◽  
Author(s):  
Jie Li ◽  
Saisai Cheng ◽  
Tianxing Du ◽  
Ningzhao Shang ◽  
Shutao Gao ◽  
...  

Pd nanoparticles anchored on g-C3N4 NS/rGO were prepared by means of a cost-effective and facile co-assembly approach. The hybrid composite showed high catalytic activity and stability for the hydrogenation of alkenes with FA and HCOONH4 as hydrogen donors.


RSC Advances ◽  
2015 ◽  
Vol 5 (97) ◽  
pp. 79348-79354 ◽  
Author(s):  
Xinhua Tang ◽  
Haoran Li ◽  
Zhuwei Du ◽  
How Yong Ng

Iron–nitrogen–carbon catalysts exhibited very high catalytic activity towards ORR and significantly enhanced power production in MFCs.


2014 ◽  
Vol 126 (47) ◽  
pp. 13069-13073 ◽  
Author(s):  
Ping Jiang ◽  
Qian Liu ◽  
Yanhui Liang ◽  
Jingqi Tian ◽  
Abdullah M. Asiri ◽  
...  

MRS Advances ◽  
2020 ◽  
Vol 5 (57-58) ◽  
pp. 2961-2972
Author(s):  
P.C. Meléndez-González ◽  
E. Garza-Duran ◽  
J.C. Martínez-Loyola ◽  
P. Quintana-Owen ◽  
I.L. Alonso-Lemus ◽  
...  

In this work, low-Pt content nanocatalysts (≈ 5 wt. %) supported on Hollow Carbon Spheres (HCS) were synthesized by two routes: i) colloidal conventional polyol, and ii) surfactant-free Bromide Anion Exchange (BAE). The nanocatalysts were labelled as Pt/HCS-P and Pt/HCS-B for polyol and BAE, respectively. The physicochemical characterization of the nanocatalysts showed that by following both methods, a good control of chemical composition was achieved, obtaining in addition well dispersed nanoparticles of less than 3 nm TEM average particle size (d) on the HCS. Pt/HCS-B contained more Pt0 species than Pt/HCS-P, an effect of the synthesis method. In addition, the structure of the HCS remains more ordered after BAE synthesis, compared to polyol. Regarding the catalytic activity for the Oxygen Reduction Reaction (ORR) in 0.5 M KOH, Pt/HCS-P and Pt/HCS-B showed a similar performance in terms of current density (j) at 0.9 V vs. RHE than the benchmark commercial 20 wt. % Pt/C. However, Pt/HCS-P and Pt/HCS-B demonstrated a 6 and 5-fold increase in mass catalytic activity compared to Pt/C, respectively. A positive effect of the high specific surface area of the HCS and its interactions with metal nanoparticles and electrolyte, which promoted the mass transfer, increased the performance of Pt/HCS-P and Pt/HCS-B. The high catalytic activity showed by Pt/HCS-B and Pt/HCS-P for the ORR, even with a low-Pt content, make them promising cathode nanocatalysts for Anion Exchange Membrane Fuel Cells (AEMFC).


2019 ◽  
Author(s):  
Du Sun ◽  
yunfei wang ◽  
Kenneth Livi ◽  
chuhong wang ◽  
ruichun luo ◽  
...  

<div> <p>The synthesis of alloys with long range atomic scale ordering (ordered intermetallics) is an emerging field of nanochemistry. Ordered intermetallic nanoparticles are useful for a wide variety of applications such as catalysis, superconductors, and magnetic devices. However, the preparation of nanostructured ordered intermetallics is challenging in comparison to disordered alloys, hindering progress in materials development. We report a process for converting colloidally synthesized ordered intermetallic PdBi<sub>2</sub> to ordered intermetallic Pd<sub>3</sub>Bi nanoparticles under ambient conditions by an electrochemically induced phase transition. The low melting point of PdBi<sub>2</sub> corresponds to low vacancy formation energies which enables the facile removal of the Bi from the surface, while simultaneously enabling interdiffusion of the constituent atoms via a vacancy diffusion mechanism under ambient conditions. The resulting phase-converted ordered intermetallic Pd<sub>3</sub>Bi exhibits 11x and 3.5x higher mass activty and high methanol tolerance for the oxygen reduction reaction compared to Pt/C and Pd/C, respectively,which is the highest reported for a Pd-based catalyst, to the best of our knowledge. These results establish a key development in the synthesis of noble metal rich ordered intermetallic phases with high catalytic activity, and sets forth guidelines for the design of ordered intermetallic compounds under ambient conditions.</p> </div>


Author(s):  
Nikolay S. Shulaev ◽  
◽  
Valeriya V. Pryanichnikova ◽  
Ramil R. Kadyrov ◽  
Inna V. Ovsyannikova ◽  
...  

The most essential scientifific and practical task in the area of ecological safety of pipelines operation is the development and improvement of methods of purifification and restoration of oil-contaminated soils. One of the most effificient and cost effective methods is electrochemical purifification, that does not require the use of expensive chemical reagents and soil excavation. However, the consideration of non-uniform contamination of various soil sections is required. The article examines the features of the organization and technological infrastructure for electrochemical purifification of non-uniformly contaminated soils when using a single electrical energy source, a method for calculating the design parameters of the corresponding installation is proposed. Effificient purifification of non-uniformly contaminated soil when using a specifified voltage is possible through the use of different-sized electrodes. For each soil type, the amount of transmitted electric charge required for soil purifification is determined by the concentration of the contaminant. Allocation of cathodes and anodes as parallel batteries and their connection using individual buses is an effective and energy-effificient solution, since an almost-uniform electric fifield is created in an inter-electrode space, thus allowing the reduction of the interelectrode resistance of the medium.


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