simultaneous oxidation
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2022 ◽  
Vol 3 (1) ◽  
pp. 19-34
Author(s):  
Susan Alkurdi ◽  
Raed Al-Juboori ◽  
Jochen Bundschuh ◽  
Alla Marchuk

The reuse of waste materials for water treatment purposes is an important approach for promoting the circular economy and achieving effective environmental remediation. This study examined the use of bone char/titanium dioxide nanoparticles (BC/nTiO2) composite and UV for As(III) and As(V) removal from water. The composite was produced via two ways: addition of nTiO2 to bone char during and after pyrolysis. In comparison to the uncoated bone char pyrolyzed at 900 °C (BC900), nTiO2 deposition onto bone char led to a decrease in the specific surface area and pore volume from 69 to 38 m2/g and 0.23 to 0.16 cm3/g, respectively. However, the pore size slightly increased from 14 to 17 nm upon the addition of nTiO2. The composite prepared during pyrolysis (BC/nTiO2)P had better As removal than that prepared after pyrolysis with the aid of ultrasound (BC/nTiO2)US (57.3% vs. 24.8%). The composite (BC/nTiO2)P had higher arsenate oxidation than (BC/nTiO2)US by about 3.5 times. Arsenite oxidation and consequent adsorption with UV power of 4, 8 and 12 W was examined and benchmarked against the composite with visible light and BC alone. The highest UV power was found to be the most effective treatment with adsorption capacity of 281 µg/g followed by BC alone (196 µg/g). This suggests that the effect of surface area and pore volume loss due to nTiO2 deposition can only be compensated by applying a high level of UV power.


Catalysts ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 38
Author(s):  
Seung-Hee Ryu ◽  
Cheol Hong Hwang ◽  
Hojin Jeong ◽  
Giyeong Kim ◽  
Sung Il Ahn ◽  
...  

Pt/γ-Al2O3 catalysts coated on honeycomb-shaped stainless STS-444 steel substrates with a γ-Al2O3 intermediate layer were prepared using a conventional washcoating method. The intermediate layer was formed on the substrate surface through oxidation using pack cementation. The monolithic catalysts with the intermediate layer were fabricated for potential applications to pre-turbocharger catalysts, which suffer from severe conditions such as vibrations of the engine and high flow rates of exhaust gas. Adhesive strength tests and simultaneous oxidation reactions of CO and C3H6 were carried out for the Pt/γ-Al2O3 monolithic catalysts with and without the intermediate layer. The catalysts with an intermediate layer showed much stronger adhesion than the catalysts without an intermediate layer. Thus, the formation of a γ-Al2O3 intermediate layer by surface oxidation through pack cementation facilitated a significant enhancement of the catalyst adhesion strength without catalytic performance degradation.


Chemosphere ◽  
2021 ◽  
pp. 133336
Author(s):  
Donghun Shin ◽  
Jong-Gook Kim ◽  
Hye-Bin Kim ◽  
Kitae Baek

Author(s):  
Haoyun Chen ◽  
Xingzhong Yuan ◽  
Longbo Jiang ◽  
Hou Wang ◽  
Guanjun Zeng

Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 943
Author(s):  
Kaouther Kerboua ◽  
Oualid Hamdaoui ◽  
Naoufel Haddour ◽  
Abdulaziz Alghyamah

The present paper investigates the potential of the Galvano-Fenton process as an advanced technique in terms of the simultaneous oxidation of a model pollutant, phenol, and the energy release and saving as compared to conventional electrochemical techniques, namely, Fenton, Fenton-like, and Electro-Fenton. A numerical model describing the electrochemical, electrolytic, and phenol’s mineralization reactions is presented. Simulations are conducted to predict the kinetics of ferrous and ferric ions, radicals’ formation, and phenol degradation along with released power. Parametric analysis and comparisons are also performed between the basic configuration of the Galvano-Fenton process and its upgraded version integrating a pre-immersion stage of the electrodes in the electrolyte equivalent to 25% of the total experiment’s duration. The ratio of the initial concentration of H2O2 to the concentration of the released/added Fe2+ catalyst is varied from 10 to 30. The effect of phenol concentration is inspected over the range of 0.188 to 10 mg/L as well. Compared to conventional Fenton-based techniques, the Galvano-Fenton process demonstrated a higher performance by reaching 1.34% of degradation efficiency per released J. This is associated with the generation of hydroxyl radicals of 0.047 nM/released J with initial concentrations of hydrogen peroxide and phenol of 0.187 mM and 2 µM, respectively. Moreover, the integration of the pre-immersion stage allowed the overcoming the barrier of the null degradation rate at the initial instant.


Catalysts ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 792
Author(s):  
Feidias Bairamis ◽  
Ioannis Konstantinou

A sequence of WO3/g-C3N4 composites was synthesized at various % weight ratios (1, 5, 6.5, 8, 10, and 15%) of WO3 into g-C3N4 via electrospinning and wet-mixing method. The prepared photocatalytic materials were characterized by X-ray diffraction (XRD), Fourier transform-infrared (FT-IR) spectroscopy, UV–vis diffuse reflection spectroscopy (DRS), scanning electron microscopy (SEM), N2 porosimetry and dynamic light scattering (DLS). Electrospun fibers of WO3 with diameter 250–300 nm was prepared using polyvinylpyrrolidone (PVP) polymer and used for the synthesis of composite WO3/g-C3N4 heterojunction structures. Results showed mesoporous materials with triclinic WO3 crystal phase, surface areas up to 67.7 m2g−1 and band gaps lower than 2.5 eV confirming the absorption to visible light region. The photocatalytic performance of the prepared photocatalysts were assessed towards the oxidation of phenol and reduction of Cr (VI), in single and binary systems using simulated solar light illumination, that followed first-order kinetics. The WO3/g-C3N4 composites were found to exhibit improved photocatalytic performances compared to the pure WO3 and g-C3N4 with 6.5 wt% WO3/g-C3N4 and 5 wt% WO3/g-C3N4 composites being the most efficient catalysts for the oxidation of phenolics and reduction of Cr (VI), respectively. The improved performance was explained by a Z-scheme photocatalytic mechanism which was proposed based on scavenging experiments and the determination of the corresponding energy levels of valence and conduction bands. The study demonstrated that such composites present interesting photocatalytic properties that can be further expanded to other environmental depollution applications as well as in energy applications.


Author(s):  
Xuecheng Sun ◽  
Meesam Ali ◽  
Changzheng Cui ◽  
Shuguang Lyu

Abstract The simultaneous oxidation performance of benzene, toluene, ethylbenzene, and xylene (BTEX) by nanoscale calcium peroxide particles (nCaO2) activated with ferric ions (Fe(III)) and the mechanism of the enhancement of BTEX degradation by L-cysteine (L-cys) were investigated. The batch experimental results showed that the nCaO2/Fe(III)/L-cys process was effective in the destruction of BTEX in both ultrapure water and actual groundwater. A proper amount of L-cys could enhance BTEX degradation due to the promotion of Fe(II)/Fe(III) redox cycles by the participation of L-cys, but excessive presence of L-cys would cause inhibition. Adding 1.0 mM L-cys to the nCaO2/Fe(III) system, the concentration of Fe(II) increased to 1.15 mM instantly. Simultaneously, the yield of HO• produced by 1.0 mM L-cys-containing system was 0.066 mM at 180 min reaction, higher than that without L-cys (0.049 mM). When excess L-cys (5.0 mM) was added to the system, the amount of Fe(II) increased to 3.73 mM because excessive L-cys caused a large number of Fe(III) in the system to be reduced. However, the yield of HO• decreased to 0.043 mM since excessive Fe(II) could conversely scavenge HO• to produce Fe(III) again. EPR tests and quenching results indicated that HO• was the dominant reactive species in the nCaO2/Fe(III)/L-cys system. For the removal of BTEX, the optimal molar ratio of nCaO2/Fe(III)/L-cys was 10.5/20/1 based on the calculation by RSM. Finally, the BTEX destruction pathway was proposed according to the detected intermediates by LC-MS.


Author(s):  
Karola Schühle ◽  
Martin Saft ◽  
Bastian Vögeli ◽  
Tobias J. Erb ◽  
Johann Heider

AbstractA novel acyl-CoA dehydrogenase involved in degradation of the auxin indoleacetate by Aromatoleum aromaticum was identified as a decarboxylating benzylmalonyl-CoA dehydrogenase (IaaF). It is encoded within the iaa operon coding for enzymes of indoleacetate catabolism. Using enzymatically produced benzylmalonyl-CoA, the reaction was characterized as simultaneous oxidation and decarboxylation of benzylmalonyl-CoA to cinnamoyl-CoA and CO2. Oxygen served as electron acceptor and was reduced to H2O2, whereas electron transfer flavoprotein or artificial dyes serving as electron acceptors for other acyl-CoA dehydrogenases were not used. The enzyme is homotetrameric, contains an FAD cofactor and is enantiospecific in benzylmalonyl-CoA turnover. It shows high catalytic efficiency and strong substrate inhibition with benzylmalonyl-CoA, but otherwise accepts only a few medium-chain alkylmalonyl-CoA compounds as alternative substrates with low activities. Its reactivity of oxidizing 2-carboxyacyl-CoA with simultaneous decarboxylation is unprecedented and indicates a modified reaction mechanism for acyl-CoA dehydrogenases, where elimination of the 2-carboxy group replaces proton abstraction from C2.


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