scholarly journals Catalytic ozonation of diclofenac with iron silicate-loaded pumice in aqueous solution

2017 ◽  
Vol 17 (5) ◽  
pp. 1458-1467
Author(s):  
Guoying Gao ◽  
Wei Chu ◽  
Zhonglin Chen ◽  
Jimin Shen
Keyword(s):  
Aqueous Solution ◽  
Synergetic Effect ◽  
Catalytic Ozonation ◽  
Iron Silicate ◽  
Oh Radicals ◽  
Ozone Decomposition ◽  
Impregnation Method ◽  
Toc Removal ◽  
Co Precipitation ◽  
Adsorption Desorption

The catalytic ozonation of diclofenac (DCF) with iron silicate-loaded pumice (FSO/PMC) in aqueous solution was investigated. FSO/PMC was synthesized by a co-precipitation–impregnation method and characterized using scanning electron microscope, N2 adsorption–desorption, X-ray fluorescence, and pHpzc measurements. Results showed that the FSO/PMC/O3 process obviously improved total organic carbon (TOC) removal efficiency from 32.3% (using sole ozonation) to 73.3% in 60 min. DCF mineralization in various oxidation processes was found to follow a two-stage pseudo-first-order kinetics. The presence of FSO/PMC effectively improved the mass transfer of ozone from gas to liquid phase and increased the efficiency of ozone decomposition, which results in the formation of •OH radicals. The ozonation of DCF generated large amounts of the ozone-refractory carboxylic acids, and these compounds were found to be continuously removed in the FSO/PMC/O3 process due to the catalytic activity of FSO/PMC. The synergetic effect between ozonation and FSO/PMC adsorption indicated that FSO/PMC is a promising catalyst for the ozonation process.

Degradation of p-Chloronitrobenzene in Aqueous Solution by Iron Silicate Catalytic Ozonation

2014 ◽  
Vol 955-959 ◽  
pp. 2162-2168 ◽  
Author(s):  
Yue Liu ◽  
Lei Liu ◽  
Wei Jin Gong
Keyword(s):  
Aqueous Solution ◽  
Catalytic Activity ◽  
Catalytic Ozonation ◽  
Iron Silicate ◽  
Radical Scavenger ◽  
Efficient Catalyst ◽  
Green Catalyst ◽  
Hydroxyl Radical Scavenger ◽  
Radical Type ◽  
Ozonation Process

Iron silicate, a stable and efficient catalyst prepared in the laboratory has been successfully used as a catalyst combined with ozonation in the degradation of p-Chloronitrobenzene (pCNB). The catalytic ozonation removal effectiveness of pCNB was investigated under various physicochemical conditions. Both the adsorption and the single ozonation were not effective for the degradation of pCNB, but the presence of iron silicate in ozonation process could substantially enhance the pCNB removal efficiency. The hydroxyl radical scavenger experiment confirmed that iron silicate catalytic ozonation followed a radical-type mechanism. The increasing of both the iron silicate dosage and the ozone dosage could enhance the removal effectiveness of pCNB. The iron silicate catalyst could be recycled easily without decreasing any ozone catalytic activity after four successive reuses. It is concluded that the iron silicate was an efficient green catalyst for pCNB degradation in drinking water.

Catalytic ozonation of bisphenol A in aqueous solution using Mn-Ce/HZSM-5 as catalyst

2015 ◽  
Vol 72 (5) ◽  
pp. 696-703 ◽  
Author(s):  
Yanfang Liu ◽  
Junna Zhao ◽  
Zaixing Li ◽  
Guixia Li ◽  
Wei Li ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Catalytic Activity ◽  
Bisphenol A ◽  
Heterogeneous Catalysts ◽  
Butyl Alcohol ◽  
Catalytic Ozonation ◽  
Point Of Zero Charge ◽  
Toc Removal ◽  
Tert Butyl Alcohol ◽  
Bpa Removal

Mixed manganese and cerium oxide supported on HZSM-5 were synthesized and used as heterogeneous catalysts for ozonation of bisphenol A (BPA) in aqueous solution. The prepared catalysts of Mn-Ce/HZSM-5 were characterized by X-ray diffraction, scanning electron microscopy and Fourier transform-infrared spectroscopy. The results indicated that Mn-Ce/HZSM-5 exhibits extraordinary catalytic activity for the degradation of BPA. Removal of 89.3% of BPA and 90.4% of total organic carbon (TOC) was achieved in 30 min, compared to non-catalytic ozonation, where only 50.5% BPA and 28.1% TOC removal were reached under the same conditions. Adsorption of BPA on HZSM-5 support and Mn-Ce/HZSM-5 catalysts was negligible. The strong inhibition of BPA removal by tert-butyl alcohol indicated that the attack of hydroxyl radicals was responsible for the improvement of catalytic ozonation. It was observed that at neutral pH, which is near the point of zero charge of the catalyst, the catalytic activity reached its maximum. Increasing the amount of Mn-Ce/HZSM-5 catalyst until it exceeded 3 g/L did not show a strong effect on BPA removal. The catalysts showed high stability and reusability.

scholarly journals Synthesis and Characterization of CuFe2O4 Nanoparticles Modified with Polythiophene: Applications to Mercuric Ions Removal

Nanomaterials ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 586 ◽  
Author(s):  
Ayman H. Kamel ◽  
Amr A. Hassan ◽  
Abd El-Galil E. Amr ◽  
Hadeel H. El-Shalakany ◽  
Mohamed A. Al-Omar
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solution ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
X Ray ◽  
Transmission Electron ◽  
Enhanced Adsorption ◽  
Co Precipitation ◽  
Adsorption Desorption

In this research, CuFe2O4 nanoparticles were synthesized by co-precipitation methods and modified by coating with thiophene for removal of Hg(II) ions from aqueous solution. CuFe2O4 nanoparticles, with and without thiophene, were characterized by x-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), energy dispersive x-ray (EDX), high-resolution transmission electron microscopy (HRTEM) and Brunauer–Emmett–Teller (BET). Contact time, adsorbent dose, solution pH, adsorption kinetics, adsorption isotherm and recyclability were studied. The maximum adsorption capacity towards Hg2+ ions was 7.53 and 208.77 mg/g for CuFe2O4 and CuFe2O4@Polythiophene composite, respectively. Modification of CuFe2O4 nanoparticles with thiophene revealed an enhanced adsorption towards Hg2+ removal more than CuFe2O4 nanoparticles. The promising adsorption performance of Hg2+ ions by CuFe2O4@Polythiophene composite generates from soft acid–soft base strong interaction between sulfur group of thiophene and Hg(II) ions. Furthermore, CuFe2O4@Polythiophene composite has both high stability and reusability due to its removal efficiency, has no significant decrease after five adsorption–desorption cycles and can be easily removed from aqueous solution by external magnetic field after adsorption experiments took place. Therefore, CuFe2O4@Polythiophene composite is applicable for removal Hg(II) ions from aqueous solution and may be suitable for removal other heavy metals.

Photo-catalytic Study of Malachite Green Dye Degradation Using Rice Straw Extracted Activated Carbon Supported ZnO Nano-particles

2020 ◽  
Vol 10 (6) ◽  
pp. 849-859
Author(s):  
Radwa A. El-Salamony ◽  
Abeer A. Emam ◽  
Nagwa A. Badawy ◽  
Sara F. El-Morsi
Keyword(s):  
Activated Carbon ◽  
Visible Light ◽  
Rice Straw ◽  
Malachite Green ◽  
Dye Degradation ◽  
Nano Particles ◽  
Oh Radicals ◽  
Impregnation Method ◽  
Photo Degradation ◽  
Malachite Green Dye

Objective: ZnO nanoparticles were synthesized using wet impregnation method, and activated carbon from rice straw (RS) prepared through chemical route. Methods: The nano-composites ZnO-AC series were prepared with different ZnO:AC ratio of 10, 20, 50, and 70% to optimize the zinc oxide nanoparticles used. The obtained composites were characterized by FE-SEM, XRD, SBET, and optical techniques then used for the photo-degradation of Malachite green dye (MG) under visible light. Results: It was found that 10ZnO-AC exhibited excellent visible light photo-catalytic performance. The ·OH radicals’ formation is matching with photo-activity of the prepared composites. The photo-degradation efficiency of MG increased from 63% to 93%, when the 10ZnO-AC photocatalyst amount was increased from 0.5 to 6 g/L. Conclusion: The GC-MS technique was used to analyze the intermediates formed; up to 15 kinds of chemicals were identified as the degradation products.

Recovery of Gallium from Aqueous Solution through Preconcentration by Adsorption/Desorption on Disordered Mesoporous Carbon

2021 ◽  
Vol 7 (1) ◽  
pp. 227-242
Author(s):  
E. Díez ◽  
J. M. Gómez ◽  
A. Rodríguez ◽  
I. Bernabé ◽  
J. Galán
Keyword(s):  
Aqueous Solution ◽  
Mesoporous Carbon ◽  
Adsorption Desorption

scholarly journals Chitosan/Zeolite Composite Aerogels for a Fast and Effective Removal of Both Anionic and Cationic Dyes from Water

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1691
Author(s):  
Angela Marotta ◽  
Enrica Luzzi ◽  
Martina Salzano de Luna ◽  
Paolo Aprea ◽  
Veronica Ambrogi ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Broad Spectrum ◽  
Organic Dyes ◽  
Indigo Carmine ◽  
Zeolite 13X ◽  
Industrial Sectors ◽  
Effective Removal ◽  
Composite Aerogels ◽  
Zeolite Composite ◽  
Adsorption Desorption

Organic dyes are extensively used in many industrial sectors, and their uncontrolled disposal into wastewaters raises serious concerns for environmental and human health. Due to the large variety of such pollutants, an effective remediation strategy should be characterized by a broad-spectrum efficacy. A promising strategy is represented by the combination of different adsorbent materials with complementary functionalities to develop composite materials that are expected to remove different contaminants. In the present work, a broad-spectrum adsorbent was developed by embedding zeolite 13X powder (ZX) in a chitosan (CS) aerogel (1:1 by weight). The CS–ZX composite adsorbent removes both anionic (indigo carmine, IC) and cationic (methylene blue, MB) dyes effectively, with a maximum uptake capacity of 221 mg/g and 108 mg/g, respectively. In addition, the adsorption kinetics are rather fast, with equilibrium conditions attained in less than 2 h. The composite exhibits good mechanical properties in both dry and wet state, which enables its handling for reusability purposes. In this regard, preliminary tests show that the full restoration of the IC removal ability over three adsorption–desorption cycles is achieved using a 0.1 M NaOH aqueous solution, while a 1 M NaCl aqueous solution allows one to preserve >60% of the MB removal ability.

Effect of Fe and Co promoters on CO methanation activity of nickel catalyst prepared by impregnation – co-precipitation method

2020 ◽  
Vol 18 (5-6) ◽  
Author(s):  
Buyan-Ulzii Battulga ◽  
Tungalagtamir Bold ◽  
Enkhsaruul Byambajav
Keyword(s):  
Synergetic Effect ◽  
Space Velocity ◽  
Catalytic Performance ◽  
Precipitation Method ◽  
Molar Ratio ◽  
Alumina Support ◽  
Co Methanation ◽  
Temperature Range ◽  
Co Precipitation ◽  
Catalyst Distribution

AbstractNi based catalysts supported on γ-Al2O3 that was unpromoted (Ni/γAl2O3) or promoted (Ni–Fe/γAl2O3, Ni–Co/γAl2O3, and Ni–Fe–Co/γAl2O3) were prepared using by the impregnation – co-precipitation method. Their catalytic performances for CO methanation were studied at 3 atm with a weight hourly space velocity (WHSV) of 3000 ml/g/h of syngas with a molar ratio of H2/CO = 3 and in the temperature range between 130 and 350 °C. All promoters could improve nickel distribution, and decreased its particle sizes. It was found that the Ni–Co/γAl2O3 catalyst showed the highest catalytic performance for CO methanation in a low temperature range (<250 °C). The temperatures for the 20% CO conversion over Ni–Co/γAl2O3, Ni–Fe/γAl2O3, Ni–Fe–Co/γAl2O3 and Ni/γAl2O3 catalysts were 205, 253, 263 and 270 °C, respectively. The improved catalyst distribution by the addition of cobalt promoter caused the formation of β type nickel species which had an appropriate interacting strength with alumina support in the Ni–Co/γAl2O3. Though an addition of iron promoter improved catalyst distribution, the methane selectivity was lowered due to acceleration of both CO methanation and WGS reaction with the Ni–Fe/γAl2O3. Moreover, it was found that there was no synergetic effect from the binary Fe–Co promotors in the Ni–Fe–Co/γAl2O3 on catalytic activity for CO methanation.

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