scholarly journals Anthocyanin-Sensitized TiO2 Nanoparticles for Phenazopyridine Photodegradation under Solar Simulated Light

2018 ◽  
Vol 2018 ◽  
pp. 1-14 ◽  
Author(s):  
Ahed H. Zyoud ◽  
Fedaa Saleh ◽  
Muath H. Helal ◽  
Ramzi Shawahna ◽  
Hikmat S. Hilal

Pharmaceutical wastes are emerging as water contaminants. Like other organic contaminants, it is necessary to find safe and economic methods to remove them from the water. In this work, anthocyanin was used as a natural dye sensitizer for the wide band gap nanosize rutile TiO2. The TiO2/Anthocyanin particles were supported on activated carbon particle surfaces. The resulting composite, which was prepared and characterized by different methods, was then used as a catalyst in the photodegradation of phenazopyridine (a model pharmaceutical contaminant) under a solar simulated light. Depending on experimental conditions, up to 90% of the contaminant was mineralized leaving no new organic products in the reaction mixture. The results show the feasibility of using the activated carbon-supported TiO2/Anthocyanin photocatalyst for pharmaceutical contaminant removal in water. The natural dye anthocyanin readily sensitized the TiO2 to visible light. The unsupported TiO2, with its nanosize particles, was not easy to recover by simple separation methods, while the activated carbon-supported catalyst was easily isolated by decantation after reaction cessation. Moreover, the recovered AC/TiO2 catalyst could also be regenerated by adding fresh anthocyanin sensitizer after recovery for further reuse. Keeping the contaminant molecules closer to the catalytic sites by adsorption, the support also enhanced the efficiency of photocatalyst.

2020 ◽  
Vol 74 (3) ◽  
pp. 108-114
Author(s):  
Charlotte E. Bopp ◽  
Hans-Peter E. Kohler ◽  
Thomas B. Hofstetter

Enzymatic oxygenations initiate biodegradation processes of many organic soil and water contaminants. Even though many biochemical aspects of oxygenation reactions are well-known, quantifying rates of oxidative contaminant removal as well as the extent of oxygenation remains a major challenge. Because enzymes use different strategies to activate O2, reactions leading to substrate oxygenation are not necessarily limiting the rate of contaminant removal. Moreover, oxygenases react along unproductive pathways without substrate metabolism leading to O2 uncoupling. Here, we identify the critical features of the catalytic cycles of selected oxygenases that determine rates and extents of biodegradation. We focus most specifically on Rieske dioxygenases, a subfamily of mononuclear non-heme ferrous iron oxygenases, because of their ability to hydroxylate unactivated aromatic structures and thus initiate the transformation of the most persistent organic contaminants. We illustrate that the rate-determining steps in their catalytic cycles range from O2 activation to substrate hydroxylation, depending on the extent of O–O cleavage that is required for generating the reactive Fe-oxygen species. The extent of O2 uncoupling, on the other hand, is highly substrate-specific and potentially modulated by adaptive responses to oxidative stress. Understanding the kinetic mechanisms of oxygenases will be key to assess organic contaminant biotransformation quantitatively.


2018 ◽  
Vol 9 (1) ◽  
pp. 124 ◽  
Author(s):  
Zhiliang Cheng ◽  
Mingxing Dai ◽  
Xuejun Quan ◽  
Shuo Li ◽  
Daomin Zheng ◽  
...  

The Merox process was widely applied in the fine chemical industry to convert mercaptans into disulfides by oxidation with oxygen, including dimethyl disulfide (DMDS). In this paper, a new activated carbon (AC)-supported sulfonated cobalt phthalocyanine (AC-CoPcS) catalyst was prepared through the chemical linkage of ethylenediamine between them. UV−VIS, FT-IR, BET, and XPS were used to characterize the structure of the new catalyst. Then AC-CoPcS was applied to catalyze sodium methylmercaptide (SMM) oxidation for the preparation of DMDS. The effect of process parameters, such as reaction time, catalyst dosage, reaction temperature, and oxygen pressure on SMM conversion per pass (CPPSMM), yield (YieldDMDS), and purity of the DMDS (PurityDMDS) product were investigated to evaluate the catalytic performance of AC-CoPcS. The new supported catalyst exhibits better catalytic performance than the commercial one and can be properly reused four times to obtain CPPSMM and YieldDMDS higher than 90% and 70%. Under the optimum experimental conditions, the CPPSMM and YieldDMDS could reach as high as 98.7% and 86.8%, respectively, and the purity of the DMDS product is as high as 99.8%. This new supported catalyst exhibits good industrial application prospects.


Minerals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 359
Author(s):  
Liping Zhang ◽  
Shengnian Wu ◽  
Nan Zhang ◽  
Ruihan Yao ◽  
Eryong Wu

Salicylic hydroxamic acid is a novel flotation reagent used in mineral processing. However, it impacts the flotation wastewater leaving behind high chromaticity which limits its reuse and affects discharge for mining enterprises. This study researched ozonation catalyzed by the granular activated carbon (GAC) method to treat the chromaticity of the simulated mineral processing wastewater with salicylic hydroxamic acid. The effects of pH value, ozone (O3) concentration, GAC dosage, and reaction time on chromaticity and chemical oxygen demand (CODCr) removal were discussed. The results of individual ozonation experiments showed that the chromaticity removal ratio reached 79% and the effluent chromaticity exceeded the requirement of reuse and discharge when the optimal experimental conditions were pH value 3, ozone concentration 6 mg/L, and reaction time 40 min. The orthogonal experimental results of catalytic ozonation with GAC on chromaticity removal explained that the chromaticity removal ratio could reach 96.36% and the chromaticity of effluent was only 20 when the optimal level of experimental parameters was pH value 2.87, O3 concentration 6 mg/L, GAC dosage 0.06 g/L, reaction time 60 min respectively. The degradation pathway of salicylic hydroxamic acid by ozonation was also considered based on an analysis with ultraviolet absorption spectrum and high-performance liquid chromatography (HPLC).


2005 ◽  
Vol 68 (3) ◽  
pp. 613-615 ◽  
Author(s):  
DANTE J. BUENO ◽  
LILIANA DI MARCO ◽  
GUILLERMO OLIVER ◽  
ALICIA BARDÓN

Zearalenone (ZEA) is a potent estrogenic metabolite produced by some Fusarium species. No treatment has been successfully employed to get rid of the ZEA contained in foods. This study was conducted to evaluate the ability (adsorptive power) of five adsorbents—activated carbon, bentonite, talc, sandstone, and calcium sulfate—to trap ZEA in vitro. Activated carbon was the best adsorbent, binding 100% ZEA (pH 3 and 7.3) at 0.1, 0.25, 0.5, and 1% dose levels. Bentonite, talc, and calcium sulfate were less efficient than activated carbon but still could bind ZEA to some extent. On the other hand, sandstone was inactive in the experimental conditions employed. Our results indicate that activated carbon could be a good candidate for detoxification of ZEA present in foods.


Water ◽  
2018 ◽  
Vol 10 (10) ◽  
pp. 1401 ◽  
Author(s):  
Ricardo Coimbra ◽  
Carla Escapa ◽  
Nadyr Vázquez ◽  
Guillermo Noriega-Hevia ◽  
Marta Otero

In the present work, the adsorptive removal of diclofenac from water by biosorption onto non-living microalgae biomass was assessed. Kinetic and equilibrium experiments were carried out using biomass of two different microalgae strains, namely Synechocystis sp. and Scenedesmus sp. Also, for comparison purposes, a commercial activated carbon was used under identical experimental conditions. The kinetics of the diclofenac adsorption fitted the pseudo-second order equation, and the corresponding kinetic constants indicating that adsorption was faster onto microalgae biomass than onto the activated carbon. Regarding the equilibrium results, which mostly fitted the Langmuir isotherm model, these pointed to significant differences between the adsorbent materials. The Langmuir maximum capacity (Qmax) of the activated carbon (232 mg∙g−1) was higher than that of Scenedesmus sp. (28 mg∙g−1) and of Synechocystis sp. (20 mg∙g−1). In any case, the Qmax values determined here were within the values published in the recent scientific literature on the utilization of different adsorbents for the removal of diclofenac from water. Still, Synechocystis sp. showed the largest KL fitted values, which points to the affinity of this strain for diclofenac at relative low equilibrium concentrations in solution. Overall, the results obtained point to the possible utilization of microalgae biomass waste in the treatment of water, namely for the adsorption of pharmaceuticals.


2020 ◽  
Vol 9 (1) ◽  
pp. 318-327

Adsorption is a widely used technique for wastewater remediation. The process is effective and economical for the removal of various pollutants from wastewater, including dyes. Moreover, Besides commercial activated carbon, different low-cost materials such as agricultural and industrial wastes are now used as adsorbents. The present review focused on the removal of a teratogenic and carcinogenic dye, orange G (OG) via adsorption using several adsorbents, together with the experimental conditions and their adsorption capacities. Based on the information compiled, various adsorbents have shown promising potential for OG removal.


Author(s):  
Sharmin Akter ◽  
Ferdousi Sultana ◽  
Md. Rakibul Kabir ◽  
Partha Pratim Brahma ◽  
Atkeeya Tasneem ◽  
...  

Pharmaceutical industries in Bangladesh are considered as one major industrial as well as environmental pollution problems which discharge a significant amount of organic contaminants in the environment hence require advanced treatment technologies to decontaminate pharmaceutical wastewater. In the present investigation, areca nut husk treated activated carbon (ANHC) was used as an adsorbent to remove chemical oxygen demand (COD) from pharmaceutical effluent as well as a comparative adsorption efficiency with commercial activated carbon (CAC) was performed.  The batch experiments were carried out in a laboratory scale. The materials also evaluated for different adsorbent dosages and contact times. The experiment revealed a removal percentage up to 70% for ANHC and 90% for CAC for 3g of adsorbents in 180 min. The adsorption processes were satisfactorily described by pseudo-second-order (PSO) kinetic model which shows a better fitting with the maximum regression coefficient for both adsorbents. The results show that Langmuir model best described the experimental data with a highest correlation coefficient (R2=0.9856 for ANHC and 0.9993 for CAC) compared to Freundlich model and the experimental data showed asorption capacity of 36.549 and 64.935 mg/g for ANHC and CAC, correspondingly. According to the adsorption studies, the results revealed that COD adsorption process followed by the monolayer chemisorption mechanisms. The results revealed that ANHC adsorbent is potentially low cost and environmental friendly adsorbent for the removal of organic matter from pharmaceutical effluent.


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