Rapid removal of phenol from aqueous solutions by AC_Fe3O4 nano-composite: Kinetics and equilibrium studies

Background and purpose: Phenol and its derivatives are used as raw material in many chemical, pharmaceutical and petrochemical industries. It is classified as priority pollutant, due to its high toxicity. In this study, the magnetic activated carbon nano-composite was used for quick removal of phenol. Materials and methods: The activated carbon was modified by magnetic nano-particles. Then physical properties of the adsorbent were investigated using BET, XRD and SEM. Afterwards, adsorption behavior of phenol onto the adsorbent was studied considering various parameters such as: pH, phenol concentration, contact time and adsorbent dosage. Also, the isotherms and adsorption kinetics model was studied. Results: BET analysis showed 10.25% decrease in the specific area of activated carbon after being amended by the Fe3O4 nano-particles. SEM and XRD confirmed the presence of Fe3O4 nanoparticles on the activated carbon. Optimum absorption points in this process were pH=8, contact time of 15 min and adsorbent dose 2 g/L. The Longmuir isotherm and pseudo-second-order kinetics were fitted to the data. The maximum adsorption capacity of phenol on AC_Fe3O4 was 84.033 mg/g. Conclusion: Creating magnetic properties on the activated carbon which has a high adsorption capacity of phenol could result in quick separation of phenol from aqueous solutions. Also, this adsorbent could be widely applied since it is inexpensive and simple to use. © 2015, Mazandaran University of Medical Sciences. All rights reserved

Catalytic Ozonation of Phenolic Wastewater: Identification and Toxicity of Intermediates

A new strategy in catalytic ozonation removal method for degradation and detoxification of phenol from industrial wastewater was investigated. Magnetic carbon nanocomposite, as a novel catalyst, was synthesized and then used in the catalytic ozonation process (COP) and the effects of operational conditions such as initial pH, reaction time, and initial concentration of phenol on the degradation efficiency and the toxicity assay have been investigated. The results showed that the highest catalytic potential was achieved at optimal neutral pH and the removal efficiency of phenol and COD is 98.5% and 69.8%, respectively. First-order modeling demonstrated that the reactions were dependent on the initial concentration of phenol, with kinetic constants varying from 0.038 min−1 ([phenol]o = 1500mg/L) to 1.273 min−1 ([phenol]o = 50mg/L). Bioassay analysis showed that phenol was highly toxic to Daphnia magna (LC50 96 h = 5.6mg/L). Comparison of toxicity units (TU) of row wastewater (36.01) and the treated effluent showed that TU value, after slightly increasing in the first steps of ozonation for construction of more toxic intermediates, severely reduced at the end of reaction (2.23).Thus, COP was able to effectively remove the toxicity of intermediates which were formed during the chemical oxidation of phenolic wastewaters

Photocatalytic degradation and mineralization of diazinon in aqueous solution using nano-TiO2(Degussa, P25): kinetic and statistical analysis

Abstract: In this study, photocatalytic degradation of diazinon was investigated using nano-TiO2, Degussa P25, as a photocatalyst and the effects of some operational parameters such as aeration, pH, photocatalyst concentration, and the irradiation time were also examined. Dispersive liquid-liquid microextraction technique was used to extract and pre-concentration of residual diazinon from the liquid samples and all experiments were carried out by gas chromatography. Amount of degradation and mineralization were determined by gas chromatograph with flame ionization detector (GC/FID) and COD measurements, respectively. The optimum condition for degradation of diazinon has been obtained in the pH 6, [nano-TiO2] = 0.2 g/L, and [time] = 120 min. In the optimal condition the removal efficiency of diazinon and COD were 99.64 and 65%, respectively. The results have shown that the nano-TiO2, aeration and time of reaction have a positive effect on photocatalytic degradation of diazinon and COD removal. Statistical analysis showed that the maximum removal of diazinon and COD were due to UV irradiation (71%, 41%), exposure time (16%, 39%), aeration (7%, 4%), and increased concentration of nano-TiO2 (0.4%, 2%), respectively; and the kinetics of photodegradation were found to follow a first-order kinetic model and the constant rate, at optimal condition, was 0.038 (min−1). © 2014 Balaban Desalination Publications. All rights reserved

Effects of Low Frequency-Low Voltage Alternating Electric Current on Apoptosis Progression in Bioelectrical Reactor Biofilm

Bioelectrochemical systems have undergone several modifications to promote the enzymes or pathways used to reduce the energy required for microbial metabolism. Changes in dominant bacteria, population, and growth rates occur when an electric current is applied intermittently. Applying electricity to bioelectrical reactor (BER) biofilms can either stimulate cells or lead to cell death; therefore, determining the applied voltage range that leads to viable and stimulated bacteria is crucial. We investigated the progression of apoptosis induced by a low frequency-low voltage alternating electric current (AC) in a BER biofilm and found that biofilms on carbon cloth (CC) and stainless steel (SS) 304 electrodes had pHzpc values of 8.67. The pHzpc of the biofilms increased by two compared to that of the inoculant bacteria mass. Furthermore, the Henderson�Hasselbalch equation reveals that the compositions of cell walls of the biofilms that formed on the CC and SS304 electrodes are very similar. In contrast, the CC and SS304 biofilms differ from the inoculant biomass without the influence of an AC field; this indicates that there are differences in the compositions of the cell walls in the present bacteria. Fourier transform infrared spectroscopy was used to compare spectra of the biofilms with that of the inoculation mass, and there were differences in shape and absorbance intensity, indicating variability in the composition, and quantity of each individual biofilm component. In addition, the dehydrogenase activity (DHA) content varied under different applied voltages; the highest DHA was obtained at 8 Vpp. A flow cytometry analysis showed a relatively low number of apoptotic cells (10.93 ± 5.19) for the AC amplitudes studied. Thus, a low voltage-low frequency AC likely induces significant changes in bacterial metabolic activity but causes no significant change in their viability. © Copyright © 2020 Hoseinzadeh, Wei, Farzadkia and Rezaee

The Effect of Organic Loading on Propylene Glycol Removal Using Fixed Bed Activated Sludge Hybrid Reactor

Propylene glycol is discharged to the surface and underground waters and vicinity soils via industrial wastewater effluents, posing many health and environmental risks. The main goal of this study was to remove propylene glycol from synthetic wastewater in a fixed bed activated sludge reactor. To observe the effects of organic loading on bioreactor performance, the organic loading was increased by two sequencing stages: first by hydraulic retention time (HRT) depletion and second via propylene glycol concentration increase. Propylene glycol removal efficiency in HRTs of 8, 6, 4 and 2 h was 95.86, 95.12, 93.96 and 79.08 % respectively. A constant HRT of 6 h was selected for the second stage; propylene glycol concentrations of 500, 1000, 1500, 2000 and 2500 mg L–1 were used. The removal efficiency for these concentrations was 95.12, 95.95, 88.54, 75.95 and 35.69 % respectively. Thus, the integrated fixed bed activated sludge reactor is an efficient, viable and promising technology for treating wastewaters containing propylene glycol

Iron-silver oxide nanoadsorbent synthesized by co-precipitation process for fluoride removal from aqueous solution and its adsorption mechanism

Fe-Ag magnetic binary oxide nanoparticles (Fe-Ag MBON) are prepared with co-precipitation of ferric and ferrous chloride solutions, and used for the adsorption of fluoride from aqueous solution. The surface morphology of the adsorbent was characterized by XRD, SEM, TEM, FTIR, XPS, EDX, BET, DLS and VSM techniques. Batch method was followed to optimize the conditions for the removal of fluoride. The results showed maximum removal occurred at pH 3.0 and adsorption equilibrium was achieved within 20 min. Chemical kinetics of the adsorption were well fitted by pseudo-second order models (R2 > 0.968) and the adsorption process followed the Langmuir isotherm model well (R2 > 0.976). The fluoride adsorption capacity of Fe-Ag MBON was 22.883 mg g-1, and decreased with increasing the temperature. Thermodynamic values revealed that the fluoride adsorption process was spontaneous and exothermic. Regeneration experiments were carried out for six cycles and the results indicate a removal efficiency loss of <22. © 2015 The Royal Society of Chemistry

Exposure to nanoscale diesel exhaust particles: Oxidative stress, neuroinflammation, anxiety and depression on adult male mice

ABSTRACT Exposure to nanoscale diesel engines exhausted particles (DEPs) is a well-recognized risk factor for respiratory and cardiovascular diseases. Rodents as commonly used models for urban air pollution in health effect studies demonstrate constant stimulation of inflammatory responses in the main areas of the brain. Nevertheless, the primary effect of diesel exhaust particulate matter on some of the brain regions and relation by behavioral alterations still remains untouched. We evaluated the brain regional in flammatory responses to a nanosized subfraction of diesel engines exhaust particulate matter (DEPs < 200 nm) in an adult male mice brain. Adult male mice were exposed to DEPs for 3, 6, and 8 h per day, 12 weeks and five days per week. Degree of anxiety and the depression by elevated plus maze and Forced Swimming Test respectively (FST) did measurement. After behavior tests, the plasma and some of the brain regions such as olfactory bulb (OB) and hippocampus (HI) were analyzed for oxidative stress and in flammatory responses. The inflammation and oxidative stress changes in OB and HI, markedly coincides with the results of behavioral alterations. These responses corresponded with rapid induction of MDA and nitrite oxide (NO) in brain regions and neuronal nitric oxide synthase (nNOS) mRNA followed by IL6, IL1 α , and TNF α in OB and HI. The different times of DEPs exposure, leads to oxidative stress and inflammatory in plasma and brain regions. That this cumulative transport of inhaled nanoscale DEPs into the brain and creating to inflammation responses of brain regions may cause problems of brain function and anxiety and depression. Keywords: Air pollution Nanoscale diesel exhaust particles Oxidative stress Nanotoxicology Anxiety Depressio

Kinetic and isotherm studies of adsorption and biosorption processes in the removal of phenolic compounds from aqueous solutions: Comparative study

The phenolic compounds are known by their carcinogenicity and high toxicity as well as creating unpleasant taste and odor in water resources. The present study develops a cost-effective technology for the treatment of water contaminated with phenolic compounds, including Phenol (Ph), 2-chlorophenol (2-CP), and 4-chlorophenol (4-CP). So, two sorbents, rice bran ash (RBA) and biomass of brown algae, Cystoseiraindica, were used and results were compared with the commercially granular activated carbon (GAC). The phenolic compounds were determined using a high performance liquid chromatography (HPLC) under batch equilibrium conditions. The effects of contact time, pH, initial adsorbate concentration, and adsorbent dosages on the removal efficiency were studied. The adsorption data were simulated by isotherm and kinetic models. Results indicated that RBA and GAC had the lowest efficiency for the removal of 2-CP, while the order of removal efficiency for C. indica biomass was as follows: 2-CP > 4-CP > phenol. The efficiency of GAC was higher than those of other adsorbents for all of the phenolic compounds. Furthermore, the adsorption capacity of RBA was found to be higher than that of C. indica biomass. The optimal initial pH for the removal of phenol, 2-CP and 4-CP was determined to be 5, 7, and 7 for RBA, GAC, and algal biomass, respectively. Kinetic studies suggested that the pseudo-second order best fitted the kinetic data. © 2013 Gholizadeh et al.; licensee BioMed Central Ltd

Comparison of Aerobic and Lime Stabilization Methods for Evaluation of Sewage Sludge Reuse

The main objective of this research was the examination of effectiveness of lime dose in order to stabilization of sewage sludge and comparison of lime stabilized sludge reuse with aerobic digested sludge reuse. Lime and aerobic stabilization were carried out in two laboratory reactor with 40 L capacity. The sludge samples were taken from the return activated sludge line in four times. Lime was used at various ratios and the mixture was stabilized for 30 days. During the lime hydrated stabilization pH values were significantly increased from 7 to 12.5. Also, aerobic digester was loaded with raw sludge and mixed by sufficient amount of air for 30 days. The results indicate that the lime addition with the dose of 0.4 g Ca(OH)2 g-1 DS could completely inactive a high amount of fecal coliforms within 1 h and in all of the times was lower than 1000 MPN g-1 DS after 30 days (p&lt;0.01). But after 30 days, fecal coliforms density in aerobic digested sludge could not achieve to Class A of USEPA category. In two stabilization methods, density of viable helminths ova could not reduce to 1 ova/4 g DS and could not achieve to Class A of USEPA category. Therefore, these methods could be achieved the reduction requirement set by USEPA for class B (p&lt;0.01) and the products could be well used as a landfill cover or a soil conditioner. Finally, our study confirmed that lime sludge stabilization has a higher hygienic effect and more cost-effective than aerobic stabilization, specially, when such sludge is used to dung and modify acid soils.© 2011 Asian Network For Scientific Information

Experimental design approach to the optimization of PAHs bioremediation from artificially contaminated soil: Application of variables screening development

Background: The effectiveness of bioremediation systems for PAH-contaminated soil may be constrained by physicochemical properties of contaminants and environmental factors. Information on what is the most effective factor in bioremediation process is essential in the decision of what stimulations can be taken to assist the biodegradation efficacy. Methods: In this study, four factors of surfactant (Tween 80), humic acid (HA), salinity and nutrients in a 24 full factorial design were screened in bioremediation of phenanthrene contaminated soil by using a consortium of bacteria. Results: Between the employed levels of the factors only salinity had not significant effect. Optimal concentrations of surfactant, HA and nutrient were obtained by a response surface design. For phenanthrene biodegradation, a central composite face centred design (CCFD) showed that nutrient, surfactant and HA concentrations had highly significant, significant and insignificant effects, respectively. The best conditions with 87.1 phenanthrene biodegradation were 150 mg HA/Kg soil, 12.68 μg/L surfactant, and nutrients as K2HPO4, 0.8; KH2PO4, 0.2 and KNO3, 1 g/L. A high similarity was between the model prediction and experimental results. Conclusions: This study showed that nutrient with 81.27 efficiency could be considered as the most effective factor for practical implications of bioremediation process for PAHs contaminated soil cleanup strategies. © 2015 Ravanipour et al.; licensee BioMed Central