Highly effective and reusable Ni-Al oxide/Zn0.4Co0.6Fe2O4 superparamagnetic aerogel for oil-water separation.

Oily wastewater from the oil industry and oil spill accidents has become a serious environmental problem and has attracted worldwide attention. The present study reports on the successful preparation of a novel magnetic Ni-Al oxide/Zn0.4Co0.6F2O4 mesoporous aerogel (MNA) as a highly selective adsorbent for oil removal from water. Oleic acid (OA) and Triton X-100 (TX) were used as hydrophobic agents for MNA surface modification. It was found that the attached amount of OA on the mesoporous MNA aerogel is 3.5 times larger than that of TX, giving an advantage to MNA-OA in oil separation. The MNA-OA displayed superhydrophobicity (contact angle ∼150°) and superparamagnetism properties that allowed the adsorbent to be used selectively for oil removal. The MNA-OA was found to have a high oil removal efficiency of ∼97% with an adsorption capacity of ∼2 g/g. Furthermore, the produced magnetic adsorbent has high stability due to the strong chemical binding of OA, which is demonstrated by its good reusability performance. Throughout five separate runs, the MNA-OA was shown to be a very efficient and reusable adsorbent for oily wastewater.

SiO2/Zn0.4Co0.6Fe2O4 aerogel: an efficient and reusable superparamagnetic adsorbent for oily water remediation.

Magnetic SiO2/Zn0.4Co0.6Fe2O4 aerogels were successfully prepared by sol-gel method with two different drying steps: ambient pressure drying (APD) and freeze-drying (FD). The surface chemistry of silica was modified to be hydrophobic by oleic acid. The prepared materials were fully characterized, displaying superparamagnetic behavior with saturation magnetizations of 10.2 and 15.1 emu g-1, and contact angles of ∼130° and ∼140° for the materials prepared by the APD and FD methods, respectively, indicating the hydrophobic surfaces of the prepared materials. This hydrophobicity allows the efficient separation of oil. Specifically, as high as 1.7 and 2 g g-1 adsorption capacities were obtained when using APD-dried and FD-dried silica aerogels, respectively, suggesting the preference for the FD method. Additionally, magnetic recovery and reuse of the adsorbents were successfully implemented in an attempt to reduce the overall practical application costs. To sum up, the prepared materials are good candidates for oil removal from wastewater and the protection of the environment.

Nanomaterials: a review of emerging contaminants with potential health or environmental impact.

Nanotechnologies have been advantageous in many sectors and gaining much concern due to the unique physical, chemical and biological properties of nanomaterials (NMs). We have surveyed peer-reviewed publications related to "nanotechnology", "NMs", "NMs water treatment", "NMs air treatment", and "NMs environmental risk" in the last 23 years. We found that most of the research work is focused on developing novel applications for NMs and new products with peculiar features. In contrast, there are relatively few of publications concerning NMs as environmental contaminants relative to that for NMs applications. Thus, we devoted this review for NMs as emerging environmental contaminants. The definition and classification of NMs will be presented first to demonstrate the importance of unifying the NMs definition. The information provided here should facilitate the detection, control, and regulation of NMs contaminants in the environment. The high surface-area-to-volume ratio and the reactivity of NMs contaminants cause the prediction of the chemical properties and potential toxicities of NPs to be extremely difficult; therefore, we found that there are marked knowledge gaps in the fate, impact, toxicity, and risk of NMs. Consequently, developing and modifying extraction methods, detection tools, and characterization technologies are essential for complete risk assessment of NMs contaminants in the environment. This will help also in setting regulations and standards for releasing and handling NMs as there are no specific regulations. Finally, the integrated treatment technologies are necessary for the removal of NMs contaminants in water. Also, membrane technology is recommended for NMs remediation in air.

Mass flow and consumption calculations of pharmaceuticals in sewage treatment plant with emphasis on the fate and risk quotient assessment.

In Egypt, pharmaceuticals consumption increased dramatically owing to the population growth and the unrestricted sale manner. Accordingly, the occurrence and fate of nine common pharmaceutical active compounds (PhACs) were scrutinized at a sewage treatment plant (STP) in Giza, Egypt. The levels of these PhACs were assessed in different the wastewater treatment stages and dewatered sludge phase using high-performance liquid chromatography coupled with photodiode arrays detector. The average concentrations of the total PhACs detected in influent, primary sedimentation effluent (PSE) and final effluent (FE) were 227, 155 and 89 µg L-1, respectively. The overall removal efficiency of the individual PhACs ranged from 18 to 72% removal. The occurrence trend revealed that biodegradation and adsorption are the concurrently removal mechanisms of the studied PhACs. The overall consumption per day in West of Greater Cairo was estimated based on influent concentration of STP. Sulfamethoxazole, paracetamol and diclofenac were detected with the highest levels in the influent of STP, PSE and FE as well as in the dewatered sludge. Furthermore, the high concentrations of these compounds in the sludge confirm the adsorption pathway removal of theses PhACs. The risk quotient (RQ) assessment for the detected PhACs in FE is greatly higher than the predicted non-effect concentration (PNEC). Conclusively, the FE of STP is considered a risky source for PhACs in adjacent surface water.

Bi2O3-BiFeO3 Glass-Ceramic: Controllable ß-/γ-Bi2O3 Transformation and Application as Magnetic Solar-Driven Photocatalyst for Water Decontamination.

Glass and glass-ceramic materials containing photoactive and magnetic crystalline phases were prepared from Fe2O3 and Bi2O3 using the conventional melt method. All samples were characterized in terms of formed phases, morphological analyses, optical properties, and magnetic properties. Formation of the photoactive tetragonal ß- and body-centered cubic γ-Bi2O3 phases along with the magnetic BiFeO3 and Fe3O4 phases was revealed. However, the crystalline structure relied on the composition and the applied heat-treatment time. ß-/γ-Bi2O3 transformation could be controlled by the heat-treatment time. The samples exhibited variable magnetic properties depending on their composition. All of the samples showed excellent absorbance in visible light with an optical band gap of 1.90-2.22 eV, making them ideal for solar-light-driven photocatalysis. The best performance was recorded for the sample containing equal amounts of Fe2O3 and Bi2O3 due to the formation of γ-Bi2O3/BiFeO3 heterojunction in this sample.

Probing protein rejection behavior of blended PES-based flat-sheet ultrafiltration membranes: A density functional theory (DFT) study.

Membrane fouling is a common problem in membrane technology and causes detrimental effects for the applied membranes such as loss of integrity and productivity. Henceforward, we devoted this work to fabricate membranes that pose favored criteria in the direction of alleviating membrane fouling incidence. Herein, the fabricated membranes were traced via an assortment of both experimental and molecular modeling verifications to understand the mechanism of interaction. To do so, firstly, three different ultrafiltration (UF) membranes had been prepared via facile wet phase inversion method thru dipping a casting solution composed of polyethersulfone-polyvinyl pyrrolidone (PES-PVP) and polyethersulfone-Pluronic P31R1 (PES-P31R1) in a water coagulation bath. Regarding the practical-based data, the pristine PES membrane exhibited the highest rejection of bovine serum albumin (BSA) protein (model foulant) compared with the modified PES-based membranes. The membrane chemical compositions were elucidated with ATR-FTIR Spectroscopy. On the other hand, molecular modeling has been carried out via calculating thermodynamic parameters, level parametric method, and density functional theory (DFT). Thermodynamic parameters analysis indicated that the noticeable difference of BSA rejection may be ascribed to different entropy behavior for the fabricated membranes. In addition, the level parametric method (PM6) and density functional theory DFT: B3LYP with 6-31g (d,p) basis set models clarified the interaction manner of BSA molecules to membrane surfaces.

Synthesis, characterization and adsorption properties of microcrystalline cellulose based nanogel for dyes and heavy metals removal.

Recently, naturally occurring biopolymers have attracted the attention as potential adsorbents for the removal of water contaminants. In this work, we present the development of microcrystalline cellulose (MCC)-based nanogel grafted with acrylamide and acrylic acid in the presence of methylene bisacrylamide and potassium persulphate as a crosslinking agent and initiator, respectively. World-class facilities such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), surface analysis, field emission scanning electron microscopy (FE-SEM), high resolution transmission electron microscopy (HR-TEM) and zeta sizer were used to characterize the synthesized MCC based nanogel. The prepared nanogel was applied to remove reactive red 195 (RR195) dye and Cd (II) from aqueous medium at different operational conditions. The adsorption experiments showed that the feed concentration of monomers has a significant effect on the removal of RR195 which peaked (93% removal) after 10min of contact time at pH2 and a dose of 1.5g/L. On contrary, the feed concentration has insignificant effect on the removal of Cd (II) which peaked (97% removal) after 30min of contact time at pH6 and a dose of 0.5g/L. The adsorption equilibrium data of RR195 and Cd (II) was best described by Freundlich and Langmuir, respectively. Conclusively, the prepared MCC based nanogels were proved as promising adsorbents for the removal of organic pollutants as well as heavy metals.

Minimization of the formation of disinfection by-products.

The drinking water industry is required to minimize DBPs levels while ensuring adequate disinfection. In this study, efficient and appropriate treatment scheme for the reduction of disinfection by-product (DBPs) formation in drinking water containing natural organic matter has been established. This was carried out by the investigation of different treatment schemes consisting of enhanced coagulation, sedimentation, disinfection by using chlorine dioxide/ozone, filtration by sand filter, or granular activated carbon (GAC). Bench scale treatment schemes were applied on actual samples from different selected sites to identify the best conditions for the treatment of water. Samples were collected from effluent of each step in the treatment train in order to analyze pH, UV absorbance at 254 nm (UVA(254)), specific UV absorbance at 254 nm (SUVA(254)), dissolved organic carbon (DOC), haloacetic acids (HAAs) and trihalomethanes (THMs). The obtained results indicated that using pre-ozonation/enhanced coagulation/activated carbon filtration treatment train appears to be the most effective method for reducing DBPs precursors in drinking water treatment.

Power generation using spinel manganese-cobalt oxide as a cathode catalyst for microbial fuel cell applications.

This study focused on the use of spinel manganese-cobalt (Mn-Co) oxide, prepared by a solid state reaction, as a cathode catalyst to replace platinum in microbial fuel cells (MFCs) applications. Spinel Mn-Co oxides, with an Mn/Co atomic ratios of 0.5, 1, and 2, were prepared and examined in an air cathode MFCs which was fed with a molasses-laden synthetic wastewater and operated in batch mode. Among the three Mn-Co oxide cathodes and after 300 h of operation, the Mn-Co oxide catalyst with Mn/Co atomic ratio of 2 (MnCo-2) exhibited the highest power generation 113 mW/m2 at cell potential of 279 mV, which were lower than those for the Pt catalyst (148 mW/m2 and 325 mV, respectively). This study indicated that using spinel Mn-Co oxide to replace platinum as a cathodic catalyst enhances power generation, increases contaminant removal, and substantially reduces the cost of MFCs.

Photocatalytic oxidation of ciprofloxacin under simulated sunlight.

Ciprofloxacin (CIP) is a famous synthetic chemotherapeutic antibiotic. It is widely found either in water or wastewater. In this study ciprofloxacin was photocatalytically degraded using commercial anatase titanium dioxide (TiO(2)) under simulated sunlight. The rate of reaction was found to be affected by pH, TiO(2) concentration and antibiotic concentration. The best reaction rate was obtained in natural ciprofloxacin pH (5.8) and 1000 mg/L TiO(2). More titania concentration was found to reduce the reaction rate because of the limitation in light transmittance. From kinetic studies, the reaction was proved to proceed through adsorption step then photooxidation and obeys pseudo-first order kinetics.

Preparation and characterization of magnetically separable photocatalyst (TiO2/SiO2/Fe3O4): effect of carbon coating and calcination temperature.

TiO2/SiO2/Fe3O4 composite was synthesized by sol-gel technique for silica and titania coatings on magnetite core to enable recovery after photocatalytic degradation. Carbon coating was also carried out by calcination of TiO2/SiO2/Fe3O4 under nitrogen atmosphere in presence of PVA as a source of carbon to enhance the adsorption of organic compounds on catalyst surface and to get better activity. All prepared samples were characterized using EDX, CN analyzer, XRD, BET and SEM. Degradation of methyl orange dye was used to assess the photocatalytic performance of the prepared samples. Calcination temperature was found to affect rate of reaction because of the formation of rutile phase at high calcination temperature. Carbon coated samples unexpectedly exhibited lower rate of reaction at almost all calcination temperatures.