The extremely high levels of water pollution caused by various industrial activities represent one of the most important environmental problems. Efficient techniques and advanced materials have been extensively developed for the removal of highly toxic organic pollutants, including pesticides. This study investigated the photocatalytic degradation of the fungicide carbendazim (Czm) using composite track-etched membranes (TeMs) in an aqueous solution. Copper(I) oxide (Cu2O) and zinc oxide (ZnO) microtubes (MTs) were prepared using an electroless template deposition technique in porous poly(ethylene terephthalate) (PET) TeMs with nanochannels with a density of 4 × 107 pores/cm−2 and diameter of 385 ± 9 nm to yield Cu2O@PET and ZnO@PET composite membranes, respectively. A mixed Cu2O/ZnO@PET composite was prepared via a two-step deposition process, containing ZnO (87%) and CuZ (13%) as crystalline phases. The structure and composition of all composite membranes were elucidated using scanning electron microscopy (SEM), atomic force microscopy (AFM), energy-dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) techniques. Under UV–visible light irradiation, the Cu2O/ZnO@PET composite displayed enhanced photocatalytic activity, reaching 98% Czm degradation, higher than Cu2O@PET and ZnO@PET composites. The maximum Czm degradation efficiency from aqueous solution was obtained at an optimal pH of 6 and contact time of 140 min. The effects of various parameters such as temperature, catalyst dosage and sample exposure time on the photocatalytic degradation process were studied. The degradation reaction of Czm was found to follow the Langmuir–Hinshelwood mechanism and a pseudo-first order kinetic model. The degradation kinetics of Czm accelerated with increasing temperature, and the activation energy (Ea) levels were calculated as 11.9 kJ/mol, 14.22 kJ/mol and 15.82 kJ/mol for Cu2O/ZnO@PET, ZnO@PET and Cu2O@PET composite membranes, respectively. The reusability of the Cu2O/ZnO@PET catalyst was also investigated at different temperatures for 10 consecutive runs, without any activation or regeneration processes. The Cu2O/ZnO@PET composite exhibited degradation efficiency levels of over 50% at 14 °C and over 30% at 52 °C after 5 consecutive uses.
Understanding the efficiency of different wastewater treatment technologies tested under real conditions is essential for successful decision making by engineers and managers. In this study, real poultry slaughterhouse wastewater coming from defeathering, cooling, and evisceration processes was treated using a lab-scale electrochemical process by use of iron-iron (Fe-Fe), iron-graphite (Fe-Gr) and aluminum-graphite (Al-Gr) electrode combinations. A water quality index (WQI) was developed and used as a tool for evaluating and classifying the effectiveness of different electrode combinations. The Al-Gr electrode combination showed an impressive performance achieving an “excellent” status for all of the three studied sources of wastewater with a WQI ranging from 13 to 34. The Fe-Gr electrode combination showed an “excellent” status performance for the wastewater from the cooling process as classified by the WQI and “good water” class for the defeathering and evisceration processes. The lower performance, which was highly affected by the increase in turbidity, was observed for the Fe-Fe electrode combination with a “poor water” status for the wastewater coming from defeathering and cooling processes and “good water” status for evisceration process.
Nanoporous track-etched membranes (TeM) are promising materials as adsorbents to remove toxic pollutants, but control over the pore diameter and density in addition to precise functionalization of nanochannels is crucial for controlling the surface area and efficiency of TeMs. This study reported the synthesis of functionalized PET TeMs as high-capacity sorbents for the removal of trivalent arsenic, As(III), which is more mobile and about 60 times more toxic than As(V). Nanochannels of PET-TeMs were functionalized by UV-initiated reversible addition fragmentation chain transfer (RAFT)-mediated grafting of 2-(dimethyamino)ethyl methacrylate (DMAEMA), allowing precise control of the degree of grafting and graft lengths within the nanochannels. Ag NPs were then loaded onto PDMAEMA-g-PET to provide a hybrid sorbent for As(III) removal. The As(III) removal efficiency of Ag@PDMAEMA-g-PET, PDMAEMA-g-PET, and pristine PET TeM was compared by adsorption kinetics studies at various pH and sorption times. The adsorption of As(III) by Ag@DMAEMA-g-PET and DMAEMA-g-PET TeMs was found to follow the Freundlich mechanism and a pseudo-second-order kinetic model. After 10 h, As(III) removal efficiencies were 85.6% and 56% for Ag@PDMAEMA-g-PET and PDMAEMA-g-PET, respectively, while PET template had a very low arsenic sorption capacity of 17.5% at optimal pH of 4.0, indicating that both PDMAEMA grafting and Ag-NPs loading significantly increased the As(III) removal capacity of PET-TeMs.
With the interest to reuse and recycle the wastewater for technological use, this project aims to test the treatment of wastewater from poultry slaughterhouse industry from three main sections of the poultry slaughtering process, defeathering, eviscerating and cooling processes. The samples for the project were obtained from Izhevskoe a Kazakhstani company. The technology used is a combination of electrocoagulation, ultrafiltration, and photochemical system and its goal is to provide treated water that can be re-utilized in the poultry industry for sterilization of technical equipment without contaminating and affecting the quality of the poultry products. The treatment of wastewater samples lasted in total for 40 min. From the results, it was found that indicators such as BOD, COD, and phosphates had removal efficiency of almost 100%, while the microbiological colonies were all eradicated from then wastewater making the treated water microbes free. Hence, proving this system to be effective for the treatment of poultry slaughterhouse wastewater and safe for technological reutilization.
A detailed synthetic procedure based on the use of urea, dichlorophthalic acid, respective transition metal halides and [NH4]2[MoO4] as a catalyst in the melt or by using 1,2,4-trichlorobenzene as a high-boiling inert solvent is described to gain 2,3,9,10,16,17,23,24-metallooctachlorophthalocyanines (MPcCl8 compounds with M=Mn, Fe, Co, Ni, Cu). In cases that a first purification by subsequent treatment of the crude materials with HCl, NaOH and HCl would not give rise to analytically pure compounds, a second novel purification by using pyridine is described. The degree of purity, exceeding always 98%, is determined by thermogravimetric analysis. Comparative IR, UV/Vis and PXRD studies of the MPcCl8 compounds are reported.
Effective removal of toxic inorganic and organic pollutants is one of the current leading challenges of wastewater treatment. In this study, the decomposition of methylene blue (MB) under UV light irradiation was investigated in the presence of copper nanoclusters (NCs)-deposited polyethylene terephthalate (PET) track-etched hybrid membranes. PET track-etched membranes (TeMs) with an average pore size of ~400 nm were grafted by functional acrylic acid (AA) monomer under electron beam irradiation after oxidation with H2O2/UV system. The radiation dose varied between 46 and 200 kGy. For the deposition of copper NCs, poly(acrylic acid) (PAA)-grafted membranes saturated with Cu(II) ions were irradiated either by electron beam or γ-rays to obtain copper-based NCs for the catalytic degradation of MB. Irradiation to 100 kGy with accelerated electrons resulted in the formation of small and uniform copper hydroxide (Cu(OH)2) nanoparticles homogeneously distributed over the entire volume of the template. On the other hand, irradiation under γ-rays yielded composites with copper NCs with a high degree of crystallinity. However, the size of the deposited NCs obtained by γ-irradiation was not uniform. Nanoparticles with the highest uniformity were obtained at 150 kGy dose. Detailed analysis by X-ray diffraction (XRD) and scanning electron microscopy (SEM) confirmed the loading of copper nanoparticles with an average size of 100 nm on the inner walls of nanochannels and on the surface of PET TeMs. Under UV light irradiation, composite membranes loaded with NCs exhibited high photocatalytic activity. It was determined that the highest catalytic activity was observed in the presence of Cu(OH)2@PET-g-PAA membrane obtained at 250 kGy. More than 91.9% of the initial dye was degraded when this hybrid membrane was employed for 180 min, while only 83.9% of MB was degraded under UV light using Cu@PET-g-PAA membrane. Cu(OH)2@PET-g-PAA membranes obtained under electron beam irradiation demonstrated a higher photocatalytic activity compared to Cu@PET-g-PAA membranes attained by γ-rays.
АННОТАЦИЯ В статье проведено исследование физико-химиче ских характеристик нефти, пластовой воды и водонефтяной системы с целью поиска способов эффективной выработки трудноизвлекаемых запасов нефти. Проведена идентификация характеристик месторождений уникальных по площади, плотности запасов, высоковязких, высокопарафинистых, с высоким содержанием смол и асфальтенов. № 3 (3), сентябрь, 2019 г.
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