Simultaneously energy production and dairy wastewater treatment using bioelectrochemical cells: In different environmental and hydrodynamic modes

A successful design, previously adapted for treatment of complex wastewaters in a microbial fuel cell (MFC), was used to fabricate two MFCs, with a few changes for cost reduction and ease of construction. Performance and electrochemical characteristics of MFCs were evaluated in different environmental conditions (in complete darkness and presence of light), and different flow patterns of batch and continuous in four hydraulic retention times from 8 to 30 h. Changes in chemical oxygen demand, and nitrate and phosphate concentrations were evaluated. In contrast to the microbial fuel cell operated in darkness (D-MFC) with a stable open circuit voltage of 700 mV, presence of light led to growth of other species, and consecutively low and unsteady open circuit voltage. Although the performance of theMFC subjected to light (L-MFC)was quite lowand unsteady in dynamic state (internal resistance = 100 Ω, power density = 5.15 W·m^-3), it reached power density of 9.2 W·m^-3 which was close to performance of D-MFC (internal resistance = 50 Ω, power density = 10.3 W·m^-3). Evaluated only for D-MFC, the coulombic efficiency observed in batch mode (30%) was quite higher than the maximum acquired in continuous mode (9.6%) even at the highest hydraulic retention time. In this study, changes in phosphate and different types of nitrogen existing in dairy wastewater were investigated for the first time. At hydraulic retention time of 8 h, the orthophosphate concentration in effluent was 84% higher compared to influent. Total nitrogen and total Kjeldahl nitrogen were reduced 70% and 99% respectively at hydraulic retention time of 30 h, while nitrate and nitrite concentrations increased. The microbial electrolysis cell (MEC), revamped from D-MFC, showed the maximum gas production of 0.2 m³ H₂·m^-3·d^-1 at 700 mV applied voltage.     

Rheological and mechanical properties of composites made from wood flour and recycled LDPE/HDPE blend

The effect of compounding method is studied with respect to the rheological behavior and mechanical properties of composites made of wood flour and a blend of two main components of plastics waste in municipal solid waste, low-density polyethylene (LDPE) and high-density polyethylene (HDPE). The effects of recycling process on the rheological behavior of LDPE and HDPE blends were investigated. Initially, samples of virgin LDPE and HDPE were thermo-mechanically degraded twice under controlled conditions in an extruder. The recycled materials and wood flour were then compounded by two different mixing methods: simultaneous mixing of all components and pre-mixing, including the blending of polymers in molten state, grinding and subsequent compounding with wood flour. The rheological and mechanical properties of the LDPE/HDPE blend and resultant composites were determined. The results showed that recycling increased the complex viscosity of the LDPE/HDPE blend and it exhibited miscible behavior in a molten state. Rheological testing indicated that the complex viscosity and storage modulus of the composites made by pre-mixing method were higher than that made by the simultaneous method. The results also showed that melt pre-mixing of the polymeric matrix (recycled LDPE and HDPE) improved the mechanical properties of the wood–plastic composites.     

Synthesis and characterization of Ag nanoparticles embedded in PVA via UV-photoreduction technique for synthesis of Prussian blue pigment

Silver nanoparticles doped in polyvinyl alcohol (AgNps/PVA) were synthesized via polymer-promoted reductive reaction of AgNO₃ and PVA under time-dependent exposure to UV radiation. The AgNps/PVA composites were characterized by X-ray photoelectron spectroscopy (XPS), X-ray diffraction, UV–Vis spectroscopy, and transmission electron microscopy to describe the structure, nuclearity, and distribution of Ag Nps within the PVA matrix. The UV–Vis spectrum of AgNps/PVA exhibited a broad surface plasmon absorption around 425–443 nm which originated from the formation of Ag NPs. Surface analysis by XPS indicated that the Ag NPs were grown solely on the PVA surface at UV exposure time of 2 h (2.0AgNPs/PVA). Increasing the UV exposure time to 4 h will cause the transformation of metallic nanosilver to oxidized nanosilver. UV–Vis absorption spectra were in situ recorded to follow the synthesis of Prussian blue (PB) on 2.0AgNPs/PVA (PB@2.0AgNPs/PVA). The colloidal dispersion of 2.0AgNPs/PVA in an acidic medium containing free Fe(III) ions and potassium hexacyanoferrate(III) revealed an additional band centered at 720 nm due to the intermetal charge-transfer absorbance of the polymeric Fe(II)-C-N-Fe(III) of the PB@2.0AgNPs/PVA nanocomposite. Control experiments were shown to involve a spontaneous electron transfer reaction between 2.0AgNPs/PVA and Fe(III) ions, with a concomitant decomposition of hexacyanoferrate(III) and formation of PB was observed. Moreover, IR gave clear cut evidence for the synthesis of PB@2.0AgNPs/PVA from the appearance of a band for the cyano group at 2090 cm^?1.     

In vivo study of hybrid biomaterial scaffold bioactive glass–chitosan after incorporation of Ciprofloxacin

The present study aimed to evaluate the effect of bioactive glass as well as the presence of Ciprofloxacin drug (%Cip) into bioactive glass–chitosan composite on the in vivo behavior of these scaffolds. These scaffolds were implanted in the femoral condyl of an ovariectomized rat. The serum and organs (liver and kidney) of the under investigated rats were analyzed. Also the physicochemical properties of the prepared implants were assessed using Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) before and after implantation (at different periods of implantation). Biochemical and histological analyses of the under investigated rats proved the biocompatibility of the prepared scaffolds. The hydroxyapatite like layer was significantly precipitated on the surface of BG–CH scaffold than BG–CH–20Cip. In this same period, FT-IR of BG–CH shows complete disappearance of Si–O–Si. Their characteristics bands were replaced by P–O group arisen form bone apatite bands. Physicochemical results show progressive degradation of BG–CH and BG–CH–20Cip that occurred at the same time as replacement of the implant by an apatite layer. However, the bioresorbability and bioactivity of BG–CH are faster than those of BG–CH–20Cip. Therefore, the incorporation of the Ciprofloxacin in the BG–CH induces a retarding effect on the formation of the hydroxyapatite, and consequently on the ossification, without any side effects on the liver–kidney.     

Study on single and binary catalytic systems of pyridine-imine catalysts based on nickel and iron in synthesis of reactor blends and low-density polyethylene nanocomposites

In the presence of modified methylaluminoxane as cocatalyst, the behavior of a binary catalytic system based on pyridine-imine nickel ( N ) and iron ( F ) catalysts was evaluated in order to reach a proper mixture of polyethylene (PE). A computational study along with kinetic profile suggested that the catalyst F with higher electron affinity (A) and electrophilicity (ω) in the methyl cationic active center and stronger interaction with the monomer led to high integrated monomer consumption and higher activity. In addition, the samples produced by the mixture of catalysts showed a higher value of [19.4 × 10⁴ g (PE) mol (Fe+Ni)⁻¹ h⁻¹)], melting point (127.8 °C), and crystallinity extent (41.29%) than the samples produced by the single catalysts. The addition of multiwalled carbon nanotubes (MWCNT) into the polymerization media reduced the activity of catalysts [from 7.50 × 10⁴ to 0.66 × 10⁴ g (PE) mol (Fe+Ni)⁻¹ h⁻¹] and the thermal properties of the low-density polyethylene nanocomposite samples. However, the sample containing 2.33% MWCNT_20-30 improved the total thermal stability of the neat polyethylene blend up to 400 °C. Scanning electron microscope images of the samples demonstrated irregular to virtually uniform morphologies were obtained through the in situ and solution-mixing techniques. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47376.     

冷加工和时效处理顺序对6061铝合金力学性能的影响(英文)

研究不同的析出硬化和冷加工组合对6061铝合金拉伸性能的影响。结果表明,在不同的热处理过程中,在180℃单时效4h能提高合金的强度和伸长率。然而,双时效处理不能改善其力学性能。另外,预时效对随后的析出硬化有负面影响。合金力学性能的变化归因于析出硬化、应变硬化和加工软化的竞争而引起的显微组织演变。     

Tool point dynamics prediction by a three-component model utilizing distributed joint interfaces

In machine dynamics the tool point frequency response functions (FRFs) are employed to predict the stable machining conditions. In this paper, a combined analytical–experimental substructuring procedure is proposed to determine the tool point FRFs for different holder–tool configurations. The method employs the measured spindle-machine FRFs and analytical models of the tool and the holder to predict the tool tip FRFs for different sets of tools and holders mounted on the machine spindle without the need for repeated experimental measurements. Distributed joint interfaces are used to couple the three-component model of the machine. The machine tool tip FRFs with different tool–holder combinations are obtained assuming the clamping conditions at joint interfaces remain unchanged. An experimental case study is provided to demonstrate the applicability of the proposed method in dynamic modeling of machine tool.     

Numerical simulation of heat transfer and fluid flow of molten metal in MMA–St copolymer lost foam casting process

In this study, a computational fluid dynamics (CFD) code was developed to calculate the filling pattern using volume of fluid (VOF) algorithm with donor–acceptor method for free surface simulation. This algorithm has been modified to include the pressure of the gas produced from foam degradation. For this purpose a heat transfer model and 2D foam degradation model were developed. In heat transfer model, radiation and conduction between foam and molten metal; and convection between gas and molten metal were considered. In order to evaluate the results of simulation, a bench scale casting apparatus was assembled and the casting was conducted in a transparent mold. The effect of several parameters such as coating thickness, foam density and vacuum level on the gap temperature, gap pressure and filling speed was studied with the developed software. It was found that the simulated results are in good agreement with experimental results.     

Synthesis of Molybdenum Oxide Nanohybrids as Efficient Catalysts in Oxidation of Alcohols

Novel layered materials based on molybdenum oxide have been synthesized using three amino-carboxylate ligands; terephetalic acid, p-aminobezoic acid and diaminobenzene. On the basis of X-ray diffraction, scanning electron microscopy, thermogravimetry, and infrared results, the insertion of organic ligands into the interlayer space of molybdenum oxide has been proposed. Moreover, the influence of organic guests on the oxide structure and also their catalytic performance are discussed. Furthermore, fabrication of the nanostructured molybdenum oxide is achieved by calcinations of these hybrid materials at 600 °C. Somewhat oriented nanoplatelets are viewed with different catalytic activity.     

Chemical modification of polypropylene fibers grafted vinyl imidazole/acrylonitrile copolymer prepared by gamma radiation and its possible use for the removal of some heavy metal ions

The chemical modification of polypropylene (PP) fibers by graft copolymerization with vinylimidazole (VIm) and acrylonitrile (AN) was carried out using γ‐radiation. Preparation conditions, such as irradiation dose, comonomer concentration and composition and type of solvent, affecting the degree of grafting were investigated. The suitable diluent for obtaining reasonable graft VIm/AN copolymer yield was acetone. The higher grafted yield was achieved by increasing the amount of vinylimidazole in comonomer feed solution as well as irradiation dose. The derivatives of PP‐g‐P(VIm/AN) grafted fibers of different functional groups were obtained by treating the grafted fibers with various organic reagents containing reactive amino groups, such as sulpha‐drug compounds, aliphatic‐ and aromatic amines. Characterization of the obtained graft copolymers and their chemical treatments with different amines was also investigated. It was observed that the nitrile group in PP‐g‐P(VIm/AN) polymer undergoes simple addition reaction via nucleophilic interaction mechanism to produce the corresponding PP‐graft‐P(vinylimidazole/acrylomidine) derivatives. The ability of the grafted fibers and their treated forms to absorb some metal ions as Cd, Hg, and Pb from their individual and mixture solutions was evaluated. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009.