Municipal solid waste compost application improves productivity, polyphenol content, and antioxidant capacity of Mesembryanthemum edule

Organic wastes were successfully used as soil amendment to improve agrosystems productivity. Yet, the effectiveness of this practice to enhance plant antioxidant capacities has received little attention. Here, we assess the effect of municipal solid waste (MSW) compost (at 40 t ha(-1)) on growth, polyphenol contents and antioxidant activities of Mesembryanthemum edule. MSW compost application significantly increased the soil contents of carbon, nitrogen, calcium, phosphorus and potassium. This was associated with higher nutrient (N, P, and K) uptake, which likely led to the significant improvement of the plant biomass and relative growth rate (RGR) (+93% on average) as compared to the control. In the same way, the fertilizing effect of the added organic matter significantly enhanced the antioxidant potential M. edule, assessed by radical scavenging activity, iron reducing power and β-carotene bleaching capacity. This was associated with significantly higher antioxidant contents, mainly total phenols and flavonoids. Heavy metal (Pb, Cd, Cu, and Zn) concentrations were slightly increased upon compost application, but remained lower than phytotoxic values. Overall, our results point out that short-term MSW compost application at 40 t ha(-1) is efficient in enhancing the productivity together with the antioxidant potentiality of M. edule without any adverse environmental impact.     

Sequencing Batch Reactor (SBR) for the removal of Hg2+ and Cd2+ from synthetic petrochemical factory wastewater

Petrochemical factories which manufacture vinyl chloride monomer and poly vinyl chloride (PVC) are among the largest industries which produce wastewater contains mercury and cadmium. The objective of this research is to evaluate the performance of a lab-scale Sequencing Batch Reactor (SBR) to treat a synthetic petrochemical wastewater containing mercury and cadmium. After acclimatization of the system which lasted 60 days, the SBR was introduced to mercury and cadmium in low concentrations which then was increased gradually to 9.03±0.02 mg/L Hg and 15.52±0.02 mg/L Cd until day 110. The SBR performance was assessed by measuring Chemical Oxygen Demand, Total and Volatile Suspended Solids as well as Sludge Volume Index. At maximum concentrations of the heavy metals, the SBR was able to remove 76-90% of Hg(2+) and 96-98% of Cd(2+). The COD removal efficiency and MLVSS (microorganism population) in the SBR was affected by mercury and cadmium concentrations in influent. Different species of microorganisms such as Rhodospirilium-like bacteria, Gomphonema-like algae, and sulfate reducing-like bacteria were identified in the system. While COD removal efficiency and MLVSS concentration declined during addition of heavy metals, the appreciable performance of SBR in removal of Hg(2+) and Cd(2+) implies that the removal in SBR was not only a biological process, but also by the biosorption process of the sludge.     

Grating-coupled surface plasmon enhanced short-circuit current in organic thin-film photovoltaic cells

In this study, we demonstrate the fabrication of grating-coupled surface plasmon resonance (SPR) enhanced organic thin-film photovoltaic cells and their improved photocurrent properties. The cell consists of a grating substrate/silver/P3HT:PCBM/PEDOT:PSS structure. Blu-ray disk recordable substrates are used as the diffraction grating substrates on which silver films are deposited by vacuum evaporation. P3HT:PCBM films are spin-coated on silver/grating substrates. Low conductivity PEDOT:PSS/PDADMAC layer-by-layer ultrathin films deposited on P3HT:PCBM films act as the hole transport layer, whereas high conductivity PEDOT:PSS films deposited by spin-coating act as the anode. SPR excitations are observed in the fabricated cells upon irradiation with white light. Up to a 2-fold increase in the short-circuit photocurrent is observed when the surface plasmon (SP) is excited on the silver gratings as compared to that without SP excitation. The finite-difference time-domain simulation indicates that the electric field in the P3HT:PCBM layer can be increased using the grating-coupled SP technique.     

Application of nanofiltration for chromium concentration in the tannery wastewater

The article presents results of investigation concerning an influence of tannery wastewater composition on chromium(III) concentration in the wastewaters during the nanofiltration process (NF). The effectiveness of this process strongly depends on mutual relation between chloride and sulfate ions concentration in tannery wastewater. For this reason, the optimum composition of the tannery wastewater should consist chloride/sulfate ions ratio close to 1. Moreover, an influence of transmembrane pressure (TMP) and the "ageing" of chromium tannery wastewater on the efficiency of the process has been investigated. Optimal range of TMP equal to 14-16 bar has been assumed for the process. It is necessary to point out that the optimum transmembrane pressure can be changed in the case of the membranes with different permeation properties. "Ageing" of the tannery wastewater reduces only a little an efficiency of the process. Experimental results demonstrated that the NF process could be successfully used for the concentration of chromium in the tannery wastewater with high permeate flux, selectivity and performance stability.     

Terrestrial gamma radioactivity levels and their corresponding extent exposure of environmental samples from Wadi El Assuity protective area, Assuit, Upper Egypt

Representative environmental samples (sandy soil, limestone, marble and gravels) collected from Wadi El Assuity, protective area, Assuit governorate in Upper Egypt have been investigated radiometrically using NaI (Tl) gamma-ray spectrometer. The specific activity of the radionuclides in Bq kg?1 for soil ranged between 10.5 and 18.7 for 22?Ra, 1.5 to 4.6 for 232Th and from 94 to 107 for ??K, for limestone ranged between 19 and 27.1 for 22?Ra, 32.9 to 50 for 232Th and from 49 to 7 3 for ??K, where, for marble ranged between 12.2 and 30.7 for 22?Ra, 32.6 to 59.5 for 232Th and 55 to 70 for ??K and for gravels ranged between 7.8 and 21.8 for 22?Ra, 19.8 to 30.0 for 232Th and from 151 to 260 for ??K. The mean activity concentrations of measured radionuclides were compared with other literature values. The absorbed dose rate, radium equivalent activity and external hazard index were calculated and compared with internationally recommended values. The gamma absorbed dose rates in the samples ranged between 8.44 and 50.89 nGy h?1. These dose rates are consistent with the accepted worldwide average 55 nGy h?1 for the public. All values obtained for radium equivalent activity are < 370 Bq kg?1, which are acceptable for safe use. The calculated values of external hazard index obtained varied from 0.12 to 0.24. Since these values are lower than unity, one can say that the radiation hazard is insignificant for the population living in the investigated area. This permits the use of these materials sediments as building materials in any probable development projects at this area.     

Microwave-assisted photochemical reactor for the online oxidative decomposition and determination of p-hydroxymercurybenzoate and its thiolic complexes by cold vapor generation atomic fluorescence detection

We developed a photochemical method for the online oxidation of p-hydroxymercurybenzoate (PHMB), an organic mercury species widely used for mercaptan and thiolic compound labeling. The method is based on a fully integrated online UV/microwave (MW) photochemical reactor for the digestion of PHMB, followed by cold vapor generation atomic fluorescence spectrometry (CVG-AFS) detection. The MW/UV process led to the quantitative conversion of PHMB and thiol-PHMB complexes to Hg(II), with a yield between 91% and 98%, without using chemical oxidizing reagents and avoiding the use of toxic carcinogenic compounds. This reaction was followed by the reduction of Hg(II) to Hg(0), performed in a knitted reaction coil with NaBH(4) solution, and AFS detection in an Ar/H(2) miniaturized flame. The low MW power applied (18 W) allowed us to keep constant the temperature of the photochemical reactor (21 ± 1 °C), using a flowing water bath. This avoided peak widening due to diffusion processes generally occurring at high temperatures and in the additional cooling coil. This method has been applied to the determination of thiols in human plasma, blood, and wine.     

Photosensitized degradation in water of the phenolic pesticides bromoxynil and dichlorophen in the presence of riboflavin, as a model of their natural photodecomposition in the environment

Within the context of environmentally friendly methods for the elimination of surface-water pollutants, the photodegradation of the phenolic pesticides bromoxynil (BXN) and dichlorophen (DCP) under simulated natural conditions has been studied. The work was done in the presence of the visible-light absorber photosensitizer riboflavin (Rf), usually present in trace quantities in natural waters. Under aerobic conditions, an efficient photooxidation of both pesticides was observed. The relatively intricate photochemical mechanism involves pesticide and oxygen consumption and, to a lesser extent, Rf degradation. The kinetic and mechanistic study supports that both H(2)O(2) and singlet molecular oxygen, O(2)((1)Δ(g)), are involved in the process. Kinetic data for the O(2)((1)Δ(g))-mediated oxidation indicate that BXN and DCP are photodegraded with this species faster than the parent compound phenol, very frequently employed as a model for aquatic contaminants, likely due to their lower pK(a) values. This observation allows the design of phenolic pesticides with different photodegradation rates under environmental conditions.     

Engineering spin propagation across a hybrid organic/inorganic interface using a polar layer

Spintronics has shown a remarkable and rapid development, for example from the initial discovery of giant magnetoresistance in spin valves to their ubiquity in hard-disk read heads in a relatively short time. However, the ability to fully harness electron spin as another degree of freedom in semiconductor devices has been slower to take off. One future avenue that may expand the spintronic technology base is to take advantage of the flexibility intrinsic to organic semiconductors (OSCs), where it is possible to engineer and control their electronic properties and tailor them to obtain new device concepts. Here we show that we can control the spin polarization of extracted charge carriers from an OSC by the inclusion of a thin interfacial layer of polar material. The electric dipole moment brought about by this layer shifts the OSC highest occupied molecular orbital with respect to the Fermi energy of the ferromagnetic contact. This approach allows us full control of the spin band appropriate for charge-carrier extraction, opening up new spintronic device concepts for future exploitation.