Highly sensitive electrochemical determination of nitric oxide using fused spherical gold nanoparticles modified ITO electrode

This paper describes the highly sensitive electrochemical determination of nitric oxide (NO) using the fused spherical gold nanoparticles (FAuNPs) modified ITO electrode. The FAuNPs were self-assembled on a (3-mercaptopropyl)-trimethoxysilane (MPTS) sol-gel film, which was preassembled on ITO electrode. The attachment of FAuNPs on MPTS sol-gel film was confirmed by UV-vis absorption spectroscopy, atomic force microscopy (AFM) and cyclic voltammetry (CV). The AFM image shows that the AuNPs retain their fused morphology after immobilized on MPTS sol-gel film. The FAuNPs modified ITO electrode shows an excellent electrocatalytic activity towards the oxidation of NO. Using FAuNPs modified electrode, the detection of 12 nM NO was achieved for the first time by amperometry method. Further, the current response was increased linearly with increasing NO concentration in the range of 1.2 × 10⁻⁸ to 7 × 10⁻⁴ M and the detection limit was found to be 3.1 × 10⁻¹⁰ M (S/N = 3). The FAuNPs modified ITO electrode displays an excellent selectivity towards the determination of 12 nM NO even in the presence of 1000-fold excess common interfering agents.     

Effect of nonstoichiometry on mechanical properties of reactive hot‐pressed monolithic ZrCx Ceramic

The reactive hot pressing (RHP) of Zr:C powder mixture at various molar ratios (1:0.5, 1:0.6, and 1:0.67) at applied pressures of 4‐7 MPa and 1200°C resulted in dense ZrC_x ceramics. Nano‐hardness values of ZrC_x are reported to be 21‐31 GPa as “x” was varied from 0.5 to 1.0. However, indentation modulus for all ZrC_x compositions remained at ~350 GPa. Microhardness of the ZrC_x increased from 13 to 15 GPa as the stoichiometry was increased from 0.5 to 1.0. The indentation fracture toughness for ZrC_0.5 was 4 MPa m^1/2, and for ZrC_0.67 it was reduced to 3.6 MPa m^1/2. The 3‐point flexural strength for ZrC_0.5 was determined to be 386 ± 26 MPa, which decreased to 316 ± 20 MPa as the carbon content (ZrC_0.67) was increased. The dry sliding wear of ZrC_0.5 to ZrC_0.6 indicated that the coefficient of friction was increased from 0.73 to 0.86 at 5 N load and 500 m sliding distance. Further, ZrC_0.67 showed a reduction in friction coefficient of 0.81, and this was due to the increase of strong Zr–C covalent bond and unreacted graphite.     

Photocatalytic degradation of phenol in a rotating annular reactor

Batch photocatalytic degradation studies of phenol were conducted in an annular slurry reactor, to evaluate its performance under different operating and design conditions. The reactor had two concentric cylinders with the inner one rotating at specified revolutions per minute. The reactor also had provisions for aerating the slurry present in the annular gap. The inner cylinder housed the UV-lamps. The effects of catalyst loading (0–8 g/L), inner cylinder rotation speed (0–50 rpm), annular gap-width (7.5, 17.5 and 32.5 mm), initial pollutant concentration (10–50 mg/L) and mode of illumination (continuous or periodic) were studied. Light intensity received by the slurry was measured using Actinometry. Depending on the catalyst loading, annular gap-width and number of illuminated lamps the intensity values ranged from 0.58×10^?4 to 6.4×10^?4 Einsteins/L min. Under well mixed conditions, the reactor performance was found to increase with increase in catalyst loading. At low/medium annular gap width configurations, agitation induced by continuous aeration was found to provide sufficient mixing even when the inner cylinder was stationary. Rotation of the inner cylinder was required only in the high gap width configuration at high catalyst loadings. Scale-up of the reactor was investigated by increasing the gap-width of the annulus and hence increasing the quantity of feed processed. Controlled periodic illumination created by Taylor vortices did not show any improved performance over the regular continuous illumination. Modeling of reaction kinetics was investigated with different approaches and their efficacy in fitting the concentration–time trends of both the primary pollutant and the intermediates are discussed.     

Comparative assessment of human exposure to phthalate esters from house dust in China and the United States

Because of volatilization and leaching from their application in consumer and personal care products, phthalate esters are ubiquitous contaminants in the indoor environment. In this study, we measured concentrations and profiles of 9 phthalate esters in indoor dust samples collected from six cities in China (n = 75). For comparison, we also analyzed samples collected from Albany, New York, USA (n = 33). The results indicated that concentrations, except for dicyclohexyl phthalate (DCHP) and bis(2-ethylhexyl) phthalate (DEHP), and profiles of phthalate esters varied significantly between the two countries. Concentrations of diethyl phthalate (DEP), di-n-hexyl phthalate (DNHP), and benzyl butyl phthalate (BzBP) were 5 to 10 times higher in dust samples collected from Albany than those from the Chinese cities. In contrast, concentrations of di-iso-butyl phthalate (DIBP) in dust samples from Albany were 5 times lower than those from the Chinese cities. We estimated the daily intake (DI) of phthalate esters through the routes of dust ingestion and dermal dust absorption. The extent of contribution of indoor dust to human exposures varied, depending on the type of phthalate esters. The contribution of dust to DEHP exposure was 2-5% and 10-58% of the estimated total DIs in China and the USA, respectively. On the basis of the estimates of total DIs of phthalates, extrapolated from urinary metabolite concentrations, the contributions of inhalation, dermal absorption, and dietary intake to total DIs were estimated. The results indicated that dietary intake is the main source of exposure to DEHP (especially in China), whereas dermal exposure was a major source for DEP. This is the first study to elucidate sources of human exposure to phthalates among the general population in China.     

Enhanced Photocatalytic and Antibacterial Activities of ZnSe Nanoparticles

Water and microbial contamination is a serious issues to aquatic system and human health. The metal selenide has a tremendous technique to degrade the dyes and bacteria.The present work reports the synthesis of ZnSe nanoparticles in a simple co-precipitation method. The synthesized samples were analyzed by structural, optical, morphological, catalytic and biological activity. The size and bandgap by annealing temperature tuning which are confirm by X-ray Diffraction and UV–Visible spectrometer. The quasi-spherical shapes were confirmed by Scanning Electron Microscope and Transmission Electron Microscope.The photo excited electrons have trapped the metals and promoting the degradation system. The release of ions to the surface was acknowledged by Photo Luminescence spectroscopy. The photocatalytic dye degradation of the Methyl Orange showed that the enhanced activity in high temperature. The photocatalytic dye degradation activity suggested that the temperature change the production of free radicals and ROS formation. The hydroxyl radicals were slewing the dye molecules and bacteria. The obtained results giving the information of ZnSe nanoparticles are one of the fascinating research areas in the current research world. Because of its large application in different field it acts as a promoting catalytic and biological application.

Graphical Abstract

     

PYRENE ENCAPSULATED ALGINATE BEAD TYPE FOR SUSTAINED RELEASE IN BIODEGRADATION: PREPARATION AND CHARACTERISTICS

A novel method for preparation of pyrene encapsulated alginate beads for controlled release delivery of pyrene is reported in this study. Five different bead types that varied on the organic phase for pyrene delivery, presence or absence of polyvinyl alcohol (PVA) and boric acid treatment were prepared. Based on the pyrene release profile, silicone oil encapsulated in PVA-alginate bead was selected where encapsulation efficiency was more than 99% without any solvent leakage. Silicone oil encapsulation was further confirmed in microscopy observations. Pyrene release behavior from the beads was explained by a diffusion controlled first order release (R² > 0.96). Reusability of this bead was demonstrated, where pyrene was loaded from an external medium in a non-destructive way. Application of the system was finally established in a biodegradation study using Mycobacterium frederiksbergense, where simultaneous release and removal of pyrene along with appearance of pyrene metabolites was observed.     

Various strategies for reducing Nox emissions of biodiesel fuel used in conventional diesel engines: A review

Energy demand, decreasing fossil fuel reserves, and health-related issues about pollutants have led researchers to search for renewable alternative fuels to either partially or fully replace fossil fuels. Among many alternative fuels, biodiesel became one of the most popular choices due to similar properties to that of conventional diesel. Biodiesel produces slightly lower brake thermal efficiency compared to that of conventional biodiesel, but has an advantage of reduced emissions of CO₂, CO, HC, and smoke. However, biodiesel shows higher NOx emission which, when used in increased biodiesel market, may become a serious problem. Various strategies were attempted by different researcher to reduce NOx emissions. In this paper, various strategies, adapted for reducing NOx emissions of biodiesel fuel used in diesel engines for automobile applications, are reviewed and discussed. The strategies are grouped into three major groups, namely combustion treatments, exhaust after-treatments, and fuel treatments. Among various strategies discussed, fuel treatments, such as low temperature combustion, mixing fuel additives and reformulating fuel composition, reduce NOx emission without compromising other emission and performance characteristics and they seem to be promising for future biodiesel fuel.     

Photophysical and photochemical investigations on triazole ring linked chalcone containing polymethacrylates

A series of polymethacrylates containing triazole ring linked chalcone were designed and synthesized. These conjugated chalcone polymers are modulate under the light depending on the pendant substituents (–N(CH₃)₂, CH₃, OCH₃, Br, H & NO₂). The steady-state absorption and emission spectroscopic techniques have been used to investigate intramolecular charge transfer (ICT) behaviour of the polymers. Absorption spectra in different organic solvents demonstrate the presence of ICT in polymer 5a. On the other hand, its excited singlet state exhibits high ICT characters as manifested by polarity of solvents. Interestingly, ICT emission maximum is strongly red shifted (53 nm). The emission intensities of fluorophore are compared with those measured after crosslinking, suggesting that the statically quenched fluorophores are entirely non-emissive. The emission decay of polymer 5a displays bi-exponentially with life time of 0.52 and 1.62 ns ascribed to presence of locally excited ICT state. Cyclic voltammogram demonstrates irreversible oxidation potential at 0.9 V indicates formation mono-radical cation.     

Tracer design for magnetic particle imaging (invited)

Magnetic particle imaging (MPI) uses safe iron oxide nanoparticle tracers to offer fundamentally new capabilities for medical imaging, in applications as vascular imaging and ultra-sensitive cancer therapeutics. MPI is perhaps the first medical imaging platform to intrinsically exploit nanoscale material properties. MPI tracers contain magnetic nanoparticles whose tunable, size-dependent magnetic properties can be optimized by selecting a particular particle size and narrow size-distribution. In this paper we present experimental MPI measurements acquired using a homemade MPI magnetometer: a zero-dimensional MPI imaging system designed to characterize tracer performance by measuring the derivative of the time-varying tracer magnetization, M'(H(t)), at a driving frequency of 25 kHz. We show that MPI performance is optimized by selecting phase-pure magnetite tracers of a particular size and narrow size distribution; in this work, tracers with 20 nm median diameter, log-normal distribution shape parameter, σ(v), equal to 0.26, and hydrodynamic diameter equal to 30 nm showed the best performance. Furthermore, these optimized MPI tracers show 4?×?greater signal intensity (measured at the third harmonic) and 20% better spatial resolution compared with commercial nanoparticles developed for MRI.     

Brazil’s new national policy on solid waste: challenges and opportunities

Brazil, one of the world’s largest developing countries, has recently introduced a new solid waste management regulatory policy. This new regulatory policy will have implications for a wide variety of stakeholders and sets the stage for opportunities and lessons to be learned. These issues are discussed in this article.