Impact of Zinc oxide nanoparticles on eggplant (S. melongena): studies on growth and the accumulation of nanoparticles

The increasing use of nanoparticles and their occurrence in the environment has made it imperative to elucidate their impact on the environment. Although several studies have advanced the authors’ understanding of nanoparticle–plant interactions, their knowledge of the exposure of plants to nanoparticles and their effects on edible crop plants remain meager and is often paradoxical. The aim of this study was to increase their knowledge on the effect of zinc oxide (ZnO) nanoparticles on eggplant seed germination and seedling growth. ZnO nanoparticles had a negative effect on the growth of eggplant in plant tissue‐culture conditions, as the growth of seedlings decreased with the increase in the concentration of ZnO nanoparticles. In contrast, ZnO nanoparticles enhanced eggplant growth under greenhouse conditions. The accumulation of ZnO nanoparticles in various parts of eggplant was observed through scanning electron microscopy of both plant tissue‐culture and greenhouse‐raised eggplant seedlings. To the best of their knowledge, this is the first study to report on ZnO nanoparticle accumulation in eggplant and its effect on seed germination and seedling growth.Inspec keywords: crops, zinc compounds, scanning electron microscopy, II‐VI semiconductors, nanoparticles, agriculture, cellular biophysics, nanofabricationOther keywords: plant tissue‐culture, greenhouse‐raised eggplant seedlings, ZnO nanoparticle accumulation, seedling growth, ZnO nanoparticles, nanoparticle–plant interactions, zinc oxide nanoparticles, eggplant seed germination, eggplant growth, ZnO     

Metol as Corrosion Inhibitor for zinc

The inhibition behavior of metol (N-methyl-p-aminophenol sulphate) on zinc in different corrosive solutions at room temperature was investigated by various techniques such as weight loss, polarization and linear polarization methods. The percentage inhibition efficiencies were evaluated at different concentrations of the inhibitors. The corrosion rate, inhibition efficiency and surface coverage were dependent on metol concentration. The electrochemical data indicated a basic modification of zinc surface resulting in a decrease in the corrosion rate. Corrosion inhibition was explained by considering an interaction between metal surface and the inhibitor. SEM images and FT-IR profiles confirmed the formation of passive film on the metal surface.     

Generation of nanocrystalline NiO particles by solution combustion method and its Zn?NiO composite coating for corrosion protection

The nanocrystalline nickel oxide (NiO) particles have been successfully prepared by a simple, fast, economical, and eco‐friendly solution‐combustion method using Ni(NO₃)₂ · 6H₂O (oxidizer) and sugar (dextrose as fuel). The as‐prepared compound was calcined for an hour at different temperatures. The synthesized NiO was characterized by XRD, TGA, SEM/EDX, TEM, XPS, FT‐IR, and UV–Vis spectral methods. The crystallite sizes of the NiO particles were measured. Rietveld refinement of X‐ray data matches the cubic structure with space group of Fm3m (No. 225). The thermal behavior of as‐prepared compound was examined. Scanning electron micrographs show uniform cubic like morphology of NiO and its chemical composition was measured. The TEM results reveal that the particle sizes were in the order of 70–80 nm. The red shift was noticed in UV–Vis absorption spectra. As an application part the Zn? NiO composite coating was prepared by electrodeposition method and its corrosion behavior was analyzed by Tafel, impedance and anodic polarization in aggressive medium.     

Morphology‐dependent electrocatalytic activity of nanostructured Pt/C particles from hybrid aerosol–colloid process

An optimum nanostructure and pore size of catalyst supports is very important in achieving high catalytic performances. In this instance, we evaluated the effects of various carbon nanostructures on the catalytic performances of carbon‐supported platinum (Pt/C) electrocatalysts experimentally and numerically. The Pt/C catalysts were prepared using a hybrid method involving the preparation of dense, hollow, and porous nanostructured carbon particle via aerosol spray pyrolysis followed by microwave‐assisted Pt deposition. Electrochemical characterization of the catalysts showed that the porous Pt/C catalyst gave the best performance; its electrochemical surface area was much higher, more than twice than those of hollow or dense Pt/C. The effects of pore size on electrocatalysis were also studied. The results showed the importance of a balance between mesopores and macropores for effective catalysis with a high charge transfer rate. A fluid flow model showed that good oxygen transport contributed to the catalytic activity. © 2015 American Institute of Chemical Engineers AIChE J, 62: 440–450, 2016     

Studies on spinel cobaltites,MCo2O4 (M = Mn,Zn, Fe,Ni and Co) and their functional properties

Optimization of electrodes for charge storage with appropriate processing conditions places significant challenges in the developments for high performance charge storage devices. In this article, metal cobaltite spinels of formula MCo₂O₄ (where M = Mn, Zn, Fe, Ni and Co) are synthesized by oxalate decomposition method followed by calcination at three typical temperatures, viz. 350, 550, and 750 °C and examined their performance variation when used as anodes in lithium ion batteries. Phase and structure of the materials are studied by powder x-ray diffraction (XRD) technique. Single phase MnCo2O4,ZnCo2O4 and Co3O4 are obtained for all different temperatures 350 °C, 550 °C and 750 °C; whereas FeCo₂O₄ and NiCo₂O₄ contained their constituent binary phases even after repeated calcination. Morphologies of the materials are studied via scanning electron microscopy (SEM): needle-shaped particles of MnCo₂O₄ and ZnCo₂O₄, submicron sized particles of FeCo₂O₄ and agglomerated submicron particle of NiCo₂O₄ are observed. Galvanostatic cycling has been conducted in the voltage range 0.005–3.0 V vs. Li at a current density of 60 mA g^?1 up to 50 cycles to study their Li storage capabilities. Highest observed charge capacities are: MnCo₂O₄ – 365 mA h g^?1 (750 °C); ZnCo₂O₄ – 516 mA h g^?1 (550 °C); FeCo₂O₄ – 480 mA h g^?1 (550 °C); NiCo₂O₄ – 384 mA h g^?1 (750 °C); and Co₃O₄ – 675 mA h g^?1 (350 °C). The Co₃O₄ showed the highest reversible capacity of 675 mA h g^?1; the NiO present in NiCo₂O₄ acts as a buffer layer that results in improved cycling stability; the ZnCo₂O₄ with long needle-like shows good cycling stability.     

Strategies for stereocontrol at C1 or C2 in syntheses of α-glucosaminides

The C1 and C2 stereocenters of α-glucosaminides can be prepared by establishing the stereocenters in either order. For the former, a C2-azido glucosyl donor is prepared first, and the restraining effect of a 4,6-O-benzylidene ring is used to induce α-coupling. For the latter, the C1 linkage is prepared first by use of an n-pentenyl-manno-1,2-orthoester donor which ensures (a) clean α-coupling and (b) a convenient C2-ester. The C2-ester is replaced with a triflate leaving group, and nucleophilic displacement is effected by use of a hypervalent silicon azide.     

Surfactant free hydrothermally derived ZnO nanowires,nanorods, microrods and their characterization

ZnO nanowires, nanorods and microrods have been prepared by an organic-free hydrothermal process using ZnSO₄ and NaOH/NH₄OH solutions. The powder X-ray diffraction (PXRD) patterns reveal that the ZnO nano/microrods are of hexagonal wurtzite structure. The Fourier transform infrared (FT-IR) spectrum of ZnO powder shows only one significant spectroscopic band at around 417 cm^?1 associated with the characteristic vibrational mode of Zn–O bonding. The thickness 75–300 nm for ZnO nanorods and 0.2–1.8 μm for microrods are identified from SEM/TEM images. UV–visible absorption spectra of ZnO nano/microrods show the blue shift. The UV band and green emission observed in photoluminescence (PL) spectra are due to free exciton emission and singly ionized oxygen vacancy in ZnO. Finally, the mechanism for organic-free hydrothermal synthesis of the ZnO nano/microrods is discussed.     

Polyphosphazenes—A Promising Candidate for Drug Delivery,Bioimaging, and Tissue Engineering: A Review

Synthetic polymer materials have been surged to the forefront of research in the fields of tissue engineering, drug delivery, and biomonitoring in recent years. Biodegradable synthetic polymers are increasingly needed as transient substrates for tissue regeneration and medicine delivery. In contrast to commonly used polymers including polyesters, polylactones, polyanhydrides, poly(propylene fumarates), polyorthoesters, and polyurethanes, biodegradable polyphosphazenes (PPZs) hold great potential for the purposes indicated above. PPZ's versatility in the synthetic process has enabled the production of a variety of polymers with various physico-chemical, and biological properties have been produced, making them appropriate for biomedical applications. Biocompatible PPZs are often used as scaffolds in the regeneration of skeleton, bones, and other tissues. PPZs have also received special attention as potential drug vehicles of high-value biopharmaceuticals such as anticancer drugs. Additionally, by incorporating fluorophores into the PPZ backbone to produce photoluminescent biodegradable PPZs, the utility of polyphosphazenes is further expanded as they are used in tracking the regeneration of the target tissue as well as the fate of PPZ based scaffolds or drug delivery vehicles. This review provides a summary of the evolution of PPZ applications in the fields of tissue engineering, drug delivery, and bioimaging in recent 5 years.     

Comparative examination of adhesive and cohesive properties of fluorinated coatings on stone/tile surfaces

A NanoScratch methodology was used to evaluate the relative adhesive and cohesive strength of fluorinated poly(methyl methacrylate-co-methacrylic acid) and fluorinated phosphate coatings on stone and tile surfaces. In general, all coatings showed ability to bind to the stone and tile surfaces, and polymer-based coatings expressed stronger adhesion compared to a small-molecule fluorinated phosphate coating. Also, anionic fluorinated polymers containing methacrylic acid (MAA) residues in the ammonium carboxylate form adhered more strongly compared to corresponding acidic polymer counterparts. In addition, anionic fluorinated polymers, shown to adhere more strongly to granite than marble, possibly due to strong Lewis acid-base interaction between carboxylate and aluminosilicates. Conversely, the fluorinated polymers, bearing the MAA side-chains in their free-acid form, bound more strongly to marble via possible Brønsted acid-base interactions between carboxylic acid and calcium carbonate. Lastly, in most cases, comparable fracture thresholds were observed for the same coating material on different substrates. This was expected since fracture threshold is a measure of the mechanical strength of the coating material, independent of the substrate difference.