Influence of Substrate Temperature on the Properties of Cobalt Oxide Thin Films Prepared by Nebulizer Spray Pyrolysis (NSP) Technique

Cobalt oxide thin films are prepared by the nebulizer spray pyrolysis technique using cobalt chloride as the precursor material. The structural, optical, morphological and electrical properties are investigated as a function of substrate temperature (300–450 °C). The X-ray diffraction (XRD) analysis reveals that all the films are polycrystalline in nature, having cubic structure with preferential orientation along the (111) plane. The optical spectra show that the films are transparent (68 %) in the IR region. The optical band gap values are calculated for different substrate temperature. Photoluminescence (PL) spectra of the films indicate the presence of indigo, blue and green emission peaks with an ultraviolet emission peak centered around 368nm. SEM images reveals small sphere-like structures for the prepared Co3O4 films. The maximum conductivity obtained is 1.48 x 10?3 S/cm at 350 °C. The activation energy varies between 0.039 and 0.138 eV for the substrate temperature variation from 300-450 Q°C.     

Oviposition Preference and Performance of a Specialist Herbivore Is Modulated by Natural Enemies,Larval Odors,and Immune Status

Journal of Chemical Ecology - Insect herbivores frequently must balance host plant quality and the risk of attack by their natural enemies when making oviposition decisions. Yet, which factor is...     

Synthesis,Characterization, and Application of Mesoporous Silica Functionalized with Alkyl‐Hydroperoxides

A variety of alkyl hydroperoxides such as tert‐butyl‐, tert‐octyl‐, 1‐cyclopentyl‐, 1‐cyclohexyl‐, 3,4‐disubstituted‐1‐cyclohexyl‐, n‐propyl, and n‐undecyl‐hydroperoxides have been functionalized onto ordered mesoporous silica, SBA‐15, from the corresponding covalently anchored synthons. All the tert‐hydroperoxides are prepared by autoxidation using molecular O₂ and an initiator, whereas other hydroperoxides are obtained by reaction with H₂O₂. For autoxidation, the use of a combination of an azoinitiator (AIBN) and N‐hydroxyphthalimide increased the hydroperoxide yield compared with using the azoinitiator alone. Synthons containing two or more tert‐ and sec‐hydrogens lead to higher peroxide yield compared to synthons with a single reactive site. Oxidation of Si–OH (silanol groups) with acidic H₂O₂ at low temperature produces Si–OOH. Reusability of these alkyl hydroperoxides is carried out by oxidation of alcohols obtained from the corresponding alkyl hydroperoxides using H₂O₂. Both the covalently anchored synthons and the resulting hydroperoxides are thoroughly characterized by powder X‐ray diffraction, ¹³C cross‐polarized magic angle spinning NMR, TG/DTA, Fourier transform IR spectroscopy, sorption, and surface area measurements. The quantification of the amount of alkyl hydroperoxide was carried out by iodometric titration using a thio solution. The hydroperoxides exhibit high activity for the epoxidation of styrene to styrene oxide and exhibit reasonably high efficiency for oxygen transfer.     

Fertilizer requirements for specified yield targets. II. Field verification of mathematical models for the estimation of soil and fertilizer nutrient efficiencies

Sugarcane response data from field experiments conducted between May 1979 and August 1981 on a sandy clay loam soil (Udic Haplustalf) of Coimbatore district, Tamil Nadu State, India were used in the present investigation. Soil () and fertilizer () nutrient efficiencies for the amount of fertilizer required for specified cane yield targets were computed from this data by three procedures, viz., conventional deduction procedure, Tamil Nadu Agricultural University Model I [TNAU Model I] and Model II [TNAU Model II].In the case of nitrogen, both TNAU Model I and TNAU Model II gave more realistic estimates of and than those determined by the conventional deduction procedure. The differences in the predicted amounts of fertilizer nitrogen required between these two models were well within the permissible limits of variation indicating that both these approaches can be followed for the amount of nitrogen required for specified yield targets.The Olsen's procedure for available phosphorus estimation was inadequate to explain the relationship between soil available phosphorus and sugarcane response as indicated by results obtained using the TNAU Model II. The incorporation of the term in this model caters for the actual situation in the field in respect of the relationship between soil and fertilizer phosphorus availabilities and phosphorus uptake by sugarcane proving usefulness of this model for assessing the amount of phosphorus required for specified cane yield targets.The results indicated that a considerable amount of potassium from the soil reserve was released into the soil available pool due to a priming effect. This fraction was preferentially absorbed by sugarcane compared to the fractions extracted by 0.1 N HNO₃ as indicated by results obtained using the TNAU Model II. In this case too, the actual situation regarding the relationship between soil and fertilizer potassium availabilities and potassium uptake by sugarcane is catered for by this model proving its superiority over the other two procedures for assessing the amount of potassium required for specified yield targets.     

Chemical Amplification of a Triphenylene Molecular Electron Beam Resist

Molecular resists, such as triphenylene derivatives, are small carbon rich molecules, and thus give the potential for higher lithographic resolution and etch durability, and lower line width roughness than traditional polymeric compounds. Their main limitation to date has been poor sensitivity. A new triphenylene derivative molecular resist, with pendant epoxy groups to aid chemically amplified crosslinking, was synthesized and characterized. The sensitivity of the negative tone, pure triphenylene derivative when exposed to an electron beam with energy 20 keV was ～ 6 × 10^–4 C cm^–2, which increased substantially to ～ 1.5 × 10^–5 C cm^–2 after chemical amplification (CA) using a cationic photoinitiator. This was further improved, by the addition of a second triphenylene derivative, to ～ 7 × 10^–6 C cm^–2. The chemically amplified resist demonstrated a high etch durability comparable with the novolac resist SAL 601. Patterns with a minimum feature size of ～ 40 nm were realized in the resist with a 30 keV electron beam.     

Corrosion behavior of metals and alloys in marine-industrial environment

This work deals with atmospheric corrosion to assess the degrading effects of air pollutants on ferrous and non-ferrous metals and alloys, which are mostly used as engineering materials. An exposure study was conducted in the Tuticorin port area located on the east coast of South India, in the Gulf of Mannar with Sri Lanka to the southeast. Common engineering materials, namely mild steel, galvanized iron, Zn, Al, Cu and Cu–Zn alloys (Cu–27Zn, Cu–30Zn and Cu–37Zn), were used in the investigation. The site was chosen where the metals are exposed to marine and industrial atmospheres. Seasonal 1 to 12 month corrosion losses of these metals and alloys were determined by a weight loss method. The weight losses showed strong corrosion of mild steel, galvanized iron, Cu and Zn and minor effect on Al and Cu–Zn alloys. Linear regression analysis was conducted to study the mechanism of corrosion. The composition of corrosion products formed on the metal surfaces was identified by x-ray diffraction and Fourier transform infrared spectroscopy.     

Ascorbic Acid-Assisted Eco-friendly Synthesis of NiCo<Subscript>2</Subscript>O<Subscript>4</Subscript> Nanoparticles as an Anode Material for High-Performance Lithium-Ion Batteries

We have synthesized NiCo₂O₄ nanoparticles (NCO NPs) using an ascorbic acid-assisted co-precipitation method for the first time. When NCO NPs are used as an anode material for lithium-ion batteries, the cell exhibits superior lithium storage properties, such as high capacity (700 mA h g^?1 after 300 cycles at 200 mA g^?1), excellent rate capabilities (applied current density range 100–1200 mA g^?1), and impressive cycling stability (at 1200 mA g^?1 up to 650 cycles). The enhanced electrochemical properties of NCO NPs are due to the nanometer dimensions which not only offers a smooth charge-transport pathway and short diffusion paths of the lithium ions but also adequate spaces for volume expansion during Li storage. Hence, this eco-friendly synthesis approach will provide a new strategy for the synthesis of various nanostructured metal oxide compounds, for energy conversion and storage systems applications.     

Crystal Structure and Improved Synthesis of 1‐(2H‐Tetrazol‐5‐yl)guanidium Nitrate

Energetic derivatives of tetrazoles are one of the key areas of research focus in pursuit of novel high energy materials, useful as propellants and explosives. Herein, the crystal structure and an improved synthetic procedure of 1‐(2H‐tetrazol‐5‐yl)guanidine ( 1 ) and its nitrate salt ( 2 ) are reported. The compounds were structurally characterized by spectroscopic (FT‐IR, ¹H NMR, ¹³C NMR) and elemental analysis. The molecular structure of tetrazolyl guanidium nitrate ( 2 ) was solved using low temperature single‐crystal X‐ray diffraction. 2 crystallized as its hemihydrate in the orthorhombic space group Fdd2, with a crystal density of 1.69 g cm⁻³. Thermal behavior and decomposition of the molecules were studied with differential scanning calorimetry (DSC). Molar enthalpy of formation (Δ_fH^m) of compound 2 was back calculated from heat of combustion (Δ_cH⁰) value obtained experimentally using bomb calorimetric measurements. Lattice enthalpy of 1‐(2H‐tetrazol‐5‐yl)guanidium nitrate was directly calculated from measured crystal density using Jenkins equation. Preliminary ballistic parameters of the compound were predicted and compared with reported high nitrogen tetrazole derivatives.     

Synthesis and characterization of olivine LiNiPO4 for aqueous rechargeable battery

LiNiPO₄ belongs to a family of olivine type compounds, with members LiMPO₄ where M = Fe, Mn, Co or Ni are transition metals. The lithium nickel phosphate was prepared and characterized in order to evaluate a new potential cathode material for our ongoing research in aqueous rechargeable batteries. Annealing the final product is critical in obtaining the stoichiometric LiNiPO₄ pure phase; conventional cooling to a room temperature leads to an indication of Li₃PO₄ and NiO secondary phases as impurities. The synchrotron infrared radiation (SR-IR) as a source for IR spectroscopy pins down the differences in the chemical bonding for annealed and conventional cooled LiNiPO₄ samples. The cyclic voltammetric and galvanostatic studies showed annealed LiNiPO₄ is electrochemically active from which lithium ions can be de-intercalated during oxidation process leading to an amorphous NiPO₄ and a minor product of nickel(II) hydroxide (β-NiOOH). During subsequent reduction, lithium ions are not fully intercalated, however, the structure is reversible and adequate for multiple cycles. The high potential in LiNiPO₄ looks to be very attractive in terms of high energy density, given the efficiency is improved.     

Proposing a multi-agency development framework

Systems used in complex, multi-agency environments have a number of inherent problems and challenges that in many cases, lead to systems failure. The area of system failure has been the subject of extensive research in the past. It has been well documented in a number of places that information systems are difficult to build and are prone to failure. This paper examines system failure from a social perspective in the context of building systems in complex environments. Through a case study modelling approach, a framework has been developed to assist in building information systems in such complex multi-agency environments. The paper introduces this framework through a study of a number of challenges confronting the builder of information systems in complex, social, multi-agency environments. We examine the role of task accountability and problems identifying authority as key reasons why systems are rejected by users. We introduce a task accountability model to help understand this problem. We conclude by identifying work still to be carried out within the study.