Cyclic voltammetric study of zinc and zinc oxide electrodes in 5.3 M KOH

The behaviour of zinc and zinc oxide in 5.3 M KOH in the presence of alkaline earth oxides, SnO, Ni(OH)₂ and Co(OH)₂ was examined by cyclic voltammetry. The influence of the alkaline earth oxides was compared with additives of established effects (Bi₂O₃, LiOH, Na₂CO₃ and CdO). The alkaline earth oxide each exhibits a distinct behaviour towards zincate. Whereas, a single process of interaction with zincate was shown by CaO; two modes of reaction were obtained with SrO and BaO. Solid solution formation was noticed with BeO and MgO. The other additives forming solid solution with ZnO were CdO, SnO. The ionic sizes of Ni(OH)₂ and Co(OH)₂ allow solid solution formation with Zn(OH)₂. Both Bi₂O₃ and Na₂CO₃ enter into complexation with zincate. LiOH forms two distinct zincates, of which one is an oxo zincate leaching the `hydroxyl' functionality. Cyclic voltammetry revealed the deposition of the oxide/hydroxide additives as metal prior to the onset of zinc deposition and the potential range for this additive metal deposition is almost the same for different additives (SnO, CdO, Ni(OH)₂). The beneficial action of these additives to zinc alkaline cells is associated with a substrate effect. The implication of this electrocatalytic deposition of metals on a zinc oxide electrode is also discussed.     

The hydrothermal synthesis and structure of a one-dimensional Fe(II)molybdophosphate

A new one-dimensional Fe(II)molybdophosphate of the formula, [(C₁₀H₈N₂)H₂]₂[Fe₄^(II)Mo₁₂^(V)(HPO₄)₆(PO₄)₂(H₂O)₈(OH)₆O₂₄]·8H₂O, (1), has been synthesized by employing hydrothermal methods and characterized by single crystal X-ray diffraction. The structure consists of a network of MO₆ (M = Fe, Mo) octahedra and (H)PO₄ tetrahedra linked through their vertices. The connectivity between the polyhedral units gives rise to one-dimensional chains with eight-membered apertures. The hydrogen bonded interactions between the chains form pseudo two-dimensional layers. Extensive hydrogen bonding also exists between the amine molecule, 4,4^′-bipyridine, water molecule and framework oxygen atoms. Crystal data for 1: monoclinic, space group = P2₁ (no. 4), a=12.549(3) (Å), b=23.496(5) (Å), c=14.551(3) (Å), β=114.87(3)°, , and Z=2.     

Second row transition metal sulfides for the hydrotreatment of coal-derived naphtha I. Catalyst preparation, characterization and comparison of rate of simultaneous removal of total sulfur, nitrogen and oxygen

Naphtha derived from an Illinois No. 6 coal contains appreciable quantities of sulfur-, nitrogen- and oxygen-containing compounds. The hydrotreatment of this naphtha has been evaluated over unsupported transition metal sulfide catalysts of the second row in the Periodic Table. The catalysts were prepared by a room temperature precipitation reaction. Surface areas, crystalline phase and particle size distributions were determined by Brunauer-Emmet-Teller (BET), X-ray diffraction (XRD) and transmission electron microscopy (TEM), respectively. A comparison of average particle sizes calculated from these three techniques has enabled the understanding of the morphology of the transition metal sulfides. The catalysts exhibit a so-called volcano plot for the HDS of dibenzothiophene. Similar so-called volcano plots are also exhibited for the simultaneous hydrodesulfurization (HDS), hydrodenitrogenation (HDN) and the hydrodeoxygenation (HDO) of the coal-derived naphtha containing a mixture of heteroatoms. The order of reactivity of the transition metal catalysts is the same for all three of the processes. Ruthenium sulfide (RuS₂) is the most active catalyst for HDS, HDN and HDO of the coal-derived naphtha.     

Studies on Silicon Containing Nano-hybrid Epoxy Coatings for the Protection of Corrosion and Bio-Fouling on Mild Steel

An epoxy nano-composite coating was developed using amine functionalized nZnO (in the amount of 2.5 %, 5.0 % and 7.5 wt %) as the dispersed phase and a commercially available epoxy resin as the matrix phase. The structural features of these materials were ascertained by FT-IR spectral studies. The anti-corrosive properties of the epoxy/nZnO hybrid coatings in comparison with a virgin coating were investigated by a salt spray test and electrochemical impedance spectroscopy technique. The surface morphology determined by SEM, indicates that nZnO particles were dispersed homogenously through the epoxy polymer matrix. The results showed improved antifouling and anticorrosive properties for epoxy-nZnO hybrid coatings.     

KINETICS OF URANIUM EXTRACTION BY MACROPOROUS BIFUNCTIONAL PHOSPHINIC ACID RESIN

ABSTRACT

The rate of extraction of uranium by macroporous bifunctional phosphinic acid (MPBPA) resin from nitric acid medium has been studied under particle diffusion controlled conditions. The internal diffusion coefficient was found to increase with increase in temperature and decrease with increase in particle size. The activation energies and entropies suggest that the extraction of uranium essentially follows ion exchange mechanism at low concentration of nitric acid while it is through linkage of >P=0 group of the resin at high concentrations.     

One‐Dimensional Pseudo‐Homogeneous Packed‐Bed Reactor Modeling: I. Chemical Species Equation and Effective Diffusivity

Packed‐bed reactor experimentation is a key tool used in order to formulate chemical kinetics. The chemical species equation and overall methodology are described for a one‐dimensional pseudo‐homogeneous packed‐bed reactor model useful for experimental calibration of chemical kinetics. Over the history of simulation development for this equation there exist numerous different effective diffusivity correlations. The included historical review and parametric study of these correlations help to determine the correct choice based on numerical simplicity and model outcomes. A subsequent review paper describes the energy equation and effective thermal conductivity correlations while coming to a generalized conclusion regarding modeling efforts.     

Impact of density gradients on the fluid flow inside a vibrating cavity subjected to soret effect

Computational fluid dynamics simulations of thermovibrational flows in a square cavity filled with a water–isopropanol mixture has shown that inaccurate density calculations can predict very different flow behaviours. Specifically, comparison has been made between two density calculation models, viz., a weighted‐average scheme and the Perturbed Chain Statistical Associating Fluid Theory equation of state. While the latter approach predicts a stronger flow in the cavity due to the convective instabilities that are induced by the large spatial gradients in density, the weighted‐average scheme cannot predict this since it does not explicitly depend on the temperature of the mixture. © 2012 Canadian Society for Chemical Engineering     

Contribution of organomodified clay on hybrid microstructures and properties of epoxidized natural rubber‐based nanocomposites

Influence of organic modifying agent of clay on dispersion, distribution, hybrid microstructure formation, and associated performance properties of epoxidized natural rubber‐based composites was evaluated. Binary and ternary composites of carbon black (CB) and two organomodified layered silicates (i.e., nanomer I30E and Cloisite 30B) were prepared and characterized based on small angle X‐ray scattering, transmission electron microscopy, hydrodynamic swelling, tensile measurement, and dynamic mechanical analyses. Greater extent of exfoliation and “nanounit” formation was noted in ternary composites containing nanomer I30E, which was reflected in higher interfacial roughness (d_s = 2.82) and lower radius of gyration (R_g = 205 Å). Morphological observations suggested higher nanomer I30E–CB interactions than that of Cloisite 30B–CB. The interplatelet distance in Cloisite 30B (d = 1.83 nm) stacks was lower than that of nanomer I30E (d = 2.26 nm). These two factors jointly contributed in higher breakdown of nanomer I30E stacks by CB than that of Cloisite 30B stacks. Greater exfoliation and nanounit formation in I30E–CB‐filled nanocomposite was also reflected in increased degree of crosslinking (n = 20 × 10^?5%), tensile modulus/strength, half height width of damping peak (20.3°C), and filler effectiveness (C = 0.33). POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

Review of Chemical Reactions in the NO Reduction by CO on Rhodium/Alumina Catalysts

The emissions of nitric oxide and carbon monoxide from internal combustion engines are of primary concern due to their impact on the environment and people's health. Since rhodium has proven to be an important catalyst for the reduction of nitric oxide by carbon monoxide, its accurate modeling is of significant value to industry. This paper reviews the literature with respect to this interaction in order to explain the history of the detailed reactions occurring on the surface. This review was accomplished in the absence of other species in order to focus the efforts and reduce the complexity of the task. In addition, this work presents an appropriate global reaction expression based on these detailed reactions for use in one-dimensional aftertreatment catalyst models.