Application of local error method to SSSF simulation of vector propagation in dispersion compensated optical links

A local error method based on an analytical scheme previously developed for the scalar optical fiber channel is applied to the second-order symmetrized split-step Fourier simulation of polarization multiplexed signal propagation through dispersion compensated optical fiber links. It is found that the global simulation accuracy for the vector propagation can be satisfied using the local error bound from a scalar propagation model for the same global error over a large range of simulation accuracy, chromatic dispersion, and differential group delay. Furthermore, carefully designed numerical simulations are used to show that similar local simulation error are obtained for vector simulations and that the similar local error leads to higher computational efficiency compared to other prevalent step-size selection schemes. The scaling of the global simulation error with respect to the number of optical fiber spans is demonstrated, and global error control for multi-span simulations is proposed. Combining the local error and global error control, the developed simulation scheme can significantly speed up the time-consuming simulations in coherent optical fiber communication system analysis and design.     

Composite Nanostructures of TiO2 and ZnO for Water Splitting Application: Atomic Layer Deposition Growth and Density Functional Theory Investigation

The commercialization of solar fuel devices requires the development of novel engineered photoelectrodes for water splitting applications which are based on redundant, cheap, and environmentally friendly materials. In the current study, a combination of titanium dioxide (TiO₂) and zinc oxide (ZnO) onto nanotextured silicon is utilized for a composite electrode with the aim to overcome the individual shortcomings of the respective materials. The properties of conformal coverage of TiO₂ and ZnO layers are designed on the atomic scale by the atomic layer deposition technique. The resulting photoanode shows not only promising stability but also nine times higher photocurrents than an equivalent photoanode with a pure TiO₂ encapsulation onto the nanostructured silicon. Density functional theory calculations indicate that segregation of TiO₂ at the ZnO surfaces is favorable and leads to the stabilization of the ZnO layers in water environments. In conclusion, the novel designed composite material constitutes a promising base for a stable and effective photoanode for the water oxidation reaction.     

Mathematical Model for Isothermal Wire-Coating From a Bath of Giesekus Viscoelastic Fluid

A mathematical model of wire-coating based on Giesekus constitutive equation is analyzed under isothermal conditions. It is desired to see the functional dependence of Giesekus model parameters on the important operating variables in the wire-coating process, which include volumetric flow rate (later referred to as flow rate), shear stress at the wire surface (later referred to as shear stress), force required for pulling the wire (later referred to as force), and radius of the coated wire (later referred to as coated wire thickness). To this end, the equation governing the laminar, incompressible, and rectilinear flow is first derived and then solved analytically for the case of vanishing axial pressure gradient. A numerical procedure is described to obtain the solution for the case of nonvanishing pressure gradient. Our results indicate that the magnitude of shear stress and force follow a decreasing trend with increasing Giesekus model parameters in both cases. The flow rate and coated wire thickness decrease on increasing the Giesekus model parameters when there is no imposed pressure gradient. However, in the presence of pressure gradient these variables first decrease with increasing Giesekus model parameters and then follow an increasing trend.     

Design of a user anonymous password authentication scheme without smart card

Recently, Jiang et al. and He et al. independently found security problems in Chen et al.'s remote user authentication scheme for non‐tamper‐proof storage devices like Universal Serial Bus stick and proposed improvements. Nonetheless, we detect that the schemes proposed by Jiang et al. and He et al. overlook a user's privacy. We also observe that Jiang et al.'s scheme is vulnerable to insider attack and denial of service attacks and lacks forward secrecy. We point out that the password changing facility in He et al.'s scheme is equivalent to undergoing registration, whereas in Jiang et al.'s scheme, it is unsuitable. Moreover, the login phase of both the schemes is incapable to prevent the use of wrong password leading to the computation of an unworkable login request. Therefore, we design a new scheme with user anonymity to surmount the identified weaknesses. Without adding much in communication/computational cost, our scheme provides more security characteristics and keeps the merits of the original schemes. As compared with its predecessor schemes, the proposed scheme stands out as a more apt user authentication method for common storage devices. We have also presented a formal proof of security of the proposed scheme based on the logic proposed by Burrows, Abadi and Needham (BAN logic). Copyright © 2014 John Wiley & Sons, Ltd.     

Development and application of C60-fullerene bound silica for solid-phase extraction of biomolecules

Sample pretreatment is the most important procedure to remove the matrix for interfacing with mass spectrometry (MS). Additionally, for the samples with low concentration, the process of preconcentration is required before MS analysis. We have newly developed a solid-phase extraction stationary phase based on C60-fullerene covalently bound to silica for purification of biomolecules of different characteristics. Silica particles of different porosity are modified with aminopropyl linker and then covalently bound to C60-fullerenoacetic acid or C60-epoxyfullerenes. The developed materials have been successfully applied as an alternative to commercially available reversed-phase materials for solid-phase extraction. C60-fullerene silica is able to retain small and hydrophilic molecules like phosphopeptides, which can be easily lost by reversed-phase sorbents. The novel materials are applied for desalting and preconcentration of proteins and peptides, especially phosphopeptides. In addition, the C60-fullerene silica is applied for the solid-phase extraction of selected flavonoids with recoveries of approximately 99%. The recoveries are compared with the commercially available solid-phase extraction materials.     

Adsorption of dyes from aqueous solutions on activated charcoal

Adsorption of industrially important dyes namely bromophenol blue, alizarine red-S, methyl blue, methylene blue, eriochrome black-T, malachite green, phenol red and methyl violet from aqueous media on activated charcoal has been investigated. The effect of shaking time, pH and temperature on the adsorption behaviour of these dyes has been studied. It was noted that adsorption of all the dyes on activated charcoal decreases with an increase in the pH and the temperature. The adsorption isotherms at different temperatures were found to be of L-type. Adsorption data was fitted to Freundlich, BET and Langmuir isotherms and various adsorption parameters have been calculated. The thermodynamic parameters such as DeltaG, DeltaH and DeltaS were calculated from the slopes and intercepts of the linear variation of lnK against 1/T, where K is the adsorption coefficient obtained from Langmuir equation, was used. The calculated values for the heat of adsorption and the free energy indicate that adsorption of dyes is favored at low temperatures and the dyes are chemisorbed on activated charcoal.     

Hybrid biosorbent: An innovative matrix to enhance the biosorption of Cd(II) from aqueous solution

To enhance the metal removing capacity of a fungus biosorbent, a new idea of producing a hybrid biosorbent (HB) matrix by combining two different biosorbents using a simple and low-cost immobilization technique was tested for the sorption of Cd(II). The two biosorbents, used as the building block for the production of HB matrix, were the fungal biomass of Phanerochaete chrysosporium (B1) and fibrous network of papaya wood (B2). Maximum independent biosorption capacity of B1 and B2 was noted, respectively, to be 71.36 and 17.62 mgCd(II)g(-1) biosorbent. However, when two biosorbents were hybridized to form HB matrix, the combined biosorption capacity (141.63 mgCd(II)g(-1) biosorbent) was increased by 98.47, 703.80%, respectively, as compared to the ability of B1 and B2 when used alone, and by 59.17% than the sum of separate individual abilities of biosorbents B1 and B2. The kinetics of equilibrium was fast, approximately 88% of Cd(II) biosorption taking place within 30 min. Biosorption kinetics and equilibria followed the pseudo-second order kinetics and Langmuir adsorption isotherms model. HB matrix was also shown to be highly effective in removing Cd(II) from aqueous solution in a continuous flow fixed-bed column bioreactor, both in batch and repeated cycles.     

Imaging of selective nuclear receptor modulator-induced conformational changes in the nuclear receptor to allow interaction with coactivator and corepressor proteins in living cells

Selective nuclear receptor modulators (SNRMs), which are used clinically for the treatment of NR-related diseases, display mixed agonistic/antagonistic activity in a tissue-selective manner depending on the cellular concentrations of coregulator proteins, that is, coactivators and corepressors. The molecular details of the SNRM function provided us with an idea for a rational method for the high-throughput screening of SNRMs in real time in intact living cells. We have developed genetically encoded fluorescent indicators based on the principle of ligand-induced coactivator and/or corepressor recruitment to NR ligand binding domain in single living cells. We demonstrated that an SNRM induces a distinct conformational change in the NR LBD, which is different from that induced by a full agonist or antagonist, but favorable for the recruitment of a coactivator or corepressor protein to the NR. The molecular details of an SNRM binding to a NR, and the subsequently induced conformational changes and recruitment of coregulator protein(s) are important features for the understanding of SNRM action in the living body. Our fluorescent indicators are capable of distinguishing among agonists, antagonists, and SNRMs, and can therefore serve as versatile molecular sensors that predict the pharmacological character of ligands, which is important for an accurate cure of a disease.