Numerical Study of Cattaneo-Christov Heat Flux Model for Viscoelastic Flow Due to an Exponentially Stretching Surface

This work deals with the flow and heat transfer in upper-convected Maxwell fluid above an exponentially stretching surface. Cattaneo-Christov heat flux model is employed for the formulation of the energy equation. This model can predict the effects of thermal relaxation time on the boundary layer. Similarity approach is utilized to normalize the governing boundary layer equations. Local similarity solutions are achieved by shooting approach together with fourth-fifth-order Runge-Kutta integration technique and Newton’s method. Our computations reveal that fluid temperature has inverse relationship with the thermal relaxation time. Further the fluid velocity is a decreasing function of the fluid relaxation time. A comparison of Fourier’s law and the Cattaneo-Christov’s law is also presented. Present attempt even in the case of Newtonian fluid is not yet available in the literature.     

Three-Dimensional Flow of Nanofluid Induced by an Exponentially Stretching Sheet: An Application to Solar Energy

This work deals with the three-dimensional flow of nanofluid over a bi-directional exponentially stretching sheet. The effects of Brownian motion and thermophoretic diffusion of nanoparticles are considered in the mathematical model. The temperature and nanoparticle volume fraction at the sheet are also distributed exponentially. Local similarity solutions are obtained by an implicit finite difference scheme known as Keller-box method. The results are compared with the existing studies in some limiting cases and found in good agreement. The results reveal the existence of interesting Sparrow-Gregg-type hills for temperature distribution corresponding to some range of parametric values.     

Volkamer Lemon Tetraploid Rootstock Transmits the Salt Tolerance When Grafted with Diploid Kinnow Mandarin by Strong Antioxidant Defense Mechanism and Efficient Osmotic Adjustment

Salinity restricts plant growth and production by specific ions toxicity to particular plants. Cl ion is exceptionally toxic to citrus. Citrus rootstock and scion has a significant effect on each other under unfavourable conditions. Nevertheless, their specific response can be different depending on the way to translocate and compartment the toxic ions, or to induce antioxidant systems. In this paper, we studied the behaviour of diploid (2x) and tetraploid (4x) Volkamer lemon rootstocks grafted with commercial cultivar Kinnow mandarin (KM/VM2x and KM/VM4x, respectively) when exposed to moderate (75 mM) and high salt stress (150 mM). Both genotypes showed a decrease in their photosynthetic variables (Pn, gs, E, Fv/Fm, Fv′/Fm′, NPQ), and the decline was more significant in KM/VM2x plants as compared to KM/VM4x. The highest increase in the concentration of stress indicators (MDA and H₂O₂) was observed in leaves and roots of KM/VM2x at 75 and 150 mM of salt stress. The KM/VM4× showed the maximum increase in antioxidative enzymes (SOD, CAT, POD, APx, GR) and osmolytes (PRO, GB) in leaves and roots at 75 and 150 mM. Minerals (Cl ion, Na, K, P, N, Ca) accumulation was also significantly affected in leaves and roots of KM/VM2x and KM/VM4x under moderate and high NaCl stress. Overall, our results showed that Cl ion accumulation presents a robust correlation with stress indicators and their scavenging enzymes in leaves and roots. Moreover, 2x scion significantly mitigated by the 4x rootstock and showed more tolerance as compared to grafted on 2x rootstock.

     

Structural and functional comparison of hexahistidine tagged and untagged forms of small multidrug resistance protein,EmrE

EmrE is a member of the small multidrug resistance (SMR) protein family in Escherichia coli. EmrE confers resistance to a wide variety of quaternary cation compounds (QCCs) as an efflux transporter driven by proton motive force. The purification yield of most membrane proteins are challenging because of difficulties in over expressing, isolating and solubilizing them and the addition of an affinity tag often improves purification. The purpose of this study is to compare the structure and function of hexahistidinyl (His₆) tagged (T-EmrE) and untagged (UT-EmrE) versions of EmrE. In vivo QCC resistance assays determined that T-EmrE demonstrated reduced resistance as compared to UT-EmrE. We isolated EmrE using the two different purification methods, an organic solvent extraction method used to isolate UT-EmrE and nickel affinity chromatography of T-EmrE. All proteins were solubilized in the same buffered n-dodecyl-β-d-maltopyranoside (DDM) detergent and their conformations were examined in the presence/absence of different QCCs. In vitro analysis of protein multimerization using SDS-Tricine PAGE and dynamic light scattering analysis revealed that both proteins predominated as monomers, but the formation of dimers was more constant and uniform in T-EmrE compared to UT-EmrE. The aromatic residue conformations of both proteins indicate that T-EmrE form is more aqueous exposed than UT-EmrE, but UT-EmrE appeared to have a more dynamic environment surrounding its aromatic residues. Using fluorescence to obtain QCC ligand-binding curves indicated that the two forms had differences in dissociation constants (K_d) and maximum specific one-site binding (B_max) values for particular QCCs. In vitro analyses of both proteins demonstrated subtle but significant differences in multimerization and QCC binding. In vivo analysis indicates differences caused by the addition of the tag, we also observed differences in vitro that could be a result of the tag and/or the different purification methods.     

Study of the migration behaviours of imidazoline corrosion inhibitor in concrete using UV–vis spectrophotometry

In this study, UV–visible light spectrophotometry was used for the first time to examine the migration behaviours of cationic and nonionic imidazoline corrosion inhibitors in concrete. Imidazoline can react with bromocresol purple resulting in a reduction in absorbance, which can be used to calculate quantitatively imidazoline concentration. The results showed that the migration rate of nonionic imidazoline was faster than that of cationic imidazoline with or without the presence of an electric field, possibly because of the better water solubility of nonionic imidazoline. The electric field could significantly accelerate the migration rate of the cationic and nonionic imidazoline. However, the penetration performance of nonionic imidazoline was much improved compared with that of cationic imidazoline in concrete. From X‐ray photoelectron spectroscopy analysis, the N element could be detected on steel, verifying the migration behaviour of the nonionic imidazoline. This nonionic imidazoline could markedly retard steel corrosion according to potentiodynamic polarization.