Experimental and theoretical cooling velocity profile inside laser welded metals using keyhole approximation and Boubaker polynomials expansion

In this paper we are concerned with the t-dependent cooling velocity during laser welding sequences. The temperature profile has been yielded by using keyhole approximation for the melted zone and solving the heat transfer equation. A polynomial expansion has been adopted as a guide to determining the cooling velocity during welding cut-off stage. A thorough comparison with experimental results and recently published profiles has been carried out.     

Electrochemical determination of tyrosine in the presence of uric acid at a carbon paste electrode modified with multi-walled carbon nanotubes enhanced by sodium dodecyl sulfate

Tyrosine (Tyr) was quantitated with high sensitivity and selectivity in the presence of uric acid (UA) using a carbon paste electrode modified with multi-walled carbon nanotubes. Tyr and UA were catalytically oxidized with diffusion-controlled characteristics. They were determined simultaneously by differential pulse voltammetry with a potential difference of 350 mV. The electrocatalytic currents increase linearly with Tyr and UA concentrations 4×10^?7?1×10^?4 M and 3×10^?7?2×10^?4 M. Their detection limits were 1×10^?7 and 5.1×10^?8 M respectively. In the presence of sodium dodecyl sulfate the Tyr detection limit improved from 1×10^?7 to 6.9×10^?8 M. The electrode was successfully used to quantitate Tyr and UA in serum.      

Phytochemical analysis and Enzyme Inhibition Assay of Aerva javanica for Ulcer

Background

Nickel ferrite, a kind of soft magnetic materials is one of the most attracting class of materials due to its interesting and important properties and has many technical applications, such as in catalysis, sensors and so on. In this paper the synthesis of NiFe₂O₄ nanoparticles by the hydrothermal method is reported and the inhibition of surfactant (Glycerol or Sodium dodecyl sulfate) on the particles growth is investigated.

Methods

For investigation of the inhibition effect of surfactant on NiFe₂O₄ particles growth, the samples were prepared in presence of Glycerol and Sodium dodecyl sulfate. The X-ray powder diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), vibrating sample magnetometer (VSM) and inductively coupled plasma atomic emission spectrometer (ICP-AES) techniques were used to characterize the samples.

Results

The results of XRD and ICP-AES show that the products were pure NiFe₂O₄ and also nanoparticles grow with increasing the temperature, while surfactant prevents the particle growth under the same condition. The average particle size was determined from the Scherrer's equation and TEM micrographs and found to be in the range of 50-60 nm that decreased up to 10-15 nm in presence of surfactant. The FT-IR results show two absorption bands near to 603 and 490 cm^-1 for the tetrahedral and octahedral sites respectively. Furthermore, the saturated magnetization and coercivity of NiFe₂O₄ nanoparticles were in the range of 39.60 emu/g and 15.67 Q_e that decreased for samples prepared in presence of surfactant. As well as, the nanoparticles exhibited a superparamagnetic behavior at room temperature.

Conclusions

Nanosized nickel ferrite particles were synthesized with and without surfactant assisted hydrothermal methods. The results show that with increasing of temperature, the crystallinity of nanoparticles is increased. In the presence of surfactants, the crystallinity of NiFe₂O₄ nanoparticles decreased in comparison with surfactant- free prepared samples. All of the nickel ferrite nanoparticles were superparamagnetic at room temperature.

Graphical abstract

     

Surface science approach to the solid-liquid interface: surface-dependent precipitation of Ni(OH)2 on α-Al2O3 surfaces

Surface-dependent precipitation: The adsorption of Ni(II) complexes in aqueous solution on (0001) and (1102) α-Al(2)O(3) single-crystal surfaces has been studied (see the X-ray absorption spectra obtained for parallel and perpendicular polarization directions). The use of planar model systems emphasizes the crucial role of the Al(2)O(3) orientation for Ni dispersion with practical implications in catalyst preparation procedures.     

Alpha-glucosidase inhibitory and antioxidant acridone alkaloids from the stem bark of Oriciopsis glaberrima ENGL. (Rutaceae)

The CH2Cl2/MeOH extract of the stem bark of Oriciopsis glaberrima ENGL. afforded four new acridone alkaloids namely oriciacridone C, D, E and F along with six known compounds: atalaphyllidine, oleanolic acid, butulinic acid, beta-sitosterol, stigmasterol, glucoside of stigmasterol and one synthetically known acridone: 1,3,5-trihydroxy-4-prenylacridone. The structures were established on the basis of MS, 1D and 2D NMR experiments. The acridones 1, 4 and 5 showed potent activity against alpha-glucosidase, while the acridones 1-5 showed moderate free radical scavenging activity against 1,1-diphenyl-2-picrylhydrazyl (DPPH).     

A new approach to decoupling of bacterial adhesion energies measured by AFM into specific and nonspecific components

A new method to decoupling of bacterial interactions measured by atomic force microscopy (AFM) into specific and nonspecific components is proposed. The new method is based on computing the areas under the approach and retraction curves. To test the efficacy of the new method, AFM was used to probe the repulsion and adhesion energies present between Listeria monocytogenes cells cultured at five pH values (5, 6, 7, 8, and 9) and silicon nitride (Si₃N₄). Overall adhesion energy was then decoupled into its specific and nonspecific components using the new method as well as using Poisson statistical approach. Poisson statistical method represents the most commonly used approach to decouple bacterial interactions into their components. For all pH conditions investigated, specific energies dominated the adhesion, and a transition in adhesion and repulsion energies for cells cultured at pH 7 was observed. When compared, the differences in the specific and nonspecific energies obtained using Poisson analysis and the new method were on average 2.2 % and 6.7 %, respectively. The relatively close energies obtained using the two approaches demonstrate the efficacy of the new method as an alternative way to decouple adhesion energies into their specific and nonspecific components.     

Aqueous Urea Solution Promoted Resolution of Five-Component Mixture of Amino Acids on Silica TLC Plates

JPC – Journal of Planar Chromatography – Modern TLC - A thin-layer chromatographic system comprising of silica gel as stationary phase and 1.0% aqueous urea solution as mobile phase (pH...     

Generalized Skew Derivations with Nilpotent Values in Prime Rings

Let ? be a prime ring, 𝒞 the extended centroid of ?, ? a Lie ideal of ?, F be a nonzero generalized skew derivation of ? with associated automorphism α, and n ≥ 1 be a fixed integer. If (F(xy) ? yx) ⁿ  = 0 for all x, y ∈ ?, then ? is commutative and one of the following statements holds:

(1) Either ? is central;

(2) Or ? ? M ₂(𝒞), the 2 × 2 matrix ring over 𝒞, with char(𝒞) = 2.     

On one sided ideals of a semiprime ring with generalized derivations

Let R be a ring with center Z(R). An additive mapping ${F : R \longrightarrow R}$ is said to be a generalized derivation on R if there exists a derivation ${d : R \longrightarrow R}$ such that F(xy) = F(x)y + xd(y), for all ${x, y \in R}$ (the map d is called the derivation associated with F). Let R be a semiprime ring and U be a nonzero left ideal of R. In the present note we prove that if R admits a generalized derivation F, d is the derivation associated with F such that d(U) ≠ (0) then R contains some nonzero central ideal, if one of the following conditions holds: (1) R is 2-torsion free and ${F(xy) \in Z(R)}$ , for all ${x, y \in U}$ , unless F(U)U = UF(U) = Ud(U) = (0); (2) ${F(xy) \mp yx \in Z(R)}$ , for all ${x,y \in U}$ ; (3) ${F(xy) \mp [x,y] \in Z(R)}$ , for all ${x,y \in U}$ ; (4) F ≠ 0 and F([x,y]) = 0, for all ${x, y \in U}$ , unless Ud(U) = (0); (5) F ≠ 0 and ${F([x, y]) \in Z(R)}$ , for all ${x, y \in U}$ , unless either d(Z(R))U = (0) or Ud(U) = (0)n.     

Controlled Assembly of Cu/Co-Oxide Beaded Nanoclusters on Thiolated Graphene Oxide Nanosheets for High-Performance Oxygen Evolution Catalysts

The use of water splitting modules is highly desired for the sustainable production of H₂ as a future energy carrier. However, the sluggish kinetics and demand of high anodic potential are the bottlenecks for half-the cell oxygen evolution reaction (OER), which severely hamper the overall conversion efficiency. Although transition metal oxides based electrocatalysts have been envisioned as cost-effective and potential contenders for this quest, nevertheless, their low conductivity, instability, and limited number of active sites are among the common impediments that need to be addressed to eventually enhance their inherent catalytic potential for enhanced OER activity. Herein, the controlled assembly of transition metal oxides, that is, Cu@CuO_x nanoclusters (NCs, ≈2 nm) and Co@CoO_x beaded nanoclusters (BNCs, ≈2 nm), on thiol-functionalized graphene oxide (G-SH) nanosheets is reported to form novel and highly efficient electrocatalysts for OER. The thiol (-SH) functionality was incorporated by selective epoxidation on the surface of graphene oxide (GO) to achieve chemically exfoliated nanosheets to enhance its conductivity and trapping ability for metal oxides in nanoscale dimensions (≈2 nm). During the electrocatalytic reaction, overpotentials of 290 mV and 310 mV are required to achieve a current density of 10 mA cm⁻² for BNCs and NCs, respectively, and the catalysts exhibit tremendous long-term stability (≈50 h) in purified alkaline medium (1 m KOH) with no dissolution in the electrolyte. Moreover, the smaller Tafel slopes (54 mV/dec for BNCs and 66 mV/dec for NCs), and a Faradic efficiency of approximately 96 % indicate not only the selectivity but also the tailored heterogeneous electrons transfer (HET) rate, which is required for fast electrode kinetics. It is anticipated that such ultrasmall metal oxide nanoclusters and their controlled assembly on a conducting surface (G-SH) may offer high electrochemical accessibility and a plethora of active sites owing to the drastic decrease in dimensions and thus can synergistically ameliorate the challenging OER process.