Spectrophotometric determination of Mercury(II) ions in laboratory and Zamzam water using bis Schiff base ligand based on 1,2,4-Triazole-3,5-diamine and o-Vaniline

The current study presents the development of a simple and direct spectrophotometric approach for Hg(II) ions determination. This method has the significant advantage of being a simple procedure where no further solvent purification or pre-concentration is needed. The concentration of Hg(II) ions was determined in the presence of the Schiff base ligand named 2-((5-(2-hydroxy-3-methoxybenzylideneamino)–2H-1,2,4-triazole-3-ylimino)methyl)-6-methoxyphenol (HMBT), at pH 10 using Briton Robinson Buffer. The method Obey Beer's law in concentration range 0.1–6 µg mL^{- 1} of Hg with (LOD) 0 0.016 µg L ^-1 and (LOQ) 0.051 µg/L. The molar ratio ensured the formation of a metal complex between HMBT and Hg ions was in the molar ratio 2:1 (HMBT: Hg²⁺). The method was used for the determination of mercury ions in tap water and Zamzam water samples. The applied method has many advantages, such as simplicity, low cost, ease of operation, rapid detection, low-ligand consumption, and high sensitivity. The analytical method sensitivity was confirmed via the suitable selection of experimental circumstances. More information about the structure and stoichiometry of the complex formed in solution between Hg(II) and HMBT ligand has been gained through the isolation and investigation of solid complex (HMBT-Hg). The structure of the solid complex, HMBT-Hg, has been elucidated by applying analytical routes such as elemental analysis and the spectral mass, UV–vis spectra, and thermal analysis.     

Atropine-selective membrane electrodes and relative selectivity concept

TFPB was introduced as a charged ionophore for atropine selective electrodes. Typical Nernstian responses were found (57.78, 58.95 and 58.41 mV/decade) for PVC-membrane electrodes incorporating NPOE, DOS, and DDP as plasticizers. They exhibited practical linear ranges of 9.1 x 10(-3) - 10(-6), 9.1 x 10(-3) - 10(-6) and 9.1 x 10(-3) - 10(-7) M, respectively. It works in the sub-micro scale of atropine concentrations. The optimum pH-range was 3.18 - 8.97. The selectivity coefficient values were estimated for different organic and inorganic cations. They were interpreted by using the "Relative Selectivity Concept", which was introduced for the first time. The new concept was applied for comparing the selectivity properties of previously reported electrodes. The effect of the presence of ephedrine, caffeine, glucose, Na(+), Ca(2+), and Mg(2+) on the calibration graphs of the electrodes was studied.     

Lamellar molybdenum oxide as a molecular sieve towards nitrogen containing molecules: intercalation compounds with pyridazine, acrylamid and tris(hydroxymethyl)aminomethane

The synthesis and characterization (by CHN elemental analysis, FTIR spectroscopy, XRD diffractometry, thermogravimetry and SEM microscopy) of MoO₃ intercalation compounds with pyridazine (pdz), acrylamid (ald) and tris(hydroxymethyl)aminomethane (tham) is reported. Such investigation was performed taking into account the possible uses of molybdenum trioxide as a molecular sieve towards nitrogen containing compounds. It is verified that the affinity of MoO₃ towards the investigated species follows the sequence: ald ? tham > pdz.     

Spectrophotometric determination of some histamine H1-antagonists drugs in their pharmaceutical preparations

Two rapid, simple and sensitive extractive specrophotometric methods has been developed for the determination of three histamine H1-antagonists drugs, e.g., chlorphenoxamine hydrochloride (CPX), diphenhydramine hydrochloride (DPH) and clemastine (CMT) in bulk and in their pharmaceutical formulations. The first method depend upon the reaction of molybdenum(V) thiocyanate ions (Method A) with the cited drugs to form stable ion-pair complexes which extractable with methylene chloride, the orange red color complex was determined colorimetrically at lambda(max) 470nm. The second method is based on the formation of an ion-association complex with alizarin red S as chromogenic reagents in acidic medium (Method B), which is extracted into chloroform. The complexes have a maximum absorbance at 425 and 426nm for (DPH or CMT) and CPX, respectively. Regression analysis of Beer-Lambert plots showed a good correlation in the concentration ranges of 5.0-40 and 5-70microgmL(-1) for molybdenum(V) thiocyanate (Method A) and alizarin red S (Method B), respectively. For more accurate analysis, Ringbom optimum concentration ranges were calculated. The molar absorptivity, Sandell sensitivity, detection and quantification limits were calculated. Applications of the procedure to the analysis of various pharmaceutical preparations gave reproducible and accurate results. Further, the validity of the procedure was confirmed by applying the standard addition technique and the results obtained in good agreement well with those obtained by the official method.     

Synthesis, spectroscopic and thermal characterization of some transition metal complexes of folic acid

Compounds having general formula: [M(FO)(Cl)(x)(H(2)O)(y)].zH(2)O, where (M=Mn(II), Fe(III), Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Hg(II), FO=folate anion, x=2 or 4, y=2 or 4 and z=0, 1, 2, 3, 5 or 15) were prepared. The obtained compounds were characterized by elemental analysis, infrared as well as electronic spectra, thermogravimetric analysis and the conductivity measurements. The results suggested that all folate complexes were formed by 2:1 molar ratio (metal:folic acid) as a bidentate through both of the two carboxylic groups. The molar conductance measurements proved that the folate complexes are electrolytes. The kinetic thermodynamic parameters such as: E*, DeltaH*, DeltaS* and DeltaG* were estimated from the DTG curves. The antibacterial evaluation of the folic acid and their complexes was also done against some Gram positive/negative bacteria as well as fungi.     

Effects of variable properties on MHD heat and mass transfer flow near a stagnation point towards a stretching sheet in a porous medium with thermal radiation

The effect of variable viscosity and thermal conductivity on steady magnetohydrodynamic(MHD) heat and mass transfer flow of viscous and incompressible fluid near a stagnation point towards a permeable stretching sheet embedded in a porous medium are presented,taking into account thermal radiation and internal heat genberation/absorbtion.The stretching velocity and the ambient fluid velocity are assumed to vary linearly with the distance from the stagnation point.The Rosseland approximation is used to describe the radiative heat flux in the energy equation.The governing fundamental equations are first transformed into a system of ordinary differential equations using a scaling group of transformations and are solved numerically by using the fourth-order Rung-Kutta method with the shooting technique.A comparison with previously published work has been carried out and the results are found to be in good agreement.The results are analyzed for the effect of different physical parameters,such as the variable viscosity and thermal conductivity,the ratio of free stream velocity to stretching velocity,the magnetic field,the porosity,the radiation and suction/injection on the flow,and the heat and mass transfer characteristics.The results indicate that the inclusion of variable viscosity and thermal conductivity into the fluids of light and medium molecular weight is able to change the boundary-layer behavior for all values of the velocity ratio parameter λ except for λ = 1.In addition,the imposition of fluid suction increases both the rate of heat and mass transfer,whereas fluid injection shows the opposite effect.     

Exact solutions for nonlinear partial fractional differential equations

In this article,we use the fractional complex transformation to convert nonlinear partial fractional differential equations to nonlinear ordinary differential equations.We use the improved(G’/G)-expansion function method to calculate the exact solutions to the time-and space-fractional derivative foam drainage equation and the time-and space-fractional derivative nonlinear KdV equation.This method is efficient and powerful for solving wide classes of nonlinear evolution fractional order equations.     

N-halamines from rice straw

The cellulosic part of rice straw was modified to develop N-halamine derivatives for disinfection. The process involved cross-linking of the cellulosic material with amino/amide/imide containing compounds; cyclic and acyclic. The structures of the prepared materials were identified using FTIR and solid state ¹³CNMR. The modified materials were halogenated to form N-halamines and the antimicrobial activity of each evaluated against examples of Gram-positive (Staphylococcus aureus) and Gram-negative bacteria (Escherichia coli) using a variety of methods; agar plate, blended agar, stirred flask and in columns. One of the N-halamines achieved a 9 log reduction against both E. coli and S. aureus in 4 h. In addition, no S. aureus growth was recorded on agar plates blended with 0.5 g of this same material.     

Mild and strong solutions to few types of fractional order nonlinear equations with periodic boundary conditions

In this paper, the two fractional periodic boundary value problems $$_0^C D_{0 + }^\alpha u\left( t \right) - \lambda u\left( t \right) = f\left( {t,u\left( t \right)} \right), u\left( 0 \right) = u\left( 1 \right), 0 < \alpha < 1,$$ and $$_0^C D_{0 + }^\beta u\left( t \right) - \lambda u\left( t \right) = f\left( {t,u\left( t \right)} \right), u\left( 0 \right) = u\left( 1 \right),u'\left( 0 \right) = 0 1 < \beta < 2,$$ will be studied where ₀ ^C D _t ^α is the ordinary Caputo fractional derivative and λ ∈ ? ?{0}. Under some suitable assumptions on the function f, the existence of at least one mild solution will be proved. Under some conditions, the uniqueness of this mild solution will be proved to both problems. Finally, these mild solutions will be strong solutions under certain conditions.