Nano Sized Moringa oleifera an Effective Strategy for Pb(II) ions Removal from Aqueous Solution

Nano-sized  Moringa oleifera is considered an effective   biosorbent  with  high surface area from agricultural waste, low coast and environment-friendly which can be used for removal of  Pb2+ from waste water. Thus our study stem to investigate the ability of natural nano-sized biosorbents for removing  very toxic Pb2+ ions from aqueous solution. The investigated biosorbent (Moringa oleifera) was characterized by FTIR, SEM, TEM, XRD and EDX techniques. Moreover, the influence of pH, temperature, adsorbent dosage, contact time and initial metal ion concentration on adsorption process were investigated. The maximum biosorption capacities (qm) of Pb2+ ions by Moringa oleifera was 37.9 mg/g. The lowest biosorption was observed (61.4%) for Pb2+ ions at pH 2.0 while the highest one (94.36%) at pH 5. The optimum contact time for the adsorption process was found to be at 60 minutes. The amount of Pb2+ ions adsorbed increases with increasing in initial metal ion concentration. Moreover, biosorption capacity (qe) and removal efficiency of Pb2+ ions solutions increase as temperature increases. FT-IR data indicated that the adsorption of metal ions occurs on the surface of Moringa oleifera powder as the main functional groups that are responsible for metal ions binding are involved in the process. Furthermore, Thermodynamic studies confirmed that the biosorption process was endothermic and the positive value of ΔG° is quite common when an ion-exchan­­ge mechanism applies in the biosorption. The Positive value of ΔS◦ suggested an increase in randomness during the biosorption. The kinetics study of sorption indicates that the pseudo second-order model provides better correlation of the sorption data (R2=0.99) than the pseudo first-order model (R2 = 0.91), confirming the chemisorption of metal ions solutions on Moringa oleifera. The Freundlich isotherm has agood fit with the experimental data (R2 close to 1) compared to Langmuir isotherm (R2=0.99). This study shows that Moringa oleifera are available, low cost, effective and environment friendlly biosorbent for the removal of Pb2+ ions from aqueous environment. Keywords: Lead, biosorption, Thermodynamics, kinetics, removal efficiency, Moringa oleifera, isother

Kinetic investigation of hydroxide ion and DNA attack on some high spin iron (II) chelates Bearing ONO Donors amino acid Schiff bases

The reactivity of few novel high spin Fe(II) complexes of Schiff base ligands derived from 2-hydroxynaphthaldehyde and some variety of amino acids with OH- ion has been examined in aqueous mixture at temperature in the range 10–40 Co. Based on the kinetic investigations, the rate law and a plausible mechanism were proposed and discussed. The general rate equation was suggested as follows: rate = kobs [Complex], where kobs.= k1 + k2 [OH-]. Base catalyzed hydrolysis kinetics measurements imply pseudo-first order doubly stage rates due the presence of merand fac-isomers. The observed rate constants kobs are correlated the effect of substituent R in the structure of the ligands. From the effect of temperature on the rate; various thermodynamic parameters have been evaluated. The evaluated rate constants and activation parameters are in a good agreement with the stability constants of the investigated complexes

Enhancement of Exchange Bias and Perpendicular Magnetic Anisotropy in CoO/Co Multilayer Thin Films by Tuning the Alumina Template Nanohole Size

The interest in magnetic nanostructures exhibiting perpendicular magnetic anisotropy and exchange bias (EB) effect has increased in recent years owing to their applications in a new generation of spintronic devices that combine several functionalities. We present a nanofabrication process used to induce a significant out-of-plane component of the magnetic easy axis and EB. In this study, 30 nm thick CoO/Co multilayers were deposited on nanostructured alumina templates with a broad range of pore diameters, 34 nm ≤ Dp ≤ 96 nm, maintaining the hexagonal lattice parameter at 107 nm. Increase of the exchange bias field (HEB) and the coercivity (HC) (12 times and 27 times, respectively) was observed in the nanostructured films compared to the non-patterned film. The marked dependence of HEB and HC with antidot hole diameters pinpoints an in-plane to out-of-plane changeover of the magnetic anisotropy at a nanohole diameter of ∼75 nm. Micromagnetic simulation shows the existence of antiferromagnetic layers that generate an exceptional magnetic configuration around the holes, named as antivortex-state. This configuration induces extra high-energy superdomain walls for edge-to-edge distance >27 nm and high-energy stripe magnetic domains below 27 nm, which could play an important role in the change of the magnetic easy axis towards the perpendicular directionEl interés por las nanoestructuras magnéticas que exhiben anisotropía magnética perpendicular y efecto de sesgo de intercambio (EB) ha aumentado en los últimos años debido a sus aplicaciones en una nueva generación de dispositivos espintrónicos que combinan varias funcionalidades. Presentamos un proceso de nanofabricación utilizado para inducir una componente significativa fuera del plano del eje magnético fácil y del EB. En este estudio, se depositaron multicapas de CoO/Co de 30 nm de espesor sobre plantillas de alúmina nanoestructurada con un amplio rango de diámetros de poro, 34 nm ≤ Dp ≤ 96 nm, manteniendo el parámetro de red hexagonal en 107 nm. Se observó un aumento del campo de polarización de intercambio (HEB) y de la coercitividad (HC) (12 veces y 27 veces, respectivamente) en las películas nanoestructuradas en comparación con la película sin patrón. La marcada dependencia de HEB y HC con los diámetros de los agujeros antidotados señala un cambio de la anisotropía magnética de dentro a fuera del plano a un diámetro de nanoagujero de ∼75 nm. La simulación micromagnética muestra la existencia de capas antiferromagnéticas que generan una configuración magnética excepcional alrededor de los agujeros, denominada estado de antivórtice. Esta configuración induce paredes de superdominio extra de alta energía para la distancia de borde a borde >27 nm y dominios magnéticos de franja de alta energía por debajo de 27 nm, que podrían desempeñar un papel importante en el cambio del eje magnético fácil hacia la dirección perpendicula

Synthesis, characterization and antibacterial activity studies of new 2‑pyrral‑L‑amino acid Schif base palladium (II) complexes.

Three new 2-pyrral amino acid Schif base palladium (II) complexes were synthesized, characterized and their activity against six bacterial species was investigated. The ligands: Potassium 2-pyrrolidine-L-methioninate (L1), Potassium 2-pyrrolidine-L-histidinate (L2) and Potassium 2-pyrrolidine-L-tryptophanate (L3) were synthesized and reacted with dichloro(1,5- cyclooctadiene)palladium(II) to form new palladium (II) complexes C1, C2 and C3, respectively. 1 NMR, FTIR, UV–Vis,elemental analysis and conductivity measurements were used to characterize the products. The antibacterial activities of the compounds were evaluated against Gram-positive Staphylococcus aureus (S. aureus, ATCC 25923), methicillin-resistant Staphylococcus aureus (MRSA, ATCC 33591), Staphylococcus epidermidis (S. epidermidis, ATCC 12228) and Streptococcus pyogenes (S. pyogenes, ATCC 19615) and, gram-negative Pseudomonas aeruginosa (P. aeruginosa, ATCC 27853) and Klebsiella pneumoniae (K. pneumoniae, ATCC 13883) using the agar well difusion assay and microtitre plate serial dilution method. The palladium complexes were active against the selected bacteria with the imidazole ring containing complex C2 and indole heterocyclic ring containing complex C3 showing the highest activity

Kinetic investigation of hydroxide ion and DNA attack on some high spin iron (II) chelates Bearing ONO Donors amino acid Schiff bases

The reactivity of few novel high spin Fe(II) complexes of Schiff base ligands derived from 2-hydroxynaphthaldehyde and some variety of amino acids with OH- ion has been examined in aqueous mixture at temperature in the range 10–40 Co. Based on the kinetic investigations, the rate law and a plausible mechanism were proposed and discussed. The general rate equation was suggested as follows: rate = kobs [Complex], where kobs.= k1 + k2 [OH-]. Base catalyzed hydrolysis kinetics measurements imply pseudo-first-order doubly stage rates due the presence of merandfac-isomers. The observed rate constants kobs are correlated the effect of substituent R in the structure of the ligands.From the effect of temperature on the rate; various thermodynamic parameters have been evaluated. The evaluated rate constants and activation parameters are in a good agreement with the stability constants of the investigated complexes.Keywords: Base catalyzed hydrolysis, Isomer, Reaction mechanism, Thermodynamic parameters

Kinetics, reactivity, initial-transition state analysis and thermodynamic parameters of base-catalyzed hydrolysis of coumalic acid in solvents with different polarities

Base-catalyzed hydrolysis of coumalic acid (COU) in binary aqueous-methanol and aqueous-acetone mixtures has been studied kinetically at a temperature range from 283 to 313 K. Moreover, the change in the activation energy barrier of COU from water to water–methanol and water–acetone mixtures is estimated from the kinetic data. Solvent effects on reactivity trends have been analyzed into initial and transition state components by using transfer chemical potentials of the reactants and kinetic data. The transfer chemical potentials δmμθ for COU− anion are derived from solubility data from its calcium, cerium and lanthanum salts. The decrease in rate constant of the base hydrolysis reaction of COU as the percentage of methanol or acetone increases is dominated by transition state (TS). The base hydrolysis reaction of COU follows a rate law with kobs = k2[OH−] and the reaction mechanism was suggested. The high negative values of entropy of activation support the proposal mechanism, i.e. the investigated reaction takes place via the formation of an intermediate complex. Thus, the ring opening of the intermediate complex would be the rate controlling step

Hydrophobicity and kinetic inspection of hydroxide ion attack on some chromen-2-one laser dyes in binary aqueous–methanol and aqueous–acetone mixtures: Initial state-transition state analysis

AbstractIn the present study, reactivity base-catalyzed hydrolysis of 7-dimethylamino-4-methyl-2H-chromen-2-one (DMAC) and 7-diethylamino-4-methyl-2H-chromen-2-one (DEAC) in binary aqueous–methanol and aqueous–acetone mixtures was examined at 298K. Kinetic results, rate laws and reaction mechanisms were established. Moreover, the change in the activation energy barrier of the investigated compounds from water to water–methanol and water–acetone mixtures was estimated from the kinetic data. Base-catalyzed hydrolysis of (DMAC) and (DEAC) in aqueous–methanol and aqueous–acetone mixtures follows a rate law with kobs=k2[OH]. The decrease in the rate constants of (DMAC) and (DEAC) as the proportion of methanol and acetone is due to the destabilization of OH− ion. The solubilities of the studied compounds, DMAC and DEAC in water–methanol and water–acetone mixtures were established and their transfer chemical potentials were calculated. Solvent effect on reactivity trends of the investigated compounds has been analyzed into initial and transition state components by using the transfer chemical potentials of the reactants and the kinetic data of the studied compounds. The decrease in the observed rate constant values (kobs) of the base hydrolysis of DMAC and DEAC with increasing of methanol% or acetone% is dominated by the initial state (IS)