Photocatalytic ozonation degradation of ciprofloxacin using ZnO nanoparticles immobilized on the surface of stones

Ciprofloxacin is used in the treatment of bacterial infections. Because ciprofloxacin is not effectively degraded by biological processes, advanced oxidation processes such as photocatalytic ozonation are applied to remove this antibiotic from wastewater. The aim of this study was to investigate photocatalytic ozonation for the removal of ciprofloxacin from aquatic environments and optimization of the effective parameters of the process. For this purpose, ZnO nanoparticles were synthesized using the thermal method and immobilized on the surface of stones. The structural properties of the nanoparticles were determined by XRD, TEM, Photoluminescence (PL) and SEM. Experiments were carried out in a Plexiglas reactor supported with the continuous injection of ozone. The effective parameters for removal efficiency were reaction time, initial concentration of ciprofloxacin, pH, photocatalyst concentration and reaction kinetics. The highest ciprofloxacin removal efficiency occurred at the following optimal conditions: pH of 7, reaction time of 30?min, photocatalyst concentration of 3?g/L and initial ciprofloxacin concentration of 10?mg/L. Removal efficiency of 96% was obtained under these conditions. Linear kinetic models showed that the process followed pseudo-first order and Langmuir-Hinshelwood kinetics. This process had a high removal efficiency and suitable for removal of ciprofloxacin from aquatic environments.GRAPHICAL ABSTRACT     

Influence of polymeric coating on capillary electrophoresis of iron oxide nanoparticles

In this work, electrophoresis was successfully used to separate three different polymer-coated magnetic iron oxide nanoparticles with similar sizes (nominally 50 nm) using high-pH borate buffer system. The coating polymers were dextran, polyethylene glycol, or carboxymethyl dextran. The results showed that the migration time of carboxymethyl dextran coated nanoparticles is the longest due to relatively more negative surface charges. Investigation of the effects of buffer concentration, pH, electric field strength and the capillary temperature, on electrophoretic properties of samples was also carried out. The results showed that pH, electric field strength and the capillary temperature had indirect relations with both of the migration time and the separation resolution of three different polymer-coated nanoparticles while the buffer concentration had a direct relation.     

Synthesis of Fe3O4-supported Schiff base Cu (II) complex: a novel efficient and recyclable magnetic nanocatalyst for one-pot three-component synthesis of quinolin-5-one,chromene-3-carbonitrile and phthalazine-5,10-dione derivatives

Research on Chemical Intermediates - In this research, synthesis and characterization of a novel Schiff base Cu (II) complex immobilized on Fe3O4@SiO2 nanoparticles are reported. Then, the...     

Hexamethylenetetramine-based ionic liquid anchored onto the metal–organic framework MIL-101(Cr) as a superior and reusable heterogeneous catalyst for the preparation of hexahydroquinolines

Research on Chemical Intermediates - Regarding the significance of medicinal and pharmacological sciences, we explored one-pot multicomponent reaction of aromatic aldehydes, aryl amines,...     

Finely dispersed palladium on silk‐fibroin as an efficient and ligand‐free catalyst for Heck cross‐coupling reaction

A palladium–fibroin complex (Pd/Fib.) was prepared by the addition of sonicated fibroin fiber in water to palladium acetate solution. Pd (OAc)₂ was absorbed by fibroin and reduced with NaBH₄ at room temperature to the Pd(0) nanoparticles. Powder‐X‐ray diffraction, scanning electron microscopy–energy‐dispersive X‐ray spectroscopy, Fourier transform‐infrared, CHN elemental analysis and inductively coupled plasma‐atomic emission spectroscopy were carried out to characterize the Pd/Fib. catalyst. Catalytic activity of this finely dispersed palladium was examined in the Heck coupling reaction. The catalytic coupling of aryl halides (‐Cl, ‐Br, ‐I) and olefins led to the formation of the corresponding coupled products in moderate to high yields under air atmosphere. A variety of substrates, including electron‐rich and electron‐poor aryl halides, were converted smoothly to the targeted products in simple procedure. Heterogeneous supported Pd catalyst can be recycled and reused several times.     

Chaos and reproduction in sea level

Prediction of sea-level is an important task for navigation, coastal engineering and geodetic applications, as well as recreational activities. This study presents a comparison of Chaos theory and Auto-Regressive Integrated Moving Average (ARIMA) techniques for sea level modelling for daily, weekly, 10-day and monthly time scale at the Cocos (Keeling) islands from 1992 to 2001. The state space reconstruction of the unknown underlying process is directly employed from time series data, through Takens delay embedding method: optimal embedding dimension and delay time are obtained from false nearest neighbours and average mutual information techniques, respectively. Optimal values are then used for the estimation of the correlation dimension and the largest Lyapunov exponent, for inspecting possible signatures of chaotic dynamics. We find a positive Lyapunov exponent an evident feature of chaos. Indeed, the nonlinear prediction of sea level, in the period ranging from January 2001 to December 2001, is in an excellent agreement with the data for the same period, evidencing the nonlinear nature of the process. ARIMA method is also used for sea level modelling, for the same time scales; the performances of the two models are compared using such statistical indices as the root mean square error (RMSE) and correlation coefficient (CC). The comparative analyses show that the chaos theory model has a slight edge over ARIMA while both models are in principal acceptable.     

Spectroscopic studies on Solvatochromism of mixed-chelate copper(II) complexes using MLR technique

Mixed-chelate copper(II) complexes with a general formula [Cu(acac)(diamine)]X where acac=acetylacetonate ion, diamine=N,N-dimethyl,N'-benzyl-1,2-diaminoethane and X=BPh(4)(-), PF(6)(-), ClO(4)(-) and BF(4)(-) have been prepared. The complexes were characterized on the basis of elemental analysis, molar conductance, UV-vis and IR spectroscopies. The complexes are solvatochromic and their solvatochromism were investigated by visible spectroscopy. All complexes demonstrated the positive solvatochromism and among the complexes [Cu(acac)(diamine)]BPh(4)·H(2)O showed the highest Δν(max) value. To explore the mechanism of interaction between solvent molecules and the complexes, different solvent parameters such as DN, AN, α and β using multiple linear regression (MLR) method were employed. The statistical results suggested that the DN parameter of the solvent plays a dominate contribution to the shift of the d-d absorption band of the complexes.     

Crossed Andreev reflection in graphene normal-superconductor-normal structures with pseudo-diffusive interfaces

In this Letter graphene normal-superconductor-normal heterostructures are modeled for studying the crossed Andreev reflection. A thin layer of undoped graphene with Fermi energy at the Dirac point at is assumed the interface between superconductor layer and each normal lead. The resulting contribution of the crossed Andreev reflection to the nonlocal conductance equals that of the electron elastic cotunneling. We explain this as another figure of merit for pseudodiffusive conduction at the Dirac point of the undoped layers. Also structures with only one undoped layer at the interface between the superconductor and one of the normal leads, as well as structures in which one of the leads is ferromagnetic, show pseudodiffusive conduction at the Dirac points.     

The role of the Rashba coupling in spin-current of monolayer gapped graphene

In the current work, based on a semiclassical Boltzmann approach, we have investigatedthe influence of the Rashba spin-orbit coupling on spin-current of a single layer gappedgraphene. It was shown that the Rashba coupling plays a considerable role in thegeneration of the spin-current of vertical spins in mono-layer graphene. The behavior ofthe spin-current is determined by the density of impurities. It was also shown that thespin-current of the system could increase by increasing the Rashba coupling strength andband-gap of the graphene and the sign of the spin-current could be controlled by thedirection of the current-driving electric field.