Determination of acidic sites and binding toxic metal ions on cumin surface using nonideal competitive adsorption model

A fundamental study of the application of cumin biomass in the recovery of Cu and Zn metal ion uptake from food and drinks is carried out at different pH's and at fixed ionic strength. The chemical characteristics of protein in cumin seeds were investigated. Results showed that cumin contains 18.25% crude protein, which includes 18 amino acids. The main reactive groups on protein cumin are amino and carboxylic groups of dicarboxylic amino acids, leading to a pH-dependent charge. Therefore, the cumin surface is considered as a heterogeneous system. To describe protonation behavior in a heterogeneous cumin biomass (cumin/0.1 M NaNO(3)) system, acid-base titrations have been performed with conductometric and potentiometric titration. Measurement of the reactivity of cumin surface in the adsorption of Cu and Zn metal ions and determination of metal binding at different pH's were also carried out. To solve broad and ill-defined titration curves, a simplified version of nonideal competitive analysis (NICA) by Plette et al.) was applied. The results show that the sorption of the bivalent metal ions onto the whole surface of cumin could be attributed to a monodentate binding to one site mainly carboxylic-type site.     

Simultaneous effects of magnetic field and space porosity on compressible Maxwell fluid transport induced by a surface acoustic wave in a microchannel

Peristaltic motion induced by a surface acoustic wave of a viscous, compressible and electrically conducting Maxwell fluid in a confined parallel-plane microchannel through a porous medium is investigated in the presence of a constant magnetic field. The slip velocity is considered and the problem is discussed only for the free pumping case. A perturbation technique is employed to analyze the problem in terms of a small amplitude ratio. The phenomenon of a “backward flow” is found to exist in the center and at the boundaries of the channel. In the second order approximation, the net axial velocity is calculated for various values of the fluid parameters. Finally, the effects of the parameters of interest on the mean axial velocity, the reversal flow, and the perturbation function are discussed and shown graphically. We find that in the non-Newtonian regime, there is a possibility of a fluid flow in the direction opposite to the propagation of the traveling wave. This work is the most general model of peristalsis created to date with wide-ranging applications in biological, geophysical and industrial fluid dynamics.     

Erratum to “Simultaneous effects of magnetic field and space porosity on compressible Maxwell fluid transport induced by a surface acoustic wave in a microchannel”

We would like to acknowledge the misprinted terms in our published paper “Simultaneous effects of magnetic field and space porosity on compressible Maxwell fluid transport induced by a surface acoustic wave in a microchannel” [Chin. Phys. B 22 124702 (2013)]. Since only two misprints exist and the main results of the published paper are correct, we present the correct equations in this erratum.     

A study of the weathering of an historic building

Various bulk and surface analytical techniques were used to study the chemical deterioration of the 13th-to-15th century limestone cathedral in Mechelen, Belgium. The weathering crust on the walls was found to be rich in sulfate, regardless of the geographic orientation. Nitrate and chloride were only detected in minor amounts in the crust and run-off samples. Attack by gaseous sulfur compounds seems to play a dominant role in the stone deterioration mechanism. Electron microprobe analysis showed predominantly bar-shaped gypsum crystals in the crust, and laser microprobe mass spectrometry showed that carbon seems to be responsible for the blackness of most crust samples. Automated electron microprobe analysis also indicated significant differences in the analytical composition of suspensions in run-off water and in rain-water.     

Characterization of TiO2 Microparticle-Blended Polymer-Based Hybrid Wood Particulate Composites

Mechanics of Composite Materials - The effects of TiO2 microparticle blending on the mechanical and thermal properties and the water absorption behavior of hybrid Pinus/Shorea robusta wood...     

DPASV Method for Determination of Trace Concentrations of Manganese in Non-Buffered Chloride Solutions by Addition of Cyanide as a Masking Agent

 A highly sensitive, selective, and rapid differential pulse anodic stripping voltammetric method at HMDE is described for the determination of trace concentrations of Mn²⁺. The determination of Mn²⁺ in non-buffered chloride solution is seriously disturbed by the presence of Ni²⁺, Co²⁺, Cr³⁺, Zn²⁺ and Cu²⁺ due to intermetallic compound formation. The procedure is based on the addition of low amounts of cyanide as a masking agent. The interference of < 20 μgL⁻¹ of Ni²⁺, Co²⁺ and Cr³⁺ and < 75 μgL⁻¹ of Cu²⁺ and Zn²⁺ can thus be avoided, as the formed cyanide complexes prevent intermetallic compound formation during the short accumulation period. Thus, the addition of cyanide greatly improves the DPASV determination of manganese in non-buffered medium. A comparison between the determination of Mn²⁺ in the presence of a mixed cyanide/non-buffered chloride and in the ammoniacal buffer solution shows that the peak current of manganese in the presence of cyanide is four times higher with the same peak potential. The proposed method is shown to be applicable for the Mn²⁺ determination in both ground and tap water. A good agreement is obtained between the results by DPASV and AAS. Received May 14, 1999. Revision May 25, 2000.     

Analysis of rain water by differential-pulse stripping voltammetry in nitric acid medium

Differential-pulse anodic stripping voltammetry is applied to determine cadmium, lead and copper in rain water acidified with nitric acid to pH 1.5, and zinc after partial neutralization to pH 4.5. Subsequently, cobalt and nickel are measured in the adsorptive mode after formation of their dimethylglyoximates. The effects of pH on the stripping peaks for Zn, Cd, Pb and Cu and of chloride on the stripping peak of copper are reported. Good agreement is found with d.p.s.v. determinations in hydrochloric acid medium and with a.a.s. measurements in most cases. Excellent accuracy is demonstrated; the average relative standard deviation per measurement appears to be between 12 and 22% for the overall analytical procedure for concentrations of 0.15–50 μgl^?1 of the various metals in the samples.     

Kinetic,solvation and reactivity studies of iron(II) complexes of monoxime and dioxime ligands

Complexes of Fe^II with monoxime and dioxime ligands have been isolated and characterised. Kinetic results and rate laws are reported for acid aquation and base hydrolysis of these complexes in H₂O and in MeOH–H₂O mixtures. Kinetics of acid catalysed aquation of Fe^II–monoxime complexes follow a rate law with k_obs = k₂[H⁺] + k₃[H⁺]², while kinetics of acid dissociation and base hydrolysis of the Fe^II–dioxime complex follow rate laws with k_obs = k₂[H⁺] and k_obs = k₂[OH⁻]. Acid aquation and base hydrolysis mechanisms are proposed. The solubilities of Fe^II–monoxime and –dioxime complex salts are reported and transfer chemical potentials of their complex cations are calculated. Solvent effects on reactivity trends have been analysed into initial and transition state components. These are determined from transfer chemical potentials of reactant and kinetic data. Rate constant trends from these complexes are compared and discussed in terms of ligand structure and solvation properties. Our kinetic results give information relevant to the application of these ligands as analytical reagents for trace Fe^II in acidic and neutral media, in water and in aqueous alcohols.     

Determination of trace metals in rain water by differential-pulse stripping voltammetry

Differential-pulse stripping voltammetry is applied to measure zinc, cadmium, lead and copper by anodic stripping and selenium(IV) by cathodic stripping in rain water at pH 2; subsequently, at pH 9,1, manganese is measured by anodic stripping on the same portion, and cobalt and nickel are measured in the adsorptive mode after formation of their dimethylglyoximates. The instrumental parameters are optimized. The linear ranges, mutual interferences and detection limits are studied. Excellent accuracy is demonstrated; the standard deviation is around 15% at 2.5–50 μg l^?1 levels. The method is shown to be applicable for rain water.     

Determination of trace metals in Nile River and ground water by differential pulse stripping voltammetry

The determination of trace metals in river water and ground water by DPSV is seriously disturbed by the presence of organic complexes. The influence of these substances can be eliminated by acidification of the samples with acids. Cd, Pb and Cu were determined at pH 1.1 (HNO₃ medium) and Zn, Cd, Pb and Cu at pH 2 (HCl medium), in both the Nile river and ground water. Zn was determined at pH 3.5 in HCl and pH 4.5 in HNO₃, after neutralizing the samples with NH₃/NH₄Cl buffer. Manganese could then be determined, after further addition of ammoniacal buffer solution up to pH 7.5 and 8.5. Ni and Co were determined in the adsorptive mode after formation of dimethylglyoximates at pH 9.2. The effect of pH on the stripping peaks of manganese was studied. Good agreement was observed between DPSV and AAS results for Zn, Cd, Pb, Cu and Mn, but the concentrations of Ni and Co were below the detection limits for AAS. Good agreement was obtained between DPSV results in HCl and HNO₃ for Ni and Co. The results indicate that decomposition of organic complexes by acidification with HNO₃ is better than in the case with HCl for Zn, Pb, Cu, Ni and Co, but HCl is better than HNO₃ for Cd and Mn.