Determination of mercury(II) ions in seafood samples after extraction and preconcentration by a novel functionalized magnetic metal–organic framework nanocomposite

This work describes a novel functionalized magnetic metal–organic framework nanocomposite [(Fe₃O₄‐2,5‐dimercapto‐1,3,4‐thiadiazole)/metal–organic framework] and its application in the preconcentration of Hg(II) ions. The parameters affecting the preconcentration procedure were optimized by a Box–Behnken design through response surface methodology. Three variables (uptake time, magnetic nanosorbent amount, and pH value) were selected as the main factors affecting the sorption step, while four variables (type, volume, and concentration of the eluent; and elution time) were selected as main factors in the optimization study of the elution step. Following the sorption and elution of analytes, the ions were quantified by cold vapor atomic absorption spectrometry. Under the optimum conditions, the limit of detection was 0.01 ng/mL and all the relative standard deviations were less than 10%. The obtained sorption capacity (in mg/g) of this new sorbent was 124. Ultimately, this nanocomposite was successfully applied to the rapid extraction of trace quantities of Hg(II) ions in seafood samples and satisfactory results were obtained.     

Electrocatalytic Oxidation and Determination of Cysteamine by Poly‐N,N‐dimethylaniline/Ferrocyanide Film Modified Carbon Paste Electrode

Functionalized poly‐N,N‐dimethylaniline film was prepared by adsorption of ferrocyanide onto the polymer forming at the surface of carbon paste electrode (CPE) in aqueous solution by using potentiostatic method. The electrocatalytic ability of poly‐N,N‐dimethylaniline/ferrocyanide film modified carbon paste electrode (PDMA/FMCPE) was demonstrated by oxidation of cysteamine. Cyclic voltammetry and chronoamperometry techniques were used to investigate this ability. Results showed that pH 7.00 is the most suitable for this purpose. It is found that the catalytic reaction rate constant, (k_h), is equal to 2.142×10³ M^?1 s^?1 by the data of chronoamperometry. The catalytic reduction peak current was linearly dependent on the cysteamine concentration and the linearity range obtained was 8.00×10^?5 M–1.14×10^?2 M. Detection limit was determined 7.97×10^?5 M (2σ). This method has been successfully employed for quantification of cysteamine in real sample.     

Quality management in research: management process of the laboratories of Moroccan faculties of sciences and techniques

Accreditation and Quality Assurance - The implementation of a quality management system including management tools in the industrial sector has several advantages. In this perspective, can we use...     

Prediction and experimental determination of the binary and ternary phase diagrams of (±)medetomidine hydrochloride

The binary phase diagram of medetomidine hydrochloride was determined based on thermogravimetric differential thermal (TGA/DTA) measurements. The binary phase diagram presented a eutectic point in the 19:81 [(R)/(S)] composition and the ternary phase diagram in the presence of 2-propanol showed a eutectic point in the 75:25 [(S)/(R)] composition, both characterizing the product as a racemic compound forming system. The solubility of enantiomeric mixtures in 2-propanol was measured at 10, 20 and 30 °C. The ideal solubility curves of the mixtures were calculated and the activity coefficients derived. A semi-empirical thermodynamic model UNIversal QUAsi-Chemical (UNIQUAC) was used to predict the solubility of various compositions of enantiomers at different temperatures. There was good agreement between the experimental solubility data of medetomidine hydrochloride and the results obtained from the UNIQUAC equation.     

A one-pot three-component reactions for the synthesis of fully substituted spiro indeno[1,2-b]quinoxaline derivatives

An efficient and simple approach of the synthesis of some spiro indeno[1,2-b]quinoxalines via a one-pot three-component reaction of 11H-indeno[1,2-b]quinoxalin-11-one, pyrazolone, and malononitrile in the presence of Na₂CO₃ at 70 °C is reported. This reaction has shown to have high atom economy.     

Synthesis of New Multibenzo Oxygen–Sulfur Donor Macrocycles Containing Lactams at Room Temperature

Some new oxygen–sulfur, multibenzo macrocyclic ligands containing amide groups have been prepared using the macrocyclization process with the reaction of 2,2′-thiobis-[4-methyl(2-aminophenoxy)phenyl ether] as a symmetrical diamine with appropriate dicarboxylicacid dichlorides in moderate yields. This macrocyclization led to the formation of di- and tetramide macrocycles. These reactions were routinely carried out at ambient temperature in CH₂Cl₂ as solvent in high dilution without template effect conditions. It is found that sulfur the atom affects the rigidity of the macrocycles and diastereotopicity of nuclei in the ring of these series of macrocyclic compounds.     

Tetrakis [<Emphasis Type="Italic">N</Emphasis>-(2-pyridyl) sulfonamide] di palladium: synthesize,X-ray diffraction,antibacterial properties and as a novel binuclear Pd-complex for coupling reactions

The N-(2-pyridyl) 4-toluene sulfonamide as a free ligand (PTS) was prepared from the reaction of 2-amino pyridine and 4-toluenesulfonyl chloride in the presence of potassium hydroxide solution 1 M as a base and THF was used as a solvent. The complex tetrakis [N-(2-pyridyl) sulfonamide] di palladium (1) (Pd₂L₄) was also prepared from the reaction of PdCl₂(CH₃CN)₂ using (PTS) in the presence of NaOH 0.5 M and its application in Heck and Suzuki reactions. This complex consists of a binuclear unit consisting of four ligands linked to two palladium atoms via the nitrogen of pyridines ring and the nitrogen of sulfonamides. These compounds were confirmed by FT-IR and ¹H NMR spectroscopy. Moreover, the structure of the complex was studied by single-crystal X-ray diffraction method. The green crystal of Pd₂L₄ [L = N-(2-pyridyl) sulfonamide](1) was found to crystallize in the monoclinic space group C2/c with a = 18.2013(19), b = 19.7544(16), c = 17.2898(19) Å, β = 120.179(8) °; V = 5374.0(9) ų; Z = 4; the final R ₁ = 0.0894, wR ₂ = 0.1754 (or 5867 observed reflections and 318 variables). The Pd–Pd distance is 2.567(2) Å. In addition, PTS and Pd₂L₄ presented different antibacterial behaviors. The free ligand was active against Staphylococcus aureus and Escherichia coli, but the complex was inactive against them.     

Effect of CH3NH3I/CH3NH3Br precursors on the structural and surface morphology properties of the electrodeposited methylammonium lead–mixed halide perovskite films

Journal of Solid State Electrochemistry - Organometallic halide perovskites have been arisen as a class of multi-purpose materials with exciting applications in optoelectronic devices such as solar...     

Surfactant Assisted Electrochemical Determination of Noscapine and Papaverine by TiO2 Nanoparticles/Multi-Walled Carbon Nanotubes Modified Carbon Paste Electrode

Russian Journal of Electrochemistry - In the present study, simultaneous voltammetric determination of noscapine and papaverine as two important alkaloids in opium was studied for the first time. A...