Sharif Digital Repository

Argon is often considered as an innocent probe that can be attached and detached to study the structure of a particular species without perturbing the species too much. We have investigated whether this assumption also holds for small copper cationic clusters and demonstrated that small but significant charge transfer from argon to metal changes the remaining binding positions, leading in general, to weaker binding of other argon atoms. The exception is binding to just one copper ion, where the binding of the first argon facilitates the binding of the second. © 2020 American Chemical Society  

An efficient, green, novel and rapid vortex-assisted dispersive solid-phase extraction (VADSPE) technique was used for the preconcentration and determination of trace levels of Cu2+ followed by flame atomic absorption spectrometry. Graphene oxide (GO) was synthesized from graphite and then modified by pectic acid (poly-d-galacturonic acid, PA) to synthesize the pectic acid–graphene oxide (PA-GO) nanocomposite. The Fourier transform infrared spectrophotometry, field emission scanning electron microcopy, energy-dispersive X-ray spectroscopy and X-ray diffraction analysis were used to characterize the synthesized GO-PA nanocomposite. By using VADSPE technique, PA-GO was used as an adsorbent for... 

A highly sensitive and selective colorimetric method for detection of copper ions, based on anti-aggregation of D-penicillamine (D-PC) induced aggregated gold nanoparticles (AuNPs) was developed. Copper ions can hinder the aggregation of AuNPs induced by D-PC, through formation of mixed-valence complex with D-PC that is a selective copper chelator. In the presence of a fixed amount of D-PC, the aggregation of AuNPs decreases with increasing concentrations of Cu2+ along with a color change from blue to red in AuNPs solution and an increase in the absorption ratio (A520/A 650). Under the optimum experimental conditions (pH 7, [AuNPs] =3.0 nmol L-1 and [NaCl]=25 mmol L-1), a linear calibration... 

Co/Cu multilayers were deposited in a sulfate solution by controlling the current and potential for the deposition of cobalt and copper layer respectively. The electrochemical behavior of these multilayers was studied by cyclic voltammetry and current transients. In addition, a mathematical analysis was used to characterize the electrodeposition system. Simultaneously, the nucleation and growth mechanisms were monitored by these techniques. In this case, the results clearly showed that electrodeposition of cobalt layers was a kinetically controlled process while the reduction of copper ions was a diffusion-control process. Although nucleation mechanism of the single Co deposit was found as a...