Search results for "solution"

Spatially limited diffusion coupled with ohmic potential drop and/or slow interfacial exchange: a new method to determine the diffusion time constant…

2004

Abstract We have analyzed chronoamperometric curves, I ( t ), after small-amplitude potential steps Δ E (PITT technique) for the model of linear diffusion of a species inside an electroactive film, taking into account ohmic effects in the external media (solution and electrode) as well as a finite rate of the interfacial exchange. For its short-time interval, t ≪ τ d ( τ d is the diffusion time constant, corresponding to unlimited diffusion from the interface), three approximate analytical expressions have been proposed. One of these represents an interpolation formula between the value of the current at the start of the diffusion process, I (0)=Δ E / R ext (after the end of the EDL chargin…

The anodic and cathodic dissolution of Al and Al–Cu–Mg alloy

2010

Abstract Atomic emission spectroelectrochemistry (AESEC) was used to monitor the release of Al from 99.99% aluminum (1199 alloy) and Al, Mg, and Cu from 2024 Al alloy in 30 g/l NaCl electrolyte as a function of pH. The cathodic dissolution of Al was demonstrated and attributed to an increase in the pH at the interface due to the water reduction reaction. The dissolution of Mg was also observed but was a more complex function of current probably depending on the interfacial pH and the Al dissolution rate. The detachment of copper-rich particles was observed as very rapid spectroscopic emission transients (peak width

A kinetic interpretation of a negative time constant in impedance equivalent circuits for the dissolution/passive transition

2007

Abstract A theoretical impedance function is proposed for the active/passive transition of nickel in an acid sulphate medium. It is considered that passivating species progressively covers the electrode surface. This approximated model predicts the appearance of negative time constants in the impedance spectra when coverage coefficient θ values for passive species are greater than 0.5.

Voltammetry of microparticles, scanning electrochemical microscopy and scanning tunneling microscopy applied to the study of dsDNA binding and damage…

2014

Abstract Microparticulate deposits of scorpiand-like azamacrocyclic receptors (L1–L4) attached to graphite electrodes provide distinctive voltammetric features in contact with aqueous DNA solutions at biological pH, denoting the formation of DNA surface complexes. This voltammetry allows for screening dsDNA, ssDNA and G-Quadruplex DNA using L4-modified electrodes. Scanning electrochemical microscopy and scanning tunneling microscopy examination of dsDNA fibers attached to the substrate electrode in contact with DMSO solutions containing ferrocene and receptor indicate that a synergic effect is exerted between electrochemically generated ferrocenium ion and the receptors so that they increas…

A POWERFUL TOOL TO STUDY COLLISIONAL PHENOMENA AND FOR COMBUSTION APPLICATIONS : THE HIGH RESOLUTION STIMULATED RAMAN SPECTROSCOPY

1987

Transportation of complexing agents released by pulp and paper industry: A Finnish lake case

1996

Complexing agents (EDTA, DTPA) are used to bind metal ions in pulp and paper industry. Their role will increase significantly when the total chlorine free (TCF) processes will be applied to a larger extent. EDTA and DTPA were analysed in the waters from the southern part of the Lake Saimaa (SE Finland) influenced by the effluents of three pulp and paper mills. The samples were collected at different distances from the points of emission. The results of analyses suggest that EDTA can persist in lake water and is able to propagate for considerable distances, while DTPA can be detected only in the near surroundings of the site of release. Some EDTA was found even in the sampling points that we…

Determination of mineral and trace element concentrations in pine needles by ICP-OES: evaluation of different sample pre-treatment methods

2008

In the present study, the determination of mineral and trace elements (Al, B, Ca, Cu, Fe, K, Mg, Mn, Na, P and Zn) from pine needles using three sample pre-treatment methods followed by inductively coupled plasma optical emission spectrometry, was examined. Sample pre-treatment methods tested were microwave digestion, ultrasound-assisted digestion and dry ashing. The new ultrasound-assisted digestion method was optimised by the analysis of the standard reference material (SRM) 1575a (pine needles) sample. The speed of dry ashing method was significantly increased by ultrasound dissolution after ashing. All the ICP-OES measurements were performed in robust plasma conditions which were tested…

The infrared spectrum of CH 3 D between 900 and 3200 cm −1 : extended assignment and modeling

2000

Abstract The high resolution infrared spectrum of CH 3 D in the region from 900 to 3200 cm −1 has been analyzed on the basis of Fourier transform spectra recorded at Kitt Peak and at Giessen. A theoretical model for an effective hamiltonian in terms of irreducible tensor operators recently adapted to symmetric top molecules has been used in order to consider simultaneously all available transitions between the lowest three polyads of the molecule: the Ground State (G.S.), the Triad (three interacting fundamental bands in the 8 μm region) and the Nonad (nine interacting bands in the 4 μm region). A preliminary simultaneous fit of 3467 Triad–G.S., 5208 Nonad–G.S., and 2487 Nonad–Triad (hot ba…

Ionic conductivity in monophasic Ag2xNa2(1 − x)ZnSiO4 materials with 0 ≤ x ≤ 1

1996

Abstract Solid solution samples Ag 2 x Na 2(1 − x ) ZnSiO 4 with 0 ≤ x ≤ 1 have been prepared by heat treating powder mixtures of Na 2 ZnSiO 4 and Ag 2 ZnSiO 4 at 300 °C and characterised by X-ray powder diffraction. The ionic conductivity of the solid solution has been determined as a function of composition and temperature by means of impedance measurements. The ionic conductivity of the mixed-mobile ion compositions (0 ≤ x ≤ 1) shows no substantial deviation from the mutually similar conductivities of the end compositions Na 2 ZnSiO 4 and Ag 2 ZnSiO 4 , and neither activation energy nor conductivity pre-factor varies significantly with composition. The results indicate that the mixed-alk…

Structural Evolution and Vanadium Distribution in the Preparation of V4+-ZrSiO4 Solid Solutions from Gels

2004

Vanadium-containing ZrSiO4-gel precursors with nominal compositions Vx-ZrSiO4 with x= 0.0, 0.002, 0.004, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.1, and 0.2 were prepared using a previously reported procedure and thermally treated over a range of temperature up to the formation of the V4+-ZrSiO4 solid solution. The structural evolution and the V4+ location and its homogenous distribution were followed using powder X-ray diffractometry and electron spin resonance spectroscopy (ESR). Our experiments showed that a tetragonal form of V4+-ZrO2 was the first crystalline phase obtained on heating the gels. On further heating, a phase transformation to the monoclinic form of V4+-ZrO2 took place. Final…