Glassy-carbon electrodes (GCEs) are modified with preoxidized multiwalled carbon nanotubes (CNTs). According to the data of atomic force microscopy, the layers of CNTs on GCEs possess a homogeneous ...nanostructurized surface. The voltammetric properties of a GCE/CNT depend on the modifier load. Guanine and deoxyguanosine monophosphate are strongly adsorbed on GCE/CNT and oxidized at +690 and +930 mV (pH 7.0), respectively. The oxidation current of guanine DNA nucleotides adsorbed on a GCE/CNT is significantly higher for the thermally denaturated biopolymer than for the native one. Our results are of interest for the development of sensors based on the electrochemical properties of nucleic acids.
Solving a Deconvolution Problem in Photon Spectrometry Aleksandrov, D.; Alme, J.; Basmanov, V. ...
Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment,
2010, Letnik:
620, Številka:
2
Journal Article
Recenzirano
We solve numerically a deconvolution problem to extract the undisturbed spectrum from the measured distribution contaminated by the finite resolution of the measuring device. A problem of this kind ...emerges when one wants to infer the momentum distribution of the neutral pions by detecting the
π
0
decay photons using the photon spectrometer of the ALICE LHC experiment at CERN
1. The underlying integral equation connecting the sought for pion spectrum and the measured gamma spectrum has been discretized and subsequently reduced to a system of linear algebraic equations. The latter system, however, is known to be ill-posed and must be regularized to obtain a stable solution. This task has been accomplished here by means of the Tikhonov regularization scheme combined with the L-curve method. The resulting pion spectrum is in an excellent quantitative agreement with the pion spectrum obtained from a Monte Carlo simulation.
The catalytic effect of Se(IV) was first observed in the reaction of the reduction of Nile Blue with sulfide ions. Optimal conditions for the determination of selenium by this reaction were found. ...The dependence of the reaction rate on the concentration of Se(IV) was linear in the concentration range 0.008-0.16 μg/mL. Solvent extraction with dithiophosphoric acids was proposed for the separation of selenium from the interferents. A procedure for the extraction-kinetic determination of selenium with the detection limit 0.006 μg/mL was developed.
