NADH Electrooxidation Using Bis(1,10-phenanthroline-5,6-dione) (2,2'-bipyridine)ruthenium(II)-Exchanged Zirconium Phosphate Modified Carbon Paste Electrodes

We present a carbon paste electrode (CPE) modified using the electron mediator bis(1,10‐phenanthroline‐5,6‐dione)(2,2′‐bipyridine)ruthenium(II) ([Ru(phend)₂bpy]²⁺) exchanged into the inorganic layered material zirconium phosphate (ZrP). X‐Ray powder diffraction showed that the interlayer distance of ZrP increases upon [Ru(phend)₂bpy]²⁺ intercalation from 10.3 Å to 14.2 Å. The UV‐vis and IR spectroscopies results showed the characteristic peaks expected for [Ru(phend)₂bpy]²⁺. The UV‐vis spectrophotometric results indicate that the [Ru(phend)₂bpy]²⁺ concentration inside the ZrP layers increased as a function of the loading level. The exchanged [Ru(phend)₂bpy]²⁺ exhibited luminescence even at low concentration. Modified CPEs were constructed and analyzed using cyclic voltammetry. The intercalated mediator remained electroactive within the layers (E°′=–38.5 mV vs. Ag/AgCl, 3.5 M NaCl) and electrocatalysis of NADH oxidation was observed. The kinetics of the modified CPE shows a Michaelis–Menten behavior. This CPE was used for the oxidation of NADH in the presence of Bakers' yeast alcohol dehydrogenase. A calibration plot for ethanol is presented.     

An algorithm for the calculation of the electrostatic repulsion between surface coated with a charge membrane

We propose a numerical procedure for the calculation of the electrostatic repulsion force between two identical, parallel surfaces immersed in anab electrolyte solution. These surfaces are coated with an ion-penetrable membrane carrying fixed charges. The amount of fixed charges is governed by the dissociation of the functional groups in the membrane phase. The effect of pH on the degree of dissociation of these functional groups is taken into account. The difficulty of extensive use of Jacobi elliptic function in the numerical treatment of Poisson-Boltzmann equation can be circumvented by resorting to the present algorithm.     

Adsorption on stepped substrates

An analysis is given of the behavior of an interface above a stepped substrate in the presence of an external pinning potential for the lattice solid-on-solid (SOS) interface model in 2D. Step-free energy including step-step interaction free energy is calculated, for large step separation. It is found it vanishes at temperatures lower thanT _w (wetting transition temperature), which is different from the case having only one step on a substrate where, as it is well known, step-free energy vanishes at the wetting transition.     

Study of the yrast band in the doubly odd156Tm

The yrast band in the doubly odd¹⁵⁶Tm nucleus was studied through¹⁴⁴Sm(¹⁹F,2p5n)¹⁵⁶Tm reaction at beam energy of 105MeV. Several high-spin states of¹⁵⁶Tm were identified and the highest spin of the band with configuration7/2^–[523] v1/2⁺[660] could be built up to spin 25. The level structure shows the onset of a non- or weak collectivity which generally appears at neutron number of 87 in neutron-deficient rare-earth nuclei.This work was supported in part by the Fok Ying Tung Education Foundation and the Natural Science Fund of China.     

Study of short-lived silver isotopes with a laser ion source

The continuum part of the⁶Li (a,a)⁶Li (1.47–2.47 MeV) scattering data at E_a=50 MeV are extracted in two discretized bins. Coupled-channel calculations are carried out coupling the 1⁺ ground state of⁶Li with both the resonant, 3⁺ ₁ state, and two non-resonant continuum states. The discretized continuum of the⁶Li (p,p)⁶Li (1.75–3.25 MeV) scattering data at E_p=65 MeV are also analysed on the same footing. In both the cases the effect of coupling is found to be minimal.     

Yrast excitations in129Te

Using an 11.4MeV/u¹³⁶Xe beam of the UNILAC accelerator of GSI and a^natW target, A=184 isobars were produced and separated by using an on-line mass separator. A new isomeric state was found in¹⁸⁴Hf. This state decays with a half-life of 48(10) s and emits three -rays of 73, 482, and 555 keV as well as lower-lying cascade transitions. The hindrance of the 73 keV-E1 transition with K=8 is compared with those of other even-even hafnium isotopes. The half-life of¹⁸⁴Lu was estimated to be between 15 and 25s.     

Multiple scattering of narrow light beams in aerosols

A multiple scattering propagation model of narrow light beams in aerosol media is described. It is based on a paraxial approximation of the radiative transfer equation in which the flux normal to the incident beam direction is modeled by a diffusion process. The model solutions are the forward- and backscattered intensity profiles for the specified geometry and receiver aperture and field of view. The required inputs are the system parameters, and the aerosol single scattering angular phase function and extinction and scattering coefficients which are allowed to vary along the beam axis. Good agreement is shown with measurements performed in the laboratory over scales ranging from a few tens of mm to a few m, and in the atmosphere over a scale of the order of 1 km. The solutions are valid for optical depths smaller than 10, for phase functions corresponding to average size parameters of order one or greater, and for off-axis positions not exceeding 25% of the reciprocal of the scattering coefficient.     

An explicit description of the fundamental unitary for SU(2) q

In this paper we study the Cauchy problem for the generalized equation of finite-depth fluids

Gas-discharge XeF* (B→X) laser with high specific output energy

The discharge characteristics of the XeF* (BX) laser are investigated. The NF₃ and Xe partial pressure of the laser gas mixture and the total gas pressure have been varied. A highest specific output energy of 4.7 J/l with an efficiency of 0.5% was obtained from a X-ray preionized Ne/Xe/NF₃ gas mixture at 6 bar with single-pulse excitation through a multichannel spark gap.     

Regioselective Synthesis of Mixed Indole 2,3-Bis(sulfides). A Study of the Mechanism of the Second Sulfenylation of Indole

Sulfenylation of indole using sulfenyl chlorides leads to the initial formation of a 3-indolyl sulfide, while excess reagent introduces a second sulfide at the 2-position of the ring. The mechanism of this second sulfenylation has not, to date, been rigorously elucidated. The development of the first, regioselective synthesis of mixed indole 2,3-bis(sulfides) has allowed the study of the sulfenylation of 3-indolyl sulfides using a different sulfenyl chloride. Our results afford evidence that the reaction proceeds via an intermediate 3,3-disulfenylated indolenine species, with subsequent migration of one of the sulfide groups to the 2-position.