Thermal neutron induced charged particle reactions on58,59,61Ni

The thermal neutron induced charged particle spectroscopy on^{58, 59, 61}Ni (target nuclei) was done at the 87 m thermal neutron curved guide of the Grenoble high flux reactor. In the⁵⁹Nu(n, α)⁵⁶Fe reaction two lines showed up corresponding toα-particle transitions to the ground and first excited states in⁵⁶Fe with σ_α0=13.1±1.1 b and σ_α1 =0.188±0.01 b. A value of σ_γα≦13 mb was obtained for the two-step⁵⁹Ni(n, γα)⁵⁶Fe reaction. The technique to unfold theγα-spectrum and to get information on the primary low energyγ-rays is given and the present and our previous data on the¹⁴³Nd(n, γα)¹⁴⁰Ce reaction are analysed. For the⁵⁹Ni(n, p)⁵⁹Co reaction _p0=1.34±0.18b,σ _p1<0.30 b were determined. The cross-sections for the⁵⁸Ni(n,α)⁵⁵Fe and⁶¹Ni(n,α)⁵⁸Fe reactions were σ_α0≦30 Μb and σ_α0≦30 Μb respectively; these andσ _p1upper limit value are about 20–1500 times lower than the existing data. The other results are compared with the existing data and the differences are explained. The experimental data are compared with the values obtained from the statistical model.     

Morphological,rheological, and mechanical properties of ethylene propylene diene monomer/carboxylated styrene-butadiene rubber/multiwall carbon nanotube nanocomposites

Abstract

A hybrid nanocomposite based on ethylene propylene diene monomer/carboxylated styrene-butadiene rubber (EPDM/XSBR) blend with different concentrations (0–7 phr) of multiwall carbon nanotube (MWCNT) was prepared on a two-roll mill. The role of grafted maleic anhydride (EPDM-g-MA) as compatibilizer and the effect of different concentrations of MWCNT on mechanical properties, morphology, rheological and curing characteristics of nanocomposites were investigated. The curing behavior of the prepared nanocomposites was studied using a rheometer. Also, the microstructure of nanocomposites was observed using TEM. By increasing the MWCNT concentration in the compatible blends, the curing time and scorch time of the blends decreased, while the maximum and minimum torque increased. Failure surface morphology studies showed that the existence of EPDM-g-MAH compatibilizer improved the distribution of MWCNT within the polymer matrix and uniform distribution of MWCNT with a small amount of aggregation was obtained. On the other hand, the presence of MWCNT in the matrix led to a sharper surface of the fracture. Also, mechanical properties such as modulus, tensile strength, hardness, fatigue, resilience and elongation-at-break for compatible EPDM/XSBR nanocomposite showed better results than those for incompatible composite.     

Photoinduced Electron Transfer in Clicked Ferrocene-BODIPY-Fullerene Conjugates

Ferrocene-BODIPY (Fc-BDP) conjugates in which one or two ferrocene entities are linked to the β-positions of the BODIPY core by an ethynyl bridge have been developed. These derivatives were easily and efficiently grafted onto a dual-clickable fullerene platform using CuAAC reactions, leading to a clickable Fc-BDP-C₆₀ triad and a clickable [Fc]₂-BDP-C₆₀ tetrad which can be used for further derivatization with complex structures. Due to the extended π-conjugation and the presence of an intramolecular charge transfer band from Fc to BDP, all these conjugates display a broad absorption in the visible region, which is bathochromically shifted when two Fc are appended to the BDP core. Ultrafast multistep electron transfers leading to charge stabilization were demonstrated in the Fc-BDP-C₆₀ triad and [Fc]₂-BDP-C₆₀ tetrad by femtosecond transient absorption studies.     

A three-component novel synthesis of 1-carbamato-alkyl-2-naphthol derivatives

A new one-pot, efficient three-component condensation of benzaldehydes, 2-naphthol, and carbamates in the presence of silica supported sodium hydrogen sulfate as an effective heterogeneous catalyst for the synthesis of novel 1-carbamato-alkyl-2-naphthol derivatives under solvent-free conditions is described. The present methodology offers several advantages, such as high yields, short reaction times, and very easy workup.     

Electrocatalytic Determination of 6‐Tioguanine at a p‐Aminophenol Modified Carbon Paste Electrode

A p‐aminophenol modified carbon paste electrode (p‐APMCPE) was constructed for determination of an anticancer drug 6‐thioguanine (6‐TG). The cyclic voltammogram showed that the electrocatalytic oxidation of 6‐TG at the surface of p‐APMCPE occurs at a potential about 840 mV less positive than at an unmodified electrode. Square‐wave voltammetry results presented that the electrocatalytic oxidation peak currents of 6‐TG in pH 9.0 had two linear dynamic ranges in the range of 0.2 to 8.0 and 8.0 to 350.0 μM 6‐TG with a detection limit of 0.08 μM. The kinetic parameters such as electron transfer coefficient (α) and rate constant were determined for the chemical reaction between 6‐TG and p‐aminophenol. Finally, this method was evaluated for the determination of 6‐TG in 6‐thioguanine tablets and urine samples.     

Rate-limiting proton-transfer in the sigma-adduct forming reactions of 1,3,5-trinitrobenzene and 4-nitrobenzofuroxan with substituted anilines in dimethyl sulfoxide

Kinetic and equilibrium results are compared for the reactions in dimethyl sulfoxide of 1,3,5-trinitrobenzene, 1, and 4-nitrobenzofuroxan, 4, with a series of substituted anilines in the presence of Dabco or in, some cases, quinuclidine. pKa values for the corresponding anilinium ions are reported. The reactions of 1and 4 are likely to proceed through nucleophilic attack by the aniline to yield zwitterionic intermediates which may transfer an acidic proton to the bases present to yield the anionic adducts 9 or 12 respectively. In the formation of 9 from 1 the proton transfer step is rate-limiting; however, the slower interconversion of 4 and its zwitterion leads to only partial rate-limiting proton transfer in the formation of 12. Results with substituted anilines including 2-substituted and N-methyl aniline indicate that steric effects are not a major factor in determining rates of proton-transfer in these systems. Contrary to previous reports no evidence was found for a strong interaction between 1 and Dabco in DMSO.     

Nuclear charge distribution of mass-separated isobars from thermal-neutron-induced fission of 235U

The nuclear charge distribution of fission products with mass numbers A = 90, 91, 94, 99, 100, 101 and 104 provided by the mass separator “Lohengrin” was measured. Adjacent elements in the group of the light fission products could be separated by their different energy loss in a carbon absorber. The Z-yields were found to be strongly dependent on the kinetic energy of the fission products. The widths of the nuclear charge distributions are very small, in general, and strongly dependent on A as well as on the kinetic energy. The influence of the neutron evaporation and odd-even effects are clearly detected. An asymmetric nuclear charge distribution was found for A = 104 indicating the suppression of fission fragments with Z = 43. The average nuclear charges of the fission products at their average kinetic energy are in good agreement with the results from measurements of the number of β-decays and K X-ray measurements. The average nuclear charge of the isobar A = 132 was measured at its average kinetic energy with a calibrated secondary electron detector to be Z = 51.14 ± 0.15 which is in very good agreement with the radiochemical results. Thus previous physical measurements indicating a large independent yield for the doubly magic nucleus ¹³²Sn could not be confirmed.     

Flow-Injection Determination of Cephalosporin Antibiotic Cefixime in Pharmaceutical Formulations with Luminol-Diperiodatoargentate(III) Chemiluminescence Detection

Journal of Analytical Chemistry - A simple and sensitive flow injection chemiluminescence method was developed for the determination of cefixime trihydrate (CFX) based on its enhancing effect on...     

Time-Resolved Spectroscopy and High-Efficiency Light-Driven Hydrogen Evolution of a {Mo3S4}-Containing Polyoxometalate-Based System

Polyoxothiometalate ions (ThioPOM) are active hydrogen-evolution reaction (HER) catalysts based on modular assembly built from electrophilic clusters {MoS_x} and vacant polyoxotungstates. Herein, the dumbbell-like anion [{(PW₁₁O₃₉)Mo₃S₄(H₂O)₃(OH)}₂]⁸⁻ exhibits very high light-driven HER activity, while the active cores {Mo₃S₄} do not contain any exposed disulfido ligands, which were suspected to be the origin of the HER activity. Moreover, in the catalyst architecture, the two central {Mo₃S₄} cores are sandwiched by two {PW₁₁O₃₉}⁷⁻ subunits that act as oxidant-resistant protecting groups and behave as electron-collecting units. A detailed photophysical study was carried out confirming the reductive quenching mechanism of the photosensitizer [Ir(ppy)₂(dtbbpy)]⁺ by the sacrificial donor triethanolamine (TEOA) and highlighting the very high rate constant of the electron transfer from the reduced photosensitizer to the ThioPOM catalyst. Such results provide new insights into the field of molecular catalytic systems able to promote high HER activity.