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161.
J. D. Pinheiro Filho E. S. De Almeida E. Z. Bilbao R. C. Santos A. X. Da Silva V. Sciani P. R. Rela 《Radiation measurements》1994,23(4):743-748
In this paper, we study the thermal annealing of proton tracks of 4 and 6 MeV at temperatures ranging from 150 to 240°C in CR-39 polymer detectors. A special experimental set-up for irradiating the detectors was arranged to obtain adequate proton beams from the Cyclotron CV-28 at IPEN/SP, Brazil. We report experimental data on track densities, track diameters, and activation energies based on current annealing models for the annealing of proton tracks in the energy range investigated. A value of (0.20±0.02)eV was determined as the mean activation energy of the annealing process in CR-39 detectors. 相似文献
162.
L. Lupan Rodica Bandula Marilena Vasilescu Cristiana Bercu 《Fresenius' Journal of Analytical Chemistry》1996,355(3-4):409-411
Conformational transformations of the tetraenic nystatin chromophore under the influence of solvents and UV irradiation have been studied by absorption, fluorescence and wide-line NMR spectroscopy. 相似文献
163.
Ferreira C.M. Alves L.L. Pinheiro M. Sa A.B. 《IEEE transactions on plasma science. IEEE Nuclear and Plasma Sciences Society》1991,19(2):229-239
A kinetic study of low-pressure microwave discharges in Ar, He, and O2 is carried out using electron-transport parameters and rate coefficients derived from solutions to the Boltzmann equation, together with the continuity and transport equations for the charged particles, taking into account stepwise-ionization processes. The Boltzmann equation is solved over a wide range of the applied frequency, ω/2π, but assuming that the angular frequency ω>τ e-1, with τe, denoting the characteristic time for electron-energy relaxation by collisions. The formulation provides discharge characteristics for the maintenance field and for mean absorbed power per electron in the three gases, which are shown to agree satisfactorily with experimental data obtained from surface-wave discharges. It is shown that such an agreement would not always be obtained without consideration of the role played by stepwise-ionization processes in sustaining the discharge 相似文献
164.
Haibo Wu Cristiana Margarita Jira Jongcharoenkamol Mark D. Nolan Thishana Singh Pher G. Andersson 《Chemical science》2021,12(5):1937
Asymmetric hydrogenation is one of the most commonly used tools in organic synthesis, whereas, kinetic resolution via asymmetric hydrogenation is less developed. Herein, we describe the first iridium catalyzed kinetic resolution of a wide range of trisubstituted secondary and tertiary allylic alcohols. Large selectivity factors were observed in most cases (s up to 211), providing the unreacted starting materials in good yield with high levels of enantiopurity (ee up to >99%). The utility of this method is highlighted in the enantioselective formal synthesis of some bioactive natural products including pumiliotoxin A, inthomycin A and B. DFT studies and a selectivity model concerning the origin of selectivity are presented.Asymmetric hydrogenation is one of the most commonly used tools in organic synthesis, whereas, kinetic resolution via asymmetric hydrogenation was less developed. 相似文献
165.
A. G. de Souza Fe. de Souza Neto J. H. de Souza R. O. Macedo J. B. L. de Oliveira C. D. Pinheiro 《Journal of Thermal Analysis and Calorimetry》1997,49(2):679-684
The standard molar enthalpy of formation of crystalline di-isobutyldithiocarbamate complexes of P, As, Sb and Bi(III) has been derived by solution calorimetry at 298.15 K. The corresponding standard molar enthalpies of sublimation were estimated by means of differential scanning calorimetry. From the standard molar enthalpies of formation of the gaseous chelates the homolytic and heterolytic mean metal-sulphur bond-dissociation enthalpies were calculated.We thank to CNPq and to PADCT for financial support of this work and also to Dr. Claudio Airoldi (UNICAMP) by facility offered for obtaining of the solution-reaction calorimetric measurements. 相似文献
166.
Horswell SL Pinheiro AL Savinova ER Danckwerts M Pettinger B Zei MS Ertl G 《Langmuir : the ACS journal of surfaces and colloids》2004,20(25):10970-10981
Hydroxide adsorption on the (111), (110), and (100) faces of silver electrodes from mixed NaOH/NaF solution is studied using cyclic voltammetry and in situ second harmonic generation (SHG). Cyclic voltammograms for the three low index silver planes in alkaline electrolytes are for the first time compared. They show two pairs of anodic and cathodic peaks in the potential interval below the equilibrium Ag/Ag(2)O potential. These are attributed to the specific adsorption of hydroxide ions followed by submonolayer oxide formation. The differences in the cyclic voltammograms for the (111), (110), and (100) planes are attributed to different (i) work functions, (ii) surface atomic densities, and (iii) corrugation potentials for these surfaces. Ex situ low energy electron diffraction (LEED) and reflection high energy electron diffraction (RHEED) show that disordered adlayers are formed on Ag(111) and Ag(100), in contrast to Ag(110), where ordered structures are produced in the region of the first pair of current peaks. In the region of the second pair of peaks, LEED indicates disordered oxide phases on each crystal plane and RHEED shows the presence of small islands of c(2 x 2) structure at some potentials on (110) and (100). SHG measurements were performed (i) in the potential scan mode at constant rotational angle and (ii) at constant potential as a function of the rotational angle. The isotropic (for the (111), (110), and (100) planes) and anisotropic (for the (110) and (111) planes) contributions to the SHG intensity were calculated by fitting the experimental data and are discussed in terms of their dependence on the charge density at the interface, on hydroxide adsorption, and on submonolayer oxide formation. 相似文献
167.
In this work, a solid phase spectrophotometric method in association with flow injection analysis for formaldehyde determination has been developed with direct measurement of light-absorption in C18 material. The 3,5-diacetyl-1,4-dihydrolutidine produced from the reaction between formaldehyde and fluoral P was quantitatively retained on C18 support and the spectrophotometric detection was performed simultaneously at 412 nm. The retained complex was quickly eluted from C18 material with the eluent stream consisting of a 50% (v/v) ethanol solution. The results showed that the proposed method is simple, rapid and the analytical response is linear in the concentration range of 0.050-1.5 mg L−1. The limit of detection was estimated as 30 μg L−1 and the R.S.D. 2.2% using a sample volume of 625 μL. The system presented an analytical throughput of 20 determinations per hour. The method was successfully applied in the determination of formaldehyde in ethanol fuel. 相似文献
168.
This paper deals with the microscopic mechanism of nanolithography of self-assembled monolayers (SAM) of alkanethiol molecules on Au(111) induced by the exposure of the film to a beam of "cold" Cs atoms. Density functional theory calculations have been carried out to elucidate the mechanism of interaction of the Cs atoms with the SAM. We found that the film damage occurs in two steps: the Cs atom penetrates the SAM and at a distance of 10-12 Angstrom from the surface donates one electron to Au, forming a Cs(+) cation which binds strongly to the surface and interacts with the polar head of the SR molecule. The thermal energy released in this process largely exceeds the energy required to stimulate the desorption of RS-SR disulfide molecules from the Au surface with consequent damage of the film. No chemical interaction occurs between Cs or Cs(+) and the hydrocarbon chain of the thiol molecule. 相似文献
169.
Detection of 2,4,6-trichloroanisole in chlorinated water at nanogram per litre levels by SPME–GC–ECD
A method involving solid-phase micro extraction (SPME) and gas chromatography with electron capture detection (SPME–GC–ECD) has been optimised for identification and quantification of 2,4,6-trichloroanisole (TCA) at ng L–1 concentrations in disinfected (chlorinated) water samples. A central composite design was used for factorial analysis of four factors, three factors related to the SPME (PDMS fibre) procedure (adsorption time, temperature of the sample during headspace sampling, and desorption time) and one related to the GC operation (the rate of increase of the temperature of the GC oven). Good linearity (linear correlation coefficient greater than 0.999) was observed for TCA concentrations up to 50 ng L–1, limits of detection and quantification of 0.7 and 2.3 ng L–1, respectively, and good precision (relative standard deviation 2.8% and 3.4% for 5 and 30 ng L–1 of TCA, respectively). Besides TCA, this system also enables the detection and quantification of the four trihalomethanes in the g L–1 concentration range with limits of detection and quantification of approximately 0.3 g L–1 and 1 g L–1, respectively. 相似文献
170.
Débora de Oliveira Irajá do Nascimento Filho Marco di Luccio Carina Faccio Clarissa Dalla Rosa João Paulo Bender Nádia Lipke Cristiana Amroginski Cláudio Dariva José Vladimir de Oliveira 《Applied biochemistry and biotechnology》2005,121(1-3):231-241
This work investigated the production of fatty acid ethyl esters (FAEEs) from soybean oil using n-hexane as solvent and two commercial lipases as catalysts, Novozym 435 and Lipozyme IM. A Taguchi experimental design was
adopted considering the variables temperature (35–65°C), addition of water (0–10 wt/wt%), enzyme (5–20 wt/wt%) concentration,
and oil-to-ethanol molar ratio (1:3–1:10). It is shown that complete conversion in FAEE is achieved for some experimental
conditions. The effects of process variables on reaction conversion and kinetics of the enzymatic reactions are presented
for all experimental conditions investigated in the factorial design. 相似文献