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951.
Rollie J. Myers 《Journal of solution chemistry》2007,36(3):395-403
We have measured the second acid dissociation constant, K
2a
, at several ionic strengths for hydrogen telluride (H2Te) using the Charge Transfer to Solvent (CTTS) uv spectra of its anions HTe− and Te2−. Since it is produced in our solutions, we have also determined the spectra of Te2
2− both in the uv and in the visible regions. At 25 ∘C, K
2a
= (1.28 ± 0.02) × 10−12 by extrapolation to zero ionic strength. Its value at an ionic strength equal to 0.5 mol.dm-3 was estimated to be (8.7 ± 0.2) × 10−12. The solution thermodynamics of these species are also discussed and comparisons are made to related acids. 相似文献
952.
Dagmara Jacewicz Agnieszka Łapińska Aleksandra Dąbrowska Lech Chmurzyński 《Transition Metal Chemistry》2006,31(1):111-117
The kinetics of the reaction between gaseous CO2 and the cis-[Cr(phen)2(OH2)2]3+ ion leading to the formation of the carbonato complex ion, have been studied over the pH and temperature ranges: 3 < pH <
6 and 5 < T < 25 °C, respectively, at a constant ionic strength of 1 m (NaClO4). Investigations were carried out using the stopped-flow spectrophotometry technique in the UV–Vis range: 340–700 nm. The
major reactant species in the pH range studied was cis-[Cr(phen)2(OH)(OH2)]2+ ion, which underwent reaction with CO2 to form cis-[Cr(phen)2(OH2)(HCO3)]2+ ion. Subsequently, slower ring closure of the latter species to form the bidentate carbonato chelate was observed. The possible
mechanism has been discussed and the activation parameters ΔH† and ΔS† were also determined for the reaction studied. 相似文献
953.
Naomi Masuda Yatsuhisa Nagano T. Kimura 《Journal of Thermal Analysis and Calorimetry》2005,81(3):533-535
Summary The standard molar enthalpy of formation of methyl methylthiomethyl sulfoxide, CH3(CH3SCH2)SO, at T=298.15 K in the liquid state was determined to be -199.4±1.5 kJ mol-1 by means of oxygen rotating-bomb combustion calorimetry. 相似文献
954.
The enthalpy change of formation of the reaction of hydrous dysprosium chloride with ammonium pyrrolidinedithiocarbamate (APDC) and 1,10-phenanthroline (o-phen?H2O) in absolute ethanol at 298.15 K has been determined as (-16.12 ± 0.05) kJ?mol-1 by a microcalormeter. Thermodynamic parameters (the activation enthalpy, the activation entropy and the activation free energy), rate constant and kinetics parameters (the apparent activation energy, the pre-exponential constant and the reaction order) of the reaction have also been calculated. The enthalpy change of the solid-phase reaction at 298.15 K has been obtained as (53.59 ± 0.29) kJ?molt-1 by a thermochemistry cycle. The values of the enthalpy change of formation both in liquid-phase and solid-phase reaction indicated that the complex could only be synthesized in liquid-phase reaction. 相似文献
955.
Zebrowska A Krysiński P 《Langmuir : the ACS journal of surfaces and colloids》2004,20(25):11127-11133
The black lipid membranes (BLMs) are artificial membrane systems that have been widely used in the study of different biological processes. In this paper the planar bilayer lipid membranes have been used to study the behavior of thiolipid molecules-dipalmitoyl-phosphatidyl-ethanolamine-mercaptopropionamide (DPPE-MPA) and cholesteryl 3-mercaptopropionate (Chs-MPA)-as compared to classical BLM made of natural lipids. We present our experiments on black thiolipid bilayer (BTM) formation from a thiolipid solution and basic results of pump currents generated by sodium-potassium pump-Na(+),K(+)-ATP-ase-introduced to such bilayer systems via proteoliposome adsorption with subsequent fusion. Our results imply that no substantial difference exists between BLMs formed from classical lipids and those made from thiolipids used in this study. The same thiolipid molecules were subsequently used for the formation of covalently bound, tethered bilayer lipid membranes (t-BLMs) on polycrystalline gold electrodes. Similarly, as in the case of BLMs, we took advantage of proteoliposome adsorption/fusion to obtain a t-BLM system with reconstituted enzyme. The vesicle fusion on hydrophobic or hydrophilic substrates is one of the main ways to obtain a bilayer system with incorporated biological species. In this paper we present also our preliminary results of electrochemical experiments using rapid solution exchange technique on such t-BLMs systems and their comparison with painted solid supported membranes (SSMs) and BLMs. We have also followed the process of vesicles fusion onto thiolipid monolayer by means of in situ atomic force microscopy in tapping mode (TM-AFM). On the basis of these experiments, we conclude that DPPE-MPA and Chs-MPA molecules used in our experiments preserve lipid properties, allowing for at least partial reconstitution of Na(+),K(+)-ATP-ase into such t-BLMs. On the other hand, the relatively compact organization on polycrystalline gold and the hydrophobic nature of the first monolayer of tethered thiolipids slows down the proteoliposome fusion onto such monolayers and consequently hinders the protein insertion. However, this effect can be overcome by mechanical stimulus that facilitates proteoliposome delamination onto the self-assembled monolayer. 相似文献
956.
Zong ChunYan Gao QingYu Wang YuMei Feng JiaMin Mao ShanCheng Zhang Lu 《中国科学B辑(英文版)》2007,50(2):205-211
The ferroin-catalyzed Belousov-Zhabotinsky(BZ) reaction,the oxidation of malonic acid by acidic bromate,is the most commonly investigated chemical system for understanding spatial pattern forma-tion. Various oscillatory behaviors were found from such as mixed-mode and simple period-doubling oscillations and chaos on both Pt electrode and Br-ISE at high flow rates to mixed-mode oscillations on Br-ISE only at low flow rates. The complex dynamic behaviors were qualitatively reproduced with a two-cycle coupling model proposed initially by Gy?rgyi and Field. This investigation offered a proper medium for studying pattern formation under complex temporal dynamics. In addition,it also shows that complex oscillations and chaos in the BZ reaction can be extended to other bromate-driven nonlinear reaction systems with different metal catalysts. 相似文献
957.
Virginie Gueu Hongpeng You Tomokatsu Hayakawa Masayuki Nogami 《Journal of Sol-Gel Science and Technology》2007,41(3):231-236
Fluorescence and spectral hole burning properties of Eu3+ ions were studied in nanocrystals-precipitated SnO2-SiO2 glasses. The glasses were prepared to contain various amount of Eu2O3 using the sol-gel method, in which SnO2 nanocrystals were precipitated by heating in air. In the glasses containing Eu2O3 less than 1%, the Eu3+ ions were preferentially doped in the SnO2 nanocrystals and their fluorescence intensities were enhanced by the energy transfer due to the recombination of electrons
and holes excited in SnO2 crystals. The SnO2 nanocrystals-precipitated glasses exhibited the persistent spectral holes with the depth of ∼25% of the total fluorescence
intensities of the Eu3+ ions. With the increasing Eu2O3 concentration, the amount of SnO2 nanocrystals decreased and the Sn4+ ions formed the random glass structure together with the silica network. This structure change induced the fluorescence intensities
and the hole depth to decrease. 相似文献
958.
Mesoporous amorphous MnO<Subscript>2</Subscript> as electrode material for supercapacitor 总被引:1,自引:0,他引:1
Mao-Wen Xu Dan-Dan Zhao Shu-Juan Bao Hu-Lin Li 《Journal of Solid State Electrochemistry》2007,11(8):1101-1107
A kind of novel mesoporous, electrochemical active material, amorphous MnO2 has been synthesized by an improved reduction reaction and using supramolecular as template. The synthesized sample was characterized
physically by thermogravimetric analysis, X-ray diffraction, transmission electron microscope (TEM), and Brunauer–Emmett–Teller
(BET) surface area measurement, respectively. Electrochemical characterization was performed using cyclic voltammetry and
chronopotentiometry in 2 mol/l KOH aqueous solution electrolyte. The results of BET and TEM analysis indicated that supramolecular
template plays an important role in the process of big specific surface area mesoporous material forming. After sintering
at 200 °C, the sample still remained an amorphous structure, and its specific capacitance reached 298.7 F/g and presented
a very stable capacitance after 500 cycles. In addition, the electrochemical process, such as ion transfer and electrical
condition, was also investigated with electrochemical impedance spectroscopy. 相似文献
959.
Endre Nagy 《Central European Journal of Chemistry》2003,1(2):160-177
A heterogeneous, multi-layer mass transfer model is proposed for prediction of the effect of multi-layer packing of catalyst
particles adhered to the gas-liquid interface. The behavior of the mass transfer rate with respect to the multi-layer packing,
to the particle size and mass transfer coefficient without particles is discussed. It is shown that enhancement can be considerably
increased by multi-layer packing compared to that of mono-layer packing, depending on the values of particle size and mass
transfer coefficient. The predicted mass transfer rates using the proposed model was verified with experimental data taken
from the literature. The model presented should be superior to that of published in the literature. 相似文献
960.
Ab initio molecular orbital theory and density functional theory have been used to study nine isomers of N7 ionic clusters with low spin at the HF/6-31G*, MP2/6-31G*, B3LYP/6-31G*, and B3LYP/6-311(+)G* levels of theory. All stationary
points are examined with harmonic vibrational frequency analyses. Four N7
+ isomers and five N7
− isomers are determined to be local minima or very close to the minima on their potential-energy hypersurfaces, respectively.
For N7
+ and N7
−, the energetically low lying isomers are open-chain structures (C
2
v
and C
2
v
or C2). The results are very similar to those of other known odd-number nitrogen ions, such as N5
+, N9
+, and N9
−, for which the open-chain structures are also the global minima. This research suggests that the N7 ionic clusters are likely to be stable and to be potential high-energy-density materials if they could be synthesized.
Received: 16 July 2001 / Accepted: 8 October 2001 / Published online: 21 January 2002 相似文献