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141.
The thermal decarboxylation of three dicarboxylic perfluoropolyether potassium salts of relatively short chain length has been investigated and the products and kinetics of the main reactions have been defined. From the rate constants and Arrhenius parameters data, the second decarboxylation appears to be quantitatively rather close to the first. 相似文献
142.
The pressure dependence of thelo-to phonons in InAs has been investigated by Raman scattering using the diamond anvil cell. Indium arsenide transforms, presumably
to the rock-salt structure at 70±1 kbar. The mode Grüneisen parameters for thelo-to phonons are γ
lo
=0.99±0.03, γ
to
=1.2±0.03 respectively. The effective charge,e*
T
, for InAs decreases slightly with pressure and this trend is in accordance with the behaviour of other III–V zinc blende
structured semiconductors: The structural phase transition is discussed in the light of theoretical calculations for phase
stability of III–V compounds, as well as recent high pressure x-ray diffraction studies. 相似文献
143.
Jerald R. Izatt Bimal K. Deka 《International Journal of Infrared and Millimeter Waves》1984,5(11):1473-1482
Using the isotopic species13CH3F in the methyl-fluoride Raman laser, we have observed kilowatt-level laser pulses which can be tuned over a series of intervals that are centered on pure-rotational transitions in thev
3 ground state with initial-state J values between 35 and 43, inclusively. Taken together, these tuning intervals cover 35% of the spectrum between 142 and 174 m. Several straightforward improvements in the experimental setup, including the use of isotopically purer13CH3F, should enhance the spectral coverage in this region. 相似文献
144.
M. Yakup Arca Meltem Ylmaz Emine Yaln Gülay Bayramo
lu 《Journal of membrane science》2004,240(1-2):167-178
Poly(hydroxyethyl methacrylate), pHEMA, and a composite pHEMA/chitosan networks were synthesized in the membrane form via UV initiated photo-polymerisation in the presence of an initiator ,′-azoisobutyronitrile. Reactive Yellow 2 (RY-2) was covalently immobilised as a dye–ligand onto both membranes. The polarity and surface energy of the investigated membranes were determined by contact angle measurement. The incorporation of chitosan in the pHEMA networks produced more hydrophilic surface, as indicated by contact angle analysis. The binding characteristics of lysozyme, γ-globulins, human serum albumin (HSA) and bovine serum albumin (BSA) to pHEMA-RY-2 and pHEMA/chitosan-RY-2 affinity membranes have been investigated from aqueous solution and their dye–ligand free forms were used as control systems. When chitosan was incorporated in the pHEMA network as a cationic polymer led to higher adsorption capacity for the lysozyme. Selective adsorption behaviour was also observed in the case of pHEMA/chitosan-RY-2 membrane for the lysozyme. The non-specific adsorptions of the lysozyme on the pHEMA and pHEMA/chitosan membranes were about 1.9 and 7.2 mg/ml, respectively. These were negligible for all others investigated proteins. The lysozyme adsorption data was analysed using the first-order and the second-order models. The first-order equation in both affinity membrane systems is the most appropriate equation to predict the adsorption capacities of the adsorbents. The adsorption isotherms well fitted the combined Langmuir–Freundlich model. A theoretical analysis has been conducted to estimate the thermodynamic contributions (changes in enthalpy, entropy and Gibbs free energy) for the adsorption of lysozyme to both dye–ligand immobilised membranes. The adsorption capacities of both dye–ligand immobilised membranes increased with increasing the temperature while decreased with increasing the NaCl concentration. Both affinity membranes are stable when subjected to sanitization with sodium hydroxide after repeated separation–elution cycles. 相似文献
145.
Lebedev B. V. Kulagina T. G. Smirnova N. N. Shifrina Z. B. Averina M. S. Rusanov A. L. 《Journal of Thermal Analysis and Calorimetry》2003,74(3):735-748
In an adiabatic vacuum calorimeter, the temperature dependence of the heat capacity C
p of phenylated polyphenylene and initial comonomer 1,4-bis(2,4,5-triphenylcyclopentadienone-3-yl)benzene was studied between
6 and 340 K with an uncertainty of about 0.2%. In a calorimeter with a static bomb and an isothermal shield their energies
of combustion DUcomb were measured. From the experimental data, the thermodynamic functions C
p
0 (T), H
0(T)-H
0(0), S
0(T)-S0(0), G
0(T)-H
0(0) were calculated from 0 to 340 K, and standard enthalpies of combustion ΔH
comb
0 and thermodynamic parameters of formation-enthalpies ΔH
f
0, entropies ΔH
f
0, Gibbs functions ΔG
f
0 - of the substances studied were estimated at T=298.15 K at standard pressure. The results were used to calculate the thermodynamic characteristics (ΔH
f
0 ,ΔS
f
0, ΔG
f
0) of phenylated polyphenylene synthesis in the range from 0 to 340 K.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
146.
H. Morais C. Ramos E. Forgasc T. Cserháti N. Matos V. Almeida J. Oliveira 《Chromatographia》2002,56(1):S173-S175
Summary The extractability and stability of anthocyanins from the skins ofVitis vinifera were determined at different pH values. Anthocyanins were extracted using acetone, partitioned with chloroform and pre-purified
by solid-phase extraction (SPE). They were analysed by RP-HPLC, and the kinetic parameters of decomposition were calculated.
The total monomeric anthocyanin content was determined by spectrophotometry. Anthocianins were well separated by RP-HPLC.
The efficiency of extraction depended strongly on the pH of the extracting agent and on the character of the pigment to be
extracted. The amount of anthocyanins decreased with increasing duration of storage, more so at elevated temperatures.
Presented at Balaton Symposium '01 on High-Performance Separation Methods Siófok, Hungary, September 2–4, 2001. 相似文献
147.
Fatma M. Elzawawy 《Monatshefte für Chemie / Chemical Monthly》1991,122(11):921-925
Summary The stoichiometric stability constants for La(III) and Y(III)L-serine complexes were determined by potentiometric methods at different ionic strengths adjusted with NaClO4 and at different temperatures. The overall changes in free energy (G
o), enthalpy (H
o), and entropy (S
o) during the protonation ofL-serine and that accompanying the complex formation with the metal ions have been evaluated.
Komplexbildungskonstanten und thermodynamische Parameter für La(III)- und Y(III)-L-Serin-Komplexe
Zusammenfassung Die stöchiometrischen Komplexbildungskonstanten für La(III)- und Y(III)-L-Serin-Komplexe wurden mittels potentiometrischer Methoden bei verschiedenen Ionenstärken (mit NaClO4 adjustiert) und bei verschiedenen Temperaturen bestimmt. Die Änderungen in der freien Energie (G o), Enthalpie (H o) und Entropie (S o) während der Protonierung und der Komplexbildung mit den Metallionen wurden ermittelt.相似文献
148.
The conditions of formation of complex lanthanide chromate(VI)-phosphates K2R(CrO4)(PO4) were found and these compounds were synthesized by solid-state synthesis with variation of the starting compounds, the temperature
of synthesis (500–800 °C), and the annealing time (6–200 h). These salts are typical of late lanthanides, R = Dy-Lu, Y. Using
lutetium derivatives as examples, it was shown that no similar compounds with lithium or sodium are formed. All the complex
chromate(VI)-phosphates obtained decompose under static conditions at temperatures above 550 °C. They are isostructural and crystallize
in the monoclinic system. The unit cell parameters for thulium, ytterbium, and lutetium compounds were calculated. It is shown
by IR spectroscopy that PO4 tetrahedra in the crystal lattice of potassium lanthanide chromate(VI)-phosphates are substantially distorted, whereas the CrO4 tetrahedra retain the regular tetrahedron symmetry (T
d
).
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 622–626, April, 2006. 相似文献
149.
Dhanpat Rai Dean A. Moore Nancy J. Hess Kevin M. Rosso Linfeng Rao Steve M. Heald 《Journal of solution chemistry》2007,36(10):1261-1285
Chromium(III)-carbonate reactions are expected to be important in managing high-level radioactive wastes. Extensive studies
on the solubility of amorphous Cr(III) hydroxide solid in a wide range of pH (3–13) at two different fixed partial pressures
of CO2(g) (0.003 or 0.03 atm.), and as functions of K2CO3 concentrations (0.01 to 5.8 mol⋅kg−1) in the presence of 0.01 mol⋅dm−3 KOH and KHCO3 concentrations (0.001 to 0.826 mol⋅kg−1) at room temperature (22±2 °C) were carried out to obtain reliable thermodynamic data for important Cr(III)-carbonate reactions.
A combination of techniques (XRD, XANES, EXAFS, UV-Vis-NIR spectroscopy, thermodynamic analyses of solubility data, and quantum
mechanical calculations) was used to characterize the solid and aqueous species. The Pitzer ion-interaction approach was used
to interpret the solubility data. Only two aqueous species [Cr(OH)(CO3)22− and Cr(OH)4CO33−] are required to explain Cr(III)-carbonate reactions in a wide range of pH, CO2(g) partial pressures, and bicarbonate and carbonate concentrations. Calculations based on density functional theory support
the existence of these species. The log 10
K° values of reactions involving these species [{Cr(OH)3(am) + 2CO2(g)⇌Cr(OH)(CO3)22−+2H+} and {Cr(OH)3(am) + OH−+CO32−
⇌Cr(OH)4CO33−}] were found to be −(19.07±0.41) and −(4.19±0.19), respectively. No other data on any Cr(III)-carbonato complexes are available
for comparisons. 相似文献
150.
把取代基电性、立体及疏水性物化参数组合建立一种新取代基描述方法, 对环尿素类和N,N-二甲基-2-溴苯乙胺类衍生物进行结构表征. 对训练样本集通过逐步回归筛选变量, 所建多元线性回归方程R2分别为0.853和0.960, 留一法交互检验Rcv2分别为0.723和0.901;用预测集样本作外部预测, 所得Qext2分别为0.7617和0.7653. 结果显示:环尿素类化合物结构中苯环邻位立体、间位疏水、对位疏水及立体因素对该类药物抗HIV活性产生阻抑作用; N,N-二甲基-2-溴苯乙胺类苯环上取代基立体因素及对位给电子效应有利于提高肾上腺素能阻断活性. 相似文献