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951.
Summary Micromolar analyses of the nitrogen species NH3, NO
2
–
, and NO
3
–
in soil and other samples are usually accomplished by extracting several samples and testing each for a different species. This procedure is not viable when the quantity of the initial sample is limited. An improved method of separating and analysing for ammonia NH3(aq), nitrite NO
2
–
(aq), and nitrate NO
3
–
(aq) from a single small sample with concentrations of 0–50 mol/l is reported. No interferences or carryovers among the three nitrogen containing species were found. Uncertainties were ±2–5 mol/l and accuracies with respect to standards were ±3 mol/l. 相似文献
952.
采用INDO方法计算了{Fe[P(OMe)_3]_3(C_8H_(13))}~+的简化离子[Fe(PH_3)_3(C_8H_(13))]~+,将正则分子轨道用Edmiston-Ruedenberg定域化方法变换为定域分子轨道,结果表明:在对应C_1-H_(1A)键的定域分子轨道中,明显包含有铁原子轨道成分(7.8%),Fe-H_(1A)和Fe—C_1键级分别为0.190和0.302。指出C_1-H_(1A)键是以一对成键σ电子配位到铁原子上的。C_8H_(13)环以包含三个碳原子的η~4—共轭体系与铁原子相互作用。铁以二价(d~6-Fe(Ⅱ)的形式存在于该离子中。C_1-H_(1A)键的配位满足了文献[15]提出的Fe(Ⅱ)的共价12价。 相似文献
953.
The selectivity of the oxides under consideration to the oxidation of methanol to formaldehyde is shown to increase in the sequence V2O5–Nb2O5–Ta2O5. The same sequence corresponds to the decrease in specific activity. The activation energy of the reaction is 12 kcal/mol for V2O5, 14 kcal/mol for Nb2O5 and 22 kcal/mol for Ta2O5.
, V2O5–Nb2O5–Ta2O5. . : V2O5 12 /, Nb2O5 14 / Ta2O5 22 /.相似文献
954.
T. M. Gairbekov Ya. S. Yakhyaev S. N. Khadzhiev 《Reaction Kinetics and Catalysis Letters》1986,31(1):127-131
Regularities in n-hexane conversion on decationized Y zeolites under cracking and aromatization conditions have been studied. Possible formation of lower olefins and benzenes in parallel reactions following different mechanisms at low conversion degrees is suggested. The effect of thermosteam treatment on the activity and selectivity of Y zeolites in n-hexane conversion has been examined.
- Y . , . Y -.相似文献
955.
Summary The semi-empirical theory on the retention volume in gas chromatography recently developed by some experiments, was found to require partial correction. It was newly refined and summarized. Overall experimental checking was performed by the use of Cl2, Br2, and I2.
Gas-Chromatographie von Halogenen
Zusammenfassung Die halbempirische Theorie über das Retentionsvolumen in der Gas-Chromatographie, die kürzlich an Hand einiger Versuche entwickelt wurde, erforderte eine teilweise Korrektur. Sie wurde verbessert und zusammenfassend dargestellt. Kontrollversuche wurden mit Hilfe von Chlor, Brom und Jod durchgeführt.相似文献
956.
M. Kuzmanovi M. A. Khakoo V. Bojovi A. Anti-Jovanovi 《Russian Journal of Physical Chemistry A, Focus on Chemistry》2007,81(9):1438-1442
An array of Franck-Condon factors and r-centroids is reported for the bands of the E
1Πu-X
1Σ
g
+
system of the Ag2 molecule. Both parameters were calculated using the Morse and Rydberg-Klein-Rees potentials. The results showed a reasonable
agreement between the two sets of data for transitions, including lower vibrational levels (v ≤ 6). Differences appear with increasing v, but two sets of calculated Franck-Condon factors follow the same pattern. The predicted intensity distribution was compared
with the estimated band intensity in the experimental spectrum.
The text was submitted by the authors in English. 相似文献
957.
Maria-Teresa Clavaguera-Mora Narcís Clavaguera Javier Rodríguez-Viejo 《Monatshefte für Chemie / Chemical Monthly》2005,12(8):1947-1953
The primary crystallization of molten alloy systems at high undercooling is studied by a precise quantitative analysis of
the calorimetric signal obtained during the transformation in terms of the reaction rate under isothermal and continuous heating
regimes. It is shown that, under specific conditions, namely, stoechiometric primary precipitates, generalized relationships
for the crystallization enthalpy and the reaction rate may be obtained. 相似文献
958.
Joeng-Shein Chen Harald Berndt Günther T?lg 《Fresenius' Journal of Analytical Chemistry》1992,344(12):526-534
Summary Various possibilities for the determination of trace impurities in high-purity iron by atomic spectrometry were investigated in detail. For Ba, Bi, Cd, Co, Cr, Cu, Mn, Ni, Pb, Ti and V, flame AAS, furnace AAS and ICP-OES were firstly evaluated in terms of their power of detection. Detection limits in the g/g-range could be achieved by direct determination. For determination in the ng/g-range a removal of iron by a solvent extraction technique prior to the instrumental measurement was required. The power of detection of direct determination, and of combined procedures were compared with regard to routine applicability and a minimization of systematic errors. 相似文献
959.
960.