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41.
42.
The determination of carbonyl compounds in gaseous samples is usually accomplished by enrichment methods, in which 2,4-dinitrophenyl-hydrazine (DNPH) as a derivatization reagent has become established to a large extent. However, the conventional methods of DNPH-impingers and of DNPH-cartridges are applicable to emission measurements in a limited way only, depending on the NO2-concentration in the exhaust gas. It could be proved that DNPH-derivatives, as well as DNPH, are also decomposed by NO2 at a different speed, in which the hydrazones of unsaturated carbonyl compounds are probably more sensitive than those of the saturated carbonyl compounds. In view of this fact, the collecting methods had to be modified to avoid losses with the enrichment. The analysis of the compounds is carried out by HPLC with an effective gradient-system which is able to separate and detect the carbonyl compounds in exhaust gas within 16 min. Furthermore, a simple working-up procedure is presented which facilitates a parallel analysis by GC. 相似文献
43.
SGTx1 is a new neurotoxin from the venom of Scodra griseipes. Because of the small quantity of this natural peptide available, mass spectrometry was used to obtain information on its higher-order structure. The kinetics of reduction by 1,4-dithiothreitol (DTT) was monitored by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS), and showed that one of the three disulfide bridges was appreciably more accessible to the DTT. Studies based on the charge state distribution (CSD) and H/D exchange of the non-reduced peptide, under neutral and acidic conditions, were performed using electrospray mass spectrometry (ES-MS). In neutral solution, SGTx1 showed a maximum charge state of four compared with seven potentially protonated basic residues, and all labile hydrogens were exchanged. However, under acidic conditions, a maximum charge state of only five was observed, and four of the labile hydrogens could not be deuterated. These observations are interpreted in terms of a rigid structure maintained by the disulfide bridges, which can be temporarily relaxed by disulfide bridge scrambling only at higher pH values. 相似文献
44.
R. S. A. de Lange K. -N. P. Kumar J. H. A. Hekkink G. M. H. van de Velde K. Keizer A. J. Burggraaf W. H. Dokter H. F. van Garderen T. P. M. Beelen 《Journal of Sol-Gel Science and Technology》1994,2(1-3):489-495
Microporous SiO2 and SiO2/MO2 (M=Ti, Zr, Al; 10 mol% MOx) materials for gas separation membrane applications have been prepared from polymeric sols. Characterization of these sols with SAXS showed that the mean fractal dimension of the SiO2 sols is 1.3–1.4 with a radius of gyration of approximately 2.5 nm. The dried and calcined films are microporous and the pore size distribution was bimodal with maxima at diameters of 0.5 nm and 0.75 nm. For the SiO2/TiO2, SiO2/ZrO2 and SiO2/Al2O3 systems, much milder reaction conditions proved to be necessary to obtain sols with comparable fractal dimensions due to the high reactivity of the Ti/Zr/Al-alkoxides. Microporous supported membranes with molecular sieve-like gas transport properties can be prepared from a relatively wide range of sol structures: from polymers too small to characterize with SAXS to structures with fractal dimensions: 1<d
f<2.04. 相似文献
45.
Brigitte Sarry und Arno Lange 《Fresenius' Journal of Analytical Chemistry》1968,241(3):186-196
Zusammenfassung Die optimalen Bedingungen für die photometrische Bestimmung von Tantal mit Pyrogallol in schwefelsaurer Lösung bei 405 nm wurden ausgearbeitet. Das Verfahren wurde statistisch überprüft.
Für die Durchführung der Untersuchungen standen Mittel aus dem ERP-Sondervermögen und dem Fonds der Chemischen Industrie zur Verfügung, für die wir auch an dieser Stelle bestens danken.
Herrn Professor Dr. E. Asmus zum 60. Geburtstag gewidmet. 相似文献
Investigations on the photometric determination of tantalum with pyrogallol
The optimum conditions for the photometric determination of tantalum with pyrogallol in sulphuric acid solution at 405 nm have been elaborated. The method has been checked statistically.
Für die Durchführung der Untersuchungen standen Mittel aus dem ERP-Sondervermögen und dem Fonds der Chemischen Industrie zur Verfügung, für die wir auch an dieser Stelle bestens danken.
Herrn Professor Dr. E. Asmus zum 60. Geburtstag gewidmet. 相似文献
46.
Boesten WH Seerden JP de Lange B Dielemans HJ Elsenberg HL Kaptein B Moody HM Kellogg RM Broxterman QB 《Organic letters》2001,3(8):1121-1124
[reaction: see text]. Diastereoselective Strecker reactions based on (R)-phenylglycine amide as chiral auxiliary are reported. The Strecker reaction is accompanied by an in situ crystallization-induced asymmetric transformation, whereby one diastereomer selectively precipitates and can be isolated in 76-93% yield and dr > 99/1. The diastereomerically pure alpha-amino nitrile obtained from pivaldehyde (R1 = t-Bu, R2 = H) was converted in three steps to (S)-tert-leucine in 73% yield and >98% ee. 相似文献
47.
John D. Mertens Katharina Kohse-Hinghaus Ronald K. Hanson Craig T. Bowman 《国际化学动力学杂志》1991,23(8):655-668
The reaction of atomic hydrogen with isocyanic acid (HNCO) to produce the amidogen radical (NH2) and carbon monoxide, has been studied in shock-heated mixtures of HNCO dilute in argon. Time-histories of the ground-state NH2 radical were measured behind reflected shock waves using cw, narrowlinewidth laser absorption at 597 nm, and HNCO time-histories were measured using infrared emission from the fundamental v2-band of HNCO near 5 μm. The second-order rate coefficient of reaction (2(a)) was determined to be: cm3 mol?1 s?1, where f and F define the lower and upper uncertainty limits, respectively. An upper limit on the rate coefficient of was determined to be: 相似文献
48.
49.
Novel l -tartaric acid based stereodynamic biphenylbisphosphinite ligands with anilino linkers were prepared as cyclic diamide compounds. The influence of the constitutional substitution pattern of the amino group at the aniline moiety on the diastereoselective formation of the ligand was investigated. While the meta-anilino bridged ligands showed a highly dynamic behavior and no discrimination between (Rax) and (Sax) configuration, l -tartaric acid substitution on ortho-anilino bridged ligands leads to diastereoselective self-alignment of the central biphenol axis, which controls the stereoselectivity of the ligand and catalyst. The experimental findings were corroborated by theoretical calculations. In the rhodium-catalyzed enantioselective hydrogenation of methyl 2-acetamidoacrylate (MAA), an enantiomeric ratio of 75 : 25 (R/S) was obtained for the ortho-substituted ligand. 相似文献