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1.
Planar laser-induced fluorescence visualisation is used to investigate nonuniformities in the flow of a hypersonic conical nozzle. Possible causes for the nonuniformity are outlined and investigated, and the problem is shown to be due to a small step at the nozzle throat. Entrainment of cold boundary layer gas is postulated as the cause of the signal nonuniformity.
PACS 47.80.Jk, 47.40.Ki, 47.60.+i 相似文献
2.
A one-dimensional bulk reaction model for the oxidation of nickeltitanium is formulated, with preferential oxidation of titaniumbeing included. The modelling is directed at the better understandingof the dominant mechanisms involved in the oxidation processand their significance for the biocompatibility of the alloy.Two different regimes for the relative diffusivities of oxygenand the metals are investigated. By assuming fast bulk reactions,different asymptotic structures emerge in different parameterregimes and the resulting models take the form of moving boundaryproblems. Different profiles of nickel concentration are obtained:in particular a nickel-rich layer (observed in practice) ispresent below the oxide/metal interface for the case when oxygenand the metals diffuse at comparable rates. 相似文献
3.
A. E. Stuchbery C. E. Doran A. P. Byrne H. H. Bolotin G. D. Dracoulis 《Hyperfine Interactions》1987,36(1):75-96
Transient-field strengths were measured for52Cr ions traversing polarized Fe hosts at velocities up to 12υ0 (12υ0 =c/137 = Bohr velocity). The results are compared with predictions of various transient-field parametrizations and discussed
in terms of possible mechanisms by which polarization might be transferred from the Fe host to inner vacancies of the moving
Cr ions. Theg-factor of the first 2+ state of52Cr was also measured by the transient-field technique and found to be in accord with shell model calculations. 相似文献
4.
5.
The use of temporary tethers in facilitating meta photocycloaddition reactions between phenol and allyl alcohol derivatives has been investigated. The merits of silicon, carbonate and methylene acetal tethers were assessed, whilst considering strategies for the preparation of the natural products gymnomitrol and gelsemine. The photoadducts were epoxidised, and then subjected to acid catalysed fragmentation with concomitant cleavage of the tether. Depending on whether water or methanol was used during the fragmentation stage of the methylene tethers, the methylene group was either removed altogether or transformed into a MOM group. 相似文献
6.
Declan J. Maher 《Tetrahedron letters》2004,45(6):1301-1305
It has been shown that catalytic amounts (20-40 mol %) of bis-aryl (thio)ureas greatly accelerate the DABCO-promoted Baylis-Hillman reaction between a range of aromatic aldehydes and methyl acrylate in the absence of solvent. These robust organocatalysts are superior mole per mole promoters of the reaction than either methanol or water and are recoverable in high yield after the reaction by column chromatography. 相似文献
7.
Roucoules V Fail CA Schofield WC Teare DO Badyal JP 《Langmuir : the ACS journal of surfaces and colloids》2005,21(4):1412-1415
A substrate-independent method has been devised for ring formation at solid surfaces. This entails the aminolysis reaction of allylamine with maleic anhydride pulsed plasma polymer films to yield terminal alkene groups at the surface. Subsequent exposure to 1,3-cyclohexadiene leads to a Diels-Alder type (4 + 2) cycloaddition reaction to give a mixture of endo- and exo-bicyclo[2.2.2]oct-2-ene rings. 相似文献
8.
The super-macromolecular complex, succinate:quinone oxidoreductase (SQR, Complex II, succinate dehydrogenase) couples the oxidation of succinate in the matrix / cytoplasm to the reduction of quinone in the membrane. This function directly connects the Krebs cycle and the aerobic respiratory chain. Until the recent first report of the structure of SQR from Escherichia coli (E. coli) the structure-function relationships in SQR have been inferred from the structures of the homologous QFR, which catalyses the same reaction in the opposite direction. The structure of SQR from E. coli, analogous to the mitochondrial respiratory Complex II, has provided new insight into SQR's molecular design and mechanism, revealing the electron transport pathway through the enzyme. Comparison of the structures of SQR, QFR and other related flavoproteins shows how common amino acid residues at the interface of two domains facilitate the inter-conversion of succinate and fumarate. Additionally, the structure has provided a possible explanation as to why certain organisms utilise both SQR and QFR despite the fact that both can catalyse the inter-conversion of succinate and fumarate, in vitro and in vivo. Here we review how this structure has advanced our knowledge of this important enzyme and compare the structural information to other members of the Complex II superfamily and related flavoproteins. 相似文献
9.
The carbobenzyloxy (cbz) protecting group is evaluated for it's potential to enhance the resolution of chiral amine enantiomers using high-performance liquid chromatography (HPLC) and supercritical fluid chromatography (SFC). A series of cbz derivatives of commercially available racemates was prepared and analyzed by enantioselective chromatography using a variety of mobile phases and polysaccharide and Pirkle-type chiral stationary phases (CSPs). The cbz-derivatized product consistently demonstrated enhanced chiral resolution under HPLC and SFC conditions. Improved selectivity and resolution combined with an automated preparative HPLC or SFC system can lead to the rapid generation of highly purified enantiomers of desirable starting materials, intermediates or final products. 相似文献
10.
L. Kosta V. Ravnik A. R. Byrne J. Štirn M. Dermelj P. Stegnar 《Journal of Radioanalytical and Nuclear Chemistry》1978,44(2):317-332
A number of investigations of trace elements in the waters, organisms and sediments of the Adriatic, using neutron activation
analysis with radiochemical, separations are reported. These include studies of Hg in mussels from the Northern Adriatic,
of Hg and Se in edible animals from the Rijeka region, and of seven elements (As, Cd, Cu, Hg, Mn, Se and Zn) in marine invertebrates
from the Slovene coast. Additionally, plankton, sediment cores and water samples were taken from a grid of stations covering
the whole Adriatic and analyzed for 6 to 11 of the trace elements As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Sb and Zn (Hg only in water).
Generally, levels found were not indicative of pollution as compared with oceanic samples, but some evidence of locally increased
levels was found, especially for Hg. The levels of eleven trace elements in three marine Intercomparison samples prepared
by the IAEA Monaco Laboratory are also presented. 相似文献