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41.
For molecular imprinting of oxidatively electroactive analytes by electropolymerization, we used herein reductively electroactive functional monomers. As a proof of concept, we applied C60 fullerene adducts as such for the first time. For that, we derivatized C60 to bear either an uracil or an amide, or a carboxy addend for recognition of the adenosine-5′-triphosphate (ATP) oxidizable analyte with the ATP-templated molecularly imprinted polymer (MIP-ATP). Accordingly, the ATP complex with all of the functional monomers formed in solution was potentiodynamically electropolymerized to deposit an MIP-ATP film either on an Au electrode of the quartz crystal resonator or on a Pt disk electrode for the piezoelectric microgravimetry (PM) or capacitive impedimetry (CI) determination of ATP, respectively, under the flow-injection analysis (FIA) conditions. The apparent imprinting factor for ATP was ∼4.0. After extraction of the ATP template, analytical performance of the resulting chemosensors, including detectability, sensitivity, and selectivity, was characterized. The limit of detection was 0.3 and 0.03 mM ATP for the PM and CI chemosensor, respectively. The MIP-ATP film discriminated structural analogues of ATP quite well. The Langmuir, Freundlich, and Langmuir–Freundlich isotherms were fitted to the experimental data of the ATP sorption and sorption stability constants appeared to be nearly independent of the adopted sorption model.  相似文献   
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Measurements of solar radiation in the millimetre and submillimetre spectral range (100 m–10 mm) yield the variation of brightness temperature with wavelength and disk position. Such information imposes important constraints on models of the structure of the solar chromosphere. This paper reviews the observational data and discusses the models derived from them.Review paper presented at the Symposium on Millimetre and Sub-millimetre Wave Research in Australia, Canberra, September 12th–14th, 1983.  相似文献   
49.
Alkali metals absorbed into silica gel yield three stages of unique loose black powders (M-SG) that are strong reducing agents. All react nearly quantitatively with water to form hydrogen. Liquid Na-K alloys form air-sensitive powders at room temperature that can be converted at 150 degrees C to a form that is sensitive to moisture but not to dry air. Slowly heating sodium and silica gel to 400 degrees C yields a third type that can be handled in ambient air with only slow degradation by atmospheric moisture. These materials eliminate many hazards associated with pure alkali metals and provide easily handled reducing agents and hydrogen sources. They could be used in continuous-flow reactors to reduce and protonate aromatics, dechlorinate alkyl and aryl halides, and desulfurize various compounds.  相似文献   
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Assessment of three regularization-based and two eddy-viscosity-based subgrid-scale (SGS) turbulence models for large eddy simulations (LES) are carried out in the context of magnetohydrodynamic (MHD) decaying homogeneous turbulence (DHT) with a Taylor scale Reynolds number (Reλ) of 120 and a MHD transition-to-turbulence Taylor-Green vortex (TGV) problems with a Reynolds number of 3000, through direct comparisons to direct numerical simulations (DNS). Simulations are conducted using the low-magnetic Reynolds number approximation (Rem<<1). LES predictions using the regularization-based Leray- α,LANS- α, and Clark- α SGS models, along with the eddy viscosity-based non-dynamic Smagorinsky and the dynamic Smagorinsky models are compared to in-house DNS for DHT and previous results for TGV. With regard to the regularization models, this work represents their first application to MHD turbulence. Analyses of turbulent kinetic energy decay rates, energy spectra, and vorticity fields made between the varying magnetic field cases demonstrated that the regularization models performed poorly compared to the eddy-viscosity models for all MHD cases, but the comparisons improved with increase in magnitude of magnetic field, due to a decrease in the population of SGS eddies within the flow field.  相似文献   
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