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In many basins, hydrogen-emitting structures are now observed, but the estimation of the H2 flow leading to their formation remains poorly constrained since all data show that the H2 emissions are variable in space and time. We present here the data of a long-term monitoring campaign with a high density of permanent hydrogen detectors installed in 2 structures in the Minas Gerais State (Brazil). Results show that two kinds of signals are recorded, large sporadic pulses that affect the H2 content of the soil for one or two days and smaller ones, with a daily periodicity, that last 6 h and during which the near surface soil concentration usually does not exceed 200 ppm. This last signal is very regular in frequency, less in amount, and the daily maximum happens around noon or in the early afternoon. We interpret the large pulses as evidences of a deep hydrogen flux, leaking either from a reservoir located in the subsurface, from an aquifer which is degassing or, although it seems unlikely, directly from the H2 generation area.The time correlation between the pulse and the increase of the daily signal suggests that this last one corresponds to the slow release of the gas that has been captured by the soil during its transport towards the surface. This daily signal is most likely influenced by external factors such as atmospheric pressure and sub-surface bacterial activity. In map view, the lack of correlation between the highest hydrogen concentrations over time suggests that the soil is very heterogeneous and that preferential pathways exist. The results confirm that long-term monitoring, over a few months, is mandatory to catch a certain number of high pulses and so to have a better estimation of the real flow. Data also suggests that sensors with a large concentration range should be used (from 10 to several 104 ppm). Even if quantification of leakage doesn't help to quantify the subsurface reserves, these new data allow a more precise evaluation of the quantity of H2 released in surface by these structures, few hundred of kilo per day, and confirm the high H2 prospectivity of this basin.  相似文献   
2.
In order to check its possible acute toxicity, C60 was incorporated into living human phagocytes. It was observed that C60 has no influence on the survival of human leukocytes.  相似文献   
3.
Abstract

High amounts of micronized C60 have been injected intraperitoneally into Swiss mice. Until the fourteenth day, they were still alive without any behaviour trouble. C60 was well absorbed, and found localized in spleen and liver. Inside the liver, C60 was  相似文献   
4.
PURPOSE: Sulfanilamide was chosen as a model compound in order to gain insights on the stability hierarchy of drug polymorphs from structural and thermodynamic criteria. Despite numerous studies, disagreements remained on the reported enthalpies associated with the mutual interconvertions of the alpha-, beta-, and gamma-forms of sulfanilamide. Therefore, the unambiguous determination of these enthalpies was the purpose of this work. METHODS: Samples, free of solvent inclusions and made of only one form, were prepared, and analyzed combining X-ray powder diffraction and Differential Scanning Calorimetry (DSC). RESULTS: The enthalpy values associated with the alpha- to gamma- and beta- to gamma-transitions were found to be + 10.2 and + 10.9 J g-1, respectively. The calculated enthalpy of the beta- to alpha-transition is consistent with the experimental one (+ 1 J g-1). CONCLUSIONS: The monotropy of the alpha-form was ascertained over the explored temperature range at ordinary pressure.  相似文献   
5.
Cultured human monocytes have been incubated with powdered cubic [60] fullerene. No modification has been observed with [60] fullerene when compared with negative control (monocytes alone).  相似文献   
6.
At room temperature, the hexagonal C60. 2(CH3)CCl3 solvate (a = 10.13(1) Å, c = 10.84(1) Å), made of alternating layers of C60 and solvent molecules, forms with a negative excess volume, and its desolvation enthalpy is virtually the same as the sublimation enthalpy of the pure solvent. Crystallographic and calorimetric studies vs temperature indicate that hexagonal C60. 2(CH3)CCl3 changes at 211.7 K (1.3 kJ mol−1 of solvate) into an intermediate triclinic phase which transforms at 189.7 K (4.1 kJ mol−1 of solvate) into another triclinic phase.A crystallographic analysis in the series of hexagonal C60. 2 YCCl3 solvates (Y = H, Cl, Br, CH3) reveals that: (i) the change in the unit-cell volume values is due to a change in axis c whose value depends on the size of Y, (ii) the molar volume of the solvates depends linearly on the molar volume of the solvents.Ageing studies at room temperature show that C60. 2(CH3)CCl3 loses its solvent molecules within a few days or a few months, depending on storage conditions.  相似文献   
7.
The pseudo-binary system AgI-BiI3 has been studied by differential thermal analysis (DTA) and by microcalorimetry. An eutectic point was found at 389°C for the composition BiI3 : 85 mol.BiI3 p.cent. Two new solid solutions have been discovered. Their existence has been confirmed by X-ray diffraction.  相似文献   
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