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71.
Densities, refractive indices and dynamic viscosities of binary and ternary mixtures composed of isopropyl acetate, isopropanol, 1-octyl-3-methyl-imidazolium bis(trifluoromethylsulfonyl)imide ([C8mim][NTf2]) have been determined at 298.15 K and atmospheric pressure. The excess molar volumes and dynamic viscosity changes of mixing have been calculated and correlated using the Redlich–Kister polynomial equation. Isobaric vapour–liquid equilibrium (VLE) data have been determined experimentally for these binary and ternary systems at 101.32 kPa. The equilibrium data have been adequately correlated by means of Wilson, NRTL, and UNIQUAC equations for the liquid phase activity coefficient.  相似文献   
72.
This study deals with some microstructural and crystallographic aspects of the thermally induced transformation of goethite (α-FeOOH) into hematite (α-Fe2O3), occurring at about 300 °C. Powder specimens of goethite have been annealed in air at different temperatures, ranging from 200 °C up to 1,000 °C. The resulting products have been analyzed for a complete characterization of the changes brought about by the thermal treatments, using a multianalytical approach, based on: thermogravimetry, differential thermal analysis, transmission electron microscopy, Raman spectroscopy, and X-ray diffraction. At lower temperatures, the transition to hematite produces no important changes in size and shape of the original goethite grains. Recrystallization, and partial sintering, occurs only at temperatures in excess of 800 °C. The relevant evolution of pores present in both phases has been also considered, as it may provide important indications on the actual formation mechanism of hematite.  相似文献   
73.
Lipopeptide biosurfactants produced by the Bacillus licheniformis V9T14 strain showed an interesting anti‐adhesion activity against biofilm formation of human pathogenic bacterial strains. The chemical characterisation of the crude extract of V9T14 strain was first developed through electrospray ionisation mass spectrometry (ESI‐MS) and ESI‐MS/MS direct infusions: two sets of molecular ion species belonging to the fengycin and surfactin families were revealed and their structures defined, interpreting their product ion spectra. The LC/ESI‐MS analysis of the crude extract allowed to separate in different chromatogram ranges the homologues and the isoforms of the two lipopeptide families. The extract was then fractionated by silica gel chromatography in two main fractions, I and II. The purified biosurfactants were analysed through a new, rapid and suitable LC/ESI‐MS/MS method, which allowed characterising the composition and the structures of the produced lipopeptides. LC/ESI‐MS/MS analysis of fraction I showed the presence of C13, C14 and C15 surfactin homologues, whose structures were confirmed by the product ion spectra of the sodiated molecules [M + Na]+ at m/z 1030, 1044 and 1058. LC/ESI‐MS/MS analysis of fraction II confirmed the presence of two main fengycin isoforms, with the protonated molecules [M + H]+ at m/z 1478 and 1506 corresponding to C17 fengycin A and C17 fengycin B, respectively. Other homologues (C14 to C16) were revealed and confirmed as belonging to fengycin A or B according to the retention times and the product ions generated, although with the same nominal mass. Finally, a relative percentage content of each homologue for both lipopeptides families in the whole extract was proposed. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   
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The mineral inclusions of two orange glass tesserae from paleo-Christian mosaics were investigated in order to derive the melting temperature reached during their production (sourced from Padua and Vicenza, Veneto region, Italy). In particular, clinopyroxene crystals were studied by single-crystal X-ray diffraction and electron microprobe WDS analysis. The crystals show C2/c symmetry, typical of disordered Ca/Na and Mg/Al distributions indicating high-temperature of formation (>700°C). The cation site populations were obtained by combining results from the two experimental techniques enabled us to derive the following stoichiometric formula:
lM2[Ca0.819Na0.172Mn0.006K0.003]M1[Mg0.765Fe3+0.210   Cu0.015Ti0.006Zn0.006]T[Si1.933Al0.037Sn0.024]O6\begin{array}{l}{}^{M2}[\mathrm{Ca}_{0.819}\mathrm{Na}_{0.172}\mathrm{Mn}_{0.006}\mathrm{K}_{0.003}]{}^{M1}[\mathrm{Mg}_{0.765}\mathrm{Fe}^{3+}_{0.210}\\[3pt]\quad{}\mathrm{Cu}_{0.015}\mathrm{Ti}_{0.006}\mathrm{Zn}_{0.006}]{}^{T}[\mathrm{Si}_{1.933}\mathrm{Al}_{0.037}\mathrm{Sn}_{0.024}]\mathrm{O}_{6}\end{array}  相似文献   
77.
The optical frequency sweep of an actively linearized, ultrabroadband, chirped laser source is characterized through optical heterodyne detection against a fiber-laser frequency comb. Frequency sweeps were measured over approximately 5 THz bandwidths from 1530 nm to 1570 nm. The dominant deviation from linearity resulted from the nonzero dispersion of the fiber delay used as a reference for the sweep linearization. Removing the low-order dispersion effects, the residual sweep nonlinearity was less than 60 kHz rms, corresponding to a constant chirp with less than 15 ppb deviation across the 5 THz sweep.  相似文献   
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79.
We provide details for the proof of Fujita's second theorem and prove that for a Kähler fibre space f:X→Bf:XB over a smooth projective curve B  , the direct image of the relative dualizing sheaf V:=f?ωX/BV:=f?ωX/B is the direct sum of an ample and a unitary flat bundle. We also show that V needs not be semiample, which is our main result.  相似文献   
80.
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