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11.
Juhani Riihentaus 《Mathematische Zeitschrift》1983,182(2):159-165
12.
Katja Lappalainen Mikko Manninen Ville Alopaeus Juhani Aittamaa John Dodds 《Transport in Porous Media》2009,77(1):17-40
Capillary pressure is considered in packed-beds of spherical particles. In the case of gas–liquid flows in packed-bed reactors,
capillary pressure gradients can have a significant influence on liquid distribution and, consequently, on the overall reactor
performance. In particular, capillary pressure is important for non-uniform liquid distribution, causing liquid spreading
as it flows down the packing. An analytical model for capillary pressure–saturation relation is developed for the pendular
and funicular regions and the factors affecting capillary pressure in the capillary region are discussed. The present model
is compared to the capillary pressure models of Grosser et al. (AIChE J., 34:1850–1860, 1988) and Attou and Ferschneider (Chem.
Eng. Sci., 55:491–511, 2000) and to the experiments of Dodds and Srivastava (Part Part Syst. Charact., 23:29–39, 2006) and
Dullien et al. (J. Colloid Interface Sci., 127:362–372, 1989). The non-homogeneity of real packings is considered through
particle size and porosity distributions. The model is based on the assumption that the particles are covered with a liquid
film, which provides hydrodynamic continuity. This makes the model more suitable for porous or rough particles than for non-porous
smooth particles. The main improvements of the present model are found in the pendular region, where the liquid dispersion
due to capillary pressure gradients is most significant. The model can be used to improve the hydrodynamic models (e.g., CFD
and cellular automata models) for packed-bed reactors, such as trickle-bed reactors, where gas, liquid, and solid phases are
present. Models for such reactors have become quite common lately (Sáez and Carbonell, AIChE J., 31:52–62, 1985; Holub et al.,
Chem. Eng. Sci, 47, 2343–2348, 1992; Attou et al., Chem. Eng. Sci., 54:785–802, 1999; Iliuta and Larachi, Chem. Eng. Sci.,
54:5039–5045, 1999, IJCRE 3:R4, 2005; Narasimhan et al., AIChE J., 48:2459–2474, 2002), but they still lack proper terms causing
liquid dispersion. 相似文献
13.
The structural similarities and differences between the original DOM and the eight size fractions separated were studied in detail with the pyrolysis technique in combination with gas chromatography and mass spectrometry (Py-GC-MS) using two alkylating reagents: TMAH (tetramethylammonium hydroxide), to find both esterified and free carboxylic acids; and TMAAc (tetramethylammonium acetate), to specify only free carboxylic acids. A statistical analysis of the original multidimensional TMAH and TMAAc pyrograms disclosed that the overall structural compositions of the five most important size fractions, accounting for 84% of the original DOM, greatly resembled each other. The remaining three minor size fractions were not classified as homogeneous associations, but they also contained the same total, covalently bound and free carboxylic acid species as the other size fractions and the original DOM mixture, thus representing some kind of intermediate forms. This fundamental outcome strongly supports the opinion that the native dissolved humic-like macromolecules resemble supramolecular associations of smaller molecular size moieties with similar structural functionalities. The concentrations of free aliphatic and aromatic dicarboxylic acids in the DOM solution were so low that their effects on the potential formation of multiply charged ions in electrospray ionization-MS (ESI-MS) studies are likely insignificant. 相似文献
14.
MR imaging of fatigue stress injuries to bones: intra- and interobserver agreement 总被引:11,自引:0,他引:11
Ahovuo JA Kiuru MJ Kinnunen JJ Haapamaki V Pihlajamaki HK 《Magnetic resonance imaging》2002,20(5):401-406
The aim of this study was to determine the validity of MR imaging (MRI) in the assessment of stress-related injuries to bone.MR images of 50 military recruits (8 females and 42 males; 18-27 (mean 20) years of age) were retrospectively evaluated twice for stress injuries to bone by 4 radiologists (2 musculoskeletal radiologists, 2 radiology residents). Coronal T1-weighed (T1W) and STIR images, as well as axial and coronal T2-weighted (T2W) fat-suppressed images were taken using a 1.0T scanner. Rates for sensitivity, specificity, and accuracy of MRI of the stress-related injuries were calculated. Intraobserver and interobserver agreement was determined with kappa statistics.Rates for MRI sensitivity were 27-96%, for specificity 65-100%, and for diagnostic accuracy 58-97%. Lowest rates were seen when reading T1W images and highest when reading STIR images. Readers showed moderate to excellent intraobserver agreement (kappa 0.75-0.95). Interobserver agreement was fair to excellent (kappa 0.41-0.91), and the lowest values were seen in the interpretation of T1W images. Normal findings could be differentiated from various grades of stress injury to bone.MRI is a valid means of revealing the presence of stress injuries to bone and their staging. Observer agreement is good to excellent when using T2W images and STIR images, while T1W images are of lesser value. 相似文献
15.
Sharp peaks were observed in the IR spectra of allyl alcohol dimers in the νOH and τOH regions in low-temperature Ar and N2 matrices. In Ar a peak at 3587 cm?1 was found to increase in intensity upon annealing and decrease upon IR irradiation; it is concluded that this peak is due to an OH...π interaction (of a cyclic structure) present in part of the dimers. This is the first time such an interaction and photoprocess have been found for an alcohol in matrices. Also a faster photo-process was found. Confomer changes in the monomers accompany the photoprocess in allyl alcohol dimers. 相似文献
16.
17.
A simple method of deformational correction for the N.M.R. spectral parameters of molecules dissolved in liquid crystals is described. The method is applicable to the different isotopically substituted derivatives of the molecules belonging to the cubic point groups. Its validity is verified for the dipolar and quadrupolar couplings observed in the molecules CH4, CD4 and CH3D dissolved in the liquid crystals Merck Phase IV, Merck ZLI 1167 and their mixtures. 相似文献
18.
Aquatic humic-type solutes were separated in parallel from the same fresh water source by four different procedures: non-ionic polymethyl methacrylate (DAX-8) and functional cross-linked polyvinylpyrrolidone (PVP) resins, functional diethylaminoethyl cellulose (DEAE) and tangential ultrafiltration completed with a weakly basic anion exchange resin (IRA-67). The similarity-dissimilarity between the quantities and qualities of the different humic samples is discussed, especially in the light of the original dissolved organic matter (DOM). During the past two decades, a significant progress has occurred in the aquatic humic research due to the so-called hydrophobic-hydrophilic properties possessed by certain non-ionic sorbing solids. As a result of many coincidences, it may be justifiable to examine critically the prevailing isolation techniques of aquatic humic solutes and to try to update their complicated definitions. For that reason, it is reasonable to summarize the leading principles of different isolation techniques in Section 1 of this article. The results of the present study strongly support the applicability of the PVP resin, alone or completed in sequence with a suitable non-ionic sorbing solid, for isolation of aquatic humic-type solutes from both quantitative and qualitative points of view. In certain cases, the DEAE cellulose gives a useful alternative for conventional sorbing solids in the isolation of the bulk of aquatic humic solutes. The base-catalyzed ester hydrolysis of the HM during the chromatographic isolation of the DOM seems to be relative minor. 相似文献
19.
Derivatives of 2-chloro-2′-deoxyadenosine ( 1a ) containing secondary 6-NH2 groups ( 5a-c ) or a 8-Br substituent ( 9 ) were synthesized. They were tested together with ring-modified congeners containing a pyrrolo[2,3-b]pyridine, pyrrolo[3,2-c]pyridine, or pyrazolo[3,4-d]pyrimidine ring system as inhibitors of various leukemic cell lines. Only the 8-Br derivatives 9 showed inhibitory activity, whereas the base-modified congeners were not active. Compound 1a was protonated at a pKa = 1.4 (2′-deoxyadenosine at pKa = 3.8). Protonation occurred at N(7) and not at N(1) as observed for dA. 相似文献
20.