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The Milne-Thomson circle theorem is extended to give a simplegeneral expression for the image system in an elliptical cylinderintroduced into an otherwise specified unbounded potential flowwhich contains no singularities in the region to be occupiedby the ellipse. This image system is used to obtain an expressionfor the corresponding source-sink surface singularity distributionon the ellipse, thus providing new benchmark test cases forsource-sink solutions as obtained numerically by a panel method.Several typical examples are given to illustrate the generaltheoretical approach.  相似文献   
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Cellulose powder was found to be a substrate favoring the deposition of calcite crystals from stable supersaturated solutions at pH 8.50 and at 25 degrees C. Kinetic analysis of the initial rates showed that they were proportional with the relative supersaturation with respect to calcite. Analysis of the dependence of the induction periods on the initial solution conditions showed that the number of ions forming the critical nucleus was 5. The second-order dependence of the rate of precipitation of calcite on cellulose on the solution supersaturation suggested a surface controlled mechanism. The surface energy of the calcite nuclei growing on cellulose was calculated to be 46 mJ m(-2) from the dependence of the induction time on the solution supersaturation. The overgrowth of calcite on cellulose was done selectively on the macromolecules possibly through active sites formation at ionizable functional groups (-OH). The nucleating capability of cellulose was found to be comparable with that of sulfonated polystyrene and significantly lower in comparison with sulfonated polystyrene divinyl benzene copolymer on which vaterite was formed. This fact together with the selective growth of the most stable calcite suggested that stereochemical factors are very important in determining both the kinetics and the nature of the polymorph formed. Copyright 2000 Academic Press.  相似文献   
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The effect of L-serine in supersaturated solutions of calcium phosphate was investigated under plethostatic conditions. The rates of crystal growth measured in the presence of L-serine at relatively high concentrations and in the range between 2x10(-3) and 1x10(-2) mol dm(-3) were appreciably reduced. The inhibitory effect of L-serine was found to be due to blocking of a portion of the active growth sites by adsorption. Kinetics measurements in the presence of L-serine as well as adsorption isotherm analysis suggested Langmuir-type adsorption of L-serine on the surface of hydroxyapatite (HAP) with a relatively low affinity for the substrate. Adsorption experiments showed that at pH 7.4 considerable adsorption of L-serine onto HAP takes place, whereas at pH 10.0 the adsorption was negligible, suggesting that electrostatic interactions are dominant. Attraction between the positively charged protonated amino group of the L-serine molecule and the negatively charged HAP surface contributed largely to the adsorption. This was corroborated by the fact that, in the presence of L-serine in the solution, a significant shift of zeta-potential of the HAP particles to less negative values was found at pH values close to 7.4. At pH values higher than 10.0 essentially no shift of zeta-potential takes place. On the basis of the experimental results, a model was proposed according to which L-serine absorbs on the surface of HAP through electrostatic attractions exerted between one negative site of the HAP surface, i.e., phosphate or hydroxyl ion, and the positively charged protonated amino group of one L-serine molecule, forming a surface ion pair. Copyright 2001 Academic Press.  相似文献   
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