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Working capillary tubes

In this section we present the system of quasi-one-dimensional equations, describing the unsteady flow in the heated capillary tube. They are valid for flows with weakly curved meniscus when the ratio of its depth to curvature radius is sufficiently small. The detailed description of a quasi-one-dimensional model of capillary flow with distinct meniscus, as well as the estimation conditions of its application for calculation of thermohydrodynamic characteristics of two-phase flow in a heated capillary are presented in the works by Peles et al. (2000,2001) and Yarin et al. (2002). In this model the set of equations including the mass, momentum and energy balances is ... [Pg.440]

The experimental set-up used for porous chromatography is virtually identical, to that used for HDC as described elsewhere (i6,1T). The use of stainless steel columns for the LEG work required 3l6 stainless steel column end-fittings and l/l6 O.D. capillary tubing. [Pg.7]

Working capillary tubing requires a slightly different technique from the working of normal tubing. This is principally due to the small bore of the tube and the very thick walls. Generally speaking it is necessary to use a smaller, hotter flame for capillary than would be... [Pg.39]

Since fluid shear rates vary enormously across the radius of a capillary tube, this type of instrument is perhaps not well suited to the quantitative study of thixotropy. For this purpose, rotational instruments with a very small clearance between the cup and bob are usually excellent. They enable the determination of hysteresis loops on a shear-stress-shear-rate diagram, the shapes of which may be taken as quantitative measures of the degree of thixotropy (G3). Since the applicability of such loops to equipment design has not yet been shown, and since even their theoretical value is disputed by other rheologists (L4), they are not discussed here. These factors tend to indicate that the experimental study of flow of thixotropic materials in pipes might constitute the most direct approach to this problem, since theoretical work on thixotropy appears to be reasonably far from application. Preliminary estimates of the experimental approach may be taken from the one paper available on flow of thixotropic fluids in pipes (A4). In addition, a recent contribution by Schultz-Grunow (S6) has presented an empirical procedure for correlation of unsteady state flow phenomena in rotational viscometers which can perhaps be extended to this problem in pipe lines. [Pg.143]

High-Performance Liquid Chromatography. A Varian 5060 delivery system was used for this work with detection by UV absorption. Either a Varian UV-50 variable wavelength detector or a Hewlett Packard 1040A scanning diode array detector was used. All HPLC columns were packed in our laboratory (10) with 5-/um particle size Spherisorb-ODS, Spherisorb-CN (Phase Separations), or 8-pm particle size Zorbax-CN (Dupont Ltd). HPLC columns (20 or 25 cm X 4.6 mm i.d.) were coupled via short lengths of stainless steel capillary tubing (5 cm X 0.25 mm i.d.). Separation conditions were as follows ... [Pg.641]

Experimental methods presented in the literature may prove of value in combustion studies of both solid and liquid suspensions. Such suspensions include the common liquid spray. Uniform droplets can be produced by aerosol generators, spinning disks, vibrating capillary tubes, and other techniques. Mechanical, physicochemical, optical, and electrical means are available for determination of droplet size and distribution. The size distribution, aggregation, and electrical properties of suspended particles are discussed as well as their flow and metering characteristics. The study of continuous fuel sprays includes both analytical and experimental procedures. Rayleigh s work on liquid jet breakup is reviewed and its subsequent verification and limitations are shown. [Pg.137]

Two types of columns are used. A packed column is one filled with inert, solid particles coated with a liquid stationary phase. Standard tubing is about 0.5 cm in diameter, with lengths ranging from 1 m to 20 m however, columns for large-scale preparative work may be up to 5 cm in diameter and several meters long. Commonly used solid supports are diatomaceous earth, Teflon powder, and glass beads. The stationary liquid must be chosen on the basis of the compounds to be analyzed. A more recently developed and more widely used type of column is the open-tubular or capillary column. This is prepared by coating the inner wall of the column with the stationary liquid phase. The inside diameter of a typical capillary tube is 0.25 mm, and... [Pg.65]

Volatile reactive liquids present few problems since they generally can be distilled from the vacuum line into a tube equipped with a serum bottle cap (Fig. 9.26). Nitrogen is then admitted to the tube, and the sample is taken with a syringe. Another scheme involves an inlet with a capillary tube or ampule breaker.33 35 This method is potentially useful for vacuum line work, since it is relatively simple to fill and seal off a sample tube attached to the vacuum line. [Pg.104]

Figure 7.11 illustrates a suitable apparatus for studying electro-osmotic flow through a porous plug. Reversible working electrodes are used to avoid gas evolution. A closed system is employed, the electro-osmotic flow rate being determined by measuring the velocity of an air bubble in a capillary tube (c. 1 mm diameter) which provides a return path for the electrolyte solution. [Pg.198]


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Capillary tubes

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