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Measurement of density

FIGURE 5-38 Density calibration results for two wedge materials, polyetherimide and aluminum. A wedge correction function of 4% is determined. [Pg.204]

Liquid Chemical Constituents Density, g/cm3 Longitudinal-Wave Phase Velocity, cm/usec [Pg.204]

FIGURE 5-39 Measured reflection coefficients as a function of viscosity with a polyetherimide wedge at two operating frequencies. [Pg.205]


Gas bubble separation time of petroleum oils NFT 60-149 ASTM D 3427 Time for air liberation after supersaturation (measurement of density)... [Pg.448]

Three frequently specified properties are density—specific gravity—API gravity, characterization factor, and sulfur content (2,6,7). The API (American Petroleum Institute) gravity is a measure of density or specific gravity (sp gr) ... [Pg.202]

Density. Measurement of density is widely used in the sugar industry to determine the sugar concentration of symps, Hquors, juices, and molasses. The instmment used is called a hydrometer or a spindle. When it is graduated in sucrose concentration (percent sucrose by weight), it is called a Brix hydrometer or a Brix spindle. Brix is defined as the percent of dry substance by hydrometry, using an instmment or table caUbrated in terms of percent sucrose by weight in water solution. Hydrometers are also graduated in °BaumH, stiU in use in some industries. The relationship between °BaumH and density, ing/cm, is °Baumn Baum e = 145(1 — 1/d). [Pg.10]

The principal methods for deterrnination of the deuterium content of hydrogen and water are based upon measurements of density, mass, or infrared spectra. Other methods are based on proton magnetic resonance techniques (77,78), F nuclear magnetic resonance (79), interferometry (80), osmometry (81), nuclear reaction (82), combustion (83), and falling drop methods (84). [Pg.8]

Shock-wave data have seen most applications in the measurement of density at high pressure. Other properties of compressed condensed materials whose measurements are discussed in this chapter include sound speed and temperature. Review articles by Grady (1977), Yakushev (1978), Davison and Graham (1979), Murri et al. (1974), Al tshuler (1965), and Miller and Ahrens (1991) summarize experimental techniques for measuring dynamic yielding. [Pg.75]

The °AP1 gravity measures the density of a hydrocarbon liquid. Specific gravity (SG) is another common measurement of density. The liquid SG is the relative weight of a volume of sample to the weight of the same volume of water at 60°F (15.5°C). [Pg.45]

Other methods for estimating the volume percentage of the interphases in a composition have been proposed, too, for example, measurements of density variations [76, 77], volume of compressed sample [78], the dielectric constant [77], etc. The important thing is that the interphase thickness determined in one way or another is an effective value dependent upon the conditions and type of the experiment by which it was determined [51]. [Pg.9]

CTP is a relatively recent development in acute stroke imaging that is already in routine clinical use in many centers. CTP and MRP are similar in that both techniques are based on rapid serial image acquisition during intravenous injection of a bolus of contrast material. In both techniques, measurements of density over time (for CTP) or signal intensity over time (for MRP) are converted to contrast agent-versus-time curves, and these are processed in similar ways to yield the same perfusion measurements (most often CBV, CBF, and MTT). Example CTP images are shown in Figure 2.12. [Pg.23]

Most measurements of densities of liquids below their normal boiling points are made in the presence of air. Densities reported here refer to liquids in equilibrium with a gas phase consisting of a mixture or air and vapor at a total pressure of one atmosphere below the normal boiling point and of vapor at the equilibrium vapor pressure above the boiling point. Thus air is not regarded as an impurity. [Pg.11]

The terms in Eq. (6) include the gravitational constant, g, the tube radius, R, the fluid viscosity, p, the solute concentration in the donor phase, C0, and the penetration depth, The density difference between the solution and solvent (ps - p0) is critical to the calculation of a. Thus, this method is dependent upon accurate measurement of density values and close temperature control, particularly when C0 represents a dilute solution. This method has been shown to be sensitive to different diffusion coefficients for various ionic species of citrate and phosphate [5], The variability of this method in terms of the coefficient of variation ranged from 19% for glycine to 2.9% for ortho-aminobenzoic acid. [Pg.107]

Tables 2.1 and 2.2 show that theory enables detonation velocities to be calculated in close agreement with those observed experimentally. This, unfortunately, is not a critical test of the theory as velocities when calculated are rather insensitive to the nature of the equation of state used. A better test would be to calculate the peak pressures, densities and temperatures encountered in detonation, and compare these with experimental results. The major difficulties here are experimental. Attempts to measure temperatures in the detonation zone have not been very successful, but better results have been obtained in the measurement of densities and pressures. Schall introduced density measurement by very short X-ray flash radiography and showed that TNT at an initial density of 1 -50 increased 22% in density in the detonation wave. More recently detonation pressures have been measured by Duff and Houston using a method (introduced by Goranson) in which the pressure is deduced from the velocity imparted to a metal plate placed at the end of the column of explosive. Using this method, for example, Deal obtains the detonation pressures for some military explosives recorded in Table 2.3. More... Tables 2.1 and 2.2 show that theory enables detonation velocities to be calculated in close agreement with those observed experimentally. This, unfortunately, is not a critical test of the theory as velocities when calculated are rather insensitive to the nature of the equation of state used. A better test would be to calculate the peak pressures, densities and temperatures encountered in detonation, and compare these with experimental results. The major difficulties here are experimental. Attempts to measure temperatures in the detonation zone have not been very successful, but better results have been obtained in the measurement of densities and pressures. Schall introduced density measurement by very short X-ray flash radiography and showed that TNT at an initial density of 1 -50 increased 22% in density in the detonation wave. More recently detonation pressures have been measured by Duff and Houston using a method (introduced by Goranson) in which the pressure is deduced from the velocity imparted to a metal plate placed at the end of the column of explosive. Using this method, for example, Deal obtains the detonation pressures for some military explosives recorded in Table 2.3. More...
Sola, M., J. Mestres, R. Carbo, and M. Duran. 1996. A Comparative Analysis by Means of Quantum Molecular Similarity Measures of Density Distributions Derived from Conventional ab initio and Density Functional Methods. J. Chem. Phys. 104, 636. [Pg.83]

The density of sugar syrups is used as a method of measuring the quantity of sugar present. Very accurate measurements of density are possible with the best equipment confectioners often use simple hygrometers. The available data give very accurate information relating density to sugar concentration. [Pg.18]

As a blast wave passes through the air or interacts with and loads a structure or target, rapid variations in pressure, density, temperature and particle velocity occur. The properties of blast waves which are usually defined are related both to the properties which can be easily measured or observed and to properties which can be correlated with blast damage patterns. It is relatively easy to measure shock front arrival times and velocities and entire time histories of overpressures. Measurement of density variations and time histories of particle velocity are more difficult, and few reliable measurements of temperature variations exist. [Pg.3]

Measurement of density is often a rapid and easily mastered technique. Different procedures are used for liquids, solids and gases. [Pg.62]

The general features of the model in which a shock, or at least a steep pressure and temperature rise, creates conditions for reaction and in which the subsequent energy release causes a drop in pressure and density have been verified by measurements in a detonation tube [18], Most of these experiments were measurements of density variation by x-ray absorption. The possible effect of reaction rates on this structure is depicted in Fig. 5.14 as well [19],... [Pg.296]

Density or specific gravity (relative density) is used whenever conversions must be made between mass (weight) and volume measurements. This property is often used in combination with other test results to predict oil quality, and several methods are available for measurement of density (or specific gravity). However, the density (specific gravity) (ASTM D1298 IP 160) is probably of... [Pg.271]

Blends of poly (ethylene terephthalate) (PETP) and polypropylene (PP) with different rheological properties were dry blended or compounded, and extrusion foamed using both physical blowing and chemical agents, and the foam properties compared with those of foam produced from the individual components in the absence of compatibilisers and rheology modifiers. The foams were characterised by measurement of density, cell size and thermal properties. Low density foam with a fine cell size was obtained by addition of a compatibiliser and a co-agent, and foamed using carbon dioxide. The presence of PP or a polyolefin-based compatibiliser did not effect... [Pg.45]

Kistiakowsky P.H. Kydd "The Measurement of Density Charges in Gaseous Detonations , 2nd ONRSympDeton (1955) and JChemPhys 25, 824... [Pg.726]

Side-Chain Chlorination of Toluene. Benzyl chloride, used mainly in the manufacture of plasticizers, may be prepared by the thermal or photochemical chlorination of toluene.191,192 In the thermal process chlorine is passed through toluene at 65-100°C. To minimize the formation of benzal chloride and benzotrichloride, the conversion is limited to about 50%. Since the density of the reaction mixture increases linearly with the formation of benzyl chloride,145 measurement of density is used to monitor the progress of the reaction. The overall yield based on toluene is about 90%, and the maximum conversion to benzyl chloride is above 70%. Higher yields in photochemical chlorination may be achieved. [Pg.594]

The molecular volume at the ordinary temperature13 is 111 c.c., and the ratio of this value to the sum of the atomic volumes of the constituent elements14 is 1-21. From measurements of density and coefficient of expansion at -194° C. the molecular volume at 0° Abs. has been calculated15 to be 76-1. The molecular weight determined by... [Pg.111]

The vapour density2 is 16-1 (air = l) corresponding to the molecular formula Asl3 (15-8), but the vapour, which is yellow, generally contains the products of thermal decomposition (see below). The heat of formation, according to Berthelot,3 is (As, 8lgas) 28,800 calories and (As, 3lsona) 12,600 calories. From measurements of density and coefficient of expansion at low temperatures the molecular volume at 0° Abs. has been calculated 4 to be 98-2, a value which corresponds with that similarly derived for the molecular volume of phosphorus triiodide. [Pg.118]

Most glasses can be made to crystallize if they are subjected io the right conditions of temperature and rate of cooling, which suggests that the glassy stale is like a supercooled liquid. This is not home out by measurements of density and other volume properties, which do not decrease in a linear manner as glass is cooled below its crystallization temperature. [Pg.723]

A preliminary step necessary to precise work with the pycnometer is the determination of its two volume constants that is, the constants of the linear equation expressing die capacity as a function of die temperature. This is done by filling with distilled water and weighing accurately several times at each of two temperatures near the ends of the range for which the pycnometer is to be used. The bottle form is also adapted to the precise measurement of densities of solids. See also Specific Gravity. [Pg.1382]

Higham, E. H., in Instrumentation Reference Book (ed. Noltingk, B. E.), Chapter 8, Measurement of density (Butterworths, London, 1988). [Pg.553]

Molecular refractivity. Molecular refractivity is an additive quantity which is often used to assist in determining molecular structures via the Lorentz-Lorentz equation. This generally gives good agreement between values derived from experimental measurements of density and refractive index and values... [Pg.85]

Nevertheless, it was decided to make the measurements of density and of refractive index for specimens after different times of curing. Since the molecular weight of the polymerized silane was not known, the molecular refractivity could not be calculated but only the ratio of this to the molecular weight. Nevertheless, interesting results were obtained with a linear relationship between the cure time and refractive index up to 18 h. The relationship between the cure time and the ratio of molecular refractivity to molecular weight is shown in Fig. 3 and indicates a steady increase in molecular complexity up to 24 h, when it approaches a constant value suggesting a final state of crosslinking. [Pg.86]

The ring-opening metathesis polymerization of dicyclopentadiene was monitored by ultrasonic spectroscopy.16 The thermoset poly(dicyclopentadiene) is formed by ringopening and cross-linking in a reaction injection molding system. A reaction cell with a plastic window was constructed for use with pulse echo ultrasonic spectroscopy. Realtime measurements of density, longitudinal velocity, acoustic modulus and attenuation were monitored. Reaction kinetics were successfully determined and monitored using this technique. [Pg.430]

Preliminary Measurements of Density, MOE, and MOR for Neat, Degradel, and Degrade2 Straw Stems Extruded at 75 wt% Straw Stems,... [Pg.92]

These are made from one piece of material and have no compensating added materials. They are required when a precise measurement of density must be made. These can be made of multiple materials for purposes of correcting the weight. This can be done by adding material or adding rings or hooks. The added material must not be able to separate from the weight. [Pg.139]


See other pages where Measurement of density is mentioned: [Pg.272]    [Pg.192]    [Pg.108]    [Pg.30]    [Pg.68]    [Pg.256]    [Pg.62]    [Pg.272]    [Pg.292]    [Pg.44]    [Pg.85]    [Pg.365]    [Pg.10]    [Pg.192]    [Pg.103]    [Pg.484]    [Pg.431]    [Pg.170]   
See also in sourсe #XX -- [ Pg.191 ]




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Density measuring

Density units of measurement

Effect of Solvent Used for Density Measurement

Indirect measurement of relative density by SPT testing

Indirect measurement of relative density by cone penetration testing

Measurement of Bulk Density

Measurement of Current Density and Coating Resistance

Measurement of Particle Density

Measurement of reference densities (minimum and maximum density)

Measuring the Density of Irregularly Shaped Solids

Measuring the Density of Liquids

Practical Hints on Measurement of Densities and Excess Molar Volumes

The measurement of density (specific gravity)

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