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Patterson’s equation

Furthermore, Helfferich (1962) gives Patterson s equation, which can be used as an approximation ... [Pg.277]

Use Patterson s equation to model the kinetic data. Furthermore, propose a design for the agitated batch reactor. [Pg.298]

Equation (8.47), with t = 0 and the composition of lead from meteoritic troilite used for the initial isotopic ratio of lead, was used by Clair Patterson (1955,1956) to determine the age of the Earth. In the 1950s, the largest uncertainty in determining the age of the Earth was the composition of primordial lead. In 1953, Patterson solved this problem by using state-of-the-art analytical techniques to measure the composition of lead from troilite (FeS) in iron meteorites. Troilite has an extremely low U/Pb ratio because uranium was separated from the lead in troilite at near the time of solar-system formation. Patterson (1955) then measured the composition of lead from stony meteorites. In 1956, he demonstrated that the data from stony meteorites, iron meteorites, and terrestrial oceanic sediments all fell on the same isochron (Fig. 8.20). He interpreted the isochron age (4.55+0.07 Ga) as the age of the Earth and of the meteorites. The value for the age of the Earth has remained essentially unchanged since Patterson s determination, although the age of the solar system has been pushed back by —20 Myr. [Pg.270]

Even Davisson and Germer s first work on the reflection of slow electrons by crystal lattices made it clear that the facts could not be accurately represented by equations (3) and (5) on the contrary, definite deviations from Bragg s law of reflection occur. These were first explained by Patterson as being due to a diminution of the distance between the lattice planes at the surface. Bethe has shown, however, that better agreement with experiment is obtained by expressing the action of the crystal on the electrons by means of a mean lattice potential V. Schrodinger s equation for the de Broglie waves with an internal lattice potential is then... [Pg.35]

Many scientists thought that Earth must have formed as long as 3.3 billion years ago, but their evidence was confusing and inconsistent. They knew that some of the lead on Earth was primordial, i.e., it dated from the time the planet formed. But they also understood that some lead had formed later from the radioactive decay of uranium and thorium. Different isotopes of uranium decay at different rates into two distinctive forms or isotopes of lead lead-206 and lead-207. In addition, radioactive thorium decays into lead-208. Thus, far from being static, the isotopic composition of lead on Earth was dynamic and constantly changing, and the various proportions of lead isotopes over hundreds of millions of years in different regions of the planet were keys to dating Earth s past. A comparison of the ratio of various lead isotopes in Earth s crust today with the ratio of lead isotopes in meteorites formed at the same time as the solar system would establish Earth s age. Early twentieth century physicists had worked out the equation for the planet s age, but they could not solve it because they did not know the isotopic composition of Earth s primordial lead. Once that number was measured, it could be inserted into the equation and blip, as Patterson put it, out would come the age of the Earth. ... [Pg.170]

Another method used to evaluate the ultrasonic velocity is the Flory statistical theory, which, as it happens, has no direct link with ultrasonic velocity. Patterson and Rastogi (1970) have used this theory to calculate a characteristic surface tension using appropriately defined characteristic pressure and temperature. Equation 3.47 can then be used to calculate s. [Pg.51]

The perturbed-hard-ehain (PHC) theory developed by Prausnitz and coworkers in the late 1970s was the first successful application of thermodynamic perturbation theory to polymer systems. Sinee Wertheim s perturbation theory of polymerization was formulated about 10 years later, PHC theory combines results fi om hard-sphere equations of simple liquids with the eoneept of density-dependent external degrees of fi eedom in the Prigogine-Flory-Patterson model for taking into account the chain character of real polymeric fluids. For the hard-sphere reference equation the result derived by Carnahan and Starling was applied, as this expression is a good approximation for low-molecular hard-sphere fluids. For the attractive perturbation term, a modified Alder s fourth-order perturbation result for square-well fluids was chosen. Its constants were refitted to the thermodynamic equilibrium data of pure methane. The final equation of state reads ... [Pg.208]

All our discussion of theories of polymer surface tensions up to now has relied ultimately on the van der Waals theory in conjunction with some equation of state. There is, however, another possible approach, which starts out from a principle of corresponding states, as was first applied to polymers by Patterson and Rastogi (1970). We start by assuming spherical molecules interacting via an attractive potential, which is described by the depth of the energy minimum (s ) and a hard core or impenetrable radius (r ). The partition function is written in terms of variables scaled by the characteristic energy and length scale and thus all physical properties can be described in terms of these scaled variables. Clear corollaries with the equation of state... [Pg.41]

P(x) is the radial distribution function (RDF) as introduced in Section I.I.2.I.4. It is the product of electronic densities attached to two points of the real space separated by vector x, with x being the distance between a pair of atoms in a set of atoms arranged disorderly. P(x) is thus a probability it is a generalization of the Patterson function of a crystal [10]. It corresponds to the Fourier transform of I(s). Reciprocally to Equation (1.8),... [Pg.9]


See other pages where Patterson’s equation is mentioned: [Pg.49]    [Pg.16]    [Pg.203]    [Pg.266]    [Pg.475]    [Pg.129]    [Pg.153]    [Pg.117]    [Pg.125]    [Pg.43]    [Pg.149]    [Pg.81]    [Pg.517]    [Pg.604]    [Pg.41]    [Pg.183]    [Pg.156]    [Pg.209]    [Pg.118]    [Pg.200]    [Pg.231]    [Pg.175]    [Pg.209]    [Pg.70]    [Pg.111]    [Pg.280]    [Pg.42]    [Pg.1319]    [Pg.607]    [Pg.231]   
See also in sourсe #XX -- [ Pg.277 , Pg.282 ]

See also in sourсe #XX -- [ Pg.277 , Pg.282 ]




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Patterson

Patterson equation

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