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Absolute magnetic susceptibility

An empirical temperature scale is based on some arbitrary physical property (such as density, electrical resistance, magnetic susceptibility, etc.) that changes in a way that is continuous and single valued. The ITS-90 temperature scale described in Appendix 2 is an empirical scale that is designed to closely approximate the absolute (ideal gas) temperature scale. [Pg.58]

In summary, it is non-trivial to implement magnetic resonance pulse sequences which allow us to monitor unambiguously the decrease in absolute concentration of reactant species and associated increase in product species, but measures of relative concentrations from which conversion and selectivity are calculated are much easier to obtain. However, if such measurements are to be deemed quantitative the spectra must be free of (or at least corrected for) relaxation time and magnetic susceptibility effects. [Pg.591]

The function (a) is known as the Langevin function, after Paul Langevin, French physicist (1872-1946). The magnetic susceptibility of a paramagnetic substance can be expressed as (jim(B/kT). where fim is the magnetic moment, (S the magnetic flux, k the B and T die absolute temperature. [Pg.246]

Figure 7 The original plot of magnetic susceptibility versus log absolute temperature (T / K) for CuCl under 5 kbar pressure. Reference 26. Figure 7 The original plot of magnetic susceptibility versus log absolute temperature (T / K) for CuCl under 5 kbar pressure. Reference 26.
Figure 19 A plot of the magnetic susceptibility (black circles) and the relative resistance (black triangles) as a function of absolute temperature (T/K) for LiQ gTi2 204. From Reference 20. Figure 19 A plot of the magnetic susceptibility (black circles) and the relative resistance (black triangles) as a function of absolute temperature (T/K) for LiQ gTi2 204. From Reference 20.
JFiq. X-l.—Curves showing the reciprocal of molar magnetic susceptibility of compounds of cobalt(II) as a function of the absolute temperature. [Pg.614]

At the end of this section on the relationship between the electronic properties and the stereochemistry of complexes of the copper(II) ion, it is worth summarizing the most useful physical techniques which offer a criterion for the presence of a polynuclear copper(II) complex rather than a mononuclear complex. These are (i) magnetic susceptibility measurements down to near absolute zero, for the determination of O or / values (ii) ESR spectra of magnetically dilute systems, in the solid state or in solution, to obtain hyperfine data and (iii) cyclic voltammetry to show evidence for a one-step reduction process in a Cu2 species. [Pg.690]

CURIE-WEISS LAW. The transition from ferromagnetic to paramagnetic properties, which occurs in iron and other ferromagnetic substances at the Curie point, is accompanied by a change in the relationship of Ihe magnetic susceptibility lo the temperature. P. Curie stated in 1895 that above this point the susceptibility varies inversely as the absolute temperature. But this was found in be not generally true, and was modified in 1907 by P. Weiss to stare that the susceptibility uf a paramagnetic substance above the Curie point varies inversely as the excess of the temperature above that point. At or below the Curie point, the Curie-Weiss law does not hold. [Pg.463]

The contribution to the absolute chemical shift from the magnetic susceptibility of a sample is given by the following equation [17] ... [Pg.138]

It should be apparent that the magnetic susceptibility x of a paramagnetic sample (corrected for diamagnetism) should be infinite at absolute zero (with perfect alignment of the magnetic dipoles, or 100% population of the lowest Zeeman state) and zero at infinite temperature (random alignment of dipoles, equal population of Zeeman states). An obvious expression which embodies these conditions is ... [Pg.73]

Fig. 34. Inverse magnetic susceptibility vs. absolute temperature for several samples Ro jCao sMuOj compared with LaMnOj and LaojBaojMnC, alter Goodenough and Zhou (1998). Fig. 34. Inverse magnetic susceptibility vs. absolute temperature for several samples Ro jCao sMuOj compared with LaMnOj and LaojBaojMnC, alter Goodenough and Zhou (1998).
The absolute values of the differential magnetic susceptibilities were measured for samples of different shape in the critical range of magnetic fields and angles Under the conditions of magnetic stratification, the magnitudes of the susceptibilities appeared to be close to those expected... [Pg.76]

Figure 2. Magnetic susceptibility (y) and resistivity (p) of the bilayer hydrate as a function of absolute temperature T. Figure 2. Magnetic susceptibility (y) and resistivity (p) of the bilayer hydrate as a function of absolute temperature T.
Static H Multiple Quantum (MQ) NMR spectroscopy, on the other hand, has shown the ability to more reliably quantitatively characterize elastomer network structure and heterogeneities (14-19). H MQ NMR methods allow for the measurement of absolute residual dipolar couplings (cooperative dynamics without interference from magnetic susceptibility and field gradients which complicate relaxation measurements (13, 14, 20,21). It has previously been shown that the residual dipolar couplings are directly related to the dynamic order parameter, Sb, and the crosslink density (1/N)(P) ... [Pg.197]

Curie law. The magnetic susceptibility of a paramagnetic substance varies inversely as the absolute temperature. [Pg.353]

Photoelectron spectroscopy and measurements of the specific heat and magnetic susceptibility are methods available to gain information about the DOS. In disordered systems, the former gives electron-distribution curves (EDC) reflecting the band density of states [5.61]. Whereas the UPS-method reveals the shape of the DOS and hardly gives the absolute value of the density of states, specific heat as well as susceptibility measurements, on the other hand, give only N(EF). [Pg.182]


See other pages where Absolute magnetic susceptibility is mentioned: [Pg.247]    [Pg.671]    [Pg.230]    [Pg.522]    [Pg.400]    [Pg.491]    [Pg.604]    [Pg.41]    [Pg.383]    [Pg.759]    [Pg.199]    [Pg.23]    [Pg.657]    [Pg.138]    [Pg.157]    [Pg.97]    [Pg.73]    [Pg.77]    [Pg.78]    [Pg.604]    [Pg.12]    [Pg.103]    [Pg.7]    [Pg.318]    [Pg.267]    [Pg.2498]    [Pg.97]    [Pg.172]    [Pg.24]    [Pg.205]    [Pg.56]    [Pg.286]    [Pg.114]    [Pg.117]   
See also in sourсe #XX -- [ Pg.491 ]




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