Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Mechanical velocity

Mossbauer spectra are usually recorded in transmission geometry, whereby the sample, representing the absorber, contains the stable Mossbauer isotope, i.e., it is not radioactive. A scheme of a typical spectrometer setup is depicted in Fig. 3.1. The radioactive Mossbauer source is attached to the electro-mechanical velocity transducer, or Mossbauer drive, which is moved in a controlled manner for the modulation of the emitted y-radiation by the Doppler effect. The Mossbauer drive is powered by the electronic drive control unit according to a reference voltage (Fr), provided by the digital function generator. Most Mossbauer spectrometers are operated in constant-acceleration mode, in which the drive velocity is linearly swept up and down, either in a saw-tooth or in a triangular mode. In either case. [Pg.25]

The quantum-mechanical ionization cross section is derived using one of several approximations—for example, the Born, Ochkur, two-state, or semi-classical approximations—and numerical computations (Mott and Massey, 1965). In some cases, a binary encounter approximation proves useful, which means that scattering between the incident particle and individual electrons is considered classically, followed by averaging over the quantum-mechanical velocity distribution of the electrons in the atom (Gryzinski, 1965a-c). However, Born s approximation is the most widely used one. This is discussed in the following paragraphs. [Pg.95]

Cross-section curves ) obtained in this way constitute probably the most reliable and most detailed experimental information on total ionization cross sections available at present. It is available for the Pgl systems He(2 5)-Ar,Kr,Xe,N2 and He(23S)-Ar,Kr,Xe,N2.34 Unnormalized cross-section curves arel(t>) are available for the systems He(21S ) Hg,Ba He(23S)-Hg,Ba Ne(3/>20)-Hg and ArC -Hg34 44. Cross-section curves directly measured on an absolute scale, using a mechanical velocity selector, are available for the systems Ne( 2/3) -Ar,Kr,Xe 45 As examples, we show cross-section curves for He(2 S), He(235)-Ar, He(2 S), He(23S)-Hg, and Ne -Kr in Figs. 6 to 8. In Fig. 8 results of the TOF method34 are compared with results using mechanical velocity selection 45 For the system He(23S)-Ar, it is shown in Fig. 9 that the temperature... [Pg.428]

In MD, a force field is used to calculate the forces on each atom of the simulated system. Then, following Newtonian mechanics, velocities and accelerations are calculated, and the atoms are slightly moved with respect to a given time step. Introducing molecular dynamics and force fields is clearly beyond the scope of this chapter, so we refer the reader to earlier reviews in this book series.118-123 However, some aspects of docking based on MD simulations should be briefly mentioned. [Pg.16]

The intensity of signal transmitted to the detector is greatly improved by using time-of-flight methods instead of mechanical velocity selectors. The beam of product molecules is chopped into a sequence of short pulses and the molecules then travel a known distance before being detected. The time-of-arrival spectrum at the detector gives the velocity distribution of the products [30]. This method of velocity analysis is now widely used in studies of crossed-beam reactions [111]. [Pg.373]

For the reactions K + HBr and K + DBr, the KBr recoil energy distribution has been determined in a crossed-molecular beam experiment using a mechanical velocity selector. No difference was found in the form of the translational energy distributions for the two reactions for which a value of 0.30 may be derived. Although all the angular momentum appears in the product rotation, the moments of inertia for the alkali halides are large, which implies that the mean product rotational energy is quite small ( 0.21, 0.21 and 0.09 for K, Rb, Cs + HBr, respectively [3] these values are derived from the rotational temperatures obtained by electric deflection analysis). [Pg.410]

To see more fringes we have to increase the coherence length and therefore decrease the velocity spread. For this purpose we employ a mechanical velocity selector, as shown after the oven in Fig. 1. It consists of four slotted disks that rotate around a common axis. The first disk chops the fullerene beam. Only those molecules are transmitted which traverse the distance from one disk to the next in the same time that the disks rotate from one open slot to the next. Although two disks would suffice for this purpose, the additional disks decrease the velocity spread even further and help to eliminate velocity sidebands. By varying the rotation frequency of the selector, the desired velocity class of the transmitted molecules can be adjusted. To measure the time of flight distribution we chopped the fullerene beam with the chopper right behind the source (see Fig. 1). The selection is of course accompanied by a significant loss in count rate, but we can still retain about 7% of the unselected molecules. [Pg.337]

The reaction of K with HBr was reinvestigated by Beck et ai [23] using a mechanical velocity selector to obtain nearly monoenergetic K beams. (If was the maximum in a narrow band of selected velocities, at half... [Pg.118]

The laser spectroscopic techniques provide much more detailed information about the state-dependent velocity distribution than measurements with mechanical velocity selectors. Note that in Fig. 4.13 not only Up(Na2) > t p(Na) but the velocity distribution of the Na2 molecules differs for different vibration-rotation levels (v, J). This is due to the fact that molecules are being formed by stabilizing collisions during the adiabatic expansion. Molecules in lower states have suffered more collisions with atoms of the cold bath. Their distribution n(v) becomes narrower and their most probable velocity Vp more closely approaches the flow velocity u. [Pg.195]

In the continuous-scan mode, a Michelson interferometer generates modulation of the radiation at each wavenumber v with a frequency F = 2Vv, where V is the mechanical velocity of the scanning mirror in centimeters per second. The frequency F is called the Fourier frequency. A typical speed of the scanning mirror is 0.1-10 cm s so that signals within the IR spectral region fall into the 10 -10" -Hz range. Since in most measurement schemes a low-pass filter is used to separate the Fourier and modulation frequencies, the modulation frequency should satisfy the sampling theorem. Specifically, the modulation rate... [Pg.376]

For a Michelson interferometer, the rate of change of retardation is twice the mechanical velocity of the mirror. This parameter is often known as the optical velocity, V, and has the units of centimeters (retardation) per second. Some FT-IR vendors specify the velocity of the moving mirror in their interferometer in terms of its mechanical velocity and some in terms of its optical velocity. Note Users should make sure which of these two parameters is in fact specified.) Still others specify the optical velocity in terms of the corresponding modulation frequency of the laser interferogram although a few commercial interferometers no longer use HeNe lasers, we will denote the frequency of the laser interferogram as /neNe-... [Pg.105]


See other pages where Mechanical velocity is mentioned: [Pg.214]    [Pg.16]    [Pg.86]    [Pg.48]    [Pg.153]    [Pg.157]    [Pg.13]    [Pg.11]    [Pg.347]    [Pg.52]    [Pg.1545]    [Pg.235]    [Pg.209]    [Pg.330]    [Pg.168]    [Pg.713]    [Pg.208]    [Pg.472]    [Pg.215]    [Pg.344]    [Pg.358]   
See also in sourсe #XX -- [ Pg.105 ]




SEARCH



© 2024 chempedia.info