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Cross-section of collisions

In another limiting case of highly inertial particles, it is possible to assume that particles move along straight trajectories. Then the cross section of collision can be found from simple geometrical arguments ... [Pg.288]

Since in the case considered the direction Eq is parallel to g Oo = 0), the cross section of collision represents a circle of radius d. Shown in Fig. 13.4 is the dependence of dimensionless radius of collision cross section d/Ri on parameter of electro-hydrodynamic interaction S2 and the ratio of drop radiuses k = R2/R1. The collision cross section grows with k and S2. [Pg.400]

Fig. 13.12 Dependence of the radius of cross section of collision of a small charged drop with a big uncharged drop on N2 for /c = 0.1 ... Fig. 13.12 Dependence of the radius of cross section of collision of a small charged drop with a big uncharged drop on N2 for /c = 0.1 ...
Explaining the cross sections of collisions and the photoabsorption spectra of molecules is fundamental to understand the properties of materials, but it is even more important to be able to manipulate and control these properties. In traditional chemistry, this is achieved by adjusting external parameters such as temperature, pressure, concentration, solvent, or by adding catalysts. A higher selectivity and precision could be obtained by a systematic use of lasers. In addition, the latter can offer the possibility to control quantum effects such as quantum coherence. In traditional chemistry, the quantum states involved in the chemical process are, in general, populated in a incoherent way described as a mixed state in quanmm statistical mechanics. The systematic use of laser pulses to induce chemical process opens the possibility to create coherent superpositions of the same quantum states, what is called a pure state in quantum statistical mechanics. Such coherent superpositions might drastically increase the efficiency and the control of... [Pg.15]

Figure 8.12 shows evaluated (ADO) cross section of collisions of Ar+ with H2, CH4 and NH3 as a function of kinetic energy. At low energy, the interaction is defined by charge-dipole interaction and the cross section is many times larger than hard-sphere cross section. Under these conditions, the difference in collision cross sections of atomic and polyatomic ions of the same charge and mass is diminished. [Pg.359]

Figure B3.3.13. Intersecting stacking faults in a fee crystal at the impact plane induced by collision with a momentum mirror for a square cross section of side 100 unit cells. The shock wave has advanced half way to the rear ( 250 planes). Atom shading indicates potential energy. Thanks are due to B Holian for tliis figure. Figure B3.3.13. Intersecting stacking faults in a fee crystal at the impact plane induced by collision with a momentum mirror for a square cross section of side 100 unit cells. The shock wave has advanced half way to the rear ( 250 planes). Atom shading indicates potential energy. Thanks are due to B Holian for tliis figure.
At low energies the abstraction process dominates and at higher energies the exchange mechanism becomes more important. The cross-sections for the two processes crossing at 10 eV. The END calculations yield absolute cross-sections that show the same trend as the experimentally determined relative cross-sections for the two processes. The theory predicts that a substantial fraction of the abstraction product NHjD, which are excited above the dissociation threshold for an N—H bond actually dissociates to NH2D" + H or NH3 during the almost 50-ps travel from the collision chamber to the detector, and thus affects the measured relative cross-sections of the two processes. [Pg.237]

The cross-section of 7-changing collisions found in Eq. (3.44) is sufficient for conversion of any gas density value to the quantity... [Pg.108]

Tusa J., Sulkes M., Rice S. A. Very low energy cross sections for collision-induced rotational relaxation of I2 seeded in a supersonic free jet, Proc. Natl. Acad. Sci. USA 77, 2367-9 (1980). [Pg.289]

Figure 10. Comparison of the velocity dependence of the disappearance cross-section of CHa+, formation cross-section of CH0 +, and Langevin orbiting collision cross-section, all as a function of reciprocal average kinetic energy of ions in the mass spectrometer source... Figure 10. Comparison of the velocity dependence of the disappearance cross-section of CHa+, formation cross-section of CH0 +, and Langevin orbiting collision cross-section, all as a function of reciprocal average kinetic energy of ions in the mass spectrometer source...
Figure 11. Ratio of experimental values of formation cross-section of CH0 + to calculated Langevin cross-section for collision of CH + with CH as a function of average ion kinetic energy... Figure 11. Ratio of experimental values of formation cross-section of CH0 + to calculated Langevin cross-section for collision of CH + with CH as a function of average ion kinetic energy...
Some of the rate constants discussed above are summarized in Table VI. The uncertainties (often very large) in these rate constants have already been indicated. Most of the rate constants have preexponential factors somewhat greater than the corresponding factors for neutral species reactions, which agrees with theory. At 2000°K. for two molecules each of mass 20 atomic units and a collision cross-section of 15 A2, simple bimolecular collision theory gives a pre-exponential factor of 3 X 10-10 cm.3 molecule-1 sec.-1... [Pg.318]

However, other data such as the small difference observed in the Si NMR chemical shift (0.9 ppm upheld from TgPhg) and the absence of any measurable Si-F coupling show that the interaction between the huoride ion and the silicon atoms is small. Studies to evaluate the collision cross section of TgPhg using Na show that the cation attaches itself to the outside of the POSS cage and does not significantly distort the structure. [Pg.33]

The cross section of the collision region that the particle impacts with the Si surface with an incident angle of 45° at a speed of 2,100 m/s is shown in Fig. 16 [28]. As the particle impacts into the Si surface layer, the contact region of the Si surface layer transforms from crystal into amorphous phase immediately. The area of the depressed region and the thickness of the amorphous layer increase with the penetration depth of the particle (Figs. 16(a)-16(c)). After it reaches the deepest position, the particle then moves both upwards and rightwards, and some silicon atoms ahead of the particle are extruded out and result in a pileup of atoms. Then the released elastic deformation energy of the Si surface pushes... [Pg.242]

The relaxation of gaseous methane, ethane and propane is by the spin-rotation mechanism and each pure component can be correlated with density and temperature [15]. However, the relaxation rate is also a function of the collision cross section of each component and this must be taken into account for mixtures [16]. This is in contrast to the liquid hydrocarbons and their mixtures that relax by dipole-dipole interactions and thus correlate with the viscosity/temperature ratio. [Pg.325]

FIGURE 4.5 Inelastic collision cross section of water vapor versus electron energy (LaVerne and Mozumder, 1992). Circles compilation of Hayashi (1989) dashed line unmodified theoretical formula (Pimblott et al., 1990) dot-dashed line theoretical formula scaled to match compilation full curve theoretical formula scaled to match experimental W values. [Pg.110]

Figure 4. The experimental [50] total and three-state resolved differential cross-sections of vibrational excitations of the water molecule in collisions with 46-eV protons. Figure 4. The experimental [50] total and three-state resolved differential cross-sections of vibrational excitations of the water molecule in collisions with 46-eV protons.

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See also in sourсe #XX -- [ Pg.80 , Pg.92 ]




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