Big Chemical Encyclopedia

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

Articles Figures Tables About

Particle intensity

The specimen intensity transform X is a type of convolution product of the particle intensity transform Ip and the particle orientation density function ( 1,2). The procedure that we have used to simulate Ip involves firstly the calculation of the intensity transform for an infinite particle, with appropriate allowances for random fluctuations in atomic positions and for matrix scattering. A mapping of Xp is then carried out which includes the effects of finite particle dimensions and of intraparticle lattice disorder, if this is present. A mapping of Is is then obtained from Tp by incorporating the effects of imperfect particle orientation. [Pg.62]

Crystalline Particles. Usually, one of the unit cell edges is preferentially oriented parallel to the fiber axis and the particle intensity transform corresponds to a single-crystal rotation pattern and the reflections are confined to layer lines spaced at intervals of Z/o where a is the dimension of the unit cell parallel to the fiber axis (3). [Pg.62]

The cylindrically averaged particle intensity transform is obtained by evaluating... [Pg.63]

Figure 2. Intensity transforms for points uniformly distributed on a helix with radius r = 4.5 A, unit height h = 3 A, and unit twist t = 108°. (a) Particle intensity transform for p = 500 A (b) particle intensity transform for p = 100 A (c) specimen intensity transform for p = 100A,ao = 3°. Figure 2. Intensity transforms for points uniformly distributed on a helix with radius r = 4.5 A, unit height h = 3 A, and unit twist t = 108°. (a) Particle intensity transform for p = 500 A (b) particle intensity transform for p = 100 A (c) specimen intensity transform for p = 100A,ao = 3°.
The first problem area occurs at a 7 for I2°/6° ratio for weakly absorbing particles where, as exemplified by Figure I, an "S in the characteristic curve precludes a unique determination of a for a measured intensity ratio of 0.5. This results in an uncertainty of about 20% in determined diameter, roughly the same as that from index-of-refraction effects discussed above. In fact, the uniqueness problem adds no new uncertainties since the S phenomenon is covered by the uncertainty band introduced when the absorbing particle intensity ratio curve is assumed to be caused by unknown particle composition. Conversely, this problem must be dealt with when analyzing nonabsorbing particles of a known composition, for instance in a study of cooling tower droplet size distributions. [Pg.202]

HIV-P is a symmetrical homodimer of identical 99 residue monomers, structurally and mechanistically similar to the pseudosymmet-ric pepsin family of proteases (92-94), whose members include renin. Because the protease is a minor component of the virion particle, intensive structural studies required overproduction through recombinant DNA methods. One of the first structures was determined with material synthesized nonbiologically (through peptide synthesis). As of June 2002, there were over 100 X-ray structures repre-... [Pg.433]

In an ideal scattering experiment the collisions are assumed to occur at a fixed point in space. In practice the collision volume is finite and the part viewed by the detecting system generally depends on the scattering angle. Care must therefore be taken in relating the scattered particle intensity to the cross section. [Pg.17]

Experimental evidence for the existence of intrinsic precursor states is rather more difficult to come by. The common observation that the initial sticking probability, s0, often decreases with increaing substrate temperature is consistent with the existence of such a state, as discussed here. Indirect evidence is also provided by molecular beam studies, for example, Hayward and Walters [401] (for H2 on W 001 ) and Engel [402] (for 02 on Pd 111 ) have observed scattered particle intensity distributions which, even at a fractional coverage in the chemisorbed layer close to zero, exhibit a strong directional lobe in the specular direction superimposed on a cosine law distribution. The specular lobe clearly contains molecules scattered at the first collision, while the cosine law component is most readily attributed to the particles which are trapped in the precursor state and then scattered back into the gas phase. Of... [Pg.63]

FiG. S.13. Plot of relative particle intensities for H, D, and T versus EdEldx in a two-detector telescc, where the first detector records d /dr and the second E. [Pg.215]

At increase in speed of movement larger nanoparticle absorbs smaller, and the uniform nanoparticle (3,4) is formed. At further increase in speed of movement of nanoparticles, owing to blow, the smaller particle intensively takes root in big and destroys it. [Pg.275]

Another way to quantify the intensity of a beam of radiation is to measure the particle intensity Ip, which is defined as the particle flux solid angle A72 of the beam. The subscript p stands for particle . The particle flux itself is measured by counting... [Pg.15]

Particle intensity 7p = A p/A72 (Time times solid angle)" (second times steradian)" l/(ssr)... [Pg.16]

Another way to quantify the intensity of a beam of radiation is to measure the particle intensity 7p, which is defined as the particle flux

solid angle A12 of the beam. The subscript p stands for particle . The particle flux <7>p itself is measured by counting the number of particles per unit time in the beam in the case of a light beam, for example, the particles are photons. The corresponding SI unit for the particle flux is seconds" (1/s). The quantity particle intensity 7p therefore has the dimensions of number per time per solid angle the corresponding derived SI unit for the particle intensity 7p is seconds" times steradian h/(ssr)). [Pg.18]


See other pages where Particle intensity is mentioned: [Pg.136]    [Pg.330]    [Pg.63]    [Pg.66]    [Pg.33]    [Pg.322]    [Pg.324]    [Pg.1057]    [Pg.1064]    [Pg.2857]    [Pg.15]    [Pg.123]    [Pg.124]    [Pg.639]    [Pg.642]    [Pg.170]    [Pg.198]    [Pg.74]    [Pg.435]   
See also in sourсe #XX -- [ Pg.7 ]

See also in sourсe #XX -- [ Pg.7 ]




SEARCH



© 2024 chempedia.info