Big Chemical Encyclopedia

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

Articles Figures Tables About

Intensity of bonds

The characteristic opening size or pore size, O95, and the pore-size distribution of a non-woven geotextile are determined not only by the quantity of the fibres forming the web and the intensity of bonding used, but also by the fibre diameter, or diameters, and their orientation in the web. Various mathematical models for pore-size prediction have been derived based largely on the open spaces viewed normal to the plane of the deposited web layers. [Pg.284]

Figure 25. Effect of exposing the originai giass surface to moisture, (a) bond angle distributions before and after exposnre to water, (b) difference between intensity of bond angle distribution before and after exposure Note loss of intensity at bond angles less than 140°. Figure 25. Effect of exposing the originai giass surface to moisture, (a) bond angle distributions before and after exposnre to water, (b) difference between intensity of bond angle distribution before and after exposure Note loss of intensity at bond angles less than 140°.
To obtain spacings between atomic layers and bond lengdis or angles between atoms, it is necessary to measure and analyse the intensity of diffraction spots. This is analogous to measuring the intensity of XRD reflections. [Pg.1770]

Intensive use of cross-terms is important in force fields designed to predict vibrational spectra, whereas for the calculation of molecular structure only a limited set of cross-terms was found to be necessary. For the above-mentioned example, the coupling of bond-stretching (f and / and angle-bending (B) within a water molecule (see Figure 7-1.3, top left) can be calculated according to Eq. (30). [Pg.348]

The vibration frequencies of C-H bond are noticeably higher for gaseous thiazole than for its dilute solutions in carbon tetrachloride or tor liquid samples (Table 1-27). The molar extinction coefficient and especially the integrated intensity of the same peaks decrease dramatically with dilution (203). Inversely, the y(C(2jH) and y(C(5(H) frequencies are lower for gaseous thiazole than for its solutions, and still lower than for liquid samples (cf. Table 1-27). [Pg.61]

Molar absorptivity (Section 13 21) Ameasure of the intensity of a peak usually in UV VIS spectroscopy Molecular dipole moment (Section 1 11) The overall mea sured dipole moment of a molecule It can be calculated as the resultant (or vector sum) of all the individual bond di pole moments... [Pg.1288]

As discussed earlier in Section lOC.l, ultraviolet, visible and infrared absorption bands result from the absorption of electromagnetic radiation by specific valence electrons or bonds. The energy at which the absorption occurs, as well as the intensity of the absorption, is determined by the chemical environment of the absorbing moiety. Eor example, benzene has several ultraviolet absorption bands due to 7t —> 71 transitions. The position and intensity of two of these bands, 203.5 nm (8 = 7400) and 254 nm (8 = 204), are very sensitive to substitution. Eor benzoic acid, in which a carboxylic acid group replaces one of the aromatic hydrogens, the... [Pg.402]

The main area of interest for plasticizers in PET is in the area of dyeing. Due to its lack of hydrogen bonds PET is relatively difficult to dye. Plasticizers used in this process can increase the speed and intensity of the dyeing process. The compounds used, however, tend to be of low molecular weight since high volatiHty is required to enable rapid removal of plasticizer from the product (see Dye carriers). [Pg.129]

Signal assignment is then no problem the C atoms whieh are bonded to the nitro groups C-2,6 and C-4 are elearly distinguishable in the C NMR speetrum by the intensities of their signals. [Pg.193]

The vibrational motions of the chemically bound constituents of matter have fre-quencies in the infrared regime. The oscillations induced by certain vibrational modes provide a means for matter to couple with an impinging beam of infrared electromagnetic radiation and to exchange energy with it when the frequencies are in resonance. In the infrared experiment, the intensity of a beam of infrared radiation is measured before (Iq) and after (7) it interacts with the sample as a function of light frequency, w[. A plot of I/Iq versus frequency is the infrared spectrum. The identities, surrounding environments, and concentrations of the chemical bonds that are present can be determined. [Pg.32]


See other pages where Intensity of bonds is mentioned: [Pg.320]    [Pg.396]    [Pg.313]    [Pg.218]    [Pg.618]    [Pg.100]    [Pg.320]    [Pg.396]    [Pg.313]    [Pg.218]    [Pg.618]    [Pg.100]    [Pg.308]    [Pg.1119]    [Pg.1150]    [Pg.1460]    [Pg.81]    [Pg.1130]    [Pg.158]    [Pg.470]    [Pg.49]    [Pg.258]    [Pg.250]    [Pg.130]    [Pg.147]    [Pg.22]    [Pg.491]    [Pg.543]    [Pg.97]    [Pg.383]    [Pg.324]    [Pg.19]    [Pg.22]    [Pg.16]    [Pg.143]    [Pg.80]    [Pg.311]    [Pg.51]    [Pg.219]    [Pg.18]    [Pg.228]    [Pg.236]    [Pg.237]   
See also in sourсe #XX -- [ Pg.218 ]




SEARCH



© 2024 chempedia.info