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Absorption Dynamics

The approximate differential equation used for calculation of reaction and mass transfer rate is given below[85] [Pg.93]

Absorption involves separation of a solute from gas phase to liquid phase. Absorption can involve reactions also. Batch absorption equipment is used to find reaction rate constants and mass transfer coefficients by measuring concentration changes for the liquid composition with respect to time. [Pg.94]

Sg surface area of gas bubbfes per volume of liquid [length [Pg.94]


Where a number of properties are relevant to a product the testing may be carried out with a sequence of tests without superimposing any ageing. Where environmental effects have to be accounted for they are applied separately and the rig tests repeated. An example of this approach is artificial sports surfaces where such characteristics as ball bounce, energy absorption, dynamic stiffness and spike resistance are measured using specifically developed rigs. [Pg.53]

McKim, J. Schmieder, P. Veith, G. 1985, Absorption dynamics of organic cherrrrcal transport across trout gills as related to rx tanol-water partition coefficient. Toxicol. Appl. PharrrL 77 1-10. [Pg.165]

Fig. 1. The transient absorption dynamics of nitrate in neutral aqueous solution 3. RESULTS AND DISCUSSION... Fig. 1. The transient absorption dynamics of nitrate in neutral aqueous solution 3. RESULTS AND DISCUSSION...
Fig. 2. The transient absorption dynamics of aqueous nitrate at a. [Ft] = 10 7 M and b. [Ft] = 0.140 M. Notice that the time scale is linear from 0-10 ps, while it is logarithmic from 10-100 ps. Fig. 2. The transient absorption dynamics of aqueous nitrate at a. [Ft] = 10 7 M and b. [Ft] = 0.140 M. Notice that the time scale is linear from 0-10 ps, while it is logarithmic from 10-100 ps.
Figure 11.9 Normalised comparison of electron absorption dynamics of N3-sensitised Ti02 films in ethylene/propylene carbonates (1 1) following excitation at different wavelengths. Inset the same data plotted on a shorter time scale. The solid lines are fits using the two-state injection model. The fast component is well described by a <100 fs rise and the slow component is fitted by a stretched exponential function with a 50 ps time constant. Reproduced with permission from J. Phys. Chem. B 107, 7376 (2003) (Asbury et al, 2003). Copyright 2003 American Chemical Society. Figure 11.9 Normalised comparison of electron absorption dynamics of N3-sensitised Ti02 films in ethylene/propylene carbonates (1 1) following excitation at different wavelengths. Inset the same data plotted on a shorter time scale. The solid lines are fits using the two-state injection model. The fast component is well described by a <100 fs rise and the slow component is fitted by a stretched exponential function with a 50 ps time constant. Reproduced with permission from J. Phys. Chem. B 107, 7376 (2003) (Asbury et al, 2003). Copyright 2003 American Chemical Society.
The various ultrafast reaction techniques have inevitably been used in a number of the reported investigations on dyes. A study of the saturation absorption dynamics of a cyanovinyldiethylamine dye has yielded a measured lifetime of 3 1 ps, a value which is determined by very rapid internal conversion of the Sj state. ... [Pg.17]

The time-dependent absorption dynamics of photogenerated electrons in water is a basic study for the understanding of the whole range of charge transfer effects. Missmer and Simon have compared various models for this system using published data for this fs time range process. [Pg.15]

FIGURE 1.25 Ultrafast transient absorption dynamics of MEH-PPV in different environments probed at 800 nm after excitation at 490 nm, normalized to the same intensity at time 0. All four curves (solution, film, VVV, and VHH) were taken under identical excitation conditions. (Source Ref. [35].)... [Pg.22]

J. Scholkopf, P. A. C. Gane, The moment ink contacts the surface a fresh look at the absorption dynamic into coated paper. Das Papier, 2004-T26pp. [Pg.382]

Figure 8.1 Ultrafast transient absorption dynamics, (a) Positive-going signal is the absorption of charge carriers which is affected by the amount of solvent additive (DIO). Negative-going features are the photobleaching signals of the neutral donor molecule, and are unaffected by solvent additives, (b) Qualitative charge transfer timescales obtained by fitting the traces of panel (a) with a model which accounts for a pulse width of 100 fs. Reproduced from ref. 10. Copyright 2012 American Chemical Society. Figure 8.1 Ultrafast transient absorption dynamics, (a) Positive-going signal is the absorption of charge carriers which is affected by the amount of solvent additive (DIO). Negative-going features are the photobleaching signals of the neutral donor molecule, and are unaffected by solvent additives, (b) Qualitative charge transfer timescales obtained by fitting the traces of panel (a) with a model which accounts for a pulse width of 100 fs. Reproduced from ref. 10. Copyright 2012 American Chemical Society.

See other pages where Absorption Dynamics is mentioned: [Pg.36]    [Pg.104]    [Pg.376]    [Pg.437]    [Pg.546]    [Pg.18]    [Pg.148]    [Pg.338]    [Pg.376]    [Pg.437]    [Pg.546]    [Pg.112]    [Pg.87]    [Pg.4520]    [Pg.75]    [Pg.85]    [Pg.149]    [Pg.93]    [Pg.93]    [Pg.513]    [Pg.168]    [Pg.173]   


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