Big Chemical Encyclopedia

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

Articles Figures Tables About

Quenching distortions

An advantage of pack carburizing is that the charcoal pack supports the workload which minimizes distortion. However, the components must be removed from the pack for quenching, or the mass cooled to room temperature and then the components reaustenitized and quenched. [Pg.217]

Quenching. After solution treatment, the product is generally cooled to room temperature at such a rate to retain essentially all of the solute in solution. The central portions of thicker products caimot be cooled at a sufficient rate to prevent extensive precipitation in some alloys. Moreover, some forgings and castings are dehberately cooled slowly to minimize distortion and residual stress produced by differential cooling in different portions of the products. Cold water, either by immersion or by sprays, is the most commonly used cooling medium. Hot water or a solution of a polymer in cold water is used when the highest rates are not desired. Dilute Al—Mg—Si and Al—Mg—Zn extmsions can be effectively solution heat treated by the extmsion process therefore, they may be quenched at the extmsion press by either air or water. [Pg.123]

Rapid cooling can cause residual stresses (leading to accelerated corrosion), distortion and quench cracks. The orientation of the component during processing is important in this respect. Sustained high temperatures can cause warping and softening. [Pg.51]

Another point of view is that exciplex formation can in some cases involve bonding changes in the acceptor. Solomon, Steel, and Weller 104 proposed that the quenching by quadricyclene leads to an exciplex where the quadricyclene is distorted. [Pg.158]

It has been important to determine if the neoxanthin distortion signature could be detected during the nonphotochemical quenching in vivo. Resonance Raman measurements on leaves and chlo-roplasts of various Arabidopsis mutants have revealed a small increase in the 950 cm 1 region. The relationship between the amplitude of this transition and the amount of NPQ suggests that the LHCII aggregation may be the sole cause of the protective chlorophyll fluorescence quenching in vivo (Ruban et al., 2007). [Pg.127]

Recall that we are assuming faem "C faff (°r fax, if turbulent flow). Anyone who has carefully observed a laminar diffusion flame - preferably one with little soot, e.g. burning a small amount of alcohol, say, in a whiskey glass of Sambucca - can perceive of a thin flame (sheet) of blue incandescence from CH radicals or some yellow from heated soot in the reaction zone. As in the premixed flame (laminar deflagration), this flame is of the order of 1 mm in thickness. A quenched candle flame produced by the insertion of a metal screen would also reveal this thin yellow (soot) luminous cup-shaped sheet of flame. Although wind or turbulence would distort and convolute this flame sheet, locally its structure would be preserved provided that faem fax. As a consequence of the fast chemical kinetics time, we can idealize the flame sheet as an infinitessimal sheet. The reaction then occurs at y = yf in our one dimensional model. [Pg.244]

Figure 6 illustrates a more complicated situation. The sample was a plain iron-carbon steel—an iron foil carburized to about 5 atomic % carbon and then quenched. One sees a rather complex pattern. There is a large central peak from some untransformed high temperature face-centered phase of iron containing carbon in solid solution, retained austenite. There is a strong six-line pattern coming from martensite, a distorted body-centered solid solution of carbon in iron. We also see a... [Pg.30]

An apparent decrease in the emission quantum yield and/or distortion of the band shape due to the reabsorption of emitted radiation. If such an effect is not corrected or compensated for, results of an emission experiment may prove to be incorrect. This is especially true in fluorescence quenching experiments conducted to evaluate the stoichiometry and affinity of ligand binding. 2. In a light irradiation experiment, the absorption of incident radiation by a species or molecular entity other than the intended primary absorber. See Fluorescence... [Pg.367]


See other pages where Quenching distortions is mentioned: [Pg.110]    [Pg.110]    [Pg.328]    [Pg.237]    [Pg.54]    [Pg.138]    [Pg.388]    [Pg.390]    [Pg.391]    [Pg.397]    [Pg.117]    [Pg.334]    [Pg.122]    [Pg.533]    [Pg.330]    [Pg.530]    [Pg.1288]    [Pg.87]    [Pg.539]    [Pg.212]    [Pg.6]    [Pg.123]    [Pg.305]    [Pg.13]    [Pg.126]    [Pg.126]    [Pg.127]    [Pg.98]    [Pg.99]    [Pg.101]    [Pg.111]    [Pg.121]    [Pg.115]    [Pg.115]    [Pg.223]    [Pg.323]    [Pg.302]    [Pg.545]    [Pg.64]    [Pg.66]    [Pg.92]    [Pg.210]    [Pg.50]    [Pg.6]   
See also in sourсe #XX -- [ Pg.9 ]




SEARCH



Jahn-Teller distortion, spin-orbit quenching

© 2024 chempedia.info