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Reduction without Phase Change

The reduction of the heat transfer coefficient ratio using a limiting resistance described above is very powerful but must be used with care. It is not valid for all situations. It is most likely valid when one resistance is for a boiling liquid or condensing steam and the other resistance is for a liquid or gas without phase change. In other situations, the base-case ratio can be determined from Equation 17.8 only if the relative magnitude for each resistance is known for the base case, as is illustrated in Example 17.4. [Pg.563]

In the test period Feb.—April 84, in which the temperature of the slurry in the tanks was lower than 7°C, during the first 2 months (it in creased to 17°-18°C only during the final phase), changes in the parameters under observation were less marked, except in the tank where aeration had been carried out. In this predominantly winteiy testing period, further reductions in the various parameters were observed after the tanks had been filled. The C.O.D. for example was reduced by 20% in the tank without treatment by 30% in the one with agitation and by 50% in the aerated tank. [Pg.279]

In addition to the productivity, the stability of the working oxide is a key issue. Ideally, the cycle possesses unlimited repeatability without loss of performance and capacity [4]. This requirement implies that the working oxide must not be trapped in an inactive form as a consequence of high-temperature reduction and oxidation by C02- Scenarios accounting for deactivation are phase changes, for example the formation of more dense phases with lower gas diffusivity, or the formation of mixed oxides by the reaction with surrounding insulation materials. These are usually less prone to thermal reduction or possess unfavorable material properties. [Pg.406]

Several findings in the above results are not consistent with earlier reports (Yoshikawa et al., 1995 Van Gelder, 1966 Tiesjema et al., 1973 Schroedl and Hartzell, 1977 Babcock et al., 1978 Blair et al., 1986 Steffens et al., 1993). It has been widely accepted that four electron equivalents are sufficient for complete reduction of the fuUy oxidized enzyme as prepared. However, most of the previous titrations were performed in the presence of electron transfer mediators. In the presence of electron transfer mediators, such as phenazine methosulfate (PMS) under anaerobic conditions, the bovine heart enzyme purified with crystallization also showed a four-electron reduction without the initial lag phase as observed in Fig. 9. A catalytic amount of PMS induced a small spectral change corresponding to the initial lag phase. These results suggest that electron transfer mediators in other titration experiments also induce autoreductions to provide the enzyme form that receives four electrons for the complete reduction. [Pg.362]

Further, oxides that are characterized by the possibility of metal ion reduction without oxide state modification have the greatest ability to promote oxidizing dehydrogenation processes. Oxide such as Iu203 is inclined to the changing of the metal ion oxidizing state In(III) In(II), while the oxide phase remains original. Due to this fact, sensors based on heterojunction oxide composites show considerable response to alcohol vapors (methanol, ethanol). The heterojunction between an oxide and solid solution phases appears to be very active in both adsorption and oxidation of alcohol. [Pg.250]

Gradual reduction in pressure from the supercritical state leads into a gas phase, without any noticeable physical changes. Gradual reduction in temperature from the supercritical state leads into the liquid state, without any changes in physical appearance. [Pg.115]

Although transition across a critical point may proceed without any first-order discontinuity, the fact that there is a change of symmetry implies that the two phases must be described by different functions of the thermodynamic variables, which cannot be continued analytically across the critical point. The order parameter serves to compensate for the reduction in symmetry. Although it is a regular function of temperature it can develop a discontinuous derivative at the critical temperature. Likewise, several measurable... [Pg.503]


See other pages where Reduction without Phase Change is mentioned: [Pg.156]    [Pg.292]    [Pg.156]    [Pg.292]    [Pg.176]    [Pg.301]    [Pg.469]    [Pg.284]    [Pg.365]    [Pg.146]    [Pg.332]    [Pg.99]    [Pg.146]    [Pg.194]    [Pg.111]    [Pg.58]    [Pg.764]    [Pg.1025]    [Pg.84]    [Pg.721]    [Pg.146]    [Pg.488]    [Pg.128]    [Pg.581]    [Pg.89]    [Pg.419]    [Pg.160]    [Pg.10]    [Pg.859]    [Pg.452]    [Pg.136]    [Pg.482]    [Pg.108]    [Pg.197]    [Pg.102]    [Pg.228]    [Pg.180]    [Pg.240]    [Pg.113]    [Pg.19]    [Pg.209]    [Pg.278]    [Pg.438]    [Pg.921]    [Pg.195]   


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Phase changes

Reduction change

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