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Phase-change difference

An example of phase-change difference is water evaporating (changing from liquid to gas) on or behind a target surface and temporarily cooling the surface. This results in a real temperature change at the target surface. [Pg.65]


The third, fourth, and fifth assumptions inherent in the Hertz-Knudsen equation are also used in the derivation of Eq. (60). Maa (M3) has shown by experimental studies that Eq. (60) provides a good model for predicting the net rate of phase change. Maa (M4) and O Connor (Ol) have shown that if these assumptions are replaced by significantly less restrictive ones, and the derivation repeated, the calculated values of the net rate of phase change differ by less than 10% under the most extreme conditions. [Pg.357]

After amplification both signals change their initial phases due to the delay r of the amplifier unblank (r = 0.1 - 0.5 ms), phase shift in it and wave propagation in passive vibrator s elements. All the mentioned phase changes are proportional to the frequency. The most contribution of them has unblank delay z. Thus frequency variations changes the initial phases) f/, and j(/c) of both signals and their difference A - Vi ... [Pg.828]

Above 81.5 K the C(2x 1) structure becomes the more stable. Two important points are, first, that a change from one surface structure to another can occur without any bulk phase change being required and, second, that the energy difference between dtemative surface structures may not be very large, and the free energy difference can be quite temperature-dependent. [Pg.304]

Calorimetry is the basic experimental method employed in thennochemistry and thennal physics which enables the measurement of the difference in the energy U or enthalpy //of a system as a result of some process being done on the system. The instrument that is used to measure this energy or enthalpy difference (At/ or AH) is called a calorimeter. In the first section the relationships between the thennodynamic fiinctions and calorunetry are established. The second section gives a general classification of calorimeters in tenns of the principle of operation. The third section describes selected calorimeters used to measure thennodynamic properties such as heat capacity, enthalpies of phase change, reaction, solution and adsorption. [Pg.1899]

The Phase Change Upon CycUzadou of Different s-cis Cyclobutadiene Isomers ... [Pg.369]

Writing Techniques. WORM disks differ depending on their data writing techniques, which can be divided into three classes (3) ablative writing, bubble forming, and phase change. [Pg.140]

Fig. 16. Maximum achievable signal-to-noise ratio (SNR) on read-out of different writable optical data storage systems as a function of the writing energy (laser power) (121). SQS = Organic dye system (WORM) PC = phase change system (TeSeSb) MO = magnetooptical system (GbTbFe). See text. Fig. 16. Maximum achievable signal-to-noise ratio (SNR) on read-out of different writable optical data storage systems as a function of the writing energy (laser power) (121). SQS = Organic dye system (WORM) PC = phase change system (TeSeSb) MO = magnetooptical system (GbTbFe). See text.
Sohd ammonium nitrate occurs in five different crystalline forms (19) (Table 6) detectable by time—temperature cooling curves. Because all phase changes involve either shrinkage or expansion of the crystals, there can be a considerable effect on the physical condition of the sohd material. This is particularly tme of the 32.3°C transition point which is so close to normal storage temperature during hot weather. [Pg.365]

Other factors also impact the type of crystals formed upon cooling of hot soap. Water activity or moisture content contribute to the final crystal state as a result of the different phases containing different levels of hydration. Any additive that changes the water activity changes the crystallization pathway. For example, the addition of salt reduces the water activity of the mixture and pushes the equiUbrium state toward the lower moisture crystal stmcture. Additionally, the replacement of sodium with other counter cations influences the crystallization. For example, the replacement of sodium with potassium drives toward the formation of 5-phase. [Pg.152]

Advantages to Membrane Separation This subsertion covers the commercially important membrane applications. AU except electrodialysis are pressure driven. All except pervaporation involve no phase change. All tend to be inherently low-energy consumers in the-oiy if not in practice. They operate by a different mechanism than do other separation methods, so they have a unique profile of strengths and weaknesses. In some cases they provide unusual sharpness of separation, but in most cases they perform a separation at lower cost, provide more valuable products, and do so with fewer undesirable side effects than older separations methods. The membrane interposes a new phase between feed and product. It controls the transfer of mass between feed and product. It is a kinetic, not an equihbrium process. In a separation, a membrane will be selective because it passes some components much more rapidly than others. Many membranes are veiy selective. Membrane separations are often simpler than the alternatives. [Pg.2024]

A copper-antimony alloy containing 95 weight% antimony is allowed to cool from 650°C to room temperature. Describe the different phase changes which take place as the alloy is cooled and make labelled sketches of the microstructure to illustrate your answer. [Pg.33]


See other pages where Phase-change difference is mentioned: [Pg.95]    [Pg.155]    [Pg.65]    [Pg.95]    [Pg.155]    [Pg.65]    [Pg.288]    [Pg.1635]    [Pg.1878]    [Pg.1916]    [Pg.2525]    [Pg.2526]    [Pg.2913]    [Pg.10]    [Pg.46]    [Pg.53]    [Pg.98]    [Pg.109]    [Pg.130]    [Pg.390]    [Pg.115]    [Pg.148]    [Pg.336]    [Pg.144]    [Pg.473]    [Pg.95]    [Pg.152]    [Pg.307]    [Pg.99]    [Pg.652]    [Pg.2423]    [Pg.99]    [Pg.260]    [Pg.334]    [Pg.62]    [Pg.104]    [Pg.53]    [Pg.252]   


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Phase changes

Phase difference

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