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Phase Dependence

The aim of the experiment was to study the transmission of a signal through the weld and to measure the frequency and phase dependencies of parameters of acoustic signals from the angle of incidence and beam path within the weld volume. One of the shift of the spectral characteristics the signal is shown in Figure 4(a,b). [Pg.732]

The scope of this section restricts the discussion. One omitted topic is the collision and interaction of molecules with surfaces (see [20, 21] and section A3.9). This topic coimects quantum molecular dynamics in gas and condensed phases. Depending on the time scales of the interaction of a molecule witli a surface, the... [Pg.2291]

Eigure 6 illustrates how the three tensions among the top, middle, and bottom phases depend on temperature for a system of nonionic surfactant—oil—water (38), or on salinity for a representative system of anionic surfactant—cosurfactant—oil—water and electrolyte (39). As T approaches from lower temperatures, the composition of M approaches the composition of T, and the iaterfacial teasioa betweea them, goes to 2ero at T =. ... [Pg.151]

Iron, cobalt, and nickel catalyze this reaction. The rate depends on temperature and sodium concentration. At —33.5°C, 0.251 kg sodium is soluble in 1 kg ammonia. Concentrated solutions of sodium in ammonia separate into two Hquid phases when cooled below the consolute temperature of —41.6°C. The compositions of the phases depend on the temperature. At the peak of the conjugate solutions curve, the composition is 4.15 atom % sodium. The density decreases with increasing concentration of sodium. Thus, in the two-phase region the dilute bottom phase, low in sodium concentration, has a deep-blue color the light top phase, high in sodium concentration, has a metallic bronze appearance (9—13). [Pg.162]

A spray comprises a cloud of liquid droplets randomly dispersed ia a gas phase. Depending on the appHcation, sprays may be produced ia many different ways. The purposes of most sprays are (/) creation of a spectmm of droplet sizes to iacrease the Hquid surface-to-volume ratio, (2) metering or control of the hquid throughput, (J) dispersion of the Hquid ia a certain pattern, or (4) generation of droplet velocity and momentum. [Pg.327]

Droplet Dispersion. The primary feature of the dispersed flow regime is that the spray contains generally spherical droplets. In most practical sprays, the volume fraction of the Hquid droplets in the dispersed region is relatively small compared with the continuous gas phase. Depending on the gas-phase conditions, Hquid droplets can encounter acceleration, deceleration, coUision, coalescence, evaporation, and secondary breakup during thein evolution. Through droplet and gas-phase interaction, turbulence plays a significant role in the redistribution of droplets and spray characteristics. [Pg.330]

However, it is not practical to set the gas temperature in steady state without equally setting the temperature of the surface and bulk phases hounding the gas. Consideration of the response of the system as a vacuum environment can then provide a sufftciendy precise prediction of the pressure P and the surface coverage 9 at temperature Tfor molecules of a known species in a known state on a known surface. For example, an isotherm is estabhshed between the surface of the condensed and the gaseous phases, depending, eg, on the heat of desorption. For submonolayer coverage on a... [Pg.366]

Since there may well be chemical or biological reactions happening on or in the solid phase, depending upon the size of the process participants, macro- or micro-scale effects may or may not be appropriate to consider. [Pg.1634]

The properties of an alloy (yield strength, toughness, oxidation resistance, etc.) depend critically on its constitution and on two further features of its structure the scale (nm or ym or mm) and shape (round, or rod-like, or plate-like) of the phases, not described by the constitution. The constitution, and the scale and shape of the phases, depend on the thermal treatment that the material has had. [Pg.324]

Metallic materials consist of one or more metallic phases, depending on their composition, and very small amounts of nonmetallic inclusions. In the metallic state, atoms donate some of their outer electrons to the electron gas that permeates the entire volume of the metal and is responsible for good electrical conductivity (10 S cm ). Pure elements do not react electrochemically as a single component. A mesomeric state can be approximately assumed... [Pg.30]

The evolution of a. star after it leaves the red-giant phase depends to some extent on its mass. If it is not more than about 1.4 M it may contract appreciably again and then enter an oscillatory phase of its life before becoming a white dwarf (p. 7). When core contraction following helium and carbon depletion raises the temperature above I0 K the y-ray.s in the stellar assembly become sufficiently energetic to promote the (endothermic) reaction Ne(y,a) 0. The a-paiticle released can penetrate the coulomb barrier of other neon nuclei to form " Mg in a strongly exothermic reaction ... [Pg.11]

Another important issue that must be considered in the development of CSPs for preparative separations is the solubility of enantiomers in the mobile phase. For example, the mixtures of hexane and polar solvents such as tetrahydrofuran, ethyl acetate, and 2-propanol typically used for normal-phase HPLC may not dissolve enough compound to overload the column. Since the selectivity of chiral recognition is strongly mobile phase-dependent, the development and optimization of the selector must be carried out in such a solvent that is well suited for the analytes. In contrast to analytical separations, separations on process scale do not require selectivity for a broad variety of racemates, since the unit often separates only a unique mixture of enantiomers. Therefore, a very high key-and-lock type selectivity, well known in the recognition of biosystems, would be most advantageous for the separation of a specific pair of enantiomers in large-scale production. [Pg.61]

The particle size of the dispersed phase depends upon the viscosity of the elastomer-monomer solution. Preferably the molecular weight of the polybutadiene elastomer should be around 2 x 10 and should have reasonable branching to reduce cold flow. Furthermore, the microstructure of the elastomer provides an important contribution toward the low-temperature impact behavior of the final product. It should also be emphasized that the use of EPDM rubber [136] or acrylate rubber [137] may provide improved weatherability. It has been observed that with an increase in agitator speed the mean diameter of the dispersed phase (D) decreases, which subsequently levels out at high shear [138-141]. However, reagglomeration may occur in the case of bulk... [Pg.657]

Because flashing steam-condensate lines represent two-phase flow, with the quantity of liquid phase depending on die system conditions, these can be designed following the previously described two-phase flow methods. An alternate by Ruskin [28] uses the concept but assumes a single homogeneous phase of fine liquid droplets dispersed in the flashed vapor. Pressure drop was calculated by the Darcy equation ... [Pg.141]

A number of authors have reported studies of the oxidation of low-alloy steel in steam. The general observations indicate strong similarities with oxidation in air, the kinetics being typically parabolic and the scales typically comprising FcjO, Fej04, FeO and spinel phases, dependent upon alloy composition, temperature and oxygen partial pressure of the environment... [Pg.985]

For lock-in amplification the pump is modulated at a reference frequency w (see Fig. 7-1), which means that AT is not constant over time. Rather, its magnitude (and its phase) depends on the modulation frequency [8. In order to find the frequency-dependent A7 (cu), let us assume that the recombination dynamics are monomolecular with a single lifetime r. Then we can write for the number density of excitations N at time / ... [Pg.423]

This potential reflects itself in the titration curves of weak polyacids such as poly(acrylic acid) and poly(methacrylic acid) [32]. Apparent dissociation constants of such polyacids change with the dissociation degree of the polyacid because the work to remove a proton from the acid site into the bulk water phase depends on the surface potential of the polyelectrolyte. [Pg.55]

Table 3.1 shows the kinetic parameters for cell growth, rate models with or without inhibition and mass transfer coefficient calculation at various acetate concentrations in the culture media. The Monod constant value, KM, in the liquid phase depends on some parameters such as temperature, initial concentration of the carbon source, presence of trace metals, vitamin B solution, light intensity and agitation speeds. The initial acetate concentrations in the liquid phase reflected the value of the Monod constants, Kp and Kp. The average value for maximum specific growth rate (/xm) was 0.01 h. The value... [Pg.64]

The isotherms represented in Fig. 1 give a general idea of the equilibria in the Pd-H system under different p-T conditions. Most experimental evidence shows, however, that the equilibrium pressure over a + /3 coexisting phases depends on the direction of the phase transformation process p a-p > pp-a (T, H/Pd constant). This hysteresis effect at 100°... [Pg.248]

To answer the question whether the ds-transisomerization of the bridged polypeptides with a Ala-Gly-Pro sequence represents the rate-determining step, the following experiment was carried out The polypeptide with a chain length n = 8 was denaturated in a rapid reaction with a temperature jump from 9.2 to 30 °C and subjected to renatura-tion at 9.2 °C after an incubation time of 25 s. In a second and a third experiment, the incubation in the coiled state was prolonged respectively to 75 and 125 s. It could be observed that the amplitude of the rapid phase depends on the time that lapses between the denaturation and renaturation (Fig. 32). [Pg.185]


See other pages where Phase Dependence is mentioned: [Pg.151]    [Pg.927]    [Pg.2557]    [Pg.93]    [Pg.572]    [Pg.93]    [Pg.202]    [Pg.420]    [Pg.420]    [Pg.1244]    [Pg.876]    [Pg.271]    [Pg.28]    [Pg.82]    [Pg.864]    [Pg.570]    [Pg.572]    [Pg.65]    [Pg.4]    [Pg.73]    [Pg.210]    [Pg.369]    [Pg.469]    [Pg.702]    [Pg.312]    [Pg.53]    [Pg.81]    [Pg.256]    [Pg.201]    [Pg.937]   


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Anchoring phase substrate dependence

Chemical shift dependent phase correction

Chemical shift dependent phase errors

Dehydrogenation Mechanism and Gas-Phase HO)-Dependent Elementary Reactions

Direction-dependent phase error

Energy-dependent phase shift

Enthalpy phase dependency

Equilibrium field-dependent phase

Equilibrium pressure-dependent phase

Frequency-dependent phase

Frequency-dependent phase, definition

Liquid phase reactions ionic strength dependence

Magnetic phase transitions pressure dependence

Membranes lipid temperature dependent phase

Mobile phase dependence

Molar Mass Dependence of Phase Diagrams

Pattern film thickness-dependent phase

Phase System Dependent on Solubility

Phase dependence of molecular structures

Phase dependence, comet

Phase dependency

Phase dependency

Phase factor time-dependent

Phase frequency dependence

Phase transformation rate temperature dependence

Phase transitions temperature dependence

Phase-dependent structures

Position-dependent phase shift

Pressure dependence of phase

Pressure dependence, phase equilibria

Schematic illustration of elution chromatography. Three solutes are separating depending on the affinity to stationary phase at different times

Sequence dependent phasing

Temperature dependence liquid crystalline phase modelling

Temperature dependence of the phase structure

Temperature dependence phase boundary

Temperature dependence phase-space transition states

Temperature dependence transformation, phase coexistence

Temperature dependence, phase

Temperature dependence, phase equilibria

Time-dependent Hartree-Fock random phase approximation

Time-dependent equations phase-space transition states

Time-dependent phase space compressibility

Wave function phase-isolated, time-dependent

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