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Vaporization temperatures

The column is swept continuously by a carrier gas such as helium, hydrogen, nitrogen or argon. The sample is injected into the head of the column where it is vaporized and picked up by the carrier gas. In packed columns, the injected volume is on the order of a microliter, whereas in a capillary column a flow divider (split) is installed at the head of the column and only a tiny fraction of the volume injected, about one per cent, is carried into the column. The different components migrate through the length of the column by a continuous succession of equilibria between the stationary and mobile phases. The components are held up by their attraction for the stationary phase and their vaporization temperatures. [Pg.20]

The process operates at 1 kPa (10 mbars) and 450 kW of power. When the condenser temperature reaches 580°C, the power is reduced to 350 kW. Cooling water is appHed to the condenser, throughout distillation, by means of sprays. Normally distillation takes 10—12 hours and the end point is signified by an increase in furnace temperature and a decrease in vapor temperature to 500—520°C. At this point the power is turned off and the vacuum pump is shut down. Nitrogen is then bled into the system to prevent oxidation of 2inc. [Pg.46]

Processing variables that affect the properties of the thermal CVD material include the precursor vapors being used, substrate temperature, precursor vapor temperature gradient above substrate, gas flow pattern and velocity, gas composition and pressure, vapor saturation above substrate, diffusion rate through the boundary layer, substrate material, and impurities in the gases. Eor PECVD, plasma uniformity, plasma properties such as ion and electron temperature and densities, and concurrent energetic particle bombardment during deposition are also important. [Pg.525]

T Absolute temperature T, for bulk temperature T, for wall temperature T, for vapor temperature for coolant temperature Tg for temperature of emitter T,. for temperature of receiver K ... [Pg.551]

The example vehicle has been run through the test sequence using a two liter carbon canister and a 150 BV purge level. Fig. 22 presents the results for both a return and retum-less fuel system used in the vehicle. As shown, the fuel vapor temperature and the amount of fuel vapor generated are both lower for the retum-less system. This reduces the amount of HC adsorption required in the carbon canister, and it also reduces the amount of HC emissions in the test sequence, fhe return fuel system used with the stated purge volume and canister size emits an unacceptable level of HC during one of the diurnal sequences (2.12 grams), while the retum-less system emission values are well below the acceptable level. [Pg.262]

Because of the continuous water flow through a condensible blowdown drum, it can safely handle cold or autorerrigerating releases only to the extent that effluent liquid and vapor temperatures remain above 0°C. [Pg.237]

Output mass rate and vapor temperature of release, mass rate of air entrained, density of mixtu >1 mass fraction in cloud. Limitations single chemical source terms, limited chemical... [Pg.347]

Thermocouple entry points on about every other tray measure either liquid of vapor temperature. [Pg.219]

ATy,j,3,5 = Maximum possible vapor temperature decrease (to liquid inlet temperature). [Pg.277]

Under the laws of vapor, the maximum quantity of a particular vapor a given space can contain is dependent solely upon the vapor temperature. As the compressed water vapor is cooled, it will eventually reach the temperature at which the space becomes saturated, now containing the maximum it can hold. Any further cooling will force part of the vapor to condense into its liquid form - water. [Pg.638]

Ny lon-6 (108 g) carpet backed with calcium-carbonate-filled latex and polypropylene was charged to a 1000-mL three-neck round-bottom flask (equipped with a condenser) with 6 mL of 85% phosphoric acid. Superheated steam was injected continuously during a 45-min period. The vapor temperature of the reaction medium was 250-300°C. The volume of distillate collected was 1065 mL. The distillate contained 1.9% e-caprolactam (as determined by GC), which corresponded to a crude yield of 37.5%. The distillate was fractionated in a distillation column and the nonaqueous phase removed. The remaining aqueous phase was treated with 2% potassium permanganate at 40-50°C for 2 h. Evaporation of... [Pg.565]

The submitters concentrated the reaction mixture by vacuum distillation (100 mm, bath temperature 70°C, vapor temperature 51°C). The weight after concentration was ca. 120 g. The checkers used rotary evaporation with a bath temperature of 65 to 70°C without any problems, and employed an explosion shield as a safety precaution. [Pg.133]

The submitters removed solvent by vacuum distillation (100 mm, bath temperature 70°C, vapor temperature 51 °C). [Pg.133]

Azeotropic removal of water was complete when the vapor temperature reached 111 °C. [Pg.134]

The first approach developed by Hsu (1962) is widely used to determine ONE in conventional size channels and in micro-channels (Sato and Matsumura 1964 Davis and Anderson 1966 Celata et al. 1997 Qu and Mudawar 2002 Ghiaasiaan and Chedester 2002 Li and Cheng 2004 Liu et al. 2005). These models consider the behavior of a single bubble by solving the one-dimensional heat conduction equation with constant wall temperature as a boundary condition. The temperature distribution inside the surrounding liquid is the same as in the undisturbed near-wall flow, and the temperature of the embryo tip corresponds to the saturation temperature in the bubble 7s,b- The vapor temperature in the bubble can be determined from the Young-Laplace equation and the Clausius-Clapeyron equation (assuming a spherical bubble) ... [Pg.260]

Thermodynamic and mechanical equilibrium on a curved vapor-liquid interface requires a certain degree of superheat in order to maintain a given curvature. Characteristics of homogeneous and heterogeneous nucleation can be estimated in the frame of classical theory of kinetics of nucleation (Volmer and Weber 1926 Earkas 1927 Becker and Doring 1935 Zel dovich 1943). The vapor temperature in the bubble Ts.b can be computed from equations (Bankoff and Flaute 1957 Cole 1974 Blander and Katz 1975 Li and Cheng 2004) for homogeneous nucleation in superheated liquids... [Pg.261]

Figure 8.2a,b shows the character of the liquid and the vapor pressure distribution along the evaporation region. It is found that for the above-mentioned parameters, the vapor pressure is practically independent from x. Accordingly, the vapor temperature, as well as the density, are also approximately constant. The latter makes it possible to reduce the number of equations by three. The remaining five equations consist of four equations that contain only four unknowns and... [Pg.364]

Fig. 8.9a-c The dependencies of vapor temperature, pressure and velocity in the outlet cross-section of the capillary on the inlet liquid temperature (a) the dependence of Ar(r ), (b) the... [Pg.370]

At Eu > 10 the wall temperature Tw depends on the liquid (vapor) temperature, the heat transfer intensity and the wall heat flux. [Pg.372]


See other pages where Vaporization temperatures is mentioned: [Pg.182]    [Pg.299]    [Pg.280]    [Pg.516]    [Pg.525]    [Pg.477]    [Pg.477]    [Pg.551]    [Pg.1042]    [Pg.1145]    [Pg.1147]    [Pg.1324]    [Pg.53]    [Pg.257]    [Pg.262]    [Pg.203]    [Pg.323]    [Pg.421]    [Pg.97]    [Pg.60]    [Pg.135]    [Pg.1173]    [Pg.337]    [Pg.339]    [Pg.341]    [Pg.130]    [Pg.251]    [Pg.352]    [Pg.369]    [Pg.371]    [Pg.372]   
See also in sourсe #XX -- [ Pg.113 ]

See also in sourсe #XX -- [ Pg.29 ]




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