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Pressure of gases

Langmuir adsorption isotherm A theoretical equation, derived from the kinetic theory of gases, which relates the amount of gas adsorbed at a plane solid surface to the pressure of gas in equilibrium with the surface. In the derivation it is assumed that the adsorption is restricted to a monolayer at the surface, which is considered to be energetically uniform. It is also assumed that there is no interaction between the adsorbed species. The equation shows that at a gas pressure, p, the fraction, 0, of the surface covered by the adsorbate is given by ... [Pg.234]

A powerful technique in studying both adsorption and desorption rates is that of programmed desorption. The general procedure (see Refs. 36, 84) is to expose a clean metal filament or a surface to a known, low pressure of gas that flows steadily over it. The pressure may be quite low, for example, 10 mm Hg or less, so that even nonactivated adsorption can take some minutes for... [Pg.694]

It is interesting to note that a similar specttum of the 0-0 band of the a-X system, leading to the same value of the absorption intensity, has been obtained using a Fourier transform spectrometer (see Section 3.3.3.2) but with an absorption path, using a multiple reflection cell, of 129 m and half the pressure of gas. [Pg.385]

Fig. 2. Schematic representation for the two-film theory of gas transfer = partial pressure of gas Pj = partial pressure of the gas at the interface Cj = concentration of gas at time t, Cj = initial concentration of gas at the interface Cg = initial concentration of gas at t = 0 and S = gas saturation. Fig. 2. Schematic representation for the two-film theory of gas transfer = partial pressure of gas Pj = partial pressure of the gas at the interface Cj = concentration of gas at time t, Cj = initial concentration of gas at the interface Cg = initial concentration of gas at t = 0 and S = gas saturation.
The events are so fine-tuned and the size of chamber, pressure of gas, travel, distance of the moving contact and the size of blast nozzle so designed and adjusted that a near-slrike-free interruption can be achieved for low reactive currents (inductive or capacitive) as well as fullload and very heavy fault currents. The advance compression of gas through the movement of main contact plays an important role by storing a part of the gas even before opening of the arcing contacts. [Pg.641]

Noble gas hydrates are formed similarly when water is frozen under a high pressure of gas (p. 626). They have the ideal composition, [Gg(H20)46], and again are formed by Ar, Kr and Xe but not by He or Ne. A comparable phenomenon occurs when synthetic zeolites (molecular sieves) are cooled under a high pressure of gas, and Ar and Kr have been encapsulated in this way (p. 358). Samples containing up to 20% by weight of Ar have been obtained. [Pg.893]

In the aqueous biphasic hydroformylation reaction, the site of the reaction has been much discussed (and contested) and is dependent on reaction conditions (temperature, partial pressure of gas, stirring, use of additives) and reaction partners (type of alkene) [35, 36]. It has been suggested that the positive effects of cosolvents indicate that the bulk of the aqueous liquid phase is the reaction site. By contrast, the addition of surfactants or other surface- or micelle-active compounds accelerates the reaction, which apparently indicates that the reaction occurs at the interfacial layer. [Pg.270]

Z = height of packed section in tower, ft Apim = log mean partial pressure of gas in inlet and exit gas streams, atm... [Pg.361]

An adsorption isotherm gives the relatiortship between the coverage of an interface With an adsorbed species (the amount adsorbed) and the pressure of gas or concentration of the species in solution in electrochemical reactions the coverage will depend alisO on the potential diHbrcnce at the... [Pg.1185]

Recall from Chapter 5 that the partial pressure of gas, /, in a mixture is given by the expression... [Pg.323]

Kinetic-molecular theory provides an explanation on a molecular level for this equilibrium. Evaporation from the liquid occurs as fast moving molecules on the surface escape from the liquid. In turn, molecules in the gas phase strike the liquid and condense, As the concentration (pressure) of gas molecules builds up in the gas phase, the rate of condensation increases. Eventually, a pressure is reached where the rate of condensation and rate of evaporation just balance, and equilibrium is achieved. The equilibrium pressure is denoted by p and is known as the vapor pressure. The magnitude ofp depends upon the substance, composition of the liquid, and any two of our thermodynamic variables such as temperature and total pressure. The criteria for equilibrium that we will now derive provide the thermodynamic relationships that will help... [Pg.225]

A domestic water-carbonating kit uses steel cylinders of carbon dioxide, each with a volume of 250. mL. Each weighs 1.04 kg when full and 0.74 kg when empty. What is the pressure of gas (in bar) in a full cylinder at 20.°C ... [Pg.293]

The pressure of gas in the source chamber was determined from the pressure in the gas reservoir (measured with a McLeod gage) by using Dushman s (11) relations for viscous and molecular flow in the higher and lower ranges of pressure, respectively. [Pg.201]

Factors may be classified as quantitative when they take particular values, e.g. concentration or temperature, or qualitative when their presence or absence is of interest. As mentioned previously, for an LC-MS experiment the factors could include the composition of the mobile phase employed, its pH and flow rate [3], the nature and concentration of any mobile-phase additive, e.g. buffer or ion-pair reagent, the make-up of the solution in which the sample is injected [4], the ionization technique, spray voltage for electrospray, nebulizer temperature for APCI, nebulizing gas pressure, mass spectrometer source temperature, cone voltage in the mass spectrometer source, and the nature and pressure of gas in the collision cell if MS-MS is employed. For quantification, the assessment of results is likely to be on the basis of the selectivity and sensitivity of the analysis, i.e. the chromatographic separation and the maximum production of molecular species or product ions if MS-MS is employed. [Pg.189]

Based on this experience, a computerized program was further developed on related topics to examine how students solved problems in particle distribution with a different orientation of the apparatus and pressures of gas particles. Case 2 below states the major design and findings of this follow-up study. [Pg.265]

Figure 12-10 is a molecular view showing that the equilibrium concentration of a dissolved gas varies with the partial pressure of that gas. An increase in the partial pressure of gas results in an increase in the rate at which gas molecules enter the solution. This increases the concentration of gas in solution. The increased concentration in solution, in turn, results in an increase in the rate at which gas molecules escape from the solution. Equilibrium is reestablished when the solute concentration is high enough that the rate of escape equals the rate of capture. [Pg.851]

At different types of adsorption isotherms plotted for adsorption of donor particles on oxides (see section 1.5) expressions (1.112) - (1.115) provide the rise in and decrease in with the growth of partial pressure of gas P, the functions themselves being different. Thus, in case of applicability of the Henry isotherm at small P we have the function oi - exp const-P becoming a power function <7s P with the rise in P which is often observed in experiments [154, 155, 169]. [Pg.71]

Fig. 1.19. The comparison of theoretical predictions (1.81) and (1.83) describing kinetics of ait) and flit) in case of large pressures of gas of acceptors with experimental results ( Pq = 300 Torr a = 0.16 nA/V t c 120 min)... Fig. 1.19. The comparison of theoretical predictions (1.81) and (1.83) describing kinetics of ait) and flit) in case of large pressures of gas of acceptors with experimental results ( Pq = 300 Torr a = 0.16 nA/V t c 120 min)...
The gas permeability constants (P) are generally expressed by the amount of the gas at standard temperature and pressure normalized for the thickness, membrane area, time and differential pressure of gas as in the following equation ... [Pg.48]

It is important to model a correlation spectroscopy system, firstly to predict performance, and also to aid the very important choice of optical filter (or choose the best LED or super-luminescent optical fibre source to give the optimal spectral output), in order to achieve the best detection performance or best selectivity possible. The length of the cells and the pressure of gas (or gas concentration) are also important parameters (although all simulated results described below are based on use of lm long cells). [Pg.466]


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Accumulatory pressure measurements of evolved gas

Behavior of Gases Under Pressure

Case Study Risk Assessment for the Failure of a Natural Gas High Pressure Pipeline

Condensation of Butane Gas Under Pressure

Correction of vapour pressure data for pad gas

Current of Gas or under Reduced Pressure

Dalton s law of partial pressures For that each gas would exert if it were alone

Effect of Gas Pressure on Discharge

Effect of liquid pressure on gas fugacity

Estimation of diffusivity in a gas mixture at low pressure

Evolution of the rate according to time and gas pressure

Gas Motion Under the Action of Short-Duration Pressure (Impulse)

Gases Dalton’s law of partial pressures

Heat Capacity at Constant Pressure of Inorganic and Organic Compounds in the Ideal Gas State Fit to Hyperbolic Functions Cp

Heat Capacity at Constant Pressure of Inorganic and Organic Compounds in the Ideal Gas State Fit to a Polynomial Cp

Mixtures of Gases and Partial Pressures

Operating defects while pumping with gas ballast Potential sources of error where the required ultimate pressure is not achieved

Partial pressure of a gas

Partial pressure of the reagent gas

Partial pressures of gas species

Pressure drop of gas

Pressure of a gas

Pressure of an ideal gas

Pressure of gases developed on expln

Pressure of gases vapor

Pressure of real gases

Properties of Gases Gas Pressure

Sizing of High-Pressure Safety Valves for Gas Service

Solutions of Gases in Liquids at High Pressures

The Effect of an Inert Gas on Vapor Pressure

The Influence of Gas Pressure upon Conductivity

The Pressure of a Dilute Gas

The Pressure of a Gas

The reactions of gases at very low pressures on heated metallic filaments

Why pressurize the contents of a gas canister

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