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Standard pressure

Enthalpies are referred to the ideal vapor. The enthalpy of the real vapor is found from zero-pressure heat capacities and from the virial equation of state for non-associated species or, for vapors containing highly dimerized vapors (e.g. organic acids), from the chemical theory of vapor imperfections, as discussed in Chapter 3. For pure components, liquid-phase enthalpies (relative to the ideal vapor) are found from differentiation of the zero-pressure standard-state fugacities these, in turn, are determined from vapor-pressure data, from vapor-phase corrections and liquid-phase densities. If good experimental data are used to determine the standard-state fugacity, the derivative gives enthalpies of liquids to nearly the same precision as that obtained with calorimetric data, and provides reliable heats of vaporization. [Pg.82]

The previous equation is only valid as long as there is no compositional change of the gas between the subsurface and the surface. The value of E is typically in the order of 200, in other words the gas expands by a factor of around 200 from subsurface to surface conditions. The actual value of course depends upon both the gas composition and the reservoir temperature and pressure. Standard conditions of temperature and pressure are commonly defined as 60°F (298K) and one atmosphere (14.7 psia or 101.3 kPa), but may vary from location to location, and between gas sales contracts. [Pg.107]

Pressure. Standard atmospheric pressure is defined to be the force exerted by a column of mercury 760-mm high at 0°C. This corresponds to 0.101325 MPa (14.695 psi). Reference or fixed points for pressure caUbration exist and are analogous to the temperature standards cited (23). These points are based on phase changes or resistance jumps in selected materials. For the highest pressures, the most rehable technique is the correlation of the wavelength shift, /SX with pressure of the mby, R, fluorescence line and is determined by simultaneous specific volume measurements on cubic metals... [Pg.20]

A number of units are used to express a pressure measurement. Some are based on a force per unit area for e.xample, pound (force) per square inch (psi) or dyne per square centimeter (dyne/enr). Otliers are based on a fluid height, such as inches of water (in H O) or millimeters of mercury (iimiHg) units such as these are convenient when tlie pressure is indicated by a difference between two levels of a liquid, as in a imuiometer or barometer. Barometric pressure is a measure of the ambient air pressure. Standard barometric pressure is 1 atm and is equivalent to 14.696 psi and 29.921 in Hg. [Pg.112]

Normal-, normal, standard, -bedingungen, /.pi. normal conditions standard specifications. -benzin, n. a special gasoline free from aromatics, -druck, m. normal pressure standard pressure. [Pg.321]

The contribution by each constituent gas to the total air pressure. Standard air pressure is 1013 mbar. [Pg.437]

For reactions at atmospheric pressure, standard laboratory glassware such as round-bottomed flasks or simple beakers from 0.25 to 2 L can be used. A protective mount in the ceiling of the cavity enables the connection of reflux condensers or distillation equipment. An additional mount in the sidewall allows for sample withdrawal, flushing with gas to create inert atmospheres, or live monitoring of the reaction with a video camera. Most of the published results in controlled MAOS have been obtained from reactions in sealed vessels, and thus in the following mostly accessories for sealed-vessel reaction conditions are described. [Pg.35]

For reactions at atmospheric pressure, standard laboratory glassware such as round-bottomed flasks from 0.5 to 3 L can be used. A protective mount in the ceil-... [Pg.40]

This method is invalid because the temperature in the denominator of the equation must be the temperature at which the liquid-vapor transition is at equilibrium. Liquid water and water vapor at 1 atm pressure (standard state, indicated by ) are in equilibrium only at 100° C = 373 K. [Pg.491]

Constant pressure standard heat capacity per mole... [Pg.800]

The index of refraction of air varies with temperature and pressure standard air is defined as dry air at 15°C and 1 atmosphere pressure, with 0.03 percent C02. To correct wavelengths measured in air to vacuum, we add (n — l)Aair. Some values of n — 1 for standard air are6... [Pg.71]

The Standard DIN EN or ANSI ASME components are generally only used for the pressure range below 200 bar in the process industry and will not be discussed further here. There are historical roots which have generated special high-pressure standards for the chemical industries earlier than was the case for other industrial applications, e.g., for the power engineering sector. The technical reasons for this fact are numerous and are based on the special requirements in the process industries ... [Pg.190]

One of the most applied high-pressure standards for the piping components is based on the so--called IG-Standard, which was established by an association of the German Chemical Industry beginning with 1930. Similar developments took place in the US and elsewhere. The pipes applied are of seamless design. The joints and seals which have been approved for high-pressure are shown in Fig. 4.2-1. [Pg.190]

Physical appearance White to cream colored if pulverized, free from lumps that do not break up under slight pressure (extra grade) moderate pressure (standard grade) ... [Pg.73]

You may wonder how a reaction, such as combustion of methane, can occur at 25°. The fact is that the reaction can be carried out at any desired temperature. The important thing is that the AH° value we are talking about here is the heat liberated or absorbed when you start with the reactants at 25° and finish with the products at 25°. As long as AH0 is defined this way, it does not matter at what temperature the reaction actually occurs. Standard states for gases are 1 atm partial pressure. Standard states for liquids or solids usually are the pure liquid or solid at 1 atm external pressure. [Pg.76]

Hydrogenation at atmospheric pressure standard procedure. This method for effecting hydrogenation at atmospheric pressure employs the apparatus shown semi-diagrammatically in Fig. 2.63(a) it is supported on a suitable metal rod framework. The essential features are a long-necked hydrogenation flask A fitted to the apparatus with sufficient flexible tube to allow shaking, a series of... [Pg.89]

Because air has weight, it exerts a pressure. The composition of the air tends to vary, leading to changes in the weight of the air (changes in atmospheric pressure). Standard pressure, also called a standard atmosphere, is... [Pg.63]

Manometers consisting of liquid columns of, commonly, mercury or a fluid such as silicone oil, have been used extensively in the past to measure gas mixtures in, for example, experimental, static investigations of the overall kinetics of gas-phase reactions. They continue to be used in many applications, including the establishment of primary pressure standards in several countries. [Pg.149]

In chemistry the term STP does not refer to an oil additive for cars but rather is an acronym for standard temperature and pressure. Standard temperature has been set by the scientific community to be 0°C, and standard pressure to be 1 atmosphere or 760 mm or 760 torr. Because gas experiments are performed under a variety of temperature and pressure conditions in laboratories all over the world, it is necessary that scientists have some type of standard so that they can compare results. STP is this standard, and results are often said to be corrected to STP. That is, the results have been calculated to be the values that they would be at STP. [Pg.78]

Table II gives the standard deviations of pressure, vapor composition and temperature, and the corresponding bias and D-value as each variable is changed randomly and then as all four are changed simultaneously. We see that the random error of x contributes ca. 75% of the induced error in the value of the standard deviation of both the pressure and temperature while the random error of T and tt only contribute about 12% each. On the other hand the random errors of x and y contribute equally to the induced-vapor composition standard deviation with the pressure making a negligible contribution. The bias values are negligibly small except for the pressure standard deviations where they are still not large. The final column has D-values at least equal to two and this gives one confidence in the model and suggests it is adequate for good quality data as in this particular case the only source of error is caused by random behavior. Table II gives the standard deviations of pressure, vapor composition and temperature, and the corresponding bias and D-value as each variable is changed randomly and then as all four are changed simultaneously. We see that the random error of x contributes ca. 75% of the induced error in the value of the standard deviation of both the pressure and temperature while the random error of T and tt only contribute about 12% each. On the other hand the random errors of x and y contribute equally to the induced-vapor composition standard deviation with the pressure making a negligible contribution. The bias values are negligibly small except for the pressure standard deviations where they are still not large. The final column has D-values at least equal to two and this gives one confidence in the model and suggests it is adequate for good quality data as in this particular case the only source of error is caused by random behavior.

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