High vacuum pressure range

In Table I the high-vacuum (HV) range means a pressure of 10 to 10 Torr entries designated by Torr mean pressures between 0.1 and 10 Torr flow refers to an unspecified steady-state flow pattern. It is apparent from Table I that there is a great diversity in the different oscillation conditions and catalytic systems. The pressures under which oscillations have been observed vary from 10 Torr for the CO/NO reaction on Pt(lOO) 141, 142) to atmospheric pressure for a large number of systems. The reactors used in these studies include ultrahigh-vacuum (UHV) systems, continuous stirred tank reactors (CSTRs), flow reactors, and reactors designed as infrared (IR) cells, calorimeters, and ellipsometric systems. 

The pressure range is the pressure difference of the maximum pressure and the minimum pressure in which a vacuum pump can work efficiently. It is necessary to combine the different types of pumps together to generate high vacuum pressure. 

Consider high vacuum distillation when material is temperature-sensitive at normal pressure ranges. 

In the static method the powder is isolated under high vacuum and surface gases driven off by heating the container. The container is next immersed in hquid nitrogen and known amounts of nitrogen vapor are admitted into the container at measured increasing pressures in the relative pressure range 0.05 to 0.35. 

If the pump is a filter pump off a high-pressure water supply, its performance will be limited by the temperature of the water because the vapour pressure of water at 10°, 15°, 20° and 25° is 9.2, 12.8, 17.5 and 23.8 mm Hg respectively. The pressure can be measured with an ordinary manometer. For vacuums in the range lO" mm Hg to 10 mm Hg, rotary mechanical pumps (oil pumps) are used and the pressure can be measured with a Vacustat McLeod type gauge. If still higher vacuums are required, for example for high vacuum sublimations, a mercury diffusion pump is suitable. Such a pump can provide a vacuum up to 10" mm Hg. For better efficiencies, the pump can be backed up by a mechanical pump. In all cases, the mercury pump is connected to the distillation apparatus through several traps to remove mercury vapours. These traps may operate by chemical action, for example the use of sodium hydroxide pellets to react with acids, or by condensation, in which case empty tubes cooled in solid carbon dioxide-ethanol or liquid nitrogen (contained in wide-mouthed Dewar flasks) are used. 

The pressure in the scattering chamber should be below approximately 10 Pa (high vacuum). Lower pressures in the UHV range are usually not necessary, because PRDA is not surface-sensitive. 

Vibrational spectroscopic studies of heterogeneously catalyzed reactions refer to experiments with low area metals in ultra high vacuum (UHV) as well as experiments with high area, supported metal oxides over wide ranges of pressure, temperature and composition [1]. There is clearly a need for this experimental diversity. UHV studies lead to a better understanding of the fundamental structure and chemistry of the surface-adsorbate system. Supported metals and metal oxides are utilized in a variety of reactions. Their study leads to a better understanding of the chemistry, kinetics and mechanisms in the reaction. Unfortunately, the most widely used technique for determining adsorbate molecular structure in UHV,... 

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