Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Porous materials, cooling

This design has a strut-supported porous shell (Figure 9-19). The shell attached to the strut is of wire from porous material. Cooling air flows up the central plenum of the strut, which is hollow with various-size metered holes on the strut surface. The metered air then passes through the porous shell. The shell material is cooled by a combination of convection and film cooling. This process is effective due to the infinite number of pores on the blade surface. The temperature distribution is shown in Figure 9-20. [Pg.358]

The most important evaluation of an ANG storage systems performance is the measurement of the amount of usable gas which can be delivered from the system. This is frequently defined as the volume of gas obtained from the storage vessel when the pressure is reduced from the storage pressure of 3.5 MPa (35 bar) to one bar, usually at 298 K. This parameter is referred to as the delivered V/V and is easy to determine directly and free from ambiguity. Moreover, it is independent of the ratio of gas adsorbed to that which remains in the gaseous state. To determine the delivered V/V an adsorbent filled vessel of at least several hundred cubic centimeters is pressurized at 3.5 MPa and allowed to cool under that pressure to 298 K. The gas is then released over a time period sufficient to allow the bed temperature to return to 298 K. A blank, where the vessel is filled with a volume of non-porous material, such as copper shot. [Pg.284]

Drying-Cooling Final Vacuum. This is produced by restarting the vacuum pump until a preset vacuum (e.g., lOOmbar) is reached. The pump is then kept running for a preset time. Porous materials (and non-porous materials also) are thus dried and cooled quickly. [Pg.3534]

STORAGE Keep in a cool, dry, well-ventilated area away from acids, oxidizers, halogens, air, heat, porous materials and open flame store under nitrogen detached or outside preferred. [Pg.144]

DISPOSAL AND STORAGE METHODS absorb liquid in sand or inert absorbent, and place in a secured, sanitary landfill dispose of container and unused contents in accordance with federal, state and local regulations store in a cool, dry location maintain adequate ventilation outside storage is preferred keep in tightly closed containers keep under inert gas separate from acids oxidizing materials, metal oxides, halogens, and porous materials. [Pg.748]

Last but not least, a class of porous materials closely related to zeolites is addressed in Chapter 9 P, Cool and E.F. Vansant discuss the basic principles of preparing pillared clays, and methods for the proper characterization of these fascinating materials are outlined. [Pg.314]

The supersaturation can be produced by cooling, evaporation and drying and wetting cycle. If the temperature dependence of the solubihty of a salt is high, a drop of temperature can result in supersaturation. Supersaturation caused by evaporation always occurs when one face of the porous material is in contact with the solution and the other face is exposed to relatively dry conditions, i.e., the salt weathering process. [Pg.434]

Spray chambers can be cooled via a water jacket or Peltier cooling to reduce the amount of solvent vapor introduced into the ICP [31, 32). A further reduction in the amount of solvent introduced can be realized via a desolvation system. Traditionally, such a desolvation system consisted of a sequence of a heated and a cooled tube. In the heated tube, the solvent is vaporized, after which it condenses on the inner wall of the cooled tube and is thus removed. Nowadays, desolvation systems equipped with a membrane desolvator are often used [33, 34). These basically consist of a tube manufactured from a semipermeable porous material, around which heated Ar gas is flowing in the opposite direction to the sample aerosol flow. The solvent is vaporized, and the gaseous solvent molecules leave the central tube via the pores and are carried off by the heated Ar flow. Desolvation of the sample aerosol can lead to an 10-fold increase in signal intensity. For rather volatile analyte elements, (partial) analyte loss needs to be taken into account [35]. [Pg.49]


See other pages where Porous materials, cooling is mentioned: [Pg.453]    [Pg.148]    [Pg.78]    [Pg.428]    [Pg.53]    [Pg.272]    [Pg.455]    [Pg.332]    [Pg.133]    [Pg.46]    [Pg.20]    [Pg.31]    [Pg.237]    [Pg.24]    [Pg.107]    [Pg.109]    [Pg.839]    [Pg.98]    [Pg.218]    [Pg.417]    [Pg.236]    [Pg.543]    [Pg.33]    [Pg.370]    [Pg.33]    [Pg.8]    [Pg.173]    [Pg.163]    [Pg.131]    [Pg.63]    [Pg.180]    [Pg.25]    [Pg.564]    [Pg.95]    [Pg.168]    [Pg.77]    [Pg.551]    [Pg.99]    [Pg.22]    [Pg.564]   
See also in sourсe #XX -- [ Pg.3534 ]




SEARCH



Cooling materials

© 2024 chempedia.info