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Vacuum pumps temperature reduction

These reactions are thermodynamically unfavorable at temperatures below ca 1500°C. However, at temperatures in the range from 1000 to 1200°C a small but finite equiUbrium pressure of barium vapor is formed at the reaction site. By means of a vacuum pump, the barium vapor can be transported to a cooled region of the reactor where condensation takes place. This destroys the equiUbrium at the reaction site and allows more barium vapor to be formed. The process is completely analogous to that used in the thermal reduction of CaO with aluminum to produce metallic calcium (see Calcium AND CALCIUM alloys). [Pg.472]

The simplest designs are volume separators in which droplets of pump fluid are separated from the exhaust gas flow by the reduction in the flow speed. These separators are used in liquid ring vacuum systems. The separation can be improved by fitting swirl bodies. A mixture of saturated vapours that varies according to the operating temperature of the vacuum pump always emerges from the exhaust gas nozzle. [Pg.319]

With a vacuum-capable enclosed vapor degreaser, this relationship is easily arranged. Vapor flows easily within whatever torturous paths there are within the arrangement of parts (Chapter 2.15). Reduction of chamber pressure by engaging the vacuum pump, reduces the temperature of the parts (Chapter 2.3). [Pg.89]

Install a cooling tower and rednce the seal water temperature on hquid-ring vacuum pumps, allowing resheaving and reduction in horsepower to achieve the same vacuum level. [Pg.458]

This means, the vacuum pump must extract 15kgh steam and the 10kgh air from 60 mbar. It can be seen that the quantities of saturation steam are considerable in vacuum. The importance of good cooling of the outlet flow from a condenser is shown by the fact that for the above example a decrease in the outlet temperature from 30 to 25 °C would mean a reduction of the steam mass flow rate to only 7 kgh . ... [Pg.20]

Lower distillation temperatures can be obtained by the use of steam. In this case the steam does not usually condense in the tower, and the plates contain only the high boiling organic material. The steam acts as an inert carrier that is easily condensed and does not have to pass through the vacuum pump. In some cases the temperature gradient in the distillation column may be so great that the steam will condense in the upper portions, and it should be withdrawn. If too much water collects on a plate, it may seriously interfere with the fractionation if the water runs down the tower, it will vaporize on the lower plates and this steam recycle in the tower can overload the unit and seriously interfere with the fractionation. Theoretically it is possible to fractionate a material with a very low vapor pressure by the use of steam distillation, but the steam consumption increases as the vapor pressure on the component decreases. Reduction of the total pressure reduces the steam consumption, but if the vapor pressure of the com-... [Pg.396]

Cooling is done by spraying water on the outside of the mold (Figure 1.197) until a temperature of about 95 °C is reached. The water, which adheres in a thin film on the molded part and mold surface, evaporates by reducing the pressure in the chamber. The water removes the evaporation enthalpy (which is needed for evaporation) from the molded part and from the mold. The necessary pressure reduction in the pressure chamber to about 200 mbar absolute pressure is mostly done using vacuum pumps. At the end of this process step, the foam parts are dimensionally stable and can be demolded. [Pg.213]

To maximize turbine efficiency (by minimizing turbine back-pressure). This is achieved by condensing steam and creating an adequate vacuum. The level of vacuum created by the reduction in steam-to-water volume is typically on the order of 26 to 29 inches of mercury and is in large part a function of the cooling water inlet temperature. A contribution to the maintenance of the vacuum is obtained through the mechanical pumps and air ejectors, which form part of the condenser system. [Pg.116]

Having established the feasibility of niobium metal production by the carbothermic reduction of niobium pentoxide under temperature and pressure conditions readily attainable in the laboratory and in industry, the principles of efficient process execution may now be examined. In a high-temperature vacuum furnace operation, the quantity of gas that is to be pumped off can influence the choice of the vacuum process. When the reduction of niobium pentoxide with either carbon or niobium carbide is attempted according to the following overall equations ... [Pg.371]

Substances which boil at too high a temperature, even in the vacuum of the water pump, can often be distilled without decomposition in a high vacuum, i.e. at pressures of 1 mm. or less. Reduction of pressure... [Pg.25]

The wet disks are immediately immersed into the vapor of refluxing isopropanol. Once they reach the reflux temperature, as noted by a reduction in the rate of alcohol condensation on the disks, they are removed into the room air where they rapidly become dry and slowly cool to room temperature. At this point, the disks are individually weighed to the nearest 0.1 mg. The disks are then loaded into a metal tray with large circular regions on their bottom faces exposed and the tray placed in the load lock of a vacuum chamber. The load lock is pumped to about 10 torr and then the tray is translated into the chamber and the load lock sealed off from the chamber. The chamber is pumped to about 10 torr with a cryopump. The major residual gas is water from the rotatable rubber seal used between the evacuated space in the chamber and the water flow path into and out of the rotatable copper crucible mentioned below. Titanium vapor is sublimed from a Ti ingot by bombardment with about 8 keV electrons while the periphery of the ingot is cooled by sparse physical contacts with the water-cooled copper crucible in which it rests. The Ti vapor condenses in the line of sight from the source onto the exposed bottoms of the disks. The thickness of the deposited titanium, is monitored by a calibrated quartz crystal balance close to the quartz disks. Typically (iji 5 x 10 cm. [Pg.149]


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See also in sourсe #XX -- [ Pg.75 , Pg.77 ]




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