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Solids Adjustment

When extended surfaces such as fins are used to enhance natural convection heat transfer between a solid and a fluid, the flow rate of the fluid in the vicinity of the solid adjusts itself to incorporate the changes in buoyancy and friction. It is obvious that this enhancement technique will work to advantage only when the increase in btroyancy is greater than the additional friction introduced. One does not need to be concerned with pressure drop or pumping power when studying natural convection since no pumps or blowers are used in (his case. Therefore, an enhancement technique in natural convection is evaluated on heat transfer performance alone. [Pg.537]

It is important to note that most treatments using the matrix method for the lattice dynamical treatment of molecular solids adjust the parameters of the potential model to fit observed frequencies. In this case, the formal error in the treatment is minimized in its importance. It may be of importance only inasmuch as the same potential model is assumed to be useful to interpret other physical properties such as gas phase second virial coefficients. It may also be important when one attempts to determine parameters for intermolecular potentials in terms of atom-atom interactions which are general to a class of molecules rather than specific to one substance. It is also evident that the error will be very serious in every case involving low-frequency librations (as for a-Ng). The reason for the small effect of the first derivative term in many cases is as follows. Both repulsive and attractive terms of the potential usually contribute significantly to the first derivative but their contributions have opposite sign and cancel. By comparison, the contribution to the second derivative of the potential is usually much larger for the repulsive potential term than for the attractive term (Shimanouchi, 1970),... [Pg.225]

Sodium gluconate can be recovered from fermentation filtrate by concentrating to 42 to 45 percent solids, adjusting to pH 7.5 with sodium hydroxide, and drum-drying. [Pg.946]

In the last years one can find a strong reorientation of most microscopical methods to study objects in natural (or adjustable) conditions without preparation. Microscopical visualization without vacuum and coating allows maintaining the natural specimen structure as well as examining its behavior under external influences (loading, chemical reactions, interaction with other solids, liquids, gases etc.)... [Pg.579]

Fig. 1 shows the block diagram of the vibrometer, in which the most sensible to small phase variations interferometric scheme is employed. It consists of the microwave and the display units. The display unit consists of the power supply 1, controller 2 of the phase modulator 3, microprocessor unit 9 and low-frequency amplifier 10. The microwave unit contains the electromechanical phase modulator 3, a solid-state microwave oscillator 4, an attenuator 5, a bidirectional coupler 6, a horn antenna 7 and a microwave detector 11. The horn antenna is used for transmitting the microwave and receiving the reflected signal, which is mixed with the reference signal in the bidirectional coupler. In the reference channel the electromechanical phase modulator is used to provide automatic calibration of the instrument. To adjust the antenna beam to the object under test, the microwave unit is placed on the platform which can be shifted in vertical and horizontal planes. [Pg.655]

This weight assumes 100 per cent, purity of the sodium hydroxide. If the commercial solid is used, its purity should be determined and a corresponding adjustment made in the weight. [Pg.637]

Diethylbarbituric acid. In a dry 250 ml. distilling flask, fitted with a thermometer reaching to within 3-4 cm. of the bottom and a condenser, place 51 g. of clean sodium and add 110 g. (140 ml.) of super-dr ethyl alcohol (Section 11,47,5). When all the sodium has reacted, introduce 20 g. of ethyl diethylmalonate and 7 0 g. of dry imea (dried at 60 for 4 hours). Heat the flask in an oil bath and slowly distil off the ethyl alcohol. As soon as the temperature of the liquid reaches 110-115°, adjust the flame beneath the bath so that the contents of the flask are maintained at this temperature for at least 4 hours. Allow the flask to cool somewhat, add 100 ml. of water and warm until the solid (veronal-sodium) dissolves. Pour the solution into a beaker, and add a further 100 ml. of water but containing 7 0 ml. of concentrated siilplmric acid this will hberate the veronal from the sodium derivative. The veronal usually crystallises out if it does not, add a few more drops of dilute sulphuric acid until the solution is acid to Congo red. Heat the contents of the beaker, with stirring and the addition of more water if necessary, until all the veronal dissolves at the boiling point. Allow the hot solution to cool, filter off the crystals of veronal and diy in the air. The yield is 12 g., m.p. 190°. [Pg.1003]

Ethyl 2-nitro-3-(5-benzyloxyindoT3-yl)propanoate (3.7 g, 0.01 mol) was dissolved in abs. ethanol (50 ml) and hydrogenated over PtO catalyst (EOg) until H2 uptake ceased (about 1.75 h). The solution was purged with nitrogen and 20% aq. NaOH solution (4.0 g) w as added. A hydrogen atmosphere was re-established and the hydrolysis was allowed to proceed overnight. The solution was diluted with water (20 ml) and filtered. The pH of the filtrate was adjusted to 6 with HOAc and heated to provide a solid precipitate. The mixture was cooled and filtered to provide 5-benzyloxytryptophan (2.64 g). [Pg.133]

Power Supplies and Controls. Induction heating furnace loads rarely can be connected directiy to the user s electric power distribution system. If the load is to operate at the supply frequency, a transformer is used to provide the proper load voltage as weU as isolation from the supply system. Adjustment of the load voltage can be achieved by means of a tapped transformer or by use of a solid-state switch. The low power factor of an induction load can be corrected by installing a capacitor bank in the primary or secondary circuit. [Pg.127]

A cocurrent evaporator train with its controls is illustrated in Fig. 8-54. The control system applies equally well to countercurrent or mixed-feed evaporators, the princip difference being the tuning of the dynamic compensator/(t), which must be done in the field to minimize the short-term effects of changes in feed flow on product quality. Solid concentration in the product is usually measured as density feedback trim is applied by the AC adjusting slope m of the density function, which is the only term related to x. This recahbrates the system whenever x must move to a new set point. [Pg.750]


See other pages where Solids Adjustment is mentioned: [Pg.67]    [Pg.1350]    [Pg.35]    [Pg.36]    [Pg.26]    [Pg.412]    [Pg.450]    [Pg.405]    [Pg.284]    [Pg.583]    [Pg.351]    [Pg.87]    [Pg.383]    [Pg.67]    [Pg.1350]    [Pg.35]    [Pg.36]    [Pg.26]    [Pg.412]    [Pg.450]    [Pg.405]    [Pg.284]    [Pg.583]    [Pg.351]    [Pg.87]    [Pg.383]    [Pg.49]    [Pg.610]    [Pg.632]    [Pg.1559]    [Pg.1930]    [Pg.2766]    [Pg.67]    [Pg.339]    [Pg.339]    [Pg.717]    [Pg.1008]    [Pg.91]    [Pg.73]    [Pg.91]    [Pg.145]    [Pg.467]    [Pg.366]    [Pg.68]    [Pg.297]    [Pg.375]    [Pg.342]    [Pg.1440]    [Pg.1570]    [Pg.1572]    [Pg.1679]   
See also in sourсe #XX -- [ Pg.405 ]

See also in sourсe #XX -- [ Pg.351 ]




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