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Temperature of atmosphere

Monthly consumption of water steam was measured in a production plant. Simultaneously the monthly average temperature of atmosphere was taken. The obtained pairs of values are in the table ... [Pg.128]

Corrosion rate of steel vs temperature of atmospheric tower sour condensate water. 19... [Pg.1]

Example 1 LNG Vaporization and Compression A port facility for unloading liquefied natural gas (LNG) is under consideration. The LNG arrives by ship, stored as saturated liquid at 115 K and 1.325 bar, and is unloaded at the rate of 450 kg s h It is proposed to vaporize the LNG with heat discarded from a heat engine operating between 300 K, the temperature of atmospheric air, and 115 K, the temperature of the vaporizing LNG. The saturated-vapor LNG so produced is compressed adiabatically to 20 bar, using the work produced by the heat engine to supply part of the compression work. Estimate the work to be supplied from an external source. [Pg.660]

Measurements of the rotational and vibrational temperatures of atmospheric molecules provide direct information on the molecular processes in the upper atmosphere. These temperatures are obtained from high resolution vibrational and rotational spectral profiles. [Pg.302]

Yuji, T. Suzaki, Y. Yamawaki, T. Sakaue, H. Akatsuka, H. (2007). Experimental Study of Temperatures of Atmospheric-Pressure Nonequilibrium Ar/N2 Plasma Jets and Poly(ethylene terephtalate)-Surface Processing. Jpn. J. Appl Phys., Vol. 46, No. 2, (February 2007), pp. 795-798, ISSN 1347-4065... [Pg.308]

Ambient temperature Temperature of atmosphere in intimate contact with the electrical part/device. [Pg.1348]

Figure 6.30 shows the grand composite curve plotted from the problem table cascade in Fig. 6.186. The starting point for the flue gas is an actual temperature of 1800 C, which corresponds to a shifl ed temperature of (1800 — 25) = mS C on the grand composite curve. The flue gas profile is not restricted above the pinch and can be cooled to pinch temperature corresponding to a shifted temperature of 145 C before venting to the atmosphere. The actual stack temperature is thus 145 + 25= 170°C. This is just above the acid dew point of 160 C. Now calculate the fuel consumption ... Figure 6.30 shows the grand composite curve plotted from the problem table cascade in Fig. 6.186. The starting point for the flue gas is an actual temperature of 1800 C, which corresponds to a shifl ed temperature of (1800 — 25) = mS C on the grand composite curve. The flue gas profile is not restricted above the pinch and can be cooled to pinch temperature corresponding to a shifted temperature of 145 C before venting to the atmosphere. The actual stack temperature is thus 145 + 25= 170°C. This is just above the acid dew point of 160 C. Now calculate the fuel consumption ...
Commercial equipment is available which automatically switches from atmospheric distillation to vacuum distillation and calculates the distillation curve as temperatures under atmospheric pressure conditions as a function of weight or volume per cent recovery. [Pg.18]

Measuring the gross heating value (mass) is done in the laboratory using the ASTM D 240 procedure by combustion of the fuel sample under an oxygen atmosphere, in a bomb calorimeter surrounded by water. The thermal effects are calculated from the rise in temperature of the surrounding medium and the thermal characteristics of the apparatus. [Pg.180]

Certain curves, T = f(% distilled), level off at high temperatures due to the change in pressure and to the utilization of charts for converting temperatures under reduced pressure to equivalent temperatures under atmospheric pressure. [Pg.332]

The nitrogenase system reduces hundreds of millions of kilograms of nitrogen gas to ammonia each year, catalysing tire reaction at ambient temperatures and atmospheric pressure. Nitrogenase consists of two proteins tliat contain... [Pg.2990]

Appreciable quantities are also obtained as a by-product in the manufacture of hydrogen from naphtha-gaseous hydrocarbons. In this process the gaseous hydrocarbon and superheated steam under a pressure of about 10 atmospheres and at a temperature of 1000 K are passed over a nickel-chromium catalyst. Carbon monoxide and hydrogen are produced ... [Pg.180]

Ammonia is a colourless gas at room temperature and atmospheric pressure with a characteristic pungent smell. It is easily liquefied either by cooling (b.p. 240 K) or under a pressure of 8-9 atmospheres at ordinary temperature. Some of its physical and many of its chemical properties are best understood in terms of its structure. Like the other group head elements, nitrogen has no d orbitals available for bond formation and it is limited to a maximum of four single bonds. Ammonia has a basic tetrahedral arrangement with a lone pair occupying one position ... [Pg.216]

Effect of impurities upon the melting point. Let us take a specific example and examine the effect of the addition of a small quantity of naphthalene to an equilibrium mixture of pure solid and liquid a-naphthol at the temperature of the true melting point (95 5°) at atmospheric pressure. [Pg.23]

Vinylacetic acid. Place 134 g. (161 ml.) of allyl cyanide (3) and 200 ml. of concentrated hydrochloric acid in a 1-htre round-bottomed flask attached to a reflux condenser. Warm the mixture cautiously with a small flame and shake from time to time. After 7-10 minutes, a vigorous reaction sets in and the mixture refluxes remove the flame and cool the flask, if necessary, in cold water. Ammonium chloride crystallises out. When the reaction subsides, reflux the mixture for 15 minutes. Then add 200 ml. of water, cool and separate the upper layer of acid. Extract the aqueous layer with three 100 ml. portions of ether. Combine the acid and the ether extracts, and remove the ether under atmospheric pressure in a 250 ml. Claisen flask with fractionating side arm (compare Fig. II, 13, 4) continue the heating on a water bath until the temperature of the vapour reaches 70°. Allow the apparatus to cool and distil under diminished pressure (compare Fig. II, 20, 1) , collect the fraction (a) distilling up to 71°/14 mm. and (6) at 72-74°/14 mm. (chiefly at 72 5°/ 14 mm.). A dark residue (about 10 ml.) and some white sohd ( crotonio acid) remains in the flask. Fraction (6) weighs 100 g. and is analytically pure vinylacetic acid. Fraction (a) weighs about 50 g. and separates into two layers remove the water layer, dry with anhydrous sodium sulphate and distil from a 50 ml. Claisen flask with fractionating side arm a further 15 g. of reasonably pure acid, b.p. 69-70°/12 mm., is obtained. [Pg.465]

P-Cyanopyridine. Mix 25 g. of powdered nicotinamide with 30g. of phosphoric oxide in a 150 ml. distilling flask by shaking. Immerse the flask in an oil bath and arrange for distillation under a pressure of about 30 mm. Raise the temperature of the oil bath rapidly to 300°, then remove the oil bath and continue the heating with a free flame as long as a distillate is obtained. The nitrile crystallises on cooling to a snow-white solid. Redistil the solid at atmospheric pressure practically all of it passes over at 201° and crystallises completely on cooling. The yield of p-cyanopyridine, m.p. 49°, is 20 g. [Pg.850]

A somewhat different type of high pressure reaction vessel is illustrated in Figs. VI, 4, 3-5. This is designed for hydrogenation reactions at working pressures from 1 to 300 atmospheres (4,500 lb. per square inch) and at temperatures from atmospheric up to 400°. Fig. VI, 4, 3... [Pg.869]

Add 40 ml. of ethyl alcohol to 21 -5 g. of 70 per cent, ethylenediamine solution (0 -25 mol) dissolve 36 -5 g. of adipic acid (0 -25 mol) in 50 ml. of a 6 1 mixture of ethyl alcohol and water. Mix the two solutions, stir and cool. Filter off the resulting salt and recrystalliae it from 60 ml. of a 6 1 ethyl alcohol - water mixture, and dry the salt in the air. Heat the salt in an atmosphere of oxygen-free nitrogen or of carbon dioxide in an oil bath until it melts (ca. 160°) the product will sohdify after a short time. Reduce the pressure to 15 mm. of mercury or less and raise the temperature of the oil bath until the product remelts (about 290°) and continue the heating for 4r-5 hours. Upon coohng, a nylon type polymer is obtained. [Pg.1025]

Alkenes resemble alkanes m most of their physical properties The lower molecular weight alkenes through 4 are gases at room temperature and atmospheric pressure The dipole moments of most alkenes are quite small Among the 4 isomers 1 butene cis 2 butene and 2 methylpropene have dipole moments m the 0 3-05 D range trans 2 butene has no dipole moment Nevertheless we can learn some things about alkenes by looking at the effect of substituents on dipole moments... [Pg.196]


See other pages where Temperature of atmosphere is mentioned: [Pg.569]    [Pg.47]    [Pg.158]    [Pg.158]    [Pg.123]    [Pg.390]    [Pg.391]    [Pg.916]    [Pg.513]    [Pg.569]    [Pg.47]    [Pg.158]    [Pg.158]    [Pg.123]    [Pg.390]    [Pg.391]    [Pg.916]    [Pg.513]    [Pg.77]    [Pg.15]    [Pg.2767]    [Pg.215]    [Pg.180]    [Pg.199]    [Pg.3]    [Pg.4]    [Pg.39]    [Pg.105]    [Pg.196]    [Pg.257]    [Pg.305]    [Pg.337]    [Pg.374]    [Pg.16]    [Pg.512]    [Pg.214]    [Pg.215]   
See also in sourсe #XX -- [ Pg.147 ]

See also in sourсe #XX -- [ Pg.750 ]

See also in sourсe #XX -- [ Pg.776 ]




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