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Actual temperature

The grand composite curve is obtained by plotting the problem table cascade. A typical grand composite curve is shown in Fig. 6.24. It shows the heat flow through the process against temperature. It should be noted that the temperature plotted here is shifted temperature T and not actual temperature. Hot streams are represented ATn,in/2 colder and cold streams AT iJ2 hotter than they are in practice. Thus an allowance for ATj in is built into the construction. [Pg.185]

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 ...
Figure 15.1a shows a single-stage evaporator represented on both actual and shifted temperature scales. Note that in shifted temperature scale, the evaporation and condensjftion duties are shown at different temperatures even though they are at the same actual temperature. Figure 15.16 shows a similar plot for a three-stage evaporator. [Pg.355]

T(f) corresponds to the actual temperature at the time t, At is the integration time step, and the relaxation time represents the strength of the coupling (smaller values mean stronger coupling to the bafli). If the coupling is too strong (r smaller... [Pg.367]

The temperature compensator on a pH meter varies the instrument definition of a pH unit from 54.20 mV at 0°C to perhaps 66.10 mV at 60°C. This permits one to measure the pH of the sample (and reference buffer standard) at its actual temperature and thus avoid error due to dissociation equilibria and to junction potentials which have significant temperature coefficients. [Pg.942]

The enthalpy hberated on the VDP of parylene is real and in an adiabatic situation causes a rise in temperature of the coated substrate. For Parylene C, 229.1 kj/mol (54.7 cal/mol) corresponds to 1654 J/g (395 cal/g) whereas its specific heat at 25°C is only 1.00 J/(g-K) [0.239 cal/(g-K)] (33). In most practical situations, however, the mass of parylene deposited is dwarfed by the substrate mass, and the heat of polymeriza tion is dissipated within the coated substrate over the time required to deposit the coating with minimal actual temperature rise. [Pg.432]

When the actual temperature-decline-with-altitude is greater than 9.8°C/1000 m, the atmosphere is unstable, the Cj s become larger, and the concentrations of poUutants lower. As the lapse rate becomes smaUer, the dispersive capacity of the atmosphere declines and reaches a minimum when the lapse rate becomes positive. At that point, a temperature inversion exists. Temperature inversions form every evening in most places. However, these inversions are usuaUy destroyed the next morning as the sun heats the earth s surface. Most episodes of high poUutant concentrations are associated with multiday inversions. [Pg.367]

Fig. 7. Constitutional supercooling, (a) impurity concentration profile during solidification (b) actual temperature T and equilibrium freezing temperature T... Fig. 7. Constitutional supercooling, (a) impurity concentration profile during solidification (b) actual temperature T and equilibrium freezing temperature T...
Actual temperatures in practical flames are lower than calculated values as a result of the heat losses by radiation, thermal conduction, and diffusion. At high temperatures, dissociation of products of combustion into species such as OH, O, and H reduces the theoretical flame temperature (7). Increasing the pressure tends to suppress dissociation of the products and thus generally raises the adiabatic flame temperature (4). [Pg.517]

Expressions of supersaturation can then be formulated as follows (/) the difference between the chemical potential of the system and the chemical potential of at saturation, ji — ji where the chemical potential is a function of both temperature and concentration (2) the difference between the solute concentration and the concentration at equiUbrium, c — c (J) the difference between the system temperature at equiUbrium and the actual temperature,... [Pg.341]

Consistent Data-Recording Procedures. Clear procedures for recording all pertinent data from the experiment must be developed and documented, and unambiguous data recording forms estabUshed. These should include provisions not only for recording the values of the measured responses and the desired experimental conditions, but also the conditions that resulted, if these differ from those plaimed. It is generally preferable to use the values of the actual conditions in the statistical analysis of the experimental results. For example, if a test was supposed to have been conducted at 150°C but was mn at 148.3°C, the actual temperature would be used in the analysis. In experimentation with industrial processes, process equiUbrium should be reached before the responses are measured. This is particularly important when complex chemical reactions are involved. [Pg.522]

Cog enera.tion in a. Steam System. The value of energy in a process stream can always be estimated from the theoretical work potential, ie, the deterrnination of how much power can be obtained by miming an ideal cycle between the actual temperature and the rejection temperature. However, in a steam system a more tangible approach is possible, because steam at high pressure can be let down through a turbine for power. The shaft work developed by the turbine is sometimes referred to as by-product power, and the process is referred to as cogeneration. [Pg.223]

Analysts should review the technical basis for uncertainties in the measurements. They should develop judgments for the uncertainties based on the plant experience and statistical interpretation of plant measurements. The most difficult aspect of establishing the measurement errors is estabhshing that the measurements are representative of what they purport to oe. Internal reactor CSTR conditions are rarely the same as the effluent flow. Thermocouples in catalyst beds may be representative of near-waU instead of bulk conditions. Heat leakage around thermowells results in lower than actual temperature measurements. [Pg.2563]

AH = latent heat of solidification T, = absolute melting temperature T = actual temperature (absolute). [Pg.372]

With gases, flow rates must be available at standard temperature and pressure as well as actual temperature and pressure. The range of gas flow must be given, as well as whether the mixer is to be operated at full horsepower for all gas ranges or operated with the gas on. [Pg.208]

One significant practical difference in use of polytropic head is that the temperature rise in the equation is the actual temperature rise when there is no jacket cooling. The other practical uses of the equation will be covered as they apply to each compressor in the later chapters. [Pg.34]

PRESSURE SYSTEM Defined in the Pressure System Safety Regulations 2000 as a system containing one or more pressure vessels of rigid construction, any associated pipework and protective devices the pipework with its protective devices to which a transportable gas container is, or is intended to be, connected or a pipeline and its protective devices which contains or is liable to contain a relevant fluid, but does not include a transportable gas container. Here relevant fluid is steam any fluid or mixture of fluids which is at a pressure of >0.5 bar above atmospheric pressure, and which fluid or a mixture of fluids is a gas, or a liquid which would have a vapour pressure of >0.5 bar above atmospheric pressure when in equilibrium with its vapour at either tlie actual temperature of the liquid or 17.5°C or a gas dissolved under pressure in a solvent contained in a porous substance at ambient temperamre and which could be released from the solvent with the application of heat. [Pg.17]

Indoor climate The actual temperature, moisture content, and air velocity within a space. [Pg.1450]

Finally, both the state of the material and the state of stress affect the laminate strength evaluation. That is, the actual temperature and moisture conditions influence the laminae strengths. Taken together with the laminae stresses, the laminae strengths and the laminate loads lead to an evaluation of the laminate capabilities. [Pg.240]

The application of information in Figure 6.19 requires some explanation. The decision as to which calculation method to choose should be based upon the phase of the vessel s contents, its boiling point at ambient pressure T its critical temperature Tf, and its actual temperature T. For the purpose of selecting a calculation method, three different phases can be distinguished liquid, vapor or nonideal gas, and ideal gas. Should more than be performed separately for each phase, and the... [Pg.202]

S° = Degrees of superheat in a steam condition, degrees I above saturated (not the actual temperature)... [Pg.155]

Wdien specifying the material at the disk temperature, the heat loss at the disk/disk holder as well as in a flowing pipe must be recognized and the assembly may need to be insulated. This is important as it relates to the actual temperature at the bursting pressure. Establishing this burst temperature is an essential part of the system Sctfety and must not be guessed at or taken lightly. [Pg.459]

Convert the free air rates to the proper product in the tanks using the corrections outlined in a previous paragraph. Keep in mind that the manufacturer s rating tables are in free air however, the actual process calculations provide flows in terms of the actual liquids at actual temperatures and pressures. It is important that the manufacturer be given the actual fluid conditions to ensure proper capacity rating. [Pg.476]

This is close enough to 1,533 mm actual temperature might be 265°F, although plotted data are probably not that accurate. Because the feed enters at 158°F and its bubble point is 266°F, the feed is considered sub-cooled. [Pg.39]

PVg = saturated vapor pressure of water at actual temperature (psi) ... [Pg.522]

A = cross-section area of piston rod, in. acfm = actual fF/min, actual temperature and pressure B = constant bhp = brake horsepower... [Pg.573]

For ready identification, actual temperature levels are expressed in degrees Celsius (°C) while temperature difference, interval or gradient is expressed in Kelvin (K). [Pg.111]

This is defined as the percentage ratio of the water vapour pressure in the atmosphere compared to that which would saturate the atmosphere at the same temperature. Alternatively, the difference in temperature between the ambient atmosphere and that to which it would have to be cooled before moisture condensed from it, is also used as a measure of moisture content. This difference in temperature is called the dew point depression. The actual temperature at which condensation takes place is known as the dew point. The relative humidity is then expressed as ... [Pg.338]

Test heat exchangers can be fitted to side-stream circuits in process plant which simulate actual temperatures existing in the plant . Condenser tubes can be removed and corrosion assessed. [Pg.1141]


See other pages where Actual temperature is mentioned: [Pg.212]    [Pg.429]    [Pg.165]    [Pg.194]    [Pg.284]    [Pg.166]    [Pg.449]    [Pg.91]    [Pg.57]    [Pg.373]    [Pg.156]    [Pg.6]    [Pg.97]    [Pg.240]    [Pg.300]    [Pg.422]    [Pg.486]    [Pg.509]    [Pg.522]    [Pg.545]    [Pg.546]    [Pg.243]   
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