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To Wall temperature

Pw Saturation vapour pressure corresponding to wall temperature ML T... [Pg.788]

In a batch forge furnace, the space above the load(s) was held at 2250 F, wall to wall. High-velocity stirring burners were fired between the 8 in. tall piers supporting the load(s). The burners were operated with fuel turndown only to minimize the concentration of triatomic molecules while inducing a high mass of inert gas from above the load. The wall-to-wall temperature drop under the product was very low—a maximum of 6°C (3.3°C). Chapter 8 discusses temperature uniformity in more detail. [Pg.57]

With reference to Fig. 2, the thermal boundary condition for which the outer wall temperature (Lw,o) is considered axially constant while the wall heat flux is considered as linearly proportional to wall temperature peripherally is referred to as the T3 boundary condition ... [Pg.493]

Figure 7.16 Radiative heat transfer coefficient from exposed bed to exposed wall as a function of gas-to-wall temperature difference (Barr et al., 1989). Figure 7.16 Radiative heat transfer coefficient from exposed bed to exposed wall as a function of gas-to-wall temperature difference (Barr et al., 1989).
Reactor temperature responds to wall temperature with a time constant of Tl and a steady-state gain of 1. If kiA is not directly known, Q/(T — Tl) may be substituted ... [Pg.76]

Vehicle Fa.ctors. Because knock is a chemical reaction, it is sensitive to temperature and reaction time. Temperature can in turn be affected either by external factors such as the wall temperature or by the amount of heat released in the combustion process itself, which is directiy related to the density of the fuel—air mixture. A vehicle factor which increases charge density, combustion chamber temperatures, or available reaction time promotes the tendency to knock. Engine operating and design factors which affect the tendency to produce knocking are... [Pg.180]

The equations presented herein do not include any viscosity correction to reflect the difference between the viscosity at the wall temperature and the bulk fluid temperature. This effect is generally negligible, except at low temperatures for organic fluids having viscosities that are strongly temperature dependent. For such conditions, the values tabulated in Table 2 should be appropriately modified. [Pg.508]

Creep of Thick-walled Cylinders. The design of relatively thick-walled pressure vessels for operation at elevated temperatures where creep caimot be ignored is of interest to the oil, chemical, and power industries. In steam power plants, pressures of 35 MPa (5000 psi) and 650°C are used. Quart2 crystals are grown hydrothermaHy, using a batch process, in vessels operating at a temperature of 340—400°C and a pressure of 170 MPa (25,000 psi). In general, in the chemical industry creep is not a problem provided the wall temperature of vessels made of Ni—Cr—Mo steel is below 350°C. [Pg.86]

Burners and combustion air ports are located in the walls of the furnace to introduce either heat or air where needed. The air path is countercurrent to the sohds, flowing up from the bottom and across each hearth. The top hearth operates at 310—540°C and dries the feed material. The middle hearths, at 760—980°C, provide the combustion of the waste, whereas the bottom hearth cools the ash and preheats the air. If the gas leaving the top hearth is odorous or detrimental to the environment, afterburning is required. The moving parts in such a system are exposed to high temperatures. The hoUow central shaft is cooled by passing combustion air through it. [Pg.46]

The time constants characterizing heat transfer in convection or radiation dominated rotary kilns are readily developed using less general heat-transfer models than that presented herein. These time constants define simple scaling laws which can be used to estimate the effects of fill fraction, kiln diameter, moisture, and rotation rate on the temperatures of the soHds. Criteria can also be estabHshed for estimating the relative importance of radiation and convection. In the following analysis, the kiln wall temperature, and the kiln gas temperature, T, are considered constant. Separate analyses are conducted for dry and wet conditions. [Pg.49]

Extruded Rigid Foa.m. In addition to low temperature thermal insulation, foamed PSs are used for insulation against ambient temperatures in the form of perimeter insulation and insulation under floors and in walls and roofs. The upside-down roof system has been patented (256), in which foamed plastic such as Styrofoam (Dow) plastic foam is appHed above the tar-paper vapor seal, thereby protecting the tar paper from extreme thermal stresses that cause cracking. The foam is covered with gravel or some other wear-resistant topping (see Roofing materials). [Pg.527]

Regenerator Vessel and Internals. The FCCU regenerator is one of the largest vessels ia the refinery (up to 18 m ia diameter) and operates at temperatures up to 775°C. The regenerator is usually a carbon steel vessel lined with refractory iasulation to maintain the wall temperature ia the area of 350°C, which is suitable for carbon steel. The usual refractory thickness ia the regenerator is 10 cm. [Pg.217]

Furnaces for Oil and Natural Gas Firing. Natural gas furnaces are relatively small in size because of the ease of mixing the fuel and the air, hence the relatively rapid combustion of gas. Oil also bums rapidly with a luminous flame. To prevent excessive metal wall temperatures resulting from high radiation rates, oil-fired furnaces are designed slightly larger in size than gas-fired units in order to reduce the heat absorption rates. [Pg.528]

Operabihty (ie, pellet formation and avoidance of agglomeration and adhesion) during kiln pyrolysis of urea can be improved by low heat rates and peripheral speeds (105), sufficiently high wall temperatures (105,106), radiant heating (107), multiple urea injection ports (106), use of heat transfer fluids (106), recycling 60—90% of the cmde CA to the urea feed to the kilns (105), and prior formation of urea cyanurate (108). [Pg.421]

Fig. 2. Profiles of conversion, A, having pressure P and gas temperature T along the reactor length. Residence time, B, where W = maximum wall temperature. To convert kPa to bar, divide by 100. Fig. 2. Profiles of conversion, A, having pressure P and gas temperature T along the reactor length. Residence time, B, where W = maximum wall temperature. To convert kPa to bar, divide by 100.
Equation (5-47b) is based on the work of Bays and McAdams [Jnd. Eng. Chem., 29, 1240 (1937)]. The significance of the term L is not clear. When L = 0, the coefficient is definitely not infinite. When E is large and the fluid temperature has not yet closely approached the wall temperature, it does not appear that the coefficient should necessarily decrease. Within the finite limits of 0.12 to 1.8 m (0.4 to 6 ft), this equation should give results of the proper order of magnitude. [Pg.562]


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