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Reactor electrical heated

Reactor electrical heat input(l) Coil/jacket heat balance Condenser heat extract rate (1) Reactor heat loss... [Pg.460]

If an electric current flows through a wire, ihe heat generated internally will result in a temperature distribution between the central axis and the surface of the wire. This type of problem will also arise in chemical or nuclear reactors where heat is generated internally. It is necessary to determine the temperature distribution in such a system and the maximum temperature which will occur. [Pg.412]

Figure 5.2. Two of the more common types of low pressure CVD reactor, (a) Hot Filament Reactor - these utilise a continually pumped vacuum chamber, while process gases are metered in at carefully controlled rates (typically a total flow rate of a few hundred cubic centimetres per minute). Throttle valves maintain the pressure in the chamber at typically 20-30 torr, while a heater is used to bring the substrate up to a temperature of 700-900°C. The substrate to be coated - e.g. a piece of silicon or molybdenum - sits on the heater, a few millimetres beneath a tungsten filament, which is electrically heated to temperatures in excess of 2200 °C. (b) Microwave Plasma Reactor - in these systems, microwave power is coupled into the process gases via an antenna pointing into the chamber. The size of the chamber is altered by a sliding barrier to achieve maximum microwave power transfer, which results in a ball of hot, ionised gas (a plasma ball) sitting on top of the heated substrate, onto which the diamond film is deposited. Figure 5.2. Two of the more common types of low pressure CVD reactor, (a) Hot Filament Reactor - these utilise a continually pumped vacuum chamber, while process gases are metered in at carefully controlled rates (typically a total flow rate of a few hundred cubic centimetres per minute). Throttle valves maintain the pressure in the chamber at typically 20-30 torr, while a heater is used to bring the substrate up to a temperature of 700-900°C. The substrate to be coated - e.g. a piece of silicon or molybdenum - sits on the heater, a few millimetres beneath a tungsten filament, which is electrically heated to temperatures in excess of 2200 °C. (b) Microwave Plasma Reactor - in these systems, microwave power is coupled into the process gases via an antenna pointing into the chamber. The size of the chamber is altered by a sliding barrier to achieve maximum microwave power transfer, which results in a ball of hot, ionised gas (a plasma ball) sitting on top of the heated substrate, onto which the diamond film is deposited.
Reactor 18 [R 18] Modular Int ated 3D System with Electrically Heated pCauze... [Pg.285]

Three different types of furnaces are generally in use for calcination. The shaft furnace is considered to be the most suited for calcining coarse limestone. Furnaces of the rotary kiln type are used for handling materials of mixed particle sizes and lumps which disintegrate during the process. Calcination can be carried out in a fluidized bed-reactor for materials of small and uniform particle size. These furnaces are usually fired with gas, oil or coke in some cases electric heating is resorted to. [Pg.348]

The maximum heat flux achievable with nucleate boiling is known as the critical heat flux. In a system where the surface temperature is not self-limiting, such as a nuclear reactor fuel element, operation above the critical flux will result in a rapid increase in the surface temperature, and in the extreme situation the surface will melt. This phenomenon is known as burn-out . The heating media used for process plant are normally self-limiting for example, with steam the surface temperature can never exceed the saturation temperature. Care must be taken in the design of electrically heated vaporisers to ensure that the critical flux can never be exceeded. [Pg.732]

Heat from all the hot exhaust gas streams is used for steam generation to drive the steam turbine. Thus, the final products from the GE fuel-flexible process are pure hydrogen from the first reactor, C02 from the second reactor, and heat for electricity production from the third reactor. A portion of the solids in the chemical loops needs to be purged to avoid ash accumulation and maintain solid reactivity (Rizeq et al., 2002). The overall energy conversion efficiency for the GE fuel-flexible process is estimated to be 60% (Rizeq et al., 2003). [Pg.582]

Armaou and Christofides (1999) present a two-electrode design for the deposition of 500-A films on an 8-cm wafer, which sits on top of the lower electrode, as shown in Fig. 10.4-2. The reactor is fed with 10% SiEE (silane) in He at 1 torr through a showerhead. An RF power source, at 13.56 MHz frequency, is used to generate the plasma, which is transported by convection and diffusion to the surface of the wafer where reaction occurs to deposit amorphous silicon. Electrical heating elements are positioned below the wafer and along the walls to achieve a uniform temperature of the plasma and wafer at 500 K. [Pg.295]

The pyrolysis apparatus consists of a vertical, electrically-heated Vycor tube (25 mm. I.D.) packed with 6-mm. lengths of Pyrex tubing (10 mm. O.D.) and mounted in an electric furnace about 45 cm. long (Notes 1 and 2). Attached to the top is a 100-ml. dropping funnel with a pressure-equalizing side arm that has an inlet for nitrogen (Note 3). A thermocouple well inside the tube holds a movable thermocouple and extends to the bottom of the heated section (Note 4). The bottom of the reactor is fitted to a 500-ml. side-arm flask packed in ice. The side arm leads to tw o traps in series cooled in ice and to a final trap cooled in a bath of dry ice and acetone (Note 5). [Pg.26]

Five biomass samples (hazelnut shell, cotton cocoon shell, tea factory waste, olive husk and sprace wood) were pyrolyzed in a laboratory-scale apparatus designed for the purpose of pyrolysis (Demirbas, 2001, 2002a). Figure 6.4 shows the simple experimental setup of pyrolysis. The main element of the experimental device is a vertical cylindrical reactor of stainless steel, 127.0 nun in height, 17.0 nun iimer diameter and 25.0 mm outer diameter inserted vertically into an electrically heated tubular furnace and provided with an electrical heating system power source, with a heating rate of about 5 K/s. The biomass samples ground... [Pg.180]

The reformer reactor performance as an ammonia cracker was evaluated. The experiments were conducted using a reformer feed composed of 6 seem ammonia. The reactor was heated with the electric heaters to determine the heater power required to achieve high conversion. In these experiments, approximately 97% of the ammonia feed was converted to hydrogen at 900 °C (approximately 1.8 W) when operating at atmospheric pressure. - °... [Pg.539]

The pyrolytic reforming reactor was a packed bed in a quartz tube reactor. Quartz was selected to reduce the effect of the reactor construction material on the hydrocarbon decomposition rate. ° The reactor was packed with 5.0 0.1 g of AC (Darco KB-B) or CB (BP2000) carbon-based catalyst. The reactor was heated electrically and operated at 850—950 °C, and the reactants had a residence time of 20—50 s, depending on the fuel. The reactor was tested with propane, natural gas, and gasoline as the fuels. Experiments showed that a flow of 80% hydrogen, with the remainder being methane, was produced for over 180 min of continuous operation.The carbon produced was fine particles that could be blown out... [Pg.546]

Heinzel et al. [77] compared the performance of a natural gas autothermal reformer with that of a steam reformer. The ATR reactor was loaded with a Pt catalyst on a metallic substrate followed by a fixed bed of Pt catalyst. In the start-up phase, the metallic substrate was electrically heated until the catalytic combustion of a stoichiometric methane-air mixture occurred. The reactor temperature was increased by the heat of the combustion reaction and later water was added to limit the temperature rise in the catalyst, while the air flow was reduced to sub-stoichiometric settings. With respect to the steam reformer, the behavior of the ATR reactor was more flexible regarding the start-up time and the load change, thus being more suitable for small-scale stationary applications. [Pg.298]

Fig. 1, the metal atoms may be generated in an electrically heated crucible and co-condensed with the substrate on the cold walls of the reaction vessel. To minimize gas-phase reactions, a good vacuum must be maintained in the reactor during this codeposition. An alternative procedure is to condense the metal vapor into a well-stirred solution of the reactant in a suitable solvent cooled to a temperature at which the vapor pressure of the solution is <10 3 torr. This method has special advantages for the preparation of unstable organometallic compounds and for reacting metal atoms with nonvolatile substrates.2... [Pg.60]


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