Chemical reactors tubular reactor

Example 9.11 Modeling of a nonisothermal plug flow reactor Tubular reactors are not homogeneous, and may involve multiphase flows. These systems are called diffusion convection reaction systems. Consider the chemical reaction A -> bB described by a first-order kinetics with respect to the reactant A. For a nonisothermal plug flow reactor, modeling equations are derived from mass and energy balances... 

The constant-flux reactor Tubular reactors control better than batch STR Stable temperature control when scaled up and fine chemical reactions... 

Five reactor designs are commonly used in the chemical processing industry stirred reactors, fixed-bed reactors, fluidized-bed reactors, tubular reactors, and furnace reactors. Nuclear reactors are also used to produce steam for power generation. 

Reactors are used to combine raw materials, heat, pressure, and catalysts in the right proportions. Five reactor designs are commonly used in the chemical processing industry stirred reactors, fixed-bed reactors, fluidized-bed reactors, tubular reactors, and furnace reactors. The basic components of a reactor include a shell, a heating or cooling device, two or more product inlet ports, and one outlet port. Critical process variables in reactor operation include temperature, pressure, concentration of reactants, catalysts, and time. 

Classification of the many different encapsulation processes is usehil. Previous schemes employing the categories chemical or physical are unsatisfactory because many so-called chemical processes involve exclusively physical phenomena, whereas so-called physical processes can utilize chemical phenomena. An alternative approach is to classify all encapsulation processes as either Type A or Type B processes. Type A processes are defined as those in which capsule formation occurs entirely in a Hquid-filled stirred tank or tubular reactor. Emulsion and dispersion stabiUty play a key role in determining the success of such processes. Type B processes are processes in which capsule formation occurs because a coating is sprayed or deposited in some manner onto the surface of a Hquid or soHd core material dispersed in a gas phase or vacuum. This category also includes processes in which Hquid droplets containing core material are sprayed into a gas phase and subsequentiy solidified to produce microcapsules. Emulsion and dispersion stabilization can play a key role in the success of Type B processes also. 

The epitaxy reactor is a specialized variant of the tubular reactor in which gas-phase precursors are produced and transported to a heated surface where thin crystalline films and gaseous by-products are produced by further reaction on the surface. Similar to this chemical vapor deposition (CVE)) are physical vapor depositions (PVE)) and molecular beam generated deposits. Reactor details are critical to assuring uniform, impurity-free deposits and numerous designs have evolved (Fig. 22) (89). 

Biphenyl has been produced commercially in the United States since 1926, mainly by The Dow Chemical Co., Monsanto Co., and Sun Oil Co. Currently, Dow, Monsanto, and Koch Chemical Co. are the principal biphenyl producers, with lesser amounts coming from Sybron Corp. and Chemol, Inc. With the exception of Monsanto, the above suppHers recover biphenyl from high boiler fractions that accompany the hydrodealkylation of toluene [108-88-3] to benzene (6). Hydrodealkylation of alkylbenzenes, usually toluene, C Hg, is an important source of benzene, C H, in the United States. Numerous hydrodealkylation (HDA) processes have been developed. Most have the common feature that toluene or other alkylbenzene plus hydrogen is passed under pressure through a tubular reactor at high temperature (34). Methane and benzene are the principal products formed. Dealkylation conditions are sufficiently severe to cause some dehydrocondensation of benzene and toluene molecules. 

Tubular reactors have empty spaces only between the catalyst particles. This eliminates one big disadvantage of CSTRs. On the other hand, the mathematical description and analysis of the data become more complicated. For chemical reaction studies it is still useful to detect major changes or differences in reaction mechanism. 

Fig ure 4-16. Trickle-bed (tubular reactor) for hydrodesulfurization. (Source J. M. Smith, Chemical Engineering Kinetics, 3rd ed., McGraw-Hill, Inc., 1981.)... 

Hannon, J., Mixing and Chemical Reaction in Tubular Reactors and Stirred Tanks, PhD. Thesis, Cranfield Institute of Technology, U.K., 1992. 

Continuous chemical reaction processes in a tubular reactor. 

Similar approaches are applicable in the chemical industry. For example, maleic anhydride is manufactured by partial oxidation of benzene in a fixed catalyst bed tubular reactor. There is a potential for extremely high temperatures due to thermal runaway if feed ratios are not maintained within safe limits. Catalyst geometry, heat capacity, and partial catalyst deactivation have been used to create a self-regulatory mechanism to prevent excessive temperature (Raghaven, 1992). 

Donnet, M., Jongen, N., Lemaitre, J., Bowen, P. and Hofmann, H., 1999. Better control of nucleation and phase purity using a new segmented flow tubular reactor Model system Precipitation of calcium oxalate. In 14th International Symposium on Industrial Crystallization. Cambridge, U.K., September 12-16, Institution of Chemical Engineers, CD ROM, pp. 1-13. 

The advantages of continuous tubular reactors are well known. They include the elimination of batch to batch variations, a large heat transfer area and minimal handling of chemical products. Despite these advantages there are no reported commercial instances of emulsion polymerizations done in a tubular reactor instead the continuous emulsion process has been realized in series-connected stirred tank reactors (1, . ... 

Walker, R. E., Chemical reaction and diffusion in a catalytic tubular reactor, Phys. Fluids 4 (1961) 1211-1216. 

This section is concerned with batch, semi-batch, continuous stirred tanks and continuous stirred-tank-reactor cascades, as represented in Fig. 3.1 Tubular chemical reactor systems are discussed in Chapter 4. 

Mathematical models of tubular chemical reactor behaviour can be used to predict the dynamic variations in concentration, temperature and flow rate at various locations within the reactor. A complete tubular reactor model would however be extremely complex, involving variations in both radial and axial... 

Chapter 4 eoncerns differential applications, which take place with respect to both time and position and which are normally formulated as partial differential equations. Applications include diffusion and conduction, tubular chemical reactors, differential mass transfer and shell and tube heat exchange. It is shown that such problems can be solved with relative ease, by utilising a finite-differencing solution technique in the simulation approach. 

Chemical Kinetics, Tank and Tubular Reactor Fundamentals, Residence Time Distributions, Multiphase Reaction Systems, Basic Reactor Types, Batch Reactor Dynamics, Semi-batch Reactors, Control and Stability of Nonisotheimal Reactors. Complex Reactions with Feeding Strategies, Liquid Phase Tubular Reactors, Gas Phase Tubular Reactors, Axial Dispersion, Unsteady State Tubular Reactor Models... 

Other advantages of the tubular reactor relative to stirred tanks include suitability for use at higher pressures and temperatures, and the fact that severe energy transfer constraints may be readily surmounted using this configuration. The tubular reactor is usually employed for liquid phase reactions when relatively short residence times are needed to effect the desired chemical transformation. It is the reactor of choice for continuous gas phase operations. 

Tubular reactors are normally used in the chemical industry for extremely large-scale processes. When filled with solid catalyst particles, such reactors are referred to as fixed or packed bed reactors. This section treats general design relationships for tubular reactors in... 

This chapter contains a discussion of two intermediate level problems in chemical reactor design that indicate how the principles developed in previous chapters are applied in making preliminary design calculations for industrial scale units. The problems considered are the thermal cracking of propane in a tubular reactor and the production of phthalic anhydride in a fixed bed catalytic reactor. Space limitations preclude detailed case studies of these problems. In such studies one would systematically vary all relevant process parameters to arrive at an optimum reactor design. However, sufficient detail is provided within the illustrative problems to indicate the basic principles involved and to make it easy to extend the analysis to studies of other process variables. The conditions employed in these problems are not necessarily those used in current industrial practice, since the data are based on literature values that date back some years. 

This review paper is restricted to stirred vessels operated in the turbulent-flow regime and exploited for various physical operations and chemical processes. The developments in the field of computational simulations of stirred vessels, however, are not separated from similar developments in the fields of, e.g., turbulent combustion, flames, jets and sprays, tubular reactors, and multiphase reactors and separators. Fortunately, there is a strong degree of synergy and mutual cross-fertilization between these various fields. This review paper focuses on aspects specific to stirred vessels (such as the revolving impeller, the resulting strong spatial variations in turbulence properties, and the macroinstabilities) and on the processes carried out in them. 

Particular attention is to be paid to closure models exploiting various types of PDFs such as beta, presumed, or full PDFs (e.g., Baldyga, 1994 Fox, 1996, 2003 Ranade, 2002). While PDFs have successfully been exploited for describing chemical reactions in turbulent flames, tubular reactors (Baldyga and Henczka, 1997), and a Taylor-Couette reactor (Marchisio and Barresi, 2003), they have never been used successfully in stirred reactors so far. 

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