Biomedical Engineering Reference
In-Depth Information
CHAPTER
5
I deal Flow Reacto rs
OUTLINE
5.1. Flow Rate, Residence Time,
Space Time, Space Velocity,
Dilution Rate
5.8. PFR or CSTR?
226
5.9. Steady Nonisothermal
Flow Reactors
178
230
5.2. Plug Flow Reactor
180
5.10. Reactive Extraction
237
5.3. Gasification and Fischere
Tropsch Technology
5.11. Graphic Solutions using Batch
Concentration Data
189
239
5.4. Continuous Stirred Tank Reactor
(CSTR) and Chemostat
5.11.1. Solution of a PFR using
Batch Concentration Data
194
239
5.11.2. Solution of a CSTR using
Batch Concentration Data
5.5. Multiple Reactors
206
241
5.6. Recycle Reactors
211
5.12. Summary
242
5.7. Distributed Feed and Withdraw
215
Problems
245
5.7.1. Distributed Feed
215
5.7.2. Reactive Distillation
222
5.7.3. Membrane Reactor
224
In this chapter, we deal with the fundamentals of reaction in continuous flow reactors. For
simplicity, we shall focus on the ideal isothermal reactors. Most industrial reactors are operated
in a continuous mode instead of batch because continuous reactors produce more products
with smaller equipment, require less labor and maintenance, and frequently produce better
quality control. Continuous processes are more difficult to start and stop than batch reactors,
but they make product without stopping to change batches and they require minimum labor.
Batch processes can be tailored to produce small amounts of product when needed. Batch
processes are also ideal to measure rates and kinetics in order to design continuous processes:
Here one only wants to obtain information rapidly without generating too much product that
must be disposed of. In pharmaceuticals, batch processes are sometimes desired to assure
 
Search WWH ::




Custom Search