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REACTIVE DISTILLATION
Presented By:
Jay Jawalge (11920039)
Rupali Kadam (11920081)
Karthik Iyer (11810069)
Payal Khandagale (11920014)
Arjun Phad (11920021) 1Group 7
Content
• Reactive Separation Technology
• What is Reactive Distillation?
• History of Reactive Distillation?
• Why reactive Distillation?
• Why not Reactive Distillation?
• Principle
• Hardware aspect
• Process alternative
• Case study
• Applications
• References
Group 7 2
Reactive Separation Technology
Group 7 3
Fig.1, Multi-functional reactor [5]
• Traditional flow sheet of a
chemical process consists of a
reactor.
• Development and application
of integrated processes.
• Better process economy.
• Multi-functional reactor.
What is Reactive Distillation?
• Chemical reaction and conventional distillation are integrated
• Example of process intensification
• Substantially smaller, cleaner, safer, and energy efficient technology
4Group 7
History of Reactive Distillation
Homogeneously catalysed esterification
Heterogeneously catalysed process, methyl tert-butyl ether
(MTBE)
The intensified (Eastman-Kodak) process, Methyl Acetate
Group 7 5
1920
1978
1984
Continued…
Fig.2, Conventional (left) and intensified (right) methyl acetate synthesis processes. The conventional process consists of one reactor followed by eight distillation columns
and one extraction column. The intensified (Eastman-Kodak) process uses reactive distillation technology, Ref. [1].
6Group 7
Example
Group 7 7
Fig. 3, Processing schemes for a reaction sequence where C and D are both desired products, [5]
Why Reactive Distillation?
Increased conversion
Increased selectivity
Reduced energy consumption
Overcoming of azeotropes
Simplified separation of close-boiling components
Capital savings
8Group 7
Why NOT Reactive Distillation?
Volatility constraints
Operating-window constraints
Occurrence of reactive azeotropes
Occurrence of multiple steady states
9Group 7
Principle
• Le chatelier’s principle
Group 7 10
• Semi-batch reactor • Reactive distillation
Group 7 11
Fig. 4 Semi-batch reactor, Ref. [3] Fig. 5 Reactive distillation, Ref. [3]
Continued…
Hardware Aspect
Group 7 12
Fig. 6, Non-catalytic column internals for Reactive distillation, Ref.[1]
Group 7 13Fig. 7, Non-catalytic column internals for Reactive distillation, Ref.[1]
Fig.6, Hybrid structure
Process alternative
Group 7 14
Fig.8, Equipment for Processes that Combine Reaction and Distillation Steps, Ref. destillation in der Prozesssynthese (Ph.D. thesis), TU Dortmund,1998
Case Study: A reactive distillation process for deep
hydrodesulphurization of diesel
Group 7
15
Fig. 9, Reactive distillation column configuration for ultra-low sulfur diesel
production
• equilibrium stage model
• H2 to hydrocarbon (HC) feed
ratio of 3.
under optimal design and operating conditions,
reactive distillation could be considered as a viable
technological alternative to produce ULSD.
Reactive Distillatory Unit: Video
Group 7 16
Applications of Reactive Distillation
Group 7 17
Table.1, Industrial applications of reactive distillation, Ref. [4]
References
[1] Keller, T. (2014). Reactive Distillation. Distillation, 261–294
[2] Reaction Distilation Unit by Goel Scientific Glass Works Ltd
[3] http://umich.edu/~elements/5e/web_mod/distill/index.htm
[4] Nguyen, Quy & Nguyen, Kim & Nguyen, Tuan-Anh & Tetsuo, Fuchino. (2020).
Overcome the equilibrium limitation in para-Xylene production by using reactive
distillation method
[5] Shah, Binoy & Shah, Parin. (2015). Reactive Distillation In Process Industries.
18Group 7
Continued…
[6] D.W. Agar, Multifunctional reactors: old preconceptions and new
dimensions, Chem. Eng. Sci. 54 (1999) 1299e1305.
[7] B. Bessling, Zur Reaktivdestillation in der Prozesssynthese (Ph.D. thesis), TU
Dortmund, 1998.
[8] G. Schembecker, S. Tlatlik, Process synthesis for reactive separations,
Chem. Eng. Process. 42 (2003) 179e189.
[9] W. Song, R.S. Huss, M.F. Doherty, M.F. Malone, Discovery of a reactive
azeotrope, Nature 388 (1997) 561e563.
Group 7 19
Thank You
Group 7 20

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Reactive Distillation: An Efficient Process Intensification Technology

  • 1. REACTIVE DISTILLATION Presented By: Jay Jawalge (11920039) Rupali Kadam (11920081) Karthik Iyer (11810069) Payal Khandagale (11920014) Arjun Phad (11920021) 1Group 7
  • 2. Content • Reactive Separation Technology • What is Reactive Distillation? • History of Reactive Distillation? • Why reactive Distillation? • Why not Reactive Distillation? • Principle • Hardware aspect • Process alternative • Case study • Applications • References Group 7 2
  • 3. Reactive Separation Technology Group 7 3 Fig.1, Multi-functional reactor [5] • Traditional flow sheet of a chemical process consists of a reactor. • Development and application of integrated processes. • Better process economy. • Multi-functional reactor.
  • 4. What is Reactive Distillation? • Chemical reaction and conventional distillation are integrated • Example of process intensification • Substantially smaller, cleaner, safer, and energy efficient technology 4Group 7
  • 5. History of Reactive Distillation Homogeneously catalysed esterification Heterogeneously catalysed process, methyl tert-butyl ether (MTBE) The intensified (Eastman-Kodak) process, Methyl Acetate Group 7 5 1920 1978 1984
  • 6. Continued… Fig.2, Conventional (left) and intensified (right) methyl acetate synthesis processes. The conventional process consists of one reactor followed by eight distillation columns and one extraction column. The intensified (Eastman-Kodak) process uses reactive distillation technology, Ref. [1]. 6Group 7
  • 7. Example Group 7 7 Fig. 3, Processing schemes for a reaction sequence where C and D are both desired products, [5]
  • 8. Why Reactive Distillation? Increased conversion Increased selectivity Reduced energy consumption Overcoming of azeotropes Simplified separation of close-boiling components Capital savings 8Group 7
  • 9. Why NOT Reactive Distillation? Volatility constraints Operating-window constraints Occurrence of reactive azeotropes Occurrence of multiple steady states 9Group 7
  • 10. Principle • Le chatelier’s principle Group 7 10
  • 11. • Semi-batch reactor • Reactive distillation Group 7 11 Fig. 4 Semi-batch reactor, Ref. [3] Fig. 5 Reactive distillation, Ref. [3] Continued…
  • 12. Hardware Aspect Group 7 12 Fig. 6, Non-catalytic column internals for Reactive distillation, Ref.[1]
  • 13. Group 7 13Fig. 7, Non-catalytic column internals for Reactive distillation, Ref.[1] Fig.6, Hybrid structure
  • 14. Process alternative Group 7 14 Fig.8, Equipment for Processes that Combine Reaction and Distillation Steps, Ref. destillation in der Prozesssynthese (Ph.D. thesis), TU Dortmund,1998
  • 15. Case Study: A reactive distillation process for deep hydrodesulphurization of diesel Group 7 15 Fig. 9, Reactive distillation column configuration for ultra-low sulfur diesel production • equilibrium stage model • H2 to hydrocarbon (HC) feed ratio of 3. under optimal design and operating conditions, reactive distillation could be considered as a viable technological alternative to produce ULSD.
  • 16. Reactive Distillatory Unit: Video Group 7 16
  • 17. Applications of Reactive Distillation Group 7 17 Table.1, Industrial applications of reactive distillation, Ref. [4]
  • 18. References [1] Keller, T. (2014). Reactive Distillation. Distillation, 261–294 [2] Reaction Distilation Unit by Goel Scientific Glass Works Ltd [3] http://umich.edu/~elements/5e/web_mod/distill/index.htm [4] Nguyen, Quy & Nguyen, Kim & Nguyen, Tuan-Anh & Tetsuo, Fuchino. (2020). Overcome the equilibrium limitation in para-Xylene production by using reactive distillation method [5] Shah, Binoy & Shah, Parin. (2015). Reactive Distillation In Process Industries. 18Group 7
  • 19. Continued… [6] D.W. Agar, Multifunctional reactors: old preconceptions and new dimensions, Chem. Eng. Sci. 54 (1999) 1299e1305. [7] B. Bessling, Zur Reaktivdestillation in der Prozesssynthese (Ph.D. thesis), TU Dortmund, 1998. [8] G. Schembecker, S. Tlatlik, Process synthesis for reactive separations, Chem. Eng. Process. 42 (2003) 179e189. [9] W. Song, R.S. Huss, M.F. Doherty, M.F. Malone, Discovery of a reactive azeotrope, Nature 388 (1997) 561e563. Group 7 19