Design and control of a gas-phase adiabatic tubular reactor process with liquid recycle

Citation
F. Reyes et Wl. Luyben, Design and control of a gas-phase adiabatic tubular reactor process with liquid recycle, IND ENG RES, 40(17), 2001, pp. 3762-3774
Citations number
7
Categorie Soggetti
Chemical Engineering
Journal title
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
ISSN journal
08885885 → ACNP
Volume
40
Issue
17
Year of publication
2001
Pages
3762 - 3774
Database
ISI
SICI code
0888-5885(20010822)40:17<3762:DACOAG>2.0.ZU;2-X
Abstract
Previous studies have explored the design and control of processes with gas -phase adiabatic tubular reactors that feature a gas recycle and a simple s eparation section consisting of a single ideal separator vessel. The gas re cycle leads to high compressor capital and operating costs. This paper exte nds this work to the case in which a distillation column is required in the separation section and the recycle stream is liquid. The liquid recycle me ans that there are no compressor costs to counterbalance the reactor costs. However, there are large capital and energy costs associated with the vapo rization/condensation of the recycle stream. For the numerical case studied , the liquid recycle process is more expensive than the gas recycle process , and it is more difficult to control. The basic reaction is A + B --> C. T hree reaction systems are considered: case 1 (irreversible with moderate ac tivation energy), case 2 (irreversible with high activation energy), and ca se 3 (reversible). The optimum steady-state designs for cases 1 and 3 can b e effectively controlled by the same control structure. The optimum steady- state design for case 2 cannot be controlled, and the process has to be red esigned to prevent reactor runaways. The concentration of one of the reacta nts has to be reduced so that it becomes a limiting reactant, thus providin g self-regulation. This self-regulation in the liquid recycle process is no t as effective as that in the gas recycle system because of the slower chan ges in concentrations due to the larger holdups of material in the liquid p hase.