State multiplicity in CSTR-separator-recycle polymerisation systems

被引:40
作者
Kiss, AA [1 ]
Bildea, CS [1 ]
Dimian, AC [1 ]
Iedema, PD [1 ]
机构
[1] Univ Amsterdam, Dept Chem Engn, NL-1018 WV Amsterdam, Netherlands
关键词
reaction engineering; polymerisation; kinetics; recycle systems; nonlinear dynamics;
D O I
10.1016/S0009-2509(01)00405-5
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This article continues earlier work (Comput. Chem. Eng. 24 (2000) 209) concerning the design and control of isothermal reactor-separator-recycle systems. The multiplicity behaviour of six reaction systems of increasing complexity, from one-reactant, first-order reaction to chain-growth polymerisation, is investigated. Below a critical value of the plant Damkohler number, Da < Da(cr), the only steady state involves infinite flow rates. Feasible steady states become possible if the critical value is exceeded, Da > Da(cr). For one-reaction systems, one stable steady state is born at a transcritical bifurcation. For consecutive-reaction systems, including polymerisation, a fold bifurcation can lead to two feasible steady states. Moreover, the transcritical bifurcation is destroyed when two reactants are involved. If the gel-effect is included, a maximum of four steady states are possible. When multiple steady states exist, the achievable conversion is constrained by the instability of the low-conversion branch. This has practical importance for polymerisation systems when the radicals' quasi-steady state assumption is not valid or the gel effect is significant. (C) 2002 Elsevier Science Ltd. All rights reserved.
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页码:535 / 546
页数:12
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