Czasopismo
Tytuł artykułu
Autorzy
Warianty tytułu
Języki publikacji
Abstrakty
The first part of this approach is concerned with the elaboration of a radical polymerization model of styrenne, based on a kinetic diagram that includes chemical and thermal initiation, propagation, termination by recombination and chain transfer to the monomer. Furthermore, volume contraction during polymerization is considered, as well as the gel and glass effects. The mathematical formalism that describes the model in terms of moments is explored in detail. The model was then used to predict the changes in monomer conversion and molecular weight after intermediate addition of initiator and monomer. The results of this operation are dependent on the conditions of the reaction mass, quantity, and moment of substance addition. Therefore, the simulations were performed at different times with respect to the gel effect; before, during and after this phenomenon, and also with respect to different temperatures and initiators. Increasing the initiator concentration before the gel effect leads to an earlier appearance of the phenomenon and to a decrease in molecular weight. The ratio $$\bar M_w /\bar M_n $$ reveals a polydispersity index smaller for the intermediate addition of initiator. No significant changes take place during or after the gel effect. If along with the initiator, unreacted monomver (used to dissolve the initiator) enters the reactor, a small dip in conversion is observed. The general conclusion of this paper reveals the intermediate addition of initiator as a method to control polymer properties and to prevent the “dead-end” polymerization of styrene.
Czasopismo
Rocznik
Tom
Numer
Strony
69-90
Opis fizyczny
Daty
wydano
2003-03-01
online
2003-03-01
Twórcy
autor
- Department of Chemical Engineering, Technical University “Gh. Asachi”, IASI, B-dul D. Mangeron No. 71A, 6600 IASI, Romania, scurtean@ch.tuiasi.ro
Bibliografia
- [1] D.S. Achilias and C. Kiparissides: “Development of a General Mathematical Framework for Modeling Diffusion-Controled Free Radical Polymerization Reactions”, Macromolecules, Vol. 25, (1992), pp. 3739–3750. http://dx.doi.org/10.1021/ma00040a021[Crossref]
- [2] R.G. Gilbert, J.F. Anstey, N. Subramanian, M.J. Monteiro: “Emulsion Polymerization as a novel tool in controlled free-radical polymerization”, Polym. Prepr., Vol. 40, (1999), pp. 297–298.
- [3] A. Sirohi and K. Ravindranath: “Modeling of Ionic Polymerization Processes: Styrene and Butadiene”, AIChE, Spring 99 Meeting, Houston, 1999.
- [4] K.J. Kim: Modeling and Control of Continuous Free Radical Polymerization Reactors, Thesis (PhD), University of Maryland, 1991.
- [5] S. Curteanu, V. Bulacovschi, R. Diaconescu: “Modeling of Free Radical Polymerization of Styrene Using a Binary Mixture of Initiarors”, Proc. Rom. Acad., Vol. 3, (2001), pp. 207–213.
- [6] S. Curteanu and V. Bulacovschi: “Modeling of Free Radical Polymerization of Styrene Using a Binary Mixture of Initiators and Isothermal Steps of Temperature”, Rev. Roum. Chim., in press.
- [7] W.Y. Chiu, G.M. Carratt, D.S. Soong: “A Computer Model for the Gel effect in Free Radical Polymerization”, Macromolecules, Vol. 16, (1983), pp. 348–357. http://dx.doi.org/10.1021/ma00237a002[Crossref]
- [8] M. Constantinescu, V. Bulacovschi, S. Curteanu: “Free Radical Polymerization of Styrene. Modeling and Simulation”, Bul. Polyt. Inst. Iasi, Tom XLIII (XLVII), 3–4, (1997), pp. 91–103.
- [9] G.A. O'Neil, M.B. Wisnudel, J.M. Torkelson: “An Evaluation of Free Volume Approaches to Describe the Gel Effect in Free Radical Polymerization”, Macromolecules, Vol. 31, (1998), pp. 4537–4545. http://dx.doi.org/10.1021/ma9713670[Crossref]
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_2478_BF02479259