Reactor Operating Strategy and Secondary Nucleation in Emulsion Polymerization

Author(s):  
Joseph Zeaiter ◽  
Jose Romagnoli ◽  
Vincent G Gomes

Particle formation is a key step in emulsion polymerization reactions and has been the subject of extensive investigations in the past few decades. The main aim of this work was to investigate, both theoretically and experimentally, the conditions for secondary nucleation and particle evolution in batch and semi-batch emulsion polymerization. The effects of variation in monomer and emulsifier concentration in the feed, the distribution between the charge and the feed, temperature and the emulsion feed rate on polystyrene particle size distribution were investigated both theoretically and experimentally. The population balance and kinetic models developed were employed for predicting the product attributes for a range of reactor operating conditions. The sets of nonlinear algebraic and integro-differential evolution equations were solved efficiently for this work.Monomer and surfactant feed rates were found to have significant effects on the growth of polymer particles and consequently on the particle size. Different particle sizes and distributions were obtained using the same procedure with variable operating mode. A semi-batch reactor with variable monomer emulsion feed can produce latexes with variable polydispersity. A high initial rate of particle formation could lead to reduction in secondary nucleation and hence to the formation of a mono-modal PSD. This can be achieved by using high initiator and emulsifier concentrations in the feed, a high temperature, or a low monomer concentration in the charge. A low initial rate of nucleation increases the possibility of secondary nucleation and the formation of a bimodal PSD. The evolution of a bimodal PSD requires secondary nucleation after primary nucleation occurs.

2006 ◽  
Vol 6 (2) ◽  
pp. 82
Author(s):  
Iwan Harsono ◽  
Herman Hindarso ◽  
Nani Indraswati

It has been long recognized that emulsion polymerization is a complex heterogeneous process involving transport of monomers and other species and free radicals between aqueous phase and organic phases. Though there are a number of models available in the literature, most of them deal only with specific aspects in emulsion polymerization and are far from being general. To simulate this complicated process and to achieve an adequate level of understanding, a Polymer Plus' software from Aspen Technology, Inc. has been used. The objective of this work is to illustrate the principle use of Polymers Plus' and to simulate and analysis the free-radical seeded emulsion copolymerization of styrene-butadiene process model in a semi-batch reactor. The base case simulation can be used to gain process understanding by analyzing how process variables and operating conditions during the course of a semi-batch reactor affect product quality.


e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Amel Chaabouni ◽  
Valerie Massardier-Nageotte ◽  
Boubaker Elleuch ◽  
Mohamed M. Chehimi ◽  
Abdelhamid Elaissari

AbstractPolystyrene latexes were prepared, in the presence of, vinyl benzyl chloride (VBC) monomer. These particles were synthesized in surfactant-free batch radical emulsion polymerization of styrene and VBC monomer mixture, with 2,2’- azobis(2-amidino propane)di-hydrochloride (V50) initiator. The polymerization kinetics was found to be rapid, as a function of VBC monomer concentration in the polymerization recipe. It is interesting to notice that high VBC amount leads to marked coagulum formation. The final hydrodynamic particle size was found to be slightly sensitive to the VBC concentration in the investigated range. The presence of VBC at the surface of the particles was investigated by XPS analysis.


2018 ◽  
Vol 4 (3) ◽  
pp. 304
Author(s):  
I Harsono ◽  
H Hindarso ◽  
N Indraswati

It has been long recognized that emulsion polymerization is a complex heterogeneous process involving transport of monomers, free radicals, and other species between aqueous phase and organic phase. Though there are a number of models available in the literature, most of them deal only with specific aspects in emulsion polymerization and are far from being general. To simulate this complicated process and to achieve an adequate level of understanding, a Polymers Plus software from Aspen Technology. Inc. was used. The objective of this work is to illustrate the principle of use of Polymers Plus, simulate, and analyze the free-radical seeded emulsion copolymerization of styrene­butadiene process model in a semi-batch reactor. The base case simulation can be used to gain process understanding by analyzing how process variables and operating conditions during the course of a semi-batch reactor affect the product quality.Keywords: Polymers Plus, Emulsion Copolymerization, Simulation, Semi Batch Reactor, Styrene/ butadiene AbstrakTelah diketahui sejak lama bahwa polimerisasi emulsi merupakan sebuah proses heterogen yang kompleks, yang meliputi perpindahan monomer, radikal bebas, dan senyawa lainnya dalam fasa air dan fasa organik. Walaupun dalam literatur terdapat berbagai model, sebagian besar hanya membahas tentang aspek-aspek khusus dalam polimerisasi emulsi yang belurn berlaku umum. Untuk melakukan simulasi serta meningkatkan pemahaman tentang proses yang kompleks ini, digunakan perangkat lunak Polymers Plus dari Aspen Technology, Inc. Penelitian ini bertujuan untuk memberikan ilustrasi tentang prinsip penggunaan Polymers Plus serta melakukan simulasi dan analisis tentang model untuk proses kopolimerisasi emulsi styrene-butadiene dengan free radical seeded dalam reaktor semi batch. Simulasi ini dapat digunakan untuk memperoleh pemahaman proses dengan menganalisis pengaruh variabel-variabel proses dan kondisi operasi dalam reaktor semi batch terhadap kualitas produk.Kata Kunci: Polymers Plus, Kopolimerisasi Emulsi, Simulasi, Reaktor Semi Batch, Stiren/ butadien


1977 ◽  
Vol 50 (3) ◽  
pp. 601-638 ◽  
Author(s):  
G. W. Poehlein ◽  
D. J. Dougherty

Abstract The theories presented can be used for prediction of particle size, particle formation, rate of polymerization, and molecular weight for the emulsion polymerization of styrene in continuous stirred-tank reactors. The incorporation of Stockmayer's modification of the Smith-Ewart theory into Gershberg's continuous reactor model has helped to account for the formation of fewer but larger particles when the reactor is operated at long mean residence times. The use of a different particle generation relation by Nomura and coworkers has led to better agreement between theory and experiment for particle number and polymerization rate at low values of mean, residence time. Their model also fits transient data better than Gershberg's. However, the prediction that free-radical movement into particles is independent of particle size is not very satisfactory. Perhaps the better agreement between theory and experiment results because of the introduction of an additional experimentally determined parameter. Data for other monomers do not follow theoretical predictions as closely as styrene. For methyl acrylate the particle number data are in reasonable agreement with theory but the polymerization rate data show completely different trends. An improved, more general, theory will undoubtedly require a more complete understanding of particle formation and particle growth mechanisms. Particle size distribution measurements would be a valuable asset in developing improved competitive particle growth models.


2020 ◽  
Vol 13 (1) ◽  
pp. 11-24
Author(s):  
Acharya Neela ◽  
Thakur Chandrakant ◽  
Chaudhari Parmesh Kumar

Wastewater treatment is challengeable in today’s scenario, as it contains many types and varying physical and chemical pollutants which enormously effect the environment and its living beings. The current review elaborates treatment of various organic effluents using sequential batch reactor (SBR). Reactor operating conditions like anaerobic, anoxic and aerobic in single or mixed forms have been covered in the review. Literatures say that SBR can be used to treat many organic, industrial and municipal wastewater (MWW) successfully. Strict effluent characteristics from government force the individuals to treat the effluent to such extent so that it can match the discharge norms of wastewater.


1976 ◽  
Vol 49 (3) ◽  
pp. 536-609 ◽  
Author(s):  
J. Ugelstad ◽  
F. K. Hansen

Abstract The course of emulsion polymerization may be considered as involving three intervals: Interval I, where particle formation takes place. The end of this interval is not dependent upon the degree of conversion, but on the total amount of polymer formed. With usual recipes, it ends at about 1-5% conversion. Interval II lasts from the end of Interval I until monomer disappears as a separate phase. In this interval, the particle number is usually found to be constant, the particle volume increases proportional to conversion, the monomer concentration in the particles is approximately constant, and therefore the termination is also constant within the particles. Interval III starts when the monomer disappears as a separate phase. The transition from Intervals II to III is determined by the degree of conversion and differs for different monomers. In cases where the solubility of monomer in the water phase is low, the monomer present in the aqueous phase may usually be neglected compared to the monomer present in the polymer particles. This will usually hold with most monomers at ordinary conditions, where the amount of polymer per unit of water is relatively high, and when the concentration of monomer in the particles is much higher than in the aqueous phase. In this case, the particle volume during Interval III will decrease slightly due to the contraction by polymerization. The concentration of monomer in the particles generally decreases during Interval III, which leads to an increased viscosity within the particles and thereby also to a decrease in the value of the termination constant. The present paper deals chiefly with the kinetics of emulsion polymerization in the three intervals and the application of kinetics to the study of the mechanism. Several review articles on emulsion polymerization have recently appeared in the literature. The reason for presenting a new review article is that a vast number of papers on emulsion polymerization have recently been published, which have broadened the theoretical and experimental knowledge of the process. Several experimental and theoretical studies on the mechanisms of particle formation have appeared. New theories for particle formation outside the micelles have appeared. Also the relative effectiveness of micelles and particles in capturing radicals from the aqueous phase has been discussed in several papers.


2005 ◽  
Vol 39 (16) ◽  
pp. 4011-4019 ◽  
Author(s):  
Ewan McAdam ◽  
Simon J. Judd ◽  
René Gildemeister ◽  
Anja Drews ◽  
Matthias Kraume

1994 ◽  
Vol 30 (6) ◽  
pp. 237-246 ◽  
Author(s):  
A. Carucci ◽  
M. Majone ◽  
R. Ramadori ◽  
S. Rossetti

This paper describes a lab-scale experimentation carried out to study enhanced biological phosphate removal (EBPR) in a sequencing batch reactor (SBR). The synthetic feed used was based on peptone and glucose as organic substrate to simulate the readily biodegradable fraction of a municipal wastewater (Wentzel et al., 1991). The experimental work was divided into two runs, each characterized by different operating conditions. The phosphorus removal efficiency was considerably higher in the absence of competition for organic substrate between P-accumulating and denitrifying bacteria. The activated sludge consisted mainly of peculiar microorganisms recently described by Cech and Hartman (1990) and called “G bacteria”. The results obtained seem to be inconsistent with the general assumption that the G bacteria are characterized by anaerobic substrate uptake not connected with any polyphosphate metabolism. Supplementary anaerobic batch tests utilizing glucose, peptone and acetate as organic substrates show that the role of acetate in the biochemical mechanisms promoting EBPR may not be so essential as it has been assumed till now.


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