Stirring: Theory and Practice
Marko Zlokarnik
Murk0 
Zlokurnik 
Stirring 
Theory 
and 
Practice 
@WILEY-VCH 
Weinheim 
- 
New York 
- 
Chichester 
- 
Brisbane 
- 
Singapore 
- 
Toronto 
Prof: 
Dr. 
Marko 
Zlokarnik 
GrillparzerstraBe 
58 
8010 
Graz 
Austria 
This 
book was carefully produced. 
Nevertheless, editors, authors and 
publisher do not warrant the 
information contained therein to 
be 
free of errors. Readers are advised to 
keep in mind that statements, data, 
illustrations, procedural details or other 
items may inadvertently be inaccurate. 
Library 
of 
Congress Card No.: applied 
for 
A 
catalogue record for this book is 
available from the British Library. 
Die Deutsche Bibliothek 
- 
CIP 
Cataloguing-in-Publication-Data 
A 
catalogue record for this publication 
is available from Die Deutsche 
Bibliothek 
0 
Wiley-VCH Verlag GmbH, 
D-69469 Weinheim (Federal 
Republic of Germany). 
2001 
All rights reserved (including those of 
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of 
this 
book may 
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- 
by photoprinting, microfilm, or 
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- 
nor transmitted or 
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Germany. 
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Co. 
KG, 
67269 Griinstadt 
ISBN 
3-527-29996-3 
Con 
tents 
Preface 
xii 
Symbols 
xu 
1 
1.1 
1.2 
1.2.1 
1.2.2 
1.2.3 
1.2.4 
1.3 
1.3.1 
1.3.2 
1.3.3 
1.3.4 
1.3.5 
1.4 
1.4.1 
1.4.2 
1.4.2.1 
1.4.2.2 
1.4.3 
1.4.3.1 
1.4.3.2 
1.4.3.3 
1.4.4 
1.4.5 
1.4.5.1 
1.4.5.2 
1.4.6 
1.4.6.1 
1.4.6.2 
1.4.6.3 
Stirring, 
general 
1 
Stirring operations 
1 
Mixing equipment 
2 
Mixing tanks and their fittings 
Stirrer types and their operating characteristics 
Nozzles and spargers 
11 
Sealing of stirrer shafts 
12 
Mechanical stress 
14 
Stress on baffles 
14 
Stress on stirrer heads 
14 
Tank vibrations 
15 
Wear of stirrer heads 
15 
Shear stress on the particulate material beinig mixed 
Flow and Turbulence 
20 
Introduction 
20 
Statistical theory of turbulence 
21 
Description 
of 
turbulent flow 
23 
Energy spectra 
25 
Experimental determination of state 
of 
flow flow and its mathematical 
modeling 
27 
Homogeneous material systems 
27 
Heterogeneous 
G/L 
material systems 
34 
Heterogeneous 
L/L 
material systems 
34 
Pumping capacity 
of 
stirrers 
34 
Surface motion 
36 
Vortex formation. Definition of geometric parameters 
Gas entrainment via vortex 
39 
Micro-mixing and reactions 
40 
Introduction 
40 
Theoretical prediction 
of 
micro-mixing 
43 
Chemical reactions for determining micro-mixing 
2 
G 
16 
3G 
45 
vi 
I 
Contents 
1.4.6.4 
1.5 
1.5.1 
1.5.2 
1.5.3 
1.6 
1.6.1 
1.6.2 
1.6.2.1 
1.6.2.2 
1.6.2.3 
1.6.2.4 
1.6.2.5 
1.6.2.6 
1.6.3 
1 h.3.1 
1.6.3.2 
1.6.3.3 
1.6.3.4 
1.6.4 
1.6.4.1 
1.6.4.2 
1.6.5 
1.6.5.1 
1.6.5.2 
1.6.5.3 
1.6.5.4 
1.6.6 
1.6.6.1 
1.6.6.2 
2 
2.1 
2.1.1 
2.1.2 
2.2 
2.2.1 
2.2.2 
2.3 
Experimental determination of micro-mixing 48 
Short introduction to rheology 
50 
Newtonian liquids 
50 
Non-Newtonian liquids 
51 
Dimensionless representation of material functions 
Short introduction to dimensional analysis and scale-up 
Introduction 60 
Dimensional analysis 
62 
Fundamentals 
62 
Dimensions and physical quantities 
62 
Primary and secondary quantities; dimensional constants 
Dimensional systems 
63 
Dimensional homogeneity of 
a 
physical relationship 63 
The pi theorem 66 
Construction of pi sets using matrix transformation 
66 
Drawing-up of a relevance list for 
a 
problem 
Determination of the characteristic geometric parameter 
Constructing and solving of the dimensional matrix 
Determination of the process characteristics 
Fundamentals of the model theory and scale-up 
Model theory 70 
Model experiments and scale-up 
71 
Remarks regarding the relevance list and experimental technique 
Taking into consideration of the acceleration due to gravity 
g 
72 
Introduction 
of 
intermediate quantities 
72 
Dealing with material systems with 
unknown 
physical properties 
Experimental methods for scale-up 73 
Conclusions 
73 
Advantages of use 
of 
dimensional analysis 
Range of applicability of dimensional analysis 
57 
60 
62 
66 
67 
68 
69 
70 
72 
72 
73 
74 
Stirrer power 
76 
Stirrer power in a homogeneous liquid 
Newtonian liquids 76 
Non-Newtonian liquids 82 
Stirrer power in 
G/L 
systems 
Newtonian liquids 83 
Non-Newtonian liquids 90 
Flooding point 
94 
; 
83 
76 
3 
Homogenization 
97 
3.1 
Definition of macro- and micro-mixing 
97 
3.2 
Definition of degree of mixing 
98 
3.3 
3.3.1 
Physical methods 
101 
Determination of the degree of mixing and the mixing time 
100 
3.3.2 
3.3.3 
3.4 
3.4.1 
3.4.2 
3.4.3 
3.5 
3.6 
3.7 
3.7.1 
3.7.2 
3.7.3 
4 
4.1 
4.2 
4.2.1 
4.2.2 
4.2.3 
4.2.4 
4.2.5 
4.3 
4.3.1 
4.3.1.1 
4.3.1.2 
4.3.1.3 
4.3.2 
4.3.2.1 
4.3.2.2 
4.3.2.3 
4.3.2.4 
4.4 
4.4.1 
4.4.2 
4.4.3 
4.4.4 
4.4.5 
4.4.6 
4.5 
4.5.1 
4.5.2 
4.5.2.1 
4.5.2.2 
4.5.3 
Chemical measurement methods 
102 
Degree of mixing and molar excess 
Homogenization characteristics 
104 
Material systems without density and viscosity differences 
Material systems with density and viscosity differences 
Non-Newtonian mixtures 
11 
2 
Optimization to minimum mixing work 
Scale-up of the homogenization process 
Homogenization in storage tanks 
122 
Homogenization with propellers 
122 
Homogenization with liquid jets 
123 
Homogenization through rising up gas bubbles 
102 
104 
110 
116 
118 
123 
Gas-liquid contacting 
126 
Introduction 
126 
Physical fundamentals of mass transfer 
Determining the driving force 
126 
Temperature dependence of 
kLa 
129 
Saturation concentration 
c, 
of the gas in the liquid 
Definition of the characteristic concentration difference 
Ac 
Consideration of the absorption process from 
a 
physical and industrial 
viewpoint 
132 
Determination of 
k~a 
132 
Unsteady-state measurement methods 
132 
Measurement with oxygen electrodes 
133 
Pressure gauge method 
133 
Dynamic response methods 
134 
Steady-state methods 
134 
Sulfite methods 
134 
Hydrazine methods 
136 
Sodium sulfite feed technique 
137 
Hydrogen peroxide method 
137 
Mass transfer characteristics for the 
G/L 
system 
Establishing mass transfer relationships 
138 
Mass transfer relationship: experimental data 
Sorption characteristics in the coalescing system water/air 
Sorption characteristics in coalescence-inhibited systems 
Sorption characteristics in rheological material systems 
Sorption characteristic in biological material systems 
Interfacial area per unit volume 
a 
Definition of 
a 
151 
Determination of 
a 
152 
Physical methods 
152 
Chemical methods 
152 
Process relationships for 
a 
152 
126 
130 
130 
138 
139 
141 
143 
145 
149 
151 
4.6 
Gas fraction (gas hold-up) in gassed liquids 153 
4.6.1 
Definition 
of 
E 
154 
4.6.2 
Determination of 
E 
154 
4.6.3 
Process relationships for 
c 
155 
4.7 
Gas bubble diameter 
db 
and its effect upon 
k~ 
4.8 
Gas-absorption in oil/water dispersions 
161 
4.9 
Chemisorption 
162 
4.10 
Bubble coalescence 165 
4.11 
Foam breaking 175 
4.11.1 
Methods and devices for foam breaking 
176 
4.11.2 
Foam centrifuge and foam turbine 
177 
4.11.3 
Minimum rotor tip speed 
179 
4.11.4 
4.12 
Special gas-liquid contacting techniques 
183 
4.12.1 
Hollow stirrers 183 
4.12.1.1 
Application areas 
183 
4.12.1.2 
Suction, power and efficiency characteristics 
4.12.1.3 
Comparison of hollow stirrer and turbine stirrer 
4.12.1.4 
Sorption characteristics 
190 
4.12.2 
Surface aerators 190 
4.12.2.1 
Centrifugal surface aerators 
190 
4.12.2.2 
Power characteristic 
191 
4.12.2.3 
Sorption characteristic 
192 
4.12.2.4 
Plunging water jet aerators 
4.12.2.5 
Horizontal blade-wheel reactor 197 
4.12.3 
Gas spargers 
199 
4.12.3.1 
Sintered glass or ceramics plates, perforated metal plates and static 
4.12.3.2 
Injectors 
(G/L 
nozzles) 
201 
4.12.3.3 
Funnel shaped nozzle as ejectors 
156 
Process characteristic of the foam centrifuge and its scale-up 
180 
185 
187 
194 
mixers 200 
205 
5 
5.1 
5.1.1 
5.1.2 
5.2 
5.3 
5.3.1 
5.3.1.1 
5.3.1.2 
5.3.2 
5.3.2.1 
5.3.2.2 
5.3.2.3 
Suspension 
of 
Solids in Liquids 
(S/L 
System) 
Classification of the suspension condition 
Complete suspension 
206 
Homogeneous suspension 
207 
Distribution of solids upon suspension 
Suspension characteristics 
21 
1 
Relevance lists and pi spaces 
Specification according to the nature of the target quantity 
n, 
Specification according to particle property 
d, 
and/or 
w,, 
21 
1 
Suspension characteristics with 
d, 
as the characteristic particle 
dimension 
21 
2 
Relevance list and pi space 
212 
The process relationship 
213 
Power requirements upon suspension 
206 
206 
208 
211 
211 
21 
6 
Contents 
I 
ix 
5.3.2.4 
5.3.2.5 
5.3.3 
5.3.3.1 
5.3.3.2 
5.3.3.3 
5.3.3.4 
5.3.3.5 
5.3.4 
5.3.5 
5.4 
5.5 
5.5.1 
5.5.2 
5.6 
5.7 
6 
6.1 
6.2 
6.2.1 
6.2.2 
6.2.3 
6.2.4 
6.2.5 
6.2.6 
6.2.7 
6.2.8 
6.3 
6.3.1 
6.3.2 
6.3.3 
6.3.4 
6.4 
6.5 
6.6 
6.7 
Power requirement for the critical stirrer speed 
n, 
Scaling up in suspension according to the criterion 
n, 
Suspension characteristic with 
w,, 
as the characteristic particle 
property 217 
Determination of the particle sinking velocity in the swarm 
w,, 
The relevance list and the pi space 
The process relationship 
220 
Final discussion from the viewpoint of the dimensional analysis 
Establishing of scale-up criteria 230 
Suspension characteristic with the energy dissipation number 
E* 
Effect of geometric and device-related factors on the suspension 
characteristic 233 
Homogenization of the liquid in the 
S/L 
system 
Mass 
transfer in the 
S/L 
system 
Physical basis of mass transfer in the 
S/L 
system 
Process characteristics of mass transfer in the 
S/L 
system 
Suspension in the 
S/ 
L/G-system: hydrodynamics and power 
requirement 
241 
Mass transfer in the S/L/G system 
217 
227 
21 
7 
220 
229 
231 
235 
236 
236 
237 
241 
Dispersion in 
L/L 
Systems 
244 
Lowest stirrer speed for dispersion 
Dispersion characteristics 
246 
The target quantity 
d32 
246 
Coalescence in the 
L/L 
system 247 
Determination method for 
djz 
247 
Dimensional-analytical description 248 
The process characteristics 
249 
Effect of coalescence and of 
pv 
on 
d3z 
Effect of viscosity 251 
Effect of stirring duration 252 
Droplet size distribution 253 
Fundamentals 253 
Effect of stirrer speed 254 
Effect of stirrer type and material system 
Effect of the mixing time 
Stirrer power for dispersion 263 
Scaling up of dispersion processes 
Mass and heat transfer upon dispersion 
Mathematical modeling of the dispersion process 
244 
250 
255 
262 
263 
264 
267 
7 
Intensification 
of 
heat transfer 
by 
stirring 
272 
7.1 
Physical fundamentals of heat transfer 
272 
7.1.1 
Determination of 
cli 
273 
7.1.2 
Dimensional-analytical description 
273 
x 
I 
Contents 
7.2 
7.2.1 
7.2.2 
7.3 
7.4 
7.4.1 
7.5 
7.6 
7.6.1 
7.7 
7.7.1 
7.7.2 
7.7.3 
7.8 
7.8.1 
7.8.2 
7.9 
8 
8.1 
8.1.1 
8.1.2 
8.1.2.1 
8.1.2.2 
8.1.3 
8.2 
8.2.1 
8.2.2 
8.3 
8.3.1 
8.3.2 
8.4 
8.4.1 
8.4.2 
8.5 
8.5.1 
8.5.2 
8.5.3 
8.6 
8.6.1 
Heat transfer between a homogeneous liquid and a heat transfer 
surface 275 
Flow range 
Re 
= 
102-106 
Flow range 
Re 
< 
lo2 
Generalized representation of the heat transfer characteristic 
by 
including the stirrer power per unit volume 282 
Effect of the Vis-term 284 
Taking non-Newtonian viscosity into consideration 
Optimization 
of 
stirrers for a maximum removal of reaction heat 
Heat transfer for G/L material systems 
Dimensionally analytical description 
291 
Heat transfer in S/L systems 
Direct heat exchange ice cubes/water 
293 
Indirect heat exchange for 
Ap 
> 
0 
Indirect heat exchange at 
Ap 
0 
295 
Heat transfer in 
L/ 
L 
material systems 
Direct heat exchange 298 
Indirect heat exchange 298 
Heat transfer in G/L/S material systems 
275 
278 
286 
288 
291 
293 
294 
298 
299 
Mixing and stirring in 
pipes 
Mixing and homogenization 300 
Straight, smooth or rough pipe without fittings 
Pipe with a jet mixer or with a Tee piece 
302 
Jet mixers 302 
Tee pieces 
304 
Flow deflecting fittings (“motionless or static mixers”) 
300 
300 
305 
Kenics mixer 307 
Sulzer mixers SMV and 
SMX 
[533] 
Ross-ISG mixer 309 
G/L-mass transfer 309 
Mass transfer in pipe flow 
Mass transfer 
in 
pipe with static mixer 
Heat transfer 3 
11 
Heat transfer in pipe flow 311 
Heat transfer in pipe with static mixer 
Dispersion in 
L/L 
system 314 
Dispersion in pipe flow 314 
Dispersion in pipe with static mixer 
Micro-mixing and chemical reaction 
Pipe reactor 317 
Pipe reactor with a jet mixer 
Pipe reactor with static mixer 
Modeling of mixing processes in pipes 
Pipe flow 322 
308 
309 
310 
311 
315 
31 
6 
319 
320 
322 
Contents 
I 
xi 
8.6.2 
Pipe with Tee mixer 
323 
8.6.3 
Pipe with static mixer 
323 
8.7 
Stirring in pipes and mixing columns 
324 
Literature 
328 
Subject 
Index 
360 
xii 
I 
Preface 
Stirring is one of the unifying processes which form part of the mechanical unit 
operations in process technology. It is an important operation which has been used 
by man since time immemorial in preparing food and drink and in constructing 
his dwelling. Since the emergence of manufacturing and the advent 
of 
industrial 
production, stirring has been used in almost all branches of industry (metallurgy, 
building materials, glass, paper, chemicals, food, pharmaceuticals, etc.). 
Permeation of scientific method into this field largely took place in the second 
half of the twentieth century, during which all the other disciplines in process 
technology evolved from “arts into sciences”. Particularly chemical and process 
engineers in the chemical industry and in research have studied this topic in- 
tensively, since chemical, biochemical and biological processes can only take place 
when all the reaction partners are brought into close contact. 
This book represents 
a 
brief summary of the state of the art in the field of stir- 
ring technology from the viewpoint of the author. It particularly focuses on recent 
research results, account being taken of scientific literature published up to the 
summer of 
2000. 
Only someone who has studied this topic intensively since the 
1950’s 
can fully 
appreciate the immense advances made feasible by new physical measuring methods 
and computers. 
Forty 
years ago determination of the stirrer speed still required 
a 
stop-watch or a stroboscope! 
Today, the whole field of classical stirring technology can be regarded as largely 
accessible to scientific method, 
so 
that a standard design for stirrers for any stirring 
operation on an industrial scale is ensured. Research is shifting increasingly to 
mathematical simulation of stirring processes. In the future, interesting sugges- 
tions for industrial practice can be expected from this work. 
I 
wish to express my sincere thanks to my friend Dr. Dr Ing. e.h. Juri Pawlowski 
for his many helpful suggestions, to my long-standing colleague and co-worker, 
Dr Ing Helmut Judat from Bayer-Leverkusen for putting at my disposal the exten- 
sive, partly jointly collected, scientific literature from the 
1950’s 
to the 
1970’s, 
and 
to Dr Ing. H J. Henzler from Bayer-Elberfeld and to Dr Ing. habil. Peter Zehner 
from BASF-Ludwigshafen for the critical reading of 
a 
chapter of the manuscript. 
Classification 
of 
Unifying Processes with Regard to the Material 
Systems 
Involved in the 
Unit Operations Mixing, Stirring and Kneading 
It 
is obvious that mixing of wine with water or the preparation of an aqueous solu- 
tion of common salt from powdered or crystalline common salt and water require 
different equipment and different procedures from those used for the preparation 
of bread dough, modelling paste with coarse or fine clay, or 
a 
concrete mixture. 
It is standard practice to classify mixing operations with regard to the state of 
aggregation 
of 
the major component in the mixture, since the same state of ag- 
gregation will generally be present in the final mixture. From the standpoint of 
process technology it is relevant, whether 
a 
gas is sparged into a liquid or a liquid is 
sprayed into a gas. 
A 
further distinction must be made with regard to the degree of uniformity 
of 
the liquid phase: low viscosity liquids will be much easier to handle than highly 
viscous paste-ldce liquids. 
In 
this respect the classification 
of 
fields of work given in 
Table 
0.1 
is recommended. 
Tab. 
0.1 
aggregation 
of 
the major component 
Classification 
of 
mixing operations according to the state 
of 
State ofoggregotion Unit operotion 
Stondord 
mixing equipment 
gaseous mixing, spraying 
mixing chamber, nozzle 
liquid stirring 
stirrer, static mixing elements 
paste-like kneading kneader, screw extruder 
solid (particulate) mixing, blending mixer 
To 
avoid misunderstandings, it should be pointed out that the above-used mixing 
terms do not enable 
a 
clear distinction to be made between the unit operation as 
action and as aim. Thus the term mixing includes both the unit operation of blend- 
ing or intermingling and the result 
of 
this unit operation namely the preparation 
of a (stochastically or molecularly homogeneous) mixture. Finally one can mix a 
heap 
on 
a pan granulator only by moistening with atomized liquid or in a rotary 
furnace preferably by supplying heat. (This is also the case with the English terms 
mixing and blending.) 
When 
a 
material system, in which liquid phases predominate, 
is 
stirred, this 
action can result in miscible liquid phases 
forming 
a molecularly homogeneous 
mixture (“solution”). In the case of immiscible liquids, 
on 
the other hand, a dis- 
persion (possibly an “emulsion”) will result. 
If 
stirring is performed to increase 
heat or mass transfer, the purpose is to accelerate this operation and the inherent 
mixing of the liquid phases is of secondary importance. 
A 
similar situation exists in the case 
of 
the term kneading. There are screw 
machines whose primarily task are the mixing or conveying of paste-like compo- 
sitions. 
In 
such cases the kneading itself is of secondary importance, although it 
cannot be ignored. 
It 
should therefore be borne in mind that the available terms such as mixing, 
blendmg, stirring, kneading denote the unit operations 
of 
unifylng processes, but 
tell 
us 
little or nothing about the result of the operation. (In this they differ from 
other unit operations such as grinding, filtration, distillation, etc. Here, the expected 
result is fully described by the term used.) 
This book has been exclusively devoted to stirring for 
a 
number of reasons: in- 
tensive research in this field has been carried out in the last 
10-15 
years, largely 
driven by the development 
of 
biotechnology, meriting a separate book and several 
books devoted to the other unifying operations (mixing of solids, mixing in ex- 
truders) have been published’) in the German language literature, making consid- 
eration 
of 
these topics unnecessary. 
It is neither the task nor in the ambit of the author, to mention all the significant 
scientific contributions over the last 
50 
years within the field covered by this book, 
much less, 
to 
honour them properly. This task has already been carried out at reg- 
ular intervals in various reviews over the years. It is therefore appropriate, to refer 
to these reviews”. 
A 
researcher is very well advised to consult them before he begins 
his own research in 
a 
special field 
of 
stirring technology. 
1) 
Ralf 
Weinekotter 
- 
Hermann Gericke: 
Juri 
Pawlowski: 
Mischen von Feststoffen (Mixing 
of 
particulate solids) 
Springer-Verlag 
1995 
Salle+Sauerlander 
1990 
Transportvorgange in Einwellen-Schnecken 
(Transfer proceses in single-screw extruders) 
ISBN 
3-540-58567-2 
ISBN 
3-79 
3 
5 
-5 
5 
28-3 
2) 
Mixing 
- 
Theory 
and 
Practice, Vol. 
1 
+ 
2 
+ 
3 
(Ed.: V.W. Uhl, Y.B. 
Gray) 
Academic Press, New 
York 
1966, 1967, 1968 
Nagata, 
S.: 
Mixing 
- 
Prinaples and 
Application 
Kodansha Ltd. 
Tokyo 
& 
John 
Willey, New 
York 
1975 
ISBN 
0-470-62863-4 
Kneule, 
F.: 
Riihren (Stirring) 
3. 
Adage, Decherna Frankfurt/Main, 
1986 
Verfahrenstechnische Berechnungsrnethoden 
Teil4 Stofiereinigen 
in 
fluiden Phasen 
(Unifying processes 
in 
fluid phases) 
Authors: 
F. 
Liepe, W. Meusel, 
H 0. 
M&kel, 
B. 
Platzer, 
H. 
WeiBgerber 
VCH Verlagsges., Weinheim 
1988 
ISBN 
3-527-26 205-9 
ISBN 
3-921567-48-3 
I 
xv 
List 
of 
Symbols 
Latin Characters 
interfacial area per unit volume, 
a 
= 
A/V 
thermal diffusivity; 
a 
= 
k/(pCp) 
area, interfacial area 
Hamaker constant 
height of stirer (paddle) blade 
concentration 
saturation concentration 
drag coefficient of 
a 
sphere in a fluid flow 
pipe flow friction factor 
heat capacity at constant pressure 
stirrer diameter 
bubble diameter, usually represented by 
d32 
mean gas bubble or liquid droplet diameter (“Sauter diameter”; eq. (6.8)) 
particle or droplet diameter 
terminal (final) bubble diameter 
inside tank or pipe diameter 
diffusion coeficient 
effective dispersion coefficient (in axial direction) 
difference 
enhancement factor in chemisorption; eq. (4.76) 
energy spectrum of vortices 
energy dissipation density spectrum, eq. 
(1.14) 
activation energy in chemical reactions 
force 
mass flow (rate of mass transfer, oxygen uptake) 
stirrer distance from bottom of the vessel (bottom clearance) 
heat transfer coefficient, definition eq. 
(7.1) 
total liquid depth (liquid height) in vessel 
momentum 
mass 
flux; 
eq. 
(4.7) 
heat flux, eq. (7.1) 
rate constant in eq. 
(1.1) 
k 
k 
R 
kG 
kL 
kLa 
L 
L 
Lrn 
m 
m 
m 
M 
M 
n 
N 
Nx 
P? 
AP 
4’ 
Q 
P 
4 
R 
S 
T 
T 
Tu 
t 
U 
Ui 
U 
U! 
LJ 
V 
VG 
V 
WS 
ws 
s 
X 
Z 
proportionality constant, eq. 
(1.45) 
thermal conductivity 
wave number of vortices 
gas side mass transfer coefficient 
liquid side mass transfer coefficient 
volume-related over-all mass transport coefficient, eq. 
(4.9) 
base dimension of length 
pipe length 
mixing length in pipe flow 
flow index in pseudoplastic fluids 
mass, 
rn 
= 
pV 
enhancement factor in physical absorption; eq. 
(4.88) 
base dimension of mass 
degree of mixedness, definition 
p. 
100 
stirrer speed 
number of stages 
normal stress 
(x 
= 
1 
or 
2); 
eq. (1.50, 
1.51) 
pressure, pressure difference (pressure drop) 
power, stirrer power 
volume throughput 
liquid throughput, brought about by a stirrer 
heat flow (rate of heat transfer) 
heat of reaction 
surface; cross-sectional area 
time 
base dimension 
of 
time 
temperature 
degree of turbulence, definition p. 
23 
tip velocity 
(u 
= 
nnd) 
velocity components in the 
x-, 
y-, 
z-direction 
mean flow velocity 
mean values of velocity fluctuations 
(u; 
= 
@) 
over-all heat transfer coefficient, eq. (7.2) 
velocity; superficial velocity 
superficial flow velocity 
(uG 
K 
qG/Dz) 
liquid volume (ungassed) 
sinking velocity of single particles; eq. (5.17) 
sinking velocity of 
a 
particle swarm; eq. (5.20)-(5.22) 
chemical conversion 
X 
= 
(co 
- 
ct)/co 
number 
Creek 
Characters 
a 
angle 
/lo 
temperaturc coefficient of the density 
deformation 
shear rate, eq. 
(1.41) 
temperature coefficient of the viscosity, eq. 
(7.6) 
thickness (of film, layer, wall) 
mixing power per unit mass 
e 
= 
P/pV 
gas hold-up (gas fraction in liquid) 
mixing time 
kinetic energy per unit mass, 
Ekin/m 
= 
(1/2)ma2/m 
= 
v2/2 
Kolmogorods micro-scale 
of 
turbulence; 
2 
= 
(v3/&)'I4; 
eq. 
(1.6) 
relaxation time, eq. 
(1.53) 
macro-scale of turbulence; 
A 
K 
d 
dynamic viscosity 
chemical potential 
scale factor 
p 
= 
LT/LM 
kinematic viscosity 
density 
I 
xvii 
List 
of 
Symbols 
heat capacity per unit volume at constant pressure 
interfacial, surface tension 
standard deviation under given conditions 
(,) 
variance 
variance coefficient 
mean residence time 
r 
= 
V/q 
shear stress, eq. 
(1.41) 
yield stress 
volume or 
mass 
fraction 
Subscripts 
0 
ax 
C 
d 
F 
G 
h 
i 
bulk 
kin 
L 
min 
M 
n 
0 
P 
'I 
outer 
axial 
continuous phase 
dispersed phase 
flake 
gas, gas phase 
hydraulic 
inner 
bulk 
of 
liquid 
kinetic 
liquid 
minimum 
model scale 
related to stirrer speed 
start condition, initial value 
particle (solid or liquid) 
related to throughput 
I 
P'Pe 
S 
baf 
S 
foam 
t 
t 
T 
voli 
W 
x. 
y. 
z 
radial 
Pipe 
saturation value 
baffles 
solid, solid phase 
foam 
terminal (final) value 
value 
at 
the time 
t 
technological scale, full-scale 
vortex 
wall 
space coordinates in the vessel 
Dimensionless 
Numbers 
Ar 
Bd 
Bo 
cd 
Cf 
De 
E' 
Eu 
Fo 
Fr 
Fr' 
Ga 
Gr 
Archimedes number 
Bond number 
Bodenstein number 
drag coefficient of 
a 
sphere in fluid flow 
friction factor in pipe 
flow 
Deborah number 
energy dissipation number 
Euler number 
Fourier number 
Froude number 
Froude number, modified by 
Ap 
Galilei number 
Grashof number 
Hat1 
Hatta number, 1.order reaction 
Hat2 
Hatta number, 2.order reaction 
Ne 
Newton number 
Nu 
Nusselt number 
no 
Mixing number 
Pr 
Prandtl number 
Pe 
PCclet number 
Q 
Throughput number 
Re 
Reynolds number 
Ri 
Richardson number 
Wi 
Weigenberg number 
We 
Weber number 
cr* 
physical properties number 
S: 
physical properties numbers describing 
Sc 
Schmidt number 
bubble coalescence behaviour 
Ar 
= 
Re2/Fr' 
Bd 
= 
WeFr 
Bo 
= 
nd2/D,tf 
and 
vD/D,R, 
resp. 
Cd 
E 
2Eu 
Cf 
2Eu 
d/L 
De 
= 
?/A& 
nl 
E' 
= 
(EA~/v~)'/~ 
Eu 
= 
Ap/(pv2) 
Fo 
= 
at/d2 
Fr 
= 
n2d/g 
Fr' 
= 
Frp/Ap 
Ga 
= 
Re2/Fr 
Gr 
= 
pATgd3/v2 
Hatl 
E 
m/kL 
Hat2 
= 
dz/kL 
Ne 
= 
P/(pn3d5) 
NU 
E 
hiD/k 
Pr 
= 
v/a 
= 
C,p/k 
Pe 
= 
RePr 
= 
nd2/a 
= 
nd2pCp/k 
Re 
= 
nd2p/p 
Ri 
= 
[Fr'd/H]-' 
Wi 
= 
Nl/r 
We 
= 
pn2d3/a 
We/(FrRe4) 
'I3 
structure unknown 
Q 
= 
w3) 
Sc 
= 
Sh 
Sherwood number 
St 
Stanton number 
Vis 
Viscosity number 
I' 
Sorption number 
I 
xix 
list 
of 
Symbols 
Sh 
= 
kLdp/D 
St 
= 
Nu/RePr 
= 
h/(vpCp) 
Vis 
= 
h/p 
see 
definition 
eq. 
4.72 
Stirring 
Theory and Practice 
Marko 
Zlokarnik 
0 
Wiley-VCH 
Verlag 
GmbH, 
2001 
I’ 
1 
Stirring, General 
1.1 
Stirring Operations 
If the liquid component predominates in the mixture of substances to be mixed, 
the mixing operation is named stirring and a stirrer (an impeller) is used as the 
mixing device. The following five stimng operations can be distinguished 
[Gll]: 
- 
Homogenization, i.e. equalization of concentration and temperature differences; 
- 
Intensification 
of 
heat transfer between a liquid and a heat transfer surface; 
- 
Suspension (and possible dissolution) of 
a 
solid 
in 
a liquid or slurry formation; 
- 
Dispersion (or sparging) of a gas in a liquid (gas-liquid contacting). 
Dispersion (or emulsification) of 
two 
immiscible liquids; 
The term homogenization is used, if 
a 
uniform liquid phase has to be realized, 
e.g. a molecularly homogeneous mixture of several miscible liquids or equalization 
of concentration and temperature differences during a chemical reaction in the 
liquid phase. (The same term is used in the food industry for 
a 
completely different 
operation, namely for 
L/ 
L 
(liquid/liquid) dispersion under extreme shear condi- 
tions; e.g. the “homogenization” of 
milk). 
Intensification of heat transfer in 
a 
stirred tank can represent, especially in case 
of viscous liquids, an important stimng operation, particularly if a strongly exo- 
thermic reaction takes place (e.g. block polymerization). 
In 
such cases the stimng 
operation consists of reducing the thickness of the liquid boundary layer on the 
tank wall and realizing liquid transport to and from the heat exchanger surface. 
If 
particulate matter has to be dissolved in 
a 
liquid or if a chemical reaction cata- 
lyzed by 
a 
solid is involved, the particles must be suspended from the vessel bottom, 
so 
that the total surface can participate in the process. In continuous processes a 
stochastically homogeneous distribution of the solid in the bulk of the liquid is 
required, 
so 
that the solid particles can be transported with the liquid from stage to 
stage (for example in a cascade crystallization process). In this intensive suspen- 
sion process, the solid is, as a rule, subjected to high mechanical stress, which can 
result in its attrition. 
In 
the case of dispersion in 
a 
L/L 
or 
L/G 
(liquid/gas) systems, one fluid phase is 
distributed in the other in the form of fine droplets 
or 
gas bubbles to accelerate 
mass transport between the 
two 
phases. 
In 
suspension polymerization the stirring 
conditions are adjusted 
so 
that 
a 
particular desired droplet size distribution results. 
Often different stirring operations must be carried out simultaneosly, an example 
being solids-catalyzed hydrogenation, in which the stirrer disperses the gas (hydro- 
gen) in the liquid phase, swirls up the catalyst particles (e.g. Raney nickel) from the 
bottom 
of 
the reactor and intensifies the removal 
of 
reaction heat. 
In 
such cases the 
stirring conditions are determined by that stirring operation which is the bottle- 
neck in the process. 
1.2 
Mixing Equipment 
1.2.1 
Mixing Tanks and Auxiliary Equipment 
The mixing tank or stirred vessel 
is 
the most commonly used piece of stirring 
equipment. (It is also the most commonly used chemical reactor). This is due to 
its considerable flexibility as regards the flow conditions, which can be realized in 
it. Mixing tubs and storage tanks are the second most commonly used pieces of 
mixing apparatus. 
The tank diameter is restricted to 
D 
5 
4.6 
m on transport grounds. 
A 
further 
increase in liquid volume is therefore only possible by an enlargement of the vessel 
height. Two disadvantages have thereby to be taken into account: 
a) 
the stirrer shaft 
becomes longer and support bearings may be required along its length; b) mixing 
times increase (see Fig. 
3.6). 
(For most stirring operations the most favorable aspect 
ratio 
HID 
(liquid height to vessel diameter) is 
HID 
z 
1). 
The design of mixing tanks is standardized 
DIN 
28 
130 [161, 
5061, 
ASME Code 
Section 
VIII. 
Internal fittings include: baffles, coils, probes (e.g. thermometer, level 
indicators) and feed and drain pipes. All of these fittings can influence the stirring 
process. 
If an axially positioned stirrer is operated in a vessel without inserts, the liquid is 
set 
in 
rotation and a vortex is produced. In the case of rapidly rotating stirrers and 
low 
viscosity liquids, the vortex can reach the stirrer head with the result that the 
stirrer entrains the gas in the liquid (see section 
1.4.5.2). 
This 
is 
generally unde- 
sirable because it results in an extraordinarily high mechanical stress 
on 
the stirrer 
shaft, bearings and seal, due to the absence of the “liquid bearing”. This ofien 
leads to the destruction of the stirrer. Even when the vortex formation causes 
no 
gas entrainment, rotation of the liquid is always undesirable if a two-phase system 
with different densities is concerned, since the centrifugal force counteracts the 
stirring process. 
The rotation of liquid in cylindrical tanks is prevented by the installation of 
baffles. So-called “complete baffling” is realized with four baffles (flow interrupting 
strips) 
D/10 
in width, where 
D 
is the inner diameter of the vessel, arranged along 
the entire vessel wall. Dead zones in the 
flow 
direction behind the baffles can be 
13 
7.2 
Mixing 
Equipment 
A 
B 
Fig. 
1.1 
Baffle design 
A 
- 
Standard design 
B 
- 
For 
glass and coated vessels (baffle basket 
with 
pressure- 
fitted ring) 
avoided by using baffles Dl12 in width, set at 
a 
clearance of D/50 from the vessel 
wall. Baffles are usually attached to the vessel wall by means of welded brackets 
(Fig. 1.1a). 
In 
enamel-coated vessels they are attached to the vessel lid. If this 
is 
not 
possible (glass tanks, wooden vats), they are made in the form of a basket with 
pressure-fitted rings (Fig. 1.1b). 
Baffles are not necessary, if stirring is carried out in a container with rectangular 
cross-section (e.g. basins or pits) or when the stirrer 
is 
mounted laterally in the 
tank wall. 
In 
the case of weak stirring, rotation of the liquid can be prevented even 
in cylindrical 
tanks 
by installing the stirrer eccentrically and/or at an angle to the 
tank axis. In this case, however, uneven mechanical stress in the stirrer shaft must 
be accepted. 
A 
jacketed vessel wall is sufficient to supply or remove relatively small quantities 
of heat. The usual configurations are shown in Fig. 
1.2. 
To 
transfer larger quantities of heat, the installation 
of 
coils is necessary. 
A 
helical 
coil (Fig. 1.3a) is only efficient 
with 
axially working stirrers, since they produce 
good liquid circulation in the annular space between the helical coil and the wall. 
On 
the other hand, the liquid circulation produced by radially working stirrers is 
strongly deflected by a helical coil, 
so 
that the flow through the annulus between 
the coil and wall is suppressed. For such stirrer types, it is advantageous to arrange 
the coil in vertical loops along the vessel wall (meander coil, Fig. 2b). This arrange- 
ment does not deflect the radial flow pattern, but prevents bulk rotation of the liquid 
to such an extent that baffles are often superfluous. 
Fig. 
1.2 
A 
- 
Jacketed vessel 
B 
- 
Cast iron vessel with integral steel tubes 
C 
-Welded helical coil with intercolated copper plates 
D 
-Welded half pipe coil 
E 
- 
Welded corner iron channels 
F 
-Jacketed bolt welding 
Design 
of 
the vessel wall for heat transfer 
[102]. 
15 
1.2 
Mixing 
Equipment 
6 
I 
1 
Stirring, 
General 
The heat-exchange tubes can also be arranged into bundles and installed instead 
of baffles. (Fig. 
1.3~). 
These heat exchangers possess 
a 
particularly large surface 
area and are therefore mainly used in biotechnology, e.g. in penicillin and enzyme 
production, because the operating temperature in such processes has to be kept 
below 40°C, resulting in extremely small temperature differences. 
1.2.2 
Stirrer Types and Their Operating Characteristics 
The stirring operations discussed in the introduction can obviously not be per- 
formed with a single type of stirrer. There are many types of stirrers appropriate 
for particular stirring operations and particular material systems. In this section 
only those stirrer types will be discussed which are widely used in the chemical 
industry and for which reliable design guidelines exist. The dimensions of stirrer 
types have also been standardized to a large extent 
[ 
1611. 
In Fig. 
1.4 
the stirrer types are arranged according to the predominant flow pat- 
tern they produce, as well as to the range 
of 
viscosities over which they can be 
effectively used. 
90% 
of all stirring operations can be carried out with these stan- 
dard stirrer types. The flow patterns obtained with typical radially and axially con- 
veying stirrers are shown in Fig. 1.5. 
Of 
the stirrer types which set the liquid in a radlal motion 
- 
or into a tangential 
flow in the case of high viscosities 
- 
only the turbine stirrer*) (so-called “Rushton 
turbine”, 
a 
disk 2d/3 in diameter supporting 
6 
blades each 
d/5 
high and 
d/4 
wide 
[474]) 
belongs to the high speed stirrers. 
It 
can be sensibly utilized only with low 
viscosity liquids and in baffled tanks. Its diameter ratio Dld is 
3-5. 
The turbine 
stirrer causes high levels of shear and hence is well suited for dispersion processes. 
The 
PFAUDLER 
impeller stirrer was developed for use in enamel-coated vessels 
[438] 
and thus has rounded stirring arms. It is installed with small bottom clear- 
ance at a Dld ratio of 
1.5 
and can be used both with and without baffles. Due to the 
small bottom clearance it can be used with strongly fluctuating filling levels (e.g. 
during emptying), since it can efficiently mix even small liquid volumes. 
PFAUDLER 
[438] 
has developed the so-called “Cryo-Lock-System”, enabling enamel- 
coated-BE vessels according to 
DIN 
28136 
to be equipped with impellers of 
d 
> 
600 
mm via 
a 
manhole of 
I 
600 
mm in diameter. It is 
a 
stirrer with four paddles of 
different design (straight, pitched paddles, TurbofoilJ-o) its paddles being arranged 
on the hub in an X-configuration rather than in a cross configuration. The fasten- 
ing of the impeller hub to the impeller shaft is realized inside the tank by first con- 
tracting the shaft in liquid nitrogen 
(-196”C), 
then mounting the impeller hub and 
finally heating to produce the connection 
[316]. 
Cross-beam, grid and blade stirrers are slow-speed stirrers and are used 
at 
D/d 
= 
1.5 
to 
2 
both with and (in the case of viscous liquids) without baffles. They 
are particularly suitable for homogenization. 
* 
In the German literature on mixing the 
Rushton turbine is referred 
to 
as 
Scheibenriihrer: 
“disk stirrer”. 
This 
is a 
misleading choice of words, since it 
is 
not the 
disk which effects the stirring, but 
the 
blades 
it 
supports 
[ 
G37]. 
17 
7.2 
Mixing Equipment 
c 
500 
~ 
P 
I 
Turbine 
'itched blade 
Impeller@ 
(Pfaudler) 
4 
Propeller 
Liquid 
viscosity 
[m 
Pa 
s] 
500 
- 
5 
000 
CrOS 
beam Frame 
L 
MIG@ 
(Ekato) 
Fig. 
1.4 
Classification 
of 
stirrers according to the predominant 
flow pattern they produce and 
to 
the range 
of 
viscosities over 
which they can 
be 
effectively used 
Fig. 
1.5 
baffled tank, generated by 
A 
- 
axial-flow propeller and a 
B 
- 
radial-flow turbine stirrer 
Flow patterns in a 
;I: 
Blade 
INERMIG@ 
(Ekato) 
jx 
103-5x 
104 
Anchor 
ielical ribbon