Chapter 5.

Reactors

• Reactors
 many different types exist for environmental engineering
 generally designed to emphasize suspended growth or biofilms

 that make use of suspended growth are also called:

- , - ,
 that make use of biofilms are also called:
fixed-film, attached-growth, immobilized reactors

• En ineer must understand

1) kinetics of substrate removal by different types of microorganisms

un amen a proper es o eren reac or ypes
5. Reactors
• Factors influencing the choice among the different
reactor types :
 physical & chemical characteristics of the waste being considered
 concentration of contaminants being treated
 presence or absence of oxygen
 efficiency of treatment and system reliability required
 climatic conditions under which the reactor will operate
 number of different biological processes involved in the overall treatment system
 skills & experience of those who will operate the system
 relative costs at a given location and time for construction and
operation of different possible reactor configurations

• The aim of this chapter :

i) how to construct mass balances for different reactors,
ii) how to use of mass balances to derive basic equations that describe the
relationshi between reactor size and treatment erformance.
5. 1 Reactor Types

Typical reactors used in environmental application

Basic reactors

Biofilm reactors
5.1 Reactor Types
5.1.1 Suspended-Growth Reactors

A) Batch reactors:

 the simplest suspended-growth reactor

 biochemical reactions take place without new additions until

e reac on s comp e e

 kinetics of contaminant removal is similar to that of

an ideal plug-flow reactor
5.1.1 B) Sequencing Batch Reactor (SBR)

1) Fill, 2) React (aerobic/anoxic or anoxic/aerobic),

e e, raw, e

can a so emp oy severa a c reac ors opera e n para e

filling

drawing
5.1.1 B) Sequencing Batch Reactor (SBR)
5.1.1 B) Sequencing Batch Reactor (SBR)
5.1.1 B) Sequencing Batch Reactor (SBR)

• Advantages of SBR:
1) Total capital costs are significantly reduced due to the elimination of clarifiers
and recirculation facilities.

modified at any time to offset i)change in process conditions, ii)influent

characteristics or iii)effluent objectives.
rocess re a y s grea y mprove ecause e process s no
affected by hourly, daily, or seasonal feed variations.
4) Since only one vessel is used for all proces operations, plant extension is
simplified.
5) Better resistance to sludge bulking, since the biomass undergoes cyclic feast-
,
sludge than continuous flow.
5.1.1 C) Continuous-flow stirred-tank reactor(CSTR),
or com letel mixed reactor :

 used to culture organisms or to study basic biochemical phenomena in

laboratory (chemostat )
 liquid or slurry stream is continuously introduced, and liquid contents are
continuously removed from the reactor
 concentration of substrates and microorganisms are the same everywhere
throughout the reactor (Ideal CSTR) ; it makes analysis of CSTR comparatively
smpe.
5.1.1 D) plug-flow reactor (PFR)

 Sometimes referred to tubular reactor or piston-flow reactor.

 In the ideal PFR,the flow moves through the reactor with no mixing with
earlier or later entering flows.
Hence if one knows the flow rate to the reactor and its size,
e oca on o e e emen a any me can e ca cu a e .
 Unlike the CSTR, the concentartions of substrates and microorganisms vary
throu hout the reactor.
 An ideal PFR is difficult to realize in practice, because mixing in the direction
of flow is impossible to prevent .
5.1.1 Comparison of CSTR and PFR

1) The high rate of substrate utilization at the entrance of reactor in PFR

because the substrate concentrations are highest at the entrance.

 If other conditions are the same, a higher S gives a higher rate of reaction.
So a PFR generally produces a higher conversion of S in a given volume
. .

 It exceeds the ability to supply sufficient oxygen (high DO demand

at the entrance and low DO demand at the exit) in an aerobic system.
Thus the aerators for PFR should be designed to provide more oxygen
in the inlet region. (disadvantage of PFR)

, e.g., destruction of methanogens at low pH in an anaerobic system.

(disadvantage of PFR)
5.1.1 Comparison of CSTR and PFR

2) In CSTR, the S in the reactor is the same as S in the effluent.

So the fresh feed is immediately dispersed into an environment of low S.
, .

 If no biomass enters PFR, no biological reaction would occur and the reactor
washes out.

 On the other hand, the influent to a CSTR is mixed with reactor fluid
containing biomass so that a CSTR can be sustained even in the absence
o omass n e ee .

 Processes for in situ biodegradation of contaminants in ground waters often

.
Here, mixing in the direction of flow (longitudinal) is generally small,
making plug flow the natural outcome.
5.1.1 Comparison of CSTR and PFR

3) The CSTR is more stable than a PFR in response to toxic and shock
loadings.

 If a concentrated ulse of a toxic substance enters a PFR, the concentration

remains high as it moves along the PFR. Because of high concentration,
the toxic substance may destroy an appreciable quantity of the biomass
in the system and cause a long term upset in PFR performance.

 With a CSTR, the pulse of toxin is dispersed rapidly throughout the CSTR
and its concentration level is reduced so that the metabolic processes of
microorganisms may be only slightly affected by the diluted toxin.

 In general, a CSTR gives a more uniform effluent under varying feed conditions.
5.1.1 Comparison of CSTR and PFR

4) The CSTR and PFR are idealized models that are difficult to achieve in
large scale biological reactors.

 In actual CSTR, short-circuiting of fluid and stagnant zones may occur because
of incomplete mixing with the bulk of the reactor fluid.

 In PFR, aeration of the fluid causes longitudinal mixing and a distribution of

residence times. Thus, long biological reactors with aeration are often better
simulated b an axial dis ersion model or a CSTR in series model.

 Tracer techniques are useful in establishing an appropriate hydraulic model for

a biological reactor.
5.1.1 Practical Aspects of Reactor Design

• The deviation from two idealized flow patterns :

I) Dead Zone (Stagnant zone)

2 Channelin of fluid
3) Short-circuiting caused by
i) density current in plug-flow reactor
ii) inadequate mixing in a CSTR

• This type of flow should be avoided since it always lowers the

erformance of the unit.

• The problems of non-ideal flow are intimately tied to those of scale-up.

• Often the uncontrolled factor differs widely between large and small
units. Therefore ignoring this factor may lead to gross errors in design.
5. 1.3 Reactor Arrangements

Reactor arrangements
5. 1.3 Reactor Arrangements
5. 1.3 Reactor Arrangements

1) Reactors in series :
- .
For example, organic oxidation (1st reactor)  nitrification (2nd reactor)
 denitrification (3rd reactor)
- To create plug-flow characteristics.

- to provide redundancy in the system so that some reactors can be

out of service, while others on a parallel track remain in operation.
- w en t e tota ow to e treate ar excee s t e capac ty o t e argest
practical units available.
- it maintains more of a completely mixed nature, compared to the more
plug- flow nature of reactors in series.
5.2 Mass Balances
• Reactor design

processes.

- It provides the critical information on what must be added to

and removed from the process.
- It makes determine the amount of chemicals to satisfy the energy, nutrient,
and environmental needs of the microorganisms.

For example: process for biological denitrification

0.0333C6 H 5COO − + 0.12 NO3− + 0.02 NH 4+ + 0.12 H + →
electron donor elector acce tor nitro en source
0.02C5 H 7O2 N + 0.06 N 2 + 0.12CO2 + 0.0133HCO3− + 0.1067 H 2O [2.34]
bacteria
. mo e ac er a represen s an s ca e ;
sludge, waste biomass, waste biosolids, excess biosolids
 5.2 Mass Balances

2 S stem boundar a control volume

(b)
(a)

(c)

• Figure 5.2 - Three possible control volume

 5.2 A component may enter /or leave the control volume

Component
omponen
Destroyed or
entered left
formed
By way of e uen s ream or n e
Fig.5.2-a
influent stream sludge waste stream reactor system
. . -

Settling tank effluent

Reactor effluent In the settling
Fi .5.2-c stream or
s ream tank
sludge recycle line
 5.2 Mass Balances
3) Reaction rates affect the size of the treatment system.

-The mass balance is defined in terms of rates of mass change in the control volume.

-Each component must have its own mass balance

componen s : , , omass, oxygen, e ec ron accep or,

nit rate, ammonium etc.

-In the development of equations useful for a reactor system, mass balances on
several different components of interest and around several different control volumes
sometimes are required.
5.2 Mass Balances
3) Reaction rates affect the size of the treatment system.

Rate of mass accumulation in control volume =

-

( the reactor volume x the concentration ; d(VC)/dt)

ass n ou : mass crosse e con ro -vo ume oun ar es

Generation : formation of the com onent of interest within the control volume
: negative – component destroyed rather than being formed
– endogenous respiration or predation
–
5.2 Mass Balances

Rate of mass accumulation in control volume =

rate(s) of mass in - rate(s) of mass out + rate(s) of mass generation

This e uation ma take man mathematical forms de endin u on

i) the nature of control volume,

ii) the manner in which mass flows into and out of the control volume,

iii) what kind of reactions generate or destroy the component.

 5.3 A Batch Reactor

• A batch reactor operated with mixing

- the control volume consists of the entire reactor
- uniformly distribution of components throughout the reactor

- only component concentrations changing with time.

The rate of mass accumulation = Vdc/dt

• Selection of the components

-
- limiting substrate – the electron donor
• Assumption
- sufficiently high concentration of all other bacterial requirements
such as electron acceptor and nutrients

- at time=0, microorganisms’ concentration in the reactor = X0 (mg/l),

rate limiting substrate in the reactor = S0 (mg/l)
5. 1 Reactor Types

Typical reactors used in environmental application

Basic reactors

Biofilm reactors
5.3 A Batch Reactor
• Mass balance for substrate

a e o mass accumu a on n con ro vo ume =

rate of mass in - rate of mass out + rate(s) of mass generation
=0 =0

: mass of substrate accumulating = mass of substrate generated

if no substrate added or removed

dS
V =Vrut [5.3]
If rate of substrate utilization follows Monod kinetics
dS ⎛ qˆS ⎞
V = ⎜−
V Xa ⎟
qˆS
rut = − Xa
K +S dS ˆS
=− a .
dt K+S
 5.3 A Batch Reactor
• Mass balance for microorganisms

a e o mass accumu a on n con ro vo ume =

rate of mass in - rate of mass out + rate(s) of mass generation
=0 =0

dX a
V =V X 5.6
t
If the organism growth rate follows Monod kinetics,
1 dX a S
syn dec
ˆ −
X a dt K +S

dX ⎛ S ⎞
V a
= V ⎜ μˆ − b⎟X a

dX ⎛ S ⎞
a
= ˆ − .
⎝ K + S
a
dt ⎠
 5.3 A Batch Reactor
- Initial conditions
Xa = Xa S =S .

dS qˆS
=− .
K +S
a
dt
dX ⎛ S ⎞
a
= ⎜ μˆ − b⎟X a [5 . 7 ]

Remark: 1) Interdependence between Xa and S, both of which vary with time

2) In order to solve for Xa and S as functions of time, eq 5.4, 5.7and 5.8
should be considered simultaneously.

3) Due to the nonlinear Monod forms, the systems of eq 5.4, 5.7and 5.8
cannot be solved analytically. It must be done with a numerical solution.
4) if organism decay is considered to be negligible (b =0 in eq 5.7 ),
an analytical solution can be obtained. This is reasonable for cases of
a c grow w ere organ sm ecay s sma w e ey are grow ng rap y.
 5.3 A Batch Reactor
Assumption : organism decay is negligible while the microorganisms
are growing rapidly

Initial conditions
X a (0 ) = X
0
a S (0 ) = S
0
[5 .8 ]

X a = X a0 + Y Δ S or X a = X a0 + Y (S 0 − S ) [5 . 9 ]
y su s u on o eq . n o eq .
dS qˆS
=− Xa [5.4]
dt K +S

dS qˆ S
=− [X 0
a + Y (S 0 − S )] [5 .10 ]
By integration, subject to the boundary conditions by eq 5.8
1⎧ ⎪⎛ K 1⎞ ⎛ K ⎞ SX a0 1 ⎫⎪
= 0
a
0
− − − 0
a .
⎩⎝ X a + YS
qˆ ⎪ ⎝ X + YS ⎠ ⎪⎭
0 0 0 0 0
Y⎠ a S Y
5.3 A Batch Reactor

1⎧⎪⎛⎜ K 1⎞ ⎛ K ⎞ SXa0 1 0 ⎪
⎫
t= ⎨ 0 0
+ ⎟ ln(Xa + YS −YS) − ⎜
0 0
0 0
⎟ ln 0 − ln Xa }⎬ [5.11]
ˆ a a

X = X 0 +Y S0 − S 5 .9

- When t is known, S can be solved by eq 5.11.

a .
 5.3 A Batch Reactor
0
X a affecting bacterial growth and the substrate concentration
la eriod

- The hi her the intial concentration of biomass the lower the substrate utilization time.
- For the lowest initial organism con., a lag period occurs before the onset of
significant substrate utilization.
-The increase of biomass between t=0 and t = t at S=0 is the same in all cases
( = ( Xa – Xa0 ) = Y S0 = 0.6 X 100 = 60 mg / L )

X a = X a0 + Y S 0 − S = X a0 + 0 . 6 (100 − 0 ) [5 . 9 ]