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Transcript
CE 548
II
Fundamentals of Biological Treatment
1
Modeling Suspended Growth
Treatment Processes
 Description of treatment process:
 All biological treatment reactor designs are based on using
mass balances across a defined volume for each constituent of
interest (i.e., biomass, substrate, etc.)
 Biomass mass balance:
Accumulation = inflow – outflow + net growth
dX
V  QX o  Q  Qw X e  Qw X r   rgV
dt
eq (7 - 32)
2
Modeling Suspended Growth
Treatment Processes
3
Modeling Suspended Growth
Treatment Processes
Assuming stead-state and Xo = 0, equation 7-32 can be
simplified:
Q  Qw X e  Qw X r  rgV
rg  Yrsu  k d X
Q  Qw X e  Qw X r
VX
SRT 
Eq (7 - 33)
Eq (7 - 21)
rsu
 Y
 kd
X
Eq (7 - 34)
mass of organisms in the reactor
mass of organisms removed form the system each day
4
Modeling Suspended Growth
Treatment Processes
VX
SRT 
Q  Qw X e  Qw X r
Eq (7 - 35)
Equation 7-34 can be written as:
rsu
1
 Y
 kd
SRT
X
Eq (7 - 36)
The term 1/SRT is related to µ, the specific biomass growth rate:
1

SRT
Eq (7 - 37)
5
Modeling Suspended Growth
Treatment Processes
In Eq. (7-36) the term (-rsu/X) is known as the specific substrate
utilization rate U and can be calculated as the following:
rsu Q( S o  S ) S o  S
U


X
VX
X
Substituting Eq. (7-12) rsu  
1
YkS

 kd
SRT K s  S
Eq (7 - 38)
kXS
Ks  S
into Eq. (7-36) yields:
Eq (7 - 39)
Solving Eq. (7-39) for S yields:
S
K s 1  k d SRT 
SRT Yk  k d   1
Eq (7 - 40)
6
Modeling Suspended Growth
Treatment Processes
 Substrate mass balance:
Accumulation = inflow – outflow + generation
0
dS
V  QS o  QS  Qw S  rsuV
eq (7 - 41)
dt
Substituting for rsu and assuming steady-state, Eq. (7-41) can be
written as:
 V  kXS 

So  S   
 Q  K s  S 
 SRT
X 
 
 Y So  S  




1

k
SRT

d

eq (7 - 42)
eq (7 - 43)
7
Modeling Suspended Growth
Treatment Processes
8
Modeling Suspended Growth
Treatment Processes
 Mixed liquor solids concentration and solids production:
The solids production from a biological reactor represents the
mass of material that must be removed each day to maintain
the process:
X TV
eq (7 - 45)
SRT
where; PX T ,VSS  total solids wasted daily, g VSS/d
PX T ,VSS 
X T  total MLVSS in areation tank, g VSS/m3
Eq. (7-45) can be used to calculate the amount of solids
wasted for any of the mixed liquor components. For the
amount of biomass wasted (PX), the biomass concentration X
can be used in place of XT in Eq. (7-45).
9
Modeling Suspended Growth
Treatment Processes
 Mixed liquor solids concentration:
The total MLVSS equals the biomass concentration X plus the
nbVSS concentration Xi :
XT  X  Xi
eq (7 - 46)
A mass balance is needed to determine the nbVSS conc.:
Accumulation = inflow – outflow + generation
dX i / dt V  QX o,i  X iV / SRT  rX ,iV
eq (7 - 47)
Where X o ,i  nbVSS concentrat ion in influent, g/m
3
X i  nbVSS concentrat ion in areation tank, g/m3
rX ,i  rate of nbVSS production from cell debris, g/m3  d
10
Modeling Suspended Growth
Treatment Processes
 Mixed liquor solids concentration:
At steady-state
dX i / dt  0 and
substituting Eq. (7-25)
rXd  f d (kd ) X for rX ,i in Eq. (7-47) yields:
X i  X o ,i ( SRT ) /   ( f d )( k d ) X ( SRT )
eq (7 - 49)
Combining Eq. (7-43) and Eq. (7-49) for X and Xi produces the
following equation that can be used to determine XT :
 SRT
XT  
 

X o,i SRT
  Y So  S  

   f d kd  X SRT 

 1  kd SRT 
(A)
(B)
Hetrotroph ic
biomass
Cell debris
eq (7 - 50)
(C)
Nonbiodegr adable
VSS in influent
11
Modeling Suspended Growth
Treatment Processes
 Solids production:
The amount of VSS produced and wasted daily is as follows:
PX ,VSS 
QY S o  S 
 f d k d X V   QX o ,i
1  k d SRT
eq (7 - 51)
Eq. (7-43) is substituted for biomass concentration (X) in Eq. (7-51)
to show VSS production rate in terms of the substrate removal,
influent VSS, and kinetic coefficients as follows:
PX ,VSS
QY S o  S  f d k d QY S o  S SRT


 QX o ,i
1  k d SRT
1  k d SRT
(A)
(B)
Hetrotroph ic
biomass
Cell debris
eq (7 - 52)
(C)
Nonbiodegr adable
VSS in influent
12
Modeling Suspended Growth
Treatment Processes
 Solids production:
The effect of SRT on the performance of an activated sludge system
for soluble substrate removal is shown in figure 7-13
The total suspended solids (TSS) production can be calculated by
modifying Eq. (7-52) assuming that a typical biomass VSS/TSS ratio
of 0.85 as follows:
PX ,TSS
A
B


 C  Q(TSSo  VSSo )
0.85 0.85
eq (7 - 53)

influent inorganic solids
13
14
Modeling Suspended Growth
Treatment Processes
 The observed yield:
The observed yield for VSS can be calculated by dividing Eq. (7-52)
by the substrate removal rate Q(So-S):
X o ,i
( f d )(kd )(Y ) SRT
Y
Yobs 


1  (kd )SRT
1  (kd ) SRT
So  S
eq (7 - 56)
 Oxygen requirements:
Oxygen used = bCOD removed – COD of waste sludge
Ro  Q( S o  S )  1.42 PX ,bio
eq (7 - 59)
where
Ro  Oxygen required, kg/d
PX ,bio  biomass as VSS wasted per day, kg/d
Study example 7-6
1.42  COD of cell tissues, g O 2 / g cells
15
Modeling Suspended Growth
Treatment Processes
 Design and operating parameters:
Following are the design and operating parameters that are
fundamentals to treatment and performance of the process:
 SRT
Food to microorganisms (F/M) ratio
F /M 
total applied substrate rate
total microbial biomass
QS o S o


VX X
eq (7 - 60)
The SRT can be related to F/M by the following equation:
1
E
 Y (F / M )
 kd
SRT
100
eq (7 - 66)
16
Modeling Suspended Growth
Treatment Processes
 Design and operating parameters:
Organic volumetric loading rate.
Defined as the amount of BOD or COD applied to the
aeration tank volume per day:
Lorg
QS o

(V )(103 g / kg)
eq (7 - 67)
Where
Lorg  volumetric organic loading, kg BOD/m 3  d
Q  influent flowrate, m3 /d
S o  influent BOD concentrat ion, g/m 3
V  aeration tank volume, m3
17
Modeling Suspended Growth
Treatment Processes
 Modeling plug-flow reactors:
Developing a kinetic model for the plug-flow reactor is
mathematically difficult (X vary along the reactor). Two assumptions
are made to simplify the modeling:
 The concentration of microorganisms is uniform along the reactor  X 
This assumption applies only when SRT/  5.
 The rate of substrate utilization is given by:
rsu 
kSX
Ks  S
eq (7 - 72)
18
Modeling Suspended Growth
Treatment Processes
19
Modeling Suspended Growth
Treatment Processes
 Modeling plug-flow reactors:
Integrating Eq. (7-72) over the retention time in the tank gives:
Yk S o  S 
1

 kd
SRT S o  S   1   K s ln Si / S 
eq (7 - 73)
X 
where;
S o  influent concentrat ion
S  effluent concentrat ion
Si  influent concentrat ion to reactor after dilution with recycle flow

S o  S
1 
  recycle ratio
20
Biological Nitrification
 Nitrification is the conversion (by oxidation) of Ammonia (NH4N) to nitrite (NO2-N) and then to nitrate (NO3-N).
 The need for nitrification arises from water quality concerns:
 Effect of ammonia on receiving water; DO demand, toxicity.
 Need to provide nitrogen removal for eutrophication control.
 Need to provide nitrogen removal for reuse applications.
 The current drinking water MCL for nitrate is 45 mg/l as
nitrate or 10 mg/l as nitrogen.
 The total concentration of organic and ammonia nitrogen in
municipal wastewater is typically in the range of 25-45 mg/l as
nitrogen.
21
Biological Nitrification
 Process description:
 Nitrification is commonly achieved with BOD removal in the same
single-sludge process.
 In case of the presence of toxic substances in the wastewater, a
two-sludge system is considered.
 Stoichiometry:
Nitritebacteria
( Nitrosomonas )
2 NH 4  3O2    2 NO2  4 H   2 H 2O
Nitratebacteria
( Nitrobacter )
2 NO2  O2    2 NO3
Overall reaction :
NH 4  2 HCO3  2O2  2 NO3  2CO2  3H 2O
22
Biological Nitrification
 Process description:
Overall reaction :
NH 4  2HCO3  2O2  2 NO3  2CO2  3H 2O
 The oxygen required for complete oxidation of ammonia is 4.57 g
O2/g N oxidized.
 The alkalinity (alk) requirement is 7.14 g alk as CaCO3 for each g of
ammonia nitrogen (as N).
23
24
Biological Denitrification
 Process description:
 Denitrification is the biological reduction of nitrate (NO3) to nitric
oxide (NO), nitrous oxide (N2O), and nitrogen (N).
 The purpose is to remove Nitrogen from wastewater.
 Compared to alternatives of ammonia stripping, breakpoint
chlorination, and ion exchange, biological nitrogen removal is more
cost-effective and used more often.
 Concerns over eutrophication and protection of groundwater against
elevated NO3-N concentration.
25
26
Biological Denitrification
 Stoichiometry:
 In denitrification, nitrate is used as the electron acceptor instead of
oxygen and the COD or BOD as the carbon source (electron donor).
 The carbon source can be the influent wastewater COD or external
source (Methanol).
Wastewater
C10 H19O3 N  10 NO3  5 N 2  10CO2  3H 2O  NH 3  10OH 
Methanol
5CH 3OH  6 NO3  2 N 2  5CO2  7 H 2O  6OH 
 One equivalent of alkalinity is produced per equivalent of nitrate
reduced. (3.57 g alk per g nitrate)
27
Biological Phosphorus Removal
 Process description:
 Phosphorous removal is done to control eutrophication.
 Chemical treatment using alum or iron salts is the most commonly
used technology for phosphorous removal.
 The principle advantages of biological phosphorous removal are
reduced chemical costs and less sludge production.
 In the biological removal of phosphorous, the phosphorous in the
influent is incorporated into cell biomass which is removed by sludge
wasting.
 Phosphorous accumulating organisms (PAOs) are encouraged to
grow and consume phosphorous. Therefore, the system is designed
so that the reactor configuration provides advantage for PAOs to
grow over other bacteria.
28
Biological Phosphorus Removal
29
Biological Phosphorus Removal
30
Anaerobic Fermentation and Oxidation
 Process description:
 Used primarily for the treatment of waste sludge and high strength
organic waste.
 Advantages include low biomass yield and recovery of energy in the
form of methane.
 Conversion of organic matter occurs in three steps:
– Step1 (Hydrolysis): involves the hydrolysis of higher-molecularmass compounds into compounds suitable for use as a source of
energy and carbon.
– Step2 (Acidogenesis): conversion of compounds from step1 into
lower-molecular-mass intermediate compounds.
(nonmethanogenic bacteria)
– Step3 (Methanogenesis): conversion of intermediates into
simpler end products (CH4 & CO2).
31
Anaerobic Fermentation and Oxidation
 Process description:
 For efficient anaerobic treatment, the reactor content should be:
– void of O2
– free of inhibiting conc. of heavy metals and sulfides
– pH ~ 6.6 – 7.6
– sufficient alkalinity to ensure pH is not <6.2 (methane bacteria
will not function below 6.2).
 Methanogenic bacteria has slow growth rate, therefore:
– require long detention time for waste stabilization
– yield is low: less sludge production and most organic matter is
converted to CH4 gas.
– sludge produced is stable: suitable for composting
– require relatively high temp for adequate treat.
32