Argaman 1984
Argaman 1984
Argaman 1984
00
Printed in Great Britain. All rights reserved Copyright © 1984 Pergamon Press Ltd
AImtrlct--Activated sludge systems of the oxidation ditch configuration are uniquely suitable for the
single-sludge nitrification and denitrification process. This is due to the high recycle flow generated by the
aeration system. Existing systems, originally designed for carbonaceous organic removal and nitrification,
can be modified to the complete nitrogen removal mode, through the control of oxygen supply. This paper
discusses the conditions required for such modification along with the necessary calculation procedures.
A case study of a full-scale industrial plant is presented. Calculations based on the principles outlined
herein illustrate the capability of the existing system to operate successfully under the single-sludge mode.
Actual data over a 15 months period support these results.
PROCESS DESCRIPTION AND REQUIREMENTS pair will be considered (as shown in Fig. I) although
the principles apply to any number of such pairs,
The oxidation ditch is an activated sludge biologi- Process formulation and design procedures which,
cal treatment process which can be operated at with appropriate modifications, may be utilized for
standard rate or in the extended aeration mode, The such systems have been presented by Barnard (1974),
typical system consists of a closed loop channel as Argaman and Miller (1979) and Argaman t1981,
shown in Fig. 1, or is shaped like a race track. The 1982). In general, the system design and operation
wastewater is aerated using mechanical aerators must meet the following requirements:
mounted across the channel. Horizontal brush, cage
or disc-type aerators are typically used. The aerator, (1) The solids retention time (SRT) must exceed the
apart from transfering atmospheric oxygen to the minimum required for nitrification in the aerobic
wastewater, provides mixing and circulation thus zone.
maintaining the biomass in suspension. Mixed liquor (2) The anoxic zone must have adequate residence
from the ditch is passed to a secondary clarifier of time and biomass concentration to allow for
conventional design. The clarifier's underflow is split denitrification.
into two parts, one returned to the ditch the other (3) The oxygen supply system must deliver ade-
carrying the excess sludge. Unlike conventional com- quate oxygen for both the carbonaceous and nitrog-
pletely mixed aeration basins the dissolved oxygen enous demand, yet assuring the absence of oxygen in
(DO) concentration in the ditch is not uniform. the anoxic zone.
Normally the highest DO levels are found just below (4) The influent carbon/nitrogen ratio must be
the aerators, and the concentration drops gradually within an appropriate range.
as the liquid moves along the channel. The DO levels (5) Flow in the ditch must generate adequate
depend on the oxygen transfer capability of the recycle rate.
aerators and the oxygen demand exerted by the (6) Appropriate environmental conditions, condu-
biochemical reaction. If the oxygen demand exceeds cive to nitrification and denitrification must exist in
the aerators maximum oxygen transfer capacity, the system.
zones of anaerobic or anoxic conditions will develop. These requirements will be discussed in more detail.
Oxygen demand in an oxidation ditch consists of
that which is utilized for carbonaceous B a D removal Solids retention time
and, in many cases, for nitrification. Nitrification is In a single stage activated sludge system the min-
often required by regulatory agencies in order to imum SRT required in order to avoid washout of
reduce toxicity and oxygen demand in receiving nitrifiers is given by
waters. Yet in other instances nitrification occurs
unintentionally as the sysem is operated under low SRT~i. = / J I (1)
organic loading for complete carbonaceous B a D where:
removal. If complete nitrogen removal is required by
SRT'min = minimum SRT required lbr
regulatory agencies, nitrate removal must also be
nitrification in a single stage activated
provided. As will be shown subsequently, the ox-
sludge (day)
idation ditch sysem is uniquely suitable lbr a com-
fi = maximum growth rate of nitrifiers
bined nitrification and denitrification process regard-
(day 1).
less of whether or not denitrification is required. As
long as nitrification occurs, it is advantageous to In deriving equation (1), it was asssumed that the
operate the system for complete nitrogen removal. nitrifier's actual specific growth rate is at its max-
This can be done at the original design phase or by imum value and that the decay rate approaches zero.
modifying the operation of an existing system. Since in reality neither of these assumptions is true,
The key to such operation is adjustment of the it is common to apply a safety factor for selecting the
aeration system so that one or more pairs of aerobic design SRT. This safety factor typically ranges from
and anoxic zones are created. In this paper, a single 2to3.
Standby aerator
Influent /
end return sludge/f
A e r o b i c zone
D o probe
To clarifier Operating
aerator
The nitrifiers maximum growth rate is temperature organics and the environmental condition to which
dependent and can be expressed by the biomass is exposed. Values reported in the litera-
ture vary from less than 1.0 day -1 for poorly de-
fz (T) = ~ (To)exp[Os(T - T0)l (2)
gradable industrial wastes to over 20.0 day -1 for
where: highly degradable organics.
The reported values of a range from 0.4 to 0.7 (g
/~ (T) a n d / i (To) are the nitrifiers maximum growth
VSS) (g BOD) -l and b from 0.02 to 0.05 day -1.
rates at temperatures T°C and
Equation (4) is based on an apparent first order
T0°C, respectively (day -1)
reaction law as suggested by Adams et al. (1975). The
0N = temperature coefficient for
overall nominal hydraulic residence time required for
nitrifiers growth rate.
nitrification in an aerobic/anoxic system can be calcu-
Values of /~ (T) vary over a wide range, mainly lated from equation (4) using the design SRT, i.e.
because of variations in environmental factors. In the (SRT)mi, multiplied by a safety factor.
absence of experimental data the value can be se- The reaction rate coefficient k is also temperature
lected from the reported range of 0.21-1.44 day -1 at dependent. Thus:
temperatures ranging from 8 to 25°C. (U.S. EPA,
k ( T ) = k(To)O r - ro (5)
1975). Reported values of 0N are less scattered and
vary from 0.069 to 0.116 (U.S. EPA, 1975). where:
In an aerobic/anoxic oxidation ditch nitrifying
k ( T ) and k(To)are the rate coefficient at tem-
microorganisms grow in the aerobic zone only. Hence
perature T and To, respectively
it can be shown that the minimum SRT required for
(day-~)
nitrification should be
0 = temperature coefficient for carbo-
(SRT)m,n = ~t-1 (SRT)~, (3) naceous organics removal rate.
where: Typical values of 0 range from 1.03 to 1.07.
(SRT)min = minimum SRT required for nitrifi- Anoxic zone
cation in an aerobic/anoxic system
The volume and biomass concentration in the
(day)
anoxic zone must be such that complete denitrific-
ct = aerobic volume fraction
ation can be achieved. The rate of denitrification
Since ~t is always less than 1.0 the minimum SRT depends primarily on the rate of organic removal
required for nitrification in an aerobic/anoxic system which, in turn, depends on the nature of the organics,
is always higher than in a single stage activated sludge temperature and other environmental factors.
system. Although the exact expression for the
Under most circumstances encountered in practice denitrification rate is given by a multi substrate
the concentration of carbonaceous organics in the Monod equation, under many situations the concen-
raw wastewater greatly exceeds that of nitrogenous trations of both nitrates and BOD in the anoxic zone
matter. Moreover, the cellular yield and growth rate allow a zero order approximation (Beccari et al.,
of heterotrophic microorganisms is considerably 1983). Thus, for adequate denitrification the biomass
higher than the corresponding values for the auto- concentration and the nominal hydraulic residence
trophs. Thus the design and operation parameters time in the anoxic zone must satisfy the following
required for maintaining a desired SRT are con- condition:
trolled by the heterotrophic biomass characteristics
Xvto >1A N o k ~ I (6)
and the carbonaceous organic removal kinetics.
Assuming that the rate of organic removal, micro- where:
organism decay and cellular yield are the same in
tD = nominal hydraulic residence time in the
both the aerobic and anoxic zones, the hydraulic
anoxic zone (day)
residence time can be related to the SRT through
AN D = denitrified nitrogen concentration (rag 1-1)
t = So(ak SRT - b SRT - 1)[kXv(1 + b SRT)] -1 (4) kz~ = zero order denitrification rate coefficient,
[(rag NOa-N ) (rag VSS) -t day-I].
where:
t = nominal hydraulic residence time (day) Reported values of ko, summarized by Eckenfelder
So = influent concentration of BOD (mg 1-1) and Argaman (1978) range from 0.03 to 0.60 (mg
a = sludge yield coefficient [(g VSS)(g BOD) -I] NO3-N) (mg VSS)- i day- 1. Values in the lower range
k = organic removal rate coefficient (day -I) refer to endogenous denitrification with domestic
b = endogenous decay rate coefficient (day -I) sewage whereas the high rates were derived from
Xv = active biomass concentration in the system denitrification systems using methanol or other
(mg 1-~). readily degradable carbon sources. The temperature
dependence of ko is similar to that of k, thus equation
The rate coefficient k depends on the nature of the (5) applies to the denitrification rate coefficient too.
1496 YERACHMIELARGAMAN
August 82 when production dropped markedly due difference between influent TKN and effluent nitrate,
to summer vacation. The data of Table 2 indicate subtracting the nitrogen used for assimilation. The
almost complete removal of BOD and ammonia latter value was estimated at 2.5~ of the removed
nitrogen. Nitrates were reduced to less than 20 mg l- BOD. Excluding the month of July 82 the calculated
in all but one month (July 82). Examination of the anoxic residence time ranged from 0.77 to 1.32 day
daily data during the month of July 82 shows very with an average of 0.99 day. For the month of July
low influent BOD ( < 1 0 0 m g l -~) and very high 82 with its unusually low influent concentration, the
effluent nitrate ( > 60 mg 1- ~) towards the end of the required anoxic residence time was 0.44 day.
month. During this period the influent BOD was
below the carbon requirements for denitrification, Overall residence time
The required overall residence time was estimated
Comparison of actual and required values
using equations (1)-(4). A safety factor of 2.5 was
The observed values of various operation parame- applied in calculating the minimum required SRT to
ters were compared to those required according to the be substituted in equation (4). A trial and error
principles outlined in the preceding presentation. solution was used since the aerobic volume fraction,
Values of the various coefficients were selected from ~, must be specified in order to calculate SRTm~n in
the literature. Where a range of values is given in the equation (3). Hence a value of ~ was assumed, the
literature, the typical, or more conservative numbers overall residence time was calculated, and the re-
were selected, as shown in Table 3. suiting 7 was compared with the assumed one. This
sequence was repeated until the two values agreed to
Anoxic residence time within 10~°/o. The resulting values of ~ ranged from
The required residence time in the anoxic zone was 0.23 to 0.58 with an average of 0.39, again excluding
calculated using equation (6). Since the system was the month of July 82. The required overall residence
operated at very low organic loading it was assumed time is compared to the actual residence time in Fig.
that the fraction of the biomass is 0.3. Thus, only 30~ 2. As can be seen the actual residence time was always
of the MLVSS of Table 2 was substituted for Xv in considerably higher than the calculated minimum
equation (6). The value of ANo was calculated as the requirement.
5.0
Actual
o 4.0 r
"o
¢) ij .
E
~. 3.0
Minimum required ['equations(I)-(4)]
c
"~ 2 . 0
,\
1 , [___ J
o6 1.0
0
! I I I. I l I I I
I I I I I I
X Xl Xll I II III IV V Vl
VII VIII IX X Xl X l l
1981 1982 Month
Fig. 2. A c t u a l a n d r e q u i r e d o v e r a l l r e s i d e n c e t i m e .
Single sludge nitrogen removal in an oxidation ditch 1499
0 0.6
m
Z
v o.4
h-
_fL LI_._ Argaman Y. (1981) Design and performance charts for
single sludge nitrogen removal systems. Water Res. 15,
841-847.
Argaman Y. (1982) Single sludge nitrogen removal from
industrial wastewater. Wat. Sci. Technol. 14, 7-20.
Argaman Y. and Miller E. (1979) Modelling recycled sys-
f~ tems for biological nitrification and denitrification. J.
_~ 0.2
E R a n g e of m i n i m u m ratio Wat. Pollut. Control Fed. 51, 749-758.
Argaman Y. and Spivak E. (1974) Engineering aspects of
eL~
X
. . . . . .
Xl xll I II
.
III IV
1 i i i
V V l V I I VIII I x
i i i
X Xl Xll
i wastewater treatment in aerated ring-shaped channels.
1981 1982 Month
Water Res. 8, 317-322.
Barnard J. L. (1974) Cut P and N without chemicals. Wat.
Fig. 4. Actual and required influent composition. Wastewat. Engng 11, 33-36, 41~14.
1500 YFRACHMIEL ARGAMAN
Beccari M., Passino R., Ramadori R. and Tandoi V. (1983) Sutton P. M., Jank B. E. and Vachon D. (1980) Nutrient
Kinetics of dissimilatory nitrate and nitrite reduction in removal in suspended growth systems without chemical
suspended growth culture. J. Wat. Pollut. Control Fed. 55, addition. J. War. PoUut. Control Fed. 52, 98- 109.
58-64. Sutton P. M., Bridle T. R., Bedford W. K. and Arnold J.
Henze Christensen M. (1975) Denitrification of sewage by (1981t Nitrification and denitrification of an industrial
alternating process operation. Prog. Wat. Technot. 7, wastewater. J. Wat. Pollut. Control Fed. 53, 176 184.
339-347. Tholander B. (1977) An example of design of activated
Matsche N. F. (1980) Influencing parameters on the sludge plants with denitrification. Prog. Wat. Technol. 8,
nitrification---denitrification performance of a single stage 661-672.
activated sludge plant. Prog. Wat. Technol. 12, 551-563. U.S. EPA (1974) Process Design Manual ,[br Nitrogen
Matsche N. F. and Spatziemer G. (1975) Austrian plant Removal, U.S. EPA, Office of Technology Transfer,
knocks out nitrogen. Wat. Engng 12, 18-24. Washington, DC.