performances of mesophilic anaerobic digestion systems treating poultry mortalities
TRANSCRIPT
This article was downloaded by: [Colorado College]On: 25 November 2014, At: 16:11Publisher: Taylor & FrancisInforma Ltd Registered in England and Wales Registered Number:1072954 Registered office: Mortimer House, 37-41 Mortimer Street,London W1T 3JH, UK
Journal of EnvironmentalScience and Health,Part B: Pesticides, FoodContaminants, andAgricultural WastesPublication details, including instructionsfor authors and subscription information:http://www.tandfonline.com/loi/lesb20
Performances ofmesophilic anaerobicdigestion systems treatingpoultry mortalitiesTen‐Hong Chen a & Jia‐Chern Wang a
a Department of Agricultural MachineryEngineering , National Chung‐HsingUniversity , Taichung, 40227, Taiwan,Republic of ChinaPublished online: 21 Nov 2008.
To cite this article: Ten‐Hong Chen & Jia‐Chern Wang (1998) Performancesof mesophilic anaerobic digestion systems treating poultry mortalities,Journal of Environmental Science and Health, Part B: Pesticides, FoodContaminants, and Agricultural Wastes, 33:4, 487-510
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J. ENVIRON. SCI. HEALTH, B33(4), 487-510 (1998)
PERFORMANCES OF MESOPHILIC ANAEROBIC DIGESTION
SYSTEMS TREATING POULTRY MORTALITIES
Key Words: Poultry mortalities, anaerobic digestion, leachbed, upflowanaerobic sludge blanket, leachate recirculation
Ten-Hong Chen and Jia-Chern Wang
Department of Agricultural Machinery Engineering,National Chung-Hsing University,
Taichung, Taiwan 40227Republic of China
ABSTRACT
A closed-loop anaerobic digestion system consisting of a leachbed (LB) and an
upflow anaerobic sludge blanket (UASB) was tested as an alternative for the
disposal of poultry mortalities. This paper compares the performances of three LB-
UASB treatment systems with different initial moisture contents in the LBs. Each
LB was loaded with one chicken and 5, 10 or 18 liters of water. The LBs initially
carried out the hydrolysis/acidification phase while the UASBs the methanogenesis
phase. Due to repeated inoculation by the UASBs, the LBs with 10 and 18 liters of
water started producing methane on day 5, while the one with 5 liters of water on
day 19. However, methane production rates were low before day 40 for the LB
with 10 liters of water and day 60 for the other LBs. Methane production gradually
487
Copyright © 1998 by Marcel Dekker, Inc. www.dekker.com
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488 CHEN AND WANG
improved as the LBs continued to receive ungranulated sludge from the UASBs.
The LBs eventually became balanced methane reactors. Continued balanced
fermentation in the LBs resulted in leachates with very low substrate concentrations
that could no longer support high-rate methanogenesis in the UASBs.
Consequently, methane production rates from the UASBs decreased quickly while
that from the LBs reached peak levels. Cumulative methane production from each
LB eventually exceeded that from its connecting UASB. After 118 days of
digestion, 414, 437 and 470 liters of methane were produced from the three
systems, respectively. Cumulative methane production from the LBs with 5 and 18
liters of water accounted for 63% of the total methane produced from their
respective systems. The LB with 10 liters of water produced 75% of the total
methane from that system. Methane yields ranged from 0.485 to 0.554 m3 (Kg TS)
1. About 86% of the initial dry weight was biodegraded. All three systems
performed very well with little operational problems. Overall, the system that
started with 10 liters of water in the LB performed the best. Strategy for enhancing
system performances and implementing farm applications are discussed.
INTRODUCTION
Chicken population in Taiwan was 101.8 million in 1995 (Taiwan Provincial
Government, 1996). At an average mortality rate of about 9.3%, about 8.6
million birds need to be disposed of annually. Being easily putrefiable, potential
of causing sanitary problems, spreading of diseases and, in the worst scenario,
smuggling of tainted meat into the market are of great concerns. To dispose of
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MESOPHILIC ANAEROBIC DIGESTION SYSTEMS 489
mortalities properly is crucial to improving public health, sustaining animal
industry and protecting the environment.
In addition to the conventional disposal methods of burial, incineration and
rendering, aerobic composting is becoming popular in America (Donald and
Blake, 1992) and accepted by many states (Proctor, 1992). Chen and Shyu
(1998) proposed anaerobic digestion as yet another alternative for mortality
disposal. The advantage of anaerobic treatment is that it couples waste treatment
with methane production. Additionally, the process kills pathogens (Lee and
Shih, 1988; Shih, 1987; Turner et al., 1983). However, a thermophilic (55°C)
LB-UASB system treating poultry mortalities was severely inhibited due to high
concentrations of long-chained fatty acids (LCFA) arising from lipid hydrolysis
(Chen and Shyu, 1998). Furthermore, operation of the system was problematic
due to frequent feeding or recycling line breakage as a result of prolonged, almost
continuous recirculation. Methane production and conversion efficiency seemed
to improve with higher initial moisture content in the LB. Digestion at 35°C was
less inhibited, although there were still rooms for further improvements. The
objective of this study was to further examine the effects of initial moisture
contents in the LB and a smaller recycle ratio on performances of a mesophilic
LB-UASB system.
MATERIALS AND METHODS
Poultry Mortalities
Chickens were purchased from a local market when needed. The average live
weight of the chickens was 2192 grams. The chickens were slaughtered, their
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490 CHEN AND WANG
blood drained and collected and their feathers plucked. Each dead bird,
simulating mortalities, was divided into four components for the experiments:
'carcasses, blood, viscera and feathers. ••'••
Experimental Set-up
The anaerobic digestion system used consisted of a leachbed (LB) and an
UASB reactor connected in a closed loop (Figure 1). Three systems were set up,
hereafter designated systems A, B and C. The reactors were made of Plexiglas.
Dimensions for the reactors are presented in Table 1. The reactors were
incubated in temperature-controlled chambers maintained at 35±1°C. Biogas
from each reactor was collected in a water displacement system, filled with
solution containing 25% NaCl and 0.5% citric acid.
Start-up
Chicken components, each in a No. 32 mesh nylon bag, were placed in the
LBs to start the experiment. One bird per LB. Five, ten and eighteen liters of
water were added to LB-A, LB-B and LB-C, respectively, to allow extra liquid
for recirculation. Each UASB was inoculated with about 50% (by volume) of
granular sludge obtained from I-Lan Brewery Plant (Taiwan Tobacco and Wine
Co.). The inoculum contained 40.47 grams of volatile suspended solids (VSS)
and had a specific methanogenic activity of 1.43 g COD (g VSS)'1 day1.
Operation
Liquid in both the LB and the UASB were recirculated by peristaltic pumps
six times daily at 30 minutes each. Liquid in the LB was recirculated by
pumping from the bottom and distributing over the chicken components from the
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MESOPHILIC ANAEROBIC DIGESTION SYSTEMS 491
- Gas Sampling
35X
BiotasCollection
Feed Pump
Leachbed UASB
FIGURE 1
Schematics of experimental setup of an LB-UASB system.
top to promote leaching. Pumping recirculating liquid created an upflow velocity
of 0.7-0.9 m h"1 in the UASB. Leachate from the LB was fed to the UASB six
times per day. During feeding, appropriate volume of the leachate was pumped
to the UASB as influent while effluent from the UASB overflowed to the LB to
maintain constant liquid volumes in both reactors. Loading rates (LR) to the
UASB determined the volume of liquid to be transferred. The chemical oxygen
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492 , CHEN AND WANG
TABLE 1
Reactors Dimensions and Some Operational Parameters
Reactor
DimensionDiameter(mm)Height(mm)Working volume
(dm3)
Recycle ratio
Liquid upflowvelocity(m h"1)
Svstem ALeachbed UASB
1950
5
NA
NA
960
3
1.4-304
0.7-0.9
Svstem BLeachbed UASB
2355
10
NA
NA
960
3
1.4-162
0.7-0.9
Svstem CLeachbed UASB
2360
18
NA
NA
960
3
1.4-132
0.7-0.9
demand (COD) of the leachate was monitored frequently and the data used for
calculating LRs to the UASB. The UASBs were started at an LR of 0.5 g COD
I"1 day"1 to avoid shock-loading the inoculum. The LR to the UASB was raised
in small steps (< 0.5 g COD I"1 week'1) if digestor performance remained
acceptable. Feeding of the UASB was discontinued when leachate concentration
became very low, but, the experiment continued until day 118.
Sampling and Analyses
Daily biogas production was determined from the volume of saline solution
displaced. Gas samples for composition analyses were taken through a septum
on top of the liquid displacement system (Figure 1). Gas composition was
analyzed with a thermal conductivity detector on a gas Chromatograph (GC,
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MESOPHILIC ANAEROBIC DIGESTION SYSTEMS 493
Shimadzu GC-14A). A 3mm by 3m column packed with 60/80 mesh
Chromosorb 102 (Supelco Inc.) was used.
The initial dry weights of the chickens were determined. Additional chickens
were used to determine the COD of chicken components. Each of these chicken
was divided into five components: bones, meats, blood, viscera and feathers. The
components were freeze-dried and ground through a 0.5mm screen in a Cyclone
Sample Mill (UDY Corp.) before analyses. The COD analyses were performed
according to the Standard Methods (APHA, 1992).
Effluent from the LB and the UASB were sampled periodically for total solids
(TS), volatile solids (VS), pH, COD, volatile fatty acids (VFA) and long-chained
fatty acids (LCFA, Cg-C24) analyses. Liquid lost through sampling and
evaporation was replaced with tap water. The CODs of both filtered (through
Supoi*-450 filters, Gelman Sei.) and unfiltered samples were determined. The
difference between the filtered and the unfiltered CODs was taken to be the
sludge concentration. The TS and VS were analyzed according to the Standard
Methods. The pH was determined with a pH electrode. The VFA and LCFAs
were determined with a flame ionization detector on a GC (Hitachi 5000A). The
column and GC conditions for VFA analyses were as previously described (Chen
and Shyu, 1996). Samples for LCFA analyses were prepared in a two-hour one-
step extraction-transesterification procedure (Sukhija and Palmquist, 1988) and
frozen (-20°C) until analyzed. A 3mm by 2m column packed with 100/120
Chromosorb WAW, GP 10% SP-2330 was used for the LCFA analyses.
Nitrogen gas at a flow rate of 20 ml min"1 was the carrier gas. The injector,
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494 CHEN AND WANG
column and detector temperatures were 220, 200 and 250°C, respectively.
Standards (Catalog nos. O 7756, 7506 and 7631) for the LCFAs analyses came
from Sigma (Sigma Chem. Co.). Individual LCFAs were calculated by
comparing peak areas of the samples to those of the standards.
On termination of the experiment, all nylon bags were retrieved from the
LBs, rinsed with water and dried to determine weight losses. The CODs of the
residual solids, the final fermentation liquid including the rinsate were also
determined for mass balancing purposes.
RESULTS
The average dry weight of the chickens was 853 grams. Addition of 5, 10
and 18 liters of water resulted in initial TS contents of 13.3%, 7.5% and 4.4%
for LB-A, LB-B and LB-C, respectively. The dry weight compositions of the
meat, bones, feathers, viscera and collected blood were 50.7, 29.1, 11, 8.3 and
0.9%, respectively. On a COD basis, meats, bones, feathers, viscera and blood
constituted 57.3, 23, 9.7, 9.3 and 0.6%, respectively, of a chicken.
Leachbed Performance
The mortalities started solubilizing quickly and produced a concentrated
leachate. A layer of oil appeared on the surface of the fermentation liquid on day
4, an indication that adipose tissues were being released from decomposing
chicken components. The leachate contained LCFAs, suggesting lipids hydrolysis
since lipids are hydrolyzed to LCFAs and glycerol (Hanaki et al., 1981).
However, the LCFA concentrations were low, at less than 1.4 g COD equivalent
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MESOPHILIC ANAEROBIC DIGESTION SYSTEMS 495
per liter. Leachate CODs reached the maximum levels within 5 days after start-
up (Figure 2). With 5, 10 and 18 liters of water added, leachate COD
concentrations reached 44, 20 and 18 g I"1, respectively. Volatile fatty acids
(mostly acetate) contributed up to 70% of the CODs. The pH levels were
between 6-6.5. There was no CH4 in the biogas. Apparently, the fermentation
was unbalanced and the LBs were carrying out hydrolysis/acidification phase up
to this point.
The LB-B and the LB-C started producing methane on day 5, while methane
appeared in the biogas from LB-A on the 19th day. Thereafter, methane contents
of the biogas increased gradually. Concurrently, leachate CODs and VFAs were
decreasing while pH was increasing. Methane contents of the biogas levelled off
at about 80%, indicating that the LBs had matured as balanced methane reactors.
It took LB-B about 50 days to reach this level, while LB-A and LB-C took about
65 days. Methane production rates reached the maximum levels on days 70, 50
and 75 for LB-A, LB-B and LB-C, respectively, and remained at those levels
until day 87 (Figure 3). During these periods, LB-A was producing an average
of 6 1 CH4 day"1, while LB-B and LB-C were averaging 5 and 7.9 1 CH4 day"1,
respectively. Leachate COD concentrations from LB-B dropped below 400 mg
I"1 after day 57 (Figure 2). The LB-A and the LB-C reached the same stage on
days 68 and 80, respectively. Methane production rate from LB-B dropped below
2 1 day"1 when the operation was terminated on day 118.
On termination of the experiment, floating oil in LB-C disappeared almost
completely, while LB-B and LB-C still contained a thin layer of oil and fats. The
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496 CHEN AND WANG
oOo
ou -
40 -
3 0 -
20-
10-
0 -
A A A Í - A ALB-ALB-B
- • • • LB-C
20 40 60Time, day
80 100 120
FIGURE 2
Leachate characteristics (COD, TVA and pH) and %CH4 in biogas from the LBs.
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MESOPHILIC ANAEROBIC DIGESTION SYSTEMS 497
500
CH4 production rate
Cum. sludge
20 40 60 80
Time, day
FIGURE 3
100 120
Methane production rate and sludge accumulation in the LBs.
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498 CHEN AND WANG
blood and viscera components disappeared completely. An average of 86.3% of
the carcasses was degraded. The remains were mostly bones. The feathers lost
77.3% weight. Overall, 14.1 % of the mortalities remained to be treated. Of the
remaining solids, 84.6% was bones and 15.4% feathers. Table 2 shows COD
distribution for the experiment. The many samples, residual solids, final
fermentation liquid and methane production accounted for 3.9%, 11.7%, 0.6%
and 83.7%, respectively of the total COD.
UASB Performance
Figures 4, 5 and 6 show the operating conditions and performances of UASB-
A, UASB-B and UASB-C, respectively. For the first 25 days, all UASBs
maintained nearly 100% COD reduction efficiencies even though influent CODs
were high and the LRs were increasing. Methane production rates continued to
follow the LRs closely, indicating stable methanogenesis and that methanogenesis
was not rate-limiting. As influent concentrations were decreasing due to efficient
COD reduction in the LBs, increasingly higher feeding rates were used to achieve
increasingly higher LRs. Consequently, the hydraulic retention times (HRT) were
becoming increasingly shorter. Prior to day 40, UASB-C had the shortest HRTs,
followed by UASB-B, then UASB-A. The LRs reached a maximum of about 4
g I'1 day"1 and could not be increased any further without lowering the HRT to
below 0.25 days after influent COD concentrations had dropped below 400 mg
I'1. A minimum HRT of 0.25 days was maintained to prevent excessive washout
from the UASBs. The LRs and methane production rates started to decrease due
to further decreases in influent concentrations. Feeding of UASB-B was
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MESOPHILIC ANAEROBIC DIGESTION SYSTEMS 499
TABLE 2
COD Distribution during the Experiment
System
ALeachbed (w/ 5 1 H2O)UASBLB-UASB
BLeachbed (w/ 10 1 H2O)UASBLB-UASB
Leachbed (w/ 18 1 H2O)UASBLB-UASB
Average LB-UASB
as % of total
Chen and Shyu (1998)Leachbed (w/ 3 1 H2O)UASBLB-UASB
Sampling
83.92.2
86.1
43.81.3
45.1
43.21.9
45.1
58.8
3.9
11613.5
129.5
COD distribution, eram
CH4 prod.
750432
1182
929.3318.7
1248
854.6496.4
1351
1260.3
83.7
117369.1486.1
CODFinal residual
Liquid
6.2-0.41
5.8
11.3-1.5'9.8
13.8-0.3'13.5
9.7
0.6
103.54.7
108.2
Solids
1870
187
196.90
196.9
145.30
145.3
176.4
11.7
———
Total
1461
1499.8
1554.9
1505.2
100
'Calculated as (final COD concentration - initial COD concentration) x (liquidvolume). The final COD concentration was lower than the initial CODconcentration.
discontinued on day 65 while feeding of UASB-A and UASB-C stopped on days
75 and 84, respectively. At these times, the COD concentrations in the UASBs
were below 200 mg I'1. Throughout the experiment, the CODs of UASB-B were
generally lower than those of UASB-A and UASB-C. The LCFA (mostly
myristate) and VF A concentrations never exceeded 450 and 1400 mg COD
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500 CHEN AND WANG
X
100
8.5
8 -
7.5-
o>ooo
ooo
3 -
2 -
1-
20 40 60Time, day
80 100
-o
oo
ou
100
-80
-60
-40
-20
co t¡¡
o3
•o<DCCDOO
120
FIGURE 4
Operating conditions (HRT and LR) and reactor performance for UASB-A.
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MESOPHILIC ANAEROBIC DIGESTION SYSTEMS 501
>•v
HI,
X
4 0 -
30 -
2 0 -
10 -
0 -
11
\ I ' ̂\
20 40 60Time, day
80 100
4.5 >-4 S
ooo
-2 S
-1
- 6 0
- 4 0
- 2 0
ctüo
n
3
œirDco
120
FIGURE 5
Operating conditions (HRT and LR) and reactor performance for UASB-B.*
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502 CHEN AND WANG
X
32-r30-
2 0 -
1 0 -
0 -
ñ J/ i
^ — •
. ^ ~
/
Ai
- 6
- 5
- 4
- 3
- 2
-1
- 0
100
40 60Time, day
80 100
a-ooo
cH5
120
FIGURE 6
Operating conditions (HRT and LR) and reactor performance for UASB-C.
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MESOPHILIC ANAEROBIC DIGESTION SYSTEMS 503
equivalent per liter, respectively. The pH profiles of all UASBs were similar.
After dropping slightly to around 7.2, the pH rised gradually and levelled off at
above 7.5. Upon termination, UASB-A, UASB-B and UASB-C contained 73.5,
65.5 and 48.4 grams of VSS, respectively.
LB-UASB System Performance
The LB-UASB system initially behaved like a two-phase system with the LB
serving as the hydrolysis/acidification phase and the UASB the methanogenesis
phase. There was a lag of 45 days for system B and 60 days for systems A and
C before accelerated methanogenesis started in the LBs (Figure 7). As the LBs
progressed to become matured methane reactors, increasingly more substrate was
bioconverted into methane in the LBs before reaching the UASBs. Cumulative
methane production from each LB eventually exceeded that from its connecting
UASB. The cross-over points occurred on days 86, 64 and 84 for systems A, B
and C, respectively. After 118 days of fermentation, system A produced a total
of 414 liters of methane while system B produced 437 liters and system C
produced 470 liters. About 63% of the total methane from each system came
from the LB for systems A and C, while cumulative methane production from
LB-B accounted for 74.5% of the total from system B. Methane yields ranged
from 0.485 to 0.551 m3 (kg TS)"1, about two to three times that reported
previously (Chen and Shyu, 1998). Additionally, there was little operational
problems, such as foaming and feeding or recycling line breakage due to
prolonged recirculation. Shorter recycling time proved desirable.
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504 CHEN AND WANG
400
cg
•oO
o
|
300 -
200-
Oa>
I 100 -
0400
300 -
200-
-£ 100 -
0400
o 300 -
200 -
o
3
u
System A
LBUASB
System B
System C
'
20 40 60Time, day
80 100 120
FIGURE 7
Cumulative methane production from the LB and UASB of each system.
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MESOPHILIC ANAEROBIC DIGESTION SYSTEMS 505
DISCUSSION
The UASBs performed very well. They were able to generate methane
efficiently over the full range of LRs applied, keeping VFAs and LCFAs at low
levels throughout the experiment. The LBs produced at least 63 % of the methane
from each system, making significant contribution to the overall stabilization of
the mortalities. Together, the performances of the present LB-UASB systems
represent a significant improvement from that reported previously (Chen and
Shyu, 1998).
The LBs in this study started producing methane earlier than the 27 days
reported previously for a similar system but with 3 liters of water in the LB and
25% (v/v) inoculum in the UASB (Chen and Shyu, 1998). One could probably
attribute the faster start of methanogenesis to more granular sludge in the UASB
as it is well accepted that a large inoculum can reduce the duration of lag phase
in batch digestion. However, it must be pointed out that very little of the
granules overflowed to the LB. Thus, the granular sludge in the UASB
contributed, at best, indirectly to methanogenesis in the LB. Perhaps more
importantly, a higher inoculation rate and a more favorable LB environment
resulting from higher moisture contents effected the faster start of
methanogenesis; Since the LBs were batch-loaded with mortalities without
inoculum, bacteria needed for methanogenesis had to come primarily from
connecting UASBs during feeding operations. Less concentrated leachate from
an LB with a higher moisture content allowed higher flow rates through its
connecting UASB while maintaining the same LR. The resultant larger effluent
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506 CHEN AND WANG
volume from the UASB carried more un-granulated methanogens to the LB to
effect a higher inoculation rate. Furthermore, an LB with a less concentrated
fermentation liquid was less inhibitory, hence more conducive to methanogenesis.
These explanations would also support the observation that the LBs with 10 and
18 liters of water started producing methane much earlier than the LB with 5
liters of water, although all three UASBs contained the same amount of inoculum.
Although the LBs started producing methane earlier than reported previously,
methane production rates were low until each LB had received about 100 g of
sludge from their respective UASB (Figure 3). The LB-B reached this level the
fastest, at around day 40, followed by LB-A and LB-C, at around day 60.
Possibly, had the LBs been inoculated with that amount of sludge from the start,
the lag periods could be much shorter. However, since large amount of inoculum
may not always be available in a real farm application, producing biomass in situ
as was the.case in this study may be a necessity. In addition to being the initial
methanogenic phase of the system, the UASBs were, in effect, vessels for
continuous biomass production for the LBs.
The time it took to transfer enough sludge to each LB depended on the sludge
concentration of effluent from respective UASB and volume of liquid transferred.
Both gas production rates and biomass growth rate of an UASB affected the
sludge concentration of its effluent while its HRT determined the volume of liquid
transferred; Biogas production and upflowing liquid during feeding and recycling
operations expanded its sludge bed, moving finer particles toward bed surfaces.
Gas bubbles erupting at bed surfaces suspended these particles, causing some of
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MESOPHILIC ANAEROBIC DIGESTION SYSTEMS 507
which to be carried over to its connecting LB during feeding operations. Sludge
concentration of effluent from UASB-B peaked on day 42 at 22 g COD 1' (Figure
8), about twice that from UASB-A. Since gas production rates were similar for
all UASBs before day 45, the higher sludge concentrations of effluent from
UASB-B most likely reflected its higher growth rate under shorter HRTs (Figures
4 and 5). On the other hand, UASB-C had the lowest growth rate before day 50,
probably because its HRTs were too short for efficient biomass growth. Thus,
considering the inverse relationship between HRTs and leachate concentrations,
the initial moisture content of an LB may provide a tool for controlling growth
rate in the UASB and inoculation rate to the LB.
Although the UASBs in this study performed very well, yet their potentials
as high-rate digestors and as vessels for continuous inoculum production for the
LBs had not been fully exploited. The UASBs became idle once their connecting
LBs started accelerated methanogenesis, causing leachate concentrations to drop.
The operation can be made more efficient by scheduling several LBs in sequence
to maintain peak LRs to the UASB; Initially, the UASB and an LB would be
operated as described in this study. As methane production from the UASB
becomes marginal when leachate COD concentration from the LB becomes low,
the UASB would be disconnected and used to start up a second LB with next
batch of mortalities. Meanwhile, the off-line LB would continue independently
as a balanced methane reactor. The UASB moves on to a third LB when the
second LB becomes a balanced reactor and leachate from it can no longer support
high-rate methanogenesis in the UASB, and so on. A cycle is complete when the
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508 CHEN AND WANG
QOUTO
CO
ocoOIDTO
_24co3
¿z -
20-18-
16-
14-
12-
10-
8-
6 -
4 -
2 -
0 -
JA ti
: •*:
IIÜ i
Vi Í
—•' —UASB-AUASB-BUASB-C
20 40 60Time, day
80 100
FIGURE 8
Sludge concentrations of effluents from the UASBs.
first LB stops active methane production. The LBs then operating and the UASB
constitute the system. The residual solid materials from the completed LB should
be removed and disposed of through other methods (such as incineration, burial,
etc.) while the liquid used to start up the next batch of mortalities. As for the
oils and fats, due to their slower stabilization, they can be skimmed off and
digested in a separate sludge digestor. The process then repeats itself. Reusing
the liquid not only reduces the volume of water used and wastewater needing
post-treatment, but should also facilitate a quick start-up since the liquid contains
un-granulated methanogens and associated enzymes.
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MESOPHILIC ANAEROBIC DIGESTION SYSTEMS 509
With the above-mentioned operational scheme in mind, the objective in
operating an LB-UASB system is to achieve high-rate methanogenesis in the LB
in the shortest possible time while sustaining performances of the UASB. Net
increases in VSS in the UASBs at the end of the experiment indicate that
excessive wash-out did not occur and the performances of the UASBs should be
sustainable. By the above criteria, system B performed the best by being the first
one to achieve the operational goal of the LB-UASB system, followed by systems
A and C.
CONCLUSIONS
The results from the present study represent a significant improvement from
that reported previously. After 118 days of anaerobic digestion in the LB-UASB
system, about 86% of the poultry mortalities was biodegraded. Methane
accounted for 83.7% of the total COD. The LBs made significant contribution
to the overall stabilization of the mortalities, accounting for at least 63% of the
bioconversion in each system. The UASBs performed very well. In addition to
being the initial methanogenic phase of the systems, the UASBs served as a vessel
for continuous inoculum production for the LBs. Ungranulated sludge from the
UASBs was crucial to the start-up and maturation of the LBs. Moisture content
in the LBs played an important role in the development of the LBs. The system
with 7.5% TS in the LB performed the best. The capacity of the system can be
further expanded by scheduling several LBs in sequence for one UASB to fully
exploit the UASB's potential as a high-rate digestor.
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510 CHEN AND WANG
ACKNOWLEDGMENTS
Funding for this project was provided by the National Science Council of the
Republic of China through Grant No. NSCSó^H-B-OOS^S.
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Received: February 13, 1998
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