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ABSTRACT. Mitigation of ammonia (NH3 ) emissions from animal production buildings has been a challenge because of the
large volume of low NH3 concentration laden air being released. Among emission mitigation technologies for concentrated
animal feeding operations, acid spray scrubbers have the greatest potential for adaptation to the existing large animal
facilities because of their lower fan airflow reduction, ability to simultaneously remove particulate and gaseous pollutants,
and viability for zero or less waste generation by recycling effluents as liquid fertilizer. A multi‐stage wet scrubber prototype
that can be operated with a maximum of three stages was developed and optimized for reducing NH3 emissions using simulated
conditions typically encountered at an animal building exhaust. The parameters optimized for a single‐stage wet scrubber
include nozzle type, nozzle operating pressure, sulfuric acid concentration, spray coverage, and air retention time. The
optimized single‐stage wet scrubber settings can remove emissions from 60% ±1% at 5 ppmv inlet NH3 concentration (IAC)
to 27% ±2% at 100 ppmv IAC at a normal exhaust superficial air velocity (SAV) of 6.6 m s-1. A high concentration of droplets
inside the contact chamber increased the rate of inter‐collision between droplets, which led to high droplet coagulation and
decreased surface area for gas‐liquid contact. These phenomena were prevented by operating the nozzles in the higher stages
co‐current to the airflow and by using fewer nozzles in higher stage. The two‐stage and three‐stage wet scrubbers were
therefore optimized by determining the least number of nozzles in each stage that provided the most effective NH3 removal.
The optimized two‐stage scrubber could remove NH3 emissions from 60% ±0% at 5 ppmv IAC and 35% ±1% at 100 ppmv
IAC. The optimized three‐stage scrubber could remove emissions from 63% ±3% at 5 ppmv IAC and 36% ±3% at 100 ppmv
IAC. Airflow retention time was found to significantly affect NH3 absorption. Reducing the superficial air velocity to 3.3 m
s-1 from 6.6 m s-1, which increased the air retention time from 0.2 s to 0.4 s, improved NH3 removal efficiencies to 98% ±3%
at 5 ppmv IAC and 46% ±2% at 100 ppmv IAC for the single‐stage scrubber. Similarly, the performance of the two‐stage
scrubber at a SAV of 3.3 m s-1 improved to 77% ±0% at 20 ppmv IAC and 57% ±1% at 100 ppm IAC. Lastly, the performance
of the three‐stage scrubber at a SAV of 3.3 m s-1 improved to 70% ±1% at 30 ppmv IAC and 64% ±1% at 100 ppmv IAC.
It was observed that the three‐stage wet scrubber did not increase the overall wet scrubber performance, as predicted
theoretically. Further studies are needed so that the application of these scrubber designs becomes feasible for treating air
emissions from animal buildings. The wet scrubber caused an additional backpressure of 27.5 Pa, resulting in about 8%
airflow reduction for a fan operating at 12.5 Pa.
Keywords. Air emissions, Air treatment, Ammonia absorption, Ammonia emissions, Animal buildings.
A
mmonia (NH3), an odorous and fast‐diffusing mal industry, especially those involving concentrated animal
lung irritant, is a detrimental agent in chemical feeding operations (CAFOs). About 50% of the total anthro‐
reactions responsible for eutrophication, forma‐ pogenic NH3 emissions in the U.S. are from animal agricul‐
tion of fine particulate matter, and ecosystem ture (NRC, 2003). A typical 250,000 hen, deep‐pit layer
acidification (De Nevers, 2000; NRC, 2003). Ammonia house can emit 387 kg NH3 per day (Lim et al., 2004). Cur‐
emissions are one of the major air quality concerns of the ani‐ rently, two supplemental air quality laws, the Comprehensive
Environmental Response, Compensation and Liability Act
(CERCLA) and the Environmental Planning and Community
Submitted for review in August 2006 as manuscript number SE 6655;
Right‐to‐Know Act (EPCRA), require any stationary major
approved for publication by the Structures & Environment Division of source to report NH3 emissions exceeding 45.4 kg (100 lb) in
ASABE in May 2007. any 24 h period (USEPA, 2006; Zhao, 2005). Idaho has
The authors are Roderick B. Manuzon, ASABE Member, Graduate started to regulate ammonia emissions from dairy operations
Research Associate, and Lingying Zhao, ASABE Member Engineer, that emit 100 tons or more NH3 per year (Dunlop, 2006).
Assistant Professor, Department of Food, Agricultural, and Biological
Engineering, The Ohio State University, Columbus, Ohio; Harold M. Therefore, effective and feasible NH3 control technologies
Keener, ASABE Member Engineer, Professor, Department of Food, for animal feeding operations (AFOs) are highly needed.
Agricultural, and Biological Engineering, OARDC, Wooster, Ohio; and Mitigation technologies that have been developed for
Matthew J. Darr, ASABE Member, Research Associate, Department of treating air emissions from mechanically ventilated build‐
Food, Agricultural, and Biological Engineering, The Ohio State University,
Columbus, Ohio. Corresponding author: Lingying Zhao, 590 Woody
ings include carbon and bio‐filtration, centrifugal separation
Hayes Dr., Columbus, OH 43210‐1057; phone: 614‐292‐2366; fax: using cyclones, and wet scrubbing. Although activated car‐
614‐292‐9448; e‐mail: zhao.119@osu.edu. bon is frequently used to capture volatile organics (De Nev‐
0.991 m
Exit transition (b) mists on its surface, was mounted after the 9° exhaust
transition (b). The mist eliminator, measuring 0.94 × 0.94 m
was designed to remove 99% of 27 m droplets at an airflow
rate of 2.8 standard cubic meters per second (sm3 s-1) and
X Stage 3 contributed a 15 Pa differential pressure drop. The 0.99 m
exit transition unit was necessary to reduce the air velocity
X = 0.457 m
1.524 m
Contact from 6.6 to 3.5 m s-1, which was specified by the mist
Stage 2
X
Stage 1 pressure drop came from the elbow (d), while 15 Pa of the
0.610 m total pressure drop came from mist eliminator.
Air ID
inlet
Elbow EXHAUST AIRFLOW SIMULATION
(d) An exhaust simulation system (fig. 2) was designed to
obtain a uniformly mixed NH3 laden air stream. A 0.61 m
Liquid inlet
Effluent (24in.) axial fan (AT24Z, Aerotech, Inc., Mason, Mich.) (g)
Liquid
outlet
downspout was used to generate airflow. The fan was operated as a
(f) variable‐speed fan using a variable‐voltage speed controller
(SSC‐1, Aerotech, Inc., Mason, Mich.). Pure anhydrous NH3
Scrubbing liquid
gas (k) was introduced into the air stream using perforated
supply tank (e) pipe distributors at a distance of nearly four fan diameters
from the fan inlet. Propeller fans (i) placed right after the
Figure 1. Schematic diagram of the spray scrubber prototype (not to distributors were used to completely mix the air. Turbulence
scale).
in the inlet was minimized using a 9° entrance transition (j).
The major part of the spray scrubber was the contact
MEASUREMENTS AND INSTRUMENTATION
chamber (c), where NH3 was absorbed into the liquid from
Ammonia Measurement
the airflow. It had a diameter of 0.61 m (24 in) and height of
The concentration of gaseous NH3 was measured using a
1.52 m (5 ft). Absorption of NH3 was accomplished by
photoacoustic sensor calibrated for NH3 (MSA Chilgard RT
atomizing the liquid inside the contact chamber with three
NH3 analyzer, MSA, Inc., Pittsburgh, Pa.), with an accuracy
stages of spray nozzles spaced 0.46 m apart. The average path
of ±2 ppmv. It draws a sample at a flow rate of 0.75 L min-1
traveled by the spray droplets spanned 0.15 m; hence, a
and responds 90% in 70 s to a sample concentration step
0.31m space allowance was provided as the separation
change. It operates at temperatures from 0°C to 50°C and
distance between stages. Longer contact height was more
relative humidities from 0% to 95%. Data were acquired
desirable according to equation 4 if the droplets can travel far
through the 4 to 20 mA analog output from the equipment and
enough through the contact height.
digitized using a 10‐bit analog‐to‐digital converter. Data
The spray supply system delivered scrubbing liquid into
collection was enabled by a personal computer running a
each stage of nozzles. The 114 L tank (e) supplying the
customized Visual Basic (Microsoft, Inc., Redmond, Wash.)
acidified scrubbing liquid was attached to a pump whose
data logging program.
pressure could vary from 0 to 689 kPa (0 to 100 psig). Gate
Gaseous NH3 concentrations were measured before and
valves installed before each nozzle inlet line served as the
after the wet scrubber for determining the absorption
coarse flow control, while needle valves mounted at the
efficiency of the prototype. Three equally spaced sampling
bypass lines going back to the supply tank served as the fine
points (sections A‐A and B‐B of figure 3) at both the inlet and
flow control. Pressure gauges were also mounted in each line.
0.610 m
Figure 2. Schematic diagram of the ammonia exhaust simulation chamber (not to scale).
0.94 x 0.94 m
B B
y
Sampling
MSA NH 3 switch
analyzer line
Inlet sampling
A location
A 0.71 x 0.71 m
Figure 3. Ammonia sampling locations and schematic diagram of the measurement system.
outlet sampling locations were diverged into one before the and full of the fan speed controller. These settings correspond
sampling tube entered the NH3 analyzer. Measurements were to an airflow range of 0.74 to 1.93 m3 s-1. The airflow
manually cycled between the inlet and outlet sampling measurements were done at the beginning of the study.
locations at 10 min intervals. However, only the final 2 min Water flow rates of each nozzle were obtained from their
data were used to ensure that the data were obtained after the technical data sheets and were verified by measuring effluent
instrument's full response. It was verified that the NH3 flow rate using a graduated cylinder and a stopwatch. Fan
concentrations were equal in the inlet and outlet sampling backpressure was measured with 0 to 75 Pa colored tube
locations before the spray was turned on for every run. inclined manometer (Dwyer Instruments, Michigan City,
To verify gaseous NH3 removal efficiency measurements, Ind.) using pressure taps at one fan diameter from the fan inlet
water samples from three representative runs each operated and outlet. Water flow rate and pressure drop were measured
with three equidistant PJ20 nozzles spaced 0.30 m apart, for each test run.
spraying 0.2 N H2SO4 at 620 kPa in a single‐stage scrubber,
were collected to obtain collection efficiency data based on AMMONIA REMOVAL EFFICIENCY CALCULATIONS
the NH3 absorbed by the scrubbing liquid. Ammonia removal efficiency, which was used as the
Liquid NH3 concentration of the effluents was analyzed criteria for determining the scrubber performance, was
by the Service Testing and Research Laboratory (STAR Lab) defined as:
of the Ohio Agricultural Research and Development Center
(OARDC) according to methods described by Mulvaney Cin − Cout
ηtotal = × 100% (7)
(1996). The efficiencies calculated from the airflow and Cin
liquid phase balance were then compared.
where
Measurement of Airflow, Water Flow, and Fan total = NH3 collection efficiency (%)
Differential Static Pressure Cin = airflow NH3 concentration before the scrubber
Airflow was determined using the equal area method (ppmv NH3)
(ASHRAE, 2000) through section A‐A. The square inlet duct Cout = airflow NH3 concentration after the scrubber
was divided into 5 × 5 equally sized grids. The air velocities (ppmv NH3).
at the center of each grid were determined using a hot‐wire Ammonia removal efficiency was also verified from
anemometer (TSI Velocicalc, TSI, Inc., Shoreview, Minn.). liquid effluent NH3 sample analysis. Liquid samples were
The airflow rate was calculated by multiplying the average collected from three single‐stage runs with the scrubber
velocity with the cross‐sectional area of the duct. Airflow operated at the following setting: three evenly distributed
measurements were done for the fan set at full speed working counter‐currently mounted PJ20 nozzles spraying 0.2 N
against various flow resistances resulting in pressure drops of H2SO4 solution at 620 kPa. The following equation was used
12, 40, 45, 50, 55, 57, 62, and 67 Pa. The resistances were to calculate the NH3 removal efficiency from the liquid
varied by controlling the opening at the inlet of the simulation sample analysis:
chamber. Three airflow measurements were done at each
pressure. Airflow rate, fan back pressure, and the controller ηtotal =
(M out − M in )QL × 103 RT × 100%
(8)
output voltage were also measured at settings 7, 8, 8.5, 9, 10, Cin QG P
h total (%)
Excess H + (%)
PJ20 75
20
PJ15
50 0
L40
10
UM300M
25 -50
0
0.00 0.01 0.02 0.03 0.04 0 -100
0.0 0.1 0.2 0.3 0.4 0.5 0.6
QL /D32 (L min-1 m m-1 )
H 2 SO4 concentration (N)
Figure 5. Ammonia scrubbing performance using single nozzles with Figure 6. Effect of scrubbing liquid H2SO4 concentration on the NH3
different liquid flow rate and mean droplet size (QL /D32) characteristics, absorption efficiency of a single‐stage scrubber (conditions: air with
0.2 N sulfuric acid, and 30 ppmv IAC. 30ppmv IAC, single PJ20 nozzle sprayed at 620 kPa).
However, removal efficiency per liter of scrubbing liquid balance using the stoichiometric equations (eqs. 1 and 2)
declined with increasing pressure, indicating that more compared with the actual amount of acid supplied per unit
scrubbing liquid was required for the hollow‐cone nozzles time. It should be noted that in a continuous operation, where
(L40 and UM300M) to match the performance of the full‐ the scrubbing liquid is recycled to economize scrubbing
cone nozzles (PJ20 and PJ15). These results are clearly liquid consumption, the driving force can only be maintained
shown in figure 5, where the efficiency obtained from each by acid replenishment to 0.2 N [H+] or higher.
nozzle is plotted as a function of liquid flow rate and mean
drop size ratio (QL /D32). Effect of Spray Coverage
The ratio QL /D32 was chosen to characterize the nozzle Appropriate spray coverage of the cross‐sectional area for
operating condition since changing the type of nozzle and its airflow through the scrubber was determined by evenly
operating pressure essentially affected only the liquid flow distributing one to four nozzles in stage 1 (fig. 7) using the
rate and mean drop size ratio. Increasing the ratio should optimized single‐nozzle setting (PJ20 at 620 kPa with 0.2 N
increase scrubbing efficiency, which can be derived from H2SO4). The maximum efficiency of 44% ±1% was attained
equation 4. Figure 5 shows the same linearly increasing trend using three nozzles spaced 0.3 m apart. Statistical analysis
for the ratio QL /D32 for all nozzles except for the L40 nozzle. showed that mean collection efficiencies using two to four
Despite having the highest liquid flow rate and mean drop nozzles were not significantly different. However from
size ratio, the mean collection efficiency of the high‐flow, visual examination of the actual spray, the optimized single‐
hollow‐cone L40 nozzle was not significantly different from stage run was conducted with three nozzles in the lowest
the collection efficiency using the full‐cone PJ20 nozzle with stage as a safety factor for ensuring full coverage. Further
about a third the flow rate of the L40. This difference was attempts to attain better coverage led to the same collection
presumably caused by the droplets concentrated on the edge performance as the three‐nozzle setting.
of the conic spray paving the way for higher rates of droplet
coagulation. The high‐flow, full‐cone PJ20 nozzle was 50
selected as the best nozzle based on these results.
40
Effect of Scrubbing Liquid Acid Concentration
Addition of acids greatly enhances the mass transfer
h total (%)
30
coefficient and Henry's law constant, which are both
important for the absorption process. However, increasing 20
the sulfuric acid concentration of the scrubbing liquid beyond
0.2 N H2SO4 did not increase scrubbing efficiency (fig. 6). 10
Pairwise mean comparisons of these values showed that the
mean efficiencies using 0.2 N acid and above were not 0
significantly different. The maximum collection efficiency 0 20 40 60 80 100
was 35% ±2% at 30 ppmv IAC using a single PJ20 nozzle set Estimated total coverage (% TC)
at 620 kPa. Using pure water, the collection efficiency was
11% ±1%. The efficiency increased to 18% ±1% and 22%
±1% using 0.05 N and 0.1 N H2SO4, respectively. From
12 in.
0.2N to 0.6 N H2SO4, the collection efficiency ranged from
35% ±1% to 37% ±4%.
The actual and maximum absorption efficiency curves
illustrate the relationship between absorption performance 1 nozzle 2 nozzles 3 nozzles 4 nozzles
(25% TC) (50% TC) (71% TC) (82% TC)
and the available amount of acid. The maximum efficiency
was calculated from equilibrium relationships using Figure 7. Effect of spray coverage on single‐stage NH3 collection
equations 1, 2, and 3 assuming enough air and liquid contact efficiency of the prototype scrubber (conditions: PJ20 sprayed at 620 kPa,
occurred. The excess acid was obtained from the material 0.2 N H2SO4, and 30 ppmv IAC).
60
These results suggested the presence of stage interactions.
40 Based on equation 5, if each stage had acted independently,
10 ppm
30 ppm
then one‐, two‐, and three‐stage operation would have
20
100 ppm
achieved 34%, 57%, and 72% removal efficiency,
respectively. The results also suggest that droplet interactions
0 were greater in the three‐stage operation compared to the
0.0 0.2 0.4 0.6 0.8
two‐stage operation. This is because increasing the number
Gas retention time (s)
of stages increases the number of dispersed liquid inside the
Figure 9. Ammonia collection efficiencies of the single‐stage scrubber scrubber chamber, thereby causing more drops to coagulate.
prototype at various air retention times at 10, 30, and 100 ppmv inlet NH3 Figure 10 illustrates how mixed‐flow configurations for
concentrations (conditions: PJ20 sprayed at 620 kPa, 0.2 N H2SO4). the two‐ and three‐stage scrubbers can improve NH3
absorption capacity. Optimization of the multi‐stage designs,
Figure 11. Performance of two‐stage mixed‐flow scrubber designs at 30 ppmv inlet NH3 concentration and 0.2 s airflow retention time (conditions: PJ20
sprayed at 620 kPa, 0.2 N H2SO4). ?Values followed by the same superscript (a or b) are not significantly different. ??Numbers (1, 2, and 3) in the
schematic diagrams refer to scrubber stages.
Figure 12. Performance of four three‐stage mixed flow scrubber designs at 30 ppmv inlet NH3 concentration and 0.2 s airflow retention time
(conditions: PJ20 sprayed at 620 kPa, 0.2 N H2SO4). ?Values followed by the same superscript (a or b) are not significantly different. ??Numbers (1,2,
and 3) in the schematic diagrams refer to scrubber stages.
0 0.0
0 20 40 60 80 100 0 20 40 60 80
Inlet NH 3 concentration (ppmv) Fan differential pressure (Pa)
100
Figure 14. Fan airflow curve at 120 V input.
80
Scrubbing liquid consumption continues to be a concern
60
for this type of scrubber. Under the non‐recycling mode used
h total (%)