al., 1999).
How to reduce and eliminate the swine odour that
evokes health complaints and impairs quality of life
in neighbouring communities has attracted attention
of researchers worldwide. Several techniques have
been developed to reduce the swine odour emission,
such as biofiltration, ozonation, covering the manure
storage, and ultraviolet light (DeBruyn et al., 2001;
Mann et al., 2002; Riley et al., 1989; Vohra et al.,
2006).
The existing technologies have various
drawbacks. For example, it is known that the ozone
itself contributes to air pollution although ozone can
oxidize odour compounds. In other words, the use of
ozone to reduce swine odour may cause secondary
pollution. Ultraviolet light used in the pig barn over
a period of time may be harmful to both the pigs and
operators and it is also expensive. The Biofiltration
have been used to treat exhaust air from pig barns for
odour reduction, but it might cause cross
contamination if used inside the pig barns.
Plant-based aromatic materials have been used as
air fresheners in many different parts of the world
(Heath et al., 1992; Zeng et al., 2003). Recently, a
process has been developed to produce a nano-
crystalline material from extracts of several plants
(or herbs) to air purification (Zhao et al., 2006). All
the constituents in this material are naturally existing
organic materials and environmentally friendly. The
objectives of this study were to design and test a
plant material-based air purification system to verify
the efficiency of this systems in PMAP reducing the
swine odour.
2 MATERIALS AND METHODS
Two identical plastic boxes with dimensions of 64
cm X 45 cm X 40 cm were used to conduct the
experiment. Equal quantities of odour generating
materials (sources) were placed into the two boxes,
respectively. The boxes were then carefully sealed to
prevent any air exchange with the ambient. A hole
of 6 mm diameter was drilled on the center of the
box lids for taking odour measurements from the
boxes. The hole was sealed between the two
measurements. For each test, one box was equipped
with the PMAP. A small device, which includes
about 18 g of PMAP material and a micro electrical
fan to enhance the evaporation of material, was
placed into only one of the boxes. The evaporation
rate of PMAP material is about 1.5 mg per hour. The
other box without PMAP used was the control.
Two sets of tests were performed; one used pig
manure to generate odour and the other used pure
hydrogen sulphide or ammonia as the odour source.
In the first set of tests, about 80 ml of pig manure
from the Animal Research Unit of the Department of
Animal Science, University of Manitoba was
transferred into a glass bottle, and shacked for
homogeneity purposes. Then it was divided equally
into two wide mouthed glass bottles, which were
then placed into the two boxes, respectively as the
swine odour sources. In the second set of tests, the
pure H
2
S was generated by the reaction of Al
2
S
3
and
H
2
O in the wide mouthed glass bottles and the pure
NH
3
from an ammonia water solution.
An AC’ SCENT International Olfactometer (St.
Croix Sensory, Inc., Stillwater, MN, USA) was used
to measure the odour concentration of air in the test
boxes. Five panelists were selected following the EU
Standard EN 13725 (CEN 2003) based on their
specific sensitivity to reference odourant n-butanol.
The odour concentration was determined by the
triangular forces choice method (ASTM E679-04).
Table 1: Concentration of swine odour with and without
PMAP for the 2 sets of the samples.
Sample
Odour
concen.
(OU/m
3
)
Reducing
(%)
S1- with PMAP 1413
S1- without PMAP 2825
50.0
S2- with PMAP 1072
S2- without PMAP 3235
66.9
In the tests with pig manure, two sets of samples
were taken from the two boxes for the olfactometer
analysis. For the first set, the odour samples were
taken from the two boxes after the swine manure
was sealed 18 hours, into two 10-L Tedlar bags
using a vacuum chamber (AC’SCENT Vacuum
chamber, St. Croix Sensory Inc., Stillwater, MN,
USA). When sampling, a bag was placed in the
chamber and the inlet of the bag was connected to a
Teflon probe which was inserted into one of the two
boxes through the hole on the box lid. Each sample
was taken in two steps: (i) fill the bag with 2 L of
odorous air and then evacuated to “coat” the bag,
and (ii) draw odorous air into the bag until the bag
was 75% full. Following the same sampling
procedure, the second set of samples was taken 8
hours after the first set of sample. Each set of sample
has two samples from the two boxes, respectively.
The H
2
S concentration was measured with a
Jerome Meter (JEROME 631-X Hydrogen Sulfide
Analyzer manufactured by Arizona Instruments) in
ppm with an accuracy of 0.001 ppm. After the two
A PLANT MATERIAL-BASED AIR PURIFICATION SYSTEM FOR SWINE ODOUR REDUCTION
121