rexresearch.com
Rohit KARNIK, et al.
Xylem Water Filter
Pine stick filter eliminates 99%+ of E.
coli; 1 sq. cm @ 5 psi produces up to 4 liters of potable
water per day.
http://newsoffice.mit.edu/2014/need-a-water-filter-peel-a-tree-branch-0226
February 26, 2014
Need a water filter? Peel a tree
branch
MIT group shows xylem tissue in sapwood can filter bacteria
from contaminated water.
by Jennifer Chu, MIT News Office
If you’ve run out of drinking water during a lakeside camping
trip, there’s a simple solution: Break off a branch from the
nearest pine tree, peel away the bark, and slowly pour lake water
through the stick. The improvised filter should trap any bacteria,
producing fresh, uncontaminated water.
In fact, an MIT team has discovered that this low-tech filtration
system can produce up to four liters of drinking water a day —
enough to quench the thirst of a typical person.
In a paper published this week in the journal PLoS ONE, the
researchers demonstrate that a small piece of sapwood can filter
out more than 99 percent of the bacteria E. coli from water. They
say the size of the pores in sapwood — which contains xylem tissue
evolved to transport sap up the length of a tree — also allows
water through while blocking most types of bacteria.
Co-author Rohit Karnik, an associate professor of mechanical
engineering at MIT, says sapwood is a promising, low-cost, and
efficient material for water filtration, particularly for rural
communities where more advanced filtration systems are not readily
accessible.
“Today’s filtration membranes have nanoscale pores that are not
something you can manufacture in a garage very easily,” Karnik
says. “The idea here is that we don’t need to fabricate a
membrane, because it’s easily available. You can just take a piece
of wood and make a filter out of it.”
The paper’s co-authors include Michael Boutilier and Jongho Lee
from MIT, Valerie Chambers from Fletcher-Maynard Academy in
Cambridge, Mass., and Varsha Venkatesh from Jericho High School in
Jericho, N.Y.
Tapping the flow of sap
There are a number of water-purification technologies on the
market today, although many come with drawbacks: Systems that rely
on chlorine treatment work well at large scales, but are
expensive. Boiling water to remove contaminants requires a great
deal of fuel to heat the water. Membrane-based filters, while able
to remove microbes, are expensive, require a pump, and can become
easily clogged.
Sapwood may offer a low-cost, small-scale alternative. The wood is
comprised of xylem, porous tissue that conducts sap from a tree’s
roots to its crown through a system of vessels and pores. Each
vessel wall is pockmarked with tiny pores called pit membranes,
through which sap can essentially hopscotch, flowing from one
vessel to another as it feeds structures along a tree’s length.
The pores also limit cavitation, a process by which air bubbles
can grow and spread in xylem, eventually killing a tree. The
xylem’s tiny pores can trap bubbles, preventing them from
spreading in the wood.
“Plants have had to figure out how to filter out bubbles but allow
easy flow of sap,” Karnik observes. “It’s the same problem with
water filtration where we want to filter out microbes but maintain
a high flow rate. So it’s a nice coincidence that the problems are
similar.”
Seeing red
To study sapwood’s water-filtering potential, the researchers
collected branches of white pine and stripped off the outer bark.
They cut small sections of sapwood measuring about an inch long
and half an inch wide, and mounted each in plastic tubing, sealed
with epoxy and secured with clamps.
Before experimenting with contaminated water, the group used water
mixed with red ink particles ranging from 70 to 500 nanometers in
size. After all the liquid passed through, the researchers sliced
the sapwood in half lengthwise, and observed that much of the red
dye was contained within the very top layers of the wood, while
the filtrate, or filtered water, was clear. This experiment showed
that sapwood is naturally able to filter out particles bigger than
about 70 nanometers.
However, in another experiment, the team found that sapwood was
unable to separate out 20-nanometer particles from water,
suggesting that there is a limit to the size of particles
coniferous sapwood can filter.
Picking the right plant
Finally, the team flowed inactivated, E. coli-contaminated water
through the wood filter. When they examined the xylem under a
fluorescent microscope, they saw that bacteria had accumulated
around pit membranes in the first few millimeters of the wood.
Counting the bacterial cells in the filtered water, the
researchers found that the sapwood was able to filter out more
than 99 percent of E. coli from water.
Karnik says sapwood likely can filter most types of bacteria, the
smallest of which measure about 200 nanometers. However, the
filter probably cannot trap most viruses, which are much smaller
in size.
Karnik says his group now plans to evaluate the filtering
potential of other types of sapwood. In general, flowering trees
have smaller pores than coniferous trees, suggesting that they may
be able to filter out even smaller particles. However, vessels in
flowering trees tend to be much longer, which may be less
practical for designing a compact water filter.
Designers interested in using sapwood as a filtering material will
also have to find ways to keep the wood damp, or to dry it while
retaining the xylem function. In other experiments with dried
sapwood, Karnik found that water either did not flow through well,
or flowed through cracks, but did not filter out contaminants.
“There’s huge variation between plants,” Karnik says. “There could
be much better plants out there that are suitable for this
process. Ideally, a filter would be a thin slice of wood you could
use for a few days, then throw it away and replace at almost no
cost. It’s orders of magnitude cheaper than the high-end membranes
on the market today.”
While the pores in sapwood are too big to filter out salts, Saurya
Prakash, an assistant professor of mechanical engineering at Ohio
State University, says the design could be useful in parts of the
world where people collect surface water, which can be polluted
with fine dust and particles of decaying plant and animal matter.
Most of this detritus, Prakash says, could easily be filtered out
by the group’s design.
“The xylem tissue acts as a natural filter, similar to a manmade
membrane,” says Prakash, who was not involved in the research.
“The study by the Karnik group shows that use of abundant,
naturally occurring materials could pave the way for a new
generation of water filters that are potentially low-cost enough
to be disposable.”
This research was supported by the James H. Ferry Jr. Fund for
Innovation in Research Education.
http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0089934
February 26, 2014
DOI: 10.1371/journal.pone.0089934
Water Filtration Using Plant Xylem
Michael S. H. Boutilier, Jongho Lee, Valerie Chambers, Varsha
Venkatesh, Rohit Karnik
Abstract
Effective point-of-use devices for providing safe drinking water
are urgently needed to reduce the global burden of waterborne
disease. Here we show that plant xylem from the sapwood of
coniferous trees – a readily available, inexpensive,
biodegradable, and disposable material – can remove bacteria from
water by simple pressure-driven filtration. Approximately 3 cm3 of
sapwood can filter water at the rate of several liters per day,
sufficient to meet the clean drinking water needs of one person.
The results demonstrate the potential of plant xylem to address
the need for pathogen-free drinking water in developing countries
and resource-limited settings.
Introduction
The scarcity of clean and safe drinking water is one of the major
causes of human mortality in the developing world. Potable or
drinking water is defined as having acceptable quality in terms of
its physical, chemical, and bacteriological parameters so that it
can be safely used for drinking and cooking [1]. Among the water
pollutants, the most deadly ones are of biological origin:
infectious diseases caused by pathogenic bacteria, viruses,
protozoa, or parasites are the most common and widespread health
risk associated with drinking water [1], [2]. The most common
water-borne pathogens are bacteria (e.g. Escherichia coli,
Salmonella typhi, Vibrio cholerae), viruses (e.g. adenoviruses,
enteroviruses, hepatitis, rotavirus), and protozoa (e.g. giardia)
[1]. These pathogens cause child mortality and also contribute to
malnutrition and stunted growth of children. The World Health
Organization reports [3] that 1.6 million people die every year
from diarrheal diseases attributable to lack of access to safe
drinking water and basic sanitation. 90% of these are children
under the age of 5, mostly in developing countries. Multiple
barriers including prevention of contamination, sanitation, and
disinfection are necessary to effectively prevent the spread of
waterborne diseases [1]. However, if only one barrier is possible,
it has to be disinfection unless evidence exists that chemical
contaminants are more harmful than the risk from ingestion of
microbial pathogens [1]. Furthermore, controlling water quality at
the point-of-use is often most effective due to the issues of
microbial regrowth, byproducts of disinfectants, pipeline
corrosion, and contamination in the distribution system [2], [4].
Common technologies for water disinfection include chlorination,
filtration, UV-disinfection, pasteurization or boiling, and ozone
treatment [1], [2], [5]. Chlorine treatment is effective on a
large scale, but becomes expensive for smaller towns and villages.
Boiling is an effective method to disinfect water; however, the
amount of fuel required to disinfect water by boiling is several
times more than what a typical family will use for cooking [1].
UV-disinfection is a promising point-of-use technology available
[1], yet it does require access to electricity and some
maintenance of the UV lamp, or sufficient sunlight. While small
and inexpensive filtration devices can potentially address the
issue of point-of-use disinfection, an ideal technology does not
currently exist. Inexpensive household carbon-based filters are
not effective at removing pathogens and can be used only when the
water is already biologically safe [1]. Sand filters that can
remove pathogens require large area and knowledge of how to
maintain them [1], while membrane filters capable of removing
pathogens [2], [4] suffer from high costs, fouling, and often
require pumping power due to low flow rates [6] that prevents
their wide implementation in developing countries. In this
context, new approaches that can improve upon current technologies
are urgently needed. Specifically, membrane materials that are
inexpensive, readily available, disposable, and effective at
pathogen removal could greatly impact our ability to provide safe
drinking water to the global population.
If we look to nature for inspiration, we find that a potential
solution exists in the form of plant xylem – a porous material
that conducts fluid in plants [7]. Plants have evolved specialized
xylem tissues to conduct sap from their roots to their shoots.
Xylem has evolved under the competing pressures of offering
minimal resistance to the ascent of sap while maintaining small
nanoscale pores to prevent cavitation. The size distribution of
these pores – typically a few nanometers to a maximum of around
500 nm, depending on the plant species [8] – also happens to be
ideal for filtering out pathogens, which raises the interesting
question of whether plant xylem can be used to make inexpensive
water filtration devices. Although scientists have extensively
studied plant xylem and the ascent of sap, use of plant xylem in
the context of water filtration remains to be explored.
Measurements of sap flow in plants suggest that flow rates in the
range of several liters per hour may be feasible with less than 10
cm-sized filters, using only gravitational pressure to drive the
flow [7].
We therefore investigated whether plant xylem could be used to
create water filtration devices. First, we reason which type of
plant xylem tissue is most suitable for filtration. We then
construct a simple water filter from plant xylem and study the
resulting flow rates and filtration characteristics. Finally, we
show that the xylem filter can effectively remove bacteria from
water and discuss directions for further development of these
filters.
Materials and Methods
Branches were excised from white pine growing on private property
in Massachusetts, USA, with permission of the owner and placed in
water. The pine was identified as pinus strobus based on the
5-fold grouping of its needles, the average needle length of 4.5
inches, and the cone shape. Deionized water (Millipore) was used
throughout the experiments unless specified otherwise. Red pigment
(pigment-based carmine drawing ink, Higgins Inks) was dissolved in
deionized water. Nile-red coated 20 nm fluorescent polystyrene
nanospheres were obtained from Life Technologies. Inactivated,
Alexa 488 fluorescent dye labeled Escherichia coli were obtained
from Life Technologies. Wood sections were inserted into the end
of 3/8 inch internal diameter PVC tubing, sealed with 5 Minute
Epoxy, secured with hose clamps, and allowed to cure for ten
minutes before conducting flow rate experiments.
Construction of the Xylem Filter
1 inch-long sections were cut from a branch with approximately 1
cm diameter. The bark and cambium were peeled off, and the piece
was mounted at the end of a tube and sealed with epoxy. The
filters were flushed with 10 mL of deionized water before
experiments. Care was taken to avoid drying of the filter.
Filtration and Flow Rate Experiments
Approximately 5 mL of deionized water or solution was placed in
the tube. Pressure was supplied using a nitrogen tank with a
pressure regulator. For filtration experiments, 5 psi (34.5 kPa)
pressure was used. The filtrate was collected in glass vials. For
dye filtration, size distribution of the pigments was measured for
the input solution and the filtrate. Higgins pigment-based carmine
drawing ink, diluted ~1000× in deionized water, was used as the
input dye solution. For bacteria filtration, the feed solution was
prepared by mixing 0.08 mg of inactivated Escherichia coli in 20
mL of deionized water (~1.6×107 mL-1) after which the solution was
sonicated for 1 min. The concentration of bacteria was measured in
the feed solution and filtrate by enumeration with a hemacytometer
(inCyto C-chip) mounted on a Nikon TE2000-U inverted
epifluorescence microscope. Before measurement of concentration
and filtration experiments, the feed solution was sonicated for 1
min and vigorously mixed.
Imaging
Xylem structure was visualized in a scanning electron microscope
(SEM, Zeiss Supra55VP). Samples were coated with gold of 5 nm
thickness before imaging. To visualize bacteria filtration, 5 mL
of solution at a bacteria concentration of ~1.6×107 mL-1 was
flowed into the filter. The filter was then cut longitudinally
with a sharp blade. One side of the sample was imaged using a
Nikon TE2000-U inverted epifluorescence microscope and the other
was coated with gold and imaged with the SEM. Optical images were
acquired of the cross section of a filter following filtration of
5 mL of the dye at a dilution of ~100×.
Particle Sizing
Dynamic light scattering measurements of particle size
distributions were performed using a Malvern Zetasizer Nano-ZS.
Results
Xylem Structure and Rationale for use of Conifer Xylem
The flow of sap in plants is driven primarily by transpiration
from the leaves to the atmosphere, which creates negative pressure
in the xylem. Therefore, xylem evolution has occurred under
competing pressures of providing minimal resistance to the flow of
sap, while protecting against cavitation (i.e. nucleation) and
growth of bubbles that could stop the flow of sap and kill the
plant, and to do this while maintaining mechanical strength [7].
The xylem structure comprises many small conduits that work in
parallel and operate in a manner that is robust to cavitation [7],
[8] (Figure 1). In woody plants, the xylem tissue is called the
sapwood, which often surrounds the heartwood (i.e. inactive,
non-conducting lignified tissue found in older branches and
trunks) and is in turn surrounded by the bark (Figure 1b,c). The
xylem conduits in gymnosperms (conifers) are formed from single
dead cells and are called tracheids (Figure 1c), with the largest
tracheids reaching diameters up to 80 µm and lengths up to 10 mm
[7]. Angiosperms (flowering plants) have xylem conduits called
vessels that are derived from several cells arranged in a single
file, having diameters up to 0.5 mm and lengths ranging from a few
millimeters to several meters [7]. These parallel conduits have
closed ends and are connected to adjacent conduits via “pits” [8]
(Figure 1d,e). The pits have membranes with nanoscale pores that
perform the critical function of preventing bubbles from crossing
over from one conduit to another. Pits occur in a variety of
configurations; Figure 1d,e shows torus-margo pit membranes that
consist of a highly porous part shaped like a donut (margo) and an
impermeable part in the center called torus, occurring in conifers
[8]. The porosity of the pit membranes ranges in size from a few
nanometers to a few hundred nanometers, with pore sizes in the
case of angiosperms tending to be smaller than those in
gymnosperms [8], [9]. Pit membrane pore sizes have been estimated
by examining whether gold colloids or particles of different sizes
can flow through [8], [10]. Remarkably, it was observed that 20 nm
gold colloids could not pass through inter-vessel pit membranes of
some deciduous tree species [10], indicating an adequate size
rejection to remove viruses from water. Furthermore,
inter-tracheid pit membranes were found to exclude particles in
the 200 nm range [8], as required for removal of bacteria and
protozoa.
Figure 1. Xylem structure.
a) Structure of xylem vessels in flowering plants and tracheids in
conifers. Longer length of the vessels can provide pathways that
can bypass filtration through pit membranes that decorate their
circumference. b) Photograph of ~1 cm diameter pine (pinus
strobus) branch used in the present study.
c) Scanning electron microscope (SEM) image of cut section showing
tracheid cross section and lengthwise profile. Scale bar is 40 µm.
d) SEM image showing pits and pit membranes. Scale bar is 20 µm.
e) Pit membrane with inset showing a cartoon of the pit
cross-section. The pit cover has been sliced away to reveal the
permeable margo surrounding the impermeable torus. Arrow indicates
observed hole-like structures that may be defects. The margo
comprises radial spoke-like structures that suspend the torus,
which are only barely visible overlaying the cell wall in the
background. Scale bar is 1 µm. f) Dependence of area
amplification, defined as the pit membrane area divided by the
nominal filter area, on the tracheid aspect ratio L/D and
fractional area a occupied by pit membranes.
Since angiosperms (flowering plants, including hardwood trees)
have larger xylem vessels that are more effective at conducting
sap, xylem tissue constitutes a smaller fraction of the
cross-section area of their trunks or branches, which is not ideal
in the context of filtration. The long length of their xylem
vessels also implies that a large thickness (centimeters to
meters) of xylem tissue will be required to achieve any filtration
effect at all – filters that are thinner than the average vessel
length will just allow water to flow through the vessels without
filtering it through pit membranes (Figure 1a). In contrast,
gymnosperms (conifers, including softwood trees) have short
tracheids that would force water to flow through pit membranes
even for small thicknesses (<1 cm) of xylem tissue (Figure 1a).
Since tracheids have smaller diameters and are shorter, they offer
higher resistance to flow, but typically a greater fraction of the
stem cross-section area is devoted to conducting xylem tissue. For
example, in the pine branch shown in Figure 1b used in this study,
fluid-conducting xylem constitutes the majority of the
cross-section. This reasoning leads us to the conclusion that in
general the xylem tissue of coniferous trees – i.e. the sapwood –
is likely to be the most suitable xylem tissue for construction of
a water filtration device, at least for filtration of bacteria,
protozoa, and other pathogens on the micron or larger scale.
The resistance to fluid flow is an important consideration for
filtration. Pits can contribute a significant fraction (as much as
30–80%) [7], [8] of the resistance to sap flow, but this is
remarkably small considering that pit membrane pore sizes are
several orders of magnitude smaller than the tracheid or vessel
diameter. The pits and pit membranes form a hierarchical structure
where the thin, highly-permeable pit membranes are supported
across the microscale pits that are arranged around the
circumference of the tracheids (Figure 1a). This arrangement
permits the pit membranes to be thin, offering low resistance to
fluid flow. Furthermore, the parallel arrangement of tracheids
with pits around their circumference provides a high packing
density for the pit membranes. For a given tracheid with diameter
D and length L, where pit membranes occupy a fraction a of the
tracheid wall area, each tracheid effectively contributes a pit
membrane area of pDLa/2, where the factor of 2 arises as each
membrane is shared by two tracheids. However, the nominal area of
the tracheid is only pD2/4, and therefore, the structure
effectively amplifies the nominal filter area by a factor of
2a(L/D) (Figure 1f). The images in Figure 1c indicate that typical
D ~ 10–15 µm and a ~ 0.2 yield an effective area amplification of
~20 for tracheid lengths of 1–2 mm. Therefore, for a filter made
by cutting a slice of thickness ~L of the xylem, the actual
membrane area is greater by a large factor due to vertical packing
of the pit membranes. Larger filter thicknesses further increase
the total membrane area, but the additional area of the membrane
is positioned in series rather than in parallel and therefore
reduces the flow rate, but potentially improves the rejection
performance of the filter due to multiple filtration steps as
shown in Figure 1a.
Construction of the Xylem Filter and Measurement of Flow Rate
The xylem filter device was constructed by simply peeling off the
bark and cambium from a section of the pine branch and inserting
it into a tube (Figure 2a). Although a simple tube fastener could
provide a leak-tight seal between the tube and the xylem, we used
epoxy to ensure that there was no inadvertent leakage. When
deionized water was loaded into the tube above the xylem and
subjected to pressure in the 0.5–5 psi (3.45 to 34.5 kPa) range,
we found that water readily flowed through the xylem. The flow
rate was proportional to applied pressure (Figure 2b), which
allowed for the extraction of the hydrodynamic conductivity K (m2
Pa-1 s-1) of the filter, defined by(1) where Q is the volumetric
flow rate (in m3 s-1) under pressure difference ?P across the
filter, while l and A are the thickness and the cross-section area
of the filter, respectively. The observed conductivities for three
different filters were in the range of ~5–6×10-10 m2 Pa-1 s-1
(Figure 2c), or equivalently, ~0.5–0.6 kg s-1 m-1 MPa-1 when
defined with respect to mass flow rate of water.
Figure 2. Xylem filter.
a) Construction of xylem filter.
b) Effect of applied pressure on the water flux through the xylem
filter.
c) Hydrodynamic conductivity of the filter extracted at each
measured pressure using the total filter cross-section area and
thickness as defined by Equation 1. Error bars indicate ±S.D. for
measurements on three different xylem filters.
Biologists have performed similar flow rate measurements by
cutting a section of a plant stem under water, flushing to remove
any bubbles, and applying a pressure difference to measure the
flow rate [11], [12]. Xylem conductivities of conifers [7]
typically range from 1–4 kg s-1 m-1 MPa-1, which compares very
well with the conductivities measured in our experiments. Lower
conductivities can easily result from introduction of bubbles [11]
or the presence of some non-conducting heartwood. We can therefore
conclude that the flow rate measurements in our devices are
consistent with those expected from prior literature on
conductivity of conifer xylem.
Filtration of Pigment Dye
After construction of the filter, we tested its ability to filter
a pigment dye with a broad particle size distribution. The red
color of the feed solution disappeared upon filtration (Figure 3a)
indicating that the xylem filter could effectively filter out the
dye.
Figure 3. Filtration performance of the xylem filter.
a) Feed solution of a pigment dye before filtration (left),
compared to the filtrate (right).
b) Size distribution of the pigment particles in the feed and
filtrate solutions measured by dynamic light scattering.
c) Dependence of the rejection on the particle size estimated from
the data in (b).
d) Cross-section of the xylem filter after filtration. Scale is in
centimeters and inches.
Since the dye had a broad pigment size distribution, we
investigated the size-dependence of filtration by quantifying the
pigment size distribution before and after filtration using
dynamic light scattering. We found that the feed solution
comprised particles ranging in size from ~70 nm to ~500 nm, with
some larger aggregates (Figure 3b). In contrast, the filtrate
particle size distribution peaked at ~80 nm, indicating that
larger particles were filtered out. In a separate experiment, we
observed that 20 nm fluorescent polystyrene nanoparticles could
not be filtered by the xylem filter, confirming this size
dependence of filtration. Assuming that pigment particles 70 nm or
less in size were not rejected, the size distributions before and
after filtration enable calculation of the rejection performance
of the xylem filter as a function of particle size (Figure 3c). We
find that the xylem filter exhibits excellent rejection for
particles with diameters exceeding 100 nm, with the estimated
rejection exceeding 99% for particles over 150 nm. Smaller
particles are expected to pass through the larger porosity of the
pit membrane: SEM images in Figure 1e indicate sub-micron spacing
between the radial spoke-like margo membrane through which the
pigment particles can pass, although the porosity is difficult to
resolve in the SEM image.
After filtration, we cut the xylem filter parallel to the
direction of flow to investigate the distribution of dye in the
filter. We observed that the dye was confined to the top 2–3
millimeters of the xylem filter (Figure 3d), which compares well
with the tracheid lengths on the millimeter scale expected for
coniferous trees [7]. These results show that the majority of the
filtration occurred within this length scale, and suggests that
the thickness of the xylem filter may be reduced to below 1 cm
while still rejecting the majority of the dye.
Filtration of Bacteria from Water
Finally, we investigated the ability of the xylem filter to remove
bacteria from water. As a model bacterium, we used fluorescently
labeled and inactivated Escherichia coli bacteria that are
cylindrical in shape with a diameter of ~1 µm. Use of
fluorescently labeled bacteria enabled easy enumeration of their
concentrations, and also allowed us to track the location in the
xylem filter where they were trapped. Since filtration is
dominated by size-exclusion at this length scale, we do not expect
modification with the dye to significantly affect filtration
characteristics. Filtration using three different xylem filters
showed nearly complete rejection of the bacteria (Figure 4a).
Using a hemacytometer to count the bacteria, we estimate that the
rejection was at least 99.9%.
Figure 4. Filtration of model bacteria by the xylem filter.
a) Concentrations of bacteria in the feed and filtrate solutions.
Inset shows fluorescence images of the two solutions. Scale bar is
200 µm. Error bars indicate ±S.D. for experiments performed on
three different xylem filters.
b) Fluorescence image of xylem filter cross-section showing
accumulation of bacteria over the margo pit membranes. Scale bar
is 20 µm. c) Low-magnification fluorescence image shows that
bacteria are trapped at the bottoms of tracheids within the first
few millimeters of the top surface. Scale bar is 400 µm. Arrow
indicates top surface of the xylem filter and also the direction
of flow during filtration. Autofluorescence of the xylem tissue
also contributes to the fluorescence signal in (b) and (c). d), e)
SEM images showing bacteria accumulated on the margo pit membranes
after filtration. Scale bars are 10 µm and 2 µm, respectively.
To investigate the mechanism of filtration, the xylem filter was
cut parallel to the direction of flow after filtration. When
examined under a fluorescence microscope, we observed that the
bacteria accumulated over the donut-shaped margo pit membranes
(Figure 4b). This distribution is consistent with the expectation
that the bacteria are filtered by the porous margo of the pit
membranes. The distribution of trapped bacteria was not uniform
across the cross section of the filter. Similar to the case of the
dye, bacteria were observed only within the first few millimeters
from the end through which the solution was infused (indicated by
the white arrow in Figure 4c). In addition, the low-magnification
fluorescence image shows that the bacteria had accumulated
primarily over pit membranes at the bottom of the tracheids, which
is again not unexpected. Further investigation by SEM clearly
showed individual bacterial cells accumulated on the pit membranes
over the porous margo (Figure 4d,e). These results confirm the pit
membranes as the functional units that provide the filtration
effect in the xylem filter.
Discussion
Wood has been investigated recently as a potential filtration
material [13], showing moderate improvement of turbidity. While we
showed filtration using freshly cut xylem, we found that the flow
rate dropped irreversibly by over a factor of 100 if the xylem was
dried, even when the xylem was flushed with water before drying.
We also examined flow through commercially available kiln-dried
wood samples cut to similar dimensions. Wood samples that
exhibited filtration showed two orders of magnitude smaller flow
rates than in the fresh xylem filter, while those that had high
flow rates did not exhibit much filtration effect and seemed to
have ruptured tracheids and membranes when observed under SEM.
Wetting with ethanol or vacuuming to remove air did not
significantly increase the flow rate in the wood samples that
exhibited the filtration effect, suggesting that the pit membranes
may have a tendency to become clogged during drying. These results
are consistent with literature showing that the pit membranes can
become irreversibly aspirated against the cell wall, blocking the
flow [14]. In fact, the pit membranes in the SEM images (Figure
1d,e and Figure 4d,e), which were acquired after drying the
samples, appear to be stuck to the walls. Regardless, our results
demonstrate that excellent rejection (>99.9%) of bacteria is
possible using the pit membranes of fresh plant xylem, and also
provide insight into the mechanism of filtration as well as
guidelines for selection of the xylem material.
Peter-Varbanets et al. [2] have outlined the key requirements for
point-of-use devices for water disinfection:
a) performance (ability to effectively remove pathogens),
b) ease of use (no time-consuming maintenance or operation steps),
c) sustainability (produced locally with limited use of chemicals
and non-renewable energy), and
d) social acceptability.
Meeting all of these requirements has proved to be challenging,
but point-of-use methods that have been successfully used for
low-cost water treatment in developing countries include
free-chlorine/solar disinfections, combined coagulant-chlorine
disinfection, and biosand/ceramic filtrations [5]. While chlorine
is a very effective biocide, its reaction with organic matter can
produce carcinogenic by-products [15] and some waterborne
pathogens such as Cryptosporidium parvum and Mycobacterium avium
are resistant to the chlorine [16]. Solar disinfection based on
ultraviolet irradiation can effectively inactivate C. parvum, but
this requires low turbidity of source water [17] and is not
effective for control of viruses [16]. Filtration based on biosand
and ceramic filters is also effective at removing pathogens, but
the effectiveness against viruses is low or unknown [18].
Coagulation combined with chlorine disinfection removes or
inactivates viruses and pathogens effectively. However, necessity
of an additional filtration step and relatively high cost are
potential barriers for practical use [18]. Among these methods, a
review on field studies by Sobsey et al. [5] suggested that
biosand and ceramic filtration are the most effective methods in
practice, because once the apparatus is installed, the effort for
use and dosage is significantly reduced and therefore promotes
persistent use compared to disinfection approaches. Although
membrane-based filtration is the most widely used for water
treatment in industrialized nations and the cost of membranes has
significantly decreased, membranes are still unaffordable to poor
communities in the developing world [2]. Ultrafiltration systems
run by hydrostatic pressure [19] and some recently invented
point-of-use devices using ultrafiltration membranes may provide
water to developing regions at reasonable cost [2]. However,
membranes still require specialized chemicals and processes for
manufacture, and need cleaning or replacement.
Xylem filter technology could be an attractive option for low-cost
and highly efficient point-of-use water treatment by filtration,
overcoming some of the challenges associated with conventional
membranes. Xylem filters could provide the advantage of reduced
human effort compared to existing point-of-use water treatment
options, requiring only simple periodic filter replacement. In
addition, the pressures of 1–5 psi used here are easily achievable
using a gravitational pressure head of 0.7–3.5 m, implying that no
pumps are necessary for filtration. The measured flow rates of
about 0.05 mL/s using only ~1 cm2 filter area correspond to a flow
rate of over 4 L/d, sufficient to meet the drinking water
requirements of one person [20]. This is comparable to
chlorination and biosand filtration, which have the highest
production rates of prevalent point-of-use water treatment
methods, and far exceeds typical production rates for solar
disinfection. Xylem filters could potentially be produced locally
and inexpensively, and disposed of easily owing to their
biodegradability. The high flow rates and low cost would certainly
help address the issues of maintenance and replacement. For
example, 200 filters of 10 cm2 area and 0.5 cm thickness could be
packaged into a volume of about 1 L, which will be inexpensive and
last a few years even with weekly replacement. Furthermore, as
suggested by the dye filtration experiment, xylem filters should
be able to significantly reduce water turbidity, enhancing the
aesthetic qualities of the drinking water, which is hardly
achieved by chlorination and solar disinfection.
Wood is an easily available material. While use of fresh xylem
does not preclude its use as a filter material, dried membranes
have definite practical advantages. Therefore, the process of wood
drying and its influence on xylem conductivity needs further
study. In particular, processes that yield intact yet permeable
xylem tissues that can be stored long-term will be helpful for
improving the supply chain if these filters are to be widely
adopted. In addition, flow through xylem of different plants needs
to be studied to identify locally available sources of xylem,
which will truly enable construction of filters from locally
available materials. In the present study, we report results using
xylem derived from only one species. These xylem filters could not
filter out 20 nm nanoparticles, which is a size comparable to that
of the smallest viruses. It will be interesting to explore whether
there exist any coniferous species that have pit membranes with
smaller pore sizes that can filter out viruses, or whether conifer
xylem can be impregnated with particles such as carbon black to
improve rejection of viruses. In their absence, angiosperms with
short vessels that yield practical filter lengths may be the best
alternative due to their smaller pit membrane pore sizes [8].
Further exploration of xylem tissues from different plants with an
engineering perspective is needed to construct xylem filters that
can effectively reject viruses, exhibit improved flow rates, or
that are amenable to easy storage. It is also conceivable that
plants could be selected or developed for enhanced filtration
characteristics, as has been the norm in agriculture for
enhancement of many desirable characteristics including resistance
to pests, flavor, or productivity.
Conclusions
Plant xylem is a porous material with membranes comprising
nanoscale pores. We have reasoned that xylem from the sapwood of
coniferous trees is suitable for disinfection by filtration of
water. The hierarchical arrangement of the membranes in the xylem
tissue effectively amplifies the available membrane area for
filtration, providing high flow rates. Xylem filters were prepared
by simply removing the bark of pine tree branches and inserting
the xylem tissue into a tube. Pigment filtration experiments
revealed a size cutoff of about 100 nm, with most of the
filtration occurring within the first 2–3 mm of the xylem filter.
The xylem filter could effectively filter out bacteria from water
with rejection exceeding 99.9%. Pit membranes were identified as
the functional unit where actual filtration of the bacteria
occurred. Flow rates of about 4 L/d were obtained through ~1 cm2
filter areas at applied pressures of about 5 psi, which is
sufficient to meet the drinking water needs of one person. The
simple construction of xylem filters, combined with their
fabrication from an inexpensive, biodegradable, and disposable
material suggests that further research and development of xylem
filters could potentially lead to their widespread use and greatly
reduce the incidence of waterborne infectious disease in the
world.
Acknowledgments
The authors thank Yukiko Oka for assistance with preparation of
illustrations and Sunandini Chopra for help with dynamic light
scattering measurements.
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