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Methodology: 2. Developing Pre-Model Design
Methodology: 2. Developing Pre-Model Design
Methodology: 2. Developing Pre-Model Design
According to WHO [11] and Pottery for peace (PFP), a family of four would consume 10 litres
of water per day. Therefore, for an extended family (the common pattern in developing
countries) and taking into account peak demand, the need for water per person should be
assumed to be 20 litres per day.
with the help of AUTO CAD software expert,it is aimed to develop pre and final model design of
ceramic pot water filter(CPWF) based on the Ceramics Manufacturing Working Group (2011) and
different parameters which control filter performance. The sectional side view of pre- designed
ceramic filter element is shown in Figure 1. The capacity of the finished product is 10 litres.
Before a final design of the water filter was created, it was necessary to ensure that the
filter works as described.
I. 5 TEST-A samples will be prepared with the same processing technique but only by varying
their composition
II. 5 TEST-B samples will be prepared with the same processing technique but only by varying
their rate and firing temperature
III. 5 TEST-C samples will be prepared with the same processing technique but only by varying
their wall thickness and depth.
But, all the fifteen pot sample will undergo/follow the same envestigation techniques listed below :-
In this project, two types of silver impregnated clay filters were made to determine their time
dependence of flow. The first kind of filters was made from clay and saw dust while the second kind was
made from clay, saw dust and hydroxyapatite. This therefore makes the raw materials that were used
for this project to be clay, sawdust and hydroxyapatite. The clay used for the moulding of the filters was
obtained from Olorunda Ayehro, Ogun State in the South-western part of Nigeria. The clay was obtained
in its raw wet lumpy form. It was therefore dried for two weeks to remove the water from it. This was
then followed by crushing of the clay into powder form using a hammer mill 121 (Munson, Utica, New
York, U.S.A). This was followed by sieving to obtain finer particles using a screen mesh (2mm). The saw
dust used in this project was obtained from a saw mill in Abeokuta, Ogun State, Nigeria. This was
prepared by sieving it to isolate the large particles of the saw dust. This was achieved using a sieve with
a 1mm screen mesh.
The filters were processed at Filtron Nigeria in Abeokuta, Nigeria. During processing, 50 vol.% of the
processed clay was measured onto a clean surface. Then 50 vol.% of saw dust was measured out and
added to the clay. The two materials were then mixed well. Water was then slowly added to the clay
and saw dust mixture during mixing. This was done periodically to ensure that a homogenous consistent
mixture was obtained. This homogenous mixture was then pressed into the filter shape using a hydraulic
press with a purpose-built mould.
After pressing, the moulds were marked with unique codes for identification. They were then left in the
open to sundry for two weeks. After drying, filters were fired in a kiln at approximately 780 0C for a
period of between 6 to 9 hours. They were then allowed to furnace cool down to room temperature. A
mixture of water and colloidal silver, that is 2 ml of colloidal silver at 3.2% added to 250 ml of water. The
dried filters were then dipped into this mixture. This resulted in the coverage of the surface with the
colloidal silver. The dipped filter was then allowed to dry in the open air under ambient conditions.
These pressed filters were marked with unique codes for identification. They were then left in the open
to sundry for two weeks. After drying, the filters were fired in a kiln at approximately 780 0C for a period
of between 6 to 9 hours. This actually burns the saw dust in the filters and therefore creating the pore
needed for the filtration. After firing, the filters were allowed to furnace cool down to room
temperature. They were then dipped in a mixture of water and colloidal silver, that is 2 ml of colloidal
silver at 3.2% added to 250 ml of water. This resulted in the coating of the filter surface with colloidal
silver. The coated filters were then dried in air under ambient condition.
Reference
[21] Souza G.P., Souza S.J.G., Terrones L.A.H., Holanda J.N.F., Mineralogical analysis of Brazilian ceramic sedimentary
clay used in red ceramic, Ceramica,
Vol.51, pp. 381-386, 2005.
[22] Sutherland K., Filters and Filtration Handbook. Butterworth-Heinemann, Elsevier Press, Atlanta, GA, 2008.
The materials that were used in the manufacturing of the filters were sampled for characterization.
These samples include; clay, sawdust and hydroxyapatite. Samples of the finished filters were also taken
for characterization. The characterization experiment was used to determine the surface morphologies,
structure and the elemental compositions of the samples. The surface morphologies were characterized
using the Scanning Electron Microscope (SEM), while the elemental compositions of the samples were
obtained using the X-Ray diffraction (XRD) and Energy Dispersive X-ray Spectroscopy (EDS).
The initial samples of clay and hydroxyapatite were in powder form while the samples of the finished
filters were not in powder form. In the XRD analysis, the samples that were already in the powder for
were only sieved through a 270 mesh sieve. However, the filter samples were first ground before sieving
them through the 270 mesh sieve. The ground/powder samples were then mounted on the XRD sample
holder before conducting the XRD analysis in a model MD-10 precision mini X-ray diffractometer
(Radicon, Russia).
In the case of the SEM and EDS analysis, the samples were characterized in their unprocessed states.
Hence, the powdered sawdust, clay and hydroxyapatite samples were characterized without special
specimen preparation. The SEM/EDS analysis was carried out at the Sheddah Science Center in
Gwagwalada, Abuja, Federal Capital Territory, Nigeria. They were conducted on the Model Zeiss Evo 60
Environment scanning electron microscope (Carl Zeisis Canada Ltd., Canada) that was instrumented with
a model Bruker AXS Quantax 4010 energy dispersive X-ray spectroscopy (EDS) system (Carl Zeisis Canada
Ltd., Canada).
The flow of water was studied in the two types of filters that were made using procedure described in
section 3. The flow experiments were used to study the time dependence of flow. Foe each type of
filter, five filters were selected randomly and each placed in a plastic container with a tap at the base.
They were then set up on a flat raised platform. Each filter had a beaker placed directly below the tap in
the plastic container to collect the water flowed through. The taps were then fully opened before filling
each filter with water. The time-dependence of flow was then recorded by measuring the volume of
water that dripped out of the tap into the beaker. It is important to note that the receptacle was filled
pre-filled to appoint where a single drip of water into receptacle resulted in a drop of water from the tap
into the beaker. The flow of water into the beaker was recorded after 15 minutes, and then after two
hours, the interval for the measurement of the water was increased to 30 minutes. This was then
increased to 1 hour, then to 1 hour 30minutes, and then finally to 2 hour intervals. The timing for the
increment of the interval for the measurement of the water depends on the measuring apparatus that is
being used in the measurement of the volume of water that flow out of the tap. This interval is
increased because, as the level of water reduces in the filter, the volume flow rate of water filtered also
reduces. Hence, large volumes are needed to measure the flow rate.
The E.coli test was conducted to determine the effectiveness of the manufactured filters in the removal
of bacteria in the water being filtered. The test was conducted for pre-filtered water and filtered water.
And in both cases, the test was conducted for 1ml and 0.5 ml of sample water and ten petrifilm plates
was used. Therefore for the 1ml of sample water, five petrifilm plates were used and the remaining five
petriflm plates were used for the 0.5ml sample water. The plates were incubated for 24 hours and the
colony forming units (CFU) was countered. Coliform tests were also conducted using 3M petrifilm Rapid
Coliform Count (RCC) plates (Microbiology Products, St. Paul, Minnesota, U.S.A). These are culture
media that have already being made. They contain Violet Red Bile (VRB) nutrients, a cold-water-soluble
gelling agent, a pH indicator, which is to detect acid and finally tetrazolium indicator, which facilitates
colony enumeration.
For the testing, a petrifilm Rapid Coliform count (RCC) plate was placed on a level surface. This was then
followed lifting the top film of the RCC. A 1 mL sample water was then dispensed onto the center of the
bottom of five films each. It was then followed by dispensing 0.5 mL of sample water onto the center of
bottom of another set of five fimls. This was done for both filtered and pre-filtered water. The top film
was then slowly rolled down onto the sample, making sure that no air bubbles were trapped in the
process. The smooth side of the plate was then turned face down, before placing the plastic spreader on
the center of the plate and pressing gently in the center to distribute the sample evenly. Caution was
taken not to slide the spreader across the film. After the press, the spreader was removed and the plates
were left undisturbed for at least one minute to permit the gel to solidify. This process was repeated for
each of the water samples that were taken.
After the whole process described above, the petrifilm RCC plates were incubated at 35 0C ± 1 0C for 6 to
24 hours in a horizontal position, making sure that the moisture lost form the plate did not exceed 15%
during this process. The plates were then examined for coliform growth after 24 ± 2 hours of incubation.
Water samples were collected randomly in properly washed and rinsed appropriate sampling bottles.
The pH meter, Cyber scan, PC300PH, Temp., TDS and EC meter having electrodes were used
immediately on spot to measure pH, Temperature, Total Dissolved Solids (TDS), and Electrical
Conductivity (EC), respectively. These electrodes were immersed in the samples and then the measured
parameters were displayed on the LCD screen of the instruments.
The physiochemical tests were performed using DR/2400 spectrophotometer. A powder reagent
chemical was dissolved in 10ml of water sample in a cylindrical sample cell and allowed to react. Color
develops with intensity proportional to the amount of the target element was measured. Each element
has a unique maximum absorption wavelength at which the spectrophotometer was adjusted. Light was
allowed to pass through the sample cell so that light is absorbed at the required wavelength. The results
were displayed on the LCD screen in mg/l in proportion to the amount of light absorbed at that
particular wavelength.
3.5.1.2 Titration
In the total hardness test procedure, the water sample is first buffered (using an organic amine and one
of its salts) to a pH of 10.1. An organic dye, calmagite, is added as the indicator for the test. The organic
dye reacts with calcium and magnesium ions to give a red-colored complex.
EDTA (ethylene di-amine tetra acetic acid) is added as a titrant. The EDTA reacts with all free calcium
and magnesium in the sample. At the end of the titration, when free magnesium ions are no longer
available, EDTA removes magnesium ions from the indicator changes its color from red to blue.
Water samples were collected in pre-sterilized plastic bags and were filtered on the spot using
membrane filters with a spore size of 45µm. The filters were incubated in an ELE Paqualab 25 field
incubator, in sterilized aluminum Petridis with a bacterial medium of m-Coli Blue24 on absorbent pad, at
37oC and 44oC for total coli forms and E-coli/fecal coli forms, respectively. The filters were examined for
24 hours to assess bacterial growth. The results were compared with WHO guidelines maximum
permissible limit value.
Table 4 Equipment and Machinery Required for Building Ceramic Filter Elements
Preparation for Ceramic Mixture – Bricks
1. Pulverizing (crushing) stage :-The ceramic media of the filter requires the incorporation of rice husks.
This allows the water flow rate through the ceramic, while maintaining the effectiveness of filtering
water [33].To obtain the main source of material for the mixture, bricks are initially crushed into
pieces with a sledge hammer. The industries put the crushed bricks into a hammer mill to turn the
pieces into powder, which will be used in the following steps. Note that the fineness of the powder
is not important. If a hammer mill cannot be provided by the thesis industrial partner, bricks will be
crushed manually with hammers.Preparation for Ceramic Mixture – Rice Husks Rice husks can be
purchased from suppliers. Preparation of rice husks requires crushing the rice husks into small
pieces. The bigger the husk size, the bigger the pore [33]. For small amounts of rice husks, crushing
is performed manually. The use of machines is recommended when mass-producing the filters.
According to Resource Development International (RDI), a rice husks-to-clay powder ratio of 1:3 is
required for the mixture [33]. Water needs to be added in the middle of the mixing process. 1.25L of
water is required for every kilogram of rice husks [33]. Clay powder and rice husks must be
processed through dry mixing for 10 minutes before water is added. Water is then evenly
distributed over the mixture with a gardening bucket, and the mixture
should be mixed for 10 additional minutes. Manual mixing is to be used for this project. The use
of automatic ceramic mixing machines is recommended for mass production.
Wet clay is then formed manually into shapes of the design. The prototype for this project is to be
formed manually. In industries, this step is carried out by hydraulic press machines to form identical
shapes for mass production.
Drying and Surface Finishing
Surface finishing is critical. The ceramic surface must be smooth and free of cracks. This ensures the
effectiveness of the water filtering process [33]. Scraping tools are useful in this step to scrape off any
rough surfaces. After the shape of this particular filter level is formed, the filter is to be air dried. Drying
time of the element depends to the size of the filter as well as the drying environment. With filter
building experience, RDI recommends to place the filter under a shaded area to ensure a more uniform
drying process [33]. Once the filter element is completely dried and hardened it is ready for firing.
Firing
The ceramic part is to be placed in a kiln or pottery oven to complete the firing process. There are two
stages in the firing process – dehydration and vitrification. Water molecules are dried off in dehydration
under low temperature firing. Vitrification is the process of creating the firm bonds of the ceramics – this
is done in higher temperature firing [37]. Rice husks mixed into the clay also burn off, thus creating
pores in the pot to allow water to pass through. In industries, numerous filter elements are fired at the
same time in a large kiln. The elements are heated at 100 oC for two hours for drying off water excess
within the ceramics [33]. Then, the temperature is gradually increased to 866 oC over 8 to 10 hours. The
firing temperature and time depends heavily on the number of elements and the unique properties of
the clay mixture.
For the thesis prototype, the time and temperature for firing will be determined afterconsultation with
pottery experts.
Silver Coating
After the ceramic filter element is fired and cooled, a coating of silver nitrate can be applied on all
surface of the element. However, during the water filtration process, there is a risk for the silver solution
to dissolve in the filtered water [38]. Investigations have been carried out by Alethia Environmental on
how much silver concentration appears in ceramic filtered water. Results have shown that the amount
of silver concentration in filtered water depends on the methodology of applying the silver coating onto
the ceramic element instead of the initial silver solution concentration [38]. Dartmouth Toxic Metals
Research Program also states that silver is not toxic to humans and will not cause cancer or other
chronic advert effects [39]. As a result, it is safe to apply a coating of silver solution onto the walls of the
filter element. The following procedure is developed by RDI in the production of their ceramic filters
[33]. The amounts used are for approximately 60 flower pot sized ceramic filters by RDI.
1. Add 100g of AgNO3 (99.8% purity) to 500mL of de-ionized water and then mix well.
2. Add 1L of de-ionized water and mix for 1 minute. Silver solution is complete.
3. Dilution of Silver solution is done with a silver solution to distilled water ratio of 1:180. (i.e. For
every 100mL of silver solution used, it should be diluted with 18L distilled water)
4. Using a paint brush, silver solution is coated on the inside and outside of the filter.
5. Let dry.
Results were compared to the standards from World Health Organization (WHO) and to the reference
sample of tap water going through
carbon filtering.
- Ice pack
- Cooler
The following procedure was carried out to complete the effectiveness test on the dual filter.
1. Place activated carbon elements into a fully built ceramic filter element.
2. Fill up the dual filter with water from Lake Ontario. Ensure absolutely no spilling on the
apparatus for accurate analysis. Due to a relatively slow flow rate, it is recommended to
setup a number of dual filters and allow them to filter in parallel.
3. To ensure minimal evaporation, enclose the setup of the testing filter with a cap and
seal off the openings with plastic food wrap.
4. Fill the two 200mL plastic bottles with filtered water. One bottle is for metals test while
the other for nutrients test.
5. Fully close the bottles with the screw-cap and place in refrigerator at less than 10°C until
shipment as per Maxxam Analytics instructions.
6. Fill the 500mL plastic bottle with filtered water. This bottle is for the general test.
7. Fully close the bottle with the screw-cap and place in refrigerator at less than 10°C until
shipment as per Maxxam Analytics instructions.
8. Repeat steps 2-7, if necessary, until the bottles are filled up to the fill-line indicator on
the bottles.
9. Package the sample bottles in the provided cooler with an ice pack. This maintains the
required low temperature condition during the shipment of the samples to Maxxam
Analytics.
10. Ship samples to Maxxam Analytics for analysis.
The following procedure was carried out to complete the effectiveness test on the carbon filter
with Lake Ontario water and tap water.
1. Pour unfiltered Lake Ontario water into a typical home-use carbon filter (eg. Brita
carbon filter).
2. Allow it to complete the filtering and fill up to the fill-line indicator on the two 200mL
plastic bottles with filtered water. One bottle is for metals test while the other for
nutrients test.
3. Fully close the bottles with the screw-cap and place in refrigerator at less than 10°C until
shipment as per Maxxam Analytics instructions.
4. Fill up to the fill-line indicator on the 500mL plastic bottle with filtered water. This bottle
is for the general test.
5. Fully close the bottle with the screw-cap and place in refrigerator at less than 10°C until
shipment as per Maxxam Analytics instructions.
6. Package the sample bottles in the provided cooler with an ice pack. This maintains the
required low temperature condition during the shipment of the samples to Maxxam
Analytics.
7. Repeat steps 1-6 for unfiltered tap water.
8. Ship samples to Maxxam Analytics for analysis.
The following procedure was carried out to complete the effectiveness test on the unfiltered
Lake Ontario water.
1. Fill up to the fill-line indicator on the two 200mL plastic bottles with unfiltered water.
One bottle is for metals test while the other for nutrients test.
2. Fully close the bottles with the screw-cap and place in refrigerator at less than 10°C until
shipment as per Maxxam Analytics instructions.
3. Fill up to the fill-line indicator on the 500mL plastic bottle with unfiltered water. This
bottle is for the general test.
4. Fully close the bottle with the screw-cap and place in refrigerator at less than 10°C until
shipment as per Maxxam Analytics instructions.
5. Package the sample bottles in the provided cooler with an ice pack. This maintains the
required low temperature condition during the shipment of the samples to Maxxam
Analytics.
6. Ship samples to Maxxam Analytics for analysis.
N.B The pH, alkalinity, TOC, and turbidity had risen for Lake Ontario
water processing through just the carbon level.
Monthly analyses were conducted on the water from various rivers that links to
Lake Victoria in Kenya. Zinc, lead, copper, cadmium, iron, chromium, manganese, and
aluminum were measured. Table 9 compares the metals concentration in Kenya’s water to the
concentrations measured from Lake Ontario’s samples.
Table 9 Comparison of Detected Metals with Water from Lake Victoria, Kenya
Iron helps transport oxygen through human blood. While it is not considered hazardous to
human health, it leaves a reddish colour to the water [45]. The USEPA limit of 300μg/L ensures
that water meets aesthetic expectations [46].
Table A3 WHO disinfectant and disinfectant by-products guideline for safe drinking water [40]
Table A4 WHO pesticides guideline for safe drinking water [40]
Reference
[8] “Dietary Reference Intakes,” 2004. [Online]. Available:
http://www.iom.edu/Object.File/Master/21/372/0.pdf
[33] RDI Cambodia, “Ceramic Water Filter Play a Major Role for Cambodian!,” rdic.org, [Online].
Available: http://www.rdic.org/waterceramicfiltration.htm
[34] A. Yehaskel, Activated Carbon: Manufacture and Regeneration, New Jersey: Noyes Data
Coporation, 1978
[36] Food & Fertilizer Technology Center, “Processing of Coconut Shell into Activated Carbon /
Charcoal,” fftc.agnet.org, November 1, 2004 [Online]. Available:
http://www.fftc.agnet.org/library/pt/2004003/
[37] University of Iowa, “Ceramics Process,” uiowa.edu, [Online]. Available:
http://www.uiowa.edu/~intl/rft/chemistry_ceramics.html
[38] “Investigation of the Potters for Peace Colloidal Silver Impregnated Ceramic Filter,” December 21,
2001. [Online]. Available: http://www.edc-cu.org/pdf/report1-final.pdf
[39] Dartmouth College, “Dartmouth Toxic Metal Research – Toxic Metals!,” dartmouth.edu, March 30,
2005. [Online]. Available: http://www.uiowa.edu/~intl/rft/chemistry_ceramics.html
[40] Lenntech, “WHO’s Drinking Water Standards 2006,” lenntech.com, 2008. [Online]. Available:
http://www.lenntech.com/WHO%27s-drinking-water-standards06.htm
[41] United States Environmental Protection Agency, “Is Total Organic Compound (TOC) a
Concern?,” epa.gov, March 2009. [Online]. Available:
http://safewater.custhelp.com/cgibin/safewater.cfg/php/enduser/std_adp.php?
p_faqid=1367&p_created=1099198920
[42] “Fact Sheet: Orthophosphate, Drinking Water and Public Health,” September 3, 2004.
[Online]. Available: http://www.epa.gov/dclead/phosphoric_acid_health_effects_sheet_FINAL.pdf
[45] Wisconsin Department of Natural Resources, “Iron in Drinking Water,” dnr.state.wi.us, January 28,
2003. [Online]. Available: http://www.dnr.state.wi.us/org/water/dwg/iron.htm
[46] United States Environmental Protection Agency, “Ground Water & Drinking Water,”
epa.gov, July 1992. [Online]. Available:
http://www.epa.gov/OGWDW/consumer/2ndstandards.html [Accessed: March 17, 2009]
[47] Government of Saskatchewan, “Conductivity - Health,” health.gov.sk.ca, 2007. [Online].
Available: http://www.health.gov.sk.ca/water-quality-parameters-conductivity
[48] “The Drop on Water pH and Alkalinity,” March 5, 2008. [Online]. Available:
http://www.gov.ns.ca/nse/water/docs/droponwaterFAQ_pH.pdf
[49] “Activated Charcoal,” September 30, 2002. [Online]. Available:
http://www.omri.org/AC_livestock.pdf