PRODUCT LAB TESTING and REVIEWS
THE TESTING OF POLY-BIO-MARINE INC.'S FILTER MEDIA
AND SYSTEM UNDER EPA STANDARDS AND ANALYSIS METHODS
PERFORMED IN STATE & FEDERAL CERTIFIED
TOXICOLOGY LABORATORY
FOREWORD:
Sampling:
All product samples, with the exception of Poly-Bio-Marine, Inc.'s Discs,
carbons, carbon-resin mixtures, ion exchange resins, and synthetic marine
salt were purchased through a single supplier. The supplier's name "That
Fish Place" and their wholesale operation "Fish Net, Inc." is located at 237
Centerville Rd., Lancaster, PA. In addition, all copper disease treatments
were purchased via "Fish Net, Inc." These products were shipped into
Poly-Bio-Marine, Inc., through ground freight, carrier United Parcel
Service. The products were then transported, in total, down to UMDNJ
Toxicology Lab and stored until required for testing. All product seals were
broken by the laboratory technician (C.A.P. Certified) performing the tests.
Due to the high levels of particulates anticipated during carbon usage and
the ion-exchange resins' lack of containment, Poly-Bio-Marine's Inc.
provided all other products one additional item. This item was a die-cut
(2.75" diameter) polyester micro-rated fiber (2,300 microns thick) three
micron (99.9%) autoclaved, pre-rinsed in sterile, pyrogen-free 1.0
microSiemens/cm conductivity water. This 99.9% particulate retention filter
may have increased the competitive products' performance slightly. This
would have occurred through particulates of chemical sorbents performing
additional chemical filtration.
Poly-Bio-Marine, Inc. provided the following samples: Regular Poly-Filter
(resale package), size: 4"x 8", custom die-cut into 2.75" diameter discs.
Hand cutting of the rectangular Poly-Filters would have resulted in cutting
abrasions releasing particulate matter. These misshapen, poorly fitting
discs would have allowed fluid bypass. We avoided these problems by taking
standard-finished Poly-Filters (resale grade), size: 4" x 8", placing them
on a platen receiver covered by a (ultra high molecular weight polyethylene)
plastic in a hydraulic press and compressing the Poly-Filters against a
sharpened stainless steel rule die under 12,000 psig force. This produced
smooth-cut particulate-free discs for testing. The next product we provided
were standard PMA-1 12/Pks. The last product we provided PMA 12/Pks
specially processed in sterile, pyrogen-free 1.0 microSiemens/cm
conductivity water. All products were placed into heat-sealed 8-mil
polyethylene plastic bags and transported directly to UMDNJ Toxicology Lab.
All product seals were broken by the laboratory technician (C.A.P.
Certified) performing the tests. We did not use a pre-filter media for
particulate control post Poly-Filter discs.
BACKGROUND INFORMATION
Sample Filtration
A ten-gallon plastic tank (Nalgene) polyethylene food grade was pre-fitted
with bulkhead fittings (food grade) with 3/8" Npt hose fitting outside the
tank. All flexible tubing consisted of PVC tubing (reinforced) nontoxic FDA,
NSF Approved capable of 200 psig. All pipe fittings (except for those
directly connected to the Nalgene tank) were polypropylene (threaded) FDA
Approved for potable water and ultra pure water contact. East fitting was
wrapped with FDA Approved virgin Teflon tape for leak containment. All
tubing was carefully piped in series, on the positive (pressure) side to the
pump, into the above test apparatus. However, upon exiting the second
Fin-L-Filter canister, the water fitting was pushed onto a Teflon wrapped
fitting and then clamped via 316 stainless hose clamps. The test filter
media apparatus consisted of two Fin-L-Filter Model PMA-1cl canisters piped
together in series, controlled by a two-way ball valve which, when open,
allowed the water to continue back into the tank (continuous loop) or to
exit the system (if a containment ball valve was in the open position). This
system draws water from the bottom side of the ten-gallon tank (suction
side) into the pump and then through two Fin-L-Filter canisters, continuing
back into the top of the 10-gallon Nalgene tank. The pump is designed for
providing pressured potable water for recreational vehicles and
week-ending/live-aboard boats. It is an all-plastic (food grade) four stage
piston pump available in both 115 volt AC/12 volt DC, designed to provide
3.78 gallons per minute constant flow rate, and pressuring up an entire
system to its 40 psig shut-off point.
The 3.78 gallons per minute (14.20 liters per minute) flow rate offers a
realistic flow rate for drinking water, showers, and fish tanks. Note: A
small aquarium power filter (hang-on-the-back type) flows more than 226.8
gallons per hour. The NSF International requires all canister filters be
tested at 0.60 gallons per minute (2.271 liters per minute) or 136.26 liters
per hour (36 gallons per hour) for potable water testing. We thought 630%
faster flow rates than NSF Standards required should be sufficient to
demonstrate the systems' unique properties.
Sampling and Supervision
Water samples were taken in 1000ml glass jars previously prepared via
hydrochloric acid washes and ultra-pure water rinses, oven-dried and
remaining in the oven until sample usage. All samples were taken and labeled
by an instructor at Toxicology Center of UMDNJ. Each set(s) of samples were
prepared for cold storage according to methods provided via the EPA
Standards. In addition, dual controls were independently prepared for each
test method. Mohamed S. Abdel-Rahman, Ph.D., B.C.F.E., Director of the
Toxicology School and a Professor of Pharmacology, University of Medicine
and Dentistry New Jersey, directly supervised all test procedures, reviewed
all data, and confirmed the final report. Dr. Abdel-Rahman trained at Ohio
State for his Masters of Science and Doctorate of Pharmacology and
Toxicology and has over three hundred published papers and chapters of books
concerning water, drinking water, chlorination, and trihalomethane toxicity.
TAP WATER FILTRATION
The System
Kold-Ster-il® Filtration System (U.S. Patent Pending). Consisting of the
following: (#1) PMA-1 canister filled with 12 specially prepared (sterile,
1.0 microSiemens/cm water) discs. (#2) PSM-1 canister filled with 1
specially prepared (sterile, 1.0 microSiemens/cm water) 0.20 micron bag
99.9%. (#3) 0.50 micron carbon core filled with a special molecular sieve
media for heavy metals, pre-rinsed in double distilled water and
specifically designed for low hardness water applications, i.e., post
nanofiltration and hyperfiltration.
Method of Spike [Test Contaminate(s)] Preparation: Metal dissolved in
acid(s) solution, prepared standards for check/calibration of AA/ICP1
equipment, manufactured by Aldrich Chemical Co.3 Concentrations(s) 990µ/ml2,
995µg/ml2, 1010µg/ml2.
Lead(Pb) 1010 µg/ml Lot No. 07307PG
Cadmium (Cd) 995 µg/ml Lot No. 07823AN
Mercury (Hg) 990 µg/ml Lot No. 04111A
Copper (Cu) 1010 µg/ml Lot No. 05224CN
Zinc (Zn) 990 µg/ml Lot No. 05313DF
Iron (Fe) 1010 µg/ml Lot No. 05212BP
1 AA/equipment Atomic Absorption, Graphite Furnace Technique Spectroscopy.
ICP Inductively
Coupled Argon Plasma Emissin Spectroscopy.
2 990,995, 1010µg/ml. To convert µg/ml into mg/L, multiply each side by
1000. Therefore, 990µg/ml = 990mg/L, 995µg/ml = 995mg/L, 1010µg/ml =
1010mg/L.
3 A small calculated sample of the standard solution was added to he Nalgene
tank containing 10 gallons (37.85 Liters) of pre-filtered water, producing a
known concentration of contaminate(s) (spike solution) in 10 gallons volume
of water.
Lead Testing at 3.78 gpm fluid flow
We prepared 10 gallons (37.85 Liters) of highly filtered tap water. The base
tap water* filtered by the Kold Ster-il ® contained 6.04µg/L (ng/ml lead.
Key: Ng/ml=µg/L* (Newark City tapwater: 6.19 pH, Conductivity 125
microSiemens/cm).
We added a calculated amount (115ng/ml of pure Lead in a nitric acid
solution) to the 10 gallons plus 1.5ml (2.5N) of sodium hydroxide buffer.
116.85ng/ml (Spike) Lead Solution. The lead spike solution now tested at
7.75pH. This solution contained 7.79 times more than the 15/ng/ml federal
lead limit.
We filtered all test solutions through a 4-stage piston pump that delivered
a constant 3.78 gpm (14.2 Liters per minute) fluid flow into (2) canister
filters (Fin-L-Filter Model PMA-1). Resale grade Poly-Filters were cut into
(s) 12/pks, run for 34 seconds filtering (>7.1 Liters of test solution).
This demonstrated 62.45% lead removal (lead filtrate) 43.87ng/ml @ 3.78 gpm
(14.2 Liters per minute) flow rate.
Important Note:
All other filter media test@ 0.60 gpm or 2.271 Liters per minute.
This means 15.9% of our 14.2 Liters per minute flow rate. Reason for lower
flow rate testing: van der Waal's Forces prevent all other media from
sorbing Lead effectively at the higher flow rates.
Our next test demonstrated the van der Waal's Forces effect. (Base Lead
level 12.34ng/ml and how one higher grade 12/Pk will outperform Two lower
grade 12/Pks.) We added a calculated amount of pure Lead in nitric acid
solution 248.38ng/ml Lead into 10 gallons of synthetic seawater (1.023
specific gravity @ 60°F). This is 16.5 times more than the potable water
limit of 15/ng/ml lead concentration. We recirculated (18.9L) of the
solution through (1) 12/Pk of discs for 14 minutes and 16 seconds or (53.44
total gallons) reducing the lead to 90.72ng/ml concentration. A 63.47% lead
reduction occurred @ 3.78 gpm flow rate or 645% faster flow rate than NSF
Standard 53lb. To clearly demonstrate the difference between our filter
media and ion-exchange resins, at the higher flow rate (van der Waal's
Forces), we took the other half of the original synthetic seawater solution
(18.9 Liters) containing 248.38ng/ml of lead and filtered it through 500 ml
volume of ion exchange resin (10" cartridge) for 14 minutes and 16 seconds @
3.78 gpm or 53.44 total gallons. The resin only sorbed 16.68% of 248.38ng/ml
of lead to produce 206.94ng/ml lead filtrate. In addition, the ion-exchange
resin, strong cation resin, acidified the filtrate dramatically from the
original 8.12 pH down to 3.26 pH. In comparison, our (1) 12/Pk raised the pH
slightly (8.12) to 8.39 pH.
Conversions: ng/ml (nonogram per milliliter) equals µg/L (microgram per
liter) Part-Per-billion. To convert ng/ml to mg/L, multiply each side of the
equation by 1000, Part-per million or Milligrams per Liter. Example:
100ng/ml = 0.100mg/L.
Formation of a Synergistic Solution Comprising Three Metals: Lead, Mercury,
and Cadmium in Potable Water.
After having performed Lead, Mercury, and Cadmium tests in Potable Water, it
was determined that testing of mixed solution should be performed to
determine if any synergistic reactions occurred. This test series offered
several unique parts: first, the acidity of the test solution decreased the
normally low pH tap water (6.12 pH) to a 5.90 pH level. Since our previous
work was buffered to 7.75 pH Lead, 7.76 pH Mercury, it was decided to
perform filtration on a naturally acid sample. We would also perform another
synergistic filtration test in synthetic seawater which was naturally
alkaline (8.12-8.35 pH Range).
Several unique features occurred during the synergistic solution tests. Lead
adsoption/absorption decreased more than 3% during the initial 65 seconds of
filtration. Mercury intake into the filter media increased dramatically from
14.73ng/ml sorbed (36.74%) of 40.09ng/ml to 78.32ng/ml (63.74%) of
122.86ng/ml. Cadmium performed similar remarkable increases in
absorption/adsorption. Initially, Cadmium was not sorbed out of potable
water at a 6.30 pH. However, in the synergistic solution (5.90 pH) Cadmium
was sorbed 50.22 ng/ml (63.21%) of 79.44ng/ml over 85 seconds filtration
time and the filtrate's pH increased to 6.40 pH. During previous filtration
tests the media seemed to prefer sorbing the metal + hydroxide [OH-] yet,
here we see the solution's pH increase. We then continued the test with the
same filter media installed in the test apparatus. The new test solution was
not the filtrate but rather, the other half of the originally prepared test
solution.
As we continued the experiment this time for 14 minutes and 16 seconds, the
following was noted: Lead sorption continued to 88.95 (75.45%) reduction of
a 117.89 Lead concentration. Mercury sorption decreased less than 3%
(44.54ng/ml) to (48.04ng/ml) out of 122.86ng/ml Mercury concentration.
Cadmium sorption continued 58.51ng/ml (73.65%) out of 79.44ng/ml Cadmium
concentration. This clearly demonstrated that the Poly-Filter PMA-1 disc
media sorbed 88.95ng/ml Lead + 74.82ng/ml Mercury + 58.52ng/ml Cadmium
during 14 minutes and 16 seconds filtration @ 3.8 gpm flow rate. This means
the Poly-Filter disc media sorbed 222.28ng/ml of Lead, Mercury, Cadmium @
5.90 pH. In comparison, a top rated NSF filter contained carbon block +
molecular sieve media saturated with only 213.70ng/ml of Cadmium during 14
minutes and 16 seconds of filtration. The solution's pH increased from 8.11
pH to 9/1 pH during the 14 minutes and 16 seconds of filtration. This
clearly demonstrates how van der Waal's forces effect filtration media
performance. The carbon block + molecular sieve media is rated under NSF
Standard 53b to deliver a minimum of 1,000 gallons of water >91% removal of
Cadmium flow rate 0.60 gpm. Subjected to 3.8 gpm flow rate the van der
Waal's Forces effect stopped the NSF Certified Filter after 54 gallons.
Synergistic Heavy Metals Solution Sorbed at 3.78 gpm Fluid Flow
We prepared 20 gallons of filtered tap water containing 27.26ng/ml Lead,
4.12ng/ml Cadmium, and 0.0ng/ml Mercury. *The Lead base normally was
6.05ng/ml *Note: The extra Lead and Cadmium can be attributed to the high
concentration of nitric acid (during storage) dissolved part of the glass
bottle used for sampling. Added: 100ng/ml of Lead, 100ng/ml of Mercury,
100ng/ml Cadmium pure metals dissolved in nitric acid to the prepared 20
gallons. Spike level concentration: 117.89ng/ml Lead, 122.86ng/ml Mercury,
79.44ng/ml Cadmium. The filtered tap water solution further acidified from
6.12-6.90 pH. The mixture was pumped through (2) 12/Pks of discs @ 3.78gpm.
Only 10 gallons of the mixture was used during the first series.
The first sample was taken 65 seconds of 3.78 gpm (14.2 Liters) fluid flow,
which produced 48.52ng/ml Lead filtrate.1
(1) This demonstrated 58.84% Lead reduction.
The third sample was taken after 90 seconds (18.925 + Liters) fluid flow
which produced 44.54 ng/ml Mercury filtrate.3
(3) This demonstrated 63.74% Mercury reduction.
The second sample was taken 85 seconds (18.925 Liters) fluid flow which
produced 29.22ng/ml Cadmium filtrate.2
(2) This demonstrated 63.27% Cadmium reduction.
The next series was to demonstrate how well the (2) 12/Pks, used in the
first test series, would filter during 14 minutes and 16 seconds.
Recirculation of a new additional 10 gallons (unused) of the original
synergistic solution. Flow rate 3.78 gpm. New volume filtered: 53.44
gallons. The fourth test sample was taken for lead (53.44 gals). 28.94ng/ml
Pb=75.45% reduction. The fifth test sample was taken for Mercury (53.44
gals) 48.04ng/ml Hg = 60.89% reduction. The sixth test sample was taken for
Cadmium (53.44 gals) 20.93 ng/ml Cd = 73.65% reduction. There is no
published data on any other filter media that has tested a synergistic
mixture for heavy metals removal under any A.S.T.M. or E.P.A. Standard.
We tested under Clinical Standards for Human Blood and Urine Concentrations
under C.A.P. Regulations (College of American Pathology) in a similar method
to EPA with stricter quality controls on operators, supervisors, and
analytical equipment.
Our media sorbed 222.28ng/ml mixture (Pb, Hg, Cd) @ 3.78 gpm flow rate and
was still able to filter additional heavy metals. We also tested a top rated
filter cartridge certified under NSF Standards 42, 53, 53b, 63 the Ametek
CBR2-10. The Ametek CBR2-10 saturated with 213ng/ml Cadmium only (not the
synergistic mixture) allowing 29.50ng/ml Cadmium to break through the filter
and appear in the filtrate. The Ametek CBR2-10, the best cartridge fijlter
certified by NSF, International, clearly demonstrated the effect of 3.78 gpm
flowrates on van der Waal's Forces which inhibits adsorption.
Lead Controls: 75ng/ml detected as 70.90ng/ml Lead
150ng/ml detected as 157.05ng.ml Lead
Mercury Controls: 10ng/ml detected as 11.16ng/ml Mercury
Dilutions (1:2), 1:5 spike: 20ng/ml detected as 21.83 ng/ml Mercury
Cadmium Controls: 15ng/ml detected as 16.14ng/ml Cadmium
Dilutions (1:2) x3: 30ng/ml detected as 29.88ng/ml Cadmium
Copper Testing at 3.78 gpm Fluid Flow
We prepared 10 gallons (37.85 Liters) NSF filtered tap water. Base level;
105.866ng/ml Copper. Source: Newark City tapwater through copper pipe
7.78pH, Conductivity 135 µSiemens/cm. We added a calculated 600ng/ml of pure
Copper in solution (HCl acid) 718.951ng/ml Copper. We also added a small
quantity of sodium hydroxide to buffer the solution to 8.00 pH. We took (1)
Poly-Filter 12/Pk (dry) and pumped the solution for 17 seconds throught eh
12/Pk, producing 489.04ng/ml filtrate with a 31.97% reduction in Copper and
a 7.76 pH. We then took (2) PolyFilter 12/Pk (dry) and pumped spike solution
for 20 seconds through the (2) 12/Pks, producing 374.09ng/ml filtrate, a
47.96% Copper reduction and a 7.30 pH. The dry filter (disc) media had not
completely wetted during 17-20 seconds of filtration. We next tested 170
grams of a prewetted zeolite synthetic resin for 17 seconds, producing
613.577ng/ml filtrate, a 14.65% Copper reduction, and an 8.80 pH. This
zeolite resin was similar to resins for Iron and Copper used in water
softeners. The last test was a 283 grams of a prewetted carbon/resin run for
30 seconds, producing 575.259ng/ml filtrate, a 19.98% Copper reduction, and
a 7.17 pH. The carbon/resin mix released a large amount of particulate
matter (i.e., carbon dust). During testing: a 1.0µm sterile polyester filter
was placed after the zeolite and carbon/resin filter for particulate control
which may actually have enhanced their sorbent performance.
Copper Controls: 95ng/ml detected as 96.286ng/ml
1100ng/ml detected as 1102.130ng/ml
Analysis Method: Atomic Absorption with chelation-extraction preocess
ASTM D1688-90: Test Method B (2ng/ml -- 500ng/ml) low range
EPA Method 7201: (200ng/ml--5000ng/ml) high range
We prepared 10 gallons of NSF filtered tap water ++ added synthetic sea
(33,000 µSiemens/cm Conductivity), pH 8.18, 31.700ng/ml base Copper level.
Mardel's proprietary chelated Copper sulfate solution, when added, produced
1570.160ng/ml Copper spike solution and a pH 8.19. For this test, we used
(2) 12/Pks and recirculated 5 gals. Of spike solutions for 14 minutes and 16
seconds, which produced 841.85ng/ml filtrate, a 46.38% reduction in chelated
copper, and a 8.50 pH. The solution(s) normal pH range = 8.30-8.50 pH 3.78
gpm x 14 minutes and 16 seconds = = 53.44 gallons total fluid volume passing
through filter media. For a valid comparison of ion-exchange resin behavior
at 3.78 gpm, we doubled the resin volume to 1000ml (filling [2] test
cylinders) + added (1) 1.00µm sterile polyester filter to the bottom of each
cylinder for resin containment. The 5 gallons of spike solution recirculated
for 14 minutes and 16 seconds. The filtrate contained 1365.580ng/ml chelated
Copper, for a reduction of 13.02% chelated copper with a more acidic 7.91
pH. Note: this resin is a commercial product presently selling into the
Aquarium Industry for heavy metals removal. 3.78 gpm x 14 minutes and 16
seconds = 53.44 gallons total fluid volume passing through filter media.
Copper Controls: 650ng/ml detected as 637.270ng/ml
1300ng/ml detected as 1324.660ng/ml
Analysis Method: Atomic Absorption EPA Method 7201
Iron and Zinc Testing at 3.78 gpm Fluid Flow
We prepared 10 gallons (37.85 Liters) NSF filtered tap water containing an
Iron level. Newark City tap water: 6.65 pH, conductivity 122µ/Siemens/cm,
42.923ng/ml Iron. We added 200ng/ml concentration of pure Iron in solution
(Hydrochloric acid) + added 1 milliLiter of NaOH(2.5N) (sodium hydroxide -
electronics grade) to slightly rebuffer to 8.00 pH. The spike solution
contained 272.136ng/ml Iron. We took (1) 12/Pk (prewet) and pumped the
solution through for 34 seconds, which produced 243.485ng/ml Iron filtrate.
This resulted in 10.53% Iron reduction and dropped the pH slightly to 7.86
pH. Next we tested (2) 12/Pks (prewet), pumping the solution for 34 seconds,
which resulted in 214.833ng/ml Iron filtrate, a 21.05% reduction and a drop
in pH to 7.29 pH. This clearly demonstrates a unique property: heavy metals
removal without loading up on dissolved Iron solute. Next, 10 gallons of
synthetic seawater were prepared via NSF filtered tap water containing a
358.09lng/ml base Iron level. These phenomena only occur in low dissolved
solids solutions! For example, when 300ng/ml of Iron is added to synthetic
seawater, 630.282ng/ml total Iron results as the spike concentration. The
same (2) 12Pks (used) sorbed all the soluble Iron within 14 minutes and 16
seconds of filtration (53.44 gallons total volume). The (2) used 12/Pks
reduced the Iron to the 358.091ng/ml Iron base level.
Iron Controls: 450ng/ml detected as 444.06ng/ml
1020ng/ml detected as 1301.40ng/ml
Analysis Method: Atomic Absorption EPA Method 7380
We prepared 10 gallons (37.85 Liters) of NSF Filtered tap water. The Newark
city water contained: 125µ/Siemens/cm, 00.00 zinc, and 6.11 pH. We added 2ml
(NaOH2.5N) as a buffer along with the pure Zinc in solution (HCl acid). This
produced 242.12ng/ml Zinc spike at a 7.09 pH. We took (2) 12/Pks (dry) and
pumped (open system) the solution for 34 seconds, which resulted in
200.62ng/ml filtrate or 17.14% Zinc reduction. The buffer depleted to 6.34
pH. Next, we took te (2) 12/Pks (used) and pumped the remaining 8.10 gallons
for 14 minute and 16 seconds of recirculation filtration (53.44 gallons
total volume). This produced 150.63ng/ml filtrate or a 37.78 Zinc reduction.
The filtrate further acidified to 6.16 pH.
Note: It was noted during additional testing in synthetic seawater that
Zinc, a very reactive metal, prefers to combine and form complexes. When we
formed 140.72ng/ml Zinc spike as part of a synergistic solution of Copper,
Iron, and Zinc. The Zinc was well sorbed 21.57ng/ml Zinc filtrate (84.7%
within 60 seconds) even in a very high TDS situation (33,000µS/cm).
Previously, no Zinc absorption (390.09ng/ml spike solution) had occurred
during a 14 minute and 16 seconds of recirculated synthetic seawater
filtration (386.60ng/ml filtrate).
Zinc Controls: 330ng/ml detected as 337.60ng/ml
EPA Method 7950: 600ng/ml detected as 648.56ng/ml
Atomic Absorption: 150ng/ml detected as 179.02ng/ml
300ng/ml detected as 319.45ng/ml
Volatile Organic Chemicals (VOC's) Background:
For this type of testing, due to the nature of VOC's, one volatile organic
chemical has been picked as a surrogate due to its ubiquitous nature. That
chemical is the trihalomethane Chloroform (CHCl3). Chloroform naturally
forms through the chlorination of organic matter (specifically tannins and
humic acids) the common color agents found in groundwater. Under current
federal regulations 100ng/ml or 100µg/L or 0.100mg/L (weighted average) is
the current action level or allowable limit. Due to the nature of the
regulation, and the weighted average term, levels can be found considerably
higher than the 100ng/ml Chloroform ceiling. The weighted average is done
over four quarters with each week's testing averaged into a month, which is
again averaged and further averaged. Chloroform is a known cancer causing
agent - not a suspected agent.
Testing:
We attempted to filter a Chloroform solution under pressure at our regular
test-flow rates (3.78 gpm); however, due to Chloroform's volatile nature,
much of the Chloroform vaporized during the filtration process. In order to
perform proper filtration, Dr. Abdel-Rahman, Director of UMDNJ's Toxicology
Department and Laboratory devised a method for filtration.
Spike Solution:
Spectrograde Chloroform (highest grade) (68 microliters) was added to 100ml
volumetric flash to make 1mg/ml Chloroform concentration in ethanol. This
was further diluted until 30.28ml of 100µg/ml Chloroform was added to 7.57
Liters of .243µS/cm conductivity (sterile, pyrogen-free) water.
This formed our Chloroform spike solution containing 347.01ng/ml Chloroform.
We added sufficient sodium hydroxide (electronics grade) to the water to
raise the 6.53 pH to 8.00 pH. Very high grade water gives a false or
non-readable pH value.
Our Chloroform spike solution was 347.01ng/ml Chloroform concentration. We
poured this solution through our PMA-1 Assembly filled with only one (1)
12/Pk at maximum gravity flow rate and produced 90.71ng/ml filtrate. Next,
we poured the initial filtrate (90.71ng/ml) through another PMA-1 Assembly
filled with (1) 12/Pk at maximum gravity flow rat and produced 66.39ng/ml
Chloroform concentration filtrate. We estimate the flow rate @
3.785L/minute.
This filter (1) 12/Pk sorbed 73.85% or 256.30ng/ml Chloroform on a single
pass. Under Federal Regulations, for Drinking Water, the spike solution
after passing through (1) 12/Pk was now safe for drinking.
Formation of a Synergistic Solution Comprising Three Metals Copper, Iron,
and Zinc in a Synthetic Seawater Solution.
The three metals copper, Iron, and Zinc had been tested in potable water and
synthetic seawater for reductions during previous filtration tests. In
addition, we tested chelated Copper (Mardel's Copper Safe)
adsorption/absorption under both high and low concentration. We decided to
see if Copper or Iron would act as Lead had done during our previous
synergistic tests.
The Copper Ion was Aldrich Chemical Co. AA/ICP calibration/check standard,
pure dissolved Copper, concentration 1010µG/ML. Lot No. 05224CN.
The Iron Ion was Aldrich Chemical Co. AA/ICP calibration/check standard,
pure dissolved Iron, concentration 1010µg/ml. Lot No. 05212BP.
The Zinc Ion was Aldrich Chemical Co. AA/ICP calibration/check standard,
pure dissolved Zinc, concentration 990µg/ml Lot No. 05313DF.
Note: For information purposes, we should add that the Nalgene tank was
washed with a 10% Nitric Acid solution which was flushed through the entire
test apparatus/system. Next, the system was flushed with D.I. Water
(.243µSiemens/cm conductivity). The Nalgene tank was then flushed with a 10%
HCl solution which ran through the entire system to discharge. Finally,
ultra pure water (0.56µSiemens/cm) was run through the entire system. This
was done after each major metals test - to remove residual contamination.
The system was ready for the synthetic seawater solution which was prepared
as follows: highly filtered tap water (125µ/Siemens/cm) was added to the
Nalgene tank (37.85L0, we added Instant Ocean Salt as per the manufacturer's
literature and stirred with a large acid-washed glass rod for 15 minutes.
Specific gravity was checked via certified hydrometer calibrated at 60
degrees F. When the specific gravity was between 1.023-1.025, we checked the
solution's pH. We found freshly hydrated Instant Ocean normally produced
8.17-8.20 pH on our calibrated daily Orion Research digital ion analyzer
with the probe maintained in standard solution (7.000 pH) between
measurements.