The Keypad ····················································································· 20
Sample Holders················································································ 20
The Display & the Menus ······························································· 21
Looping Menus ················································································ 23
TESTING
Testing Menu ·················································································· 24
Sequences of Tests ··········································································· 25
General Testing Procedures ····························································· 26
Testing With the LaMotte Pre-Programmed Tests ·························· 26
Measuring in the %T/ABS Mode ···················································· 28
1SMART 2 COLORIMETER OPERATOR’S MANUAL
TABLE OF CONTENTS (cont.)
EDITING MENU
Edit a Sequence ·············································································· 30
Adding or Deleting Tests ································································· 31
Edit User Tests ················································································ 34
Naming the Test ·············································································· 35
Selecting the Vial and Wavelength ················································· 37
Entering a New Calibration ···························································· 38
Selecting the Numerical Format of the Result ································ 40
Selecting Units of Concentration····················································· 41
Setting the Clock ············································································· 42
Turning the Data Logger On and Off ·············································· 43
Factory Setup ··················································································· 44
Setting the Power Saver Function···················································· 44
Experienced packaging personnel at LaMotte Company assure adequate
protection against normal hazards encountered in transportation of shipments.
After the product leaves the manufacturer, all responsibility for its safe delivery
is assured by the transportation company. Damage claims must be filed
immediately with the transportation company to receive compensation for
damaged goods.
Should it be necessary to return the instrument for repair or servicing, pack
instrument carefully in suitable container with adequate packing material. A
return authorization number must be obtained from LaMotte Company by
calling 1-800-344-3100. Attach a letter with the authorization number to the
shipping carton which describes the kind of trouble experienced. This valuable
information will enable the service department to make the required repairs
more efficiently.
GENERAL PRECAUTIONS
n
Before attempting to set up or operate this instrument it is important to read
the instruction manual. Failure to do so could result in personal injury or
damage to the equipment.
The SMART 2 Colorimeter should not be stored or used in a wet or corrosive
environment. Care should be taken to prevent water or reagent chemicals from
wet colorimeter tubes from entering the colorimeter chamber.
NEVER PUT WET TUBES IN COLORIMETER.
SAFETY PRECAUTIONS
n
Read the labels on all LaMotte reagent containers prior to use. Some
containers include precautionary notices and first aid information. Certain
reagents are considered hazardous substances and are designated with a * in the
instruction manual. Material Safety Data Sheets (MSDS) are supplied for these
reagents. Read the accompanying MSDS before using these reagents.
Additional emergency information for all LaMotte reagents is available 24
hours a day from the Poison Control Center listed in the front of the phone
book. Be prepared to supply the name and four-digit LaMotte code number
found on the container label or at the top of the MSDS. LaMotte reagents are
registered with a computerized poison control information system available to
all local poison control centers.
Keep equipment and reagent chemicals out of the reach of young children.
Protect Yourself and Equipment: Use Proper Analytical Techniques
LIMITS OF LIABILITY
n
Under no circumstances shall LaMotte Company be liable for loss of life,
property, profits, or other damages incurred through the use or misuse of its
products.
3SMART 2 COLORIMETER OPERATOR’S MANUAL
SPECIFICATIONS
n
n
INSTRUMENT TYPE: Colorimeter
ReadoutGraphical 4 line, 16 character per line LCD
Wavelengths430nm, 520 nm, 570 nm, 620 nm
Wavelength Accuracy± 2 nm
Readable ResolutionDetermined by reagent system
Wavelength Bandwidth10 nm typical
Photometric Range−2 to +2A
Photometric Precision± 0.001Α
Sample ChamberAccepts 25 mm diameter flat-bottomed test tubes, 10
mm square cuvettes, 16 mm COD test tubes
Light Sources4 LEDs
Detectors4 silicon photodiodes with integrated interference
filters
ModesAbsorbance, pre-programmed tests
Pre-Programmed TestsYES, with automatic wavelength selection
User Defined TestsUp to 10 user tests can be input
RS232 Port8 pin mDIN, 9600b, 8, 1, n
Power RequirementsBattery Operation: 9 volt alkaline
Line Operation: 120/220V, 50/60 Hz with adapter
Dimensions (LxWxH)8.5 x 16.2 x 16.7 cm, 3.4 x 6.4 x 2.6 inches
Weight312 g, 11 oz (meter only)
Data Logger350 test results stored for download to a PC
SMART 2 COLORIMETER OPERATOR’S MANUAL4
CONTENTS AND ACCESSORIES
n
n
CONTENTS
SMART 2 Colorimeter
Test Tubes, with Caps
Sample Cell Holder, Universal
Sample Cell Holder, 10 mm Square
Power Cable
Battery Charger
Power Supply, 110/220V
SMART 2 Colorimeter Quick Start Guide
SMART 2 Colorimeter Manual
n
ACCESSORIES
Cigarette Lighter Adapter
Carrying Case
SMARTLink 2 Software with Cable
EPA COMPLIANCE
n
The SMART 2 Colorimeter is an EPA-Accepted instrument. EPA-Accepted
means that the instrument meets the requirements for instrumentation as
found in test procedures that are approved for the National Primary Drinking
Water Regulations (NPDWR) or National Pollutant Discharge Elimination
System (NPDES) compliance monitoring programs. EPA-Accepted
instruments may be used with approved test procedures without additional
approval.
5SMART 2 COLORIMETER OPERATOR’S MANUAL
CE COMPLIANCE
Standards to which
Conformity Declared:
Manufacturer's Name:
Manufacturer's Address:
Type of Equipment:
Model Name:
Year of Manufacture:
Testing Performed By:
Place
Date
Signature
Name
Position
n
The SMART 2 Colorimeter has earned the European CE Mark of Compliance
for electromagnetic compatibility and safety.
SMART 2 COLORIMETER OPERATOR’S MANUAL6
CHEMICAL TESTING
WATER SAMPLING FOR CHEMICAL ANALYSIS
n
n
Taking Representative Samples
The underlying factor to be considered for any type of water sampling is
whether or not the sample is truly representative of the source. To properly
collect a representative sample:
l
Sample as frequently as possible.
l
Collect a large sample or at least enough to conduct whatever tests are
necessary.
l
Make a composite sample for the same sampling area.
l
Handle the sample in such a way as to prevent deterioration or
contamination before the analysis is performed.
l
Perform analysis for dissolved gases such as dissolved oxygen, carbon
dioxide, and hydrogen sulfide immediately at the site of sampling. These
factors, as well as samples for pH, cannot be stored for later examination.
l
Make a list of conditions or observations which may affect the sample.
Other considerations for taking representative samples are dependent
upon the source of the sample. Taking samples from surface waters
involves different considerations than taking samples from impounded and
sub-surface waters.
n
Sampling of Open Water Systems
Surface waters, such as those found in streams and rivers, are usually well
mixed. The sample should be taken downstream from any tributary, industrial
or sewage pollution source. For comparison purposes samples may be taken
upstream and at the source of the pollution before mixing.
In ponds, lakes, and reservoirs with restricted flow, it is necessary to collect a
number of samples in a cross section of the body of water, and where possible
composite samples should be made to ensure representative samples.
To collect samples from surface waters, select a suitable plastic container with a
tight fitting screw cap. Rinse the container several times with the sample to be
tested, then immerse the container below the surface until it is filled to
overflowing and replace the cap. If the sample is not to be tested immediately,
pour a small part of the sample out and reseal. This will allow for any
expansion. Any condition which might affect the sample should be listed.
Sub-surface sampling is required to obtain a vertical profile of streams, lakes,
ponds, and reservoirs at specific depths. This type of sampling requires more
sophisticated sampling equipment.
For dissolved oxygen studies, or for tests requiring small sample sizes, a Water
Sampler (LaMotte Code 1060) will serve as a subsurface or in-depth sampler.
7SMART 2 COLORIMETER OPERATOR’S MANUAL
This weighted device is lowered to the sampling depth and allowed to rest at
this depth for a few minutes. The water percolates into the sample chamber
displacing the air which bubbles to the surface. When the bubbles cease to rise,
the device has flushed itself approximately five times and it may be raised to
the surface for examination. The inner chamber of the sampling device is lifted
out and portions of the water sample are carefully dispensed for subsequent
chemical analysis.
A Snap-Plunger Water Sampler (LaMotte Code 1077) is another “in-depth”
sampling device which is designed to collect large samples which can be used
for a multitude of tests. Basically, this collection apparatus is a hollow cylinder
with a spring loaded plunger attached to each end. The device is cocked above
the surface of the water and lowered to the desired depth. A weighted
messenger is sent down the calibrated line to trip the closing mechanism and
the plungers seal the sample from mixing with intermediate layers as it is
brought to the surface. A special drain outlet is provided to draw off samples for
chemical analysis.
n
Sampling of Closed System
To obtain representative samples from confined water systems, such as pipe
lines, tanks, vats, filters, water softeners, evaporators and condensers, different
considerations are required because of chemical changes which occur between
the inlet and outlet water. One must have a basic understanding of the type of
chemical changes which occur for the type of equipment used. Also,
consideration should be given to the rate of passage and retaining time for the
process water.
Temperature changes play an important part in deciding exactly what test
should be performed. Process water should be allowed to come to room
temperature, 20–25°C, before conducting any tests.
When drawing off samples from an outlet pipe such as a tap, allow sample to
run for several minutes, rinsing the container several times before taking the
final sample. Avoid splashing and introduction of any contaminating material.
FILTRATION
n
When testing natural waters that contain significant turbidity due to suspended
solids and algae, filtration is an option. Reagent systems, whether EPA,
Standard Methods, LaMotte or any others, will generally only determine
dissolved constituents. Both EPA and Standard Methods suggest filtration
through a 0.45 micron filter membrane, to remove turbidity, for the
determination of dissolved constituents.** To test for total constituents,
organically bound and suspended or colloidal materials, a rigorous high
temperature acid digestion is necessary.
**LaMotte offers a filtering apparatus: syringe assembly (Code 1050) and membrane
filters, 0.45 micron, (Code 1103).
SMART 2 COLORIMETER OPERATOR’S MANUAL8
AN INTRODUCTION TO COLORIMETRIC ANALYSIS
n
Most test substances in water are colorless and undetectable to the human eye.
To test for their presence we must find a way to “see” them. The SMART 2
Colorimeter can be used to measure any test substance that is itself colored or
can be reacted to produce a color. In fact a simple definition of colorimetry is
“the measurement of color” and a colorimetric method is “any technique used
to evaluate an unknown color in reference to known colors”. In a colorimetric
chemical test the intensity of the color from the reaction must be proportional
to the concentration of the substance being tested. Some reactions have
limitations or variances inherent to them that may give misleading results.
Many such interferences are discussed with each particular test instruction. In
the most basic colorimetric method the reacted test sample is visually
compared to a known color standard. However, accurate and reproducible
results are limited by the eyesight of the analyst, inconsistencies in the light
sources, and the fading of color standards.
To avoid these sources of error, a colorimeter can be used to photoelectrically
measure the amount of colored light absorbed by a colored sample in reference
to a colorless sample (blank).
White light is made up of many different colors or wavelengths of light. A
colored sample typically absorbs only one color or one band of wavelengths
from the white light. Only a small difference would be measured between white
light before it passes through a colored sample versus after it passes through a
colored sample. The reason for this is that the one color absorbed by the sample
is only a small portion of the total amount of light passing through the sample.
However, if we could select only that one color or band of wavelengths of light
to which the test sample is most sensitive, we would see a large difference
between the light before it passes through the sample and after it passes
through the sample.
The SMART 2 Colorimeter passes one of four colored light beams through one
of four optical filters which transmits only one particular color or band of
wavelengths of light to the photodectector where it is measured. The difference
in the amount of colored light transmitted by a colored sample is a
measurement of the amount of colored light absorbed by the sample. In most
colorimetric tests the amount of colored light absorbed is directly proportional
to the concentration of the test factor producing the color and the path length
through the sample. However, for some tests the amount of colored light
absorbed is inversely proportional to the concentration.
The choice of the correct wavelength for testing is important. It is interesting
to note that the wavelength that gives the most sensitivity (lower detection
limit) for a test factor is the complementary color of the test sample. For
example the Nitrate-Nitrogen test produces a pink color proportional to the
nitrate concentration in the sample (the greater the nitrate concentration, the
darker the pink color). A wavelength in the green region should be selected to
analyze this sample since a pinkish-red solution absorbs mostly green light.
9SMART 2 COLORIMETER OPERATOR’S MANUAL
REAGENT BLANK
n
Some tests will provide greater accuracy if a reagent blank is determined to
compensate for any color or turbidity resulting from the reagents themselves. A
reagent blank is performed by running the test procedure on 10 mL of
demineralized water. Use sample water to SCAN BLANK. Insert the reagent
blank in the colorimeter chamber and select SCAN SAMPLE. Note result of
reagent blank. Perform the tests on the sample water as described. Subtract
results of reagent blank from all subsequent test results. NOTE: Some tests
require a reagent blank to be used to SCAN BLANK.
COLORIMETER TUBES
n
Colorimeter tubes which have been scratched through excessive use should be
discarded and replaced with new ones. Dirty tubes should be cleaned on both
the inside and outside. Fingerprints on the exterior of the tubes can cause
excessive light scattering and result in errors. Handle the tubes carefully,
making sure the bottom half of the tube is not handled.
LaMotte Company makes every effort to provide high quality colorimeter
tubes. However, wall thicknesses and diameter of tubes may still vary slightly.
This may lead to slight variations in results (e.g. if a tube is turned while in the
sample chamber, the reading will likely change slightly). To eliminate this error
put the tubes into the sample chamber with the same orientation every time.
The tubes that are included with the colorimeter have an index mark to
facilitate this. If possible, use the same tube to SCAN BLANK and SCANSAMPLE.
SELECTING AN APPROPRIATE WAVELENGTH
n
The most appropriate wavelength to use when creating a calibration curve is
usually the one which gives the greatest change from the lowest reacted
standard concentration to the highest reacted standard concentration.
However, the absorbance of the highest reacted standard concentration should
never be greater than 2.0 absorbance units. Scan the lowest and highest reacted
standards at different wavelengths using the absorbance mode to find the
wavelength which gives the greatest change in absorbance without exceeding
2.0 absorbance units. Use this wavelength to create a calibration curve.
SMART 2 COLORIMETER OPERATOR’S MANUAL10
Below is a list of suggested wavelengths for the color of the reacted samples.
Use these as a starting point.
Green and Blue620
CALIBRATION CURVES
n
Sample
Color
Yellow430
Pink520
Red570
Wavelength
Range
The SMART 2 Colorimeter contains precalibrated tests for the LaMotte
reagent systems (see Page 45). The first step in using a non-LaMotte reagent
system with your SMART 2 Colorimeter is to create a calibration curve for the
reagent system. To create a calibration curve, prepare standard solutions of the
test factor and use the reagent system to test the standard solutions with the
SMART 2 Colorimeter. Select a wavelength for the test as described above.
Plot the results (in ABS or %Transmittance) versus concentration to create a
calibration curve. The calibration curve may then be used to identify the
concentration of an unknown sample by testing the unknown, reading
Absorbance or %T, and finding the corresponding concentration from the
curve. The linear range of the reagent system can be determined and this
information can be used to input a User Test into the SMART 2 Colorimeter
(see EDIT USER TESTS, page 34).
n
PROCEDURE
1. Prepare 5 or 6 standard solutions of the factor being tested. The
concentration of these standards should be evenly distributed throughout
the range of the reagent system, and should include a 0 ppm standard
(distilled water). For instance, the solutions could measure 0, 10%, 30%,
50%, 70%, and 90% of the system’s maximum range.
2. Turn on the SMART 2 Colorimeter. Select the appropriate wavelength from
the absorbance mode. Be sure to select the appropriate wavelength for the
color produced by the reagent system.
3. Use the unreacted 0 ppm standard to standardize the colorimeter by using it
to scan blank.
4. Following the individual reagent system instructions, react each standard
solution beginning with 0 ppm. Continue with standards in increasing
concentration. Record the reading and the standard solution concentration
on a chart. Readings can be recorded as percent transmittance (%T) or
absorbance (A).
11SMART 2 COLORIMETER OPERATOR’S MANUAL
5. Plot results on graph paper or computer using any available plotting
0
1
10
100
123456
Concentration in ppm
%T vs. Concentration
CALIBRATION CURVE
891070
0.0
0.2
0.4
0.6
0.8
1.0
1.2
1.4
1.6
1.8
2.0
123456
Concentration in ppm
Absorbance vs. Concentration
CALIBRATION CURVE
89107
program. If results are as %T versus concentration, semilog graph paper
must be used. Plot the standard solution concentrations on the horizontal,
linear axis, and the %T on the vertical, logarithmic axis. If results are as
absorbance versus standard solution concentration, simple linear graph
paper can be used. Plot the standard solution concentration on the
horizontal axis, and the absorbance on the vertical axis.
6. After plotting the results, draw a line, or curve, of best fit through the
plotted points. The best fit may not connect the points. There should be
approximately an equal number of points above the curve as below the
curve. Some reagent systems will produce a straight line, while others
produce a curve. Many computer spreadsheet programs can produce the
curve of best fit by regression analysis of the standard solution data.
NOTE: Only reagent systems which produce a straight line can be used for a
User Test.
A sample of each type of graph appears below:
SMART 2 COLORIMETER OPERATOR’S MANUAL12
n
PREPARING DILUTE STANDARD SOLUTIONS
Standard solutions should be prepared to create a calibration curve. Standard
solutions can be prepared by diluting a known concentrated standard by
specified amounts. A chart or computer spreadsheet can be created to
determine the proper dilutions. Use volumetric flasks and volumetric pipets for
all dilutions.
1. In Column A – Record the maximum concentration of test as determined
by the range and path length.
2. In Column B – Record the percent of the maximum concentration the
standard solution will be.
3. In Column C – Calculate the final concentration of the diluted standard
solutions by multiplying the maximum concentration (In Column A) by the
% of maximum concentration divided by 100. (C = A x
B
).
100
4. In Column D – Record the final volume of the diluted sample (i.e. volume
of volumetric flask).
5. In Column E – Record the concentration of the original standard.
6. In Column F – Calculate the milliliters of original standard required
(C x
D
E
= F).
A sample chart appears below:
ABC = A x
B
I 00
DEF = C x
Final
Maximum
concentration
of test
% of
Maximum
concentration
concentration
of Diluted
Standard
Volume of
Standard
Concentration
of Original
Standard
Standard
Required
10.0 ppm909.0 ppm100 mL1000 ppm0.90 mL
10.0 ppm707.0 ppm100 mL1000 ppm0.70 mL
10.0 ppm505.0 ppm100 mL1000 ppm0.50 mL
10.0 ppm303.0 ppm100 mL1000 ppm0.30 mL
10.0 ppm101.0 ppm100 mL1000 ppm0.10 mL
10.0 ppm00 ppm100 mL1000 ppm0 mL
mL of
Original
D
E
STANDARD ADDITIONS
n
A common method to check the accuracy and precision of a test is by standard
additions. In this method a sample is tested to determine the concentration of
the test substance. A second sample is then “spiked” by the addition of a
known quantity of the test substance. The second sample is then tested. The
determined concentration of the spiked sample should equal the concentration
of the first plus the amount added with the spike. The procedure can be
repeated with larger and larger “spikes.” If the determined concentrations do
not equal the concentration of the sample plus that added with the “spike”,
then an interference may exist.
13SMART 2 COLORIMETER OPERATOR’S MANUAL
For example, a 10.0 mL water sample was determined to contain 0.3 ppm iron.
To a second 10.0 mL sample, 0.1 mL of 50 ppm iron standard was added. The
concentration of iron due to the “spike” was (0.10 mL x 50 ppm)/10.0 mL =
0.50 ppm. The concentration of iron determined in the spiked sample should
be 0.3 + 0.5 = 0.8 ppm iron. (Note: any error due to the increased volume from
the “spike” is negligible).
LaMotte offers a line of calibration standards which can be used to generate
calibration curves and perform standard additions.
SAMPLE DILUTION TECHNIQUES
n
& VOLUMETRIC MEASUREMENTS
If a test result using the SMART 2 Colorimeter gives an OVERRANGE message
then the sample concentration could be over range or under range. If it is over
range, the sample must be diluted. Then the test should be repeated on the
diluted sample to obtain a reading which is in the concentration range for the
test. (Note: This is not true for colorimetric determination of pH.)
Example:
Measure 5 mL of the water sample into a graduated cylinder. Add
demineralized water until the cylinder is filled to the 10 mL line. The sample
has been diluted by one-half, and the dilution factor is therefore 2. Perform the
test procedure, then multiply the resulting concentration by 2 to obtain the test
result.
The following table gives quick reference guidelines on dilutions of various
proportions. All dilutions are based on a 10 mL volume, so several dilutions
will require small volumes of the water sample. Graduated pipets should be
used for all dilutions.
Deionized Water to Bring
Size of Sample
10 mL0 mL1
5 mL5 mL2
2.5 mL7.5 mL4
1 mL9 mL10
0.5 mL9.5 mL20
Volume to 10 mLMultiplication Factor
If the above glassware is not available, dilutions can be made with the
colorimeter tube. Fill the tube to the 10 mL line with the sample then transfer
it to another container. Add 10 mL volumes of demineralized water to the
container and mix. Transfer back 10 mL of the diluted sample to the tube and
follow the test procedure. Continue diluting and testing until a reading, which
is in the concentration range for the test, is obtained. Be sure to multiply the
concentration found by the dilution factor (the number of total 10 mL volumes
used).
Example:
10 mL of sample is diluted with three 10 mL volumes of demineralized water;
the dilution factor is four.
SMART 2 COLORIMETER OPERATOR’S MANUAL14
INTERFERENCES
n
LaMotte reagent systems are designed to minimize most common interferences.
Each individual test instruction discusses interferences unique to that test. Be
aware of possible interferences in the water being tested.
The reagent systems also contain buffers to adjust the water sample to the ideal
pH for the reaction. It is possible that the buffer capacity of the water sample
may exceed the buffer capacity of the reagent system and the ideal pH will not
be obtained. If this is suspected, measure the pH of a reacted distilled water
reagent blank using a pH meter. This is the ideal pH for the test. Measure the
pH of a reacted water sample using the pH meter. If the pH is significantly
different from the ideal value, the pH of the sample should be adjusted before
testing.
Interferences due to high concentration of the substance being tested, can be
overcome by sample dilution (see page 14).
STRAY LIGHT INTERFERENCE
n
When scanning samples in 16 mm tubes, such as COD, the sample chamber lid
can not be closed. The COD adapter minimizes stray light. To further reduce
stray light interference, do not scan sample in direct sunlight.
15SMART 2 COLORIMETER OPERATOR’S MANUAL
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