Section 9 Contact Information ......................................................................45
4
Section 1Specifications
Specifications are subject to change without notice.
Table 1 Specifications
General
RangeSelectable, 0 to 35, 0 to 70, 0 to 350, 0 to 700 mg/L
3
Dimensions28.9 x 26 x 9.8 cm (11
External power supply
CapacitySix 492 mL bottles
Shipping weight4 kg (8.8 lb)
Operating temperature20 ºC (68 ºF)
Storage temperature0 to 40 ºC (104 ºF)
Input: 110 to 240 V, 50/60 Hz, Output: 24 V, UL CSA, and
TUV approved
Method performance specifications
On a standard containing 150 mg/L each of glucose and
glutamic acid, a single analyst using 6 BODTrak™ II
Precision
Drift Less than 3 mg/L BOD in 5 days
Resolution1 mg/L BOD
instruments and testing 44 samples obtained a mean of
235 mg/L BOD with a 95% confidence limit of distribution
of 11 mg/L or a range of
224 to 246 mg/L BOD.
/8 x 10 ¼ x 3 7/8 inches)
Table 2 Certification
Certification
Hach Company certifies this instrument was tested thoroughly, inspected and found to meet
its published specifications when it was shipped from the factory. The BODTrak II has been
tested and is certified as indicated to the following instrumentation standards:
FCC Part 15, Sub-Part B, Class A Limits: Supporting test records by Intellistor, certified
compliance by Hach Company
Canadian Interference-Causing Equipment Regulation, ICES-003, Class A: Supporting
test records by Intellistor, certified compliance by Hach Company
EN 55011/CISPR 11(EMI) “B” Limits per 89/336/EEC EMC: Supporting test records by
Intellistor, certified compliance by Hach Company
EN 50082-1 (Immunity) per 89/336/EEC EMC: Supporting test records by Hach Company,
certified compliance by Hach Company. Standards include:
•IEC 801-2 and EN 61000-4-2 (ESD)
•IEC 801-3 and EN V50140 (RF & EM Field)
•IEC 801-4 and EN 61000-4-4 (Fast Transient)
•EN 61000-4-5 (Surge)
Warranty: US 1 year; EU 2 year
5
Specifications
Table 2 Certification (continued)
Radio frequency interference
This Class A digital apparatus meets all requirements of the Canadian Interference-Causing
Equipment Regulations. This device complies with Part 15 of the FCC Rules. Operation is
subject to the following two conditions:
(1) This device may not cause harmful interference, and (2) this device must accept any
interference received, including interference that may cause undesired operation.
Warning
Changes or modifications to this unit not expressly approved by the party
responsible for compliance could void the user’s authority to operate the equipment.
This equipment has been tested and found to comply with the limits for a Class A digital
device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide
reasonable protection against harmful interference when the equipment is operated in a
commercial environment. This equipment generates, uses and can radiate radio frequency
energy and, if not installed and used in accordance with the instruction manual, may cause
harmful interference to radio communications. Operation of this equipment in a residential
area is likely to cause harmful interference, in which case the user will be required to correct
the interference at their own expense. Shielded cables must be used with this unit to ensure
compliance with the Class A FCC limits. Because this instrument operates on and
generates radio frequency energy, interference to radio and television reception may occur.
If such interference does occur, the operator should take the necessary steps to correct the
interference. The following techniques of reducing the interference problems are easily
applied:
•Disconnect power from the BODTrak II instrument to verify the instrument is
the source of the interference.
•If the BODTrak II is plugged into the same outlet as the device with which it is
interfering, try another outlet.
•Move the BODTrak II away from the device receiving the interference.
•Reposition the receiving antenna for the device receiving the interference.
•Try combinations of the above.
6
Section 2General information
2.1Safety information
Please read this entire manual before unpacking, setting up or operating this
equipment. Pay attention to all danger and caution statements. Failure to do so
could result in serious injury to the operator or damage to the equipment.
Make sure that the protection provided by this equipment is not impaired, do not
use or install this equipment in any manner other than that specified in this manual.
2.1.1Use of hazard information
DANGER
Indicates a potentially or imminently hazardous situation which, if not
avoided, will result in death or serious injury.
WARNING
Indicates a potentially or imminently hazardous situation which, if not
avoided, could result in death or serious injury.
CAUTION
Indicates a potentially hazardous situation that may result in minor or
moderate injury.
Important Note: Indicates a situation which, if not avoided, may cause damage to
the instrument. Information that requires special emphasis.
Note: Information that supplements points in the main text.
2.1.2Precautionary labels
Read all labels and tags attached to the instrument. Personal injury or damage to
the instrument could occur if not observed. A symbol, if noted on the instrument, will
be included with a danger or caution statement in the manual.
This symbol, if noted on the instrument, references the instruction manual for
operation and/or safety information.
Electrical equipment marked with this symbol may not be disposed of in
European public disposal systems after 12 August of 2005. In conformity with
European local and national regulations (EU Directive 2002/96/EC), European
electrical equipment users must now return old or end-of life equipment to the
Producer for disposal at no charge to the user.
Note: For return for recycling, please contact the equipment producer or supplier
for instructions on how to return end-of-life equipment, producer-supplied
electrical accessories, and all auxiliary items for proper disposal.
7
General information
2.2Theory of operation
Respirometric Biochemical Oxygen Demand (BOD) is a test done at 20 °C (68 °F)
in a controlled environment. The test period can be 5, 7 or 10 days, contingent on
the analysis or protocol. The BOD test measures the quantity of oxygen consumed
by bacteria that oxidize organic matter in a water sample. The test is used to
measure waste loadings at wastewater treatment plants and to examine the
efficiency of wastewater treatment.
BOD test results help find general oxygen uptake patterns. This lets operators
estimate plant operating efficiency and find correct treatment procedures.
Advantages to the BODTrak™ II as an alternative to the dilution method are:
•Minimal time to prepare a sample.
•Decreased total test time.
•The BODTrak II method gives results comparable to the diluton method (BOD5)
in 2 to 3 days.
•Calibration and dissolved oxygen measurement are not necessary.
•The BODTrak II test is easy to monitor.
•The sample is stirred constantly and kept in natural conditions. This makes the
BODTrak II results similar to occurrences found in a natural environment. The
dilution method supplies no additional oxygen to the sample. This causes a
higher percentage of oxygen depletion and possible retardation of biochemical
reactions.
•The BOD can be monitored at any time because the instrument continuously
shows the BOD result. Pressure changes in the closed BODTrak II system are
shown graphically in milligrams per liter (mg/L) on an LCD. The system supplies
360 uniform data points over the selected time period.
•The BODTrak II system continuously removes carbon dioxide from the system
so that the pressure difference monitored is proportional to the quantity of
oxygen used.
•Degassing can cause negative errors when heat is applied to a sample to
achieve experimental temperature. The BODTrak II adjusts for this occurrence.
The BODTrak II does not start the test until the temperature gets to equilibrium.
2.2.1Oxygen transfer to sample
Bacteria in the sample use oxygen while consuming organic matter in the sample
bottles. The air in the bottle above the sample contains 21% oxygen and
replenishes the dissolved oxygen used by the bacteria. During the test period, stir
bars continually mix the sample in each bottle. This moves oxygen from the air to
the sample and helps simulate natural conditions.
8
General information
2.2.2Pressure sensor function
The BODTrak II is sealed to prevent external atmospheric pressure changes in the
test bottle. Pressure sensors monitor air pressure in the sample bottles. When
oxygen is consumed, the pressure in the bottle head space drops. The pressure
drop correlates directly to BOD.
2.2.3Removing carbon dioxide
Carbon dioxide is made when microorganisms oxidize organic matter in the
sample. The carbon dioxide must be removed from the system so it does not
interfere with the measurement. Potassium hydroxide pellets put in the seal cup of
each sample bottle before the test remove the carbon dioxide.
9
10
Section 3Installation
3.1Component list
Compare each item below to the items in the shipment. If an item is missing or
damaged, refer to the manufacturer.
•BODTrak™ II instrument
•A UL/CSA approved 115 VAC power cord with a NEMA 5-15P style plug
•A 230 VAC harmonized power cord with a continental European plug
•Power supply, auto–switching between 115 V and 230 V
•6 seal cups
•6 BODTrak II amber sample bottles
•6 BODTrak II magnetic stir bars
•Spatula scoop
•One package nutrient buffer solution pillows
•One container potassium hydroxide pellets
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Installation
3.2Electrical installation
The power adaptor supplies AC power to the IEC universal connector (Figure 1).
The power switch powers the instrument on and off.
Figure 1 External connections
1 Power switch3 RS232 connector
2 IEC universal connector
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Section 4Operation
4.1Operational controls
The BODTrak™ II operator controls are shown in Figure 2.
The display shows a graph of BOD values on the vertical axis and time in days on
the horizontal axis. Push the left and right arrow keys to move the cursor along the
BOD curve to show the approximate coordinates (time, BOD) of the selected data
point.
The time interval and BOD value of the data point are shown in the lower right of
the display. The cursor is automatically placed at the most recently collected data
point in a channel display.
Push and hold the two arrow keys at the same time to go into the instrument setup
menu. The arrow keys are also used to change the time, date, test length and
range.
4.1.3The ON key
To access the range selection menu, push the ON key from a channel display
screen. Then push and hold the ON key to start the test for the selected channel.
4.1.4The OFF key
When a test is in DELAY or RUN modes, pushing and holding the OFF key
manually ends the test. The instrument will display END. The OFF key is also used
to exit the instrument setup menu or range selection menu. Any changes made
prior to exit will be saved.
4.2Bottle connections
Each bottle position/channel has the applicable tube numbered with a plastic
sleeve. The bottle positions are numbered 1 though 6 with number 1 in the back left
corner of the chassis. Use the channel selection keys as a guide.
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