Table of Contents Specifications ....................................5 General information ..................................6 Safety information ....................................7 Use of hazard information .................................. 7 Precautionary labels ..................................7 Certification ......................................7 Product overview ....................................8 Product components ..................................9 Installation ....................................... 10 Put paper in the printer ..................................10 User interface ....................................
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Table of Contents Clean the sample cell ................................19 Indexing a single sample cell ..............................20 Matching sample cells ................................22 Prepare dilution water ................................24 Prepare the sample ..................................24 Prepare a representative sample .............................. 24 Remove air bubbles from the sample ............................24 Apply a vacuum .................................
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Table of Contents Using a manual flow cell ..............................36 Using an automated flow cell ............................. 36 Measurement notes ................................37 Static or dynamic measurement procedure ........................38 Use a cell adapter ..................................39 Install a cell adapter ................................40 Remove a cell adapter ...............................
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Table of Contents Delete all the ASC data points ..............................50 Maintenance ....................................50 Clean the instrument ..................................50 Change the filter assembly ................................50 Clean the filter assembly .................................. 50 Replace the lamp ..................................... 50 Replace a fuse ....................................53 Troubleshooting ..................................
Safety information on the instrument, will be included with a danger or caution statement in the manual. N O T I C E This symbol, if noted on the instrument, references the instruction The manufacturer is not responsible for any damages due to misapplication or manual for operation and/or safety information.
Installation User interface D A N G E R Figure 4 Keypad Multiple hazards. Only qualified personnel must conduct the tasks described in this section of the document. Put paper in the printer N O T I C E Use only the provided thermal paper. Use of other thermal paper may cause poor print quality and decrease the life of the print-head.
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Table 1 Key descriptions (continued) Figure 5 Indicator lights Description Starts the changing of the sample number shown on the mode display. Selects automatic or manual ranging. Selects the unit of measure. Exits Calibration or Setup mode without saving changes. Turns Ratio on or off.
Table 2 Light descriptions 1. Put the instrument on a stable, level surface that is free of vibration. Do not put in direct sunlight. Light Description 2. Make sure that there is air circulation around the instrument. Keep Illuminated when the instrument light source is on. the back and area below the instrument free of material that could decrease air flow through the vents.
Prepare the StablCal standards Option Description When received and at intervals: Sets the month and day (MM-DD). 1. Clean the exterior surface of the StablCal vials with laboratory glass Sets the year (YY). cleaning detergent. 3. Push ENTER. 2. Rinse the vials with distilled or deionized water. 4.
• All nephelometric (turbidity units of measure) calibrations are done at CAL/Zero after the 4000 NTU standard is measured to complete the the same time. calibration procedure. • Ratio-on and Ratio-off calibration data is measured and recorded at • Clean the USEPA filter assembly before doing a primary calibration, the same time.
7. Use the oiling cloth 8. Put the vial in the 9. Push ENTER. 10. Remove the vial 11. Do steps 5–10 for 12. Push CAL/Zero. to apply the oil equally sample cell holder with from the sample cell the other StablCal vials The instrument display The instrument saves to the surface of the...
Measure the Gelex stray light standard Measure the Gelex stray light standard when the instrument is first received. Record the value on the Gelex vial with a permanent marker one time. 1. Clean the stray light 2. Apply a small bead 3.
Measure the Gelex secondary turbidity standards Measure the Gelex secondary turbidity standards each time the instrument is calibrated and record the new values on the Gelex vials with a water soluble marker. 1. Clean the Gelex 2. Apply a small bead 3.
7. Push RATIO to 8. Put the 0–2 NTU 9. Read the value 10. Record the value 11. Do steps 7–10 for select Ratio on or off. Gelex vial in the sample when stable. Remove on the white diamond the other Gelex vials cell holder with the the vial from the space on the vial using...
2. Fully rinse the sample cell many times with distilled or deionized Clean the sample cell water. C A U T I O N 3. Clean the internal and external surfaces of the sample cell and cap with 1:1 hydrochloric acid. 4.
Indexing a single sample cell When measuring very low turbidity samples, use a single indexed sample cell or a flow cell for all measurements to get precise and repeatable measurements. As an alternative, optically matched sample cells can be used. Refer to Matching sample cells on page 22.
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7. Repeat step 6 until 8. Put an orientation the lowest value is mark on the marking shown on the display. band near the top of the sample cell where the lowest value is shown. English 21...
Matching sample cells To decrease the effects that optical differences among sample cells can have on turbidity, transmittance, color or absorbance measurements, measure samples in matched sample cells. It may not be possible to match all sample cells due to the differences in glass. 1.
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7. Repeat step 6 until 8. Record the value. 9. Put the second 10. Remove the 11. Repeat step 10 12. Put an orientation the lowest value is Put an orientation mark sample cell in the sample cell, turn it until the value matches mark on the marking shown on the display.
The methods typically used for degassing are: Prepare dilution water Dilution water is used when indexing a sample cell or matching sample • Let the sample stand for several minutes cells and to prepare formazin standards. • Apply a vacuum •...
1. Fill a clean sample cell with sample. Do not put the cap on the Note: Warming may change the sample turbidity. Measure the sample without warming when possible. sample cell. Measure over-range samples 2. Put of the sample cell into the ultrasonic bath and let it stand until visible bubbles are removed.
Example: Dilution factor = 100 ÷ 20 = 5 For accurate turbidity readings use clean sample cells and remove air bubbles. Refer to Clean the sample cell on page 19 and Remove air 3. Calculate the actual turbidity: bubbles from the sample on page 24.
• Measure samples immediately to prevent temperature changes and Note: As an alternative, matched sample cells may be used for measurements but do not provide as good of accuracy or precision as a single indexed sample cell or settling. Before a measurement is taken, always make sure that the flow cell.
7. Read and record the value when stable. Note: To print or send (via RS232) a measurement record, push PRINT. Absorbance and transmittance measurement measured on a single sample after setting a zero reference point in one of the three modes. •...
Absorbance and transmittance measurement procedure Note: To measure samples with negative absorbance, set the analytical zero using the sample with the greatest absorbance, and measure the sample with the least absorbance. Report the reading as negative absorbance. 1. Put a clean filter 2.
To make a 15 CU standard, add deionized water on page 5. Use of a Flow Cell is especially important when low-level to 15 mL of the 500 CU standard from Hach until 500 mL. A flow cell color is measured.
Color measurement and calibration procedure 1. Make sure that the 2. Push RANGE to 3. Push SIGNAL AVG 4. Push UNITS/Exit 5. Push CAL/Zero. 6. Using the manual 455 nm filter assembly select manual or to set signal averaging until "CU" is shown on flow cell kit, install the The display shows is installed in the...
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7. Slowly put 250 mL of 8. Push ENTER. 9. Use the arrow keys 10. Slowly put 250 mL 11. Push ENTER. 12. Push UNITS/Exit deionized water down to change the display to of the CU standard in to go back to The instrument display The instrument display the interior edge of the...
Measurement techniques Push SIGNAL AVG to turn signal averaging on or off. The SIGNAL AVG light turns on when signal averaging is on. Measurements may be made with different operation mode settings and Push ENTER when signal averaging is on to erase data in the signal optional accessories.
if interferences caused by color or light absorbing particles are not Figure 8 Standard shop air present. Using the air purge system The air purge system is used to keep condensation off the external surface of the sample cell when cold samples are measured. The air purge system pushes dry air through the optical compartment to keep the outside the sample cell dry.
Install a flow cell 4. Fill the sample cell with distilled or demineralized water and immediately put the caps on the sample cell. 1. Fully clean and assemble the flow cell, tubing and stand. Refer to 5. Clean the inside and outside of the plastic parts and tubing with Clean a flow cell assembly on page 35 and the user instructions laboratory detergent and warm water.
Flow cell storage 2. The flow valve closes when the fill time interval ends. The last portion of sample flowing through the flow cell is held so that sample volume • Install the reservoir cover when the system is not in use to prevent measurements can be made for the selected measurement time.
A fill time setting of 0 seconds causes the instrument to start Select the measurement time measurement immediately. The measurement time is the time interval that the instrument measures the sample. Use the flow cell specifications in Table 3 to calculate the correct fill time. Make sure that the fill time includes time to fill the system and to fully A measurement is completed and the display is updated about once remove the previous sample from the system.
Static or dynamic measurement procedure 1. Push PRINT to turn 2. Install the automated 3. Push FLOW. 4. Push the up and 5. Push ENTER. 6. Push the arrow keys the print interval feature flow cell. Refer to Install down arrow keys to to select the fill time.
7. Push ENTER. 8. Push the arrow keys 9. Push ENTER to 10. When 11. Push and hold the to select the open the flow valve and measurements are valve-control switch to The display shows measurement time. start the fill time complete, push FLOW.
Install a cell adapter N O T I C E Note: Use the application specific calibration (ASC) ability of the instrument to Do not force the cell adapter out of the instrument as serious damage can provide direct reading of results with cell adapters installed. If the ASC ability is not occur.
Connect to a printer or computer Configure the RS232 connection Use the serial interface (RS232) connector on the back of the instrument 1. Push SETUP. The SETUP light turns on. to transmit data from the instrument to an external printer or a serial 2.
Table 5 RS232 command set (continued) Configure the data recorder output Command Description Note: The recorder minimum and maximum values are selected independently for each measurement mode. When the measurement mode changes, the previous Gets the recorder minimum value. settings are automatically used. To change the recorder minimum value, enter RMN=XXXXX (XXXXX=a number, minimum value=0), then push Enter.
Standard Step 1 Step 2 Step 3 stock solution from Hach to make formazin standards. 1000 NTU Add 50 mL of dilution With a TenSette Dilute to the mark Note: As an alternative, a 4000-NTU formazin stock solution that is prepared by water to a clean 100- Pipet, add 25.00 mL...
• Use only the provided silicone oil. This silicone oil has the same • Ratio-on and Ratio-off calibration data is measured and recorded at refractive index as the vial glass and masks minor glass differences the same time. and scratches. •...
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7. Apply a small bead 8. Use the oiling cloth 9. Put the sample cell 10. Push ENTER. 11. Remove the 12. Do steps 5–11 for of silicone oil from the provided to apply the oil in the sample cell sample cell from the the other formazin The instrument display...
Note: Making formazin stock solution from raw materials is not recommended. standards are in the range of: Preparation of formazin stock solution is temperature and technique sensitive. Use Hach formazin stock solution to get the best instrument performance and analytical • 10–30 NTU standard accuracy.
Special research applications Application specific calibration The instrument has special features and operations for special research Nephelometric analysis can result in a calibration curve that is not linear. applications. This instrument can store two application specific caibration (ASC) curves with up to eight data pairs in each. Application specific methods This instrument uses point-to-point interpolation between entered standards for the ASC calibrations.
Either ASC can be changed at any time, so recalibration is not The left digit of the display flashes. necessary. 7. Use the arrow keys to change the number on the display to the The sample is under-range if the display flashes 0s. correct NTU value.
8. Push ENTER to accept the MGL value shown on the display. Note: A print of a graph of the ASC points is also made if the internal printer is enabled. The mode display flashes the next data point (e.g., "05" for data point 4.
Change the filter assembly Delete all the ASC data points Either of the ASC calibration curves can be deleted and the ASC unit N O T I C E name changed back to the factory default. The filter assembly is fragile and must be handled with care to prevent damage. 1.
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Notes: • Turn the instrument on 30 minutes (Ratio on) or 60 minutes (Ratio off) before measurement or calibration. • Replace the lamp with the same size, style and electrical rating • Calibrate the instrument after the lamp is replaced. (4708900).
Troubleshooting Replace a fuse Refer to the tables in this section for error codes, diagnostic codes, D A N G E R common problem messages or symptoms, possible causes and corrective actions. Fire hazard. Use the same type and current rating to replace fuses. Error codes Replacement parts: Table 8...
Table 8 Error codes (continued) Table 8 Error codes (continued) Error Description Solution Error Description Solution ERR03 Low light error ERR10 System voltage out of 1. Put the sample in the instrument again. 1. Turn the instrument off and then back on. range 2.
Table 9 Diagnostic codes (continued) zero using the sample with the greatest absorbance and read the sample with the least absorbance. Record the reading as negative Code Display Description absorbance. Test results are shown. Keyboard test Replacement parts and accessories Test results are shown.
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Replacement parts (continued) Accessories (continued) Description Quantity Item no. Description Quantity Item no. Power cord, European, 230 VAC, VDE Filter assembly, 810 nm 3037600 4683600 approved Filter assembly, 860 nm Printer paper, thermal 4709000 1999900 (specified by ISO 7027 for turbidity measurement) Sample cells, 30mL, 1 in.
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