Owner's manual
Table Of Contents
- 1 Overview
- 2 Safety instructions
- 3 Commissioning
- 4 Operation
- 4.1 Switching on or off the photometer
- 4.2 General operating principles
- 4.3 Photometer settings and system administration
- 4.4 Zero adjustment
- 4.5 Measuring in Concentration mode
- 4.5.1 Measuring cell tests with barcode
- 4.5.2 Measuring reagent tests with AutoSelector
- 4.5.3 Measuring reagent-free tests and user-defined methods
- 4.5.4 Exceeding the upper or lower limits of the measuring range
- 4.5.5 Selecting a method manually
- 4.5.6 Settings for Concentration mode
- 4.5.7 Measuring diluted samples
- 4.5.8 Sample blank value
- 4.5.9 Reagent blank value
- 4.5.10 Automatic Turbidity correction
- 4.5.11 Programming / modifying user-defined methods
- 4.5.12 The IQ LabLink procedure
- 4.6 Measuring the Absorbance / % Transmission
- 4.7 Multi wavelengths methods
- 4.8 Spectrum
- 4.9 Kinetics
- 4.10 Timer
- 4.11 Memory
- 4.11.1 Overview
- 4.11.2 Instructions on using USB memory devices
- 4.11.3 Measurement datasets
- 4.11.4 Saving measurement datasets manually
- 4.11.5 Saving measurement datasets automatically
- 4.11.6 Displaying measurement data memory
- 4.11.7 Filtering measurement datasets
- 4.11.8 Inverting filters
- 4.11.9 Erasing stored measurement datasets
- 4.12 Copying files
- 4.13 Transmitting data
- 4.14 Analytical quality assurance (AQA)
- 4.15 User management
- 4.16 Reset
- 4.17 Photometer information ([Info])
- 4.18 Lamp counter
- 4.19 Software and methods update
- 5 Maintenance and cleaning
- 6 What to do if ...
- 7 Technical data
- 8 Accessories and options
- Appendix
Operation photoLab
®
6100 VIS
64
ba75847e01 08/2009
Variant 1:
Measure standard
solutions
1 Select and confirm Measure
standard solutions.
2 Enter and confirm details of the
standard solutions (optional).
3 Using [Next], accept all entries on
the page and switch to the next
page.
The table for the measurement of
standard solutions pops up.
In the first two lines of the table,
the two value pairs (measuring
points) that are at least required
for a calibration are already
prepared (reagent blank value E0
and any further nominal value).
4 Create further values pairs with
[Add] as necessary.
You can delete a highlighted value
pair with [Delete].
5 In the Target value column, enter
the nominal values of the
individual standard solutions.
Measuring the standard solutions:
6 Using the arrow keys <▲><▼>
and <W><X>, navigate to the
relevant input field in the
Absorbance column and press
<START·ENTER>.
Edit method
04/16/07 9:52
Standard ID
Standard manufacturer
Back Next
Edit method
04/16/07 9:52
Tar g et va lue Abs o r b ance
E0 0.000
1
Back Add Delete Next
Edit method
04/16/07 9:52
Tar g et va lue Abs o r b ance
E0 0.000
1 0.300
2 0.600
3 1.000
Back Add Delete Next
Edit method
04/16/07 9:52
Tar g et va lue Abs o r b ance
E0 0.000
1 0.300
2 0.600
3 1.000
Back Add Delete Next