
Cobalt solution check Photometric linearity check
If thephotometric linearity of the instrumentis
questionable,first checkyour analyticalprocedureand
technique(seeTechniquesonpage2-2). Ifproper
operationis still in doubt,usethePhotometric
Accuracy/linearity Testfrom SPECTRONIC8'
Standards(Cat.No. 333150) to testandevaluate
photometric performanceof your instrument.
To preparea stock cobaltsolution:
I. In a I-liter volumetric flask,place 200 mL distilled
water. Slowly and cautiouslyadd 10mL
concentratedhydrochloric acid (ACS grade). Mix
andmaketo volume with distilled waterto obtain
I% hydrochloric acid solution.
2. In a I-liter volumetric flask, place 22 to23 gm
cobaltchloride (CoC~, ACS grade).Dissolve in the
I% hydrochloric acid. Make to volume with 1%
hydrochloric acid to obtain cobaltchloride stock
solution.
Thealternatemethodbelowusesspeciallyprepared
potassiumdichromatesolutions.
To performthe cobalt solutioncheck:
I. Turn onthe PowerSwitch/Zero Control and allow
the instrumentto warm up for atleast15minutes.
2. If youhaveaSPECTRONIC" 20D or 20D+,setthe
displaymodeto Transmittance.
3. With the samplecompartmentemptyandthe cover
closed,adjustthe PowerSwitch/Zero Control until
the meteror displayreadsO%T.
4. SettheWavelength Control to 500nm.
5. Setthe Filter Leverto 340-599nm.
6. Inserttheglasswarefilled with distilled waterinto
thesamplecompartmentandusethe
Transmittance!Absorbance Control to setthe meter
or display to lOO%T.
7. Replacethedistilled water with the cobaltchloride
solution.
8. Insertthe glasswarefilled with the cobaltchloride
solutioninto the samplecompartment.
9. Read%T onthe meteror display.
10. Repeatsteps4 through 9 at505,510,515 and
520 nm. The instrumentis in proper calibration
whenminimum transmittance(maximum
absorbance)occurs between505 and515 nm. The
specifictransmittance (or absorbance)valuesare
unimportant.
Wavelength calibration adjustment
If the wavelength accuracyis out of tolerance,referto
theService Procedure sectiononpage3-5. Customer
recalibrationis notrecommended.
I. Turn onthe PowerSwitch/Zero Control and allow
the instrumentto warm up for at least 15minutes.
2. Make surethatthe samplecompartmentis empty
andthe coveris closed,then adjustthe Power
Switch/Zero Control until the displayreadsO%T.
3. If youhaveaSPECTRONICII200 or 200+, setthe
displaymode to Absorbance.
4. Prepare O.OINsulfuric acid diluent by adding0.3mL
of concentratedsulfuric acid to about500mL of
deionized or distilled water in a clean IL volumetric
flask. Fill to volume with deionized or distilled
water.
5. Preparea stocksolutionof potassiumdichromateby
weighing 0.500gof potassiumdichromate(e.g.,
FisherCertified A.C.S. potassiumdichromate,
formula weight294.19) anddissolving it in about
400mL ofO.OIN sulfuric acid solution in a 500mL
volumetric flask. Fill to volume with O.OINsulfuric
acid solution. This is your stock 1.0g/L potassium
dichromatesolution.
6. Measure2.5mL of the stock 1.0g/L potassium
dichromatesolutioninto a clean lOOmLvolumetric
flaskcontaining about75mL O.OINsulfuric acid
solution. Fill tovolume with O.OINsulfuric acid
solution. This is your 0.025g/L potassium
dichromatesolution.
7. Measure5.0mL of the stock 1.0g/L potassium
dichromatesolution into a clean lOOmLvolumetric
flaskcontaining about75mL O.OINsulfuric acid
solution. Fill tovolume with O.OINsulfuric acid
solution. This is your0.05g/L potassiumdichromate
solution.
8. SettheWavelength Control to350nm.
9. SetFilter Leverto 340 -950nm.