Methods – YSI 910 COD Colorimeter User Manual
Page 6

6
Methods
COD reagents
Select	the	appropriate	vial	for	the	desired	range*:
LR-Range:	
0 – 150 mg/l, part number 251990Y, 25 count
MR-Range:
0 – 1500 mg/l, part number 251991Y, 25 count
HR-Range:
0 – 15000 mg/l, part number 251992Y, 25 count
*Reagents are also availble in 150 count packages.
preparing the sample
Open	a	reaction	vial	with	a	white	cap	and	add	the	specified	volume.		
(Ensure	that	appropriate	personnel	safety	equipment	is	used.)
lr-/Mr: 2 ml water sample
Hr: 0.2 ml water sample
Prepare	a	blank	(Note	1)	by	using	deionized	water	(TOC-free)	instead	of	the	sample	 
(lr/Mr: 2 ml, Hr: 0.2 ml).
Replace	the	cap	tightly.	Invert	the	vial	gently	several	times	to	mix	the	contents	(The	vial	will	become	
hot	during	mixing!)	and	digest	the	vials	for	120	minutes	in	the	reactor	at	a	temperature	of	150°C.	
Remove	the	vials	from	the	reactor	and	allow	them	to	cool	down	to	60°C	or	less.	Mix	the	contents	by	
inverting each vial several times while still warm. Then allow the vials to cool to ambient temperature
before measuring.
Guidelines for photometric measurements
1.
Run samples and blanks with the same batch of vials.
The blank is stable when stored in the dark and can be used for further measurements with vials
from the same batch.
2.
Don‘t	place	hot	vials	in	the	adapter.	Allow	the	vials	to	cool	to	room	temperature	for	 
a minimum 45 minutes. It is recommended to leave the vials to cool over night.
3. suspended solids in the vial lead to incorrect measurements. For this reason it is important to place
the	vials	carefully	in	the	adapter.	The	precipitant	at	the	bottom	of	the	sample	should	not	be	 
suspended.
4.
Clean the outside of the vials with a towel to remove fingerprints or other marks.
5.
Avoid	spillage	of	water	or	reagent	solution	into	the	sample	chamber	because	this	can	lead	to	incor-
rect test results.
6.
Contamination of the transparent cell chamber can result in incorrect readings. Check at regular in-
tervals and – if necessary – clean the transparent cell chamber using a moist cloth or cotton swab.
7.
Large temperature differences between the instrument and the environment can lead to errors –
e.g. due to the formation of condensation in the cell chamber or on the vial.
8.
To avoid errors caused by stray light do not use the instrument in bright sunlight.
