Calibration issues Al, Na & Si

Hi,

I'm having some persistent calibration issues for an ICP-OES analyzing Al, Ca, Fe, K, Na, Ni, P, Si, V & Zn in the range of 0.05 - 1 ug/mL.

The following lines (Al 237.312, Si 185.005 and Na 589.592  nm) keep failing the calibrations due to lowered measured concentration in the highest standard (should be 1 ppm but is measured at about 0.75-0.80).

The standards are prepared using a multi-element standard containing all 10 elements at the same concentration, they are all prepared in 9% HNO3, matched with the acid content of digested samples measured with this method.
The concentrations are as follows:

Blank
0.05 ppm
0.10 ppm
0.5 ppm
1.0 ppm

For the lines mentioned above, the highest standard repeatedly falls well below the actual concentration, the calibration standards were prepared 3 times, all with comparable results. I suspect the issue to either stem from the sample introduction or the optics, as all other elements form valid calibrations over the whole range.

What could be the usual culprits in this case? The pump tubing has just been replaced, as well as the axial pre-optics window. Both the nebulizer and spray chamber have been cleaned somewhat recently, but will give them a clean next week to be sure. I was wondering if the torch could also have an influence on this. Although it is cleaned every month or so with aqua regia, there are soms signs of devitrification and an unknown brown stain that does not come of with acid or alkaline detergent.

Any tips, pointers and idea's as to what may be causing this issue are more than welcome!

Parents
  • Additional info:

    I prepare the 9% HNO3 solution in a 1 L glass bottle using trace analysis grade nitric and ultra pure water. I know one should avoid glass when measuring Si but by using the same bottle and keeping the contact time as short as possible the blank levels remain low.

    Standards are prepared in PMP volumetric flasks and are then transferred to 50 mL Perkin Elmer DigiTubes. After preparation the flasks and caps are leached with ~5% nitric acid in a stove at 40C for about 8 hours to overnight. Any glass containers used in standard preparation are leached similarly as well.

    If more info is needed please do tell!

Reply
  • Additional info:

    I prepare the 9% HNO3 solution in a 1 L glass bottle using trace analysis grade nitric and ultra pure water. I know one should avoid glass when measuring Si but by using the same bottle and keeping the contact time as short as possible the blank levels remain low.

    Standards are prepared in PMP volumetric flasks and are then transferred to 50 mL Perkin Elmer DigiTubes. After preparation the flasks and caps are leached with ~5% nitric acid in a stove at 40C for about 8 hours to overnight. Any glass containers used in standard preparation are leached similarly as well.

    If more info is needed please do tell!

Children
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