Metrohm 746 VA Trace Analyzer User Manual

Page 535

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7 Safety, Errors, Troubleshooting, Diagnosis, GLP

746 VA Trace Analyzer / 747 VA Stand

7-36

Peak displacement

•

Check and adjust the pH of the solution.

•

Check electrolyte composition and correct if necessary. Use a buffer solution

instead of an acid.

•

Carry out a standard addition to check whether the correct peak has been

evaluated.

•

Organic components interfere with the analysis: carry out a UV digestion or

other suitable sample preparation.

• Enter a new half-wave potential in the instrument and recalculate the results.

•

Check reference electrode (see section 3.6).

No peak found

•

The peak is only displaced: adjust the half-wave potential and recalculate the

results.

•

The sample concentration is too low: increase the sample volume or the

amount of sample.

•

The concentration of the ion to be determined is too low: use HMDE (inverse

voltammetry) instead of DME or SMDE.

•

Are the initial and final potentials correct?

Peak is in the highest

µ

A range

•

The concentration of the ion to be determined is too high: reduce the sample

volume and carry out the analysis again.

•

The preconcentration time under

MEAS

is too high, reduce it and try the

analysis again.

Double peak

•

Check MME. If necessary, change capillary (see section 3.4.8) or replace

sealing needle (see section 3.4.9).

•

Organic components interfere with the analysis: carry out a UV digestion or

other suitable sample preparation.

•

If a second element is present at the same potential: add this element to the

sample and carry out the analysis again. If the second peak has become

higher then the second element is present.

•

Has any substance been precipitated out in the measuring vessel (e.g. lead

perchlorate standard with KCl as electrolyte)?

•

Try out eluents with different compositions (addition of complex formers).

•

Check analysis parameters.

•

Try another measurement mode like AC1. If one substance is reversible and

the second one irreversible, only the reversible substance is detected by

AC1.

Standard addition peaks displaced

•

Standard solutions have been made too acidic.

•

Buffering capacity of the electrolyte is not sufficient: increase electrolyte vol-

ume.

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