I'm currently working on a new lead based alloy. I'm planning to use a Spark-OES for quick turnaround analysis and an ICP-OES for verification. I did a few test runs on the ICP-OES using a few of our Spark-OES's certified reference material (CRM) to see if there's a significant difference between the two. By and large, the results for most of the elements jive, except for sulfur (for example the CRM with S of 13 ppm reads on the Spark-OES as 13+0.4 ppm and ~200 ppm at the ICP-OES). I was thinking that this might be because of interference with another element, based on our lab's reference (A Manual for the Chemical Analysis of Metals, Thomas R. Dulski) errors due to digestion would translate to lower ICP-OES readings. ICP-OES wavelength tables I've found indicate that arsenic and manganese has the closest wavelengths for the intensity setting we use. Any help on eliminating or minimizing interference would be greatly appreciated. The digestion method used for the ICP-OES sample preparation is as follows: 1g sample, 10 ml deionized water + 10 ml HNO3. I'm hesitant to use hydro-halide acids because they will precipitate some of the tested elements. Elements tested for were Pb, Sn, As, Sb, Ca, Al, Fe, Na, Cr, S, Mn, Se, and Te

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