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FAQ
What causes poor chromatogram peak shape when using thermal desorption?
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FAQ
What is the baseline step near the beginning of my GC–MS run?
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FAQ
How can I prevent high air/water background when using a thermal desorber with GC–MS analysis?
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FAQ
How do I convert peak areas into toluene equivalents?
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FAQ
How do I calibrate my analytical system to quantify an analyte collected on a sorbent tube?
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FAQ
What difference does sorbent mesh size make?
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FAQ
What is the cause of extra peaks in my blanks/samples?
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FAQ
What is the cause of poor reproducibility for liquid-loaded standards?
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FAQ
How do I avoid water saturation when carrying out large-volume sampling of humid air?
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