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Module 8: Applying Chemical Ideas

Quick questions on Colourimetry, UV-vis and AAS explained: HSC Chemistry Module 8

10short Q&A pairs drawn directly from our worked dot-point answer. For full context and worked exam questions, read the parent dot-point page.

What is beer-Lambert law?
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For a solution that absorbs light, the absorbance $A$ is related to the path length $l$ and concentration $c$ by:
What is building a calibration curve?
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1. Prepare standards by serial dilution of a stock solution of the target species. Use at least five standards bracketing the expected concentration range. 2.
What is colourimetry?
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The simplest version. A coloured filter (a piece of coloured glass or plastic) selects a band of visible light a few tens of nanometres wide. A photocell measures the light passing through the cuvette. Suitable for any solution with a visible colour.
What is uV-visible spectrophotometry?
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A more capable instrument. A diffraction grating (monochromator) selects a narrow (about 1 nm) band anywhere from 200 to 800 nm. A photomultiplier or photodiode detector measures the transmitted intensity.
What is atomic absorption spectroscopy (AAS)?
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The technique of choice for trace metal analysis. Three components are unique:
What is forgetting to use $\lambda_{\max}$?
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Sensitivity drops away from the peak; using the wrong wavelength means a worse detection limit and a non-linear plot.
What is not zeroing on a matrix-matched blank?
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If your sample is in acid, your blank should be the same acid. Water-only blanks under-correct.
What is working outside the linear range?
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Beer-Lambert breaks down for $A > 2$. Dilute and re-measure.
What is reusing the wrong lamp on AAS?
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A copper lamp cannot measure lead. The lamp must match the analyte.
What is treating AAS as good for non-metals?
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AAS measures atomic absorption by metal atoms in a flame. It is not used for $Cl^-$, $SO_4^{2-}$ etc.

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