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Bone consists of the protein collagen and the mineral hydroxyapatite,Ca10(PO4)6(OH)2. The content of archaeological humanskeletons measured by graphite furnace atomic absorption shedslight on customs and economic status of individuals in historicaltimes. 37Explain why La3+ is added to bone samples to suppressmatrix interference in Pbanalysis.

Short Answer

Expert verified

La3+ appears to be a releasing agent, as it preferentially reacts with PO42-, releasing Pb2+ .

Step by step solution

01

Define release agent.

A release agent (also known as a release coating, release agent, or mould release coating) is a substance that prevents other materials from adhering to surfaces. Mould release, die-cast release, plastic release, adhesive release, tyre and web release are all procedures where it can help.

02

Explain why La3+  is added to bone samples to suppress matrix interference in  Pb analysis.

To avoid the chemical matrix effect, La3+ is employed. By creating thermally stable compounds, PO42- prevents the atomization of Pb2+ . La3+ appears to be a releasing agent, as it preferentially reacts with PO42- , releasing Pb2+ .

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Most popular questions from this chapter

Quantitative analysis by selected ion monitoring. Caffeine in beverages and urine can be measured by adding caffeine- D3as an internal standard and using selected ion monitoring to measure each compound by gas chromatography. The figure shows mass chromatograms of caffeine (m/z,194)and caffeine-DD3(m-z.197), which have nearly the same retention time.

Suppose that the following data were obtained for standard mixtures:

(a) Compute the mean response factor in the equation

role="math" localid="1664874599903" AreaofanalytesignalAreaofstandardsingle=F(concentrationofanalyteconcentrationofstandard)

(b) For analysis of a cola beverage, 1.000mL of beverage was treated with 50.0ฮผLof standard solution containing 1.11 g/Lcaffeine-D3 in methanol. The combined solution was passed through a solid-phase extraction cartridge that retains caffeine. Polar solutes were washed off with water. Then the caffeine was washed off the cartridge with an organic solvent and the solvent was evaporated to dryness. The residue was dissolved in50ฮผL of methanol for gas chromatography. Peak areas were 1144 for m/z197 and 1733 for m/z194. Find the concentration of caffeine (mg/L ) in the beverage.

28: A limitation on how many spectra per second can be recorded by a time-of-flight mass spectrometer is the time it takes the slowest ions to go from the source to the detector. Suppose we want to scan up to m/z 500. Calculate the speed of this heaviest ion if it is accelerated through 5.00 kV in the source. How long would it take to drift 2.00 m through a spectrometer? At what frequency could you record spectra if a new extraction cycle were begun each time this heaviest ion reached the detector? What would be the frequency if you wanted to scan up to m/z 1000?

The molecular ion region in the mass spectrum of a large molecule, such as a protein, consists of a cluster of peaks differing by 1 Da. This pattern occurs because a molecule with many atoms has a high probability of containing one or several atoms of C1315N,18O,2Hand 32S. In fact, the probability of finding a molecule with only C1214N,16O,1Hand 32S may be so small that the nominal molecular ion is not observed. The electrospray mass spectrum of the rat protein interleukin-8 consists of a series of clusters of peaks arising from intact molecular ions with different charge. One cluster has peaks at m/z 1 961.12, 1 961.35, 1 961.63, 1 961.88, 1 962.12 (tallest peak), 1 962.36, 1 962.60, 1 962.87, 1 963.10, 1 963.34, 1 963.59, 1 963.85, and 1 964.09. These peaks correspond to isotopic ions differing by 1 Da. From the observed peak separation, fi nd the charge of the ions in this cluster. From m/z of the tallest peak, estimate the molecular mass of the protein.

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(b)The vacuum in an orbital mass separator is 1028 Pa. Find the mean free path in the orbital for the same conditions as (a).

Measure the resolving power m/m1/2from the 31Ppeak in Figure 22 10.

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