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A sample is analyzed to determine the concentration of an analyte. Under the conditions of the analysis the sensitivity is \(17.2 \mathrm{ppm}^{-1}\). What is the analyte's concentration if \(S_{\text {total }}\) is 35.2 and \(S_{\text {reag }}\) is \(0.6 ?\)

Short Answer

Expert verified
The analyte's concentration is approximately 2.012 ppm.

Step by step solution

01

Understand the formula for concentration

The formula to calculate the concentration of an analyte is given by:\[ \text{Concentration} = \frac{S_{\text{total}} - S_{\text{reag}}}{\text{sensitivity}} \]where \( S_{\text{total}} \) is the total signal, \( S_{\text{reag}} \) is the reagent signal, and sensitivity is given.
02

Substitute the values into the formula

Given values: \( S_{\text{total}} = 35.2 \), \( S_{\text{reag}} = 0.6 \), and sensitivity = 17.2 ppm\(^{-1}\).Substitute these into the formula:\[ \text{Concentration} = \frac{35.2 - 0.6}{17.2} \]
03

Perform the calculation

First, calculate the difference between \( S_{\text{total}} \) and \( S_{\text{reag}} \):\[ 35.2 - 0.6 = 34.6 \]Next, divide the result by the sensitivity:\[ \frac{34.6}{17.2} \approx 2.012 \]
04

Conclude with the solution

The concentration of the analyte is approximately \( 2.012 \) ppm.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Analyte Concentration
An analyte concentration refers to the amount of a substance within a given sample. It's crucial in analytical chemistry to accurately determine the concentration because it provides valuable information about the sample's composition. When assessing concentration, chemists often use signal measurements, as seen in our exercise.

The formula for determining analyte concentration in this context uses three key elements:
  • **Total Signal ( S_{total} ):** This is the overall signal measurement, which includes all contributions from the analyte and other substances in the sample.
  • **Reagent Signal ( S_{reag} ):** This portion of the signal comes from substances other than the analyte, such as reagents or impurities.
  • **Sensitivity:** This is a known constant value indicating how much the signal changes per unit change in the analyte concentration.
To calculate the analyte concentration, subtract the S_{reag} from S_{total} to solely consider the contribution of the analyte, and then divide by the sensitivity. This gives a clear indication of how much analyte is present in terms of its contribution to the overall signal.
Sensitivity
In the context of analytical chemistry, sensitivity is a measure of how effectively a measurement method can detect changes in analyte concentration. It is essentially the relationship between the signal produced and the concentration of the analyte being measured.

Sensitivity is often expressed in units such as ppm, and it dictates how minute changes in concentration can alter the signal. For example, in our exercise, sensitivity is given as 17.2 ppm⁻¹, meaning for every additional ppm of analyte, the signal increases by that factor.

The sensitivity of a measurement can play a significant role in determining the reliability and precision of the results. Higher sensitivity allows for the detection of smaller changes in concentration, making it an important parameter in experiments where precision is needed. Keep in mind, though, that extremely high sensitivity can sometimes also amplify noise in measurements, so balancing it with specificity and accuracy is key.
Signal Analysis
Signal analysis in analytical chemistry involves interpreting the signals received from instruments to deduce meaningful chemical information about a sample. Signals are quantitative measurements that represent the presence or concentration of an analyte.

In signal analysis, one starts by understanding the components of the signals:
  • **Total Signal ( S_{total} ):** This is the combined result from all influencing factors, including the target analyte and background signals.
  • **Reagent Signal ( S_{reag} ):** This represents the signal contribution from reagents or any non-analyte sources in the sample.
When analyzing signals, the main goal is to isolate the analyte's contribution ( S_{analyte} ) from these other components using calculations. In the provided exercise, this is done by subtracting the reagent signal from the total signal.

This clean differentiation ensures the resulting calculation accurately reflects the analyte's concentration. Accurate signal analysis is vital for clear results, helping researchers make informed conclusions about their samples.

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Most popular questions from this chapter

Ibrahim and co-workers developed a new method for the quantitative analysis of hypoxanthine, a natural compound of some nucleic acids. As part of their study they evaluated the method's selectivity for hypoxanthine in the presence of several possible interferents, including ascorbic acid. (a) When analyzing a solution of \(1.12 \times 10^{-6} \mathrm{M}\) hypoxanthine the authors obtained a signal of \(7.45 \times 10^{-5}\) amps. What is the sensitivity for hypoxanthine? You may assume the signal has been corrected for the method blank. (b) When a solution containing \(1.12 \times 10^{-6} \mathrm{M}\) hypoxanthine and \(6.5 \times 10^{-5} \mathrm{M}\) ascorbic acid is analyzed a signal of \(4.04 \times 10^{-5}\) amps is obtained. What is the selectivity coefficient for this method? (c) Is the method more selective for hypoxanthine or for ascorbic acid? (d) What is the largest concentration of ascorbic acid that may be present if a concentration of \(1.12 \times 10^{-6} \mathrm{M}\) hypoxanthine is to be determined within \(1.0 \%\) ?

A certain concentration method works best when the analyte's concentration is approximately 10 ppb. (a) If the method requires a sample of \(0.5 \mathrm{~mL}\), about what mass of analyte is being measured? (b) If the analyte is present at \(10 \% \mathrm{w} / \mathrm{v}\), how would you prepare the sample for analysis? (c) Repeat for the case where the analyte is present at \(10 \% \mathrm{w} / \mathrm{w}\). (d) Based on your answers to parts (a)-(c), comment on the method's suitability for the determination of a major analyte.

An analyst needs to evaluate the potential effect of an interferent, \(I,\) on the quantitative analysis for an analyte, \(A\). She begins by measuring the signal for a sample in which the interferent is absent and the analyte is present with a concentration of 15 ppm, obtaining an average signal of 23.3 (arbitrary units). When she analyzes a sample in which the analyte is absent and the interferent is present with a concentration of \(25 \mathrm{ppm}\), she obtains an average signal of 13.7 . (a) What is the sensitivity for the analyte? (b) What is the sensitivity for the interferent? (c) What is the value of the selectivity coefficient? (d) Is the method more selective for the analyte or the interferent? (e) What is the maximum concentration of interferent relative to that of the analyte if the error in the analysis is to be less than \(1 \% ?\)

When working with a solid sample, often it is necessary to bring the analyte into solution by digesting the sample with a suitable solvent. Any remaining solid impurities are removed by filtration before continuing with the analysis. In a typical total analysis method, the procedure might read After digesting the sample in a beaker using approximately \(25 \mathrm{~mL}\) of solvent, remove any solid impurities that remain by passing the solution the analyte through filter paper, collecting the filtrate in a clean Erlenmeyer flask. Rinse the beaker with several small portions of solvent, passing these rinsings through the filter paper and collecting them in the same Erlenmeyer flask. Finally, rinse the filter paper with several portions of solvent, collecting the rinsings in the same Erlenmeyer flask. For a typical concentration method, however, the procedure might state After digesting the sample in a beaker using \(25.00 \mathrm{~mL}\) of solvent, remove any solid impurities by filtering a portion of the solution containing the analyte. Collect and discard the first several \(\mathrm{mL}\) of filtrate before collecting a sample of \(5.00 \mathrm{~mL}\) for further analysis. Explain why these two procedures are different.

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