/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 37 The concentration of \(\mathrm{N... [FREE SOLUTION] | 91Ó°ÊÓ

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The concentration of \(\mathrm{Na}\) in plant materials are determined by flame atomic emission. The material to be analyzed is prepared by grinding, homogenizing, and drying at \(103^{\circ} \mathrm{C}\). A sample of approximately \(4 \mathrm{~g}\) is transferred to a quartz crucible and heated on a hot plate to char the organic material. The sample is heated in a muffle furnace at \(550^{\circ} \mathrm{C}\) for several hours. After cooling to room temperature the residue is dissolved by adding \(2 \mathrm{~mL}\) of \(1: 1 \mathrm{HNO}_{3}\) and evaporated to dryness. The residue is redissolved in \(10 \mathrm{~mL}\) of \(1: 9 \mathrm{HNO}_{3},\) filtered and diluted to \(50 \mathrm{~mL}\) in a volumetric flask. The following data are obtained during a typical analysis for the concentration of \(\mathrm{Na}\) in a \(4.0264-\mathrm{g}\) sample of oat bran. $$ \begin{array}{lcc} {\text { sample }} & \mathrm{mg} \mathrm{Na} / \mathrm{L} & \text { emission (arbitrary units) } \\ \hline \text { blank } & 0.00 & 0.0 \\ \text { standard 1 } & 2.00 & 90.3 \\ \text { standard } 2 & 4.00 & 181 \\ \text { standard } 3 & 6.00 & 272 \\ \text { standard } 4 & 8.00 & 363 \\ \text { standard } 5 & 10.00 & 448 \\ \text { sample } & & 238 \end{array} $$ Report the concentration of sodium in the sample of oat bran as \mug Na/g sample.

Short Answer

Expert verified
The concentration of sodium in the oat bran sample is approximately 65.9 µg Na/g sample.

Step by step solution

01

Plot a Calibration Curve and Determine Line Equation

First, we plot a calibration curve using the given standard data: | mg Na/L | Emission ||---------|----------|| 0.00 | 0.0 || 2.00 | 90.3 || 4.00 | 181 || 6.00 | 272 || 8.00 | 363 || 10.00 | 448 |A linear regression on these points yields the equation of the line: \[y = 44.8x\]where **y** is the emission (arbitrary units) and **x** is the concentration in mg Na/L.
02

Determine Sodium Concentration in Sample Solution

Now that we have the calibration curve equation, we'll use it to find the concentration of Na in the sample. The sample emission is 238 arbitrary units.Using the line equation: \[238 = 44.8x \]Solve for **x**:\[x = \frac{238}{44.8} \approx 5.31 \text{ mg Na/L}\]
03

Convert Sodium Concentration to µg Na/g Sample

The concentration obtained from the emission is in mg Na/L for the sample solution. We need to convert it to µg Na/g sample. The sample of oat bran is diluted to a volume of 50 ml = 0.050 L. Therefore, the total mass of Na in the solution is:\[\text{Total mass} = 5.31 \text{ mg/L} \times 0.050 \text{ L} = 0.2655 \text{ mg}\]Convert this mass into micrograms (µg): \[0.2655 \text{ mg} = 265.5 \text{ µg} \]Since the sample mass is 4.0264 g, the concentration in the sample is:\[\frac{265.5 \text{ µg}}{4.0264 \text{ g}} \approx 65.9 \text{ µg Na/g sample}\]

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Key Concepts

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

Calibration Curve
In Flame Atomic Emission Spectroscopy, the calibration curve is a crucial tool used to determine the concentration of an element in a sample. This curve is created by plotting known concentrations (standards) of an element against their corresponding emission values. In our case:

- We have data points with known mg Na/L and their respective emission values in arbitrary units.
- By plotting these points on a graph, a linear relationship can be established. This is often represented by a straight line.
- The equation of this line is critical as it allows us to find unknown concentrations by inputting the sample's emission value.

The calibration curve obtained was a linear equation: \[ y = 44.8x \]where **y** is the emission value and **x** is the concentration in mg Na/L. This equation helps to translate emission values directly into concentrations.
Sodium Concentration
Once the calibration curve is established, determining the sodium concentration in the sample becomes straightforward. For the oat bran sample, its emission value is given as 238 arbitrary units. Using the line equation from the calibration curve:\[ 238 = 44.8x \]we solve for **x** to find the concentration of sodium in the sample solution.

Solving gives us:\[ x = \frac{238}{44.8} \approx 5.31 \text{ mg Na/L} \]

This concentration represents how much sodium is present in each liter of the prepared sample solution. However, to understand the amount of sodium per unit of oat bran (the actual sample), further conversion is necessary.
Sample Preparation
Sample preparation is an often overlooked but fundamental step in obtaining accurate results in Flame Atomic Emission Spectroscopy. In our exercise, the oat bran is thoroughly prepped before analysis:

- The plant material is first ground, homogenized, and then dried to ensure consistency.
- A sample is charred and ashed to decompose organic material, leaving behind an inorganic residue.
- This residue needs to be dissolved and diluted. It's initially mixed with nitric acid (HNO₃) and then converted to a solution with precise volume.

This meticulous preparation is crucial to reduce errors and ensure that the sodium measured is accurately representative of the sample. It allows us to relate the concentration of sodium in the solution back to the actual sample, leading to the final concentration expressed as micrograms \( \text{µg Na/g sample} \). Proper preparation ensures reproducibility and accuracy.

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Most popular questions from this chapter

A spectrophotometric method for the analysis of iron has a linear calibration curve for standards of \(0.00,5.00,10.00,15.00,\) and 20.00 \(\mathrm{mg} \mathrm{Fe} / \mathrm{L}\). An iron ore sample that is \(40-60 \% \mathrm{w} / \mathrm{w}\) is analyzed by this method. An approximately \(0.5-\mathrm{g}\) sample is taken, dissolved in a minimum of concentrated HCl, and diluted to \(1 \mathrm{~L}\) in a volumetric flask using distilled water. A \(5.00 \mathrm{~mL}\) aliquot is removed with a pipet. To what volume- \(10,25,50,100,250,500,\) or \(1000 \mathrm{~mL}\) - should it be diluted to minimize the uncertainty in the analysis? Explain.

A solution's transmittance is \(35.0 \%\). What is the transmittance if you dilute \(25.0 \mathrm{~mL}\) of the solution to \(50.0 \mathrm{~mL}\) ?

Bonert and Pohl reported results for the atomic absorption analysis of several metals in the caustic suspensions produced during the manufacture of soda by the ammonia-soda process. \(^{31}\) (a) The concentration of Cu is determined by acidifying a \(200.0-\mathrm{mL}\) sample of the caustic solution with \(20 \mathrm{~mL}\) of concentrated \(\mathrm{HNO}_{3}\), adding \(1 \mathrm{~mL}\) of \(27 \% \mathrm{w} / \mathrm{v} \mathrm{H}_{2} \mathrm{O}_{2},\) and boiling for \(30 \mathrm{~min} .\) The resulting solution is diluted to \(500 \mathrm{~mL}\) in a volumetric flask, filtered, and analyzed by flame atomic absorption using matrix matched standards. The results for a typical analysis are shown in the following table. $$ \begin{array}{ccc} \text { solution } & \mathrm{mg} \mathrm{Cu} / \mathrm{L} & \text { absorbance } \\ \hline \text { blank } & 0.000 & 0.007 \\ \text { standard } 1 & 0.200 & 0.014 \\ \text { standard } 2 & 0.500 & 0.036 \\ \text { standard } 3 & 1.000 & 0.072 \\ \text { standard } 4 & 2.000 & 0.146 \\ \text { sample } & & 0.027 \end{array} $$ Determine the concentration of \(\mathrm{Cu}\) in the caustic suspension. (b) The determination of \(\mathrm{Cr}\) is accomplished by acidifying a \(200.0-\mathrm{mL}\) sample of the caustic solution with \(20 \mathrm{~mL}\) of concentrated \(\mathrm{HNO}_{3}\), adding \(0.2 \mathrm{~g}\) of \(\mathrm{Na}_{2} \mathrm{SO}_{3}\) and boiling for \(30 \mathrm{~min}\). The Cr is isolated from the sample by adding \(20 \mathrm{~mL}\) of \(\mathrm{NH}_{3}\), producing a precipitate that includes the chromium as well as other oxides. The precipitate is isolated by filtration, washed, and transferred to a beaker. After acidifying with \(10 \mathrm{~mL}\) of \(\mathrm{HNO}_{3}\), the solution is evaporated to dryness. The residue is redissolved in a combination of \(\mathrm{HNO}_{3}\) and \(\mathrm{HCl}\) and evaporated to dryness. Finally, the residue is dissolved in \(5 \mathrm{~mL}\) of \(\mathrm{HCl}\), filtered, diluted to volume in a 50 -mL volumetric flask, and analyzed by atomic absorption using the method of standard additions. The atomic absorption results are summarized in the following table. $$ \begin{array}{lcc} {\text { sample }} & \mathrm{mg} \mathrm{Cr}_{\text {added }} / \mathrm{L} & \text { absorbance } \\ \hline \text { blank } & & 0.001 \\ \text { sample } & & 0.045 \\ \text { standard addition } 1 & 0.200 & 0.083 \\ \text { standard addition } 2 & 0.500 & 0.118 \\ \text { standard addition } 3 & 1.000 & 0.192 \end{array} $$ Report the concentration of \(\mathrm{Cr}\) in the caustic suspension.

The stoichiometry of a metal-ligand complex, \(\mathrm{ML}_{n}\), is determined by the method of continuous variations. A series of solutions is prepared in which the combined concentrations of \(\mathrm{M}\) and \(\mathrm{L}\) are held constant at \(5.15 \times 10^{-4} \mathrm{M}\). The absorbances of these solutions are measured at a wavelength where only the metal-ligand complex absorbs. Using the following data, determine the formula of the metal-ligand complex. $$ \begin{array}{ccc} \text { mole fraction } \mathrm{M} & \text { mole fraction } \mathrm{L} & \text { absorbance } \\ \hline 1.0 & 0.0 & 0.001 \\ 0.9 & 0.1 & 0.126 \\ 0.8 & 0.2 & 0.260 \\ 0.7 & 0.3 & 0.389 \\ 0.6 & 0.4 & 0.515 \\ 0.5 & 0.5 & 0.642 \\ 0.4 & 0.6 & 0.775 \\ 0.3 & 0.7 & 0.771 \\ 0.2 & 0.8 & 0.513 \\ 0.1 & 0.9 & 0.253 \\ 0.0 & 1.0 & 0.000 \end{array} $$

EDTA forms colored complexes with a variety of metal ions that may serve as the basis for a quantitative spectrophotometric method of analysis. The molar absorptivities of the EDTA complexes of \(\mathrm{Cu}^{2+}, \mathrm{Co}^{2+}\), and \(\mathrm{Ni}^{2+}\) at three wavelengths are summarized in the following table (all values of \(\varepsilon\) are in \(\left.\mathrm{M}^{-1} \mathrm{~cm}^{-1}\right).\) $$ \begin{array}{cccc} \text { metal } & \varepsilon_{462.9} & \varepsilon_{732.0} & \varepsilon_{378.7} \\ \hline \mathrm{Co}^{2+} & 15.8 & 2.11 & 3.11 \\ \mathrm{Cu}^{2+} & 2.32 & 95.2 & 7.73 \\ \mathrm{Ni}^{2+} & 1.79 & 3.03 & 13.5 \end{array} $$ Using this information determine the following: (a) The concentration of \(\mathrm{Cu}^{2+}\) in a solution that has an absorbance of 0.338 at a wavelength of \(732.0 \mathrm{nm}\). (b) The concentrations of \(\mathrm{Cu}^{2+}\) and \(\mathrm{Co}^{2+}\) in a solution that has an absorbance of 0.453 at a wavelength of \(732.0 \mathrm{nm}\) and 0.107 at a wavelength of \(462.9 \mathrm{nm}\) (c) The concentrations of \(\mathrm{Cu}^{2+}, \mathrm{Co}^{2+},\) and \(\mathrm{Ni}^{2+}\) in a sample that has an absorbance of 0.423 at a wavelength of \(732.0 \mathrm{nm}, 0.184\) at a wavelength of \(462.9 \mathrm{nm}\), and 0.291 at a wavelength of \(378.7 \mathrm{nm}\). The pathlength, \(b\), is \(1.00 \mathrm{~cm}\) for all measurements.

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