/*! 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 12 Wang and Taha described an inter... [FREE SOLUTION] | 91影视

91影视

Wang and Taha described an interesting application of potentiometry, which they call batch injection. \({ }^{24}\) As shown in Figure \(11.56,\) an ionselective electrode is placed in an inverted position in a large volume tank, and a fixed volume of a sample or a standard solution is injected toward the electrode's surface using a micropipet. The response of the electrode is a spike in potential that is proportional to the analyte's concentration. The following data were collected using a \(\mathrm{pH}\) electrode and a set of \(\mathrm{pH}\) standards. \begin{tabular}{cc} \(\mathrm{pH}\) & potential (mV) \\ \hline 2.0 & +300 \\ 3.0 & +240 \\ 4.0 & +168 \\ 5.0 & +81 \\ 6.0 & +35 \\ 8.0 & -92 \\ 9.0 & -168 \\ 10.0 & -235 \\ 11.0 & -279 \end{tabular} Determine the \(\mathrm{pH}\) of the following samples given the recorded peak potentials: tomato juice, \(167 \mathrm{mV} ;\) tap water, \(-27 \mathrm{mV} ;\) coffee, \(122 \mathrm{mV}\).

Short Answer

Expert verified
Tomato juice pH is approximately 4.0, tap water pH is approximately 7.0, coffee pH is approximately 4.8.

Step by step solution

01

Analyze the Given Data

Review the provided data which consist of pH values and corresponding electrode potentials. The relationship between pH and potentials is crucial for further calculations.
02

Establish the Calibration Curve

Plot the given pH values against their corresponding potentials to create a calibration curve. This graph shows potential (mV) on the Y-axis and pH on the X-axis, which should yield a roughly linear relationship.
03

Determine the Relationship Using Linear Regression

Apply linear regression on the plotted data to find the best-fit line. This will provide the equation of the line, generally in the form of \( V = a \cdot pH + b \), where \( V \) is the potential and \( a \) and \( b \) are constants derived from the regression.
04

Insert Sample Potentials Into the Calibration Equation

Using the equation derived from linear regression in Step 3, insert the recorded peak potentials for each sample (tomato juice: 167 mV, tap water: -27 mV, coffee: 122 mV) to calculate the approximate pH for each.
05

Calculate Probable pH Values

Replace the potential values into the regression equation: - For tomato juice, solve \( 167 = a \cdot pH_{tomato} + b \).- For tap water, solve \( -27 = a \cdot pH_{water} + b \).- For coffee, solve \( 122 = a \cdot pH_{coffee} + b \).
06

Solve for Each Sample's pH

Rearrange and solve the linear equations derived: - Solve for \( pH_{tomato} \), \( pH_{water} \), and \( pH_{coffee} \) by isolating the pH variable in each equation using the constants \( a \) and \( b \) estimated from the calibration curve.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91影视!

Key Concepts

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

Ion-Selective Electrode
An ion-selective electrode (ISE) is a key tool in potentiometry. It is designed to be sensitive to specific ions and measure their activity in a solution. The unique feature of an ISE is its specific membrane, which allows selective ion exchange. The electrode generates a potential difference that is directly related to the ion concentration.
ISEs are popular for their use in environments where precise ion concentration readings are essential. These electrodes are commonly used to measure the pH of a solution, where the membrane selectively interacts with hydrogen ions (H鈦). This interaction causes changes in voltage that can be interpreted to determine pH levels accurately. Understanding how an ion-selective electrode works is integral to using potentiometric methods effectively.
Calibration Curve
Creating a calibration curve is a fundamental step in potentiometric measurements. This curve is essential as it establishes the relationship between the known pH values and their corresponding potential readings.
To create a calibration curve, one would plot the potential (in mV) on the y-axis and the pH on the x-axis. This graph visually represents how changes in pH correspond to changes in electrode potential. The calibration curve is usually a straight line in the case of ion-selective electrodes, reflecting their linear response over a particular range.
This curve is crucial during analysis because it allows the computation of unknown sample pH values by comparing potential measurements against the established line.
Linear Regression
Linear regression is a statistical method used to find the best-fit line through a set of data points. In the context of potentiometry, linear regression helps determine the mathematical equation that represents the relationship between pH and potential.
By applying linear regression to the plotted calibration data, we obtain an equation of the form:\[ V = a \cdot pH + b \]
where \( V \) is the potential in millivolts, \( a \) is the slope of the line, and \( b \) is the y-intercept.
This equation allows for precise determination of unknown pH values by substituting the potential readings from sample measurements. Linear regression provides a mathematical way to interpret the graphical data obtained from the calibration curve, ensuring accurate pH readings.
pH Measurement
pH measurement using potentiometry is a practical application of ion-selective electrodes. It focuses on determining the hydrogen ion concentration, or "power of hydrogen," in various solutions.
The process involves using a pH electrode that reacts with H鈦 ions, producing a potential difference measurable in millivolts. By referencing the calibration curve and using the linear regression equation, one can accurately compute the pH of unknown samples.
This method is widely used in different fields, from laboratory testing to environmental monitoring, due to its precision and adaptability. With an understanding of how pH measurements work, users can confidently analyze the acidity or basicity of various substances and apply this knowledge in practical scenarios.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Thioamide drugs are determined by cathodic stripping analysis. \(^{30}\) Deposition occurs at \(+0.05 \mathrm{~V}\) versus an \(\mathrm{SCE}\). During the stripping step the potential is scanned cathodically and a stripping peak is observed at \(-0.52 \mathrm{~V}\). In a typical application a 2.00 -mL sample of urine is mixed with \(2.00 \mathrm{~mL}\) of a \(\mathrm{pH} 4.78\) buffer. Following a \(2.00 \mathrm{~min}\) deposition, a peak current of \(0.562 \mu \mathrm{A}\) is measured. A \(0.10-\mathrm{mL}\) addition of \(a 5.00 \mu \mathrm{M}\) solution of the drug is added to the same solution. A peak current of \(0.837 \mu \mathrm{A}\) is recorded using the same deposition and stripping conditions. Report the drug's molar concentration in the urine sample.

Baldwin and co-workers report the following data from a cyclic voltammetry study of the electrochemical behavior of \(p\) -phenylenediamine in a \(\mathrm{pH} 7\) buffer \(^{32}\) All potentials are measured relative to an \(\mathrm{SCE}\). \begin{tabular}{rcccc} scan rate \((\mathrm{mV} / \mathrm{s})\) & \(E_{\mathrm{p}, \mathrm{a}}(\mathrm{V})\) & \(E_{\mathrm{p}, \mathrm{C}}(\mathrm{V})\) & \(i_{\mathrm{p}, \mathrm{a}}(\mathrm{mA})\) & \(i_{\mathrm{p}, \mathrm{C}}(\mathrm{mA})\) \\ \hline 2 & 0.148 & 0.104 & 0.34 & 0.30 \\ 5 & 0.149 & 0.098 & 0.56 & 0.53 \\ 10 & 0.152 & 0.095 & 1.00 & 0.94 \\ 20 & 0.161 & 0.095 & 1.44 & 1.44 \\ 50 & 0.167 & 0.082 & 2.12 & 1.81 \\ 100 & 0.180 & 0.063 & 2.50 & 2.19 \end{tabular} The initial scan is toward more positive potentials, leading to the oxidation reaction shown here. Use this data to show that the reaction is electrochemically irreversible. A reaction may show electrochemical irreversibility because of slow electron transfer kinetics or because the product of the oxidation reaction participates in a chemical reaction that produces an nonelectroactive species. Based on the data in this problem, what is the likely source of \(p\) -phenylenediamine's electrochemical irreversibility?

The purity of a sample of \(\mathrm{K}_{3} \mathrm{Fe}(\mathrm{CN})_{6}\) is determined using linear-potential scan hydrodynamic voltammetry at a glassy carbon electrode. The following data were obtained for a set of external calibration standards. \begin{tabular}{cc} {\(\left[\mathrm{K}_{3} \mathrm{Fe}(\mathrm{CN})_{6}\right](\mathrm{mM})\)} & limiting current \((\mu \mathrm{A})\) \\ \hline 2.0 & 127 \\ 4.0 & 252 \\ 6.0 & 376 \\ 8.0 & 500 \\ 10.0 & 624 \end{tabular} A sample of impure \(\mathrm{K}_{3} \mathrm{Fe}(\mathrm{CN})_{6}\) is prepared for analysis by diluting a \(0.246-\mathrm{g}\) portion to volume in a \(100-\mathrm{mL}\) volumetric flask. The limiting current for the sample is \(444 \mu \mathrm{A}\). Report the purity of this sample of \(\mathrm{K}_{3} \mathrm{Fe}(\mathrm{CN})_{6}\)

What reaction prevents us from using \(Z n\) as an electrode of the first kind in an acidic solution? Which other metals do you expect to behave in the same manner as Zn when immersed in an acidic solution?

An ion-selective electrode can be placed in a flow cell into which we inject samples or standards. As the analyte passes through the cell, a potential spike is recorded instead of a steady-state potential. The concentration of \(\mathrm{K}^{+}\) in serum has been determined in this fashion using standards prepared in a matrix of \(0.014 \mathrm{M} \mathrm{NaCl}^{23}\) \begin{tabular}{cccc} {\(\left[\mathrm{K}^{+}\right](\mathrm{mM})\)} & \(E\) (arb. units) & {\(\left[\mathrm{K}^{+}\right](\mathrm{mM})\)} & \(E(\) arb. units \()\) \\ \hline 0.10 & 25.5 & 0.60 & 58.7 \\ 0.20 & 37.2 & 0.80 & 64.0 \\ 0.40 & 50.8 & 1.00 & 66.8 \end{tabular} A \(1.00-\mathrm{mL}\) sample of serum is diluted to volume in a \(10-\mathrm{mL}\) volumetric flask and analyzed, giving a potential of 51.1 (arbitrary units). Report the concentration of \(\mathrm{K}^{+}\) in the sample of serum.

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.