Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

Use the following data to determine the half-life of \(^{218} 80\) and the rate constant for the decay of \(^{218} 84\) Po. $$\begin{array}{lllllll} \hline \text { Time } / \mathrm{s} & 0 & 200 & 400 & 600 & 800 & 1000 \\ \text { Moles }_{84}^{218} \mathrm{Po} & 0.250 & 0.110 & 0.057 & 0.025 & 0.012 & 0.005 \\ \hline \end{array}$$

Short Answer

Expert verified
The half-life of \(^{218} 84\)Po is approximately 187.47 s, and the rate constant is \(0.0037 \, \text{s}^{-1}\).

Step by step solution

01

Understanding the Decay Process

The decay of a radioactive substance is a first-order reaction. This means that the rate of reaction is directly proportional to the concentration of the substance. The rate constant \( k \) can be found using the formula for first-order kinetics: \[ k = \frac{1}{t} \ln \left( \frac{[A]_0}{[A]} \right) \]where \( [A]_0 \) is the initial concentration, \( [A] \) is the concentration at time \( t \), and \( \ln \) represents the natural logarithm.
02

Calculating the Rate Constant

Using the given data, select two points: at time \( t = 0 \) s, \( [A]_0 = 0.250 \) moles; at time \( t = 400 \) s, \( [A] = 0.057 \) moles. Plug these into the formula for \( k \):\[ k = \frac{1}{400} \ln \left( \frac{0.250}{0.057} \right) \]Calculating gives \( \ln(4.386) \approx 1.4790 \), so \[ k \approx \frac{1.4790}{400} = 0.0036975 \, \text{s}^{-1} \]
03

Calculating the Half-life

The half-life \( t_{1/2} \) of a first-order reaction is given by the formula: \[ t_{1/2} = \frac{0.693}{k} \]Substitute \( k = 0.0036975 \, \text{s}^{-1} \):\[ t_{1/2} = \frac{0.693}{0.0036975} \approx 187.47 \, \text{s} \]
04

Verification Using Additional Data Points

For accuracy, repeat the calculation of \( k \) with different pairs of points from the dataset to ensure consistency. The pattern of radioactive decay should result in the same \( k \) value irrespective of the time points chosen, reinforcing the validity of \( k \) and ensuring any variations in calculations are accounted for.

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 Vaia!

Key Concepts

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

First-order Kinetics
Radioactive decay often follows a first-order kinetic model. This type of kinetic reaction indicates that the rate at which a substance decays is directly proportional to its current concentration. To understand it easily, consider that as you have more of a radioactive substance, the decay happens faster; less substance results in slower decay.
For first-order kinetics, the equation used is \[ k = \frac{1}{t} \ln \left( \frac{[A]_0}{[A]} \right) \]where:
  • \( k \) is the rate constant, indicating how fast the reaction occurs.
  • \( t \) is the elapsed time during which the reaction progresses.
  • \([A]_0\) is the initial concentration of the substance.
  • \([A]\) is the concentration at time \( t \).
  • The function \( \ln \) is the natural logarithm.
This formula helps us calculate how fast a radioactive substance decays and allows us to quantify the process under first-order kinetics.
Rate Constant
The rate constant \( k \) is crucial in understanding the speed of a radioactive decay process. In first-order kinetics, the rate constant provides insight into how rapidly the reaction progresses. With the rate constant, we can predict how long it will take for a certain amount of the substance to decay over time.
In our exercise, we determine \( k \) using specific data points: the initial amount of \( ^{218}_{84} \text{Po} \) and its amount after a given period. By applying the formula \[ k = \frac{1}{t} \ln \left( \frac{[A]_0}{[A]} \right) \],we can compute \( k \) between any two data points:
  • For instance, at \( t = 0 \) s, \([A]_0 = 0.250\) moles, and at \( t = 400 \) s, \([A] = 0.057\) moles.Calculating the rate constant yields \( k \approx 0.0036975 \, \text{s}^{-1} \).
By calculating \( k \) across various time intervals, we ensure accurate and consistent results, underscoring the reliability of our calculations.
Half-life Calculation
Half-life is a fundamental concept in radioactive decay, representing the time required for half the amount of a radioactive substance to decay. It's a critical measure that helps understand and predict the behavior of radioactive materials over time.
For first-order reactions like radioactive decay, the half-life can be calculated using the formula \[ t_{1/2} = \frac{0.693}{k} \],where \( k \) is the rate constant calculated earlier.

In our problem, using the given rate constant \( k = 0.0036975 \, \text{s}^{-1} \), the half-life is determined as:
  • \[ t_{1/2} = \frac{0.693}{0.0036975} \approx 187.47 \, \text{s} \]
Therefore, the half-life represents the decay process's slow and consistent pace, providing essential information about the durability of the radioactive substance and its potential applications or risks in real-world 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

Interpret the following notational forms of nuclear reactions: (a) \(\frac{58}{26} \mathrm{Fe}(2 \mathrm{n}, \beta)_{27}^{60} \mathrm{Co} ;(\mathrm{b}) \frac{55}{25} \mathrm{Mn}(\mathrm{n}, \gamma)_{25}^{56} \mathrm{Mn}\) \((\mathrm{c})_{16}^{32} \mathrm{S}(\mathrm{n}, \mathrm{p})_{15}^{32} \mathrm{P}\) (d) 233 11 \(\mathrm{Na}(\gamma, 3 \mathrm{n})_{11}^{20} \mathrm{Na}\)

The half-life of strontium-90 is 29.1 years. Determine the rate constant for the decay of strontium-90 in units of \(s^{-1}\) [The SI unit of time is the second.]

Determine the half-life of Bk given that a plot of \(\ln N\) against \(t\) is linear with a gradient of -0.0023 day \(^{-1}\) where \(N\) is the number of nuclides present at time \(t\)

Why is a coupling constant measured in \(\mathrm{Hz}\) and is not recorded as a chemical shift difference? Long-range couplings are often observed between \(^{31} \mathrm{P}\) and \(^{19} \mathrm{F}\) nuclei, between \(^{31} \mathrm{P}\) and \(^{1} \mathrm{H}\) nuclei, but not between remote non-equivalent \(^{1} \mathrm{H}\) nuclei. What does this tell you about the relative magnitudes of values of \(J_{\mathrm{PF}}, J_{\mathrm{PH}}\) and \(J_{\mathrm{HH}}\) for the respective pairs of nuclei when they are directly attached?

The \(^{19} \mathrm{F}\) NM \(\mathrm{R}\) spectrum of each of the following molecules exhibits one signal. For which species is this observation consistent with a static molecular structure as predicted by the VSEPR model: (a) \(\mathrm{SiF}_{4}\) i; (b) \(P F_{5} ;\) (c) \(\mathrm{SF}_{6}\) (d) \(\operatorname{SOF}_{2}\) (e) \(\mathrm{CF}_{4} ?\)

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.

Sign-up for free