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The decomposition of many substances on the surface of a heterogeneous catalyst shows the following behaviour:

How do you account for the rate law changing from first order to zero order in the concentration of reactant?

a. Determine the first-order rate constants for thermal degradation of silk for each of the three experiments.

b. Does either of the two additives appear to retard the degradation of silk?

c. Calculate the half-life for the thermal degradation of silk for each of the three experiments.

Short Answer

Expert verified

Heterogeneous catalysisby solids plays a key role in chemical industry due to the ability to accelerate a chemical reaction to reach the equilibrium and to selectively accelerate a desirable chemical reaction in a complex chemical reaction network to reach the equilibrium.

a) untreatedK=0.465day-1

deacidifying K=0.659day-1

antioxidantK=0.779day-1

b) Both additives are increasing the rate of degradation process

c) untreatedt1/2=ln20.465days=1.49days

deacidifying t1/2=ln20.659days-1=1.05days

antioxidantt1/2=ln20.779days-1=0.890days

Step by step solution

01

Determine the reaction between the reactant and the catalyst

The reaction happens on the surface of the catalyst followed by desorption of the product. The rate of reaction is represented as follows:

Rate=k1k2CA1+k1CA

Here,CA is the concentration of reactant A and Csis the active site on the catalyst S.

The reaction is represented as follows:

Rate=k1k2CAK1CA

Rate=k1k2k1

Here, no reactant molecule is involved in the rate expression; therefore, the reaction is zero-order in this case.

02

Determine the zero-order reaction.

The integrated rate law for the zero-order reaction A → products is [A]_t = -kt + [A]. Because this equation has the form y = mx + b, a plot of the concentration of A as a function of time yields a straight line.

The rate constant for the reaction can be determined from the slope of the line, which is equal to -k.

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Most popular questions from this chapter

The following mechanism has been proposed to account for the rate law of the decomposition of ozone to O2(g):

O3+MK-1K1O2+O+MO+O3K22O2

Apply the steady-state hypothesis to the concentration of atomic oxygen, and derive the rate law for the decomposition of ozone. (M stands for an atom or molecule that can exchange kinetic energy with the particles undergoing the chemical reaction) .

The decomposition of hydrogen peroxide was studied at a particular temperature. The following data were obtained, where Rate=-d[H2O2]dt

Time (s)[H2O2](mol/L)
01.00
120±1
0.91
300±1
0.78
600±1
0.59
1200±1
0.37
1800±1
0.22
2400±1
0.13
3000±1
0.082
3600±1
0.050

Determine the integrated state law, the differential state law, and the value of the rate constant. Calculate theH2O2at4000.5after the start of the reaction.

Determine the forms of the integrated and the differential rate laws for the decomposition of benzene diazonium chloride C6H5N2Cl(aq)C6H5Cl(l)+N2(g)

from the following data, which were collected at50.0oCand1.00atm:

Time (s)N2Evolved (ml)
619.3
926.0
1436.0
2245.0
3050.4

58.3

The total solution volume was 40.0ml.

Question: Consider a sample containing 2.00 moles of a monatomic ideal gas that undergoes the following changes:

For each step, assume that the external pressure is constant and equals the final pressure of the gas for that step. Calculate q, w, ΔE, and ΔH for each step and for the overall change from state A to state D

Small quantities of hydrogen gas can be prepared in the laboratory by the addition of aqueous hydrochloric acid to metallic zinc.

Zns+2HClaqZnCl2aq+H2g

Typically, the hydrogen gas is bubbled through water for collection and becomes saturated with water vapor. Suppose 240. mL of hydrogen gas is collected at 30.oC and has a total pressure of 1.032 atm by this process. What is the partial pressure of hydrogen gas in the sample? How many grams of zinc must have reacted to produce this quantity of hydrogen? (The vapor pressure of water is 32 torr at 30oC.)

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