Chapter 12 Kinetics
12.7 Catalysis
Learning Objectives
By the end of this section, you will be able to:
- Explain the function of a catalyst in terms of reaction mechanisms and potential energy diagrams
- List examples of catalysis in natural and industrial processes
Among the factors affecting chemical reaction rates discussed earlier in this chapter was the presence of a catalyst, a substance that can increase the reaction rate without being consumed in the reaction. The concepts introduced in the previous section on reaction mechanisms provide the basis for understanding how catalysts are able to accomplish this very important function.
Figure 12.19 shows reaction diagrams for a chemical process in the absence and presence of a catalyst. Inspection of the diagrams reveals several traits of these reactions. Consistent with the fact that the two diagrams represent the same overall reaction, both curves begin and end at the same energies (in this case, because products are more energetic than reactants, the reaction is endothermic). The reaction mechanisms, however, are clearly different. The uncatalyzed reaction proceeds via a one-step mechanism (one transition state observed), whereas the catalyzed reaction follows a two-step mechanism (two transition states observed) with a notably lesser activation energy. This difference illustrates the means by which a catalyst functions to accelerate reactions, namely, by providing an alternative reaction mechanism with a lower activation energy. Although the catalyzed reaction mechanism for a reaction needn’t necessarily involve a different number of steps than the uncatalyzed mechanism, it must provide a reaction path whose rate determining step is faster (lower Ea).
Example 12.15 – Reaction Diagrams for Catalyzed Reactions
The two reaction diagrams here represent the same reaction: one without a catalyst and one with a catalyst. Estimate the activation energy for each process, and identify which one involves a catalyst.
Solution
Activation energies are calculated by subtracting the reactant energy from the transition state energy.
[latex]\text{diagram (a):} \; E_a = 32 \: kJ \: - \: 6 \: kJ = 26 \: kJ[/latex]
[latex]\text{diagram (b):} \; E_a = 20 \: kJ \: - \: 6 \: kJ = 14 \: kJ[/latex]
The catalyzed reaction is the one with lesser activation energy, in this case represented by diagram b.
Check Your Learning
Reaction diagrams for a chemical process with and without a catalyst are shown below. Both reactions involve a two-step mechanism with a rate-determining first step. 
Homogeneous Catalysts
A homogeneous catalyst is present in the same phase as the reactants. It interacts with a reactant to form an intermediate substance, which then decomposes or reacts with another reactant in one or more steps to regenerate the original catalyst and form product.
As an important illustration of homogeneous catalysis, consider the earth’s ozone layer. Ozone in the upper atmosphere, which protects the earth from ultraviolet radiation, is formed when oxygen molecules absorb ultraviolet light and undergo the reaction:
Ozone is a relatively unstable molecule that decomposes to yield diatomic oxygen by the reverse of this equation. This decomposition reaction is consistent with the following two-step mechanism:
O3 → O2 + O
A number of substances can catalyze the decomposition of ozone. For example, the nitric oxide–catalyzed decomposition of ozone is believed to occur via the following three-step mechanism:
NO(g) + O3(g) → NO2(g) + O2(g)
As required, the overall reaction is the same for both the two-step uncatalyzed mechanism and the three-step NO-catalyzed mechanism:
Notice that NO is a reactant in the first step of the mechanism and a product in the last step. This is another characteristic trait of a catalyst: though it participates in the chemical reaction, it is not consumed by the reaction.
Portrait of a Chemist
Mario J. Molina
The 1995 Nobel Prize in Chemistry was shared by Paul J. Crutzen, Mario J. Molina, a Mexican citizen (Figure 12.20), and F. Sherwood “Sherry” Rowland “for their work in atmospheric chemistry, particularly concerning the formation and decomposition of ozone”1 completed at the University of California, Irvine.
1 “The Nobel Prize in Chemistry 1995,” Nobel Prize.org, accessed February 18, 2015, http://www.nobelprize.org/nobel_prizes/chemistry/laureates/1995/.
In 1974, Molina and Rowland published a paper in the journal Nature detailing the threat of chlorofluorocarbon gases to the stability of the ozone layer in earth’s upper atmosphere. The ozone layer protects earth from solar radiation by absorbing ultraviolet light. As chemical reactions deplete the amount of ozone in the upper atmosphere, a measurable “hole” forms above Antarctica, and an increase in the amount of solar ultraviolet radiation— strongly linked to the prevalence of skin cancers—reaches earth’s surface. The work of Molina and Rowland was instrumental in the adoption of the Montreal Protocol, an international treaty signed in 1987 that successfully began phasing out production of chemicals linked to ozone destruction.
Molina and Rowland demonstrated that chlorine atoms from human-made chemicals can catalyze ozone destruction in a process similar to that by which NO accelerates the depletion of ozone. Chlorine atoms are generated when chlorocarbons or chlorofluorocarbons—once widely used as refrigerants and propellants—are photochemically decomposed by ultraviolet light or react with hydroxyl radicals. A sample mechanism is shown here using methyl chloride:
Chlorine radicals break down ozone and are regenerated by the following catalytic cycle:
Cl + O3 → ClO + O2
A single monatomic chlorine can break down thousands of ozone molecules. Luckily, the majority of atmospheric chlorine exists as the catalytically inactive forms Cl2 and ClONO2.
How Sciences Interconnect
Glucose-6-Phosphate Dehydrogenase Deficiency
Enzymes in the human body act as catalysts for important chemical reactions in cellular metabolism. As such, a deficiency of a particular enzyme can translate to a life-threatening disease. G6PD (glucose-6-phosphate dehydrogenase) deficiency, a genetic condition that results in a shortage of the enzyme glucose-6-phosphate dehydrogenase, is the most common enzyme deficiency in humans. This enzyme, shown in Figure 12.21, is the rate-limiting enzyme for the metabolic pathway that supplies NADPH to cells (Figure 12.22).
A disruption in this pathway can lead to reduced glutathione in red blood cells; once all glutathione is consumed, enzymes and other proteins such as hemoglobin are susceptible to damage. For example, hemoglobin can be metabolized to bilirubin, which leads to jaundice, a condition that can become severe. People who suffer from G6PD deficiency must avoid certain foods and medicines containing chemicals that can trigger damage their glutathione-deficient red blood cells.
Heterogeneous Catalysts
A heterogeneous catalyst is a catalyst that is present in a different phase (usually a solid) than the reactants. Such catalysts generally function by furnishing an active surface upon which a reaction can occur. Gas and liquid phase reactions catalyzed by heterogeneous catalysts occur on the surface of the catalyst rather than within the gas or liquid phase.
Heterogeneous catalysis typically involves the following processes:
- Adsorption of the reactant(s) onto the surface of the catalyst
- Activation of the adsorbed reactant(s)
- Reaction of the adsorbed reactant(s)
- Desorption of product(s) from the surface of the catalyst
Figure 12.23 illustrates the steps of a mechanism for the reaction of compounds containing a carbon–carbon double bond with hydrogen on a nickel catalyst. Nickel is the catalyst used in the hydrogenation of polyunsaturated fats and oils (which contain several carbon–carbon double bonds) to produce saturated fats and oils (which contain only carbon–carbon single bonds).
Many important chemical products are prepared via industrial processes that use heterogeneous catalysts, including ammonia, nitric acid, sulfuric acid, and methanol. Heterogeneous catalysts are also used in the catalytic converters found on most gasoline-powered automobiles (Figure 12.24).
Chemistry in Everyday Life
Automobile Catalytic Converters
Scientists developed catalytic converters to reduce the amount of toxic emissions produced by burning gasoline in internal combustion engines. By utilizing a carefully selected blend of catalytically active metals, it is possible to effect complete combustion of all carbon-containing compounds to carbon dioxide while also reducing the output of nitrogen oxides. This is particularly impressive when we consider that one step involves adding more oxygen to the molecule and the other involves removing the oxygen (Figure 12.24).
Most modern, three-way catalytic converters possess a surface impregnated with a platinum-rhodium catalyst, which catalyzes the conversion of nitric oxide into dinitrogen and oxygen as well as the conversion of carbon monoxide and hydrocarbons such as octane into carbon dioxide and water vapor:
2 NO2(g) → N2(g) + 2 O2(g)
In order to be as efficient as possible, most catalytic converters are preheated by an electric heater. This ensures that the metals in the catalyst are fully active even before the automobile exhaust is hot enough to maintain appropriate reaction temperatures.
Link to Learning
If you are intrested in learning more, here is a thorough explanation of how catalytic converters work.
How Sciences Interconnect
Enzyme Structure and Function
The study of enzymes is an important interconnection between biology and chemistry. Enzymes are usually proteins (polypeptides) that help to control the rate of chemical reactions between biologically important compounds, particularly those that are involved in cellular metabolism. Different classes of enzymes perform a variety of functions, as shown in Table 12.3.
|
Class |
Function |
|
oxidoreductases |
redox reactions |
|
transferases |
transfer of functional groups |
|
hydrolases |
hydrolysis reactions |
|
lyases |
group elimination to form double bonds |
|
isomerases |
isomerization |
|
ligases |
bond formation with ATP hydrolysis |
Enzyme molecules possess an active site, a part of the molecule with a shape that allows it to bond to a specific substrate (a reactant molecule), forming an enzyme-substrate complex as a reaction intermediate. There are two models that attempt to explain how this active site works. The most simplistic model is referred to as the lock-and-key hypothesis, which suggests that the molecular shapes of the active site and substrate are complementary, fitting together like a key in a lock. The induced fit hypothesis, on the other hand, suggests that the enzyme molecule is flexible and changes shape to accommodate a bond with the substrate. This is not to suggest that an enzyme’s active site is completely malleable, however. Both the lock-and-key model and the induced fit model account for the fact that enzymes can only bind with specific substrates, since in general a particular enzyme only catalyzes a particular reaction (Figure 12.25).
Link to Learning
The Royal Society of Chemistry provides an excellent introduction to enzymes for students and teachers.