TYPES OF CATALYSIS
This page looks at the the different types of catalyst (heterogeneous and homogeneous) with examples of each kind, and explanations of how they work. You will also find a description of one example of autocatalysis - a reaction which is catalysed by one of its products.
Note: This page doesn't deal with the effect of catalysts on rates of reaction. If you don't already know about that, you might like to follow this link first. Return to this page via the BACK button on your browser.
Types of catalytic reactions
Catalysts can be divided into two main types - heterogeneous and homogeneous. In a heterogeneous reaction, the catalyst is in a different phase from the reactants. In a homogeneous reaction, the catalyst is in the same phase as the reactants.
What is a phase?
If you look at a mixture and can see a boundary between two of the components, those substances are in different phases. A mixture containing a solid and a liquid consists of two phases. A mixture of various chemicals in a single solution consists of only one phase, because you can't see any boundary between them.
You might wonder why phase differs from the term physical state (solid, liquid or gas). It includes solids, liquids and gases, but is actually a bit more general. It can also apply to two liquids (oil and water, for example) which don't dissolve in each other. You could see the boundary between the two liquids.
If you want to be fussy about things, the diagrams actually show more phases than are labelled. Each, for example, also has the glass beaker as a solid phase. All probably have a gas above the liquid - that's another phase. We don't count these extra phases because they aren't a part of the reaction.
This involves the use of a catalyst in a different phase from the reactants. Typical examples involve a solid catalyst with the reactants as either liquids or gases.
Note: It is important that you remember the difference between the two terms heterogeneous and homogeneous.
hetero implies different (as in heterosexual). Heterogeneous catalysis has the catalyst in a different phase from the reactants.
homo implies the same (as in homosexual). Homogeneous catalysis has the catalyst in the same phase as the reactants.
How the heterogeneous catalyst works (in general terms)
Most examples of heterogeneous catalysis go through the same stages:
A good catalyst needs to adsorb the reactant molecules strongly enough for them to react, but not so strongly that the product molecules stick more or less permanently to the surface.
Silver, for example, isn't a good catalyst because it doesn't form strong enough attachments with reactant molecules. Tungsten, on the other hand, isn't a good catalyst because it adsorbs too strongly.
Metals like platinum and nickel make good catalysts because they adsorb strongly enough to hold and activate the reactants, but not so strongly that the products can't break away.
Examples of heterogeneous catalysis
The hydrogenation of a carbon-carbon double bond
The simplest example of this is the reaction between ethene and hydrogen in the presence of a nickel catalyst.
In practice, this is a pointless reaction, because you are converting the extremely useful ethene into the relatively useless ethane. However, the same reaction will happen with any compound containing a carbon-carbon double bond.
One important industrial use is in the hydrogenation of vegetable oils to make margarine, which also involves reacting a carbon-carbon double bond in the vegetable oil with hydrogen in the presence of a nickel catalyst.
Ethene molecules are adsorbed on the surface of the nickel. The double bond between the carbon atoms breaks and the electrons are used to bond it to the nickel surface.
Hydrogen molecules are also adsorbed on to the surface of the nickel. When this happens, the hydrogen molecules are broken into atoms. These can move around on the surface of the nickel.
If a hydrogen atom diffuses close to one of the bonded carbons, the bond between the carbon and the nickel is replaced by one between the carbon and hydrogen.
That end of the original ethene now breaks free of the surface, and eventually the same thing will happen at the other end.
As before, one of the hydrogen atoms forms a bond with the carbon, and that end also breaks free. There is now space on the surface of the nickel for new reactant molecules to go through the whole process again.
Note: Several metals, including nickel, have the ability to absorb hydrogen into their structure as well as adsorb it on to the surface. In these cases, the hydrogen molecules are also converted into atoms which can diffuse through the metal structure.
This happens with nickel if the hydrogen is under high pressures, but I haven't been able to find any information about whether it is also absorbed under the lower pressures usually used for these hydrogenation reactions. I have therefore stuck with the usual explanation in terms of adsorption.
If anyone has any firm information about this, could they contact me via the address on the about this site page.
Catalytic converters change poisonous molecules like carbon monoxide and various nitrogen oxides in car exhausts into more harmless molecules like carbon dioxide and nitrogen. They use expensive metals like platinum, palladium and rhodium as the heterogeneous catalyst.
The metals are deposited as thin layers onto a ceramic honeycomb. This maximises the surface area and keeps the amount of metal used to a minimum.
Taking the reaction between carbon monoxide and nitrogen monoxide as typical:
Note: This is a simplification which is adequate for what most examiners at this level ask. The equation represents an overall change in the catalytic converter, but takes place in more than one stage. If you were interested, you could follow this up by reading this Wikipedia page
Catalytic converters can be affected by catalyst poisoning. This happens when something which isn't a part of the reaction gets very strongly adsorbed onto the surface of the catalyst, preventing the normal reactants from reaching it.
Lead is a familiar catalyst poison for catalytic converters. It coats the honeycomb of expensive metals and stops it working.
In the past, lead compounds were added to petrol (gasoline) to make it burn more smoothly in the engine. But you can't use a catalytic converter if you are using leaded fuel. So catalytic converters have not only helped remove poisonous gases like carbon monoxide and nitrogen oxides, but have also forced the removal of poisonous lead compounds from petrol.
The use of vanadium(V) oxide in the Contact Process
During the Contact Process for manufacturing sulphuric acid, sulphur dioxide has to be converted into sulphur trioxide. This is done by passing sulphur dioxide and oxygen over a solid vanadium(V) oxide catalyst.
Note: The equation is written with the half in it to make the explanation below tidier. You may well be familiar with the equation written as twice that shown, but the present version is perfectly acceptable. It is also shown as a one-way rather than a reversible reaction to avoid complicating things.
This example is slightly different from the previous ones because the gases actually react with the surface of the catalyst, temporarily changing it. It is a good example of the ability of transition metals and their compounds to act as catalysts because of their ability to change their oxidation state.
Note: If you aren't sure about oxidation states, it might be useful to follow this link before you go on. Use the BACK button on your browser to return to this page.
The sulphur dioxide is oxidised to sulphur trioxide by the vanadium(V) oxide. In the process, the vanadium(V) oxide is reduced to vanadium(IV) oxide.
The vanadium(IV) oxide is then re-oxidised by the oxygen.
This is a good example of the way that a catalyst can be changed during the course of a reaction. At the end of the reaction, though, it will be chemically the same as it started.
Note: If you want more detail about the Contact Process, you will find a full description of the conditions used and the reasons for them by following this link.
This has the catalyst in the same phase as the reactants. Typically everything will be present as a gas or contained in a single liquid phase. The examples contain one of each of these . . .
Examples of homogeneous catalysis
The reaction between persulphate ions and iodide ions
This is a solution reaction that you may well only meet in the context of catalysis, but it is a lovely example!
Persulphate ions (peroxodisulphate ions), S2O82-, are very powerful oxidising agents. Iodide ions are very easily oxidised to iodine. And yet the reaction between them in solution in water is very slow.
If you look at the equation, it is easy to see why that is:
The reaction needs a collision between two negative ions. Repulsion is going to get seriously in the way of that!
The catalysed reaction avoids that problem completely. The catalyst can be either iron(II) or iron(III) ions which are added to the same solution. This is another good example of the use of transition metal compounds as catalysts because of their ability to change oxidation state.
For the sake of argument, we'll take the catalyst to be iron(II) ions. As you will see shortly, it doesn't actually matter whether you use iron(II) or iron(III) ions.
The persulphate ions oxidise the iron(II) ions to iron(III) ions. In the process the persulphate ions are reduced to sulphate ions.
The iron(III) ions are strong enough oxidising agents to oxidise iodide ions to iodine. In the process, they are reduced back to iron(II) ions again.
Both of these individual stages in the overall reaction involve collision between positive and negative ions. This will be much more likely to be successful than collision between two negative ions in the uncatalysed reaction.
What happens if you use iron(III) ions as the catalyst instead of iron(II) ions? The reactions simply happen in a different order.
The destruction of atmospheric ozone
This is a good example of homogeneous catalysis where everything is present as a gas.
Ozone, O3, is constantly being formed and broken up again in the high atmosphere by the action of ultraviolet light. Ordinary oxygen molecules absorb ultraviolet light and break into individual oxygen atoms. These have unpaired electrons, and are known as free radicals. They are very reactive.
The oxygen radicals can then combine with ordinary oxygen molecules to make ozone.
Ozone can also be split up again into ordinary oxygen and an oxygen radical by absorbing ultraviolet light.
This formation and breaking up of ozone is going on all the time. Taken together, these reactions stop a lot of harmful ultraviolet radiation penetrating the atmosphere to reach the surface of the Earth.
The catalytic reaction we are interested in destroys the ozone and so stops it absorbing UV in this way.
Chlorofluorocarbons (CFCs) like CF2Cl2, for example, were used extensively in aerosols and as refrigerants. Their slow breakdown in the atmosphere produces chlorine atoms - chlorine free radicals. These catalyse the destruction of the ozone.
This happens in two stages. In the first, the ozone is broken up and a new free radical is produced.
The chlorine radical catalyst is regenerated by a second reaction. This can happen in two ways depending on whether the ClO radical hits an ozone molecule or an oxygen radical.
If it hits an oxygen radical (produced from one of the reactions we've looked at previously):
Or if it hits an ozone molecule:
Because the chlorine radical keeps on being regenerated, each one can destroy thousands of ozone molecules.
Note: If you are a UK A level student it is probable that you will only want one of these last two equations depending on what your syllabus says. Unfortunately, at the time of writing, different A level syllabuses were quoting different final equations. You need to check your current syllabus. If you don't have a copy of your syllabus, follow this link to find out how to get one.
The oxidation of ethanedioic acid by manganate(VII) ions
In autocatalysis, the reaction is catalysed by one of its products. One of the simplest examples of this is in the oxidation of a solution of ethanedioic acid (oxalic acid) by an acidified solution of potassium manganate(VII) (potassium permanganate).
The reaction is very slow at room temperature. It is used as a titration to find the concentration of potassium manganate(VII) solution and is usually carried out at a temperature of about 60°C. Even so, it is quite slow to start with.
The reaction is catalysed by manganese(II) ions. There obviously aren't any of those present before the reaction starts, and so it starts off extremely slowly at room temperature. However, if you look at the equation, you will find manganese(II) ions amongst the products. More and more catalyst is produced as the reaction proceeds and so the reaction speeds up.
You can measure this effect by plotting the concentration of one of the reactants as time goes on. You get a graph quite unlike the normal rate curve for a reaction.
Most reactions give a rate curve which looks like this:
Concentrations are high at the beginning and so the reaction is fast - shown by a rapid fall in the reactant concentration. As things get used up, the reaction slows down and eventually stops as one or more of the reactants are completely used up.
An example of autocatalysis gives a curve like this:
You can see the slow (uncatalysed) reaction at the beginning. As catalyst begins to be formed in the mixture, the reaction speeds up - getting faster and faster as more and more catalyst is formed. Eventually, of course, the rate falls again as things get used up.
Don't assume that a rate curve which looks like this necessarily shows an example of autocatalysis. There are other effects which might produce a similar graph.
For example, if the reaction involved a solid reacting with a liquid, there might be some sort of surface coating on the solid which the liquid has to penetrate before the expected reaction can happen.
A more common possibility is that you have a strongly exothermic reaction and aren't controlling the temperature properly. The heat evolved during the reaction speeds the reaction up.
© Jim Clark 2002 (last modified September 2012)