Catalysts 1
Catalysts 1
Catalysts 1
College of Engineering
Chemical Engineering Department
Chemical Process Engineering
Report of Catalysts
Student preparation
Omar qasim lafta
2023-2024
The aim of this presentation is to provide a
general overview of the catalyst
Additional information for each Unit is provided within issued project documentation.
1.2 Properties
• Heterogeneous catalysis
• Homogeneous catalysis
(A) Homogenous catalysis: reaction where the catalysts are in the same phase as the
reactants.
(B) Heterogeneous catalysis: reaction where the catalyst and reactant are in different
phases.
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1.2 Properties:
A small quantity of the catalyst is enough to catalyze a large quantity of reactants into
products .Though reactants are same, the type of catalyst used may decide the products
formed.
• If 2 catalysts can catalyze the same reaction, the better catalyst is the one which
produces a greater reduction in activation energy.e.g. activation energy for the
decomposition of H₂O, for different catalysts.
This alternate pathway requires lower activation energy and is easier to achieve and a
larger number of molecules can react and yield products.
• 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.
• Heterogeneous catalysis
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.
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 carboncarbon 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.
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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.
• heterogeneous catalyst.
The metals are deposited as thin layers onto a ceramic honeycomb. This maximizes
the surface area and keeps the amount of metal used to a minimum.
Taking the reaction between carbon monoxide and nitrogen monoxide as typical:
In the same sort of way as the previous example, the carbon monoxide and nitrogen
monoxide will be adsorbed on the surface of the catalyst, where they react. The
carbon dioxide and nitrogen are then desorbed
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• 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
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.
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 .
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.
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
What happens if you use iron(III) ions as the catalyst instead of iron(II) ions? The reactions
simply happen in a different order.
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.
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.