In
chemistry and
biology,
catalysis is the acceleration (increase in
rate) of a
chemical reaction by means of a substance, called a
catalyst, which is itself not consumed by the overall reaction. The word is derived from the
Greek noun κατάλυσις, related to the
verb καταλύειν, meaning
to annul or
to untie or
to pick up.
A catalyst provides an alternative route of reaction where the
activation energy is lower than the original
chemical reaction. Catalysts participate in reactions but are neither reactants nor products of the reaction they catalyze. An exception is the process of
autocatalysis where the product of a reaction helps to accelerate the same reaction. They work by providing an alternative pathway for the reaction to occur, thus reducing the
activation energy and increasing the
reaction rate. More generally, one may at times call anything that accelerates a reaction, without itself being consumed or changed, a "catalyst" (for example, a "catalyst for political change").
A good example of a catalyst is in the
disproportionation of
hydrogen peroxide. Hydrogen peroxide reacts to give water and
oxygen gas by itself:
2 H
2O
2 → 2 H
2O + O
2 Usually, this reaction is slow. On the addition of
manganese dioxide to a dilute solution of hydrogen peroxide, an
effervescence is observed, and much oxygen, detectable by a glowing splint, is evolved. The manganese dioxide may be recovered, and re-used indefinitely, thus it is a catalyst — it is not consumed by the reaction.
A promoter is an accelerator of catalysis, but not a catalyst by itself. An
inhibitor inhibits the working of a catalyst.
Definitions Main article: catalytic cycle Catalytic cycles Catalysts work by providing an (alternative) mechanism involving a different transition state and lower
activation energy. The effect of this is that more molecular collisions have the energy needed to reach the transition state. Hence, catalysts can perform reactions that, albeit thermodynamically feasible, would not run without the presence of a catalyst, or perform them much faster, more specific, or at lower temperatures. This can be observed on a
Boltzmann distribution and
energy profile diagram. This means that catalysts reduce the amount of energy needed to start a chemical reaction.
Catalysts
cannot make energetically unfavorable reactions possible — they have
no effect on the
chemical equilibrium of a reaction because the rate of both the forward and the reverse reaction are equally affected (see also
thermodynamics). The net free energy change of a reaction is the same whether a catalyst is used or not; the catalyst just makes it easier to activate.
The
SI derived unit for measuring the
catalytic activity of a catalyst is the
katal, which is moles per second. The degree of activity of a catalyst can also be described by the
turn over number (or TON) and the catalytic efficiency by the
turn over frequency (TOF). The biochemical equivalent is the
enzyme unit.
Catalysts and reaction energetics Catalysts can be either
heterogeneous or
homogeneous.
Biocatalysts are often seen as a separate group.
Heterogeneous catalysts are present in different
phases from the
reactants (for example, a
solid catalyst in a
liquid reaction mixture), whereas homogeneous catalysts are in the same phase (for example, a
dissolved catalyst in a liquid reaction mixture).
Types of catalysts Main article: Heterogeneous catalysis Heterogeneous catalysts Main article: Homogeneous catalysis Homogeneous catalysts Main article: Biocatalysis Biocatalysts In the context of
electrochemistry, specifically in
fuel cell engineering, various metal-rich catalysts are used to promote the efficiency of a
half reaction that occurs within the fuel cell. One common type of fuel cell electrocatalyst is based upon tiny
nanoparticles of
platinum which adorn slightly larger
carbon particles. When this type of platinum electrocatalyst is in contact with one of the
electrodes in a fuel cell, it increases the rate of the
redox half reaction in which
oxygen gas is reduced to water (or
hydroxide or
hydrogen peroxide).
Electrocatalysts Catalysis is of paramount importance in the chemical industry. The production of most industrially important chemicals involves catalysis. The earliest commercial processes are the
Haber process for
ammonia synthesis and the
Fischer-Tropsch synthesis. Research into catalysis is a major field in applied science, and involves many fields of chemistry, notably in
organometallic chemistry, and physics. Catalysis is important in many aspects of
environmental science, from the
catalytic converter in automobiles to the causes of the
ozone hole. Catalytic, rather than
stoichiometric reactions are preferred in environmentally friendly
green chemistry due to the reduced amount of waste generated.
Significance Estimates are that 60% of all commercially produced chemical products involve catalysts at some stage in the process of their manufacture.
Manganese dioxide is used in the laboratory to prepare
oxygen by the decomposition of
hydrogen peroxide to
oxygen and
water.
Some of the most famous catalysts ever developed are:
Some examples of (famous) catalysts that perform specific transformations on functional groups:
These given examples show that different catalysts perform other transformations on the same functional groups, where the reaction would not run, run very slowly, or not run in a specific manner
without the presence of the catalyst.
The most effective catalysts are usually
transition metals or transition metal
complexes.
Catalytic converters made from
platinum and
manganese break down some of the more harmful byproducts of automobile exhaust.
the
Haber process for the synthesis of
ammonia from
nitrogen and
hydrogen, where ordinary
iron is used as a catalyst.
Transformations of
olefinic groups:
- the Ziegler-Natta catalyst used to mass produce polyethylene and polypropylene.
the Grubbs' catalyst for olefin metathesis. Notable examples
While transition metal catalysts are well established, a new trend is toward organocatalysis which use comparatively simple organic molecules as catalysts. While typically, catalyst loading is much higher than transition metal-based catalysts, the catalysts are usually commercially available in bulk, helping to reduce costs drastically. Organocatalysts of the "new generation" are competitive to traditional metal-containing catalysts and are owing to low product inhibion applicable in substoichiomertric quantities. The chemical character of organocatalysts offers new and attractive perspectives and advantages to synthetically working chemists.
Catalytic processes
The journal Catalysts and Catalysed Reactions
Autocatalysis
Enzyme
Enzyme catalysis
Phase Boundary Catalysis
SUMO enzymes
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