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with a ''fast'' reaction rate.]]

The reaction rate or '''rate of reaction''' for a Reactant or Product in a particular Reaction is intuitively defined as how fast a reaction takes place. For example the Oxidation of iron under the atmosphere is a slow reaction which can take years, the combustion of butane in a fire is a reaction that takes place in fractions of a second.

Chemical Kinetics is the part of Physical Chemistry that studies reaction rates. The concepts of chemical kinetics are applied in many disciplines, such as Chemical Engineering , Enzymology or Environmental Engineering .


FORMAL DEFINITION OF REACTION RATE

According to IUPAC 's Gold Book definition IUPAC definition of rate of reaction the reaction rate ''v'' (also ''r'' or ''R'') for the general chemical reaction
aA + bB → pP + qQ, occurring in a Closed System under constant-volume conditions, without a build-up of Reaction Intermediate s, is defined as:ccv

:v = - rac{1}{a} rac{d = - rac{1}{b} rac{d[B }{dt} = rac{1}{p} rac{d = rac{1}{q} rac{d[Q }{dt}

The IUPAC recommends that the unit of time should always be the second. In such a case the rate of reaction differs from the rate of increase of concentration of a product P by a constant factor (the reciprocal of its Stoichiometric Number ) and for a reactant A by minus the reciprocal of the stoichiometric number. Reaction rate usually has the units of mol dm-3 s-1.
It is important to bear in mind that the previous definition is only valid for a ''single reaction'', in a '' Closed System '' of ''constant volume''. This most usually implicit assumption must be stated explicitly, otherwise the definition is incorrect: If water is added to a pot containing salty water, the concentration of salt decreases, although there is no chemical reaction.

For any system in general the full Mass Balance must be taken into account: IN - OUT + GENERATION = ACCUMULATION

:F_{A0} - F_A + \int_{0}^{V} r\, dV = rac{dN_A}{dt}

When applied to the simple case stated previously this equation reduces to: v= rac{d {Link without Title} }{dt}

For a single reaction in a closed system of varying volume the so called ''rate of conversion'' can be is used, in order to avoid handling concentrations. It is defined as the derivative of the Extent Of Reaction with respect to time.

\dot{\xi} = rac{d\xi}{dt} = rac{1}{
u_i} rac{dn_i}{dt} = rac{1}{
u_i} \left(V rac{dC_i}{dt} + C_i rac{dV}{dt} ight)

\scriptstyle
u_i is the stoichiometric coefficient for substance i, \scriptstyle V is the volume of reaction and \scriptstyle C_i is the concentration of substance i.

When side products or reaction intermediates are formed, the IUPAC recommends the use of the terms rate of appearance and '''rate of disappearance''' for products and reactants, respectively.

Reaction rates may also be defined on a basis that is not the volume of the reactor. When a Catalyst is used the reaction rate may be stated on a catalyst weight (mol g-1 s-1) or surface area (mol m-2 s-1) basis. If the basis is a specific catalyst site that may be rigorously counted by a specified method, the rate is given in units of s-1 and is called a turnover frequency.


FACTORS INFLUENCING RATE OF REACTION

There are several factors that affect the rate of reaction:
  • '' and explained by Collision Theory . As reactant concentration increases, the Frequency of Collision increases.

  • ''The nature of the reaction'': Some reactions are naturally faster than others. The number of reacting species, their Physical State (the particles that form solids move much more slowly than those of gases or those in Solution ), the complexity of the reaction and other factors can influence greatly the rate of a reaction.

  • '' resulting in more successful collisions (when bonds are formed between reactants). The influence of temperature is described by the Arrhenius Equation . As a Rule Of Thumb , reaction rates for many reactions double or triple for every 10 degrees Celsius increase in temperature,Kenneth Connors, Chemical Kinetics, 1990, VCH Publishers, pg. 14 though the effect of temperature may be very much larger or smaller than this (to the extent that reaction rates can be independent of temperature or decrease with increasing temperature!)

    • For example, coal burns in a fireplace in the presence of oxygen but it doesn't when it is stored at Room Temperature . The reaction is spontaneous at low and high temperatures but at room temperature its rate is so slow that it is negligible. The increase in temperature, as created by a match, allows the reaction to start and then it heats itself, because it is Exothermic .

That is valid for many other fuels, such as Methane , Butane , Hydrogen ...
  • '' as well has an effect on reaction rate.

  • '' Pressure '': The rate of gaseous reactions increases with pressure, which is, in fact, equivalent to an increase in concentration of the gas.

  • '' Electromagnetic Radiation '': Electromagnetic radiation is a form of energy so it may speed up the rate or even make a reaction spontaneous, as it provides the particles of the reactants with more energy. This energy is in one way or another stored in the reacting particles (it may break bonds, promote molecules to electronically or vibrationally excited states...) creating intermediate species that react easily.

    • For example when Methane reacts with Chlorine in the dark, the reaction rate is very slow. It can be sped up when the Mixture is put under diffused light. In bright sunlight, the reaction is explosive.

  • ''A .

    • For example, Platinum catalyzes the combustion of hydrogen with oxygen at room temperature.

  • '' consists in a different reaction rate for the same molecule if it has different isotopes, usually Hydrogen isotopes, because of the mass difference between hydrogen and deuterium.

  • ''Surface Area'': In Reactions On Surfaces , which take place for example during Heterogeneous Catalysis , the rate of reaction increases as the surface area does. That is due to the fact that more particles of the solid are exposed and can be hit by reactant molecules.

  • '' Order '': The order of the reaction controls how the reactant concentration affects reaction rate.


All the factors that affect a reaction rate are taken into account in the rate equation of the reaction.


RATE EQUATION

See Also: rate equation


For a Chemical Reaction ''n'' A + ''m'' B → C + D, the rate equation or '''rate law''' is a Mathematical Expression used in chemical kinetics to link the rate of a reaction to the Concentration of each reactant. It is of the kind:

:\,r = k(T) {Link without Title} ^{n'} {Link without Title} ^{m'}

In this equation k(T) is the ''reaction rate coefficient'' or ''rate constant'', although it is not really a constant, because it includes all the parameters that affect reaction rate, except for concentration, which is explicitly taken into account. Of all the parameters described before, temperature is normally the most important one.

The exponents ''n''' and ''m''' are called reaction Orders and depend on the Reaction Mechanism . They sometimes are the same as the Stoichiometric Coefficient s of A and B, but not necessarily.

Stoichiometry , Molecularity (the actual number of molecules colliding) and Reaction Order only coincide necessarily in elementary reactions, that is, those reactions that take place in just one step. The reaction equation for elementary reactions coincides with the process taking place at the atomic level, i.e. n molecules of type A are colliding with m molecules of type B (n plus m is the molecularity).

For gases the rate law can also be expressed in pressure units using e.g. the Ideal Gas Law .

By combining the rate law with a Mass Balance for the system in which the reaction occurs, an expression for the rate of change in concentration can be derived. For a closed system with constant volume such an expression can look like

: rac{d = k(T)[A ^{n'}[B]^{m'}


TEMPERATURE DEPENDENCE

See Also: Arrhenius equation


Each reaction rate coefficient k has a temperature dependency, which is usually given by the Arrhenius Equation :

: k = A e^{ - rac{E_a}{RT} }

''Ea'' is the Activation Energy and ''R'' is the Gas Constant . Since at Temperature ''T'' the molecules have energies given by a Boltzmann Distribution , one can expect the number of collisions with energy greater than ''Ea'' to be proportional to e^{ rac{-E_a}{RT}}. ''A'' is the pre-exponential factor or Frequency Factor .

The values for ''A'' and ''E''a are dependent on the reaction. There are also more complex equations possible, which describe temperature dependence of other rate constants which do not follow this pattern.


EXAMPLE

For the reaction
: 2H_2 (g) + 2 NO(g) arr N_2 (g) + 2 H_2O (g)
The rate equation is:
: r = k {Link without Title} ^1 {Link without Title} ^2 \,

The rate equation does not simply reflect the reactants stoichiometric coefficients in the overall reaction: it is first order in H2, although the stoichiometric coefficient is 2 and it is second order in NO.

In chemical kinetics the overall reaction is usually proposed to occur through a number of elementary steps. Not all of these steps affect the rate of reaction; normally it is only the slowest elementary step that affect the reation rate. For example, in:

# 2 NO \ \overrightarrow\longleftarrow \ N_2O_2 (fast equilibrium)
#N_2O_2 + H_2 arr N_2O + H_2O (slow)
#N_2O + H_2 arr N_2 + H_2O (fast)

Reactions 1 and 3 are very rapid compared to the second, so it is the slowest reaction that is reflected in the rate equation. The slow step is considered the rate determining step. The orders of the rate equation are those from the rate determining step.


SEE ALSO




NOTES



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