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Catalyst poisoning refers to the partial or total deactivation of a catalyst by a chemical compound. An important historic example was the poisoning of catalytic converters by leaded fuel. Poisoning refers specifically to chemical deactivation, rather than other mechanism of catalyst degradation such as thermal decomposition or physical damage.[1][2] Although usually undesirable, poisoning may be helpful when it results in improved catalyst selectivity (e.g. Lindlar's catalyst).


Poisoning processEdit

Poisoning often involves compounds that bond chemically to the active surface sites of a catalyst. Poisoning decreases the number of catalytic sites or the fraction of the total surface area that has the capability of promoting reaction always decreases, and the average distance that a reactant molecule must diffuse through the pore structure before undergoing reaction may increase.[3] Poisoned sites can no longer accelerate the reaction with which the catalyst was supposed to catalyze.[4] Large scale production of substances such as ammonia in the Haber–Bosch process include steps to remove potential poisons from the product stream.

When the poisoning reaction rate is slow relative to the rate of diffusion, the poison will be evenly distributed throughout the catalyst and will result in homogeneous poisoning of the catalyst. Conversely, if the reaction rate is fast compared to the rate of diffusion, a poisoned shell will form on the exterior layers of the catalyst, a situation known as "pore-mouth" poisoning, and the rate of catalytic reaction may become limited by the rate of diffusion through the inactive shell.[3]

Common catalyst poisonsEdit

Organic functional groups and inorganic anions often have the ability to strongly adsorb to metal surfaces, i.e. they are poisons. Common catalyst poisons include the following: carbon monoxide, halide, cyanide, sulfide, sulfite, and phosphite and organic molecules such as nitriles, nitros, oximes and nitrogen-containing heterocycles. Agents vary their catalytic properties because of the nature of the transition metal.

Selective poisoningEdit

If the catalyst and reaction conditions are indicative of a low effectiveness factor, selective poisoning may be observed, which is a phenomenon where poisoning of only a small fraction of the catalyst surface gives a disproportionately large drop in activity. Mathematical models exist which describe the cases where the interaction of the poisoning process with the influence of the intraparticle diffusion on the rates of the primary and poisoning reactions leads to an interesting relations between observed catalytic activity and the fraction of surface poisoned.[3]

By combining a material balance over a differential element of pore length and the Thiele modulus, the equation is found:


where η is the effectiveness factor of the poisoned surface and hp is the Thiele modulus for the poisoned case.

When the ratio of the reaction rate for the poisoned pore to the unpoisoned pore is considered, the following equation can be found:


where F is the ratio of rates of poisoned and unpoisoned pores, hT is the Thiele modulus for the unpoisoned case, and α is the fraction of the surface that is poisoned.

The above equation simplifies depending on the value of hT. When hT is small, meaning that the surface is available, the equation becomes:


This represents the "classical case" of nonselective poisoning where the fraction of the activity remaining is equal to the fraction of the unpoisoned surface remaining.

When hT is very large, it becomes:


In this case, the catalyst effectiveness factors are considerably less than unity, and the effects of the portion of the poison adsorbed near the closed end of the pore are not as apparent as when hT is small.

Delving further into the mathematical relationships of selective poisoning, or "Pore-Mouth" poisoning, looking at the steady-state conditions, the rate of diffusion of the reactant through the poisoned region is equal to the rate of reaction. The rate of diffusion is given by:


And the rate of reaction within a pore is given by:


Through further manipulation and substitution, the fraction of the catalyst surface available for reaction can be obtained from the ratio of the poisoned reaction rate to the unpoisoned reaction rate:




where, as before, hT is the Thiele modulus for the unpoisoned case, and α is the fraction of the surface that is poisoned.[3]:465

Benefits of selective poisoningEdit

Usually, catalyst poisoning is undesirable as it leads to a loss of usefulness of expensive noble metals or their complexes. However, poisoning of catalysts can be used to improve selectivity of reactions. Poisoning can allow for selective intermediates to be isolated and final products with desirable stereochemistry to be achieved.


Palladium catalystEdit

Poisoning of palladium and platinum catalysts has been extensively researched. As a rule of thumb, platinum (as Adams' catalyst, platinum oxide finely divided on carbon) is less susceptible. Common poisons for these two metals are sulfur and nitrogen-heterocycles like pyridine and quinoline.

Intentional palladium catalyst poisoningEdit

In some cases, a highly active catalyst can lead to undesirable secondary reactions with the desired product. In some of these cases, the addition of a small amount of a catalyst poison increases the yield of the desired product by lower the catalyst activity. For example, in the classical "Rosenmund reduction" of an acyl chloride to the corresponding aldehyde, the palladium catalyst (over barium sulfate or calcium carbonate) is intentionally poisoned by the addition of sulfur or quinoline in order to lower the catalyst activity and thereby prevent further reduction of the aldehyde product to yield a primary alcohol. In the case of Lindlar's catalyst, palladium is poisoned with a lead salt to allow reduction of an alkyne to the corresponding alkene while preventing reduction of the alkene product to the corresponding alkane.

Hydrodesulfurization catalystsEdit

In the purification of crude petroleum products the process of hydrodesulfurization is utilized.[5] Thiol containing hydrocarbons, such as thiophene, are reduced using H2 in order to produce H2S and different length chains of hydrocarbons. Common catalyst used are tungsten and molybdenum sulfide particles. By adding cobalt and nickel [6] nuclei to either edge s or partially incorporating them into the crystal lattice structure can create more efficient catalyst. The synthesis of the catalyst creates a supported hybrid that prevents poisoning of the cobalt nuclei that may be unstable in the mono-nuclear form.

Catalytic converterEdit

A catalytic converter for an automobile can be poisoned if the vehicle is operated on gasoline containing lead additives. Fuel cells running on hydrogen must use very pure reactants, free of sulfur and carbon compounds.

Example of Catalytic Converter used in the Automotive Industry


Raney nickel catalysts have reduced activity when it is in combination with mild steel. The loss in activity of the catalyst can be overcome by having a lining of epoxy or other substances.

See alsoEdit


  1. ^ Forzatti, P.; Lietti, L. (1999). "Catalyst Deactivation". Catalysis Today. 52 (2–3): 165–181. doi:10.1016/S0920-5861(99)00074-7.CS1 maint: Uses authors parameter (link)
  2. ^ Bartholomew, Calvin H (2001). "Mechanisms of Catalyst Deactivation". Applied Catalysis A: General. 212 (1–2): 17–60. doi:10.1016/S0926-860X(00)00843-7.
  3. ^ a b c d Charles G. Hill, An Introduction To Chemical EngineDesign, John Wiley & Sons Inc., 1977 ISBN 0-471-39609-5, page 464
  4. ^ Jens Hagen, Industrial catalysis: a practical approach ,Wiley-VCH, 2006 ISBN 3-527-31144-0, page 197
  5. ^ Cheng, F. Y; Chen, J; Gou, X. L (2006). "MoS2–Ni Nanocomposites as Catalysts for Hydrodesulfurization of Thiophene and Thiophene Derivatives". Advanced Materials. 18 (19): 2561. doi:10.1002/adma.200600912.
  6. ^ Kishan, G; Coulier, L; Van Veen, J.A.R; Niemantsverdriet, J.W (2001). "Promoting Synergy in CoW Sulfide Hydrotreating Catalysts by Chelating Agents". Journal of Catalysis. 200: 194–196. doi:10.1006/jcat.2001.3203.