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  2. Catalysis - Wikipedia

    en.wikipedia.org/wiki/Catalysis

    An illustrative example is the effect of catalysts to speed the decomposition of hydrogen peroxide into water and oxygen: . 2 H 2 O 2 → 2 H 2 O + O 2. This reaction proceeds because the reaction products are more stable than the starting compound, but this decomposition is so slow that hydrogen peroxide solutions are commercially available.

  3. Industrial catalysts - Wikipedia

    en.wikipedia.org/wiki/Industrial_catalysts

    The disadvantage with a copper catalysts is that it is very sensitive when it comes to sulfide poisoning, a future use of for example a cobalt- molybdenum catalyst could solve this problem. The catalyst mainly used in the industry today is a copper-zinc-alumina (Cu/ZnO/Al 2 O 3) based catalyst.

  4. Heterogeneous catalysis - Wikipedia

    en.wikipedia.org/wiki/Heterogeneous_catalysis

    Typical energies for physisorption are from 3 to 10 kcal/mol. [2] In heterogeneous catalysis, when a reactant molecule physisorbs to a catalyst, it is commonly said to be in a precursor state, an intermediate energy state before chemisorption, a more strongly bound adsorption. [6]

  5. Organocatalysis - Wikipedia

    en.wikipedia.org/wiki/Organocatalysis

    In this context, simple organic acids have been used as catalyst for the modification of cellulose in water on multi-ton scale. [9] When the organocatalyst is chiral an avenue is opened to asymmetric catalysis; for example, the use of proline in aldol reactions is an example of chirality and green chemistry. [10]

  6. Catalytic cycle - Wikipedia

    en.wikipedia.org/wiki/Catalytic_cycle

    Usually the true catalyst is an expensive and complex molecule and added in quantities as small as possible. The stoichiometric catalyst on the other hand should be cheap and abundant. [citation needed] "Sacrificial catalysts" are more accurately referred to by their actual role in the catalytic cycle, for example as a reductant.

  7. Gomberg–Bachmann reaction - Wikipedia

    en.wikipedia.org/wiki/Gomberg–Bachmann_reaction

    For example, p-bromobiphenyl may be prepared from 4-bromoaniline and benzene: [4] BrC 6 H 4 NH 2 + C 6 H 6 → BrC 6 H 4 −C 6 H 5. The reaction offers a wide scope for both diazonium component and arene component but yields are generally low following the original procedure (less than 40%), given the many side-reactions of diazonium salts.

  8. Hydrogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrogenation

    Thus, a carefully chosen catalyst can be used to hydrogenate some functional groups without affecting others, such as the hydrogenation of alkenes without touching aromatic rings, or the selective hydrogenation of alkynes to alkenes using Lindlar's catalyst. For example, when the catalyst palladium is placed on barium sulfate and then treated ...

  9. Catalytic oxidation - Wikipedia

    en.wikipedia.org/wiki/Catalytic_oxidation

    Typical catalysts are platinum, and redox-active oxides of iron, vanadium, and molybdenum. In many cases, catalysts are modified with a host of additives or promoters that enhance rates or selectivities. Important homogeneous catalysts for the oxidation of organic compounds are carboxylates of cobalt, iron, and manganese