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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. Catalyst poisoning - Wikipedia

    en.wikipedia.org/wiki/Catalyst_poisoning

    Common catalysts used are tungsten and molybdenum sulfide. Adding cobalt and nickel [8] to either edges or partially incorporating them into the crystal lattice structure can improve the catalyst's efficiency. The synthesis of the catalyst creates a supported hybrid that prevents poisoning of the cobalt nuclei.

  4. Frustrated Lewis pair - Wikipedia

    en.wikipedia.org/wiki/Frustrated_Lewis_pair

    Hydrogenations of these unsaturated substrates can be effected by metal-catalyzed reactions. Metal-free catalytic hydrogenation was carried out using the phosphonium borate catalyst (R 2 PH)(C 6 F 4)BH(C 6 F 5) 2 (R = 2,4,6-Me 3 C 6 H 2) 1. This type of metal-free hydrogenation has the potential to replace high cost metal catalyst.

  5. 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

  6. Autocatalysis - Wikipedia

    en.wikipedia.org/wiki/Autocatalysis

    Autocatalytic cycle of formose reaction showing how glyceraldehyde can be both the catalyst and the product of one portion of this complex reaction type. An early example of autocatalysis is the formose reaction, in which formaldehyde and base produce sugars and related polyols. Characteristic of autocatalysis, this reaction rate is extremely ...

  7. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    Catalysts are often based on palladium, which is frequently selected due to high functional group tolerance. Organopalladium compounds are generally stable towards water and air. Palladium catalysts can be problematic for the pharmaceutical industry, which faces extensive regulation regarding heavy metals.

  8. Pfizer Stock Has Positive and Negative Catalysts Going ... - AOL

    www.aol.com/news/pfizer-stock-positive-negative...

    Pfizer (NYSE:PFE) stock has missed out on the exuberant bull market this year, as the indexes have hit all-time highs, but Pfizer stock has fallen about 10% in 2019.Source: Shutterstock Then again ...

  9. Reactions on surfaces - Wikipedia

    en.wikipedia.org/wiki/Reactions_on_surfaces

    C 2 H 2 + H 2 (ads.) → C 2 H 4 on nickel or iron catalysts The Langmuir-Rideal mechanism is often, incorrectly, attributed to Dan Eley as the Eley-Rideal mechanism. [ 5 ] The actual Eley-Rideal mechanism, studied in the thesis of Dan Eley and proposed by Eric Rideal in 1939, was the reaction between a chemisorbed and a physisorbed molecule. [ 6 ]