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  2. Palladium - Wikipedia

    en.wikipedia.org/wiki/Palladium

    Global palladium sales were 8.84 million troy ounces (275 t) in 2017, [96] of which 86% was used in the manufacturing of automotive catalytic converters, followed by industrial, jewelry, and investment usages. [97]

  3. Wacker process - Wikipedia

    en.wikipedia.org/wiki/Wacker_process

    The construction of a new oil refinery in Cologne by Esso close to a Wacker site, combined with the realization that ethylene would be a cheaper feedstock prompted Wacker to investigate its potential uses. As part of the ensuing research effort, a reaction of ethylene and oxygen over palladium on carbon in a quest for ethylene oxide ...

  4. Organopalladium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organopalladium_chemistry

    Organopalladium chemistry is a branch of organometallic chemistry that deals with organic palladium compounds and their reactions. Palladium is often used as a catalyst in the reduction of alkenes and alkynes with hydrogen. This process involves the formation of a palladium-carbon covalent bond.

  5. Nanomaterial-based catalyst - Wikipedia

    en.wikipedia.org/wiki/Nanomaterial-based_catalyst

    The compound Pd 2 (dba) 3 is a source of Pd(0), which is the catalytically active source of palladium used for many reactions, including cross coupling reactions. [4] Pd2(dba)3 was thought to be a homogeneous catalytic precursor, but recent articles suggest that palladium nanoparticles are formed, making it a heterogeneous catalytic precursor. [4]

  6. Palladium compounds - Wikipedia

    en.wikipedia.org/wiki/Palladium_compounds

    Palladium forms a variety of ionic, coordination, and organopalladium compounds, typically with oxidation state Pd 0 or Pd 2+. Palladium(III) compounds have also been reported. Palladium compounds are frequently used as catalysts in cross-coupling reactions such as the Sonogashira coupling and Suzuki reaction.

  7. Suzuki reaction - Wikipedia

    en.wikipedia.org/wiki/Suzuki_reaction

    The Suzuki reaction or Suzuki coupling is an organic reaction that uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide. [1] [2] [3] It was first published in 1979 by Akira Suzuki, and he shared the 2010 Nobel Prize in Chemistry with Richard F. Heck and Ei-ichi Negishi for their contribution to the discovery and development of noble metal catalysis in organic ...

  8. Palladium on carbon - Wikipedia

    en.wikipedia.org/wiki/Palladium_on_carbon

    Palladium on carbon, often referred to as Pd/C, is a form of palladium used as a catalyst. [1] The metal is supported on activated carbon to maximize its surface area ...

  9. Fission products (by element) - Wikipedia

    en.wikipedia.org/wiki/Fission_products_(by_element)

    The palladium forms an alloy with the fission tellurium. This alloy can separate from the glass. 107 Pd is the only long-living radioactive isotope among the fission products and its beta decay has a long half life and low energy, this allows industrial use of extracted palladium without isotope separation. [9]