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  2. Cracking (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Cracking_(chemistry)

    In modern cracking furnaces, the residence time is reduced to milliseconds to improve yield, resulting in gas velocities up to the speed of sound. After the cracking temperature has been reached, the gas is quickly quenched to stop the reaction in a transfer line heat exchanger or inside a quenching header using quench oil. [citation needed] [8]

  3. Steam cracking - Wikipedia

    en.wikipedia.org/wiki/Steam_cracking

    Steam cracking is a petrochemical process in which saturated hydrocarbons are broken down into smaller, often unsaturated, hydrocarbons. It is the principal industrial method for producing the lighter alkenes (or commonly olefins ), including ethene (or ethylene ) and propene (or propylene ).

  4. Fluid catalytic cracking - Wikipedia

    en.wikipedia.org/wiki/Fluid_catalytic_cracking

    [1] [2] [3] The cracking of petroleum hydrocarbons was originally done by thermal cracking, now virtually replaced by catalytic cracking, which yields greater volumes of high octane rating gasoline; and produces by-product gases, with more carbon-carbon double bonds (i.e. alkenes), that are of greater economic value than the gases produced by ...

  5. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    Alkanes have the general chemical formula C n H 2n+2. The alkanes range in complexity from the simplest case of methane (CH 4), where n = 1 (sometimes called the parent molecule), to arbitrarily large and complex molecules, like pentacontane (C 50 H 102) or 6-ethyl-2-methyl-5-(1-methylethyl) octane, an isomer of tetradecane (C 14 H 30).

  6. Fischer–Tropsch process - Wikipedia

    en.wikipedia.org/wiki/Fischer–Tropsch_process

    The Fischer–Tropsch process involves a series of chemical reactions that produce a variety of hydrocarbons, ideally having the formula (C n H 2n+2). The more useful reactions produce alkanes as follows: [7] (2n + 1) H 2 + n CO → C n H 2n+2 + n H 2 O. where n is typically 10–20. The formation of methane (n = 1) is unwanted.

  7. Dehydrogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrogenation

    Relative to thermal cracking of alkanes, oxidative dehydrogenation (ODH) is of interest for two reasons: (1) undesired reactions take place at high temperature leading to coking and catalyst deactivation, making frequent regeneration of the catalyst unavoidable, (2) thermal dehydrogenation is expensive as it requires a large amount of heat ...

  8. Catalytic reforming - Wikipedia

    en.wikipedia.org/wiki/Catalytic_reforming

    [12] [page needed] Chlorination requires finesse, lest it affect the Pt or Re component. The platinum and/or rhenium are very susceptible to poisoning by sulfur and nitrogen compounds. Therefore, the naphtha feedstock to a catalytic reformer is always pre-processed in a hydrodesulfurization unit which removes both the sulfur and the nitrogen ...

  9. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    The compound with the formula (C 5 H 5) 2 Fe 2 (CO) 4 exists as three isomers in solution. In one isomer the CO ligands are terminal. When a pair of CO are bridging, cis and trans isomers are possible depending on the location of the C 5 H 5 groups. [7] Another example in organometallic chemistry is the linkage isomerization of ...