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  2. C1 chemistry - Wikipedia

    en.wikipedia.org/wiki/C1_Chemistry

    Together with hydrogen, it is the feed for the Fischer–Tropsch process, which affords liquid fuels. Methanol is the precursor to acetic acid, dimethyl ether, formaldehyde, and many methyl compounds (esters, amines, halides). A larger scale application is methanol to olefins, which produces ethylene and propylene. [2]

  3. Gas to liquids - Wikipedia

    en.wikipedia.org/wiki/Gas_to_liquids

    The Mobil MTG process is practiced from coal-derived methanol in China by JAMG. A more modern implementation of MTG is the Topsøe improved gasoline synthesis (TiGAS). [5] Methanol can be converted to olefins using zeolite and SAPO-based heterogeneous catalysts. Depending on the catalyst pore size, this process can afford either C2 or C3 ...

  4. Shell higher olefin process - Wikipedia

    en.wikipedia.org/wiki/Shell_higher_olefin_process

    The Shell higher olefin process (SHOP) is a chemical process for the production of linear alpha olefins via ethylene oligomerization and olefin metathesis invented and exploited by Shell plc. [1] The olefin products are converted to fatty aldehydes and then to fatty alcohols , which are precursors to plasticizers and detergents .

  5. Olefin metathesis - Wikipedia

    en.wikipedia.org/wiki/Olefin_metathesis

    In organic chemistry, olefin metathesis is an organic reaction that entails the redistribution of fragments of alkenes (olefins) by the scission and regeneration of carbon-carbon double bonds. [ 1 ] [ 2 ] Because of the relative simplicity of olefin metathesis, it often creates fewer undesired by-products and hazardous wastes than alternative ...

  6. Ethenolysis - Wikipedia

    en.wikipedia.org/wiki/Ethenolysis

    The Shell higher olefin process (SHOP process) uses ethenolysis on an industrial scale. SHOP α-olefin mixtures are first separated by distillation. Higher molecular weight fractions are isomerized by alkaline alumina catalysts in the liquid phase. The resulting internal olefins are reacted with ethylene to regenerate α-olefins.

  7. Methanol - Wikipedia

    en.wikipedia.org/wiki/Methanol

    Methanol and its vapours are flammable. Moderately toxic for small animals – Highly toxic to large animals and humans (in high concentrations) – May be fatal/lethal or cause blindness and damage to the liver, kidneys, and heart if swallowed – Toxicity effects from repeated over exposure have an accumulative effect on the central nervous system, especially the optic nerve – Symptoms may ...

  8. Ring-opening metathesis polymerisation - Wikipedia

    en.wikipedia.org/wiki/Ring-opening_metathesis...

    The mechanism of homogeneous ring-opening metathesis polymerization is well-studied. It is similar to any olefin metathesis reaction. Initiation occurs by forming an open coordination site on the catalyst. Propagation happens via a metallacycle intermediate formed after a 2+2 cycloaddition. When using a G3 catalyst, 2+2 cycloaddition is the ...

  9. Methanol-to-olefin - Wikipedia

    en.wikipedia.org/?title=Methanol-to-olefin&...

    This page was last edited on 22 April 2018, at 14:36 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may ...