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  2. Thermoplastic olefin - Wikipedia

    en.wikipedia.org/wiki/ThermoPlastic_Olefin

    If PP and PE are the dominant component of a TPO blend then the rubber fraction will be dispersed into a continuous matrix of "crystalline" polypropylene. If the fraction of rubber is greater than 40% phase inversion may be possible when the blend cools, resulting in an amorphous continuous phase, and a crystalline dispersed phase.

  3. Functionalized polyolefins - Wikipedia

    en.wikipedia.org/wiki/Functionalized_polyolefins

    Randomly functionalized polyolefins have differing types, location, and amount of functionality on the polyolefin backbone. Randomly functionalized polyolefins can be synthesized through many familiar combination of polymerization techniques including: post-functionalization, ROMP/hydrogenation, ADMET/hydrogenation, radical polymerization, and catalytic copolymerization.

  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. Polyolefin - Wikipedia

    en.wikipedia.org/wiki/Polyolefin

    An alpha-olefin (or α-olefin) is an alkene where the carbon-carbon double bond starts at the α-carbon atom, i.e. the double bond is between the #1 and #2 carbons in the molecule. Alpha-olefins such as 1-hexene may be used as co-monomers to give an alkyl branched polymer (see chemical structure below), although 1-decene is most commonly used ...

  6. Straight-chain terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Straight-chain_terminal_alkene

    Straight-chain terminal alkenes, also called linear alpha olefins (LAO) or normal alpha olefins (NAO), are alkenes (olefins) having a chemical formula C n H 2n, distinguished from other alkenes with a similar molecular formula by being terminal alkenes, in which the double bond occurs at the alpha (α-, 1-or primary) position, and by having a linear (unbranched) hydrocarbon chain.

  7. 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 ...

  8. Ziegler–Natta catalyst - Wikipedia

    en.wikipedia.org/wiki/Ziegler–Natta_catalyst

    A Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, is a catalyst used in the synthesis of polymers of 1-alkenes (alpha-olefins).Two broad classes of Ziegler–Natta catalysts are employed, distinguished by their solubility:

  9. Terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Terminal_alkene

    The double bond of an alpha olefin is between the #1 and #2 (IUPAC) or α and β (common) carbon atoms. In organic chemistry , terminal alkenes ( alpha-olefins , α-olefins , or 1-alkenes ) are a family of organic compounds which are alkenes (also known as olefins) with a chemical formula C x H 2 x , distinguished by having a double bond at the ...