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Alpha olefins processes Ziegler process

Another source, catalytic oligomerization, which produces the alpha olefins using the Ziegler process mentioned above, has its own treatment in Chapter 21. But then the Oxo process really only replaces steps-three and four in Figure 15-3. Besides, Oxo higher alcohols still have branches. [Pg.221]

Ziegler process. The chemistry of the Ziegler catalyst route to alpha olefins is the same as. you read in Chapter 15, The Higher Alcohols. The treatment here is another approach, and you might find it instructive. Or not. [Pg.304]

What is the difference between the Ziegler process for producing alpha olefins and the one described in Chapter 15 for producing higher alcohols ... [Pg.313]

In the Ziegler process, why do you think there is a distribution of different carbon count alpha olefins rather than just one ... [Pg.313]

In the higher alcohol process, the displacement is affected by oxidizing the trialkyl aluminum and then hydrolyzing, to form aluminum hydroxide and the linear alcohol. In the Ziegler process for alpha olefins, ethylene is used to displace the alpha olefin. [Pg.433]

The Ziegler process produces the full range of alpha olefins, from C4 to C2o The Alpha Select process produces C4 through Cio-... [Pg.433]

Compounds with 6 to 18 carbons are the most common alpha olefins (a-olefins) and Ziegler catalysts are used in this process. Certain olefins such as nonene (C9) and dodecene (C12) can also be made by cracking and dehydrogenation of n-paraffins, as practiced in the petrochemical section of a refinery. [Pg.295]

With the Ziegler displacement process the higher alkyl group is displaced from the chain growth product by ethylene. This yields a mixture of even-numbered linear alpha olefins with the trialkyl aluminum being recycled. The odd-numbered linear alcohols are produced through hydroformylation of the olefin and hydrogenation of the odd-numbered aldehydes. [Pg.5704]

For decades, linear dialkyl phthalate plasticizers with sidechains between seven and eleven carbons in length, averaging 9 carbons (71 IP and more recently L9P), have been widely used in many North American made flexible PVC products for outdoor applications. Linear dialkyl phthalates are defined as those derived from commercial alcohols with very little side chain branching. These alcohols range from 100% normal products made by ethylene growth in the Ziegler process to 65% normal, 35% 2-methyl branched products made from oxonation of normal alpha olefins.[l] (91 IP and 1 IP have also been available, but at a premium price.) The relatively less branched alkyl sidechains in a linear, as opposed to a branched, dialkyl phthalate afford measurably improved... [Pg.156]


See other pages where Alpha olefins processes Ziegler process is mentioned: [Pg.169]    [Pg.161]    [Pg.53]    [Pg.401]    [Pg.10]    [Pg.38]    [Pg.409]    [Pg.66]    [Pg.156]    [Pg.79]    [Pg.80]    [Pg.295]    [Pg.204]    [Pg.6]    [Pg.9]    [Pg.338]    [Pg.2918]   
See also in sourсe #XX -- [ Pg.304 , Pg.305 ]




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Alpha olefins

Ziegler process

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