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Polyethylene naphthalene structure

Poro-xylene is an industrially important petrochemical. It is the precursor chemical for polyester and polyethylene terephthalate. It usually is found in mixtures containing all three isomers of xylene (ortho-, meta-, para-) as well as ethylbenzene. The isomers are very difficult to separate from each other by conventional distillation because the boiling points are very close. Certain zeoHtes or mol sieves can be used to preferentially adsorb one isomer from a mixture. Suitable desorbents exist which have boiling points much higher or lower than the xylene and displace the adsorbed species. The boihng point difference then allows easy recovery of the xylene isomer from the desorbent by distillation. Because of the basic electronic structure of the benzene ring, adsorptive separations can be used to separate the isomers of famihes of substituted aromatics as weU as substituted naphthalenes. [Pg.174]

At pressures of 13 GPa many carbonaceous materials decompose when heated and the carbon eventually turns into diamond. The molecular structure of the starting material strongly affects this process. Thus condensed aromatic molecules, such as naphthalene or anthracene, first form graphite even though diamond is the stable form. On the other hand, aliphatic substances such as camphor, paraffin wax, or polyethylene lose hydrogen and condense to diamond via soft, white, solid intermediates with a rudimentary diamond structure (29). [Pg.564]


See other pages where Polyethylene naphthalene structure is mentioned: [Pg.389]    [Pg.456]    [Pg.314]    [Pg.228]    [Pg.207]    [Pg.462]    [Pg.257]    [Pg.360]    [Pg.180]    [Pg.561]    [Pg.170]    [Pg.183]    [Pg.155]   
See also in sourсe #XX -- [ Pg.10 ]




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Naphthalene structure

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