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Polypolar aromatics

The results in Figure 1 can be interpreted in terms of general ring structures with the hydrocarbon classes. The peak for the polypolar aromatic fraction at 160° C probably is caused by polar-monocyclic compounds and the peak at 240° C is probably the result of polar dicyclic compounds. The broad curve in the monoaromatics centering at 275°C is probably mainly caused by alkyl-substituted tetralins while the peaks... [Pg.85]

Saturates Monoaromatics Diaromatics Polypolar Aromatics Loss... [Pg.80]

See other pages where Polypolar aromatics is mentioned: [Pg.84]    [Pg.85]    [Pg.86]    [Pg.87]    [Pg.81]    [Pg.82]    [Pg.84]    [Pg.85]    [Pg.86]    [Pg.87]    [Pg.81]    [Pg.82]   
See also in sourсe #XX -- [ Pg.81 , Pg.82 ]

See also in sourсe #XX -- [ Pg.81 , Pg.82 ]



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Aromatic polypolar

Aromatic polypolar

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