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Liquid chromatographic separation of aromatic hydrocarbons with chemically bonded (2,4-dinitroanilinopropyl) silica

Journal Article · · Anal. Chem.; (United States)
DOI:https://doi.org/10.1021/ac00244a013· OSTI ID:7119623
A detailed comparison of alumina and chemically bonded silica-R(NH/sub 2/)/sub 2/ and (2,4-dinitroanilinopropyl)silica (DNAP-silica) for the compound-class (ring-numbered) high-performance liquid chromatographic separation of aromatic hydrocarbons was made with 86 model compounds either expected or known to be present in petroleums, coal liquids, or shale oils. Model compounds ranged from one-ring aromatic hydrocarbons to highly condensed polyaromatic hydrocarbons containing six aromatic rings. The importance of substituent and structure effects on separations was determined by varying the degree of alkyl and naphthenic substitution on the basic ring structures. Determination of the best system was based upon the relative retention strengths, grouping tendencies, and the observed structure and substituent effects. The silica-DNAP and alumina were determined to be more sensitive to molecular structure but less sensitive to substituent effects than the silica-R(NH/sub 2/)/sub 2/. The retention characteristics of all three systems are strongly dependent upon steric effects. On the basis of retention strengths and grouping tendencies, the DNAP-silica is considered superior to alumina and silica-R(NH/sub 2/)/sub 2/.
Research Organization:
Bartlesville Energy Technology Center, OK
OSTI ID:
7119623
Journal Information:
Anal. Chem.; (United States), Journal Name: Anal. Chem.; (United States) Vol. 54:7; ISSN ANCHA
Country of Publication:
United States
Language:
English

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