1998
DOI: 10.1002/(sici)1521-4087(199804)23:2<111::aid-prep111>3.0.co;2-j
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Stationary Phases 45(1). Chromatographic Separation of High Energetic Materials with C60-Fullerene Stationary Phase

Abstract: A method for the chromatographic separation of nitroaromatic high energetic materials on C60‐fullerene stationary phase is discussed. Special selectivity on this phase using methanol/water(80/20) as mobile phase leads to have a wider separating space so that its retention power is much greater than that of a commercial RP‐18 phase. This advantage can be used to identify the isomers of some nitroaromatic high energetic materials.

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Cited by 7 publications
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“…For example, Chang et al, have reported the immobilisation of C 60 -fullerenes on silica substrates, and applied the modied phase as a reversed-phase substrate for use in the HPLC separation of high energetic materials (explosives). 47 The retention behaviour for a total of 23 explosives was studied, and a well resolved separation of 6 explosives was achieved in $35 min, using isocratic elution with methanol-water (80/20) mixture. This was directly compared to the separation of the same analytes, under the same conditions on an ODS stationary phase, where no separation was achieved due to co-elution of 4 of the 6 analytes.…”
Section: Fullerenesmentioning
confidence: 99%
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“…For example, Chang et al, have reported the immobilisation of C 60 -fullerenes on silica substrates, and applied the modied phase as a reversed-phase substrate for use in the HPLC separation of high energetic materials (explosives). 47 The retention behaviour for a total of 23 explosives was studied, and a well resolved separation of 6 explosives was achieved in $35 min, using isocratic elution with methanol-water (80/20) mixture. This was directly compared to the separation of the same analytes, under the same conditions on an ODS stationary phase, where no separation was achieved due to co-elution of 4 of the 6 analytes.…”
Section: Fullerenesmentioning
confidence: 99%
“…These results clearly highlight the much higher specicity for substituted aromatic compounds afforded by the immobilised fullerenes, and is supported by similar studies reporting high selectivity for PAHs using such phases. 48 More recently, Bonn and co-workers have explored the selectivity of C 60 -fullerene modied silica gels, using a similar immobilisation approach to that of Chang et al, 47,48 but here fullerenes were immobilised onto 3-aminopropylsilica (APS) using either C 60 -fullerenoacetic acid or C 60 -epoxyfullerene as the starting materials. [49][50][51] Characterising selectivity of the modied phases towards various biomolecules, including amino acids, carbohydrates, proteins, peptides and phospholipids was the main aim of this work, and particular selectivity for phosphorylated peptides was noted by the researchers.…”
Section: Fullerenesmentioning
confidence: 99%