Abstract
To assess the impact of environmental toxicants on human health, researchers routinely use GC/MS, and the compounds they use for analytical reference standards must be synthesized, purified, and characterized. Reversed-phase HPLC separation and structure identification of polychlorinated dibenzo-p-dioxin (PCDD) isomers (potentially hazardous environmental contaminants) in synthesis reaction mixtures were accomplished by taking advantage of the different retention mechanisms at work on four different stationary phases bonded to silica gel. Hydrophobic, charge-transfer, and dipole-dipole interactions characterize the analyte elution orders of the positional isomers of PCDDs from columns packed with C18, pyrenylethyl, (nitrophenyl)ethyl, and (nitrophenoxy)-propyl stationary phases.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 2502-2509 |
| Number of pages | 8 |
| Journal | Analytical Chemistry |
| Volume | 65 |
| Issue number | 18 |
| DOIs | |
| State | Published - Sep 1 1993 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
All Science Journal Classification (ASJC) codes
- Analytical Chemistry
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