High nitrile content cyano-substituted polymethylsiloxane encapsulated particles were prepared for double bond selectivity in packed capillary column supercritical fluid chromatography (SFC). Silica particles were deactivated with 50% cyanopropyl-substituted polymethylhydrosiloxane, and coated with
Cyanobiphenyl-substituted polymethylsiloxane encapsulated particles for packed capillary column supercritical fluid chromatography
✍ Scribed by Yufeng Shen; Wenbao Li; Abdul Malik; Shawn L. Reese; Bryant E. Rossiter; Milton L. Lee
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 590 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1040-7685
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Nine isomeric cyanobiphenyl‐substituted (25%) polymethylsiloxane (CBP) stationary phases were coated and immobilized by free‐radical crosslinking on silica packing materials for use in supercritical fluid chromatography (SFC). The selectivities of these packing materials to benzene derivatives, polycyclic aromatic hydrocarbons (PAHs), and double bonds in fatty acid methylesters (FAMEs) were determined. Among the nine isomeric CBP‐coated packing materials, the o, p‐CBP phase was found to be the most selective to both double bonds and aromatic isomers under SFC conditions. The durability of the packing materials was evaluated by measuring the changes in selectivity with SFC use. The loss in selectivity was less than 0.20% after being continuously washed by supercritical carbon dioxide at 100°C and 300 atm for more than 100 h.
📜 SIMILAR VOLUMES
Strongly basic polyethylenimines (PEI) were coated on both untreated and diol-bonded silica particles. The resultant basic surface was found suitable for the separation of strongly basic alkylamines such as a-phenylethylamines with a pK, of ca. 4, under supercritical fluid chromatography (SFC) condi