Dynamic in situ growth of bonded-phase silica nanospheres on silica capillary inner walls for open-tubular liquid chromatography

Silica nanospheres (SNS) were grown on the inner walls of silica capillaries through a dynamic in situ nucleation process to prepare a highly porous and large accessible surface area substrate. The SNS were then functionalized with octadecyl (C-18), 3-aminopropyltriethoxysilane (APTES), beta-cyclodextrin (beta-CD), and amino groups to develop robust and efficient chromatographic stationary phases. The modified silica capillaries were exploited for open-tubular liquid chromatography (OT-LC) and open-tubular capillary electrochromatography (OT-CEC) applications. The prepared stationary phases were compared to conventional capillaries in terms of separation performance. The synthesis process was optimized, and the bonded-phase stationary phases were characterized by the electron microscopy technique. The effects of different solvents, additives, and functional groups on the geometry and chromatographic resolving power of the SNS were envisaged. The capillaries modified with octadecyl groups were evaluated for the separation of non-steroidal anti-inflammatory drugs, phenones, alkenylbenzenes, and enantiomers of chlorophenoxy herbicides. As an application instance, an SNS-C-18-coated capillary was utilized for the separation of alkenylbenzenes from clove extract and protein digest medium, through OT-LC and OT-CEC techniques, respectively. The beta-CD functionalized capillary was applied for the OT-CEC separation of a dichlorprop racemic mixture.

Automated summary

Silica nanospheres (SNS) were grown on the inner walls of silica capillaries through a dynamic in situ nucleation process, resulting in highly porous and large accessible surface area substrate. The SNS were functionalized with various groups to develop robust and efficient chromatographic stationary phases, which were compared to conventional capillaries in terms of separation performance. The effects of different solvents, additives, and functional groups on the SNS were studied.