Using inverse exclusion chromatography, the porous structure of four polyme
ric stationary phases has been investigated. Three of the copolymers were c
haracterized by a high degree of crosslinking because they were synthesized
from two tetrafunctional monomers. The fourth copolymer was obtained from
styrene (bifunctional monomer) and divinylbenzene (tetrafunctional monomer)
and has a significantly smaller degree of crosslinking.
To determine the pore size distribution of the copolymers, toluene, alkylph
enones, phthalates, and polystyrene standards were used as probes, Addition
ally, changes of the volume of the copolymers when changing from water to t
etrahydrofuran were determined. The results show that more stable porous st
ructures were obtained from tetrafunctional monomers. All polymeric station
ary phases have micropores in their internal structure but their contributi
ons are different.