Silica gel is the most widely used as a packing material for HPLC. It posse
sses the advantages of high mechanical strength, a large number of theoreti
cal plates, ease of chemical modification of the surface and availability;
at a relatively low price. The demand for further improvements in the perfo
rmance of silica-based packing materials has been increasing. In this study
, improvements of reversed phase packing materials, restricted access media
(RAM) and child stationary phases were achieved through the development of
new methods for silica surface modification. Art end-capping method using
high-temperature silylation was developed, which produced octadecylsilylate
d silica gel (ODS) without and undesirable effects of residual silanol grou
ps. In a study on RAM, glycerylalkylsilylated silica gels with alkyl moiety
ranging from C-3 to C-6 were prepared as a new type of RAM. These packing
materials did not adsorb proteins, but could retain small molecules, such a
s drugs, in direct injection analysis of serum samples. This is one of the
simplest methods for preparing RAM. In the addition, a low-temperature plas
ma treatment was applied to the preparation of RAM. The plasma more easily
removed octadecyl groups on the external surface of ODS; to produce silanol
groups than those on the internal surface. The silanol groups were glycery
lpropylsilylated to produce RAM. Furthermore, some novel chiral stationary
phases were prepared by covalently bonding chiral binaphthol and its deriva
tives to silica gels. These stationary phases showed enantioselectivity mai
nly basic compounds. The hydroxyl groups of binaphthol played a dominant ro
le in chiral recognition and retention.