The diffusion of cyclohexane and several alkylcyclohexanes in silicali
te was studied using a simultaneous thermal analyzer. This apparatus a
llowed for the determination of heats of sorption and diffusion coeffi
cients. Zero length chromatography was also used to determine diffusiv
ities of some of the adsorbates. The trend in diffusion rates observed
was trans-1,4-dimethylcyclohexane >> methylcyclohexane > cyclohexane
> ethylcyclohexane, cis-1,4-dimethylcyclohexane. This is in qualitativ
e agreement with the previous results of Chon and Park. A comprehensiv
e interpretation of the experimental results was developed, using the
basic qualitative arguments of transition state theory. The fast diffu
sion of trans-1,4-dimethylcyclohexane is associated with a relatively
low energy barrier for channel crossing. The transition entropy for di
ffusion appears to be the reason for the more rapid diffusion of methy
lcyclohexane relative to cyclohexane.