The fluxes of aromatic molecules (p-xylene, o-xylene, and benzene) were mea
sured as a function of temperature and feed partial pressure through severa
l molecular sieve membranes (SAPO-5, SAPO-11, and mordenite) and three type
s of MFI membranes (silicalite-1, ZSM-5, and boron-substituted ZSM-5). Sing
le-file diffusion appeared to control transport through the SAPO and morden
ite membranes. Hence, those membranes showed ideal selectivities greater th
an 1 for benzene over the xylene isomers but no separation selectivities fo
r the mixtures. Surface diffusion and activated gaseous transport were the
controlling mechanisms for the MFI membranes. The highest p-xylene/o-xylene
selectivities were obtained for a boron-substituted ZSM-5 membrane. At fee
d partial pressures of 2.1 kPa and at a temperature of 425 K, the best sele
ctivities were 130 (ideal) and 60 (separation). Zeolite pores preferentiall
y permeated p-xylene and took as long as 8 h to reach steady state. Nonzeol
ite pores preferentially permeated o-xylene after much shorter breakthrough
times. Higher pressures of p-xylene distorted the membrane framework, resu
lting in increased o-xylene permeation and reduced selectivity. After reach
ing steady state, the flux of p-xylene through zeolite pores was stable for
at least 10 h. The flux of o-xylene through nonzeolite pores was similarly
stable at 373 K but continuously decreased for at least 12 h at 405 K.