Hh. Funke et al., SEPARATIONS OF CYCLIC, BRANCHED, AND LINEAR HYDROCARBON MIXTURES THROUGH SILICALITE MEMBRANES, Industrial & engineering chemistry research, 36(1), 1997, pp. 137-143
Binary and ternary mixtures of organic vapors were separated at elevat
ed temperatures with a silicalite zeolite membrane on a porous, tubula
r, gamma-alumina support. Linear alkanes (C-5-C-9), branched alkanes,
aromatics, and saturated ring compounds were used as feeds, and permea
nces of pure compounds and mixtures were measured between similar to 3
60 and 510 K. Pure compound permeances of the linear alkanes strongly
decrease with increasing chain length, whereas the branched and cyclic
compounds]permeate at rates similar to those of n-hexane and n-heptan
e. Almost all permeances increase with increasing temperature. Mixture
s of branched or cyclic molecules with small linear alkanes were readi
ly separated with high selectivities (over 200 for n-hexane/benzene),
even though the ratios of pure component permeances were small. The se
paration behavior is not due to molecular sieving but instead appears
to be due to preferential adsorption (adsorption on external surface,
pore entering, adsorption in pores) of one species, which prevents the
other organics from adsorbing and transporting through the membrane.
Mixtures of cyclic or branched molecules showed small or no separation
s. For all systems, separations factors decrease as temperature increa
ses apparently because preferential adsorption becomes less important
at elevated temperatures. For mixtures of benzene or methylyclohexane
with 2,2,4-trimethylpentane and for mixtures of 2,2-dimethylbutane wit
h 3-methylpentane, both compounds permeated at similar rates and no se
parations were obtained. Single-file transport in the zeolite channels
is suspected to limit transport. The membranes have intercrystalline
regions in parallel with the zeolite pores that may also permeate the
organics.