Carbon molecular sieve transport mechanisms

Gas separation membranes combining the desirable gas transport properties of molecular sieving media and the attractive mechanical and low cost properties of polymers are considered. A fundamental analysis of predicted mixed matrix membrane performance based on intrinsic molecular sieve and polymer matrix gas transport properties is discussed. This assists in proper materials selection for the given gas separation. In addition, to explore the practical applications of this concept, this paper describes the experimental incorporation of 4A zeolites and carbon molecular sieves in a Matrimid matrix with subsequent characterization of the gas transport properties. There is a discrepancy between the predicted and the observed permeabilities of O2/N2 in the mixed matrix membranes. This discrepancy is analyzed. Some conclusions are drawn and directions for further investigations are given. 

Figure 22.7 Descriptions of nanoporous carbon membranes (a) mechanism of transport through the molecular sieve carbon (MSC) membrane, (b) mechanism of transport through the selective surface flow (SSF) membrane, (c) separation performance of H2S—H2 mixtures by the SSF membrane, (d) schematic drawing of a two-stage SSF membrane operation for Fl2S—FI2/CH4 separation.

To surpass Robeson s upper bound, materials are emerging that rely on transport mechanisms other than solution-diffusion through glassy or rubbery polymeric materials. In particular, a number of materials have been developed that possess fixed microporosity (2 nm or less) in contrast to the activated, transient molecular gaps that give rise to diffusion in most polymers. These materials include amorphous and crystalline (zeolite) ceramics [68-69], molecular sieve carbons [70], polymers that possess intrinsic microporosity [71-72], and carbon nanotube membranes [73-76]. Transport in such materials is determined primarily by the average size and size distribution of the microporosity - the porosity can be tuned to allow discrimination between species that differ by less than one Angstrom in size. However, surface... 

Mass transfer of gas through a porous membrane can involve several processes depending on the pore stmcture and the solid [1]. There are four different mechanisms for the transport Poiseuille flow Knndsendiflusion partial condensation/capillaiy diffusion/selective adsorption and molecular sieving [2, 3]. The transport mechanism exhibited by most of carbon membranes is the molecular sieving mechanism as shown in Fig. 2.1. The carbon membranes contain constrictions in the carbon matrix, which approach the molecular dimensions of the absorbing species [4],... 

Rao and Sircar [5-7] introduced nanoporous supported carbon membranes which were prepared by pyrolysis of PVDC layer coated on a macroporous graphite disk support. The diameter of the macropores of the dried polymer film was reduced to the order of nanometer as a result of a heat treatment at 1,000°C for 3 h. These membranes with mesopores could be used to separate hydrogen-hydrocarbon mixtures by the surface diffusion mechanism, in which gas molecules were selectively adsorbed on the pore wall. This transport mechanism is different from the molecular sieving mechanism. Therefore, these membranes were named as selective sitrface flow (SSF ) membranes. It consists of a thin (2-5 pm) layer of nanoporous carbon (effective pore diameter in the range of 5-6 A) supported on a mesoporous inert support such as graphite or alumina (effective pore diameter in the range of 0.3-1.0 pm). The procedures for making the selective surface flow membranes were described in [5, 7]. In particular, the requirements to produce a surface diffusion membrane were shown clearly in [7]. 

Gas transport in zeolites, some molecular sieve carbons, and polymers is described by a sorption-diffusion mechanism. In these cases, the permeability coefficient, P, of penetrant A is the product of a kinetic parameter, the average diffusion coefficient and a thermodynamic parameter, S, the solubility coefficient (2). 

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