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H. Morgner, “Computer Simulation on Static and Dynamic Properties during Transient Sorption of Fluids in Mesoporous Materials,” The Journal of Physical Chem-istry C, Vol. 114, 2010, pp. 8877-83. doi:org/10.1021/jp903717b

has been cited by the following article:

• TITLE: On a New Mechanism for Separating two Components in a Stationary Flow through Mesopores

  AUTHORS: Harald Morgner

  KEYWORDS: Fluids in Mesopores, Negative Pressure States, Pressure Dependence of Miscibility

  JOURNAL NAME: American Journal of Analytical Chemistry, Vol.2 No.5, September 22, 2011

  ABSTRACT: When simulating the behavior of fluids in a stationary flow through mesopores we have observed a phenomenon that may prove useful in some cases as basis for separating fluid components. The scheme works at constant temperature which makes it energy efficient as are other schemes like (molecular) sieves or chromatography. Sieves rely on differences in molecular size and chromatography on different affinity of components to the solid material of the ‘packing’. The scheme presented here may sometimes complement the established techniques in that it is based on a different mechanism. The fluids to be separated can have the same molecular size and the same affinity to solid material they are in contact with. The only requirement for the scheme to work is that the miscibility behavior varies somewhat with pressure or density. From literature it is known that virtually any mixture reacts on strong variations of pressure. Even a mixture that behaves almost ideally at ambient pressure will show slight deviations from ideal miscibility when exposed to extreme pressure. The strong differences in pressure are not created by external means but by exploiting the spontaneous behavior of fluids in mesopores. If the experiment is designed correctly, strong pressure gradients show up in mesopores that are far beyond any gradient that could be established by technical means. Our simulations are carried out for situations where pressure inside the pores varies between a few hundred bar positive pressure and a few hundred bar negative pressure while the pressure in the gas phase outside the pores amounts to ca.170 mbar.