Issue 0, 1971

Zeolitic water content and adsorptive capacity for ammonia of microporous sepiolite

Abstract

Sepiolite from Amboseli, Tanzania, possesses a high adsorptive capacity for ammonia at 273 K and 298 K after outgassing below 378 K; the B.E.T. (N2) area is ca. 360 m2 g–1. The adsorption of NH3 and N2 is greatly decreased by prior exposure of outgassed sepiolite to NH3 followed by outgassing at 373 K, or by outgassing fresh sepiolite above 383 K. Desorption of NH3 from the solid is accompanied by the loss of H2O previously strongly held. Exchange of NH3 with up to half the co-ordinately bound H2O in sepiolite is postulated. A classification of ‘acidic sites’ on the surface on the basis of NH3 retention is thus not possible. The adsorptive capacities for NH3 and N2 of sepiolite exposed to NH3 can be restored to the original values by exposure to H2O vapour for 24 h. Only partial regeneration is possible for sepiolite outgassed above 393 K.

Thermogravimetric studies in a vacuum and in air yield results which are compared with other data and with theoretical models of the sepiolite structure. The above effects are discussed in terms of reversible and irreversible bonding of adsorbed NH3, of the exchange of NH3 and structural H2O, and of the ‘tilting’ of lattice channels of the sepiolite structure when it is heated in vacuo above 390 K.

Article information

Article type
Paper

J. Chem. Soc. A, 1971, 2383-2387

Zeolitic water content and adsorptive capacity for ammonia of microporous sepiolite

A. J. Dandy, J. Chem. Soc. A, 1971, 2383 DOI: 10.1039/J19710002383

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements