Publicaties

Skip Navigation Links.
Recent verschenen
Expand per documenttypeper documenttype
Expand per Unitper Unit
Expand per Clusterper Cluster

Zoeken naar publicaties:
Beperk het zoeken tot de velden:

ECN publicatie:
Titel:
Tuning the nanopore structure and separation behavior of hybrid organosilica membranes
 
Auteur(s):
Castricum, H.L.; Paradis, G.G.; Mittelmeijer-Hazeleger, M.C.; Bras, W.; Eeckhaut, G.; Vente, J.F.; Rothenberg, G.; Elshof, J.E. ten
 
Gepubliceerd door: Publicatie datum:
ECN Biomass & Energy Efficiency 20-12-2013
 
ECN publicatienummer: Publicatie type:
ECN-W--13-064 Artikel wetenschap tijdschrift
 
Aantal pagina's:
13  

Gepubliceerd in: Microporous and Mesoporous Materials (Elsevier), , 2014, Vol.185, p.224-234.

Samenvatting:
The exceptional hydrothermal- and solvent stability of organically linked silica makes it a promising candidate material for molecular separation membranes. Tailoring towards specific separation properties however requires precise control over the pore structure. Here we show that this can be achieved by adjusting the acid-to-Si ratio immediately before the onset of physical drying of the 1,2-bis(triethoxysilyl) ethane-based polymeric colloidal sols. This procedure provides uniform coating conditions and results in defect-free films. The structure development is investigated with in-situ Small-Angle X-ray Scattering, both in a solvent and during film drying. Acid-catalyzed colloidal growth in a solvent is governed by diffusion- limited cluster aggregation for all studied acid concentrations. Upon solvent evaporation, micropores (<2 nm) are formed at low acid concentrations (H+:Si 6 0.1). This can be explained by compressive capillary forces exerted by the receding pore liquid. At H+:Si = 1, reaction-limited cluster aggregation is observed during drying, followed by the formation of pores >2 nm. The compressive forces are balanced by a network strengthened by ongoing condensation reactions, and by the positive charge on the hybrid organosilica. This results in a larger pore size under more acidic conditions. The permselectivity of the supported membranes correlates with the pore structure of the unsupported materials. Thus, the adaptability of the pore structure allows a wider applicability of organosilica membranes in energy-efficient industrial molecular separations.


Terug naar overzicht.