TY - JOUR

T1 - The change of the unit cell dimension of different zeolite types by heating and its influence on supported membrane layers

AU - Noack, M.

AU - Schneider, M.

AU - Dittmar, A.

AU - Georgi, G.

AU - Caro, J.

PY - 2009/1/1

Y1 - 2009/1/1

N2 - In comparison with the well-known swelling of organic polymer membranes, zeolite membranes have been considered for a long time as relatively stiff. The problem of the different thermal expansion coefficients of the α-Al2O3 support and the zeolite layer was usually reduced on a possible crack formation during the template removal of MFI membranes. However, the crack formation could be avoided by an extremely slow heating rate and by membrane layers formed of small and non-oriented zeolite crystallites. Several papers have shown that the isomorphous incorporation of Al into the MFI structure (silicalite → ZSM-5) results in an increase of the non-selective intercrystalline transport and - as a consequence - the separation selectivity drops. In accordance with this observation, no shape-selective gas separation is reported for the Al-rich zeolite membranes MOR, FAU and LTA. On the other hand, these membranes allow the highly selective separation of water from organic mixtures due to hydrophilic interactions. In the present paper the change of the unit cell dimension (UCD) for zeolites LTA, FAU, MOR and MFI was studied as a function of temperature and water content using Rietveld refinement. Parallel to the determination of the linear and volume expansion coefficients by in situ-heating XRD, the de-watering and de-templating was studied by thermogravimetry (TGA). A strong UCD-change was found for all Al-rich zeolite types as a result of the de-watering. In contrast, the smallest changes of the UCD in the temperature range 50-450 °C were found for MFI crystals. Nevertheless, also for MFI membrane layers with rising temperature an increasing tension between the expanding α-Al2O3 support and the slightly shrinking membrane layer takes place. Zeolite layers of small crystals with either a random or a preferential crystal orientation relative to the support and an only partial de-watering in the case of Al-rich zeolite layers can minimize the tension in the support-membrane system. Thus, the irreversible formation of macroscopic cracks can be avoided and the formation of small intercrystalline pores in the mesopore region becomes reversible.

AB - In comparison with the well-known swelling of organic polymer membranes, zeolite membranes have been considered for a long time as relatively stiff. The problem of the different thermal expansion coefficients of the α-Al2O3 support and the zeolite layer was usually reduced on a possible crack formation during the template removal of MFI membranes. However, the crack formation could be avoided by an extremely slow heating rate and by membrane layers formed of small and non-oriented zeolite crystallites. Several papers have shown that the isomorphous incorporation of Al into the MFI structure (silicalite → ZSM-5) results in an increase of the non-selective intercrystalline transport and - as a consequence - the separation selectivity drops. In accordance with this observation, no shape-selective gas separation is reported for the Al-rich zeolite membranes MOR, FAU and LTA. On the other hand, these membranes allow the highly selective separation of water from organic mixtures due to hydrophilic interactions. In the present paper the change of the unit cell dimension (UCD) for zeolites LTA, FAU, MOR and MFI was studied as a function of temperature and water content using Rietveld refinement. Parallel to the determination of the linear and volume expansion coefficients by in situ-heating XRD, the de-watering and de-templating was studied by thermogravimetry (TGA). A strong UCD-change was found for all Al-rich zeolite types as a result of the de-watering. In contrast, the smallest changes of the UCD in the temperature range 50-450 °C were found for MFI crystals. Nevertheless, also for MFI membrane layers with rising temperature an increasing tension between the expanding α-Al2O3 support and the slightly shrinking membrane layer takes place. Zeolite layers of small crystals with either a random or a preferential crystal orientation relative to the support and an only partial de-watering in the case of Al-rich zeolite layers can minimize the tension in the support-membrane system. Thus, the irreversible formation of macroscopic cracks can be avoided and the formation of small intercrystalline pores in the mesopore region becomes reversible.

KW - FAU crystals

KW - Hydrophilicity

KW - Intercrystalline mesopores

KW - LTA

KW - MFI

KW - MOR

KW - Unit cell dimension

KW - Water loading

KW - Zeolite membranes

UR - http://www.scopus.com/inward/record.url?scp=55749104201&partnerID=8YFLogxK

U2 - 10.1016/j.micromeso.2008.05.013

DO - 10.1016/j.micromeso.2008.05.013

M3 - Article

AN - SCOPUS:55749104201

VL - 117

SP - 10

EP - 21

JO - Microporous and Mesoporous Materials

JF - Microporous and Mesoporous Materials

SN - 1387-1811

IS - 1-2

ER -