In situ dehydration behavior of zeolite-like pentagonite: A single-crystal X-ray study

Danisi, Rosa Micaela; Armbruster, Thomas; Lazic, Biljana (2013). In situ dehydration behavior of zeolite-like pentagonite: A single-crystal X-ray study. Journal of solid state chemistry, 197, pp. 508-516. Elsevier 10.1016/j.jssc.2012.09.002

[img] Text
danisi_armbruster.pdf - Published Version
Restricted to registered users only
Available under License Publisher holds Copyright.

Download (1MB) | Request a copy

The structural modifications upon heating of pentagonite, Ca(VO)(Si4O10)·4H2O (space group Ccm21, a=10.3708(2), b=14.0643(2), c=8.97810(10) Å, V=1309.53(3) Å3) were investigated by in situ temperature dependent single-crystal X-ray structure refinements. Diffraction data of a sample from Poona district (India) have been measured in steps of 25 up to 250 °C and in steps of 50 °C between 250 and 400 °C. Pentagonite has a porous framework structure made up by layers of silicate tetrahedra connected by V4+O5 square pyramids. Ca and H2O molecules are extraframework occupants. Room temperature diffraction data allowed refinement of H positions. The hydrogen-bond system links the extraframework occupants to the silicate layers and also interconnects the H2O molecules located inside the channels. Ca is seven-fold coordinated forming four bonds to O of the tetrahedral framework and three bonds to extraframework H2O. The H2O molecule at O9 showing a high displacement parameter is not bonded to Ca. The dehydration in pentagonite proceeds in three steps. At 100 °C the H2O molecule at O8 was released while O9 moved towards Ca. As a consequence the displacement parameter of H2O at O9 halved compared to that at room temperature. The unit-cell volume decreased to 1287.33(3) Å3 leading to a formula with 3H2O per formula unit (pfu). Ca remained seven-fold coordinated. At 175 °C Ca(VO)(Si4O10)·3H2O transformed into a new phase with 1H2O molecule pfu characterized by doubling of the c axis and the monoclinic space group Pn. Severe bending of specific TOT angles led to contraction of the porous three-dimensional framework. In addition, H2O at O9 was expelled while H2O at O7 approached a position in the center of the channel. The normalized volume decreased to 1069.44(9) Å3. The Ca coordination reduced from seven- to six-fold. At 225 °C a new anhydrous phase with space group Pna21 but without doubling of c had formed. Release of H2O at O7 caused additional contraction of TOT angles and volume reduction (V=1036.31(9) Å3). Ca adopted five-fold coordination. During heating excursion up to 400 °C this anhydrous phase remained preserved. Between room temperature and 225 °C the unit-cell volume decreased by 21% due to dehydration. The dehydration steps compare well with the thermo-gravimetric data reported in the literature.

Item Type:

Journal Article (Original Article)

Division/Institute:

08 Faculty of Science > Institute of Geological Sciences > Mineralogical Crystallography (discontinued)

UniBE Contributor:

Danisi, Rosa Micaela and Armbruster, Thomas Michael

Subjects:

500 Science > 540 Chemistry
500 Science > 550 Earth sciences & geology

ISSN:

0022-4596

Publisher:

Elsevier

Language:

English

Submitter:

Frank Gfeller

Date Deposited:

18 Jun 2014 11:15

Last Modified:

26 Jun 2016 01:48

Publisher DOI:

10.1016/j.jssc.2012.09.002

Uncontrolled Keywords:

Pentagonite, Dehydration, Crystal structure, Hydrogen bonding

BORIS DOI:

10.7892/boris.45446

URI:

https://boris.unibe.ch/id/eprint/45446

Actions (login required)

Edit item Edit item
Provide Feedback