Dynamics of supercooled water in highly compacted clays studied by neutron scattering
Creators
- 1. Laboratory for Waste Management, Paul Scherrer Institute, CH-5232 Villigen PSI (Switzerland)
- 2. Laboratory for Neutron Scattering, Paul Scherrer Institute, CH-5232 Villigen PSI (Switzerland)
- 3. Institut Laue-Langevin, 38042 Grenoble (France)
- 4. Forschungsneutronenquelle Heinz Maier-Leibnitz (FRM II), 85747 Garching (Germany)
Description
The freezing behavior of water confined in compacted charged and uncharged clays (montmorillonite in Na- and Ca-forms, illite in Na- and Ca-forms, kaolinite and pyrophyllite) was investigated by neutron scattering. Firstly, the amount of frozen (immobile) water was measured as a function of temperature at the IN16 backscattering spectrometer, Institute Laue-Langevin (ILL). Water in uncharged, partly hydrophobic (kaolinite) and fully hydrophobic (pyrophyllite) clays exhibited a similar freezing and melting behavior to that of bulk water. In contrast, water in charged clays which are hydrophilic could be significantly supercooled. To observe the water dynamics in these clays, further experiments were performed using quasielastic neutron scattering. At temperatures of 250, 260 and 270 K the diffusive motion of water could still be observed, but with a strong reduction in the water mobility as compared with the values obtained above 273 K. The diffusion coefficients followed a non-Arrhenius temperature dependence well described by the Vogel-Fulcher-Tammann and the fractional power relations. The fits revealed that Na- and Ca-montmorillonite and Ca-illite have similar Vogel-Fulcher-Tammann temperatures (TVFT, often referred to as the glass transition temperature) of ∼120 K and similar temperatures at which the water undergoes the 'strong-fragile' transition, Ts∼210 K. On the other hand, Na-illite had significantly larger values of TVFT∼180 K and Ts∼240 K. Surprisingly, Ca-illite has a similar freezing behavior of water to that of montmorillonites, even though it has a rather different structure. We attribute this to the stronger hydration of Ca ions as compared with the Na ions occurring in the illite clays
Availability note (English)
Available from http://dx.doi.org/10.1088/0953-8984/20/41/415102Additional details
Identifiers
- DOI
- 10.1088/0953-8984/20/41/415102;
- PII
- S0953-8984(08)78713-7;
Publishing Information
- Journal Title
- Journal of Physics. Condensed Matter
- Journal Volume
- 20
- Journal Issue
- 41
- Journal Page Range
- [9 p.]
- ISSN
- 0953-8984
- CODEN
- JCOMEL
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 40035385
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- BACKSCATTERING; CALCIUM IONS; FREEZING; GLASS; HYDRATION; ILLITE; KAOLINITE; MELTING; MONTMORILLONITE; NEUTRON DIFFRACTION; NEUTRON REACTIONS; PYROPHYLLITE; QUASI-ELASTIC SCATTERING; SODIUM IONS; SPECTROMETERS; TEMPERATURE DEPENDENCE; TEMPERATURE RANGE 0065-0273 K; TRANSITION TEMPERATURE; WATER
- Descriptors DEC
- BARYON REACTIONS; CHARGED PARTICLES; CLAYS; COHERENT SCATTERING; DIFFRACTION; DIRECT REACTIONS; HADRON REACTIONS; HYDROGEN COMPOUNDS; INORGANIC ION EXCHANGERS; ION EXCHANGE MATERIALS; IONS; MATERIALS; MEASURING INSTRUMENTS; MINERALS; NUCLEAR REACTIONS; NUCLEON REACTIONS; OXYGEN COMPOUNDS; PHASE TRANSFORMATIONS; PHYSICAL PROPERTIES; QUASI-FREE REACTIONS; SCATTERING; SILICATE MINERALS; SOLVATION; TEMPERATURE RANGE; THERMODYNAMIC PROPERTIES