Encapsulation of Hydrated Salt Phase Change Materials within Polymer Monoliths through Emulsion-templating

Seminars
16.12.2018
14:30
David Wang Auditorium, 3rd floor Dalia Maydan Bldg
MSc Candidate Natalie Rosen

MSc Candidate Natalie Rosen

Department of Materials Science and Engineering,
Technion, Haifa, Israel

Phase change materials (PCMs) store and release thermal energy through their relatively high latent heat associated with melting and crystallization. Salt hydrates PCMs have several advantages over organic PCMs such as paraffins and over fatty acids: a relatively high latent heat per volume, high thermal conductivity, non-flammability, and the availability of a wide range of transition temperatures. Since salt hydrates tend to melt incongruently, resulting in irreversible melt-freeze processes, and exhibit significant supercooling, their utilization in energy storage applications has been limited.

The objective of this research was to develop an innovative method of encapsulating an inorganic salt hydrate PCM within polymer monoliths, templating within molten-salt-in-oil high internal phase emulsions (HIPEs). This work focused on calcium chloride hexahydrate (CaCl2·6H2O, CC‑HH), with a melting point of 30 ˚C and a latent heat of fusion of 176 J/g, that was encapsulated within an elastomeric polyacrylate based on 2-ethylexyl acrylate (EHA). The effects of HIPE stabilization, locus of polymer initiation, nucleation, crosslinking strategy, and polymerization procedures were investigated. The emulsion-templated structures were characterized using scanning electron microscopy and the thermal properties were characterized using differential scanning calorimetry. Based on the results of thermal cycling tests, the most promising encapsulation system exhibited a CC‑HH content of 79% dispersed within droplets of 100 to 300 µm, with melting and crystallization heats of ~120 J/gsample (~160 J/gCC‑HH). The addition of 3 wt % SCl2·6H2O as a nucleating agent reduced the extent of supercooling to 14 °C, in contrast to 43 °C for pure CC‑HH. The resulting average melting and crystallization temperatures were 34 °C and 20 °C, respectively. Unfortunately, the relatively interconnected droplet structure had a negative effect on the long-term thermal stability of the encapsulated CC‑HH, with irreversible phase separation and CaCl2·4H2O formation producing a 40% reduction in latent heat.   

Prof. Michael S. Silverstein