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Barocaloric material
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Barocaloric materials are characterized by strong, reversible thermic responses to changes in pressure. Many involve solid-to-solid phase changes from disordered to ordered and rigid under increased pressure, releasing heat. Barocaloric solids undergo solid-to-solid phase change.[1] One barocaloric material processes heat without a phase change: natural rubber.[2]

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Barocaloric effects can be achieved at pressures above 200 MPa for intermetallics or about 100 MPa in plastic crystals. However, NH4I changes phase at pressures of 80 MPa.[3] The hybrid organic–inorganic layered perovskite (CH3–(CH2)n−1–NH3)2MnCl4 (n = 9,10), shows reversible barocaloric entropy change of ΔSr ~ 218, 230 J kg−1 K−1 at 0.08 GPa at 294-311.5 K (transition temperature).[4]

Barocaloric materials are one of several classes of materials that undergo caloric phase transitions. The others are magnetocaloric, electrocaloric, and elastocaloric. Magnetocaloric effects typically require field strengths larger than 2 T, while electrocaloric materials require field strengths in the kV to MV/m range. Elastocaloric materials may require force levels as large as 700 MPa.

Potential applications

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Barocaloric materials have potential use as refrigerants in cooling systems instead of gases such as hydrofluorocarbons. cycles, the pressure then drives a solid-to-solid phase change.[5] A prototype air conditioner was made from a metal tube filled with a metal-halide perovskite (the refrigerant) and water or oil (heat/pressure transport material). A piston pressurizes the liquid.[1][6]

Another project used NH4I as the refrigerant. It achieved reversible entropy changes of ~71 J K−1 kg−1 at ambient temperature. The phase transition temperature is a function of pressure, varying at a rate of ~0.79 K MPa−1. The accompanying saturation driving pressure is ~40 MPa, a barocaloric strength of ~1.78 J K−1 kg−1 MPa−1, and a temperature span of ~41 K under 80 MPa. Neutron scattering characterizations of crystal structures/atomic dynamics show that reorientation-vibration coupling is responsible for the pressure sensitivity.[3]

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References

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