ABSTRACT
Phase change materials that leverage the latent heat of solid-liquid transition have many applications in thermal energy transport and storage. When employed as particles within a carrier fluid, the resulting phase change slurries (PCSs) could outperform present-day single-phase working fluidsâprovided that viscous losses can be minimized. This work investigates the rheological behavior of encapsulated and nonencapsulated phase change slurries (PCSs) for applicability in flowing thermal energy systems. The physical and thermal properties of the PCS candidates, along with their rheological behavior, are investigated below and above their phase transition points at shear rates of 1-300 s-1, temperatures of 20-80 °C, and concentrations of 15-37.5 wt %. The effect of shell robustness and melting on local shear thickening and global shear thinning is discussed, followed by an analysis of the required pumping power. A hysteresis analysis is performed to test the transient response of the PCS under a range of shear rates. We assess the complex viscoelastic behavior by employing oscillatory flow tests and by delineating the flow indicesâflow consistency index (K) and flow behavior index (n). We identify a viscosity limit of 0.1 Pa·s for optimal thermal performance in high-flow applications such as renewable geothermal energy.
ABSTRACT
The complexation of MgII with adenosine 5'-triphosphate (ATP) is omnipresent in biochemical energy conversion, but is difficult to interrogate directly. Here we use the spin- 1/2 ß-emitter 31 Mg to study MgII -ATP complexation in 1-ethyl-3-methylimidazolium acetate (EMIM-Ac) solutions using ß-radiation-detected nuclear magnetic resonance (ß-NMR). We demonstrate that (nuclear) spin-polarized 31 Mg, following ion-implantation from an accelerator beamline into EMIM-Ac, binds to ATP within its radioactive lifetime before depolarizing. The evolution of the spectra with solute concentration indicates that the implanted 31 Mg initially bind to the solvent acetate anions, whereafter they undergo dynamic exchange and form either a mono- (31 Mg-ATP) or di-nuclear (31 MgMg-ATP) complex. The chemical shift of 31 Mg-ATP is observed up-field of 31 MgMg-ATP, in accord with quantum chemical calculations. These observations constitute a crucial advance towards using ß-NMR to probe chemistry and biochemistry in solution.
Subject(s)
Adenosine Triphosphate , Magnesium , Adenosine Triphosphate/chemistry , Imidazoles , Magnetic Resonance Spectroscopy/methodsABSTRACT
Correction for 'Solution-processed wrinkled electrodes enable the development of stretchable electrochemical biosensors' by Yuting Chan et al., Analyst, 2019, 144, 172-179.
ABSTRACT
Wearable biosensors are critical for enabling real-time and continuous health monitoring and disease management. Conductors that retain their conductivity under strain are an essential building block of these systems. Strategies based on stretchable materials or structures have enabled the development of electrodes that can withstand impressive strains before loss of conductivity. In spite of this, it remains challenging to develop three-dimensional and high surface area electrodes that combine stretchability with high analytical sensitivity. Here, we develop stretchable electrochemical biosensors using solution-processed wrinkled gold electrodes. Wrinkling enhances the surface area of the electrodes and allows glucose to be detected with a sensitivity of 750-810 µA M-1 cm-2. Furthermore, wrinkling enables electrodes to be strained by up to 230% without significant loss in conductivity.
