Magnetic resonance imaging: an innovative approach to observe rare metal extraction using ionic liquid.

In the present work, a novel approach has been made to evaluate the extraction mechanism of neodymium (Nd) using trihexyl-tetradecyl-phosphonium benzoate (TTPB) ionic liquid through nuclear magnetic resonance (NMR) techniques. A detailed study on the interactions between the extractant (Nd) and the ionic liquid (IL) is presented. The 1H NMR spectral analysis confirmed that Nd extraction took place through the benzoate anion. Furthermore, the NMR relaxation time of the anion is greatly affected affirming that Nd extraction indeed took place through the benzoate anion. This change in the relaxation time caused by the Nd ion on the protons in the anion and cation in TTPB has been used to visualize the extraction mechanism using 1H MRI. A strong change in the image intensity with respect to the time observed in the IL phase validates the extraction of Nd from the aqueous phase into the IL phase. Also, combining the 1H NMR, diffusion coefficient, Karl-Fischer and ultraviolet-visible absorption spectroscopic (UV-Vis) results, we have elucidated the co-ordination structure around Nd during the extraction process.

Drug formulation augments the therapeutic response of carboplatin administered through a lymphatic drug delivery system.

Treatment of metastatic lymph nodes (LNs) is challenging due to their unique architecture and biophysical traits. Systemic chemotherapy fails to impede tumor progression in LNs due to poor drug uptake and retention by LNs, resulting in fatal systemic metastasis. To effectively treat LN metastasis, achieving specific and prolonged retention of chemotherapy drugs in the tumor-draining LNs is essential. The lymphatic drug-delivery system (LDDS) is an ultrasound-guided drug-delivery methodology for administration of drugs to LNs that addresses these requirements. However, early-stage metastatic LNs have an additional set of drug transport barriers, such as elevated intranodal pressure and viscosity, that negatively impact drug diffusion. In the present study, using formulations of elevated osmotic pressure and viscosity relative to saline, we sought to favorably alter the LN's physical environment and study its impact on pharmacokinetics and consequently the therapeutic efficacy of carboplatin delivered using the LDDS. Our study confirmed the capability of a drug formulation with elevated osmotic pressure and viscosity to alter the architecture of LNs, as it caused notable expansion of the lymphatic sinus. Additionally, the study delineated an optimal range of osmotic pressure and viscosity, centered around 1897 kPa and 11.5 mPa·s, above and below which therapeutic efficacy was found to decline markedly. These findings suggest that formulation osmotic pressure and viscosity are parameters that require critical consideration as they can both hinder and promote tumorigenesis. The facile formulation reported here has wide-ranging applicability across cancer spectrums and is thus anticipated to be of great clinical benefit.

Understanding Ion Dynamics in Closoborate-Type Lithium-Ion Conductors on Different Time-Scales.

The lithium-ion transport mechanism in 0.7Li(CB9H10)-0.3Li(CB11H12) complex hydride solid electrolyte was studied over a wide time-scale (ns-ms) by choosing appropriate techniques for assessing ionic motion on the desired time-scale using nuclear magnetic resonance (NMR) relaxation, AC impedance, and pulsed field gradient-NMR (PFG-NMR) measurements. The 7Li NMR line width decreased with increasing temperature, and the spin-lattice relaxation time T1 for the cation and anions showed a minimum near 303 K, indicating that the lithium ions and the anions were highly mobile. The activation energy estimated from the analysis of the NMR relaxation time matched well with the values estimated from the AC impedance and PFG-NMR. This confirms that the lithium-ion motion in 0.7Li(CB9H10)-0.3Li(CB11H12) is the same over a wide time-scale, suggesting steady Li-ion motion over a wide transport range. This understanding offers insights into strategies for designing complex hydride lithium superionic conductors.

Complex Hydride-Based Gel Polymer Electrolytes for Rechargeable Ca-Metal Batteries.

Rechargeable Ca batteries offer the advantages of high energy density, low cost, and earth-abundant constituents, presenting a viable alternative to lithium-ion batteries. However, using polymer electrolytes in practical Ca batteries is not often reported, despite its potential to prevent leakage and preserve battery flexibility. Herein, a Ca(BH4)2-based gel-polymer electrolyte (GPE) is prepared from Ca(BH4)2 and poly(tetrahydrofuran) (pTHF) and tested its performance in Ca batteries. The electrolyte demonstrates excellent stability against Ca-metal anodes and high ionic conductivity. The results of infrared spectroscopy and 1H and 11B NMR indicate that the terminal ─OH groups of pTHF reacted with BH4 - anions to form B─H─(pTHF)3 moieties, achieving cross-linking and solidification. Cyclic voltammetry measurements indicate the occurrence of reversible Ca plating/stripping. To improve the performance at high current densities, the GPE is supplemented with LiBH4 to achieve a lower overpotential in the Ca plating/stripping process. An all-solid-state Ca-metal battery with a dual-cation (Ca2+ and Li+) GPE, a Ca-metal anode, and a Li4Ti5O12 cathode sustained >200 cycles, confirming their feasibility. The results pave the way for further developing lithium salt-free Ca batteries by developing electrolyte salts with high oxidation stability and optimal electrochemical properties.

Synthesis of Li(1+x)V3O8 by chemical route and its characterization.

Lithium trivanadate (Li(1+x)V3O8) nanorods have been synthesized by the simple polymer precursor route using the polymer, polyvinyl pyrrolidone (PVP) as the complexing agent. Thermal behavior of the precursor has been studied by the differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and differential thermal analysis (DTA) techniques. X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR) studies confirm the formation of the compound. High resolution scanning electron microscopy (HRSEM) analysis reveals the synthesized Li1.2V3O8 particles to be nanorods with an average diameter of 50 nm.