The modulation of coupled relaxation in porous media.

This work investigates the effects of modulation of the transverse and longitudinal relaxation of the surface-fluid/pore-fluid spin system in porous media. Important new NMR well logging applications identify pore fluids by varying the CPMG T(2) pulse spacing to discriminate on the basis of fluid diffusivities in applied and local static magnetic field gradients. However, anomalous laboratory CPMG T(2) results have been reported repeatedly over 25 years for various porous media filled with a single fluid. In relatively large pores, at near bulk conditions, the transverse relaxation of diffusing molecular spins should be proportional to the square of the CPMG pulse spacing tau, the susceptibility contrast at the pore wall and the applied gradient. Observed is a markedly linear tau dependence that saturates at a plateau for large tau. The effect is not quadratic in applied gradient or susceptibility. For large pores, the tau dependence and the saturation value are proportional to the surface-to-volume ratio of the pores. This is in distinct contrast to the behavior observed by Borgia, Brown and Fantazzini for systems with much smaller pores at higher magnetic fields. The large-pore anomalous behaviors can be explained as a modulation of the exchange between surface-fluid and pore-fluid spins, such as observed by Luz and Meiboom in 1963 for water enriched with quadrupolar 17O. Scalar coupling of the solid-surface spins to the fluid-surface spins was postulated by Kleinberg, Kenyon and Mitra as a dominant relaxation mechanism for the surface fluid. The CPMG tau effect can be described as the modulation of the exchange coupling by the CPMG pi pulses, which mix the magnetizations between the exchanging, strongly coupled spin systems of the pore-fluid and the surface-fluid, which is, in turn, weakly coupled by scalar or pseudo-scalar interactions to the fast-relaxing solid surface.     

A lithium ion battery using nanostructured Sn-C anode, LiFePO4 cathode and polyethylene oxide-based electrolyte

In this work we report a lithium ion battery based on a nanostructured Sn-C anode, an improved lithium iron phosphate, LiFePO₄, cathode and a polyethylene oxide-based electrolyte. The battery has a solid-like configuration, high safety and can operate at room temperature with a stable capacity of the order of 120 mAh g^− 1 at a voltage of 2.8 V. These properties candidate the battery as very appealing energy accumulation system suitable for environmentally friendly, safe, applications.     

Total Fluorescence Fingerprinting of Pesticides: A Reliable Approach for Continuous Monitoring of Soils and Waters

The present work relates to the creation/extension of a database of Total Excitation-Emission and Total Synchronous Fluorescence Matrices (TEEMs and TSFMs) along with optimal Synchronous Fluorescence Spectra (SFS) to fingerprint pesticides widely used in Morocco. This spectrometric multi-component fingerprinting may permit the direct detection of pesticides persisting in soil or water. The objective of the current investigation is to detect four pesticide remains in agricultural soils by applying the spectrometric fingerprinting results. They are the commercial: i) insecticide Axlera 5G (carbamate), ii) fungicide Orsalis 5% SC (triazole), iii) insecticide Force 0,5 G (pyrethrinoid) and iv) insecticide Proclaim 05 SG (non-assigned). The agricultural plantations monitored are located in the great agricultural Doukkala region at the western Atlantic side of Morocco, where these chemicals are in large sale and use.     

Using the liquid nature of the stationary phase in countercurrent chromatography. IV. The cocurrent CCC method

The retention volumes of solutes in countercurrent chromatography (CCC) are directly proportional to their distribution coefficients, K(D) in the biphasic liquid system used as mobile and stationary phase in the CCC column. The cocurrent CCC method consists in putting the liquid "stationary" phase in slow motion in the same direction as the mobile phase. A mixture of five steroid compounds of widely differing polarities was used as a test mixture to evaluate the capabilities of the method with the biphasic liquid system made of water/methanol/ethyl acetate/heptane 6/5/6/5 (v/v) and a 53 mL CCC column of the coil planet centrifuge type. It is shown that the chromatographic resolution obtained in cocurrent CCC is very good because the solute band broadening is minimized as long as the solute is located inside the "stationary" phase. Pushing the method at its limits, it is demonstrated that the five steroids can still be (partly) separated when the flow rate of the two liquid phases is the same (2 mL/min). This is due to the higher volume of upper phase (72% of the column volume) contained inside the CCC column producing a lower linear speed compared to the aqueous lower phase linear speed. The capabilities of the cocurrent CCC method compare well with those of the gradient elution method in HPLC. Continuous detection is a problem due to the fact that two immiscible liquid phases elute from the column. It was partly solved using an evaporative light scattering detector.     

Alkane effect in the Arizona liquid systems used in countercurrent chromatography

Countercurrent chromatography (CCC) is a separation technique that uses a biphasic liquid system; one liquid phase is the mobile phase, the other liquid phase is the stationary phase. Selection of the appropriate liquid system can be a problem in CCC, since it is necessary to select both the “column” and the mobile phase at the same time as the first is completely dependent on the second. A range of systems with various proportions of solvents were developed to ease this choice; 23 variations of the heptane/ethyl acetate/methanol/water biphasic liquid system were labeled A to Z. This range proved to be extremely useful and became the popular Arizona (AZ) liquid system. However, authors often replace the heptane with hexane. In this work, the chemical compositions of the upper phases and the lower phases of 55 Arizona systems made with various alkanes (pentane, hexane, heptane, isooctane and cyclohexane) were determined by gas chromatography and Karl Fischer titration. The test mixture separated consisted of five steroid compounds. The lower phases were found to have similar compositions when different alkanes were used, but the upper phases were found to change. Exchanging heptane for hexane or isooctane produced minimal changes in the CCC chromatogram, while changing the proportions of the solvents resulted in an exponential change in the retention volumes. The high density of cyclohexane made liquid stationary phase retention difficult. All Arizona systems equilibrated within 30 min, but were not stable: water slowly hydrolyzed the ethyl acetate (as shown by a continuous decrease in the pH of the lower aqueous phase), especially in the water-rich systems (early alphabet letters).     

A Long‐Life Lithium Ion Battery with Enhanced Electrode/Electrolyte Interface by Using an Ionic Liquid Solution

In this paper, we report an advanced long‐life lithium ion battery, employing a Pyr₁₄TFSI‐LiTFSI non‐flammable ionic liquid (IL) electrolyte, a nanostructured tin carbon (Sn‐C) nanocomposite anode, and a layered LiNi_1/3Co_1/3Mn_1/3O₂ (NMC) cathode. The IL‐based electrolyte is characterized in terms of conductivity and viscosity at various temperatures, revealing a Vogel–Tammann–Fulcher (VTF) trend. Lithium half‐cells employing the Sn‐C anode and NMC cathode in the Pyr₁₄TFSI‐LiTFSI electrolyte are investigated by galvanostatic cycling at various temperatures, demonstrating the full compatibility of the electrolyte with the selected electrode materials. The NMC and Sn‐C electrodes are combined into a cathode‐limited full cell, which is subjected to prolonged cycling at 40 °C, revealing a very stable capacity of about 140 mAh g^?1 and retention above 99 % over 400 cycles. The electrode/electrolyte interface is further characterized through a combination of electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM) investigations upon cell cycling. The remarkable performances reported here definitively indicate that IL‐based lithium ion cells are suitable batteries for application in electric vehicles.     

A tetraethylene glycol dimethylether-lithium bis(oxalate)borate (TEGDME-LiBOB) electrolyte for advanced lithium ion batteries

Tetraethylene glycol dimethylether-lithium bis(oxalate)borate (TEGDME-LiBOB) electrolyte is here studied. Electrochemical impedance spectroscopy (EIS) measurements demonstrate that the electrolyte has conductivity higher than 10^− 3 S cm^− 1 at room temperature and about 10^− 2 S cm^− 1 at 60 °C, while thermogravimetry indicates a stability extending up to 180 °C. Sweep voltammetry of the electrolyte shows anodic stability extending over 4.6 V vs. Li and cathodic peak at about 1.5 V vs. Li/Li⁺, caused by a decomposition of LiBOB salt, and following prevented by using a pre-treated Sn-C anode. Furthermore, LiFePO₄ electrode is successfully used as cathode in a lithium cell using the TEGDME-LiBOB electrolyte. The promising electrochemical results, the low cost and the very high safety level candidate the electrolyte here reported as a valid alternative to the conventional electrolyte based on fluorinated salts presently used in the lithium ion battery field.     

96 mW longitudinal single mode red-emitting distributed Bragg reflector ridge waveguide laser with tenth order surface gratings

Red-emitting ridge waveguide lasers with integrated tenth order surface distributed Bragg reflector gratings were developed. The grating was implemented by the use of a BCl3-Ar-plasma, while the shape of the grating trench was controlled by additional He-backside cooling of the wafer. The devices exhibit longitudinal single mode operation up to 96 mW at 635.3 nm with a side mode suppression ratio of 18 dB and a good beam quality of M2<3. The spectrum is free of mode hops for a span of more than 55 pm.