Ionic Nitrate Research Articles

The infrared spectrum of the protic ionic liquid 1-methylimidazolium nitrate: An ab initio molecular dynamics simulation study

Complex features observed in the infrared (IR) spectrum of the protic ionic liquid 1-methylimidazolium nitrate, [C1im][NO3], are assigned using ab initio molecular dynamics (AIMD) simulation. AIMD is used at the same level of theory to simulate the known X-ray crystal structure of [C1im][NO3] and a cluster of ionic pairs representing the liquid phase. The calculation of several single particle and collective time correlation functions of velocity forms the basis for the AIMD simulation assignment of the infrared spectra. The AIMD simulation demonstrates that the lift of the degeneracy of the anion asymmetric stretching mode, νas(NO3), due to symmetry breaking and coupling to external modes result in multiple band splitting in the crystal spectrum in the region of the νas(NO3) mode. Owing of the intrinsic anharmonic characteristic of the AIMD simulation, the calculation accounts for the broad band in the high-frequency range of the IR spectrum caused by the cation ν(NH) stretching mode in strong cation–anion hydrogen bond. The AIMD simulation of the liquid captures spectral changes upon melting of [C1im][NO3] due to loosening of the NH···O hydrogen bond and changes in the [NO3]- interaction with other hydrogen atoms of the imidazolium ring. The AIMD simulation assigns the intermolecular stretching mode of the hydrogen bond, ν(NH…O), as the band at 183 cm−1 in the far infrared spectrum of the [C1im][NO3] crystal.

Electrochemical degradation of acetaminophen in urine matrices: Unraveling complexity and implications for realistic treatment strategies

Urine has an intricate composition with high concentrations of organic compounds like urea, creatinine, and uric acid. Urine poses a formidable challenge for advanced effluent treatment processes following urine diversion strategies. Urine matrix complexity is heightened when dealing with pharmaceutical residues like acetaminophen (ACT) and metabolized pharmaceuticals. This work explores ACT degradation in synthetic, fresh real, and hydrolyzed real urines using electrochemical oxidation with a dimensional stable anode (DSA). Analyzing drug concentration (2.5 - 40 mg L−1) over 180 min at various current densities in fresh synthetic effluent revealed a noteworthy 75% removal at 48 mA cm−2. ACT degradation kinetics and that of the other organic components followed a pseudo-first-order reaction. Uric acid degradation competed with ACT degradation, whereas urea and creatinine possessed higher oxidation resistance. Fresh real urine presented the most challenging scenario for the electrochemical process. Whereas, hydrolyzed real urine achieved higher ACT removal than fresh synthetic urine. Carboxylic acids like acetic, tartaric, maleic, and oxalic were detected as main by-products. Inorganic ionic species nitrate, nitrite, and ammonium ions were released to the medium from N-containing organic compounds. These findings underscore the importance of considering urine composition complexities and provide significant advancements in strategies for efficiently addressing trace pharmaceutical contamination.

Novel crosslinked gum tragacanth electrolyte with enhanced thermal, mechanical and water resistive properties

Although electrolytes prepared from natural substances have taken up research towards a greener future, practical difficulties in their mechanical and water resistive properties are yet to be addressed by many. In this current paper, a natural gum tragacanth is graft copolymerized with tertiary butyl acrylate utilising glutaraldehyde as the crosslinker and ascorbic acid and potassium persulfate as the initiators. From the TGA analysis, enhanced thermal stability is observed in the crosslinked membrane. The DSC analysis reveals that the crosslinked gum exhibits a glass transition temperature (Tg) of 66 °C and a melting temperature (Tm) of 86 °C. The water uptake of the crosslinked membrane was found to be lower than the pure non-crosslinked membrane. The stress-strain curves of the crosslinked electrolyte showed a tensile strength of 3.58Mpa and a percent elongation of 302%. The effect of the crosslinker glutaraldehyde and the ionic salt lithium nitrate is studied with the help of XRD and FTIR. The electrolyte is characterised to be a good ionic conductive membrane as its conductivity value is found to be 4.72 ×10−4 Scm−1 through EIS measurements. The Arrhenius behaviour of temperature-dependent conductivity was studied and the activation energy values for all the films were calculated.

Thermal Characterization of [C2Im][NO3] and Multivalent Nitrate Salts Mixtures

Due to their intrinsic properties, the current applicability of ionic liquids is enormous. In particular, their use in electrochemistry is beyond question. Numerous studies on these compounds and their mixtures, especially with lithium salts, focus on their use as electrolytes for batteries and other energy storage devices. This includes thermal energy storage devices, where 4th generation ionic liquids and their derivatives show a huge potential. Nevertheless, considering the uneven availability of the raw materials, such as lithium, research has extended to mixtures of these compounds with other salts of different metals that are more abundant and widely distributed, such as magnesium or aluminum. This work presents a comprehensive thermal characterization, using differential scanning calorimetry and thermogravimetry, of the protic ionic liquid ethylimidazolium nitrate and its mixture with magnesium and aluminum nitrate salts at different concentrations. Additionally, a comparison between these results and previous studies of mixtures of this ionic liquid with lithium nitrate, as well as mixtures of the protic ionic liquid EAN with the same metal salts, was also performed. The results indicated that the salt addition tends to broaden and reduce crystallization and melting peaks, while the glass transition becomes more visible and shifts to higher temperatures with increasing salt concentration. This is due to the disorder generated by the rearrangement of ions in the polar domains, which erodes the hydrogen bond network of the protic ionic liquid. Nevertheless, the thermal stability of the blended samples does not change significantly compared to the bulk ionic liquid.

Characterization of the H2/NOx reaction process over the La0.9Ce0.1Co0.9Pd0.1O3-BaO/Al2O3 catalyst

An excellent textual properties and performance La0.9Ce0.1Co0.9Pd0.1O3-BaO/Al2O3 catalyst was synthesized. The reaction mechanism of H2/NOx over the La0.9Ce0.1Co0.9Pd0.1O3-BaO/Al2O3 catalyst was investigated by temperature programmed reduction/ desorption/ surface reaction (TPR/D/SR) technologies and in-situ diffuse reflectance Fourier transform (DRIFT) technology. The results show that cerium or palladium species are inserted into the cells of LaCoO3, as well as they synergetic promote the redox properties of the La0.9Ce0.1Co0.9Pd0.1O3-BaO/Al2O3 catalyst. Surface activated nitrates exist over the La0.9Ce0.1Co0.9Pd0.1O3-BaO/Al2O3 catalyst, with thermal stable increasing in the order: absorbed N2O4 < monodentate nitrates < chelating bidentate nitrates < nitrates unidentate < free ionic nitrates < bulk free ionic nitrates. H2 preferentially reacted with absorbed N2O4 and monodentate nitrates at low temperatures, due to their high activity. The concentration of generated NH3 from the redox reaction of H2/NOx achieves the maximum value between 350 and 450 °C over the La0.9Ce0.1Co0.9Pd0.1O3-BaO/Al2O3 catalyst. Compared with the NOx adsorption process at 50 °C, monodentate nitrates and absorbed N2O4 disappeared due to their low thermal stability, chelating bidentate nitrates become stronger, as well as free ionic nitrates converted to bulk free ionic nitrates with higher thermal stability at 350 °C. When H2 is exposed to NOx species adsorbed on La0.9Ce0.1Co0.9Pd0.1O3-BaO/Al2O3, chelating bidentate nitrates and bulk free ionic nitrates are consumed gradually, indicating that although the bulk free ionic nitrates own high stability, it also could be consumed by involving in the H2/NOx reaction at 350 °C. The quantitative H2/NO reaction experiments confirmed the results of H2-TPSR and NSR. It is beneficial to the formation of NH3 when the H2/NO ratio is more than 2.5. Comparing traditional Pt-BaO/Al2O3 catalyst, the La0.9Ce0.1Co0.9Pd0.1O3-BaO/Al2O3 catalyst exhibit an excellent performance, including considerable NH3 production property, lower N2O selectivity, and the precious metal saving.

Laser-induced fluorescence detection of nitroxyl (HNO) formed from the thermal decomposition of hydroxylammonium nitrate vapor

The decomposition of the ionic liquid hydroxylammonium nitrate (HAN) produces gas phase products which have utility in spacecraft propulsion systems. Among the various gas phase species generated from HAN decomposition is the nitroxyl (HNO) radical, a highly reactive molecule with implications in both chemical and electric propulsion applications. The work described here used a laser-induced fluorescence platform to directly detect the relative density of the HNO radical formed by passing HAN vapor through heated porous disks of varying composition. The use of heated porous 316-stainless steel and aluminum disks showed significant HNO density production and is attributed to a surface hydrogen abstraction mechanism. There was also evidence of surface modification to the metal disks which resulted in a shift in the HNO density temperature profiles. The results reported demonstrate that use of a heated porous material can easily generate a molecular vapor at moderate temperatures for combustion and electric propulsion applications.

On the formation of ammonia from the thermal decomposition of hydroxylammonium nitrate vapor

The ionic liquid hydroxylammonium nitrate (HAN) is a promising propellant for various types of spacecraft propulsion systems. With respect to combustion and plasma-based electric propulsion, the thermal decomposition of HAN into gas phase species provides a convenient feed gas supply. While the decomposition of HAN in the liquid phase has been extensively studied, little is known about the decomposition chemistry of HAN vapor interacting with heated surfaces. The ability to decompose HAN vapor on a reactive surface could provide a means to control the feed gas composition and enhance the performance of spacecraft propulsion systems.In this initial qualitative study, HAN was vaporized and thermally decomposed using porous 316-stainless-steel and quartz disks under vacuum conditions. Decomposition products with low vapor pressures would condense on an in-line quartz tube which was subsequently collected and analyzed with Raman spectroscopy, NMR spectroscopy, and FT-IR spectroscopy. At temperatures above 440 K the 316-stainless-steel system produced significant quantities of ammonia which reacted with vaporized nitric acid to form ammonium nitrate. Temperatures below 440 K yielded partial HAN decomposition which resulted in a binary mixture of HAN and ammonium nitrate. The degree to which HAN was consumed was determined by analysis of the 1008 cm−1N-OH asymmetric Raman band of HAN and the 1049 cm−1 symmetric stretching Raman band of the nitrate ion, NO3−. The quartz system yielded significantly different results with no ammonium nitrate detected at temperatures above 440 K. Reformed HAN was the primary product detected at lower temperatures. The difference in reported measurements and visual observations highlights the distinct differences in HAN vapor decomposition chemistry from the two materials examined.

Hofmeister effects influence bulk nanostructure in a protic ionic liquid

HypothesisThe origins and behaviour of specific ion effects have been studied in water for more than a century, and more recently in nonaqueous molecular solvents. However, the impacts of specific ion effects on more complex solvents such as nanostructured ionic liquids remains unclear. Here, we hypothesise that the influence of dissolved ions on the hydrogen bonding in the nanostructured ionic liquid propylammonium nitrate (PAN) constitutes a specific ion effect. ExperimentsWe performed molecular dynamics simulations of bulk PAN and 1–50 mol% PAN-PAX (X = halide anions F−, Cl−, Br−, I−) and PAN-YNO3 (Y = alkali metal cations, Li+, Na+, K+ and Rb+) solutions to investigate how monovalent salts influence the bulk nanostructure in PAN. FindingsThe key structural characteristic in PAN is a well-defined hydrogen bond network formed within the polar and non-polar domains in its nanostructure. We show that dissolved alkali metal cations and halide anions have significant and unique influences on the strength of this network. Cations (Li+, Na+, K+ and Rb+) consistently promote hydrogen bonding in the PAN polar domain. Conversely, the influence of halide anions (F−, Cl−, Br−, I−) is ion specific; while F− disrupts PAN hydrogen bonding, I− promotes it. The manipulation of PAN hydrogen bonding therefore constitutes a specific ion effect – i.e. a physicochemical phenomena caused by the presence of dissolved ions, which are dependent on these ions’ identity. We analyse these results using a recently proposed predictor of specific ion effects developed for molecular solvents, and show that it is also capable of rationalising specific ion effects in the more complex solvent environment of an ionic liquid.

Separation of americium from highly active raffinates by an innovative variant of the AmSel process based on the ionic liquid Aliquat-336 nitrate

A new variant of the AmSel (Americium Selective Separation) system for the separation of Am(iii) from a PUREX raffinate was tested in which the aliphatic diluent was replaced by the ionic liquid Aliquat-336 nitrate.

ATOMIZATION AND MIXING OF BLENDED ENERGETIC IONIC LIQUID HYDROXYETHYLHYDRAZINIUM NITRATE

Hypergolic propellants are widely used in liquid rocket propulsion. Instantaneous control of combustion, lack of requirement of an ignition system, and storability for long durations are the major advantages of hypergolic propellants. The propellant community is on the lookout for replacements for the currently utilized toxic hydrazine and its derivatives. Energetic hypergolic ionic liquids are excellent candidates for such replacement. However, their high viscosity and surface tension render atomization difficult, and hence, increase the ignition delays in the combustion chamber and reduce combustion efficiency. The current study focuses on the geometrical aspects of injector design and other injection conditions that control the ignition process and combustion efficiency. These mainly depend on the extent of mixing and atomization. Shadowgraphy and patternator-based experiments were performed on doublet and triplet impingement injectors under variable injection conditions, such as impingement angle, jet diameters, and injection velocities. A blend of 50&amp;#37; unsymmetrical dimethylhydrazine in the energetic ionic liquid hydroxyethylhydrazinium nitrate (UHN50) shows promise as a candidate for a hydrazine replacement. A blend of 38&amp;#37; ethanol in glycerol (GE6238) was used as a surrogate for UHN50, whereas water was used as a surrogate for nitrogen tetroxide. The effect of variation of injection conditions was found to be contradictory for achieving atomization and mixing. An optimum criterion was obtained for both atomization and mixing.

Collective Effects in Ionic Liquid [emim][Tf2N] and Ionic Paramagnetic Nitrate Solutions without Long-Range Structuring.

Mesoscopic shear elasticity has been revealed in ordinary liquids both experimentally by reinforcing the liquid/surface interfacial energy and theoretically by nonextensive models. The elastic effects are here examined in the frame of small molecules with strong electrostatic interactions such as room temperature ionic liquids [emim][Tf2N] and nitrate solutions exhibiting paramagnetic properties. We first show that these charged fluids also exhibit a nonzero low-frequency shear elasticity at the submillimeter scale, highlighting their resistance to shear stress. A neutron scattering study completes the dynamic mechanical analysis of the paramagnetic nitrate solution, evidencing that the magnetic properties do not induce the formation of a structure in the solution. We conclude that the elastic correlations contained in liquids usually considered as viscous away from any phase transition contribute in an effective way to collective effects under external stress whether mechanical or magnetic fields.

Assessment of traffic-related chemical components in ultrafine and fine particles in urban areas in Vietnam

Ultrafine particles (UFPs or PM0.1; aerodynamic diameter ≤ 0.1 μm) were monitored at a roadside site (RS) in a populated area of Hanoi, Vietnam. Meanwhile, UFPs and fine particles (FPs or PM2.5, aerodynamic diameter ≤ 2.5 μm) were monitored at an ambient site (AS), located at an on-campus a university, approximately 200 m away from the RS. Sampling was conducted in different seasons–summer, winter, and the transitional periods of summer-to-winter and winter-to-summer (STP and WTP, respectively). Carbonaceous and ionic species in UFPs and FPs–rarely investigated in the study area–were analyzed to observe the seasonal variations, characteristics of UFPs near the roadway, and spatial differences between the sites. The UFPs concentration at the AS was in the order of winter > STP > WTP > summer, whereas that of the FPs was winter > WTP > STP > summer. This seasonal variation of particle concentration was possibly affected by the meteorological conditions, which contribute to the highest concentration in winter. The higher FPs concentration in WTP than in STP resulted from the substantial increase in ionic concentrations, particularly sulfate, nitrate, and ammonium. This result indicates the effect of secondary formation processes under drizzle-like weather, which is typical during WTP in northern Vietnam. Compared with UFPs at the AS, traffic-related emissions were more noticeable in UFPs at the RS, including a higher EC concentration and lower OC/EC ratio. The possibility of particle growth under favorable conditions, including the presence of gas-phase pollutants and the availability of surface areas owing to high UFPs concentration in Hanoi, may explain the low correlation of the chemical components between UFPs and FPs in the sites. This study serves as a reference for further investigation of the relationship between UFPs and FPs under highly polluted conditions in big cities in Vietnam in future studies.

Silver as an Antibiotic-Independent Antimicrobial: Review of Current Formulations and Clinical Relevance.

Background: The increase of multi-drug-resistant organisms has revived the use of silver as an alternative antibiotic-independent antimicrobial. Although silver's multimodal mechanism of action provides low risk for bacterial resistance, high local and uncontrolled concentrations have shown toxicity. This has resulted in efforts to develop novel silver formulations that are safer and more predictable in their application. Optimization of silver as an antimicrobial is crucial given the growing resistance profile against antibiotics. This article reviews formulations of silver used as antimicrobials, focusing on the mechanisms of action, potential for toxicity, and clinical applications. Methods: A search of four electronic databases (PubMed, Embase, MEDLINE, and Cochrane Library) was conducted for relevant studies up to January 2022. Searches were conducted for the following types of silver: ionic, nanoparticles, colloidal, silver nitrate, silver sulfadiazine, silver oxide, silver carboxylate, and AQUACEL® (ConvaTec, Berkshire, UK). Sources were compiled based on title and abstract and screened for inclusion based on relevance and study design. Results: A review of the antimicrobial activity and uses of ionic silver, silver nanoparticles, colloidal silver, silver nitrate, silver sulfadiazine, silver oxide, Aquacel, and silver carboxylate was conducted. The mechanisms of action, clinical uses, and potential for toxicity were studied, and general trends between earlier and more advanced formulations noted. Conclusions: Early forms of silver have more limited utility because of their uncontrolled release of silver ions and potential for systemic toxicity. Multiple new formulations show promise; however, there is a need for more prospective in vivo studies to validate the clinical potential of these formulations.

L-Proline Nitrate: An Efficient Amino Acid Ionic Liquid Catalyzed Synthesis of 5-aryl-[1, 2, 4]-triazolidine-3-thiones

Abstract: An environmentally benign, simple, rapid synthesis of 1,2,4-triazolidine-3-thiones at room temperature is reported using amino acid-derived Brønsted acidic ionic liquid L-proline nitrate [Pro+NO3 -] from aldehyde and thiosemicarbazide in an aqueous medium. A cost-effective and energy-efficient catalyst with the reusability of up to five cycles without significant loss in the catalytic activity makes this protocol superior. A faster reaction and easy work-up with excellent yields are the added advantages of this protocol.

The gas phase reaction of iridium and iridium carbide anions with 2-hydoxyethylhydrazine (HEH)

Understanding the chemistry of compounds that are similar to hydrazine has two advantages. First, it helps to identify less hazardous propellants to replace hydrazine as the most widely used monopropellant. And second, it helps to gain insight into the reaction mechanism that could be analogous to the decomposition of hydrazine into ammonia and nitrogen. Ionic liquids have already shown to be promising candidates to replace hydrazine. The molecule investigated in this study is 2-hydroxyethlyhydrazine (HOCH2CH2NHNH2; HEH), which is a neutral precursor to the ionic liquid 2-hydroxyethylhydrazinium nitrate (HEHN) and differs from hydrazine by the substitution of a hydrogen with a hydroxyethyl group. Gas phase photoelectron spectroscopy and density functional theory were used to examine the reaction between a HEH molecule and an Ir− anion as well as with IrC−. Suggested by the experimental and theoretical data, Ir− and IrC− react with HEH and can attack the C–N, C–O, N–N, C–H and the C–C bond in HEH.

Hydrogen-bonding and symmetry breaking in the protic ionic liquid 1-ethylimidazolium nitrate

The strong cation-anion interaction in the protic ionic liquid 1-ethylimidazolium nitrate, [C2im][NO3], is revealed in different regions of the infrared spectrum (IR). The IR band related to the anion asymmetric stretching mode νas(NO3) splits due to degeneracy lifting, the symmetry forbidden symmetric stretching mode νs(NO3) acquires significant IR activity, and the cation ν(NH) stretching mode produces a broad band characteristic of strong hydrogen bond (H-bond). At high temperatures (up to 120 °C), these spectral features remain in the IR spectrum, indicating the strong cation-anion interaction. The size of the νas(NO3) splitting, the relative strength of νs(NO3), and the intermolecular H-bond stretching mode ν(NH…O) seen in the far-IR range are all accounted for in a quantum chemistry calculation of an ionic pair. The complex spectral pattern in the high-frequency range of the IR spectrum, where NH and CH stretching modes occur in overlapping bands, can be explained using a simple model coupling the ν(N–H) and ν(NH…O) modes. The parameters of the model, including the dependence of the ν(NH) frequency on the N…O distance of the H-bond, are also derived from the ionic pair calculation. The IR spectrum thus gives experimental evidence that using an ionic pair to explore the H-bond influence on the electronic structure of [C2im][NO3] is reasonable.

Experimental and density functional theory studies on Cu/Ba-coimpregnated γ-Al2O3 for low-temperature NOx storage and adsorbent regeneration

Although the lean-NOx trap (LNT) has been used to reduce NOx emissions from diesel-powered vehicles, LNT application is limited because its performance degrades at low temperatures (e.g., during cold starting). Therefore, to enhance low-temperature NOx storage and adsorbent regeneration, γ-Al2O3 was coimpregnated with both Cu and Ba (Cu–Ba/γ-Al2O3). The experimentally measured NOx storage capacities (NSCs) and NOx storage efficiencies (NSEs) were compared. Density-functional-theory (DFT) calculations were performed to reveal the NOx storage mechanism. The Cu/Ba-coimpregnated γ-Al2O3 improved both NSC and NSE of NO storage and enhanced NSE of NO2 storage at initial stage. In addition, it desorbed NOx at lower temperatures than the conventional Ba-impregnated γ-Al2O3 (Ba/γ-Al2O3). The in-situ diffuse reflectance infrared Fourier-transform spectroscopy analysis and DFT calculations for NO storage showed that NO adsorption was superior on the Cu-compound surfaces and that stable hyponitrite was stored on the Ba-compound surfaces. In NO2 storage, Cu/Ba coimpregnation offered high preferential NO2 coverage on the CuO surface and produced the most stable ionic nitrate on the Ba-compound surfaces. The experimental and theoretical results confirmed that the Cu/Ba-coimpregnated adsorbent exhibited both superior NOx storage and adsorbent regeneration compared to the conventional Ba-containing LNT adsorbent.

Hydrogen bonding effect on the thermal behavior of acidic ionic liquids

A relationship between the thermal performance (melting and thermal decomposition) and the internal hydrogen bonds for the protic ionic liquids pyridinium nitrate ([H–Pyr]+[NO3]–), pyridinium hydrogen sulfate ([H–Pyr]+[HSO4]–), pyridinium dihydrogen phosphate ([H–Pyr]+[H2PO4]–) and 4-amino-1H-1,2,4-triazolium nitrate ([4-AT]+[NO3]–) is investigated in the current work. For that purpose, melting/decomposition points, non-covalent bonding and intermolecular interaction are studied by means of TGA/DSC, reduced density gradient method and a Hirshfeld surface analysis.Results established that strong hydrogen bonds, rather than van der Waals interactions, influence the thermal behavior of the aforementioned ionic liquids in a great extent. Melting points of the compounds under investigation are found to decrease in order [H–Pyr]+[NO3]– > [4-AT]+[NO3]– > [H–Pyr]+[H2PO4]– > [H–Pyr]+[HSO4]– due a various hydrogen bonding degree. Overall decomposition of the pyridinium-based ionic liquids includes simple pyridine evaporation and protic acid (HNO3, H2SO4 and H3PO4) decay. However, decomposition of 2-aminotriazolium fragment (except HNO3) is also detected during [4-AT]+[NO3]– decay upon heating.

Electrocatalytic activity enhancement of N,P-doped carbon nanosheets derived from polymerizable ionic liquids

A facile preparation method was developed to obtain two-dimensional (2D) metal-free N, P-co-doped carbon nanosheets with sp2/sp3 interface derived from polymerizable ionic liquids (PIL) and ammonium nitrate (NH4NO3), exhibiting better electrocatalytic activity than that of the commercial Pt/C toward oxygen reduction reaction (ORR). The introduction of NH4NO3 can benefit the formation of carbon nanosheets structure and hierarchical porous structure due to decomposition and carbonization of polymer and gases emission resulting from ammonia nitrate, which can be confirmed by the SEM, TEM and BET results. The sp3 carbon and doping effect of heteroatoms of N, P can be investigated with the XPS, Raman and NEXAFS spectroscopy. The present work developed a facile method to prepare heteroatom-co-doped carbon as metal-free catalyst toward ORR with superior catalytic performance. Two-dimensional carbon nanosheets doped with N, P atoms can be successfully prepared via pyrolysis process of the polymerizable ionic liquids ([Hvim]DHP) and NH4NO3, demonstrating superior electrocatalytic performance toward oxygen reduction in alkaline media.

Selective extraction of trivalent actinides using CyMe4BTPhen in the ionic liquid Aliquat-336 nitrate.

The extraction of Am(iii), Cm(iii) and Eu(iii) by 2,9-bis(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-1,2,4-benzotriazin-3-yl)-1,10-phenanthroline (CyMe4BTPhen) from nitric acid solution was studied using the ionic liquid Aliquat-336 nitrate ([A336][NO3]) as diluent. Results show a high selectivity of the solvent for Am(iii) and Cm(iii) over Eu(iii), but rather slow extraction kinetics. The kinetics of CyMe4BTPhen were largely improved by the addition of 0.005 mol L−1N,N,N′,N′-tetra-n-octyl-diglycolamide (TODGA) as a phase transfer reagent and by the use of 1-octanol as co-diluent. The addition of the phase transfer catalyst and co-diluent did not compromise the selectivity towards the actinide/lanthanide separation and thus this four-component system can be successfully applied to separate Am(iii) and Cm(iii) from the lanthanides.