Non-ionic Components Research Articles

Simultaneously converting synthetic fresh urine into high-quality artificial phosphate ores and urea solution: A novel coupled system of electrochemical selective separation plus induced precipitation

Both the sustainable development and environmental protection urge a demand of new paradigm to recover high-quality nutrients from source-separated urine, but the simultaneous recovery of phosphorus and nitrogen is difficult due to the complex composition. Herein, a coupled system consisting of a flow-electrode capacitive desalination and magnesium-air fuel cell (FCDI-MAFC) was proposed to accomplish electrochemical selective separation plus induced precipitation. The results showed that ionic species in urine were effectively separated from the non-ionic components to generate a urea solution with purity up to 99.7%. Ionic species were converted into artificial phosphate ores (APOs) with a phosphate content of 98.2%. The mass proportion of struvite in the APOs exceeded 90%. The energy consumption also decreased by 13% over five batches of operation. The overall results provide a novel method for the electrochemical selective separation and recovery of high-quality nutrients from complex wastewater.

Effects of UVC irradiation on polystyrene for healthcare packaging: Study by FTIR and Raman spectroscopy with thermoluminescence

The interaction between ultraviolet C radiation (UVC) and polystyrene (PS) materials has been investigated, particularly in post-packaging irradiation processes for healthcare applications. Effective UVC penetration through PS materials, regardless of their thickness (0.16 and 0.40 mm) has been observed. However, the penetration effectiveness could be affected by the thickness of the PS material. Achieving optimal post-packaging UVC treatment requires a thorough evaluation of chemical composition and material thickness, especially in pharmaceutical and medical packaging industries.Preliminary results reveal minimal degradation in UVC-irradiated PS packaging samples, as supported by FTIR and Raman spectroscopy characterization. Minor variations could be attributed to intrinsic PS materials properties and/or their respective background, rather than the influence of UVC radiation. Consequently, PS materials exhibit resilience under the experimental conditions following UVC irradiation treatment. Furthermore, a comprehensive analysis of thermoluminescence (TL) emissions evaluates several commercial dosimeter materials for UVC radiation detection. The TLD-100 and TLD-200 dosimeters show potential as UVC detectors, displaying distinct responses linked to the non-ionizing component of UVC radiation at 310 °C and in the range of 150–250 °C, respectively. However, the TLD-400 and GR-200 dosimeters are not suitable for UVC detection due to their spread TL emissions considering intensity and curve shape.This UVC-TL analysis consistently detects radiation in the proposed commercial dosimeter materials one-hour post-exposure, providing assurance that healthcare materials have been irradiated. Such analysis enhances reliability during extended UVC exposures, offering valuable insights for industries employing UVC-irradiated materials, particularly in healthcare applications.

Cooperative Self-Assembly Process Involving Giant Toroidal Polyoxometalate as a Membrane Building Block in Nanoscale Vesicles.

The self-assembly of organic amphiphilic species into various aggregates such as spherical or elongated micelles and cylinders up to the formation of lyotropic hexagonal or lamellar phases results from cooperative processes orchestrated by the hydrophobic effect, while those involving ionic inorganic polynuclear entities and nonionic organic components are still intriguing. Herein, we report on the supramolecular behavior of giant toroidal molybdenum blue-type polyoxometalate, namely, the {Mo154} species in the presence of n-octyl-β-glucoside (C8G1), widely used as a surfactant in biochemistry. Structural investigations were carried out using a set of complementary multiscale methods including single-crystal X-ray diffraction analysis supported by molecular modeling, small-angle X-ray scattering and cryo-TEM observations. In addition, liquid NMR, viscosimetry, surface tension measurement, and isothermal titration calorimetry provided further information to decipher the complex aggregation pathway. Elucidation of the assembly process reveals a rich scenario where the presence of the large {Mo154} anion disrupts the self-assembly of the C8G1, well-known to produce micelles, and induces striking successive phase transitions from fluid-to-gel and from gel-to-fluid. Herein, intimate organic-inorganic primary interactions arising from the superchaotropic nature of the {Mo154} lead to versatile nanoscopic hybrid C8G1-{Mo154} aggregates including crystalline discrete assemblies, smectic lamellar liquid crystals, and large uni- or multilamellar vesicles where the large torus {Mo154} acts a trans-membrane component.

Solute dynamics of a hydrophobic molecule in a menthol-thymol based type-V deep eutectic solvent: effect of composition of the components.

Type-V deep eutectic solvents (DESs) are a newly emerging unique class of solvents obtained by physical mixing and heating of non-ionic components. These solvents show deviation from the thermodynamic ideality. Compared to type-I to IV DESs, type-V DESs are less explored and their physical chemistry is in its nascent stage. In this work, we have chosen a type-V DES based on menthol-thymol (MT) for our working media. Solvent and rotational dynamics were studied with varying temperature using a well-known solvatochromic probe, Coumarin 153 (C153). We prepared the MT-based DES using a reported procedure at three molar ratios: 1 : 1 (M1T1), 1 : 1.5 (M1T1.5), and 2 : 1 (M2T1) of menthol (M) and thymol (T). Time-resolved emission spectra (TRES) were constructed with varying temperature. Utilizing TRES, the decay of the solvent correlation function (C(t)) was plotted. We have correlated the solvent relaxation time in these DESs as a function of viscosity. The time-resolved anisotropy decays were also collected to perceive the rotational relaxation dynamics of C153 as a function of temperature. The decay of solvent relaxation was found to be bi-exponential, and the average solvation time (〈τs〉) in M2T1 was found to be longer than those of M1T1.5 and M1T1. The rotational reorientation times (〈τrot〉) also follow the same trend. We have analysed the rotational dynamics of C153 in type-V DESs employing the Stokes-Einstein-Debye (SED) hydrodynamic model. The rotational dynamics in DESs demonstrate a good correlation with the SED model with a little deviation. In MT-based DESs, the solute's rotational relaxation times approach hydrodynamic stick boundary condition at low viscosity (or at high temperatures) for all molar compositions. Using the Arrhenius-type equations, we have correlated the activation energies for the rotational motion of C153, along with the viscous flow and non-radiative pathways for all the DESs.

Polymer Screening for Efficient Water Cut Reduction in a Sandstone Oilfield in Kazakhstan.

Polymer flooding is one of the most widely used and effective enhanced oil recovery techniques. It can improve the macroscopic sweep efficiency of a reservoir by controlling the fractional flow of water. The applicability of polymer flooding for one of the sandstone fields in Kazakhstan was evaluated in this study and polymer screening was carried out to choose the most appropriate polymer among four hydrolyzed polyacrylamide polymer samples. Polymer samples were prepared in Caspian seawater (CSW) and assessed based on rheology, thermal stability, sensitivity to non-ionic materials and oxygen, and static adsorption. All the tests were performed at a reservoir temperature of 63 °C. Based on the results of the screening study, tolerance of a polymer towards high-temperature reservoir conditions, resistance to bacterial activity and dissolved oxygen present in make-up brine, chemical degradation, and reduced adsorption on rock surface were considered the most important screening parameters. As a result of this screening study, one out of four polymers was selected for the target field as it showed a negligible effect of bacterial activity on thermal stability. The results of static adsorption also showed 13-14% lower adsorption of the selected polymer compared to other polymers tested in the study. The results of this study demonstrate important screening criteria to be followed during polymer selection for an oilfield as the polymer should be selected based on not only polymer characteristics but also the polymer interactions with the ionic and non-ionic components of the make-up brine.

The Influence of Dissolved Organic Matter to the Seawater Refractive Index Using Optical Refractometer

Optic refractive index is a good proxy for in situ salinity measurement of seawater according to TEOS-10. Currently, salinity of seawater is estimated by practical salinity (SP), which is calculated by measuring electric conductivity, temperature and pressure using Conductivity-Temperature-Depth (CTD) sensors. However, the electric conductivity method only takes into account the conductive compositions to seawater salinity and ignores the contribution of non-ionic components. However, non-ionic components in seawater affect seawater salinity according to the definition of salinity of seawater, but they could not be measured by conductivity sensor. Optical refractive index is sensitive to all dissolved matters of seawater including ionic and non-ionic components. Here, we take the dissolved organic matter (DOM) extracted from Aoshan Bay seawater as the representative sample to experimentally study the contribution of the non-ionic component to the refractive index of the standard seawater. Seawater refractive indices with different DOM concentrations were measured by a home-made V-shaped groove refractometer. The experimental results show that refractive index of seawater increases linearly with increasing DOM concentration at rate of 1.19 × 10-4/1(g/kg) DOM.

Salinity Tolerance, Ion Accumulation Potential and Osmotic Adjustment In Vitro and In Planta of Different Armeria maritima Accessions from a Dry Coastal Meadow.

The aim of the present study was to compare tolerance to salinity and ion accumulation potential of Armeria maritima subsp. elongata. Three accessions (AM1 and AM2, both from Latvia, and AM3 from Sweden) from relatively dry sandy soil habitats in the Baltic Sea region were selected and compared using both in vitro cultivated shoot explants and long-term soil-cultivated plants at flowering stage. Growth of root non-forming explants treated with increasing concentrations of NaCl was significantly inhibited starting from 110 mmol L−1, and the rate of shoot formation was even more sensitive. Significant differences in morphology and responses to salinity were found between different accessions. For soil-grown plants, biomass accumulation in above-ground parts was relatively little affected by salinity in AM1 and AM2 in comparison to that in AM3. Differences in ion accumulation were evident between the accessions as well as in respect to cultivation system used. Maximum accumulation capacity for Na+ was up to 2.5 mol kg−1 both in shoot explant tissues and in old leaves of soil-grown plants treated with NaCl, but that for K+ reached 4.0 mol kg−1 in old leaves of soil-grown plants treated with KCl. Non-ionic component of osmotic value was relatively high in old leaves and significantly increased under NaCl treatment, especially for AM2 and AM3 plants at moderate salinity, but in AM1 only at high salinity. In contrast, it significantly decreased in old leaves of AM2 plants treated with increasing concentration of KCl. It can be concluded that a wide salinity tolerance exists within A. maritima accessions from dry sandy soil habitats, associated with the ability to accumulate surplus ions both in salt glands and old leaves.

Lipid-Based Formulations Containing Labrafil M2125-CS: A Deep Investigation on Nanosystem Stability

Labrafil M2125-CS is a non-ionic surfactant component widely used for improving the solubilization of poor water-soluble drugs and as component of lipid-based nanosystem formulation. The aim of this research work was to evaluate in depth the stability of lipid-based nanosystems when exposed at several experimental conditions, such as temperature- and pH-variations, and during a specific storage process—lyophilization. Dynamic light scattering was the main analysis carried out during this research work for investigating eventual physico-chemical variations of nanosystem properties after different storage phases. We demonstrated that many of prepared formulations were able to maintain almost unchanged mean size and polydispersity index values, resisting acid and basic pH or high and low temperature, as well as the freeze-drying process. Finally, the results showed that there are no univocal experimental conditions suitable for the storage of all formulation types, but each sample requires customized conditions.

The interaction of the surface active ionic liquid with nonionic surfactants (Triton X-100 and Triton X-405) in aqueous solution by using tensiometry method

The synergistic interactions of the surface active ionic liquid (1-dodecyl-3-methylimidazolium bromide, IL) with non-ionic surfactants TritonX-100 (TX-100) and TritonX-405 (TX-405) were investigated in aqueous solution at various mole fractions by using the surface tension technique at 298.15 K. In this work, the pendant drop method was used for surface tension measurement of solutions. The surfactant properties such as critical micelle concentration (CMC), micellar mole fractions (X1Rub), interaction parameter (βm), and activity coefficients of components in the mixed micelle (f1Rub and f2Rub) were calculated by theoretical Clint and Rubingh models. Also, surface and adsorption parameters, maximum surface excess values (Γmax), minimum area per molecule (Amin), surface tension at CMC (σCMC), and surface pressure at the CMC (πCMC) values have been estimated in (TX-405/TX-100 + IL + water) systems. The synergistic effects operating in these amphiphile mixtures were confirmed by the negative values of the interaction parameter. Generally, the CMC value of surfactant solution increases with the addition of ionic liquid in the mixture. It was demonstrated that IL can be judiciously used at different mole fractions for modifying the physicochemical properties of (TX-100 and TX-405). Different thermodynamics parameters were computed for mixtures and were also discussed in detail. The Gibbs free energy change of micellization (ΔGmo), the standard Gibbs energy of adsorption (ΔGado) and the excess free energy of micellization (ΔGexRub) values have been estimated at different compositions. The calculation of thermodynamic parameters shows that the micellization process is spontaneous and becomes more favorable with addition of the non-ionic component in mixture.

Thermodynamic Affinity and Nature of Forces Defining Glycosaminoglycan-Protein Systems Using Fluorescence Spectroscopy.

Among the biophysical techniques used to study glycosaminoglycan (GAG)-protein interactions, fluorescence spectroscopy is a quantitative tool that has been extensively used to provide structural and dynamical information. Its advantages include high sensitivity, relative ease of applicability, and wide range of available fluorescence labels and probes. A large majority of protein-GAG systems have been studied using either intrinsic (e.g., Trp) or extrinsic (e.g., a noncovalent fluorophore) probes. It forms the basis for measurement of dissociation constant and stoichiometry of GAG-protein complexes. We describe step-by-step procedures to measure the affinity of GAG-protein complexes, parse the ionic and non-ionic components of the free energy of binding, and identify the site of GAG binding through competitive binding experiments.

Playing Favorites: Preferential Adsorption of Nonionic over Anionic Surfactants at the Liquid/Liquid Interface.

While many studies have investigated synergic interactions between surfactants in mixed systems, understanding possible competitive behaviors between interfacial components of binary surfactant systems is necessary for the optimized efficacy of applications dependent on surface properties. Such is the focus of these studies in which the surface behavior of a binary surfactant mixture containing nonionic (Span-80) and anionic (AOT) components adsorbing to the oil/water interface was investigated with vibrational sum-frequency (VSF) spectroscopy and surface tensiometry experimental methods. Time-dependent spectroscopic studies reveal that while both nonionic and anionic surfactants initially adsorb to the interface, anionic surfactants desorb over time as the nonionic surfactant continues to adsorb. Concentration studies that vary the ratio of Span-80 to AOT in bulk solution show that the nonionic surfactant preferentially adsorbs to the oil/water interface over the anionic surfactant. These studies have important implications for applications in which mixed surfactant systems are used to alter interfacial properties, such as pharmaceuticals, industrial films, and environmental remediation.

MUSE observations of the blue compact dwarf galaxy Haro 14

Investigations of blue compact galaxies (BCGs) are essential to advancing our understanding of galaxy formation and evolution. BCGs are low-luminosity, low-metallicity, gas-rich objects that form stars at extremely high rates, meaning they are good analogs to the high-redshift star-forming galaxy population. Being low-mass starburst systems, they also constitute excellent laboratories in which to investigate the star formation process and the interplay between massive stars and their surroundings. This work presents results from integral field spectroscopic observations of the BCG Haro 14 taken with the Multi Unit Spectroscopic Explorer (MUSE) at the Very Large Telescope in wide-field adaptive optics mode. The large MUSE field of view (1′×1′ = 3.8 × 3.8 kpc2 at the adopted distance of 13 Mpc) enables simultaneous observations of the central starburst and the low-surface-brightness host galaxy, which is a huge improvement with respect to previous integral field spectroscopy of BCGs. From these data we built galaxy maps in continuum and in the brightest emission lines. We also generated synthetic broad-band images in the VRI bands, from which we produced color index maps and surface brightness profiles. We detected numerous clumps spread throughout the galaxy, both in continuum and in emission lines, and produced a catalog with their position, size, and photometry. This analysis allowed us to study the morphology and stellar populations of Haro 14 in detail. The stellar distribution shows a pronounced asymmetry; the intensity peak in continuum is not centered with respect to the underlying stellar host but is displaced by about 500 pc southwest. At the position of the continuum peak we find a bright stellar cluster that with Mv = −12.18 appears as a strong super stellar cluster candidate. We also find a highly asymmetric, blue, but nonionizing stellar component that occupies almost the whole eastern part of the galaxy. We conclude that there are at least three different stellar populations in Haro 14: the current starburst of about 6 Myr; an intermediate-age component of between ten and several hundred million years; and a red and regular host of several gigayears. The pronounced lopsidedness in the continuum and also in the color maps, and the presence of numerous stellar clusters, are consistent with a scenario of mergers or interactions acting in Haro 14.

Electromembrane extraction using deep eutectic solvents as the liquid membrane

In this work, we investigated for the first time hydrophobic deep eutectic solvents (DES) as supported liquid membrane (SLM) for electromembrane extraction (EME). Camphor, coumarin, DL-menthol, and thymol were used as non-ionic DES components. Different DESs compositions were tested, to study systematically the importance of hydrogen bonding and dispersion/aromatic interactions during mass transfer across the SLM. Unexpectedly, mixtures of coumarin and thymol were highly efficient SLMs, and provided exhaustive or near-exhaustive extraction of non-polar bases, non-polar acids, and polar bases. SLMs with such performance for both bases and acids, in a large polarity window, are not found in current literature. The SLMs were highly aromatic, very strong hydrogen bonding donors, and moderately strong hydrogen bonding acceptors. Aromatic (π type) interactions were apparently very important for transfer of bases, while hydrogen bonding were dominant for acids. EME of six polar basic drugs from plasma, with a coumarin and thymol mixture as SLM, and combined with UHPLC-MS/MS analysis, was evaluated to test the potential for analytical applications. Plasma was diluted 1:1 with phosphate buffer pH 2.0. Calibration curves were linear in the therapeutic ranges (0.970 < R2 < 0.999), recoveries ranged between 47 and 93%, and repeatability was within 1.6–10.7% RSD. The clean-up efficiency was excellent and no matrix effects from plasma were seen. Presence of trace levels of coumarin in the acceptor phase was however found to cause some ion enhancement. Based on the current work, we foresee more research on the use of DES in EME.

Синергизм действия в бинарном растворе неионогенного и анионного ПАВ.

Adsorption at the gas —air interface and micelle formation in binary solutions of ethoxylated alkyl phenol (Neonol AF 9-10) and sodium oleate have been studied. The Rubin and Rosen equations were used to determine the interaction parameters and the composition of mixed micelles and adsorption layers depending on the initial solution composition. The authors have found out that the micelles and the adsorption layer at the interface are enriched in a non-ionic component. The maximum synergistic effect during micelle formation was found for solutions containing 20–30 % molar of reagent Neonol AF 9-10, and during adsorption —20 and 50 %.

Do Deep Eutectic Solvents Form Uniform Mixtures Beyond Molecular Microheterogeneities?

We have performed small-angle neutron scattering in a momentum transfer range (0.05 < Q < 0.5 Å-1) to study long-range order and concentration fluctuations in deep eutectic solvents (DESs) and their aqueous solutions. Ethaline (choline chloride/ethylene glycol), glycerol/lactic acid, and menthol/decanoic acid mixtures were selected to illustrate individually the case of ionic, nonionic, and hydrophobic mixtures. Carefully designed isotopic labeling was used to emphasize selectively the spatial correlations between the different solvent components. For ethaline DESs and their aqueous solutions, a weak low-Q peak observed only for certain compositions and some partial structure factors revealed the mesoscopic segregation of ethylene glycol molecules that do not participate in the solvation of ionic units, either because they are in excess with respect to the eutectic stoichiometry (1:4 neat ethaline) or substituted by water (4w-ethaline and higher aqueous dilutions). For the nonionic hydrophilic solutions, such a mesoscopic segregation was not observed. This indicates that the better balanced interactions between the three nonionic H-bonded components (water, lactic acid, and glycerol) favor homogeneous mixing. For the hydrophobic DESs, we observed an excess of coherent scattering intensity centered at Q = 0, which could be reproduced by a model of noninteracting spherical domains. Local concentration fluctuations are not excluded either. However, unlike liquid mixtures with a tendency to demix, we have found no evidence of expansion of domains with different compositions to a large scale.

Concentration-dependent physicochemical behaviors and micellar interactions in polyalkoxylated fatty alcohol-based binary surfactant systems

The concentration-dependent physicochemical behaviors of the binary mixtures of polyalkoxylated fatty alcohol (PAFA)-AS (alkyl sulfonate), PAFA-CB (cocamidopropyl betaine) and PAFA-APG (alkyl polyglucosides) and their micellar interactions were determined at the ratios of 9:1, 8:2, 7:3 and 6:4 (w/w). At concentrated level, the rheological study of all the PAFA-mixed surfactants display a Newtonian behavior at low viscosities. Prominent discrepancies among the mixed surfactant systems were observed after stepwise dilution of the samples. In tensiometry study, the types of mutual interaction in the mixed surfactant systems were evaluated by regular solution theory (RST). The CMCexp curves of PAFA-AS and PAFA-CB systems demonstrate lower position than their CMCtheo curves signifying that these nonionic–anionic and nonionic–zwitterionic samples behave nonideal showing synergistic interaction between individual components in the mixed micelles, as further verified by the negative values of interaction parameter β and activity coefficients f1 and f2 are less than 1. Meanwhile, the PAFA-APG system shows no significant mutual interaction between the nonionic–nonionic components in the mixed micelles. TEM micrographs depict the formations of branched wormlike micelles and multiconnected threadlike networks for the PAFA-AS and PAFA-CB systems, respectively, while gigantic multilamellar vesicles for the PAFA-APG system. Upon dilution of these mixed surfactants to CMC, the mixed micelles are in monodisperse sizes of less than 15 nm and in various magnitudes of zeta potential ranging from –2.92 to –21.87 mV.

Тemplate synthesis of multidimensional porous silica

Isothermal data of superficial tension of solutions of surfactant mixture and low-temperature nitrogen sorption of multidimensional porous silica received by template synthesis prove complementarity of its properties and properties of SAA micelles. The measured isotherms of gas sorption belong to IV Type inherent in mesoporous adsorbents. The BET specific surface area is 600–800 m2/g, and the Gurvich pore volume is 0.7–1.0 cm3/g. With increase in mole fraction of nonionic component these values decrease, the ordered texture of SiO2, characteristic of MCM-48 mesoporous molecular sieve, collapses, d211-spacing becomes &lt; 3.31 nm, and NLDFT distribution is transformed from monomodal to polymodal one.

Molecular characterization of nonionic surfactant components of the Corexit® 9500 oil spill dispersant by high-resolution mass spectrometry.

Approximately 7 million liters of Corexit® dispersants were applied during the 2010 Deepwater Horizon oil spill to facilitate the dispersion of crude oil. At the time of application, the exact chemical composition of Corexit® was relatively unknown. Characterization of Corexit® 9500 was performed using high-resolution mass spectrometry to further understand the complexity of the nonionic surfactant components of this mixture. Corexit®9500 was analyzed by ultra-high-performance liquid chromatography (UHPLC) coupled to a high resolution Orbitrap Fusion Lumos mass spectrometer operated in positive electrospray ionization mode and a charged aerosol detector. Chromatographic conditions were optimized to efficiently separate isobaric and isomeric compounds. Polyethoxylated nonionic surfactants in Corexit® 9500 were identified using the following criteria: accurate mass (<3 ppm), retention time, and homologue series; in addition, interpretation of high-resolution tandem mass spectra was used to annotate tentative component structures. More than 2000 polysorbate nonionic surfactants in 87 homologue series were detected. Polysorbate surfactants were characterized by the type of molecular basis group (sorbitan, isosorbide, or fatty acid), degree of esterification (n= 0-4), ester chain length (C6-C24), and ester saturation, in addition to polydispersion by ethoxylation. Isomeric compounds were differentiated by LC/HRMS/MS analysis with product ion assignment. Results from the charged aerosol detector showed that the diesters (23.9 ± 0.78%) were the most abundant component in Corexit® 9500 followed by dioctyl sodium sulfosuccinate (DOSS) (19.2 ± 1.5%), triesters (17.3 ± 1.5%), and monoesters (15.7 ± 2.3%). Our analytical approach facilitated the characterization of polysorbate surfactants within Corexit® 9500 and allowed a systematic study to differentiate isomeric and isobaric compounds, when standards were not available. The characterized composition of Corexit® 9500 will facilitate future studies to determine the chemical and biological transformation kinetics and byproducts of Corexit® 9500 under environmental conditions.

Solid phase extraction of pesticides from environmental waters using an MSU-1 mesoporous material and determination by UPLC-MS/MS

This paper describes the synthesis of a silica based MSU-1 mesoporous solid and its application as sorbent in solid-phase extraction to pre-concentrate thirteen pesticides of low-high polarity (methomyl, cymoxanil, carbofuran, monolinuron, isoproturon, methidathion, methiocarb, malathion, phosalone, diazinon, penconazole, neburon and chlorotoluron) in ground and river water. The synthesis was based in an H-bonding interaction assembling (I0N0) between two non-ionic components (the inorganic silica surface, I0 and the polyethylene oxide template, N0) by adding tetraethoxysilane to the non-ionic surfactant Brij®100, the latter previously dissolved in HCl 1 M. 50 mL water samples adjusted at pH= 3.5 were passed, at a flow rate of 5 mL/min, through a home-made cartridge containing 50 mg of MSU-1 sorbent, pre-conditioned with 5 mL of ultrapure water; then, the cartridge was washed with 5 mL of ultrapure water. Following elution with 5 mL of acetonitrile, the pesticides were determined by ultra performance liquid chromatography coupled to triple quadrupole-mass spectrometry. Two selected reaction monitoring transitions were monitored per compound, the most intense one being used for quantification and the second one for confirmation. Three points were used for identification, as established in the Directive 96/23/EC for LC-MS/MS analysis, which deals with confirmatory methods for organic residues and contaminants listed in the Group B (veterinary drugs and contaminants). Medium matrix effect (|20%|<ME<|50%|) was found for methiocarb and malathion, whereas diazinon and phosalone showed strong matrix effect (ME≥>|50%|). Therefore, the standard addition methodology was applied by adding an adequate amount of the pesticide standard mixture to the final sample extract. All pesticides were quantified using this approach for practical reasons, thus avoiding two different calibrations. The method quantification limit (MQL) of pesticides was 0.01 μg/L for all of them, except for diazinon (0.1 μg/L). Recoveries of the target pesticides at MQL and 0.25 µg/L concentration levels in blank river water were in the range 70.1–113.5% and 86.7–107.3%, respectively, with RSDs lower than 16.3% and 15.7%, respectively. Four ground water samples and three river water samples, taken from Almería (Spain), were analyzed by the proposed method and only phosalone at a concentration level of 0.05 µg/L was found in one river water sample.

Sustainable preparation of sunlight active α-Fe2O3 nanoparticles using iron containing ionic liquids for photocatalytic applications.

Inspired by the nano-segregation of ionic liquids (ILs) into bi-continuous structures constituting of arrays of ionic and non-ionic components, herein, a new and sustainable strategy for preparation of mesh-like nano-sheet α-Fe2O3 nanoparticles and their photo-catalytic activity under sunlight, is presented. For the purpose, metal (iron) containing ionic liquids (MILs), 1-alkyl-3-methylimidazolium tetrachloroferrates, [Cnmim][FeCl4], (n = 4, 8 and 16), which not only act as precursors and solvents but also as structure directing agents have been used. Thus prepared NPs show MIL dependent structural, photophysical and magnetic properties. The catalytic efficiency of NPs has been tested for the photo-degradation of organic dyes (Rhodamine B) in aqueous solution under sunlight. The NPs are found to exhibit comparable catalytic efficiency under sunlight as compared to that observed under high intensity visible lamplight, without showing a decline in their catalytic efficiency even after 4 catalytic cycles. It is anticipated that the present work will provide a new platform for preparation of sunlight active nanomaterials for photo-catalytic applications with control over the structural and physical properties via varying the molecular structure of MILs.