Biochar-based polymeric film as sustainable and efficient sorptive phase for preconcentration of steroid hormones in environmental waters and wastewaters.

BACKGROUND: The environmental impact of sample preparation should be minimized through simplification of the procedures and the use of natural, renewable and/or reusable materials. In such scenario, thin-film microextraction fulfils the former criteria, as it enables few steps and miniaturization, thus small amount of extraction phase. At the same time, the use of sorbents such as biochars obtained from biomass waste is even more promoted due to their availability at low cost and increased life-cycle in a circular economy vision. However, it is not always easy to combine these criteria in sample preparation. RESULTS: A thin film microextraction was developed for the determination of steroids in aqueous samples, entailing a membrane made of cellulose triacetate and a wood-derived biochar (Nuchar®) as carbon precursor. Different characterization techniques showed the successful preparation, whereas the sorption kinetics experiments demonstrated that biochar is responsible for the extraction with the polymer acting as a smart support. After a study about membranes' composition in terms of biochar amounts (4 %, 10 %, 16 % wt) and type of synthesis set up, the ceramic 3D-mold was selected, achieving reproducible and ready-to-use membranes with composition fixed as 10 %. Different elution conditions, viz. type and time of agitation, type, composition and volume of eluent, were evaluated. The final microextraction followed by HPLC-MS/MS quantification was successfully validated in river and wastewater treatment plant effluent samples in terms of accuracy (R% 64-123 %, RSD<19 % in river; R% 61-118 %, RSD <18 % in effluent, n = 4), sensitivity (MQLs 0.2-8.5 ng L-1) and robustness. SIGNIFICANCE: This novel biochar-based polymeric film proved to be a valid and sustainable sorbent, in terms of extraction capability, ease of preparation and greenness. By comparison with literature and the greenness evaluation with the most recent metric tools, this method expands the potential applicability of the thin-film microextraction and opens up innovative scenarios for sustainable procedures entailing the use of biochars entrapped in bio-polymers.

A Comprehensive Study on the Effect of Plasticizers on the Characteristics of Polymer Inclusion Membranes (PIMs): Exploring Butyl Stearate as a Promising Alternative.

This study investigated the influence of various plasticizers commonly used in the manufacture of polymer inclusion membranes (PIMs), such as 2-nitrophenyl octyl ether (NPOE), phthalates, adipates, and sebacates on the mechanical, thermal, and transport properties of membranes. Additionally, butyl stearate (BTS), chosen for its non-toxic nature compared to phthalates and its cost-effectiveness relative to adipates and sebacates, was evaluated as a plasticizer in PIMs for the first time. All plasticizers were incorporated in PIMs made of either cellulose triacetate (CTA) or poly(vinyl chloride) (PVC) as the base polymers and the task-specific ionic liquid trioctylmethylammonium thiosalicylate (TOMATS) as the carrier. The plasticizers were found to significantly affect the characteristics of membrane hydrophilicity, mechanical flexibility, and thermal stability. Transport experiments using Hg(II) as a model target ion revealed that, for CTA-based PIMs, the plasticizer did not significantly affect transport efficiency. However, for PVC-based PIMs, BTS exhibited better efficiency when compared to NPOE. These findings highlight the potential of BTS as an attractive alternative to currently used plasticizers in PVC-based PIM formulations.

Multiwalled Carbon Nanotubes Embedded in a Polymeric Matrix as a New Material for Thin Film Microextraction (TFME) in Organic Pollutant Monitoring.

It is essential to monitor organic pollutants to control contamination levels in environmental water bodies. In this respect, the development of new materials based on functionalised polymeric films for the measurement of toxic compounds is of interest. In this study, we prepare new films based on polymer cellulose triacetate modified with multi-walled carbon nanotubes for the monitoring of selected compounds: a fungicide (chlorpyrifos) and two emerging contaminants, the musk tonalide and the bactericide triclosan, which are used in the formulation of personal care products. The films, upon contact with water samples and following the principles of thin film microextraction, allow the determination of organic pollutants at low concentration levels. The contact time of the film with a predetermined volume of water is fixed at 60 min, and the compounds are eluted with a small volume (1 mL) of organic solvent for GC-MS analysis. Parameters such as repeatability for different films and detection limits are found to be satisfactory. Applying the method to river water demonstrates its suitability and, in the cases of chlorpyrifos and tonalide, the absence of a significant matrix effect.

New Insights on the Effects of Water on Polymer Inclusion Membranes Containing Aliquat 336 Derivatives as Carriers.

Surface characterization of polymer inclusion membranes (PIMs) using the polymers cellulose triacetate and polyvinyl chloride, containing different ionic liquids (ILs) as carriers, has been performed. Three different ILs have been tested: commercial trioctyl methylammonium chloride (Aliquat 336-AlqCl-) and two derivatives bearing the counter anion NO3- or SCN- (AlqNO3 and AlqSCN, respectively). Surface analysis was performed by scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) for both dry membranes and PIMs immersed for 4 days in ultrapure water to investigate the effect of the interaction of water with the membrane's morphology and composition. XPS analysis of the PIMs revealed that immersion in ultrapure water causes a decrease in the atomic concentration percentage (A.C.%) of the specific IL atoms (Cl, S, and N) when compared with dry samples. Moreover, SEM images of the PIMs containing the IL AlqNO3 showed an alteration in the morphology of the membrane due to water contact at surface level, whereas no changes were observed at a bulk level. These changes in the surface composition of the water equilibrated PIMs may be associated with the solubilization of the IL in the water solution, which, therefore, may affect the reactivity of the membrane's surface. To better understand this effect, PIMs containing both AlqCl and AlqNO3 as carriers were used for arsenic (V) transport. It was found that AlqCl was the most effective IL and that the effectivity of the PIM on As(V) removal was not affected after five cycles of the membrane's reuse.

Determination of elemental bioavailability in soils and sediments by microwave induced plasma optical emission spectrometry (MIP-OES): Matrix effects and calibration strategies.

In the past few years, microwave induced plasma optical emission spectrometry (MIP-OES) has generated great interest as an alternative technique to inductively coupled plasma-based techniques due to its lower operational cost. Since MIP-OES suffers from severe matrix effects due to easily ionizable elements (EIEs) (Na, Ca, etc.), it is unclear whether this technique could be employed for elemental bioavailability studies in soils and sediments since the main extractant solutions employed in such works may contain high levels of these elements. Thus, the aim of this work was to evaluate the feasibility of MIP-OES as a detector for such applications. To this end, the influence of different extractant solutions (0.25 mol L-1 MgCl2, 0.25 mol L-1 CaCl2, 0.10 mol L-1 acetic acid, 0.05 mol L-1 Na2EDTA, 0.25 mol L-1 NaNO3, 0.25 mol L-1 NaOAc/HOAc and 0.10 mol L-1 NH2OH·HCl) on the analyte emission of several elements (As, Cd, Co, Cr, Cu, Fe, Mg, Mn, Mo, Ni, Pb, Rh, Se, Sr and Zn) was investigated. Results were compared to those obtained using a reference solution made of 5% w w-1 HNO3 solution. For saline extractant solutions, both the optimum nebulizer gas flow rate (Qg) and analyte emission were modified with regard to the reference solution. In general, the optimum Qg was reduced by between 0.1 and 0.2 L min-1 for both ionic and atomic lines. Under optimum Qg conditions, analyte emission was supressed by saline solutions except for atomic lines with an upper electronic state below 4 eV, which were enhanced. The magnitude of matrix effects was strongly dependent on EIE ionization energy. The lower the ionization energy, the greater the matrix effects were registered. No measurable matrix effects were registered on both Qg and analyte emission within experimental uncertainties for NH2OH·HCl and acetic acid extractant solutions. Experimental data suggest that matrix effects were related to changes in plasma characteristics and the analyte excitation/ionization mechanism. To mitigate matrix effects and improve long-term MIP-OES performance, internal standardization using either Rh (343.489 nm and 369.236 nm) or OH molecular emission band (308.958 nm) was required. This calibration methodology was successfully applied to the study of the elemental bioavailability in soil samples from a vineyard affected by copper-based fungicides and sediment samples from an area affected by mining waste.

Effective concentration signature of Zn in a natural water derived from various speciation techniques.

The uptake of nutrients or toxicants by different organisms in aquatic systems is known to correlate with different fractions of the nutrient's or toxicant's total concentration. These fractions can be provided by different analytical techniques, from which the better correlation is expected to be found for those with a characteristic length comparable to that in the considered organism uptake. An effective concentration signature can be built up with the concentration values associated to the availability (i.e. fluxes in dynamic techniques) of the nutrient or toxicant measured by various analytical techniques with different characteristic lengths. Here, this new representation was obtained for the pool of Zn complexes in the Mediterranean stream Riera d'Osor (Girona, Catalonia, Spain) with a suite of four analytical techniques. Absence of Gradients and Nernstian Equilibrium Stripping (AGNES) and Polymer Inclusion Membrane (PIM) devices provided the free Zn concentration. Linear Anodic Stripping Voltammetry provided a labile fraction (defined here as cLASV, higher than the free concentration), related to the diffusion layer scale. Diffusion Gradients in Thin-films provided higher labile fractions (known as DGT concentrations, cDGT) connected to the different characteristic lengths of different configurations (e.g. one or two resin discs) longer, in any case, than that corresponding to LASV. The combination of the information retrieved by the techniques allowed to quantify lability degrees of the pool of Zn complexes and to build up the effective concentration signature for this water.

Preparation and Characterization of Nanoparticle-Doped Polymer Inclusion Membranes. Application to the Removal of Arsenate and Phosphate from Waters.

Nanoparticle-doped polymer inclusion membranes (NP-PIMs) have been prepared and characterized as new materials for the removal of arsenate and phosphate from waters. PIMs are made of a polymer, cellulose triacetate (CTA), and an extractant, which interacts with the compound of interest. We have used the ionic liquid (IL) trioctylmethylammonium chloride (Aliquat 336) as the extractant and have investigated how the addition of nanoparticles can modify membrane properties. To this end, inorganic nanoparticles, such as ferrite (Fe3O4), SiO2 and TiO2, and multiwalled carbon nanotubes (MWCNTs), were blended with the polymer/extractant mixture. Scanning electron microscopy (SEM), infrared spectroscopy (FT-IR), and contact angle measurements have been used to characterize the material. Moreover, PIM stability was checked by measuring the mass loss during the experiments. Since Aliquat 336 acts as an anion exchanger, the NP-PIMs have been explored in two different applications: (i) as sorbent materials for the extraction of arsenate and phosphate anions; (ii) as an organic phase for the separation of arsenate and phosphate in a three-phase system. The presence of oleate-coated ferrite NP in the PIM formulation represents an improvement in the efficiency of NP-PIMs used as sorbents; nevertheless, a decrease in the transport efficiency for arsenate but not for phosphate was obtained. The ease with which the NP-PIMs are prepared suggests good potential for future applications in the treatment of polluted water. Future work will address three main aspects: firstly, the implementation of the Fe3O4-PIMs for the removal of As(V) in real water containing complex matrices; secondly, the study of phosphate recovery with other cell designs that allow large volumes of contaminated water to be treated; and thirdly, the investigation of the role of MWCNTs in PIM stability.

Evaluation and optimization of the derivatization reaction conditions of glyphosate and aminomethylphosphonic acid with 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate using reversed-phase liquid chromatography.

Due to the polar and ionic characteristics of glyphosate and its main metabolite, aminomethylphosphonic acid, a derivatization reaction is required before performing liquid chromatographic determination of these compounds. In this study, reaction conditions using 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate as the derivatization reagent are assessed. A two-level full-factorial design is applied here to optimize the derivatization time (ranging from 0.5 to 20 min) and temperature (from 24 to 55°C). It is found that neither of these two variables have a significant effect on the derivatization process and that the reaction is quantitatively achieved in a few seconds at room temperature (24°C). The results obtained indicate that derivatization reaction with 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate is achieved in milder conditions, with a faster kinetic reaction, than those required with the most conventional derivatization reagents used today, and the derivatives are more stable. It has been found that the most important parameter affecting the chromatographic separation is the pH of the mobile phase, as it has a significant effect on the retention time of the hydrolyzed excess of reagent. When ammonium acetate is used in the mobile phase, buffered solutions at pH around 5.0 are required.

Development of a new binding phase for the diffusive gradients in thin films technique based on an ionic liquid for mercury determination.

Determining bioavailable trace concentrations of mercury (Hg) in water is still a challenging analytical task. In this study, we report a methodology for determining labile Hg in natural waters using newly developed sorbents. Silicon dioxide at a nanoparticle range (Si-np) and cellulose powder at a microparticle range (Cel-p), both modified with the ionic liquid trioctylmethylammonium thiosalicylate (TOMATS), have been tested as sorbents (sorb-TOMATS) for Hg(II) uptake from solution. These novel sorb-TOMATS materials were characterized, and parameters affecting the uptake were examined. A similar Hg(II) uptake efficiency (97%) and binding capacity (9 mg Hg/g) was obtained for both sorb-TOMATS, while only a 25% of Hg(II) was taken up using non-impregnated materials. Moreover, these sorb-TOMATS were effectively embedded in agarose gel and were tested as a novel binding phase for the Diffusive Gradients in Thin Films (DGT) technique. Research revealed Si(np)-TOMATS sorbent as a suitable binding phase in the DGT technique for Hg(II) measurements, since it also allowed the efficient elution of the bound Hg(II). This new binding phase showed strong linear correlation between the accumulated Hg(II) mass and deployment time, which is in agreement with the DGT principle. In summary, this novel sorbent has a great potential to improve Hg monitoring in natural waters when integrated it in the DGT design.

First Report on a Solvent-Free Preparation of Polymer Inclusion Membranes with an Ionic Liquid.

A novel and environmentally-friendly procedure for the preparation of polymer inclusion membranes (PIMs) containing an ionic liquid is presented for the first time. Traditionally, PIMs are prepared by a solvent casting method with the use of harmful organic solvents. Here we report a new solvent-free procedure based on a thermal-compression technique which involve the melting of the components of the PIM and the application of a high pressure to the melted specimen to form a flat-sheet film. In our study, we have tested different polymers, such as two cellulose derivatives as well as two thermoplastic polymers, polyurethane (TPU) and poli ε-caprolactone (PCL). The ionic liquid (IL) trioctylmethylammonium chloride (Aliquat 336) has been used to produce PIMs with a fixed composition of 70% polymer-30% IL (w/w). Both TPU and PCL polymers provide successful membranes, which have been thoroughly characterized. PIMs based on the polymer PCL showed a high stability. To test whether the properties of the IL were affected by the preparation conditions, the extraction ability of Aliquat 336 was investigated for both PCL and TPU membranes in terms of Cr(VI) extraction. Satisfactory values (90% extraction) were obtained for both membranes tested, showing this novel procedure as a green alternative for the preparation of PIMs with ILs.

System for mercury preconcentration in natural waters based on a polymer inclusion membrane incorporating an ionic liquid.

In this study, we have evaluated two different ionic liquids (IL) as extractants based on the same cation (trioctylmethylammonium) but bearing the anion thiosalicylate (TOMATS) or salicylate (TOMAS). Both IL have been incorporated as carriers in polymer inclusion membranes (PIMs), and mercury (Hg) has been preconcentrated using a special device. Results show that among the tested IL, TOMATS has given better results. A PIM made of 50% cellulose triacetate, 30% TOMATS and 20% nitrophenyl octyl ether as a plasticizer enabled the effective transport of Hg to a 10-3M cysteine solution used as a stripping phase. This novel and simple PIM-device system allows the transport of Hg at low concentration levels in different types of natural waters such as rivers, groundwater and seawater without any previous treatment. Since no matrix effect was observed on Hg transport efficiency with different waters, this newly developed PIM-system could be used as a global detection system for this metal. The effect of biofilm growth on the surface of PIMs has been investigated for the first time, and no significant differences on Hg transport have been found when using a fresh PIM and a PIM deployed for 7 days in a pond.

Conventional and novel techniques for the determination of Hg uptake by lettuce in amended agricultural peri-urban soils.

Peri-urban agriculture provides environmental benefits to the nearby urban areas. However, domestic and industrial infrastructures can be sources of pollution that can affect agricultural production. In this work, the diffusive gradient in thin film (DGT) technique was used to assess the bioavailability of mercury (Hg) in organic-amended agricultural soils, and uptake by lettuce. Two different amendments were studied individually in three different sets using a wood-based biochar at two rates (3% and 6%, w/w), and compost at one rate (30% w/w). The effect of the amendments on Hg bioavailability, mobility and uptake was investigated by means of both DGT analyses and accumulation of Hg by lettuce. DGT manufactured in-house devices with polyacrylamide gel using both open and restricted diffusive layers (ODL and RDL, respectively) were used to determine organic and inorganic Hg labile species in soils, respectively. The Hg concentration in lettuce leaves and roots were analyzed and compared with DGT measurements to predict the uptake of Hg from the different organic-amended soils and the non-amended soils. Results show that the application of biochar reduces the bioavailability of Hg in soil and, in consequence, the Hg uptake by lettuce. Inorganic Hg species were predominant in all the different sets of the experiment (62-97%), although the addition of the different amendments reduced the free ionic species in soil.

Automatic determination of arsenate in drinking water by flow analysis with dual membrane-based separation.

The sequential application of a polymer inclusion membrane (PIM), composed of poly(vinylidenefluoride-co-hexafluoropropylene) and the anionic extractant Aliquat 336, and a microporous polytetrafluoroethylene (PTFE) gas-permeable membrane was utilized for the first time to develop a flow analysis (FA) system, for the automatic determination of trace levels of arsenate (As(V)) in drinking water as arsine. The system incorporated a flow-through extraction cell for separation and preconcentration of arsenate and a gas-diffusion cell for the separation of arsine prior to its spectrophotometric determination based on the discoloration of a potassium permanganate solution. Under optimal conditions the FA system is characterized by a limit of detection of 3.0 µg L-1 As(V) and repeatability of 1.8% (n = 5, 25 µg L-1 As(V)) and 2.8% (n = 5, 50 µg L-1 As(V)). The newly developed FA method was successfully applied to the determination of arsenate in drinking water samples in the µg L-1 concentration range.

Design of a Hollow Fiber Supported Liquid Membrane System for Zn Speciation in Natural Waters.

A supported liquid membrane-hollow fiber system (HFSLM) has been developed to determine zinc speciation in aquatic environments. The liquid membrane consisted of an organic solution of bis-(2-ethylhexyl)phosphoric acid (D2EHPA) impregnated in the microporous of a polypropylene hollow fiber. The membrane contacted both the donor solution, that contained the metal and the stripping solution, placed in the lumen of the hollow fiber, where the metal was preconcentrated. Different parameters affecting the Zn2+ transport efficiency have been evaluated such as the composition of both the donor and stripping solutions as well as the membrane phase. Extraction and transport efficiencies of free Zn(II) higher than 90% were obtained with a liquid membrane consisting of a 0.1 M D2EHPA solution in dodecane and a 0.1 M HNO3 solution as the stripping phase. The developed HFSLM was used to study the effect of different ligands (EDTA and citric acid) in the donor phase of Zn(II) transport and to investigate the selectivity of the membrane towards Zn when other metals were also present. Finally, the HFSLM system was successfully applied to estimate the free Zn(II) concentrations in three water samples from a mining area. Moreover, the HFSLM system facilitates the analytical determination of trace Zn(II) levels allowing the achievement of enrichment factors of around 700 in the stripping phase.

Comparison of different speciation techniques to measure Zn availability in hydroponic media.

Four analytical techniques are compared: AGNES (Absence of Gradients and Nernstian Equilibrium Stripping), LASV (Anodic Stripping Voltammetry with Linear stripping), DGT (Diffusive Gradients in Thin films) and PIM (Polymer Inclusion Membranes). These techniques have been designed to provide the free ion concentration or a labile fraction, complementarily contributing to an integrated description of speciation and availability. Their simultaneous application to the determination of free Zn concentrations or labile fluxes in seven solutions of a hydroponic medium reveals characteristics of each technique and correlations between their results. All dynamic results can be interpreted in terms of a general theoretical framework on fluxes. Indeed, in techniques under diffusion-limited conditions in the sample, the flux can be split into the free contribution (linearly proportional to the free fraction), plus the contribution of the complexes (where mobility, lability and abundance of complexation are intertwined). A methodology to compute lability degrees is developed. Measurements with PIM devices confirm that diffusion in the sample solution is not rate limiting, so its flux is proportional to the free metal in the donor solution. A proportionality between the responses of any given two techniques is observed, which suggests that, for the low ligand-to-metal concentration ratios used in the present work, any of these techniques would correlate similarly with uptake, toxic or nutritional measurements.

An Efficient Polymer Inclusion Membrane-Based Device for Cd Monitoring in Seawater.

A novel and simple device that includes a polymer inclusion membrane (PIM) has been prepared and tested for the first time to detect low concentration levels of cadmium in seawater. The ionic liquid trihexyl (tetradecyl) phosphonium chloride (THTDPCl) has been shown to be an effective extractant when incorporated in a PIM that uses cellulose triacetate (CTA) as a polymer. However, it has been reported that the use of a plasticizer is mandatory to ensure an effective transport, which uses both ultrapure water and a nitric acid solution as a stripping phase. A special device incorporating a PIM made of 50% CTA, 40% nitrophenyl octyl ether (as a plasticizer), and 10% THTDPCl, effectively allows the quantitative transport and preconcentration of 10 µg L-1 Cd from seawater samples to a stripping phase consisting of 0.5 M HNO3 solution. This study shows that the efficiency of the PIM system is not affected by high salinity nor the presence of large amounts of other ions, and can thus facilitate Cd monitoring in seawater samples.

A new extraction phase based on a polymer inclusion membrane for the detection of chlorpyrifos, diazinon and cyprodinil in natural water samples.

A simple and effective method for the detection of three pesticides (chlorpyrifos, diazinon and cyprodinil) is developed using a polymer inclusion membrane (PIM) prior to gas chromatography and mass spectrometry detection (GC-MS). Analytes are extracted from natural water samples using a 3 cm2 PIM made of the polymer, cellulose triacetate (CTA), and the plasticizer, nitrophenyl octyl ether (NPOE). Addition of the plasticizer to the CTA matrix is found to be necessary for the extraction of pesticides. After extraction, analytes are recovered from the membrane with 1 mL of acetonitrile and injected into the GC-MS system. The main factors affecting the extraction efficiency are evaluated, including membrane composition, stirring mode, extraction and elution time. Ultrasonic assisted elution of the extracted pesticides is accomplished after 15 min of contact. The PIM-assisted extraction method makes it possible for pesticides to be determined in the range of 50-1000 ng L-1 with good linearity (coefficient of determination ≥0.995) and suitable recoveries (85-119%) and precision (<21%, n = 3) using 100 mL of a water sample. This methodology is shown to be suitable for the detection of chlorpyrifos in local river waters.

Applicability of a Supported Liquid Membrane in the Enrichment and Determination of Cadmium from Complex Aqueous Samples.

A supported liquid membrane is developed for the separation of Cd from either high in salinity or acidity aqueous media. The membrane consisted of a durapore (polyvinylidene difluoride) polymeric support impregnated with a 0.5 M Aliquat 336 solution in decaline. The effect of carrier concentration, organic solvent and feed and receiving solutions on the metal permeability is studied. This system allows the effective transport of trace levels of Cd through the formation of CdCl42−, which is the predominant species responsible for the extraction process, in both NaCl and HCl solutions. The supported liquid membrane system in a hollow fibre configuration allows the enrichment and separation of trace levels of Cd from spiked seawater samples, facilitating the analytical determination of this toxic metal.

Polymer Inclusion Membrane as an Effective Sorbent To Facilitate Mercury Storage and Detection by X-ray Fluorescence in Natural Waters.

A novel and simple method is presented for the preconcentration and determination of mercury (Hg) from natural waters through its extraction into a polymer inclusion membrane (PIM) containing the task-specific ionic liquid trioctylmethylammonium thiosalicylate (TOMATS) followed by Energy Dispersive X-ray fluorescence (EDXRF) analysis. The determination was made directly on the membrane without any treatment or elution step, and due to the characteristics of the PIM no matrix or thickness corrections were required in EDXRF analysis. Under the best extracting and EDXRF operating conditions, a Hg limit of detection of 0.2 µg Hg L-1 was obtained. Moreover, no water matrix effect was observed when Hg was extracted from different types of water such as river, seawater, groundwater, and tap water, showing this extraction system as a global solution when dealing with natural waters. Interestingly, this Hg collected in the PIM has shown to be stable for at least 6 months without the use of any preservative. This fact is of prime importance taking into account the usual stability problems of Hg during sample storage.

Polymer inclusion membrane to access Zn speciation: Comparison with root uptake.

Metal speciation studies can be performed with a new technique based on a functionalized membrane. The estimation of not only the total amount of metal, but also the metal available to living organisms is very important. In this context, we have investigated the use of a polymer inclusion membrane (PIM) in a new tool for the determination of free metal ion concentration. In order to check the usefulness of PIM devices in metal speciation studies and metal availability to potato plants (Solanum tuberosum), Zn has been chosen as a case study. The PIM designed for Zn transport uses polyvinyl chloride (PVC) as polymer and di-(2-ethylhexyl) phosphoric acid (D2EHPA) as carrier, with 0.01M nitric acid in the receiving solution. The stability of the PIM has been demonstrated and good linearity of PIM-device fluxes (JPIM) with free metal concentration was observed for total metal concentrations ranging from 3µM up to 70µM. The presence of different ligands, such as ethylenediaminetetraacetic acid (EDTA), humic acid (HA) and citrate, greatly influences the measured JPIM because the formation of metal complexes in the donor phase decreases the free Zn concentration in the sample. Good correlation has been found when comparing PIM fluxes and metal accumulation in potato plants roots in the presence of EDTA. But, the root uptake did not change when adding citrate and HA to the hydroponic medium, so the uptake does not always follows the Free Ion Activity Model (FIAM). These ligands might induce physiological changes in the roots and enhance metal uptake.