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Ligia Maria Moretto

Bio: Ligia Maria Moretto is an academic researcher from Ca' Foscari University of Venice. The author has contributed to research in topics: Voltammetry & Cyclic voltammetry. The author has an hindex of 28, co-authored 100 publications receiving 2315 citations. Previous affiliations of Ligia Maria Moretto include University of Caxias do Sul & Federal University of Rio Grande do Norte.


Papers
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TL;DR: In this article, a review describes principles and analytical applications of ion exchange voltammetry (IEV) at polymer modified electrodes, and results of mechanistic studies which are relevant to the development and optimization of IEV methods are discussed.
Abstract: This review describes principles and analytical applications of ion-exchange voltammetry (IEV) at polymer modified electrodes. Results of mechanistic studies which are relevant to the development and optimization of IEV methods are discussed. Useful examples of IEV determinations of traces of inorganic and organic electroactive ions of interest for environmental, biomedical or pharmaceutical analysis are given along with future prospects for this technique.

107 citations

Journal ArticleDOI
TL;DR: This Minireview focuses on recent advances in the use of ionomer-coated electrodes and nanoelectrode ensembles for the determination of redox ions at trace concentration level with special stress on applications for environmental monitoring.
Abstract: This Minireview focuses on recent advances in the use of ionomer-coated electrodes and nanoelectrode ensembles for the determination of redox ions at trace concentration level with special stress on applications for environmental monitoring. After an overview on the most recent developments of ionomer-coated electrodes, attention is directed towards their use for speciation analysis in environmental samples. In particular, some examples such as the selective determination of inorganic and metallorganic species of different toxicity and the redox state speciation of multiply charged ions are discussed. The second part of the Minireview deals with the development and electroanalytical use of a new kind of nanostructured electrode, named nanoelectrode ensembles, which are prepared by template synthesis within the pores of microporous guest membranes. Advantages, peculiarities, and limits of such devices are discussed together with perspectives for their use in electroanalytical sensing at trace and ultratrace concentration levels in environmental samples.

102 citations

Journal ArticleDOI
TL;DR: In this article, the results of a study on the determination of trace levels of mercury in natural saltwaters using screen-printed carbon electrodes modified with Sumichelate Q10R, a chelating resin containing dithiocarbamate groups, which binds mercury strongly and selectively are reported.
Abstract: The results of a study on the determination of trace levels of mercury in natural saltwaters using screen-printed carbon electrodes modified with Sumichelate Q10R, a chelating resin containing dithiocarbamate groups, which binds mercury strongly and selectively are reported. Cyclic voltammetric measurements indicate that mercury(II) is preconcentrated by complexation at the modified electrode, giving peak currents which are about one order of magnitude higher than those obtained at an unmodifed screen-printed electrode. The voltammetric pattern is characterized by a broad reduction peak to which a sharp and well-resolved reoxidation peak is associated. Trace (subnanomolar) concentrations of mercury can be determined at the screen-printed modified electrode by adopting a complexation-anodic stripping procedure with detection via differential pulse voltammetry. The method is characterized by a low detection limit (3j blank/sensitivity) of 12 pM with 20 min complexation and 5 min reduction at ‐0.5 V. Excess copper interferes in the analysis of mercury only when present in more than hundred-fold excess. Data concerning the application of modified screen-printed electrodes to the analysis of mercury in water samples from the channels of Venice (Italy) are presented and discussed.

99 citations

Journal ArticleDOI
TL;DR: In this article, three different preparation methods are compared showing that the better results in terms of sensor durability and reproducibility are achieved by pre-sputtering a thin gold film on the templating membrane and attaching it to a supporting electrode by exploiting the adhesion property and ionic conductivity of a thin Nafion interlayer.
Abstract: Ensembles of copper nanowire electrodes (CuWNEEs) are prepared via electrodeposition in track-etched polycarbonate membranes. Three different preparation methods are compared showing that the better results in terms of sensor durability and reproducibility are achieved by pre-sputtering a thin gold film on the templating membrane and attaching it to a supporting electrode by exploiting the adhesion property and ionic conductivity of a thin Nafion interlayer. SEM-EDS analyses together with double layer charging currents measurements indicate that these arrays are formed by copper nanowires with 400 nm diameter, 10 μm length distributed with a spatial density of 1 × 10 8 nanowires/cm 2 . The voltammetric reduction of nitrate at CuWNEEs is characterized by a well-resolved cathodic peak at approximately −0.680 V vs Ag/AgCl, whose current scales linearly with the nitrate concentration in the 10–400 μM range. The limit of detection (LOD) achieved by simple linear sweep voltammetry is in the 1.7–3.0 μM range, depending on the CuWNEE preparation method, such LOD values being among the lowest reported up to now in the literature. The possibility to use CuWNEEs in chloride and nitrite containing water samples is demonstrated.

94 citations

Journal ArticleDOI
TL;DR: In this paper, the electrochemistry of three electron transfer mediators used for biosensors based on reductase enzymes was investigated at gold nanoelectrode ensembles.

90 citations


Cited by
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Journal ArticleDOI
01 Apr 1988-Nature
TL;DR: In this paper, a sedimentological core and petrographic characterisation of samples from eleven boreholes from the Lower Carboniferous of Bowland Basin (Northwest England) is presented.
Abstract: Deposits of clastic carbonate-dominated (calciclastic) sedimentary slope systems in the rock record have been identified mostly as linearly-consistent carbonate apron deposits, even though most ancient clastic carbonate slope deposits fit the submarine fan systems better. Calciclastic submarine fans are consequently rarely described and are poorly understood. Subsequently, very little is known especially in mud-dominated calciclastic submarine fan systems. Presented in this study are a sedimentological core and petrographic characterisation of samples from eleven boreholes from the Lower Carboniferous of Bowland Basin (Northwest England) that reveals a >250 m thick calciturbidite complex deposited in a calciclastic submarine fan setting. Seven facies are recognised from core and thin section characterisation and are grouped into three carbonate turbidite sequences. They include: 1) Calciturbidites, comprising mostly of highto low-density, wavy-laminated bioclast-rich facies; 2) low-density densite mudstones which are characterised by planar laminated and unlaminated muddominated facies; and 3) Calcidebrites which are muddy or hyper-concentrated debrisflow deposits occurring as poorly-sorted, chaotic, mud-supported floatstones. These

9,929 citations

Journal ArticleDOI
TL;DR: The construction of controlled architectures based on spatially segregated multilayers, exhibiting complementary biological activities is described, and the attachment of biomolecules to biotinylated polymers through affinity interactions based on avidin-biotin bridge is presented.

731 citations

Journal ArticleDOI
TL;DR: The selectivity experiments reveal that the fluorescent sensor is specific for Hg(2+) even with interference by high concentrations of other metal ions, and can be successfully applied to the determination of Hg (2+) in tap water and real lake water samples.

725 citations