This study developed a new type of all-solid-state ion-selective electrode based on a transducing layer of a network of single-walled carbon nanotubes. The extraordinary capacity of carbon nanotubes to promote electron transfer between heterogeneous phases made the presence of electroactive polymers or any other ion-to-electron-transfer promoter unnecessary. The new transducer layer was characterized by environmental scanning electron microscopy and electrochemical impedance spectroscopy. The stability of the electrical potential of the new solid-contact electrode was examined by performing current-reversal chronopotentiometry, and the influence of the interfacial water film was assessed by the potentiometric water layer test. The performance of the new electrode was evaluated by determining K+ with an ion-selective membrane that contained the well-known valinomycin ion carrier. The new electrode had a Nernstian slope (58.4 mV/decade), dynamic ranges of four logarithmic units, and selectivities and limits of detection comparable to other solid-contact electrodes. The short response time (less than 10 s for activities higher than 10(-5.5) M) and the stability of the signal over several days makes these new electrodes very promising candidates for attaining true miniaturization.

Porous carbon materials and carbon nanotubes were recently used as solid contacts in ion-selective electrodes (ISE), and the signal transduction mechanism of these carbon-based materials is therefore of great interest. In this work the ion-to-electron transduction mechanism of carbon nanotubes is studied by using electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). Single-walled carbon nanotubes (SWCNT) are deposited on glassy carbon (GC) disk electrodes by repetitive spraying, resulting in SWCNT layers with thicknesses of 10, 35, and 50 mum. The impedance spectra of these GC/SWCNT electrodes in contact with aqueous electrolyte solution show a very small resistance and a large bulk capacitance that is related to a large effective double layer at the SWCNT/electrolyte interface. Interestingly, the impedance response of GC/SWCNT is very similar to that of poly(3,4-ethylenedioxythiophene) (PEDOT) film electrodes studied earlier under the same experimental conditions. The same equivalent circuit is valid for both types of materials. The reason is that both materials can be described schematically as an asymmetric capacitor where one side is formed by electronic charge (electrons/holes) in the SWCNT wall or along the conjugated polymer chain of PEDOT and the other side is formed by ions (anions/cations) in the solution (or in the ion-selective membrane when used as a solid contact in ISE).

Gas detection is important for controlling industrial and vehicle emissions, household security and environmental monitoring. In recent decades many devices have been developed for detecting CO(2), CO, SO(2), O(2), O(3), H(2), Ar, N(2), NH(3), H(2)O and several organic vapours. However, the low selectivity or the high operation temperatures required when most gas sensors are used have prompted the study of new materials and the new properties that come about from using traditional materials in a nanostructured mode. In this paper, we have reviewed the main research studies that have been made of gas sensors that use nanomaterials. The main quality characteristics of these new sensing devices have enabled us to make a critical review of the possible advantages and drawbacks of these nanostructured material-based sensors.

A simple and generalized approach to build electrochemical sensors for wearable devices is presented. Commercial cotton yarns are first turned into electrical conductors through a simple dyeing process using a carbon nanotube ink. These conductive yarns are then partially coated with a suitable polymeric membrane to build ion-selective electrodes. Potentiometric measurements using these yarn-potentiometric sensors are demonstrated. Examples of yarns that can sense pH, K(+) and NH4(+) are presented. In all cases, these sensing yarns show limits of detection and linear ranges that are similar to those obtained with lab-made solid-state ion-selective electrodes. Through the immobilization of these sensors in a band-aid, it is shown that this approach could be easily implemented in a wearable device. Factors affecting the performance of the sensors and future potential applications are discussed.

A new approach to develop ultra low-cost, robust, rugged, and disposable potentiometric sensors is presented. A suspension of carbon nanotubes in a water-surfactant mixture (carbon nanotubes ink) is applied on conventional filter papers to turn them into conductive papers, which are then used as a substrate to build ion-selective electrodes. The electrodes are made by drop casting a membrane on a small circular area of the conductive paper. In this way, the carbon nanotubes act as both electric conductors and ion-to-electron transducers of the potentiometric signal. Electrodes for sensing K(+), NH(4)(+), and pH were built and tested using this approach, and the results were compared with classical solid-state ion selective electrodes using carbon nanotubes as transducers and glassy carbon as a substrate. In all cases, the analytical performance (sensitivity, linear ranges, limits of detection, selectivity, etc.) of these disposable paper electrodes was similar to that obtained for the more conventional type of ion-selective-electrodes. This opens new avenues for very low-cost platforms for generation of chemical information.

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Keeping the doctor away: An aptamer attached to an electrode coated with single‐walled carbon nanotubes interacts selectively with bacteria (see picture). The resulting electrochemical response is highly accurate and reproducible and starts at ultralow bacteria concentrations, thus providing a simple, selective method for pathogen detection.

This paper overviews the application of multivariate curve resolution (optimized by alternating least squares) to spectroscopic data acquired by monitoring chemical reactions and other processes. The goals of the resolution methods and the principles for understanding their applications are described. Some of the problems arising from these evolving systems and the limitations of the multivariate curve resolution methods are also discussed. This article reviews most of the applications of multivariate curve resolution applied to reacting systems published between January 2000 and June 2007. Some basic papers dated before 2000 have also been included.