Extraction and pre-concentration of platinum and palladium from microwave-digested road dust via ion exchanging mesoporous silica microparticles prior to their quantification by quadrupole ICP-MS

We report on the use of mesoporous silica microparticles (mu Ps) functionalized with quarternary amino groups for the isolation of platinum and palladium tetrachloro complexes from aqueous road dust digests. The mu Ps have a size ranging from 450 to 850 nm and are suspended directly in the aqueous digests, upon which the anionic Pt and Pd complexes are retained on the cationic surface. Subsequently, the mu Ps are separated by centrifugation. Elements that cause spectral interferences in ICP-MS determination of Pt and Pd can be quantitatively removed by adding fresh 0.240 mol L-1 HCl to the mu Ps and by repeating the centrifugation step. The analyte-loaded mu Ps are then dissolved in 0.1 mL of 2 mol L-1 HF, diluted to 2 mL, and the solutions thus obtained are analyzed by quadrupole ICP-MS. This method avoids analyte elution from the sorbent. This "dispersed particle extraction" approach yielded a run-to-run relative standard deviation a parts per thousand currency signaEuro parts per thousand 5 % for Pt and a parts per thousand currency signaEuro parts per thousand 4 % for Pd (at 0.1 ng mL(-1), n = 4 road dust digests). Method detection limits (expressed as concentrations in the dust samples) are 2 and 1 ng g(-1) for Pt and Pd, respectively. The method was validated by analysis of a reference material (BCR CRM 723) and applied to the analysis of road dust samples collected in downtown Vienna. Pt and Pd concentrations in samples collected in summer and in winter were compared, with concentrations ranging from 205 to 1445 ng g(-1) for Pt and from 201 to 1230 ng g(-1) for Pd

Quelle bibliothèque numérique pour une bibliothèque patrimoniale ? : l\u27exemple de la bibliothèque centrale du Museum d\u27Histoire naturelle de Paris

"nous verrons donc dans une première partie comment cette logique permet d’aborder plus facilement l’élaboration d’une « bibliothèque numérique patrimoniale 3 » en suivant les premiers principes d’une politique documentaire traditionnelle , ceux d’une politique d’acquisition. Cependant, force est de constater que la poursuite du processus, la politique de gestion des collections, appelle des exigences nouvelles et particulières, que l’on rapproche beaucoup plus difficilement de celles d’une bibliothèque matérielle. Serait -ce la fin d’une analogie rassurante ? Telle est la question que traite la seconde partie. Enfin, nous verrons dans quelle mesure cette démarche analogique et théorique permet effectivement à la Bibliothèque centrale de trouver un canevas général pour son projet et de déterminer des pistes de réflexion pour une réalisation concrète à venir.

Real-time sweat pH monitoring based on a wearable chemical barcode micro-fluidic platform incorporating ionic liquids

This work presents the fabrication, characterisation and the performance of a wearable, robust, flexible and disposable chemical barcode device based on a micro-fluidic platform that incorporates ionic liquid polymer gels (ionogels). The device has been applied to the monitoring of the pH of sweat in real time during an exercise period. The device is an ideal wearable sensor for measuring the pH of sweat since it does not contents any electronic part for fluidic handle or pH detection and because it can be directly incorporated into clothing, head- or wristbands, which are in continuous contact with the skin. In addition, due to the micro-fluidic structure, fresh sweat is continuously passing through the sensing area providing the capability to perform continuous real time analysis. The approach presented here ensures immediate feedback regarding sweat composition. Sweat analysis is attractive for monitoring purposes as it can provide physiological information directly relevant to the health and performance of the wearer without the need for an invasive sampling approac

Photopatternable ionogels for electrochromic applications

This work describes the development of photopatternable ionogels based on a hybrid organic/inorganic sol–gel material and both phosphonium (trihexyltetradecylphosphonium dicyanamide [P6,6,6,14][dca], trihexyltetradecylphosphonium bis(trifluoromethanesulfonyl)-amide [P6,6,6,14][NTf2]) and imidazolium (1-ethyl-3-methylimidazolium tris(pentafluoroethyl)trifluorophosphate [emIm][FAP]) room temperature ionic liquids (RTILs). Ionogels were prepared via a two step process with the RTIL content varied between 40 and 80 w/w%, and characterised via Raman and Electrochemical Impedance Spectroscopy. 1 and 2 photon polymerisation was performed on the hybrid ionogels using photolithography, resulting in three dimensional structures that were characterised using scanning electron microscopy. Electrochromic ionogels were prepared by addition of ethyl viologen dibromide (EV) to an ionogel containing [emIm][FAP] and hybrid sol–gel material. This composition was photopolymerised on ITO electrodes by UV irradiation and subsequentially characterised via UV/Vis spectroelectrochemistry. It was also possible to fabricate a solid state electrochromic device based on EV and switch between the colourless (oxidised) and blue (reduced) forms using a perturbation signalof 1 V

An electrochromic ionic liquid: design, characterisation and performance in a solid state platform

This work describes the synthesis and characteristics of a novel electrochromic ionic liquid (IL) based on a phosphonium core tethered to a viologen moiety. When integrated into a solid-state electrochromic platform, the viologen modified IL behaved as both the electrolyte and the electrochromic material. Platform fabrication was achieved through in situ photo-polymerisation and encapsulation of this novel IL within a hybrid sol-gel. Important parameters of the platform performance, including its coloration efficiency, switching kinetics and optical properties were characterised using UV/Vis spectroscopy and cyclic voltammetry in tandem. The electrochromic platform exhibits a coloration efficiency of 10.72 cm2C-1, and a varied optical output as a function of the incident current. Despite the rather viscous nature of the material, the platform exhibited approximately two orders of magnitude faster switching kinetics (221 seconds to reach 95 % absorbance) when compared to previously reported electrochromic ILs (18,000 seconds)

Nanomaterials From Imogolite: Structure, Properties, and Functional Materials

International audienceHollow cylinders with a diameter in the nanometer range are carving out prime positions in nanoscience. Thanks to their physico-chemical properties, they could be key elements for next-generation nanofluidics devices, for selective molecular sieving, energy conversion or as catalytic nanoreactors. Several difficult problems such as fine diameter and interface control are solved for imogolite nanotubes. This chapter will present an overview of this unique class of clay nanotubes, from their geological occurrence to their synthesis and their applications. In particular, emphasis will be put on providing an up-to-date description of their structure and properties, their synthesis and the strategies developed to modify their interfaces in a controlled manner. Developments on their applications, in particular for polymer/imogolite nanotubes composites, molecular confinement or catalysis, are presented