10 research outputs found

    LACTOSE TO NATURALIZE TEXTILE DYES

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    Many natural dyes, for example carminic acid, are soluble in water. We present a simple strategy to naturalize synthetic azadyes through their linkage with lactose to induce their water solubility. The dyeing process of textile fibres then becomes possible in water without additives such as surfactants and mordants, which result in products that are difficult to eliminate. Glyco-azadyes (GADs) we are presenting here are obtained through a diether linker to bond the azadye and the sugar. Tinctorial tests were carried out with fabrics containing wool, polyester, cotton, nylon, and acetate. GADs were found to be multipurpose and capable of dyeing many fabrics efficiently under mild conditions

    Efficient double glycoconjugation to naturalize high molecular weight disperse dyes

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    Commercially available Disperse Orange 29 (1a) and Disperse Red 1 (2a) were elaborated to glycoconjugated species, following a new version of a previously-described ‘naturalisation’ procedure. Glutamic acid was chosen to achieve a double glycoconjugation, which is essential to give to the original disperse dye a water solubility suitable for reaching optimal dyeing conditions. UV–vis plot of the ‘naturalised’ species showed negligible differences when compared to those of the commercial dye

    Amine-Grafted Pomegranate Peels for the Simultaneous Removal of Nitrate and Phosphate Anions from Wastewater

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    Pomegranate peel (PP), a by-product of agro-food consumption, has a low adsorption capacity for nitrate and phosphate ions in aqueous media, but its surface is very rich in alcohol functional groups. In this work, the surface of pomegranate peels was functionalized by chemo-grafting 3-(2-Aminoethylamino) propyl] trimethoxy silane (AEAPTES) using the availability of alcohol groups to increase the adsorption capacity of the resulting adsorbent (PP/AEAPTES) towards nitrate and phosphate ions. The prepared PP/AEAPTES adsorbent was analyzed by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), Zeta potential, and X-ray photoelectron spectrometry (XPS). Under experimental conditions, the adsorption capacity of PP/AEAPTES has been found to be 124.57 mg/g and 94.65 mg/g for NO3− and PO43−, respectively, at pH 6 over a wide temperature range, and adsorption is exothermic for NO3− and endothermic for PO43−, as well as spontaneous and physical in nature. The adsorptions of NO3− and PO43− were also correctly described by the Langmuir isotherm and followed the pseudo-second-order model. The ability of PP/AEAPTES to adsorb NO3− and PO43− ions under real conditions was evaluated, and efficient regeneration and repetitive use of PP/AEAPTES was successfully achieved up to 5 cycles

    Recent advances in electrochemical sensors and biosensors for monitoring drugs and metabolites in pharmaceutical and biological samples

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    Various applications of electrochemical sensors and biosensors have been reported in many fields. These include pharmaceuticals, drug detection, cancer detection, and analysis of toxic elements in tap water. Electrochemical sensors are characterised by their low cost, ease of manufacture, rapid analysis, small size and ability to detect multiple elements simultaneously. They also allow the reaction mechanisms of analytes, such as drugs, to be taken into account, giving a first indication of their fate in the body or their pharmaceutical preparation. Several materials are used in the construction of sensors, such as graphene, fullerene, carbon nanotubes, carbon graphite, glassy carbon, carbon clay, graphene oxide, reduced graphene oxide, and metals. This review covers the most recent progress in electrochemical sensors used to analyze drugs and metabolites in pharmaceutical and biological samples. We have highlighted carbon paste electrodes (CPE), glassy carbon electrodes (GCE), screen-printed carbon electrodes (SPCE) and reduced graphene oxide electrodes (rGOE). The sensitivity and analysis speed of electrochemical sensors can be improved by modifying them with conductive materials. Different materials used for modification have been reported and demonstrated, such as molecularly imprinted polymers, multiwalled carbon nanotubes, fullerene (C60), iron(III) nanoparticles (Fe3O4NP), and CuO micro-fragments (CuO MF). Manufacturing strategies and the detection limit of each sensor have been reported
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