A mesoporous, high surface area and conductive silica/titania graphite composite modified with chitosan and functionalized with tyrosinase was prepared. The composite was obtained by the sol-gel method and the surface of the resultant material was modified with chitosan solutions containing 5, 10 and 15% by mass. The textural characterization showed that even after modification with chitosan, the composite maintains a pore volume near 0.70 cm 3 g -1 and pore diameter between 10 and 50 nm, adequate for enzyme immobilization. The tyrosinase was immobilized on the composite that was modified with 5% chitosan solution. A carbon ceramic electrode was manufactured with this material and was used as an electrochemical biosensor for phenolic compounds, showing low detection limits in the linear range from 40 to 350 µmol L -1 and good sensitivity of 0.284, 0.141 and 0.165 µA µmol -1 L for catechol, dopamine and pyrogallol, respectively. In this composite the enzyme showed to be operative and stable after several months.

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The design and development of efficient and electrocatalytic sensitive nickel oxide nanomaterials have attracted attention as they are considered cost-effective, stable, and abundant electrocatalytic sensors. However, although innumerable electrocatalysts have been reported, their large-scale production with the same activity and sensitivity remains challenging. In this study, we report a simple protocol for the gram-scale synthesis of uniform NiO nanoflowers (approximately 1.75 g) via a hydrothermal method for highly selective and sensitive electrocatalytic detection of hydrazine. The resultant material was characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, and X-ray diffraction. For the production of the modified electrode, NiO nanoflowers were dispersed in Nafion and drop-cast onto the surface of a glassy carbon electrode (NiO NF/GCE). By cyclic voltammetry, it was possible to observe the excellent performance of the modified electrode toward hydrazine oxidation in alkaline media, providing an oxidation overpotential of only +0.08 V vs Ag/AgCl. In these conditions, the peak current response increased linearly with hydrazine concentration ranging from 0.99 to 98.13 μmol L–1. The electrocatalytic sensor showed a high sensitivity value of 0.10866 μA L μmol–1. The limits of detection and quantification were 0.026 and 0.0898 μmol L–1, respectively. Considering these results, NiO nanoflowers can be regarded as promising surfaces for the electrochemical determination of hydrazine, providing interesting features to explore in the electrocatalytic sensor field.

Here, we report multiwalled carbon nanotubes (MWCNTs) functionalized with γ‐cyclodextrins (γCD) as a novel electrochemical strategy for Rutin determination, showing superior performance than β‐cyclodextrins (βCD) modified MWCNTs, suggesting an adequate environment for host‐guest interactions. Under optimized conditions, the sensor showed a linear range of 39–975 nmol L−1 and a limit of detection of 7 nmol L−1. When tested with quercetin, catechin, and caffeine, the platform presented high selectivity with an interference response <10 %. The method was employed to quantify Rutin in spiked pharmaceutical and herbal extracts, providing recovery of 93–98.4 %. Also, HPLC‐PDA confirmed the method‘s accuracy.