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Functionalized silica nanotubes with azo-chromophore for enhanced Pd2+ and Co2+ ions monitoring in E-wastes

Silica nanotubes (SNTs) were utilized as a scaffold for designing a novel solid chemical sensor. The optical nanosensor was designed by direct immobilization of novel azo-chromophore with two carboxylic acid groups called (Z)-2-((2-hydroxynaphthalen-1-yl)diazenyl)terephthalic acid (azo-HNTA) onto th...

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Bibliographic Details
Published in:Journal of molecular liquids 2021-05, Vol.329, p.115585, Article 115585
Main Authors: Abou-Melha, Khlood S., Al-Hazmi, Gamil A.A., Habeebullah, Turki M., Althagafi, Ismail, Othman, Abdullah, El-Metwaly, Nashwa M., Shaaban, Fathy, Shahat, Ahmed
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Language:English
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Summary:Silica nanotubes (SNTs) were utilized as a scaffold for designing a novel solid chemical sensor. The optical nanosensor was designed by direct immobilization of novel azo-chromophore with two carboxylic acid groups called (Z)-2-((2-hydroxynaphthalen-1-yl)diazenyl)terephthalic acid (azo-HNTA) onto the SNTs. Beer's law was obeyed in the ranges of 5–240 and 5–150 ppb for Pd2+ and Co2+ ions, with linear correlation coefficients of 0.999 and 0.971, respectively. The novel nanosensor presented high sensitivity for very low concentrations up to 1.10 × 10−7 mol L−1 (11.7 ppb for Pd2+). The proficiency of this chemosensor for utilizing as an adsorber was tested. The (azo-HNTA) sensor presented a very quick adsorption property for the elimination of Pd2+ and Co2+ ions without preconcentration. The capacities of adsorption were 69.83 and 161.03 mg/g for Pd2+ and Co2+ ions, respectively. Additionally, this nanosensor has efficient recognition and selective recovery of Pd2+ and Co2+ ions in E-wastes. [Display omitted] •SNT was used for accommodating azo-chromophore for designing a unique chemosensor.•The novel nanosensor presented high sensitivity for very low concentrations.•The sensor presented a very quick adsorption property for the Pd2+ and Co2+ ions.•It displayed high efficiency for recovery of Pd2+ and Co2+ ions from E-wastes.
ISSN:0167-7322
DOI:10.1016/j.molliq.2021.115585