Herein, a novel poly(2-mercaptobenzothiazole) coated magnetic nanoadsorbent derived from zeolitic-imidazole framework-8 (ZIF-8) was synthesized and then employed for the extraction/preconcentration of trace amounts of palladium and silver in various real matrixes. In this way, magnetite was fabricated first, and then functionalized with tetraethyl orthosilicate. After that, the synthesized magnetite@silica was coated with the ZIF-8 to obtain magnetic ZIF-8. Afterward, the magnetic ZIF-8 was pyrolyzed under the protection of a nitrogen atmosphere to get a magnetic carbon nanoadsorbent. Finally, the magnetic carbon was functionalized with a conductive polymer (poly-2-mercaptobenzothiazole). Fabrication of the nanoadsorbent was affirmed with scanning and transmission electron microscopies, elemental analysis, X-ray diffraction, Fourier transform infrared spectroscopy, and vibrating sample magnetometry. The method is linear from 0.25 to 200 μg L for silver, and from 0.5 to 250 μg L for palladium. The detection limits are 0.07 and 0.15 μg L for Ag and Pd, respectively. The precision was evaluated at three concentration levels (1, 75, 200 μg L, = 5) and all the relative standard deviation (RSD) values were lower than 10.3%. In the end, the new method was utilized for the preconcentration/determination of trace amounts of palladium and silver in various real matrixes, satisfactorily (relative recovery: 86% to 104%; RSD%: 4.0-9.5%).
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http://dx.doi.org/10.1039/d2ra06193g | DOI Listing |
Langmuir
January 2025
Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering, Kansai University, Suita, Osaka 564-8680, Japan.
In recent years, the advancement of high-frequency communication systems, particularly 5G and future 6G technologies, has increased the need for substrates that minimize signal loss and electromagnetic interference. Glass substrates are highly desirable for these applications due to their low dielectric constant and excellent surface smoothness. However, conventional electroless Cu plating methods struggle to achieve strong adhesion between Cu and the smooth, low-polarity surface of glass, making this an important challenge to address.
View Article and Find Full Text PDFInt J Mol Sci
November 2024
Research Institute of Hydrogen Energy, Kuban State University, Krasnodar 350040, Russia.
Thin-film membranes of Pd-Ag and Pd-Cu alloys capable of releasing hydrogen in a wide temperature range have been developed. The surface activation of the membranes with a nanostructured coating made it possible to intensify hydrogen transport through Pd-containing membranes at low temperatures. This effect was achieved by accelerating limiting surface processes by increasing the active area of the membrane.
View Article and Find Full Text PDFPharm Nanotechnol
December 2024
BIOMCI, Faculty of Medicine and Pharmacy of Agadir, University Ibn Zohr, Agadir, Morocco.
Nanotechnology is rapidly transforming various fields, including medicine, environmental conservation, agriculture, and pharmaceuticals. The production of metallic nanoparticles is a key area within this field, known for its innovative applications. However, traditional chemical and physical methods used for nanoparticle synthesis often involve toxic chemicals and are expensive, making them unsuitable for large-scale production.
View Article and Find Full Text PDFJ Colloid Interface Sci
March 2025
Key Lab for Colloid and Interface Science of Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China. Electronic address:
Metal hydrides are sensitive to HO and O, which reduces the atom efficiency of the hydride donors. Silver (Ag) is an inexpensive coinage metal; however, its lower activity compared to gold, platinum, and palladium limits its application in catalytic hydrogenation. Here, electron-deficient metallic single-atom Ag (AgSA) was loaded onto γ-AlO using a benzoquinone- and KNO- assisted photolysis approach.
View Article and Find Full Text PDFChemistryOpen
November 2024
Departamento de Química Inorgánica, Universidad de Santiago de Compostela, E-, 15782, Santiago de Compostela, Spain.
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