BackgroundThis study aims to investigate the influence of different stirring time for synthesis of silver nanoparticles in glutathione (GSH) aqueous solution. The silver nanoparticles (Ag-NPs) were prepared by green synthesis method using GSH as reducing agent and stabilizer, under moderate temperature at different stirring times. Silver nitrate (AgNO3) was taken as the metal precursor while Ag-NPs were prepared in the over reaction time.ResultsFormation of Ag-NPs was determined by UV–vis spectroscopy where surface plasmon absorption maxima can be observed at 344–354 nm from the UV–vis spectrum. The synthesized nanoparticles were also characterized by X-ray diffraction (XRD). The peaks in the XRD pattern confirmed that the Ag-NPs possessed a face-centered cubic and peaks of contaminated crystalline phases were unable to be located. Transmission electron microscopy (TEM) revealed that Ag-NPs synthesized were in spherical shape. Zeta potential results indicate that the stability of the Ag-NPs is increases at the 72 h stirring time of reaction comparison to GSH. The Fourier transform infrared (FT-IR) spectrum suggested the complexation present between GSH and Ag-NPs. The use of green chemistry reagents, such as peptide, provides green and economic features to this work.ConclusionsAg-NPs were successfully synthesized in GSH aqueous solution under moderate temperature at different stirring times. The study clearly showed that the Ag-NPs synthesized in the long times of stirring, thus, the kinetic of GSH reaction is very slow. TEM results shows that with the increase of stirring times the mean particle size of Ag-NPs become increases. The FT-IR spectrum suggested the complexation present between GSH and Ag-NPs. These suggest that Ag-NPs can be employed as an effective bacteria inhibitor and can be applied in medical field.
The effects of noncovalent bonding and mechanical interlocking of carbon nanotubes (CNT) coating on tensile and interfacial strength of glass fiber were investigated. CNT were coated over glass fiber by a simple dip coating method. Acid treated CNT were suspended in isopropanol solution containing Nafion as binding agent. To achieve uniform distribution of CNT over the glass fiber, an optimized dispersion process was developed by two parameters: CNT concentration and soaking time. CNT concentration was varied from 0.4 to 2 mg/mL and soaking time was varied from 1 to 180 min. The provided micrographs demonstrated appropriate coating of CNT on glass fiber by use of CNT-Nafion mixture. The effects of CNT concentration and soaking time on coating layer were studied by performing single fiber tensile test and pull-out test. The obtained results showed that the optimum CNT concentration and soaking time were 1 mg/mL and 60 min, respectively, which led to significant improvement of tensile strength and interfacial shear stress. It was found that, at other concentrations and soaking times, CNT agglomeration or acutely curly tubes appeared over the fiber surface which caused a reduction of nanotubes interaction on the glass fiber.
In the last 5 years, additive manufacturing (three-dimensional printing) has emerged as a highly valuable technology to advance the field of analytical sample preparation. Three-dimensional printing enabled the cost-effective and rapid fabrication of devices for sample preparation, especially in flow-based mode, opening new possibilities for the development of automated analytical methods. Recent advances involve membrane-based three-dimensional printed separation devices fabricated by print-pause-print and multi-material three-dimensional printing, or improved three-dimensional printed holders for solid-phase extraction containing sorbent bead packings, extraction disks, fibers, and magnetic particles. Other recent developments rely on the direct three-dimensional printing of extraction sorbents, the functionalization of commercial three-dimensional printable resins, or the coating of three-dimensional printed devices with functional micro/nanomaterials. In addition, improved devices for liquid-liquid extraction such as extraction chambers, or phase separators are opening new possibilities for analytical method development combined with high-performance liquid chromatography. The present review outlines the current state-of-the-art of three-dimensional printing in analytical sample preparation.
K E Y W O R D S3D printing, liquid-liquid extraction, membrane separation, sample preparation, solid-phase extraction 1854
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