Abstract:A facile one-step synthesis of Ag nanoparticles (NPs) with particle sizes less than 5 nm is presented. The average size, size distribution and morphology of the NPs were determined using a number of techniques, including UV-visible absorption spectroscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy (EDX) and a particle size analyzer (PSA). Furthermore, the resulting Ag NPs, without extra treatment, could be used as a probe to detect Hg(II) ions in aqueous media. The response in abso… Show more
“…Room temperature synthesis routes for the fabrication of Ag nanoparticles have been investigated recently, showing promising application feasibility and reliability for largescale manufacture with energy saving and safety. Zhang et al [5] and Huang et al [6] prepared Ag nanoparticles at room temperature, showing excellent antibacterial properties; Li et al [22] prepared Ag nanoparticles at room temperature, which was confirmed to be effective for detecting mercury ion with high sensitivity and selectivity; snowflake-like dendritic Ag Nanostructures [23] and Ag nanowires [24] were also prepared at room temperature. As the concept of "green methods" has become more and more important since the last decade [6], nanomaterials scientists start to pay more attention to facile, safe, and environmentally friendly routes for synthesizing Ag nanoparticles, and room temperature is one of the most promising routes to realize this goal.…”
Well-dispersed Ag nanoparticles with size of 20–30 nm were synthesized in water at room temperature with a self-made novel imidazoline Gemini surfactant quaternary ammonium salt of di (2-heptadecyl-1-formyl aminoethyl imidazoline) hexanediamine. Transmission electron microscopy, X-ray powder diffraction, ultraviolet-visible absorption spectra, and Fourier transform infrared ray were used to characterize the Ag nanoparticles. Results showed that the micellized aggregation of imidazoline Gemini surfactant in water, the growth of Ag initial particles, and the interaction (adsorption and coordination) between surfactant and Ag+/Ag nanoparticles took place simultaneously to form the well-dispersed Ag nanoparticles. Catalytic results show that the surface-modified Ag product was an active metal catalyst for methyl orange reduction reaction due to the effective adsorption between Ag nanoparticles and methyl orange molecules, which was of promising application in environmental protection.
“…Room temperature synthesis routes for the fabrication of Ag nanoparticles have been investigated recently, showing promising application feasibility and reliability for largescale manufacture with energy saving and safety. Zhang et al [5] and Huang et al [6] prepared Ag nanoparticles at room temperature, showing excellent antibacterial properties; Li et al [22] prepared Ag nanoparticles at room temperature, which was confirmed to be effective for detecting mercury ion with high sensitivity and selectivity; snowflake-like dendritic Ag Nanostructures [23] and Ag nanowires [24] were also prepared at room temperature. As the concept of "green methods" has become more and more important since the last decade [6], nanomaterials scientists start to pay more attention to facile, safe, and environmentally friendly routes for synthesizing Ag nanoparticles, and room temperature is one of the most promising routes to realize this goal.…”
Well-dispersed Ag nanoparticles with size of 20–30 nm were synthesized in water at room temperature with a self-made novel imidazoline Gemini surfactant quaternary ammonium salt of di (2-heptadecyl-1-formyl aminoethyl imidazoline) hexanediamine. Transmission electron microscopy, X-ray powder diffraction, ultraviolet-visible absorption spectra, and Fourier transform infrared ray were used to characterize the Ag nanoparticles. Results showed that the micellized aggregation of imidazoline Gemini surfactant in water, the growth of Ag initial particles, and the interaction (adsorption and coordination) between surfactant and Ag+/Ag nanoparticles took place simultaneously to form the well-dispersed Ag nanoparticles. Catalytic results show that the surface-modified Ag product was an active metal catalyst for methyl orange reduction reaction due to the effective adsorption between Ag nanoparticles and methyl orange molecules, which was of promising application in environmental protection.
“…The luminescence enhancement displayed a linear range of Hg(II) concentration from 0 to 180 nM with a correlation coefficient of 0.997 (Figure S8 (ESI†)), indicating the potential capability of this system in quantitative analysis of Hg(II). Notably, a limit of detection (LOD) for Hg(II) was calculated to be 5 nM according to the equation C
lim = 3δ/ k , which is lower than the maximum permissible level (10 nM) of Hg(II) in drinking water specified by the U.S. Environmental Protection Agency (EPA) 7, 46 . Additionally, the sensitivity of this proposed method is also found to be comparable to other reported methods for Hg(II) detection as summarized in Table S2 (ESI†) 6–8, 12, 13, 17,19–22, 47–53 .…”
A novel luminescent turn-on detection method for Hg(II) was developed. The method was based on the silver nanoparticle (AgNP)-mediated quenching of Ir(III) complex 1. The addition of Hg(II) ions causes the luminescence of complex 1 to be recovered due to the oxidation of AgNPs by Hg(II) ions to form Ag(I) and Ag/Hg amalgam. The luminescence intensity of 1 increased in accord with an increased Hg(II) concentration ranging from 0 nM to 180 nM, with the detection limit of 5 nM. This approach offers an innovative method for the quantification of Hg(II).
“…Among them, silver nanoparticle (AgNP) has been extensively studied due to their beneficial catalytic, electrical, optical and properties [16][17][18]. With the vast progress of awareness in the field of nanotechnologies and the spectral theories, the luminescence properties of metal NP have also been testified [19][20][21][22].…”
Silver nanoparticles have been synthesized and were utilized for the enhanced luminometric estimation of moxifloxacin antibiotic. During the experimental procedure, it was clearly found that the addition of silver nanoparticles intensifies the weak chemiluminescence signal intensity of calcein-KMnO4 system by several folds. It was also obvious that the intensity enhancement was linearly proportional to the moxifloxacin concentration and this phenomenon was further utilized for the quantitative determination of target analyte. Effects of the different chemical variables during the experiment were studied to achieve best chemiluminescence signal. Under the optimized experimental parameters, the linear calibration graph was established over the moxifloxacin concentration range of 6.0 × 10(-8) M to 2.5 × 10(-6) M with coefficient of correlation (r (2)) value 0.9998. The lower detection limit was found to be 5.6 × 10(-9) M. The percentage relative standard deviation calculated from five replicate chemiluminescence measurements was found to be 2.63 %. The developed chemiluminescence technique was successfully applied to the determination of moxifloxacin in tablet formulation and spiked human urine sample.
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