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Kinetic and Mechanistic Studies of the Formation of Silver Nanoparticles by Nicotinamide as a Reducing Agent

[Image: see text] Here, in the present study, silver nanoparticles (SNPs) in the size range 6–10 nm have been synthesized by a chemical reduction method using nicotinamide (NTA), an anti-inflammatory agent, and cetyltrimethylammonium bromide (CTAB), a good stabilizing agent, to preparing the nanopar...

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Autores principales: Kumar, Indresh, Gangwar, Chinky, Yaseen, Bushra, Pandey, Pradeep Kumar, Mishra, Sheo K., Naik, Radhey Mohan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088940/
https://www.ncbi.nlm.nih.gov/pubmed/35559139
http://dx.doi.org/10.1021/acsomega.2c00046
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author Kumar, Indresh
Gangwar, Chinky
Yaseen, Bushra
Pandey, Pradeep Kumar
Mishra, Sheo K.
Naik, Radhey Mohan
author_facet Kumar, Indresh
Gangwar, Chinky
Yaseen, Bushra
Pandey, Pradeep Kumar
Mishra, Sheo K.
Naik, Radhey Mohan
author_sort Kumar, Indresh
collection PubMed
description [Image: see text] Here, in the present study, silver nanoparticles (SNPs) in the size range 6–10 nm have been synthesized by a chemical reduction method using nicotinamide (NTA), an anti-inflammatory agent, and cetyltrimethylammonium bromide (CTAB), a good stabilizing agent, to preparing the nanoparticles in the 6–10 nm size range. Kinetic studies on the formation of SNPs have been performed spectrophotometrically at 410 nm (strong plasmon band) in aqueous medium as a function of [AgNO(3)], [NTA], [NaOH], and [CTAB]. The plot of ln(A(∞) – A(t)) versus time exhibited a straight line and the pseudo-first-order rate constants of different variables were calculated from its slope. On the basis of experimental findings, a plausible mechanism was proposed for the formation of SNPs colloid. From the mechanism, it is proved that the reduction of silver ions proceeded through the formation of silver oxide in colloidal form by their reaction with hydroxide ions and NTA after performing their function and readily undergo hydrolysis to form nicotinic acid as a hydrolysis product with the release of ammonia gas. The preliminary characterization of the SNPs was carried out by using a UV–visible spectrophotometer. The detailed characterization of SNPs was also carried out using other experimental techniques such as Fourier transform infrared spectroscopy (FTIR), field-emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and powder X-ray diffraction (PXRD). SNPs show a remarkable catalytic activity of up to 90% for the reduction of the cationic dye methylene blue.
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spelling pubmed-90889402022-05-11 Kinetic and Mechanistic Studies of the Formation of Silver Nanoparticles by Nicotinamide as a Reducing Agent Kumar, Indresh Gangwar, Chinky Yaseen, Bushra Pandey, Pradeep Kumar Mishra, Sheo K. Naik, Radhey Mohan ACS Omega [Image: see text] Here, in the present study, silver nanoparticles (SNPs) in the size range 6–10 nm have been synthesized by a chemical reduction method using nicotinamide (NTA), an anti-inflammatory agent, and cetyltrimethylammonium bromide (CTAB), a good stabilizing agent, to preparing the nanoparticles in the 6–10 nm size range. Kinetic studies on the formation of SNPs have been performed spectrophotometrically at 410 nm (strong plasmon band) in aqueous medium as a function of [AgNO(3)], [NTA], [NaOH], and [CTAB]. The plot of ln(A(∞) – A(t)) versus time exhibited a straight line and the pseudo-first-order rate constants of different variables were calculated from its slope. On the basis of experimental findings, a plausible mechanism was proposed for the formation of SNPs colloid. From the mechanism, it is proved that the reduction of silver ions proceeded through the formation of silver oxide in colloidal form by their reaction with hydroxide ions and NTA after performing their function and readily undergo hydrolysis to form nicotinic acid as a hydrolysis product with the release of ammonia gas. The preliminary characterization of the SNPs was carried out by using a UV–visible spectrophotometer. The detailed characterization of SNPs was also carried out using other experimental techniques such as Fourier transform infrared spectroscopy (FTIR), field-emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and powder X-ray diffraction (PXRD). SNPs show a remarkable catalytic activity of up to 90% for the reduction of the cationic dye methylene blue. American Chemical Society 2022-04-14 /pmc/articles/PMC9088940/ /pubmed/35559139 http://dx.doi.org/10.1021/acsomega.2c00046 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Kumar, Indresh
Gangwar, Chinky
Yaseen, Bushra
Pandey, Pradeep Kumar
Mishra, Sheo K.
Naik, Radhey Mohan
Kinetic and Mechanistic Studies of the Formation of Silver Nanoparticles by Nicotinamide as a Reducing Agent
title Kinetic and Mechanistic Studies of the Formation of Silver Nanoparticles by Nicotinamide as a Reducing Agent
title_full Kinetic and Mechanistic Studies of the Formation of Silver Nanoparticles by Nicotinamide as a Reducing Agent
title_fullStr Kinetic and Mechanistic Studies of the Formation of Silver Nanoparticles by Nicotinamide as a Reducing Agent
title_full_unstemmed Kinetic and Mechanistic Studies of the Formation of Silver Nanoparticles by Nicotinamide as a Reducing Agent
title_short Kinetic and Mechanistic Studies of the Formation of Silver Nanoparticles by Nicotinamide as a Reducing Agent
title_sort kinetic and mechanistic studies of the formation of silver nanoparticles by nicotinamide as a reducing agent
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088940/
https://www.ncbi.nlm.nih.gov/pubmed/35559139
http://dx.doi.org/10.1021/acsomega.2c00046
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