Synthesis of Silver Nanoparticles at the Liquid–Liquid Using Ultrasonic Wave

2013 ◽  
Vol 135 (1) ◽  
Author(s):  
Seong-Ik Hong ◽  
Alma Duarte ◽  
Gabriel A. Gonzalez ◽  
Nam-Soo Kim

The high demand of flexible electronics and the miniaturization of electronic components have been increasing very rapidly. Nanotechnology and in particular nanoparticles have become very important for the development of new technologies and applications which depend on the synthesis and characterization of nanoparticles with specific properties. Significant attention has been focused on the characteristics of the nanoparticles since their properties, particle size and shape are very different when compared to those of the bulk materials. In order to produce nanoparticles with more efficient structures and electronic properties for nano ink, it is necessary to control the particle size to avoid agglomeration. Currently, the nanoparticle size and its agglomeration is controlled by surfactants, but some studies have shown that adding surfactants have negative effects on the conductivity of the nanoparticles along with the high curing temperatures of nano-ink. In this study, silver nanoparticles were synthesized by adding methanol to water instead of surfactants in order to control the silver nanoparticle size. The water and methanol solution was prepared by using different ratios v/v of water/methanol obtaining a liquid–liquid interface and forming a molecular–molecular interface restricting the silver ion movement in the solution. In addition to the liquid–liquid interface, the ion concentration and movement were also restricted through a spraying mist by using ultrasonic waves. The silver ion and the reducing agent were found to have a difference in concentration by the spraying mist method. The movement of the silver ions and the reducing agents were controlled by the difference in concentration. It was observed that the control of the nanoparticles and ion movement was more efficient by spraying silver ion solution than using a reducing agent solution. We confirmed that by increasing the volumetric ratios of methanol the silver nanoparticle size also increased. The mist particle size and the concentration were also calculated at different volumetric ratios of methanol.

2017 ◽  
Vol 901 ◽  
pp. 26-31 ◽  
Author(s):  
Dian Susanthy ◽  
Fadliah ◽  
Endang Tri Wahyuni ◽  
Sri Juari Santosa

Synthesis of silver nanoparticles (AgNPs) by reduction of AgNO3 with o-hydroxybenzoic, p-hydroxybenzoic and o,p-dihydroxybenzoic acids as reducing agents was investigated. This research was conducted to determine the effect of the position and number of hydroxyl groups towards the size, shape and stability of the resulted AgNPs. Surface Plasmon Resonance (SPR) of AgNPs was characterized by UV/Vis spectrophotometer, the shape and size of AgNPs was determined by Transmission Electron Microscope (TEM). The results showed that the reducing agent that has substituents in the para position (p-hydroxybenzoic acid) has the higher reduction ability than the others. AgNPs were yielded by all types of reducing agents in alkaline system. Reducing agents which have greater number of substituents (o,p-dihydroxybenzoic acid) could produce AgNPs with smaller concentration of AgNO3 than the others. AgNPs that was produced by reducing agent having substituents on the para position (p-hydroxybenzoic acid) was more stable and smaller particle size, i.e. 34 ± 1.78 nm than reducing agent that has substituent on the ortho para positions (with particle size 45 + 3.67 nm) and ortho positions (with particle size 70 ± 4.96 nm).


2010 ◽  
Vol 644 ◽  
pp. 85-90 ◽  
Author(s):  
Rebeca G. Melendez ◽  
Karla J. Moreno ◽  
Ivana Moggio ◽  
Eduardo Arias ◽  
Arturo Ponce ◽  
...  

In this paper, we studied the influence of the silver nanoparticles size on the electrical conductivity of PEDOT:PSS in Ag(PEDOT:PSS) films. The silver nanoparticles were synthesized in presence of PEDOT:PSS by varying the molar ratio between AgNO3 and the reducing agent (NaBH4). Both the particle size determined by TEM and the plasmon band obtained by UV-Vis spectroscopy were found to be strongly dependent on the reducing agent concentration. The electrical conductivity increases inversely with the concentration of reducing agent from 5.24 x 10-4 up to 1.63 S/cm; three orders of magnitude higher than pristine PEDOT:PSS.


2016 ◽  
Vol 4 (3) ◽  
Author(s):  
Yong X. Gan ◽  
Gustavo R. Tavares ◽  
Rafhael S. Gonzaga ◽  
Ryan N. Gan

Silver nanoparticles were electrodeposited from 0.3 M oxalic acid electrolyte on a pure aluminum working electrode under silver ion concentration-limited condition. A silver wire was held in a glass tube containing 1.0 M KCl solution as the counter electrode. Ion exchange between the glass tube and the main electrodeposition bath through a capillary was driven by the overpotentials as high as 10 V supplied by an electrochemical workstation. Due to the reaction between chlorine anion and silver cation to form AgCl solid at the Ag/AgCl electrode, the silver ion concentration-limited condition holds in the electrolyte. It is found that silver grows at the aluminum working electrode to form nanoparticles with an average size of about 52.4 ± 13.6 nm. With the increasing of the deposition time, the silver nanoparticles aggregate into clusters. The silver particle clusters are separated with approximately 112.6 ± 19.7 nm due to the hydrogen bubble-induced self-assembling, which is shown by the confined deposition of silver on a gold coating. The surface roughness of the aluminum substrate leads to the reduced uniformity of silver nanoparticle nucleation and growth.


2012 ◽  
Vol 622-623 ◽  
pp. 864-868
Author(s):  
Sirirat Mookriang ◽  
Ampa Jimtaisong ◽  
Nisakorn Saewan ◽  
Krisada Kittigowittana ◽  
Pornchai Rachtanapun ◽  
...  

Silver nanoparticles were prepared by treating a solution of AgNO3 dissolved in deionized water with Emblica (Phyllanthus emblica) extract as reducing agent. The factors that affect the synthesis of silver nanoparticles (time, temperature and concentration of silver nitrate and reducing agent) were investigated. The high concentration of silver nitrate and reducing agent showed the higher in concentration of silver nanoparticles. The heating temperature help increase the yield of silver nanoparticles at shorter reaction time. Their structure, shape and size distribution were characterized by UV-vis spectrophotometer, SEM and TEM technique. The UV-vis spectrophotometer show peaks located of silver-Emblica nanoparticle at 430 nm and the particle size of silver-Emblica is 41.2 nm in average diameter determined by TEM.


2020 ◽  
Vol 32 (8) ◽  
pp. 2079-2083
Author(s):  
Paweena Porrawatkul ◽  
Rungnapa Pimsen ◽  
Saksit Chanthai ◽  
Prawit Nuengmatcha

In this study, silver nanoparticles (AgNPs) were successfully synthesized from aqueous Terminalia catappa leaf extract that acts as a novel reducing agent. Various parameters, including pH, temperature and reaction time, were determined. The UV-visible spectra showed the main peak at 416 nm, which was the characteristic surface plasmon resonance of AgNPs. The spherical shape and particle size of 49 ± 0.01 nm were observed from SEM, TEM and laser particle size analysis (LPSA). FTIR spectra of the leaf extract exhibited the characteristic functional groups that should be responsible for Ag+ ion reduction. The EDX spectrum proved that the obtained sample is silver. The antioxidant activity of AgNPs treated with the leaf extract as determined by the DPPH assay was higher compared to that of Terminalia catappa leaf extract, and the treated AgNP sample exhibited high antibacterial potential against both Gram-positive and Gram-negative bacteria.


2018 ◽  
Vol 5 (2) ◽  
pp. 304-312 ◽  
Author(s):  
Kathryn A. Johnston ◽  
Lisa M. Stabryla ◽  
Ashley M. Smith ◽  
Xing Yee Gan ◽  
Leanne M. Gilbertson ◽  
...  

We determine the impact of bacterial growth media on silver nanoparticle surface chemistry, this surface chemistry on silver ion release from the nanoparticles, and ultimately the antimicrobial implications of those parameters.


2017 ◽  
Vol 14 (4) ◽  
pp. 742-750 ◽  
Author(s):  
Baghdad Science Journal

The present research included synthesis of silver nanoparticle from(1*10-3,1*10-4 and1*10-5) M aqueous AgNO3 solution through the extract of M.parviflora reducing agent. In the process of synthesizing silver nanoparticles we detected a rapid reduction of silver ions leading to the formation of stable crystalline silver nanoparticles in the solution.


2011 ◽  
Vol 119 (1) ◽  
pp. 37-44 ◽  
Author(s):  
Christina M. Powers ◽  
Appala R. Badireddy ◽  
Ian T. Ryde ◽  
Frederic J. Seidler ◽  
Theodore A. Slotkin

2013 ◽  
Vol 12 (02) ◽  
pp. 1350012
Author(s):  
A. G. DEMISSIE ◽  
S. S. LELE

The present study reports a rapid plant-based biosynthesis of silver nanoparticles using callus extract of Jatropha curcas L. The particle size and morphological analyses were carried out using Zetasizer, SEM, TEM. The physicochemical properties were monitored using UV-Vis spectroscopic, IR and DSC. The formation of silver nanoparticle was confirmed by using UV-Vis spectrophotometer and absorbance peaks at 421 nm. The silver nanoparticle was found to be a negatively charged with size ranging from 2 nm to 50 nm. The morphology of the nanoparticle is uniformly spherical and has a dispersion ratio of 0.14. The physicochemical study using DSC indicated significant thermal stability and crystalline nature of the nanoparticle. This intracellular biosynthesis of silver nanoparticles is simple, cheap and eco-friendly than other mechanical and chemical approaches.


2021 ◽  
Vol 33 (9) ◽  
pp. 2049-2052
Author(s):  
D. Muralidharan ◽  
A. Jaculin Raiza ◽  
K. Pandian

A single pot synthesis of gellan gum coated silver nanoparticles using aniline as a reducing agent has been investigated in present study. The reaction was facile at 80 ºC under reflux condition and the complete reduction of silver ions was noted within 2 h. The resulting gellan gum protected silver nanoparticle was isolated and analyzed with various analytical tools. The antimicrobial activity of the prepared nanocomposite had shown an excellent activity against some selected pathogenic microorganisms.


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