scholarly journals Optical Properties of Linoleic Acid Protected Gold Nanoparticles

2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
Ratan Das ◽  
Siddartha S. Nath ◽  
Ramendu Bhattacharjee

Linoleic acid-protected gold nanoparticles have been synthesized through the chemical reduction of tetrachloroaurate ions by ethanol in presence of sodium linoleate. The structure of these nanoparticles is investigated using transmission electron microscopy, which shows that the Au nanoparticles are spherical in shape with a narrow size distribution which ranges from 8 to 15 nm. Colloidal dispersion of gold nanoparticles in cyclohexane exhibits absorption bands in the ultraviolet-visible range due to surface plasmon resonance, with absorption maximum at 530 nm. Fluorescence spectra of gold nanoparticles also show an emission peak at 610 nm when illuminated at 450 nm. UV-Vis spectroscopy reveals that these nanoparticles remain stable for 10 days.

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Min Song ◽  
Juan Xu ◽  
Changzi Wu

In our study, graphene oxide is synthesized by Hummers method. And then, carboxylic acid functionalized graphene (graphene-COOH), thiol-functionalized graphene (graphene-SH), and highly dispersive graphene are prepared by chemical modification of respective groups on the graphene surface. Furthermore, we explore a solution-based approach to prepare three differently functionalized graphene-gold composites by one-step chemical reduction ofAuCl4 -ions in respective functionalized graphene suspensions, where the gold nanoparticles are deposited on the functionalized graphene surface during their synthesis process. In addition, we compare the influence of surface functionalization on the growth of gold nanoparticles on graphene surface. Transmission electron morphology (TEM) and ultraviolet-visible (UV-Vis) spectroscopy are employed to study the effect of surface functionalities on AuNPs distribution onto the graphene surface and demonstrate the successful immobilization of AuNPs on graphene surface.


Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 2937
Author(s):  
Muhammad Zulfajri ◽  
Wei-Jie Huang ◽  
Genin-Gary Huang ◽  
Hui-Fen Chen

The laser ablation synthesis in solution (LASiS) method has been widely utilized due to its significant prospects in laser microprocessing of nanomaterials. In this study, the LASiS method with the addition of different surfactant charges (cationic CTAB, nonionic TX-100, and anionic SDS) was used to produce Au NPs. An Nd:YAG laser system at 532 nm excitation with some synthetic parameters, including different laser fluences, ablation times, and surfactant concentrations was performed. The obtained Au NPs were characterized by UV-Vis spectroscopy, transmission electron microscopy, and zeta potential analyzer. The Au NPs exhibited the maximum absorption peak at around 520 nm for all samples. The color of Au NPs was changed from red to reddish by increasing the laser fluence. The surfactant charges also played different roles in the Au NPs’ growth during the synthesis process. The average sizes of Au NPs were found to be 8.5 nm, 5.5 nm, and 15.5 nm with the medium containing CTAB, TX-100, and SDS, respectively. Besides, the different surfactant charges induced different performances to protect Au NPs from agglomeration. Overall, the SDS and CTAB surfactants exhibited higher stability of the Au NPs compared to the Au NPs with TX-100 surfactant.


Author(s):  
Utkarsh Jain ◽  
CS Pundir ◽  
Shaivya Gupta ◽  
Nidhi Chauhan

Recent advancements in nanotechnology, for the biosynthesis of metal nanoparticles through enormous techniques, showed multidimensional developments. One among many facets of nanotechnology is to procure and adopt new advancements for green technology over chemical reduction synthesis. This adaptation for acquiring green nanotechnology leads us to a new dimension of nanobiotechnology. In order to imply one such efforts, in this study the emphasis is being laid on the synthesis of MgO nanoparticles using green technology and eliminating chemical reduction methods. Different characterization techniques such as UV–Vis spectroscopy, transmission electron microscopy, and dynamic light scattering were used to carry out the experiments. The average size of MgO nanoparticles were obtained in the range of 85–95 nm, when synthesized by various sources. The extracts of plants were capable of producing MgO nanoparticles efficiently and exhibited good results during cyclic voltammetry and electrochemical impedance spectroscopy study. The electrode modified with MgO nanoparticles (plant extract) showed good stability (90 days) and high conductivity. This study reports cost-effective and environment-friendly method for synthesis of MgO nanoparticles using plant extracts. The process is rapid, simple, and convenient and can be used as an alternative to chemical method.


Polymers ◽  
2021 ◽  
Vol 13 (23) ◽  
pp. 4066
Author(s):  
David Herrera Robalino ◽  
María del Mar Durán del Amor ◽  
Carmen María Almagro Gómez ◽  
José Ginés Hernández Cifre

The adsorption of the thermoresponsive positively charged copolymer poly(N-isopropylacrylamide)-block-poly(3-acrylamidopropyl)trimethylammonium chloride, PNIPAAM48-b-PAMPTMA6(+), onto negatively charged gold nanoparticles can provide stability to the nanoparticles and make the emerging structure tunable by temperature. In this work, we characterize the nanocomposite formed by gold nanoparticles and copolymer chains and study the influence of the copolymer on the expected aggregation process that undergoes those nanoparticles at high ionic strength. We also determine the lower critical solution temperature (LCST) of the copolymer (around 42 °C) and evaluate the influence of the temperature on the nanocomposite. For those purposes, we use dynamic light scattering, UV-vis spectroscopy and transmission electron microscopy. At the working PNIPAAM48-b-PAMPTMA6(+) concentration, we observe the existence of copolymer structures that trap the gold nanoparticles and avoid the formation of nanoparticles aggregates. Finally, we discuss how these structures can be useful in catalysis and nanoparticles recovery.


Author(s):  
Is Fatimah ◽  
Putwi Widya Citradewi ◽  
Amri Yahya ◽  
Bambang Nugroho ◽  
Habibi Hidayat ◽  
...  

Abstract The composite of green synthesized gold nanoparticles (Au NPs)-doped hydroxyapatite (HA) has been prepared. The gold nanoparticles were produced via bioreduction of HAuCl4 with Clitoria ternatea flower extract, and utilized in the synthesis of hydroxyapatite using Ca(OH)2 and ammonium diphosphate as precursor. The aim of this research is to study the structural analysis of the composite and antibacterial activity test toward Eschericia coli, Staphylococcus aureus, Klebsiela pneumoniae, and Streptococcus pyogenes. In addition, the antioxidant activity was evaluated using 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging method. The monitoring of gold nanoparticles formation was conducted by UV–vis spectroscopy and particle size analyses, meanwhile the synthesized composite was studied using X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The results showed that homogeneously dispersed gold nanoparticles in HA structure was obtained with the particle size ranging at 5-80 nm. The nanocomposite demonstrated antibacterial activity against tested bacteria. The nanocomposite expressed an antioxidant activity as shown by the DPPH scavenging activity of 66 and 58% at the concentration of 100 μg/mL and 50 μg/mL, respectively.


2016 ◽  
Vol 15 (01n02) ◽  
pp. 1650008 ◽  
Author(s):  
Anal K. Jha ◽  
K. Prasad

Aquatic pteridophyte (Azolla sp.) was taken to assess its potential to synthesize the metal (Au) nanoparticles. The synthesized particles were characterized using X-ray, UV-visible, scanning and transmission electron microscopy analyses. Nanoparticles almost spherical in shape having the sizes of 5–17[Formula: see text]nm are found. UV-visible study revealed the surface plasmon resonance at 538[Formula: see text]nm. Responsible phytochemicals for the transformation were principally phenolics, tannins, anthraquinone glycosides and sugars present abundantly in the plant thereby bestowing it adaptive prodigality. Also, the use of Azolla sp. for the synthesis of gold nanoparticles offers the benefit of eco-friendliness.


2016 ◽  
Vol 09 (03) ◽  
pp. 1650045 ◽  
Author(s):  
Pei-Ying Li ◽  
Kai-Yu Cheng ◽  
Xiu-Cheng Zheng ◽  
Pu Liu ◽  
Xiu-Juan Xu

Chitosan-ionic liquid conjugation (CILC), which was prepared through the reaction of 1-(4-bromobutyl)-3-methylimidazolium bromide (BBMIB) with chitosan, was firstly used to prepare functionalized graphene composite via the chemical reduction of graphene oxide (GO). The obtained water soluble graphene-based composite was characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), ultraviolet-visible (UV–Vis) spectroscopy and so on. CILC-RGO showed excellent dispersion stability in water at the concentration of 2.0 mg/mL, which was stable for several months without any precipitate. This may be ascribed to the electrostatic attraction and [Formula: see text]–[Formula: see text] interaction between CILC and graphene.


2013 ◽  
Vol 313-314 ◽  
pp. 232-236
Author(s):  
Dan Zhang

Activated carbon supported gold nanoparticles (Au/C) were prepared by a chemical reduction process using NaBH4as a reducing agent. The characterization of transmission electron microscope indicated that the Au nanoparticles (AuNPs) in the Au/C catalyst were highly well dispersed on the carbon support. The catalytic activity of the Au/C catalyst for the methanol electrooxidation (MEO) was investigated by the cyclic voltammetry (CV). The results displayed that the Au/C catalyst exhibited a favorable catalytic activity towards the MEO in alkaline solution. Moreover, the competitive adsorption between OH-and CH3OH on the surface of the AuNPs in the Au/C catalyst existed in the course of the MEO. Based on this competitive adsorption, the mechanism of the MEO on the Au/C catalyst was further investigated.


2020 ◽  
Vol 2020 ◽  
pp. 1-11
Author(s):  
Kamonpan Wongyai ◽  
Phitchayapak Wintachai ◽  
Rasimate Maungchang ◽  
Parawee Rattanakit

A green, simple, and rapid synthesis of gold nanoparticles using plant extract, Cryptolepis buchanani Roem. and Schult, and their applications are first described in this paper. The formation of gold nanoparticles was visually observed by the appearance of a ruby red color, which was further indicated by an absorption peak at 530 nm in UV-Vis spectroscopy. Optimization of reaction parameters for the gold nanoparticles was also investigated. Various analytical techniques were employed as part of the process of characterizing the resulting gold nanoparticles. Fourier transform infrared (FTIR) analysis revealed that the phenol compounds present in the extract were responsible for gold(III) reduction and stabilization of gold nanoparticles. Transmission electron microscopy (TEM) analysis showed that the gold nanoparticles were spherical in shape with an average diameter of 11 nm. Powder X-ray diffraction (XRD) pattern indicated that the green synthesis approach produced highly crystalline, face-centered cubic gold nanoparticles. Energy-dispersive X-ray spectroscopy (EDS) measurements confirmed the presence of elemental gold in the prepared nanoparticles. The negative zeta potential value of gold nanoparticles was found to be -30.28 mV. The green synthesized gold nanoparticles expressed effective antibacterial activity against Staphylococcus aureus, methicillin-resistant Staphylococcus aureus, and Acinetobacter baumannii and exhibited an excellent catalytic property in terms of its reduction ability of methylene blue.


2018 ◽  
Vol 7 (5) ◽  
pp. 433-440 ◽  
Author(s):  
Zafer Çıplak ◽  
Ceren Gökalp ◽  
Bengü Getiren ◽  
Atila Yıldız ◽  
Nuray Yıldız

Abstract In the present study, the green chemistry approach for the biosynthesis of Ag, Au and Ag-Au bimetallic nanoparticles (NPs) was applied using lichen extract [Cetraria islandica (L.) Ach.]. The lichen extract acts both as a reducing and stabilizing agent. The monometallic and bimetallic NPs were characterized by transmission electron microscopy (TEM), ultraviolet-visible (UV-Vis) spectroscopy and Fourier transform infrared (FTIR) spectroscopy. The results showed that NPs were successfully synthesized and the prepared structures were generally spherical. The synthesized nanostructures exhibited excellent catalytic activities towards reduction of nitrophenols (4-nitrophenol; 4-NP) to aminophenols (4-aminophenol; 4-AP) with sodium borohydride (NaBH4). It was determined that bimetallic NPs exhibit more effective catalytic activity than monometallic Ag and Au nanostructures. This is the first report on 4-NP reduction with Ag, Au and Au-Ag NP catalysts prepared by lichen extract.


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