scholarly journals Catalytic performance of Ag, Au and Ag-Au nanoparticles synthesized by lichen extract

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.

2016 ◽  
Vol 2016 ◽  
pp. 1-17 ◽  
Author(s):  
Noura El-Ahmady El-Naggar ◽  
Attiya Mohamedin ◽  
Sarah Shawqi Hamza ◽  
Abdel-Dayem Sherief

Biological method for silver nanoparticles synthesis has been developed to obtain cost effective, clean, nontoxic, and ecofriendly size-controlled nanoparticles. The objective of this study is extracellular biosynthesis of antimicrobial AgNPs using cell-free supernatant of a localStreptomycessp. strain SSHH-1E. Different medium composition and fermentation conditions were screened for maximal AgNPs biosynthesis using Plackett-Burman experimental design and the variables with statistically significant effects were selected to study their combined effects and to find out the optimum values using a Box-Behnken design. The synthesized AgNPs were characterized using UV-visible spectroscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, and energy dispersive X-ray spectroscopy. Rapid biosynthesis of AgNPs was achieved by addition of 1 mM AgNO3solution to the cell-free supernatant. The produced particles showed a single surface plasmon resonance peak at 400 nm by UV-Vis spectroscopy which confirmed the presence of AgNPs.Streptomycessp. SSHH-1E was identified asStreptomyces narbonensisSSHH-1E. Transmission electron microscopy study indicated that the shape of AgNPs is spherical and the size is ranging from 20 to 40 nm. Fourier transform infrared spectroscopy analysis provides evidence for proteins as possible reducing and capping agents. Furthermore, the biosynthesized AgNPs significantly inhibited the growth of medically important pathogenic Gram-positive and Gram-negative bacteria and yeast. The maximum biosynthesis of AgNPs was achieved at initial pH of 8, peptone of 0.5 g, and inoculum age of 48 h. The statistical optimization resulted in a 4.5-fold increase in the production of AgNPs byStreptomyces narbonensisSSHH-1E.


2008 ◽  
Vol 1082 ◽  
Author(s):  
Robert William James Scott ◽  
Priyabrat Dash

ABSTRACTWe will show that metallic and bimetallic nanoparticles solubilized in 1-butyl-3-methylimidazolium hexafluorophosphate ionic liquids (IL) can be used as catalysts for a variety of oxidation and hydrogenation reactions. Nanoparticles were either directly synthesized in the IL or transferred to the IL from other solvents. Characterization was carried out by UV-Vis spectroscopy and transmission electron microscopy. Both the activity and selectivity of the hydrogenation reactions could be tuned by varying the composition of AuPd bimetallic nanoparticles. We will also show that the nanoparticle/IL catalysts can be recycled and then reused for further catalytic reactions with minimal loss in activity. In addition, new insights into the stabilization of nanoparticles in ionic liquids will be presented.


2019 ◽  
Vol 150 (1) ◽  
pp. 49-55 ◽  
Author(s):  
Laura Abis ◽  
Nikolaos Dimitratos ◽  
Meenakshisundaram Sankar ◽  
Simon J. Freakley ◽  
Graham J. Hutchings

Abstract Au nanoparticles supported on P25 TiO2 (Au/TiO2) were prepared by a facile sol-immobilisation method and investigated for the surface plasmon-assisted glycerol oxidation under base-free conditions. The Au/TiO2 samples were characterized by UV–vis spectroscopy and transmission electron microscopy. Catalysts were prepared using polyvinyl alcohol as stabiliser as well as in the absence of polymer stabiliser. Both the conversion and the reaction selectivity are affected by the plasmon-assisted oxidation and there is an interplay between the presence of the stabiliser and the Au nanoparticle size. Graphic Abstract


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.


2010 ◽  
Vol 09 (05) ◽  
pp. 399-406 ◽  
Author(s):  
A. A. EL-DALY

In this paper, we report a convenient and informative procedure for detecting the morphology and surface structure of individual gold nanocrystals using digital Crystal Image Software (CIS) processing of transmission electron microscopy (TEM) image, which comprises coalescence phenomena of these nanoparticles. The results show that the internal structure of Au nanoparticles has a core of gold atoms arranged as a Marks decahedron, surrounded by additional gold–organic compound layers forming a rigid surface layer, and its outer layer comprises four staple motif bridge molecules that resemble handles, formed an unusual pattern. The obtained results improved our understanding of the basics of the coalescence phenomena such as the driving mechanisms acting at different particle sizes. However, these discrete natures of the nanoparticles will assist in the understanding of principles of nanocore assembly and opens a new window for nanoparticles chemistry.


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.


2013 ◽  
Vol 750-752 ◽  
pp. 336-339
Author(s):  
Fa Chao Wu ◽  
Teng Fei Shen

In this work, CaCO3 nanoparticles have been synthesized via heat-treatment of a new precursor. Effect of calcinations temperature on particle size has been investigated. The products were characterized by Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). nanoCaCO3 was modified using chloroform as solvent and fatty acid as modifier atroom temperature. The advantage of this modification is that it can be proceed at room temperature and it can reduce energy consumption.


2019 ◽  
Vol 2019 ◽  
pp. 1-16 ◽  
Author(s):  
Shohreh Hemmati ◽  
Erin Retzlaff-Roberts ◽  
Corren Scott ◽  
Michael T. Harris

An environmentally friendly technique has been developed to produce metal nanoparticles using green synthesis methods. In this study, silver nanostructures were synthesized using different sugar substitutes and artificial sweeteners as green reducing agents in an aqueous solution at low temperature. The main ingredients (such as maltodextrin, sucrose, saccharin, and sucralose) of the artificial sweeteners acting as reducing agents were used to reduce Ag+ ions to Ag0. The pH of the solution was controlled during synthesis through the addition of sodium hydroxide (NaOH) to increase the strength of the reducing agents by converting nonreducing sugars to reducing ones and consequently increasing the rate of silver nanoparticle formation. The size and morphology of the synthesized nanostructures were characterized by transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX). The formation of nanostructures during the course of the reactions was investigated by UV-visible (UV-vis) spectroscopy characterization of an aliquot of sample at specific intervals. The function of each artificial sweetener and corresponding ingredients as a reducing agent and capping agent was investigated by Fourier-transform infrared spectroscopy (FTIR) and mass spectrometry (MS).


Sign in / Sign up

Export Citation Format

Share Document