scholarly journals Advancement of Microwave-Assisted Biosynthesis for Preparing Au Nanoparticles Using Ganoderma lucidum Extract and Evaluation of Their Catalytic Reduction of 4-Nitrophenol

ACS Omega ◽  
2021 ◽  
Author(s):  
Vinh Phu Nguyen ◽  
Hieu Le Trung ◽  
Thu Huong Nguyen ◽  
DongQuy Hoang ◽  
Thai Hoa Tran
RSC Advances ◽  
2015 ◽  
Vol 5 (10) ◽  
pp. 7554-7558 ◽  
Author(s):  
Hyunje Woo ◽  
Ji Woong Kim ◽  
Miran Kim ◽  
Sungkyun Park ◽  
Kang Hyun Park

A one-pot hydrothermal synthesis approach was developed to prepare FeSO4·(H2O)–graphene oxide (GO) nanosheets. Au nanoparticles were immobilized onto this support, giving Au/Fe2O3–GO nanocomposites.


2020 ◽  
Vol 01 ◽  
Author(s):  
Huiying Wu ◽  
Feng Liang

Background: Porous Au nanomaterials show great potential in the fields of biomedicine, drug delivery and catalysis for the merits of low density, large void space and large specific surface area. The preparation of porous Au nanomaterials is usually carried out by using a hard-templating method which is cumbersome. Methods: Dandelion-like porous Au nanoparticles were synthesized through a soft-templating method in our work. The synthesized porous Au nanoparticles were characterized via transmission electron microscopy (TEM), X-ray diffraction (XRD), energy-dispersive X-ray (EDX) and cyclic voltammetry (CV). The reduction of nitrophenol was carried out to evaluate the catalytic behavior of porous Au nanoparticles. Results: Porous Au nanoparticles prepared were in uniform size (47.9±6.4 nm) and the morphology could be regulated by adjusting the molar ratio of reactants. The apparent rate constant (kapp) value of reducing nitrophenol catalyzed by porous Au nanoparticles was higher than Au nanospheres and nanobranches in similar size. It could be attributed to the large amount of active sites and high proportion of high-order crystal faces proved by CV and XRD. Conclusion: We developed a facile and reproducible method for synthesizing porous Au nanoparticles. The morphology of porous Au nanoparticles can be ajusted by changing the molar ratio of reactants. Porous Au nanoparticles we prepared behaved better in catalysis compared with Au nanospheres and Au nanobranches.


2011 ◽  
Vol 2011 ◽  
pp. 1-3
Author(s):  
Manuel Ramos ◽  
Karina Castillo ◽  
Domingo A. Ferrer ◽  
Rurik J. Farias ◽  
Sergio Flores ◽  
...  

Core-Shell (Fe3O4/Au) nanoparticles were synthesized using iron II chloride tetrahydrate (FeCl2H2O) and potassium tetrachloroaurate III (AuCl4K) precursors under microwave-assisted conditions. Products were analyzed using field emission gun electron microscope in transmission and scanning modes; energy disperse X-ray spectroscopy performed during STEM measurements indicated a signal for gold K and M signals at 9 keV and 13 keV, respectively, confirming Au atoms at nanoparticle's perimeter and Fe-L signal at 8 keV to be at the center.


Chemija ◽  
2019 ◽  
Vol 30 (1) ◽  
Author(s):  
Daina Upskuvienė ◽  
Aldona Balčiūnaitė ◽  
Jūratė Vaičiūnienė ◽  
Algirdas Selskis ◽  
Rimantas Vaitkus ◽  
...  

In this study, the gold nanoparticles (AuNPs) without carbon support were prepared using the well-known citrate reduction method. The carbon supported AuNPs nanocomposites were fabricated by two different approaches: chemical adsorption of AuNPs from the prepared citrate stabilized AuNP colloidal solution on the carbon powder surface and one-pot microwave-assisted synthesis. The nanocomposites were characterized using scanning electron microscopy (SEM) and inductively coupled plasma optical emission spectroscopy (ICP-OES). The electrocatalytic activity of the prepared catalysts was evaluated for the electrooxidation of glucose in an alkaline media using cyclic voltammetry. The highest electrocatalytic activity was observed for the catalyst of carbon supported Au nanoparticles prepared by microwave-assisted synthesis, followed by the catalyst of carbon supported Au nanoparticles prepared by means of the adsorption method, whereas the pure Au nanoparticles without carbon support exhibited the lowest electrocatalytic properties for glucose electrooxidation.


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