Gold Nanoparticles Formation via Au(III) Complex Ions Reduction with l -Ascorbic Acid

2017 ◽  
Vol 49 (11) ◽  
pp. 789-797 ◽  
Author(s):  
M. Luty-Błocho ◽  
M. Wojnicki ◽  
K. Fitzner
2020 ◽  
Vol 16 (7) ◽  
pp. 905-913
Author(s):  
Youyuan Peng ◽  
Qingshan Miao

Background: L-Ascorbic acid (AA) is a kind of water soluble vitamin, which is mainly present in fruits, vegetables and biological fluids. As a low cost antioxidant and effective scavenger of free radicals, AA may help to prevent diseases such as cancer and Parkinson’s disease. Owing to its role in the biological metabolism, AA has also been utilized for the therapy of mental illness, common cold and for improving the immunity. Therefore, it is very necessary and urgent to develop a simple, rapid and selective strategy for the detection of AA in various samples. Methods: The molecularly imprinted poly(o-phenylenediamine) (PoPD) film was prepared for the analysis of L-ascorbic acid (AA) on gold nanoparticles (AuNPs) - multiwalled carbon nanotubes (MWCNTs) modified glass carbon electrode (GCE) by electropolymerization of o-phenylenediamine (oPD) and AA. Experimental parameters including pH value of running buffer and scan rates were optimized. Scanning electron microscope (SEM), fourier-transform infrared (FTIR) spectra, cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were utilized for the characterization of the imprinted polymer film. Results: Under the selected experimental conditions, the DPV peak currents of AA exhibit two distinct linear responses ranging from 0.01 to 2 μmol L-1 and 2 to 100 μmol L-1 towards the concentrations of AA, and the detection limit was 2 nmol L-1 (S/N=3). Conclusion: The proposed electrochemical sensor possesses excellent selectivity for AA, along with good reproducibility and stability. The results obtained from the analysis of AA in real samples demonstrated the applicability of the proposed sensor to practical analysis.


2010 ◽  
Vol 43 (18) ◽  
pp. 2809-2822 ◽  
Author(s):  
T. G. Satheesh Babu ◽  
P. V. Suneesh ◽  
T. Ramachandran ◽  
Bipin Nair

2015 ◽  
Vol 1115 ◽  
pp. 386-389
Author(s):  
Haroon Haiza ◽  
I.I. Yaacob ◽  
Ahmad Zahirani Ahmad Azhar

Colloidal gold nanoparticles have been successfully prepared using a simple two-electrode cells connected to a DC power supply. During the electro-dissolution-reduction process, the bulk gold at the anode oxidized into gold cations which then reacted with the chloride ions to form aurochloride complex. The complex ions were then reduced by the citrate ion to form colloidal gold nanoparticles. The size and shape of the nanoparticles were modulated by varying the terminal voltages. The colloidal gold nanoparticles obtained were characterized by field-emission scanning electron microscope (FESEM), transmission electron microscope (TEM) and ultraviolet-visible spectrophotometer (UV-Vis). From FESEM analysis, it was found that by increasing the voltage, the size of colloidal gold nanoparticles produced marginally decreased. The mean sizes of gold nanoparticles were roughly about 23.5 nm, 23.2 nm and 19.3 nm for 32 V, 36 V and 40 V, respectively. TEM micrograph showed that the shape of gold nanoparticles obtained is almost spherical. The characteristic peaks of UV-Vis spectra revealed that the suspension was indeed colloidal gold nanoparticles. Keywords: Gold, Nanoparticles, Electro-dissolution-reduction


1998 ◽  
Vol 76 (11) ◽  
pp. 1707-1716 ◽  
Author(s):  
I Coulthard ◽  
S Degen ◽  
Y -J Zhu ◽  
T K Sham

Utilizing porous silicon as a reducing agent and a substrate, gold complex ions [AuCl4]- were reduced from aqueous solution to produce nanoparticles of gold upon the surface of porous silicon. Scanning electron microscopy (SEM) was utilized to study the morphology of the porous silicon layers and the deposits of gold nanoparticles. It is found that preparation conditions have a profound effect on the morphology of the deposits, especially on porous silicon prepared from a p-type wafer. The gold nanoparticles, varying from micrometric aggregates of clusters of the order of 10 nm, to a distribution of nearly spherical clusters of the order of 10 nm, to strings of ~10 nm were observed and compared to bulk gold metal using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and X-ray absorption spectroscopy (XAS). These techniques confirm and complement the SEM findings. The potential for this reductive deposition technique is noted.Key words: gold nanostructures, reductive deposition, porous silicon, morphology, X-ray spectroscopy.


Talanta ◽  
2017 ◽  
Vol 174 ◽  
pp. 733-737 ◽  
Author(s):  
M. Asunción Alonso-Lomillo ◽  
Olga Domínguez-Renedo ◽  
Abraham Saldaña-Botín ◽  
M. Julia Arcos-Martínez

Author(s):  
Humaira Razzaq ◽  
Farhat Saira ◽  
Azra Yaqub ◽  
Rumana Qureshi ◽  
Misbah Mumtaz ◽  
...  

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