scholarly journals Microwave-assisted Synthesis of Hexagonal Gold Nanoparticles Reduced by Organosilane (3-Mercaptopropyl)trimethoxysilane

Materials ◽  
2019 ◽  
Vol 12 (10) ◽  
pp. 1680 ◽  
Author(s):  
Kwok Wei Shah ◽  
Long Zheng
Keyword(s):  
Electron Microscopy ◽  
Gold Nanoparticles ◽  
Microwave Irradiation ◽  
Irradiation Time ◽  
Chemical Reduction ◽  
Microwave Assisted Synthesis ◽  
Au Nps ◽  
One Step ◽  
The Impact ◽  
First Time

A novel synthesis of hexagonal gold nanoparticles (Au NPs) via hydrolyzed organosilane (3-mercaptopropyl)trimethoxysilane (MPTMS) using an ultrafast and environmentally friendly method is presented in this study. For the first time, organosilane MPTMS is used for chemical reduction of auric acid under ultrafast microwave irradiation. To the best of our knowledge, the use of organosilane for the synthesis of Au NPs has not been reported. The entire one-step process is convenient, rapid and cost-effective, as well as eco-friendly under alcohol-free aqueous media. Different characterization methods were carried out to investigate the properties of synthesized gold nanoparticles. transmission electron microscopy and scanning electron microscopy were used to investigate the morphology of as-synthesized Au NPs, while X-ray powder diffraction was applied to obtain the crystalline nature. Nuclear magnetic resonance was used to track the hydrolysis of organosilane MPTMS, which is employed for the first time as a reducing agent for the synthesis of Au NPs. The impact from microwave irradiation time and power, as well as the catalytic property of as-synthesized Au NPs, was investigated via ultraviolet–visible spectroscopy. The as-synthesized products include gold nanohexagon and two-dimensional hexagonal gold nanoplatelets, both of which are single-crystal with (1 1 1) planes as basal surfaces. From UV-vis spectra, it is found that the facile water-based fabrication of hexagonal Au NPs began within seconds of microwave irradiation and the size growth increased with the microwave power and time. Moreover, the efficient reduction of 4-nitrophenol to 4-aminophenol in the presence of as-synthesized Au NPs was observed, exhibiting a remarkable catalytic activity. The present simple, rapid and convenient one-step microwave process possess high scalability and useful for future applications such as catalysis, medical, biological, plasmonic sensors and electronics.

scholarly journals Effects of Different Surfactant Charges on the Formation of Gold Nanoparticles by the LASiS Method

Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 2937
Author(s):  
Muhammad Zulfajri ◽  
Wei-Jie Huang ◽  
Genin-Gary Huang ◽  
Hui-Fen Chen
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Gold Nanoparticles ◽  
Laser System ◽  
Synthesis Process ◽  
Au Nps ◽  
Laser Fluences ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
532 Nm

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.

Microwave-Irradiated Preparation of Super Absorbent Resin by Graft Copolymerization of Starch and Acrylic Acid

2011 ◽  
Vol 291-294 ◽  
pp. 1335-1338
Author(s):  
Da Biao Zhao
Keyword(s):  
Acrylic Acid ◽  
Microwave Irradiation ◽  
Graft Copolymerization ◽  
Irradiation Time ◽  
Low Cost ◽  
Power Level ◽  
Conventional Heating ◽  
Simple Process ◽  
One Step ◽  
Microwave Power Level

Graft copolymerization of acrylic acid(AA) on starch to prepare super absorbent resin (SAR) under microwave irradiation were investigated using N,N-methylene bis-acrylamide as crosslinker and potassium persulfate as initiator. The influences of the amount of initiator and crosslinker, neutralization degree of acrylic acid(AA), ratio of starch to AA, microwave power level and irradiation time on the distilled water absorption amount of resin were investigated. The results indicated that it only needed 4min under the microwave level of 231W to obtain the resin with the maximum absorption amount of 1110g×g-1, under the conditions that 0.3wt% initiator, 0.02wt% crosslinker, 60% neutralization degree of acrylic acid, the ratio of starch to acrylic acid of 0.25. Under microwave irradiation, the synthesis and drying of super absorbent resin could be completed at one step without nitrogen. Compared to conventional heating method, the methods had the striking advantages of short reaction time, simple process and low cost.

scholarly journals Electrophoretic deposition of Au NPs on CNT networks for sensitive NO<sub>2</sub> detection

2014 ◽  
Vol 3 (2) ◽  
pp. 245-252 ◽  
Author(s):  
E. Dilonardo ◽  
M. Penza ◽  
M. Alvisi ◽  
C. Di Franco ◽  
D. Suriano ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Gas Sensing ◽  
Spectroscopic Characterization ◽  
Core Diameter ◽  
Au Nps ◽  
Transmission Electron ◽  
P Type ◽  
Reducing Gases ◽  
The Impact

Abstract. In the present study, Au-surfactant core-shell colloidal nanoparticles (NPs) with controlled dimension and composition were synthesized by sacrificial anode electrolysis. Transmission electron microscopy (TEM) revealed that Au NPs core diameter is between 8 and 12 nm, as a function of the electrosynthesis conditions. Moreover, surface spectroscopic characterization by X-ray photoelectron spectroscopy (XPS) analysis confirmed the presence of nanosized gold phase. Controlled amounts of Au NPs were then deposited electrophoretically on carbon nanotube (CNT) networked films. The resulting hybrid materials were morphologically and chemically characterized using TEM, SEM (scanning electron microscopy) and XPS analyses, which revealed the presence of nanoscale gold, and its successful deposition on CNTs. Au NP/CNT networked films were tested as active layers in a two-pole resistive NO2 sensor for sub-ppm detection in the temperature range of 100–200 °C. Au NP/CNT exhibited a p-type response with a decrease in the electrical resistance upon exposure to oxidizing NO2 gas and an increase in resistance upon exposure to reducing gases (e.g. NH3). It was also demonstrated that the sensitivity of the Au NP/CNT-based sensors depends on Au loading; therefore, the impact of the Au loading on gas sensing performance was investigated as a function of the working temperature, gas concentration and interfering gases.

scholarly journals Ionic Liquids-Containing Silica Microcapsules: A Potential Tunable Platform for Shaping-Up Epoxy-Based Composite Materials?

Nanomaterials ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 881
Author(s):  
Ting Shi ◽  
Sébastien Livi ◽  
Jannick Duchet ◽  
Jean-François Gérard
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Diameter Distribution ◽  
Excellent Thermal Stability ◽  
Transmission Electron ◽  
Micron Size ◽  
Phosphonium Ionic Liquid ◽  
One Step ◽  
The One ◽  
First Time

In this work, silica microcapsules containing phosphonium ionic liquid (IL), denoted SiO2@IL, were successfully synthesized for the first time using the one step sol-gel method in IL/H20 emulsion. The morphologies of the obtained micron-size microcapsules, including their diameter distribution, were characterized using dynamic light scattering (DLS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The thermal behavior of these microcapsules and the mass fraction of the encapsulated IL in the silica microcapsules were determined using thermogravimetric analysis, showing an excellent thermal stability (up to 220 °C) and highlighting that an amount of 20 wt.% of IL is contained in the silica microcapsules. In a second step, SiO2@IL microcapsules (1 wt.%) were dispersed into epoxy-amine networks to provide proof of concept of the ability of such microcapsules to act as healing agents as microcracks propagate into the epoxy networks.

scholarly journals A Sustainable Approach to the Low-Cost Recycling of Waste Glass Fibres Composites towards Circular Economy

2020 ◽  
Vol 12 (2) ◽  
pp. 641 ◽  
Author(s):  
Omid Zabihi ◽  
Mojtaba Ahmadi ◽  
Chao Liu ◽  
Roya Mahmoodi ◽  
Quanxiang Li ◽  
...  
Keyword(s):  
Microwave Irradiation ◽  
End Of Life ◽  
Epoxy Polymer ◽  
Irradiation Time ◽  
Low Cost ◽  
Chemical Oxidation ◽  
Reinforced Polymers ◽  
Practical Applications ◽  
Low Energy Consumption ◽  
One Step

For practical applications, both environmental and economic aspects are highly required to consider in the development of recycling of fibre reinforced polymers (FRPs) encountering their end-of-life. Here, a sustainable, low cost, and efficient approach for the recycling of the glass fibre (GF) from GF reinforced epoxy polymer (GFRP) waste is introduced, based on a microwave-assisted chemical oxidation method. It was found that in a one-step process using microwave irradiation, a mixture of hydrogen peroxide (H2O2) as a green oxidiser and tartaric acid (TA) as a natural organic acid could be used to decompose the epoxy matrix of a waste GFRP up to 90% yield. The recycled GFs with ~92.7% tensile strength, ~99.0% Young’s modulus, and ~96.2% strain-to-failure retentions were obtained when compared to virgin GFs (VGFs). This short microwave irradiation time using these green and sustainable recycling solvents makes this a significantly low energy consumption approach for the recycling of end-of-life GFRPs.

scholarly journals Surface-Modified Titanium Dioxide Nanofibers with Gold Nanoparticles for Enhanced Photoelectrochemical Water Splitting

Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 261 ◽  
Author(s):  
Van Nghia Nguyen ◽  
Minh Vuong Nguyen ◽  
Thi Hong Trang Nguyen ◽  
Minh Thuy Doan ◽  
Loan Le Thi Ngoc ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Gold Nanoparticles ◽  
Titanium Dioxide ◽  
Water Splitting ◽  
Xenon Lamp ◽  
Hydrogen Energy ◽  
Au Nps ◽  
X Ray ◽  
Tio2 Nanofiber ◽  
Surface Modified

High-stability, high-efficiency, and low-cost solar photoelectrochemical (PEC) water splitting has great potential for hydrogen-energy applications. Here, we report on gold/titanium dioxide (Au/TiO2) nanofiber structures grown directly on a conductive indium tin oxide substrate, and used as photoelectrodes in PEC cells for hydrogen generation. The titanium dioxide nanofibers (TiO2 NFs) are synthesized using electrospinning, and are surface-modified by the deposition of gold nanoparticles (Au NPs) using a simple photoreduction method. The structure and morphology of the materials were characterized by field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The surface plasmon resonance (SPR) of the Au NPs was investigated by ultraviolet-visible (UV-Vis) diffuse reflectance spectroscopy. The PEC properties of the as-prepared photoelectrodes were measured. The obtained photoconversion efficiency of 0.52% under simulated-sunlight illumination by a 150 W xenon lamp of the Au/TiO2 NFs structure with 15 min UV irradiation for Au NP deposition was the highest value from comparable structures. Working photoelectrode stability was tested, and the mechanism of the enhanced PEC performance is discussed.

Preparation of Cellulose Acetate Ultra-Fine Fibers Containing Quasi-Spherical Gold Nanoparticles by Electrospinning Method

2011 ◽  
Vol 391-392 ◽  
pp. 400-403
Author(s):  
Dong Mei Zhao ◽  
Li Guo Sun ◽  
Li Li Lv ◽  
Jian Li
Keyword(s):  
Electron Microscopy ◽  
Gold Nanoparticles ◽  
Cellulose Acetate ◽  
Trisodium Citrate ◽  
X Ray Diffraction ◽  
Au Nps ◽  
Transmission Electron ◽  
Electrospinning Method ◽  
Before And After ◽  
Spherical Gold Nanoparticles

Quasi-spherical gold nanoparticles(Au NPs) prepared by trisodium citrate reduction of HAuCl4were dispersed into cellulose acetate(CA) ultra-fine fibers by electrospinning. The optical properties of Au NPs before and after electrospinning were measured by UV-vis spectrometer. The morphology and distribution of Au NPs in CA ultra-fine fibers were observed by transmission electron microscopy (TEM). The morphology and diameter of Au NPs/CA fibers were studied by scanning electron microscopy (SEM). The crystallinity change of CA fiber before and after adding Au NPs was characterized by X-ray diffraction (XRD).

2,3,4-Trihydroxy benzophenone as a novel reducing agent for one-step synthesis of size-optimized gold nanoparticles and their application in colorimetric sensing of adenine at nanomolar concentration

RSC Advances ◽  
2016 ◽  
Vol 6 (14) ◽  
pp. 11099-11108 ◽  
Author(s):  
Karuna A. Rawat ◽  
Suresh Kumar Kailasa
Keyword(s):  
Gold Nanoparticles ◽  
Reducing Agent ◽  
Colorimetric Sensing ◽  
Au Nps ◽  
Stabilizing Agent ◽  
Nanomolar Concentration ◽  
One Step

2,3,4-trihydroxy benzophenone acts as a novel reducing and stabilizing agent for one-step synthesis of size-optimized Au NPs and used as a probe for colorimetric sensing of adenine.

Microwave-Assisted Synthesis of Unmodified Gold Nanoparticles for Colorimetric Detection of Dopamine

2017 ◽  
Vol 730 ◽  
pp. 167-171 ◽  
Author(s):  
Ekarat Detsri ◽  
Kanrayasiri Kamhom ◽  
Chatsuda Detsri
Keyword(s):  
Gold Nanoparticles ◽  
Sodium Citrate ◽  
Limit Of Detection ◽  
Signal To Noise Ratio ◽  
Chemical Reduction ◽  
Colorimetric Detection ◽  
Random Coil ◽  
Microwave Assisted Synthesis ◽  
Microwave Assisted ◽  
Transmission Electron

Unmodified gold nanoparticles (AuNPs) have been successfully synthesized by the chemical reduction of tetrachloride gold (III) ions ([AuCl4]-) in the presence of sodium citrate based on the rapid microwave−assisted approach. The diameter of the synthesized nanoparticles was found in the range of 16.50±2.75 nm. The AuNPs were characterized using UV−vis spectrophotometer, zeta potential analyzer and transmission electron microscope (TEM). The sodium citrate protected AuNPs were found to be selective and sensitive for the detection of dopamine. It was based on the aggregation change of the nanoparticles from random coil to hairpin structure upon the addition of dopamine concentration. The red shift of the plasmonic peak wavelength of AuNPs could be used for the detection of dopamine. The response to dopamine allows for a linear range from 10 to 125 mg⋅L-1 (R2 = 0.9804) with a limit of detection (LOD) at a signal to noise ratio of 3 of 12.85±1.38 mg⋅L-1. The colorimetric sensor was evaluated with 98.0−99.9% recovery of added dopamine in urine sample. The proposed sensor was successfully applied to the determination of dopamine in biological samples.

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