scholarly journals Rapid and Green Preparation of Multi-Branched Gold Nanoparticles Using Surfactant-Free, Combined Ultrasound-Assisted Method

Processes ◽  
2021 ◽  
Vol 9 (1) ◽  
pp. 112
Author(s):  
Phat Trong Huynh ◽  
Giang Dang Nguyen ◽  
Khanh Thi Le Tran ◽  
Thu Minh Ho ◽  
Vinh Quang Lam ◽  
...  

The conventional seed-mediated preparation of multi-branched gold nanoparticles uses either cetyltrimethylammonium bromide or sodium dodecyl sulfate. However, both surfactants are toxic to cells so they have to be removed before the multi-branched gold nanoparticles can be used in biomedical applications. This study describes a green and facile method for the preparation of multi-branched gold nanoparticles using hydroquinone as a reducing agent and chitosan as a stabilizer, through ultrasound irradiation to improve the multi-branched shape and stability. The influence of pH, mass concentration of chitosan, hydroquinone concentration, as well as sonication conditions such as amplitude and time of US on the growth of multi-branched gold nanoparticles, were also investigated. The spectra showed a broad band from 500 to over 1100 nm, an indication of the effects of both aggregation and contribution of multi-branches to the surface plasmon resonance signal. Transmission electron microscopy measurements of GNS under optimum conditions showed an average core diameter of 64.85 ± 6.79 nm and 76.11 ± 14.23 nm of the branches of multi-branched particles. Fourier Transfer Infrared Spectroscopy was employed to characterize the interaction between colloidal gold nanoparticles and chitosan, and the results showed the presence of the latter on the surface of the GNS. The cytotoxicity of chitosan capped GNS was tested on normal rat fibroblast NIH/3T3 and normal human fibroblast BJ-5ta using MTT assay concentrations from 50–125 µg/mL, with no adverse effect on cell viability.

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Abhishek Das ◽  
Ridhima Chadha ◽  
Nandita Maiti ◽  
Sudhir Kapoor

The stability of gold nanoparticles is a major issue which decides their impending usage in nanobiotechnological applications. Often biomimetically synthesized nanoparticles are deemed useless owing to their instability in aqueous medium. So, surfactants are used to stabilize the nanoparticles. But does the surfactant only stabilize by being adsorbed to the surface of the nanoparticles and not play significantly in moulding the size and shape of the nanoparticles? Keeping this idea in mind, gold nanoparticles (GNPs) synthesized by l-tryptophan (Trp) mediated reduction of chloroauric acid (HAuCl4) were stabilized by anionic surfactant, sodium dodecyl sulphate (SDS), and its effect on the moulding of size and properties of the GNPs was studied. Interestingly, unlike most of the gold nanoparticles synthesis mechanism showing saturation growth mechanism, inclusion of SDS in the reaction mixture for GNPs synthesis resulted in a bimodal mechanism which was studied by UV-Vis spectroscopy. The mechanism was further substantiated with transmission electron microscopy. Zeta potential of GNPs solutions was measured to corroborate stability observations recorded visually.


Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 118
Author(s):  
Qui Quach ◽  
Erik Biehler ◽  
Ahmed Elzamzami ◽  
Clay Huff ◽  
Julia M. Long ◽  
...  

The current climate crisis warrants investigation into alternative fuel sources. The hydrolysis reaction of an aqueous hydride precursor, and the subsequent production of hydrogen gas, prove to be a viable option. A network of beta-cyclodextrin capped gold nanoparticles (BCD-AuNP) was synthesized and subsequently characterized by Powder X-Ray Diffraction (P-XRD), Fourier Transform Infrared (FTIR), Transmission Electron Microscopy (TEM), and Ultraviolet-Visible Spectroscopy (UV-VIS) to confirm the presence of gold nanoparticles as well as their size of approximately 8 nm. The catalytic activity of the nanoparticles was tested in the hydrolysis reaction of sodium borohydride. The gold catalyst performed best at 303 K producing 1.377 mL min−1 mLcat−1 of hydrogen. The activation energy of the catalyst was calculated to be 54.7 kJ/mol. The catalyst resisted degradation in reusability trials, continuing to produce hydrogen gas in up to five trials.


Nanomaterials ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 132
Author(s):  
Jumoke A. Aboyewa ◽  
Nicole R. S. Sibuyi ◽  
Mervin Meyer ◽  
Oluwafemi O. Oguntibeju

Cyclopia intermedia (C. intermedia) is an indigenous South African shrub used to prepare the popular medicinal honeybush (HB) tea. This plant contains high levels of mangiferin (MGF), a xanthonoid that was reported to have numerous biological activities, including anti-tumor activity. MGF and extracts that contain high concentrations of MGF, such as extracts from Mangifera indica L. or mango have been used to synthesize gold nanoparticles (AuNPs) using green nanotechnology. It has previously been shown that when AuNPs synthesized from M. indica L. extracts are used in combination with doxorubicin (DOX) and Ayurvedic medicine, the anti-tumor effects appear to be augmented. It has also been demonstrated that MGF used in combination with DOX resulted in enhanced anti-tumor effects. In this study, C. intermedia (HB) and MGF were used to synthesize HB-AuNPs and MGF-AuNPs, respectively. The physicochemical properties of the AuNPs were characterized by the UV-Visible Spectroscopy (UV-Vis), dynamic light scattering (DLS), Fourier transform infra-red spectroscopy (FTIR), X-ray diffraction spectroscopy (XRD) and high-resolution transmission electron microscopy (HR-TEM). The cytotoxicity of HB-AuNPs and MGF-AuNPs were assessed on human colon (Caco-2), prostate (PC-3) and glioblastoma (U87) cancer cells; as well as normal breast epithelial (MCF-12A) cells using the MTT assay. Both HB-AuNPs and MGF-AuNPs demonstrated relatively low cytotoxicity in these cells. However, when these nanoparticles were used in combination with DOX, the cytotoxicity of DOX was significantly augmented.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Phitchan Sricharoen ◽  
Supalak Kongsri ◽  
Chunyapuk Kukusamude ◽  
Yonrapach Areerob ◽  
Prawit Nuengmatcha ◽  
...  

AbstractWe report a novel method for the synthesis of 3-mercaptopropyl trimethoxysilane-modified hydroxyapatite (FHAP-SH) derived from fish-scale residues by using ultrasound irradiation. Scanning electron microscopy, transmission electron microscopy, energy-dispersive spectroscopy, X-ray diffraction, and Fourier transform infrared spectroscopy were used for the FHAP-SH characterization. Then, the organic dye adsorption on the FHAP-SH was monitored through an ultrasound process. After the dye removal optimization, significant improvements were observed in the maximum adsorption capacities for Congo Red (CR, 500 mg g−1), Coomassie Brilliant Blue G 250 (CB, 235 mg g−1), and Malachite Green (MG, 625 mg g−1). The adsorption behaviors of these dyes were fitted by using the Langmuir isotherm model with a high coefficient of determination values ranging from 0.9985 to 0.9969. The adsorption of the three dyes onto FHAP-SH was an endothermic process based on the adsorption thermodynamics model, while the adsorption kinetics analysis of the dyes presented a good alignment with the pseudo-second-order kinetics. The FHAP-SH exhibits a remarkably high adsorption capacity, is inexpensive, and fulfills the ecofriendly requirements of dye wastewater treatment, especially in the textile industry.


2011 ◽  
Vol 415-417 ◽  
pp. 617-620 ◽  
Author(s):  
Yan Su ◽  
Ying Yun Lin ◽  
Yu Li Fu ◽  
Fan Qian ◽  
Xiu Pei Yang ◽  
...  

Water-soluble gold nanoparticles (AuNPs) were prepared using 2-mercapto-4-methyl-5- thiazoleacetic acid (MMTA) as a stabilizing agent and sodium borohydride (NaBH4) as a reducing agent. The AuNPs product was analyzed by transmission electron microscopy (TEM), UV-vis absorption spectroscopy and Fourier transform infrared spectroscopy (FTIR). The TEM image shows that the particles were well-dispersed and their average particle size is about 5 nm. The UV-vis absorption and FTIR spectra confirm that the MMTA-AuNPs was stabilized by the carboxylate ions present on the surface of the AuNPs.


1998 ◽  
Vol 536 ◽  
Author(s):  
S. B. Aldabergenova ◽  
M. Albrecht ◽  
A. A. Andreev ◽  
C. Inglefield ◽  
J. Viner ◽  
...  

AbstractWe report on strong Er3+ luminescence in the visible and infra-red regions at room temperature in amorphous GaN:Er thin films prepared by DC magnetron co-sputtering. The intensity of the Er3+ luminescence at 1.535 μm corresponding to 4I13/2 → 4I15/2 transitions is greatly enhanced after annealing at 750°C. In this material GaN crystallites have formed and embedded in the continuous amorphous matrix. The crystallites are 4 to 7 nm in diameter as analyzed by high resolution transmission electron microscopy. The absorption edge, extending three orders of magnitude in absorption coefficient in the spectral range from 0.5 to 3.5 eV, is superimposed on resonant absorption bands of Er3+ ions.The total photoluminescence spectrum consists of welldefined Er3+ luminescence peaks imposed on a broad band edge luminescence from the amorphous GaN host matrix.


2011 ◽  
Vol 311-313 ◽  
pp. 1044-1048
Author(s):  
Hong Long Xing ◽  
Shui Lin Chen

Polyacrylate microgel emulsion was prepared by emulsion polymerization using styrene, α-n-butyl acrylate and methyl methacrylate as monomer, polyoxyethylene octylphenol ether (TX-30) and sodium dodecyl sulfate(SDS) as combine emulsifier, divinyl benzene and ammonium persulfate (APS) as initiator,respectively. The prepared microgel was analyzed by a variety of measurment methods, such as Fourier transform infrared spectroscopy and transmission electron microscopy. The effect of microgel on the rheological properties of adhesives, leveling, mechanical properties and pigment printing performance was studied. The rhelogy and the color fastness of the pigment printing binder of printed fabrics were measured by rheometer and friction color fastness test instruments, respectively. At the same time, the mechanical properties of the adhesive film was measured by strength tester. The results show that the thixotropy, leveling and mechanical properties of adhesive printing binder and pringting quality of coating fabrics were improved when the microgel was added.


Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 347
Author(s):  
Beomjin Kim ◽  
Woo Chang Song ◽  
Sun Young Park ◽  
Geuntae Park

The green synthesis of inorganic nanoparticles (NPs) using bio-materials has attained enormous attention in recent years due to its simple, eco-friendly, low-cost and non-toxic nature. In this work, silver nanoparticles (AgNPs) and gold nanoparticles (AuNPs) were synthesized by the marine algae extract, Sargassum serratifolium (SS). The characteristic studies of bio-synthesized SS-AgNPs and SS-AuNPs were carried out by using ultraviolet–visible (UV–Vis) absorption spectroscopy, dynamic light scattering (DLS), high-resolution transmission electron microscope (HR-TEM), selected area electron diffraction (SAED), energy-dispersive X-ray spectroscopy (EDX), X-ray powder diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). Phytochemicals in the algae extract, such as meroterpenoids, acted as a capping agent for the NPs’ growth. The synthesized Ag and Au NPs were found to have important catalytic activity for the degradation of organic dyes, including methylene blue, rhodamine B and methyl orange. The reduction of dyes by SS-AgNPs and -AuNPs followed the pseudo-first order kinetics.


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.


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