One-Step Microwave-Assisted Aqueous Synthesis of Silver-Based Nanoparticles Functionalized by Glutathione

2014 ◽  
Vol 1675 ◽  
pp. 163-168
Author(s):  
Myrna Reyes Blas ◽  
Maricely Ramírez-Hernandez ◽  
Danielle Rentas ◽  
Oscar Perales-Perez ◽  
Felix R. Román

ABSTRACTThe use of nano-sized silver and its alloys represents an interesting alternative to common food preservation methods, which are based on radiation, heat treatment and low temperature storage. These metal nanoparticles, embedded within a polymeric matrix for instance, would extend the shelf life of perishable foods while acting as a bactericidal agent to prevent food-borne illnesses. Common methods used in the synthesis of metal nanoparticles require toxic solvents and reagents that could be harmful to health and the food itself. In addition, several steps are required to obtain aqueous stable, i.e. dispersible, silver nanoparticles. In this work we propose the microwave-assisted aqueous synthesis of silver-based nanoparticles, (Ag Based NP) functionalized by glutathione (GSH) in a single-step using sodium sulfite (Na2SO3), as reducing agent. Ag-Based nanoparticles were synthesized at pH 6 and 1:3:1 (AgNO3/GSH/ Na2SO3) molar ratio. UV-Vis measurement clearly showed the plasmon peak attributed to silver-based nanoparticles (374 nm). Highly monodispersed water stable Ag-based nanoparticles were observed and 3.897 ± 0.167 nm particle size was determined through Transmission Electron Microscopy. FT-IR measurements suggested the actual GSH-Ag based surface interaction through –SH and –COOH groups; the functionalization by GSH explained the high stability of the nanoparticles in aqueous suspensions. These Ag-GSH nanoparticles exhibited remarkable antimicrobial activity against E. Coli.

2006 ◽  
Vol 61 (12) ◽  
pp. 1566-1572 ◽  
Author(s):  
Dongsheng Li ◽  
Sridhar Komarneni

Platinum nanoparticles and nanorods were synthesized by microwave-assisted solvothermal techniques. Changing the reaction conditions controlled particle size and morphology. The effects of the reaction conditions, such as the molar ratio of the polyvinylpyrrolidone (PVP) repeating unit to the metal sources, the concentration of metal sources, the reaction temperature, and the presence of distilled water were investigated. Nanoparticles of Pt were approximately 3 nm in size. Produced nanoparticles and nanorods were characterized by transmission electron microscopy. Image JTM software was used to calculate the particle size and size distribution.


2021 ◽  
Vol 11 (19) ◽  
pp. 8949
Author(s):  
Vittorio Scardaci ◽  
Marcello Condorelli ◽  
Matteo Barcellona ◽  
Luca Salemi ◽  
Mario Pulvirenti ◽  
...  

The shape control of metal nanoparticles, along with the size, is critical for most of their applications as they control their optical properties. Anisotropic metal nanoparticles show superior performance in a number of applications compared to spherical ones. Shape control is usually achieved by a two-step process, where the first involves the formation of spherical nanoparticles and the second is about the actual shape transformation. In this paper, we report on a fast and facile synthesis of silver nanoplates in a single step, involving laser ablation of a silver target in a liquid medium while this is exposed to light irradiation and hydrogen peroxide flow. We obtained anisotropic particles with a mixture of shapes, of 70–80 nm in size and 10–20 nm in thickness, which showed a plasmon sensitivity greater than 200 nm/RIU.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Diego Alberto Lomelí-Rosales ◽  
Adalberto Zamudio-Ojeda ◽  
Sara Angélica Cortes-Llamas ◽  
Gilberto Velázquez-Juárez

AbstractNowadays, there are several approaches reported to accomplish the green synthesis of metal nanoparticles by using bacterial and fungi supernatants or by-products generated by these microorganisms. Therefore, agars as solely reductive regents have started to be used in order to obtain metal nanoparticles. This paper shows the results of the synthesis of gold and silver nanoparticles with different morphology, mainly triangular and truncated triangular, using Eosin Methylene Blue (EMB) agar as reducing agent. To control the reaction process, the necessary activation energy for the reducer was provided by three different techniques: microwave radiation, using a domestic microwave oven, ultraviolet radiation, and heating on a conventional plate. The evolution of the reduction process and stability of the samples was performed by ultraviolet visible spectroscopy. Morphology was carefully analyzed using high-resolution transmission electron microscopy (HRTEM) and Transmission electron microscopy (TEM). A one step synthesis for gold and silver nanoparticles was optimized with an eco-friendly and economic process.


2011 ◽  
Vol 239-242 ◽  
pp. 1643-1648 ◽  
Author(s):  
Qin Tang ◽  
Xiang Yong Chen ◽  
Wei Bing Hu ◽  
Gui Yun Zhou

Calcium carbonate was obtained by the microwave-assisted hydrothermal synthesized technique using calcium chloride and urea as the raw materials. The uniform aragonite hexagonal columnar-shaped calcium carbonate with a diameter of 3.0~4.0μm and 70~120μm in length were produced without any additives at the molar ratio of urea and calcium chloride 1.5:1, microwave power 600W. The morphology, size and crystal structure were characterized by means of scanning electron microscope (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FT-IR).The formation process of aragonite hexagonal columnar-shaped calcium carbonate was discussed.


2013 ◽  
Vol 457-458 ◽  
pp. 270-275
Author(s):  
Guang Jian Xing ◽  
Yi Wang ◽  
Chun Na Yu ◽  
Chang Zhao ◽  
Guang Ming Wu

Well-crystallized SrWO4 mesocrystals with different shapes including flower-like sphere, bundle, peanut, dumbbell, and notched sphere were controllably synthesized via a simple microwave-assisted precipitation method. X-ray powder diffraction (XRD), field-emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), and photoluminescence (PL) measurements were used to characterize these mesocrystals. XRD patterns indicate that the SrWO4 mesocrystals present a scheelite-type tetragonal structure. FESEM and HRTEM micrographs showed different shapes for the SrWO4 mesocrystals. The molar ratio of [WO42-] to [Sr2+] was found to play an important role in the morphological controlling of the resulting SrWO4 mesocrystals. With the increase of the molar ratio, the shape of the SrWO4 mesocrystals changed from flower-like sphere assembled with nanorods to notched sphere with intermediate peanut and dumbbell shapes. PL spectra measurements showed that the luminescence properties of the SrWO4 mesocrystals strongly relied on its shapes.


Author(s):  
R.P. Goehner ◽  
W.T. Hatfield ◽  
Prakash Rao

Computer programs are now available in various laboratories for the indexing and simulation of transmission electron diffraction patterns. Although these programs address themselves to the solution of various aspects of the indexing and simulation process, the ultimate goal is to perform real time diffraction pattern analysis directly off of the imaging screen of the transmission electron microscope. The program to be described in this paper represents one step prior to real time analysis. It involves the combination of two programs, described in an earlier paper(l), into a single program for use on an interactive basis with a minicomputer. In our case, the minicomputer is an INTERDATA 70 equipped with a Tektronix 4010-1 graphical display terminal and hard copy unit.A simplified flow diagram of the combined program, written in Fortran IV, is shown in Figure 1. It consists of two programs INDEX and TEDP which index and simulate electron diffraction patterns respectively. The user has the option of choosing either the indexing or simulating aspects of the combined program.


Author(s):  
H. J. Bender ◽  
R. A. Donaton

Abstract The characteristics of an organic low-k dielectric during investigation by focused ion beam (FIB) are discussed for the different FIB application modes: cross-section imaging, specimen preparation for transmission electron microscopy, and via milling for device modification. It is shown that the material is more stable under the ion beam than under the electron beam in the scanning electron microscope (SEM) or in the transmission electron microscope (TEM). The milling of the material by H2O vapor assistance is strongly enhanced. Also by applying XeF2 etching an enhanced milling rate can be obtained so that both the polymer layer and the intermediate oxides can be etched in a single step.


Materials ◽  
2020 ◽  
Vol 13 (21) ◽  
pp. 4715
Author(s):  
Adam Kubiak ◽  
Marta Kubacka ◽  
Elżbieta Gabała ◽  
Anna Dobrowolska ◽  
Karol Synoradzki ◽  
...  

The TiO2-Fe3O4 composite materials were fabricated via the hydrothermal-assisted technique. It was determined how the molar ratio of TiO2 to Fe3O4 influences the crystalline structure and morphology of the synthesized composite materials. The effect of the molar ratio of components on the antibacterial activity was also analyzed. On the basis of XRD patterns for the obtained titanium(IV) oxide-iron(II, III) oxide composites, the two separate crystalline forms—anatase and magnetite —were observed. Transmission electron microscopy revealed particles of cubic and tetragonal shape for TiO2 and spherical for Fe3O4. The results of low-temperature nitrogen sorption analysis indicated that an increase in the iron(II, III) oxide content leads to a decrease in the BET surface area. Moreover, the superparamagnetic properties of titanium(IV) oxide-iron(II, III) oxide composites should be noted. An important aim of the work was to determine the antibacterial activity of selected TiO2-Fe3O4 materials. For this purpose, two representative strains of bacteria, the Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus, were used. The titanium(IV) oxide-iron(II, III) oxide composites demonstrated a large zone of growth inhibition for both Gram-positive and Gram-negative bacteria. Moreover, it was found that the analyzed materials can be reused as antibacterial agents in three consecutive cycles with good results.


Synthesis ◽  
2021 ◽  
Author(s):  
Sambasivarao Kotha ◽  
Sunil Pulletikurti ◽  
Ambareen Fatma ◽  
gopal dhangar ◽  
gonna somu Naidu

Here, we have demonstrated that the presence of a carbonyl group at C7 position is preventing the olefin metathesis of endo-norbornene derivatives due to the complexation of the metal alkylidene. Time-dependent NMR studies showed the presence of new proton signals in the metal alkylidene region, which indicate the formation of metal complex with the carbonyl group of the substrate. These observations were further proved by ESI-MS analysis. Whereas, computational studies provided that the catalyst was interacting with the C7 carbonyl group and aligned perpendicular to that of norbornene olefin. Later, these endo-keto norbornene derivatives were reduced to hydroxyl derivatives diastereoselectively. Ring-rearrangement metathesis (RRM) of these hydroxyl derivatives, produced the [6/5/6], and [5/6/5] carbo-tricyclic cores of the natural products in one step. Whereas the RRM of O-allyl derivatives, delivered the oxa-tricyclic compounds in a single step with excellent yields.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shella Permatasari Santoso ◽  
Vania Bundjaja ◽  
Artik Elisa Angkawijaya ◽  
Chintya Gunarto ◽  
Alchris Woo Go ◽  
...  

AbstractNitrogen-grafting through the addition of glycine (Gly) was performed on a metal- phenolic network (MPN) of copper (Cu2+) and gallic acid (GA) to increase its adsorption capacity. Herein, we reported a one-step synthesis method of MPN, which was developed according to the metal–ligand complexation principle. The nitrogen grafted CuGA (Ng-CuGA) MPN was obtained by reacting Cu2+, GA, and Gly in an aqueous solution at a molar ratio of 1:1:1 and a pH of 8. Several physicochemical measurements, such as Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), N2 sorption, X-ray diffraction (XRD), and thermal gravimetry analysis (TGA), were done on Ng-CuGA to elucidate its characteristics. The analysis revealed that the Ng-CuGA has non-uniform spherical shaped morphology with a pore volume of 0.56 cc/g, a pore size of 23.25 nm, and thermal stability up to 205 °C. The applicational potential of the Ng-CuGA was determined based on its adsorption capacity against methylene blue (MB). The Ng-CuGA was able to adsorb 190.81 mg MB per g adsorbent at a pH of 6 and temperature of 30 °C, which is 1.53 times higher than the non-grafted CuGA. Detailed assessment of Ng-CuGA adsorption properties revealed their pH- and temperature-dependent nature. The adsorption capacity and affinity were found to decrease at a higher temperature, demonstrating the exothermic adsorption behavior.


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