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The unique properties of zinc oxide nanoparticles (ZnO-NPs) produced using plant extract make them attractive for use in medical as well as industrial applications, and it is necessary to develop environmentally friendly methods for their synthesis. This can be accomplished by replacing the traditional chemical compounds for the reduction of the zinc ions to ZnO-NPs during synthesis with natural plant extracts. Here, the biosynthesis of ZnO-NPs using Punica granatum (P. granatum) fruit peels extract was investigated as the reducing and stabilizing agent. The P. granatum /ZnO-NPs with spherical and hexagonal shapes were biosynthesized at different annealing temperatures. The X-ray diffraction analysis confirmed the synthesis of highly pure ZnO-NPs with increasing crystallinity in higher annealing temperatures. The ZnO-NPs displayed characteristic absorption peaks between 370 and 378 nm in the UV–vis spectra. Transmission electron microscopy (TEM) imaging showed the formation of mostly spherical and hexagonal-shaped ZnO-NPs in the mean size of 32.98 nm and 81.84 nm at 600 °C and 700 °C respectively. According to FTIR spectrum, strong absorption bands in the range of 462–487 cm−1 corresponding to Zn O bond stretching can be seen. Antibacterial activities of P. granatum /ZnO-NPs against Escherichia coli (E. coli) and Enterococcus faecalis (E. faecalis) were investigated and compared. Results obtained show that smaller-sized P. granatum /ZnO-NPs are more effective in inhibiting growth of both bacteria. In addition, cytotoxicity assays were performed for P. granatum /ZnO-NPs against human colon normal and cancerous cells. P. granatum /ZnO-NPs exhibited similar killing activities of both cell lines at the concentration of ≥31.25 μg/mL. The biosynthesized ZnO-NPs could offer potential applications in bio-medical field. Image 1 • ZnO nanoparticles were prepared using Punica granatum fruit peels extract by sol-gel and thermal decomposition methods. • The ZnO-NPs were characterized by XRD, UV–visible spectroscopy, TEM, FESEM, and FTIR. • P. granatum /ZnO-NPs exhibited excellent antibacterial activities against Escherichia coli and Enterococcus faecalis. [ABSTRACT FROM AUTHOR]

This paper presents a green, facile and rapid method to prepare magnetite/zeolite-nanocomposites (NCs) in one step procedure at ambient temperature. The powder X-ray diffraction (PXRD) pattern of iron oxide nanoparticles (NPs) with the sole zeolite showed the broadening of zeolite peaks attributed to the incorporation of Fe 3 O 4 . Field-emission scanning electron microscopy (FESEM) analysis depicted that the Fe 3 O 4 ‒NPs were formed on the surface of porous zeolite framework. Transmission electron microscopy (TEM) analysis displayed the Fe 3 O 4 nanoparticles (NPs) were mostly in spherical shape with a mean diameter and standard deviation of 2.40 ± 0.41 nm. The selected-area electron diffraction (SAED) pattern confirmed the presence of cubic Fe 3 O 4 phase. The vibrating sample magnetometer (VSM) results indicated the as-synthesized sample has a saturation magnetization of around 6.52 emu g −1 . The magnetite/zeolite-NCs can be considered as a low-cost alternative catalyst for oxygen reduction reaction (ORR) process. The electrochemical measurement showed that the performance of magnetite/zeolite-NCs towards the ORR increased as the scan rate increased from 20 mV s −1 to 500 mV s −1 . The ORR is a diffusion-controlled process in the alkaline medium. [ABSTRACT FROM AUTHOR]

Background This study aims to investigate the influence of different stirring time for synthesis of silver nanoparticles in glutathione (GSH) aqueous solution. The silver nanoparticles (Ag-NPs) were prepared by green synthesis method using GSH as reducing agent and stabilizer, under moderate temperature at different stirring times. Silver nitrate (AgNO3) was taken as the metal precursor while Ag-NPs were prepared in the over reaction time. Results Formation of Ag-NPs was determined by UV-vis spectroscopy where surface plasmon absorption maxima can be observed at 344-354 nm from the UV-vis spectrum. The synthesized nanoparticles were also characterized by X-ray diffraction (XRD). The peaks in the XRD pattern confirmed that the Ag-NPs possessed a face-centered cubic and peaks of contaminated crystalline phases were unable to be located. Transmission electron microscopy (TEM) revealed that Ag-NPs synthesized were in spherical shape. Zeta potential results indicate that the stability of the Ag-NPs is increases at the 72 h stirring time of reaction comparison to GSH. The Fourier transform infrared (FT-IR) spectrum suggested the complexation present between GSH and Ag-NPs. The use of green chemistry reagents, such as peptide, provides green and economic features to this work. Conclusions Ag-NPs were successfully synthesized in GSH aqueous solution under moderate temperature at different stirring times. The study clearly showed that the Ag-NPs synthesized in the long times of stirring, thus, the kinetic of GSH reaction is very slow. TEM results shows that with the increase of stirring times the mean particle size of Ag-NPs become increases. The FT-IR spectrum suggested the complexation present between GSH and Ag-NPs. These suggest that Ag-NPs can be employed as an effective bacteria inhibitor and can be applied in medical field. [ABSTRACT FROM AUTHOR]

Different biological methods are gaining recognition for the production of silver nanoparticles (Ag-NPs) due to their multiple applications. The use of plants in the green synthesis of nanoparticles emerges as a cost effective and eco-friendly approach. In this study the green biosynthesis of silver nanoparticles using Callicarpa maingayi stem bark extract has been reported. Characterizations of nanoparticles were done using different methods, which include; ultraviolet-visible spectroscopy (UV-Vis), powder X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy dispersive X-ray fluorescence (EDXF) spectrometry, zeta potential measurements and Fourier transform infrared (FT-IR) spectroscopy. UV-visible spectrum of the aqueous medium containing silver nanoparticles showed absorption peak at around 456 nm. The TEM study showed that mean diameter and standard deviation for the formation of silver nanoparticles were 12.40 ± 3.27 nm. The XRD study showed that the particles are crystalline in nature, with a face centered cubic (fcc) structure. The most needed outcome of this work will be the development of value added products from Callicarpa maingayi for biomedical and nanotechnology based industries. [ABSTRACT FROM AUTHOR]

The roles of green chemistry in nanotechnology and nanoscience fields are very significant in the synthesis of diverse nanomaterials. Herein, we report a green chemistry method for synthesized colloidal silver nanoparticles (Ag NPs) in polymeric media. The colloidal Ag NPs were synthesized in an aqueous solution using silver nitrate, polyethylene glycol (PEG), and ß-D-glucose as a silver precursor, stabilizer, and reducing agent, respectively. The properties of synthesized colloidal Ag NPs were studied at different reaction times. The ultraviolet-visible spectra were in excellent agreement with the obtained nanostructure studies performed by transmission electron microscopy (TEM) and their size distributions. The Ag NPs were characterized by utilizing X-ray diffraction (XRD), zeta potential measurements and Fourier transform infrared (FT-IR). The use of green chemistry reagents, such as glucose, provides green and economic features to this work. [ABSTRACT FROM AUTHOR]

Superparamagnetic magnetite nanocomposites (Fe 3 O 4 -NCs) were successfully synthesized, which comprised of montmorillonite (MMT) as matrix support, Kappaphycus alvarezii (SW) as bio-stabilizer and Fe 3 O 4 as filler in the composites to form MMT/SW/Fe 3 O 4 -NCs. Nanocomposite with 0.5 g Fe 3 O 4 (MMT/SW/0.5Fe 3 O 4) was selected for anticancer activity study because it revealed high crystallinity, particle size of 7.2 ± 1.7 nm with majority of spherical shape, and M s = 5.85 emu/g with negligible coercivity. Drug loading and release studies were carried out using protocatechuic acid (PCA) as the model for anticancer drug, which showed 19% and 87% of PCA release in pH 7.4 and 4.8, respectively. Monolayer anticancer assay showed that PCA-loaded MMT/SW/Fe 3 O 4 (MMT/SW/Fe 3 O 4 -PCA) had selectivity towards HCT116 (colorectal cancer cell line). Although MMT/SW/Fe 3 O 4 -PCA (0.64 mg/mL) showed higher IC 50 than PCA (0.148 mg/mL) and MMT/SW/Fe 3 O 4 (0.306 mg/mL, MMT/SW/Fe 3 O 4 -PCA showed more effective killing towards tumour spheroid model generated from HCT116. The IC 50 for MMT/SW/Fe 3 O 4 -PCA, MMT/SW/Fe 3 O 4 and PCA were 0.132, 0.23 and 0.55 mg/mL, respectively. This suggests the improved penetration efficiency and drug release of MMT/SW/Fe 3 O 4 -PCA towards HCT116 spheroids. Moreover, concentration that lower than 2 mg/mL MMT/SW/Fe 3 O 4 -PCA did not result any hemolysis in human blood, which suggests them to be ideal for intravenous injection. This study highlights the potential of MMT/SW/Fe 3 O 4 -NCs as drug delivery agent. [ABSTRACT FROM AUTHOR]

In this study, a comparative study of effect using honey on copper nanoparticles (Cu-NPs) via simple, environmentally friendly process and inexpensive route was reported. Honey and ascorbic acid act as stabilizing and reducing agents with the assistance of sonochemical method. The products were characterized using UV–visible (UV–vis) spectroscopy, X-Ray Diffraction (XRD), High-Resolution Transmission Electron Microscopy (HRTEM), Field-Emission Scanning Electron Microscopy (FESEM) and Fourier Transform Infrared (FTIR) spectroscopy. The reddish brown colour demonstrated the formation of Cu-NPs and UV–visible proved the plasmon resonance of Cu-NPs. XRD also confirmed a highly pure Cu-NPs obtained with absence of copper oxide in which the structure is crystalline. The spherical size of the Cu-NPs was acquire in the presence of honey which is 3.68 ± 0.78 nm with narrow particle distribution. The antibacterial activity was seen against gram-positive and gram-negative bacteria which are Enterococcus faecalis (E. faecalis) and Escherichia coli (E. coli). At higher concentration of Cu-NPs, they were more effective in killing both bacteria. The Cu-NPs without and with honey exhibited toxicities toward normal and cancerous cells. However, Cu-NPs without honey showed more potent killing activity against normal and cancer cells. Unlabelled Image • Honey as capping and reducing agent for Cu-NPs • Ultrasonic irradiation assistance reduced the time of reaction. • Cu-NPs show potential antibacterial against gram positive and negative bacteria. • Cytotoxic of Cu-NPs toward CCD 112 and HCT 116 are reported in this study. [ABSTRACT FROM AUTHOR]

In this research, gold nanoparticles (Au-NPs) are biosynthesized from tetrachloroaurate (AuCl4−) aqueous solution through a simple and ecofriendly route using water extract of black Camellia sinensis leaf (C. sinensis L.) which acted as a reductant and stabilizer simultaneously. The prepared gold nanoparticles are characterized using UV-visible spectroscopy, X-ray diffraction (XRD), and transmission electron microscopy (TEM). Also, determination of the accurate predictor model for chemical reactions is particularly important because of high cost of the chemical materials and measurement devices. While the artificial neural networks (ANNs) are one of the appropriate tools to forecast any phenomena, due to the low number of data set related to chemical experimental was caused to provide appropriate model is a time-consuming iterative process. With the aim to improve the accuracy of the ANN model and overcome the local convergence of this problem, a global search technique, biogeography-based optimization (BBO) method which integrated by chaotic map is employed. The improved model showed minimum mean squared error (MSE) of 0.0134 and maximum coefficient of determination (R2) equal to 0.9822 compared with several other famous ANN training algorithm, utilizing output experimental data obtained from biosynthesis proceeding. [ABSTRACT FROM AUTHOR]

Background: Green approach in synthesizing metal nanoparticles has gain new interest from the researchers as metal nanoparticles were widely applied in medical equipment and household products. The use of plants in the synthesis of nanoparticles emerges as a cost effective and eco-friendly approach. A green synthetic route for the production of stable silver nanoparticles (Ag-NPs) by using aqueous silver nitrate as metal precursor and Artocarpus elasticus stem bark extract act both as reductant and stabilizer is being reported for the first time. Results: The resultant Ag-NPs were characterized by UV-vis spectroscopy, powder X-Ray diffraction, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and Fourier-transform infra-red (FT-IR). The morphological study by TEM and SEM shows resultant Ag-NPs in spherical form with an average size of 5.81 ± 3.80, 6.95 ± 5.50, 12.39 ± 9.51, and 19.74 ± 9.70 nm at 3, 6, 24, and 48 h. Powder X-ray diffraction showed that the particles are crystalline in nature, with a face-centered cubic structure. The FT-IR spectrum shows prominent peaks appeared corresponds to different functional groups involved in synthesizing Ag-NPs. Conclusions: Ag-NPs were synthesized using a simple and biosynthetic method by using methanolic extract of A. elasticus under room temperature, at different reaction time. The diameters of the biosynthesis Ag-NPs depended on the time of reaction. Thus, with the increase of reaction time in the room temperature the size of Ag-NPs increases. From the results obtained in this effort, one can affirm that A. elasticus can play an important role in the bioreduction and stabilization of silver ions to Ag-NPs. [ABSTRACT FROM AUTHOR]

The goal of this study was to prepare nanocomposites of rice straw coated with different percentages of Fe3O4 nanoparticles (Fe3O4-NPs) [1.0, 5.0, 10.0, and 20.0 wt. %]. In this process, the size of Fe3O4-NPs changed with varying volumes of NaOH (2M). The Fe3O4-NPs were precipitated with sodium hydroxide from a solution of Fe(II) and (III) chloride in water under ambient conditions and N2 gas by the quick precipitation method using urea as a stabilizer. The rice straw/Fe3O4 nanocomposites (NCs) prepared by this method had magnetic properties in percentages higher than ten (10 wt. %). When the volume of NaOH increased, Fe3O4-NPs with uniform size and better distribution could be prepared, which means that the size of the NPs decreased as the reducing agent was increased. Transmission electron microscopy (TEM) showed that Fe3O4-NPs in rice straw were spherical with diameters from 18.47 to 9.93 nm. The SEM results show that the structure of rice straw underwent no particular change. EDX indicated the presence of Fe3O4- NPs on the surface of rice straw. X-ray powder diffraction (PXRD) indicated that the magnetic Fe3O4-NPs were pure and that the particles were small. The FT-IR results showed that the Fe3O4-NPs were successfully coated on the surface of rice straw. [ABSTRACT FROM AUTHOR]

Iron oxide nanoparticles (Fe3O4-NPs) were synthesized using chemical coprecipitation method. Fe3O4-NPs are located in interlamellar space and external surfaces of montmorillonite (MMT) as a solid supported at room temperature. The size of magnetite nanoparticles could be controlled by varying the amount of NaOH as reducing agent in the medium. The interlamellar space changed from 1.24 nm to 2.85 nm and average diameter of Fe3O4 nanoparticles was from 12.88nm to 8.24 nm. The synthesized nanoparticles were characterized using some instruments such as transmission electron microscopy, powder X-ray diffraction, energy dispersive X-ray spectroscopy, field emission scanning electron microscopy, vibrating sample magnetometer, and Fourier transform infrared spectroscopy. [ABSTRACT FROM AUTHOR]

Small sized magnetite iron oxide nanoparticles (Fe3O4-NPs) with were successfully synthesized on the surface of rice straw using the quick precipitation method in the absence of any heat treatment. Ferric chloride (FeCl3.6H2O), ferrous chloride (FeCl2.4H2O), sodium hydroxide (NaOH) and urea (CH4N2O) were used as Fe3O4-NPs precursors, reducing agent and stabilizer, respectively. The rice straw fibers were dispersed in deionized water, and then urea was added to the suspension, after that ferric and ferrous chloride were added to this mixture and stirred. After the absorption of iron ions on the surface layer of the fibers, the ions were reduced with NaOH by a quick precipitation method. The reaction was carried out under N2 gas. The mean diameter and standard deviation of metal oxide NPs synthesized in rice straw/Fe3O4 nanocomposites (NCs) were 9.93 ± 2.42 nm. The prepared rice straw/Fe3O4-NCS were characterized using powder X-ray diffraction (PXRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy dispersive X-ray fluorescence (EDXF) and Fourier transforms infrared spectroscopy (FT-IR). The rice straw/Fe3O4-NCs prepared by this method have magnetic properties. [ABSTRACT FROM AUTHOR]

This paper presents the green synthesis of silver nanoparticles (Ag NPs) in aqueous medium. This method was performed by reducing AgNO3 in different stirring times of reaction at a moderate temperature using green agents, chitosan (Cts) and polyethylene glycol (PEG). In this work, silver nitrate (AgNO3) was used as the silver precursor while Cts and PEG were used as the solid support and polymeric stabilizer. The properties of Ag/Cts/PEG nanocomposites (NCs) were studied under different stirring times of reaction. The developed Ag/Cts/PEG NCs were then characterized by the ultraviolet-visible (UV-Vis) spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy. [ABSTRACT FROM AUTHOR]

A green quick precipitation method was successfully used for synthesis of magnetic iron oxide nanoparticles (Fe3O4-NPs) on the surface of sodium/potassium type zeolite. Ferric chloride, ferrous chloride and sodium hydroxide aqueous solutions were used in the synthesis and coating of the Fe3O4-NPs on the surface of the zeolite to produce the zeolite/magnetic iron oxide nanocomposite (zeolite/Fe3O4 -NCs). The reaction was performed in aqueous suspension phase under the ambient condition as green chemistry method. Characterization with Fourier transforms infrared spectroscopy (FT-IR), powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), energy dispersive X-ray fluorescence (EDXF) and transmission electron microscopy (TEM) confirmed the formation of Fe3O4-NPs with mean particle sizes of 3.55±1.02 nm on the surface of the zeolite. [ABSTRACT FROM AUTHOR]

In this paper, Polyimide/Montmorillonite Nanocomposites (PI/MMT NCs), based on aromatic diamine (4-Aminophenyl sulfone) (APS) and aromatic dianhydride (3,3',4,4'-benzophenonetetracarboxylic dianhydride) (BTDA) were prepared using in situ polymerization and solution-dispersion techniques. The prepared PI/MMT NCs films were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM) and thermogravimetric analysis (TGA). The XRD results showed that at the content of 1.0 wt % Organo Montmorillonite (OMMT) for two techniques and 3.0 wt % OMMT for the in situ polymerization technique, the OMMT was well-intercalated, exfoliated and dispersed into polyimide matrix. The OMMT agglomerated when its amount exceeded 10 wt % and 3.0 wt % for solution-dispersion and in situ polymerization techniques respectively. These results were confirmed by the TEM images of the prepared PI/MMT NCs. The TGA thermograms indicated that thermal stability of prepared PI/MMT NCs were increased with the increase of loading that, the effect is higher for the samples prepared by in situ polymerization technique. [ABSTRACT FROM AUTHOR]

Different biological methods are gaining recognition for the production of silver nanoparticles (Ag-NPs) due to their multiple applications. One of the most important applications of Ag-NPs is their use as an anti-bacterial agent. The use of plants in the synthesis of nanoparticles emerges as a cost effective and eco-friendly approach. In this study the biosynthesis of silver nanoparticles using Vitex negundo L. extract and its antimicrobial properties has been reported. The resulting silver particles are characterized using transmission electron microscopy (TEM), X-ray diffraction (XRD) and UV-Visible (UV-Vis) spectroscopic techniques. The TEM study showed the formation of silver nanoparticles in the 10-30 nm range and average 18.2 nm in size. The XRD study showed that the particles are crystalline in nature, with a face centered cubic (fcc) structure. The silver nanoparticles showed the antimicrobial activity against Gram positive and Gram negative bacteria. Vitex negundo L. was found to display strong potential for the synthesis of silver nanoparticles as antimicrobial agents by rapid reduction of silver ions (Ag+ to Ag0). [ABSTRACT FROM AUTHOR]