scholarly journals Green Synthesis of Gold Nanoparticles from Coprinus comatus, Agaricaceae, and the Effect of Ultraviolet Irradiation on Their Characteristics

Author(s):  
Ghassan Adnan NAEEM ◽  
Ahmed Saadoun JALOOT ◽  
Mustafa Nadhim OWAID ◽  
Rasim Farraj MUSLIM

The present research aims to produce gold nanoparticles (AuNPs) from the aqueous extract of locally isolated mushroom Coprinus comatus from Hit city, Iraq. Its properties were studied using the optical vision, UV-Vis, EDX, XRD, FTIR, AFM, and Zetasizer analyses. The exposure of the colloidal solution of AuNPs to UV radiation was investigated for 1, 2, and 3 h. The results showed the color change of the interaction mixture from light yellow to purple after 25 min. The lambda max of the absorbance reached 530 nm using UV-Visible spectrum as evident in the formation of AuNPs. FTIR spectra revealed the presence of functional groups related to peptides, proteins, flavonoids, monosaccharides, and phenolic compounds, which reduced gold ions. The EDX technique showed that the formed nanoparticles were AuNPs. XRD results showed that AuNPs have a face-centered cubic (fcc) crystal. The UV irradiation at different times led to an increase in the intensity of absorbance and sizes of AuNPs from 17.39 nm before the irradiation and switched to 58.16, 59.13, and 47.35 nm after 1, 2, and 3 h, respectively, but their sizes remained within the nanoscale range (less than 100 nm). In conclusion, the best result was observed after about an hour on the effects of UV irradiation on sizes of AuNPs, which reached smaller nanoparticles compared with times 2 and 3 h.

2018 ◽  
Vol 17 (2) ◽  
pp. 75-87
Author(s):  
Mustafa Nadhim OWAID ◽  
Ghassan Adnan NAEEM ◽  
Rasim Farraj MUSLIM ◽  
Raheel Saeed OLEIWI

The object of this study is to synthesize and characterize silver nanoparticles from Agaricus bisporus pileus extracts and their applications. Agaricus bisporus-mediated synthesis of AgNPs was characterized using changing the color solution, UV-Visible spectroscopy, SEM, AFM, SPM, FTIR spectrum, XRD, and EDS analyses. The change of the mixture color of 10-3 M AgNO3 with the watery extract of fresh A. bisporus caps from colorless to brown color is an indicator for the formation of silver nanoparticles (AgNPs). The UV-Visible spectrum exhibits the absorption peak at 418 nm. The FTIR spectra exhibited that the structures of amino acids, polysaccharides, and polyphenols in the crude extract of A. bisporus are not affected because of the joining and interaction of their functional groups with silver ions, and act as reducing and capping agents to the biosynthesized Ag nanoparticles. SEM and EDS refer to the formation of AgNPs with irregular or spherical shapes. The XRD pattern exhibits face-centered cubic (fcc) silver nanocrystals, with crystalline AgNPs size of 43.9 nm. The biosynthesized AgNPs play a suitable role against mouse cell line, which has receptors for polioviruses (L20B). After exposure of the colloid AgNPs to UV radiation (256 nm), the absorption band transferred from 418 nm to 435 nm, indicating that UV rays affect on physical properties of AgNPs. Roughness average of the biosynthesized AgNPs from A. bisporus caps is 15.4 nm, but the roughness is increased after UV irradiation for 1 h to average 33.6 nm. Histograms of particle size distribution of AgNPs show the average of AgNPs is 103.57 nm, while the size of nanoparticles reaches 69.47 nm after exposure to UV radiation of 256 nm. The use of UV radiation leads to enhanced characteristics of silver nanoparticles.


2019 ◽  
Vol 0 (0) ◽  
Author(s):  
R. Krishnamurthy ◽  
V. Revathy ◽  
K. S. Joseph Wilson ◽  
Sofyan A. Taya ◽  
I. S. Amiri

AbstractCopper nanoparticles (Cu) anchored lithium niobate (LiNbO3) nanostructures were prepared by a simple hydrothermal technique. The fine and sparse Cu nanoparticles were homogeneously dispersed over the surface of LiNbO3. An effectual anchoring of Cu was evidenced from the acquired reflection planes in diffraction analysis, which clearly indicate the face-centered cubic structure of Cu. The UV-Visible spectrum of LiNbO3 and Cu/LiNbO3 nanocomposites were also studied. When the Cu nanoparticles were doped with LiNbO3/LiTaO3 superlattice system, the change in the dispersion relation was observed theoretically. The characteristics of the polariton dispersion variation with filling factor of Cu nanoparticles concentration were investigated systematically. The importance of the polariton modes in communication sector was analyzed and the occurrence of new modes on the polaritonic gap, where the propagation of the electromagnetic wave is forbidden, were obtained in the system due to the presence of copper nanoparticles.


MRS Advances ◽  
2019 ◽  
Vol 4 (38-39) ◽  
pp. 2109-2117
Author(s):  
Rossymar Rivera Colón ◽  
Wilfred Fonseca Ferrer ◽  
Sonia J. Bailón-Ruiz

ABSTRACTThe generation of AuNPs was realized in presence of gold chloride (Au3+), and citrate solution as reducing agent. The production of AuNPs was proved by the color change in the solution; from yellow to red wine. Purified nanostructures synthesized at citrate/Au3+ molar ratio of 1.0/10.0 evidenced an absorption peak at 526 nm attributed to the localized surface Plasmon Resonance (LSPR) which suggested the formation of small gold nanoparticles (NPs). The decrease of citrate/Au3+ molar ratio at 1.0/3.0 provoked a growing of gold nanostructures, which was evidenced by a red shift in the SPR at 546nm. High Resolution Transmission Electron Microscopy technique evidenced the spherical form and sizes for both nanoparticles at the range 10-15 nm (small NPs) and 20-25 nm (big NPs), respectively. Electron Diffraction (ED) patterns for both sizes evidenced the (111), (200), (220), (311), and (222) reflections of face centered cubic (FCC) gold nanostructures. Studies of energy-dispersive X-ray Spectroscopy indicated peaks at 1.65, 2.12, 9.71, 11.58 and 13.38 keV for both nanostructures, which suggests the presence of gold into the crystalline structure of the nanoparticles. Interaction tests were carried out in presence of marine crustaceans and different concentrations of gold nanoparticles; including a control test. Both sizes evidenced to be toxic when the concentration and exposure time were increased.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Somayeh Safat ◽  
Foad Buazar ◽  
Salim Albukhaty ◽  
Soheila Matroodi

AbstractThis contribution presents the biosynthesis, physiochemical properties, toxicity and photocatalytic activity of biogenic CeO2 NPs using, for the first time, marine oyster extract as an effective and rich source of bioreducing and capping/stabilizing agents in a one-pot recipe. CeO2 NPs formation was initially confirmed through the color change from light green to pale yellow and subsequently, their corresponding absorption peak was spectroscopically determined at 310 nm with an optical band-gap of 4.67 eV using the DR-UV technique. Further, XRD and Raman analyses indicated that nanoceria possessed face-centered cubic arrangements without any impurities, having an average crystallite size of 10 nm. TEM and SEM results revealed that biogenic CeO2 NPs was approximately spherical in shape with a median particle size of 15 ± 1 nm. The presence of various bioorganic substances on the surface of nanoparticles was deduced by FTIR and TGA results. It is found that marine-based nanoceria shows no cytotoxic effect on the normal cell, thus indicating their enhanced biocompatibility and biosafety to living organisms. Environmentally, due to energy band gap, visible light-activated CeO2 nanocatalyst revealed superior photocatalytic performance on degradation of methylene blue pollutant with removal rate of 99%. Owing to the simplicity, cost-effectiveness, and environmentally friendly nature, this novel marine biosynthetic route paves the way for prospective applications of nanoparticles in various areas.


Materials ◽  
2019 ◽  
Vol 12 (15) ◽  
pp. 2382 ◽  
Author(s):  
Muhammad Jamshed Khan ◽  
Suriya Kumari ◽  
Kamyar Shameli ◽  
Jinap Selamat ◽  
Awis Qurni Sazili

Nanoparticles (NPs) are, frequently, being utilized in multi-dimensional enterprises. Silver nanoparticles (AgNPs) have attracted researchers in the last decade due to their exceptional efficacy at very low volume and stability at higher temperatures. Due to certain limitations of the chemical method of synthesis, AgNPs can be obtained by physical methods including sun rays, microwaves and ultraviolet (UV) radiation. In the current study, the synthesis of pullulan mediated silver nanoparticles (P-AgNPs) was achieved through ultraviolet (UV) irradiation, with a wavelength of 365 nm, for 96 h. P-AgNPs were formed after 24 h of UV-irradiation time and expressed spectra maxima as 415 nm, after 96 h, in UV-vis spectroscopy. The crystallographic structure was “face centered cubic (fcc)” as confirmed by powder X-ray diffraction (PXRD). Furthermore, high resolution transmission electron microscopy (HRTEM) proved that P-AgNPs were covered with a thin layer of pullulan, with a mean crystalline size of 6.02 ± 2.37. The average lattice fringe spacing of nanoparticles was confirmed as 0.235 nm with quasi-spherical characteristics, by selected area electron diffraction (SAED) analysis. These green synthesized P-AgNPs can be utilized efficiently, as an active food and meat preservative, when incorporated into the edible films.


2019 ◽  
Vol 290 ◽  
pp. 87-92
Author(s):  
Adamu Ibrahim Usman ◽  
Azlan Abdul Aziz ◽  
Osama Abu Noqta

A simple method to synthesized nanoparticles was satisfied by reduction of tetrachloroauric acid in the presence of palm oil fronds extracts as capping and reduced agents. The as-synthesized gold nanoparticles structures have a triangular and hexagonal shape that are of tens of nanometre in size. It was realized that good control shape of nano-hexagonal gold nanoparticles were obtained from nano-triangular gold nanoparticles in the absence of any soft template. The production techniques of the gold nanoparticles were examined by using UV-vis spectroscopy, EFTEM and XRD patterns, which showed peaks at (111), (200), (220), (311) and (222), that described the preferential structure of the AuNPs as face-centered cubic crystal


2020 ◽  
Vol 2020 ◽  
pp. 1-11
Author(s):  
Kamonpan Wongyai ◽  
Phitchayapak Wintachai ◽  
Rasimate Maungchang ◽  
Parawee Rattanakit

A green, simple, and rapid synthesis of gold nanoparticles using plant extract, Cryptolepis buchanani Roem. and Schult, and their applications are first described in this paper. The formation of gold nanoparticles was visually observed by the appearance of a ruby red color, which was further indicated by an absorption peak at 530 nm in UV-Vis spectroscopy. Optimization of reaction parameters for the gold nanoparticles was also investigated. Various analytical techniques were employed as part of the process of characterizing the resulting gold nanoparticles. Fourier transform infrared (FTIR) analysis revealed that the phenol compounds present in the extract were responsible for gold(III) reduction and stabilization of gold nanoparticles. Transmission electron microscopy (TEM) analysis showed that the gold nanoparticles were spherical in shape with an average diameter of 11 nm. Powder X-ray diffraction (XRD) pattern indicated that the green synthesis approach produced highly crystalline, face-centered cubic gold nanoparticles. Energy-dispersive X-ray spectroscopy (EDS) measurements confirmed the presence of elemental gold in the prepared nanoparticles. The negative zeta potential value of gold nanoparticles was found to be -30.28 mV. The green synthesized gold nanoparticles expressed effective antibacterial activity against Staphylococcus aureus, methicillin-resistant Staphylococcus aureus, and Acinetobacter baumannii and exhibited an excellent catalytic property in terms of its reduction ability of methylene blue.


2020 ◽  
Vol 840 ◽  
pp. 472-477
Author(s):  
Naura Nadhifah ◽  
Wening Rara Pratita ◽  
Eko Sri Kunarti ◽  
Nuryono Nuryono ◽  
Sri Juari Santosa

The synthesis of gold nanoparticles (AuNPs) was carried out by reacting chloroauric acid [AuCl4]‒ and glutamic acid solution in a water bath at 80 °C. The reaction was confirmed by the color change from colorless solution into pink. Various concentrations of the glutamic acid solution, reaction times and pH were examined to determine the optimum condition of AuNPs synthesis. The AuNPs colloid was characterized by UV-Visible spectrophotometer at wavelength 350-800 nm, particle size analyzer (PSA) and transmission electron microscope (TEM). The optimum synthesis condition for obtained [AuCl4]‒ was 4 mM glutamic acid solution at pH 11 and 60 min reaction. TEM results showed that the particles were round in shape with the article size indicated by PSA was 40 nm.


2021 ◽  
Vol 37 (1) ◽  
pp. 157-161
Author(s):  
Namita Bharadwaj ◽  
Jaishri Kaushik

The stability constant Kf for the complexation of Ag(Ⅰ) metal ion with Midodrine hydrochloride were determinedby spectrophotometric method at room temperature .The colored complexes were measured at 300 nm. The stability constant of the complexes were found to be 5.47 by mole ratio method. The stoichiometry of the complexes formed between the Midodrine drug and Ag (Ⅰ) metal ion are 1:1 M/L ratio. Silver conjugated Midodrine hydrochloride Nano synthesized and characterized by UV/Visible spectroscopy, SEM, XRD and FT-IR. The UV/Visible spectra of Midodrine –Ag nanoparticle in the range of 322 nm. XRD conformThe crystallite size of Midodrine - Ag (Ⅰ) nanoparticles are found to be 64.5 nmfrom Debye Scherer formula.Thecrystallinity of nanoparticles is Face centered cubic structure. SEM conform of particle size and surface morphology, FTIR analyzed involvement of -NH2 group in Midodrine is the stabilized of silver nanoparticle. This research is focuses on complexation, Nano synthesis and characterization of Drug-silver nanoparticle for antihypotention therapy.


2013 ◽  
Vol 662 ◽  
pp. 80-83 ◽  
Author(s):  
Mana Intarasawang ◽  
Kheamrutai Thamaphat

In the present study, we demonstrated an effective cost and environmentally benign method to synthesize the silver nanoparticles (AgNPs) using aquatic weed namely water hyacinth as a reducing agent. Ultraviolet irradiation was also combined in the process to enhance the reaction rate. The aqueous silver ions mixed with water hyacinth leaf extract under UV irradiation were reduced to AgNPs. The mixture color was changed from light yellow to yellowish-brown color within 5 min due to excitation of surface plasmon vibrations in AgNPs. The formation of AgNPs was confirmed by UV-visible spectroscopy, X-ray diffraction (XRD) spectrometry, energy dispersive X-ray (EDX) analysis and transmission electron microscopy (TEM). The AgNPs were found to be polycrystalline in nature and spherical particles with mean diameter of 12.54 ± 0.19 nm. The XRD pattern peaked at different diffraction angles corresponding to the (111), (200), (220), and (311) planes indicated that AgNPs have face-centered cubic (fcc) unit cell structure. This proposed method revealed that unwanted plant can utilize in nano-manufacturing as well.


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