scholarly journals Simultaneous Sonochemical Coloration and Antibacterial Functionalization of Leather with Selenium Nanoparticles (SeNPs)

Polymers ◽  
2021 ◽  
Vol 14 (1) ◽  
pp. 74
Author(s):  
Tarek Abou Elmaaty ◽  
Khaled Sayed-Ahmed ◽  
Radwan Mohamed Ali ◽  
Kholoud El-Khodary ◽  
Shereen A. Abdeldayem
Keyword(s):  
Electron Microscopy ◽  
Antibacterial Activity ◽  
Antibacterial Properties ◽  
Salmonella Typhi ◽  
Point Of View ◽  
Selenium Nanoparticles ◽  
Footwear Industry ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Low Cytotoxicity

The development of antibacterial coatings for footwear components is of great interest both from an industry and consumer point of view. In this work, the leather material was developed taking advantage of the intrinsic antibacterial activity and coloring ability of selenium nanoparticles (SeNPs). The SeNPs were synthesized and implemented into the leather surface by using ultrasonic techniques to obtain simultaneous coloring and functionalization. The formation of SeNPs in the solutions was evaluated using UV/Vis spectroscopy and the morphology of the NPs was determined by transmission electron microscopy (TEM). The treated leather material (leather/SeNPs) was characterized by scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). The effects of SeNPs on the coloration and antibacterial properties of the leather material were evaluated. The results revealed that the NPs were mostly spherical in shape, regularly distributed, and closely anchored to the leather surface. The particle size distribution of SeNPs at concentrations of 25 mM and 50 mM was in the range of 36–77 nm and 41–149 nm, respectively. It was observed that leather/SeNPs exhibited a higher depth of shade compared to untreated ones, as well as excellent fastness properties. The results showed that leather/SeNPs can significantly enhance the antibacterial activity against model of bacteria, including Gram-positive bacteria (Bacillus cereus) and Gram-negative bacteria (Pseudomonas aeruginosa, Salmonella typhi and Escherichia coli). Moreover, the resulting leather exhibited low cytotoxicity against HFB4 cell lines. This achievement should be quite appealing to the footwear industry as a way to prevent the spread of bacterial infection promoted by humidity, poor breathability and temperature which promote the expansion of the microflora of the skin.

scholarly journals Biosynthesized gold nanoparticles-doped hydroxyapatite as antibacterial and antioxidant nanocomposite

2021 ◽  
Author(s):  
Is Fatimah ◽  
Putwi Widya Citradewi ◽  
Amri Yahya ◽  
Bambang Nugroho ◽  
Habibi Hidayat ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Antioxidant Activity ◽  
Particle Size ◽  
Gold Nanoparticles ◽  
Antibacterial Activity ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Dpph Scavenging Activity ◽  
Dpph Scavenging

Abstract The composite of green synthesized gold nanoparticles (Au NPs)-doped hydroxyapatite (HA) has been prepared. The gold nanoparticles were produced via bioreduction of HAuCl4 with Clitoria ternatea flower extract, and utilized in the synthesis of hydroxyapatite using Ca(OH)2 and ammonium diphosphate as precursor. The aim of this research is to study the structural analysis of the composite and antibacterial activity test toward Eschericia coli, Staphylococcus aureus, Klebsiela pneumoniae, and Streptococcus pyogenes. In addition, the antioxidant activity was evaluated using 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging method. The monitoring of gold nanoparticles formation was conducted by UV–vis spectroscopy and particle size analyses, meanwhile the synthesized composite was studied using X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The results showed that homogeneously dispersed gold nanoparticles in HA structure was obtained with the particle size ranging at 5-80 nm. The nanocomposite demonstrated antibacterial activity against tested bacteria. The nanocomposite expressed an antioxidant activity as shown by the DPPH scavenging activity of 66 and 58% at the concentration of 100 μg/mL and 50 μg/mL, respectively.

scholarly journals Manganese ferrite graphene nanocomposite synthesis and the investigation of its antibacterial properties for water treatment purposes

2020 ◽  
Vol 15 (4) ◽  
pp. 1
Author(s):  
Lara De Souza Soletti ◽  
Maria Eliana Camargo Ferreira ◽  
Alex Toshio Kassada ◽  
Benício Alves de Abreu Filho ◽  
Rosangela Bergamasco ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Antibacterial Activity ◽  
Water Treatment ◽  
Graphene Nanosheets ◽  
Antibacterial Properties ◽  
Morphological Characteristics ◽  
Manganese Ferrite ◽  
Transmission Electron ◽  
Cutting Effect ◽  
Mnfe2o4 Nanoparticles

The main objective of this study was to synthesize a nanocomposite using graphene and manganese ferrite nanoparticles (MnFe2O4-G) and to evaluate its antibacterial activity for water treatment purposes. Its morphological characteristics were evaluated by instrumental techniques, such as scanning electron microscopy and transmission electron microscopy. The characterization results indicated that the nanocomposite presented nanoparticles of approximately 25 nm well dispersed in transparent and large (14 μm) graphene nanosheets. The antibacterial activity was evaluated in a batch experiment using a concentration of 40 μg mL-1 of nanocomposite (MnFe2O4-G, bare MnFe2O4 nanoparticles or graphene oxide), 1x105 CFU mL-1 of Escherichia coli, and 8 h of contact time at room temperature. The highest antibacterial capacity was observed for the hybrid nanocomposite (91.91%), due to the synergic effect of graphene and MnFe2O4 nanoparticles. Various mechanisms were proposed to explain the effective antibacterial activity of MnFe2O4-G, such as wrapping, oxidative stress, sharp-edge cutting effect, among others. The results showed that MnFe2O4-G is a potential alternative in water treatment processes as an antibacterial agent.

scholarly journals Fortunella japonica extract as a reducing agent for green synthesis of silver nanoparticles

2018 ◽  
Vol 7 (3) ◽  
pp. 1570
Author(s):  
Nguyen Phung Anh ◽  
Truong Thi Ai Mi ◽  
Duong Huynh Thanh Linh ◽  
Nguyen Thi Thuy Van ◽  
Hoang Tien Cuong ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Silver Nanoparticles ◽  
Antibacterial Activity ◽  
Volume Ratio ◽  
Diffusion Method ◽  
High Antibacterial Activity ◽  
Agno3 Solution ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Average Size

A rapid way of synthesizing silver nanoparticles (AgNPs) by treating Ag+ ions with a green Fortunella Japonica (F.J.) extract as a combined reducing and stabilizing agent was investigated. The reaction solutions were monitored using UV-Vis spectroscopy, the size and shape of crystals were determined by scanning electron microscopy and transmission electron microscopy, the crystalline phases of AgNPs were presented by X–ray diffraction, and the relation of nanoparticles with Fortunella Japonica extract was confirmed using fourier transform infrared spectroscopy. The results indicated that no formation of AgNPs had taken place in the dark during 24 hours at room temperature and 40 oC. Meanwhile, it was found that the rate of AgNPs formation increased rapidly under the sunlight. The effects of the synthesis factors on the AgNPs formation were investigated. The suitable conditions for the synthesis of AgNPs using F.J. extract were determined as follows: F.J. extract was mixed with AgNO3 1.75 mM solution with the volume ratio of 3.5 AgNO3 solution/1.5 F.J. Extract, stirred 300 rpm for 150 minutes at 40 oC under sunlight illumination. At these conditions, AgNPs showed high crystalline structure with the average size of 15.9 nm. The antibacterial activity of silver nanoparticles was determined by agar well diffusion method against E. coli and B. subtilis bacteria. The green synthesized AgNPs performed high antibacterial activity against both bacteria.  

scholarly journals Green preparation and characterization of silver nanocolloids used as antibacterial material in soap

2022 ◽  
Author(s):  
M. Nowak ◽  
A. Tolińska ◽  
L. Marciniak ◽  
M. Skrobańska ◽  
B. Tylkowski ◽  
...  
Keyword(s):  
Silver Nanoparticles ◽  
Antibacterial Activity ◽  
Inductively Coupled Plasma ◽  
Antibacterial Properties ◽  
Dirty Hands ◽  
Inductively Coupled ◽  
Transmission Electron ◽  
Pure Soap ◽  
Vis Spectroscopy ◽  
Plasma Mass Spectrometry

AbstractThis study aimed to assess the characteristics, including morphology, physicochemical properties, and antibacterial properties, of silver nanocolloids obtained by D-glucose reduction. Silver nanoparticles were synthesized in accordance with the principles of green chemistry using D-glucose as a reductor. The obtained nanostructures were characterized by UV–vis spectroscopy, transmission electron microscopy, and dynamic light scattering. Stability tests performed after 1 month of storage revealed that the colloids prepared with and without polyvinylpyrrolidone as a stabilizer had the same properties. Distribution of the nanoparticles was tested using inductively coupled plasma mass spectrometry by doping the silver colloids into a natural soap mass. The antibacterial activity of the soap containing silver nanoparticles was tested on dirty hands. The antibacterial activity test demonstrated that the novel green soap materials improved with D-glucose-reduced silver nanoparticles possessed better antibacterial properties than a pure soap, and thus, they could be recommended for quotidian use by dermatological patients.

Antibacterial Fibers Containing Nanosilica with Immobilized Silver Nanoparticles

2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Emilia Smiechowicz ◽  
Barbara Niekraszewicz ◽  
Marta Strzelinska ◽  
Maria Zielecka
Keyword(s):  
Electron Microscopy ◽  
Silver Nanoparticles ◽  
Antibacterial Activity ◽  
Energy Dispersive Spectrometry ◽  
Antibacterial Properties ◽  
Cellulose Fiber ◽  
Cellulose Dissolution ◽  
Transmission Electron ◽  
Basic Parameters ◽  
Selection Of

AbstractThe main aim of the presented research was to obtain antibacterial fibers containing nanosilica with immobilized silver nanoparticles. The nanomodifier in an amount of 250 ppm, 500 ppm, 1,000 ppm, and 2,000 ppm were introduced into the cellulose fiber matrix during the cellulose dissolution process. In order to assess the influence of the nanomodifier's amount in the fiber on the antibacterial activity of modified fiber, a quantitative test of the antibacterial activity of the fibers was performed. The basic parameters of modified fibers, such as the mechanical and hygroscopic, were estimated. The size and shape of the nanomodifier in the selected fibers, as well as microanalysis of the polymer matrix, were examined. The investigations were conducted by Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), and Energy Dispersive Spectrometry (EDS). The obtained results allowed the selection of optimal fibers with strong antibacterial properties that can be potentially used for personal protection or medical purposes.

scholarly journals Biosynthesis of Gold Nanoparticles (AuNPs) by Diopatra claparedii Grube, 1878 (Polychaeta: Onuphidae) and Its Antibacterial Activity

2021 ◽  
Vol 50 (5) ◽  
pp. 1309-1320
Author(s):  
Chong Huai Piong ◽  
Noor Aniza Harun ◽  
Angeline Ung Ee Pei ◽  
Mohammad Asyraf Adhwa Masimen ◽  
Wan Iryani Wan Ismail ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Gold Nanoparticles ◽  
Size Range ◽  
Salmonella Typhi ◽  
Atmospheric Conditions ◽  
Environmental Friendly ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Staphyloccus Aureus ◽  
Scanning Electron

Gold nanoparticles (AuNPs) have gained attention as it possesses outstanding physicochemical properties, and utilised in variety of applications especially in biomedical and pharmaceutical. Majorly, AuNPs are produced by conventional methods (chemical and physical). However, these methods bring several drawbacks such as toxic, hazardous, low yield and non-environmental friendly. Hence, biosynthesis of AuNPs that compliance with ‘greener’ approach becomes vitals. In this study, marine tube worm of Diopatra claparedii (polychaetes) was employed as reducing agent in the biosynthesis of AuNPs. The biosynthesised of AuNPs by D. claparedii extract was successfully prepared under ambient temperature and normal atmospheric conditions. The formation of AuNPS was confirmed by the appearance of surface Plasmon resonance (SPR) bands around 540 to 560 nm characterized by UV-Vis spectroscopy. Scanning electron microscopy (SEM) showed that the AuNPs are mostly in agglomerated spherical like shapes with size ranging from 100 to 400 nm. Meanwhile, transmission electron microscopy (TEM) showed that the particles are in the size range from 25 to 60 nm, also mainly form in spherical like shape. The particle size of AuNPs in a range of 50-100 nm was showed by dynamic light scattering (DLS). Fourier-transform infrared (FTIR) spectrum of D. claparedii extract indicated the existence of several functional groups. Biosynthesised AuNPs also successfully gave inhibition on bacterial growth (Staphyloccus aureus, S. epidermidis, Escheratia coli, Salmonella typhi) through antibacterial assessment.

scholarly journals Synthesis and characterization of Fe, Co, and Ni colloids in 2-mercaptoethanol

2020 ◽  
Vol 10 ◽  
pp. 184798042096688
Author(s):  
Galo Cárdenas-Triviño ◽  
Sergio Triviño-Matus
Keyword(s):  
Electron Microscopy ◽  
Electron Diffraction ◽  
Colloidal Dispersions ◽  
Synthesis And Characterization ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Chemical Liquid Deposition ◽  
Liquid Deposition

Metal colloids in 2-mercaptoethanol using nanoparticles (NPs) of iron (Fe), cobalt (Co), and nickel (Ni) were prepared by chemical liquid deposition method. Transmission electron microscopy, electron diffraction, UV-VIS spectroscopy, and scanning electron microscopy with electron dispersive X-ray spectroscopy characterized the resulting colloidal dispersions. The NPs exhibited sizes with ranges from 9.8 nm for Fe, 3.7 nm for Co, and 7.2 nm for Ni. The electron diffraction shows the presence of the metals in its elemental state Fe (0), Co (0), and Ni (0) and also some compounds FeO (OH), CoCo2S4, and NiNi2S4.

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.

scholarly journals Antibacterial activity of zinc oxide nanoparticles obtained by pulsed laser ablation in water and air

2018 ◽  
Vol 243 ◽  
pp. 00017 ◽  
Author(s):  
Daria Goncharova ◽  
Ekaterina Gavrilenko ◽  
Anna Nemoykina ◽  
Valery Svetlichnyi
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Antibacterial Activity ◽  
Laser Ablation ◽  
Zno Nanoparticles ◽  
Antibacterial Properties ◽  
Pulsed Laser ◽  
Pulsed Laser Ablation ◽  
Composition And Structure ◽  
Scanning Electron

The paper studies physicochemical and antibacterial properties of ZnO nanoparticles obtained by pulsed laser ablation in water and air. Their composition and structure were studied by X-ray diffraction, transmission and scanning electron microscopy. Antibacterial activity of the nanoparticles was examined by its affection on Gram-positive Staphylococcus aureus (S.aureus). The dependence of nanoparticles’ physical and chemical antibacterial properties on the conditions of the ablation was shown. The model materials for the antibacterial bandage were made of cotton, filter paper and biodegradable polymer scaffolds (poly-l-lactide acid), and then they were coated with the obtained ZnO nanoparticles. The model bandage materials were examined by the scanning electron microscopy method and their antibacterial activity (ISO 20743:2013) was determined. High activity of all the samples against S.aureus was proved.

Study on Dispersion and Characterization of Functionalized MWCNTs Prepared by Wet Oxidation

2014 ◽  
Vol 661 ◽  
pp. 8-13 ◽  
Author(s):  
Intan Syaffinazzilla Zaine ◽  
N.A.M. Napiah ◽  
Azmi Mohamad Yusof ◽  
A.N. Alias ◽  
A.M.M. Ali ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Relative Intensity ◽  
Colloidal Stability ◽  
Structural Defects ◽  
Wet Oxidation ◽  
Defect Level ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Functionalized Mwcnts

The MWCNTs was functionalized by refluxing commercial MWCNTs (a-MWCNTs) in concentrated HNO3/H2SO4 (3:1 v/v) at 100°C for 6 hours. The dispersion of a-MWCNTs and functionalized MWCNTs (f-MWCNTs) were observed after 1 hour sonication in ethanol. Both samples were characterized by UV-vis spectroscopy for dispersion behavior. The dried f-MWCNTs and a-MWCNTs were characterized by Raman spectroscopy to estimate the defect level. The morphology of the samples were analyzed by Transmission Electron Microscopy (TEM). The f-MWCNTs was well dispersed in ethanol within 2 weeks of observations period. The colloidal stability of a-MWCNTs was low as it was easily sediment after 24 hours. The UV-vis spectra of f-MWCNTs show maximum absorbance at 250 nm meanwhile no absorbance was observed for a-MWCNTs. Analysis from Raman spectrum shows that the f-MWCNTs have relative intensity of 1.101 which is higher than a-MWCNTs that have relative intensity of 0.935. The image from TEM revealed that the f-MWCNTs have structural defects and the absence of amorphous carbon on sidewall meanwhile the a-MWCNTs indicate otherwise.

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