Acalypha Indica mediated MgO NPs: A novel approach in greener route with its antibacterial activity against pathogens

2020 ◽  
Vol 3 (2) ◽  
Author(s):  
Kavipriya K C ◽  
Sudha A P ◽  
Sujatha K ◽  
Sowmya Lakshmi K

The interest in miniaturization of particles revealed the hidden applications of metal oxides. The potential applications of the particles may vary when the size of the particle is reduced. One of the alternative routes to the conventional approach is the use of plant extract for the synthesis of metal oxides NPs. In the framework of this study, the ecofriendly MgO nanoparticles were synthesized using Acalypha Indica leaf extract,functioning as reducing and capping agent by co-precipitation method. The predecessor taken here was Magnesium Nitrate. The biologically synthesized MgO NPs were characterized by various techniques like X ray diffraction(XRD), Fourier Transform infrared spectroscopy(FTIR), Scanning electron microscope (SEM) with Energy Dispersive X-ray spectroscopy(EDX) profile and its antibacterial activity is evaluated against causative organisms. XRD studies confirmed the face centered cubic crystalline structure of MgO NPs and the average crystalline size of MgO NPs calculated using Scherer’s formula was found to be 13 nm. FTIR spectrum shows a significant Mg-O vibrational band. Purity, surface morphology and chemical composition of elements were confirmed by SEM with EDX. The SEM result shows the fine spherical morphology with the grain size range between 43nm to 62nm. Antimicrobial assay of MgO NPs was examined against gram positive and negative bacteria. Appreciated activity was observed on the Staphylococcus aureus bacterial species. In general, the renewed attempt of this facile approach gave the optimum results of multifunctional MgO NPs.

2020 ◽  
Vol 3 (2) ◽  
Author(s):  
Aarth R ◽  
Sudha A P ◽  
Sujatha B ◽  
Sowmya Lakshmi K

The phytosynthesis of n-type Cadmium Oxide Nanoparticles reduces the toxicity of the substance and makes it Eco-friendly. This Eco-friendly biosynthesis of CdO NPs was synthesized for the first time from the Queen of herbs, Ocimum Sanctum (holy basil).The biosynthesized Cadmium oxide was prepared using Ocimum leaf extract as a reductant and Cadmium Chloride and hydroxide as cadmium and oxide source materials by Co- Precipitation method. Thus obtained Cadmium Oxide Nanoparticles were characterized by different techniques such as X-ray diffraction (XRD), Fourier Transform infrared spectroscopy (FTIR), Scanning electron microscope (SEM),Energy dispersive X-ray spectroscopy(EDS) to study the structural and morphological properties. XRD pattern exhibited the formation of face centered cubic structure of CdO NPs with an average crystalline size of 11.5nm .The chemical bond formation of CdO NPs were confirmed by FTIR spectrum in the range of (400-4000cm-1). The SEM micrographs revealed the predominant formation of Cauliflower shape with a particle size in the range of 61-142nm. The high purity of the biosynthesized nanoparticles were confirmed by EDS analysis. Further it was tested against gram positive and gram negative bacterial strains and showed significant antibacterial activity. This biosynthetic research study opens an innovative window to progress our understanding of how CdO NPs shows resistance to different bacterial strains.


Water ◽  
2021 ◽  
Vol 13 (16) ◽  
pp. 2189
Author(s):  
V. Beena ◽  
S. L. Rayar ◽  
S. Ajitha ◽  
Awais Ahmad ◽  
Munirah D. Albaqami ◽  
...  

The development of cost-effective and ecofriendly approaches toward water purification and antibacterial activity is a hot research topic in this era. Purposely, strontium-doped zinc selenide (Sr-doped ZnSe) nanoparticles, with different molar ratios of Sr2+ cations (0.01, 0.05, and 0.1), were prepared via the co-precipitation method, in which sodium borohydride (NaBH4) and 2-mercaptoethanol were employed as reducing and stabilizing agents, respectively. The ZnSe cubic structure expanded by Sr2+ cations was indicated by X-ray diffraction (XRD) analysis. The absorption of the chemical compounds on the surface was observed via Fourier transform infrared (FT-IR) spectroscopy. The optical orientation was measured by ultraviolet–visible diffused reflectance spectroscopy (UV-DRS) analysis. The surface area, morphology, and elemental purity were analyzed using field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM), and energy-dispersive spectroscopy (EDS) analyses. The oxidation state and valency of the synthesized nanoparticles were analyzed using X-ray photoelectron spectroscopy (XPS). Sr-doped ZnSe nanoparticles were investigated for photocatalytic degradation of methyl orange (MO), and their antibacterial potential was investigated against different bacterial strains. The antibacterial activity examined against Staphylococcus aureus and Escherichia coli implied the excellent biological activity of the nanoparticles. Moreover, the Sr-doped ZnSe nanoparticles were evaluated by the successful degradation of methyl orange under visible light irradiation. Therefore, Sr-doped ZnSe nanoparticles have tremendous potential in biological and water remediation fields.


2020 ◽  
Vol 3 (1) ◽  
Author(s):  
Dhivya B ◽  
Sujatha K ◽  
Sudha A P

The conventional methods for the synthesis of metal oxides intake large amount of hazardous chemicals, the best promising alternative is the use of plant extracts. In this work, calcium oxide nanoparticles of 16 nm size with the cubic shape were synthesized using the papaya leaf extract by the simple greener route using calcium chloride as a source material by co-precipitation method. By using the XRD (X-Ray Diffraction), FTIR (Fourier Transform Infrared Spectroscopy), SEM (Scanning Electron Microscope) and EDAX (Energy Dispersive X-ray Analysis), the structural,surface morphology, functional group and the antibacterial activity of the synthesized calcium oxide nanoparticles were analyzed. The XRD pattern of the CaO nanoparticles was well matched with the standard value and the crystalline size obtained using the Scherer formula was 16 nm. The elemental composition of the prepared sample was confirmed by the EDAX result. The presence of the functional groups of the synthesized CaO nanoparticles was confirmed by the FTIR analysis (4000-400 cmˉ1). The cubic morphology was identified from the SEM image and the grain size ranges from 125-218 nm. The CaO nanoparticles were further evaluated for their antibacterial activity against Staphylococcus aureus and klebsiella pneumonia and from the result it was found that CaO nanoparticles was active against both gram positive and gram negativebacteria.Therefore, it may be an emerging platform for new medicines.


2020 ◽  
Vol 3 (3) ◽  
Author(s):  
Pavithra D ◽  
Sujatha K ◽  
Sudha A P

In the present work, cobalt oxide nanoparticles were prepared by using precipitation method. The cobalt nitrate [Co (No3)2] and ammonium oxalate [C2H8N2O4] were used as precursors for the synthesis of cobalt oxide nanoparticles and the resultant product was Calcinated at 400˚C for 2 hrs. The synthesized nanoparticles were characterized by X-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscope (SEM), Energy Dispersive X-ray Spectroscopy (EDAX) to analyze the structural and morphological properties. The XRD pattern of the synthesized cobalt oxide nanoparticles exhibits cubic structure with the average crystalline size of 8.06 nm. The functional groups of the synthesized nanoparticles were confirmed by using FTIR spectrum (400 to 4000 cm-1). In the synthesized sample and its purity were confirmed from EDAX spectrum. The surface morphology of the synthesized Co3O4 nanoparticles shows spherical morphology. The optical properties of the synthesized cobalt oxide nanoparticles were investigated by photoluminescence spectrum which shows a minor emission at around 440 nm.


2021 ◽  
Author(s):  
Alaa Abdallah ◽  
Ramadan Awad

Abstract Pure and different concentrations from (Gd, Ru) co-doped NiO nanoparticles, capped with Polyvinylpyrrolidone (PVP), were fabricated by the co-precipitation method. The nanoparticles were characterized by different techniques. The Rietveld refinements of X-Ray Diffraction (XRD) patterns confirmed the formation of the pure face-centered-cubic NiO phase. The X-ray Photo-induced Spectroscopy (XPS) assured the trivalent oxidation state of the doped ions Gd3+ and Ru3+ and unveiled the multiple oxidation states of nickel ions (Ni2+ and Ni3+), emerging from the vacancies in the samples. The Transmission Electron Microscope (TEM) images showed the pseudospherical morphology of the samples and the Energy Dispersive X-ray permitted the quantitative analysis of the presented elements and their homogeneous distribution. The Raman and Fourier Transform Infra-Red (FTIR) spectra depicted the fundamental vibrational bands of NiO nanoparticles, confirming their purity. The UV-visible spectroscopy enabled the absorption measurements and the energy gap calculations. The co-dopants increased the energy bandgap of NiO nanoparticles from 3.15 eV for pure NiO to 3.62 eV with the highest concentration of the co-dopants (x = 0.02) The photoluminescence (PL) spectra gave insights into the possible defects present in the samples, such as nickel vacancies, single and double oxygen vacancies, and oxygen interstitials. The Vibrating Sample Magnetometer (VSM) studied the room temperature M-H loops of the co-doped samples. A combination of ferromagnetic, antiferromagnetic, and paramagnetic contributions was noticed and treated according to the law of approach to saturation and bound magnetic polaron (BMP) model. The magnetic parameters, such as the saturation magnetization, exchange and anisotropy field, and the BMP concentration were extracted from the fitted models and discussed in terms of the co-dopants’ concentration. The co-doped samples showed a softer magnetic behavior, which is recommended for data storage applications.


2013 ◽  
Vol 678 ◽  
pp. 234-238 ◽  
Author(s):  
Vishwanath D. Mote ◽  
Babasaheb N. Dole

Nanosized Mn doped ZnO samples were synthesized by co-precipitation method using Polyethylene glycol (PEG) as a capping agent. X- ray diffraction patterns confirm that the pure and Mn doped ZnO nanocrystals have wurtzite structure without any seconadary phases. Lattice parameters of pure and Mn doped ZnO nanocrystals increase slightly with increasing Mn concentration. The average crystalline size of pure and Mn doped ZnO nanocrystals are in the range of 14-18 nm. The X-ray density for pure and Mn doped ZnO sample is calculated using lattice parameters. It is found that almost static for Mn doped ZnO samples. In the Zn1-xMnx samples, room temperature magnetic hysteresis is observed and the saturation magnetization increases with increasing Mn content. However, these samples show room temperature ferromagnetic in nature. Result of the present investigation compared without PEG.


2019 ◽  
Vol 31 (10) ◽  
pp. 2222-2228
Author(s):  
M. Elayaraja ◽  
I. Kartharinal Punithavathy ◽  
S. Johnson Jeyakumar ◽  
M. Jothibas

A simple and modified chemical precipitation method is used for synthesis of different PEG assisted cadmium oxide nanoparticles. The prepared products were characterized by X-ray diffraction, Fourier transform infrared, ultraviolet, scanning electron microscopy and energy dispersive X-ray analysis. The XRD patterns revealed the cubic phases and calculated particle sizes are 36.42, 34.27, 33.54 and 35.21 nm for pure CdO with 2, 4 and 6 % PEG nanoparticles respectively, From these results, it can be observed that the average crystalline size decreases with increasing PEG concentration. The functional groups and band area of the product were established by FT-IR spectroscopy. The band gap energy of CdO nanoparticles increased from 2.54 to 2.94 eV by increasing PEG concentration .The surface morphology and element composition have been confirmed form SEM with EDX analysis. In addition, the photocatalytic performance of PEG assisted CdO nanoparticles with methylene blue indicated that the CdO can be utilized a good photocatalyst for degradation of methylene blue.


2018 ◽  
Vol 10 (6) ◽  
pp. 224 ◽  
Author(s):  
Manyasree D. ◽  
Kiranmayi P. ◽  
Venkata R Kolli

Objective: In the present study the antibacterial activity of zinc oxide (ZnO) nanoparticles was investigated against gram negative (Escherichia coli and Proteus vulgaris) and gram positive (Staphylococcus aureus and Streptococcus mutans) organisms.Methods: The synthesis of ZnO nanoparticles was carried out by co-precipitation method using zinc sulfate and sodium hydroxide as precursors. These nanoparticles were characterized by XRD (X-Ray Diffraction), FTIR (Fourier Transform Infrared Radiation), UV-Visible spectroscopy and SEM (Scanning Electron Microscope) with EDX (Energy Dispersive X-ray analysis). As well as antibacterial activity and minimum inhibitory concentration of the nanoparticles were carried out by agar well diffusion method and broth dilution method respectively against gram negative (Escherichia coli and Proteus vulgaris) and gram positive (Staphylococcus aureus and Streptococcus mutans) bacteria.Results: The average crystallite size of ZnO nanoparticles was found to be 35 nm by X-ray diffraction. The vibration bands at 450 and 603 cm-1 which were assigned for ZnO stretching vibration were observed in FTIR spectrum. The optical absorption band at 383 nm was obtained from UV-Visible spectrum. Spherical shape morphology was observed in SEM studies. The antibacterial assay clearly expressed that E. coli showed a maximum zone of inhibition (32±0.20 mm) followed by Proteus vulgaris (30±0.45 nm) at 50 mg/ml concentration of ZnO nanoparticles.Conclusion: Zinc oxide nanoparticles have exhibited good antibacterial activity with gram negative bacteria when compared to gram positive bacteria.


2016 ◽  
Vol 846 ◽  
pp. 352-357 ◽  
Author(s):  
Rizuan Mohd Rosnan ◽  
Zulkafli Othaman ◽  
Ali A. Ati ◽  
Rosli Hussin ◽  
Shadab Dabagh ◽  
...  

This study evaluates the structural and magnetic properties of Ni-Mg substituted Cobalt ferrite samples prepared through the co-precipitation method. The nominal compositions Co0.5Ni0.5−xMgx Fe2O4 in the range x = 0.1 have been synthesized and then was sintered at temperature at 700 and 1000°C in the furnace for 10 hour with a heating rate of 5°C/min. The prepared nanoferrites were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and vibration sample magnetometer (VSM). XRD confirmed formation of single phase spinel ferrite with average crystalline size in the range of 27–33 nm. The lattice constant (a), cell volume (V) and X-ray density (ρx) are also calculated from XRD data. Lattice constant (a) decreases with an increase of sintering temperature. Further information about the structure and morphology of the nanoferrites was obtained from FESEM and results are in good agreement with XRD. Saturation magnetization showed increasing trend with sintering temperature from 700 to 1000°C.


2011 ◽  
Vol 9 (2) ◽  
pp. 275-282 ◽  
Author(s):  
Kristina Klemkaite ◽  
Igoris Prosycevas ◽  
Ricardas Taraskevicius ◽  
Alexander Khinsky ◽  
Aivaras Kareiva

AbstractThree layered double hydroxides (LDH) [Mg1−xAlx(OH)2]x+(Am−)x/m]·nH2O and [MII 1−xMIII x (OH)2]x+(Am−)x/m]·nH2O (MII — Mg, Co, Ni; MIII — Al; A — CO3 2−) were successfully synthesized by the low supersaturation method. The as-synthesized LDH samples were thermally decomposed and the derived mixed metal oxides reformed back to layered structures in water and magnesium nitrate media at different temperatures. All synthesized samples were characterized by X-ray diffraction (XRD) analysis, thermogravimetric (TG) analysis, X-ray fluorescence (XRF) analysis and scanning electron microscopy (SEM). The results of XRD and XRF analyses showed that single-phase layered double hydroxides were formed during synthesis and reformation. It was demonstrated, that a partially substituted by cobalt and nickel LDH samples also show memory effect. The crystallite size of regenerated LDH depends on the regeneration media, temperature and chemical composition. The LDH samples after regeneration consist of large particles with sharp edges along with a large amount of smaller particles


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