Biosynthesis, Characterization and Mechanism of Formation of ZnO Nanoparticles Using Petroselinum Crispum Leaf Extract

2020 ◽  
Vol 17 (7) ◽  
pp. 558-566
Author(s):  
Azeez Abdullah Barzinjy ◽  
Samir Mustafa Hamad ◽  
Ahmed Fattah Abdulrahman ◽  
Safiya Jameel Biro ◽  
AbdulBasit Ali Ghafor

Aims: The study aimed at synthesizing ZnO NPs using Petroselinum crispum extract, commonly known as parsley, as a source of biosynthesis without utilizing chemical agents for reducing, capping and stabilizing agent. Background: Recently, the biosynthesis of nanoparticles has been widely explored due to the wide range of vital applications in nanotechnology. Biosynthesized zinc oxide nanoparticles, ZnO NPs, have become increasingly important since they have many applications and are environmentally friendly. Methods: The innovation of this investigation is that the nanosized ZnO NPs can be formed from one-pot reaction without utilizing any external stabilizing and reducing agent which is not plausible via the current procedures. Results: The biosynthesized ZnO NPs were characterized using UV-Vis spectroscopy, FT-IR spectroscopy, X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), Energy-dispersive X-ray spectroscopy (EDX) to investigate the optical, chemical, structural, and morphological properties. Conclusion: These techniques exhibited that the property of the biosynthesized ZnO NPs is analogous with the standard NPs prepared from dissimilar methods. Investigating the plausible mechanism of formation and stabilization of ZnO NPs by biomolecules of Petroselinum crispum leaf extract was another vital feature of this study.

Author(s):  
Selma M.H. AL-Jawad ◽  
Zahraa S. Shakir ◽  
Duha S. Ahmed

ZnO/MWCNTs hybrid and doped with different concentration of Nickel element prepared by using Sol-gel been technique reported. All samples were prepared and characterized by X-Ray Diffraction Analysis (XRD), Energy Dispersive X-ray Spectroscopy (EDS), Fourier-Transform Infrared Spectroscopy (FTIR), Field-Emission Scanning Electron Microscopy (FE-SEM), and UV-Vis spectroscopy have been identified the structural, optical and morphological properties. X-ray diffraction showed the polycrystalline nature with hexagonal wutzite structure of hybrid and doped with Nickel. The crystalline size of the hybrid nanostructure was increasing from 23.73 nm to 34.59 nm. Besides, the UV-Vis spectroscopy showed a significant decrease in the band gap values from 2.97 eV to 2.01 eV. Whereas the FE-SEM analysis confirm the formation spherical shapes of ZnO NPs deposited on cylindrical tubes representing the MWCNTs. The antibacterial activity reveals that the inhibition zone of Ni doped-ZnO/MWCNTs hybrid was 28.5 mm, 26.5 mm toward E. coli and S. aureus bacteria, respectively.


2021 ◽  
Author(s):  
Santanu Maity ◽  
P.P Sahu ◽  
Tiju Thomas

Abstract ZnO nanostructures are promising for a wide range of applications, including gas sensors. Ethanol sensing using ZnO remains unexplored though. In this paper, we report ethanol-sensing using un-doped ZnO nano flowers and Mg doped ZnO nano flowers. These are grown using a rather simple chemo-thermal process, making this a plausibly scalable technology. To study the structural and morphological properties of undoped ZnO and Mg doped ZnO nanoflowers, Raman spectroscopy, Fourier Transform Infrared Spectroscopy (FTIR), x-ray diffraction and Field Emission Scanning Electron Microscopy (FESEM) are carried out. Ethanol sensing properties of undoped ZnO and Mg doped ZnO nanoflower devices are investigated toward different ethanol concentration (concentration range of 1–600 ppm at 100°C–200°C). Our findings show that 15% Mg doped ZnO nano flower is better than ZnO nano flower for ethanol gas-sensing applications.


2016 ◽  
Vol 8 (1) ◽  
pp. 1523-1532 ◽  
Author(s):  
Sujata D Wangkheirakpam ◽  
Wangkheirakpam Radhapiyari Devi ◽  
Chingakham Brajakishore Singh ◽  
Warjeet S Laitonjam

The leaf extract of Strobilanthes flaccidifolius Nees. was used for the synthesis of silver nanoparticles through a green technique of synthesis. The nanoparticles was characterized by UV-VIS spectroscopy which proves the formation silver nanoparticles. FTIR (Fourier Transmission infra red spectroscopy) study was carried out to assess the biomolecule as indigo precursors, Energy dispersion X-ray analysis(EDX) data further proves it. EPR (Electron paramagnetic resonance technique) shows the free radical in silver neutral state and XRD(X-ray diffraction technique) also repots silver neutral formation.The morphology and the shape of the silver nanoparticles were determined by Scanning electron microscopy(SEM) and Tunneling electron microscopy (TEM).The nanoparticles adopted spherical morphology and the size ranging from 6nm to 54.11nm and average size was determined as 12.15± 5.3nm.The nanoparticles had antimicrobial activity


Author(s):  
M Karthikeyan ◽  
A Jafar Ahamed ◽  
P Vijaya Kumar

The present investigation, the successful preparation of pure ZnO (Z1) NPs and SrBa dual doped ZnO (Z2) NPs by chemical co-precipitation technique without use of any capping agent. The structural and morphological properties of Z1 and Z2 NPs were analyzed using X-ray diffraction (XRD) studies, Field emission scanning electron microscopy (FESEM), Elemental analysis (EDAX), Fourier transform infrared spectroscopy (FTIR). An optical property was studied by UV–Vis spectroscopy and Photoluminescence (PL) spectra. The antimicrobial activity of Z1 and Z2 NPs has been investigated against Staphylococcus aureus and Klebsiella pneumoniae bacterial strains. It has been interestingly observed that Z2 NPs has enhanced the inhibitory activity than that of Z1 NPs against S. aureus and more efficiently than the K. pneumoniae bacterial strain.


2020 ◽  
Vol 76 (1) ◽  
pp. 37-43
Author(s):  
Zhi-Qiang Shi ◽  
Ning-Ning Ji ◽  
Hai-Liang Hu

By employing the conjugated bithiophene ligand 5,5′-bis(1H-imidazol-1-yl)-2,2′-bithiophene (bibp), which can exhibit trans and cis conformations, two different CuII coordination polymers, namely, poly[[μ-5,5′-bis(1H-imidazol-1-yl)-2,2′-bithiophene-κ2 N:N′](μ2-4,4′-oxydibenzoato-κ2 O:O′)copper(II)], [Cu(C14H8O5)(C14H10N4S2)] n or [Cu(bibp)(oba)] n , (I), and catena-poly[μ-aqua-bis[μ-5,5′-bis(1H-imidazol-1-yl)-2,2′-bithiophene-κ2 N:N′]bis(μ3-4,4′-oxydibenzoato)-κ3 O:O′:O′′;κ4 O:O′,O′′:O′-dicopper(II)], [Cu2(C14H8O5)2(C14H10N4S2)(H2O)] n or [Cu2(bibp)(oba)2(H2O)] n , (II), have been prepared through one-pot concomitant crystallization and characterized by single-crystal X-ray diffraction, IR spectroscopy, elemental analysis, powder X-ray diffraction (PXRD) and thermogravimetric (TG) analysis. Single-crystal X-ray diffraction indicates that the most interesting aspect of the structure is the existence of sole trans and cis conformations of the bibp ligand in a single net of (I) and (II), respectively. Compound (I) displays a threefold interpenetrating three-dimensional framework with a 4-connected {65.8} cds topology, whereas (II) features a one-dimensional chain structure. In the crystal of (II), the polymeric chains are further extended through C—H...O hydrogen bonds and C—H...π interactions into a three-dimensional supramolecular architecture. In addition, strong intramolecular O—H...O hydrogen bonds formed between the bridging water molecules and the carboxylate O atoms improve the stability of the framework of (II). Furthermore, solid-state UV–Vis spectroscopy experiments show that compounds (I) and (II) exhibit optical band gaps which are characteristic for optical semiconductors, with values of 2.70 and 2.26 eV, respectively.


2020 ◽  
Vol 9 (1) ◽  
pp. 469-476
Author(s):  
Hong Yu ◽  
Yingmei Mu ◽  
Lianzhi Mu

AbstractThis study showed the fabrication of gold nanoparticles (AuNPs) utilizing Erythrina senegalensis leaf extract as an effective, low-cost and eco-friendly approach. The bioconstituents existing in the E. senegalensis leaf extract are accountable for reducing and stabilization of NPs. The produced AuNPs were studied by using transmission electron microscopy, X-ray diffraction, UV-visible (UV-Vis) spectroscopy, Fourier transform infrared spectroscopy and energy-dispersive X-ray spectroscopy. In addition, this study also showed that the prepared AuNPs exhibited very good antipneumonial activity against mycoplasmal pneumonia in the investigational animals, indicating their potential for the development of new therapeutic drugs for the lung injury treatments in in the future.


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.


1961 ◽  
Vol 5 ◽  
pp. 276-284
Author(s):  
E. L. Moore ◽  
J. S. Metcalf

AbstractHigh-temperature X-ray diffraction techniques were employed to study the condensation reactions which occur when sodium orthophosphates are heated to 380°C. Crystalline Na4P2O7 and an amorphous phase were formed first from an equimolar mixture of Na2HPO4·NaH2PO4 and Na2HPO4 at temperatures above 150°C. Further heating resulted in the formation of Na5P3O10-I (high-temperature form) at the expense of the crystalline Na4P4O7 and amorphous phase. Crystalline Na5P3O10-II (low-temperature form) appears after Na5P3O10-I.Conditions which affect the yield of crystalline Na4P2O7 and amorphous phase as intermediates and their effect on the yield of Na5P3O10 are also presented.


Materials ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1786
Author(s):  
Carla Queirós ◽  
Chen Sun ◽  
Ana M. G. Silva ◽  
Baltazar de Castro ◽  
Juan Cabanillas-Gonzalez ◽  
...  

The development of straightforward reproducible methods for the preparation of new photoluminescent coordination polymers (CPs) is an important goal in luminescence and chemical sensing fields. Isophthalic acid derivatives have been reported for a wide range of applications, and in addition to their relatively low cost, have encouraged its use in the preparation of novel lanthanide-based coordination polymers (LnCPs). Considering that the photoluminescent properties of these CPs are highly dependent on the existence of water molecules in the crystal structure, our research efforts are now focused on the preparation of CP with the lowest water content possible, while considering a green chemistry approach. One- and two-dimensional (1D and 2D) LnCPs were prepared from 5-aminoisophthalic acid and Sm3+/Tb3+ using hydrothermal and/or microwave-assisted synthesis. The unprecedented LnCPs were characterized by single-crystal X-ray diffraction (SCRXD), powder X-ray diffraction (PXRD), Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM), and their photoluminescence (PL) properties were studied in the solid state, at room temperature, using the CPs as powders and encapsulated in poly(methyl methacrylate (PMMA) films, envisaging the potential preparation of devices for sensing. The materials revealed interesting PL properties that depend on the dimensionality, metal ion, co-ligand used and water content.


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