scholarly journals Synthesis of Nanocrystalline Cellulose Stabilized Copper Nanoparticles

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Aminu Musa ◽  
Mansor B. Ahmad ◽  
Mohd Zobir Hussein ◽  
Saiman Mohd Izham ◽  
Kamyar Shameli ◽  
...  

A chemical reduction method was employed for the synthesis of copper nanoparticles stabilized by nanocrystalline cellulose (NCC) using different concentrations of copper salt in aqueous solution under atmospheric air. CuSO4·5H2O salt and hydrazine were used as metal ion precursor and reducing agent, respectively. Ascorbic acid and aqueous NaOH were also used as an antioxidant and a pH moderator, respectively. The number of CuNPs increased with increasing concentration of the precursor salt. The formation of copper nanoparticles stabilized by NCC (CuNPs@NCC) was investigated by UV-visible spectroscopy (UV-vis), where the surface absorption maximum was observed at 590 nm. X-ray diffraction (XRD) analysis showed that the CuNPs@NCC are of a face-centered cubic structure. Moreover, the morphology of the CuNPs@NCC was investigated using transmission electron microscope (TEM) and field emission scanning electron microscope (FESEM), which showed well-dispersed CuNPs with an average particle size less than 4 nm and the shape of CuNPs was found to be spherical. Energy dispersive X-ray spectroscope (EDS) also confirmed the presence of CuNPs on the NCC. The results demonstrate that the stability of CuNPs decreases with an increasing concentration of the copper ions.

2005 ◽  
Vol 879 ◽  
Author(s):  
Chunwei Wu ◽  
Brian P. Mosher ◽  
Taofang Zeng

AbstractIn this paper, we describe a simple and rapid solution-phase chemical reduction method with no inert gas protection, for preparing stable copper nanoparticle colloid with average particle size of 3.4 nm and narrow size distribution. In our synthesis route, ascorbic acid, natural vitamin C (VC), serves as both a reducing agent and an antioxidant to reduce copper salt precursor and effectively prevent the general oxidation process occurring to the newborn nanoparticles. XRD and UV/vis confirm the formation of pure face-centered cubic (fcc) copper nanoparticles and the excellent antioxidant ability of ascorbic acid.


2018 ◽  
Vol 238 ◽  
pp. 02002
Author(s):  
Fangjing Sun ◽  
Yi Zhang ◽  
Jiawei Zhang ◽  
Xixi Yan ◽  
Xiaoyu Liu ◽  
...  

In this experiment, ultrafine iron phosphate micro-powder was prepared by hydrothermal method which used phosphate slag as an iron source. The effects of reaction temperature, surfactants type and amount on its particle size were explored. The samples were characterized by using Malvern Laser Particle Size Analyzer (MS2000), X-Ray Diffractometer (XRD), Scanning Electron Microscope (SEM) and Energy Dispersive X-Ray Spectroscopy (EDX).The results showed that at 160 °C, 1 wt%CTAB, monoclinic iron phosphate micro-powder was obtained with an average particle size about 0.4 μm which also has a good dispersion in aqueous solution.


2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Malathi Sampath ◽  
Ramya Vijayan ◽  
Ezhilarasu Tamilarasu ◽  
Abiraman Tamilselvan ◽  
Balasubramanian Sengottuvelan

Novel jasmine bud-shaped copper nanoparticles were synthesized by a green chemical reduction method using polyvinylpyrrolidone (PVP) as a capping agent, L-ascorbic acid (AA) as a reducing agent as well as antioxidant agent, isonicotinic acid hydrazide (INH) as a reducing agent, and water as a solvent at 60–70°C (pH-7) in the presence of air. The UV-Vis absorption maximum obtained is 573 nm. The crystal lattice (fcc) structure of Cu Nps was confirmed by X-ray diffraction (XRD). The novel jasmine bud shape was visualized in a transmission electron microscope (TEM). The height of single copper nanobud was 6.41 nm as measured by atomic force microscope (AFM). The average particle size 6.95 nm is obtained by XRD results. Antibacterial activity of the Cu nanobuds was evaluated by testing against Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria.


2015 ◽  
Vol 1107 ◽  
pp. 301-307 ◽  
Author(s):  
Salahudeen A. Gene ◽  
Elias B. Saion ◽  
Abdul Halim Shaari ◽  
Mazliana A. Kamarudeen ◽  
Naif Mohammed Al-Hada

The fabrication of nanospinel zinc chromite (ZnCr2O4) crystals by the means of thermal treatment method from an aqueous solution containing metal nitrates, polyvinyl pyrrolidone (PVP), and deionized water was described in this study. The samples were calcined at various temperatures ranging from 773 to 973 K for the decomposition of the organic compounds and crystallization of the nanocrystals. PVP was used as capping agent to control the agglomeration of the particles. The characterization studies of the fabricated samples were carried out by X-ray diffraction spectroscopy (XRD), transmission electron microscopy (TEM), energy dispersed X-ray spectroscopy (EDX) and electron spin resonance spectroscopy (ESR). The corresponding peaks of Zn, Cr and O were observed in the EDX spectrum of the sample which confirms the formation of ZnCr2O4. The XRD patterns also confirmed the formation of the single faced nanocrystallines of spinel ZnCr2O4 with a face-centered cubic structure. The average particle size of the synthesized crystals was also determined from the XRD patterns using the Scherers formula which shows that the crystallite sizes increases with increase in calcination temperature and was in good agreement with the TEM images which shows cubical ZnCr2O4 nanocrystals with uniform morphology and particle size distributions. The ESR spectra confirmed the existence of unpaired electron in the fabricated samples and the increase in g-factor and decreases in resonant magnetic field (Hr) were observed as the calcination temperature increases.


2019 ◽  
Vol 11 (11) ◽  
pp. 1064-1070 ◽  
Author(s):  
Nkosinathi G. Dlamini ◽  
Albertus K. Basson ◽  
V. S. R. Rajasekhar Pullabhotla

Bioflocculant from Alcaligenis faecalis HCB2 was used in the eco-friendly synthesis of the copper nanoparticles. Nanoparticles were characterized using a scanning electron microscope (SEM), transmission electron microscopy (TEM), UV-visible spectroscopy, thermo gravimetric analysis (TGA) and Fourier Transform Infrared Spectroscopy (FT-IR). The transmission electron microscopy images showed close to spherical shapes with an average particle size of ∼53 nm. Energy-dispersive X-ray spectroscopy analysis confirmed the presence of the Cu nanopartilces and also the other elements such as O, C, P, Ca, Cl, Na, K, Mg, and S originated from the bioflocculant. FT-IR results showed the presence of the –OH and –NH2 groups, aliphatic bonds, amide and Cu–O bonds. Powder X-ray diffraction peaks confirmed the presence of (111) and (220) planes of fcc structure at 2 of 33° and 47° respectively with no other impurity peaks.


2011 ◽  
Vol 299-300 ◽  
pp. 722-726
Author(s):  
Wen Chang Zhuang ◽  
Yu Xiao Wang

Composites have achieved much attention because of their excellent qualities. Core-shell γ-Fe2O3/Au nanoparticles were prepared by chemical reduction. Their optical properties and morphology were characterized by UV-visible spectrum (UV-vis), X-ray diffraction (XRD) and Transmission Electronic Microscopy (TEM). Furthermore, the average particle size and interface structure were also analyzed using small angle X-ray scattering (SAXS).


2020 ◽  
Vol 98 (2) ◽  
pp. 79-89 ◽  
Author(s):  
Amina Ramdani ◽  
Zoubida Taleb ◽  
Abdelkrim Guendouzi ◽  
Abdelkader Kadeche ◽  
Hayat Herbache ◽  
...  

In this study, low-cost biomaterial hydroxyapatite (N-Hap) prepared from bovine bones was tested for its potential to sorb copper Cu2+ and Fe3+ from aqueous solution and was compared with commercial hydroxyapatite (C-Hap). The structural characterization of N-Hap and C-Hap were carried out by Fourier transform infrared (FTIR) analysis, textural analysis (BET), morphology, and elemental analysis via scanning electron microscopy (SEM-EDX). The results obtained show that SEM images confirmed the formation of porous N-Hap with various morphologies and the average particle size ranges from 50 to 100 nm and the CaP ratio is 1.657. The presence of functional groups on N-Hap surface was confirmed by FTIR analysis. The specific surface areas of N-Hap and C-Hap are found to be 46.87 and 40.98 m2/g, respectively. Adsorption of two metals Cu2+ and Fe3+ was fast, with equilibrium attained within 30 min. Copper ions exhibited the greatest adsorption on both adsorbents because of their size and pH conditions. Metallic ion removal efficiency was favored at a slightly acidic solution pH and low temperature. The equilibrium and kinetic data were found to fit well the Langmuir model and the pseudo second order model with intraparticle diffusion. Thermodynamic parameters (ΔHads < 0 and ΔGads < 0) involved the exothermic, spontaneous, and physical adsorption process. The adsorption interaction of Cu2+ and Fe3+ with Hap surface was investigated by theoretical density functional theory (DFT) calculations. Therefore, the porous hydroxyapatite N-Hap displays potential as a new biocompatible adsorbent, and its use seems to be an interesting solution for the treatment of industrial wastewater.


2013 ◽  
Vol 860-863 ◽  
pp. 835-838
Author(s):  
Zhong Xu Dai ◽  
Dan Ni Tian ◽  
Xin Zhang ◽  
Si Lin Gong ◽  
Chang Ying Yang

To investigate the influence of ethanol catalyzed oxidation on activity of Pd/C with different ratio of Pd and C. Pd/C catalyst samples with Pd loads of 20, 30, 40 and 50 wt% were obtained by chemical reduction reaction of PdCl2 and NaBH4. The samples morphology and structure were characterized by XRD and SEM. The electrocatalytic oxidation activities of ethanol were examined by cyclic voltammetry in alkaline media. The results show that a face centered cubic (FCC) Pd phase can be identified in the sample powders. The average particle size of the Pd/C powder is about 10 nm. The performance of ethanol oxidation on 40 % Pd/C electro-catalyst is better than that of the other Pd/C samples.


2021 ◽  
Author(s):  
C. Nirmala ◽  
M Srid

Abstract Endophyte mediated nanoparticles fabrication was emerging as a new frontier in nanomedicines that produce high biocompatible and functionalized silver nanoparticles. In this study, silver nanoparticles were successfully biosynthesized from the extracellular extract of endophytic bacterium Pantoea anthophila isolated from the stem of Waltheria indica for the first time. The synthesised nanoparticles were characterized by UV-Visible and Fourier Transform Infra-Red spectroscopy. The structural analysis is done by X-ray diffraction and the stability was studied by dynamic light scattering and particle size analyser. The size and shape were observed by Transmission Electron Microscope, Scanning Electron Microscope and Energy Dispersive X-Ray spectrum. Further, the nanoparticles were evaluated for antimicrobial and antioxidant properties. Synthesized nanoparticle showed a strong absorption band in the UV-Visible range at 410 nm. The average particle size was found to be 16.8 nm with spherical shaped, crystalline nature. Good zones of inhibition at various ranges were detected against a broad range of human pathogenic bacteria and fungi. A strong free radical scavenging activity of silver nanoparticles with IC50 values 30.75, 19.47, 34.59, 41.12, 27.24, 28.16, 36.21 µg/ml was obtained that was comparable to the reference. The study suggests that the silver nanoparticles can be biosynthesised from endophytic P. anthophila metabolites with significant therapeutic potential. With proper validation, the biosynthesised silver nanoparticles can be developed as a promising antiviral and anticancer drug candidate.


2021 ◽  
Vol 9 (3) ◽  
pp. 220-226
Author(s):  
Bishow Regmi ◽  
Tirtha Raj Binadi ◽  
Sarb Narayan Jha ◽  
Rajib Kumar Chaudhary ◽  
Bhoj Raj Poudel ◽  
...  

Silver nanoparticles (AgNPs) have been synthesized by green synthesis using Azadirachta indica leaf extract as both reducing and stabilizing agent. Synthesis of colloidal AgNPs was monitored by UV- visible spectroscopy. The UV- visible spectrum showed a peak at 455 nm corresponding to the plasmon absorbance of the silver nanoparticles. Crystallite structure of silver nanoparticles was studied using X-ray diffraction (XRD) analysis which revealed the face-centered cubic structure (FCC) with average particle size of 8.9 nm, calculated using Debye-Scherrer’s equation. Transmission electron microscopy (TEM) image revealed the agglomeration of small grain with particle size ranging from 2 to 14 nm. FCC crystalline nature was also evident from selected area electron diffraction (SAED) analysis. High purity of as-synthesized AgNPs was analyzed using energy dispersive X-ray (EDX) spectroscopy. Band gap energy was calculated to be 2.7 eV from UV- Visible spectra. 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay was stabilized by AgNPs which reveals its antioxidant efficacy. Well diffusion method showed 7 mm to 12 mm zone of inhibition (ZOI) against Gram-positive and Gram-negative bacteria, respectively confirming the antibacterial potential of AgNPs. Int. J. Appl. Sci. Biotechnol. Vol 9(3): 220-226.


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