scholarly journals Synthesis and Characterization of Black Currant Selenium Nanoparticles (Part I)

2020 ◽  
Vol 44 (2) ◽  
pp. 25-34
Author(s):  
Masar J. Al-Kurdy

The present study aimed to synthesize selenium nanoparticles (SeNPs) using aqueous extract of black currant as a reducing agent. The green synthesized black currant selenium nanoparticles (BCSeNPs) were identified by color change. The characterization of SeNPs was achieved by Ultraviolet-visible (UV–VIS) spectroscopy, scanning electron microscopy (SEM), X–ray diffraction analysis (XRD), and Fourier transform infrared spectroscopy (FTIR). These tests were used to detect: stability, morphology, size, crystalline nature, and functional groups present on the surface of BCSeNPs. The results revealed appearance of the brick-red color indicating the specific color of selenium nanoparticles, and UV-Vis spectroscopy showed band absorbance at 265 nm of intense surface plasmon resonance manifesting the formation and stability of the prepared BCSeNPs. The SEM image showed the prevalence of spherical selenium nanosized, XRD at 2θ revealed crystallin selenium nanoparticles, the size was in the average of 18-50 nm. Furthermore, FTIR revealed the presence of functional groups of the plant which act as stabilizing and reducing agents. In conclusion, the aqueous black currant extract can act as a reducing and capping agent to synthesize BCSeNPs in nano-scale size by a simple method

2020 ◽  
Vol 1 (1) ◽  
pp. 51-58
Author(s):  
Sharmila Pradhan ◽  
Rajeswori Shrestha ◽  
Khuma Bhandari

This research is focused on bio-synthesis of Copper nanoparticles (CuNPs) using lemon extract to study the effect of various parameters on synthesis and to explore antibacterial activity. The biomolecules present in lemon extract act as self reducing and stabilizing agent. The synthesis of CuNPs was found to be affected by various parameters like volume of the lemon extract, concentration of the precursor and the temperature etc. Preliminary characterization of formation of nanoparticles were done by color change and UV-visible (UV-vis) spectroscopy. Elemental composition of the prepared sample was determined via Energy Dispersive X-ray (EDX) Spectroscopy. Presence of important functional groups associated with biomolecules is well characterized by Fourier Transform Infrared spectroscopy (FTIR). Scanning Electron Microscopy (SEM ) revealed the formation agglomerated CuNPs of different shape and sizes and the X-ray diffraction pattern showed the formation of purely crystalline nature of CuNPs. Finally, agar well diffusion method showed that CuNPs have potential antibacterial activity against Gram-ve bacteria compared to Gram +ve bacteria.


2015 ◽  
Vol 1088 ◽  
pp. 91-95
Author(s):  
Ping Li ◽  
Shan Huang ◽  
Hong Cheng Pan

This article presents a simple method for fabrication of Au-CdS composite thin films onto indium-tin-oxide (ITO) coated glass substrates. The method starts with electrodeposition of CdS thin films onto ITO substrates and followed by spontaneous growth of Au nanoparticles onto the CdS surface in solutions containing AuCl4- ions. X-ray diffraction (XRD) and UV-vis spectroscopy were used to investigate the Au-CdS thin films. The photoelectrochemical property and sensing for Hg2+ ions of the Au-CdS/ITO were studied. The electrode exhibits a low limit of detection of 2.5 μM and a high selectivity for Hg2+ ions, even in the presence of a large excess (1000-fold) of other metal (Na+, K+, Ca2+, Mg2+, Cd2+, Pb2+, and Zn2+) ions.


2015 ◽  
Vol 775 ◽  
pp. 143-146
Author(s):  
Ming Kwen Tsai ◽  
Yueh Chien Lee ◽  
Chia Chih Huang ◽  
Sheng Yao Hu ◽  
Kwong Kau Tiong ◽  
...  

In this work, the CuInS2 nanoparticles are successfully synthesized by microwave-assisted heating technique and further calcined at 400 °C. The morphological, structural, and optical properties of the synthesized CuInS2 nanoparticles are investigated by scanning electron microscope (SEM), X-ray diffraction (XRD), Raman scattering, and transmittance measurement, respectively. The SEM image shows the clear particle shape of the calcined CuInS2 nanoparticles. After calcination treatment, the fundamental (112) peak of the XRD spectrum and a broad Raman peak mixed with chalcopyrite and CuAu structures support the improved crystallinity of the calcined CuInS2 nanoparticles.


Polymers ◽  
2021 ◽  
Vol 13 (24) ◽  
pp. 4364
Author(s):  
Rutaba Amjad ◽  
Bismillah Mubeen ◽  
Syed Shahbaz Ali ◽  
Syed Sarim Imam ◽  
Sultan Alshehri ◽  
...  

The use of biomaterials in the synthesis of nanoparticles is one of the most up-to-date focuses in modern nanotechnologies and nanosciences. More and more research on green methods of producing metal oxide nanoparticles (NP) is taking place, with the goal to overcome the possible dangers of toxic chemicals for a safe and innocuous environment. In this study, we synthesized copper nanoparticles (CuNPs) using Fortunella margarita leaves’ extract, which reflects its novelty in the field of nanosciences. The visual observation of a color change from dark green to bluish green clearly shows the instant and spontaneous formation of CuNPs when the phytochemicals of F. margarita come in contact with Cu+2 ions. The synthesis of CuNPs was carried out at different conditions, including pH, temperature, concentration ratio and time, and were characterized with UV-Vis absorption spectra, scanning electron microscope (SEM) and X-ray diffraction (XRD). The UV-Vis analysis reveals the surface plasmon resonance property (SPR) of CuNPs, showing a characteristic absorption peak at 679 nm, while SEM reveals the spherical but agglomerated shape of CuNPs of the size within the range of 51.26–56.66 nm.


Polymers ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 1498 ◽  
Author(s):  
Abdul Hafeez ◽  
Zareen Akhter ◽  
John F. Gallagher ◽  
Nawazish Ali Khan ◽  
Asghari Gul ◽  
...  

Bis-aldehyde monomers 4-(4′-formyl-phenoxy)benzaldehyde (3a), 3-methoxy-4-(4′-formyl-phenoxy)benzaldehyde (3b), and 3-ethoxy-4-(4′-formyl-phenoxy)benzaldehyde (3c) were synthesized by etherification of 4-fluorobenzaldehyde (1) with 4-hydroxybenzaldehyde (2a), 3-methoxy-4-hydroxybenzaldehyde (2b), and 3-ethoxy-4-hydroxybenzaldehyde (2c), respectively. Each monomer was polymerized with p-phenylenediamine and 4,4′-diaminodiphenyl ether to yield six poly(azomethine)s. Single crystal X-ray diffraction structures of 3b and 3c were determined. The structural characterization of the monomers and poly(azomethine)s was performed by FT-IR and NMR spectroscopic techniques and elemental analysis. Physicochemical properties of polymers were investigated by powder X-ray diffraction, thermogravimetric analysis (TGA), viscometry, UV–vis, spectroscopy and photoluminescence. These polymers were subjected to electrical conductivity measurements by the four-probe method, and their conductivities were found to be in the range 4.0 × 10−5 to 6.4 × 10−5 Scm−1, which was significantly higher than the values reported so far.


2012 ◽  
Vol 31 (6) ◽  
pp. 723-725 ◽  
Author(s):  
Gholamreza Nabiyouni ◽  
Parviz Boroojerdian ◽  
Kambiz Hedayati ◽  
Davood Ghanbari

AbstractLead sulfide nanoparticles were synthesized at room temperature via a simple chemical reaction. In this synthesis, 2-mercaptoethanolwas used as the capping agent and sodium sulfide was used as a sulfur source. The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), ultraviolet-visible (UV-vis) spectroscopy and Fourier transform infrared (FT-IR) spectroscopy Electron microscopy study showed that without using a capping agent the bulk PbS is obtained, while adding the mercaptoethanol leads to production of nanoparticles. We found that the electronic absorption spectra as well as the particle sizes depend on the used capping agents. Two exitonic peaks with a large blue shift were observed when mercaptoethanol was used.


2017 ◽  
Vol 907 ◽  
pp. 56-60
Author(s):  
Ummuhanı Hilal Özer ◽  
Kerim Emre Öksüz ◽  
Ali Özer

It is well known that sol-gel technique is a simple method to produce nano sized ceramic powders. In this study, cerium oxide doped zirconia samples, with 10 mol%-12mol% and14mol% CeO2, were synthesized by sol-gel technique and characterized. The surface morphology, elemental composition, microstructure, and phase analysis, of the sintered CeO2 doped ZrO2 ceramics were characterized by field emission scanning electron microscopy (FE-SEM), energy dispersive X-ray (EDS) analysis, and X-ray diffraction (XRD) respectively. X-ray diffraction for samples sintered at 1550 °C for 4h revealed that the zirconia ceramics have a tetragonal phase structure. The addition of CeO2 can raise the content of the tetragonal phase, but the minor monoclinic phase exists even at the CeO2 content of 10 mol%. The effect of dopant concentration on the lattice parameter, average primary crystallite size and micro-strain was studied. Relative densities for CeO2 doped ZrO2 bulk ceramics varied between 95% and 99 %, depending on the CeO2 addition.


2016 ◽  
Vol 872 ◽  
pp. 81-86 ◽  
Author(s):  
Haji Aripin ◽  
Seitaro Mitsudo ◽  
I Nyoman Sudiana ◽  
Nundang Busaeri ◽  
Bambang Sunendar ◽  
...  

In this paper, we present the synthesis procedure and the results of an investigation of a novel silica xerogel (SX) glass ceramic developed from an amorphous SX derived from sago waste ash that incorporates TiO2 as an additive. The studied compositions have been prepared by adding of either 20% or 80 wt% of TiO2 into SX, respectively. The samples have been dry pressed and sintered in the temperature range between 900°C and 1500°C. Their properties have been characterized on the basis of the experimental data obtained using X-ray diffraction (XRD), Fourier transform infrared (FTIR), and ultraviolet-visible (UV-Vis) spectroscopy. It has been found that an increase of the content of SX in the composition leads to an increase of the shift of the bandgap energy of TiO2. The analysis based on the interpretation of both XRD patterns and FTIR spectrum allows one to explain the shift in the bandgap energy by an enlargement of the crystallite size of TiO2 and by forming of more Si–O–Ti bonds in the samples with a smaller loading of TiO2.


2019 ◽  
Vol 37 (3) ◽  
pp. 304-309
Author(s):  
Azeezaa Varsha Mohammed ◽  
Suresh Sagadevan

AbstractL-cysteine hydrogen fluoride (LCHF) single crystals were grown from aqueous solution. Single crystal X-ray diffraction, FT-IR, UV-Vis-NIR, and TG-DTA were used to test the grown crystals. The specimen dielectric and mechanical behaviors were also studied. Powder X-ray diffraction of the grown crystal was recorded and indexed. The optical properties of the LCHF crystal were determined using UV-Vis spectroscopy. It was found that the optical band gap of LCHF was 4.8 eV. The crystal functional groups were identified using FT-IR. Second harmonic generation (SHG) efficiency of the LCHF was three times higher than that of KDP. The dielectric constant, dielectric loss and AC conductivity were measured at different frequencies and temperatures.


2017 ◽  
Vol 18 (2) ◽  
pp. 34-41
Author(s):  
Fathilah binti Ali ◽  
Long Jiajia ◽  
Wan Wardatul Amani binti Wan Salim

Nanocomposites that consist of diblock copolymer (BCP) and gold nanoparticles (AuNPs) can be applied as a matrix to immobilize enzymes or other molecules based on the well-defined core/shell nanostructures of these composites. In this research, polylactic acid-block-poly(2-vinylpyridine) (PLA-b-P2VP)/hydrogen tetrachloroaurate(III) hydrate (HAuCl4.3H2O) composites were hybridized and then reduced in dichloromethane (DCM) solution. The hybridizations between gold precursors and the P2VP domain were prepared with different ratios of gold to P2VP block (1:1, 1:5, 1:10, 5:1, 10:1) by taking advantage of the association between the long-pair nitrogen of the pyridine group of P2VP. The reduction of the Au3+/PLA-b-P2VP composite was accomplished by hydrazine solution in order to get gold nanoparticle/PLA-b-P2VP composites, which was visually confirmed by a direct color change from bright yellow to purple. In this work, ultraviolet–visible (UV-vis) spectroscopy and Fourier transform infrared spectroscopy (FTIR) were used to confirm the association between gold precursors and pyridine groups as well as the synthesis of gold nanoparticles.The composite which labeled as R3 (Au3+: P2VP = 10:1) showed the highest peak current based on the cyclic voltammetry (CV) measurment. Furthermore, graphene oxide (GO) was added into R3 to prepare BCP/AuNPs/GO composite and reduced to BCP/AuNPs/rGO through electrochemical reduction. The resulting BCP/AuNPs/rGO showed high potential to be used in amperometric biosensor.


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