graphene nanoparticles
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Coatings ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. 91
Author(s):  
Aliah Nursyahirah Kamarudin ◽  
Mohd Mustafa Awang Kechik ◽  
Siti Nabilah Abdullah ◽  
Hussein Baqiah ◽  
Soo Kien Chen ◽  
...  

The development of high-temperature superconductor (HTS) YBa2Cu3O7~δ (Y123) bulks in industrial applications were established years ago. It is one of the developments that currently attracts great attention especially in transportation, superconductor cables and wires. This study is focused on the preparation of the Y123 bulk superconductors by the thermal treatment method due to the promising ways to develop high-quality Y123 superconductors with its simplicity, low cost, and relatively low reaction temperature used during the process. Y123 were added with graphene nanoparticles (x = (0.0–1.0) wt.%). Samples were then characterized by X-ray diffraction (XRD) analysis, field-emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), and alternating current susceptibility (ACS). It was found that Y123 confirmed that the majority of phases in all the XRD patterns was the orthorhombic crystal structure and the Pmmm space group with secondary phases belonged to Y2Ba1Cu1O5 (Y211). The highest Tc obtained when graphene nanoparticles were added in the Y123 sample was x = 1.0 wt.%, followed by x = 0.5 wt.% with 92.64 and 92.59 K, respectively. From the microstructure analysis, the average grain size significantly decreased to 4.754 µm at x = 0.5 wt.%. The addition of graphene nanoparticles had disturbed the grain growth of Y123, affecting the superconducting properties of the samples. On the other hand, the intergranular critical current density, Jcm, was found to increase with graphene nanoparticle addition and had the highest value at x = 1.0 wt.%, indicating that graphene nanoparticles acted as pinning centers in the Y123 matrix.


Surface ◽  
2021 ◽  
Vol 13(28) ◽  
pp. 166-174
Author(s):  
N. V. Sigareva ◽  
◽  
B. M. Gorelov ◽  
S. V. Shulga ◽  
◽  
...  

The participation of the electronic subsystem of graphene nanoparticles in heat transfer on the interfaphase surface with epoxy polymer, its participation in the thermodestruction processes of epoxy matrix and the concentration interval of the subsystem's influence on the thermal destruction of the polymer matrix are investigated. For such purpose, epoxy resin composites with oxidized and non-oxidized graphene nanoparticles have been used.The particles were obtained by electrochemical method and those are characterized by the same dispersion and analogical of defect spectra. The particles have the same crystal structure, however in composites with oxidized graphene, the participation of the electronic subsystem in thermophysical processes on the interfacial surface is blocked by the atomic layer of adsorbed oxygen. Сomposites of epoxy resin filled with the same particles of nonoxidized and oxidized nanoparticles in the filler content 0.0, 1.0, 2.0, and 5.0 wt%. The multilayered graphene particles were studied by X-ray diffraction analysis (XRD) and Raman spectroscopy (RS) methods. It was shown that the graphene particles are the 2D dimensional structures with about of 100 layers. Desorption curves of epoxy and its composites have been obtained using a programmable thermal desorption mass-spectroscopic (TDMS) technique for fragments with 15≤ m/z ≤108 and temperature interval 35 - 800 оС. The activation energy of desorption was determined from the Wigner-Polanyi equation as 35 - 150 kJ/mol, temperature and mass dependences of the quantity of desorbed atomic fragments have been calculated. It were established the graphene electron subsystem takes part in polymer structure thermodestruction for epoxy composites with nonoxidized graphene enhancing their heat resistance at graphene content С ≤ 1 wt%. With increasing filler content, the thermodestruction behavior in pristine epoxy and its composites with nonoxidized and oxidized graphene is analogical. The thermodestruction characterizes by the stepwise variations in the desorption intensity of atomic fragments. The electron subsystem of graphene particles does not participate in the heat resistance variations.


2021 ◽  
Vol 44 ◽  
pp. 103265
Author(s):  
Awatef Abidi ◽  
Muhyaddin Rawa ◽  
Yacine Khetib ◽  
Hatem Faiz Assad Sindi ◽  
Mohsen Sharifpur ◽  
...  

2021 ◽  
Vol 24 (2) ◽  
pp. 121-128
Author(s):  
A. Tammam ◽  
S. Ibrahim ◽  
A. Hemid ◽  
F. Abdel-Azeem ◽  
A. El-Faham ◽  
...  

2021 ◽  
Vol 19 (51) ◽  
pp. 72-78
Author(s):  
Fatima Mikdad Ahmed ◽  
Salma M. Hassan

In this work, chemical oxidation was used to polymerize conjugated polymer "Polypyrrole" at room temperature Graphene nanoparticles were added by in situ-polymerization to get (PPY-GN) nano. Optical and Electrical properties were studied for the nanocomposites. optical properties of the nanocomposites were studied by UV-Vis spectroscopy at wavelength range (200 -800 nm). The result showed optical absorption spectra were normally determined and the result showed that the maximum absorbance wave length at 280nm and 590nm. The optical energy gap has been evaluated by direct transition and the value has decreased from (2.1 eV for pure PPy) to (1.3 eV for 5 %wt. of GN). The optical constants such as the band tail width ΔE was evaluated, the value of ΔE for pure PPy was (0.0949eV) while for 5 wt. % of GN it was (0.5156 eV), It has been observed that the Urbach tail for pure PPy was smaller than that for PPy/GN nanocomposites and it increase as GN concentration increases. The A.C electrical conductivity at range of frequency (103Hz-106Hz) was increased by increasing the frequency and GN concentration about four order of magnitude. The s value was about (0.653-0.962) which means that the mechanism of conductivity is correlated hopping mechanism (C. H. P.). The dielectric constant and dielectric lose were determined and found to decrease with increasing frequency.


2021 ◽  
Vol 10 (23) ◽  
pp. 5560
Author(s):  
Magdalena Wyszyńska ◽  
Monika Nitsze-Wierzba ◽  
Ewa Białożyt-Bujak ◽  
Jacek Kasperski ◽  
Małgorzata Skucha-Nowak

The aim of this work is a review of recent information about halitosis among patients using prosthetic dentures. Halitosis is a condition in which an unpleasant smell comes out of the oral cavity, which is caused mainly by volatile sulfur and non-sulfured compounds. The etiology of halitosis may be intra- or extra-oral; in most patients, however, it is due to the activity of microorganisms in the oral cavity. The problem of the occurrence of halitosis has accompanied patients for many years. In dental prosthetics, the problem of halitosis occurs in patients using removable or fixed dentures. In both cases, new niches for the development of microorganisms may be created, including those related to halitosis. It should be noted that dentures—both fixed and removable—are a foreign body placed in the patient’s oral cavity which, in case of insufficient hygiene, may constitute a reservoir of microorganisms, causing this unpleasant condition. Conventional treatment of intraoral halitosis reduces microbial activity via chemical and/or mechanical action. Currently, the search for new strategies in the treatment of halitosis is in progress. One idea is to use photodynamic therapy, while another is to modify poly(methyl methacrylate) (PMMA) with silver and graphene nanoparticles. Additionally, attempts have been made to combine those two methods. Another unconventional method of treating halitosis is the use of probiotics.


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