scholarly journals Fractal Dimension Calculation of a Manganese-Chromium Bimetallic Nanocomposite Using Image Processing

2015 ◽  
Vol 2015 ◽  
pp. 1-9
Author(s):  
Amir Lashgari ◽  
Shahriar Ghamami ◽  
Saeedeh Shahbazkhany ◽  
Guillermo Salgado-Morán ◽  
Daniel Glossman-Mitnik

Bimetallic materials, which have the ability to convert heat change into mechanical movement, normally consist of two bonded strips of dissimilar metals that expand at different rates. We describe how we made a manganese-chromium (Mn-Cr) bimetallic nanocomposite using the centrifuge method and a low-to-high approach. We conducted scanning electron microscope (SEM) imaging, energy-dispersive X-ray spectroscopy (EDX) analysis, and X-ray diffraction spectra of the nanocomposite to prove its identity. We examined how centrifuge speed, process time, and the use of an “intruder agent” affected the properties of the material. The fractal dimension is a significant factor that can be used to approximate the surface roughness, the texture segmentation, and an image of the studied compounds. We calculated the technique of fractal dimensions using image-processing values on a computer and histogram plot with the SEM image of the Mn-Cr bimetallic nanocomposite using MATLAB software. We applied the Statistical Package for the Social Sciences software for statistics data extracted from the SEM image of the nanocomposite and obtained the following results: mean = 1.778, median = 1.770, max = 1.98, min = 1.60, skewness = 0.177, range = 0.38, and harmonic mean = 1.771 for fractal dimension of the SEM image.

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.


2011 ◽  
Vol 675-677 ◽  
pp. 1025-1029
Author(s):  
Hui Zhang ◽  
Xiao Meng Lü ◽  
Jian Lin Ding ◽  
Ji Min Xie ◽  
Chang Hao Yan

Using Y2O3, Mn(CH3COO)2·4H2O as raw materials and glacial acetic acid as solvents, YMnxFe1-xO3 precursors (x= 0, 0.05, 0.1, 0.3, 0.5) have been prepared under 80°C water bath conditions. Perovskite YMnxFe1-xO3 samples were achieved after calcination over 900 °C for 4 h. Structure of the samples was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Ultraviolet obvious diffuse reflection(UV-vis DRS), and Field-emission scanning electron microscopy (FESEM). Photocatalytic activity of the samples was also investigated. Results showed that all the samples with stable perovskite structure had high light absorption in visible-light region, suggesting good visible light harvesting. SEM image showed that the samples were sponge-like and porous agglomerates. Photodecoloration activity of 100 mL Rhodamine B (10 mg/L) was 16~56 % under illumination for 150 min. Oxygen vacancies of the perovskite may explain the high activity of x = 0.1 sample.


2008 ◽  
Vol 55-57 ◽  
pp. 645-648
Author(s):  
Phathaitep Raksa ◽  
A. Gardchareon ◽  
N. Mangkorntong ◽  
Supab Choopun

CuO nanostructures were synthesized by oxidizing copper thin films. The copper thin film was grown on alumina substrates by evaporation copper powder at pressure of 0.04 mtorr. The copper thin films were then oxidized 800, and 900oC for 12, 24 and 48 hr, respectively. The obtained CuO nanostructures were investigated by Energy Dispersive Spectroscopy (EDS), Field Emission Scanning Electron Microscope (FE-SEM) image, and X-Ray Diffraction (XRD). The diameter of CuO nanostructure is around 100-600 nanometers and it is depends on oxidation reaction time and temperature. These CuO nanostructures have a potential application for nanodevices such as nano gas sensor or dye-sensitized solar cells.


Catalysts ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 817 ◽  
Author(s):  
A. Luna-Flores ◽  
M.A. Morales ◽  
R. Agustín-Serrano ◽  
R. Portillo ◽  
J.A. Luna-López ◽  
...  

In this work, a novel route is discussed to produce in one step ZnO/Burkeite powders by the modified solution combustion method. The ZnO particles enhance the photocatalytic activity in the degradation of Rhodamine B, in which Burkeite mineral acts as a support due to the pH-dependent morphology of the particle aggregates of the as-synthesized powders. The X-ray diffraction (XRD) characterization shows the presence of a heterostructure: ZnO/Burkeite. The Scanning Electron Microscopy (SEM) image shows a morphological dependence with the pH of the solution used for the synthesis. The results show that the system with the highest degradation (92.4%) corresponds to the case in which ZnO/Burkeite heterostructure was synthesized with a pH 11.


Materials ◽  
2019 ◽  
Vol 12 (14) ◽  
pp. 2338 ◽  
Author(s):  
Jinwei Yao ◽  
Jiankang Chen ◽  
Chunsheng Lu

Sulfate attack tests were performed on concrete samples with three water-to-cement ratios, and micro-crack growth patterns on concrete surfaces were recorded. The expansive stress and crack nucleation caused by delayed ettringite formation (DEF) were studied using X-ray diffraction and scanning electron microscopy. By means of a digital image processing technology, fractal dimensions of surface cracking patterns were determined, which monotonously increase during corrosion. Moreover, it is shown that the change of fractal dimensions is directly proportional to accumulation of DEF, and therefore, a simple theoretical model could be proposed to describe the micro-crack evolution in concretes under sulfate attack.


2020 ◽  
Vol 13 ◽  
pp. 117862212093212
Author(s):  
Neway Belachew ◽  
Redeat Fekadu ◽  
Amare Ayalew Abebe

In this work, we have reported a low-cost and environmentally friendly Fe3O4-modified activated kaolin (AK-Fe3O4) composite for efficient Fenton-like degradation of 4-nitrophenol (4-NP) and optimization of the degradation variables. The AK-Fe3O4 composites were characterized by Fourier transform infrared spectroscopy, powder x-ray diffraction, scanning electron microscopy (SEM), and vibrating sample magnetometer (VSM). X-ray diffraction confirms the syntheses of pure phases of Fe3O4 and AK-Fe3O4. The SEM image of the AK-Fe3O4 composite reveals the formation of a highly porous surface. The room temperature VSM analysis describes the superparamagnetic nature of AK-Fe3O4 composites with 25 emu/g magnetization values. Response surface methodology coupled with Box-Behnken design was used to optimize the 4-NP degradation (%) variables such as contact time (10-90 minutes), 4-NP concentration (10-30 mg/L), and pH (3-8). The high regression value ( R² = 0.9964 and adjusted R² = 0.9917) and analysis of variance ( P < .0001) show that the quadratic model can sufficiently explain the 4-NP degradation (%). The optimum 4-NP degradation was found to be 96.01% ± 1.89% using 1 mg/mL of AK-Fe3O4, 20 mg/L of 4-NP, 97.9 mmol/L of H2O2, and pH of 3 at the end of 75 minutes of reaction time. Moreover, the catalyst shows good recyclability and stability after 5 successive degradations of 4-NP. In general, a low-cost and magnetically separable AK-Fe3O4 composite is an effective Fenton-like catalyst for the degradation of 4-NP.


MAPAN ◽  
2013 ◽  
Vol 28 (4) ◽  
pp. 327-333
Author(s):  
Udomchok Phromsuwan ◽  
Yaowarat Sirisathitkul ◽  
Chitnarong Sirisathitkul ◽  
Paisarn Muneesawang ◽  
Bunyarit Uyyanonvara

2013 ◽  
Vol 829 ◽  
pp. 912-916 ◽  
Author(s):  
Alireza Khanaki ◽  
Hossein Abdizadeh ◽  
Mohammad Reza Golobostanfard

Nanocrystalline CuInSe2 (CIS) powders were synthesized with a simple open-air solvothermal method as well as under conditions of applying internal imposed pressure. No post-treating processes such as annealing or selenization were used in both methods. The synthesis processes involved the reaction of precursors in an autoclave for different process times. Structural, morphological, and opto-electronic properties of CIS powders were compared. X-ray diffraction patterns (XRD) confirmed the formation of chalcopyrite structure of CIS powders in both approaches at reaction temperature of 220 °C and for short process time. Field emission scanning electron microscopy (FESEM) results show that while CIS powders synthesized under the atmospheric condition are mostly agglomerated, particles have more specific shapes in samples synthesized under internal imposed pressure. Furthermore, the band gap energies of synthesized CIS powders were obtained using diffuse reflectance UV-vis spectroscopy (DRS) measurements.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Qingfeng Sun ◽  
Yun Lu ◽  
Jinchun Tu ◽  
Dongjiang Yang ◽  
Jun Cao ◽  
...  

We report a bulky macroporous TiO2particles with cellular structure prepared in the presence of wood slices as template. Firstly, TiO2sol was coated onto the wood slices by repeated dip-coating process. Then, after calcinations at 550°C, the wood template could be removed, and the bulky TiO2structure was obtained. The prepared samples were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersive spectroscopy (EDS), and transmission electron microscope (TEM) techniques. XRD pattern confirmed the crystalline phase of the wood-templated TiO2is anatase phase. And interestingly, from the observation of SEM image, the wood-templated TiO2inherited the initial cellular structures of birch lumber (B. albosinensis Burk), and numerous macropores were observed in the sample. Meanwhile, the wood-templated TiO2presented a superior photocatalytic ability to decompose Rhodamine B (RhB) under ultraviolet irradiation.


2011 ◽  
Vol 364 ◽  
pp. 500-503 ◽  
Author(s):  
S. J. Kasim ◽  
F. H. Khaleel ◽  
F. A. Kasim ◽  
M.A. Mahdi

Ag2S nanorods and nonoparticles have been successfully prepared using chemical method. Silver nitrate with molar concentration of 0.1 M and thiourea with different molar concentration were used as a source of Ag++and S++ions, respectively. The pH of solution was in range of 10-11. Scanning electron microscopy (SEM) image showed that the nanorods length and diameter were 2.5-3 μm and 300-400 nm, respectively. X-ray diffraction results showed a monoclinic α-Ag2S phase was obtained. The atomic ratio of silver and sulphur were found using energy dispersive spectroscopy (EDS) and it was 62.39% and 37.61%, respectively.


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