scholarly journals Effect of Liquid Ga on Metal Surfaces: Characterization of Morphology and Chemical Composition of Metals Heated in Liquid Ga

2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Eun Je Lee ◽  
Min Goo Hur ◽  
Jeong Mun Son ◽  
Jeong Hoon Park ◽  
Seung Dae Yang

This study investigates the effect of liquid gallium (Ga) on metal foils made of titanium (Ti), niobium (Nb), and molybdenum (Mo). The Ti, Nb, and Mo foils were heated in liquid Ga at 120°C for a maximum of two weeks. After heating, the changes in the morphology and the chemical composition of the metal foils were analyzed by using a field emission scanning electron microscope, energy-dispersive X-ray spectrometer, X-ray diffractometer, and X-ray photoelectron spectrometer. The results of the analysis indicated that the Nb foil showed the minimum adhesion of liquid Ga to the surface while the maximum amount of liquid Ga was observed to adhere to the Ti foil. In addition, the Nb foil was oxidized and the Mo foil was reduced during the heating process. Considering these effects, we conclude that Mo may be used as an alternative encapsulation material for Ga in addition to Nb, which is used as the conventional encapsulation material, due to its chemical resistance against oxidation in hot liquid Ga.

2011 ◽  
Vol 415-417 ◽  
pp. 642-647
Author(s):  
En Zhong Li ◽  
Da Xiang Yang ◽  
Wei Ling Guo ◽  
Hai Dou Wang ◽  
Bin Shi Xu

Ultrafine fibers were electrospun from polyacrylonitrile (PAN)/N,N-dimethyl formamide (DMF) solution as a precursor of carbon nanofibers. The effects of solution concentration, applied voltage and flow rate on preparation and morphologies of electrospun PAN fibers were investigated. Morphologies of the green fibers, stabilized fibers and carbonized fibers were compared by scanning electron microscope (SEM). The diameter of PAN nanofibers is about 450nm and the distribution of diameter is well-proportioned. Characterization of the elements changes of fibers were performed by X-ray photoelectron spectroscopy (XPS).


2014 ◽  
Vol 782 ◽  
pp. 603-606 ◽  
Author(s):  
Ondrej Milkovič ◽  
Karel Saksl ◽  
Mária Hagarová ◽  
Štefan Michalik ◽  
Jana Gamcová

This paper is focused to structure characterization of two differently electrodeposited Ni-Co alloys on the copper surface. The chemical composition of the layers was determined by the EDX analysis in the scanning electron microscope. Phase analysis was realized by diffraction in the transmission mode using synchrotron radiation. Diffraction patterns also show the preferred orientation in the coating with saccharine addition.


2012 ◽  
Vol 465 ◽  
pp. 76-79 ◽  
Author(s):  
Shuang Zhan ◽  
Xia Li

The novel Y2O3 nanoflowers were synthesized through a facile hydrothermal method without using any catalyst or template. The phase composition and the microstructure of as-prepared products were characterized by field emission scanning electron microscope (FE-SEM), X-ray diffraction (XRD) as well as Fourier transform infrared spectrum. The formation mechanism for the Y2O3 flowers has been proposed.


2010 ◽  
Vol 434-435 ◽  
pp. 850-852
Author(s):  
Qi Wang ◽  
Bo Yin ◽  
Zhen Wang ◽  
Gen Li Shen ◽  
Yun Fa Chen

In present work, ceria microspheres were synthesized by template hydrothermal method. Crystalline form of the as-synthesized ceria microspheres was defined by X-ray powder diffraction (XRD) and high resolution transmission electron microscopy (HRTEM). Dispersibility of ceria microspheres was comprehensively characterized using scanning electron microscope (SEM) observation and laser particle size analyzer. Furthermore, the ultraviolet light absorption performances of ceria microspheres with several different sizes were compared by ultraviolet visible spectrophotometer. The results showed that ceria microspheres presented excellent UV absorbent property and the size influence was remarkable.


2017 ◽  
Vol 17 (2) ◽  
pp. 129-134 ◽  
Author(s):  
Dawei Gao ◽  
Lili Wang ◽  
Chunxia Wang ◽  
Yuping Chang ◽  
Pibo Ma

Abstract Polyacrylonitrile (PAN)/Co(OAc)2/carbon nanotubes (CNTs) composite nanofibers were fabricated via electrospinning with N,N-dimethylformamide (DMF) as solvent, and by carbonization and activation of the above precursor nanofibers, porous carbon composite nanofibers were successfully obtained. Scanning electron microscope, X-ray diffraction, ASAP 2020, and Solartron 1470 were used to characterize the surface morphology, the phase composition, specific surface area, and electrochemical property of the nanofibers, respectively. The result showed that some of the fibers were broken after sintering, and the surface area and pore volume of the porous C/Cu/CNTs were 771 m2/g and 0.347 cm3/g, respectively. The specific capacitance of the composite nanofibers reached up to 210 F/g at the current density of 1.0 A/g. Its energy density and power density were 3.1 Wh/Kg and 2,337 W/Kg, respectively, at the current of 0.5 and 5 mA.


2011 ◽  
Vol 675-677 ◽  
pp. 835-838
Author(s):  
Jing Wang ◽  
Si Jing Fu ◽  
Hong Cheng

The present work reported the preparation of TiC/Fe-based composite by the synthesis reaction from Ti, C and Fe. The sintered composites were characterized by X-ray diffraction, scanning electron microscope and transmission electron microscope. TiC, Fe3C and α-Fe were detected by X-ray diffraction analysis. The scanning and transmission electron micrographs revealed the morphology and distribution of the reinforcements, the microstructure of Fe matrix, the interfacial structure of TiC particle-to-Fe matrix. Moreover, the formation reason of the voids in composite was also discussed.


Abstract: The photocatalytic composite Fe doped AC/TiO2 has been prepared by sol-gel method. The prepared Fe doped AC/TiO2 composite were characterized by scanning electron microscope (SEM) and X-ray diffraction (XRD).The SEM analysis showed that Fe and TiO2 were attached to the Activated Carbon surfaces. The X-Ray Diffraction data showed that Fe doped AC/TiO2 composite mostly contained anatase phase.


2020 ◽  
Vol 16 (1) ◽  
pp. 1
Author(s):  
Ana Hidayati Mukaromah ◽  
Tulus Ariyadi ◽  
Inas Hasna Azizah ◽  
Mifbakhuddin Mifbakhuddin

<p>Telah dilakukan sintesis dan karakterisasi membran ZSM-5 dengan penyangga kasa jenis 304 ukuran 200 dan 400 mesh dan jenis kasa AISI 316 ukuran 180 mesh. Tujuan penelitian ini adalah mensintesis membran ZSM-5 dengan penyangga kasa jenis 304 ukuran 200 dan 400 mesh dan jenis kasa AISI 316 ukuran 180 mesh dan mengkarakterisasi membran ZSM-5 hasil sintesis. Sintesis membran dilakukan dengan cara melapiskan prekursor ZSM-5 (<em>coating)</em> pada penyangga kasa yang telah diberi perlakuan dan dipanaskan pada suhu 90 °C selama 4 hari. Selanjutnya, membran yang dihasilkan dikarakterisasi engan metoda <em>X-ray diffraction</em> (XRD), <em>scanning electron microscope-energy dispersive spectroscopy</em> (SEM-EDS) dan <em>Fourier-transform infrared</em> (FTIR). Hasil citra SEM-EDS menunjukkan bahwa ukuran membran ZSM-5 yang semakin besar, menghasilkan jumlah lubang atau pori semakin banyak dengan luasan pori yang semakin kecil. Pola difraksi XRD menunjukkan bahwa membran yang dihasilkan mempunyai intensitas tertinggi pada 2 8º dan 23º yang merupakan karakteristik dari ZSM-5. Hasil spektra FTIR menunjukkan adanya serapan pada bilangan gelombang 450 cm<sup>-</sup><sup>1</sup>yang merupakan ciri khas membran ZSM-5.</p><p class="Text"><strong>Characterization of ZSM-5 Membranes Synthesized by Variation of Support Types and Sizes.</strong> Synthesis and characterization of ZSM-5 membrane were carried out with 304 type 200 and 400 mesh gauze supports and 180 mesh AISI 316 gauze types. The purpose of this study was to synthesize ZSM-5 membrane with 304 type 200 and 400 mesh gauze support and AISI 316 type 180 mesh size 180 mesh and characterize the synthesized ZSM-5 membrane. Membrane synthesis was carried out by coating the pre-treated gauze support with the ZSM-5 precursor and was heated at 90 °C for 4 days. Furthermore, the resulting membrane was characterized by X-ray diffraction (XRD), scanning electron microscope-energy dispersive spectroscopy (SEM-EDS) dan Fourier-transform infrared (FTIR). The SEM-EDX analysis shows that the increasing of ZSM-5 membrane size allowed pores number to increase with smaller pore surface area. The X-ray Diffraction pattern (XRD) shows that the resulting membrane has the highest intensity at 2  of 8º and 23º as the characteristics of ZSM-5. The FTIR spectra results show absorption at wavenumbers 450 cm<sup>-1</sup> which is a characteristic of ZSM-5 membranes.</p>


2021 ◽  
Vol 12 (1) ◽  
pp. 53-64
Author(s):  
Zilfa Zilfa ◽  
Safni Safni ◽  
Febi Rahmi

An investigation on modification of natural zeolite with ZnO for the degradation of tartrazine. In this study, ZnO as a semiconductor is modified into a natural zeolite as support to form ZnO/zeolite that can increase the efficiency degradation of tartrazine. Further, the formed catalyst was added to tartrazine by determining the variation in ozonolysis time, the amount of addition of the catalyst, and the addition of a catalyst time. The results of degradation were determined by UV-Vis spectrophotometer at 424 nm. The result showed that the percentage of degradation obtained on each catalyst in the degradation. The resulted percent degradation of 20 ml of tartrazine at concentration of 15 mg/L using 20 mg ZnO/zeolite was 56.80%, while using 0.77 mg ZnO was 42.25%, and with the addition of 19.23 mg of Zeolite was 31.18%, all of that condition was proceeded by 40 minutes of ozonolysis. Thus, the result indicates that the ZnO/zeolite catalyst can increase percentages of tartrazine degradation by ozonolysis. It is known that the catalyst ZnO/zeolite is very effective in increasing the degradation of tartrazine. Analysis of tartrazine compounds using fourier-transform infrared spectroscopy (FTIR) after degradation changes in wavenumber indicates that there is a breaking of the bonds of tartrazine compounds. Characterization of ZnO/zeolite catalyst using FTIR, X-Ray diffraction (XRD) and scanning electron microscope (SEM), in each spectrum there was no shift, indicating that there is no change in ZnO/zeolite structure


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