Preparation and Synthesis of Functional Silica-Nafion Composite Materials

2012 ◽  
Vol 496 ◽  
pp. 310-313 ◽  
Author(s):  
Yu Yuan Zhi ◽  
Kai Gu ◽  
Hui Qin Lian ◽  
Xiu Guo Cui

In this study, a series of sulfonic-functionalized mesoporous silica (SMS) were synthesized and SMS-Nafion composites membranes were fabricated. The morphology of SMS was characterized by scanning electron microscopy and BET. The physical properties of SMS and composites membranes were tested in terms of ion-exchange capacity, linear expansion, and ionic conductivity. The results showed that the morphology of SMS influenced their physical properties as well as the properties of SMS-Nafion composite membranes.

2011 ◽  
Vol 335-336 ◽  
pp. 187-190
Author(s):  
Jian Jun Chen ◽  
Ji Ying Men

Abstract: Conductive polypyrrole(PPy)-polylactic Acid(PLA) composite membranes are prepared with chemical method. Membranes have been characterized by Fouier transform infrared spectroscopic(FT-IR) and scanning electron microscopy (SEM).The conductive stability of membranes has been measured by home-made multiwell direct current electrical stimulating system. The results show PPy nanparticals network embeds in PLA matrix and the conductive stability of membranes sustains in the range of 28μA~35μA between the observation time of 560h to 1146h.


2015 ◽  
Vol 825-826 ◽  
pp. 838-843
Author(s):  
Moritz Boehm ◽  
Thomas Schmoelzer ◽  
Reinhard Simon ◽  
Christian Gierl-Mayer

Chromium and molybdenum exhibit continuous solubility in the solid phase region at temperatures of 908°C and above [1]. At lower temperatures, the system exhibits a miscibility gap. Furthermore a congruent minimum in the liquidus boundary exists at 1854°C. Chromium and molybdenum powders with different particle morphologies were mixed and porous green parts were produced by pressing. Sintering experiments were performed at different temperatures and for different chromium to molybdenum ratios. To investigate the evolution of the microstructure, sintering was interrupted at different temperatures and points in time. The microstructure and morphology of the sintered parts was investigated by scanning electron microscopy as well as light optical microscopy. It was found that during sintering, a Cr-Mo solid solution is formed. Depending on the molybdenum content, this induces either shrinking or swelling of the porous parts. Samples exhibited a linear expansion of up to 10% and final porosities of up to 65%.


2012 ◽  
Vol 1372 ◽  
Author(s):  
L. Ortiz-Martínez ◽  
M. Torres-Rodríguez ◽  
M. Gutiérrez-Arzaluz

ABSTRACTIn this work, the synthesis of dense Pd/α–Al2O3 and Pd-Ag/α–Al2O3 ceramic composite membranes was done through the sequential electroless plating technique of Pd and Ag. The precursors are solutions of PdCl2 and AgNO3 and N2H4 salts, as reducing agent. The membranes were characterized by X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and Energy Dispersive Spectroscopy (EDS). The permeation tests of H2 and N2 was carried out at 20 psi of pressure and at 25°C, resulted πH2=5.2x10-9 mol H2/m2·s·Pa and πN2=8.2x10-10 mol N2/m2·s·Pa.


Author(s):  
Jinjun Shi ◽  
Bor Jang

A hydrophilic expanded poly(tetrafluoroethylene) (ePTFE) based composite membrane was prepared and tested for proton exchange fuel cell applications. The composite membrane was prepared by impregnating hydrophilic ePTFE membrane with 5% Nafion solution (equivalent weight=1000). This new composite membrane showed higher water uptake (12.7%) than that of normal hydrophobic ePTFE based composite membrane (6.3%) and better proton conductivity. Scanning electron microscopy micrographs showed that the hydrophilic ePTFE based membrane can easily form a dense composite membrane while hydrophobic ePTFE based composite membranes tend to have micropores inside. The hydrophilic ePTFE based composite membrane showed better thermal and dimensional stability than recast Nafion membrane.


2009 ◽  
Vol 79-82 ◽  
pp. 1635-1638 ◽  
Author(s):  
Qiu Ping Ma ◽  
Wen Liu ◽  
Bao Cheng Wang ◽  
Qing Sen Meng

In this paper it was investigated that silicon be electrodeposited in the room temperature from propylene carbonate solvent. Cyclic voltammograms indicated that it was possible to electrochemical reduction of silicon chloride at -2.3984V versuHg/Hg2Cl2/ KCl (saturation) quasi-reference electrode. Potentiostatic electrolysis yielded deposits, accompanied by the change in electrolyte color from transparent to brown. Scanning electron microscopy (SEM) and energy dispersion spectroscopy (EDS) were used to characterize the physical properties of the silicon. The EDS analysis performed simultaneously with SEM observation demonstrates that the deposit consists of Si, O and Cl.


Author(s):  
S. Sharma

Pectin cerium(IV) iodate (PcCeI) and cerium(IV) iodate (CeI) cation ion exchange materials were synthesized via sol–gel methods. The materials were characterized by using Fourier transform infrared spectroscopy, X-ray diffractometer, thermogravimetric analysis, and scanning electron microscopy. The ion exchange capacity (IEC), thermal stability, distribution coefficient (Kd), and pH titrations were investigated to recognize the cation exchange behavior of the materials. The IEC of pectin-cerium(IV) iodate (PcCeI and cerium(IV) iodate CeI were reported as 1.80 meq/g and 0.92 meq/g, respectively. The higher distribution coefficient values of 250.01 and 219.14 mg/L confirmed the selectivity of pectin-cerium(IV) iodate hybrid ion exchanger for As3+ and Zn2+. The antibacterial activity of synthesized ion exchangers was explored for E. coli bacteria and observed relatively higher for PcCeI as compared to CeI.


2021 ◽  
Vol 10 (4) ◽  
pp. 84-87
Author(s):  
Maya Sari ◽  
Yolanda Rati ◽  
Tetty Marta Linda ◽  
Yanuar Hamzah ◽  
Ari Sulistyo Rini

 Abstrak. Dalam rangka mengurangi pemakaian bahan kimia berbahaya, kini telah mulai dikembangkan penggunaan bahan alami pada proses pembentukan nanopartikel. Pada penelitian ini, biosintesis nanopartikel ZnO dilakukan menggunakan ekstrak kulit Ananas comosus sebagai agen capping sekaligus agen pereduksi. Seng nitrat digunakan sebagai prekursor dari ion seng, sedangkan kulit nanas dibuat menjadi ekstrak untuk dimanfaatkan kandungan antioksidannya. Sampel ZnO dipelajari sifat fisisnya dari hasil karakterisasi X-ray diffraction (XRD), scanning electron microscopy (SEM) dan spektroskopi UV-Vis. Berdasarkan pola XRD, nanopartikel ZnO memberikan fasa kristal heksagonal wurtzite dengan ukuran kristal 14 nm. Morfologi SEM masing-masing sampel didapatkan berbentuk bunga atau micro-nanoflower dengan ukuran diameter rata-rata 510 nm dan 560 nm untuk sampel 0,01 M dan 0,025 M. Hasil spektrum absorbansi UV-Vis menunjukkan peningkatan puncak penyerapan cahaya dengan penambahan konsentrasi seng nitrat. Berdasarkan informasi sifat fisis ini, sampel ZnO berpotensi diaplikasikan sebagai material fotokatalis.Abstract. In order to reduce the use of hazardous chemicals, the use of natural ingredients has now been developed in the process of forming nanoparticles. In this study, biosynthesis of ZnO nanoparticles was carried out using Ananas comosus peel extract as capping agent and reducing agent. Zinc nitrate was used as a precursor to zinc ion. The physical properties of ZnO samples were studied from the characterization result of scanning electron microscopy (SEM), UV-Vis spectroscopy, and X-ray diffraction (XRD). The SEM morphology of each different sample was obtained in the form of micro-nanoflower with an average diameter  of 510 nm and 560 nm for 0.01 M and 0.025 M samples, respectively. The UV-Vis absorbance spectrum results showed an increase in the light absorption peak as  zinc nitrate concentration increased. According to the XRD pattern, the ZnO nanoparticles possessed an hexagonal wurtzite crystal phase with a crystal size of 14 nm. Based on this information on physical properties, the ZnO sample has the potential to be applied as a photocatalyst material.


2012 ◽  
Vol 463-464 ◽  
pp. 1497-1500
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang

Na0.5Bi0.5TiO3 microcubes with the side size ca. 20-30um were successfully fabricated by a Cr3+-assisted hydrothermal method. The obtained samples were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Results show that Cr3+ played a significant role in the formation of Na0.5Bi0.5TiO3 microcubes. Possible mechanisms for the growth of Na0.5Bi0.5TiO3 microcubes are discussed. The results presented in this study would be important in investigating the correlation between morphology and basic physical properties, and may offer a route to control the morphology and size of crystals.


2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Xin-chun Zhang ◽  
Xing-zhi Wang ◽  
Gang Chen ◽  
Qiang Deng ◽  
Huarui Hao

A biglucoside (BG) was synthesized with glucose and epichlorohydrin as raw materials. The inhibition of BG against montmorillonite swelling was investigated by various methods including montmorillonite linear expansion test, mud ball immersing test, thermogravimetric analysis, and scanning electron microscopy. The results show that the BG has good inhibition ability to the hydration swelling and dispersion of montmorillonite. Under the same condition, the linear expansion ratio of montmorillonite in BG solution is much lower than that of MEG. The particle distribution measurement, thermogravimetric analysis, FT-IR, and scanning electron microscopy results all prove the efficient inhibition of BG.


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