Size-Controllable Synthesis of Worm-Like SiO2 Microspheres Using Dodecylamine as Direct Agent in Ethanol/Water Solvent System

2013 ◽  
Vol 448-453 ◽  
pp. 154-159
Author(s):  
Xue Ling Zhang ◽  
Wei Yao Zhu ◽  
Meng Jing Cao ◽  
Qiang Cai ◽  
Xiao Feng Wang ◽  
...  

Size-controllable synthesis of worm-like microporous monodispersed SiO2microspheres using dodecylamine (DDA) as direct agent in ethanol-water solvent system was firstly developed by varying the proportion of reactants. The products were characterized with scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), small angle X-ray diffraction (SAXRD) and nitrogen adsorption. The results showed that the SiO2microspheres with size of 50nm~1um could be prepared by varying the molar ratio of water/ethanol when the molar ratio of (DDA)/tetraethyl orthosilicate (TEOS) is 0.4 and the concentration of TEOS varied from 0.138 to 0.248mol/L. This method is simple and convenient, the prepared SiO2microspheres are monodispersed and uniform, the worm-like pore size is about 1.4nm. The size controllable silica microspheres could be used as an excellent additional medium to alter rheological behavior of fluid after surface modification..

NANO ◽  
2013 ◽  
Vol 08 (05) ◽  
pp. 1350050
Author(s):  
MIN GUAN ◽  
HAI-PENG BI ◽  
ZUYUAN WANG ◽  
SHAOHUA BU ◽  
LING HUANG ◽  
...  

Mesoporous silicas SBA-15 are modified with β-Cyclodextrins (β-CD) by simple grafting method. β-CD functionalized SBA-15 was characterized by Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), powder X-ray diffraction (PXRD), nitrogen adsorption–desorption measurements, thermogravimetric analysis (TGA) and X-ray photoelectron spectroscopy (XPS). Furthermore, the applicability of it is investigated through studying the adsorption properties of clenbuterol. It showed better adsorption capacities of clenbuterol than pure SBA-15. β-CD functionalized SBA-15 material has the potential applications in the treatment of clenbuterol contamination in food and environment science.


Clay Minerals ◽  
1991 ◽  
Vol 26 (4) ◽  
pp. 527-534 ◽  
Author(s):  
C. Bender Koch

AbstractThe EDTA-insoluble residues from five samples (two from the oolitic shoal facies and three from the lagoonal facies) of the Late Permian Ca-2 unit (Zechstein) have been investigated by X-ray diffraction, infrared spectroscopy, and scanning and transmission electron microscopy with energy dispersive X-ray analysis (EDXA). The results show that spheres of non-crystalline hydrous feldspathoids (with Al/Si molar ratio between 1·5 and 2·2) dominate the residues of samples from the oolitic shoal facies. Samples from the lagoonal facies are dominated by crystalline material (muscovite and quartz), but two of the samples contain a small number of spheres. Analyses of these samples by selective area diffraction and EDXA revealed the presence of small amounts of non-crystalline hydrous feldspathoids with Al/Si molar ratio between 0·1 and 1·9.


2017 ◽  
Vol 2017 ◽  
pp. 1-10 ◽  
Author(s):  
Feng Tao ◽  
Zhishun Shen ◽  
Zhijun Wang ◽  
Da Shu ◽  
Qi Liu ◽  
...  

Hexagonal NaYF4:Ln3+ micro/nanoplates were successfully synthesized via a hydrothermal method using oxalic acid as a shape modifier. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), and selected area electron diffraction (SAED) have been used to study the morphologies and crystal structure of the products. The effects of the pH values and the molar ratio of oxalic acid to NaOH on the crystal growth have been investigated in detail. The time-dependent experiments have been conducted to investigate the morphology evolution process, and based on the results, a possible growth mechanism was proposed. The photoluminescence properties of 5 mol% Eu3+ and 3 mol% Sm3+ doped NaYF4 and 20 mol% Yb3+/2 mol% Er3+ codoped NaYF4 micro/nanoplates were investigated. The experimental results showed that NaYF4:Ln3+ micro/nanoplates have excellent luminescence and can be potential application in the field of light display systems, lasers, and optoelectronic devices.


2010 ◽  
Vol 663-665 ◽  
pp. 965-968
Author(s):  
Yue Hui Wang ◽  
Dong Jun Wang ◽  
Ai Jun Song ◽  
Zhi Gang Zhang ◽  
Shi Tao Song

TiO2/Ga2O3 nanowires were successfully prepared by a sol–gel-solvothermal method using tetrabutyl titanate as precursor, alcohol as solvent, Ga2O3 as templet and dopants, alginate as dispersant. The structures, morphologies,compositions and catalytic activity of products have been characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy ( FESEM ), nitrogen adsorption test, ultraviolet-visible near-infrared spectroscopy (UV–vis–NIR ),energy dispersive X-ray (EDX) analysis and spectrophotometer. The results revealed that the as-synthesized TiO2/Ga2O3 nanowires grew along [001] direction,which is reported for the first time, and the as-prepared product had better optical activity than TiO2 nanoparticles. Finally, the nanowires have a good adsorption capacity of 128.2 m2/g tested through nitrogen adsorption.


2006 ◽  
Vol 60 (21-22) ◽  
pp. 2682-2685 ◽  
Author(s):  
Marcelo J.B. Souza ◽  
Antonio S. Araujo ◽  
Anne M.G. Pedrosa ◽  
Bojan A. Marinkovic ◽  
Paula M. Jardim ◽  
...  

2017 ◽  
Vol 727 ◽  
pp. 395-402
Author(s):  
Zi Run Wang ◽  
Xin Liu ◽  
Gui Qi Xie ◽  
Yi Wu ◽  
Ming Nie ◽  
...  

Cu-Ag alloy nanoparticles were synthesized by a liquid phase reduction method. Using sodium formaldehyde sulfoxylate (SFS) as reducing agents, copper-silver bimetallic nanoleaflets with high content of Cu were prepared. The obtained Cu-Ag bimetallic nanocrystal were characterized by powder X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), field emission scanning electron microscope (FESEM), high resolution transmission electron microscopy (HRTEM) and transmission electron microscopy (TEM). Different molar ratio of Cu-Ag bimetallic nanomaterials could produce different morphologies. The surfactant β-CD plays a crucial role on the structure of the products. The different molar ratios of Cu-Ag were also investigated. The electrochemical activity was evaluated using cyclic voltammetry (CV), electrochemical hydrogen evolution reaction (HER) in a 0.5M Na2SO4 electrolyte.


2010 ◽  
Vol 654-656 ◽  
pp. 2277-2280
Author(s):  
Xi Long ◽  
Wen Chen ◽  
Shao Jiang Chen ◽  
Chun Xia Zhao

Mesoporous carbon with MoO3 loading (MoO3/CMK-3) was obtained via ultrasonic assembly with CMK-3 as the host material and MoO3 as the guest material which was yield from MoO3ּpH2O2ּqH2O sol precursor. The microstructures of such MoO3/CMK-3 composites were characterized by X-ray diffraction (XRD), nitrogen adsorption and desorption, X-ray photoelectron spectra (XPS), Fourier-transform infrared (FTIR) and transmission electron microscopy (TEM). The results show that the method of ultrasonic assembly was efficient to highly disperse MoO3 nanoparticales into the channels of mesoporous carbon.


2007 ◽  
Vol 40 (2) ◽  
pp. 260-276 ◽  
Author(s):  
Marek Andrzej Kojdecki ◽  
Esther Ruiz de Sola ◽  
Francisco Javier Serrano ◽  
Estefanía Delgado-Pinar ◽  
María Mercedes Reventós ◽  
...  

The crystalline microstructure of mullites obtained by heating monophasic gels has been investigated. Gels with alumina to silica molar ratio of 3:2 (as in secondary mullite) and 2:1 (as in primary mullite) were prepared by gelling mixtures of aluminium nitrate and tetraethylorthosilicate. Phase transformations were induced by heating the gel precursors, with different final treatment temperatures between 1173 and 1873 K. The mullites formed as a result of thermal treatment were studied by means of X-ray diffraction, scanning electron microscopy and transmission electron microscopy. The crystalline structure (unit-cell parameters) and microstructure were determined from X-ray diffraction patterns. The formation of mullites of homogeneous chemical composition and with unit-cell parameters depending almost linearly on the treatment temperature was found. Their compositions, expressed as alumina to silica molar ratio, were determined from the unit-cell parameters and were in the range of those characterizing primary and secondary mullites. Mullites processed at lower temperatures were accompanied by small amounts of vitreous phase. The crystalline microstructure of the obtained mullites was interpreted by means of a mathematical model of polycrystalline material, involving prevalent crystallite shape, volume-weighted crystallite size distribution and second-order crystalline lattice strain distribution as model parameters. The model parameters were determined for each sample by modelling its X-ray diffraction pattern and fitting it to a measured pattern. Bimodality of the size distribution was observed and explained as a consequence of two crystallite nucleation and growth processes, which started from small alumina-rich and alumina-poor domains, spontaneously formed in a precursor gel at early stages of heating. Images produced by scanning and transmission electron microscopy agreed well with the characteristics obtained from the analysis of the X-ray diffraction patterns.


2010 ◽  
Vol 123-125 ◽  
pp. 631-634 ◽  
Author(s):  
Yu Ping Tong ◽  
Shun Bo Zhao ◽  
Feng Lan Li ◽  
Chang Yong Li

La1.6Ln0.4Zr2O7 (Ln= La, Nd, Dy, Er) nanocrystals were prepared by stearic acid combustion method. The samples were characterized by powder X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) nitrogen adsorption, transmission electron microscopy (TEM) and high-resolution transmission electron microscopy (HRTEM). The photocatalytic activity of La1.6Ln0.4Zr2O7 was evaluated by the photocatalytic degradation of methyl orange. The order of the photocatalytic activity was as following: La1.6Er0.4Zr2O7>La1.6Dy0.4Zr2O7> La1.6Nd0.4Zr2O7> La2Zr2O7. La1.6Dy0.4Zr2O7 showed that the best photocatalytic activity and the reason may be related to the big magnetic moment of Er3+. It may be considered largely to be caused by the partly occupied Ln4f levels. Since the solid samples have the same structure, the reason that La1.6Er0.4Zr2O7 shows the highest reactivity may be related to lowest Ln4f level of Er3+.


Catalysts ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1069 ◽  
Author(s):  
Abir Azara ◽  
El-Hadi Benyoussef ◽  
Faroudja Mohellebi ◽  
Mostafa Chamoumi ◽  
François Gitzhofer ◽  
...  

In this study, iron-rich mining residue (UGSO) was used as a support to prepare a new Ni-based catalyst via a solid-state reaction protocol. Ni-UGSO with different Ni weight percentages wt.% (5, 10, and 13) were tested for C2H4 dry reforming (DR) and catalytic cracking (CC) after activation with H2. The reactions were conducted in a differential fixed-bed reactor at 550–750 °C and standard atmospheric pressure, using 0.5 g of catalyst. Pure gases were fed at a molar ratio of C2H4/CO2 = 3 for the DR reaction and C2H4/Ar = 3 for the CC reaction. The flow rate is defined by a GHSV = 4800 mLSTP/h.gcat. The catalyst performance is evaluated by calculating the C2H4 conversion as well as carbon and H2 yields. All fresh, activated, and spent catalysts, as well as deposited carbon, were characterized by Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectrometry (EDX), transmission electron microscopy (TEM), temperature programmed reduction (TPR), and thermogravimetric analysis (TGA). The results so far show that the highest carbon and H2 yields are obtained with Ni-UGSO 13% at 750 °C for the CC reaction and at 650 °C for the DR reaction. The deposited carbon was found to be filamentous and of various sizes (i.e., diameters and lengths). The analyses of the results show that iron is responsible for the growth of carbon nanofilaments (CNF) and nickel is responsible for the split of C–C bonds. In terms of conversion and yield efficiencies, the performance of the catalytic formulations tested is proven at least equivalent to other Ni-based catalyst performances described by the literature.


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