Bi2WO6 Nanoparticles Prepared by Combustion Synthesis with Different Fuels and their Photocatalytic Activity

2014 ◽  
Vol 604 ◽  
pp. 93-101
Author(s):  
Maris Kodols ◽  
Sabine Didrihsone ◽  
Janis Grabis

The influence of glycine, glycerine, ethylene glycol and citric acid fuel and their ratio to NO3- on formation and dispersity of Bi2WO6 nanoparticles prepared by combustion synthesis has been studied. The pure crystalline Bi2WO6 with specific surface area 24,8 m2/g and crystallite size of 28 nm was obtained by using glycerine as fuel at its ratio to NO3- of 0,67. The photocatalytic activity of the prepared Bi2WO6 in degradation of methylene blue depended on its specific surface area of samples and solution pH.

2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Yosep Han ◽  
Hyung-Seok Kim ◽  
Hyunjung Kim

The degradation efficiency of methylene blue by TiO2nanoparticles, which were synthesized under different synthesis conditions (i.e., molar ratio of water and titanium tetraisopropoxide (TTIP), pH, and calcination temperature) in a sol-gel process, was systematically investigated. The results showed that increasing the molar ratio of water and TTIP led to the enhanced photocatalytic activity of TiO2nanoparticles, which were likely attributed to the increased specific surface area of TiO2nanoparticles synthesized with high molar ratio. The results were supported by the relative increase in the size of interaggregated pores of the aggregated TiO2nanoparticles. The best photocatalytic activity of TiO2nanoparticles was observed at acidic synthesis conditions; however, the results were not consistent with physical properties for the crystallinity and the crystallite size of TiO2nanoparticles but rather explained by the presence of abundant hydroxyl groups and water molecules existing on the surface of TiO2under acidic synthesis environments. Furthermore, methylene blue degradation experiments revealed that the photocatalytic activity of TiO2nanoparticles was maximized at the calcination temperature of 700°C. The trend was likely due to the combined effect of the anatase crystallinity which showed the highest value at 700°C and the crystallite size/specific surface area which did not excessively increase up to 700°C.


2020 ◽  
Vol 998 ◽  
pp. 78-83
Author(s):  
Yi Yi Zaw ◽  
Du Ang Dao Channei ◽  
Thotsaphon Threrujirapapong ◽  
Wilawan Khanitchaidecha ◽  
Auppatham Nakaruk

Titanium dioxide (TiO2) is known as one of the widely used catalysts in photocatalysis process. Recently, the photocatalysis of TiO2 has been implied in water purification and treatment, particularly dyes and organic compounds degradations. Naturally, the TiO2 can be found in three phases including anatase, rutile and brookite; each phase has its own specific properties such as grain size, stability and band gap energy. In this work, the effect of calcination temperature on the structure, morphology and photocatalytic activity were investigated. The data suggested that the anatase/rutile ratio of TiO2 can be controlled through the calcination process. The phase transformation data strongly indicated the liner function between percentage of rutile phase and calcination temperature. The BET analysis provided the consistent data with XRD patterns by showing that the specific surface area was decreased by increasing calcination temperature. The photodegradation of methylene blue under UV irradiation proved that the mixed phase of anatase/rutile ratio at 78.5/21.5 provided the highest photocatalytic activity. The phase composition ratio can influence the nanoparticles properties including band gap, specific surface area and energy band structure. Therefore, the control of anatase/rutile ratio was an alternative to enhance the photocatalytic activity of TiO2 nanoparticles for dyes and organic compounds degradations.


2021 ◽  
Vol 12 (2-2021) ◽  
pp. 214-218
Author(s):  
S. A. Safaryan ◽  
◽  
M. L. Belikov ◽  
V. A. Krysanova ◽  
◽  
...  

The article presents the results of the studies of the physicochemical and photocatalytic properties of titanium dioxide modified with manganese, by the example of decomposition of organic dyes — ferroin and methylene blue. The correlations between the specific surface area and phase composition of the composites with their photocatalytic activity are revealed.


2013 ◽  
Vol 838-841 ◽  
pp. 894-900 ◽  
Author(s):  
Wen Wu Chen ◽  
Yan Rong Xu ◽  
Zhi Qian Guo

The main chlorides that pollute soil are NaCl, KCl, MgCl2and CaCl2, who will change the physicochemical properties of soil. It takes Jiuzhoutai loess as the object, using methylene blue method and ethylene glycol monoethyl ether method to determinate the specific surface area of loess, which was immersed by chloride with different concentrations and cations to analyze the influence of chloride contamination, respectively. The specific surface area decrease with the increase of chloride concentration, while has the negative correlation with the affinity of cations to clay which immersed by different cations. Different absorbents that have lead to the difference of test results, and the results of ethylene glycol monoethyl ether method are always bigger than methylene blue method.


2012 ◽  
Vol 463-464 ◽  
pp. 543-547 ◽  
Author(s):  
Cheng Feng Li ◽  
Xiao Lu Ge ◽  
Shu Guang Liu ◽  
Fei Yu Liu

Core-shell structured hydroxyapatite (HA)/meso-silica was prepared and used as absorbance of methylene blue (MB). HA/meso-silica was synthesized in three steps: preparation of nano-sized HA by wet precipitation method, coating of dense silica and deposition of meso-silica shell on HA. As-received samples were characterized by Fourier transformed infare spectra, small angle X-ray diffraction, nitrogen adsorption-desorption isotherm and transmission electron microscopy. A wormhole framework mesostructure was found for HA/meso-silica. The specific surface area and pore volume were 128 m2•g-1 and 0.36 cm3•g-1, respectively. From the adsorption isotherm, HA/meso-silica with the great specific surface area exhibited a prominent adsorption capacity of MB (134.0 mg/g) in comparison with bare HA (0 mg/g). This study might shed light on surface modification of conventional low-cost adsorbents for removal of organic pollutants from aqueous solutions.


2011 ◽  
Vol 10 (2) ◽  
pp. 25
Author(s):  
Anirut Leksomboon ◽  
Bunjerd Jongsomjit

In this present study, the spherical silica support was synthesized from tetraethyloxysilane (TEOS), water, sodium hydroxide, ethylene glycol and n-dodecyltrimethyl ammonium bromide (C12TMABr). The particle size was controlled by variation of the ethylene glycol co-solvent weight ratio of a sol-gel method preparation in the range of 0.10 to 0.50. In addition, the particle size apparently increases with high weight ratio of co-solvent, but the particle size distribution was broader. The standard deviation of particle diameter is large when the co-solvent weight ratio is more than 0.35 and less than 0.15. However, the specific surface area was similar for all weight ratios ranging from 1000 to 1300 m2/g. The synthesized silica was spherical and has high specific surface area. The cobalt was impregnated onto the obtained silica to produce the cobalt catalyst used for CO2 hydrogenation.</


2018 ◽  
Vol 2018 ◽  
pp. 1-12 ◽  
Author(s):  
Asif Hussain ◽  
Jiebing Li ◽  
Jun Wang ◽  
Fei Xue ◽  
Yundan Chen ◽  
...  

Herein we demonstrate first report on fabrication, characterization, and adsorptive appraisal of graphene/cellulose nanofibers (GO/CNFs) monolith for methylene blue (MB) dye. Series of hybrid monolith (GO/CNFs) were assembled via urea assisted self-assembly method. Hybrid materials were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction patterns, Raman spectroscopy, elemental analysis, thermogravimetric curve analysis, specific surface area, surface charge density measurement, and compressional mechanical analysis. It was proposed that strong chemical interaction (mainly hydrogen bonding) was responsible for the formation of hybrid assembly. GO/CNFs monolith showed mechanically robust architecture with tunable pore structure and surface properties. GO/CNFs adsorbent could completely remove trace to moderate concentrations of MB dye and follow pseudo-second-order kinetics model. Adsorption isotherm behaviors were found in the following order: Langmuir isotherm > Freundlich isotherm > Temkin isotherm model. Maximum adsorption capacity of 227.27 mg g−1 was achieved which is much higher than reported graphene based monoliths and magnetic adsorbent. Incorporation of nanocellulose follows exponential relationship with dye uptake capacities. High surface charge density and specific surface area were main dye adsorptive mechanism. Regeneration and recycling efficiency was achieved up to four consecutive cycles with cost-effective recollection and zero recontamination of treated water.


Biochar ◽  
2020 ◽  
Author(s):  
Marlene C. Ndoun ◽  
Herschel A. Elliott ◽  
Heather E. Preisendanz ◽  
Clinton F. Williams ◽  
Allan Knopf ◽  
...  

Abstract Biochars produced from cotton gin waste (CG) and guayule bagasse (GB) were characterized and explored as potential adsorbents for the removal of pharmaceuticals (sulfapyridine-SPY, docusate-DCT and erythromycin-ETM) from aqueous solution. An increase in biochar pyrolysis temperature from 350 οC to 700 οC led to an increase in pH, specific surface area, and surface hydrophobicity. The electronegative surface of all tested biochars indicated that non-Coulombic mechanisms were involved in adsorption of the anionic or uncharged pharmaceuticals under experimental conditions. The adsorption capacities of Sulfapyridine (SPY), Docusate (DCT) and Erythromycin (ETM) on biochar were influenced by the contact time and solution pH, as well as biochar specific surface area and functional groups. Adsorption of these pharmaceutical compounds was dominated by a complex interplay of three mechanisms: hydrophobic partitioning, hydrogen bonding and π–π electron donor–acceptor (EDA) interactions. Despite weaker π–π EDA interactions, reduced hydrophobicity of SPY− and increased electrostatic repulsion between anionic SPY− and the electronegative CG biochar surface at higher pH, the adsorption of SPY unexpectedly increased from 40% to 70% with an increase in pH from 7 to 10. Under alkaline conditions, adsorption was dominated by the formation of strong negative charge-assisted H-bonding between the sulfonamide moiety of SPY and surface carboxylic groups. There seemed to be no appreciable and consistent differences in the extent of DCT and ETM adsorption as the pH changed. Results suggest the CG and GB biochars could act as effective adsorbents for the removal of pharmaceuticals from reclaimed water prior to irrigation. High surface area biochars with physico-chemical properties (e.g., presence of functional groups, high cation and anion exchange capacities) conducive to strong interactions with polar-nonpolar functionality of pharmaceuticals could be used to achieve significant contaminant removal from water. Graphic Abstract


2017 ◽  
Vol 10 (03) ◽  
pp. 1750028 ◽  
Author(s):  
Yan Zhu ◽  
Xiaoxia Yan ◽  
Yuanxin Ge ◽  
Shumin Wang ◽  
Dongmei Deng ◽  
...  

A facile approach was developed to synthesize novel Roe-like TiO2 hollow nanospheres via a template-assisted self-assembly process. These TiO2 nanospheres possessing mesoporous cavity manifest significantly improved photocatalytic activity owing to the synergistic effects of increased charge separation, more efficient use of the light and specific surface area.


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