scholarly journals Preparation of Stellerite Loading Titanium Dioxide Photocatalyst and Its Catalytic Performance on Methyl Orange

2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Hua Chen ◽  
Jianhua Wang ◽  
Huajun Wang ◽  
Fei Yang ◽  
Jia-nan Zhou ◽  
...  

TiO2/stellerite composite photocatalysts were prepared by dispersing TiO2 onto the surface of HCl, NaOH, or NaCl treated stellerite using a sol-gel method. The materials were characterized by scanning electron microscopy (SEM), energy dispersive X-ray (EDX), Fourier transform infrared spectroscopy (FT-IR), BET surface area analysis, and X-ray diffraction (XRD). HCl and NaCl modification result in the promotion of the pore formation at the stellerite surfaces and induced the microscopic changes, while the surface morphology and structure of the stellerite were almost ruined by NaOH modification. Supported TiO2 calcinated at 200°C presented anatase structure. The photocatalytic degradation activities of TiO2 loaded HCl and NaCl modified stellerite were better than that of natural stellerite, accompanied with increasing specific surface area. On the contrary, NaOH modification induced the loss of photocatalytic ability of composite due to the generation of silicates.

2018 ◽  
Vol 63 (1) ◽  
pp. 85-95 ◽  
Author(s):  
Harish Phattepur ◽  
Gowrishankar Bychapur Siddaiah ◽  
Nagaraju Ganganagappa

A sol-gel method was employed to synthesise pure titanium dioxide (TiO2) and surfactant assisted TiO2 nanoparticles (NPs). The effect of novel surfactant viz., Lauryl lactyl lactate on photocatalytic properties of TiO2 was studied. TiO2 NPs were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), UV-Vis Diffuse Reflectance spectra (DRS), Field emission scanning electron microscopy (FE-SEM), Transmission electron microscopy (TEM), Thermo gravimetric analysis (TGA), and Brunauer – Emmet - Teller (BET) surface area. Anatase phase of TiO2 was confirmed by X-Ray diffraction pattern and the crystallite size was between 9–19 nm. Addition of surfactant improved the BET surface area, surface defects, while the agglomeration of particles was reduced. DRS results revealed that the addition of surfactant to TiO2 sol induced a red shift of the absorption edge which resulted in the reduction of band gap from 3.23 to 3.21 eV. These physicochemical properties of TiO2 NPs were correlated with photocatalytic degradation of phenol. About 92% of phenol degradation was observed for surfactant assisted TiO2 NPs (SA-TiO2). Salicylic acid and caffeine were also degraded using SA-TiO2 NPs.


2016 ◽  
Vol 1141 ◽  
pp. 190-195
Author(s):  
Hitesh Saravaia ◽  
Hariom Gupta ◽  
Vaibhav Kulshreshtha

Barium Titanate (BaTiO3) nanostructures are synthesized by the molten salt-hydroxide reaction. The crystalline phase and chemical structure of the synthesized material are analyzed using powder x-ray diffraction (XRD) and FT-IR techniques, revealing the tetragonal BaTiO3 crystalline structure. Morphology and thermal stability of the material are characterized using TEM and TG-DTG analysis. BET surface area analysis shows significant active surface available for adsorption and its surface area value is found to be 14.8427 m2 g-1. The maximum adsorption of strontium metal is found to be 56.3 for the 1.2 g L-1 BaTiO3 adsorbent dose which reveals a remarkable separation property of the BaTiO3.


2019 ◽  
Vol 37 (4) ◽  
pp. 645-651
Author(s):  
Yasaman Khaksarfard ◽  
Hakimeh Ziyadi ◽  
Akbar Heydari

AbstractBecause of special characteristics of vanadate compound, such as its sustainability, magneticity, high selectivity in reactions and catalytic character, this study aimed to preparation and analyzing novel ceramic iron vanadate (FeVO4) nanofibers. The ceramic nanofibers of iron vanadate were made by the combination of sol-gel and electrospinning methods. First, polyvinyl alcohol (PVA), as a matrix polymer, was mixed separately with ammonium metavanadate (NH4VO3) and iron (III) nitrate (Fe(NO3)3). As a result, the spinnable polymeric gel was obtained from the controlled mixture of these two precursors of ceramic material. Electrospinning of PVA/iron (III) nitrate/ammonium vanadate solution was done using an Electroris setup that enabled preparation of polymeric template nanofiber. Finally, iron vanadate nanofiber was obtained by calcination of polymer nanofiber at controlled temperature. The products were characterized with scanning electron microscope (SEM), energy dispersive X-ray spectroscope (EDX), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), vibrating sample magnetometer (VSM) and Brunauer-Emmett-Teller (BET) surface area analysis.


2011 ◽  
Vol 399-401 ◽  
pp. 625-628 ◽  
Author(s):  
Juan Tan ◽  
Xu Ying Li ◽  
Fei Yang ◽  
Jing Liu

Mesostructured nickel phosphate was synthesized with urea as alkali by sol-gel method. The obtained material nominated as NiPO-3 was characterized by means of XRD, ICP, FT-IR, TEM, and N2 adsorption. In contrast to mesoporous nickel phosphate NiPO-1 and NiPO-2 we reported before, NiPO-3 exhibits relatively longer nanotubes reached up to 400~600 nm. N2 adsorption shows that NiPO-3 possesses high BET surface area (345.8 m2g-1) and pore volume (0.46 cm3g-1). The catalytic performance of NiPO-3 showed that the total selectivity of epoxycyclohexane and hexadienol was as high as 83.38%.


2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Fu Ding ◽  
Yajing Zhang ◽  
Guijin Yuan ◽  
Kangjun Wang ◽  
Ileana Dragutan ◽  
...  

A series of Ni/SiO2catalysts with different Ni content were prepared by sol-gel method for application in the synthesis of 2-methyltetrahydrofuran (2-MTHF) by hydrogenation of 2-methylfuran (2-MF). The catalyst structure was investigated by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and temperature programmed reduction (TPR). It is found that structures and catalytic performance of the catalysts were highly affected by the Ni content. The catalyst with a 25% Ni content had an appropriate size of the Ni species and larger BET surface area and produced a higher 2-MF conversion with enhanced selectivity in 2-MTHF.


Processes ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 1238
Author(s):  
Garven M. Huntley ◽  
Rudy L. Luck ◽  
Michael E. Mullins ◽  
Nick K. Newberry

Four naturally occurring zeolites were examined to verify their assignments as chabazites AZLB-Ca and AZLB-Na (Bowie, Arizona) and clinoptilolites NM-Ca (Winston, New Mexico) and NV-Na (Ash Meadows, Nevada). Based on powder X-ray diffraction, NM-Ca was discovered to be mostly quartz with some clinoptilolite residues. Treatment with concentrated HCl (12.1 M) acid resulted in AZLB-Ca and AZLB-Na, the chabazite-like species, becoming amorphous, as confirmed by powder X-ray diffraction. In contrast, NM-Ca and NV-Na, which are clinoptilolite-like species, withstood boiling in concentrated HCl acid. This treatment removes calcium, magnesium, sodium, potassium, aluminum, and iron atoms or ions from the framework while leaving the silicon framework intact as confirmed via X-ray fluorescence and diffraction. SEM images on calcined and HCl treated NV-Na were obtained. BET surface area analysis confirmed an increase in surface area for the two zeolites after treatment, NM-Ca 20.0(1) to 111(4) m2/g and NV-Na 19.0(4) to 158(7) m2/g. 29Si and 27Al MAS NMR were performed on the natural and treated NV-Na zeolite, and the data for the natural NV-Na zeolite suggested a Si:Al ratio of 4.33 similar to that determined by X-Ray fluorescence of 4.55. Removal of lead ions from solution decreased from the native NM-Ca, 0.27(14), NV-Na, 1.50(17) meq/g compared to the modified zeolites, 30 min HCl treated NM-Ca 0.06(9) and NV-Na, 0.41(23) meq/g, and also decreased upon K+ ion pretreatment in the HCl modified zeolites.


2012 ◽  
Vol 217-219 ◽  
pp. 733-736
Author(s):  
Xiu Mei Han ◽  
Shu Ai Hao ◽  
Ying Ling Wang ◽  
Gui Fang Sun ◽  
Xi Wei Qi

Zn2SiO4:Eu3+, Dy3+ phosphors have been prepared through the sol-gel process. X-ray diffraction (XRD), thermogravimetric and ddifferential thermal analysis (TG-DTA), FT-IR spectra and photoluminescence spectra were used to characterize the resulting phosphors. The results of XRD indicated that the phosphors crystallized completely at 1000oC. In Zn2SiO4:Eu3+,Dy3+ phosphors, the Eu3+ and Dy3+ show their characteristic red(613nm, 5D0-7F2), blue (481nm, 4F9/2–6H15/2) and yellow (577nm, 4F9/2–6H13/2) emissions.


2012 ◽  
Vol 518-523 ◽  
pp. 775-779 ◽  
Author(s):  
Dong Dong Tan ◽  
De Fu Bi ◽  
Peng Hui Shi ◽  
Shi Hong Xu

The TiO2/NiFe2O4 (TN) composite nanoparticles with different mass ratios of NiFe2O4 to TiO2 were prepared via sol-gel method. X-ray diffraction was used to characterize the phase structure of TN. The results indicated that adulterating a smidgen of NiFe2O4 into the TiO2 (about 0.1%) can promote the phase transformation of TiO2, however, when the doping amount of NiFe2O4 surpasses 1%, the introduction of NiFe2O4 can inhibit the growth of TiO2 crystal grain and reduce the size of TiO2 crystal grain. The degradation experiment of methyl orange solution under UV illumination (253.7 nm) showed that the content of NiFe2O4 in the TN was higher, the photocatalytic activity of TN was worse, and the 0.1% TiO2/NiFe2O4 calcined at 400 °C presented the best photocatalytic activity.


2011 ◽  
Vol 284-286 ◽  
pp. 377-381
Author(s):  
Ji Chu Zhang ◽  
Ze Peng Zhang ◽  
Bo Hu ◽  
Gang Liu

In this paper, Ca2+-montmorillonite (Ca2+-Mt) was modified with cationic surfactant hexadecyl trimethyl ammonium Bromide (CTAB) directly, without changing Ca2+-Mt into Na+-montmorillonite (Na+-Mt). X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FT-IR), contact angle tests and rotary viscosity tests were used to characterize the structure and property of the organo-montmorillonite. The results of XRD show that interlayer space (d001) of the product is 4.05nm. The results of TGA indicate the ratio of weight loss of the organic components in the product is 37.7%. The results of FT-IR indicate there are organic components and hardly any water molecules in the product. All these findings indicate that the CTAB has intercalated into the galleries of Ca2+-Mt. Contact angle tests shows the product is well hydrophobic and the hydrophobic property is as good as that of organo-montmorillonite modified from Na+-Mt. Rotary viscosity tests show that the viscosity of the product at the rotational speed of 6R/min is 1226mPa·s, much better than that of the organo- montmorillonite modified from Na+-Mt which is 1070 mPa·s. The thixotropy index of the product is 9.22, much better than that of the organo-montmorillonite modified from Na+-Mt which is 5.88. It can be concluded that organo-montmorillonite with perfect interlayer expansion and thixotropic property was prepared by modifying Ca2+-Mt with CTAB directly.


2021 ◽  
Vol 11 (3) ◽  
pp. 215
Author(s):  
Achraf El Hallaoui ◽  
Tourya Ghailane ◽  
Soukaina Chehab ◽  
Youssef Merroun ◽  
Rachida Ghailane ◽  
...  

<p>This work aims to prepare a new bimetallic phosphate catalyst using a new simple and effective method. This new catalyst was ready for the first time by a modification of Triple Super Phosphate (TSP) fertilizer with silver sulfate (AgSO<sub>4</sub>), followed by the impregnation of the aluminum atoms using aluminum nitrate (Al(NO<sub>3</sub>)<sub>3</sub>). The use of Al/Ag<sub>3</sub>PO<sub>4</sub>, for the first time as a heterogeneous catalyst in organic chemistry, offers a new, efficient, and green pathway for synthesizing 1,2-dihydro-l-phenyl-3H-naphth[1,2-e]-[1,3]oxazin-3-one derivatives by one-pot three-component cyclocondensation of b-naphthol, aryl aldehyde, and urea. The structure and the morphology of the prepared catalyst were characterized by spectroscopic methods such as X-Ray Diffraction (XRD), Fourier Transform Infrared spectroscopy (FT-IR), and dispersive X-ray spectrometry coupled with a scanning electron microscope (EDX-SEM). In addition, the optimization of the reaction parameters was carried out considering the effect of catalyst amount, the temperature, and the solvent. The procedure described herein allowed a comfortable preparation of oxazine derivatives with excellent yields, short reaction times, and in the absence of organic solvent.</p>


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