Mechanochemical-hydrothermal preparation of crystalline hydroxyapatite powders at room temperature

2001 ◽  
Vol 16 (5) ◽  
pp. 1231-1234 ◽  
Author(s):  
Pavel Shuk ◽  
Wojciech L. Suchanek ◽  
Tian Hao ◽  
Eric Gulliver ◽  
Richard E. Riman ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Room Temperature ◽  
Heterogeneous Reaction ◽  
Stoichiometric Composition ◽  
X Ray Diffraction ◽  
Hydrothermal Preparation ◽  
Hydrothermal Route ◽  
20 Nm

Crystalline hydroxyapatite (HAp) powders were prepared at room temperature from heterogeneous reaction between Ca(OH)2powders and (NH4)2HPO4 solutions via the mechanochemical-hydrothermal route. X-ray diffraction, infrared spectroscopy, thermogravimetric characterization, and chemical analysis were performed, and it was determined that the room temperature products were phase-pure, thermally stable HAp with a nearly stoichiometric composition. Dynamic light scattering revealed that the dispersed particle size distribution of the room temperature HAp powders was in the range of 0.15–3.0 μm with a specific surface area of ≈90 m2/g. Both specific surface area measurements and scanning electron microscopy confirmed that the HAp powders consisted of agglomerates containing hundreds of ≈20 nm HAp crystals.

Preparation of Photocatalytic Porous Nano-ZnO from Galvanizing Dross

2019 ◽  
Vol 298 ◽  
pp. 186-194
Author(s):  
Peng Hui Wu ◽  
Jun Lin Xie ◽  
Jia Ming Yang ◽  
Wen Hao Yang ◽  
Chi Mao ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Calcination Temperature ◽  
Specific Surface Area ◽  
Hexagonal Wurtzite Structure ◽  
Growth Direction ◽  
X Ray Diffraction ◽  
Nano Zno ◽  
20 Nm

By using an acid free wet chemical method, porous nano-ZnO with high photocatalytic performance was synthesized from galvanizing dross at room temperature. The route is an environmental way to realize high value conversion and reuse of galvanizing dross. X-ray diffraction, microstructure, electron diffraction and specific surface area analyses show, the prepared porous nano-ZnOs are hexagonal wurtzite structure ZnO strips. The strips are consist of ZnO nanoparticles, the strips growth direction is perpendicularly to the C axis when the calcination temperature is up to 350°C. With the increase of calcination temperature, the specific surface area of ZnO decreases and the crystallinity increases. The photocatalytic activity of nano-ZnO is related to its crystallinity and grain size. When the calcination temperature is 400°C and the calcination time is 2h, the nano-ZnO has been completely crystallized, the ZnO particle size is uniform and is about 20 nm, the photocatalytic activity is the best and can reach up to 95%.

Photocatalytic Efficiency for Dye Decolorization of the UV/TiO2, UV/TiO2 + In2O3 and UV/TiO2-In2O3 Systems

2013 ◽  
Vol 831 ◽  
pp. 263-266
Author(s):  
Chung Hsin Wu ◽  
Chao Yin Kuo ◽  
Chih Hao Lai ◽  
Wei Yang Chung
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Dye Decolorization ◽  
X Ray Diffraction ◽  
First Order ◽  
First Order Kinetics ◽  
Vis Spectroscopy ◽  
Reactive Red 2

This study explored the decolorization of C.I. Reactive Red 2 (RR2) by the ultraviolet (UV)/TiO2, UV/TiO2 + In2O3, and UV/TiO2-In2O3 systems. The TiO2-In2O3 was generated by the sol-gel method and TiO2 + In2O3 was created by mixing TiO2 and In2O3 powders. The surface properties of TiO2, In2O3, and TiO2-In2O3 were analyzed by X-ray diffraction, a specific surface area analyzer, UV-vis spectroscopy, and scanning electron microscopy. The specific surface area of TiO2, In2O3, and TiO2-In2O3 was 29.5, 44.6, and 35.7 m2/g, respectively; additionally, the band gap of TiO2, In2O3, and TiO2-In2O3 was 2.95, 2.64, and 2.91 eV; respectively. The decolorization rate constant fit pseudo-first-order kinetics and that of the UV/TiO2, UV/TiO2 + In2O3, and UV/TiO2-In2O3 systems was 0.0023, 0.0031, and 0.0072 min-1; respectively.

Ultrasonic-Microwave Synergistic Synthesis of RGO–Bi2WO6 Photocatalyst with High Photoactivity for Basic Nitrogen Compounds in Light Oil

NANO ◽  
2016 ◽  
Vol 11 (05) ◽  
pp. 1650052 ◽  
Author(s):  
Ying Chen ◽  
Shenglun Ji ◽  
Tengfei Qiao ◽  
Shuang Miao ◽  
Yu Zhao
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Composite Catalyst ◽  
Photogenerated Carrier ◽  
X Ray Diffraction ◽  
Composite Photocatalyst ◽  
Photocatalytic Activities ◽  
Light Oil ◽  
Ft Ir

Graphene–Bi2WO6 composite photocatalyst with excellent photocatalytic properties were synthetized by ultrasonic-microwave synergistic method. The obtained samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier infrared (FT-IR) spectrum, specific surface area analyzer (BET) and UV-Vis diffuse reflectance spectra. The photocatalytic activities of as-prepared samples were evaluated by degradation of pyridine in light oil under visible light irradiation. The results show that graphene changed appearance structure of Bi2WO6, which prevented the Bi2WO6 nanosheets reunion arrangement, and increased specific surface area of the catalyst. It can also reduce the recombination probability of photogenerated carrier, so as to improve the photocatalytic activity of the composite catalyst. The optimal amount of graphene is 2%, with the denitrification rate as high as 89.28%, much higher than that of pure Bi2WO6.

Study of Heating Effect on Specific Surface Area, and Changing Optical Properties of ZnO Nanocrystals

2011 ◽  
Vol 403-408 ◽  
pp. 1205-1210
Author(s):  
Jaleh Babak ◽  
Ashrafi Ghazaleh ◽  
Gholami Nasim ◽  
Azizian Saeid ◽  
Golbedaghi Reza ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Energy Gap ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Zno Nanocrystals ◽  
Transmission Electron ◽  
Zno Nanocrystal

In this work ZnO nanocrystal powders have been synthesized by using Zinc acetate dehydrate as a precursor and sol-gel method. Then the products have been annealed at temperature of 200-1050°C, for 2 hours. The powders were characterized using X-ray diffraction (XRD), UV-vis absorption and photoluminescence (PL) spectroscopy. The morphology of refrence ZnO nanoparticles have been studied using Transmission Electron Microscope (TEM). During the annealing process, increase in nanocrystal size, defects and energy gap quantitative, and decrease in specific surface area have been observed.

Fabrication and Characterization of Cu Doped CeO2 by Hydrothermal Process for Antimicrobial Activity

2019 ◽  
Vol 391 ◽  
pp. 114-119 ◽  
Author(s):  
Yeon Bin Choi ◽  
Jeong Hun Son ◽  
Dong Sik Bae
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Hydrothermal Process ◽  
Antibacterial Properties ◽  
Reaction Times ◽  
X Ray Diffraction ◽  
Spherical Type ◽  
Average Size

Cu doped CeO2 nanopowder was synthesized by hydrothermal process at 180°C for 2~10h. The average size and distribution of the synthesized Cu doped CeO2 nanopowder was controlled by reaction times. The crystallinity of the synthesized Cu doped CeO2 nanoparticles was investigated by X-ray diffraction (XRD). The morphology of the synthesized Cu doped CeO2 nanoparticles was observed by FE-SEM. The specific surface area of the synthesized Cu doped CeO2 nanoparticles was measured by BET. The crystal size of the synthesized Cu doped CeO2 nanoparticles decreased with decreasing reaction times. The average size of the synthesized Cu doped CeO2 nanoparticles was below 10nm and narrow, respectively. The shape of the synthesized Cu doped CeO2 nanoparticles was spherical type. The specific surface area of the synthesized Cu doped CeO2 nanoparticles increased with decreasing reaction times. Antibacterial properties of Cu doped CeO2 were analyzed by MIC method. The synthesized Cu doped CeO2 nanopowders showed antibacterial properties against E.coli and B.sub bacteria.

Synthesis and Characterization of Porous Mo-W Oxide Nanostructures

2008 ◽  
Vol 8 (12) ◽  
pp. 6445-6450
Author(s):  
F. Paraguay-Delgado ◽  
Y. Verde ◽  
E. Cizniega ◽  
J. A. Lumbreras ◽  
G. Alonso-Nuñez
Keyword(s):  
Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Synthesis Method ◽  
Atomic Ratio ◽  
High Specific Surface Area ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Before And After

The present study reports the synthesis method, microstructure characterization, and thermal stability of nanostructured porous mixed oxide (MoO3-WO3) at 550 and 900 °C of annealing. The material was synthesized using a hydrothermal method. The precursor was prepared by aqueous solution using ammonium heptamolibdate and ammonium metatungstate, with an atomic ratio of Mo/W = 1. The pH was adjusted to 5, and then the solution was transferred to a teflon-lined stainless steel autoclave and heated at 200 °C for 48 h. The resultant material was washed using deionized water. The specific surface area, morphology, composition, and microstructure before and after annealing were studied by N2 physisorption, scanning electron microscopy (SEM), analytical transmission electron microscopy (TEM), and X-Ray diffraction (XRD). The initial synthesized materials showed low crystallinity and high specific surface area around (141 m2/g). After thermal annealing the material showed higher crystallinity and diminished its specific surface area drastically.

Synthesis and Photocatalytic Property of BiVO4/FeVO4 Composite Novel Photocatalyst

2010 ◽  
Vol 129-131 ◽  
pp. 784-788 ◽  
Author(s):  
Min Wang ◽  
Qiong Liu ◽  
Dong Zhang
Keyword(s):  
Photocatalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Photocatalytic Property ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Experimental Conditions ◽  
Triclinic Phase ◽  
Xrd Patterns

BiVO4/FeVO4 composite photocatalyst samples were prepared by calcining the mixture of FeVO4 and BiVO4 precusor which were prepared through liquid phase precipitation method for further increasing the photocatalytic efficiency of FeVO4. The catalysts were characterized by X-ray diffraction (XRD), scanning electron microsoope（SEM）and specific surface area (BET). The photocatalytic activity was evaluated by photocatalytic degradation of methyl orange (MO) solution under visible light. The XRD patterns indicate that BiVO4/FeVO4 composite photocatalysts consist of triclinic phase and the lattice was not distorted beacause of doping Bi. But the morphology change greatly and the specific surface area has little change. In the experimental conditions used, the optimal photocatalytic activity for all the prepared samples was reached when BiVO4 doping was 22 at%. The degradation rate of MO was increased by 20％ or so than that of pure FeVO4.

Mineralogy, chemistry, and physical properties interrelationships of some sensitive clays from Eastern Canada

1984 ◽  
Vol 21 (3) ◽  
pp. 530-540 ◽  
Author(s):  
Jacques Locat ◽  
Guy Lefebvre ◽  
Gérard Ballivy
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Clay Fraction ◽  
Internal Standard ◽  
Mineralogical Composition ◽  
Index Properties ◽  
X Ray Diffraction ◽  
Eastern Canada ◽  
Quantitative Mineralogy

This paper describes the use of quantitative mineralogy and specific surface area in interpreting the index properties of clayey soils from nine sites in Eastern Canada. Samples representative of the Tyrrell, Laflamme, Champlain, and Goldthwait marine seas and Lac Barlow–Ojibway have been studied.Quantitative X-ray diffraction analyses may be satisfactorily obtained using potassium metaperiodate (Foscal-Mella 1976) as an internal standard in these soils. Determination of contained amorphous matter requires extraction procedures less brutal than those employed in the Ségalen method.Correlations between Atterberg limits and specific surface area are believed to be more useful than those between specific surface area and the grain size or clay fraction. Increases in plasticity and specific surface area are related to increases in the amount of contained phyllosilicates and amorphous matter.The mineralogical composition of the soils studied is dominated, even in the clay fraction, by felsic minerals (plagioclase, quartz, microcline, and hornblende). Samples close to the Canadian Shield contain relatively more felsic minerals than those away from it. Key words: mineralogy, index properties, sensitive clays, physicochemistry.

Study of Gamma Alumina Synthesis – Analysis of the Specific Surface Area

2014 ◽  
Vol 87 ◽  
pp. 54-60 ◽  
Author(s):  
A.H. Munhoz ◽  
H. de Paiva ◽  
L. Figueiredo de Miranda ◽  
E.C. de Oliveira ◽  
Raphael Cons Andrades ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Ageing Time ◽  
Precursor Solution ◽  
Specific Area ◽  
Gamma Alumina ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dta And Tg

Different samples of pseudoboehmite (PB) were synthesized through the sol-gel process, using aluminum nitrate as precursor. The influence of variables on the synthesis and calcinations of the PB on the specific area of the obtained gamma-Alumina were studied. The variables were the ageing temperature (25 and 130o C), addition or not of polyvinyl alcohol to the precursor solution and the ageing time of the PB. The pH adjustment of the precursor solution was made by using ammonium carbonate. The products, which were obtained on different conditions, were then characterized by x-ray diffraction, specific area measurements through the BET process, and by thermal analysis (DTA and TG). After characterization, the synthesis products were calcined at 500°C; during this process the gamma-Alumina transformation was observed. The calcination products were characterized by the same methods (x-ray diffraction, BET, DTA and TG) and the desorption-absorption curves were obtained as well, in order to measure the pore volume of the samples. Finally, the results were analyzed through an experimental factorial planning, which showed that high specific surface area gamma-Al2O3 (around 330m²/g) can be obtained through this process.

scholarly journals Preparation and Application of 2D MXene-Based Gas Sensors: A Review

Chemosensors ◽  
2021 ◽  
Vol 9 (8) ◽  
pp. 225
Author(s):  
Qingting Li ◽  
Yanqiong Li ◽  
Wen Zeng
Keyword(s):  
Composite Materials ◽  
Specific Surface ◽  
Surface Area ◽  
Gas Sensor ◽  
Specific Surface Area ◽  
Gas Sensors ◽  
Room Temperature ◽  
Gas Sensing ◽  
Interlayer Spacing ◽  
Preparation Methods

Since MXene (a two-dimensional material) was discovered in 2011, it has been favored in all aspects due to its rich surface functional groups, large specific surface area, high conductivity, large porosity, rich organic bonds, and high hydrophilicity. In this paper, the preparation of MXene is introduced first. HF etching was the first etching method for MXene; however, HF is corrosive, resulting in the development of the in situ HF method (fluoride + HCl). Due to the harmful effects of fluorine terminal on the performance of MXene, a fluorine-free preparation method was developed. The increase in interlayer spacing brought about by adding an intercalator can affect MXene’s performance. The usual preparation methods render MXene inevitably agglomerate and the resulting yields are insufficient. Many new preparation methods were researched in order to solve the problems of agglomeration and yield. Secondly, the application of MXene-based materials in gas sensors was discussed. MXene is often regarded as a flexible gas sensor, and the detection of ppb-level acetone at room temperature was observed for the first time. After the formation of composite materials, the increasing interlayer spacing and the specific surface area increased the number of active sites of gas adsorption and the gas sensitivity performance improved. Moreover, this paper discusses the gas-sensing mechanism of MXene. The gas-sensing mechanism of metallic MXene is affected by the expansion of the lamellae and will be doped with H2O and oxygen during the etching process in order to become a p-type semiconductor. A p-n heterojunction and a Schottky barrier forms due to combinations with other semiconductors; thus, the gas sensitivities of composite materials are regulated and controlled by them. Although there are only several reports on the application of MXene materials to gas sensors, MXene and its composite materials are expected to become materials that can effectively detect gases at room temperature, especially for the detection of NH3 and VOC gas. Finally, the challenges and opportunities of MXene as a gas sensor are discussed.

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