scholarly journals Influence of Activity of CaSO4·2H2O on Hydrothermal Formation of CaSO4·0.5H2O Whiskers

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
S. C. Hou ◽  
L. Xiang
Keyword(s):  
Specific Surface ◽  
Calcium Sulfate ◽  
Room Temperature ◽  
Raw Material ◽  
Particle Sizes ◽  
Grain Sizes ◽  
Surface Areas ◽  
Aspect Ratios ◽  
Calcium Sulfate Dihydrate ◽  
Specific Surface Areas

The influence of the activity of calcium sulfate dihydrate (CaSO4·2H2O) on the hydrothermal formation of CaSO4·0.5H2O whiskers was investigated in this paper, using commercial CaSO4·2H2O as the raw material. The experimental results indicated that the activity of CaSO4·2H2O was improved after calcination of the commercial CaSO4·2H2O at 150°C for 6.0 h followed by hydration at room temperature for 1.0 h, corresponding to the decrease of the agglomerated particle sizes from 29.7 μm to 15.1 μm, the increase of the specific surface areas (BET) from 4.75 m2·g−1to 19.12 m2·g−1and the grain sizes from 95 nm to 40 nm. The active CaSO4·2H2O produced by the calcination-hydration treatment favored the hydrothermal dissolution of CaSO4·2H2O, promoting the formation of hemihydrate calcium sulfate (CaSO4·0.5H2O) whiskers with high aspect ratios.

scholarly journals Ultrafine porous boron nitride nanofibers synthesized via a freeze-drying and pyrolysis process and their adsorption properties

RSC Advances ◽  
2016 ◽  
Vol 6 (2) ◽  
pp. 1253-1259 ◽  
Author(s):  
Jing Lin ◽  
Lulu Xu ◽  
Yang Huang ◽  
Jie Li ◽  
Weijia Wang ◽  
...  
Keyword(s):  
Boron Nitride ◽  
Specific Surface ◽  
Freeze Drying ◽  
Adsorption Properties ◽  
Pyrolysis Process ◽  
Surface Areas ◽  
Aspect Ratios ◽  
Large Pore ◽  
Specific Surface Areas

Ultrafine porous boron nitride nanofibers with high aspect ratios, high specific surface areas and large pore volumes has been synthesized in large quantity via a freeze-drying and post pyrolysis process.

Ageing of synthetic and natural schwertmannites at pH 2—8

Clay Minerals ◽  
2008 ◽  
Vol 43 (3) ◽  
pp. 437-448 ◽  
Author(s):  
S. Kumpulainen ◽  
M.-L. Räisänen ◽  
F. Von Der Kammer ◽  
T. Hofmann
Keyword(s):  
Trace Elements ◽  
Phase Transformation ◽  
Organic Matter ◽  
Iron Oxide ◽  
Specific Surface ◽  
Room Temperature ◽  
Synthetic Sample ◽  
Surface Areas ◽  
Specific Surface Areas ◽  
One Year

AbstractThe transformation of schwertmannite to goethite was studied by ageing one synthetic and five natural schwertmannites in water at room temperature. Additionally, one synthetic and two natural schwertmannites were kept at variable pH (2, 4, 6 and 8). After one year, only the synthetic sample and one natural schwertmannite had transformed to goethite. However, the oxalate solubility of Fe and trace elements in all the samples decreased, whereas the total Fe/S ratios and specific surface areas of all samples increased. Arsenic and organic matter appeared to suppress the schwertmannite-to-goethite phase transformation. At pH 2, synthetic schwertmannite fully-transformed to goethite, but at pH 4–6 only minor transformation occurred. Depending on pH, many trace elements were released into solution during ageing of the natural schwertmannites. In general, Co, Mn, Zn and Si were released to solution, whereas As was enriched in the remaining iron oxide fraction. Al was dissolved at pH <4.

scholarly journals Experimental Investigation of Coal Dust Wettability Based on Surface Contact Angle

2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
Gang Zhou ◽  
Han Qiu ◽  
Qi Zhang ◽  
Mao Xu ◽  
Jiayuan Wang ◽  
...  
Keyword(s):  
Surface Tension ◽  
Contact Angle ◽  
Specific Surface ◽  
Coal Dust ◽  
Single Point ◽  
Contact Angles ◽  
Critical Surface ◽  
Volume Percentage ◽  
Surface Areas ◽  
Specific Surface Areas

Wettability is one of the key chemical properties of coal dust, which is very important to dedusting. In this paper, the theory of liquid wetting solid was presented firstly; then, taking the gas coal of Xinglongzhuang coal mine in China as an example, by determination of critical surface tension of coal piece, it can be concluded that only when the surface tension of surfactant solution is less than 45 mN/m can the coal sample be fully wetted. Due to the effect of particle dispersity, compared with the contact angle of milled coal particle, not all the contact angles of screened coal powder with different sizes have a tendency to increase. Furthermore, by the experiments of coal samples’ specific surface areas and porosities, it can be achieved that the volume of single-point total pore decreases with the gradual decreasing of coal’s porosity, while the ultramicropores’ dispersities and multipoint BET specific surface areas increase. Besides, by a series of contact angle experiments with different surfactants, it can be found that with the increasing of porosity and the decreasing of volume percentage of ultramicropore, the contact angle tends to reduce gradually and the coal dust is much easier to get wetted.

Facile Method To Synthesize Mesoporous Multimetal Oxides (ATiO3, A = Sr, Ba) with Large Specific Surface Areas and Crystalline Pore walls

2010 ◽  
Vol 22 (4) ◽  
pp. 1276-1278 ◽  
Author(s):  
Xiaoxing Fan ◽  
Ying Wang ◽  
Xinyi Chen ◽  
Ling Gao ◽  
Wenjun Luo ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Areas ◽  
Specific Surface Areas

Carbon Microspheres Prepared by High Internal Phase Emulsion Polymerization

2011 ◽  
Vol 239-242 ◽  
pp. 3105-3108
Author(s):  
Ming Xian Liu ◽  
Li Hua Gan ◽  
Jun Hu ◽  
Hong Lai Liu ◽  
Long Wu Chen
Keyword(s):  
Electron Microscopy ◽  
Specific Surface ◽  
Aqueous Phase ◽  
Apparent Density ◽  
Tween 80 ◽  
Carbon Microspheres ◽  
High Internal Phase Emulsion ◽  
Surface Areas ◽  
Internal Phase ◽  
Specific Surface Areas

In this paper, we present a novel approach for the synthesis of carbon microspheres via the polymerization of a high internal phase emulsion (HIPE). By using Span 80 and Tween 80 as emulsifiers, 1iquid paraffin as oil phase, and the mixture of resorcinol/formaldehyde (R/F) solution as aqueous phase, an O/W emulsion was obtained. This emulsion phase inverted to a W/O HIPE induced by ammonia which served as the polymerization catalyst. Carbon microspheres (CMs) were prepared by polymerization of the HIPE, followed by drying and carbonization. Scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Brunauer-Emmett-Teller (BET) analyzer were used to characterize as-prepared CMs. The results indicate that, in case of 0.25 wt% ammonia of the HIPE, the diameters of CMs decreased from about 2 to 1 μm when the mass fraction of aqueous R/F decreased from 0.714 to 0.357; the apparent density and the specific surface areas of the CMs, however, did not change obviously, which are about 0.6 g/cm3and 200 m2/g, respectively. The dosage of ammonia has a significant influence on the morphology and properties of CMs. With increasing of the ammonia mass to 1 wt% of the HIPE, the resultant carbon materials comprise not only CMs, but also some carbon sheets; the apparent density of which increased to 0.9 g/cm3and the specific surface areas of which decreased to below 100 m2/g. In addition, the other parameters for CMs preparation were also investigated. It was found that the proper conditions were controlling the temperature of 303-333 K and the oil/aqueous phase mass ratio of 2.5:7.

Sign in / Sign up

Export Citation Format

Share Document