Influence of Acid Treatment on the Loading and Release Behavior of Halloysite with 2-Mercaptobenzothiazole

2019 ◽  
Vol 19 (11) ◽  
pp. 7178-7184 ◽  
Author(s):  
Xuteng Xing ◽  
Jihui Wang ◽  
Qiushi Li ◽  
Wenbin Hu
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Acid Treatment ◽  
Gas Adsorption ◽  
Treatment Time ◽  
Halloysite Nanotubes ◽  
Tubular Structure ◽  
Internal Diameter ◽  
Release Behavior

Halloysite nanotubes (HNTs) are natural clay minerals with a tubular structure. They have attracted considerable attention as a potential nanocontainer due to their abundance, biocompatibility and nontoxicity. In this study, HNTs were handled with H2SO4 at 70 °C. The morphology and structure of these acid-treated and original HNTs were investigated by scanning electron microscopy (SEM), energy dispersion spectrum (EDS), transmission electron microscope (TEM), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR), and their specific surface area was determined by automatic gas adsorption analyzer. The loading efficiency and release behavior of acid-treated HNTs for 2-Mercaptobenzothiazole (MBT) were investigated by UV-vis spectrophotometer. Results show that acid-treated HNTs retained their tubular structure, but their internal diameter expanded by 35–37 nm after 32 h of acid treatment. After 72 h of acid treatment, HNTs can be transferred into amorphous silica nanotubes. Moreover, the specific surface area of these HNTs samples initially increased with the increase in acid treatment time but then started to decrease after 32 h. The specific surface area of acid-treated HNTs at 32 h can reach 251.6 m2/g, which was much higher than that for untreated HNTs (55.3 m2/g). In addition, the loading capacity of acid-treated HNTs can reach 32.1% for HNTs-32, which is about three times higher than that of original HNTs. The acid treatment has slight effect on the release behavior.

The Effect of Hydrothermal Treatment on Samaria and Gadolinia Doped Ceria Powders Synthesized by Coprecipitation

2010 ◽  
Vol 660-661 ◽  
pp. 959-964
Author(s):  
Alexander Rodrigo Arakaki ◽  
Walter Kenji Yoshito ◽  
Valter Ussui ◽  
Dolores Ribeiro Ricci Lazar
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Hydrothermal Treatment ◽  
Specific Surface Area ◽  
Gas Adsorption ◽  
Fluorite Structure ◽  
High Specific Surface Area ◽  
Powder Synthesis ◽  
Laser Scattering ◽  
The One

One of the main applications of ceria-based (CeO2) ceramics is the manufacturing of Intermediate Temperature Solid Oxide Fuel Cells electrolytes. In order to improve ionic conductivity and densification of these materials various powder synthesis routes have been studied. In this work powders with composition Ce0.8(SmGd)0.2O1.9 have been synthesized by coprecipitation and hydrothermal treatment. A concentrate of rare earths containing 90wt% of CeO2 and other containing 51% of Sm2O3 and 30% of Gd2O3, both prepared from monazite processing, were used as precursor materials. The powders were characterized by X-ray diffraction, scanning and transmission electron microscopy, agglomerate size distribution by laser scattering and specific surface area by gas adsorption. Ceramic sinterability was evaluated by dilatometry and density measurements by Archimedes method. High specific surface area powders (~100m2/g) and cubic fluorite structure were obtained after hydrothermal treatment around 200°C. Ceramic densification was improved when compared to the one prepared from powders calcined at 800°C.

The whole-aperture pore-structure characteristics of marine-continental transitional shale facies of the Taiyuan and Shanxi Formations in the Qinshui Basin, North China

2019 ◽  
Vol 7 (2) ◽  
pp. T547-T563 ◽  
Author(s):  
Jiyuan Wang ◽  
Shaobin Guo
Keyword(s):  
High Pressure ◽  
Specific Surface ◽  
Pore Structure ◽  
Surface Area ◽  
Specific Surface Area ◽  
Gas Adsorption ◽  
Pore Morphology ◽  
Qinshui Basin ◽  
Mercury Intrusion ◽  
Structure Characteristics

To systematically study the whole-aperture pore-structure characteristics of the marine-continental transitional shale facies in the Upper Palaeozoic Taiyuan and Shanxi Formations of the Qinshui Basin, we have collected a total of 11 samples for high-pressure mercury intrusion, low-pressure gas adsorption ([Formula: see text] and [Formula: see text]), nuclear magnetic resonance (NMR), and field-emission scanning electron microscopy with argon-ion polishing experiments to determine the pore morphology and distribution characteristics of shale samples in detail and to perform quantitative analyses. Then compared the pore-development characteristics of the Taiyuan Formation samples with those of the Shanxi Formation to determine which is preferable. The experimental results indicate that the shale samples of the Qinshui Basin mainly develop three types of pores: organic pores, intergranular pores, and microfractures. High-pressure mercury intrusion and gas-adsorption experiments indicate that the pore-size distributions exhibit multiple peaks. The samples contained varying proportions of macropores, mesopores, and micropores, among which the former two are dominant, accounting for approximately 85% of the total pore volume, whereas micropores account for only 15%. However, mesopores and micropores dominate the specific surface area; between them, the micropores are much more prevalent, accounting for more than 99% of the total specific surface area. Macropores contribute less than 1% of the specific surface area and therefore can be neglected. The pore morphology resembles the slit type parallel platy pores with a ballpoint pen structure. The NMR [Formula: see text] spectra have multiple-peak values. In addition, the large difference between the curved areas before and after centrifugation indicates that the samples contain a large proportion of mesopores and macropores, which is consistent with the results presented above. The results demonstrate that the development of pores in the Taiyuan Formation is better than that in the Shanxi Formation.

scholarly journals Improve in CO2 and CH4 Adsorption Capacity on Carbon Microfibers Synthesized by Electrospinning of PAN

Fibers ◽  
2019 ◽  
Vol 7 (10) ◽  
pp. 81 ◽  
Author(s):  
Reyna Ojeda-López ◽  
J. Marcos Esparza-Schulz ◽  
Isaac J. Pérez-Hermosillo ◽  
Armin Hernández-Gordillo ◽  
Armando Domínguez-Ortiz
Keyword(s):  
Specific Surface ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Specific Surface Area ◽  
Gas Adsorption ◽  
Morphological Structure ◽  
Different Temperatures ◽  
Ch4 Adsorption ◽  
Stabilization Temperature ◽  
Carbon Microfibers

Carbon microfibers (CMF) has been used as an adsorbent material for CO2 and CH4 capture. The gas adsorption capacity depends on the chemical and morphological structure of CMF. The CMF physicochemical properties change according to the applied stabilization and carbonization temperatures. With the aim of studying the effect of stabilization temperature on the structural properties of the carbon microfibers and their CO2 and CH4 adsorption capacity, four different stabilization temperatures (250, 270, 280, and 300 °C) were explored, maintaining a constant carbonization temperature (900 °C). In materials stabilized at 250 and 270 °C, the cyclization was incomplete, in that, the nitrile groups (triple-bond structure, e.g., C≡N) were not converted to a double-bond structure (e.g., C=N), to form a six-membered cyclic pyridine ring, as a consequence the material stabilized at 300 °C resulting in fragile microfibers; therefore, the most appropriate stabilization temperature was 280 °C. Finally, to corroborate that the specific surface area (microporosity) is not the determining factor that influences the adsorption capacity of the materials, carbonization of polyacrylonitrile microfibers (PANMFs) at five different temperatures (600, 700, 800, 900, and 1000 °C) is carried, maintaining a constant temperature of 280 °C for the stabilization process. As a result, the CMF chemical composition directly affects the CO2 and CH4 adsorption capacity, even more directly than the specific surface area. Thus, the chemical variety can be useful to develop carbon microfibers with a high adsorption capacity and selectivity in materials with a low specific surface area. The amount adsorbed at 25 °C and 1.0 bar oscillate between 2.0 and 2.9 mmol/g adsorbent for CO2 and between 0.8 and 2.0 mmol/g adsorbent for CH4, depending on the calcination treatment applicated; these values are comparable with other material adsorbents of greenhouse gases.

Surface Analysis of Etched Molar Enamel by Gas Adsorption

2008 ◽  
Vol 87 (6) ◽  
pp. 532-536 ◽  
Author(s):  
M.F. Orellana ◽  
A.E. Nelson ◽  
J.P.R. Carey ◽  
G. Heo ◽  
D.G Boychuk ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Gas Adsorption ◽  
Third Molar ◽  
Dental Enamel ◽  
Total Surface Area ◽  
Gas Absorption ◽  
Etch Pattern

Much research has been devoted to the study of etched enamel, since it is critical to bonding. Currently, there are no precise data regarding the etched-enamel specific surface area. The aim of this study was to characterize, by two different methods, the surface of human dental enamel in vitro after being etched. It was hypothesized that differences would be observed between specimens in terms of specific surface area and grade of etching. Sixteen third molar enamel samples were etched for 30 sec with 37% phosphoric acid prior to being viewed by SEM. Etched enamel surfaces were graded according to the Galil and Wright classification. The total surface area of etched samples was determined by the BET gas absorption method. A substantial variability in total surface area was observed between and among samples. A Pearson’s Correlation Coefficient showed a lack of relationship between etch pattern and total surface area.

Modification of Cordierite Honeycomb Ceramics Matrix for DeNOx Catalyst

2012 ◽  
Vol 1449 ◽  
Author(s):  
Qingcai Liu ◽  
Yuanyuan He ◽  
Jian Yang ◽  
Wenchang Xi ◽  
Juan Wen ◽  
...  
Keyword(s):  
Acid Solution ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Acid Treatment ◽  
Coefficient Of Thermal Expansion ◽  
Physical Adsorption ◽  
Active Species ◽  
Treatment Temperature ◽  
Cordierite Honeycomb

ABSTRACTTo obtain highly dispersed and highly active catalysts by impregnating of active species onto the monolith directly, cordierite honeycomb ceramics were modified by nitric acid solution of 68wt%. Effects of acid treatment temperature and time on the performance of cordierite were investigated. Specific surface area, pore size distribution, morphology and structure of cordierite were characterized by N2-physical adsorption, SEM, XRD, respectively. Concentrations of ions in the acid solution were measured by AAS. It is shown that the corrosion content of cordierite increases and more micropores are generated with increasing time of acid treatment, leading to an upward trend of specific surface area. The coefficient of thermal expansion and compression strength decrease obviously at a higher temperature, which is mainly attributed to the removal of Al and Mg ions from the silicate structure and delayed formation of free amorphous silica on the surface of the cordierite. The optimal modification process of cordierite matrix acid erosion is at 110°C for 6 h.

Effects of extraction process on the dried cell wall pore structure of messmate heartwood

BioResources ◽  
2021 ◽  
Vol 16 (3) ◽  
pp. 6074-6082
Author(s):  
Weikai Wang ◽  
Minghan Li ◽  
Jiabin Cai
Keyword(s):  
Cell Wall ◽  
Specific Surface ◽  
Pore Structure ◽  
Surface Area ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Gas Adsorption ◽  
Extraction Process ◽  
Micropore Volume ◽  
Adsorption Method

In order to study the effects of a messmate heartwood extraction process on its cell wall pore structure and its drying ability, its nanopore structure was explored after via gas adsorption technology. Specifically, the messmate heartwood particles were extracted with methanol, and then the cell wall pore structure of the original and extracted samples were evaluated by N2 and CO2 sorption and pycnometer methods, respectively. Overall, compared with the original samples, the cell wall porosity, micropore volume, mesopore volume, BET specific surface area, and specific surface area of the micropores of the extracted messmate heartwoods increased by 2.55%, 0.007 cm3/g, 0.0014 cm3/g, 0.24 m2·g-1, and 21.9 m2·g-1, respectively. The cell wall pore volume measured via the gas adsorption method was smaller than the measurement from the pycnometer method. The results indicated that the presence of extractives made the messmate cell wall have a decreased pore volume and porosity, which may be one of the reasons messmate wood is difficult to dry. Messmate extractives primarily were present in the micropores of the cell wall in the range of 0.4 nm to 0.7 nm. However, gas sorption technology could not detect all the pores in the cell wall of the messmate heartwood sample.

Conjugated microporous copolymer networks with enhanced gas adsorption

2015 ◽  
Vol 6 (17) ◽  
pp. 3217-3223 ◽  
Author(s):  
Miao Yu ◽  
Xiaoyan Wang ◽  
Xiao Yang ◽  
Yang Zhao ◽  
Jia-Xing Jiang
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Gas Adsorption ◽  
High Specific Surface Area

Conjugated microporous copolymer networks show a high specific surface area of up to 2241 m2 g−1 and a high CO2 uptake of 4.57 mmol g−1 (1.13 bar/273 K) with a H2 uptake of 2.24 wt% (1.13 bar/77.3 K).

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