Double function of tris(hydroxymethyl)aminomethane (THAM) for the preparation of colloidal silica nanospheres and the conversion to ordered mesoporous carbon

2011 ◽  
Vol 47 (39) ◽  
pp. 10933 ◽  
Author(s):  
Kwang-Min Choi ◽  
Kazuyuki Kuroda
Keyword(s):  
Mesoporous Carbon ◽  
Colloidal Silica ◽  
Ordered Mesoporous Carbon ◽  
Silica Nanospheres ◽  
Ordered Mesoporous ◽  
Double Function

Advanced ordered mesoporous carbon with fast Li-ion diffusion for lithium–selenium sulfide batteries in a carbonate-based electrolyte

Carbon ◽  
2020 ◽  
Vol 170 ◽  
pp. 236-244
Author(s):  
Wonhee Kim ◽  
Jiyeon Lee ◽  
Seungmin Lee ◽  
KwangSup Eom ◽  
Chanho Pak ◽  
...  
Keyword(s):  
Mesoporous Carbon ◽  
Ordered Mesoporous Carbon ◽  
Ion Diffusion ◽  
Ordered Mesoporous ◽  
Li Ion ◽  
Selenium Sulfide

scholarly journals Efficient Batch and Fixed-Bed Sequestration of a Basic Dye using a Novel Variant of Ordered Mesoporous Carbon as Adsorbent

2021 ◽  
pp. 103186
Author(s):  
Asna Mariyam ◽  
Jyoti Mittal ◽  
Farzeen Sakina ◽  
Richard T. Baker ◽  
Ashok K. Sharma ◽  
...  
Keyword(s):  
Mesoporous Carbon ◽  
Fixed Bed ◽  
Ordered Mesoporous Carbon ◽  
Basic Dye ◽  
Ordered Mesoporous ◽  
Novel Variant

scholarly journals A Hierarchically Ordered Mesoporous-Carbon-Supported Iron Sulfide Anode for High-Rate Na-Ion Storage

Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4349
Author(s):  
Anupriya K. Haridas ◽  
Natarajan Angulakshmi ◽  
Arul Manuel Stephan ◽  
Younki Lee ◽  
Jou-Hyeon Ahn
Keyword(s):  
Mesoporous Carbon ◽  
Anode Materials ◽  
Iron Sulfide ◽  
Carbon Composite ◽  
Ordered Mesoporous Carbon ◽  
Cycle Life ◽  
High Rate ◽  
Volume Changes ◽  
Ordered Mesoporous ◽  
Ion Storage

Sodium-ion batteries (SIBs) are promising alternatives to lithium-based energy storage devices for large-scale applications, but conventional lithium-ion battery anode materials do not provide adequate reversible Na-ion storage. In contrast, conversion-based transition metal sulfides have high theoretical capacities and are suitable anode materials for SIBs. Iron sulfide (FeS) is environmentally benign and inexpensive but suffers from low conductivity and sluggish Na-ion diffusion kinetics. In addition, significant volume changes during the sodiation of FeS destroy the electrode structure and shorten the cycle life. Herein, we report the rational design of the FeS/carbon composite, specifically FeS encapsulated within a hierarchically ordered mesoporous carbon prepared via nanocasting using a SBA-15 template with stable cycle life. We evaluated the Na-ion storage properties and found that the parallel 2D mesoporous channels in the resultant FeS/carbon composite enhanced the conductivity, buffered the volume changes, and prevented unwanted side reactions. Further, high-rate Na-ion storage (363.4 mAh g−1 after 500 cycles at 2 A g−1, 132.5 mAh g−1 at 20 A g−1) was achieved, better than that of the bare FeS electrode, indicating the benefit of structural confinement for rapid ion transfer, and demonstrating the excellent electrochemical performance of this anode material at high rates.

scholarly journals Ordered Mesoporous Carbon as a Support for Palladium-Based Hydrodechlorination Catalysts

Catalysts ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 23
Author(s):  
Farzeen Sakina ◽  
Carlos Fernandez-Ruiz ◽  
Jorge Bedia ◽  
Luisa Gomez-Sainero ◽  
Richard Baker
Keyword(s):  
Photoelectron Spectroscopy ◽  
Mesoporous Carbon ◽  
Catalyst Deactivation ◽  
Average Diameter ◽  
Pd Nanoparticles ◽  
Ordered Mesoporous Carbon ◽  
Catalyst Composition ◽  
Ordered Mesoporous ◽  
Higher Hydrocarbons ◽  
Carbon Catalysts

Ordered mesoporous carbon (OMC) was employed as a support for palladium nanoparticles in catalysts for the gas phase hydrodechlorination (HDC) of trichloromethane (TCM). 1 wt% palladium was incorporated using three methods: incipient wetness (IW); a dilute solution (DS) method; and a solid-liquid (SL) method. The effect of the preparation method on catalyst structure and activity was investigated. Catalyst composition and nanostructure were studied using gas physisorption, high specification transmission electron microscopy and X-ray photoelectron spectroscopy. Catalytic conversion and product selectivities were determined in steady-state activity tests at temperatures between 70 and 300 °C. Two of the catalysts (IW and DS) showed excellent dispersion of fine Pd nanoparticles of average diameter ~2 nm. These materials showed excellent activity for HDC of TCM which compares favourably with the performance reported for Pd on amorphous carbon catalysts. In addition, they showed relatively high selectivities to the more valuable higher hydrocarbons. However, the SL method gave rise to catalysts with larger particles (~3 nm) and a less uniform palladium distribution. This resulted in lower conversion and lower selectivities to higher hydrocarbons and in more severe catalyst deactivation at the highest reaction temperatures.

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