Preparation of mesoporous carbon by steam activation of commercial activated carbon in the presence of yttrium oxide

Author(s):  
W.Z. Shen ◽  
J.T. Zheng ◽  
Y.L. Zhang ◽  
J.G. Wang ◽  
Z.F. Qin
RSC Advances ◽  
2014 ◽  
Vol 4 (104) ◽  
pp. 60168-60175 ◽  
Author(s):  
Qiaoli Peng ◽  
Zehui Zhang ◽  
Ze'ai Huang ◽  
Wei Ren ◽  
Jie Sun

N-Doped ordered mesoporous carbon (N-OMC) was successfully prepared using dicyandiamide (C2H4N4) as the nitrogen source and was grafted onto activated carbon fibres (ACFs) to form carbon composites (ACF@N-OMC).


2013 ◽  
Vol 228 ◽  
pp. 1074-1082 ◽  
Author(s):  
Kaifang Fu ◽  
Qinyan Yue ◽  
Baoyu Gao ◽  
Yuanyuan Sun ◽  
Liujia Zhu

2019 ◽  
Author(s):  
Kevin Gu ◽  
Eric J. Kim ◽  
Sunil K. Sharma ◽  

<p>Carbon aerogel possesses unique structural and electrical properties, such as high mesopore volume, specific surface area, and electrical conductivity, which make it suitable for use as a catalyst support in Proton Exchange Membrane Fuel Cells (PEMFC). In this study, we present a novel synthesis of highly mesoporous carbon aerogel via ambient-drying and investigate its application in PEMFCs. The structural effects of activation on carbon aerogel were also studied. The TEM, XRF, Non Localized Density Function Theory (NLDFT) and BJH analysis were carried out to observe the morphology and pore structure. Pt on carbon aerogel and activated carbon aerogel show efficient activity in both oxygen reduction and hydrogen oxidation reactions compared to Pt on Vulcan XC-72, with increases up to 715% and 195% in specific power density, respectively. The enhanced performance of carbon aerogel is attributed to its large specific surface area and high mesopore to micropore ratio. Accelerated stress tests show that carbon aerogel has comparable durability with Vulcan XC-72, while activated carbon aerogel is less durable than both materials. Thus, the mesoporous carbon aerogel provides an efficient, lower-cost alternative to existing microporous carbon material as a catalyst support in PEMFCs.</p><p></p>


2019 ◽  
Vol 236 ◽  
pp. 245-253 ◽  
Author(s):  
Peter Nai Yuh Yek ◽  
Rock Keey Liew ◽  
Mohammad Shahril Osman ◽  
Chern Leing Lee ◽  
Joon Huang Chuah ◽  
...  

Catalysts ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 406 ◽  
Author(s):  
Masayasu Nishi ◽  
Shih-Yuan Chen ◽  
Hideyuki Takagi

The Cs-promoted Ru nanocatalysts supported on mesoporous carbon materials (denoted as Cs-Ru/MPC) and microporous activated carbon materials (denoted as Cs-Ru/AC) were prepared for the sustainable synthesis of ammonia under mild reaction conditions (<500 °C, 1 MPa). Both Ru and Cs species were homogeneously impregnated into the mesostructures of three commercial available mesoporous carbon materials annealed at 1500, 1800 and 2100 °C (termed MPC-15, MPC-18 and MPC-21, respectively), resulting in a series of Cs-Ru/MPC catalysts with Ru loadings of 2.5–10 wt % and a fixed Cs loading of 33 wt %, corresponding to Cs/Ru molar ratios of 2.5–10. However, the Ru and Cs species are larger than the pore mouths of microporous activated carbon (shortly termed AC) and, as a consequence, were mostly aggregated on the outer surface of the Cs-Ru/AC catalysts. The Cs-Ru/MPC catalysts are superior to the Cs-Ru/AC catalyst in catalysing mild ammonia synthesis, especially for the 2.5Cs-10Ru/MPC-18 catalyst with a Ru loading of 10 wt % and a Cs/Ru ratio of 2.5, which exhibited the highest activity across a wide SV range. It also showed an excellent response and stability during cycling tests over a severe temperature jump in a short time, presumably due to the open mesoporous carbon framework and suitable surface concentrations of CsOH and metallic Ru species at the catalytically active sites. This 2.5Cs-10Ru/MPC-18 catalyst with high activity, fast responsibility and good stability has potential application in intermittently variable ammonia synthesis using CO2-free hydrogen derived from electrolysis of water using renewable energy with fast variability.


RSC Advances ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 6452-6459 ◽  
Author(s):  
Guangzhi Xin ◽  
Min Wang ◽  
Lin Chen ◽  
Yuzhou Zhang ◽  
Meicheng Wang ◽  
...  

A novel adsorbent zeolite/N-doped porous activated carbon (ZAC) was prepared by the synthesis of zeolite and mesoporous carbon to remove ammonia nitrogen (NH4+–N) and chemical oxygen demand (COD) from aqueous solution.


2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
Daouda Kouotou ◽  
Horace Ngomo Manga ◽  
Abdelaziz Baçaoui ◽  
Abdelrani Yaacoubi ◽  
Joseph Ketcha Mbadcam

In this study, activated carbons were prepared from oil palm shells by physicochemical activation. The methodology of experimental design was used to optimize the preparation conditions. The influences of the impregnation ratio (0.6–3.4) and the activation temperature between 601°C and 799°C on the following three responses: activated carbon yield (R/AC-H3PO4), the iodine adsorption (I2/AC-H3PO4), and the methylene blue adsorption (MB/AC-H3PO4) results were investigated using analysis of variance (ANOVA) to identify the significant parameters. Under the experimental conditions investigated, the activation temperature of 770°C and impregnation ratio of 2/1 leading to the R/AC-H3PO4of 52.10%, theI2/AC-H3PO4of 697.86 mg/g, and the MB/AC-H3PO4of 346.25 mg/g were found to be optimum conditions for producing activated carbon with well compromise of desirability. The two factors had both synergetic and antagonistic effects on the three responses studied. The micrographs of activated carbons examined with scanning electron microscopy revealed that the activated carbons were found to be mainly microporous and mesoporous.


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