Honeycombed activated carbon with greatly increased specific surface by direct activation of glucose for supercapacitors

2021 ◽  
pp. 160907
Author(s):  
Lu Zhang ◽  
Lixing Zhang ◽  
Huazhi Gu ◽  
Yao Chen ◽  
George Zheng Chen
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Direct Activation

scholarly journals Experimental Study on Activated Carbon-MIL-101(Cr) Composites for Ethanol Vapor Adsorption

Materials ◽  
2021 ◽  
Vol 14 (14) ◽  
pp. 3811
Author(s):  
Zhongbao Liu ◽  
Jiayang Gao ◽  
Xin Qi ◽  
Zhi Zhao ◽  
Han Sun
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Ethanol Vapor ◽  
Future Application ◽  
Working Fluid ◽  
Relative Pressure ◽  
Adsorption Refrigeration ◽  
Vapor Adsorption

In this study, the hydrothermal method was used to synthesize MIL-101(Cr), and activated carbon (AC) with different content was incorporated in to MIL-101(Cr), thereby obtaining AC-MIL-101(Cr) composite material with a huge specific surface area. The physical properties of MIL-101(Cr) and AC-MIL-101(Cr) were characterized by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), nitrogen adsorption and desorption and specific surface area testing, and ethanol vapor adsorption performance testing. The results show that with the increase of activated carbon content, the thermal stability of AC-MIL-101(Cr) is improved. Compared with the pure sample, the BET specific surface area and pore volume of AC-MIL-101(Cr) have increased; In the relative pressure range of 0–0.4, the saturated adsorption capacity of AC-MIL-101(Cr) to ethanol vapor decreases slightly. It is lower than MIL-101(Cr), but its adsorption rate is improved. Therefore, AC-MIL-101(Cr)/ethanol vapor has a good application prospect in adsorption refrigeration systems. The exploration of AC-MIL-101(Cr) composite materials in this paper provides a reference for the future application of carbon-based/MOFS composite adsorbent/ethanol vapor working fluid in adsorption refrigeration.

Increase the Microporosity and CO2 Adsorption of a Commercial Activated Carbon

2015 ◽  
Vol 749 ◽  
pp. 17-21 ◽  
Author(s):  
Joanna Sreńscek Nazzal ◽  
Karolina Glonek ◽  
Jacek Młodzik ◽  
Urszula Narkiewicz ◽  
Antoni W. Morawski ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Materials ◽  
Micropore Volume ◽  
Microporous Carbon ◽  
Microporous Carbons ◽  
Adsorption Capacities

Microporous carbons prepared from commercial activated carbon WG12 by KOH and/or ZnCl2 treatment were examined as adsorbents for CO2 capture. The micropore volume and specific surface area of the resulting carbons varied from 0.52 cm3/g (1374 m2/g) to 0.70 cm3/g (1800 m2/g), respectively. The obtained microporous carbon materials showed high CO2 adsorption capacities at 40 bar pressure reaching 16.4 mmol/g.

Study of the Porous Structure and High Adsorption Capacity of Biomass-Based Activated Carbon Prepared from Aspen Wood by Ferric Nitrate III Activation

2021 ◽  
Vol 15 (2) ◽  
pp. 131-144
Author(s):  
Chunjiang Jin ◽  
Huimin Chen ◽  
Luyuan Wang ◽  
Xingxing Cheng ◽  
Donghai An ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Mass Ratio ◽  
Aspen Wood ◽  
Surface Functional Groups ◽  
Wood Sawdust

In this study, aspen wood sawdust was used as the raw material, and Fe(NO3)3 and CO2 were used as activators. Activated carbon powder (ACP) was produced by the one-step physicochemical activation method in an open vacuum tube furnace. The effects of different mass ratios of Fe(NO3)3 and aspen wood sawdust on the pore structure of ACP were examined under single-variable experimental conditions. The mass ratio was 0–0.4. The detailed characteristics of ACP were examined by nitrogen adsorption, scanning electron microscopy, X-ray diffraction, and Fourier transform infrared spectroscopy. The adsorption capacity of ACP was established by simulating volatile organic compounds (VOCs) using ethyl acetate. The results showed that ACP has a good nanostructure with a large pore volume, specific surface area, and surface functional groups. The pore volume and specific surface area of Fe-AC-0.3 were 0.26 cm3/g and 455.36 m2/g, respectively. The activator played an important role in the formation of the pore structure and morphology of ACP. When the mass ratio was 0–0.3, the porosity increased linearly, but when it was higher than 0.3, the porosity decreased. For example, the pore volume and specific surface area of Fe-AC-0.4 reached 0.24 cm3/g and 430.87 m2/g, respectively. ACP presented good VOC adsorption performance. The Fe-AC-0.3 sample, which contained the most micropore structures, presented the best adsorption capacity for ethyl acetate at 712.58 mg/g. Under the action of the specific reaction products nitrogen dioxide (NO2) and oxygen, the surface of modified ACP samples showed different rich C/O/N surface functional groups, including C-H, C=C, C=O, C-O-C, and C-N.

scholarly journals Highly Mesoporous Carbon Aerogel as Catalyst Support in Proton Exchange Membrane Fuel Cells

2019 ◽  
Author(s):  
Kevin Gu ◽  
Eric J. Kim ◽  
Sunil K. Sharma ◽  
Keyword(s):  
Fuel Cells ◽  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Mesoporous Carbon ◽  
Proton Exchange Membrane ◽  
Catalyst Support ◽  
Carbon Aerogel ◽  
Proton Exchange ◽  
Exchange Membrane

<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>

Mesoporous Activated Carbon Filaments

1996 ◽  
Vol 454 ◽  
Author(s):  
Weiming Lu ◽  
D. D. L. Chung
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Pore Size ◽  
Surface Area ◽  
Specific Surface Area ◽  
Mesoporous Activated Carbon ◽  
Carbon Filaments

ABSTRACTActivated carbon filaments of diameter ∼0.1 μm, main pore size (BJH) 55 Å, specific surface area 1310 m2/g and yield 36.2% were obtained by activating carbon filaments of diameter ∼ 0.1 urn in C02 + N2 (1:1) at 970°C for 80 min. Prior to this activation, the filaments were surface oxidized by exposure to ozone.

Analysis of the Factors Affecting the Instrumentation of the Technological Process of the Activated Carbon Material Production

2022 ◽  
pp. 20-30
Author(s):  
A.A. Popova ◽  
I.N. Shubin
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Carbon Material ◽  
Mutual Influence ◽  
Chemical Activation ◽  
High Specific Surface Area ◽  
Laboratory Research ◽  
High Porosity ◽  
Gas Purification ◽  
Factors Affecting

The article discusses significance of the development of activated carbon materials with a high specific surface area and high porosity. The features of the course of chemical activation and the factors influencing the characteristics of the obtained material have been established. The main stages of the activation of the carbon material, including the preliminary raw carbon material carbonization, its alkaline activation, and the post-processing of the created material, have been determined. The mutual influence of temperature and flow rate of an inert gas on the characteristics of a carbon material obtained with a BET specific surface in the range of 2550–2700 m2/g is experimentally investigated. The analysis of the obtained results has been carried out. Recommendations are given for reducing ambiguity and uncertainty during the transition from laboratory research to pilot production. The resulting activated carbon material can be used as a sorbent in gas purification systems, gas accumulators and for solving various environmental problems.

scholarly journals Thermal Modification Effect on Supported Cu-Based Activated Carbon Catalyst in Hydrogenolysis of Glycerol

Materials ◽  
2020 ◽  
Vol 13 (3) ◽  
pp. 603 ◽  
Author(s):  
Juan Seguel ◽  
Rafael García ◽  
Ricardo José Chimentão ◽  
José Luis García-Fierro ◽  
I. Tyrone Ghampson ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Hydrogen Adsorption ◽  
Carbon Support ◽  
Catalytic Performance ◽  
Homogeneous Distribution ◽  
Surface Groups ◽  
Carbon Supports ◽  
Surface Areas ◽  
Oxygen Surface

Glycerol hydrogenolysis to 1,2-propanediol (1,2-PDO) was performed over activated carbon supported copper-based catalysts. The catalysts were prepared by impregnation using a pristine carbon support and thermally-treated carbon supports (450, 600, 750, and 1000 °C). The final hydrogen adsorption capacity, porous structure, and total acidity of the catalysts were found to be important descriptors to understand catalytic performance. Oxygen surface groups on the support controlled copper dispersion by modifying acidic and adsorption properties. The amount of oxygen species of thermally modified carbon supports was also found to be a function of its specific surface area. Carbon supports with high specific surface areas contained large amount of oxygen surface species, inducing homogeneous distribution of Cu species on the carbon support during impregnation. The oxygen surface groups likely acted as anchorage centers, whereby the more stable oxygen surface groups after the reduction treatment produced an increase in the interaction of the copper species with the carbon support, and determined catalytic performances.

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