514
Views
4
CrossRef citations to date
0
Altmetric
Articles

The effect of pore and surface characteristics of activated carbon produced by coal through N2 and H2O vapor/H3PO4 activation on a single step for CH4 adsorption in the low pressure

Pages 1950-1962 | Received 06 Jan 2019, Accepted 18 Feb 2019, Published online: 15 Apr 2019
 

ABSTRACT

In this study, activated carbons (AC) were produced by the activation of H3PO4 (with and without sonication) under N2 and N2+ H2O vapor at various temperatures (700–900°C). These ACs have been investigated for the effect of surface and pore property on methane adsorption at low pressure (1 atm) and 298 K. The textural, surface and porosity properties of activated carbons were determined by N2 (77 K), CO2 (273 K), and SEM-EDAX, XRD. The CH4 adsorption-desorption behavior at 298 K under low pressure was calculated using the volumetric method. According to the results obtained from N2 adsorption at 77 K, it was determined that the increase of temperature, N2+ H2O vapor and sonication increased BET surface area and pore volume of the ACs. The highest BET surface area and total pore volume were found in the H900N2+ H2O-S sample as 1881 m2/g and 1.12 cm3/g, respectively. It has been shown that narrow micropores (<10 Å) and surface oxygen groups are effective in increasing the CH4 adsorption capacity at 298 K at low pressures. Although ACs produced by N2+ H2O vapor have similar micropore volume to ACs generated by N2 activation, ACs produced with N2+ H2O vapor are found to have higher CH4 adsorption due to the lower oxygen content. The highest CH4 adsorption capacity at 298 K was found at H800N2+ H2O sample and it is 19.45 cm3/g.

Acknowledgments

This study was supported by Bülent Ecevit University Scientific Research Projects (project no: 2014-52349806-01). In addition, I would like to thank Prof. Dr. Türkan KOPAÇ who provide us the opportunity to use her laboratory.

Additional information

Funding

This work was supported by the Bülent Ecevit Üniversitesi [2014-52349806-01].

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.