For instance, as for EA data, the oxygen content of the carbons increased from 17.6 to 36.7 wt% and 41.5 wt% after oxidizing pristine CDC by HNO3 at 50°C and 80°C, respectively. The subsequent H2 reduction decreased the oxygen contents to 11.2 and 20.5 wt% for CDC-50 and CDC-80, respectively. Table 1 Specific surface areas, pore structure parameters, and oxygen contents of CDCs Sample S BET a V micro b V total c Pore sized O content (m2 g−1) (cm3 g−1) (cm3 g−1) (nm) EA (wt%) XPS (wt%) EDS (wt%) Pristine CDC 1,216 0.59 0.65 2.13 17.6 8.7 6.8 CDC-50 907 0.43 0.47 2.06 36.7 14.6
20.3 CDC-50-HR 1,115 check details 0.51 0.58 2.08 11.2 10.2 10.3 CDC-80 449 0.22 0.24 2.15 41.5 15.7 29.8 CDC-80-HR 497 0.22 0.27 2.21 20.5 14.2 16.0 aBET specific surface area. bMicropore volumes calculated by the t-plot method. cSingle-point total pore volume measured at p/p 0 = 0.995. dPore size = 4V total/S BET. Nitrogen physisorption measurements were performed at RepSox nmr 77 K to characterize the surface areas and pore structures of CDCs. The N2 adsorption isotherms of all the carbons (Additional file 1: Figure S2) exhibit type I isotherms, and no hysteresis loop can be observed for these samples, indicating the microporous nature of these carbons and the absence of mesopores. The detailed specific surface area and pore structure parameters
of these carbons are listed in Table 1. The specific surface area MycoClean Mycoplasma Removal Kit and micropore volume decrease from 1,216 m2/g and 0.59 cm3/g to 907 m2/g and 0.43 cm3/g, respectively, after
oxidizing the pristine CDC by HNO3 at 50°C, which is due to the introduction of oxygen-containing www.selleckchem.com/products/gsk2126458.html groups to the pore surface of the carbon. After H2 reduction, the specific surface area and micropore volume increase back to 1,115 m2/g and 0.51 cm3/g, indicating that the oxygen-containing groups are effectively removed from the pore surface by H2 reduction. This result coincides with the elemental analyses data. It is also suggested that the oxidation of the pristine CDC by HNO3 at 50°C did not obviously damage the pore structure of the carbon and that the decrement in the specific surface area and micropore volume due to the oxidation can be mostly recovered by H2 reduction. By contrast, oxidizing the pristine CDC by HNO3 at 80°C results in the dramatic decrease of the specific surface area and micropore volume. Although the subsequent H2 reduction can effectively remove oxygen-containing groups from CDC-80, the surface area and micropore volume cannot be recovered, indicating that HNO3 oxidation at 80°C severely damaged the micropore structure of the carbon. In order to further clarify the pore structure evolution caused by HNO3 oxidation, TEM observations were also conducted to get the microscopic morphology of the CDC.