2018
DOI: 10.1016/j.jece.2017.12.069
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Porosity enhancement of spherical activated carbon: Influence and optimization of hydrothermal synthesis conditions using response surface methodology

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Cited by 44 publications
(11 citation statements)
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“…The XRD patterns of the natural biochar depicted two broad diffraction peaks centered at 2θ = 22° and 43°, corresponding to the (0,0,2) planes of graphite and the (1,0,1) reflection stemming from the in‐plane structure of graphitic crystallites, respectively. Similar results have been reported in the literature 61‐63 . However, after the impregnation of bismuth, the diffraction intensity of Bi@WBC was notably higher than those of Bi@CBC and Bi@BBC, suggesting that Bi@WBC exhibited a stronger degree of crystallinity and graphitization than the others.…”
Section: Resultssupporting
confidence: 89%
See 1 more Smart Citation
“…The XRD patterns of the natural biochar depicted two broad diffraction peaks centered at 2θ = 22° and 43°, corresponding to the (0,0,2) planes of graphite and the (1,0,1) reflection stemming from the in‐plane structure of graphitic crystallites, respectively. Similar results have been reported in the literature 61‐63 . However, after the impregnation of bismuth, the diffraction intensity of Bi@WBC was notably higher than those of Bi@CBC and Bi@BBC, suggesting that Bi@WBC exhibited a stronger degree of crystallinity and graphitization than the others.…”
Section: Resultssupporting
confidence: 89%
“…Similar results have been reported in the literature. [61][62][63] However, after the impregnation of bismuth, the diffraction intensity of Bi@WBC was notably higher than those of Bi@CBC and Bi@BBC, suggesting that Bi@WBC exhibited a stronger degree of crystallinity and graphitization than the others. In Fig.…”
Section: Surface Chemistry Of Bibc Xrd Investigationmentioning
confidence: 98%
“…Table S2 shows the ANOVA for the response model. The response model has a reasonable F-value of 27.04 and a p-value of 0.0001 (less than 0.05), as well as a lack of fit p-value of 0.37 (higher than 0.05) 31 .…”
Section: Resultsmentioning
confidence: 91%
“…The overlapping bands with peaks at 1695 cm −1 and 1606 cm −1 are due to carbonyl (C=O) stretching vibrations and the stretching of C=C in aromatic rings, respectively [49]. The broad band at 1298 cm −1 is ascribed to C-O bending vibrations [50]. The band at 798 cm −1 is attributed to the C-H vibration in aromatic structures [49].…”
Section: Resultsmentioning
confidence: 99%