2022
DOI: 10.1016/j.fuel.2022.123277
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A low carbon footprint method for converting low-rank coals to oxygen-containing chemicals

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Cited by 25 publications
(6 citation statements)
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“…Additionally, two characteristic absorption peaks corresponding to the stretching vibration of C–O in the 1000–1260 cm –1 range and −OH around 3420 cm –1 in a-AER 500 indicated that a-AER 500 retained abundant OCFGs after activation. The absorbance of aromatic CC vibration around 1600 cm –1 in a-AER 500 was stronger than that in AER 500 , while the absorbance of −CH 2 – and −CH 3 vibration around 2900 cm –1 and 2870 cm –1 in a-AER 500 was weaker than those in AER 500, suggesting that the macromolecular aromatic structures were further polymerized at high temperature.…”
Section: Resultsmentioning
confidence: 93%
“…Additionally, two characteristic absorption peaks corresponding to the stretching vibration of C–O in the 1000–1260 cm –1 range and −OH around 3420 cm –1 in a-AER 500 indicated that a-AER 500 retained abundant OCFGs after activation. The absorbance of aromatic CC vibration around 1600 cm –1 in a-AER 500 was stronger than that in AER 500 , while the absorbance of −CH 2 – and −CH 3 vibration around 2900 cm –1 and 2870 cm –1 in a-AER 500 was weaker than those in AER 500, suggesting that the macromolecular aromatic structures were further polymerized at high temperature.…”
Section: Resultsmentioning
confidence: 93%
“…This is consistent with their higher C and H content in Table . All the SDP subfractions show the obvious carbonyl vibration peaks at 1710 cm –1 . , The peaks near 1610, 1500, and 1450 cm –1 are assigned to aromatic ring stretching vibrations. , The peaks of THFS and TS at these positions are strong while that of HS is weak, indicating abundant aromatic structures in THFS and TS. The bands at 1300–1000 cm –1 are assigned to C–O (alcohol), C–O (phenol), and C–O–C structures, and their presence suggests the rich alcohol, phenol, and/or ether group in SDP subfractions.…”
Section: Resultsmentioning
confidence: 97%
“…The strong resonance peaks at 126–128.5 ppm indicate the preponderance of phenanthrene, its methyl-substituted molecule, and anthracene. The peaks at 137–139 ppm are attributed to polycyclic species and their substituted aromatics. , The total number of carbons ( C t ) in THFS is 78.5; therefore, the number of each type of carbon of THFS can be calculated from the 13 C-NMR spectra, and the results are listed in Table . The number of carbons in the carboxyl group of an average molecule of THFS is 1.4 (Table ).…”
Section: Resultsmentioning
confidence: 99%
“…53 CBHA mainly consists of sp 2 -conjugated CQC rings connected with carboxyl (-COOH), hydroxyl (-OH), and carbonyl (CQO), which is the perfect precursor for the assembly of CDs. 53,54 The synthetic CBHA-derived CDs (HACDs) have abundant functional groups and excellent properties, which can be applied in areas such as bio-imaging, chemical analysis, photocatalysis and optoelectronic materials. 55 However, to the best of our knowledge, there are few reports on coal-based CDs as RTP materials.…”
Section: Introductionmentioning
confidence: 99%