2016
DOI: 10.1016/j.fuproc.2016.08.035
|View full text |Cite
|
Sign up to set email alerts
|

FTIR study on structural changes of different–rank coals caused by single/multiple extraction with cyclohexanone and NMP/CS 2 mixed solvent

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
29
0

Year Published

2018
2018
2023
2023

Publication Types

Select...
6
1
1

Relationship

0
8

Authors

Journals

citations
Cited by 73 publications
(31 citation statements)
references
References 58 publications
1
29
0
Order By: Relevance
“…The sample preparation work followed the procedure of Tian et al and Wang et al [71,72]. The characteristic peaks of the minerals and organic functional groups can be obtained from Figure 7d, indicating that there was a close relationship between the organic functional groups and B. licheniformis.…”
Section: Ftir Analysis Of the Minerals At A Mg/ca Molar Ratio Of 0 Anmentioning
confidence: 97%
See 1 more Smart Citation
“…The sample preparation work followed the procedure of Tian et al and Wang et al [71,72]. The characteristic peaks of the minerals and organic functional groups can be obtained from Figure 7d, indicating that there was a close relationship between the organic functional groups and B. licheniformis.…”
Section: Ftir Analysis Of the Minerals At A Mg/ca Molar Ratio Of 0 Anmentioning
confidence: 97%
“…FTIR Analysis of the Minerals at a Mg/Ca Molar Ratio of 0 and 3 Induced by BacteriaThe sample preparation work followed the procedure of Tian et al and Wang et al[71,72]. The characteristic peaks of the minerals and organic functional groups can be obtained fromFigure 7.…”
mentioning
confidence: 99%
“…The organic functional groups on/within the minerals were analyzed by FTIR (Nicolet 380, Thermo Fisher Scientific Inc., Waltham, MA, USA) [77,78] using the potassium bromide method in a scanning range of 400-4000 cm −1 with a resolution of 4 cm −1 .…”
Section: Characterization Of the Extracellular Mineral Precipitatesmentioning
confidence: 99%
“…It exhibited that HMD‐GO contained amino functional groups. The characteristic bands of GO appeared at 3,420 cm −1 (O‐H stretching vibration), 1,740 cm −1 (C = O stretching in carboxylic acid), 1,630 cm −1 (C = C stretching in aromatic ring), and 1,047 cm −1 (epoxy stretching vibration) . The reaction between GO and HMD was confirmed by the appearance of peaks at 2,836 and 2,911 cm −1 (C‐H stretching of CH 2 ) and a new peak at 1,560 cm −1 along with a broad band at 3,732 cm −1 (N‐H wagging vibration of the amine group) in FT‐IR spectra of HMD‐GO.…”
Section: Resultsmentioning
confidence: 87%