TY - JOUR
T1 - Sequential extraction and characterization of liquefaction residue from Shenmu-Fugu subbituminous coal
AU - Li, Peng
AU - Zong, Zhi Min
AU - Liu, Fang Jing
AU - Wang, Yu Gao
AU - Wei, Xian Yong
AU - Fan, Xing
AU - Zhao, Yun Peng
AU - Zhao, Wei
N1 - Publisher Copyright:
© 2014 Elsevier B.V. All rights reserved.
PY - 2015/7/28
Y1 - 2015/7/28
N2 - Liquefaction residue from Shenmu-Fugu subbituminous coal (LRSFSBC) was fractionated into extracts 1-6 (E1-E6) and inextractable portion (IEP) by sequential extraction with petroleum ether, cyclohexane, methanol, acetone, carbon disulfide (CDS), and isometric CDS and acetone mixture (ICDSAM) followed by analyses with Fourier transform infrared (FTIR) spectrometer, gas chromatography/mass spectrometer (GC/MS) and atmospheric solid analysis probe/time of flight mass spectrometer (ASAP/TOF-MS). In total, 69.06% of LRSFSBC were extracted by the sequential extraction. Large amounts of multi-substituted alkylarenes and hydroarenes were identified in LRSFSBC according to GC/MS and FTIR analyses. A series of nitrogen heterocyclic aromatics and arylamines in LRSFSBC were enriched in E3. In total 61 compounds were detected with GC/MS, including 48 arenes with a total relative content of 98.72%, while 478 organooxygens, organonitrogens, organosulfurs, and organochlorines were detected with ASAP/TOF-MS. The double bond equivalent, carbon number, and molecular mass distribution of the compounds range from 0 to 13, 6 to 23, and 230 to 511 Da, respectively, by ASAP/TOF-MS analysis. E1 with the yield of 33.47% could be converted to light oil by catalytic hydroconversion due to its high H/C ratio and low sulfur content, while E5 could be a promising precursor for preparing carbon materials because of its high carbon content and C/H ratio.
AB - Liquefaction residue from Shenmu-Fugu subbituminous coal (LRSFSBC) was fractionated into extracts 1-6 (E1-E6) and inextractable portion (IEP) by sequential extraction with petroleum ether, cyclohexane, methanol, acetone, carbon disulfide (CDS), and isometric CDS and acetone mixture (ICDSAM) followed by analyses with Fourier transform infrared (FTIR) spectrometer, gas chromatography/mass spectrometer (GC/MS) and atmospheric solid analysis probe/time of flight mass spectrometer (ASAP/TOF-MS). In total, 69.06% of LRSFSBC were extracted by the sequential extraction. Large amounts of multi-substituted alkylarenes and hydroarenes were identified in LRSFSBC according to GC/MS and FTIR analyses. A series of nitrogen heterocyclic aromatics and arylamines in LRSFSBC were enriched in E3. In total 61 compounds were detected with GC/MS, including 48 arenes with a total relative content of 98.72%, while 478 organooxygens, organonitrogens, organosulfurs, and organochlorines were detected with ASAP/TOF-MS. The double bond equivalent, carbon number, and molecular mass distribution of the compounds range from 0 to 13, 6 to 23, and 230 to 511 Da, respectively, by ASAP/TOF-MS analysis. E1 with the yield of 33.47% could be converted to light oil by catalytic hydroconversion due to its high H/C ratio and low sulfur content, while E5 could be a promising precursor for preparing carbon materials because of its high carbon content and C/H ratio.
KW - ASAP/TOF-MS analysis
KW - Coal liquefaction residue
KW - Composition
KW - Sequential extraction
UR - http://www.scopus.com/inward/record.url?scp=84944408174&partnerID=8YFLogxK
U2 - 10.1016/j.fuproc.2014.04.013
DO - 10.1016/j.fuproc.2014.04.013
M3 - Article
AN - SCOPUS:84944408174
SN - 0378-3820
VL - 136
SP - 1
EP - 7
JO - Fuel Processing Technology
JF - Fuel Processing Technology
ER -