Effect of heat reflux extraction on the structure and composition of a high-volatile bituminous coal
- 1. State Key Laboratory of Heavy Oil Processing, China University of Petroleum (East China), Qingdao 266580 (China)
- 2. Key Laboratory of Low Carbon Energy and Chemical Engineering, Shandong University of Science and Technology, Qingdao, Shandong 266590 (China)
- 3. State Key Laboratory Breeding Base of Coal Science and Technology Co-founded by Shanxi Province and the Ministry of Science and Technology, Taiyuan University of Technology, Taiyuan 030024 (China)
Description
Highlights: • A novel HRE process with CYC is proposed to dissolve coal. • Most of the aliphatic compounds in coal are extracted during HRE process. • The carbon crystallite structure of coal changes after HRE process with CYC. • The thermal degradation behavior of ER is significantly different from that of the SFHB. - Abstract: Heat reflux extraction (HRE) process with cyclohexanone (CYC) in a high-performance mass transfer extractor was applied to dissolve Shenmu-Fugu high-volatile bituminous (SFHB) coal for the first time to afford extract (E) and extract residue (ER) from the extraction. SFHB, E, and ER were characterized by elemental analysis, solid-state 13C NMR spectrometry, FTIR spectrometry, XRD, SEM, and TG-FTIR to elucidate the effect of HRE on the evolution of functional groups and macromolecular structure of coal during extraction. The soluble portion in SFHB was 24.37% in the course of HRE with CYC. The aromaticity of SFHB derived from both curve-fitting of 13C NMR and FTIR spectra was obviously increased after extraction suggesting that most of the aliphatic fractions were extracted during HRE process. It was clarified that the substituted degree of aromatic ring in SFHB became low but the substituents on aromatics were larger after extraction. Due to irreversibly swelling crystal structure of SFHB, its interlayer spacing became larger and the stacking height of crystallite decreased after extraction. Moreover, significant amounts of volatile matters were extracted, which caused relatively lower mass loss rate and contents of gaseous products (CO2, aliphatic moieties, CH4, and CO) of ER than SFHB during main pyrolysis stage.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.applthermaleng.2016.08.104Additional details
Identifiers
- DOI
- 10.1016/j.applthermaleng.2016.08.104;
- PII
- S1359-4311(16)31464-8;
Publishing Information
- Journal Title
- Applied Thermal Engineering
- Journal Volume
- 109
- Journal Issue
- Part A
- Journal Page Range
- p. 560-568
- ISSN
- 1359-4311
- CODEN
- ATENFT
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48063258
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- BITUMINOUS COAL; CARBON 13; CARBON DIOXIDE; CARBON MONOXIDE; CRYSTAL STRUCTURE; CYCLOHEXANONE; EXTRACTION; FOURIER TRANSFORM SPECTROMETERS; INFRARED SPECTRA; MASS TRANSFER; METHANE; NUCLEAR MAGNETIC RESONANCE; PYROLYSIS; RESIDUES; SCANNING ELECTRON MICROSCOPY; SOLIDS; SWELLING; THERMAL DEGRADATION; VOLATILE MATTER; X-RAY DIFFRACTION
- Descriptors DEC
- ALKANES; BLACK COAL; CARBON COMPOUNDS; CARBON ISOTOPES; CARBON OXIDES; CARBONACEOUS MATERIALS; CHALCOGENIDES; CHEMICAL REACTIONS; COAL; COHERENT SCATTERING; DECOMPOSITION; DEFORMATION; DIFFRACTION; ELECTRON MICROSCOPY; ENERGY SOURCES; EVEN-ODD NUCLEI; FOSSIL FUELS; FUELS; HYDROCARBONS; ISOTOPES; KETONES; LIGHT NUCLEI; MAGNETIC RESONANCE; MATERIALS; MATTER; MEASURING INSTRUMENTS; MICROSCOPY; NUCLEI; ORGANIC COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; RESONANCE; SCATTERING; SEPARATION PROCESSES; SPECTRA; SPECTROMETERS; STABLE ISOTOPES; THERMOCHEMICAL PROCESSES
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.