2016
DOI: 10.3103/s1068364x1608007x
|View full text |Cite
|
Sign up to set email alerts
|

Heat treatment of anthracene oil under pressure

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

1
1
0

Year Published

2017
2017
2023
2023

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 7 publications
(3 citation statements)
references
References 15 publications
1
1
0
Order By: Relevance
“…Table shows that the oil components can be divided into nine classes, i.e., alkyl aromatics, indene compounds, double-ring alkyl aromatics, biphenyl, oxygenated compounds, sulfur-containing compounds, naphthalene and its homologues, fluorene and its homologues, and tricyclic and larger PAHs. The contents of alkyl aromatics and indene compounds significantly decreased after cracking, owing to high-temperature dealkylation. , Moreover, the formation of gaseous hydrocarbons, such as CH 4 , confirmed that alkyl aromatic side chains and benzene rings underwent C–C bond cleavage during cracking, as reported previously, , which reveals that compounds containing aliphatic hydrogens (by dealkylation), acenaphthylene (on account of the double bond in the molecule), and naphthalene (less active than anthracene) broke down most vigorously in anthracene oil. The content of indene compounds was also reduced after cracking, which was ascribed to ring-opening reactions .…”
Section: Resultssupporting
confidence: 81%
“…Table shows that the oil components can be divided into nine classes, i.e., alkyl aromatics, indene compounds, double-ring alkyl aromatics, biphenyl, oxygenated compounds, sulfur-containing compounds, naphthalene and its homologues, fluorene and its homologues, and tricyclic and larger PAHs. The contents of alkyl aromatics and indene compounds significantly decreased after cracking, owing to high-temperature dealkylation. , Moreover, the formation of gaseous hydrocarbons, such as CH 4 , confirmed that alkyl aromatic side chains and benzene rings underwent C–C bond cleavage during cracking, as reported previously, , which reveals that compounds containing aliphatic hydrogens (by dealkylation), acenaphthylene (on account of the double bond in the molecule), and naphthalene (less active than anthracene) broke down most vigorously in anthracene oil. The content of indene compounds was also reduced after cracking, which was ascribed to ring-opening reactions .…”
Section: Resultssupporting
confidence: 81%
“…2 , the C/H ratio of the 1S-CT treated at 360 °C for 3 h was 0.08 lower than that of the 1S-CT treated at 330 °C for 3 h; however, the TI was higher and the QI was similar in the above mentioned conditions. In other words, these results indicate that when the 1S-CT is treated at 360 °C for 3 h, the amount of high molecular weight components corresponding to TI and QI and the amount of low molecular weight components simultaneously increase [ 26 , 28 ].…”
Section: Resultsmentioning
confidence: 99%
“…Для покрытия дефицита каменноугольного пека на российском и мировом рынках для электродной промышленности и производства пековых углеродных волокон наиболее перспективным направлением развития промышленного производства является получение пекоподобных продуктов по технологии термического растворения углей [1,2,3,4].…”
Section: Introductionunclassified