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contributor authorYang, Jingyu
contributor authorShi, Huibing
contributor authorZhao, Deming
contributor authorChen, Minghao
contributor authorLi, Ming
date accessioned2026-02-17T21:40:24Z
date available2026-02-17T21:40:24Z
date copyright5/27/2025 12:00:00 AM
date issued2025
identifier issn2998-1638
identifier otherjertb-24-1076.pdf
identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4310461
description abstractAs an excellent precursor of high-modulus carbon materials, petroleum mesophase pitches' spinning performance was limited by its high softening point. Under the premise of ensuring the order degree of mesophase microcrystalline structure, the softening point was reduced by preparing mesophase pitch via in-process hydrogenation using fluid catalytic cracking aromatic-rich oil as raw material and decahydronaphthalene as a hydrogen supplier. The effects of in-process hydrogenation on the properties of mesophase and carbonization behavior during thermal polycondensation were investigated. It was found that the two-stage hydrotreated mesophase pitch produced an optical structure that was 100% generalized, with the highest crystal order of 0.9189, the highest aromaticity Iar of 0.520, and a softening point of 176 °C. The results showed that the addition of decahydronaphthalene promoted the hydrogen transfer reaction of the reaction system, producing light components such as cycloalkyl and saturates. The system mobility was improved, which made the molecular weight of the mesophase pitch concentrated and suitable for the full development of crystals.
publisherThe American Society of Mechanical Engineers (ASME)
titleStudy on the Carbonization Behavior of Petroleum-Based Mesophase Prepared by In-Process Hydrogenation
typeJournal Paper
journal volume1
journal issue4
journal titleJournal of Energy Resources Technology, Part B: Subsurface Energy and Carbon Capture
identifier doi10.1115/1.4068702
journal fristpage41007-1
journal lastpage41007-7
page7
treeJournal of Energy Resources Technology, Part B: Subsurface Energy and Carbon Capture:;2025:;volume( 001 ):;issue: 004
contenttypeFulltext


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