dc.contributor.author |
Foss L. |
|
dc.contributor.author |
Kayukova G. |
|
dc.contributor.author |
Tumanyan B. |
|
dc.contributor.author |
Petrukhina N. |
|
dc.contributor.author |
Nikolaev V. |
|
dc.contributor.author |
Romanov G. |
|
dc.date.accessioned |
2018-04-05T07:08:52Z |
|
dc.date.available |
2018-04-05T07:08:52Z |
|
dc.date.issued |
2017 |
|
dc.identifier.issn |
0009-3092 |
|
dc.identifier.uri |
http://dspace.kpfu.ru/xmlui/handle/net/129383 |
|
dc.description.abstract |
© 2017, Springer Science+Business Media, LLC. A physical model has been developed for the aquathermolysis of heavy crude oil from the Ashalchinsk oil field at 250°, 300°, and 350°C. Nickel and cobalt carboxylates were used as oil-soluble catalyst precursors. In the presence of a hydrogen proton donor at 300°C, the oil content was found to rise considerably and the resin content was found to decrease by a factor of 1.8, which leads to a decrease in crude oil viscosity by 91% and a decrease in density from 960 to 933 kg/m 3 . The hydrocarbon composition of the liquid aquathermolysis products was studied by chromate-mass spectrometry. The average molecular weight of the asphaltenes was determined by matrix-assisted laser desorption/ionization (MALDI) spectrometry. The maximum disproportionation of the hydrocarbons into n-alkanes, alkylcyclohexanes, and alkylbenzenes occurs at 300° and 350°C. The composition of the hydrogen proton donor (tetralin) conversion products at these aquathermolysis temperatures was determined. |
|
dc.relation.ispartofseries |
Chemistry and Technology of Fuels and Oils |
|
dc.subject |
aquathermolysis |
|
dc.subject |
asphaltenes |
|
dc.subject |
catalyst precursor |
|
dc.subject |
heavy crude oil |
|
dc.subject |
hydrogen proton donor |
|
dc.title |
Change in the Hydrocarbon and Component Compositions of Heavy Crude Ashalchinsk Oil Upon Catalytic Aquathermolysis |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
2 |
|
dc.relation.ispartofseries-volume |
53 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
173 |
|
dc.source.id |
SCOPUS00093092-2017-53-2-SID85020535249 |
|