Deep oxidative desulfurization of benzothiophene and dibenzothiophene with a peroxophosphotungstate–ionic liquid brush assembly. (14th July 2015)
- Record Type:
- Journal Article
- Title:
- Deep oxidative desulfurization of benzothiophene and dibenzothiophene with a peroxophosphotungstate–ionic liquid brush assembly. (14th July 2015)
- Main Title:
- Deep oxidative desulfurization of benzothiophene and dibenzothiophene with a peroxophosphotungstate–ionic liquid brush assembly
- Authors:
- Shi, Xian‐Ying
Sun, Man
Fan, Juan
Wang, Peng‐Min
Ma, Wen‐Juan
Wei, Jun‐Fa - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>A novel, efficient and reusable heterogeneous catalytic assembly of peroxophosphotungstate held in an ionic liquid brush was synthesized and an extraction and catalytic oxidative <named-content content-type="reactionType" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">desulfurization</named-content> (ECODS) procedure was developed for a model oil of benzothiophene (BT) and dibenzothiophene (DBT) using 30 wt% <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">hydrogen peroxide</named-content> as terminal oxidant and methanol as solvent under mild conditions. Several factors that affect <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">sulfur removal</named-content> were investigated in detail. The highest <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">sulfur removal</named-content> can reach 100% for BT in 7 h at 70 °C when the molar ratio of H<sub>2</sub>O<sub>2</sub>, S and catalyst is 10:1:0.025. The <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">sulfur removal</named-content> for DBT can also reach 100% in 4 h at 50 °C with the same molar ratio of H<sub>2</sub>O<sub>2</sub>, S and catalyst. The experimental results<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>A novel, efficient and reusable heterogeneous catalytic assembly of peroxophosphotungstate held in an ionic liquid brush was synthesized and an extraction and catalytic oxidative <named-content content-type="reactionType" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">desulfurization</named-content> (ECODS) procedure was developed for a model oil of benzothiophene (BT) and dibenzothiophene (DBT) using 30 wt% <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">hydrogen peroxide</named-content> as terminal oxidant and methanol as solvent under mild conditions. Several factors that affect <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">sulfur removal</named-content> were investigated in detail. The highest <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">sulfur removal</named-content> can reach 100% for BT in 7 h at 70 °C when the molar ratio of H<sub>2</sub>O<sub>2</sub>, S and catalyst is 10:1:0.025. The <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">sulfur removal</named-content> for DBT can also reach 100% in 4 h at 50 °C with the same molar ratio of H<sub>2</sub>O<sub>2</sub>, S and catalyst. The experimental results demonstrate that this ECODS process has no apparent scale‐up effect. The catalyst can be easily recovered (via simple filtration) and recycled five times without a significant decrease in activity. Copyright © 2015 John Wiley &amp; Sons, Ltd.</p> </abstract> … (more)
- Is Part Of:
- Applied organometallic chemistry. Volume 29:Number 9(2015:Sep.)
- Journal:
- Applied organometallic chemistry
- Issue:
- Volume 29:Number 9(2015:Sep.)
- Issue Display:
- Volume 29, Issue 9 (2015)
- Year:
- 2015
- Volume:
- 29
- Issue:
- 9
- Issue Sort Value:
- 2015-0029-0009-0000
- Page Start:
- 633
- Page End:
- 637
- Publication Date:
- 2015-07-14
- Subjects:
- Organometallic chemistry -- Periodicals
Organometallic compounds -- Periodicals
547.05 - Journal URLs:
- http://www3.interscience.wiley.com/cgi-bin/jhome/109566206 ↗
http://www3.interscience.wiley.com/cgi-bin/jhome/2676 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/aoc.3344 ↗
- Languages:
- English
- ISSNs:
- 0268-2605
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1576.270000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3372.xml