2017
DOI: 10.1016/j.jhazmat.2017.06.050
|View full text |Cite
|
Sign up to set email alerts
|

L-proline-based deep eutectic solvents (DESs) for deep catalytic oxidative desulfurization (ODS) of diesel

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

2
48
0
1

Year Published

2018
2018
2024
2024

Publication Types

Select...
7
1

Relationship

1
7

Authors

Journals

citations
Cited by 129 publications
(51 citation statements)
references
References 61 publications
2
48
0
1
Order By: Relevance
“…From the FTIR spectra of BA and [TEA]/[BA],i tc an be seen that the absorption of ÀOH is significantly strengthened and widened at ñ % 3400 cm À1 of [TEA]/[BA],w hichi ndicates the formation of ah ydrogen bond between TEA and BA. [18] The blueshift of C=Oo fB Af rom ñ = 1687 to 1703 cm À1 is because the morphologyo ft he dimers is destroyedb yt he hydrogen bond between TEA and BA.T he shift of all Ha toms of [TEA]/[BA] to lower fieldi ntensities, as shown in the 1 HNMR spectra, may be because of the formation of hydrogen bonds or other interactions between TEA and BA. [18] The blueshift of C=Oo fB Af rom ñ = 1687 to 1703 cm À1 is because the morphologyo ft he dimers is destroyedb yt he hydrogen bond between TEA and BA.T he shift of all Ha toms of [TEA]/[BA] to lower fieldi ntensities, as shown in the 1 HNMR spectra, may be because of the formation of hydrogen bonds or other interactions between TEA and BA.…”
Section: Characterizationmentioning
confidence: 95%
See 1 more Smart Citation
“…From the FTIR spectra of BA and [TEA]/[BA],i tc an be seen that the absorption of ÀOH is significantly strengthened and widened at ñ % 3400 cm À1 of [TEA]/[BA],w hichi ndicates the formation of ah ydrogen bond between TEA and BA. [18] The blueshift of C=Oo fB Af rom ñ = 1687 to 1703 cm À1 is because the morphologyo ft he dimers is destroyedb yt he hydrogen bond between TEA and BA.T he shift of all Ha toms of [TEA]/[BA] to lower fieldi ntensities, as shown in the 1 HNMR spectra, may be because of the formation of hydrogen bonds or other interactions between TEA and BA. [18] The blueshift of C=Oo fB Af rom ñ = 1687 to 1703 cm À1 is because the morphologyo ft he dimers is destroyedb yt he hydrogen bond between TEA and BA.T he shift of all Ha toms of [TEA]/[BA] to lower fieldi ntensities, as shown in the 1 HNMR spectra, may be because of the formation of hydrogen bonds or other interactions between TEA and BA.…”
Section: Characterizationmentioning
confidence: 95%
“…The band at ñ = 933 cm À1 belongs to OH···O, which indicates that BA tends to exist in the morphology of dimers. [18] The blueshift of C=Oo fB Af rom ñ = 1687 to 1703 cm À1 is because the morphologyo ft he dimers is destroyedb yt he hydrogen bond between TEA and BA.T he shift of all Ha toms of [TEA]/[BA] to lower fieldi ntensities, as shown in the 1 HNMR spectra, may be because of the formation of hydrogen bonds or other interactions between TEA and BA. Therefore, more work should be carried out to study the formation mechanism of aromatica cid based DESs.…”
Section: Characterizationmentioning
confidence: 95%
“…Among these processes, the ODS has gained attention from the scientific community worldwide due to mild reaction conditions such as lower reaction temperature and atmospheric pressure, lower investment, operating costs, and simpler process . During the last few decades, the application of ODS method for removal of OSCs from liquid fuels has been confirmed to be very promising . Various types of catalysts for ODS have been reported in previous publications .…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, DESs have become suitable candidates for desulfurization processes. They were not only employed as extractants or reaction medium for desulfurization or photochemical desulfurization, but also as catalyst for extraction and catalytic oxidation desulfurization (ECODS) , .…”
Section: Introductionmentioning
confidence: 99%