2017
DOI: 10.1016/j.cattod.2016.07.007
|View full text |Cite
|
Sign up to set email alerts
|

Efficient magnetic recoverable acid-functionalized-carbon catalysts for starch valorization to multiple bio-chemicals

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
11
0

Year Published

2017
2017
2024
2024

Publication Types

Select...
6
1

Relationship

1
6

Authors

Journals

citations
Cited by 18 publications
(12 citation statements)
references
References 53 publications
1
11
0
Order By: Relevance
“…A second type of tested acid-based composites involved the oxidation of the activated carbons followed by their impregnation with triflic acid (Scheme 2). Most probably, the functionalization of the activated carbons surface with triflate groups takes place through a similar mechanism to that proposed by Perego et al [18] and confirmed by Coman et al [19], in which triflic acid reacts with vicinal hydroxyl groups yielding a bipodally anchored triflate to the carrier surface. Moreover, the resulting water from the esterification reaction may be coordinated to the grafted triflate, generating a strongly hydrated triflic acid onto the activated carbon surface, less prone to leaching.…”
Section: Resultssupporting
confidence: 64%
“…A second type of tested acid-based composites involved the oxidation of the activated carbons followed by their impregnation with triflic acid (Scheme 2). Most probably, the functionalization of the activated carbons surface with triflate groups takes place through a similar mechanism to that proposed by Perego et al [18] and confirmed by Coman et al [19], in which triflic acid reacts with vicinal hydroxyl groups yielding a bipodally anchored triflate to the carrier surface. Moreover, the resulting water from the esterification reaction may be coordinated to the grafted triflate, generating a strongly hydrated triflic acid onto the activated carbon surface, less prone to leaching.…”
Section: Resultssupporting
confidence: 64%
“…Due to their remarkably high acidity (H o = −8.2), also preserved in water, niobia-based catalysts were extensively investigated by different research groups, in various transformations of biomass derivatives [ 17 , 18 , 19 , 20 , 21 , 22 ]. The enhancement of both the hydrothermal stability and acidity in aqueous phase reactions through the deposition of niobia on oxide supports (e.g., silica, titania, alumina) is well documented in the literature [ 23 ].…”
Section: Introductionmentioning
confidence: 99%
“…The enhancement of both the hydrothermal stability and acidity in aqueous phase reactions through the deposition of niobia on oxide supports (e.g., silica, titania, alumina) is well documented in the literature [ 23 ]. Moreover, in the presence of Nb-based carbon nanotubes (CN) catalysts, levulinic acid and glucose were successfully oxidized to SA, with selectivities of 98–99% and 80%, respectively, for a total conversion of the raw material at 180 °C, 10 bar O 2 , and after 6 h [ 21 ]. However, the catalytic performances, expressed in terms of succinic acid yields, were directly correlated to the nature of the catalytic sites which, in turn, has been dictated by the niobia content and the preparation route.…”
Section: Introductionmentioning
confidence: 99%
“…Near quantitative yield of SA was achieved when the reaction was performed at 180°C for 6 h in the aqueous medium under 10 bar of O 2 pressure. [59] The two carboxylic acid functionalities in SA can be synthetically manipulated to form crucial derivatives. For example, the acid-catalyzed esterification of SA leads to succinate esters.…”
Section: La To Succinic Acid (Sa)mentioning
confidence: 99%