2008
DOI: 10.1016/j.jcis.2008.05.006
|View full text |Cite
|
Sign up to set email alerts
|

Tuning of texture and surface chemistry of carbon xerogels

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
70
0
1

Year Published

2011
2011
2023
2023

Publication Types

Select...
7
1
1

Relationship

0
9

Authors

Journals

citations
Cited by 85 publications
(72 citation statements)
references
References 7 publications
1
70
0
1
Order By: Relevance
“…Concerning the CDC-H, the amount of adsorbed N 2 is quite close to the original CDC, suggesting that the loss of surface area on CDC-H is negligible. On the other hand, air oxidization results in more adsorbed N 2 , which is attributed to the partial activation of carbon during the air oxidation process at high temperature [18,19]. This activation takes place by partial gasification of carbon to produce CO and CO 2 .…”
Section: Characterizations Of the Adsorbentsmentioning
confidence: 99%
“…Concerning the CDC-H, the amount of adsorbed N 2 is quite close to the original CDC, suggesting that the loss of surface area on CDC-H is negligible. On the other hand, air oxidization results in more adsorbed N 2 , which is attributed to the partial activation of carbon during the air oxidation process at high temperature [18,19]. This activation takes place by partial gasification of carbon to produce CO and CO 2 .…”
Section: Characterizations Of the Adsorbentsmentioning
confidence: 99%
“…Using molecular oxygen, arabinoic acid could be synthesised from arabinose, D-arabino-1,4-lactone being found as an intermediary (Scheme 4). Preliminary results showed that MWCNTs (Nanocyl-NC3100) and carbon xerogel (CX, prepared by the resorcinol/formaldehyde approach [15]), loaded with 1 wt.% Au (by the sol method [13]) were used as catalysts. Au/CNT was less active than Au/CX.…”
Section: Organic Chemistrymentioning
confidence: 99%
“…Such a carbon metal-free catalyst displays a high stability as a function of the test duration under severe reaction conditions, i.e., high space velocity, low O 2 -to-H 2 S ratio. In the literature, the incorporation of these oxygenated functional groups has generally been carried out through oxidation treatments of the pristine carbon materials with different oxidants such as liquid HNO 3 [17,18], H 2 SO 4 [19], KMnO 4 [20], and H 2 O 2 [21] or through gaseous reactants like oxygen plasma [22], ozone [23], or CO 2 [24]. The main drawbacks of the liquid-phase treatments are the generation of a large amount of acid waste and the need for a subsequent washing step to remove the residual acid adsorbed on the sample surface.…”
Section: Introductionmentioning
confidence: 99%