2020
DOI: 10.1016/j.fuel.2020.118724
|View full text |Cite
|
Sign up to set email alerts
|

An efficient process to synthesize solketal from glycerol over tin (II) silicotungstate catalyst

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
39
0
1

Year Published

2020
2020
2023
2023

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 45 publications
(40 citation statements)
references
References 51 publications
0
39
0
1
Order By: Relevance
“…For example, Da Silva et al employed an SnF 2 catalyst at 298 K, obtaining a glycerol conversion of 90 % with A/G = 8. Employing a tin(II) silicotungstate catalyst under the same conditions, they reached a glycerol conversion of 85 % (this work: 91 %) 18, 19. Rahaman et al obtained a glycerol conversion of 89 % at 303 K and A/G = 12, employing an HY zeolite (this work: 92.5 %) 1.…”
Section: Resultsmentioning
confidence: 84%
“…For example, Da Silva et al employed an SnF 2 catalyst at 298 K, obtaining a glycerol conversion of 90 % with A/G = 8. Employing a tin(II) silicotungstate catalyst under the same conditions, they reached a glycerol conversion of 85 % (this work: 91 %) 18, 19. Rahaman et al obtained a glycerol conversion of 89 % at 303 K and A/G = 12, employing an HY zeolite (this work: 92.5 %) 1.…”
Section: Resultsmentioning
confidence: 84%
“…Due to their structural versatility, various modifications on the Keggin anion have improved their catalytic activity. These are the main changes performed: (i) to convert HPAs to salts after exchange their protons by metal or organic cations, resulting in catalysts highly active in esterification, etherification, acetalization, and hydrolysis reactions; [21–29] (ii) to transform the Keggin HPAs to lacunar salts, removing one MO unit (M=W or Mo), leading to the highly active catalysts in oxidation reactions with hydrogen peroxide of olefins, alcohols, and aldehydes; [30–35] and (iii) to doping lacunar Keggin anion with a transition metal cation, resulting in efficient catalysts in oxidative transformations [36–41] …”
Section: Introductionmentioning
confidence: 99%
“…[18][19][20] Due to their structural versatility, various modifications on the Keggin anion have improved their catalytic activity. These are the main changes performed: (i) to convert HPAs to salts after exchange their protons by metal or organic cations, resulting in catalysts highly active in esterification, etherification, acetalization, and hydrolysis reactions; [21][22][23][24][25][26][27][28][29] (ii) to transform the Keggin HPAs to lacunar salts, removing one MO unit (M=W or Mo), leading to the highly active catalysts in oxidation reactions with hydrogen peroxide of olefins, alcohols, and aldehydes; [30][31][32][33][34][35] and (iii) to doping lacunar Keggin anion with a transition metal cation, resulting in efficient catalysts in oxidative transformations. [36][37][38][39][40][41] An important aspect is that the size of cation can modulate the solubility of these salts (i. e., lacunar, metal-doped); while salts containing highly charged counterions such as small-sized metal cations are soluble in a polar solvent, those having large radium cations are almost insoluble.…”
Section: Introductionmentioning
confidence: 99%
“…15 Contrarily, heteropoly acids have advantages such as strong Brønsted acidity and special Keggin-type structural properties for acid-catalyzed reactions. 19,20 However, unsupported heteropoly acids have high solubility in polar media and low surface area, which limit their industrial applications. [21][22][23] Therefore, the design of heteropoly acids encapsulation into the excellent and stable porous supported for biodiesel production is still a great challenge.…”
Section: Introductionmentioning
confidence: 99%