TY - JOUR
T1 - SO3H-containing functional carbon materials: Synthesis, structure, and acid catalysis
AU - Jyoti Konwar, Lakhya
AU - Mäki-Arvela, Päivi
AU - Mikkola, Jyri-Pekka
N1 - tk.
Publication Date: October 7, 2019
Postprint, 12 mån embargo, all rights reserved
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Har kontaktat [email protected] den 25.2.2020/LN
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PY - 2019
Y1 - 2019
N2 - The "sulfonated carbons" are a new class of metal-free solid protonic acids characterized by their unique carbon structure and Bronsted acidity (-H0 = 8-11) on par to concentrated H2SO4. These carbon materials covalently functionalized with SO3H groups via C-PhSO3H or C-SO3H linkages can act as versatile water-tolerant solid acids. Due to their low production costs, unique surface chemistry, high chemical and thermal stability, as well as tailorable pore structures they are regarded as potential substitutes to liquid H2SO4. Catalysis, in particular, biomass and large molecule catalysis, is one of the important areas in which acidic carbons have demonstrated exceptional activity and selectivity, outperforming traditional solid acid catalysts (cation-exchange resins, sulfated oxides, and acidic zeolites). In this review we address developments in the different types SO3H- and PhSO3H-functionalized acidic carbon materials, their structure, active sites, and surface properties, applications in catalysis, as well as activation and deactivation characteristics covering important literature since 2004. In particular, we aim to provide a systematic discussion on the specific merits and demerits of such materials obtained from different carbon precursors and functionalization methods which directly influence the structure-stability-acidic properties and catalytic performance.
AB - The "sulfonated carbons" are a new class of metal-free solid protonic acids characterized by their unique carbon structure and Bronsted acidity (-H0 = 8-11) on par to concentrated H2SO4. These carbon materials covalently functionalized with SO3H groups via C-PhSO3H or C-SO3H linkages can act as versatile water-tolerant solid acids. Due to their low production costs, unique surface chemistry, high chemical and thermal stability, as well as tailorable pore structures they are regarded as potential substitutes to liquid H2SO4. Catalysis, in particular, biomass and large molecule catalysis, is one of the important areas in which acidic carbons have demonstrated exceptional activity and selectivity, outperforming traditional solid acid catalysts (cation-exchange resins, sulfated oxides, and acidic zeolites). In this review we address developments in the different types SO3H- and PhSO3H-functionalized acidic carbon materials, their structure, active sites, and surface properties, applications in catalysis, as well as activation and deactivation characteristics covering important literature since 2004. In particular, we aim to provide a systematic discussion on the specific merits and demerits of such materials obtained from different carbon precursors and functionalization methods which directly influence the structure-stability-acidic properties and catalytic performance.
U2 - 10.1021/acs.chemrev.9b00199
DO - 10.1021/acs.chemrev.9b00199
M3 - Översiktsartikel
SN - 0009-2665
VL - 119
SP - 11576
EP - 11630
JO - Chemical Reviews
JF - Chemical Reviews
IS - 22
ER -