2015
DOI: 10.1016/j.fuel.2015.03.086
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Synthesis of tert -amyl methyl ether (TAME) over modified activated carbon catalysts

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Cited by 31 publications
(20 citation statements)
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“…However, as suggested in the literature, hot concentrated H2SO4 is a strong oxidizing agent; upon contact with carbonaceous materials, it can also generate carboxylic groups [29]. This phenomenon was observed by Rechnia et al [30] in the case of H2SO4-modified activated carbons. On the other hand, the reaction of TRGO with H3PO4 did not increase the oxygen content.…”
Section: Elemental and Textural Analysismentioning
confidence: 66%
“…However, as suggested in the literature, hot concentrated H2SO4 is a strong oxidizing agent; upon contact with carbonaceous materials, it can also generate carboxylic groups [29]. This phenomenon was observed by Rechnia et al [30] in the case of H2SO4-modified activated carbons. On the other hand, the reaction of TRGO with H3PO4 did not increase the oxygen content.…”
Section: Elemental and Textural Analysismentioning
confidence: 66%
“…Most importantly, the selected functionalization methods led to successful incorporation of S to CNFs (the S content in the modified samples between 0.3 and 1.0%). However, the efficiency of these modifications was considerably lower than that observed for other carbon materials, such as carbon xerogels and spheres (for which the S contents were between 1.4 and 4.3%) 17 , ordered mesoporous carbons (S = 1.4% and 7.0%) 18 , or activated carbons (the S content of 1.5–2.8%) 41 . Significantly higher amounts of sulfur were introduced to the virgin CNFs during functionalization with diazonium salt (BDS-modified CNFs contained 2–3 times more S than H 2 SO 4 -modified carbons).…”
Section: Resultsmentioning
confidence: 78%
“…In addition, the two best performing carbocatalysts (i. e. CX_P and CX_gel_P) presented high surface acidity (see Table ), as a consequence of the surface enrichment with the oxygen and phosphorus groups during their functionalisation. Importantly, these catalysts displayed Brønsted acidity originated from P−OH groups as well as from the presence of carboxylic groups and some weak acids like phenolic groups, which were shown to be active in hydrolysis reactions ,. Moreover, as was shown by the comparison of XPS, IR and ICP results, most of the phosphoric functionalities together with the oxygen groups were easily accessible for the bulky substrate (i. e. cellobiose) and in close vicinity to glycosidic bond to activate it for hydrolysis, leading to the outstanding catalytic results.…”
Section: Resultsmentioning
confidence: 97%
“…The total acidity of the samples was determined by a potentiometric back titration method as described in detail in using a Cerko Lab System microtitration unit equipped with a syringe pump, a pH combined electrode and a magnetic stirrer.…”
Section: Methodsmentioning
confidence: 99%