Ethyl -butyl ether synthesis using carbon catalysts from lignocellulose

Porous structure, surface chemistry and catalytic properties of carbon catalysts with various acid groups in ethyl tert -butyl ether synthesis were studied. Carbon catalysts were obtained by phosphoric acid activation followed by sulphonation of lignocellulosic feedstocks of different origin. Porous...

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Main Authors: Alexander M Puziy, Yuriy N Kochkin, Olga I Poddubnaya, Mykola M Tsyba
Format: Article
Language:English
Published: Hindawi - SAGE Publishing 2017-06-01
Series:Adsorption Science & Technology
Online Access:https://doi.org/10.1177/0263617417696091
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spelling doaj-af549043befc43c0ac1127d21cce241a2021-04-02T10:54:19ZengHindawi - SAGE PublishingAdsorption Science & Technology0263-61742048-40382017-06-013510.1177/0263617417696091Ethyl -butyl ether synthesis using carbon catalysts from lignocelluloseAlexander M PuziyYuriy N KochkinOlga I PoddubnayaMykola M TsybaPorous structure, surface chemistry and catalytic properties of carbon catalysts with various acid groups in ethyl tert -butyl ether synthesis were studied. Carbon catalysts were obtained by phosphoric acid activation followed by sulphonation of lignocellulosic feedstocks of different origin. Porous structure of carbon catalysts was characterized by nitrogen adsorption. Surface chemistry was investigated by potentiometric titration. Carbon catalysts obtained from lignosulphonate and sucrose showed the highest catalytic activity in ethyl tert-butyl ether synthesis (reaction rate at 120℃ is 4.3–5.2 × 10 −6  mol·g −1 ·s −1 ), is comparable to activity of Amberlyst-15 (5.0 ×10 −6  mol·g −1 ·s −1 ). Calculated turnover frequency (TOF) of sulphonic groups (pK a  = −2.5) equals 0.00116 s −1 , polyphosphate groups (pK a  = 1.9) 0.01019 s −1 , strong carboxylic (pK a  = 3.6) 0.00202 s −1 and 0 s −1 for weak carboxylic (pK a  = 6) groups. The activity of acid groups with pK a lower than 3.6 is higher than the activity of sulphonic groups of Amberlyst-15 (TOF 0.00115 s −1 ).https://doi.org/10.1177/0263617417696091
collection DOAJ
language English
format Article
sources DOAJ
author Alexander M Puziy
Yuriy N Kochkin
Olga I Poddubnaya
Mykola M Tsyba
spellingShingle Alexander M Puziy
Yuriy N Kochkin
Olga I Poddubnaya
Mykola M Tsyba
Ethyl -butyl ether synthesis using carbon catalysts from lignocellulose
Adsorption Science & Technology
author_facet Alexander M Puziy
Yuriy N Kochkin
Olga I Poddubnaya
Mykola M Tsyba
author_sort Alexander M Puziy
title Ethyl -butyl ether synthesis using carbon catalysts from lignocellulose
title_short Ethyl -butyl ether synthesis using carbon catalysts from lignocellulose
title_full Ethyl -butyl ether synthesis using carbon catalysts from lignocellulose
title_fullStr Ethyl -butyl ether synthesis using carbon catalysts from lignocellulose
title_full_unstemmed Ethyl -butyl ether synthesis using carbon catalysts from lignocellulose
title_sort ethyl -butyl ether synthesis using carbon catalysts from lignocellulose
publisher Hindawi - SAGE Publishing
series Adsorption Science & Technology
issn 0263-6174
2048-4038
publishDate 2017-06-01
description Porous structure, surface chemistry and catalytic properties of carbon catalysts with various acid groups in ethyl tert -butyl ether synthesis were studied. Carbon catalysts were obtained by phosphoric acid activation followed by sulphonation of lignocellulosic feedstocks of different origin. Porous structure of carbon catalysts was characterized by nitrogen adsorption. Surface chemistry was investigated by potentiometric titration. Carbon catalysts obtained from lignosulphonate and sucrose showed the highest catalytic activity in ethyl tert-butyl ether synthesis (reaction rate at 120℃ is 4.3–5.2 × 10 −6  mol·g −1 ·s −1 ), is comparable to activity of Amberlyst-15 (5.0 ×10 −6  mol·g −1 ·s −1 ). Calculated turnover frequency (TOF) of sulphonic groups (pK a  = −2.5) equals 0.00116 s −1 , polyphosphate groups (pK a  = 1.9) 0.01019 s −1 , strong carboxylic (pK a  = 3.6) 0.00202 s −1 and 0 s −1 for weak carboxylic (pK a  = 6) groups. The activity of acid groups with pK a lower than 3.6 is higher than the activity of sulphonic groups of Amberlyst-15 (TOF 0.00115 s −1 ).
url https://doi.org/10.1177/0263617417696091
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