Three-dimensional 10-ring zeolites: The activities in toluene alkylation and disproportionation

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F16%3A00454734" target="_blank" >RIV/61388955:_____/16:00454734 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1016/j.cattod.2015.05.019" target="_blank" >http://dx.doi.org/10.1016/j.cattod.2015.05.019</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.cattod.2015.05.019" target="_blank" >10.1016/j.cattod.2015.05.019</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Three-dimensional 10-ring zeolites: The activities in toluene alkylation and disproportionation

Popis výsledku v původním jazyce

Three-dimensional 10-ring zeolites TUN, IMF, –SVR, MFI and MEL were investigated as for their acid properties, adsorption of 2,2-dimethylbutane and in toluene disproportionation and its alkylation with isopropyl alcohol. The results were compared against zeolite *SFV, the structure of which consists mainly of MEL zeolite with some additional 12-ring channel system. With exception of –SVR synthesized with high Si/Al ratio, all other zeolites provided Si/Al ratios in a narrow region. Novel zeolites TUN, IMF, and –SVR exhibited higher conversions than MFI and MEL in toluene alkylation. TUN and IMF were substantially more active in toluene disproportionation indicating less diffusion restrictions of channel structure on the disproportionation reaction. *SFV showed a similar catalytic behavior to MEL with much lower selectivity to p-xylene and p-cymene. This could indicate that both toluene disproportionation and alkylation proceed in reaction space of *SFV being similar to those of MFI and MEL. *SFV and TUN exhibited much faster adsorption of 2,2-dimethylbutane than MFI, MEL, IMF, and –SVR. It was concluded that the presence of some larger transport pores in *SFV than in other zeolites is responsible for fast adsorption of 2,2-dimethylbutane and transport of products resulting in a low selectivity to p-xylene and p-cymene.n

Název v anglickém jazyce

Three-dimensional 10-ring zeolites: The activities in toluene alkylation and disproportionation

Popis výsledku anglicky

Three-dimensional 10-ring zeolites TUN, IMF, –SVR, MFI and MEL were investigated as for their acid properties, adsorption of 2,2-dimethylbutane and in toluene disproportionation and its alkylation with isopropyl alcohol. The results were compared against zeolite *SFV, the structure of which consists mainly of MEL zeolite with some additional 12-ring channel system. With exception of –SVR synthesized with high Si/Al ratio, all other zeolites provided Si/Al ratios in a narrow region. Novel zeolites TUN, IMF, and –SVR exhibited higher conversions than MFI and MEL in toluene alkylation. TUN and IMF were substantially more active in toluene disproportionation indicating less diffusion restrictions of channel structure on the disproportionation reaction. *SFV showed a similar catalytic behavior to MEL with much lower selectivity to p-xylene and p-cymene. This could indicate that both toluene disproportionation and alkylation proceed in reaction space of *SFV being similar to those of MFI and MEL. *SFV and TUN exhibited much faster adsorption of 2,2-dimethylbutane than MFI, MEL, IMF, and –SVR. It was concluded that the presence of some larger transport pores in *SFV than in other zeolites is responsible for fast adsorption of 2,2-dimethylbutane and transport of products resulting in a low selectivity to p-xylene and p-cymene.n

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

CF - Fyzikální chemie a teoretická chemie

OECD FORD obor

—

Projekt

<a href="/cs/project/GBP106%2F12%2FG015" target="_blank" >GBP106/12/G015: Vývoj nových nanoporézních adsorbentů a katalyzátorů</a><br>

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2016

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Catalysis Today

ISSN

0920-5861

e-ISSN

—

Svazek periodika

259

Číslo periodika v rámci svazku

JAN 2016

Stát vydavatele periodika

NL - Nizozemsko

Počet stran výsledku

10

Strana od-do

97-106

Kód UT WoS článku

000363425100012

EID výsledku v databázi Scopus

2-s2.0-84945468659