Zeolite synthesis in the presence of flexible diquaternary alkylammonium ions (C(2)H(5))(3)N(+)(CH(2))(n)N(+)(C(2)H(5))(3) with n=3-10 as structure-directing agents

Authors
Lee, SHShin, CHChoi, GJPark, TJNam, ISHan, BHong, SB
Issue Date
2003-06-19
Publisher
ELSEVIER SCIENCE BV
Citation
MICROPOROUS AND MESOPOROUS MATERIALS, v.60, no.1-3, pp.237 - 249
Abstract
The use of flexible diquaternary alkylammonium ions (C(2)H(5))(3)N(+)(CH(2))(n)N(+)(C(2)H(5))(3) (Et(6)-diquat-n with n = 3-10) as structure-directing agents for zeolite synthesis in the presence of alkali metal cation is described. Among the organic structure-directing agents studied here, a considerable diversity in the phase selectivity was observed only for the Et(6)-diquat-5 ion: this cation can produce five different zeolite structures (i.e., P1, SSZ-16, SUZ-4, ZSM-57, and mordenite), depending on the oxide composition of synthesis mixtures. Analysis of the variable-temperature (1)H CRAMPS NMR spectra obtained from the Et(6)-diquat-5 molecules in these five zeolites reveals that the host-guest interactions occurring within the respective materials maintain in a manner different from one another even at 160 degreesC at which the zeolite hosts crystallize. (C) 2003 Elsevier Science Inc. All rights reserved.
Keywords
SKELETAL ISOMERIZATION; CATALYTIC EVALUATION; FRAMEWORK TOPOLOGY; PROTON NMR; SUZ-4; ZSM-57; N,N,N,N' ,N' ,N' -HEXAETHYLPENTANEDIAMMONIUM; DEHYDRATION; REFINEMENT; CATIONS; SKELETAL ISOMERIZATION; CATALYTIC EVALUATION; FRAMEWORK TOPOLOGY; PROTON NMR; SUZ-4; ZSM-57; N,N,N,N' ,N' ,N' -HEXAETHYLPENTANEDIAMMONIUM; DEHYDRATION; REFINEMENT; CATIONS; zeolite syntheses; diquaternary ammonium ions; alkali metal cations; phase selectivity; variable-temperature (1)H CRAMPS NMR
ISSN
1387-1811
URI
https://pubs.kist.re.kr/handle/201004/138458
DOI
10.1016/S1387-1811(03)00381-0
Appears in Collections:
KIST Article > 2003
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE