(488g) Preparation of Metal Ion Modified ETS-4 Molecular Sieve with High Adsorption Performance
AIChE Annual Meeting
2011
2011 Annual Meeting
Separations Division
Adsorbent Materials
Wednesday, October 19, 2011 - 2:30pm to 2:50pm
Preparation of metal ion
modified ETS-4 molecular sieve with high adsorption performance
Liyun Song1, Hongxing
Dai1,Jian Li1, Yongling
Li2, Yingshu Liu2*, Hong He1*
1College
of Environmental and Energy Engineering,
Beijing
University of Technology, Beijing
100124,
China
2University
of Science and Technology Beijing,
Xueyuan Road
30, Beijing, 100083,
China
Key words: ETS-4, adsorption, PSA
Abstract
ETS-4
had attracted more and more attentions for many researchers because of its
potential properties in adsorption, mixed gas separation, and catalysis, which
has octahedral-tetrahedral structure with the potential properties that were different
from the conventional zeolite materials[1].
The preparation and crystallization of ETS-4 with small pores had been reportedby many researchers[2-4]. In
this paper, titanosilicate ETS-4 sieves with the Sr and Ni modification were prepared by hydrotherrmal
method using the titanium trichloride and tetraethoxysilane as the precursors. The properties and morphology
of the materials were also characterized by XRD, SEM and PSA techniques. The Sr and Ni
doping could improve the N2 and CH4 adsorption capacity
of ETS-4. The N2 and CH4adsorbance
increased in the pressurization process for ETS-4-Sr and ETS-4-Ni, but no
significant change in N2 and CH4 adsorbance
with the pressure increasing was observed over the ETS-4 sample. At the pressure
of 1200 mmHg, the N2adsorbances for ETS-4-Sr
and ETS-4-Ni were 4.2 and 3.9 times as that of ETS-4 sieve, respectively. Summary,
the metal ion doping (Sr2+ and Ni2+) can improve the
adsorption performance of ETS-4 greatly.
Reference
[1]Sankar Nair. Chem. Mater. 2001, 13,4247-4254
[2] S.M. Kuznicki. Nature. 2001, 412, 720-724
[3] B. Majumdar. Ind.
Eng.Chem. Res. 2011,
50, 3021¨C3034
[4] Moises L. Pinto. J.
Am. Chem. Soc. 2011, 133, 6396¨C6402