Abstract:High silica zeolite ZK-5 (framework Si/Al = 4.8) has been prepared by interzeolite conversion from ultrastable zeolite Y via a co-templating route using alkali metal cations and nitrate anions but without organic structure directing agents. The mechanism, which involves zeolite frameworkalkali metal cation -nitrate anion ordering, has been established by a combination of chemical and thermal analyses, Raman spectroscopy, computational modelling, and X-ray powder diffraction. Ammonium exchange gives ZK-5 with o… Show more
“… 50 Feasibility of this concept has very recently been demonstrated in the inorganic synthesis of KFI-type zeolite with unusually high silica content, by inclusion of K + –NO 3 – pairs. 59 The framework Si/Al ratio was 4.8, cation occupancy was found to be 100%, and the material remained stable after extraction of the excess ions. An earlier study 60 describing the synthesis of high silica KFI (Si/Al = 5.2–5.8) also required the use of high concentrations of KNO 3 in the synthesis batch as a source of potassium to obtain the desired product.…”
Section: Resultsmentioning
confidence: 94%
“…These ion pairs can be removed post-synthesis, simply by making the crystals to come into contact with water . Feasibility of this concept has very recently been demonstrated in the inorganic synthesis of KFI-type zeolite with unusually high silica content, by inclusion of K + –NO 3 – pairs . The framework Si/Al ratio was 4.8, cation occupancy was found to be 100%, and the material remained stable after extraction of the excess ions.…”
A guideline for zeolite phase selection in inorganic
synthesis
media is proposed, based on a systematic exploration of synthesis
from inorganic media using liquid Na+, K+, and
Cs+ aluminosilicate. Although the Si/Al ratio of the zeolites
is a continuous function of the synthesis conditions, boundaries between
topologies are sharp. The here-derived phase selection criterion relates
the obtained zeolite topology to the Si/Al ratio imposed by the synthesis
medium. For a given Si/Al ratio, the framework with the highest occupation
of topologically available cation sites is favored. The large number
of published zeolite syntheses supporting the observation provides
strong indication that the concept is applicable in a larger context.
The proposed criterion explains how minor variations in the composition
of inorganic synthesis media induce the commonly occurring, abrupt
changes in topology. It highlights underlying reasons causing the
strict demarcation of stability fields of the as-synthesized zeolites
experimentally observed in inorganic synthesis.
“… 50 Feasibility of this concept has very recently been demonstrated in the inorganic synthesis of KFI-type zeolite with unusually high silica content, by inclusion of K + –NO 3 – pairs. 59 The framework Si/Al ratio was 4.8, cation occupancy was found to be 100%, and the material remained stable after extraction of the excess ions. An earlier study 60 describing the synthesis of high silica KFI (Si/Al = 5.2–5.8) also required the use of high concentrations of KNO 3 in the synthesis batch as a source of potassium to obtain the desired product.…”
Section: Resultsmentioning
confidence: 94%
“…These ion pairs can be removed post-synthesis, simply by making the crystals to come into contact with water . Feasibility of this concept has very recently been demonstrated in the inorganic synthesis of KFI-type zeolite with unusually high silica content, by inclusion of K + –NO 3 – pairs . The framework Si/Al ratio was 4.8, cation occupancy was found to be 100%, and the material remained stable after extraction of the excess ions.…”
A guideline for zeolite phase selection in inorganic
synthesis
media is proposed, based on a systematic exploration of synthesis
from inorganic media using liquid Na+, K+, and
Cs+ aluminosilicate. Although the Si/Al ratio of the zeolites
is a continuous function of the synthesis conditions, boundaries between
topologies are sharp. The here-derived phase selection criterion relates
the obtained zeolite topology to the Si/Al ratio imposed by the synthesis
medium. For a given Si/Al ratio, the framework with the highest occupation
of topologically available cation sites is favored. The large number
of published zeolite syntheses supporting the observation provides
strong indication that the concept is applicable in a larger context.
The proposed criterion explains how minor variations in the composition
of inorganic synthesis media induce the commonly occurring, abrupt
changes in topology. It highlights underlying reasons causing the
strict demarcation of stability fields of the as-synthesized zeolites
experimentally observed in inorganic synthesis.
“…26 Inter-zeolite transformations (IZT), employing industrial zeolites as silica-alumina sources to generate another target zeolite, has recently drawn much attention. [27][28][29][30][31] The zeolite crystallization by IZT is faster and yields high. [32][33][34] The method can also provide pathways to synthesize zeolites with specific frameworks and compositions that are not possible with conventional silica and alumina sources.…”
“…On the other hand, OSDAs play a pivotal role in the hitherto synthesis of zeolites, which directly determines the morphologies, topologies, and acidities of the final products . Molecules such as quaternary ammonium salts, , ethers, , alcohols, , amines, , polymers, and even inorganic cations , are among the frequently used OSDAs, considering their intense interactions with the zeolite frameworks. , Commensurate sizes with zeolite channels and proper interactions with zeolite frameworks are critical factors of OSDAs that govern their structure-directing effect and further decide the physiochemical properties of the obtained materials . As unveiled by recent studies, the usage of OSDAs can also achieve the precise regulation of the acidity locations and the hydrothermal stabilities, which could significantly improve the catalytic performances.…”
The physiochemical properties and catalytic performance
of zeolite
rely on the judicious selection of organic structure-directing agents
(OSDAs), among which alcoholamines are rarely used. Here, we report
that 6-amino-1-hexanol (AH) can be used as an OSDA for the generation
of commercially viable ZSM-22 with a Si/Al ratio window of 35–150.
Compared with ZSM-22 derived from commonly used 1,6-diaminohexane
(DAH), the samples generated using AH possess improved crystallinity
and more intermediate-to-strong acid site, which can be attributed
to the stronger host–guest interactions between AH and zeolite
framework. In addition, the crystallization process can be accelerated
by the use of AH. ZSM-22 catalysts derived from AH outperform the
counterpart generated from DAH in hydroisomerization of n-heptane, and improved catalytic activity and isomer yield can be
achieved thanks to the presence of abundant acid sites and high crystallinity.
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