Synthesis and catalytic performance of hierarchically structured beta zeolites by a dual-functional templating approach

2017 ◽  
Vol 41 (10) ◽  
pp. 3950-3956 ◽  
Author(s):  
Kai Zhang ◽  
Zewei Liu ◽  
Min Wang ◽  
Xin Yan ◽  
Chao Li ◽  
...  

A beta zeolite possessing a hierarchical structure with excellent catalytic activity and long lifetime was obtained in the presence of a dual-functional amphiphilic surfactant.

RSC Advances ◽  
2017 ◽  
Vol 7 (16) ◽  
pp. 9551-9561 ◽  
Author(s):  
An Li ◽  
Chen Huang ◽  
Cai-Wu Luo ◽  
Wen-Jun Yi ◽  
Zi-Sheng Chao

Quinoline was synthesized via the typical Skraup approach with a vapor-phase process. The mesoporous Ni/beta zeolite catalyst exhibited high-efficiency catalytic activity and an enhanced ability of anti-deactivation.


Catalysts ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 25
Author(s):  
Su-Un Lee ◽  
You-Jin Lee ◽  
Soo-Jin Kwon ◽  
Jeong-Rang Kim ◽  
Soon-Yong Jeong

With the growing global propylene demand, propane dehydrogenation (PDH) has attracted great attention for on-purpose propylene production. However, its industrial application is limited because catalysts suffer from rapid deactivation due to coke deposition and metal catalyst sintering. To enhance metal catalyst dispersion and coke resistance, Pt-based catalysts have been widely investigated with various porous supports. In particular, zeolite can benefit from large surface area and acid sites, which favors high metal dispersion and promoting catalytic activity. In this work, we investigated the PDH catalytic properties of Beta zeolites as a support for Pt-Sn based catalysts. In comparison with Pt-Sn supported over θ-Al2O3 and amorphous silica (Q6), Beta zeolite-supported Pt-Sn catalysts exhibited a different reaction trend, achieving the best propylene selectivity after a proper period of reaction time. The different PDH catalytic behavior over Beta zeolite-supported Pt-Sn catalysts has been attributed to their physicochemical properties and reaction mechanism. Although Pt-Sn catalyst supported over Beta zeolite with low acidity showed low Pt dispersion, it formed a relatively lower amount of coke on PDH reaction and maintained a high surface area and active Pt surfaces, resulting in enhanced stability for PDH reaction. This work can provide a better understanding of zeolite-supported Pt-Sn catalysts to improve PDH catalytic activity with high selectivity and low coke formation.


Catalysts ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 318 ◽  
Author(s):  
Tian Zhao ◽  
Hexin Zhu ◽  
Ming Dong

MIL-101(Cr), as a prototypical mesoporous metal–organic framework (MOF), can be facially prepared by involving different modulators to fit various demands. In this paper, a range of MIL-101(Cr) products were prepared under similar conditions. It was found that one of the additives, phenylphosphonic acid (PPOA), could give a stable hierarchical structure material. Compared to other MIL-101(Cr)s, though hierarchical MIL-101(Cr) showed less porosity, it gave a better catalytic performance in the oxidation of indene and 1-dodecene.


Catalysts ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 504 ◽  
Author(s):  
Wenming Hao ◽  
Weimin Zhang ◽  
Zaibin Guo ◽  
Jinghong Ma ◽  
Ruifeng Li

To improve the catalytic performance of zeolite catalysts in reactions involving bulky molecules, a series of mesoporous Beta zeolite were prepared using organic functionalized fumed silica as the silicon source, which were thoroughly characterized in terms of porosity and acidity. The peaks in X-ray diffraction (XRD) patterns showed broadening, and the external surface area and mesoporosity increased progressively when the content of organic functionalization increased. An infrared (IR) spectroscopy study of adsorbed probe molecules, including pyridine (Py-IR), 2,6-ditertbutylpyridine (DTBPy-IR) and pivalonitrile (Pn-IR), showed that the improvement of mesoporosity increased the accessibility of acidic sites. In the catalytic benzylation of naphthalene with benzyl chloride (BC) over the mesoporous Beta zeolite catalysts, the conversion of BC was significantly increased when the accessibility of Brönsted acid sites improved. The increase of mesoporosity not only improved the diffusion ability of the reactants and products, but also increased the accessibility of acid sites, which greatly enhanced the activity of the mesoporous Beta zeolite catalysts. It is highlighted that the interdependence of mesoporosity, acid type, acid concentration, and strength of the mesoporous Beta zeolites on the catalytic performance in the benzylation of naphthalene with BC was comprehensively studied.


2015 ◽  
Vol 17 (5) ◽  
pp. 2732-2735 ◽  
Author(s):  
Hirokazu Kobayashi ◽  
Haruka Yokoyama ◽  
Bo Feng ◽  
Atsushi Fukuoka

H-beta zeolite with a Si/Al ratio of 75 uniquely shows high catalytic activity for the dehydration of sorbitol, giving a 76% yield of isosorbide at 400 K over 2 h.


2015 ◽  
Vol 3 (11) ◽  
pp. 5811-5814 ◽  
Author(s):  
Yanmei Liao ◽  
Shuxiang Pan ◽  
Chaoqun Bian ◽  
Xiangju Meng ◽  
Feng-Shou Xiao

Nickel forms of aluminum-rich beta zeolite modified electrodes (Ni-beta-SDS/GC) exhibit high activities in methanol electro-oxidation compared with those of the conventional beta zeolites.


2019 ◽  
Vol 9 (3) ◽  
pp. 811-821 ◽  
Author(s):  
Zhao-Meng Wang ◽  
Li-Juan Liu ◽  
Bo Xiang ◽  
Yue Wang ◽  
Ya-Jing Lyu ◽  
...  

The catalytic activity decreases as –(SiO)3Mo(OH)(O) > –(SiO)2Mo(O)2 > –(O)4–MoO.


2018 ◽  
Author(s):  
Felix Hemmann ◽  
Jonathan Hackebeil ◽  
Andreas Lißner ◽  
Florian Mertens

Molecular sieves with beta zeolite topology are promising catalysts for various reactions as they exhibits extraordinary Lewis acidity. However, their industrial application and related research in academica is hindered because their synthesis is time consuming and typically involves toxic chemicals as hydrofluoric acid. Therefore, tetraethylammonium fluorid was tested as a non-toxic fluotide source for the synthesis of beta zeolites. In combination with the previously reported nano-seeded growth method, a fast synthesis of beta zeolites only involving non-toxic chemicals was possible. Synthesized zeolites show comparable selectivity in the Bayer-Villinger oxidation as conventional zeolites synthesized with hydrofluoric acid.<br>


Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 88
Author(s):  
Diana García-Pérez ◽  
Maria Consuelo Alvarez-Galvan ◽  
Jose M. Campos-Martin ◽  
Jose L. G. Fierro

Catalysts based on zirconia- and alumina-supported tungsten oxides (15 wt % W) with a small loading of platinum (0.3 wt % Pt) were selected to study the influence of the reduction temperature and the nature of the support on the hydroisomerization of n-dodecane. The reduction temperature has a major influence on metal dispersion, which impacts the catalytic activity. In addition, alumina and zirconia supports show different catalytic properties (mainly acid site strength and surface area), which play an important role in the conversion. The NH3-TPD profiles indicate that the acidity in alumina-based catalysts is clearly higher than that in their zirconia counterparts; this acidity can be attributed to a stronger interaction of the WOx species with alumina. The PtW/Al catalyst was found to exhibit the best catalytic performance for the hydroisomerization of n-dodecane based on its higher acidity, which was ascribed to its larger surface area relative to that of its zirconia counterparts. The selectivity for different hydrocarbons (C7–10, C11 and i-C12) was very similar for all the catalysts studied, with branched C12 hydrocarbons being the main products obtained (~80%). The temperature of 350 °C was clearly the best reduction temperature for all the catalysts studied in a trickled-bed-mode reactor.


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