scholarly journals Assessment of the Location of Pt Nanoparticles in Pt/zeolite Y/γ‐Al 2 O 3 Composite Catalysts

ChemCatChem ◽  
2019 ◽  
Vol 12 (2) ◽  
pp. 615-622 ◽  
Author(s):  
Jogchum Oenema ◽  
Jan P. Hofmann ◽  
Emiel J. M. Hensen ◽  
Jovana Zečević ◽  
Krijn P. Jong
2020 ◽  
Vol 6 (2) ◽  
pp. 31
Author(s):  
Roba Saab ◽  
Kyriaki Polychronopoulou ◽  
Nikolaos Charisiou ◽  
Maria A. Goula ◽  
Andreas Schiffer

This paper examines the effect of incorporating graphene nanoplatelets (GNPs) in an Ni-based/Zeolite-Y catalyst on the hydrocracking of heptane fuel at two temperatures, 350 and 400 °C. Specifically, reduced GNP/NiO-ZY and NiO-ZY catalysts, each with a 5 wt. % Ni loading, were compared in this study. The results show that the reduced GNP/NiO-ZY enhanced the conversion percentage by 31% at 350 °C and by 6% at 400 °C as compared with the reduced NiO-ZY, and the GNP/NiO-ZY also showed superior stability, reporting a less than 2% drop in conversion over 20 h of time-on-stream. The enhancement in performance is linked to the surface and texture characteristics of both catalysts. Although the calcined GNP/NiO-ZY possessed a lower Brunauer–Emmett–Teller (BET) surface area of 458 m2/g compared with 536 m2/g for the calcined NiO-ZY, it showed a more hydrophobic nature, as deduced from the water adsorption profiles, which corroborates the hypothesis that the increased affinity between the catalyst surface and heptane molecules during the reaction leads to an improved catalytic activity.


2017 ◽  
Vol 4 (2) ◽  
pp. 141
Author(s):  
N.A. Zakarina ◽  
L.D. Volkova ◽  
O.V. Chshukina

Presented paper is devoted to the construction of cracking catalysts based on H-form zeolite Y, modifying by heteropolyacids of 12 row decationzed forms of natural clays of Tagan and Narynkol deposits. Conditions of acid activation were compared for Tagan clay. Chemical composition of clays before and after activation was detected by optical emission spectral method; phase composition was detected with X-ray<br />diffraction. It has been shown that activities of composite catalysts are related to the concentration and sequence of HPA adding. From the results the conclusion was drawn that amount of adding HPA influenced the activity and thermal stability of catalysts prepared on the base of Tagan and Narynkol clays deposits. The synthesized catalysts were studied in a laboratory microimpulse catalytic set by the model reaction of isopropylbenzene cracking at temperature 350-500 °C. The optimum compositions of zeolite containing contacts served as the base of creation of cracking catalysts for real raw (kerosene-gas-oil fraction) into quartz reactor with a fixed catalyst bed. These prepared catalysts have demonstrated enhanced thermal<br />stability and high activity. Stronger cracking activity of catalysts prepared on the base of Narynkol clay has been shown.


2020 ◽  
Vol 605 ◽  
pp. 117815
Author(s):  
Jogchum Oenema ◽  
Renée A. van Alst ◽  
Mark J. Meijerink ◽  
Jovana Zečević ◽  
Krijn P. de Jong

Author(s):  
H. Kinney ◽  
M.L. Occelli ◽  
S.A.C. Gould

For this study we have used a contact mode atomic force microscope (AFM) to study to topography of fluidized cracking catalysts (FCC), before and after contamination with 5% vanadium. We selected the AFM because of its ability to well characterize the surface roughness of materials down to the atomic level. It is believed that the cracking in the FCCs occurs mainly on the catalysts top 10-15 μm suggesting that the surface corrugation could play a key role in the FCCs microactivity properties. To test this hypothesis, we chose vanadium as a contaminate because this metal is capable of irreversibly destroying the FCC crystallinity as well as it microporous structure. In addition, we wanted to examine the extent to which steaming affects the vanadium contaminated FCC. Using the AFM, we measured the surface roughness of FCCs, before and after contamination and after steaming.We obtained our FCC (GRZ-1) from Davison. The FCC is generated so that it contains and estimated 35% rare earth exchaged zeolite Y, 50% kaolin and 15% binder.


2015 ◽  
Vol 30 (9) ◽  
pp. 931 ◽  
Author(s):  
XU Ming-Li ◽  
DUAN Ben ◽  
ZHANG Ying-Jie ◽  
YANG Guo-Tao ◽  
DONG Peng ◽  
...  

2020 ◽  
Vol 17 (2) ◽  
pp. 117-130 ◽  
Author(s):  
Mehdi Kalhor ◽  
Zohre Zarnegar ◽  
Zahra Seyedzade ◽  
Soodabeh Banibairami

Background: SO3H-functionalized zeolite-Y was prepared and used as a catalyst for the synthesis of 2-aryl-N-benzimidazole-4-thiazolidinones and tri-substituted imidazoles at ambient conditions. Objective: The goals of this catalytic method include excellent yields and high purity, inexpensive procedure and ease of product isolation, the use of nontoxic and heterogeneous acid catalyst, shorter reaction times and milder conditions. Materials and Methods: NMR spectra were recorded on Brucker spectrophotometer using Me4Si as internal standard. Mass spectra were recorded on an Agilent Technology 5975C VL MSD with tripe-axis detector. FTIR spectra were obtained with KBr disc on a galaxy series FT-IR 5000 spectrometer. The surface morphology of nanostructures was analyzed by FE-SEM (EVO LS 10, Zeiss, Carl Zeiss, Germany). BET analysis were measured at 196 °C by a Japan Belsorb II system after the samples were vacuum dried at 150°C overnight. Results: The NSZ was characterized by FT-IR, FESEM, EDX, XRF, and BET. The catalytic activity of NSZ was investigated for synthesis of 1,3-tiazolidin-4-ones in H2O/Acetone at room temperature. Moreover, NSZ was used for synthesis of tri-substituted imidazoles at 60 °C via solvent-free condensation. Different kinds of aromatic aldehydes were converted to the corresponding of products with good to excellent yields. Conclusion: Sulfonated zeolite-Y was as an efficient catalyst for the preparation of N-benzimidazole-2-aryl-1,3- thiazolidin-4-ones and 2,4,5-triaryl-1H-imidazoles. High reaction rates, elimination toxic solvent, simple experimental procedure and reusability of the catalyst are the important features of this protocol.


2020 ◽  
Vol 16 (4) ◽  
pp. 617-624 ◽  
Author(s):  
Yao Feng ◽  
Ran Wang ◽  
Juanjuan Yin ◽  
Fangke Zhan ◽  
Kaiyue Chen ◽  
...  

Background: 4-nitrophenol (4-NP) is one of the pollutants in sewage and harmful to human health and the environment. Cu is a non-noble metal with catalytic reduction effect on nitro compounds, and.has the advantages of simple preparation, abundant reserves, and low price. Carbon nanotubes (CNT) are widely used for substrate due to their excellent mechanical stability and high surface area. In this study, a simple method to prepare CNT-Cu2O by controlling different reaction time was reported. The prepared nanocomposites were used to catalyze 4-NP. Methods: CNTs and CuCl2 solution were put into a beaker, and then ascorbic acid and NaOH were added while continuously stirring. The reaction was carried out for a sufficiently long period of time at 60°C. The prepared samples were dried in a vacuum at 50°C for 48 h after washing with ethyl alcohol and deionized water. Results: Nanostructures of these composites were characterized by scanning electron microscope and transmission electron microscopy techniques, and the results at a magnification of 200 nanometers showed that Cu2O was distributed on the surface of the CNTs. In addition, X-ray diffraction was performed to further confirm the formation of Cu2O nanoparticles. The results of ultraviolet spectrophotometry showed that the catalytic effect of the compound on 4-NP was obvious. Conclusions: CNTs acted as a huge template for loading Cu2O nanoparticles, which could improve the stability and cycle performance of Cu2O. The formation of nanoparticles was greatly affected by temperature and the appropriate concentration, showing great reducibility for the 4-NP reduction reaction.


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