PdO/CuO Nanoparticles on Zeolite-Y for Nitroarene Reduction and Methanol Oxidation

2019 ◽  
Vol 2 (6) ◽  
pp. 3769-3779 ◽  
Author(s):  
Mukesh Sharma ◽  
Biraj Das ◽  
Anil Hazarika ◽  
Ankur K. Guha ◽  
Suresh K. Bhargava ◽  
...  
RSC Advances ◽  
2015 ◽  
Vol 5 (10) ◽  
pp. 7637-7646 ◽  
Author(s):  
Amal Suleiman ◽  
Christian L. Menéndez ◽  
Ramón Polanco ◽  
Esteban Rosim Fachini ◽  
Yaritza Hernández-Lebrón ◽  
...  

Platinum was electrodeposited onto Y-zeolite and Y-zeolite (Y)/Vulcan XC-72R (V) to produce Pt/Y/V and Pt/Y catalysts using a rotating disk slurry electrode technique.


2021 ◽  
Vol 397 ◽  
pp. 139313
Author(s):  
Nazimul Hoque ◽  
Manash J. Baruah ◽  
Seonghwan Lee ◽  
Young-Bin Park ◽  
Rupjyoti Dutta ◽  
...  

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.


2010 ◽  
Vol 25 (4) ◽  
pp. 359-364 ◽  
Author(s):  
Xin ZENG ◽  
Xian-Xia YUAN ◽  
Xiao-Yun XIA ◽  
Juan DU ◽  
Hui-Juan ZHANG ◽  
...  

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.


2018 ◽  
Vol 3 (2) ◽  
pp. 121-125
Author(s):  
Bhumika K. Sharma ◽  
Kinjal Patel ◽  
Debesh R. Roy

1992 ◽  
Vol 57 (12) ◽  
pp. 2529-2538 ◽  
Author(s):  
Krasimir Ivanov ◽  
Penka Litcheva ◽  
Dimitar Klissurski

Mn-Mo-O catalysts with a different Mo/Mn ratio have been prepared by precipitation. The precipitate composition as a function of solution concentration and pH was studied by X-ray, IR, thermal and chemical methods. Formation of manganese molybdates with MnMoO4.1.5H2O, Mn3Mo3O12.2.5H2O, and Mn3Mo4O15.4H2O composition has been supposed. It is concluded that pure MnMoO4 may be obtained in both acid and alkaline media, the pH values depending on the concentration of the initial solutions. The maximum Mo/Mn ratio in the precipitates is 1.33. The formation of pure Mn3Mo4O15.4H2O is possible in weakly acidic media. This process is favoured by increasing the concentration of initial solutions.


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