scholarly journals Oxidative Desulfurization of Dibenzothiophene Using Dawson Type Heteropoly Compounds/Tantalum as Catalyst

2018 ◽  
Vol 16 (1) ◽  
pp. 105 ◽  
Author(s):  
Risfidian Mohadi ◽  
Lusi Teresia ◽  
Najma Annuria Fithri ◽  
Aldes Lesbani ◽  
Nurlisa Hidayati
Keyword(s):  
Catalytic Activity ◽  
Vibration Spectrum ◽  
Oxidative Desulfurization ◽  
Heteropoly Compounds ◽  
Atmospheric Conditions ◽  
N2 Adsorption ◽  
Fresh Catalyst ◽  
Wet Impregnation ◽  
Percent Conversion ◽  
Adsorption Desorption

Catalyst (NH4)6[b-P2W18O62]/Ta has been synthesized by simple wet impregnation at 30-40 °C under atmospheric conditions using Dawson type polyoxometalate (NH4)6[b-P2W18O62] and tantalum. The catalyst was characterized by FTIR spectrophotometer, XRD, SEM, and N2 adsorption desorption methods. FTIR spectrum of (NH4)6[b-P2W18O62]/Ta showed that Dawson type polyoxometalate (NH4)6[b-P2W18O62] and Ta was successfully impregnated which was indicated by vibration spectrum at wavenumber of 900-1100 cm-1 for polyoxometalate and 550 cm-1 for Ta. The surface area of the (NH4)6[b-P2W18O62]/Ta after impregnation was higher than (NH4)6[b-P2W18O62]•nH2O and its morphology was found to be uniform. The catalytic activity of (NH4)6[b-P2W18O62]/Ta toward desulfurization of dibenzothiophene was three times higher than the original catalyst of (NH4)6[b-P2W18O62]•nH2O without impregnation. The catalytic regeneration test of catalyst (NH4)6[b-P2W18O62]/Ta showed that the catalytic activity for first regeneration of catalyst has similar catalytic activity with the fresh catalyst without loss of catalytic activity indicated by almost similar percent conversion.

Catalytic Activity of Dehydrogenation of Methanol to MF over Cu/MCM-41 and Cu-ZnO/MCM-41 Prepared by Impregnation and Grinding

2011 ◽  
Vol 396-398 ◽  
pp. 730-733
Author(s):  
Guo Ru Li ◽  
Gong Li ◽  
Shu Xi Zhou ◽  
Hui Juan Tong
Keyword(s):  
Catalytic Activity ◽  
Atmospheric Pressure ◽  
Molecular Sieves ◽  
Conversion Rate ◽  
Methyl Formate ◽  
Methanol Conversion ◽  
N2 Adsorption ◽  
Flow Microreactor ◽  
Adsorption Desorption ◽  
Mcm 41

Abstract. Using MCM-41 molecular sieves as the support, Cu-ZnO/MCM-41 and Cu/MCM-41 catalysts were prepared by impregnation and grinding. The catalysts were characterized by XRD, N2 adsorption-desorption and TPR methods. The catalytic activity of the dehydrogenation of methanol to methyl formate (MF) was evaluated using the flow microreactor under atmospheric pressure. According to the results, the catalyst prepared by impregnation had a better selectivity for the MF, but a lower methanol conversion rate. However, the product's selectivity could be improved by adding ZnO additive while the methanol conversion rate was reduced. For Cu/MCM-41 prepared by impregnation and grinding, the methanol conversion rate was 20.18% and 24.13% respectively at 250°C and the MF selectivity was 73.75% and 67.35% respectively. Likewise for Cu-ZnO/MCM-41 prepared by impregnation and grinding, the methanol conversion rate was 15.28% and 18.83% respectively at 250°C and the MF selectivity was 81.31% and 75.32% respectively.

Ammoxidation of 3-Picoline over V2O5/TiO2 Catalysts: Effects of TiO2 Supports on the Catalytic Performance

2011 ◽  
Vol 396-398 ◽  
pp. 791-797 ◽  
Author(s):  
Fu Min Zhang ◽  
Fei Chen ◽  
Qiang Xiao ◽  
Yi Jun Zhong ◽  
Wei Dong Zhu
Keyword(s):  
Catalytic Properties ◽  
External Surface ◽  
Weak Interactions ◽  
Catalytic Performance ◽  
Vanadium Oxides ◽  
Active Species ◽  
Direct Oxidation ◽  
N2 Adsorption ◽  
Wet Impregnation ◽  
Adsorption Desorption

A series of V2O5/TiO2catalysts were prepared by wet impregnation, and these prepared catalysts were characterized by XRD, N2 adsorption-desorption, H2-TPR, and TEM techniques and used in the selective ammoxidation of 3-picoline to 3-cyanopyridine. The effects of TiO2 supports on the catalytic properties of the resulting catalysts for the ammoxidation of 3-picoline to 3-cyanopyridine were investigated in detail. It is found that the V5+/V4+ transformation during ammoxidation is more favorable than the V5+/V3+ transformation for the selective ammoxidation of 3-picoline to 3-cyanopyridine. The V2O5/TiO2catalysts prepared from the nanosized TiO2particles as supports show a high activity for the direct oxidation of 3-picoline by air, resulting Subscript text Subscript textin a low selectivity for 3-cyanopyridine. This could be due to the fact that the active species vanadium oxides could be only supported on the external surface of the nano-sized TiO2particles with very minor contact area, leading to the weak interactions between active species and support.

Structure, Acid Properties and Catalysis Performance of MCM-22 “Family” Zeolites on the Alkylation of Benzene with Propylene

2012 ◽  
Vol 549 ◽  
pp. 283-286 ◽  
Author(s):  
Fei Zhao ◽  
Yu Zhang ◽  
Shu Dong Geng ◽  
Lian Fa Chen ◽  
Wei Wang
Keyword(s):  
Catalytic Activity ◽  
Liquid Phase ◽  
Reaction Temperature ◽  
Dynamic Method ◽  
N2 Adsorption ◽  
Acid Properties ◽  
Low Reaction Temperature ◽  
Alkylation Of Benzene ◽  
Adsorption Desorption

MCM-22 “family” zeolites (MCM-22, MCM-49 and MCM-56) have been synthesized hydrothermally by dynamic method. All materials were characterized by different techniques, such as XRD, N2 adsorption-desorption and NH3-TPD. The catalyst performance of MCM-22 “family” zeolites have been studied on the alkylation of benzene with propylene in liquid phase. Result shows that MCM-22 “family” zeolites are excellent alkylation catalysts for the produce of cumene. Compared to MCM-22 and MCM-49, MCM-56 shows higher catalytic activity in a relatively low reaction temperature and higher monoalkylation selectivity in a relatively low benzene-to-propylene ratio.

scholarly journals Preparation of Magnetic CuFe2O4@Ag@ZIF-8 Nanocomposites with Highly Catalytic Activity Based on Cellulose Nanocrystals

Molecules ◽  
2019 ◽  
Vol 25 (1) ◽  
pp. 124 ◽  
Author(s):  
Sufeng Zhang ◽  
Yongshe Xu ◽  
Dongyan Zhao ◽  
Wenqiang Chen ◽  
Hao Li ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Cellulose Nanocrystals ◽  
Environmental Chemistry ◽  
Magnetic Core ◽  
In Situ Reduction ◽  
Ag Nps ◽  
N2 Adsorption ◽  
Ag Catalyst ◽  
Adsorption Desorption

A facile approach was successfully developed for synthesis of cellulose nanocrystals (CNC)-supported magnetic CuFe2O4@Ag@ZIF-8 nanospheres which consist of a paramagnetic CuFe2O4@Ag core and porous ZIF-8 shell. The CuFe2O4 nanoparticles (NPs) were first prepared in the presence of CNC and dispersant. Ag NPs were then deposited on the CuFe2O4/CNC composites via an in situ reduction directed by dopamine polymerization (PDA). The CuFe2O4/CNC@Ag@ZIF-8 nanocomposite was characterized by TEM, FTIR, XRD, N2 adsorption-desorption isotherms, VSM, and XPS. Catalytic studies showed that the CuFe2O4/CNC@Ag@ZIF-8 catalyst had much higher catalytic activity than CuFe2O4@Ag catalyst with the rate constant of 0.64 min−1. Because of the integration of ZIF-8 with CuFe2O4/CNC@Ag that combines the advantaged of each component, the nanocomposites were demonstrated to have an enhanced catalytic activity in heterogeneous catalysis. Therefore, these results demonstrate a new method for the fabrication of CNC-supported magnetic core-shell catalysts, which display great potential for application in biocatalysis and environmental chemistry.

scholarly journals Synthesis, characterization and catalytic properties of SAPO-11 molecular sieve synthesized in hydrothermal media using di-isopropylamine as template

2014 ◽  
Vol 62 (3) ◽  
pp. 481-488 ◽  
Author(s):  
T. Chellappa ◽  
M. Jose Fonseca Costa ◽  
W.A. Nascimento ◽  
L. Ferreira De Lima ◽  
I. Almeida Bassan ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Molecular Sieve ◽  
Catalytic Properties ◽  
Single Agent ◽  
Catalytic Performance ◽  
Organic Template ◽  
N2 Adsorption ◽  
Bet Analysis ◽  
High Crystallization ◽  
Adsorption Desorption

Abstract A microporous SAPO-11 Molecular sieve was successfully synthesized by the hydrothermal method, using a single agent, as an organic template: di-isopropylamine (DIPA). The obtained solid was calcined at 550◦C for three hours, after which the flow of nitrogen was exchanged for that of synthetic air and submitted for another ten hours of calcination, so as to remove the single agent: di-isopropylamine, which after the removal of the template could be observed by the high crystallization of the sample. Furthermore, the molecular sieve was characterized by XRD, SEM, TG-DTG and N2 adsorption desorption (BET analysis). The obtained catalyst proved to have a high potential catalytic activity and selectivity, through the obtained characterization results, exhibiting good hydrothermal stability. The catalytic performance of SAPO-11 was tested by the deactivation/regenerability of the coked sample, furthered by cracking of n-hexane reaction and high olefins selectivity was obtained.

Catalytic Oxidation of CO over Ag-Doped Manganese Oxide Catalysts: Preparation and Catalytic Activity

2015 ◽  
Vol 1089 ◽  
pp. 133-136 ◽  
Author(s):  
Zhi Dan Fu ◽  
Qing Ye ◽  
Shui Yuan Cheng ◽  
Dao Wang
Keyword(s):  
Catalytic Activity ◽  
Co Oxidation ◽  
Manganese Oxide ◽  
Impregnation Method ◽  
Efficient Catalyst ◽  
Preparation Methods ◽  
Wet Impregnation ◽  
Adsorption Desorption ◽  
Wet Impregnation Method ◽  
Incorporation Method

The manganese oxide (MnO2) sample was synthesized by the reaction of KMnO4 with Mn (Ac)2 using the HNO3 solution as pH regulator. The Ag-doped manganese oxide, Ag/MnO2-Q and Ag/MnO2-H, were synthesized by incorporation method and typical wet impregnation method, respectively. The structure of catalysts was characterized by N2 adsorption/desorption and X-ray diffraction. The influences of preparation methods on the catalytic activity of CO oxidation were studied. The doping of Ag to MnO2 decreased the specific surface area of Ag/MnO2 catalysts, especially for Ag/MnO2-H samples prepared by traditional wet-impregnation method. The Ag/MnO2 catalysts showed higher catalytic activity for CO oxidation than that of MnO2. The catalytic activities of Ag/MnO2 samples strongly depended upon the preparing methods, among which 3Ag/MnO2-Q catalyst, prepared by the incorporation method, was the most efficient catalyst towards the addressed reactions. The excellent performance of 3Ag/MnO2-Q was mainly associated with the good low-temperature reducibility, abundant surface oxygen and broadly dispersed silver oxides species.

scholarly journals Zr-Modified ZnO for the Selective Oxidation of Cinnamaldehyde to Benzaldehyde

Catalysts ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 716 ◽  
Author(s):  
Pengju Du ◽  
Tongming Su ◽  
Xuan Luo ◽  
Xinling Xie ◽  
Zuzeng Qin ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Selective Oxidation ◽  
Active Sites ◽  
Catalyst Surface ◽  
Precipitation Method ◽  
N2 Adsorption ◽  
X Ray ◽  
Temperature Programmed ◽  
Zr Modification ◽  
Adsorption Desorption

ZnO and Zr-modified ZnO were prepared using a precipitation method and used for the selective oxidation of cinnamaldehyde to benzaldehyde in the present study. The results showed that physicochemical properties of ZnO were significantly affected by the calcination temperature, and calcination of ZnO at 400 °C demonstrated the optimum catalytic activity for the selective oxidation of cinnamaldehyde to benzaldehyde. With 0.01 g ZnO calcined at 400 °C for 2 h as a catalyst, 8.0 g ethanol and 2.0 g cinnamaldehyde reacted at an oxygen pressure of 1.0 MPa and 70 °C for 60 min, resulting in benzaldehyde selectivity of 69.2% and cinnamaldehyde conversion of 16.1%. Zr was the optimal modifier for ZnO: when Zr-modified ZnO was used as the catalyst, benzaldehyde selectivity reached 86.2%, and cinnamaldehyde conversion was 17.6%. The X-ray diffractometer and N2 adsorption–desorption characterization indicated that doping with Zr could reduce the crystallite size of ZnO (101) and increase the specific surface area of the catalyst, which provided more active sites for the reaction. X-ray photoelectron spectrometer results showed that Zr-doping could exchange the electrons with ZnO and reduce the electron density in the outer layer of Zn, which would further affect benzaldehyde selectivity. The results of CO2 temperature-programmed desorption showed that Zr-modification enhanced the alkalinity of the catalyst surface, which caused the Zr–ZnO catalyst to exhibit higher catalytic activity.

Get Rid of the Shackle from Supports: Construct Recoverable Semi-Homogeneous Catalysts with Attapulgite

2021 ◽  
Author(s):  
Ruixiang Guo ◽  
Gang Wang ◽  
Wei Liu ◽  
Zibei Yao ◽  
Wei-Sheng Liu
Keyword(s):  
Catalytic Activity ◽  
Homogeneous Catalysts ◽  
Immobilized Catalyst ◽  
Novel Strategy ◽  
Adsorption Desorption

Traditionally, the immobilized catalyst sacrifices a part of catalytic activity for its recyclability. To reproduce the catalytic activity of active specie, we construct a novel strategy called "adsorption-desorption-adsorption". Since the...

Vanadium-Chromium Oxide: Effective Catalysts for Ammoxidation of 3-Picoline

2013 ◽  
Vol 634-638 ◽  
pp. 624-627 ◽  
Author(s):  
Feng Jiang ◽  
Wei Xu ◽  
Lei Niu ◽  
Guo Min Xiao
Keyword(s):  
Raman Spectroscopy ◽  
Catalytic Activity ◽  
Chromium Oxide ◽  
Atmospheric Pressure ◽  
High Selectivity ◽  
Surface Acidity ◽  
N2 Adsorption ◽  
Composite Oxide ◽  
Highly Active

Bulk vanadium-chromium oxide (VCrO) catalyst was prepared and characterized by N2 adsorption, XRD, NH3-TPD, H2-TPR, and Raman spectroscopy. XRD and Raman results showed that the VCrO catalyst was a kind of VV-CrIII composite oxide mainly consisted of crystalline V2O5 and CrVO4-Ⅲ (orthorhombic). NH3-TPD and H2-TPR results revealed that this catalyst had negligible surface acidity, and was easily reduced due to the formation of CrVO4-Ⅲ. Their catalytic activity was evaluated in the ammoxidation of 3-picoline to nicotinonitrile. Catalytic results showed that the bulk VCrO catalyst was highly active and selective; the nicotinonitrile selectivity and yield was up to 96.1%, 88.2% respectively at atmospheric pressure and 360 °C. The high selectivity was related closely to the low surface acidity of the catalyst.

Facile Preparation of Nanoporous SnO2 for Application in Photodegradation of Methylene Blue

2011 ◽  
Vol 194-196 ◽  
pp. 385-388
Author(s):  
Hong Juan Wang ◽  
Feng Qiang Sun ◽  
Ming Zhong Ren ◽  
Qing Wei Guo
Keyword(s):  
Aqueous Solution ◽  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Photocatalytic Performance ◽  
Uv Light ◽  
High Photocatalytic Activity ◽  
N2 Adsorption ◽  
Photochemical Method ◽  
Degussa P25 ◽  
Adsorption Desorption

Nanoporous SnO2with high photocatalytic activity has been successfully prepared by a photochemical method, using SnCl2aqueous solution as a precursor. The as-synthesized sample was characterized by XRD, N2 adsorption-desorption and UV-vis. The photocatalytic activity of the sample was evaluated by degrading methylene blue (MB) aqueous solution under the UV light source and was compared with that of the commercial titania (Degussa P25). The results showed that the produced SnO2can degrade MB solution quickly and has comparative photocatalytic performance with P25 for degrading MB. This facile method supplies an effective way to prepare SnO2photocatalyst.

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