Catalytic hydrodeoxygenation of palmitic acid over a bifunctional Co-doped MoO2/CNTs catalyst: an insight into the promoting effect of cobalt

2016 ◽  
Vol 6 (7) ◽  
pp. 2065-2076 ◽  
Author(s):  
Ranran Ding ◽  
Yulong Wu ◽  
Yu Chen ◽  
Hao Chen ◽  
Jianlong Wang ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Palmitic Acid ◽  
Oxygen Vacancies ◽  
Promoting Effect ◽  
Lewis Acidic Sites ◽  
Acidic Sites ◽  
Lower Temperature ◽  
Insight Into ◽  
Co Doped

HDO of palmitic acid into C16 hydrocarbons was successfully achieved over Co doped MoO2/CNTs catalysts at a much lower temperature. Co could promote the formation of Lewis acidic sites, oxygen vacancies and Mo2C particles, which are all decisive factors for better catalytic activity.

scholarly journals Effect of Fe Additives on the Catalytic Performance of Ion-Exchanged CsX Zeolites for Side-Chain Alkylation of Toluene with Methanol

Catalysts ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 829 ◽  
Author(s):  
Zhang ◽  
Yuan ◽  
Miao ◽  
Li ◽  
Shan ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Catalytic Performance ◽  
High Yield ◽  
Side Chain ◽  
Impregnation Method ◽  
Basic Sites ◽  
Lewis Acidic Sites ◽  
X Zeolite ◽  
Acidic Sites ◽  
Negative Effect

The side-chain alkylation of toluene with methanol was investigated over some Fe-modified Cs ion-exchanged X zeolite (CsX) catalysts prepared via the impregnation method using different iron sources. The absorption/activation behaviors of the reactants on the surface of the catalysts were studied by in situ Fourier-transform infrared (FT-IR) spectroscopy and temperature programmed desorption (TPD) mass measurements. Modification of CsX with a small amount of FeCl3 could result in a considerable decrease in catalytic activity, due mainly to the remarkable decrease in the density of acidic and basic sites of the catalysts. Interestingly, the Fe(NO3)3-modified CsX with an optimum Fe loading of 0.15 wt.% shows improved catalytic activity and high yield compared to the side-chain alkylation products. Modification of CsX with Fe(NO3)3 could also result in a decrease in basic sites of the catalyst. However, such a change does not bring an obvious negative effect on the adsorption/activation of toluene, while it could effectively inhibit the generation of the undesired bidentate formate. Furthermore, the introduced FeOx species (derived from the decomposition of Fe(NO3)3) may also act as new Lewis acidic sites to participate in the activation of methanol and to stabilize the formed active intermediates (i.e., unidentate formate). Therefore, modification of CsX with a suitable amount of Fe(NO3)3 may adjust its adsorption/activation ability for reagents by changing the acid–base properties of the catalyst, which can finally enhance the catalytic performance for the side-chain alkylation of toluene with methanol.

A DFT study on direct benzene hydroxylation catalyzed by framework Fe and Al sites in zeolites

2014 ◽  
Vol 4 (8) ◽  
pp. 2490-2493 ◽  
Author(s):  
Gang Yang ◽  
Lijun Zhou
Keyword(s):  
Catalytic Activity ◽  
Dft Study ◽  
Benzene Hydroxylation ◽  
Lewis Acidic Sites ◽  
Acidic Sites

Framework Fe rather than Al Lewis acidic sites in zeolites are demonstrated to show superior catalytic activity for benzene hydroxylation.

An efficient Fe2O3/HY catalyst for Friedel–Crafts acylation of m-xylene with benzoyl chloride

RSC Advances ◽  
2014 ◽  
Vol 4 (70) ◽  
pp. 36951-36958 ◽  
Author(s):  
Manman Mu ◽  
Ligong Chen ◽  
Yunlong Liu ◽  
Wangwang Fang ◽  
Yang Li
Keyword(s):  
Catalytic Activity ◽  
Iron Oxide ◽  
Benzoyl Chloride ◽  
Catalytic Performance ◽  
Reaction Parameters ◽  
Hy Zeolite ◽  
Lewis Acidic Sites ◽  
Acidic Sites ◽  
Excellent Catalytic Performance

Iron oxide supported on HY zeolite was prepared and exhibited excellent catalytic performance in the acylation of m-xylene with benzoyl chloride. It was characterized by XRD, BET, XPS, NH3-TPD and Py-IR. The catalytic activity of Fe2O3/HY is enhanced with the increase of Lewis acidic sites. Furthermore, the reaction parameters were optimized. Finally, the catalyst was easily separated reused for five runs without appreciable loss of catalytic activity.

Strong Promoting Effect of Gold Nanoparticles on the CO Abatement Catalytic Activity of CoO x /Clay‐Bonded SiC Catalysts Produced by AA‐MOCVD Method Using Co(acac) 2 as Precursor

2020 ◽  
Vol 5 (44) ◽  
pp. 13878-13887
Author(s):  
Golnoosh MirMoghtadaei ◽  
Manoj K. Ghosalya ◽  
Luca Artiglia ◽  
Jeroen A. Bokhoven ◽  
Cavus Falamaki
Keyword(s):  
Gold Nanoparticles ◽  
Catalytic Activity ◽  
Promoting Effect

scholarly journals Insight into Active Centers and Anti-Coke Behavior of Niobium-Containing SBA-15 for Glycerol Dehydration

Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 488
Author(s):  
Katarzyna Stawicka ◽  
Maciej Trejda ◽  
Maria Ziolek
Keyword(s):  
Coke Formation ◽  
Catalytic Performance ◽  
Acid Sites ◽  
Silica Matrix ◽  
High Concentration ◽  
Active Centers ◽  
Acidic Sites ◽  
Glycerol Dehydration ◽  
Adsorption Desorption ◽  
Insight Into

Niobium containing SBA-15 was prepared by two methods: impregnation with different amounts of ammonium niobate(V) oxalate (Nb-15/SBA-15 and Nb-25/SBA-15 containing 15 wt.% and 25 wt.% of Nb, respectively) and mixing of mesoporous silica with Nb2O5 followed by heating at 500 °C (Nb2O5/SBA-15). The use of these two procedures allowed obtaining materials with different textural/surface properties determined by N2 adsorption/desorption isotherms, XRD, UV-Vis, pyridine, and NO adsorption combined with FTIR spectroscopy. Nb2O5/SBA-15 contained exclusively crystalline Nb2O5 on the SBA-15 surface, whereas the materials prepared by impregnation had both metal oxide and niobium incorporated into the silica matrix. The niobium species localized in silica framework generated Brønsted (BAS) and Lewis (LAS) acid sites. The inclusion of niobium into SBA-15 skeleton was crucial for the achievement of high catalytic performance. The strongest BAS were on Nb-25/SBA-15, whereas the highest concentration of BAS and LAS was on Nb-15/SBA-15 surface. Nb2O5/SBA-15 material possessed only weak LAS and BAS. The presence of the strongest BAS (Nb-25/SBA-15) resulted in the highest dehydration activity, whereas a high concentration of BAS was unfavorable. Silylation of niobium catalysts prepared by impregnation reduced the number of acidic sites and significantly increased acrolein yield and selectivity (from ca. 43% selectivity for Nb-25/SBA-15 to ca. 61% for silylated sample). This was accompanied by a considerable decrease in coke formation (from 47% selectivity for Nb-25/SBA-15 to 27% for silylated material).

Insight into the mechanism of intense NIR-to-red upconversion luminescence in Er3+ doped and Er3+–Yb3+ co-doped SrF2 nanoparticles

2021 ◽  
Vol 45 (14) ◽  
pp. 6469-6478
Author(s):  
Qingling Zeng ◽  
Wenxiang He ◽  
Fangfei Luan ◽  
Yu Yan ◽  
Hongli Du ◽  
...  
Keyword(s):  
Hydrothermal Method ◽  
Theoretical Basis ◽  
Upconversion Luminescence ◽  
Insight Into ◽  
Co Doped

SrF2:Yb3+,Er3+ NPs were synthesized by the hydrothermal method and their luminescence mechanism was discussed in detail, which provided a theoretical basis for further understanding the properties of the materials.

scholarly journals Highly Dispersed Pd Species Supported on CeO2 Catalyst for Lean Methane Combustion: The Effect of the Occurrence State of Surface Pd Species on the Catalytic Activity

Catalysts ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 772
Author(s):  
Yanxiong Liu ◽  
Changhua Hu ◽  
Longchun Bian
Keyword(s):  
Catalytic Activity ◽  
Oxygen Vacancies ◽  
Methane Combustion ◽  
Pd Nanoparticles ◽  
High Concentration ◽  
Ch4 Combustion ◽  
Highly Active ◽  
Δ Phase ◽  
Occurrence State ◽  
Comprehensive Characterization

The correlation between the occurrence state of surface Pd species of Pd/CeO2 for lean CH4 combustion is investigated. Herein, by using a reduction-deposition method, we have synthesized a highly active 0.5% PdO/CeO2-RE catalyst, in which the Pd nanoparticles are evenly dispersed on the CeO2 nanorods CeO2-R. Based on comprehensive characterization, we have revealed that the uniformly dispersed Pd nanoparticles with a particle size distribution of 2.3 ± 0.6 nm are responsible for the generation of PdO and PdxCe1−xO2−δ phase with –Pd2+–O2−–Ce4+– linkage, which can easily provide oxygen vacancies and facilitate the transfer of reactive oxygen species between the CeO2-R and Pd species. As a consequence, the remarkable catalytic activity of 0.5% Pd/CeO2-RE is related to the high concentration of PdO species on the surface of the catalyst and the synergistic interaction between the Pd species and the CeO2 nanorod.

scholarly journals On the Effects of Doping on the Catalytic Performance of (La,Sr)CoO3. A DFT Study of CO Oxidation

Catalysts ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 312 ◽  
Author(s):  
Antonella Glisenti ◽  
Andrea Vittadini
Keyword(s):  
Catalytic Activity ◽  
Co Oxidation ◽  
Density Functional Calculations ◽  
Density Functional ◽  
Formation Energy ◽  
Oxygen Vacancies ◽  
Catalytic Performance ◽  
Energy Profiles ◽  
High Concentrations ◽  
3D Impurities

The effects of modifying the composition of LaCoO3 on the catalytic activity are predicted by density functional calculations. Partially replacing La by Sr ions has benefical effects, causing a lowering of the formation energy of O vacancies. In contrast to that, doping at the Co site is less effective, as only 3d impurities heavier than Co are able to stabilize vacancies at high concentrations. The comparison of the energy profiles for CO oxidation of undoped and of Ni-, Cu-m and Zn-doped (La,Sr)CoO3(100) surface shows that Cu is most effective. However, the effects are less spectacular than in the SrTiO3 case, due to the different energetics for the formation of oxygen vacancies in the two hosts.

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