Abundant Lewis acidic sites of peculiar fibrous silica zeolite X enhanced toluene conversion in side chain toluene methylation

Fuel ◽  
2021 ◽  
Vol 305 ◽  
pp. 121432
Author(s):  
M.A.H Aziz ◽  
A.A Jalil ◽  
T.J Siang ◽  
I. Hussain ◽  
A.F.A Rahman ◽  
...  
Catalysts ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 829 ◽  
Author(s):  
Zhang ◽  
Yuan ◽  
Miao ◽  
Li ◽  
Shan ◽  
...  

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.


2008 ◽  
Vol 73 (8-9) ◽  
pp. 1061-1088
Author(s):  
Sule Rabiu ◽  
Sulaiman Al-Khattaf

In this work three important aromatic transformations, namely: toluene disproportionation, toluene methylation and m-xylene isomerization, were investigated in a riser simulator which closely mimics the operation of commercial fluidized bed reactors. The transformations were studied over a ZSM-5 based catalyst with medium acidity of 0.23 mmol/g and a series of Y zeolites of acidities between 0.55 and 0.03 mmol/g. For pure toluene feed, it was observed that conversion over the ZSM-5 based catalyst and the weakly acidic Y zeolite (USY-1) was very low. However, with the highly acidic Y zeolite (H-Y), significant toluene conversion was observed with paring reaction more prominent than disproportionation. On the other hand, when toluene was alkylated with methanol, higher toluene conversions were achieved over both the ZSM-5 based and the weakly acidic USY-1 catalysts as compared to when pure toluene feed was used. In addition, p-xylene/o-xylene (P/O) ratios higher than the equilibrium values were obtained in the reaction product over both catalysts. Finally, for m-xylene isomerization it was found that m-xylene conversion increased initially as the acidity of the catalyst increased up to 0.1 mmol/g beyond which any further increase in acidity resulted in a slight decrease in the m-xylene conversion.


2016 ◽  
Vol 234 ◽  
pp. 61-72 ◽  
Author(s):  
He Han ◽  
Min Liu ◽  
Xiaowa Nie ◽  
Fanshu Ding ◽  
Yiren Wang ◽  
...  

Materials ◽  
2019 ◽  
Vol 12 (22) ◽  
pp. 3654 ◽  
Author(s):  
Mingxuan Ma ◽  
Xiaoyu Ma ◽  
Suping Cui ◽  
Tingting Liu ◽  
Yingliang Tian ◽  
...  

A series of MCM-41 molecular sieves with different molar ratio of template to silicon were synthesized through hydrothermal synthesis method by using cetyltrimethylammonium bromide (CTAB) as the template, diatomite as the silicon source. By using impregnation method, the Mn-Ce/MCM-41 SCR molecular sieve-based catalysts were prepared. The results observed that when the molar ratio of template to silicon was 0.2:1, the MCM-41 as catalyst carrier has the highest surface area and largest pore volume, it also presented typically ordered hexagonal arrays of uniform channels. The denitration catalytic material based on this carrier has a high number of Lewis acidic sites, and the denitration efficiency can reach more than 93%.


Catalysts ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 44
Author(s):  
Cui Ouyang ◽  
Yingxia Li ◽  
Jianwei Li

The oxidation of benzene to phenol (BTOP) with N2O as the oxidant has been studied with a variety of Fe/ZSM-5 catalysts. The literature has conclusively proven that Fe2+ sites are the active sites. However, some studies have suggested that the Lewis acidic sites (LAS) are responsible for the generation of the active chemisorbed oxygen. Nevertheless, there is no clear relationship between the LAS and the N2O selectivity to phenol. In an effort to elucidate the effects of LAS on BTOP with various ZSM-5 catalysts, we investigated the initial N2O selectivity to phenol. Here we show that the initial N2O selectivity to phenol is negative with the amount of LAS over a certain range. The catalyst H-ZSM-5-ST (H-ZSM-5 treated with water vapor) showed a remarkable initial N2O selectivity to phenol as high as 95.9% with a 0.021 mmol g−1 LAS concentration on the surface of the catalyst, while the Fe/ZSM-5 catalyst demonstrated the lowest initial N2O selectivity to phenol (11.7%) with the highest LAS concentration (0.137 mmol g−1). Another remarkable feature is that steaming was more effective than Fe ion exchange and high temperature calcining. The samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), N2-adsorption-desorption, UV-vis, NH3-TPD and pyridine Fourier transform infrared (FT-IR) techniques. Our results demonstrate how the concentration of LAS is likely to affect the initial N2O selectivity to phenol within a certain range (0.021–0.137 mmol g−1). This research has demonstrated the synergy between the active Fe2+ sites and LAS.


2019 ◽  
Vol 31 (11) ◽  
pp. 4166-4172 ◽  
Author(s):  
Jiafei Lyu ◽  
Xuan Zhang ◽  
Peng Li ◽  
Xingjie Wang ◽  
Cassandra T. Buru ◽  
...  

2016 ◽  
Vol 18 (34) ◽  
pp. 23746-23754 ◽  
Author(s):  
Zhen Guo ◽  
De Sheng Theng ◽  
Karen Yuanting Tang ◽  
Lili Zhang ◽  
Lin Huang ◽  
...  

Lewis acidic sites on the surface of lanthanum phosphate nano-rods play a crucial role on the catalytic dehydration of lactic acid to acrylic acid.


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