Effects of crosslinking density and Lewis acidic sites on conductivity and viscoelasticity of dynamic network electrolytes

Author(s):  
Brian B. Jing ◽  
Patricia Mata ◽  
Qiujie Zhao ◽  
Christopher M. Evans
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.


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.


1984 ◽  
Vol 24 (1-2) ◽  
pp. 25-29 ◽  
Author(s):  
M. B. Fleisher ◽  
L. O. Golender ◽  
M. V. Shimanskaya

2017 ◽  
Vol 6 (1) ◽  
pp. 165-176 ◽  
Author(s):  
Xueyan Zhang ◽  
Yue Li ◽  
Lifang Xue ◽  
Shengtian Wang ◽  
Xiaohong Wang ◽  
...  

RSC Advances ◽  
2021 ◽  
Vol 11 (40) ◽  
pp. 24702-24708
Author(s):  
Gi-Baek Lee ◽  
In-Kyoung Ahn ◽  
Won-Hyo Joo ◽  
Jae-Chan Lee ◽  
Ji-Yong Kim ◽  
...  

Ag nanoparticles in Zn-embedded carbon nanofiber were synthesized by a simple one-pot, self-forming strategy. Charged Zn single atoms act as Lewis acidic sites and improving the CO2 reduction reaction performance of the Ag nanoparticles.


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