superacid catalyst
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2021 ◽  
Vol 400 (1) ◽  
pp. 2100056
Author(s):  
Raju Kagne ◽  
Sandeep Niwadange ◽  
Virbhadra Kalalawe ◽  
Gopinath Khansole ◽  
Dashrath Munde

2020 ◽  
Vol 8 (45) ◽  
pp. 16878-16888
Author(s):  
Lei Song ◽  
Hairong Yue ◽  
Kui Ma ◽  
Weizao Liu ◽  
Wen Tian ◽  
...  
Keyword(s):  
Flue Gas ◽  
Nh3 Scr ◽  

Author(s):  
Xiang Li ◽  
Rui Yang ◽  
Detang Wang ◽  
Gan Li ◽  
Meixia Zhao
Keyword(s):  

2020 ◽  
Vol 44 (32) ◽  
pp. 13669-13684 ◽  
Author(s):  
Chien-Chang Huang ◽  
Shih-Han Ho ◽  
Jo-Shu Chang ◽  
Pei-Jyuan Gao

The high catalytic reactivity and reusability of the sulfated/chlorinated Sr–Fe oxide could be ascribed to the synergistic effect of coordinated Cl− and surface SrSO4 clusters on suppressing the chemisorption of oleic acid on the surface cations.


Energies ◽  
2019 ◽  
Vol 12 (10) ◽  
pp. 1905
Author(s):  
Seong-Min Cho ◽  
Chang-Young Hong ◽  
Se-Yeong Park ◽  
Da-Song Lee ◽  
June-Ho Choi ◽  
...  

Brønsted acid-catalyzed reactions of α-pinene have been studied because of their ability to produce various types of fragrance molecules. Beyond this application, dimeric hydrocarbon products produced from coupling reactions of α-pinene have been suggested as renewable high-density fuel molecules. In this context, this paper presents the application of a sulfated tin(IV) oxide catalyst for the partial coupling reaction of α-pinene from turpentine. Brønsted acid sites inherent in this solid superacid catalyst calcined at 550 °C successfully catalyzed the reaction, giving the largest yield of dimeric products (49.6%) at 120 °C over a reaction time of 4 h. Given that the low-temperature viscosity of the mentioned dimeric products is too high for their use as a fuel in transportation engines, lowering the viscosity is an important avenue of study. Therefore, our partial coupling reaction of α-pinene provides a possible solution as a considerable amount of the isomers of α-pinene still remained after the reaction, which reduces the low-temperature viscosity. On the basis of a comparison of the reaction products, a plausible mechanism for the reaction involving coinstantaneous isomerization and coupling reaction of α-pinene was elucidated.


2019 ◽  
Vol 33 (2) ◽  
pp. 1334-1343 ◽  
Author(s):  
Natthawan Prasongthum ◽  
Paweesuda Natewong ◽  
Prasert Reubroycharoen ◽  
Raphael Idem

2017 ◽  
Vol 72 (1) ◽  
pp. 119-128 ◽  
Author(s):  
Hong K. D. Nguyen ◽  
Hung V. Vo ◽  
Tuyet Anh T. Dang ◽  
Ngo T. Dinh

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