Magnetic ZSM-5 zeolite: a selective catalyst for the valorization of furfuryl alcohol to γ-valerolactone, alkyl levulinates or levulinic acid

2016 ◽  
Vol 18 (20) ◽  
pp. 5586-5593 ◽  
Author(s):  
Thiago M. Lima ◽  
Carolina G. S. Lima ◽  
Anuj K. Rathi ◽  
Manoj B. Gawande ◽  
Jiri Tucek ◽  
...  

A magnetic ZSM-5 zeolite with a core–shell type structure was synthesized, fully characterized and had its catalytic activity evaluated on the valorization of bio-derived furfuryl alcohol.

2016 ◽  
Vol 6 (13) ◽  
pp. 5102-5115 ◽  
Author(s):  
Biplab Banerjee ◽  
Ramana Singuru ◽  
Sudipta K. Kundu ◽  
Karnekanti Dhanalaxmi ◽  
Linyi Bai ◽  
...  

Core–shell catalytic nanoreactor was designed, exhibiting high catalytic activity for levulinic acid hydrogenation.


2018 ◽  
Vol 53 (13) ◽  
pp. 9650-9661 ◽  
Author(s):  
M. Cernea ◽  
B. S. Vasile ◽  
I. V. Ciuchi ◽  
V. A. Surdu ◽  
C. Bartha ◽  
...  

2020 ◽  
Vol 56 (9) ◽  
pp. 1433-1435
Author(s):  
Yu Zhu ◽  
Jian Zhang ◽  
Lei Zhang

A large organotin-oxo arsonate cluster, {Na6Sn14As16}, with a core–shell type structure consisting of a {Na6} core and a {Sn14As16} shell is successfully constructed, which shows high water stability and has potential application as an electrode decoration material in CO2 reduction.


2021 ◽  
Vol 193 ◽  
pp. 112-116
Author(s):  
Kenji Kaneko ◽  
Takuya Maeda ◽  
Yasuhito Kawahara ◽  
Kazuhiro Ichino ◽  
Takuro Masumura ◽  
...  

2020 ◽  
Author(s):  
Kenji Kaneko ◽  
Kazuhiro Ichino ◽  
Yasuhito Kawahara ◽  
Takuya Maeda ◽  
Takuro Masumura ◽  
...  

2021 ◽  
Vol 148 ◽  
pp. 106050
Author(s):  
Wasinton Simanjuntak ◽  
Kamisah D. Pandiangan ◽  
Zipora Sembiring ◽  
Agustina Simanjuntak ◽  
Sutopo Hadi

2021 ◽  
Vol 171 ◽  
pp. 124-132
Author(s):  
Ruoqing Wang ◽  
Feng Shen ◽  
Yiwei Tang ◽  
Haixin Guo ◽  
Richard Lee Smith ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 656
Author(s):  
Henrietta Kovács ◽  
Krisztina Orosz ◽  
Gábor Papp ◽  
Ferenc Joó ◽  
Henrietta Horváth

Na2[Ir(cod)(emim)(mtppts)] (1) with high catalytic activity in various organic- and aqueous-phase hydrogenation reactions was immobilized on several types of commercially available ion-exchange supports. The resulting heterogeneous catalyst was investigated in batch reactions and in an H-Cube flow reactor in the hydrogenation of phenylacetylene, diphenylacetylene, 1-hexyne, and benzylideneacetone. Under proper conditions, the catalyst was highly selective in the hydrogenation of alkynes to alkenes, and demonstrated excellent selectivity in C=C over C=O hydrogenation; furthermore, it displayed remarkable stability. Activity of 1 in hydrogenation of levulinic acid to γ-valerolactone was also assessed.


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