Selective Hydrogenation of Maleic Anhydride to Succinic Anhydride Over Nickel-palladium Catalysts

2014 ◽  
Vol 32 (15) ◽  
pp. 1784-1790 ◽  
Author(s):  
W. -P. Tian ◽  
S. -F. Guo ◽  
L. Shi
2013 ◽  
Vol 33 (7) ◽  
pp. 1229-1235
Author(s):  
Da WANG ◽  
Yin ZHANG ◽  
Haitao LI ◽  
Lili ZHAO ◽  
Hongxi ZHANG ◽  
...  

Catalysts ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 366 ◽  
Author(s):  
Lili Zhao ◽  
Yin Zhang ◽  
Tianjie Wu ◽  
Min Zhao ◽  
Yongzhao Wang ◽  
...  

A series of Sc-doped ZrO2 supports, with Sc2O3 content in the range of 0 to 7.5% (mol/mol), were prepared using the hydrothermal method. Ni/Sc-doped ZrO2 catalysts with nickel loading of 10% (w/w) were prepared using impregnation method, and characterized with the use of XRD, Raman, H2 temperature-programmed reduction (H2-TPR), H2 temperature-programmed desorption (H2-TPD), XPS, and in situ FT-IR techniques. The catalytic performances of Ni/Sc-doped ZrO2 catalysts in maleic anhydride hydrogenation were tested. The results showed that the introduction of Sc3+ into ZrO2 support could effectively manipulate the distribution of maleic anhydride hydrogenation products. γ-butyrolactone was the major hydrogenation product over Sc-free Ni/ZrO2 catalyst with selectivity as high as 65.8% at 210 °C and 5 MPa of H2 pressure. The Ni/Sc-doped ZrO2 catalyst, with 7.5 mol% of Sc2O3 content, selectively catalyzed maleic anhydride hydrogenation to succinic anhydride, the selectivity towards succinic anhydride was up to 97.6% under the same reaction condition. The results of the catalysts’ structure–activity relationships revealed that there was an interdependence between the surface structure of ZrO2-based support and the C=O hydrogenation performance of the ZrO2-based supported nickel catalysts. By controlling the Sc2O3 content, the surface structure of ZrO2-based support could be regulated effectively. The different surface structure of ZrO2-based supports, resulted in the different degree of interaction between the nickel species and ZrO2-based supports; furthermore, the different interaction led to the different surface oxygen vacancies electron properties of ZrO2-based supported nickel catalysts and the C=O hydrogenation activity of the catalyst. This result provides new insight into the effect of ZrO2 support on the selective hydrogenation activity of ZrO2-supported metal catalysts and contributes to the design of selective hydrogenation catalysts for other unsaturated carbonyl compounds.


2012 ◽  
Vol 425-426 ◽  
pp. 205-212 ◽  
Author(s):  
Yonghai Feng ◽  
Hengbo Yin ◽  
Aili Wang ◽  
Tao Xie ◽  
Tingshun Jiang

2014 ◽  
Vol 20 (6) ◽  
pp. 4140-4145 ◽  
Author(s):  
Weitao Huo ◽  
Chunlei Zhang ◽  
Hongjing Yuan ◽  
Mingjun Jia ◽  
Chunli Ning ◽  
...  

2014 ◽  
Vol 126 (1) ◽  
pp. 141-145 ◽  
Author(s):  
HONGJING YUAN ◽  
CHUNLEI ZHANG ◽  
WEITAO HUO ◽  
CHUNLI NING ◽  
YONG TANG ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (79) ◽  
pp. 75541-75551 ◽  
Author(s):  
Feng Jiang ◽  
Jian Cai ◽  
Bing Liu ◽  
Yuebing Xu ◽  
Xiaohao Liu

Palladium particles of different sizes obtained directly and indirectly by various methods were studied to clarify the particle size effect in the selective hydrogenation of cinnamaldehyde (CAL).


2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Amal Amin ◽  
Moshera Samy

Different polyesteramides hyperbranched polymers (HPEA1-6)/montomorillonite clay (MMT) nanocomposites were prepared with three different loading contents of clay (4, 10, and 15 wt%). The obtained nanocomposites were characterized via XRD, thermal analyses, and TEM. Generally, intercalation behavior was observed. The hyperbranched polyesteramides (HPEA1-6) were originally prepared by the bulky reaction between maleic anhydride (MAn), succinic anhydride (ScAn), and phthalic anhydride (PhAn) with either diethanolamine (DEA) or diisopropanolamine (DiPA). The resulting hyperbranched polyesteramides (HPEA1-6) were characterized by GPC, IR,1H-NMR, TGA, and DSC.


Sign in / Sign up

Export Citation Format

Share Document