Cooperation between the surface hydroxyl groups of the support and organic additives in the highly selective hydrogenation of citral

2012 ◽  
Vol 445-446 ◽  
pp. 351-358 ◽  
Author(s):  
Hai-Jun Jiang ◽  
Hong-Bin Jiang ◽  
De-Ming Zhu ◽  
Xue-Li Zheng ◽  
Hai-Yan Fu ◽  
...  
2014 ◽  
Vol 881-883 ◽  
pp. 267-270 ◽  
Author(s):  
Guang Yin Fan ◽  
Chun Zhang

The Ir/AlO(OH) catalyst was prepared by sol-gel method and used for selective hydrogenation of p-chloronitrobenzene (p-CNB) to p-chloroniamine (p-CAN). The mechanism of p-CNB hydrogenation over the catalyst was discussed. The hydrogen bond between the surface hydroxyl groups of the catalyst and the nitrogen present in p-CNB facilitated the hydrogenation of nitro group. On the other hand, the formation of hydrogen bond between the hydrogenation product and water promotes the rapid desorption of the hydrogenation product on the surface of the catalyst. Thus the activity and selectivity were greatly promoted.


1986 ◽  
Vol 51 (7) ◽  
pp. 1430-1438 ◽  
Author(s):  
Alena Reissová ◽  
Zdeněk Bastl ◽  
Martin Čapka

The title complexes have been obtained by functionalization of silica with cyclopentadienylsilanes of the type Rx(CH3)3 - xSi(CH2)nC5H5 (x = 1-3, n = 0, 1, 3), trimethylsilylation of free surface hydroxyl groups, transformation of the bonded cyclopentadienyl group to the cyclopentadienyl anion, followed by coordination of (h5-cyclopentadienyl)trichlorotitanium. The effects of single steps of the above immobilization on texture of the support, the number of free hydroxyl groups, the coverage of the surface by cyclopentadienyl groups and the degree of their utilization in anchoring the titanium complex have been investigated. ESCA study has shown that the above anchoring leads to formation of the silica-supported bis(h5-cyclopentadienyl)dichlorotitanium(IV) complex.


RSC Advances ◽  
2015 ◽  
Vol 5 (121) ◽  
pp. 99712-99721 ◽  
Author(s):  
Yan Li ◽  
Yawen Wang ◽  
Yu Huang ◽  
Junji Cao ◽  
Wingkei Ho ◽  
...  

Surface modification by phosphate efficiently improves the photocatalytic performance of BiPO4 for the degradation of methylene orange (MO), by enhancing the concentration of surface hydroxyl groups and improving its hydrophilicity.


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