A facile microwave-induced synthesis of titanium pyrophosphate nanocrystals

2012 ◽  
Vol 83 ◽  
pp. 130-132 ◽  
Author(s):  
Rui Wang ◽  
Junwei Ye ◽  
Guiling Ning ◽  
Heng Jiang ◽  
Weilei Zhou ◽  
...  
ACS Nano ◽  
2019 ◽  
Vol 13 (8) ◽  
pp. 9227-9236 ◽  
Author(s):  
Zhongtao Li ◽  
Yunfa Dong ◽  
Jianze Feng ◽  
Tao Xu ◽  
Hao Ren ◽  
...  

2008 ◽  
Vol 595-598 ◽  
pp. 17-22 ◽  
Author(s):  
S.Y. Brou ◽  
G. Bonnet ◽  
Jean Luc Grosseau-Poussard

Gamma-TiAl samples were treated by phosphoric acid solutions at different concentrations. With 15 mol/dm3, a viscous deposit was left on the surface leading, after drying and high temperature oxidation, to a very heterogeneous surface aspect. Concentrations below 0.5 mol/dm3 were then used and allowed to greatly ameliorate the homogeneity of the superficial layer. After heating from ambient to oxidation temperature, however, cracks were always observed, due to the departure of gaseous molecules. Isothermal oxidation tests come out at 800°C and 900°C under reconstituted air showed that weight gains were strongly reduced when TiAl had been treated. A compound containing titanium, oxygen and phosphorus was detected at the end of the heating period, identified as titanium pyrophosphate, TiP2O7. This compound remained the only one detected for 100 h when oxidation was come out at 800°C, but evolved towards TiO2 when oxidation time was increased. In the case of oxidation at 900°C, the evolution from TiP2O7 to TiO2 also happened but appeared to go faster.


2005 ◽  
Vol 70 (6) ◽  
pp. 791-798 ◽  
Author(s):  
Ioan-Cezar Marcu ◽  
Jean Millet ◽  
Ioan Sandulescu

The catalytic properties of titanium pyrophosphate in the oxidative dehydrogenation of isobutane to isobutylene were investigated in the 400 ? 550 ?C temperature range. Asignificant change of the product distribution and of the apparent activation energy of the reaction was observed at about 490 ?C. This phenomenon, already observed in the oxidative dehydrogenation of n-butane, has been interpreted by the existence of two reaction mechanisms depending upon the reaction temperature. Comparison with the n-butane reaction allowed different activation pathways for the activation of alkanes to be proposed. The catalytic properties of TiP2O7 in the oxidative dehydrogenation of isobutane was also compared to those obtained previously with several other pyrophosphates and TiP2O7 was found to be less active and selective for this reaction.


2003 ◽  
Vol 337 (1-4) ◽  
pp. 221-229 ◽  
Author(s):  
K.E. Lipinska-Kalita ◽  
M.B. Kruger ◽  
S. Carlson ◽  
A.M.Krogh Andersen

2020 ◽  
Vol 344 ◽  
pp. 115140 ◽  
Author(s):  
Yve Xian Ooi ◽  
Kyaw Zay Ya ◽  
Keiichiro Maegawa ◽  
Wai Kian Tan ◽  
Go Kawamura ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-12 ◽  
Author(s):  
Huemantzin Balan Ortiz-Oliveros ◽  
Rosa María Flores-Espinosa ◽  
Eduardo Ordoñez-Regil ◽  
Suilma Marisela Fernández-Valverde

This work addresses the synthesis of titanium pyrophosphate, as well as the characterization and evaluation of the sorption process of europium, for removal of trivalent heavy metals and actinides simulate. The evaluation of the surface properties of titanium pyrophosphate was carried out determining the surface roughness and surface acidity constants. The values obtained from the determination of the surface roughness of the synthesized solid indicate that the surface of the material presents itself as slightly smooth. The FITEQL program was used to fit the experimental titration curves to obtain the surface acidity constants: log⁡K+=3.59±0.06 and log⁡K-=-3.90±0.05. The results of sorption kinetics evidenced that the pseudo-order model explains the retention process of europium, in which the initial sorption velocity was 8.3 × 10−4 mg g−1 min−1 and kinetic constant was 1.8 × 10−3 g mg min−1. The maximum sorption capacity was 0.6 mg g−1. The results obtained from sorption edge showed the existence of two bidentate complexes on the surface.


2020 ◽  
Vol 268 ◽  
pp. 127399 ◽  
Author(s):  
Chengcheng Li ◽  
Qingyu Han ◽  
Yufu Pan ◽  
Jingyu Zhao ◽  
Yanfang Luo ◽  
...  

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