Rapid hydrolysis of phosphate monoesters by zirconium(IV) complexes in neutral solution

Polyhedron ◽  
2012 ◽  
Vol 48 (1) ◽  
pp. 104-109 ◽  
Author(s):  
Fergal Coleman ◽  
Andrea Erxleben
2019 ◽  
Vol 118 ◽  
pp. 03048
Author(s):  
Changchun Li ◽  
Yuxin Wu

Hydrogen generation from rapid hydrolysis of aluminum in sodium fluoride solution was investigated through a hydrolysis experiment. Rapid and instant hydrogen yield were observed using sodium fluoride as additive. The experimental results demonstrate that the increase of temperature and the amount of additives in a certain range will boost the hydrogen production. The amount of additives outside the range only has an effect on the rapid hydrolysis of the aluminum during the initial stage, but the total amount of hydrogen produced doesn’t increased significantly. Theoretical analysis of the effects of the mixing ratio and the temperature on the hydrogen production rates were performed using the shrinking core model and the kinetic model. The shrinking core model parameter a and k indicate the film change degree of porosity and thickness and the effect of time on the diffusion coefficient. the kinetic model is verified and the activation energy confirming hydrogen yield control by a molecular diffusion process. Correspondingly, mechanisms of Al corrosion in NaF solutions under low and high alkalinity were proposed, respectively.


1994 ◽  
Vol 17 (5) ◽  
pp. 389-391
Author(s):  
Man Ki Park ◽  
Jeong Hill Park ◽  
Sool Yeon Cho ◽  
Seung Yong Lee ◽  
Byung Hoon Han

2016 ◽  
Vol 12 ◽  
pp. 1467-1475 ◽  
Author(s):  
Sonia L Repetto ◽  
James F Costello ◽  
Craig P Butts ◽  
Joseph K W Lam ◽  
Norman M Ratcliffe

A novel approach to protecting jet fuel against the effects of water contamination is predicated upon the coupling of the rapid hydrolysis reactions of lipophilic cyclic geminal ethers, with the concomitant production of a hydrophilic acyclic hydroxyester with de-icing properties (Fuel Dehydrating Icing Inhibitors - FDII). To this end, a kinetic appraisal of the hydrolysis reactions of representative geminal ethers was undertaken using a convenient surrogate for the fuel–water interface (D2O/CD3CN 1:4). We present here a library of acyclic and five/six-membered cyclic geminal ethers arranged according to their hydroxonium catalytic coefficients for hydrolysis, providing for the first time a framework for the development of FDII. A combination of 1H NMR, labelling and computational studies was used to assess the effects that may govern the observed relative rates of hydrolyses.


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