Using first principles calculations we unveil fundamental mechanism of hydrolysis reactions of two hazardous chemicals PCl3 and POCl3 with explicit molecular water clusters nearby. It is found that the water molecules play a key role as a catalyst significantly lowing activation barrier of the hydrolysis via transferring its protons to reaction intermediates. Interestingly, torsional angle of the molecular complex at transition state is identified as a vital descriptor on the reaction rate. Analysis of charge distribution over the complex further reinforces the finding with atomic level correlation between the torsional angle and variation of the orbital hybridization state of phosphorus (P) in the complex. Electronic charge separation (or polarization) enhances thermodynamic stability of the activated complex and reduces the activation energy through hydrogen bonding network with water molecules nearby. Calculated potential energy surfaces (PES) for the hydrolysis of PCl3 and POCl3 depict their two contrastingly different profiles of double- and triple-depth wells, respectively. It is ascribed to the unique double-bonding O = P in the POCl3. Our results on the activation free energy show well agreements with previous experimental data within 7 kcal mol−1 deviation.
|Number of pages||7|
|Journal||Journal of Hazardous Materials|
|Publication status||Published - 2018|
Bibliographical noteFunding Information:
This work was supported by the Korea Ministry of Environment (MOE) as “the Chemical Accident Prevention Technology Development Project”. Also, this subject is supported by Global Frontier Program through the Global Frontier Hybrid Interface Materials (GFHIM) ( 2013- M3A6B1078882 ) and the Defense Industry Technology Center (DITC) for financial support from contract No. UC15000ID. Appendix A
© 2017 Elsevier B.V.
All Science Journal Classification (ASJC) codes
- Environmental Engineering
- Environmental Chemistry
- Waste Management and Disposal
- Health, Toxicology and Mutagenesis