Approach to theoretical estimation of the activation energy of particle aggregation taking ionic nonclassic polarization into account
Source abstract
Abstract
The activation energy of particle aggregation in suspensions is a very important kinetic parameter in a wide range of science and engineering applications. At present, however, there is no theory that can theoretically predict the activation energy. Because the activation energy is often less than 10 kT (where k is the Boltzmann constant and T is the temperature), it is difficult to experimentally measure. In this study, a theory for calculating the activation energy is established. Experimental measurements of the activation energy of montmorillonite aggregation were performed with different electrolyte and particle concentrations using the dynamic light scattering (DLS) technique. The validity of the theory was verified by the experiments. This study confirmed that both the method for activation energy measurements by DLS and the theory for its calculation can be applied to suspensions of polydisperse nonspherical particles. The average kinetic energy at the moment of particle collision in the aggregation process was found to be 0.2 kT, which is less than the instantaneous kinetic energy of a Brownian particle (0.5 kT) because of the viscous resistance of the water medium. This study also shows that adsorbed Na+ is strongly polarized in the electric field near the particle surface, and the polarization increases the effective charge of Na+ from +1 to +1.18.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Electrostatics and Colloid Interactions · Microfluidic and Bio-sensing Technologies · Electrowetting and Microfluidic Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Southwest University Chongqing Key Laboratory of Soil Multi-Scale Interfacial Process, College of Resources and Environment, , Chongqing, PR China
Funding
major science and technology program for water pollution control and treatment · National Natural Science Foundation of China
References (25)
Show source-provided references
1. Langmuir · 2008 · 24 · 1061210.1021/la802303z ↗
2. Natl. Acad. Sci. USA · 2006 · 103 · 1573910.1073/pnas.0606422103 ↗
3. Adv. Colloid Interface Sci. · 1996 · 67 · 11910.1016/0001-8686(96)00302-8 ↗
4. Nature · 1991 · 353 · 23910.1038/353239a0 ↗
5. Surf. Sci. Rep. · 2005 · 59 · 110.1016/j.surfrep.2005.08.003 ↗
6. Langmuir · 1996 · 12 · 554110.1021/la960326e ↗
7. Phys. Chem. Chem. Phys. · 2014 · 16 · 882810.1039/c3cp54813a ↗
8. J. Phys. Chem. C · 2015 · 119 · 485610.1021/jp512078v ↗
9. J. Soil Sediment · 2013 · 13 · 32510.1007/s11368-012-0608-8 ↗
10. Adv. Colloid Interface Sci. · 2007 · 134-35 · 15110.1016/j.cis.2007.04.003 ↗
11. J. Colloid Interface Sci. · 1981 · 83 · 53110.1016/0021-9797(81)90348-9 ↗
12. J. Colloid Interface Sci. · 1984 · 97 · 44610.1016/0021-9797(84)90316-3 ↗
13. Langmuir · 1992 · 8 · 10910.1021/la00037a021 ↗
14. Langmuir · 2012 · 28 · 533910.1021/la204603y ↗
15. Soil Sci. Soc. Am. J. · 2009 · 73 · 165810.2136/sssaj2008.0017 ↗
16. J. Phys. Chem. C · 2009 · 113 · 441910.1021/jp808372r ↗
17. Soil Sci. Soc. Am. J. · 2013 · 77 · 156310.2136/sssaj2013.01.0009 ↗
18. Scientific Reports · 2014 · 4 · 504710.1038/srep05047 ↗
19. J. Phys. Chem. C · 2013 · 117 · 624510.1021/jp312682u ↗
20. PLOS ONE · 2015 · 10 · e012246010.1371/journal.pone.0122460 ↗
21. European Journal of Soil Science · 2015 · 66 · 61510.1111/ejss.12252 ↗
22. J. Phys. Chem. B · 2013 · 117 · 1086910.1021/jp405578w ↗
23. Science · 2010 · 328 · 167310.1126/science.1189403 ↗
24. Acta Phys-Chim. Sin · 2009 · 25 · 122510.3866/PKU.WHXB20090631 ↗
25. J. Colloid and Inter. Sci. · 2004 · 275 · 17210.1016/j.jcis.2003.12.055 ↗