The coagulation kinetics of composite particles

1997 ◽  
Vol 28 ◽  
pp. S647-S648 ◽  
Author(s):  
V.N. Piskunov
2015 ◽  
Vol 15 (17) ◽  
pp. 23795-23840
Author(s):  
Y.-H. Kim ◽  
S. Yiacoumi ◽  
A. Nenes ◽  
C. Tsouris

Abstract. Charging and coagulation influence one another and impact the particle charge and size distributions in the atmosphere. However, few investigations to date have focused on the coagulation kinetics of atmospheric particles accumulating charge. This study presents three approaches to include mutual effects of charging and coagulation on the microphysical evolution of atmospheric particles such as radioactive particles. The first approach employs ion balance, charge balance, and a bivariate population balance model (PBM) to comprehensively calculate both charge accumulation and coagulation rates of particles. The second approach involves a much simpler description of charging, and uses a monovariate PBM and subsequent effects of charge on particle coagulation. The third approach is further simplified assuming that particles instantaneously reach their steady-state charge distributions. It is found that compared to the other two approaches, the first approach can accurately predict time-dependent changes in the size and charge distributions of particles over a wide size range covering from the free molecule to continuum regimes. The other two approaches can reliably predict both charge accumulation and coagulation rates for particles larger than about 40 nm and atmospherically relevant conditions. These approaches are applied to investigate coagulation kinetics of particles accumulating charge in a radioactive neutralizer, the urban atmosphere, and a radioactive plume. Limitations of the approaches are discussed.


2010 ◽  
Vol 83 (5) ◽  
pp. 806-810 ◽  
Author(s):  
E. E. Bibik ◽  
A. V. Semyachkov

2011 ◽  
Vol 688 ◽  
pp. 45-50
Author(s):  
Xiao Feng Wu ◽  
Yu Chao Liao ◽  
Ren Liang Yue ◽  
Yun Fa Chen

Based on the growth kinetics of the SiO2particles, we studied the kinetic hetero-precipitation process on the interface of polystyrene (PS) microscale particles. The nanoscale SiO2shell thickness increased with increasing time and was proportional to the square root of the initial concentration of TEOS precursor while governed by hetero-precipitation process. Moreover, the hetero-precipitation process followed the first-order growth mechanism of silica onto the surface of templating PS pariticles. Properly controlling the reagent concentrations could alleviate and even avoid, to a certain extent, aggregation among PS@SiO2particles that could otherwise have an adverse effect on the properties and applications of those composite particles and the corresponding SiO2hollow products.


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