The increasing enrichment of microplastics (MPs) in the
shoreline
environment poses both ecological and social-economic risks. The alteration
and motion of MPs in the ocean under the effect of bulk nanobubbles
(NBs) have been less extensively studied. In this study, we explored
the behavior and movement of various MPs in the presence of bulk NBs.
The role of salinity and external energy in the interactions between
NBs and MPs was evaluated, and the mechanism underlying these interactions
was analyzed. In the presence of NBs, the binding of MPs and NBs resulted
in an increase in the measured average particle size and concentration.
Meanwhile, NBs reduced the aggregation between MPs, while the NBs
present combined with MPs to make them more stable in suspensions.
The velocity of motion of MPs driven by NBs varies under different
salinity conditions. The increase in ionic strength reduced the energy
barrier between particles and promoted their aggregation. Thus, the
binding of NBs and MPs became more stable, which in turn affected
the movement of MPs in suspensions. Polyethylene (PE1) with small
particle size was mainly affected by Brownian motion, and its rising
was limited; therefore, polyethylene (PE2) with large particle size
rose faster than PE1 in suspension, especially in the presence of
NBs. The rising velocity of poly(tetrafluoroethylene) (PTFE) was higher
than that of PE1 and PE2. However, when NBs were present, the trend
of the change in velocity was the opposite compared to the absence
of NBs for PTFE. Moreover, various types of MPs were found to be affected
distinctly by external energy. The presence of NBs had a clear effect
on PE under shaking conditions, whereas the effect on PTFE was less
obvious.