Unlike crystalline metals, which have a well-understood periodical structure, the amorphous structure of metallic glasses (MGs) is still poorly understood, particularly when such a structure rearranges itself at the nanoscale under external agitations.
Here, we selected three critical factors, namely, volume ratio of organic solvent phase to external aqueous phase, agitation speed, and duration of homogenization for the optimization of the experimental investigation response.
It was found that coupling elastic and magnetic properties within the 3D flexible scaffold enables continuous non-contact mode of mechanical agitation by external magnetic field.
It may also suggest that the external diffusion assisted by agitation or oscillation can benefit the adsorption process, while our work was completed under static adsorption conditions where adsorption equilibrium was established by simple diffusion.
The materials could be recovered after the reaction by an external magnetic field, and agitation of the solution via a magnetic field led to improvements of mass transfer of the substrates to the catalyst surface for hydrogenation reactions.
The call for more external directors has also caused agitation.
The effect of agitator speed, duration of agitation, xylene concentration in the membrane phase, membrane to external phase (M/E) ratio on the reduction of solute, concentration of biological oxygen demand (BOD) and chemical oxygen demand (COD) in the external phase has been studied.
This may suggest that the monotony in the positive trend is a result of an ever increasing and consistent external enhancement of the natural climate agitation.
Consequently, the well-integrated ZnO NRAs on the CT substrate could be fabricated by the ED process with the aid of ultrasonic agitation under a proper external cathodic voltage.
The ZnO NRAs were successfully integrated on the CT substrate (i.e., woven by Ni/PET fibers) by the ED process using the seed layer and ultrasonic agitation under a proper external cathodic voltage of −2 V for 1 h.
