Microplastics are sub-millimeter-sized fragments of plastics and a relatively new class of pollutant increasingly found in the environment. Due to their size and surface area to volume ratio, the physicochemical characteristics of microplastics can diverge from those of their macroscopic counterparts. This is partly why it is challenging to understand their origin, analyze their behavior, and predict their fates in the environment compared to large pollutants. We believe that adopting a view of microplastics as a colloid provides a holistic framework that connects their physical properties and surface chemistries with observations of their dynamics in the environment. In particular, we discuss the role of fundamental principles of colloid science in interpreting phenomena of wetting, adsorption, aggregation, and transport of microplastics. Colloid and interface science can provide the tools to couple or decouple the physicochemical behaviors of microplastics, which may aid in understanding the environmental challenge both from a fundamental perspective and with respect to practical remediation methods.
Suprastructures at the colloidal scale must be assembled with precise control over local interactions to accurately mimic biological complexes. The toughest design requirements include breaking the symmetry of assembly in a simple and reversible fashion to unlock functions and properties so far limited to living matter. We demonstrate a simple experimental technique to program magnetic field–induced interactions between metallodielectric patchy particles and isotropic, nonmagnetic “satellite” particles. By controlling the connectivity, composition, and distribution of building blocks, we show the assembly of three-dimensional, multicomponent supraparticles that can dynamically reconfigure in response to change in external field strength. The local arrangement of building blocks and their reconfigurability are governed by a balance of attraction and repulsion between oppositely polarized domains, which we illustrate theoretically and tune experimentally. Tunable, bulk assembly of colloidal matter with predefined symmetry provides a platform to design functional microstructured materials with preprogrammable physical and chemical properties.
Electric and magnetic fields have enabled both technological applications and fundamental discoveries in the areas of bottom-up material synthesis, dynamic phase transitions, and biophysics of living matter. Electric and magnetic fields are versatile external sources of energy that power the assembly and self-propulsion of colloidal particles. In this Invited Feature Article, we classify the mechanisms by which external fields impact the structure and dynamics in colloidal dispersions and augment their nonequilibrium behavior. The paper is purposely intended to highlight the similarities between electrically and magnetically actuated phenomena, providing a brief treatment of the origin of the two fields to understand the intrinsic analogies and differences. We survey the progress made in the static and dynamic assembly of colloids and the self-propulsion of active particles. Recent reports of assembly-driven propulsion and propulsion-driven assembly have blurred the conceptual boundaries and suggest an evolution in the research of nonequilibrium colloidal materials. We highlight the emergence of colloids powered by external fields as model systems to understand living matter and provide a perspective on future challenges in the area of field-induced colloidal phenomena.
Microplastics are ubiquitous in the environment, leading to a new form of plastic pollution crisis, which has reached an alarming level worldwide. Micron and nanoscale plastics may get integrated into ecological cycles with detrimental effects on various ecosystems. Commodity plastics are widely considered to be chemically inert, and alterations in their surface properties due to environmental weathering are often overlooked. This lack of knowledge on the dynamic changes in the surface chemistry and properties of (micro)plastics has impeded their life-cycle analysis and prediction of their fate in the environment. Through simulated weathering experiments, we delineate the role of sunlight in modifying the physicochemical properties of microplastics. Within 10 days of accelerated weathering, microplastics become dramatically more dispersible in the water column and can more than double the surface uptake of common chemical pollutants, such as malachite green and lead ions. The study provides the basis for identifying the elusive link between the surface properties of microplastics and their fate in the environment.
Active colloids are a synthetic analogue of biological microorganisms that consume external energy to swim through viscous fluids. Such motion requires breaking the symmetry of the fluid flow in the vicinity of a particle; however, it is challenging to understand how surface and shape anisotropies of the colloid lead to a particular trajectory. Here, we attempt to deconvolute the effects of particle shape and surface anisotropy on the propulsion of model ellipsoids in alternating current (AC) electric fields. We first introduce a simple process for depositing metal patches of various shapes on the surfaces of ellipsoidal particles. We show that the shape of the metal patch is governed by the assembled structure of the ellipsoids on the substrate used for physical vapor deposition. Under high-frequency AC electric field, ellipsoids dispersed in water show linear, circular, and helical trajectories which depend on the shapes of the surface patches. We demonstrate that features of the helical trajectories such as the pitch and diameter can be tuned by varying the degree of patch asymmetry along the two primary axes of the ellipsoids, namely longitudinal and transverse. Our study reveals the role of patch shape on the trajectory of ellipsoidal particles propelled by induced charge electrophoresis. We develop heuristics based on patch asymmetries that can be used to design patchy particles with specified nonlinear trajectories.
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