Magnetite (Fe3O4) forms the basis of most dispersions studied in the field of magnetic fluids and magnetic colloids. Despite extensive theory and simulations on chain formation in dipolar fluids in zero field, such structures have not yet been imaged in laboratory-made magnetite dispersions. Here, we present the first direct observation of dipolar chain formation in zero field in a ferrofluid containing the largest synthetic single-domain magnetite particles studied so far. To our knowledge, this is the only ferrofluid system available at present that allows quantifying chain length and ring-size distributions of dipolar structures as a function of concentration and particle size.

We present the first real-space analysis on a single-particle level of the dipolar chains and branched clusters self-assembling in magnetic fluids in zero field. Spatial correlations and chain-length distributions directly obtained from tracked particle positions in vitrified films of synthetic magnetic (Fe3O4) dispersions provide a quantitative test for simulations and theory of dipolar fluids. A pertinent example is the cluster-size distribution that can be analyzed with a one-dimensional aggregation model to yield a dipolar attraction energy that agrees well with the dipole moment found from independent magnetization measurements.

Field-induced structures in a ferrofluid with well-defined magnetite nanoparticles with a permanent magnetic dipole moment are analyzed on a single-particle level by in situ cryogenic transmission electron microscopy (2D). The field-induced columnar phase locally exhibits hexagonal symmetry and confirms the structures observed in simulations for ferromagnetic dipolar fluids in 2D. The columns are distorted by lens-shaped voids, due to the weak interchain attraction relative to field-directed dipole-dipole attraction. Both dipolar coupling and the dipole concentration determine the dimensions and the spatial arrangement of the columns. Their regular spacing manifests long-range end-pole repulsions that eventually dominate the fluctuation-induced attractions between dipole chains that initiate the columnar transition. DOI: 10.1103/PhysRevLett.97.185702 PACS numbers: 64.70.Nd, 75.50.Mm, 82.70.Dd Nanoparticles dispersed in a solvent and with a sufficiently large permanent magnetic dipole moment selfassemble into a variety of magnetic equilibrium structures such as (flux-closure) rings and wormlike, branched dipole chains [1,2]. The morphology of these clusters, formed in absence of an external field, has been examined in detail, together with a determination of pair correlation functions and chain-length distributions [3]. In contrast, much less is known about the structural transitions induced by an external (homogeneous) magnetic field for fluids of permanent dipoles. Interestingly, magnetic colloids in an external field are nevertheless frequently encountered in practical applications [4] and biomedicine [5,6].The structure formation and phase behavior of colloidal systems in reduced dimensions is not necessarily equivalent to that of three-dimensional (3D) systems [7][8][9]. In particular, for permanent dipolar spheres confined to two dimensions (2D) a field-induced transition to a columnar phase with local hexagonal symmetry was predicted [10], although a conclusive experimental real-space analysis is still lacking. Elongated iron-particle clusters have been imaged [1] but the irregular particle shape and the bidisperse size distribution obstruct the wanted single-particle analysis. Parallel structures have also been observed for maghemite ferrofluids dried in the presence of a homogeneous field [11,12]. However, we have shown elsewhere that drying procedures may drastically change structure morphology [2]. Moreover, dipole interactions in conventional ferrofluids are in general too weak for a realistic comparison to the purely dipolar spheres from simulations.In this Letter, we report unequivocal real-space evidence for the predicted columnar phase transition [10] from in situ cryo-TEM images of monodisperse magnetic colloids with dominating dipolar interactions. The particle positions are confined by a 2D film whereas the dipole orientations can thermally fluctuate in 3D. Our imaging results, in addition, allow to quantify positional and angular interparticle correlations showing, among other things, a pr...

Ultrathin plate-like colloidal particles are effective candidates for Pickering stabilization of water-in-water emulsions, a stabilization that is complicated by the thickness and ultralow tension of the water–water interface. Plate-like particles have the advantage of blocking much of the interface while simultaneously having a low mass. Additionally, the amount of blocked interface is practically independent of the equilibrium contact angle θ at which the water–water interface contacts the nanoplates. As a result, the adsorption of nanoplates is stronger than for spheres with the same maximal cross section, except if θ = 90°.

Glycerol is an attractive renewable building block for the synthesis of di‐ and triglycerols, which have numerous applications in the cosmetic and pharmaceutical industries. In this work, the selective etherification of glycerol to di‐ and triglycerol was studied in the presence of alkaline earth metal oxides and the data are compared with those obtained with Na2CO3 as a homogeneous catalyst. It was found that glycerol conversion increased with increasing catalyst basicity; that is, the conversion increases in the order: MgO90 % at 60 % conversion) are obtained over CaO, SrO, and BaO. For these catalysts no substantial acrolein formation was observed. Furthermore, at the start of the reaction mainly linear diglycerol was produced, whereas at higher conversion degrees branched diglycerol started to form. In another series of experiments different types of CaO materials were prepared. It was found that these CaO‐based materials not only differed in their surface area and number of basic sites, but also in their Lewis acid strength. Within this series the CaO material possessing the strongest Lewis acid sites had the highest catalytic activity, comparable to that of BaO, pointing towards the important role of Lewis acidity for this etherification reaction. Based on these observations a plausible alternative reaction scheme for glycerol etherification is presented, which considers the facilitation of the hydroxyl leaving process. Finally, the stability of the catalytic solids under study was investigated and it was found that colloidal CaO particles of about 50–100 nm can be spontaneously generated during reaction. Catalytic testing of these CaO colloids, after isolation from the reaction medium, revealed a very high etherification activity. Understanding the nature of these Ca‐based colloids opens new opportunities for investigating supported colloidal particle catalysts to take advantage of both their hetero‐ and homogeneous nature.