Fabrication of Anisotropic Porous Silica Monoliths by Means of Magnetically Controlled Phase Separation in Sol–Gel Processes

Sol–gel accompanied by phase separation is an established method for the preparation of porous silica monoliths with well-defined macroporosity, which find numerous applications. In this work, we demonstrate how the addition of (superpara)­magnetic nanocolloids as templates to a system undergoing a sol–gel transition with phase separation leads to the creation of monoliths with a strongly anisotropic structure. It is known that magnetic nanocolloids respond to the application of an external magnetic field by self-assembling into columnar structures. The application of a magnetic field during the chemically driven spinodal decomposition induced by the sol–gel transition allows one to break the symmetry of the system and promote the growth of elongated needle-like silica domains incorporating the magnetic nanocolloids, aligned in the direction of the field. It is found that this microstructure imparts a strong mechanical anisotropy to the materials, with a ratio between the Young’s modulus values measured in a direction parallel and perpendicular to the one of the field as high as 150, and an overall smaller average macropores size as compared to isotropic monoliths. The microstructure and properties of the porous monoliths can be controlled by changing both the system composition and the strength of the applied magnetic field. Our monoliths represent the first example of materials prepared by magnetically controlling a phase transition occurring via spinodal decomposition

Template-Assisted Synthesis of Janus Silica Nanobowls

The preparation of anisotropic nanoparticles has drawn much attention in the literature, with most of the efforts being dedicated to convex particles. In this work, instead, we present a reliable method to synthesis silica nanobowls with one well-defined opening, covering a broad range of sizes. The nanobowls have been obtained from asymmetrically functionalized silica–polymer Janus nanodumbbells, used as templates, by removing of the polymer. Polystyrene seeds having different sizes as well as surface chemistry have been used as starting material in a two-step seeded emulsion polymerization, which leads to polymer nanodumbbells. These dumbbells are also asymmetrically functionalized due to the presence of silane groups on only one of their two hemispheres. This allows us to selectively coat the silane-bearing hemisphere of the dumbbells with a silica layer by means of a Stoeber process. The silica nanobowls are eventually obtained after either calcination or dissolution of the polymeric template. Depending on the route followed to remove the polymer, nanobowls made of pure silica (from calcination) or hybrid Janus nanobowls with a silica outer shell and a covalently bound hydrophobic polymer layer inside the cavity (from dissolution) could be prepared. The difference between the two types of nanobowls has been proved by electrostatically binding oppositely charged silica nanoparticles, which adhere selectively only on the outer silica part of the nanobowls prepared by polymer dissolution, while they attach both inside and outside of nanobowls prepared by calcination. We also show that selective functionalization of the outer surface of the Janus nanobowls from dissolution is possible. This work is one of the first examples of concave objects bearing different functionalities in the inner and outer parts of their surface

Breakage Rate of Colloidal Aggregates in Shear Flow through Stokesian Dynamics

We study the first breakage event of colloidal aggregates exposed to shear flow by detailed numerical analysis of the process. We have formulated a model, which uses Stokesian dynamics to estimate the hydrodynamic interactions among the particles in a cluster, van der Waals interactions and Born repulsion to describe the normal interparticle interactions, and the tangential interactions through discrete element method to account for contact forces. Fractal clusters composed of monodisperse spherical particles were generated using different Monte Carlo methods, covering a wide range of cluster masses (<i>N</i>_sphere = 30–215) and fractal dimensions (<i>d</i>_f = 1.8–3.0). The breakup process of these clusters was quantified for various flow magnitudes (γ), under both simple shear and extensional flow conditions, in terms of breakage rate constant (<i>K</i>^B), mass distribution of the produced fragments (FMD, <i>f</i>_{<i>m</i>,<i>k</i>}), and critical stable aggregate mass (<i>N</i>_c), defined as the largest cluster mass that does not break under defined flow conditions. The breakage rate <i>K</i>^B showed a power law dependence on the product of the aggregate size and the applied stress, with values of the corresponding exponents depending only on the aggregate fractal dimension and the type of flow field, whereas the prefactor of the power law relation also depends on the size of the primary particles comprising a cluster. The FMD was fitted by Schultz–Zimm distribution, and the parameter values showed an analogous dependence on the product of the aggregate size and the applied stress similar to the rate constant. Finally, a power law relation between the applied stress and corresponding largest stable aggregate mass was found, with an exponent value depending on the aggregate fractal dimension. This unique and detailed analysis of the breakage process can be directly utilized to formulate a breakage kernel used in solving population balance equations

Influence of the Potential Well on the Breakage Rate of Colloidal Aggregates in Simple Shear and Uniaxial Extensional Flows

In this work we build on our previous paper (Harshe, Y. M.; Lattuada, M. <i>Langmuir</i> <b>2012</b>, <i>28</i>, 283–292) and compute the breakage rate of colloidal aggregates under the effect of shear forces by means of Stokesian dynamics simulations. A library of clusters made of identical spherical particles covering a broad range of masses and fractal dimension values (from 1.8 to 3.0) was generated by means of a combination of several Monte Carlo methods. DLVO theory has been used to describe the interparticle interactions, and contact forces have been introduced by means of the discrete element method. The aggregate breakage process was investigated by exposing them to well-defined shear forces, generated under both simple shear and uniaxial extensional flow conditions, and by recording the time required to reach the first breakage event. It has been found that the breakage rate of clusters was controlled by the potential well between particles as described by DLVO theory. A semiempirical Arrhenius-type exponential equation that relates the potential well to the breakage rate has been used to fit the simulation results. The dependence of the breakage process on the radius of gyration, on the external shear strength, and on the fractal dimension has been obtained, providing a very general relationship for the breakage rate of clusters. It was also found that the fragment mass distribution is insensitive to the presence of electrostatic repulsive interactions. We also clarify the physical reason for the large difference in the breakage rate of clusters between simple shear and the uniaxial extensional flow using a criterion based on the energy dissipation rate. Finally, in order to answer the question of the minimum cluster size that can break under simple shear conditions, a critical rotation number has been introduced, expressing the maximum number of rotations that a cluster exposed to simple shear could sustain before breakage

Influence of the Potential Well on the Breakage Rate of Colloidal Aggregates in Simple Shear and Uniaxial Extensional Flows

In this work we build on our previous paper (Harshe, Y. M.; Lattuada, M. <i>Langmuir</i> <b>2012</b>, <i>28</i>, 283–292) and compute the breakage rate of colloidal aggregates under the effect of shear forces by means of Stokesian dynamics simulations. A library of clusters made of identical spherical particles covering a broad range of masses and fractal dimension values (from 1.8 to 3.0) was generated by means of a combination of several Monte Carlo methods. DLVO theory has been used to describe the interparticle interactions, and contact forces have been introduced by means of the discrete element method. The aggregate breakage process was investigated by exposing them to well-defined shear forces, generated under both simple shear and uniaxial extensional flow conditions, and by recording the time required to reach the first breakage event. It has been found that the breakage rate of clusters was controlled by the potential well between particles as described by DLVO theory. A semiempirical Arrhenius-type exponential equation that relates the potential well to the breakage rate has been used to fit the simulation results. The dependence of the breakage process on the radius of gyration, on the external shear strength, and on the fractal dimension has been obtained, providing a very general relationship for the breakage rate of clusters. It was also found that the fragment mass distribution is insensitive to the presence of electrostatic repulsive interactions. We also clarify the physical reason for the large difference in the breakage rate of clusters between simple shear and the uniaxial extensional flow using a criterion based on the energy dissipation rate. Finally, in order to answer the question of the minimum cluster size that can break under simple shear conditions, a critical rotation number has been introduced, expressing the maximum number of rotations that a cluster exposed to simple shear could sustain before breakage

Population Balance Modeling of Antibodies Aggregation Kinetics

The aggregates morphology and the aggregation kinetics of a model monoclonal antibody under acidic conditions have been investigated. Growth occurs via irreversible cluster–cluster coagulation forming compact, fractal aggregates with fractal dimension of 2.6. We measured the time evolution of the average radius of gyration, ⟨<i>R</i>_<i>g</i>⟩, and the average hydrodynamic radius, ⟨<i>R</i>_<i>h</i>⟩, by in situ light scattering, and simulated the aggregation kinetics by a modified Smoluchowski‘s population balance equations. The analysis indicates that aggregation does not occur under diffusive control, and allows quantification of effective intermolecular interactions, expressed in terms of the Fuchs stability ratio (<i>W</i>). In particular, by introducing a dimensionless time weighed on <i>W</i>, the time evolutions of ⟨<i>R</i>_<i>h</i>⟩ measured under various operating conditions (temperature, pH, type and concentration of salt) collapse on a single master curve. The analysis applies also to data reported in the literature when growth by cluster–cluster coagulation dominates, showing a certain level of generality in the antibodies aggregation behavior. The quantification of the stability ratio gives important physical insights into the process, including the Arrhenius dependence of the aggregation rate constant and the relationship between monomer–monomer and cluster–cluster interactions. Particularly, it is found that the reactivity of non-native monomers is larger than that of non-native aggregates, likely due to the reduction of the number of available hydrophobic patches during aggregation

Modeling of the Degradation of Poly(ethylene glycol)-<i>co</i>-(lactic acid)-dimethacrylate Hydrogels

Because of their similarity with extracellular matrix, hydrogels are ideal substrates for cell growth. Hydrogels made of synthetic polymers are excellent alternatives to natural ones and offer the key advantage of precisely controllable degradation times. In this work, hydrogels have been prepared from modified poly­(ethylene glycol) macromonomers, functionalized on both ends first with a few lactic acid units, and then with methacrylate groups. A library of hydrogels has been prepared using free-radical polymerization of the macromonomers, by changing both the macromonomer concentration and their type, i.e., the number of lactic acid repeating units. The degradation kinetics of these hydrogels, caused by the hydrolysis of the lactic acid units, have been carefully monitored in terms of swelling ratio, mass loss, and Young’s modulus. A complete mathematical model, accounting for hydrogel degradation, swelling, and reverse gelation, has been developed and used to predict all the measured quantities until complete disappearance of the gels. The model is capable of accurately predicting the time evolution of all the properties investigated experimentally. To the best of our knowledge, this is the first study where such a systematic comparison between model predictions and experimental data is presented

Magnetically Guided Synthesis of Anisotropic Porous Carbons toward Efficient CO₂ Capture and Magnetic Separation of Oil

Conventional synthetic strategies do not allow one to impart structural anisotropy into porous carbons, thus leading to limited control over their textural properties. While structural anisotropy alters the mechanical properties of materials, it also introduces an additional degree of directionality to increase the pore connectivity and thus the flux in the designed direction. Accordingly, in this work the structure of porous carbons prepared from resorcinol–formaldehyde gels has been rendered anisotropic by integrating superparamagnetic colloids to the sol–gel precursor solution and by applying a uniform magnetic field during the sol–gel transition, which enables the self-assembly of magnetic colloids into chainlike structures to template the growth of the gel phase. Notably, the anisotropic pore structure is maintained upon pyrolysis of the gel, leading to hierarchically porous carbon monoliths with tunable structure and porosities. With an advantage granted to anisotropic materials, these porous carbons showed higher porosity, a higher CO2 uptake capacity of 3.45 mmol g–1 at 273 K at 1.1 bar, and faster adsorption kinetics compared to the ones synthesized in the absence of magnetic field. Moreover, these materials were also used as magnetic sorbents with fast adsorption kinetics for efficient oil-spill cleanup and retrieved easily by using an external magnetic field

Synthesis of Hetero-nanoclusters: The Case of Polymer–Magnetite Systems

Nanoclusters (NCs) composed of nanoparticles (NPs) with different functionalities and having final size in the sub-micrometer range are of great interest for biomedical imaging, drug delivery, sensors, etc. Because some of the functionalities cannot be incorporated into a single NP, e.g., high drug loading combined with strong magnetic properties, here, we present a proof of the concept using an alternative way to combine these properties using different NPs. In particular, starting from polymer and magnetite nanoparticles (MNPs), we produce NCs made out of a statistical distribution of the two components through a process based on aggregation and breakup. The effect of all involved operating parameters, i.e., primary NP size and composition, surfactant type and concentration, and applied hydrodynamic stress on the NC size and internal structure, was systematically investigated using dynamic light scattering (DLS), static light scattering (SLS), and transmission electron microscopy (TEM) analyses. It was found that, by properly tuning the balance between attractive and steric repulsive forces on one side and hydrodynamic stress on the other, NCs as small as 100 nm can be produced. In all cases, the produced NCs have a very compact internal structure characterized by fractal dimension around 2.6. The proposed production strategy to synthesize hetero-NCs composed of mixtures of various primary particles is suitable for the production of multifunctional devices of nanometer size (i.e., approximately 100 nm) for material and biomedical applications

La naissance des jeux olympiques et le sport dans l'antiquité

The ultrasound-induced cleavage of macromolecules has become a routine experiment in the emerging field of polymer mechanochemistry. To date, it has not been conclusively proven whether the molecular weight of a polymer or its contour length is the determining factor for chain scission upon ultrasonication. Here we report comparative experiments that confirm unequivocally that the contour length is the decisive parameter. We utilized postpolymerization modifications of specifically designed precursor polymers to create polymers with identical chain length but different molecular mass. To demonstrate the universality of the findings, two different polymer backbones were utilizedpoly­(styrene) and poly­(norbornene imide alkyne)whose molecular weights were altered by bromination and removal of pendant triisopropylsilyl protecting groups, respectively. Solutions of the respective polymer pairs were subjected to pulsed ultrasound at 20 kHz and 10.4 W/cm² in order to investigate the chain scission trends. The effects of cleavage and sonochemical treatments were monitored by size exclusion chromatography. In both series, experimental data and calculations show that the molecular weight reduction upon sonication is the same for polymers with the same contour length