Spherical Polystyrene Particles Research Articles

Enhancing cement hydration by core/shell PS@SiO2 nanoparticles

Nanoparticles are widely used in construction. Here, nano-SiO2 is employed, in a way that prevents agglomeration of the nanoparticles, as pozzolanic material to improve Portland cement hydration and to improve the properties of the concrete. To explore the effect of nano-SiO2 and core-shell PS@SiO2 on cement properties, spherical polystyrene particles were prepared by dispersion polymerization of styrene in polar solvents and characterized by FTIR and E-SEM. The core shells PS@SiO2 were synthesized by Stöber method. The results showed an amorphous nano-SiO2 layer can be deposited uniformly on polystyrene particles. This core/shell structure was reducing the aggregation of nano-SiO2 effectively. It was shown that PS@SiO2 particles improved the concrete performances compared to blended cement with nano-SiO2 due to the agglomeration affect. Highlights • Core/shell PS@SiO2 nanoparticles with a uniform coating layer were prepared. • As-prepared nanoparticles were characterized by a variety of advanced methods. • Nanoparticles accelerate hydration and lower the spatial weight of cement paste. • Core/shell nanoparticles improve cement hydration much better than nano-SiO2.

Dynamics of the surface growth resulted from sedimentation of spheres in a Hele–Shaw cell containing a low-viscosity fluid

In this paper, we investigate the dynamics of surface growth resulting from sedimentation of spherical granular particles in a fluid environment, using experiments and simulations. In the experimental part, spherical polystyrene particles are poured down from the top of a vertical Hele–Shaw cell and form a 1 + 1-dimensional growing surface. The surface roughness is obtained from the images, and the growth and roughness exponents are measured. In the numerical simulation part, the surface growth process is simulated using the discrete element method, considering the interactions between the grains, and the exponents are calculated. In this method, unlike conventional simulation models, instead of a discrete deposition law, the dynamics of the individual particles throughout the process are obtained, considering different forces acting on the particles. Finally, the simulation results are compared with the experiment, and we see a very good agreement between them. We find different values for the exponents using different methods, indicating that the system is multi-affine and does not obey the scaling laws of affine models.

DEDALO: Device for Enhanced Dust Analyses with Light Obscuration sensors

Instruments based on light obscuration sensors are widely used for measuring the size distribution of insoluble sub-visible particles in liquid suspensions, being fast and suitable for in situ and real-time measurements. Such instruments are typically calibrated by means of reference polystyrene spherical particles with a specific refractive index, which unavoidably leads to systematic errors when determining the size of particles of different materials. In this paper, we propose a reliable and consistent method to overcome this limitation by setting the refractive index value according to the sample, thus achieving an improved particle size distribution (PSD) measurement. An ad hoc, ready-to-use, open source code with a graphical interface able to drive an in-line instrument and obtain a real-time correction to the PSD has been developed. The method has been extensively validated with several oil emulsions characterized by different refractive index values and the results have been compared with an independent optical method. As an example of application, we have adopted this approach for the analysis of dust suspended in meltwater of an ice core from a glacier in the Aosta Valley (Italy). We believe that our approach will strongly improve the accuracy in characterizing liquid suspensions and reduce discrepancies between data obtained with different methods. The code has been made publicly available at: https://instrumentaloptics.fisica.unimi.it/dedalo/ and on the GitHub page of the corresponding author (https://github.com/LucaTeruzzi/DEDALO).

Three-Dimensional Characterization of Dry Particle Coating Structures Originating from the Mechano-fusion Process.

Dry particle coating processes are of key importance for creating functionalized materials. By a change in surface structure, initiated during coating, a surface property change and thus functionalization can be achieved. This study introduces an innovative approach employing 3D X-ray micro-computed tomography (micro-CT) to characterize coated particles, consisting of spherical alumina particles (d50 = 45.64 μm), called hosts, surrounded by spherical polystyrene particles (d50 = 3.5 μm), called guests. The formed structures, hetero-aggregates, are generated by dry particle coating using mechano-fusion (MF). A deeper understanding of the influence of MF process parameters on the coating structures is a crucial step toward tailoring of coating structure, resulting surface property and functionalization. Therefore, the influence of rotational speed, process time, and total mechanical energy input during MF is explored. Leveraging micro-CT data, acquired of coated particles, enables non-stereologically biased and quantitative coating structure analysis. The guest's coating thickness is analyzed using the maximum inscribed sphere and ray method, two different local thickness measurement approaches. Particle-discrete information of the coating structure are available after a proper image processing workflow is implemented. Coating efficiency and guest's neighboring relations (nearest neighbor distance and number of neighbors inside search radius) are evaluated.

Structure Formation in Supraparticles Composed of Spherical and Elongated Particles.

We studied the evaporation-induced formation of supraparticles from dispersions of elongated colloidal particles using experiments and computer simulations. Aqueous droplets containing a dispersion of ellipsoidal and spherical polystyrene particles were dried on superamphiphobic surfaces at different humidity values that led to varying evaporation rates. Supraparticles made from only ellipsoidal particles showed short-range lateral ordering at the supraparticle surface and random orientations in the interior regardless of the evaporation rate. Particle-based simulations corroborated the experimental observations in the evaporation-limited regime and showed an increase in the local nematic ordering as the diffusion-limited regime was reached. A thin shell of ellipsoids was observed at the surface when supraparticles were made from binary mixtures of ellipsoids and spheres. Image analysis revealed that the supraparticle porosity increased with an increasing aspect ratio of the ellipsoids.

Microplastic-induced inhibition of cell adhesion and toxicity evaluation using human dermal fibroblast-derived spheroids

Nanoplastics and microplastics (MPs) can significantly affect marine ecosystems and pose potential risks to human health. Although adverse effects stemming from direct exposure to MPs have been demonstrated at the cellular level in animal models, the potential toxicity of these materials in the human body remains uncertain. In this study, we investigated the three-dimensional (3D) behavior of dermal-derived cells exposed to MPs using artificially manufactured spherical primary polystyrene (PS) particles. To explore these effects, we used cellular spheroids as a 3D cell culture model, examined the size-dependent penetration of PS-MPs, and observed morphological alterations in the spheroids. Furthermore, we assessed changes in physiological activities, including reactive oxygen species, adenosine triphosphate, and lactate dehydrogenase, to elucidate the potential intra- and extracellular toxic reactions to PS-MPs. Additionally, our examination of cell–cell junctions and the extracellular matrix (ECM), along with analysis of the regulators involved in their decreased integrity, revealed negatively influenced changes in expression. This exposure study using spheroid models provides new insights into the potential toxicity of short-term exposure to MPs under conditions that closely resemble in vivo systems.

Preparation of Non-Spherical Janus Particles via an Orthogonal Dissolution Approach.

Post-synthesis modifications are valuable tools to alter functionalities and induce morphology changes in colloidal particles. Non-spherical polymer particles with Janus characteristics are prepared by combining seeded growth polymerization and selective dissolution. First, spherical polystyrene (PS) particles have been swollen with methyl methacrylate (MMA) with an activated swelling method. This is followed by polymerization that led to particles with two well-separated faces: one made of PS and the second of polymethyl methacrylate (PMMA). Subsequently, non-spherical particles are obtained by exposing the Janus colloids to various solvents. Using the two polymers' orthogonal solubility, solvents are identified to selectively dissolve only one face, leading to hemispherical PS or PMMA particles. It is further investigated how changing the composition of the PMMA face - by either co-polymerization with glycidyl methacrylate or by adding a cross-linker - affects the particles' morphology. The poly-methacrylate face can gain total or partial resistance towards the solvents, resulting in intriguing shapes, such as mushroom-like and Janus dimpled particles. The dissolution mechanisms are investigated via optical microscopy, where total or partial dissolutions can be directly observed. Lastly, prematurely quenching the dissolution of the particle's lobes with water can be used to control the Janus mushroom-like particle aspect ratio.

Continuous flow synthesis of plasmonic gold patches and nearly-complete nanoshells on polystyrene core particles

We describe the development of a T-mixer based continuous flow process for the coating of 86–500 nm diameter spherical polystyrene particles with thin gold patches by heterogeneous nucleation and growth. After establishing a suitable flow rate for good mixing and sufficiently uniform product morphology we systematically investigate the main reaction parameters. This reveals a considerable tunability of the patch morphology and, by virtue of the localized surface plasmon resonance of gold, the optical properties of the product dispersions. In order to further widen the range of nanostructures accessible by our process, a second T-mixer was added. This introduced new gold precursor, leading to further growth of the patches that were formed after the first mixer. By this approach, nearly-complete gold nanoshells could be produced in high yield on both small and large core particles, without the unwanted production of free-standing gold nanoparticles. Due to the pronounced optical properties of nearly-complete gold nanoshells on small core particles, we could estimate from electrodynamic simulations the equivalent shell thickness to be as low as 8.6 nm. This is significantly thinner than can be routinely achieved using the standard seeded growth approach to synthesise gold nanoshells. Our results are therefore highly promising for the gram-scale synthesis of plasmon resonant nanostructures with designed optical properties.

Shape-selective remobilization of microparticles in a mesh-based DEP filter at high throughput

In numerous of studies, dielectrophoresis (DEP) has proven that its high selectivity and versatility make it a promising separation technique in a variety of fields. So far, however, only a few processes in the bioanalytics have made it to commercial use. One of the main challenges is to achieve a technically relevant throughput while maintaining a high selectivity. We present a novel approach of a mesh-based DEP filter with ordered field disturbing structures that has a high potential for upscaling because low-cost and commercially available materials are used. In this filter, we firstly trap a mixture of particles and then selectively remobilize them via a frequency shift, which allows for multidimensional separation. Shape-selective separation is demonstrated using ellipsoidal and spherical polystyrene particles, first in established microchannels and subsequently in the mesh-based filter. Hence, particles were trapped at flow rates up to 120mLh−1 and then selectively remobilized according to their shape. These results pave the way for high-throughput multitarget separations in a single and scalable device.

Study of repellence on polymeric surfaces with two individually adjustable pore hierarchies

Highly repellent surfaces offer many interesting applications as oil-repellent textiles and self-cleaning coatings, making these surfaces highly sought-after. Engineering these repellent surfaces requires the combination of a low surface energy material with special surface geometries with multiple levels of hierarchy in roughness. Yet, the current approaches for the fabrication of these surfaces have many drawbacks (complex fabrication techniques, fragile nature of the surface features with low abrasion resistances) that preventing their wider application. Here, we present a study of a new double–hierarchical Fluoropor which allows creating a bulk-porous fluorinated polymer foam with two individually tunable pore hierarchies. We combined our previous structuring approach for the micro /nanoscale (addition of an adaptable porogen mixture to the monomer) with sacrificial templating utilizing spherical polystyrene particles to obtain a second micropore hierarchy, resulting in a novel double-hierarchical material. We found that a micro-/nanoporosity with a larger pore structure in combination with a higher volumetric loading of structuring particles was beneficial to increase the repellence. We found the highest repellence for double–hierarchical Fluoropor with a bulk–porosity with 259 nm median pore diameter structured with 50 vol% of 40 µm sized microspheres. These superhydrophobic surface showed high static contact angles for ethylene glycol of 164° with a roll–off angle of 13° and a static contact angle for n–hexadecane of 145°. The material was covalently coated onto technical substrates (glass, copper, steel) and demonstrated good self-clean abilities for inorganic as well for organic contaminants. Abrasion test with 1000 cycles showed the repellence was not affected and persisted.

Revisiting the preparation of cylindrical polystyrene particles by magnetic stirring

The cylindrical shape is one of the most common shapes in geometry. The preparation of cylindrical polystyrene (PS) particles by magnetic stirring has been previously reported (Angew. Chem. Int. Ed.2018, 57, 9936–9940) via two steps: spherical PS particles were synthesized by dispersion polymerization of styrene with polyvinylpyrrolidone (PVP) as the stabilizer, followed by stirring the spherical PS particles in a water medium in the presence of PVP. However, the effects of various parameters on the deformation were not fully investigated. Herein we report full details of the preparation of cylindrical PS particles by stirring at room temperature. The influence of PVP molecular weight in the polymerization process, and various stirring parameters such as the molecular weight of PVP for stirring, concentration of PVP for stirring, stirring time, stirring rate, size of stirrer and amount of the mixture for stirring on the morphology of the resulting particles was investigated systematically. Moreover, a larger glass vial and correspondingly a larger magnetic stirrer were used in this work, which could produce cylindrical polymer particles at a five-fold larger scale. However, the production of cylindrical polymer particles at a even (fifty-fold) larger scale was less successful and might lead to a substantial part of peanut-shaped particles. This work is expected to be useful for improved understanding of the formation of these cylindrical polymer particles.

Nonlinear charge regulation for the deposition of silica nanoparticles on polystyrene spherical surfaces

HypothesisWe describe the deposition behavior of monodispersed silica nanoparticles on polystyrene spherical particles by using modified pairwise DLVO (Derjaguin-Landau-Verwey-Overbeek) interaction force profiles at pH values between two and twelve. Our modified model contains a new nonlinear charge regulation parameter that considers redistribution of ions, which allows us to realistically express the electrical double layer (EDL) interaction forces. ExperimentsSilanol-terminated silica nanoparticles (7.6 ± 0.4 nm), l-lysine-covered silica nanoparticles (7.8 ± 0.4 nm), and polyallylamine hydrochloride-covered polystyrene (PAH/PS) particles (348 ± 1 nm) were synthesized. Then, each type of silica nanoparticle was deposited on the PAH/PS particles at a range of pH values. FindingsOur new regulation parameter describes the realistic redistribution of charges governed by pH, total salt concentration, ionic strength of solution, and separation distance of particles. We find that this regulation parameter can be roughly approximated from the absolute values of theoretically calculated surface charge density and potential distributions, as well as experimentally measured ζ-potentials. Morphological analysis using electron microscopy of the experimental systems shows that the modified pairwise DLVO interaction forces exceptionally describe the deposition behavior of the silica nanoparticles physically adsorbed on the PAH/PS particle substrates.

Reconfigurable label-free shape-sieving of submicron particles in paired chalcogenide waveguides.

Up-to-date particle sieving schemes face formidable challenges for sieving label-free submicron molecules with similar sizes and dielectric constants but diverse shapes. Herein, optical sorting of polystyrene particles with various shapes is illustrated in optofluidic nanophotonic paired waveguide (ONPW) composed of chalcogenide semiconductor Sb2Se3. The Sb2Se3-ONPW creates the coupling length (CL) between the neighboring hot spots that can be actively modulated via the transition of Sb2Se3 between amorphous (AM) and crystalline (CR) phases. Submicron particles interfere with the coupled hotspots, which can exert various optical torques on the particles according to their profiles. In the model system, spherical (diameter of 0.5 μm) and rod-shaped (diameter of 0.5 μm, length of 1.5 μm) polystyrene particles were employed to mimic two types of bacteria, namely, Staphylococcus aureus and rod-shaped Escherichia coli, respectively. For the AM state, the CL value is ∼7.0 μm, enabling the structure to trap the sphere stably in the hot spots. For the CR state, the CL value becomes ∼25 μm, leading to stable trapping of the rod-shaped particle. In this work, the working wavelength was fixed at 1.55 μm at which both AM- and CR-Sb2Se3 are transparent. Our scheme may offer a paradigm shift in shape-selective sieving of biomolecules and fulfill the requirements of the new-generation lab-on-chip techniques, where the integrated manipulation system must be much more multifunctional and flexible.

Electrical Propulsion and Cargo Transport of Microbowl Shaped Janus Particles.

Herein the effective electrical propulsion, cargo trapping, and transport capabilities of microbowl-shaped Janus particles (JPs) are demonstrated and evaluated. These active JPs are made by deposition of Au and Ti layers onto sacrificial spherical polystyrene particles, followed by oxidation of the Ti to TiO2 . In contrast to the commonly studied spherical JP, the dual broken symmetry of both geometrical and electrical properties of the microbowl renders a strong dependence of its mobility and cargo loading on the order of the layering of Au and TiO2 . Specifically, an opposite direction of motion is obtained for interchanged layers of Au and TiO2 , using only electrical propulsion as the sole mechanism of motion. The concave side of the microbowl exhibits a negative dielectrophoretic trap of large size wherein trapped cargo is protected from hydrodynamic shearing, leading to an enhanced cargo loading capacity compared to that obtained using common spherical JP. Such enhanced cargo capability of the microbowl along with the ease of engineering it by interchanging the order of the layers are very attractive for future in vitro biological and biomedical applications.

Latex agglutination analysis by novel ultrasound scattering techniques

The latex agglutination test is employed to visualize antigen–antibody reactions through the aggregation of antibody-coated particles in the presence of an antigen. In the present study, we developed an ultrasound scattering technique to detect latex agglutination in an optically turbid media. However, the ultrasonic technique had less sensitivity to the dilute particle suspension than the optical techniques because of its wavelength. Therefore, we applied a time-correlation approach to detect small amounts of these aggregates using a sophisticated noise correction algorithm in the frequency domain. The lowest concentration of avidin used to detect aggregations of the biotin-coated particle using the ultrasound scattering technique was found to be 0.625 μg/ml. Furthermore, since the density differences between the particle and liquid were larger for silica suspensions than for polystyrene (PS) suspensions, a larger signal was proposed to be expected from silica suspensions. Nevertheless, it was found that latex agglutinations with the PS particle were more sensitive than those with the silica particles. The dynamic ultrasound scattering analysis along the sedimentation direction also supported the presence of strongly scattered intensity components of the PS aggregates, which is proposed to be due to the resonance scattering from PS spherical particles. Therefore, this technique can be employed to enhance scattering signals from particles for application in the agglutination test using ultrasound.

Assembly of Colloidal Clusters Driven by the Polyhedral Shape of Metal-Organic Framework Particles.

Control of the assembly of colloidal particles into discrete or higher-dimensional architectures is important for the design of myriad materials, including plasmonic sensing systems and photonic crystals. Here, we report a new approach that uses the polyhedral shape of metal–organic-framework (MOF) particles to direct the assembly of colloidal clusters. This approach is based on controlling the attachment of a single spherical polystyrene particle on each face of a polyhedral particle via colloidal fusion synthesis, so that the polyhedral shape defines the final coordination number, which is equal to the number of faces, and geometry of the assembled colloidal cluster. As a proof of concept, we assembled six-coordinated (6-c) octahedral and 8-c cubic clusters using cubic ZIF-8 and octahedral UiO-66 core particles. Moreover, we extended this approach to synthesize a highly coordinated 12-c cuboctahedral cluster from a rhombic dodecahedral ZIF-8 particle. We anticipate that the synthesized colloidal clusters could be further evolved into spherical core–shell MOF@polystyrene particles under conditions that promote a higher fusion degree, thus expanding the methods available for the synthesis of MOF–polymer composites.

Visualization of Three-Dimensional Acoustic Streaming Flow Patterns around an Inclined Triangular Obstruction using Digital In-Line Holographic Micro-Particle Tracking Velocimetry

Acoustic Streaming is a flow phenomenon with many applications in the field of microfluidics, such as micro mixing[1, 2] and particle manipulation[3]. With the manufacturing techniques evolves, more complicated geometries can be designed for microfluidic device and 3-D acoustic streaming patterns may occurs. In this study, 3-D trajectories of particle induced by acoustic streaming around an inclined triangular obstruction in a microchannel were visualized by a volumetric tracking method using Digital Inline Holographic Microscopy (DIHM)[4-6]. The triangular obstruction has a tip angle of 20° and an inclined angle of 30°. The acoustic streaming is created under 12 kHz oscillation of a piezo plate driven by 20V voltage. Illuminated by a 450nm continuous laser, the magnified hologram of the motion of 1.79μm tracer particles was recorded by a low-cost 10X industrial microscope with a machine vision camera of 10 fps (frames per second). Using RayleighSommerfeld back-propagation method[7], particle locations was reconstructed frame by frame and 3-D tracking of individual particles was performed afterwards. The trajectories of each particle were reconstructed to reveal the vortical structure of the acoustic streaming flow. For the current system setup, the measurable range was estimated to be 550×685×840 μm3. The 3-D location reconstruction accuracy was verified with a calibration target and the location sensitivity was found to be linear throughout the measurable range. Reconstruction at different depth locations show that the dick-shaped calibration dots and the spherical polystyrene particles have different intensity profiles. The calibration dots show local minimum of intensity at the correct depth location, while polystyrene particles show local maximum of intensity instead. Resolved particle trajectories show that the acoustic streaming flows cause particles to move with 3-D spiral shaped motions near the side of the triangular obstruction, while particles away from the obstruction shows planar motions.

Frequency-responsive cooperativity of graphene oxide complexes under a low AC bulk electric field

Graphene oxide (GO) is a promising material for the construction of biological functional surfaces and corresponding biomedical applications. The physical properties of sheets of GO are determined by its conductivity, flexibility (being just a few atomic carbon layers thick), and hydrophilicity/hydrophobicity. In order to exploiting multitask surfaces, however, controlling reliable tunability of the complex formation with other macromolecules in aqueous environments is highly non-trivial due to the hydrophobic nature of GO. Thus, one effective way of complicated physical process of dealing with aqueous systems of GO is to perform the complex formation under in-situ external fields. In this paper, we report the response of GO-sheets, complexed with spherical colloidal polystyrene particles, nafion, and long and thin DNA-viruses (fd), in alternating electric fields, probed by means of novel experimental methods of image-time correlation spectroscopy and small-angle dynamic light scattering. Here, the frequency-responsive reorientations of a GO-sheet are interpreted by random orientations of particles. As results, we have found that GO carries overall local reorientations with feedback oscillations, as well in the GO-complexes (of a colloidal sphere polymerized polystyrene (PPs) and nafion solution). However, such oscillations are absent, as overdamped Brownian motion, in the mixture of DNA-virus suspension (with GO-PPs). This indicates that Brownian fluctuations of GO can be effectively stabilized, and cooperated in the membrane-based, isotropic rod-mesh network of DNA-virus (fd) suspension. We hope then the results are useful to foster better designs of processing GO-sheets in the controls of accessible biological and biomedical applications.

Quantitative analysis of the three-dimensional trap stiffness of a dielectrophoretic corral trap.

Dielectrophoresis is a robust approach for the manipulation and separation of (bio)particles using microfluidic platforms. We developed a dielectrophoretic corral trap in a microfluidic device that utilizes negative dielectrophoresis to capture single spherical polystyrene particles. Circular-shaped micron-size traps were employed inside the device and the three-dimensional trap stiffness (restoring trapping force from equilibrium trapping location) was analyzed using 4.42μm particles and 1MHz of an alternating electric field from 6 VP-P to 10 VP-P . The trap stiffness increased exponentially in the x- and y-direction, and linearly in the z-direction. Image analysis of the trapped particle movements revealed that the trap stiffness is increased 608.4, 539.3, and 79.7% by increasing the voltage from 6 VP-P to 10 VP-P in the x-, y-, and z-direction, respectively. The trap stiffness calculated from a finite element simulation of the device confirmed the experimental results. This analysis provides important insights to predict the trapping location, strength of the trapping, and optimum geometry for single particle trapping and its applications such as single-molecule analysis and drug discovery.

Разделение нефтяной эмульсии динамической мембраной с поверхностным слоем из полистирола

In this paper, we studied the parameters of the process of separation of oil emulsion using a dynamic membrane of ultrafiltration PTFEg-PSd. A polymer membrane with a dynamic layer of polystyrene particles with sizes from 55 to 72 nm was obtained on a substrate of hydrophilic polytetrafluoroethylene (PTFE). The results of scanning electron microscopy showed the formation of a layer of spherical polystyrene particles on the membrane surface. The properties of a dynamic membrane were studied: porosity, moisture capacity, and wettability. After applying the polystyrene layer, an increase in the hydrophobicity of the surface layer of the membrane was established. For membrane separation, a 1% oil emulsion was prepared by dispersing the carbonaceous oil. The retention capacity of membranes for oil products from 1% oil emulsion was 96.4%, with a specific productivity of 113 dm3/m2·h which is not inferior to the performance of a commercial UPM-100 ultrafiltration membrane. Particle sizes of the dispersed phase in a 1% oil emulsion are distributed in the range from 229 to 1476 nm, after separation of the emulsion by a dynamic membrane, oil particles with sizes from 134 to 236 nm were detected in the filtrate, which indicates the removal of the bulk of the dispersed phase from the emulsion by ultrafiltration membranes.