Types Of Colloidal Particles Research Articles

Effects of Low-Frequency Randomly Polarized Electromagnetic Radiation, as Revealed upon Swelling of Polymer Membrane in Water with Different Isotopic Compositions.

Photoluminescence from the surface of Nafion polymer membrane upon swelling in water under irradiation by electromagnetic waves at a frequency of 100 MHz was studied. In these experiments, natural deionized (DI) water with a deuterium content of 157 ppm and deuterium-depleted water (DDW, deuterium content is 1 ppm) were explored. We have studied for the first time the effect of linearly and randomly polarized low-frequency electromagnetic radiation on the luminescence excitation. To obtain low-frequency electromagnetic radiation with random polarizations, anisotropic solid submicron-sized particles, which result in depolarization effects upon scattering of the initially linearly polarized radiation, were used. We compared two types of colloidal particles: spherically symmetric (isotropic) and elongated (anisotropic). If the radiation is linearly polarized, the intensity of luminescence from the Nafion surface decreases exponentially as the polymer is soaked, and such a behavior is observed both in natural DI water and DDW. When spherically symmetric submicron-sized particles are added to a liquid sample, the luminescence intensity also decreases exponentially upon swelling in both natural DI water and DDW. At the same time, when anisotropic submicron-sized particles are added to DI water, random jumps in the luminescence intensity appear during swelling. At the same time, the exponential decrease in the luminescence intensity is retained upon swelling in DDW. A qualitative theoretical model for the occurrence of random jumps in the luminescence intensity is presented.

Unraveling the Strong Fluorescence Enhancement of HPBI Molecules by ZIF-8 Colloidal Suspensions via Adsorption Analysis.

Enhancing the fluorescence of organic dye by colloidal particles is one of the most promising routes to optimize fluorescence detection. However, in addition to metallic particles, which serve as the most frequently used particles and have been found to employ the plasmonic resonance to provide strong fluorescence enhancement, neither new types of colloidal particles nor new fluorescence mechanisms have been intensively explored in recent years. In this work, strongly enhanced fluorescence was observed when 2-(2-hydroxyphenyl)-1H-benzimidazole (HPBI) molecules were simply mixed with zeolitic imidazolate framework-8 (ZIF-8) colloidal suspensions. Moreover, the enhancement factor ΔI = IHPBI+ZIF-8/IHPBI does not increase accordingly with the increasing amount of HPBI. To find out how the strong fluorescence was triggered and affected by the amount of HPBI, multiple techniques were applied to analyze the adsorption behavior. By combining analytical ultracentrifugation with first-principles calculations, we proposed that HPBI molecules were adsorbed onto the surface of ZIF-8 particles coordinatively and electrostatically, depending on the concentration of HPBI molecules. The coordinative adsorption would result in a new kind of fluorescence emitter. The new fluorescence emitters tend to distribute on the outer surface of ZIF-8 particles periodically. The distance between each fluorescence emitter is fixed and much smaller than the wavelength of the excitation light. Thus, it can be concluded that collective spontaneous emission might be triggered.

CO2-Switchable colloids.

The development and design of CO2-switchable colloidal particles is described. A presentation of the principles of CO2 switching, especially as they apply to colloids, is followed by recent progress in the preparation of several types of colloidal particles (polymer nanoparticles, metal-organic frameworks (MOFs), quantum dots, graphene, cellulose nanocrystals, carbon nanotubes) for various applications (Pickering stabilizers, catalysts, latexes), and our perspective on future opportunities.

Dynamic density functional theory for drying colloidal suspensions: Comparison of hard-sphere free-energy functionals.

Dynamic density functional theory (DDFT) is a promising approach for predicting the structural evolution of a drying suspension containing one or more types of colloidal particles. The assumed free-energy functional is a key component of DDFT that dictates the thermodynamics of the model and, in turn, the density flux due to a concentration gradient. In this work, we compare several commonly used free-energy functionals for drying hard-sphere suspensions, including local-density approximations based on the ideal-gas, virial, and Boublík-Mansoori-Carnahan-Starling-Leland (BMCSL) equations of state as well as a weighted-density approximation based on fundamental measure theory (FMT). To determine the accuracy of each functional, we model one- and two-component hard-sphere suspensions in a drying film with varied initial heights and compositions, and we compare the DDFT-predicted volume fraction profiles to particle-based Brownian dynamics (BD) simulations. FMT accurately predicts the structure of the one-component suspensions even at high concentrations and when significant density gradients develop, but the virial and BMCSL equations of state provide reasonable approximations for smaller concentrations at a reduced computational cost. In the two-component suspensions, FMT and BMCSL are similar to each other but modestly overpredict the extent of stratification by size compared to BD simulations. This work provides helpful guidance for selecting thermodynamic models for soft materials in nonequilibrium processes, such as solvent drying, solvent freezing, and sedimentation.

Ultrafast and Irreversibly Thermochromic SiO2 -PC/PEG Double Layer for Green Thermal Printing.

Traditional thermochromic photonic crystal (PC) usually has a slow and reversible thermal response, which limits its application in thermal printing. Here, the authors develop a thermochromic "SiO2 -PC/PEG" double layer structure with a responding time of milliseconds for fast thermal printing. Controlled by the print-head, the polyethylene glycol (PEG) melts, infiltrates, and solidifies within the interparticle voids, which instantly and irreversibly changes the refractive index and produces the PC pattern. Multicolor printing can be realized by tuning the size and type of colloidal particles. Resolution as high as 300 DPI is achieved to print the high-resolution patterns and then the grayscale patterns based on the control of pixel densities. Different from fiber thermal paper, the "SiO2 -PC/PEG" film has no toxic bisphenol A and possesses superior light stability for keeping the images longer. It is fully compatible with the commercial printer, which provides a mature solution for fast and convenient preparation of PC patterns.

Pickering Emulsions Simultaneously Stabilized by Starch Nanocrystals and Zein Nanoparticles: Fabrication, Characterization, and Application.

Using two types of colloidal particles having natural origins to synergistically stabilize Pickering emulsions is essential for food, cosmetics, and pharmaceutics, especially when neither particle can stabilize the Pickering emulsions alone. The use of two natural stabilizers avoids the complicated surface treatments of particles and the introduction of poisonous or harmful chemicals. In this work, we report an all-natural Pickering emulsion stabilized synergistically by starch nanocrystals and zein protein nanoparticles. Our result shows that the electrostatic interaction between the two types of particles greatly affects their assembled structure at the oil/water interface, which is closely related to the emulsion stability. Specifically, particle bilayers could form with oppositely charged particles at the interface to endow the emulsion with improved stability. As a demonstration, the resultant Pickering emulsions effectively carry β-carotene and have high stability against high temperatures and ultraviolet radiation. This type of all-natural Pickering emulsion is a promising tool to protect and deliver liposoluble bioactive components.

The effect of morphology and particle-wall interaction on colloidal near-wall dynamics.

We investigated the near-wall Brownian dynamics of different types of colloidal particles with a typical size in the 100 nm range using evanescent wave dynamic light scattering (EWDLS). In detail we studied dilute suspensions of silica spheres and shells with a smooth surface and silica particles with controlled surface roughness. While the near wall dynamics of the particle with a smooth surface differ only slightly from the theoretical prediction for hard sphere colloids, the rough particles diffuse significantly slower. We analysed the experimental data by comparison with model calculations and suggest that the deviating dynamics of the rough particles are not due to increased hydrodynamic interaction with the wall. Rather, the particle roughness significantly changes their DLVO interaction with the wall, which in turn affects their diffusion.

Controllable synthesis of patchy particles with tunable geometry and orthogonal chemistry

HypothesisSelf-assembly using anisotropic colloidal building blocks may lead to superstructures similar to those found in molecular systems yet can have unique optical, electronic, and structural properties. To widen the spectrum of achievable superstructures and related properties, significant effort was devoted to the synthesis of new types of colloidal particles. Despite these efforts, the preparation of anisotropic colloids carrying chemically orthogonal anchor groups on distinct surface patches remains an elusive challenge. ExperimentsWe report a simple yet effective method for synthesizing patchy particles via seed-mediated heterogeneous nucleation. Key to this procedure is the use of 3-(trimethoxysilyl)propyl methacrylate (TPM) or 3-(trimethoxysilyl)propyl acrylate (TMSPA), which can form patches on a variety of functional polymer seeds via a nucleation and growth mechanism. FindingsA family of anisotropic colloids with tunable numbers of patches and patch arrangements were prepared. By continuously feeding TPM or TMSPA the geometry of the colloids could be adjusted accurately. Furthermore, the patches could be reshaped by selectively polymerizing and/or solvating the individual colloidal compartments. Relying on the chemically distinct properties of the TPM/TMSPA and seed-derived domains, both types of patches could be functionalized independently. Combining detailed control over the patch chemistry and geometry opens new avenues for colloidal self-assembly.

Independent Blue and Red Light Triggered Narcissistic Self-Sorting Self-Assembly of Colloidal Particles.

The ability of living systems to self-sort different cells into separate assemblies and the ability to independently regulate different structures are one ingredient that gives rise to their spatiotemporal complexity. Here, this self-sorting behavior is replicated in a synthetic system with two types of colloidal particles; where each particle type independently self-assembles either under blue or red light into distinct clusters, known as narcissistic self-sorting. For this purpose, each particle type is functionalized either with the light-switchable protein VVDHigh or Cph1, which homodimerize under blue and red light, respectively. The response to different wavelengths of light and the high specificity of the protein interactions allows for the independent self-assembly of each particle type with blue or red light and narcissistic self-sorting. Moreover, as both of the photoswitchable protein interactions are reversible in the dark; also, the self-sorting is reversible and dynamic. Overall, the independent blue and red light controlled self-sorting in a synthetic system opens new possibilities to assemble adaptable, smart, and advanced materials similar to the complexity observed in tissues.

Fabrication of Ordered 2D Colloidal Crystals on Flat and Patterned Substrates by Spin Coating.

Spin coating is a simple and rapid method for fabricating ordered monolayer colloidal crystals on flat as well as patterned substrates. In this article, we show how a combination of factors, particularly concentration of the dispensed colloidal solution (Cn) and spin-coating speed, influences the ordering process. We have performed systematic experiments on different types of substrates with two types of colloidal particles (polystyrene and silica). We also show that even when perfect ordering is achieved at some locations, there might be a significant spatial variation in the deposit morphology over different areas of the sample. Our experiments reveal that higher Cn is required for obtaining perfect arrays, as the diameter of the colloids (dD) increases. Interestingly, a combination of higher Cn and rotational speed (expressed as revolutions per minute) is required to achieve perfect ordering on a topographically patterned substrate, as compared to that on a flat surface, because of loss of inertia of the particles during outward flow because of impact on the substrate features. Finally, we also identify the relation between the particle diameter and the height of the pattern features to achieve topography-mediated particle ordering.

Preparation of PLGA/Rose Bengal colloidal particles by double emulsion and layer-by-layer for breast cancer treatment

The use of colloidal particles (CPs) in the transport of drugs is developing rapidly thanks to its effectiveness and biosafety, especially in the treatment of various types of cancer. In this study Rose Bengal/PLGA CPs synthesized by double emulsion (W/O/W) and by electrostatic adsorption (layer-by-layer), were characterized and evaluated as potential breast cancer treatment. CPs were evaluated in terms of size, zeta potential, drug release kinetics and cell viability inhibition efficacy with the triple negative breast cancer cell line HCC70. The results showed that both types of CPs can be an excellent alternative to conventional cancer treatment by taking advantage of the enhanced permeation and retention (EPR) effect, manifested by solid tumors; however, the double emulsion CPs showed more suitable delivery times of up to 60% within two days, while layer-by-layer showed fast release of 50% in 90 min. Both types of CPs were capable to decrease cell viability, which encourage us to further testing in in vivo models to prove their efficacy and feasible use in the treatment of triple negative breast cancer.

Asymmetrical phase separation and gelation in binary mixtures of oppositely charged colloids.

Two types of colloidal particles, which are nearly the same in chemical composition but carry opposite surface charges, are mixed in water. Depending on the relative proportion of the oppositely charged particles, the process of aggregation leads to the formation of discrete clusters of various sizes in dilute dispersions, and to the development of particle gel networks in more concentrated systems. Due to the significant difference in the absolute values of surface charges (negative particle: -48 mV, positive particle: +24 mV), the phase separation and the gelation behaviors are asymmetric with respect to the mixing ratio. Mixtures with excess negative particles are more stable, while mixtures with excess positive particles are easily affected by phase separation. The hetero-aggregation triggered by the addition of microscopically large macro-ions is similar to what is often observed in a mono-component charged colloidal system, i.e., phase separation occurs through addition of small electrolyte ions. Within the concentration region investigated here, it is clear that the gel line is buried inside the phase separation region. Gelation occurs only when the number and size of the clusters are large and big enough to connect up into a space-spanning network. Our results indicate that, in this binary mixture of oppositely charged colloids, although the interaction between unlike species is attractive and that between like species is repulsive, the onset of gelation is in fact governed by the equilibrium phase separation, as in the case of purely attractive systems with short-range isotropic interaction.

Patchy micelles based on coassembly of block copolymer chains and block copolymer brushes on silica particles.

Patchy particles are a type of colloidal particles with one or more well-defined patches on the surfaces. The patchy particles with multiple compositions and functionalities have found wide applications from the fundamental studies to practical uses. In this research patchy micelles with thiol groups in the patches were prepared based on coassembly of free block copolymer chains and block copolymer brushes on silica particles. Thiol-terminated and cyanoisopropyl-capped polystyrene-block-poly(N-isopropylacrylamide) block copolymers (PS-b-PNIPAM-SH and PS-b-PNIPAM-CIP) were synthesized by reversible addition-fragmentation chain transfer polymerization and chemical modifications. Pyridyl disulfide-functionalized silica particles (SiO2-SS-Py) were prepared by four-step surface chemical reactions. PS-b-PNIPAM brushes on silica particles were prepared by thiol-disulfide exchange reaction between PS-b-PNIPAM-SH and SiO2-SS-Py. Surface micelles on silica particles were prepared by coassembly of PS-b-PNIPAM-CIP and block copolymer brushes. Upon cleavage of the surface micelles from silica particles, patchy micelles with thiol groups in the patches were obtained. Dynamic light scattering, transmission electron microscopy, and zeta-potential measurements demonstrate the preparation of patchy micelles. Gold nanoparticles can be anchored onto the patchy micelles through S-Au bonds, and asymmetric hybrid structures are formed. The thiol groups can be oxidized to disulfides, which results in directional assembly of the patchy micelles. The self-assembly behavior of the patchy micelles was studied experimentally and by computer simulation.

An investigation of water magnetization and its influence on some concrete specificities like fluidity and compressive strength

In this paper, effects of magnetic water on different properties of cement paste including fluidity, compressive strength, time of setting and etc, has been studied in concrete laboratory of Sahand University of Technology. For production of magnetic water, three devices including an AFM called device(made in UAE) ,a device marked AC(made in Germany) and finally a device was designed and made in Concrete Laboratory of Sahand University of Technology) have been used. The results show that, intensity and direction of magnetic field, velocity and time of water passing through magnetic device, and amount and type of Colloidal particles have direct effects on properties of magnetic water and using such a water in making cement paste, increases its fluidity and compressive strength up to 10%.

Electroacoustic study of dispersions containing two types of colloidal particles

The procedure of subtraction of electrolyte background electroacoustic signal, which is a standard feature in commercially available instruments, can be used to determine the ζ potentials of particular types of colloidal particles in multi-component dispersions. A preliminary study was carried out in a few two-component dispersions (dispersions containing two types of particles). One-component dispersion with the same mass fraction of component 1 and with the same solution composition as in the two-component dispersion of interest was prepared and the electroacoustic signal of that one-component dispersion was measured and saved as the “electrolyte background”. Then, the signal of the two-component dispersion was measured, and the saved background signal was subtracted from the signal of the two-component dispersion, thus producing the ζ potential of component 2. An analogous procedure was carried out to determine the ζ potential of component 1. Two opposite types of behavior were observed in various two-component dispersions. In certain dispersions (e.g., titania-alumina in dilute solutions of 1–1 electrolytes at various pH), the behavior of the both types particles was independent, that is, their ζ potentials at certain pH in one- and two-component dispersions were equal. In other dispersions (e.g., silica-alumina at neutral pH), the apparent behavior of particles in one- and two-component dispersions was completely different. The observed difference indicates an interaction between the particles, e.g., formation of aggregates containing both types of particles, adsorption of products of dissolution or formation of new phases.

The structure of Cu–Zr glasses using a colloidal proxy system

We present a novel experimental technique for studying the structure of metallic glasses (specifically Cu–Zr) through a proxy system of charged colloidal particles. A dense suspension of two types of colloidal particles that match the relative size ratio and approximate the attractive interaction of Cu and Zr atoms is created. Confocal microscopy images are analyzed to find the location of tens of thousands of particles at each composition studied. The particle locations are used to determine the packing fraction, partial radial distribution functions and partial coordination numbers of each component as well as the shape of clusters (central atom and first shell neighbors) that form. These results are compared to experimental and simulation literature on Cu–Zr systems, with good agreement found among all structural properties.

Application of flow field-flow fractionation (FlFFF) for size characterization of carbon black particles in ink

The size and distribution of the carbon black particles play important roles with respect to application in diverse areas. When used in inks, the smaller the particle size, the better the carbon black particles are dispersed, and thus the glossiness of ink increases. Asymmetrical flow field-flow fractionation (AsFlFFF) has shown to be applicable for size characterization of various types of colloidal particles. In the present study, AsFlFFF was employed to analyze the size of carbon black particles used in ink. Carbon black suspensions were prepared by dispersing carbon black powder in aqueous media containing various types of copolymeric dispersing agents of hydrophobic (styrene) and hydrophilic (acrylic or maleic acid) monomers. Experimental parameters of AsFlFFF including the type of the surfactant added to the carrier liquid, the channel and the cross flow rates, and the ionic strength were varied to find an optimum condition for analysis of the carbon black particles. It was found that the use of FL-70 as an additive to the carrier liquid resulted in the best elution profile among the tested surfactants (cationic, anionic, and nonionic surfactant). Although the mean sizes obtained by AsFlFFF and dynamic light scattering (DLS) were generally in good agreements, DLS failed to distinguish between the carbon black suspensions having different size distributions, whereas AsFlFFF was able to differentiate easily. Results indicated that the carbon black particles were dispersed better with the copolymeric dispersing agents having the hydrophobic content of 2 to 3 times higher than the hydrophilic molecules. At the styrene:acrylic acid of 1:1, the carbon black particles tend to have larger mean sizes and the size distributions tend to become broader, probably due to poor dispersion. Furthermore, it was observed that as the mean size of the carbon black particles decreased and the size distribution became narrower, the ink became clearer and glossier.

Nanoparticle-Promoted Thermal Stabilization of Room Temperature Cholesteric Blue Phase Mixtures

A blue phase (BP*) liquid crystal mixture was stabilised via doping with three different types of colloidal particles, smaller hexane thiolate-capped gold nanoparticles (NP1) with a size around 2.2 nm, larger oleylamine capped gold nanoparticles (NP2) with an average size of 13.2 nm, and manganese oxide nanoparticles (NP3) capped with oleic acid (10 nm in core diameter). We have experimentally studied the thermal stability of the blue phases by varying the core material of the nanoparticle additives (metal vs. metal oxide), the nature of the capping agents, and the core size. We have used polarized optical microscopy (POM) and the selective reflection of blue phases to identify the type of blue phase as well as the mesomorphic range. For the doped colloidal mixtures, POM and UV-vis spectrophotometry results confirmed the thermal stabilisation of the used BP* mixtures.

A General Method to Coat Colloidal Particles with Titania

We describe a general one-pot method for coating colloidal particles with amorphous titania. Various colloidal particles such as silica particles, large silver colloids, gibbsite platelets, and polystyrene spheres were successfully coated with a titania shell. Although there are several ways of coating different particles with titania in the literature, each of these methods is applicable to only one type of material. The present method is especially useful for giving the opportunity to cover many types of colloidal particles with titania and forgoes the use of a coupling agent or a precoating step. We can produce particles with a smooth titania layer of tunable thickness. The monodispersity, which improves during particle growth, and the high refractive index of titania make these particles potential candidates for photonic crystal applications. We also describe various ways of fabricating hollow titania shells, which have been intensively studied in the literature for their applications in electronics, catalysis, separations, and diagnostics. Note that our method initially produces amorphous shells on the particles, but these can be easily turned into crystalline titania by a calcination step. We also find that the growth of titania is a surface-reaction-limited process.

Evaporative Deposition of Bacteria and Microspheres on Mica from a Sessile Drop: The Use of Surface Conditioning in a Laboratory Atmosphere to Control Drop Spreading and Particle Deposition Patterns

AbstractEvaporative deposition from a sessile drop is an appealing way to deposit materials on a surface due to the simplicity of the technique. In this work we deposit aqueous solutions of two types of colloidal particles, namely bacteria and microspheres, on mica. We show that by controlling the extent of initial drop spreading through subtle changes in surface conditioning caused by exposure to the laboratory atmosphere in a laminar flow hood it is possible to systematically vary the particle deposition patterns. On freshly cleaved mica the contact angle of water is < 5°. Drops of bacterial and microsphere solutions deposited on freshly cleaved mica spread to cover a large surface area. Drying occurs through pinning and depinning events leaving a series of colloidal particle rings. We found in our laboratory that the contact angle of water on mica exposed to a constant flow of filtered laboratory air in a laminar flow hood gradually increases with time. For drops of both bacterial and microsphere solutions there is a corresponding decrease in the extent of drop spreading with increasing exposure of the mica surface to laboratory air. This results in a profound change in the colloidal particle deposition pattern. Short exposures of minutes to hours are enough to decrease spreading and affect the resulting deposition pattern. For our longest mica surface exposure times (months to 1 year) the contact angle of water reaches values near 20°. Spreading of the bacterial and microsphere drops is substantially decreased. A portion of the colloidal particles are deposited in an outer deposition ring which marks the extent of drop spreading and the remainder of the particles are deposited in the drop interior as a honeycomb or cellular film. The fraction of the drop residue covered with the cellular film increases with particle concentration as well as the length of time the mica is exposed to the laboratory atmosphere. This work shows that evaporative deposition on mica is very sensitive to surface conditioning through atmospheric exposure and also suggests that particle deposition patterns can be tuned by small changes in drop spreading.