Nanosized titanium dioxide reduces copper toxicity--the role of organic material and the crystalline phase.

Titanium dioxide nanoparticles (nTiO2) are expected to interact with natural substances and other chemicals in the environment, however little is known about their combined effects. Therefore, this study assessed the toxicity of copper (Cu) in combination with varying crystalline phases (anatase, rutile, and the mixture) of nTiO2 and differing organic materials on Daphnia magna. The nanoparticles reduced the Cu-toxicity depending on the product (0.3- to 2-fold higher 48-h EC50). This decrease in toxicity coincided with a lowered Cu-concentration in the water column, which was driven by the adsorption of Cu to nTiO2-depending on available surface area and structure-and their subsequent sedimentation. In the presence of organic material and nTiO2, the Cu-toxicity was further reduced (up to 7-fold higher 48-h EC50). This observation can be explained by a reduced Cu-bioavailability as a result of complexation and adsorption by the organic material and nTiO2, respectively. Thus, the crystalline phase composition, which is determining the surface area and structure of nTiO2, seems to be of major importance for the toxicity reduction of heavy metals, while the influence of the organic materials was mainly driven by the quantity and quality of humic substances.

Preparation of Self-Assembled Nanoparticle-Polymer Hybrids from Modified Silica Nanoparticles and Polystyrene-Block-Polyacrylic Acid Vesicles via the Co-Precipitation Method.

Nanoparticle-polymer hybrids are becoming increasingly important because seemingly contrasting properties, such as mechanical stability and high elasticity, can be combined into one material. In particular, hybrids made of self-assembled polymers are of growing interest since they exhibit high structural precision and diversity and the subsequent reorganization of the nanoparticles is possible. In this work, we show, for the first time, how hybrids of silica nanoparticles and self-assembled vesicles of polystyrene-block-polyacrylic acid can be prepared using the simple and inexpensive method of co-precipitation, highlighting in particular the challenges of using silica instead of other previously well-researched materials, such as gold. The aim was to investigate the influence of the type of modification and the particle size of the silica nanoparticles on the encapsulation and structure of the polymer vesicles. For this purpose, we first needed to adjust the surface properties of the nanoparticles, which we achieved with a two-step modification procedure using APTES and carboxylic acids of different chain lengths. We found that silica nanoparticles modified only with APTES could be successfully encapsulated, while those modified with APTES and decanoic acid resulted in vesicle agglomeration and poor encapsulation due to their strong hydrophobicity. In contrast, no negative effects were observed when different particle sizes (20 nm and 45 nm) were examined.

The Effect of Particle Shape on the Compaction of Realistic Non-Spherical Particles-A Multi-Contact DEM Study.

The purpose of this study was to investigate the deformation behavior of non-spherical particles during high-load compaction using the multi-contact discrete element method (MC-DEM). To account for non-spherical particles, the bonded multi-sphere method (BMS), which incorporates intragranular bonds between particles, and the conventional multi-sphere (CMS), where overlaps between particles are allowed to form a rigid body, were used. Several test cases were performed to justify the conclusions of this study. The bonded multi-sphere method was first employed to study the compression of a single rubber sphere. This method's ability to naturally handle large elastic deformations is demonstrated by its agreement with experimental data. This result was validated further through detailed finite element simulations (multiple particle finite element method (MPFEM)). Furthermore, the conventional multi-sphere (CMS) approach, in which overlaps between particles are allowed to form a rigid body, was used for the same objective, and revealed the limitations of this method in successfully capturing the compression behavior of a single rubber sphere. Finally, the uniaxial compaction of a microcrystalline cellulose-grade material, Avicel® PH 200 (FMC BioPolymer, Philadelphia, PA, USA), subjected to high confining conditions was studied using the BMS method. A series of simulation results was obtained with realistic non-spherical particles and compared with the experimental data. For a system composed of non-spherical particles, the multi-contact DEM showed very good agreement with experimental data.

Influence of Process Parameters on the Kinetics of the Micelle-to-Vesicle Transition and Ripening of Polystyrene-Block-Polyacrylic Acid.

Due to their ability to self-assemble into complex structures, block copolymers are of great interest for use in a wide range of future applications, such as self-healing materials. Therefore, it is important to understand the mechanisms of their structure formation. In particular, the process engineering of the formation and transition of the polymer structures is required for ensuring reproducibility and scalability, but this has received little attention in the literature. In this article, the influence of the addition rate of the selective solvent on the homogeneity of self-assembled vesicles of polystyrene-block-polyacrylic acid is demonstrated, as well as the influence of the reaction time and the mixing intensity on the morphology of the polymer structures. For example, it was demonstrated that the higher the mixing intensity, the faster the transition from micelle to vesicle. The experimental results are further supported by CFD simulations, which visually and graphically show an increase in shear rate and narrower shear rate distributions at higher stirring rates. Furthermore, it was demonstrated that the vesicle size is not only kinetically determined, since flow forces above a critical size lead to the deformation and fission of the vesicles.

Quantification and modeling of macroparticle-induced mechanical stress for varying shake flask cultivation conditions.

In biotechnological processes, filamentous microorganisms are known for their broad product spectrum and complex cellular morphology. Product formation and cellular morphology are often closely linked, requiring a well-defined level of mechanical stress to achieve high product concentrations. Macroparticles were added to shake flask cultures of the filamentous actinomycete Lentzea aerocolonigenes to find these optimal cultivation conditions. However, there is currently no model concept for the dependence of the strength and frequency of the bead-induced stress on the process parameters. Therefore, shake flask simulations were performed for combinations of bead size, bead concentration, bead density and shaking frequency. Contact analysis showed that the highest shear stresses were caused by bead-bottom contacts. Based on this, a newly generated characteristic parameter, the stress area ratio (SAR), was defined, which relates the bead wall shear and normal stresses to the total shear area. Comparison of the SAR with previous cultivation results revealed an optimum pattern for product concentration and mean product-to-biomass related yield coefficient. Thus, this model is a suitable tool for future optimization, comparison and scaling up of shear-sensitive microorganism cultivation. Finally, the simulation results were validated using high-speed recordings of the bead motion on the bottom of the shake flask.

Colloidal aggregates tested via nanoindentation and quasi-simultaneous 3D imaging.

The mechanical properties of aggregated colloids depend on the mutual interplay of inter-particle potentials, contact forces, aggregate structure and material properties of the bare particles. Owing to this variety of influences, experimental results from macroscopic mechanical testings were mostly compared to time-consuming, microscopic simulations rather than to analytical theories. The aim of the present paper was to relate both macroscopic and microscopic mechanical data with each other and simple analytical models. We investigated dense amorphous aggregates made from monodisperse poly-methyl methacrylate (PMMA) particles (diameter: 1.6 µm via nanoindentation in combination with confocal microscopy. The resulting macroscopic information was complemented by the three-dimensional aggregate structure as well as the microscopic strain field and strain tensor. The measured strain field and tensor were in reasonable agreement with the predictions from analytical continuum theories. Consequently, the measured force-depth curves could be analyzed within a theoretical framework that had been frequently used for nanoindentation of atomic matter such as metals, ceramics and polymers. The extracted values for hardness and effective Young's modulus represented average values characteristic of the aggregate. On the basis of of these parameters we discuss the influence of the strength of particle bonds by introducing polystyrene (PS) between the particles.

Geotechnical and Shear Behavior of Novel Lunar Regolith Simulants TUBS-M, TUBS-T, and TUBS-I.

The return to the Moon is an important short-term goal of NASA and other international space agencies. To minimize mission risks, technologies, such as rovers or regolith processing systems, must be developed and tested on Earth using lunar regolith simulants that closely resemble the properties of real lunar soil. So far, no singular lunar simulant can cover the multitude of use cases that lunar regolith involves, and most available materials are poorly characterized. To overcome this major gap, a unique modular system for flexible adaptable novel lunar regolith simulants was developed and chemically characterized in earlier works. To supplement this, the present study provides comprehensive investigations regarding geotechnical properties of the three base regolith simulant systems: TUBS-M, TUBS-T, and TUBS-I. To evaluate the engineering and flow properties of these heterogeneous materials under various conditions, shear tests, particle size analyses, scanning electron microscope observations, and density investigations were conducted. It was shown that small grains <25 µm (lunar dust) are highly compressive and cohesive even at low external stress. They are particularly important as a large amount of fine dust is present in lunar regolith and simulants (x50 = 76.7 to 96.0 µm). Further, ring shear and densification tests revealed correlations with damage mechanisms caused by local stress peaks for grains in the mm range. In addition, an explanation for the occurrence of considerable differences in the literature-based data for particle sizes was established by comparing various measurement procedures. The present study shows detailed geotechnical investigations of novel lunar regolith simulants, which can be used for the development of equipment for future lunar exploration missions and in situ resource utilization under realistic conditions. The results also provide evidence about possible correlations and causes of known soil-induced mission risks that so far have mostly been described phenomenologically.

Polymer Membranes for All-Vanadium Redox Flow Batteries: A Review.

Redox flow batteries such as the all-vanadium redox flow battery (VRFB) are a technical solution for storing fluctuating renewable energies on a large scale. The optimization of cells regarding performance, cycle stability as well as cost reduction are the main areas of research which aim to enable more environmentally friendly energy conversion, especially for stationary applications. As a critical component of the electrochemical cell, the membrane influences battery performance, cycle stability, initial investment and maintenance costs. This review provides an overview about flow-battery targeted membranes in the past years (1995-2020). More than 200 membrane samples are sorted into fluoro-carbons, hydro-carbons or N-heterocycles according to the basic polymer used. Furthermore, the common description in membrane technology regarding the membrane structure is applied, whereby the samples are categorized as dense homogeneous, dense heterogeneous, symmetrical or asymmetrically porous. Moreover, these properties as well as the efficiencies achieved from VRFB cycling tests are discussed, e.g., membrane samples of fluoro-carbons, hydro-carbons and N-heterocycles as a function of current density. Membrane properties taken into consideration include membrane thickness, ion-exchange capacity, water uptake and vanadium-ion diffusion. The data on cycle stability and costs of commercial membranes, as well as membrane developments, are compared. Overall, this investigation shows that dense anion-exchange membranes (AEM) and N-heterocycle-based membranes, especially poly(benzimidazole) (PBI) membranes, are suitable for VRFB requiring low self-discharge. Symmetric and asymmetric porous membranes, as well as cation-exchange membranes (CEM) enable VRFB operation at high current densities. Amphoteric ion-exchange membranes (AIEM) and dense heterogeneous CEM are the choice for operation mode with the highest energy efficiency.

Viscosity Model for Nanoparticulate Suspensions Based on Surface Interactions.

In this paper, a widely mechanistic model was developed to depict the rheological behaviour of nanoparticulate suspensions with solids contents up to 20 wt.%, based on the increase in shear stress caused by surface interaction forces among particles. The rheological behaviour is connected to drag forces arising from an altered particle movement with respect to the surrounding fluid. In order to represent this relationship and to model the viscosity, a hybrid modelling approach was followed, in which mechanistic relationships were paired with heuristic expressions. A genetic algorithm was utilized during model development, by enabling the algorithm to choose among several hard-to-assess model options. By the combination of the newly developed model with existing models for the various physical phenomena affecting viscosity, it can be applied to model the viscosity over a broad range of solids contents, shear rates, temperatures and particle sizes. Due to its mechanistic nature, the model even allows an extrapolation beyond the limits of the data points used for calibration, allowing a prediction of the viscosity in this area. Only two parameters are required for this purpose. Experimental data of an epoxy resin filled with boehmite nanoparticles were used for calibration and comparison with modelled values.

Modeling of High-Density Compaction of Pharmaceutical Tablets Using Multi-Contact Discrete Element Method.

The purpose of this work is to simulate the powder compaction of pharmaceutical materials at the microscopic scale in order to better understand the interplay of mechanical forces between particles, and to predict their compression profiles by controlling the microstructure. For this task, the new framework of multi-contact discrete element method (MC-DEM) was applied. In contrast to the conventional discrete element method (DEM), MC-DEM interactions between multiple contacts on the same particle are now explicitly taken into account. A new adhesive elastic-plastic multi-contact model invoking neighboring contact interaction was introduced and implemented. The uniaxial compaction of two microcrystalline cellulose grades (Avicel® PH 200 (FMC BioPolymer, Philadelphia, PA, USA) and Pharmacel® 102 (DFE Pharma, Nörten-Hardenberg, Germany) subjected to high confining conditions was studied. The objectives of these simulations were: (1) to investigate the micromechanical behavior; (2) to predict the macroscopic behavior; and (3) to develop a methodology for the calibration of the model parameters needed for the MC-DEM simulations. A two-stage calibration strategy was followed: first, the model parameters were directly measured at the micro-scale (particle level) and second, a meso-scale calibration was established between MC-DEM parameters and compression profiles of the pharmaceutical powders. The new MC-DEM framework could capture the main compressibility characteristics of pharmaceutical materials and could successfully provide predictions on compression profiles at high relative densities.

Numerical Simulation of the Rheological Behavior of Nanoparticulate Suspensions.

Nanoparticles significantly alter the rheological properties of a polymer or monomeric resin with major effect on the further processing of the materials. In this matter, especially the influence of particle material and disperse properties on the viscosity is not yet understood fully, but can only be modelled to some extent empirically after extensive experimental effort. In this paper, a numerical study on an uncured monomeric epoxy resin, which is filled with boehmite nanoparticles, is presented to elucidate the working principles, which govern the rheological behavior of nanoparticulate suspensions and to simulate the suspension viscosity based on assessable material and system properties. To account for the effect of particle surface forces and hydrodynamic interactions on the rheological behavior, a resolved CFD is coupled with DEM. It can be shown that the particle interactions caused by surface forces induce velocity differences between the particles and their surrounding fluid, which result in increased drag forces and cause the additional energy dissipation during shearing. The paper points out the limits of the used simulation method and presents a correction technique with respect to the Péclet number, which broadens the range of applicability. Valuable information is gained for a future mechanistic modelling of nanoparticulate suspension viscosity by elucidating the interdependency between surface forces, shear rate and resulting drag forces on the particles.

Effect of Different Shear Rates on Particle Microstructure of Cementitious Materials in a Wide Gap Vane-in-cup Rheometer.

Rheological properties of cementitious suspensions are affected not only by their mixture composition but also by process-related factors such as shear history. To enable a model-based description, investigations were carried out on the effect of shear history (shear rate variation over time) on the cement paste agglomeration state. Therefore, a Focused Beam Reflectance Measurement (FBRM) system and a wide gap rheometer were coupled to study the relation between shear history and in-situ chord length distribution simultaneously, indicating particle agglomeration. Hence, the effect of average shear rates (resulting from the applied shear profile), as well as shear rate distribution within the gap (local shear rates) on the particle agglomeration state have been investigated. The rheological properties of cement paste were evaluated with the Reiner-Riwlin approach. Furthermore, the agglomeration state of the particles was compared for different average shear rates and local shear rates at various positions of the FBRM probe. The results show that the median chord length increases in all positions when the average shear rate is decreased, indicating increasing particle agglomeration. Moreover, due to variable local shear rates at different FBRM probe positions, different agglomeration states are observed, resulting from two factors, shear rate dependent particle agglomeration and shear-induced particle migration.

A blessing in disguise? Natural organic matter reduces the UV light-induced toxicity of nanoparticulate titanium dioxide.

Besides their economic value, engineered inorganic nanoparticles (EINPs) may pose a risk for the integrity of ecosystems. Among EINPs, titanium dioxide (nTiO2) is frequently used and released into surface waters in the µg range. There, nTiO2 interacts with environmental factors, influencing its potential to cause adverse effects on aquatic life. Although factors like ultra violet (UV) light and natural organic matter (NOM) are considered as ubiquitous, their joint impact on nTiO2-induced toxicity is poorly understood. This study addressed the acute toxicity of nTiO2 (P25; 0.00-64.00 mg/L; ~60 nm) at ambient UV light (0.00-5.20 W UVA/m2) and NOM levels (seaweed extract; 0.00-4.00 mg TOC/L), using the immobility of Daphnia magna as response variable. Confirming previous studies, effects caused by nTiO2 were elevated with increasing UV radiation (up to ~280 fold) and mitigated by higher NOM levels (up to ~12 fold), possibly due to reduced reactive oxygen species (ROS; measured as •OH radicals) formation at lower UV intensities. However, contradicting to former studies, nTiO2-mediated ROS formation was not proportional to increasing NOM levels: lower concentrations (0.04-0.40 mg TOC/L) slightly diminished, whereas a higher concentration (4.00 mg TOC/L) promoted the ROS quantity, irrespective of UV intensity. Measured ROS levels do not fully explain the observed nTiO2-induced toxicity, whereas increasing acetylcholinesterase and glutathione-S-transferase activities in daphnids (in presence of 8.00 mg/L nTiO2 and elevated UV intensity) point towards neurotoxic and oxidative stress as a driver for the observed effects. Hence, despite higher •OH levels in the treatments where 4.00 mg TOC/L were present, NOM was still capable of reducing nTiO2-induced stress and ultimately adverse effects in aquatic life.

Influence of surface modification on structure formation and micromechanical properties of spray-dried silica aggregates.

Spray drying processes were utilized for the production of hierarchical materials with defined structures. The structure formation during the spray drying process and the micromechanical properties of the obtained aggregates depend on the particle-particle interactions, the primary particle size and morphology as well as the process parameters of the spray drying process. Hence, the effect of different primary particle systems prepared as stable dispersions with various surface modifications were investigated on the colloidal structure formation and the micromechanical properties of silica particles as model aggregates and compared to theoretical considerations. The obtained results show that the structure formation of aggregates during the spray drying process for stable suspensions is almost independent on the functional groups present at the particle surface. Further, the mechanical properties of these aggregates differ considerably with the content of the bound ligand. This allows the defined adjustment of the aggregate properties, such as the strength and surface properties, as well as the formation of defined hierarchical aggregate structures.

Hierarchical Structure Formation of Nanoparticulate Spray-Dried Composite Aggregates.

The design of hierarchically structured nano- and microparticles of different sizes, porosities, surface areas, compositions, and internal structures from nanoparticle building blocks is important for new or enhanced application properties of high-quality products in a variety of industries. Spray-drying processes are well-suited for the design of hierarchical structures of multicomponent products. This structure design using various nanoparticles as building blocks is one of the most important challenges for the future to create products with optimized or completely new properties. Furthermore, the transfer of designed nanomaterials to large-scale products with favorable handling and processing can be achieved. The resultant aggregate structure depends on the utilized nanoparticle building blocks as well as on a large number of process and formulation parameters. In this study, structure formation and segregation phenomena during the spray drying process were investigated to enable the synthesis of tailor-made nanostructures with defined properties. Moreover, a theoretical model of this segregation and structure formation in nanosuspensions is presented using a discrete element method simulation.

Influence of electrostatic particle interactions on the properties of particulate coatings of titanium dioxide.

HYPOTHESIS: Particulate coatings are used in a wide range of technical applications. The application affecting properties of these coatings depend strongly on the structure formation along the production process. Thus, primary and secondary particle size, size distribution, particle morphology as well as the particle-particle and particle-fluid interactions of the used formulation affect the resulting coating properties. EXPERIMENTS: In this investigation titanium dioxide particles were dispersed in ethanol with a stirred media mill and stabilised electrostatically. Subsequently, the suspension was destabilised to reach specific pH* values and processed into coatings by dip coating. The influence of the pH* value of the suspension on the suspension's properties such as viscosity, agglomerate size and zeta potential and on its application properties such as coating thickness, micro-mechanical properties, abrasion resistance, gloss, roughness and adhesion was examined. FINDINGS: The electrostatic particle interactions show a significant influence on the structure formation as well as on the properties of nanoparticulate coatings. The coating properties are affected by the coating structures on micro-, meso- or macroscopic scale. Selective coating properties were related to the coating structure using the theoretical model of Rumpf. Besides other important process and formulation parameters, for the production of homogeneous, functional coatings with the desired properties a precise adjustment of the particle interactions is necessary.

Biological surface coating and molting inhibition as mechanisms of TiO2 nanoparticle toxicity in Daphnia magna.

The production and use of nanoparticles (NP) has steadily increased within the last decade; however, knowledge about risks of NP to human health and ecosystems is still scarce. Common knowledge concerning NP effects on freshwater organisms is largely limited to standard short-term (≤48 h) toxicity tests, which lack both NP fate characterization and an understanding of the mechanisms underlying toxicity. Employing slightly longer exposure times (72 to 96 h), we found that suspensions of nanosized (∼100 nm initial mean diameter) titanium dioxide (nTiO(2)) led to toxicity in Daphnia magna at nominal concentrations of 3.8 (72-h EC(50)) and 0.73 mg/L (96-h EC(50)). However, nTiO(2) disappeared quickly from the ISO-medium water phase, resulting in toxicity levels as low as 0.24 mg/L (96-h EC(50)) based on measured concentrations. Moreover, we showed that nTiO(2) (∼100 nm) is significantly more toxic than non-nanosized TiO(2) (∼200 nm) prepared from the same stock suspension. Most importantly, we hypothesized a mechanistic chain of events for nTiO(2) toxicity in D. magna that involves the coating of the organism surface with nTiO(2) combined with a molting disruption. Neonate D. magna (≤6 h) exposed to 2 mg/L nTiO(2) exhibited a "biological surface coating" that disappeared within 36 h, during which the first molting was successfully managed by 100% of the exposed organisms. Continued exposure up to 96 h led to a renewed formation of the surface coating and significantly reduced the molting rate to 10%, resulting in 90% mortality. Because coating of aquatic organisms by manmade NP might be ubiquitous in nature, this form of physical NP toxicity might result in widespread negative impacts on environmental health.