Experimental and mathematical investigation of cotransport of clay and microplastics in saturated porous media.

Microplastics in the subsurface cause groundwater contamination, thereby posing potential risks to human health and the ecosystem. Clay particles are ubiquitous in the subsurface and can interact and alter the transport behavior of microplastics. Hence, it is essential to understand the effect of clays on the transport behavior of microplastics to estimate the groundwater contamination potential. This study investigated the individual transport and cotransport of clay and microplastics under different pore-water velocities and sand types in saturated porous media through column experiments and mathematical modeling. Copresence of suspended microplastics retarded the transport of clay due to the preferential attachment of clay over microplastics on grain surfaces and the formation of clay-microplastic heteroaggregates which have a greater retention in sand than free clay and free microplastics. However, in contrast, cotransport with clay enhanced the transport of microplastics due to the lower affinity of microplastics than clay for deposition on grain surfaces and the lesser mass fraction of microplastics than clay in the heteroaggregates. The cotransport of clay and microplastics was successfully simulated using a two-way coupled model, which accounted for the retention of free clay and free microplastics in the sand, kinetics of clay-microplastics heteroaggregation, and heteroaggregate retention in the sand. The rates of heteroaggregation and heteroaggregate retention in sand decreased with increasing velocity and grain size, resulting in increased transport of clay and microplastics.

Effect of isomeric polysaccharides on heteroaggregation of nanoplastics in high ionic strength conditions: Synergies of morphology and molecular conformation.

Polysaccharides with various molecular structures and morphology may influence the aggregation kinetics of nanoplastics. This study used various characterization methods to elucidate the heteroaggregation mechanism of polystyrene nanoplastics (PSNPs) in the presence of polysaccharides (ionic strength (IS) 1-800 mM NaCl and 0.01-60 mM CaCl2). The results showed that under high IS, cellulose (CL) accelerated the heteroaggregation of PSNPs, and the aggregation rate of PSNPs increased by approximately 62.05 %, while amylose (AM) had little effect (10.38 %). Compared with AM (43.2 nm), the morphology of the CL (78.4 nm) gully had improved surface roughness, leading to its decisive role in the heteroaggregation of PSNPs. Quantum chemistry calculations indicated that van der Waals forces of PSNPs-CL systems (-217.28 kJ mol-1) were stronger than those of PSNPs-AM systems (-184.62 kJ mol-1) based on the subtle molecular conformation differences between CL and AM (opposite and same sides of OH groups in CL and AM, respectively). The morphology and molecular conformation of polysaccharides collaboratively controlled the heteroaggregation of PSNPs. Because the morphology of polysaccharides was based on their molecular conformation, the latter is the most critical factor. These findings provide new insights into the effects of PSNPs stability in the environment.

From Bulk to Nano: Formation, Features, and Functions of Nano-Black Carbon in Biogeochemical Processes.

Globally increasing wildfires and widespread applications of biochar have led to a growing amount of black carbon (BC) entering terrestrial ecosystems. The significance of BC in carbon sequestration, environmental remediation, and the agricultural industry has long been recognized. However, the formation, features, and environmental functions of nanosized BC, which is one of the most active fractions in the BC continuum during global climate change, are poorly understood. This review highlights the formation, surface reactivity (sorption, redox, and heteroaggregation), biotic, and abiotic transformations of nano-BC, and its major differences compared to other fractions of BC and engineered carbon nanomaterials. Potential applications of nano-BC including suspending agent, soil amendment, and nanofertilizer are elucidated based on its unique properties and functions. Future studies are suggested to develop more reliable detection techniques to provide multidimensional information on nano-BC in environmental samples, explore the critical role of nano-BC in promoting soil and planetary health from a one health perspective, and extend the multifield applications of nano-BC with a lower environmental footprint but higher efficiency.

Interfacial interactions of nanoscale zero-valent iron particles with clay minerals in the aquatic environments: Experimental and theoretical calculation study.

The environmental transport and fate of nanoscale zero-valent iron particles (nZVI) in soil and groundwater can be altered by their hetero-aggregation with clay mineral particles (CMP). This study examines the interactions between bare or carboxymethyl cellulose (CMC)-coated nZVI with typical CMP, specifically kaolinite and montmorillonite. Methods include co-settling experiments, aggregation kinetic studies, electron microscopy, Derjaguin-Landau-Verwey-Overbeek (DLVO) and extended DLVO (EDLVO) energy analysis, and density functional theory calculations, focusing on the pH dependency of these interactions. The EDLVO theory effectively described the interactions between nZVI and CMP in aquatic environments. Under acidic conditions (pH 3.5), the interfacial interaction between bare nZVI and kaolinite is regulated by van der Waals forces, while complexation, van der Waals forces, and electrostatic attraction govern the interaction of bare nZVI with montmorillonite, primarily depositing on the SiO face. In contrast, the positively charged AlO face and edge of CMP are the main deposition sites for CMC-coated nZVI through hydrogen bonding, van der Waals forces, and electrostatic attraction. At neutral (pH 6.5) and alkaline (pH 9.5) conditions, both bare and CMC-coated nZVI predominantly attach to the AlO face and edge, facilitated by complexation or hydrogen bonding, alongside van der Waals forces. The attachment of CMC-coated nZVI to CMP surfaces shows reversible aggregation or deposition due to the steric repulsion from the CMC coating. These findings hold significant implications for the environmental applications and risk of nZVI.

The impact of heteroaggregation between nZVI and SNPs on the co-transport of Cd(II) in saturated sand columns.

This study investigated the co-transport behaviors of nano zero-valent iron (nZVI) and Cd(II) in the presence of soil nanoparticles (SNPs) under various SNPs/nZVI mass ratios. It was illustrated that the mobility of colloidal Cd(II) was highly dependent on the nZVI-SNPs heteroaggregation behavior. In the case of 40 mg/L nZVI with SNPs/nZVI mass ratios > 1, the formation of stable SNPs-nZVI heteroaggregates with hydrodynamic diameters (Dh) < 500 nm facilitated the nZVI and colloidal Cd(II) transport at their effluent mass recoveries of 34.76-37.82 % and 9.81-17.17 %, respectively. However, in the case of 100 mg/L nZVI with SNPs/nZVI mass ratios of 0.4-2, the interception of nZVI-SNPs heteroaggregates with Dh > 1500 nm by quartz sands led to almost complete retention of nZVI and colloidal Cd(II) in the columns. Combined with analytical results of zeta potentials and XRD spectrum, it was revealed that the Cd(II) ions could accelerate nZVI corrosion. The positively charged Fe3O4 and γ-FeOOH on corroded nZVI surface could facilitate the heteroaggregation of nZVI-SNPs by the patch-charge attraction, which further reduced the environmental risk of colloidal Cd(II) transport. These findings revealed the important effects of heteroaggregation between nZVI and SNPs on the transport risk of Cd(II) in groundwater.

Both nanoplastic and iron mineral types determine their heteroaggregation: Aggregation kinetics and interface process.

Nanoplastics (NPs) inevitably interact with iron minerals (IMs) after being released into aquatic environments, changing their transport and fate. In this study, batch heteroaggregation kinetics of four types of NPs, i.e., polymethyl methacrylate (PMMA), polystyrene (PS-Bare), amino-polystyrene (PS-NH2), and carboxyl-polystyrene (PS-COOH), with two different IMs (hematite and magnetite) were conducted. We found that the heteroaggregation of NPs and IMs and the associated interfacial interaction mechanisms are both NPs-dependent and IMs-dependent. Specifically, the NPs had stronger heteroaggregation with hematite than magnetite; the heteroaggregation order of two IMs with NPs was PMMA > PS-NH2 > PS-Bare > PS-COOH. Moreover, hydrogen bond, complexation, hydrophobic, cation-π, and electrostatic interaction were involved in the interfacial reaction between NPs and hematite, and electrons were transferred from the NPs to the hematite, causing the reduction of Fe3+ into Fe2+. Furthermore, we first revealed that both pre-homoaggregation of NPs and IMs could affect their subsequent heteroaggregation, and the homoaggregates of IMs could be interrupted by PMMA or PS-COOH NPs introduction. Therefore, the emerging NPs pollution is likely to generate an ecological effect in terms of elemental cycles such as iron cycle. This work provides new insights into assessing the environmental transfer and ecological effects of NPs in aquatic environments.

The Identification of Structural Changes in the Lithium Hexamethyldisilazide-Toluene System via Ultrasonic Relaxation Spectroscopy and Theoretical Calculations.

Ultrasonic absorption measurements were carried out over a wide concentration and temperature range by means of a pulse technique to examine the structural mechanisms and the dynamical properties in lithium hexamethyldisilazide (LiHMDS)-toluene solutions. Acoustic spectra revealed two distinct Debye-type relaxational absorptions attributed to the formation of trimers from dimeric and monomer units and to the formation of aggregates between a LiHMDS dimer and one toluene molecule in low and high frequencies, respectively. The formation of aggregates was clarified by means of molecular docking and DFT methodologies. The aggregation number, the rate constants and the thermodynamic properties of these structural changes were determined by analyzing in detail the concentration-dependent relaxation parameters. The low-frequency relaxation mechanism dominates the acoustic spectra in the high LiHMDS mole fractions, while the high-frequency relaxation influences the spectra in the low LiHMDS mole fractions. In the intermediate mole fraction region (0.25 to 0.46), both relaxations prevail in the spectra. The adiabatic compressibility, the excess adiabatic compressibility and the theoretically estimated mean free length revealed a crossover in the 0.25 to 0.46 LiHMDS mole fractions that signified the transition from one structural mechanism related with the hetero-association of LiHMDS dimers with toluene molecules to the other structural mechanism assigned to the formation of LiHMDS trimers. The combined use of acoustic spectroscopy with theoretical calculations permitted us to disentangle the underlying structural mechanisms and evaluate the volume changes associated with each reaction. The results were compared with the corresponding theoretically predicted volume changes and discussed in the context of the concentration effect on intermolecular bonding.

Microplastics and Nanoplastics Impair the Biophysical Function of Pulmonary Surfactant by Forming Heteroaggregates at the Alveolar-Capillary Interface.

Microplastics (MPs) are ubiquitous environmental pollutants produced through the degradation of plastic products. Nanoplastics (NPs), commonly coexisting with MPs in the environment, are submicrometer debris incidentally produced from fragmentation of MPs. We studied the biophysical impacts of MPs/NPs derived from commonly used commercial plastic products on a natural pulmonary surfactant extracted from calf lung lavage. It was found that in comparison to MPs/NPs derived from lunch boxes made of polypropylene or from drinking water bottles made of poly(ethylene terephthalate), the MP/NP derived from foam packaging boxes made of polystyrene showed the highest adverse impact on the biophysical function of the pulmonary surfactant. Accordingly, intranasal exposure of MP/NP derived from the foam boxes also induced the most serious proinflammatory responses and lung injury in mice. Atomic force microscopy revealed that NP particles were adsorbed on the air-water surface and heteroaggregated with the pulmonary surfactant film. These results indicate that although the incidentally formed NPs only make up a small mass fraction, they likely play a predominant role in determining the nano-bio interactions and the lung toxicity of MPs/NPs by forming heteroaggregates at the alveolar-capillary interface. These findings may provide novel insights into understanding the health impact of MPs and NPs on the respiratory system.

A critical review on remediation of microplastics using microalgae from aqueous system.

Microplastics (MPs) are deemed to be a global concern due to their harmful negative effects on the aquatic environment and human beings. MPs have a significant impact on both fresh and marine water ecosystems. In many countries, there is concern about the deleterious consequences of MPs on human health due to the presence of MPs in aquatic life for higher intake of marine food (fish and shellfish). Exposure to MPs causes fish to suffer from growth retardation, neurotoxicity, and behavioural abnormalities and it affects human as well. It causes oxidative stress, neurotoxicity, cytotoxicity, and immune system disruption after being ingested to these contaminated fish in human body. Due to these reasons, it has become imperative to find ways to resolve this problem. This review paper represents a pioneering endeavor by consolidating comprehensive information on microplastic-polluted Indian riverine ecosystems and effective MPs removal methods into a single, cohesive document. It meticulously evaluates the principles, removal efficiency, benefits, and drawbacks of various techniques, aiming to identify the most optimal solution. Furthermore, this paper provides a comprehensive exploration of the interesting interactions between MPs and microalgae, delving into the intricate processes of hetero-aggregation. Additionally, it shines a spotlight on the latest advancements in understanding the efficacy of microalgae in removing MPs, showcasing recent breakthroughs in this field of research. Moreover, the work goes beyond conventional assessments by elucidating the characteristics of MPs and exploring diverse influencing parameters that impact MPs removal by microalgae and also addresses the potential future aspects. This thorough investigation uncovers important factors that could significantly contribute to the development of more efficient and sustainable remediation strategies.

Spray Flame Synthesis and Multiscale Characterization of Carbon Black-Silica Hetero-Aggregates.

The increasing demand for lithium-ion batteries requires constant improvements in the areas of production and recycling to reduce their environmental impact. In this context, this work presents a method for structuring carbon black aggregates by adding colloidal silica via a spray flame with the goal of opening up more choices for polymeric binders. The main focus of this research lies in the multiscale characterization of the aggregate properties via small-angle X-ray scattering, analytical disc centrifugation and electron microscopy. The results show successful formation of sinter-bridges between silica and carbon black leading to an increase in hydrodynamic aggregate diameter from 201 nm to up to 357 nm, with no significant changes in primary particle properties. However, segregation and coalescence of silica particles was identified for higher mass ratios of silica to carbon black, resulting in a reduction in the homogeneity of the hetero-aggregates. This effect was particularly evident for silica particles with larger diameters of 60 nm. Consequently, optimal conditions for hetero-aggregation were identified at mass ratios below 1 and particle sizes around 10 nm, at which homogenous distributions of silica within the carbon black structure were achieved. The results emphasise the general applicability of hetero-aggregation via spray flames with possible applications as battery materials.

Hybrid gold-silica nanoparticles for plasmonic applications: A comparison study of synthesis methods for increasing gold coverage.

The current work focuses on the synthesis of hybrid nanoparticles (NPs) made of a silica core (Si NPs) coated with discrete gold nanoparticles (Au NPs), which exhibit localized surface plasmon resonance (LSPR) properties. This plasmonic effect is directly related to the nanoparticles size and arrangement. In this paper, we explore a wide range of size for the silica cores (80, 150, 400, and 600 nm) and for the gold NPs (8, 10, and 30 nm). Some rational comparison between different functionalization techniques and different synthesis methods for the Au NPs are proposed, related to the optical properties and colloidal stability in time. An optimized, robust and reliable synthesis route is established, which improves the gold density and homogeneity. The performances of these hybrid nanoparticles are evaluated in order to be used in the shape of a dense layer for pollutant detection in gas or liquids, and find numerous applications as a cheap and new optical device.

Heteroaggregation effects on Pickering stabilization using oppositely charged cellulose nanocrystal and nanochitin.

Pickering emulsions are stabilized using complexes of cellulose nanocrystals (CNC) and nanochitin (NCh). The colloidal behavior and heteroaggregation in aqueous media are studied in relation to complex formation and net charge. The complexes are remarkably effective in stabilizing oil-in-water Pickering emulsions under conditions of slightly net positive or negative charges, as determined by the CNC/NCh mass ratio. Close to charge neutrality (CNC/NCh ~5), large heteroaggregates form, resulting in unstable emulsions. By contrast, under net cationic conditions, interfacial arrest of the complexes leads to non-deformable emulsion droplets with high stability (no creaming for 9 months). At given CNC/NCh concentrations, emulsions with up to 50% oil fraction are produced. This study shows how to control emulsion properties beyond consideration of the typical formulation variables, for instance, through adjusting CNC/NCh ratio or charge stoichiometry. We highlight the possibilities that are available for emulsion stabilization by using a combination of polysaccharide nanoparticles.

The heteroaggregation behavior of nanoplastics on goethite: Effects of surface functionalization and solution chemistry.

Nanoplastics have attracted extensive attention in recent years. However, little is known about the heteroaggregation behavior of nanoplastics on goethite (FeOOH), especially the contribution of surface functional groups. In this study, the heteroaggregation behavior between polystyrene nanoplastics (PSNPs) and FeOOH was systematically investigated under different reaction conditions. Moreover, the effect of different functional groups (-NH2, -COOH, and bare) of PSNPs and solution chemistry was evaluated. The results showed that PSNPs could heteroaggregate with FeOOH, and the heteroaggregation rate of PSNPs with surface functionalization was significantly faster. The removal of suspended PSNPs was enhanced with increasing NaCl or CaCl2 concentration. However, heteroaggregation was significantly inhibited with the increase of solution pH. The zeta potentials analysis, time-resolved dynamic light scattering (DLS) and heteroaggregation experiments suggested that the electrostatic force affected the heteroaggregation process significantly. Fourier transform infrared (FTIR) spectra proved that the adsorption affinity between PSNPs and FeOOH was stronger after surface functionalization, especially for CH, O-C=O, and -CH2- groups, indicating that chemical bonding also made a contribution during the heteroaggregation process. This work is expected to provide a theoretical basis for predicting the environmental behavior between PSNPs and FeOOH.

Impact of iron/aluminum (hydr)oxide and clay minerals on heteroaggregation and transport of nanoplastics in aquatic environment.

Nanoplastics (NPs) are emerging contaminants in the environment, where the transport and fate of NPs would be greatly affected by interactions between NPs and minerals. In the present study, the interactions of two types of polystyrene nanoplastics (PSNPs), i.e., bare-PSNPs and carboxylated PSNPs-COOH, with iron (hydr)oxides (hematite, goethite, magnetite, and ferrihydrite), aluminum (hydr)oxides (boehmite and gibbsite), and clay minerals (kaolinite, montmorillonite, and illite) were investigated. The positively charged iron/aluminum (hydr)oxide minerals could form heteroaggregates with negatively charged PSNPs. Electrostatic and hydrophobic interaction dominate for the heteroaggregation of bare-PSNPs with iron/aluminum (hydr)oxide minerals, while ligand exchange and electrostatic interaction are involved in the heteroaggregation of PSNPs-COOH with iron/aluminum (hydr)oxides minerals. However, heteroaggregation between PSNPs and negatively charged clay minerals was negligible. Humic acid markedly suppressed such heteroaggregation between PSNPs and minerals due to enhanced electrostatic repulsion, steric hindrance, and competition of surface attachment sites. The heteroaggregation rates of both bare-PSNPs and PSNPs-COOH with hematite decreased with increasing solution pH. Increased ionic strength enhanced the heteroaggregation of PSNPs-COOH but inhibited that of bare-PSNPs. The results of the present study suggested that the heteroaggregation of PSNPs in environments could be strongly affected by minerals, solution pH, humic acid, and ionic strength.

Role of heteroaggregation and internalization in the toxicity of differently sized and charged plastic nanoparticles to freshwater microalgae.

The toxic effect of waterborne nanoplastics is a manifestation of bio-nano interfacial interactions. Although nanoplastics with different physicochemical characteristics are known to exhibit distinct toxicities, it remains poorly understood how the properties of nanoplastics affect the bio-nano interface interactions. Here, polystyrene nanoparticles (PSNPs) varying in size (50, 300, and 500 nm) and surface charge (negative and positive charge) were employed to explore the interplay between PSNPs and algal cells (Chlamydomonas reinhardtii), with special focus on the heteroaggregation of PSNPs and microalgae, PSNPs cellular internalization, and cellular physiological responses. Results showed that large-sized PSNPs (300 and 500 nm) caused apparent toxicity to C. reinhardtii, mainly due to light blockage resulting from the PSNPs-microalgae heteroaggregation and the shading effect of PSNPs, which was independent of PSNPs concentrations. However, the toxicity of small-sized PSNPs (50 nm) was controlled by both particle surface charge and particle concentration. The positively charged PS-NH2 was more readily heteroaggregated with microalgae than the negatively charged PS-COOH, leading to photosynthesis damage-induced toxicity. Increasing the concentration of small-sized PSNPs stimulated the secretion of extracellular polymeric substances, allowing more PSNPs to attach on the cell surface and further to enter the cell, which was responsible for the increased toxicity. These findings provide new insights into how nanoplastics induce contact toxicity in microalgae cells through specific biointerfacial interactions.

Acute toxicity of nanoplastics on Daphnia and Gammarus neonates: Effects of surface charge, heteroaggregation, and water properties.

Despite progress in evaluation of risk assessment, knowledge gaps largely exist understanding the toxicity of nanoplastics in aquatic systems considering nanoplastics surface properties, environmental media characteristics and species ecological traits. In this study, amidine - functionalized polystyrene nanoparticles (PS-NPLs) of 20, 40, 60 and 100 nm are considered using Geneva lake water and mineral water to investigate the behavior and effects in neonate organisms of the plankton Daphnia magna and the benthos Gammarus fossarum. Key parameters including ζ-potential, z-average diameter, conductivity, polydispersity index, pH, EC50 were investigated. The results showed that the toxicity of PS-NPLs exhibited a dose-response relationship, size- and exposure condition-dependent trend. The smaller size PS-NPLs (20 and 40 nm) induced higher adverse effects than PS-NPLs of 60 and 100 nm in both water conditions and crustacean species. Moreover, PS-NPLs were found more toxic in the mineral water compared to lake water. Principal component analysis evidenced that the surface charge and aggregation behavior are the most influential toxicity of PS-NPLs factor for D. magna and Gammarus fossarum, respectively. These results highlight the relationship between PS-NPLs intrinsic properties, their transformation behavior, water properties and species-specificity in the evaluation of PS-NPLs biological effects on crustacean neonates in natural aquatic environments.

Thermodynamic investigation of nanoplastic aggregation in aquatic environments.

In this study, the aggregation behavior of polystyrene nanoplastics (PS NPs) in the absence or presence of oppositely charged particulate matters is systematically investigated for a wide range of electrolyte conditions. Herein, we used isothermal titration calorimetry combined with time-resolved dynamic light scattering to provide kinetic and thermodynamic insights into the NP aggregation. The thermodynamic profiles of homoaggregation and heteroaggregation were fit using an independent site and two independent sites models, respectively, demonstrating different interaction modes of both aggregation processes. We found that the contribution of solvation entropy was significant and variable in most cases, and this thermodynamic parameter was a large determinant of the thermodynamics of NP aggregation. Furthermore, the stability of PS NPs in natural water matrices was found to be correlated with ionic strength and the content of natural colloids (e.g., metal oxides and clay particles). These results point to the importance of considering the role of thermodynamic variables when studying the fate of NPs within various environmental conditions.

Ecotoxicity of Heteroaggregates of Polystyrene Nanospheres in Chironomidae and Amphibian.

Due to their various properties as polymeric materials, plastics have been produced, used and ultimately discharged into the environment. Although some studies have shown their negative impacts on the marine environment, the effects of plastics on freshwater organisms are still poorly studied, while they could be widely in contact with this pollution. The current work aimed to better elucidate the impact and the toxicity mechanisms of two kinds of commercial functionalized nanoplastics, i.e., carboxylated polystyrene microspheres of, respectively, 350 and 50 nm (PS350 and PS50), and heteroaggregated PS50 with humic acid with an apparent size of 350 nm (PSHA), all used at environmental concentrations (0.1 to 100 µg L-1). For this purpose, two relevant biological and aquatic models-amphibian larvae, Xenopus laevis, and dipters, Chironomus riparius-were used under normalized exposure conditions. The acute, chronic, and genetic toxicity parameters were examined and discussed with regard to the fundamental characterization in media exposures and, especially, the aggregation state of the nanoplastics. The size of PS350 and PSHA remained similar in the Xenopus and Chironomus exposure media. Inversely, PS50 aggregated in both exposition media and finally appeared to be micrometric during the exposition tests. Interestingly, this work highlighted that PS350 has no significant effect on the tested species, while PS50 is the most prone to alter the growth of Xenopus but not of Chironomus. Finally, PSHA induced a significant genotoxicity in Xenopus.

Biocompatible Nanoparticle Heteroaggregates as Stabilizers of Pickering Emulsions for Vitamin D3 Efficient Delivery.

Vitamin D3 deficiency is a major public health problem worldwide, and standard cholecalciferol formulations provide poor absorbability of the vitamin. Several biphasic formulas have been proposed to overcome the disadvantages in which Pickering emulsions stand out in particular. This paper describes olive oil-in-water Pickering emulsions stabilized by pseudoboehmite (AlOOH), cellulose nanocrystals (CNC), and their heterocoagulates. Colloidal properties were assessed by laser Doppler microelectrophoresis, potentiometric titration, and rheology. It was shown that the heterocoagulation of CNC and AlOOH led to a drastic change in surface properties (ζ-potential, pKa, and number of active centers), which promoted the formation of more stable emulsions with the smallest size of droplets and the highest viscosity among the studied samples. Simulated digestion studies showed the targeted release in the small intestine medium where cholecalciferol should be delivered. High-performance liquid chromatography showed the efficient encapsulation of cholecalciferol in emulsions (86% of initial concentration). Oral administration to laboratory mice of initial nanoparticles and emulsions stabilized by them showed nontoxicity for all of the components, and they were estimated to be class V materials. The proposed emulsions have great potential as targeted delivery systems of lipophilic drugs.

Mechanical properties, degradation behavior and cytocompatibility of biodegradable 3vol%X (X = MgO, ZnO and CuO)/Zn matrix composites with excellent dispersion property fabricated by graphene oxide-assisted hetero-aggregation.

Metal matrix composites have been recognized as a feasible approach to obtain a new generation of biodegradable Zn-based material. Nevertheless, there is a great challenge in achieving good dispersion properties of the bioactive reinforcements within zinc matrix. A novel and facile approach, namely graphene oxide (GO)-assisted hetero-aggregation, were developed to achieve uniformly dispersed nanoceramics in the Zn matrix, by using very low-content (0.03 vol%) GO as a linker between the Zn matrix and reinforcement. The negatively-charged GO becomes a suitable "bridge" connected the positively-charged metallic powder and bioactive reinforcement by charge neutralization in polarity solvent. Three kinds of reinforcements, including MgO, ZnO and CuO, were used to verify the feasibility of the above-mentioned method. As-sintered 3CuO/Zn matrix composites, which possessed uniformly distributed reinforcement, uniaxial compressive strength of 301.2 MPa, failure strain over 40%, moderate corrosion rate of 0.063 mm·y-1, acceptable cytocompatibility and antibacterial property, should be a useful material for orthopedic applications.