Toxicological Aspects of Long‐Term Treatment of Keratinocytes with ZnO and TiO2 Nanoparticles

Sunscreens containing ZnO and TiO₂ nanoparticles (NPs) are increasingly applied to skin over long time periods to reduce the risk of skin cancer. However, long‐term toxicological studies of NPs are very sparse. The in vitro toxicity of ZnO and TiO₂ NPs on keratinocytes over short‐ and long‐term applications is reported. The effects studied are intracellular formation of radicals, alterations in cell morphology, mitochondrial activity, and cell‐cycle distribution. Cellular response depends on the type of NP, concentration, and exposure time. ZnO NPs have more pronounced adverse effects on keratinocytes than TiO₂. TiO₂ has no effect on cell viability up to 100 μg mL^?1, whereas ZnO reduces viability above 15 μg mL^?1 after short‐term exposure. Prolonged exposure to ZnO NPs at 10 μg mL^?1 results in decreased mitochondrial activity, loss of normal cell morphology, and disturbances in cell‐cycle distribution. From this point of view TiO₂ has no harmful effect. More nanotubular intercellular structures are observed in keratinocytes exposed to either type of NP than in untreated cells. This observation may indicate cellular transformation from normal to tumor cells due to NP treatment. Transmission electron microscopy images show NPs in vesicles within the cell cytoplasm, particularly in early and late endosomes and amphisomes. Contrary to insoluble TiO₂, partially soluble ZnO stimulates generation of reactive oxygen species to swamp the cell redox defense system thus initiating the death processes, seen also in cell‐cycle distribution and fluorescence imaging. Long‐term exposure to NPs has adverse effects on human keratinocytes in vitro, which indicates a potential health risk.     

Mechanistic Investigation of the Biological Effects of SiO2, TiO2, and ZnO Nanoparticles on Intestinal Cells

Silicon dioxide (SiO₂), titanium dioxide (TiO₂), and zinc oxide (ZnO) are currently among the most widely used nanoparticles (NPs) in the food industry. This could potentially lead to unintended exposure of the gastrointestinal tract to these NPs. This study aims to investigate the potential side‐effects of these food‐borne NPs on intestinal cells and to mechanistically understand the observed biological responses. Among the panel of tested NPs, ZnO NPs are the most toxic. Consistently in all three tested intestinal cell models, ZnO NPs invoke the most inflammatory responses from the cells and induce the highest intracellular production of reactive oxygen species (ROS). The elevated ROS levels induce significant damage to the DNA of the cells, resulting in cell‐cycle arrest and subsequently cell death. In contrast, both SiO₂ and TiO₂ NPs elicit minimum biological responses from the intestinal cells. Overall, the study showcases the varying capability of the food‐borne NPs to induce a cellular response in the intestinal cells. In addition to physicochemical differences in the NPs, the genetic landscape of the intestinal cell models governs the toxicology profile of these food‐borne NPs.     

In Situ Synthesis of CuO and Cu Nanostructures with Promising Electrochemical and Wettability Properties

A strategy is presented for the in situ synthesis of single crystalline CuO nanorods and 3D CuO nanostructures, ultra‐long Cu nanowires and Cu nanoparticles at relatively low temperature onto various substrates (Si, SiO₂, ITO, FTO, porous nickel, carbon cotton, etc.) by one‐step thermal heating of copper foam in static air and inert gas, respectively. The density, particle sizes and morphologies of the synthesized nanostructures can be effectively controlled by simply tailoring the experimental parameters. A compressive stress based and subsequent structural rearrangements mechanism is proposed to explain the formation of the nanostructures. The as‐prepared CuO nanostructures demonstrate promising electrochemical properties as the anode materials in lithium‐ion batteries and also reversible wettability. Moreover, this strategy can be used to conveniently integrate these nanostructures with other nanostructures (ZnO nanorods, Co₃O₄ nanowires and nanowalls, TiO₂ nanotubes, and Si nanowires) to achieve various hybrid hierarchical (CuO‐ZnO, CuO‐Co₃O₄, CuO‐TiO₂, CuO‐Si) nanocomposites with promising properties. This strategy has the potential to provide the nano society with a general way to achieve a variety of nanostructures.     

The role of catalyst support on activity of copper oxide nanoparticles for reduction of 4-nitrophenol

Developing a facile and efficient method is an important approach for promising commercial catalytic applications. Toxic organic pollutants in waste waters are becoming a worldwide problem that threatens life on earth and prevents essential elements to sustain living organisms. Herein, the effect of catalyst support on the activity of copper oxide (CuO) nanoparticles for catalytic reduction of 4-nitrophenol (4-NP) in presence of sodium borohydride (NaBH₄)-aqueous medium was discussed. A simple and conventional wet impregnation method was used for the deposition of CuO nanoparticles on several metal oxides (Al₂O₃, SiO₂, MgO, CaO, ZnO, ZrO₂). The prepared catalysts were characterized via using techniques such as X-ray diffraction (XRD), nitrogen sorption, inductively coupled plasma-optical emission spectrometry (ICP-OES), scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDS), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The effect of support material on the catalytic performance of CuO nanoparticles for the reduction of 4-NP was evaluated and the performance order of support was ZrO₂ > Al₂O₃ > SiO₂ > CaO > MgO > ZnO. CuO/ZrO₂ catalyst exhibited excellent catalytic activity and the pseudo-first-order rate constant was determined as 15.97 · 10⁻³ s⁻¹. Considering the simple preparation process and the efficient catalytic reduction of 4-NP of CuO/ZrO₂, this study opens up a marvelous chance to this material for practical application of waste water treatment.     

Formation of metallic vanadium nanoparticles in SiO2 by ion implantation and of vanadium oxide nanoparticles by additional thermal oxidation

Metallic V nanoparticles (NPs) were formed in silica glass by implantation with V⁺ ions of 60 keV to a fluence of 1.0 × 10¹⁷ ions/cm². Annealing in oxygen gas at 800 °C transformed the metallic NPs to oxide NPs. While the mean diameter of the metal V NPs was 8.4 nm in the as-implanted state, the diameters steeply increased during oxidation, with some exceeding 100 nm. Since at least 15 different composition phases, such as V₂O₃, V₃O₇, V₆O₁₃, V₉O₁₇, etc., are known for vanadium oxides, identification of the oxide phase of the NPs was not easy. X-ray diffraction (XRD) was not a powerful tool for phase identification of the NPs, because the diffraction peaks were broad due to the nanometric sizes of the particles and readily shift due to stress effects. The temperature dependence of the optical absorption spectrum was measured. The observed spectra were almost unchanged between 3.3 and 370 K. Combining the spectral result and the XRD results, the candidates were narrowed down to three phases, V₂O₅, V₄O₉, and V₇O₁₃, from the 15 candidates. Among the three, the V₂O₅ phase is the most probable because the absorption spectrum and the oxygen partial pressure for its formation were both consistent.     

Influence of cerium dopant on magnetic and dielectric properties of ZnO nanoparticles

Ce-doped ZnO nanoparticles (NPs) with different Ce doping concentrations (0, 0.96, 1.96, 2.52 and 3.12 at.% of Ce) were prepared by the chemical co-precipitation method. Energy-dispersive analysis of X-rays confirms the presence of Ce in Ce-doped ZnO nanoparticles. Raman spectra revealed the hexagonal wurtzite structure of pure and Ce-doped ZnO nanoparticles and presence of various defects. The photoluminescence spectra exhibited enhanced violet and blue emission peak intensities for 0.96 at.% of Ce, while broad band green emissions decreased with Ce content. Electron paramagnetic resonance (EPR) studies revealed the presence of oxygen vacancies (V _O), zinc vacancies (V _Zn) and Ce³⁺ ions in the prepared ZnO nanoparticles. VSM studies showed room temperature ferromagnetism (RTFM) in the Ce-doped ZnO NPs. The substituted Ce³⁺ions found to induce RTFM along with V _O, V _Zn in correlation with the results obtained from the EPR, PL and Raman studies. The variation of dielectric constants (ε _r), dielectric loss (ε″) and ac conductivity (σ _ac) as a function of frequency and Ce concentration is studied using ‘Maxwell–Wagner Model.’     

In Situ Encapsulating α‐MnS into N,S‐Codoped Nanotube‐Like Carbon as Advanced Anode Material: α → β Phase Transition Promoted Cycling Stability and Superior Li/Na‐Storage Performance in Half/Full Cells

Incorporation of N,S‐codoped nanotube‐like carbon (N,S‐NTC) can endow electrode materials with superior electrochemical properties owing to the unique nanoarchitecture and improved kinetics. Herein, α‐MnS nanoparticles (NPs) are in situ encapsulated into N,S‐NTC, preparing an advanced anode material (α‐MnS@N,S‐NTC) for lithium‐ion/sodium‐ion batteries (LIBs/SIBs). It is for the first time revealed that electrochemical α → β phase transition of MnS NPs during the 1st cycle effectively promotes Li‐storage properties, which is deduced by the studies of ex situ X‐ray diffraction/high‐resolution transmission electron microscopy and electrode kinetics. As a result, the optimized α‐MnS@N,S‐NTC electrode delivers a high Li‐storage capacity (1415 mA h g^?1 at 50 mA g^?1), excellent rate capability (430 mA h g^?1 at 10 A g^?1), and long‐term cycling stability (no obvious capacity decay over 5000 cycles at 1 A g^?1) with retained morphology. In addition, the N,S‐NTC‐based encapsulation plays the key roles on enhancing the electrochemical properties due to its high conductivity and unique 1D nanoarchitecture with excellent protective effects to active MnS NPs. Furthermore, α‐MnS@N,S‐NTC also delivers high Na‐storage capacity (536 mA h g^?1 at 50 mA g^?1) without the occurrence of such α → β phase transition and excellent full‐cell performances as coupling with commercial LiFePO₄ and LiNi_0.6Co_0.2Mn_0.2O₂ cathodes in LIBs as well as Na₃V₂(PO₄)₂O₂F cathode in SIBs.     

Polymer Doping Enables a Two‐Dimensional Electron Gas for High‐Performance Homojunction Oxide Thin‐Film Transistors

High‐performance solution‐processed metal oxide (MO) thin‐film transistors (TFTs) are realized by fabricating a homojunction of indium oxide (In₂O₃) and polyethylenimine (PEI)‐doped In₂O₃ (In₂O₃:x% PEI, x = 0.5–4.0 wt%) as the channel layer. A two‐dimensional electron gas (2DEG) is thereby achieved by creating a band offset between the In₂O₃ and PEI‐In₂O₃ via work function tuning of the In₂O₃:x% PEI, from 4.00 to 3.62 eV as the PEI content is increased from 0.0 (pristine In₂O₃) to 4.0 wt%, respectively. The resulting devices achieve electron mobilities greater than 10 cm² V^?1 s^?1 on a 300 nm SiO₂ gate dielectric. Importantly, these metrics exceed those of the devices composed of the pristine In₂O₃ materials, which achieve a maximum mobility of ≈4 cm² V^?1 s^?1. Furthermore, a mobility as high as 30 cm² V^?1 s^?1 is achieved on a high‐k ZrO₂ dielectric in the homojunction devices. This is the first demonstration of 2DEG‐based homojunction oxide TFTs via band offset achieved by simple polymer doping of the same MO material.     

An Assessment of the Impact of SiO2 Nanoparticles of Different Sizes on the Rest/Wake Behavior and the Developmental Profile of Zebrafish Larvae

In this study, zebrafish larvae are introduced as an in vivo platform to examine the neurotoxicity and developmental toxicity associated with continuous exposure to a concentration gradient of different sizes of SiO₂ nanoparticles (15 nm and 50 nm diameter) to determine the dose effect and size effect of SiO₂ nanoparticle (NP)‐induced toxicity. Bovine serum albumin (BSA‐V) is utilized as a stabilizing agent to prevent coagulation of the SiO₂ nanoparticles. To the best of our knowledge, this study is the first to describe locomotor activity assays linking rest/wake behavioral profiles for the purpose of investigating the neurotoxicity of NPs. In addition, developmental toxicological endpoints including mortality, LC₅₀, malformation, and cartilaginous deformity are assessed. The results show a concentration‐dependent increase in behavioral neurotoxicity, mortality, and malformation among larvae treated with the SiO₂ nanoparticles of 15 nm and 50 nm. A comparison of the 15 nm and 50 nm NPs by K‐means clustering analysis demonstrates that the 15 nm NPs have a greater neurotoxic effect than the 50 nm NPs, with the 50 nm NPs exhibiting greater developmental toxicity on the zebrafish larvae than the 15 nm NPs.     

Synthesis and functionalization of SiO2 coated Fe3O4 nanoparticles with amine groups based on self-assembly

The purpose of this research was to synthesize amino modified Fe₃O₄/SiO₂ nanoshells for biomedical applications. Magnetic iron-oxide nanoparticles (NPs) were prepared via co-precipitation. The NPs were then modified with a thin layer of amorphous silica. The particle surface was then terminated with amine groups. The results showed that smaller particles can be synthesized by decreasing the NaOH concentration, which in our case this corresponded to 35 nm using 0.9 M of NaOH at 750 rpm with a specific surface area of 41 m² g^? 1 for uncoated Fe₃O₄ NPs and it increased to about 208 m² g^?1 for 3-aminopropyltriethoxysilane (APTS) coated Fe₃O₄/SiO₂ NPs. The total thickness and the structure of core-shell was measured and studied by transmission electron microscopy (TEM). For uncoated Fe₃O₄ NPs, the results showed an octahedral geometry with saturation magnetization range of (80–100) emu g^?1 and coercivity of (80–120) Oe for particles between (35–96) nm, respectively. The Fe₃O₄/SiO₂ NPs with 50 nm as particle size, demonstrated a magnetization value of 30 emu g^?1. The stable magnetic fluid contained well-dispersed Fe₃O₄/SiO₂/APTS nanoshells which indicated monodispersity and fast magnetic response.     

Amorphous Silica Nanoparticles Promote Monocyte Adhesion to Human Endothelial Cells: Size‐Dependent Effect

There is evidence that nanoparticles can induce endothelial dysfunction. Here, the effect of monodisperse amorphous silica nanoparticles (SiO₂‐NPs) of different diameters on endothelial cells function is examined. Human endothelial cell line (EA.hy926) or primary human pulmonary artery endothelial cells (hPAEC) are seeded in inserts introduced or not above triple cell co‐cultures (pneumocytes, macrophages, and mast cells). Endothelial cells are incubated with SiO₂‐NPs at non‐cytotoxic concentrations for 12 h. A significant increase (up to 2‐fold) in human monocytes adhesion to endothelial cells is observed for 18 and 54 nm particles. Exposure to SiO₂‐NPs induces protein expression of adhesion molecules (ICAM‐1 and VCAM‐1) as well as significant up‐regulation in mRNA expression of ICAM‐1 in both endothelial cell types. Experiments performed with fluorescent‐labelled monodisperse amorphous SiO₂‐NPs of similar size evidence nanoparticle uptake into the cytoplasm of endothelial cells. It is concluded that exposure of human endothelial cells to amorphous silica nanoparticles enhances their adhesive properties. This process is modified by the size of the nanoparticle and the presence of other co‐cultured cells.     

Interfacial Engineering of Hierarchical Transition Metal Oxide Heterostructures for Highly Sensitive Sensing of Hydrogen Peroxide

Hydrogen peroxide (H₂O₂) is a major messenger molecule in cellular signal transduction. Direct detection of H₂O₂ in complex environments provides the capability to illuminate its various biological functions. With this in mind, a novel electrochemical approach is here proposed by integrating a series of CoO nanostructures on CuO backbone at electrode interfaces. High‐resolution transmission electron microscopy (HRTEM), X‐ray diffraction, and X‐ray photoelectron spectroscopy demonstrate successful formation of core–shell CuO–CoO hetero‐nanostructures. Theoretical calculations further confirm energy‐favorable adsorption of H₂O₂ on surface sites of CuO–CoO heterostructures. Contributing to the efficient electron transfer path and enhanced capture of H₂O₂ in the unique leaf‐like CuO–CoO hierarchical 3D interface, an optimal biosensor‐based CuO–CoO‐2.5 h electrode exhibits an ultrahigh sensitivity (6349 µA m m ^?1 cm^?2), excellent selectivity, and a wide detection range for H₂O₂, and is capable of monitoring endogenous H₂O₂ derived from human lung carcinoma cells A549. The synergistic effects for enhanced H₂O₂ adsorption in integrated CuO–CoO nanostructures and performance of the sensor suggest a potential for exploring pathological and physiological roles of reactive oxygen species like H₂O₂ in biological systems.     

A High‐Rate V2O5 Hollow Microclew Cathode for an All‐Vanadium‐Based Lithium‐Ion Full Cell

V₂O₅ hollow microclews (V₂O₅‐HMs) have been fabricated through a facile solvothermal method with subsequent calcination. The synthesized V₂O₅‐HMs exhibit a 3D hierarchical structure constructed by intertangled nanowires, which could realize superior ion transport, good structural stability, and significantly improved tap density. When used as the cathodes for lithium‐ion batteries (LIBs), the V₂O₅‐HMs deliver a high capacity (145.3 mAh g^‐1) and a superior rate capability (94.8 mAh g^‐1 at 65 C). When coupled with a lithiated Li₃VO₄ anode, the all‐vanadium‐based lithium‐ion full cell exhibits remarkable cycling stability with a capacity retention of 71.7% over 1500 cycles at 6.7 C. The excellent electrochemical performance demonstrates that the V₂O₅‐HM is a promising candidate for LIBs. The insight obtained from this work also provides a novel strategy for assembling 1D materials into hierarchical microarchitectures with anti‐pulverization ability, excellent electrochemical kinetics, and enhanced tap density.     

Generic Synthesis of Carbon Nanotube Branches on Metal Oxide Arrays Exhibiting Stable High‐Rate and Long‐Cycle Sodium‐Ion Storage

A new and generic strategy to construct interwoven carbon nanotube (CNT) branches on various metal oxide nanostructure arrays (exemplified by V₂O₃ nanoflakes, Co₃O₄ nanowires, Co₃O₄–CoTiO₃ composite nanotubes, and ZnO microrods), in order to enhance their electrochemical performance, is demonstrated for the first time. In the second part, the V₂O₃/CNTs core/branch composite arrays as the host for Na⁺ storage are investigated in detail. This V₂O₃/CNTs hybrid electrode achieves a reversible charge storage capacity of 612 mAh g^?1 at 0.1 A g^?1 and outstanding high‐rate cycling stability (a capacity retention of 100% after 6000 cycles at 2 A g^?1, and 70% after 10 000 cycles at 10 A g^?1). Kinetics analysis reveals that the Na⁺ storage is a pseudocapacitive dominating process and the CNTs improve the levels of pseudocapacitive energy by providing a conductive network.     

Study of Structural and Magnetic Properties of Superparamagnetic Fe3O4–ZnO Core–Shell Nanoparticles

In this work, Fe₃O₄–ZnO core–shell nanoparticles have been successfully synthesized using a simple two-step co-precipitation method. In this regard, Fe₃O₄ (magnetite) and ZnO (zincite) nanoparticles (NPs) were synthesized separately. Then, the surface of the Fe₃O₄ NPs was modified with trisodium citrate in order to improve the attachment of ZnO NPs to the surface of Fe₃O₄ NPs. Afterwards, the modified magnetite NPs were coated with ZnO NPs. Moreover, the influence of the core to shell molar ratio on the structural and magnetic properties of the core–shell NPs has been investigated. The prepared nanoparticles have been characterized utilizing transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy and vibrating sample magnetometer (VSM). The results of XRD indicate that Fe₃O₄ NPs with inverse spinel phase were formed. The results of VSM imply that the Fe₃O₄–ZnO core–shell NPs are superparamagnetic. The saturation magnetization of prepared Fe₃O₄ NPs is 54.24 emu/g and it decreases intensively down to 29.88, 10.51 and 5.75 emu/g, after ZnO coating with various ratios of core to shell as 1:1, 1:10 and 1:20, respectively. This reduction is attributed to core–shell interface effects and shielding. TEM images and XRD results imply that ZnO-coated magnetite NPs are formed. According to the TEM images, the estimated average size for most of core–shell NPs is about 12 nm.     

Lab‐on‐a‐Chip‐Based High‐Throughput Screening of the Genotoxicity of Engineered Nanomaterials

The continuous increasing of engineered nanomaterials (ENMs) in our environment, their combinatorial diversity, and the associated genotoxic risks, highlight the urgent need to better define the possible toxicological effects of ENMs. In this context, we present a new high‐throughput screening (HTS) platform based on the cytokinesis‐block micronucleus (CBMN) assay, lab‐on‐chip cell sorting, and automated image analysis. This HTS platform has been successfully applied to the evaluation of the cytotoxic and genotoxic effects of silver nanoparticles (AgNPs) and silica nanoparticles (SiO₂NPs). In particular, our results demonstrate the high cyto‐ and genotoxicity induced by AgNPs and the biocompatibility of SiO₂NPs, in primary human lymphocytes. Moreover, our data reveal that the toxic effects are also dependent on size, surface coating, and surface charge. Most importantly, our HTS platform shows that AgNP‐induced genotoxicity is lymphocyte sub‐type dependent and is particularly pronounced in CD2+ and CD4+ cells.     

Green synthesis of ZnO and Mg doped ZnO nanoparticles,and its optical properties

The Zinc oxide nanoparticles (ZnO NPs) and Magnesium doped ZnO nanoparticles (Mg doped ZnO NPs) are synthesized by Psidium guajava leaf extract. X-ray diffraction studies confirmed that, synthesized nanoparticles were retained the wurtzite hexagonal structure. In FESEM and HRTEM image analysis, ZnO and Mg doped ZnO NPs morphology were trigonal and spherical shape. Elemental compositions were identified by EDAX analysis. From FTIR result, the Zn–O stretching was observed at 453 and 448 cm^?1 for both ZnO samples. In Raman spectra, the high intensive E₂ ^high mode observed for 438 cm^?1 for ZnO NPs. But Mg doped ZnO NPs intensity of E₂ ^high mode decreased as compared to the pure ZnO NPs, it is due to the Mg²⁺ ion in to ZnO lattice site. The photoluminescence measurements revealed that the broad emission was composed of seven different bands due to zinc vacancies, oxygen vacancies and surface defects.     

Polyhydroxylated Metallofullerenols Stimulate IL‐1β Secretion of Macrophage through TLRs/MyD88/NF‐κB Pathway and NLRP3 Inflammasome Activation

Polyhydroxylated fullerenols especially gadolinium endohedral metallofullerenols (Gd@C₈₂(OH)₂₂) are shown as a promising agent for antitumor chemotherapeutics and good immunoregulatory effects with low toxicity. However, their underlying mechanism remains largely unclear. We found for the first time the persistent uptake and subcellular distribution of metallofullerenols in macrophages by taking advantages of synchrotron‐based scanning transmission X‐ray microscopy (STXM) with high spatial resolution of 30 nm. Gd@C₈₂(OH)₂₂ can significantly activate primary mouse macrophages to produce pro‐inflammatory cytokines like IL‐1β. Small interfering RNA (siRNA) knockdown shows that NLRP3 in?ammasomes, but not NLRC4, participate in fullerenol‐induced IL‐1β production. Potassium efflux, activation of P2X₇ receptor and intracellular reactive oxygen speciesare also important factors required for fullerenols‐induced IL‐1β release. Stronger NF‐κB signal triggered by Gd@C₈₂(OH)₂₂ is in agreement with higher pro‐IL‐1β expression than C₆₀(OH)₂₂. Interestingly, TLR4/MyD88 pathway but not TLR2 mediates IL‐1β secretion in Gd@C₈₂(OH)₂₂ exposure confirmed by macrophages from MyD88^?/?/TLR4^?/?/TLR2^?/? knockout mice, which is different from C₆₀(OH)₂₂. Our work demonstrated that fullerenols can greatly activate macrophage and promote IL‐1β production via both TLRs/MyD88/NF‐κB pathway and NLRP3 inflammasome activation, while Gd@C₈₂(OH)₂₂ had stronger ability C₆₀(OH)₂₂ due to the different electron affinity on the surface of carbon cage induced by the encaged gadolinium ion.     

Characterisation of binary (Fe3O4/SiO2) biocompatible nanocomposites as magnetic fluid

This article describes coating of magnetite nanoparticles (NPs) with amorphous silica shells. Controlled co-precipitation technique under N₂ gas was used to prevent undesirable critical oxidation of Fe²⁺. The synthesised Fe₃O₄ NPs were first coated with trisodium citrate to achieve solution stability and then covered by SiO₂ layer using Stober method. For uncoated Fe₃O₄ NPs, the results showed an octahedral geometry with saturation magnetisation range of 82–96?emu/g and coercivity of 85–120?Oe for particles between 35 and 96?nm, respectively. The best value of specific surface area (41?m²/g) for Fe₃O₄ alone was obtained at 0.9?M NaOH at 750?rpm and it increased to about 81?m²/g for Fe₃O₄/SiO₂ combination. The total thickness and the structure of core–shell was measured and studied by transmission electron microscopy. The average particles size was about 50?nm, indicating the presence of about 15?nm SiO₂ layer. Finally, the stable magnetic fluid contained well-dispersed magnetite-silica nanocomposites which showed monodispersity and fast magnetic response.     

Cement-based composites endowed with novel functions through controlling interface microstructure from Fe3O4@SiO2 nanoparticles

In this paper, Fe₃O₄@SiO₂ nanoparticles (NPs) were introduced in the surface layer of cement-based materials derived by magnetic field to create a wave adsorbing layer. The cement-based materials treated with Fe₃O₄@SiO₂ NPs revealed superior microwave-absorption property comparing with the samples treated with pure Fe₃O₄ NPs. Because of a SiO₂ coating on Fe₃O₄ NPs, water absorption rates of cement mortars treated with Fe₃O₄@SiO₂ NPs have reduced by 45.3%. In addition, the SiO₂ coating on Fe₃O₄ NPs bonded wave absorbing materials on the surface of cement-based composites by forming a mass of SiO₂ and calcium silicate hydrate (C-S-H) gels. The Fe₃O₄@SiO₂ NPs can be considered as an ideal wave absorption surface-treatment agent for cement-based composites.