Inorganic replication of human hair and in situ synthesis of gold nanoparticles

The structure of hair was replicated via a solgel process using human hair as a template. When using silicate and tetraethoxysilane (TEOS) as the precursor, the cell structure of the hair cuticle was not well replicated. When using Ti(OnBu)₄ as the precursor, however, titania microtubes were obtained, with nanopores in their walls and nanoporous platelets on their outer surfaces, which were derived from cuticle cells on the hair surfaces. The nanopores in the microtubes acted as an effective nanoreactor for in situ synthesis of Au nanoparticles. The microchannels, nanopores and noble metal nanoparticles may provide a unique combination that would be attractive in applications such as catalysis, adsorption, and separation. Translated from Journal of Inorganic Materials, 2006, 21(6): 1,313–1,318 (in Chinese)     

Facile Synthesis of γ‐In2Se3 Nanoflowers toward High Performance Self‐Powered Broadband γ‐In2Se3/Si Heterojunction Photodiode

An effective colloidal process involving the hot‐injection method is developed to synthesize uniform nanoflowers consisting of 2D γ‐In₂Se₃ nanosheets. By exploiting the narrow direct bandgap and high absorption coefficient in the visible light range of In₂Se₃, a high‐quality γ‐In₂Se₃/Si heterojunction photodiode is fabricated. This photodiode shows a high photoresponse under light illumination, short response/recovery times, and long‐term durability. In addition, the γ‐In₂Se₃/Si heterojunction photodiode is self‐powered and displays a broadband spectral response ranging from UV to IR with a high responsivity and detectivity. These excellent performances make the γ‐In₂Se₃/Si heterojunction very interesting as highly efficient photodetectors.     

Preparation of composite nanofibers containing gold nanoparticles by using poly(N-vinylpyrrolidone) and β- cyclodextrin

We report a new method for preparing β-cyclodextrin/poly(N-vinylpyrrolidone) composite nanofibers containing gold nanoparticles by electrospinning. β-Cyclodextrin is mixed into fibers as a new material, and it acts as stabilized reagent and reducing reagent in the synthesis of gold nanoparticles. TEM observation confirms that the gold nanoparticles are completely encapsulated within the composite nanofibers.     

Study of autoabsorption for total α and β counting

The RaMsEs Group (Radioprotection et Mesures Environnementales) of the IPHC performs research and offers services mainly in the field of radioactivity measurements and sample analysis. This report will describe some of our recent experience using a semiautomatic evaporation system to prepare large area thin deposits for total α and β counting and gives experimental and simulated results for the autoabsorption coefficients.     

Physico/chemical characterization and preliminary human histology assessment of a β-TCP particulate material for bone augmentation

This study aimed to physico/chemically characterize and evaluate the in vivo performance of a β-TCP particulate grafting material. SEM/TEM, and EDS and XPS were used for morphology and chemistry assessment, respectively. FTIR was used to determine Ca–P phases characteristic bands. Rietveld refinement/XRD spectra was performed for secondary phase detection. Particle size distribution and specific surface were assessed by a scattering-laser based technique and BET, respectively. Mercury porosimetry was employed to determine pore-size distribution. For in vivo evaluation, the grafting material was used in 12 patients' sinus lifts, and biopsies were obtained at post-operative times of 3, 6, and 9 months. SEM/TEM revealed multigrained particles with interconnected pores. EDS showed Ca, P, and O, with stoichiometry close to theoretical values. XRD/Rietveld showed that the material presented crystalline β-TCP with ~ 9% β-Ca₂P₂O₇ secondary phase. FTIR did not detect the presence of bands related to α-TCP. Human histologic assessment showed that newly formed bone was present at 3 months, and degrees of bone organization increased as time elapsed in vivo. Human histology showed that the material is suitable for bone regeneration in a maxillofacial complex region.     

Effect of Ni-modified α-Al2O3 prepared by sol–gel and solvothermal methods on the characteristics and catalytic properties of Pd/α-Al2O3 catalysts

In the present study, Ni-modified α-Al₂O₃ with Ni/Al ratios of 0.3 and 0.5 were prepared by sol–gel and solvothermal method and then were impregnated with 0.3 wt.% Pd. Due to different crystallization mechanism of the two preparation methods used, addition of nickel during preparation of α-Al₂O₃ resulted in various species such as NiAl₂O₄, mixed phases between NiAl₂O₄ and α-Al₂O₃, and mixed phases between NiAl₂O₄ and NiO. As revealed by NH₃-temperature programmed desorption, formation of NiAl₂O₄ drastically reduced acidity of alumina, hence lower amounts of coke deposited during acetylene hydrogenation was found for the Ni-modified α-Al₂O₃ supported catalysts. For any given method, ethylene selectivity was improved in the order of Pd/Ni–Al₂O₃-0.5 > Pd/Ni–Al₂O₃-0.3 > Pd/Ni–Al₂O₃-0  Pd/α–Al₂O₃-commercial. When comparing the samples prepared by different techniques, the sol–gel-made samples showed better performances than the solvothermal-derived ones.     

A variationally consistent αFEM (VCαFEM) for solution bounds and nearly exact solution to solid mechanics problems using quadrilateral elements

A variationally consistent alpha finite element method (VC αFEM) for quadrilateral isoparametric elements is presented by constructing an assumed strain field in which the gradient of the compatible strain field is scaled with a free parameter α. The assumed strain field satisfies the orthogonal condition and the Hellinger–Reissner variational principle is used to establish the discretized system of equations. It is shown that the strain energy is a second‐order continuous function of α, and the VC αFEM can produce both lower and upper bounds to the exact solution in the strain energy for all elasticity problems by choosing a proper α∈[0, α_upper]. Based on this bound property, an exact‐α approach has been devised to give an ultra‐accurate solution that is very close to the exact one in the strain energy. Furthermore, the exact‐α approach also works well for volumetric locking problems, by simply replacing the strain gradient matrix by a stabilization matrix. In addition, a regularization‐α approach has also been suggested to overcome possible hourglass instability. Intensive numerical studies have been conducted to confirm the properties of the present VC αFEM, and a very good performance has been found in comparing to a large number of existing FEM models. Copyright © 2010 John Wiley & Sons, Ltd.     

Characterisation of blends between poly(ε-caprolactone) and polysaccharides for tissue engineering applications

In this work, bioartificial binary blends between poly(ε-caprolactone) (PCL) and a polysaccharide (chitosan (CS) or starch (S)) with different contents of the natural polymer (5–30 wt.%) were produced. Melt-mixing and double-precipitation were the methods used for the obtainment of PCL/S and PCL/CS blends, respectively. Tubular scaffolds were produced from bioartificial blends by melt-extrusion. Physico-chemical characterisation was performed by differential scanning calorimetry analysis (DSC), thermogravimetry (TGA), scanning electron microscopy (SEM), infrared analysis (FTIR-ATR and micro-ATR mapping), atomic force microscopy (AFM) and stress–strain tests. Blends were not miscible, phase-separated systems, showing a homogeneous composition and morphology only at low polysaccharide content (≤ 10 wt.%). The biocompatibility of bioartificial guides was investigated by culturing NIH-3T3 mouse fibroblasts. Cells response showed the following order: PCL/S > PCL > PCL/CS. For each blend type, biocompatibility increased with decreasing the polysaccharide content. In vitro cell tests using S5Y5 neuroblastoma cells, carried out on the most biocompatible blends, assessed their absence of cytotoxicity towards these model cells of the nervous tissue. Results showed that blends with a low chitosan or starch content (≤ 10 wt.%) are promising for the regeneration of tissues requiring tubular scaffolds, such as the peripheral nerves.     

Hydrothermal synthesis and characterization of monodisperse α-Fe2O3 nanoparticles

Monodisperse α-Fe₂O₃ nanoparticles have been successfully prepared by hydrothermal synthetic route using FeCl₃, CH₃COONa as reagents and reacted at 200 °C for 12 h. The morphology and structure of products were characterized by powder X-ray diffraction, scanning electron microscopy and transmission electron microscopy. The results showed that the α-Fe₂O₃ nanoparticles were single-crystalline hexagonal structure and average diameters were about 80 nm. Magnetic properties have been detected by a vibrating sample magnetometer at room temperature. The nanoparticles exhibited a ferromagnetic behavior with the coercive force (Hc), saturation magnetization (Ms) and remanent magnetization (Mr) was 185.28 Oe and 0.494 emu/g, 0.077 emu/g.     

Formation of η and σ phase in three polycrystalline superalloys and their impact on tensile properties

The formation and phase transformation mechanism of η and σ phases in three experimental polycrystalline superalloys were studied. It was shown that a high (Ti + Al) content in the alloys would favor the formation of η and σ phases in the interdendritic region. Different as-cast microstructures resulted in different phase transformation processes during heat treatment and thermal exposure. Influence of η and σ phase on tensile properties had been investigated as well. The tensile properties of the alloys were sensitive to γ′ volume fraction of the alloys, as well as morphologies of η and σ phases in the interdendritic area. Formation of plate-like η phase had negative impact on the low and intermediate temperature tensile properties of the polycrystalline superalloy.     

Effects of hydrolysis on dodecyl alcohol modified β-CaSiO3 particles and PDLLA/modified β-CaSiO3 composite films

In this research, β-CaSiO₃ particles were surface modified with dodecyl alcohol, and Poly-(DL-lactic acid) (PDLLA)/modified β-CaSiO₃ composite films were fabricated with a homogenous dispersion of β-CaSiO₃ particles in the PDLLA matrix. The aim of the study was to investigate the properties of the composite films before and after hydrolytic treatment. SEM images showed retained homogenous dispersion of β-CaSiO₃ particles after hydrolysis and tensile test also showed maintained mechanical property. Simulated body fluid (SBF) incubation experiment suggested that hydrolytic treatment did not affect the formation of hydroxyapatite on the surface of the composite films. The hydrophilicity of the composites was greatly recovered (from 69.82° to 50.28°) after hydrolysis. In addition, cells cultured on composite films after hydrolysis presented the highest cell proliferation rate and differentiation level. All of these results suggested that the surface modification of silicate particles with dodecyl alcohol along with reversible hydrolytic treatment was an effective and feasible approach to fabricate polymer/silicate composite materials with improved properties.     

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.     

Optoelectronic properties of β-Fe2O3 hollow nanoparticles

The effect of hollow structure on the optoelectronic properties of β-Fe₂O₃ hollow nanoparticles (HNPs) was determined. Spectrophotometry showed that the optical transmittance of the β-Fe₂O₃ HNPs was less than 40% in the visible-light region. This opaqueness was suggested to be an optical characteristic, commonly found in the authors' previous studies of TiO₂ and δ-Al₂O₃ HNPs. In addition, β-Fe₂O₃ HNPs had a band gap (1.86 eV) between amorphous (1.73 eV) and polycrystalline (1.97 eV) β-Fe₂O₃ thin films, which was a 5–7 nm thick shell that embraced an intermediate volume of the crystal phase, in-between the two thin films.     

The influence of α‐tocopherol concentration on the stability of linoleic acid and the properties of low‐density polyethylene

In food packaging applications where low‐density polyethylene (LDPE) film containing α‐tocopherol is used, the antioxidant may have a dual function, i.e. to protect the polymer from oxidative degradation during processing, and to delay the onset of oxidation of the packaged foodstuff during storage. Incorporation of high levels of α‐tocopherol into LDPE film was found to inhibit oxidation of a linoleic acid emulsion stored in contact with the film at 6°C. However, the presence of 360 ppm caused changes in mechanical properties and an increase in oxygen transmission. Levels as high as 3400 ppm α‐tocopherol also caused yellowing and reduction in crystallinity of the material. Thus, the use of high amounts of α‐tocopherol in LDPE, which might be needed in active packaging applications, requires careful consideration of the protective requirements for each specific food and the maintenance of the desired properties of the packaging material. Copyright © 2000 John Wiley & Sons, Ltd.     

Borehole indentor — A tool for assessing in-situ bulk ice strength and micromechanics

National Research Council (NRC) borehole indentor (BHI) is increasingly being used in the Arctic for measuring in-situ bulk strength of ice and its seasonal variation in conjunctions with investigations on climate change. Before NRC-BHI system was taken to the Arctic, its performance was evaluated on columnar-grained S1 ice in Dow's Lake, Ottawa. S1 ice with its huge and clear grains is ideal for microstructural analysis of indented ice and understanding the micromechanisms of failures (ductile and brittle) under three-dimensionally confined BHI conditions involving large volumes of ice. The upper yield (UY) strength was shown to exhibit power-law dependence on average stress rate to UY. This power-law is universally applicable to low-salinity (0.3 ppt) brackish-water S2 ice and various types of sea ice — first-year S3, granular and frazil, second-year S3 and multi-year ridge ice. The concept of shift function is introduced for quantifying the effect of temperature on BHI-UY strength. For 0.62 m thick S1 ice sheet at an average temperature of − 3.8 °C (or 0.986 T_m) the failure indentation is constant for strength of 15 to 30 MPa or stress of 1.5 × 10^{− 3} E to 3.0 × 10^{− 3} E — analogous to high-temperature creep failure strains under comparable normalized stresses in metal and complex alloys — thus establishing the same physics of deformation and failure processes. For BHI tests, the preferred independent and controllable variable, however, is the indentation rate. Both BHI-UY and BHI-flow strength (for 5 mm penetration, say) also obey power-law dependence on indentation rate and 0.1 mm s^{− 1} is suggested for standardization. While UY failures are characterized by parabolic zone of deformed, recrystallized and HIPed (hot isostatically pressed) ice, premature brittle fractures occurring at speeds at or higher than 0.2 mm s^{− 1}, are caused by the propagation of cracks nucleated at the ice-indentor contact surface. Two different measures of the degree of maturity in brittle fractures are proposed — one based on failure time and the other on UY stress.     

Relationship between photoluminescence and structural properties of the sputtered Zn1−xCdxO films on Si substrates

Zn_1−xCd_xO (x=0.2, 0.4) alloyed crystal thin films have been deposited on Si(1 1 1) substrates at different temperatures by using dc reactive magnetron sputtering technique. The Zn_1−xCd_xO films are of highly (0 0 2)-preferred orientation possessing the hexagonal wurtzite structure of pure ZnO. At 450 °C, the films have better crystal quality and photoluminescent characteristics. For the films with x=0.2 and 0.4, the corresponding near-band-edge (NBE) energies are 3.10 and 3.03 eV, respectively, both have red-shifts compared with that of ZnO (3.30 eV). For the substrate temperatures lower or higher than 450 °C, the other NBE emission peak appears, the X-ray diffraction intensity of (0 0 2) peak decreases and the related FWHM increases. With the Cd addition up to x=0.4 both the XRD and PL intensity of the Zn_1−xCd_xO films decrease sharply in comparison with x=0.2.     

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.     

Doping-induced microstructural, textural and optical properties of In2Ti1−xVxO5+δ semiconductors and their role in the photocatalytic splitting of water

The physicochemical properties of V-doped indium titanates (In₂Ti_1−xV_xO_5+δ, 0.0 ≤ x ≤ 0.2) were investigated by using XPS, powder XRD, UV–vis, SEM and luminescence spectroscopy techniques. The Rietveld refinement of XRD data revealed that even though the V-containing samples were isostructural with In₂TiO₅ (orthorhombic space group Pnma), a systematic x-dependent variation was noticeable in the Ti–O bond lengths in [TiO₆] octahedral units, cell parameters and in the value of δ. XPS results confirmed the coexistence of V⁵⁺ and V⁴⁺ states, leading thereby to an enhancement in oxygen non-stoichiometry in the doped samples. A loading-dependent progressive shift from 400 to 750 nm was also observed in the onset of the absorption edge, indicating a significant narrowing of the band gap. Furthermore, the samples with higher V-content were comprised of the grain clusters having larger size and an irregular shape. The UV–vis, photoluminescence and thermoluminescence studies indicate that the doping-induced lattice defects may give rise to certain closely spaced acceptor/donor energy levels in between the band gap of host matrix. The indium titanates are found to serve as stable photocatalysts for water splitting under visible light, where oxygen was the major reaction product. The role of microstructural and morphological properties in the photocatalytic activity is discussed.     

Stochastic response of linear and non-linear systems to α-stable Lévy white noises

The stochastic response of linear and non-linear systems to external α-stable Lévy white noises is investigated. In the literature, a differential equation in the characteristic function (CF) of the response has been recently derived for scalar systems only, within the theory of the so-called fractional Einstein–Smoluchowsky equations (FESEs). Herein, it is shown that the same equation may be built by rules of stochastic differential calculus, previously applied by one of the authors to systems driven by arbitrary delta-correlated processes. In this context, a straightforward formulation for multi-degree-of-freedom (MDOF) systems is also developed.Approximate CF solutions to the derived equation are sought for polynomial non-linearities, in stationary conditions. To this aim a wavelet representation is used, in conjunction with a weighted residual method. Numerical results prove in excellent agreement with exact solutions, when available, and digital simulation data.