Fibrillar collagen networks template and direct biocompatible silica mineralization to produce hybrid materials for biomedical applications. Silica mineralization kinetics is critical for precision-tuning material properties, including mechanical strength, microstructure, and interface thickness. We investigated the effect of varying collagen template fibril volume fraction (0.2–0.8) and elasticity (G′ 200–1500 Pa) on silica mineralization rates. Measurement of the depletion of mono- and disilicic acids by silicomolybdic acid titration showed that silica condensation on collagen fibrils follows third-order kinetics. Resulting third-order rate constants increased linearly with storage modulus and quadratically with fibril volume fraction. A unique rheological approach used to probe the collagen template surface elasticity in real-time during silicification suggested a two-phase mechanism with high levels of surface-localized gelation in Phase 1 and high levels of bulk solution-localized gelation in Phase 2. These results provide a tool for controlling hybrid collagen-silica material properties by controlling local silica condensation rates.

Dentinogenesis imperfecta type II (DGI-II) lacks intrafibrillar mineral with severe compromise of dentin mechanical properties. A Dspp knockout (Dspp–/–) mouse, with a phenotype similar to that of human DGI-II, was used to determine if poly-L-aspartic acid [poly(ASP)] in the “polymer-induced liquid-precursor” (PILP) system can restore its mechanical properties. Dentin from six-week old Dspp–/– and wild-type mice was treated with CaP solution containing poly(ASP) for up to 14 days. Elastic modulus and hardness before and after treatment were correlated with mineralization from Micro x-ray computed tomography (Micro-XCT). Transmission electron microscopy (TEM)/Selected area electron diffraction (SAED) were used to compare matrix mineralization and crystallography. Mechanical properties of the Dspp–/– dentin were significantly less than wild-type dentin and recovered significantly (P < 0.05) after PILP-treatment, reaching values comparable to wild-type dentin. Micro-XCT showed mineral recovery similar to wild-type dentin after PILP-treatment. TEM/SAED showed repair of patchy mineralization and complete mineralization of defective dentin. This approach may lead to new strategies for hard tissue repair.

Structural characterization, quantitative phase analysis, and morphological behavior of biomineralized deposits in human pancreas [pancreatic stones (PSs)] have been carried out using infrared (IR)-spectroscopy, scanning electron microscopy (SEM), powder x-ray diffraction, and thermogravimetry - differential scanning calorimetry (TG–DSC). The fourier transform infrared (FT-IR) spectra indicated that the primary composition of PSs was calcium carbonate. An x-ray powder diffraction phase quantification using the Rietveld method revealed that five of the pancreatic calculi were composed exclusively of calcite (CAL) and the remaining four contained small amounts of vaterite and aragonite in addition to the CAL phase. The crystallite size of CAL in the PSs study varied between 104(6) and 181(2) nm. The SEM images of pancreatic calculi showed a variety of crystal morphologies for biogenic CAL crystallites such as, thin plates, spherulites, prisms, and cylindrical laths. Thermogravimetric analysis of PS1 reveals that biogenic CAL is stable up to 910 K, above which temperature CAL transforms into calcium oxide.

The charge transport properties of anthra-tetrathiophene (ATT) and its brominated and cyanated derivatives (TBATT and TCATT) were investigated by the density functional theory (DFT) coupled with incoherent charge-hopping model. The crystal structure of TCATT is predicted by the dispersion-corrected DFT (DFT-D) method, and those of ATT and TBATT are retrieved from the Cambridge Crystallographic Data Center. The introduction of electron-withdrawing substituents of bromine and cyano decreases the frontier molecular orbital energies but increases the electron affinities, which is beneficial to electron injection and guarantees charge carrier stabilization. The π–π stacking of neighbor molecules with a short distance and large coupling area contributes to the largest transfer integral. The predicted electron mobility of TCATT reaches up to 1.851 cm2/(V·s), indicating that the cyanation of ATT is favorable for improving the electron transport. The angular dependent simulation for electron mobility shows that the electron transport is remarkably anisotropic.

Poly(lactic acid) (PLA)/graphene oxide (GO) nanocomposites were prepared by solution mixing. Differential scanning calorimetry results indicated that GO was an effective nucleating agent. The size of spherulites decreased, the density of spherulites increased with increasing GO and the crystallinity of PLA increased from 4.34 to 49.01%. For isothermal crystallization, the crystallization rates of PLA/GO nanocomposites were significantly higher than that of neat PLA, in which t 0.5 reduced from 9.0 to 2.8. Spindle-like nanopores (about 100–200 nm) that arranged like spherulites were prepared by low temperature foaming. It was found that the crystallization rate increase and spherulite morphology change were insignificant when the content of GO exceeded 0.5 wt%, because the excessive GO increased the number of nucleation sites while restricting the PLA crystal growth. Thus, the arrangement of nanopores did not mimick the spherulites because of imperfect crystal morphology.

DNA-immobilized Fe3O4 particles (DNA–Fe-particles) were prepared by mixing DNA, magnetic Fe3O4 particles, and the silane coupling reagent, bis[3-(trimethoxysilyl)propyl]amine. The DNA–inorganic hybrid material was uniformly immobilized onto magnetic Fe3O4 particles with the diameters of approximately 450 nm. These DNA–Fe-particles were stable in water. Additionally, we could simply collect the DNA–Fe-particles by a magnet from an aqueous solution. Therefore, we demonstrated the accumulation of various metal ions, such as heavy and rare-earth metal ions, by the DNA–Fe-particles. As a result, although these DNA–Fe-particles could selectively accumulate heavy and rare-earth metal ions, these materials could not accumulate the light metal ions, such as Mg(II) and Ca(II) ions. Furthermore, the metal ion-accumulated DNA–Fe-particles could be recycled by washing them with an aqueous ethylenediaminetetraacetic acid solution.

We designed a clamped beam bending test using a nanoindentation holder with help of transmission electron microscopy (TEM) and focused ion beam specimen fabrication. The microstructure evolution and crack propagation in nanocrystalline TiN were studied by electron imaging and load–displacement measurements during mechanical loading. By measuring the loads under which the crack starts and stops propagating and the time, we obtained the film's fracture toughness using the finite element method and crack propagation speed. Among these, we identified three types of crack propagation pathways, namely bridging, intergranular and a mixed mode of transgranular and intergranular fracture, and the associated microstructure changes. The measured fracture toughness is in agreement with the reported values. Thus, our in situ TEM bending test provides the first direct measurement of fracture toughness in a TEM and a correlation of fracture toughness with fracture toughening mechanisms in nanocrystalline TiN. The method is general and can be applied to other nanocrystalline materials.

The NbCr2 Laves phase was fabricated by spark plasma sintering (SPS) using spherical Nb and Cr powders. The experimental results revealed that increasing the sintering temperature to 1773 K can result in the formation of NbCr2 Laves phase as major phase, but it always appeared with trace amounts of Nb and Cr solid solutions. Based on the theoretical calculations, the residual of Nb and Cr solid solutions was attributed to the inhomogeneous distribution of temperature increase from the particle-contacting surface to the center of particle when pulsed current passed through. Moreover, the hardness and fracture toughness of the SPS-processed NbCr2 attained 14.05 ± 0.67 GPa and 8.9 MPa·m1/2, which were 1.6 and 7.4 times of the as-cast NbCr2 Laves phase (1.2 MPa·m1/2). The formation of ductile Nb and Cr solid solutions and fine grains were considered to be the reason for the remarkable enhancements in mechanical properties.

The friction and wear behaviors of reciprocatingly extruded AA 6061–SiC composites form the focal point of this study. To find the optimum way for refining the grains of the matrix, reciprocating extrusion (RE), as a deformation processes, is conducted and found to be feasible. Accordingly, RE has been applied on SiC particles reinforced AA 6061 matrix composite. Using the RE passes as a base, wear behaviors of the composites have been investigated at ambient temperature under dry and lubricated forms. Optical microscopy, transmission electron microscopy and scanning electron microscopy techniques were used to reveal the effect of the RE passes on the microstructure of the materials. As a result, it is found that there is a clear relationship between the weight loss, wear resistance and hardness of the samples. As the load and the number of passes increase, the weight loss in the samples increases. The worn surfaces of the reinforced composites have commonly adhesive and abrasive type of wear.

The refinement mechanism of alternating current pulse (ACP) on the solidification macrostructures of pure Al and the characterization of refining efficiency were investigated by embedding the wire mesh in the mold. The experiment results showed that ACP treatment during solidification led to the formation of fine equiaxed grain. There were remarkably differences with respect to the area of fine equiaxed zone inside and outside the tube. Lorentz force, induced melt flow and the rest of intrinsic effects of ACP inside and outside the tube were discussed in the present study. It demonstrated that the forced melt flow could lead to the columnar fragmentation and make the crystal nucleus on the mold wall fall off and drift in the liquid, leading to grain refinement. In addition, Reynolds number was suitable to characterize the refining efficiency of pure Al under ACP.

Electroreduction of solid V2O3 pellets (∼0.7 g) to V in molten CaCl2 at 900 °C has been studied by cyclic voltammetry and potentiostatic electrolysis, together with scanning electron microscopy, energy dispersive x-ray, and elemental analyses. The intermediate products of the potentiostatic electrolysis are various, forming some lower valence state compounds (VO, V16O3, V7O3, VO0.2) and higher valence state which are likely VO2, CaVO3, or CaV2O5. At potentials more negative than −0.6 V versus Ag/AgCl, fine vanadium powder (aggregates of nodular ∼500 nm particles) can be prepared by electrolysis of porous solid of the V2O3 pellets. The current efficiency and energy consumption were satisfactory, about 53.4% and 2.5 kW h/(kg V) at −0.6 V versus Ag/AgCl, respectively. Moreover, V–20Ti alloys were electrochemically synthesized by constant voltage electrolysis at the indicated potentials, the control of composition as well as the reduction optimization of the mixtures were demonstrated. This electrochemical route is efficient and offers a product with controlled stoichiometry, with particular advantage of manufacturing of low cost alloys and intermetallics directly from mixed oxide precursors, and has potential to produce functional vanadium alloys.