Synthesis and characterization of multiferroic BiFeO3 powders fabricated by hydrothermal method

The influence of processing parameters on phase formation and particle size of hydrothermally synthesized BiFeO₃ powders was investigated. BiFeO₃ powder was synthesized by dissolving bismuth nitrate and iron nitrate in KOH solution at temperatures ranging from 150 to 225 °C. X-ray diffraction patterns and scanning electron microscopy observation indicated that rod-like α-Bi₂O₃ phase was formed at initial stage of reaction and dissolved into ions to form thermodynamically stable BiFeO₃ phase. Single-phase perovskite BiFeO₃ has been formed using a KOH concentration of 8 M at a temperature of ≥175 °C in a 6 h reaction period. BiFeO₃ particle growth was promoted by lowering the KOH concentration, or increasing the duration time or reaction temperature. The effects of processing conditions on the formation of crystalline BiFeO₃ powders were discussed in terms of a dissolution–precipitation mechanism. The magnetization of the BiFeO₃ powders at room temperature showed a weak a ferromagnetic nature.     

Electrochemistry of Single Nanoparticles via Electrocatalytic Amplification

Recent experiments on the observation of collisions of single nanoparticles (NPs) with an electrode through amplification of the current by electrocatalysis are described. Systems in which the particles adhere to the electrode upon collision produce a step and staircase response, while those in which particles only interact for a short time with the electrode produce a spike or blip, with little change in the steady state current. Examples of both behaviors, e. g., Pt NPs on a Au electrode for hydrazine oxidation (staircase response) and IrO_x NPs on a Pt electrode for water oxidation (blip response) are shown. Controlling the nature of the electrode surface is important in generating useful responses, for example, in the case of gold NPs on an oxidized Pt electrode for borohydride oxidation.     

Polyester polyol synthesis by alternating copolymerization of propylene oxide with cyclic acid anhydrides by using double metal cyanide catalyst

Ring-opening copolymerizations of propylene oxide (PO) with cyclic acid anhydrides, succinic anhydride (SA), maleic anhydride (MA) and phthalic anhydride (PA) were carried out in the presence of a double metal cyanide (DMC) catalyst of molecular formula Zn_2.3Cl_1.0[Co(CN)₆]_1.0?2.0^tBuOH?1.0H₂O as a means of developing functional polyols bearing ester backbones. Uniform alternating copolymers are produced when [PO]/[anhydride] in the copolymer approaches unity. All resulting copolymers have moderate molecular weights (M_n = 2300–10,600) and a narrow polydispersity index (1.02–1.49). The apparent reactivity ratio of PO is 0.34, 0.28, and 0.26 for PO/SA, PO/MA, and PO/PA copolymerizations, respectively, assuming that the reactivity ratio of the anhydrides is zero. The DMC-catalyzed PO copolymerizations with anhydrides are an efficient way to produce polyester polyols, expanding the versatility of conventional polyols.     

Control of release characteristics in pH‐sensitive poly(vinyl alcohol)/poly(acrylic acid) microcapsules containing chemically treated alumina core

The pH‐sensitive poly(vinyl alcohol)/poly(acrylic acid) hydrogel microcapsules containing vitamin B₁₂‐loaded Al₂O₃ core were prepared with a three‐step emulsion polymerization. Al₂O₃ was chemically treated with HCl or NaOH solutions at room temperature for 24 h to modify the binding properties with vitamin B₁₂. The colon‐targeted release characteristics of vitamin B₁₂ from the microcapsules were evaluated at different pHs. These microcapsules showed the faster and larger release of vitamin B₁₂ due to the high swelling of microcapsule shell as the pH was changed into more basic condition. However, these microcapsules showed the slower and less release of vitamin B₁₂ as the acid value of Al₂O₃ increased due to the strong binding interaction between Al₂O₃ core and vitamin B₁₂ even though the initial loading of vitamin B₁₂ was higher. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Feasibility of creating compression‐molded biocomposite boards from berry fruit pomaces

In this study, we investigated the feasibility of creating biocomposite boards from berry fruit pomaces on the basis of a crosslinking mechanism. Blueberry, cranberry, and wine grape pomaces were ground, dried, and mixed with soy flour (SF) or pectin and xanthan gum mixture at a ratio of 1 : 1 and with the addition of 15% glycerol (w/w of pomace and SF). Blueberry pomace (BP) was also blended with NaOH‐modified soy flour (MSF) at pomace/MSF ratios of 1 : 1, 4 : 1, and 9 : 1 and with 5, 10, or 15% glycerol. The mixtures were compression‐molded at 130–140°C into biocomposite boards to evaluate their mechanical and thermal properties, water absorption and solubility, and microstructure. Among the three pomaces, the BP board was the stiffest, whereas the wine grape pomace board was the most flexible. The breaking strength and modulus of elasticity of the BP/MSF boards increased with increasing MSF concentration but decreased with increased glycerol concentration. Mixing the pomace and glycerol into SF shifted the endothermic peaks and initial degradation to lower temperatures compared to that of SF alone. Increasing the glycerol concentration decreased the water absorption but increased the water solubility of the BP/MSF board. The pomace/MSF ratio in the board did not affect (P > 0.05) the water absorption, but the water solubility increased with increasing pomace concentration. Glycerol addition in the BP/MSF board smoothed the fracture surface, as shown by scanning electron microscopy images. This study may provide an approach to reducing fruit pomace disposal through the development of new value‐added biodegradable products for industrial applications, such as nursery pots and egg cartons. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Effect of applied potential on fatigue crack propagation behavior of API X80 steel in seawater

In the present study, the fatigue crack propagation (FCP) tests were conducted on X80 steel in air and artificial seawater (ASW) under various applied potentials to establish optimum and safe working limits of cathodic protection (CP). The slow strain rate test (SSRT) was also conducted on the X80 BM specimens in ASW under CP potential to identify the susceptibility of hydrogen affecting the FCP behavior. The CP potential of ?850 and ?1,050 mV_SCE suppressed the environmental effect of seawater on the FCP behavior of X80 BM and WM specimens, showing almost identical da/dN-ΔK curves for both air and ASW environments. The SSRT in ASW under CP potential of ?1,050 mV_SCE suggested that the X80 BM specimen steel is susceptible to hydrogen embrittlement, but the effect of hydrogen was believed to be marginal in affecting the FCP behavior of the X80 specimens at a loading frequency of 10 Hz. The FCP behavior of high strength X80 steel is discussed based on the fractographic observation to understand the FCP mechanism in seawater under various CP potentials.     

Effect of the dehydrogenation speed and Nd content on the microstructure and magnetic properties of HDDR processed Nd-Fe-B magnets

The effect of Nd content and dehydrogenation speed on the microstructure and magnetic properties of hydrogenation-disproportionation-desorption-recombination (HDDR) processed Nd-Fe-B magnetic powders was studied. The Nd_xB_6.4Ga_0.3Nb_0.2Fe_bal (x=12.5–13.5, at.%) mold casting alloys were subjected to HDDR process after homogenization heat treatment. During desorption-recombination stage, dehydrogenation speed and time were systematically changed to control the speed of the desorption-recombination reaction. The higher Nd content resulted in better magnetic properties of the HDDR powder, and this was attributed to the thicker and more uniform Nd-rich phase at grain boundaries. It was also confirmed that the slow dehydrogenation speed could maximize the effect of high Nd content on the magnetic properties of HDDR powder. At the optimized dehydrogenation speed, the coercivity and remanence was 15.3 kOe and 13.0 kG, respectively, at 12.9 at.% Nd content, which resulted in a (BH)_max of 36.8 MGOe.     

Effect of electrolyte on mechanical properties of AZ31B Mg alloy in electrolytic plasma processing

Coatings on Mg alloys were prepared using NaOH + Na₂SiO₃ as basic electrolyte containing electrolyte of Na₂SiF₆ or NaF. EPP treatment was carried out on AZ31 Mg alloys matrix under a hybrid voltage of AC of 200 V combined with DC of 260 V for 30 min. Structural and morphological analyses of ceramic coatings were analyzed by XRD and SEM. Wear and hardness of coatings were measured by pin-on disk test and Vickers hardness test. The coatings formed in Na₂SiF₆ and NaF electrolytes were mainly composed of MgO and Mg₂SiO₄. The measured micro-hardness of coating formed in Na₂SiF₆ electrolyte was found to be over HV 1100, while, coating formed in NaF electrolyte possessed micro-hardness of HV ～900. These results show that the mechanical properties of AZ31B Mg alloys can be enhanced by the proper selection of electrolyte agent.