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Synroc is recognized as the second generation waste form for the disposal of high-level radioactive waste (HLW). In this research, one of the mostly studied Synroc minerals, zirconolite (CaZrTi2O7), was prepared by self-propagating high-temperature synthesis (SHS). CuO and MoO3 were employed as the oxidants with Ti as the reductant. Different TiO2/Ti ratios were selected to investigate reactivity and adiabatic temperature (Tad) of the designed SHS reactions. Zirconolite was successfully synthesized as the main phase at varied TiO2/Ti ratios using CuO and MoO3 as the oxidants. The as-synthesized samples were readily solidified with desirable density and Vickers hardness.

Electrogenerated chemiluminescence (ECL) of a novel phenyleneethynylene derivatives [4,4’-(2,5-dimethoxy-1,4-phenylene)bis(ethyne-2,1-diyl) dibenzoic acid; P-acid] possessing carboxylic acid groups at the para positions in aqueous solutions and its first immunosensing application are studied. Nanotubular mesoporous Pt–Ag alloy nanoparticles are first used to fabricate the ECL immunosensor as a signal amplification carrier. Absorption, photoluminescence, cyclic voltammetry, scanning electron microscopy, transmission electron microscopy, and electrochemical impedance spectroscopy are used as powerful tools to characterize P-acid, Pt–Ag alloy nanoparticles, and the fabrication process of the immunosensor. P-acid exhibits two ECL peaks at –1.07 (ECL-1) and 0.64 (ECL-2) V in air-saturated pH 7.4, 0.1 M PBS containing 0.1 M KCl during the cyclic sweep between 1.51 and –2.67 V at 0.1 V s−1; the ECL mechanism of these two ECL peaks is demonstrated. The electron-transfer reaction between electrochemically oxidized P-acid and tri-n-propylamine (TPrA) radical cation is also demonstrated to produce high ECL emissions and used to develop an ultrasensitive ECL immunosensor. In addition, a Pt–Ag alloy nanoparticles amplification carrier for protein ECL analysis is applied for improvement of the detection sensitivity. Thus, this ECL immunosensor exhibits high sensitivity, good reproducibility, rapid response, and long-term stability.

One-dimensional SrSn(OH) 6 nanowires were successfully synthesized through a rapid simple method-sonochemical synthesis at room temperature without using any templates or surfactants. The growth mechanism has been proposed, and the reaction conditions were carefully investigated. The experimental results revealed that both the ultrasound irradiation and the presence of Na 2 CO 3 in the synthetic process had an impact on the fast formation of the SrSn(OH) 6 nanowires. Moreover, a subsequent precipitation-hydrothermal treatment of SrSn(OH) 6 nanowires-was conducted in ethanol at 180 °C for 8 h in order to improve their crystallinity and thermal stalibity. SrSnO 3 nanorods were converted by calcination of the hydrothermally treated SrSn(OH) 6 nanowires at 700 °C for 3 h in air. In particular, it was the first attempt to test the electrochemical properties of the SrSnO 3 products as anode in a Li ion battery. The resulting SrSnO 3 nanorods exhibited a better cyclability over 50 cycles with a reversible lithium storage capacity of 200 mA h g ―1 than that of SrSnO 3 nanoparticles.

CaSn(OH)(6) nanotubes were fabricated by sonochemical precipitation method at room temperature. A direct rolling process from nanosheets to nanotubes was expected for the synthesis of CaSn(OH)(6) nanotubes. The transient CaSn(OH)(6) nanosheets are formed as intermediates produced by the spontaneous self-assembly and transformation of amorphous colloid clusters. During the crystallization process of intermediate nanosheets, the relaxation of surface strain in the nanosheet interfaces can induce the nanosheets to roll up to form nanotubes under ultrasonic conditions. In this synthesis, the addition of Na(2)CO(3) seems to play an important role in the formation, size, and shape control of the nanotubes. Investigations into the stability performance of the nanotubes indicate that the morphologies are very sensitive to pH and temperature. The method suggests a general strategy for the design and fabrication of functional single-crystalline nanotubes through an intermediate nanosheet rolling process. The in vitro fabrication of such single crystal nanotubes could shed light on fundamental mechanisms for closed hollow nanostructures. Furthermore, nanotubes produced in high yield and at low cost are envisioned to have applications in areas ranging from medicine to pharmaceuticals through to materials science.

An axial magnetic field of 0.1 T was applied to ZrF4–BaF2–LaF3–AlF3NaF fibers during heating to the glass crystallization temperature. Scanning electron microscopy and x-ray diffraction were used to identify crystal phases. It was shown that fibers exposed to the magnetic field did not crystallize, while fibers not exposed to the field did crystallize. A hypothesis based on magnetic work was proposed to explain the results, and was tested by measuring the magnetic susceptibilities of the glass and crystal.

One-dimensional SrSn(OH) 6 nanowires were successfully synthesized through a rapid simple methods sonochemical synthesis at room temperature without using any templates or surfactants. The growth mechanism has been proposed, and the reaction conditions were carefully investigated. The experimental results revealed that both the ultrasound irradiation and the presence of Na 2 CO 3 in the synthetic process had an impact on the fast formation of the SrSn(OH) 6 nanowires. Moreover, a subsequent precipitations hydrothermal treatment of SrSn(OH) 6 nanowiresswas conducted in ethanol at 180 °C for 8 h in order to improve their crystallinity and thermal stalibity. SrSnO 3 nanorods were converted by calcination of the hydrothermally treated SrSn(OH) 6 nanowires at 700°C for 3 h in air. In particular, it was the attempt to test the electrochemical properties of the SrSnO 3 products as anode in a Li ion battery. The resulting SrSnO 3 nanorods exhibited a better cyclability over 50 cycles with a reversible lithium storage capacity of 200 mA h g−1 than that of SrSnO 3 nanoparticles.

This paper describes a facile solvothermal method to synthesize self-assembled three-dimensional (3D) Ni2+-Fe3+ layered double hydroxides (LDHs) nanocrystals. Flower-like Ni2+-Fe3+ LDHs constructed of thin nanopetals were obtained using ethylene glycol (EG) as a chelating reagent and urea as a hydrolysis agent. The reaction mechanism and self-assembly process are discussed. After calcinating the as-prepared LDHs at 450 °C in nitrogen gas, porous NiO/NiFe 2 O 4 nanosheets were obtained. This work resulted in the development of a simple, cheap, and effective route for the fabrication of large area Ni2+-Fe3+ LDHs as well as porous NiO/NiFe 2 O 4 nanosheets.

In this paper, single-crystalline Ni(SO4)0.3(OH)1.4 nanocrystals could be synthesized on a large scale by a facile hydrothermal treatment without using templates or organic additives. Ammonia concentration played an important role for the composition, phase structure and shape control of the the Ni(SO4)0.3(OH)1.4 nanobelts. Electrochemical measurement revealed that the asprepared Ni(SO4)0.3(OH)1.4 nanobelts exhibited high specific capacity close to the theoretical capacity performance of β-Ni(OH)2. On the other hand, the single-crystalline porous nickel oxide nanobeltsnanobelts can be obtained through calcination of the Ni(SO4)0.3(OH)1.4. nanobelts.

This paper describes a facile solvothermal method to synthesize self-assembled three-dimensional (3D) Ni2+-Fe3+ layered double hydroxides (LDHs). Flower-like Ni2+-Fe3+ LDHs constructed of thin nanopetals were obtained using ethylene glycol (EG) as a chelating reagent and urea as a hydrolysis agent. The reaction mechanism and self-assembly process are discussed. After calcinating the as-prepared LDHs at 450 degrees C in nitrogen gas, porous NiO/NiFe2O4 nanosheets were obtained. This work resulted in the development of a simple, cheap, and effective route for the fabrication of large area Ni2+-Fe3+ LDHs as well as porous NiO/NiFe2O4 nanosheets.