Side-by-Side In(OH)<Subscript>3</Subscript> and In<Subscript>2</Subscript>O<Subscript>3</Subscript> Nanotubes: Synthesis and Optical Properties

A simple and mild wet-chemical approach was developed for the synthesis of one-dimensional (1D) In(OH)₃ nanostructures. By calcining the 1D In(OH)₃ nanocrystals in air at 250 °C, 1D In₂O₃ nanocrystals with the same morphology were obtained. TEM results show that both 1D In(OH)₃ and 1D In₂O₃ are composed of uniform nanotube bundles. SAED and XRD patterns indicate that 1D In(OH)₃ and 1D In₂O₃ nanostructures are single crystalline and possess the same bcc crystalline structure as the bulk In(OH)₃ and In₂O₃, respectively. TGA/DTA analyses of the precursor In(OH)₃ and the final product In₂O₃ confirm the existence of CTAB molecules, and its content is about 6%. The optical absorption band edge of 1D In₂O₃ exhibits an evident blueshift with respect to that of the commercial In₂O₃ powders, which is caused by the increasing energy gap resulted from decreasing the grain size. A relatively strong and broad purple-blue emission band centered at 440 nm was observed in the room temperature PL spectrum of 1D In₂O₃ nanotube bundles, which was mainly attributed to the existence of the oxygen vacancies.     

Mechanism of formation of the complex oxide Na<Subscript>2</Subscript>Nd<Subscript>2</Subscript>Ti<Subscript>3</Subscript>O<Subscript>10</Subscript>

The processes of phase formation in the Nd₂O₃-TiO₂-Na₂CO₃ system have been investigated in the temperature range 500–1100°C. The mechanism of the high-temperature solid-phase reaction of formation of the complex oxide Na₂Nd₂Ti₃O₁₀ has been studied. It has been established that the Na₂Nd₂Ti₃O₁₀ compound is formed from the intermediate product Na_0.5Nd_0.5TiO₃ with a perovskite structure in the temperature range 830–890°C and from the NaNdTiO₄ oxide with a perovskite-like layered structure in the temperature range 960–1100°C.     

Synthesis of Submicron Nanocrystalline Y<Subscript>2</Subscript>O<Subscript>3</Subscript>: Eu Particles via Solvothermal Approach Using Surface Modifiers

In this paper, solvothermal synthesis of submicron nanocrystalline Y₂O₃: Eu particles with and without surface modifier (β-alanine and Tween-80) is investigated. X-ray diffraction ananlysis confirms the one-step formation of Y₂(OH)₅NO₃H₂O phase during solvothermal process and its conversion to Y₂O₃: Eu after heat treatment at 600 °C. Fourier transformation infrared spectroscopy showed that C=C, C–C and C–H peaks are corresponded to the surface modifiers i.e. tween-80 and β-alanine. Scanning electron microscopy and transmission electron microscopy images also showed that the modifier results in the particle morphology improvement from sheet-like to submicron spherical particles. Photoluminescence experiments indicated that the emission intensity increases due to the morphology modification.     

Synthesis and optical property of one-dimensional spinel ZnMn<Subscript>2</Subscript>O<Subscript>4</Subscript> nanorods

Spinel zinc manganese oxide (ZnMn₂O₄) nanorods were successfully prepared using the previously synthesized α-MnO₂ nanorods by a hydrothermal method as template. The nanorods were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, UV-Vis absorption, X-ray photoelectron spectroscopy, surface photovoltage spectroscopy, and Fourier transform infrared spectroscopy. The ZnMn₂O₄ nanorods in well-formed crystallinity and phase purity appeared with the width in 50-100 nm and the length in 1.5-2 μm. They exhibited strong absorption below 500 nm with the threshold edges around 700 nm. A significant photovoltage response in the region below 400 nm could be observed for the nanorods calcined at 650 and 800°C.     

Synthesis and characterization of zeolite mazzite analogue in Na<Subscript>2</Subscript>O–Al<Subscript>2</Subscript>O<Subscript>3</Subscript>–SiO<Subscript>2</Subscript>–Piperazine–H<Subscript>2</Subscript>O

Zeolite Mazzite (MAZ) analogue was synthesized directly using piperazine as a structure directing agent. The reactive gel composition used was (5.0–7.0) piperazine:(6.0–7.0) Na₂O:Al₂O₃:20.0SiO₂:400H₂O. Using this composition, the reaction time was shortened greatly to 4 days and the crystallization time was reduced as well. The DTA data showed that piperazine, in as-synthesized zeolite omega decomposed easily. The decomposition of the piperazine occurred at 400–480°C. NH₃-TPD analysis proved that zeolite H-omega from piperazine had strong surface acidity with ammonia desorption temperature up to 590°C.     

Low-temperature anti-icing reagents in the Ca(NO<Subscript>3</Subscript>)<Subscript>2</Subscript>-Mg(NO<Subscript>3</Subscript>)<Subscript>2</Subscript>-CO(NH<Subscript>2</Subscript>)<Subscript>2</Subscript>-H<Subscript>2</Subscript>O system and their properties

The polytherms of ice melting in sections of the Ca(NO₃)₂-Mg(NO₃)₂-CO(NH₂)₂-H₂O system with different component ratios were studied in the temperature interval from 0 to −40°C. A series of nitrate and nitrate-carbonate reagents that are promising for the creation of anti-acing reagents were found, which form eutectics with ice at temperatures from −25 to −39°C. Their properties, viz., melting properties with respect to ice and corrosiveness on metals and alloys, were determined. An effective corrosion inhibitor was selected.     

Influence of operating temperature on CO<Subscript>2</Subscript>-NH<Subscript>3</Subscript> reaction in an aqueous solution

Although aqueous ammonia solution has been focused on the removal of CO₂ from flue gas, there have been very few reports regarding the underlying analysis of the reaction between CO₂ and NH₃. In this work, we explored the reaction of CO₂-NH₃-H₂O system at various operating temperatures: 40 °C, 20 °C, and 5 °C. The CO₂ removal efficiency and the loss of ammonia were influenced by the operating temperatures. Also, infrared spectroscopy measurement was used in order to understand the formation mechanism of ion species in absorbent, such as NH₂COO⁻, HCO₃⁻, CO₃²⁻, and NH₄⁺, during CO₂, NH₃, and H₂O reaction. The reactions of CO₂-NH₃-H₂O system at 20 °C and 40 °C have similar reaction routes. However, a different reaction route was observed at 5 °C compared to the other operating temperatures, showing the solid products of ammonium bicarbonates, relatively. The CO₂ removal efficiency and the formation of carbamate and bicarbonate were strongly influenced by the operating temperatures. In particular, the analysis of the formation carbamate and bicarbonate by infrared spectroscopy measurement provides useful information on the reaction mechanism of CO₂ in an aqueous ammonia solution.     

The nitridation of ZnO nanowires

ZnO nanowires (NWs) with diameters of 50 to 250 nm and lengths of several micrometres have been grown by reactive vapour transport via the reaction of Zn with oxygen on 1 nm Au/Si(001) at 550°C under an inert flow of Ar. These exhibited clear peaks in the X-ray diffraction corresponding to the hexagonal wurtzite crystal structure of ZnO and a photoluminescence spectrum with a peak at 3.3 eV corresponding to band edge emission close to 3.2 eV determined from the abrupt onset in the absorption-transmission through ZnO NWs grown on 0.5 nm Au/quartz. We find that the post growth nitridation of ZnO NWs under a steady flow of NH₃ at temperatures ≤600°C promotes the formation of a ZnO/Zn₃N₂ core-shell structure as suggested by the suppression of the peaks related to ZnO and the emergence of new ones corresponding to the cubic crystal structure of Zn₃N₂ while maintaining their integrity. Higher temperatures lead to the complete elimination of the ZnO NWs. We discuss the effect of nitridation time, flow of NH₃, ramp rate and hydrogen on the conversion and propose a mechanism for the nitridation.     

Facile synthesis and high rate capability of Li<Subscript>4</Subscript>Ti<Subscript>5</Subscript>O<Subscript>12</Subscript>/C composite materials with controllable carbon content

A modified ball-milling-assisted green solid reaction method is provided to prepare Li₄Ti₅O₁₂/C composite materials with controllable carbon content. Thermal analysis was utilized to investigate the reaction process and the temperature for eliminating carbon. The added carbon and the time for eliminating the carbon can affect the particle size and greatly improve the cycling stability and rate performance. Besides, the particle size can reach ~60 nm, the Li₄Ti₅O₁₂ eliminated carbon at 600 °C has ~178% higher discharge capacity than that without added carbon after 500 cycles under the same conditions. As for the Li₄Ti₅O₁₂ with a carbon weight of 10.6%, the second discharge capacity can reach 177.2 and 120.8 mAh g⁻¹ at 1 and 20 C rates, respectively. Its discharge capacity still remains at 118.3 mAh g⁻¹ after 500 cycles under various current rates. The results are comparable to those of the reported Li₄Ti₅O₁₂/PAS composite.     

Temperature programmed desorption of oxygen from Pd films interfaced with Y<Subscript>2</Subscript>O<Subscript>3</Subscript>-doped ZrO<Subscript>2</Subscript>

The origin of the effect of non-faradaic electrochemical modification of catalytic activity (NEMCA) or Electrochemical Promotion was investigated via temperature-programmed-desorption (TPD) of oxygen, from polycrystalline Pd films deposited on 8 mol%Y₂O₃–stabilized–ZrO₂ (YSZ), an O²⁻ conductor, under high-vacuum conditions and temperatures between 50 and 250 °C. Oxygen was adsorbed both via the gas phase and electrochemically, as O²⁻, via electrical current application between the Pd catalyst film and a Au counter electrode. Gaseous oxygen adsorption gives two adsorbed atomic oxygen species desorbing at about 300 °C (state β₁) and 340–500 °C (state β₂). The creation of the low temperature peak is favored at high exposure times (exposure >1 kL) and low adsorption temperatures (T_ads < 200 °C). The decrease of the open circuit potential (or catalyst work function) during the adsorption at high exposure times, indicates the formation of subsurface oxygen species which desorbs at higher temperatures (above 450 °C). The desorption peak of this subsurface oxygen is not clear due to the wide peaks of the TPD spectra. The TPD spectra after electrochemical O²⁻ pumping to the Pd catalyst film show two peaks (at 350 and 430 °C) corresponding to spillover O_ads and according to the reaction:

Study on the properties of Bi<Subscript>2</Subscript>O<Subscript>3</Subscript>-B<Subscript>2</Subscript>O<Subscript>3</Subscript>-BaO lead-free glass using in the electronic pastes

The Sb₂O₃ doping lead-free glass in Bi₂O₃-B₂O₃-BaO ternary system were prepared in the composition of several different subsystem, and the glass powder was produced through the process of water quenching. Glass transition temperatures (T _g ), glass soften temperatures(T _s ), the volume resistivity (ρ) in the temperature range of 80–200°C, and linear thermal coefficients of expansion in the temperatures range of 25–300°C (α_25–300) were measured for subsystems along with the different ratio of Bi₂O₃, B₂O₃ and BaO. For these subsystems, T _g ranged from 458 to 481°C, and T _s ranged from 490 to 512°C, both decreasing with the increasing of Bi₂O₃/B₂O₃ ratio, and increasing with the increasing of BaO/B₂O₃ ratio. The measured α_25–300 ranged from 65.3 to 76.3 × 10⁻⁷ K⁻¹, with values increasing with increasing Bi₂O₃/B₂O₃ and BaO/B₂O₃ ratio. The volume resistivity remains at a high standards, which may caused by it’s non-alkali composition, and it fluctuated from 10¹³ to 10¹¹ Ω cm with the temperature varied from 80–200°C. The structure of Bi₂O₃-B₂O₃-BaO ternary leadfree glass system was mearsured by FT-IR. The IR studies indicate that these glasses are made up of [BiO₆], [BO₃], and [BO₄] basic structural units, and it appears that Ba²⁺ acts as a glass-modifier in this ternary system, but the Bi³⁺ has entered the glass network when it is in relative high content so as to change the α_25–300, T _s and T _g .     

Sol-gel synthesis and features of the structure of Au-In<Subscript>2</Subscript>O<Subscript>3</Subscript> nanocomposites

The specific features of the chemical state of gold and indium oxide in Au-In₂O₃ (0.01–1.0 wt % Au) nanocomposites have been investigated by the methods of X-ray diffraction analysis, electron microscopy, infrared and optical spectroscopy, electron paramagnetic resonance, and thermal analysis. Xerogels, powders, and films obtained by the introduction of HAuCl₄ into the indium hydroxide sol and thermal treatment at 50–700°C have been studied. The mutual influence of the components on the size of the Au and In₂O₃ particles and the state of their surface has been established. It has been shown that the synthesis of Au-In₂O₃ by the sol-gel method leads to the formation of nanosized indium oxide particles with the high concentration of hydroxyl groups on surfaces and favors the stabilization of gold in the form of nanoclusters and ion forms.     

Preparation and characterization of spindle-like Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> mesoporous nanoparticles

Magnetic spindle-like Fe₃O₄ mesoporous nanoparticles with a length of 200 nm and diameter of 60 nm were successfully synthesized by reducing the spindle-like α-Fe₂O₃ NPs which were prepared by forced hydrolysis method. The obtained samples were characterized by transmission electron microscopy, powder X-ray diffraction, attenuated total reflection fourier transform infrared spectroscopy, field emission scanning electron microscopy, vibrating sample magnetometer, and nitrogen adsorption-desorption analysis techniques. The results show that α-Fe₂O₃ phase transformed into Fe₃O₄ phase after annealing in hydrogen atmosphere at 350°C. The as-prepared spindle-like Fe₃O₄ mesoporous NPs possess high Brunauer-Emmett-Teller (BET) surface area up to ca. 7.9 m² g^-1. In addition, the Fe₃O₄ NPs present higher saturation magnetization (85.2 emu g^-1) and excellent magnetic response behaviors, which have great potential applications in magnetic separation technology.     

Effect of annealing treatments on photoluminescence and charge storage mechanism in silicon-rich SiN<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>:H films

In this study, a wide range of a-SiN _x :H films with an excess of silicon (20 to 50%) were prepared with an electron-cyclotron resonance plasma-enhanced chemical vapor deposition system under the flows of NH₃ and SiH₄. The silicon-rich a-SiN _x :H films (SRSN) were sandwiched between a bottom thermal SiO₂ and a top Si₃N₄ layer, and subsequently annealed within the temperature range of 500-1100°C in N₂ to study the effect of annealing temperature on light-emitting and charge storage properties. A strong visible photoluminescence (PL) at room temperature has been observed for the as-deposited SRSN films as well as for films annealed up to 1100°C. The possible origins of the PL are briefly discussed. The authors have succeeded in the formation of amorphous Si quantum dots with an average size of about 3 to 3.6 nm by varying excess amount of Si and annealing temperature. Electrical properties have been investigated on Al/Si₃N₄/SRSN/SiO₂/Si structures by capacitance-voltage and conductance-voltage analysis techniques. A significant memory window of 4.45 V was obtained at a low operating voltage of ± 8 V for the sample containing 25% excess silicon and annealed at 1000°C, indicating its utility in low-power memory devices.     

Visible light-irradiated degradation of alachlor on Fe-TiO<Subscript>2</Subscript> with assistance of H<Subscript>2</Subscript>O<Subscript>2</Subscript>

0.1 Fe/Ti mole ratio of Fe-TiO₂ catalysts were synthesized via solvothermal method and calcined at various temperatures: 300, 400, and 500 °C. The calcined catalysts were characterized by XRD, N₂-adsorption-desorption, UV-DRS, XRF, and Zeta potential and tested for photocatalytic degradation of alachlor under visible light. The calcined catalysts consisted only of anatase phase. The BET specific surface area decreased with the calcination temperatures. The doping Fe ion induced a red shift of absorption capacity from UV to the visible region. The Fe-TiO₂ calcined at 400 °C showed the highest photocatalytic activity on degradation of alachlor with assistance of 30 mM H₂O₂ at pH 3 under visible light irradiation. The degradation fitted well with Langmuir-Hinshelwood model that gave adsorption coefficient and the reaction rate constant of 0.683 L mg⁻¹ and 0.136 mg/L·min, respectively.     

Growth of In2O3 Nanowires Catalyzed by Cu via a Solid–Liquid–Solid Mechanism

In₂O₃ nanowires that are 10–50 nm in diameter and several hundred nanometers to micrometers in length have been synthesized by simply annealing Cu–In compound at a relatively low temperature of 550°C. The catalysis of Cu on the growth of In₂O₃ nanowires is investigated. It is believed that the growth of In₂O₃ nanowires is via a solid–liquid–solid (SLS) mechanism. Moreover, photoluminescence (PL) peaks of In₂O₃ nanowires at 412 and 523 nm were observed at room temperature, and their mechanism is also discussed.     

Regeneration of Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>-based high-temperature coal gas desulfurization sorbent in atmosphere with sulfur dioxide

Regeneration of a high-temperature coal gas desulfurization sorbent is a key technology in its industrial applications. A Fe₂O₃-based high-temperature coal gas desulfurizer was prepared using red mud from steel factory. The influences of regeneration temperature, space velocity and regeneration gas concentration in SO₂ atmosphere on regeneration performances of the desulfurization sorbent were tested in a fixed bed reactor. The changes of phase and the composition of the Fe₂O₃-based high-temperature coal gas desulfurization sorbent before and after regeneration were examined by X-ray diffraction (XRD) and X-ray Photoelectron spectroscopy(XPS), and the changes of pore structure were characterized by the mercury intrusion method. The results show that the major products are Fe₃O₄ and elemental sulfur; the influences of regeneration temperature, space velocity and SO₂ concentration in inlet on regeneration performances and the changes of pore structure of the desulfurization sorbent before and after regeneration are visible. The desulfurization sorbent cannot be regenerated at 500°C in SO₂ atmosphere. Within the range of 600°C–800°C, the time of regeneration becomes shorter, and the regeneration conversion increases as the temperature rises. The time of regeneration also becomes shorter, and the elemental sulfur content of tail gas increases as the SO₂ concentration in inlet is increased. The increase in space velocity enhances the reactive course; the best VSP is 6000 h^?1 for regeneration conversion. At 800°C, 20 vol-% SO₂ and 6000 h^?1, the regeneration conversion can reach nearly to 90%.     

Synthesis and properties of the composite ceramics from nanocrystalline Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-30% Y<Subscript>0.1</Subscript>Zr<Subscript>0.9</Subscript>O<Subscript>2</Subscript> prepared from a water-alcohol solution

The hydrogel of the mixed oxide Al₂O₃-30% Y_0.1Zr_0.9O₂ was prepared by precipitation of ammonia from a water-alcohol mixture (1 : 5). The Al₂O₃-30% Y_0.1Zr_0.9O₂ compound thus synthesized was characterized using differential scanning calorimetry, transmission electron microscopy, and the BET adsorption method. The obtained sample consisted of spherical particles with an average size of 16–20 nm and a specific surface area of 167 m²/g. The Al₂O₃-30% Y_0.1Zr_0.9O₂ powder was pressed at 300 MPa and then calcinated at 1600°C for 2 h in air. The topographic and structural features of the prepared ceramics were determined using atomic force microscopy and X-ray electron probe microanalysis. The porosity, the Vickers microhardness, and the tensile strength were determined by mercury porometry.     

Thermomechanical properties of refractory materials of AL<Subscript>2</Subscript>O<Subscript>3</Subscript>–Si<Subscript>3</Subscript>N<Subscript>4</Subscript>–C compositions based on acpb after impregnation with a sol-gel composition

Comparative characteristics are presented for the physicomechanical properties and oxidation resistance of refractory materials of Al₂O₃–Si₃N₄–C composition based on an ACPB for the original materials (fired at 1400°C) and after impregnation with a sol-gel composition and heat treatment at 800°C. Areduction in material porosity, increase in strength and reduction in carbon burn-off are due to development of a glassy phase in the pore space and on graphite flakes due to SiO₂formation with thermal destruction of the organosilicon substance.     

Preparation of CuO-CeO<Subscript>2</Subscript>-Al<Subscript>2</Subscript>O<Subscript>3</Subscript> catalyst with mesopore structure for water gas shift reaction

The water gas shift (WGS) reaction has been investigated widely in fuel cell technologies due to the potential for high fuel efficiency and lower emissions during the production of pure hydrogen. Industrially, the WGS reaction occurs in one of the following two ways: (a) high-temperature in the range of 310–450°C with Fe-Cr catalyst, (b) low-temperature in the range of 210–250°C with Cu-ZnO-Al₂O₃. In this study, a mesoporous catalyst was prepared, with a large surface area and uniformity in both pore size and distribution, by using a one-pot synthesis method. The prepared CuO-CeO₂-Al₂O₃ brought high CO conversion (82%), and was suitable for WGS reaction at low temperature (250 °C). This article is dedicated to Professor Chang Kyun Choi for celebrating his retirement from the School of Chemical and Biological Engineering, Seoul National University.