Fe- and Co-doped lanthanum oxides catalysts for ammonia decomposition:Structure and catalytic performances

In this paper, a series of Fe- and Co-doped lanthanum（hydr）oxides catalysts were prepared by a simple coprecipitationhydrothermal method. The as-prepared catalysts were characterized with various techniques including powder X-ray diffraction（XRD）, N2 adsorption/desorption, inductively coupled plasma（ICP） and transmission electron microscopy（TEM）. The Fe-based catalysts exhibited consecutive phase changes of amorphous Fe Ox→FeLaO3→Fe2N under different stages（as-prepared→calcination→ammonia decomposition reaction）; as for Co-based catalysts, the phase transformation followed a sequence of Co（OH）2→Co3O4→metallic Co. It was revealed that Fe2N and metallic Co were most probably the active crystalline phase respectively for Feand Co-based catalysts in the decomposition of ammonia.

High Temperature XPS/AES Investigation of Mo-La_2O_3 Cathodes Ⅱ. Variation of Lanthanum During Activation Processes

The changes of the valence state of lanthanum in the Mo La 2O 3 model cathode specimens were systematically studied by in situ XPS/AES analyses from room temperature to 1550 ℃. The experimental results show that the valence of lanthanum changes during the activation processes. As the temperature increases, the lattice oxygen in La 2O 3 is dissociated, resulting in partial reduction of the lanthanum to LaO x(x <3/2). In addition, the lanthanum rich phase diffuses from bulk into the surface of the sample. The lack of lattice oxygen in this phase has a favorable effect on emission, which leads to a lower work function for the Mo La 2O 3 cathode.

Mechanochemical Reaction of Lanthanum Carbonate with Sodium Hydroxide and Preparation of Lanthanum Oxide Nanoparticle

The preparation of nano sized La 2O 3 powder by mechanochemical reaction of lanthanum carbonate with sodium hydroxide and subsequent heat treatment was studied using X ray diffraction, differential thermal and thermo gravimetric analysis and transmission electron microscopy. It was found that the mechanochemical reaction process can be divided into two steps: the first step is the multi phases mechanochemical reaction of lanthanum carbonate with NaOH to form amorphous lanthanum basic carbonate and lanthanum hydroxide, and the second step is the crystallization of basic lanthanum carbonate with the formula of La 2(OH) 2(CO 3) 2·H 2O under a quasi hydrothermal synthesis condition caused by the mechanical ball milling. The synthesized La 2O 3 powder appears clearly separated spherical like monodisperse nano size particles in which particle size ranges from 30 to 50 nm.

Hydrogen production via autothermal reforming of ethanol over noble metal catalysts supported on oxides

Hydrogen was produced over noble metal（Ir, Ru, Rh, Pd） catalysts supported on various oxides, including γ-Al2O3, CeO2, ZrO2 and La2O3, via the autothermal reforming reaction of ethanol （ATRE） and oxidative reforming reaction of ethanol （OSRE）. The conversion of ethanol and selectivites for hydrogen and byproducts such as methane, ethylene and acetaldehyde were studied. It was found that lanthana alone possessed considerable activity for the ATRE reaction, which could be used as a functional support for ATRE catalysts. It was demonstrated that Ir/La2O3 prevented the formation of methane, and Rh/La2O3 encumbered the production of ethylene and acetaldehyde. ATRE reaction was carried out over La2O3-supported catalysts （Ir/La2O3） with good stability on stream, high conversion, and excellent hydrogen selectivity approaching thermodynamic limit under autothermal condition. Typically, 3.4H2 molecules can be extracted from a pair of ethanol and water molecules over Ir（5wt%）/La2O3. The results presented in this paper indicate that Ir/La2O3 can be used as a promising catalyst for hydrogen production via ATRE reaction from renewable ethanol.

Preparation of Lanthanum Nickel Oxide-Coated Ni Sheet Anodes and Their Application to Electrolytic Production of (CF_3)_3N in (CH_3)_4NF·4.0HF Melt

A new process for electrolytic production of a perfluorinated compound, （CF3）3N, using lanthanum nickel oxide-coated Ni sheet anode in the （CH3）4NF· 4.0HF melt at room temperature, was developed. Thin films of the lanthanum nickel oxides were prepared on Ni sheets by sol-gel coating method using polyvinlylpyrrolidone（PVP）. The main components of the thin films were La2O3, LaNiO3, and La2NiO4 at 500, 750 and 1000℃, respectively. The anode performance in the （CH3）4NF·4.0HF melt depends greatly on the main component of the thin film, and the LaNiO3-coated Ni sheet anode gives the best anode performance. The potential of LaNiO3-coated Ni sheet anode remains constant at 5.9 V during electrolysis at 20 mA·cm^-2 in the （CH3）4NF·4.0HF melt for 100 h. This is because LaNiO3 and NiF3 and/or Ni2F5, the latter of which was formed during electrolysis, in the film give a high electronic conductivity to the surface film during electrolysis. The maximum mole fraction of （CF3）3N （21.4%） was obtained at 20 mA·cm^-2 in （CH3）4NF·4.0HF melt using the LaNiO3-coated Ni sheet.

Determination of Non-Rare Earth Impurities in High Purity Lanthanum Oxide by Inductively Coupled Plasma Atomic Emission Spectrometry after HPLC Separation Using P507 Resin

A new method for the determination of trace non-rare earth elements (NREEs) impurities in high-purity lanthanum oxide by HPLC combined with ICP-AES is proposed. The chromatographic retention behaviors of matrix (La) and NREEs were studied using 2-ethylhexyl hydrogen 2-ethylhexyl phosphonate (P507) chelating resin as the stationary phase and dilute nitric acid as the mobile phase. It is found that the use of pH 1.7 nitric acid enables effective elution of NREEs from HPLC column, but the lanthanum remains on the column. The experimental results show that a favorable separation between matrix lanthanum and NREEs can be obtained within 15 min. The method proposed is applied to the determination of 8 NREEs impurities in high-purity La2O3. The recoveries of 8 NREEs are in the range of 90 % similar to 110 %.

Direct Determination of Trace Silicon in Lanthanum Oxide by Using a Selective Volatility and Slurry Sampling-FETV-ICP-AES

A new method for determination of trace silicon in high purity lanthanum oxide by using electrothermal vaporization (ETV) ICP AES with polytetrafluoroethylene(PTFE) slurry as a fluorinating reagent has been proposed. Under the optimized experimental conditions, the fluorination reactions of analyte(Si) and matrix(La) with PTFE in the graphite furnace took place at high temperature, and the fractional volatilily between Si and La was observed. Based on this principle the matrix interference could be eliminated. The detection limit of Si was 4.0 μg·L -1 , and the RSD was 3.4%( C =0.2 mg·L -1 , n =10). The procedure proposed has been applied successfully to determine trace Si in La 2O 3 without any chemical pre treatment.

Spectral properties of Ce^(3+) doped yttrium lanthanum oxide transparent ceramics

Ce3＋-doped yttrium lanthanum oxide （Y0.9La0.1）2O3 transparent ceramics is fabricated with nanopowders and sintered in H2 atmosphere. The spectral properties of Ce：（Y0.9La0.1）2O3 transparent ceramics are investigated. There appear two characteristic absorption peaks of Ce3＋ ions at 230~nm and 400~nm, separately. It is found that Ce3＋ ions can efficiently produce emission at 384~nm from （Y0.9La0.1）2O3 transparent ceramic host, while the emission is completely quenched in Re2O3 （Re=Y, Lu, La） host materials.

Comparison of toxicity between lanthanum oxide nanoparticles and lanthanum chloride

Due to the wide application of rare earth elements,lanthanum(La) is gradually accumulated in our living environment.Lanthanum can enter the body through a variety of routes,which has a series of effects on various systems.As a consequence,the safety of lanthanum deserves our attention.This study aims to compare the toxicity of lanthanum oxide nanoparticles(La_(2)O_(3) NPs) and lanthanum chloride(LaCl_(3)) and enrich the toxicity evaluation of lanthanum.Therefore,a 30 d intragastal experiment was conducted.C57BL/6j mice were given by La_(2)O_(3) NPs solution and LaCl_(3) solution respectively at doses of 0,30,60 and120 mg/kg BW(lanthanum content).The results show that,compared with the control group,both La_(2)O_(3)NPs and LaCl_(3) can reduce the body weight of female mice in the high-dose group,but for male mice,the high-dose La_(2)O_(3) NPs solution can increase the body weight,while LaCl_(3) has the opposite effect.The coefficients of liver,kidney,heart,lung,uterine and ovaries increase first and then decrease with the exposure dose,but testes and epididymides coefficient keep increasing with the exposure of LaCl_(3) and La_(2)O_(3) NPs.La_(2)O_(3) NPs and LaCl_(3) can reduce the concentration of triglycerides(TG) and increase the level of low density lipoprotein(LDL),but the effect of La_(2)O_(3) NPs is more obvious.La_(2)O_(3) NPs and LaCl_(3) can reduce the concentration of malondialdehyde(MDA),increase the total antioxidant capacity(T-AOC)and enhance the activity of catalase(CAT),but LaCl_(3) has more obvious protective effects on oxidative stress.La_(2)O_(3) NPs and LaCl_(3) have potential risks to liver,and the toxicity of La_(2)O_(3) NPs might be higher than that of LaCl_(3).

High Temperature XPS/AES Investigation of Mo-La_2O_3 Cathode-Ⅰ. Species and Properties of Oxygen on Surface

In situ activation process of Mo-La2O3 prototype cathode at high temperature was systematically investigated by XPS/AES. The oxygen species produced during the process were characterized at different temperatures. The results show that there exist two kinds of oxygen ions at above 1300 ℃, the lattice oxygen with lower binding energy(Eb=530.00 eV) should be dissociated from the lattice oxygen of La2O3. It may be concluded that La2O3 was partly reduced to LaOx(x<3/2) due to the dissociation of lattice oxygen. And the oxygen may play a favorable or an unfavorable role in emission depending upon its relative quantity and position in the surface layer.

Microstructure modification by La_2O_3 and its effect on wear resistance properties of as-cast ZL107 alloy

Modification of ZL107 aluminum alloy has been successfully achieved by using La2O3. The different casting parameters, including casting temperature as well as holding time and modifier content, were carried out to investigate the modification effects. The results show that the best modifier content is 1.0 wt.%, and the casting temperature has little effect. In addition, the wear behavior of modified and unmodified ZL 107 has been compared. The wear resistance of as-cast ZL 107 aluminum alloy can be significantly improved after modification.

Carbon dioxide reforming of methane on monolithic Ni/Al_2O_3-based catalysts

Nickel-alumina catalysts supported on cordierite monoliths of honeycomb structure surpass essentially the conventional granulated ones with respect to the output in carbon dioxide reforming of methane. Adjusting the surface acid-base properties of catalysts by introduction of alkali metal （Na, K） oxides inhibits the carbonization and as a result, improves the operational stability of these catalysts. An effect of promotion of nickel-alumina based composite doped by lanthanum oxide is found. This effect, caused by an additional route for the CO2 activation on Ni-La2O3/Al2O3/cordierite catalyst, is displayed in increase of methane conversion under conditions of an oxidant excess.

High Temperature Chemical Reaction of La_2O_3 in H_3BO_3-C System

The high temperature chemical reaction process of La2O3 in H3BO3-C system was studied by means of XRD and TG-DTA.The results showed that dehydration reaction of H3BO3 occurred in the temperature range of 82～390 ℃;La2O3 and B2O3 reacted to form LaB3O6,LaBO3,and B4C in the temperature range of 836～1400℃;at 1450 ℃,B4C and LaBO3 further reacted to form LaB4,and partial LaB4 and B reacted to form LaB6;at 1500 ℃,LaB4 and B reacting into LaB6 was the main reaction,and the content of LaB6 increased with prolonging time.

CH_4 reforming with CO_2 for syngas production over La_2O_3 promoted Ni catalysts supported on mesoporous nanostructured γ-Al_2O_3

Nanostructured -y-A12O3 with high surface area and mesoporous structure was synthesized by sol-gel method and employed as catalyst support for nickel catalysts in methane reforming with carbon dioxide. The prepared samples were characterized by XRD, N2 adsorption-desorption, TPR, TPO, TPH, NH3-TPD and SEM techniques. The BET analysis showed a high surface area of 204 m2.g-1 and a narrow pore-size distribution centered at a diameter of 5.5 nm for catalyst support. The BET results revealed that addition of lanthanum oxide to aluminum oxide decreased the specific surface area. In addition, TPR results showed that addition of lanthanum oxide increased the reducibility of nickel catalyst. The catalytic evaluation results showed an increase in methane conversion with increasing lanthanum oxide to 3 mol% and further increase in lanthanum content decreased the catalytic activity. TPO analysis revealed that the coke deposition decreased with increasing lanthanum oxide to 3 mol%. SEM and TPH analyses confirmed the formation of whisker type carbon over the spent catalysts. Addition of steam and Oxide to drv reformin feed increased the methane conversion and led to carbon free ooeration in combined orocesses.

Investigation on the thermal decomposition of aged La_2O_3

The thermal decomposition process of air-aged La203 in argon atmosphere was studied using nonisothermal TG-DSC. X-ray diffraction and TG-DSC analysis showed that the aged powder was composed of La（OH）3 with small amounts of oxycarbonate. The decomposition process of air-aged La2O3 involves the two-step decomposition of La（OH）3 and the decomposition of oxycarbonate. The kinetic analysis of the two-step decomposition of La（OH）3 was carried out using Coats-Redfern and isoconversion （Ozawa） methods. The kinetics of the two-step decomposition can be described in terms of the nucleation and growth model A （m=1.5, m is the model parameter） and A （m=2.5）, respectively. The apparent activation energy for the first step is 136-144 （Coats-Redfern） and 137-164 kJ/mol （isoconversion）. The apparent activation energy for the second step is 191-194 （Coats-Redfern） and 186-213 kJ/mol （isoconversion）.

Effect of La2O3 Addition on Sintering Properties of Magnesia

Light burned magnesia powders with different particle sizes were obtained by calcining crystalline magnesite.Sintered magnesia was prepared from the light burned magnesia powders by adding different amounts of La2O3.The effect of the La2O3 addition on the densification of magnesia was studied.The results show that the densification of sintered magnesia can be promoted both by reducing the particle size of the light burned powder and by adding small amounts of La2O3.The effect of the La2O3 addition is more significant:the maximum bulk density of the sintered magnesia can reach 3.49 g·cm-3 and the apparent porosity can be reduced to 0.33%.During sintering,Ca2+from the impurities enters La2O3 lattices,causing lattice distortion of La2O3 thus promoting the formation of La4.67(SiO4)3O phase and CaLa4(SiO4)3O phase,which fill the pores between the MgO grains and promote the densification of sintered magnesia.

Performance of La203/InA1N/GaN metal-oxide-semiconductor high electron mobility transistors

We report on the performance of La203/InA1N/GaN metal-oxide-semiconductor high electron mobility transistors （MOSHEMTs） and InA1N/GaN high electron mobility transistors （HEMTs）. The MOSHEMT presents a maximum drain current of 961 mA/mm at Vgs = 4 V and a maximum transconductance of 130 mS/mm compared with 710 mA/mm at Vgs = 1 V and 131 mS/mm for the HEMT device, while the gate leakage current in the reverse direction could be reduced by four orders of magnitude. Compared with the HEMT device of a similar geometry, MOSHEMT presents a large gate voltage swing and negligible current collapse.

Kinetics of Carbothermic Reduction of MnO_2 and Catalytic Effect of La_2O_3

Kinetics of carbothermic reduction of manganese oxide and the catalyticeffect of La_2O_3 on the reduction have been studied by the measurement of mass loss in N_2atmosphere at different temperatures and followed by SEM analysis. It is concluded that the kineticsof carbothermic reduction of manganese oxide is divided into three stages: gas diffusioncontrolling stage, carbon gasification con-trolling stage and solid state diffusion controllingstage. La_2O_3 has catalytic effect on the reduction. The catalytic effect of La_2O_3 increases withthe added amount of La_2O_3. SEM analysis shows that the catalytic mechanism is that La_2O_3promotes the transfer of oxygen ions so that carbon gasifying is catalyzed and thus carbothermicreduction of MnO_2 is catalyzed.

Preparation and Characterization of La<SUB>2</SUB>O<SUB>3</SUB>Doped Ba<SUB>0.3</SUB>Sr<SUB>0.7</SUB>TiO<SUB>3</SUB>Perovskite Ceramics of Varied Sintering Temperature and Doping

In order to explore new application opportunities of Barium Strontium Titanate (BST) ceramic composite by modifying the conventional ferroelectric properties of BST through La2O3 doping in BST matrix sintered at different temperature was investigated in this current study. Unadulterated Ba0.3Sr0.7TiO3 (BST) matrix was prepared from BaTiO3 (99.95%) and SrTiO3 (99.95%) taken in stoichiometric extents which later doped by La2O3 (99.99%) in varying extents (0.05 g, 0.10 g and 0.15 g) exploiting solid state reaction route. Doping caused drag effect for the penetration of impurities and sintering temperature helped the impurities migration to BST. Dielectric constant gets lower with rising of frequency, as electrons do not get enough time to polarize at high frequency. Dielectric constant and conductance are found maximum for the sample (0.1 g La2O3 doped BST) sintered at 1460°C and reverse is found in impedance analysis. These electrical properties showed visible frequency dependent response irrespective of sintering temperature and doping.

Dependence of spectroscopic properties on doping content and temperature of bismuth-doped lanthanum aluminosilicate glass

The effects of bismuth doping content and temperature on the absorption property and near-infrared （NIR） luminescence of Bi-doped La2O3-Al2O3-SiO2 （LAS） glasses are presented. The emission intensity reaches the maximum when the Bi2O3 content in 3.0Bi-LAS is 1.83%. The emission spectra reach their peaks at 1 190 and 1 117 nm, with full-width at half-maximum （FWHM） values of 330 and 228 nm under 500 and 700-nm excitations, respectively. As the Bi203 content increases, the peak wavelengths and FWHMs of emission bands increase, but their lifetimes decrease. The lifetime of 2.0Bi-LAS is 460 μs at 9 K, and is almost temperature independent until 350 K. The NIR emission of Bi in the system has strong resistance to thermal quenching from 9 to 350 K.