Ozone Generator with Cylindrical Type of Rotating Electrode

An ozone generator using a rotating electrode to improve ozone generation efficiency is proposed. The ozone generator electrode unit consists of a rotating electrode and fixed electrode. The rotating electrode has the grounded 36 pieces of tungsten wires fixed in parallel to the rotation axis on the rotating cylinder surface. A dielectric electrode is used as a fixed electrode located on the inside of the tube of the electrode unit. The width of the apparent discharge gap is 1mm. Alternating current with a frequency of 50 Hz is applied to the electrode unit. The rotation speed can be adjusted from 0 rpm to 1200 rpm by a variable speed motor. Oxygen gas is used as the material gas. Higher ozone concentration and higher ozone generation efficiency are obtained compared with that when the rotation speed is 0 rpm. The gas temperature is measured at the inlet and outlet of the ozone generator, and the rotation speed for the cooling effect is most effective at about 500 rpm. The maximum generation efficiency is estimated to be 61 g/kWh at 800 rpm, and this value is twice as large as in the case of 0 rpm.     

Theoretical Study of the Ozone Production and NOx Molecules Processing in N2/O2 Pulsed Discharge

Environmental decontamination is a major challenge due to the rapid growth of industrial and technological development, requiring an important consumption of fossil energies. Nowadays, a new way to treat polluting molecules based on the use of nonequilibrium reactive plasmas, is under development. These plasmas are generated by electrical discharges at atmospheric pressure, for neutralizing or transforming the toxic oxides. In this respect, the goal of the present work is to analyze the possibilities of treatment of NO_x molecules and ozone generation by pulsed discharge. The study was carried out by using a one-dimensional model based on the parallel resistor network concept, consisting in dividing the discharge volume into plasma elements which are connected in no way but through their contribution to the total resistance of the plasma. The model calculations indicate the effect of gas heating and inhomogeneous preionization on the ozone production and NO_x destruction.     

Co-generation of Ammonia and H2 from H2O Vapor and N2 Using a Membrane Electrode Assembly

The direct electrochemical synthesis of NH₃ from nitrogen and water vapor without the use of a fossil carbon source is highly desired. This synthesis is a viable option to store energy and produce fertilizer precursors. Here, a new Pt-free membrane electrode assembly is presented. An electrochemical membrane reactor demonstrates the feasibility of co-generating NH₃ and H₂ directly from nitrogen and water vapor at ambient conditions. An unprecedented high NH₃-specific current efficiency of up to 27.5% using Ti as cathodic catalyst is reported. The co-generation can be tuned by the balance of process parameters.     

Reaction of NO and N2O gases with graphite in TGA

Thermal analyses were conducted in a thermogravimetric analyzer by isothermal techniques in order to characterize the carbon-nitrogen oxide reaction. The carbon samples employed in the present study were SP-1 graphite and Micro 450 graphite. Carbon-NO and carbon-N₂O reactions were carried out in a temperature range of 550–900 °C and 5–20 kPa of the partial pressure of reactant. In the NO reaction, reaction orders with respect to NO concentration and activation energy were 0.46-0.92 and 85–102 kJ/mol, respectively. The rate on the monolayer edge was higher than the rate on the multilayer edges. In the N₂O reaction, reaction orders with respect to N₂O concentration and activation energy were 0.55–1.35 and 167–190 kJ/mol, respectively.     

Experimental Study of Ozone Generation by Negative Corona Discharge in Mixtures of N2 and O2

Ozone generation by negative DC corona discharge in N₂-O₂ mixtures has been experimentally investigated using a coaxial wire-cylinder corona reactor operating at room temperature and atmospheric pressure. The experiments have been carried out under different gas flows (15 cm³ min^?1 to 200 cm³ min^?1) and gas compositions (5% to 90% of O₂), and the effect of these parameters on the corona current, the ozone density and the efficiency of the ozone generator have been analyzed. The global rate coefficients for ozone formation and destruction have also been evaluated, and their values compared with those reported by other authors. The maximum efficiency for ozone production was found in gas mixtures with oxygen content about 70–80%.     

Reaction Synthesis and Mechanical Properties of Lu4Si2O7N2

Crystallized Lu–Si–O–N phases were believed to be the grain‐boundary (GB) phases that might provide Si₃N₄ with excellent high‐temperature mechanical properties. However, little is known about the intrinsic properties, as well as the synthesis, of the Lu–Si–O–N ceramics. This work reveals the reaction paths of heating Lu₂O₃, SiO₂, and Si₃N₄ powder mixtures (with the stoichiometry of 4:0.96:1) from room temperature to 1600°C. Thereafter, dense Lu₄Si₂O₇N₂ samples are synthesized by in situ reaction/hot‐pressing method, and the mechanical properties at room temperature and elevated temperatures are reported for the first time. The Lu₄Si₂O₇N₂ samples show significant high‐temperature mechanical properties, such as the elastic stiffness remains 77% from room temperature to 1500°C; and bending strength keeps 93% from room temperature to 1400°C. The present results shine a light on Lu₄Si₂O₇N₂ as a promising target GB phase for the optimization of high‐temperature mechanical properties of Si₃N₄.     

Transfer and Reaction Performances of Selective Catalytic Reduction of N2O with CO over Monolith Catalysts

This work tries to identify the relationship between geometric configuration of monolith catalysts, and transfer and reaction performances for selective catalytic reduction of N2O with CO. Monolith cat...     

Effects of O2 and N2 Gas Concentration on the Formation of Ho2O3 Gate Oxide on 4H-SiC Substrate

Silicon - In this paper, the impacts of flow concentration of oxynitridation on the structural and electrical performance of a high-κ Ho2O3 dielectric on n-type 4H-SiC were studied. The Ho2O3...     

Li0.98Mn2O4的流变相法合成及电化学性能研究

用流变相反应法以乙酸锂、乙酸锰、柠檬酸为原料合成正极材料Li0.98Mn2O4,探讨了合成条件;经X-射线衍射表征,热重法(TG)和差热分析(DTA)以及电化学性能测试表明:Li0.98Mn2O4结晶性能很好,为尖晶石结构,其首次放电比容量高达130 mAh/g,具有较好的循环性,40次循环后还能保持初始容量的88%以上。     

Temporal and Spatial Variations in N2O Emissions from a Chinese Cabbage Field as a Function of Type of Fertilizer and Application

We conducted a field experiment in an Andosol near Tsukuba (Japan) to study the effects of the type of nitrogen fertilizer on nitrous oxide (N₂O) emissions and on nitrogen uptake by Chinese cabbage (Brassica campestris L.). We used four treatments: fertilizer containing no nitrogen (CONT), broadcast application of urea (BR-U), band application of urea (B-U), and band application of controlled-release urea (B-CU). The application rate was 250 kg N ha⁻¹, a conventional rate in the region. We measured N₂O flux two or three times a week during the 82-day growth period, then divided the cumulative emissions into three stages: early (28 days), middle (27 days), and late (27 days). The temporal variation in N₂O emissions differed among the treatments. Broadcast urea application produced 70% of N₂O emissions during the early stage. N₂O emissions increased with increasing cabbage growth in the CONT treatment, indicating that plant growth accompanied by increasing root biomass could stimulate N₂O emissions from unfertilized soil. There were no differences in the patterns of temporal variation in N₂O flux between the two band applications (B-U and B-CU); N₂O emissions in the early and middle stages were 46 and 42%, respectively, for B-U, vs. 41 and 40% for B-CU. However, the overall N₂O emission was reduced by 40.5% in the B-CU treatment compared with the B-U treatment. N₂O emissions from the soils within fertilized bands were dramatically higher than those between the fertilized bands, and this trend continued until harvesting.     

流化床燃煤过程中氧化亚氮的生成和还原机理

流化床燃烧是一种先进的燃煤技术 ,可以降低 NOx的排放。但流化床在低温下燃烧生成较多的N2 O。本文简述了 N2 O在流化床燃烧条件下的生成和还原机理 ,讨论了燃烧温度、煤阶等因素对 N2 O生成和还原的影响以及 NO- SO2 - N2 O的相互作用     

Effect of crop-specific field management and N fertilization on N2O emissions from a fine-loamy soil

Agricultural soils are a major source of atmospheric N₂O. This study was conducted to determine the effect of different crop-specific field management and N fertilization rates on N₂O emissions from a fine-loamy Dystric Eutrochrept. Fluxes of N₂O were measured for two years at least once a week on plots cropped with potatoes (Solanum tuberosum) fertilized with 50 or 150 kg N ha⁻¹ a⁻¹, winterwheat (Triticum aestivum) fertilized with 90 or 180 kg N ha⁻¹ a⁻¹, corn (Zea mays) fertilized with 65 or 130 kg N ha⁻¹ a⁻¹, and on an unfertilized, set-aside soil planted with grass (mainly Lolium perenne and Festuca rubra). The mean N₂O emission rate from the differently managed plots was closely correlated to the mean soil nitrate content in the Ap horizon for the cropping period (April to October, r ² = 0.74), the winter period (November to March, r ² = 0.93, one outlier excluded), and the whole year (r ² = 0.81). N₂O emissions outside the cropping period accounted for up to 58% of the annual emissions and were strongly affected by frost-thaw cycles. There was only a slight relationship between the amount of fertilizer N applied and the annual N₂O emission (r ² = 0.20). The mean annual N₂O-N emission from the unfertilized set-aside soil was 0.29 kg ha⁻¹. The annual N₂O-N emission from the fertilized crops for the low and the recommended rates of N fertilization were 1.34 and 2.41 kg ha⁻¹ for corn, 2.70 and 3.64 kg ha⁻¹ for wheat, and 5.74 and 6.93 kg ha⁻¹ for potatoes. The high N₂O emissions from potato plots were due to (i) high N₂O losses from the interrow area during the cropping season and (ii) high soil nitrate contents after the potato harvest. The reduction of N fertilization (fertilizer was applied in spring and early summer) resulted in decreased N₂O emissions during the cropping period. However, the emissions during the winter were not affected by the rate of N fertilization. The results show that the crop-specific field management had a great influence on the annual N₂O emissions. It also affected the emissions per unit N fertilizer applied. The main reasons for this crop effect were crop-specific differences in soil nitrate and soil moisture content. This revised version was published online in June 2006 with corrections to the Cover Date.     

The Kinetics and the Mechanism of the Reaction of 2-chloro-4,6-dialkylamino-1,3,5-triazines with Ozone

Eight 2-chloro-4,6-dialkylamino-1,3,5-triazines were reacted with ozone at pH 3. Alkyl groups were methyl, ethyl, n-propyl, i-propyl, n-butyl, t-butyl, hydrogen. Oxidative N-dealkylation and α-oxygenation to give an amide were obtained. Kinetic measurements were used to obtain second order rate constants and activation parameters. The entropy of activation and some semi empirical calculations suggests a mechanism occurring via addition to nitrogen concerted with hydrogen transfer. The α-oxygenation reaction is the metal-free oxidation of value in a green chemistry perspective.     

碳纳米管载钴氧化物催化剂制备及其分解N2O研究

用自行合成的碳纳米管(CNTs)作为载体,制备了高分散催化剂Co3O4/CNTs.通过SEM,TEM,XRD和TGA以及表面积与孔径测定仪等测试手段对该负载型催化剂的物相、粒子的形貌和粒度进行了表征.还利用反应器研究了催化剂对N2O分解的催化活性,结果证明在实验条件下载钴碳纳米管催化剂中钴以Co3O4的晶相存在,呈球状小颗粒,并均匀地分布在碳纳米管上,对N2O分解反应有良好的催化活性.     

N2O and NO emissions from different N sources and under a range of soil water contents

Emissions of nitrous oxide (N₂O) and nitric oxide (NO) have been identified as one of the most important sources of atmospheric pollution from grasslands. Soils are major sources for the production of N₂O and NO, which are by-products or intermediate products of microbial nitrification and denitrification processes. Some studies have tried to evaluate the importance of denitrification or nitrification in the formation of N₂O or NO but there are few that have considered emissions of both gases as affected by a wide range of different factors. In this study, the importance of a number of factors (soil moisture, fertiliser type and temperature) was determined for N₂O and NO emissions. Nitrous oxide and NO evolution in time and the possibility of using the ratio NO:N₂O as an indicator for the processes involved were also explored. Dinitrogen (N₂) and ammonia (NH₃) emissions were estimated and a mass balance for N fluxes was performed. Nitrous oxide and NO were produced by nitrification and denitrification in soils fertilised with and by denitrification in soils fertilised with . Water content in the soil was the most important factor affecting N₂O and NO emissions. Our N₂O and NO data were fitted to quadratic (r=0.8) and negative exponential (r=0.7) equations, respectively. A long lag phase was observed for the N₂O emitted from soils fertilised with (denitrification), which was not observed for the soils fertilised with (nitrification) and was possibly due to a greater inhibiting effect of low temperatures on microbial activity controlling denitrification rather than on nitrification. The use of the NO:N₂O ratio as a possible indicator of denitrification or nitrification in the formation of N₂O and NO was discounted for soils fertilised with . The N mass balance indicated that about 50 kg N ha⁻¹ was immobilised by microorganisms and/or taken up by plant roots, and that most of the losses ocurred in wet soils (WFPS >60%) as N₂ and NH₃ losses (>55%).     

Emissions of N2O from Scottish agricultural soils, as a function of fertilizer N

Potato fields and cut (ungrazed) grassland in SE Scotland gave greater annual N₂O emissions per ha (1.0–3.2 kg N₂O–N ha^-1) than spring barley or winter wheat fields (0.3–0.8 kg N₂O–N ha^-1), but in terms of emission per unit of N applied the order was potatoes > barley > grass > wheat. On the arable land, especially the potato fields, a large part of the emissions occurred after harvest.When the grassland data were combined with those for 2 years' earlier work at the same site, the mean emission over 3 years, for fertilization with ammonium nitrate, was 2.24 kg N₂O–N ha^-1 (0.62% of the N applied). Also, a very strong relationship between N₂O emission and soil nitrate content was found for the grassland, provided the water-filled pore space was > 70%. Significant relationships were also found between the emissions from potato fields and the soil mineral N content, with the added feature that the emission per unit of soil mineral N was an order of magnitude larger after harvest than before, possibly due to the effect of labile organic residues on denitrification.Generally the emissions measured were lower, as a function of the N applied, than those used as the basis for the current value adopted by IPCC, possibly because spring/early summer temperatures in SE Scotland are lower than those where the other data were obtained. The role of other factors contributing to emissions, e.g. winter freeze–thaw events and green manure inputs, are discussed, together with the possible implications of future increases in nitrogen fertilizer use in the tropics.     

Recovery of Lithium from Seawater Using a New Type of Ion-Sieve Adsorbent Based on MgMn2O4

Abstract

A new type of ion-sieve manganese oxide, HMnO(Mg), was prepared by an acid treatment of MgMn₂O₄. The HMnO(Mg) showed a remarkably high selectivity for lithium ions among alkali metal and alkaline earth metal ions. The selectivity sequences were Na ? K ? Li for alkali metal ions and Mg ≤ Ca ≤ Sr ≤ Ba for alkaline earth metal ions at pH 8. The HMnO(Mg) showed a high selectivity for lithium ions in seawater. The lithium uptake increased with increasing solution pH and adsorption temperature. The maximum lithium uptake from native seawater reached 8.5 mg/g, corresponding to a lithium content of 1.8% in the form of Li₂O. The adsorbed lithium could easily be eluted with a dilute acid solution. The adsorptive capacity for lithium ions gradually decreased through repeated adsorption/elution cycles. The HMnO(Mg) after 4 cycles showed a lithium adsorptivity which was about 60% of the initial value.     

The Formation of CrO2+2 in the Reaction of Cr2+ + O2 in Aqueous Acid Solutions

The reduction rate of Cr³⁺ by e_aq was determined, k₈ = 1.7 × 10¹⁰ M^?1 s^?1. The reaction of Cr²⁺ with O₂ was studied, k₂ = 1.6 × 10⁸ M^?1 s^?1. The spectrum of CrO²⁺₂ was obtained both with the pulse radiolysis method and by mixing Cr²⁺ with excess of O₂. It was shown that CrO²⁺₂ decays slowly to yield HCrO^?₄. The results suggest that the reaction of Cr²⁺ with O₂ is a two electron transfer process.     

ETX-5型脱除N_2O催化剂的性能研究

通过催化剂活性评价实验,考察了ETX-5型催化剂在模拟氨氧化炉环境下的催化活性,并研究了催化剂工艺条件对催化剂活性的影响。实验结果表明,在温度800℃~860℃、空速70 000 h~(-1)、O_2体积分数6.3%、进口N_2O体积分数为1 740×10~(-6)、压力0.4 MPa、通水量为16.5%的条件下,N_2O的转化率达99%。ETX-5型脱除N_2O催化剂的开发具有一定的社会效益和经济效益。     

Formation of Azobenzenes and Azoxybenzenes from the Aqueous Reactions of Anilines and Ozone

Azobenzenes and azoxybenzenes are two of the products identified from the aqueous reaction of anilines with ozone. Aniline concentration and functional groups on the benzene ring of aniline affected the amount of azobenzenes and azoxybenzenes formed; (1) decreasing the aniline concentration significantly increased azobenzene formation, and (2) electron-withdrawing groups increased the formation of its related azobenzene and azoxybenzene, whereas electron-donating groups had the opposite effect.