Alpha induced reactions on Sn: An experimental study of excitation functions and possible production pathways

In the frame of a systematic study of light ion induced threshold reactions on natural tin (Sn) excitation functions for alpha particles induced reactions are presented in a 12–38 MeV energy domain. Using a stacked foil activation method the following radioisotopes were identified: ¹¹⁶Te, ¹¹⁷Te, ¹¹⁸Te, ¹¹⁹Te, ¹²¹Te, ¹²³Te, ¹¹⁷Sb, ¹¹⁸Sb, ¹²⁰Sb, ¹²²Sb, ¹²⁴Sb, ¹²⁶Sb, ¹¹⁷Sn, ¹¹¹In. The experimental cross sections for these isotopes are presented for the first time in this energy range and a direct comparison with values calculated with the ALICE-IPPE code is discussed. Possible use of these data for production of some isotopes relevant in nuclear medicine is suggested.     

Electrochemical study of a hydrogen diffusion anode-membrane assembly for membrane electrolysis

The membrane electrode assembly (MEA) studied was constituted with a gas diffusion electrode (E-TEK) impregnated with Nafion^® solution which was assembled with a Nafion^® 117 cation exchange membrane under heat and pressure. The MEA was used as anode in a membrane electrolysis (ME) cell with the objective to regenerate HCl and NaOH from NaCl. Current efficiency for hydrogen oxidation was determined and its value is 100%, which indicates that the only reaction occurring at the anode is the oxidation of hydrogen. Current-potential curves, recorded in different conditions, showed a linear variation in the range 0-3000 A m⁻² when hydrochloric acid concentration is below 2 mol dm⁻³. In this case, the overvoltage was shown to be mainly due to the ohmic drop in the membrane and in the layer where Nafion^® impregnation was performed. MEA overvoltage necessary to reach 3000 A m⁻² current density was about 0.12 V. For high HCl concentration (6-8 mol dm⁻³), the MEA overvoltage increased sharply with current density due to the adsorption of chloride anions on platinum catalyst.     

Film-pore diffusion models—analytical and numerical solutions

The sorption of acid dyes from aqueous effluents onto activated carbon has been studied. The effects of initial dye concentration and activated carbon mass on the rate of Acid Blue 80 and Acid Yellow 117 removal have been investigated. Three mass transport models based on film and pore diffusion control have been applied to model the experimental concentration decay curves. The models are compared on the basis of the solid-phase loading capacity using various assumptions since the assignment of an appropriate solid-phase loading has been the subject of several papers on this topic and no comparisons have been provided on the effectiveness of each approach. The equilibrium solid-phase concentration is assumed: (i) incorporating a time-dependent solid-phase concentration Y_e,t, (ii) equal to the intersection point of the equilibrium isotherm and the operating line and (iii) the point on the equilibrium isotherm where the liquid-phase concentration equals the initial concentration in the film-pore diffusion model.     

隐身飞机F-117A单站电磁散射面积仿真分析

为满足雷达对抗隐身目标的需求,建立了单站电磁波入射角度的模型。利用电磁仿真软件XFDTD计算和分析了典型隐身目标F-117A飞机的单站雷达截面积,包括电磁波在头向入射、鼻椎向入射、正侧向入射、尾向入射条件下单站雷达截面积随频率变化的特性。通过对仿真结果的分析得出了有利于单基地雷达反隐身的入射方向和工作频段等结论及数据,具有一定的理论参考价值。     

巨大晶胞化合物Ho117Fe52Ge112的结构磁性能研究

利用X射线衍射技术和振动样品磁强计（VSM）研究了巨大晶胞三元化合物Ho117Fe52Ge112的结构与磁性能,测定了外加磁场为0．5T时该化合物的磁矩随温度的变化关系。该化合物具有Tb117Fe52Ge112结构类型,空间群为Fm3m（No．225）点阵参数为a=2．80832（8）nm。在90K到室温的范围内,Ho117Fe52Ge112的磁化率与温度关系服从居里——外斯定律,每个化学式有效磁矩的实验值为ueff=111．25us。测定了室温（300K）时磁矩随外加磁场的变化关系。当外加磁场到2．1T时,该化合物的磁矩约为3．61emu／g,还没有达到饱和状态。     

Chemical exposure and flammability risks of upholstered furniture

Upholstered furniture remains a consumer fire hazard. Flame retardant technologies are necessary but may present a health risk from chemical exposure. This study developed methodologies for measuring exposure to flame retardants and flammability performance, comparing the effectiveness of differing flammability reduction strategies on upholstered chairs with and without added flame retardants and the use of a barrier material. The chemical analysis focused on volatile organic compounds (VOCs) and flame retardants. Open flame tests were conducted on chair assemblies, and smolder resistance tests were conducted on chair materials. Results showed that VOC inhalation exposure during consumer use was low for all chair types. However, VOCs were significantly elevated during the chair burns. The organophosphorus flame retardant used in this study was found in air, settled dust and dermal transfer samples. The chairs with a barrier material demonstrated significantly lower flammability hazards when compared to the other chair types. All assembled chairs did not meet the criteria for smolder testing, suggesting a lack of correlation with open‐flame performance. This study demonstrated that combined human health and flammability advantages may be achieved for upholstered chairs constructed with an effective fire barrier material without any added flame retardants.     

HIP-Si3N4陶瓷/45#钢副干摩擦和水润滑下摩擦学性能

利用MPX-2000型盘销式摩擦磨损试验机考察了HIP—Si3N4陶瓷／45^#钢副在干摩擦和水润滑下的摩擦磨损性能；用扫描电子显微镜观察了试件表面的磨损状态；采用X射线电子能谱仪分析了摩擦表面的化学成分：结果表明：干摩擦条件下，HIP—Si3N4陶瓷的磨损速率比45^#钢小，45^#钢发生粘着磨损，HIP—Si3N4陶瓷发生了脆性断裂和脱落；水润滑条件下，摩擦表面产生了Si(OH)4反应膜，降低了磨损，主要是化学腐蚀磨损。     

Active metal-based corrosion protective coating systems for aircraft requiring no-chromate pretreatment

There has been much R&D effort expended to develop pretreatments and coatings that allow the replacement of toxic, carcinogenic, mutagenic, environmentally hazardous chromates used as pretreatments and pigments in aircraft coating systems. There have been many claims for chromate replacement in primer and pretreatment systems for aircraft, but no systems presently are in use that can function and meet specifications without some form of chromate used in the pretreatment and/or primer. The Mg-rich primer technology developed at North Dakota State University and now in final commercial development at AKZO Nobel Aerospace Coatings shows that finally aerospace Al alloys can be protected against corrosion. With simple cleaning only or a non-chromate pretreatment, the Mg-rich primer (MgRP) + aerospace topcoat provides an aircraft protection system that give corrosion protection that equals or exceeds any system using chromate in any form. About 18 peer reviewed papers have been published and at least twice that many presentations at technical meetings describing this new aircraft primer technology. There are an extensive number of samples in outdoor exposure, and in exposure on small parts of aircraft like port-hole covers and doors, and the coating system has been in accelerated exposure cabinets of all sorts. In the first versions of the magnesium primer premature blistering was noted during immersion or B117 continuous salt spray testing which may be due to hydrogen generation from water contact at a particle. Efforts to control the level of activity of the magnesium have been successfully accomplished since the testing reported in this paper which controls this phenomenon. Current formulations meet and exceed the ASTM B117 test results of full chromate primer systems. Open circuit potential (OCP) measurements indicate an extended period of cathodic protection of the Al aircraft alloys such as AA 2024 T-3 and AA 7075 T-6. After this stage of protection, a combination of Mg oxide, hydroxide and carbonate compounds seem to give protection to the system, as we have seen corrosion protection given to samples for greater than 10,000 h of cyclic exposure for Mg-rich primers with good aerospace topcoats. Preliminary data are presented for other Mg alloys as pigments in metal-rich coating systems. All data indicates that the Mg-rich (or Mg-alloy pigment-rich) primer + aircraft topcoat system gives excellent corrosion protection by mechanisms entirely different from the modes of protection for aircraft alloys given by the toxic, carcinogenic chromate compounds now in use in all corrosion protection systems for aircraft. In most cases thus far examined, the protection, especially in cyclic exposure, exceeds the present chromate-based systems.     

Membrane electrolysis of Bunsen reaction in the iodine–sulphur process for hydrogen production

In traditional IS process for production of hydrogen by water decomposition, the Bunsen reaction (SO₂ + I₂ + 2H₂O → H₂SO₄ + 2HI) was carried out by direct contact of SO₂ with aqueous solution of I₂ where a large excess of I₂ (8 mol) and H₂O (16 mol) were required. Excess amounts of these chemicals severely affected the overall thermal efficiency of the process and new ways including membrane electrolysis was reported in literature for carrying out Bunsen reaction where the amount of excess chemicals can be greatly reduced. We have carried out Bunsen reaction in a two-compartment membrane electrolysis cell containing graphite electrodes and Nafion 117 membrane as a separator between the two-compartments. Electrolysis was carried out at room temperature with continuous recirculation of anolyte and catholyte. Electrolysis was done in constant-current mode with current density in the range of 1.6 A/dm² to 4.8 A/dm². Initial concentrations of H₂SO₄ and HI were about 10 and 5 N, respectively and I₂/HI molar ratio in the catholyte was varied in the range of 0.25–1.5. Current efficiency was found to be close to 100% indicating absence of any side reaction at the electrodes. Cell voltage was found to vary linearly with current densities up to 80 A/dm² and for I₂/HI molar ratio in the range of 0.25–1.5 the cell voltage was found to be lowest for the value of 0.5.     

Transport Properties of Ion‐Exchange Membranes During Pervaporation of Water‐Alcohol Mixtures

Abstract

Pervaporation properties of PESS ion‐exchange membranes in contact with water‐aliphatic alcohol mixtures were obtained. PESS ion‐exchange membranes were prepared by chemical modification of the interpenetrating polymer network system polyethylene‐poly(styrene‐co‐divinylbenzene). PESS membranes were loaded with different alkali metal ions as counterions. The obtained data showed that properties of PESS membranes depended strongly on the kind of counterions, degree of crosslinking, and difference in the polarities between water and organic component of the binary mixture. Results obtained for PESS membranes were compared with data obtained for Nafion 117 ion‐exchange membrane.