核电异种金属焊接材料及方法研究现状

异种金属焊接接头开裂是导致核电事故的主要原因，急需开发新材料新技术，提高焊缝质量。传统电弧焊方法存在效率低、热输入大和变形严重等问题。窄间隙电弧焊的热输入、填充量、变形量等都比传统电弧焊低。与窄间隙电弧焊相比，窄间隙激光填丝焊坡口更窄、热输入更低、变形更小、精度更高。研究表明，窄间隙激光填丝焊可获得满足核电压力容器制造要求的焊缝，有望成为异种金属连接新方法。然而，现有窄间隙激光填丝焊采用常规激光及单焊丝填充，仍存在3个主要问题：一是界面容易产生未熔合问题；二是熔融金属粘度大，熔池流动性差，合金元素分布不均匀；三是低熔点共晶相沿晶界析出过多，无法兼顾焊缝抗液化裂纹、应力腐蚀裂纹和高温失塑裂纹能力。研究表明，焊接热源和焊材是解决上述问题的2个关键因素。     

Experimental analysis of internal leakage current using a 100 cm2 class planar solid oxide fuel cell

This work studies the effect of the electronic conductivity of a commercially used yttria-stabilised zirconia (YSZ) electrolyte on solid oxide fuel cell performance. For the first time, an experimental method is used to measure the electronic conductivity of YSZ in commercially manufactured and operated single cells. An inert-gas step addition (ISA) method is employed to measure the electronic conductivity in the form of voltage changes at the open-circuit state. Since the electronic conductivity allows oxide ion transfer and water generation at the anode, a reduction in open-circuit voltage (E_OCV) occurs due to the increased water partial pressure. The step increase in the anode flow rate in the ISA method reduces water partial pressure and raises E_OCV. The E_OCV change is then converted into internal leakage currents and electronic resistivities. The YSZ's electronic resistivity obtained in this work is comparable to the results obtained using the Hebb-Wagner polarisation technique and the oxygen permeation method.     

Effect of hydrogen addition on the structure and stabilization of a micro-jet methane diffusion flame

The micro-jet diffusion flame can act as the heat source for the micro power generation systems due to some advantages. The present work investigates the effect of hydrogen addition on the structure and stabilization of micro-jet methane diffusion flame by numerical simulation. The results show that the oval flame becomes more and more circular with the increase of hydrogen addition fraction. The addition of hydrogen remarkably suppresses the increase of the flame height with the inlet velocity. The methane sharply decreases around the outlet of the micro-jet tube due to the high fresh fuel temperature. The intermediate species (e.g., H₂ and CO) increase sharply before the flame front, and they are consumed sharply within the flame front. With the increase of hydrogen addition fraction, the concentration gradients of reactive species increase before the flame front, while the flame temperature decreases. In addition, with the increase of hydrogen addition fraction, the micro-jet flame root shifts toward the tube-wall and downstream direction at the radial and axial directions, respectively, and the addition of hydrogen decreases the anchoring temperature of the micro-jet flame root, which is conductive to improve the flame stabilization. Meanwhile, a large hydrogen addition fraction is detrimental for the flame stabilization in terms of the thermal interaction between the micro-jet flame and tube-wall. However, the positive effects brought by a large hydrogen addition fraction are noticeably larger than the adjunctive negative effects. This study not only provides the guideline for further expanding the operating range of the micro-jet methane diffusion flame but also helps us to gain insights into the mechanism of hydrogen addition on improving the flame stabilization.     

Production of olefins from ethanol by Fe and/or P‐modified H‐ZSM‐5 zeolite catalysts

BACKGROUND: Much attention has been paid to the catalytic conversion of ethanol to olefins, since biomass resources such as ethanol are carbon‐neutral and renewable, and olefins are useful as both fuels and chemicals. It has been reported that zeolite H‐ZSM‐5 is effective for converting ethanol to hydrocarbons, with the chief products being aromatic compounds. RESULTS: Successive addition of Fe and P to the H‐ZSM‐5 improved the initial selectivity for propylene, while the sole addition of Fe or P and co‐addition of Fe and P showed medium initial selectivity. In general, catalysts showing higher initial selectivity for propylene exhibited a steeper decrease in propylene selectivity with time on‐stream. The cause of the change in product selectivity may be carbon deposition during reaction. Addition of Fe and P can improve catalytic stability when processing both neat and aqueous ethanol. The catalytic performance was regenerated by calcination in flowing air. CONCLUSION: Fe‐ and/or P‐modified H‐ZSM‐5 zeolite catalysts efficiently produced olefins (especially propylene) from ethanol. Effective catalyst regeneration was achieved by calcination in flowing air. Copyright © 2010 Society of Chemical Industry     

Novel Tertiary Amino Containing Blinding Composite Membranes via Raft Polymerization and Their Preliminary CO2 Permeation Performance

Facile synthesis of poly (N,N-dimethylaminoethyl methacrylate) (PDMAEMA) star polymers on the basis of the prepolymer chains, PDMAEMA as the macro chain transfer agent and divinyl benzene (DVB) as the cross-linking reagent by reversible addition-fragmentation chain transfer (RAFT) polymerization was described. The RAFT polymerizations of DMAEMA at 70 °C using four RAFT agents with different R and Z group were investigated. The RAFT agents used in these polymerizations were dibenzyl trithiocarbonate (DBTTC), s-1-dodecyl-s''-(α,α''-dimethyl-α-acetic acid) trithiocarbonate (MTTCD), s,s''-bis (2-hydroxyethyl-2''-dimethylacrylate) trithiocarbonate (BDATC) and s-(2-cyanoprop-2-yl)-s-dodecyltrithiocarbonate (CPTCD). The results indicated that the structure of the end-group of RAFT agents had significant effects on the ability to control polymerization. Compared with the above-mentioned RAFT agents, CPTCD provides better control over the molecular weight and molecular weight distribution. The polydispersity index (PDI) was determined to be within the scope of 1.26 to 1.36. The yields, molecular weight, and distribution of the star polymers can be tuned by changing the molar ratio of DVB/PDMAEMA-CPTCD. The chemical composition and structure of the linear and star polymers were characterized by GPC, FTIR, ¹H NMR, XRD analysis. For the pure Chitosan membrane, a great improvement was observed for both CO₂ permeation rate and ideal selectivity of the blending composite membrane upon increasing the content of SPDMAEMA-8. At a feed gas pressure of 37.5 cmHg and 30 °C, the blinding composite membrane (Cs: SPDMAEMA-8 = 4:4) has a CO₂ permeation rate of 8.54 × 10⁻⁴ cm³ (STP) cm⁻²∙s⁻¹∙cm∙Hg⁻¹ and a N₂ permeation rate of 6.76 × 10⁻⁵ cm³ (STP) cm⁻²∙s⁻¹∙cm∙Hg⁻¹, and an ideal CO₂/N₂ selectivity of 35.2.     

Ce添加对AP65镁合金显微组织及电化学性能的影响

采用熔炼铸造法制备添加不同含量Ce的AP65镁合金。采用X射线衍射(XRD)、扫描电镜(SEM)和电子探针(EPMA)研究Ce对AP65镁合金显微组织的影响。采用恒电流放电、动电位极化扫描、化学浸泡研究不同Ce含量AP65镁合金的腐蚀电化学行为。结果表明:随Ce含量增加,合金中依次出现棒状或簇状的Al4Ce相和块状的Al2Ce相。Ce的添加导致AP65镁合金的电化学性能明显提高,添加0.6%(质量分数)的Ce使AP65镁合金的平均放电电位从-1.648 V(vs SCE)负移到-1.756 V(vs SCE);添加4%的Ce使AP65镁合金具有较小的腐蚀电流密度(19.66μA/cm2)和较高的阳极利用率(84.3%),与未添加Ce的AP65镁合金相比,阳极利用率提高16.6%。     

Effects of storage on quality of carrot juices produced with lactofermentation and acidification

In this study, effects on the yield and the quality of product properties of carrot juice produced with lactofermentation and added citric acid, and with and without total enzymatic liquefaction (Pectinex Ultra SP-L) were investigated. Samples were stored at room temperature for 6 months and analytical changes which might occur were determined at day 0 and after 2, 4 and 6 months by quality control tests. In enzyme-treated samples, the yield and the quality of mineral incrementation were determined. Accordingly, ash and water-soluble dry matter contents were increased in the samples. Galacturonic acid formed after enzymatic breakdown of pectin in the raw material increased the total acidity of the samples. Sensorial tests of the product were also carried out. According to the test results, the products produced with enzyme treatment at day 0, after 2 and 4 months storages were found to be the ones mostly preferred. However the samples without enzyme treatment were preferred by the panelists after long-term (6 months) storage.     

第28届IULTCS国际会议概况及皮革中禁用偶氮染料检测方法的最新进展

简要介绍第28届IULTCS会议概况以及欧盟在皮革中禁用偶氮染料检测方法方面的最新进展。