Enthalpy recovery of gases issued from H2 production processes: Activity and stability of oxide and noble metal catalysts in oxidation reaction under highly severe conditions

Oxidation activity and stability under reaction was investigated for a series of mixed oxide catalysts, doped or not by a precious metal (Pd, Pt). The reaction feedstock, containing CO, H₂, CH₄, CO₂ and H₂O, simulated gases issued from H₂ production processes for fuel cells. Contrarily to conventional noble metal catalysts, mixed oxide samples present generally good stability under reaction at high temperature. The activities measured for the perovskite and hexaaluminate catalysts, are however largely lower than that of the reference Pd/Al₂O₃ catalyst. High activities were obtained after impregnation of 1.1 wt.% Pd or 0.8 wt.% Pt on the hexaaluminates samples. Even if Pd/Al₂O₃ was found to present a high activity, this sample suffered from drastic deactivation at 700 °C. Better stability were obtained on perovskite. Furthermore, doping hexaaluminate by Pt led to samples with good activities and high stability. Even if better activities were obtained by doping the hexaaluminate samples by Pd, the Pd/BaAl₁₂O₁₉ strongly deactivated, as it was previously observed for the reference catalyst. Interestingly, this Pd deactivation was not observed when Pd was impregnated on the Mn substituted hexaaluminate, leading to a stable and active catalyst. This suggests that it is possible to stabilize the palladium in its oxidized form at high temperature (700 °C) on the surface of some supports.     

Mixing in the transition flow regime with helical ribbon agitators

The effects of the non-Newtonian properties on the effective deformation rate, mixing and circulation times and flow behaviour have been investigated in the transition flow regime of mixing systems. Based on the equivalent Couette flow, three models are proposed and are shown to predict similar and drastic increases of the effective deformation rate with the impeller rotational speed in the transition regime. The predictions are shown to fit very well data obtained for various non-Newtonian fluids mixed with helical ribbon agitators, and with literature data for anchor, blade turbine and flat disc agitators. The elasticity along with shear-thinning properties appear to have slight effects on the dimensionless mixing and circulation times in the transition regime, whereas their effects in the laminar regime are quite drastic, as reported by others.     

Euclidean Distance Mapping for computing microstructural gradients at interfaces in composite materials

This paper presents an image analysis procedure using Euclidean Distance Mapping to compute microstructural gradients at interfaces in composite materials. This method is capable of producing phase distribution plots at single pixel strip width very quickly and efficiently. Compared to conventional dilation-subtraction strip analysis, the new method is faster, more flexible and is not constrained by feature geometry and boundary conditions. This allows for truly random and unbiased sampling. The new method was applied to investigate microstructural gradients at the interfacial transition zone (ITZ) of an ordinary Portland cement concrete. The average results show strong gradients in anhydrous cement and detectable porosity at the ITZ, but this is highly variable from location to location. The overall ITZ characteristics depend on the amount of calcium hydroxide deposited on aggregate particles. The new method was able to measure the effect of these calcium hydroxide deposits on the porosity gradient, which has not been reported before.     

基于日志挖掘的移动应用用户访问模型建模技术研究

提出了一种基于监控日志挖掘的移动应用用户访问模型自动构造方法,该方法包括监控代码注入和界面访问模型构造两部分。首先,提出了一种监控代码自动注入方法,即通过对移动应用代码的静态分析,自动地在相应位置插入监控代码以支持在运行时动态地监控用户的访问行为。其次,提出了一种基于状态机的移动应用用户访问模型构造方法。访问模型中状态机的节点和节点间跳转上的附加属性描述了UI界面之间的跳转行为和界面内控件的使用情况。对移动应用进行的实验表明,这种基于监控日志挖掘的移动应用用户访问模型自动构造方法能够成功地自动注入移动应用的监控代码,并能够有效获得移动应用用户界面访问行为。     

Sorption of Cr(III)‐containing cations on strongly basic anion exchangers

It is shown that strongly basic anion exchangers AV‐17 and Varion‐AD in definite conditions are able to retain Cr(III)‐containing ions from Cr(III) sulfate solution. It is found that the sorption of Cr(III)‐containing ions on the polymers is essentially dependent on the pH, temperature, and Cr(III) sulfate concentration. The maximum temperature dependence of sorption was found to be about 60°C. The sorption isotherms are well described by Langmuir's equations. The sorption kinetics is determined by the diffusion of Cr(III)‐containing ions into polymer's phase. It is assumed that the Cr(III)‐containing ions are retained through formation, in polymer's phase, of the jarosite‐type mineral compounds: R₄N[Cr₃(OH)₆(SO₄)₂], H₃O[Cr₃(OH)₆(SO₄)₂], and K[Cr₃(OH)₆(SO₄)₂]. For comparison of sorptional capacities, the sorption of Cr(III)‐containing ions was determined on different cation and anion exchangers. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3978–3985, 2006     

热塑性弹性体SBS的工程开发Ⅴ．万吨级聚合装置SBS产品的性能剖析

对用国内技术建设的万吨级聚合装置生产的５种牌号产品：线型ＳＢＳ１３０１，ＳＢＳ１４０１和星形ＳＢＳ４３０３，ＳＢＳ４４０２及充油３３％的星形ＳＢＳ４４５２２进行了性能剖析。结果表明，国产ＳＢＳ的物理性质、热氧稳定、玻璃化转变温度、微观结构和相态结构与国外同类产品相当，Ｍ＿ｎ可以达到预期要求，说明该开发技术是成功的。     

Synthesis,characterization, and thermal behavior study of methyl methacrylate polymers containing 4‐carbazole substitutes

A new polymerizable monomer, [4‐(9‐ethyl)carbazolyl]methyl methacrylate ( 2 ), was synthesized by reacting of methacrylic acid and 4‐hydroxymethyl‐9‐ethyl carbazole ( 1 ) by esterification procedure in the presence of N,N′‐dicyclohexylcarbodiimide. The resulting monomer was then polymerized free‐radically to form the poly(methyl methacrylate) containing 4‐(9‐ethyl)carbazolyl pend ent groups. Also, copolymerization of monomer 2 with various acrylic monomers such as methyl methacrylate, ethyl methacrylate, methyl acrylate, ethyl acrylate, and n‐butyl acrylate by azobisisobutyronitrile as a free radical polymerization initiator gave the related copolymers in high yields. The structure of all the resulted compounds was characterized and confirmed by FTIR and ¹H NMR spectroscopic techniques. The average molecular weight of the obtained polymers was determined by gel permeation chromatography using tetrahydrofurane as the solvent. The thermal gravimetric analysis and differential scanning calorimeter instruments were used for studying of thermal properties of polymers. It was found that, with the incorporation of bulky 4‐(9‐ethyl)carbazolyl substitutes in side chains of methyl methacrylate polymers, thermal stability and glass transition temperature of polymers are increased. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4989–4995, 2006     

话题转换方式和句子长度对边界声学参数的影响

该文研究了不同话题转换方式和句子长度对边界处停顿、边界前延长量及音高重置的影响。语料是由两个句子构成的小语篇,通过改变第二个句子控制两种句子长度(短和长)和三种话题转换方式(延续、精述和转折)。20位发音人的语音分析结果显示: (1) 话题转换方式和句子长度对停顿及音高重置都有调节作用,但对边界前词的时长延长量没有显著影响。另外,两因素间没有交互作用。主要表现为: 边界后句子越长,句间停顿越长,且边界处的音高重置越大。从话题延续、话题精述到话题转折,停顿时长呈增长趋势,且音高重置度增大; (2) 停顿时长与边界前延长量存在较弱的负相关,与音高重置则存在较弱的正相关; (3) 相较于男性发音人,女性发音人对话题转换方式更为敏感,且更倾向于用停顿和音高两种声学线索标记话题转换方式。句长效应则在男女发音人中都稳定存在。以上结果表明,句长对边界处声学参数的影响基于底层发音机制,而话题转换方式的影响则是语言中信息传递的需要。     

Transition phenomena of polymers in mixed solvents in the vicinity of theta conditions: Effect of preferential adsorption

Viscosimetric measurements were obtained with the ternary systems polystyrene/dioxane/methanol, polystyrene/benzene/methanol and poly(methyl methacrylate)/dioxane/cyclohexane, changing the solvent mixture composition at constant temperature. The polystyrene and poly(methyl methacrylate) systems exhibit a transition phenomenon with solvent-mixture composition in which the polymer is just above the theta condition. In the case where two theta conditions occur ((θ-intra, θ-inter) the transition point is closely related to the intramolecular theta conditions. Moreover the intramolecular theta conditions vary with the molecular weight in the region of molecular weights where the preferential adsorption also varies. This variation induces a variation of the transition point with molecular weight which obeys a formula analogous to that giving the variation of the preferential adsorption with molecular weight.     

Confinement, composition, and spin-coating effects on the glass transition and stress relaxation of thin films of polystyrene and styrene-containing random copolymers: Sensing by intrinsic fluorescence

The glass transition temperatures (T_gs) of polystyrene (PS) and styrene/methyl methacrylate (S/MMA) random copolymer films are characterized by intrinsic fluorescence, i.e., monomer fluorescence from an excited-state phenyl ring and excimer fluorescence from an excited-state dimer of two phenyl rings. The T_g is determined from the intersection of the rubbery- and glassy-state temperature dependences of the integrated fluorescence intensity measured upon cooling from an equilibrated state. With PS, the effects of nanoconfinement on T_g and the transition strength agree with results from studies using probe fluorescence and ellipsometry. The T_g-nanoconfinement effect is “tuned” by copolymer composition. As S-content is reduced from 100 mol% to 22 mol%, the confinement effect changes from a reduction to an enhancement of T_g relative to bulk T_g. Intrinsic fluorescence is also a powerful tool for characterizing relaxation of residual stresses. Stresses induced by spin coating affect local conformations, which in turn affect excimer and monomer fluorescence and thereby integrated intensity. The heating protocol needed to achieve apparently equilibrated local conformations is determined by equivalence in the integrated intensities obtained upon heating and subsequent cooling. While partial stress relaxation occurs upon heating in the glassy state, full relaxation of local conformations requires that a film be heated above T_g for times that are long relative to the average cooperative segmental relaxation time. For example, in thin and ultrathin films, equilibration is achieved by heating slowly (∼1 K/min) to 15-20 K above T_g. Dilute solution fluorescence of PS and S/MMA copolymers is also characterized and compared to reports in the literature.