等径角挤压后Ti5553钛合金的冲蚀磨损机理演变

本文中系统研究了经等径角挤压(ECAE)处理后的Ti5553钛合金在海砂环境中的冲蚀磨损机理演变历程和失效原因.发现Ti5553钛合金在高角度冲蚀工况下,其冲蚀磨损机理从初期的微切削转变为冲击挤压变形,并保持稳定;合金显微组织中弥散的α相以及ECAE工艺影响了冲蚀机理演变过程及冲蚀磨损程度;提高合金的强度、韧塑性对于抵抗冲蚀磨损起到了促进作用.     

FRP加固梁的FRP-混凝土界面脱胶分析

为了研究纤维增强聚合物(fiber reinforced polymer, FRP) 加固梁的FRP-混凝土界面脱胶破坏过程,本文将混凝土梁和FRP 板均视为线弹性的欧拉-伯努利梁(Euler-Bernoulli beams), 且两者通过粘结层胶结在一起. 对于FRP-混凝土结构,有两种形式的脱胶破坏：板端脱胶破坏和跨中裂缝导致的脱胶破坏.对于FRP-混凝土梁,利用合理的粘结模型按第2 种脱胶失效形式,详细讨论了FRP-混凝土界面的脱胶过程,得到了不同阶段的胶结滑移、界面剪应力和FRP 轴向力的解析解. 实验研究验证了理论分析的结果,参数研究进一步探讨了胶结长度和粘结层厚度对于FRP-混凝土界面脱胶行为的影响.     

Moment redistribution in continuous reinforced concrete beams strengthened with carbon-fiber-reinforced polymer laminates

The results of tests on continuous steel-fiber-reinforced concrete (RC) beams, with and without an external strengthening, are presented. The internal flexural steel reinforcement was designed so that to allow steel yielding before the collapse of the beams. To prevent the shear failure, steel stirrups were used. The tests also included two nonstrengthened control beams; the other specimens were strengthened with different configurations of externally bonded carbon-fiber-reinforced polymer (CFRP) laminates. In order to prevent the premature failure from delamination of the CFRP strengthening, a wrapping was also applied. The experimental results obtained show that it is possible to achieve a sufficient degree of moment redistribution if the strengthening configuration is chosen properly, confirming the results provided by two simple numerical models. Russian translation published in Mekhanika Kompozitnykh Materialov, Vol. 43, No. 5, pp. 667–686, September–October, 2007.     

Thermodynamic equilibrium of the solute distribution in size-exclusion chromatography

Our understanding of the nature of solute retention in size-exclusion chromatography (SEC) is predicated upon an equilibrium, entropy-controlled, size-exclusion mechanism. The entropic nature of the separation depends, in turn, upon the solute distribution coefficient (K(SEC) being at (or close to) thermodynamic equilibrium. Classic experiments to confirm this assumption were performed over thirty years ago. Here, we combine information obtained from both flow and static mixing SEC experiments to show that the solute distribution in SEC is in thermodynamic equilibrium over a molar mass range extending one order of magnitude higher than previously measured (from 2 x 10(3) to 1.1 x 10(6) Da) using crosslinked polystyrene packing material of identical pore size (10(4) A). The differences between our observations and previous ones conducted over three decades ago are ascribed, principally, to advances in stationary phase synthesis and column technology for SEC in particular and, secondarily, to improvements in the performance of the various instrumental components of liquid chromatographic systems in general.     

Dielectric relaxation studies of binary mixtures of N-methylacetamide and N-methylformamide in benzene solutions using microwave absorption data

Using standard microwave X-band technique and by following Gopala Krishna's single frequency (9.90?GHz) concentration variational method, the dielectric relaxation times (τ) and the dipole moments (μ) of dilute solution of N-methylacetamide (NMA), N-methylformamide (NMF) and NMA?+?NMF binary mixtures in benzene solutions have been calculated at different temperatures. The energy parameters for the dielectric relaxation process for NMA?+?NMF binary mixture containing 30?mol% NMF have been calculated at 25, 30, 35 and 40°C and compared with the corresponding viscosity parameters. A good agreement between the free energy of activation from these two sets of values shows that the dielectric relaxation process like the viscous flow process can be treated as the rate process. From relaxation time behavior of NMA and NMF binary mixture in benzene solution, solute–solute types of the molecular association has been proposed.     

Effect of pressure on retention factors in HPLC using a non-porous stationary phase

Summary Pressure and temperature have significant influence on retention in HPLC. This study investigates the effect of pressure and temperature on the retention behavior of aromatic hydrocarbons (toluene, ethyl benzene, butyl benzene, pentyl benzene) and polar, acidic and basic samples (phenol, acetophenone, N,N-dimethyl aniline, benzophenone) on a reversed phase column. The effect has been studied on non-porous, tetradecyl (C₁₄) coated silica particles. We found that the adsorption-induced decrease of the partial molar volume of the solutes investigated was between ΔV _m =5–15 cm³ mol⁻¹. The increment of the decrease of the partial molar volume due to the addition of one CH₂ group, for the homologous series of the aromatic hydrocarbons is approximately ΔV _CH2 =2.3 cm³mol⁻¹. Presented at Balaton Symposium '01 on High-Performance Separation Methods, Siófok, Hungary, September 2–4, 2001.     

Effect of short-chain alcohols on surfactant-mediated reversed-phase liquid chromatographic systems

The behaviour of β-blockers in a reversed-phase liquid chromatographic (RPLC) column with mobile phases containing a short-chain alcohol (methanol, ethanol or 1-propanol), with and without the surfactant sodium dodecyl sulphate (SDS), was explored. Two surfactant-mediated RPLC modes were studied, where the mobile phases contained either micelles or only surfactant monomers at high concentration. Acetonitrile was also considered for comparison purposes. A correlation was found between the effects of the organic solvent on micelle formation (monitored by the drop weight procedure) and on the nature of the chromatographic system (as revealed by the retention, elution strength and peak shape of β-blockers). When SDS is added to the mobile phase, the free surfactant monomers bind the C18 bonded chains on the stationary phase, forming an anionic layer, which attracts strongly the cationic β-blockers. The retention is modified as a consequence of the solving power of the organic solvent, micelles and surfactant monomers. The molecules of organic solvent bind the micelles, modify their shape, and may avoid their formation. They also bind the monomers of surfactant, desorbing them from the stationary phase, which affects the retention. The remaining surfactant covers the free silanols on the siliceous support, avoiding the interaction with the cationic solutes. The retention of β-blockers results from a combination of electrostatic and hydrophobic interactions, the latter being weaker compared to the hydro-organic system. The peak efficiencies and asymmetries are excellent tools to probe the surfactant layer on the stationary phase in an SDS/organic solvent system. The peaks will be nearly symmetrical wherever enough surfactant coats the stationary phase (up to 60% methanol, 40% ethanol, 35% 1-propanol, and 50% acetonitrile).     

Excited‐State Hydrogen Bonding Strengthening and Weakening with Intramolecular Charge Transfer in Resorufin‐Water Complexes: A TD‐DFT Study

The geometric structures, infrared spectra and hydrogen bond binding energies of the various hydrogen‐bonded Res^?‐water complexes in states S0 and S1 have been calculated using the density functional theory (DFT) and time‐dependent density functional theory (TD‐DFT) methods, respectively. Based on the changes of the hydrogen bond lengths and binding energies as well as the spectral shifts of the vibrational mode of the hydroxyl groups, it is demonstrated that hydrogen bonds HB‐II, HB‐III and HB‐IV are strengthened while hydrogen bond HB‐I is weakened in the four singly hydrogen‐bonded Res^?‐Water complexes upon photoexcitation. When the four hydrogen bonds are formed simultaneously between one resorufin anion and four water molecules in the Res^?‐4Water complex, all the hydrogen bonds are weakened in both the ground and excited states compared with those in the corresponding singly hydrogen‐bonded Res^?‐Water complexes. Furthermore, in complex Res^?‐4Water, hydrogen bonds HB‐II and HB‐IV are strengthened while hydrogen bonds HB‐I and HB‐III are weakened after the electronic excitation. The hydrogen bond strengthening and weakening in the various hydrogen‐bonded Res^?‐water complexes should be due to the redistribution of the charges among the four heteroatoms (O_1‐3 and N₁) within the resorufin molecule upon the optical excitation.     

Erosion of efficiency in non-uniform linear chromatography

In linear chromatography (i.e. chromatography performed in the absence of sample overloading), when the plate height of a column is roughly uniform along its length, variations in the velocities of solutes are the only possible causes of erosion of efficiency. The sources of these variations (variations in capacity ratio and in the density of the mobile phase, etc.) play no direct role in the erosion of efficiency except through their effect on solute velocities. In other words, what eventually causes the erosion of efficiency is merely variation in the time required for solutes to traverse equally small segments of a column. Significant erosion can only arise from abrupt and deep deceleration of solutes in one or several relatively small segments of a column. If erosion of efficiency caused by pressure gradients in linear SFC is to be large, the depth and the sharpness of the deceleration of a solute must go beyond that hitherto confirmed experimentally. Many relevant examples are analyzed graphically.