Enthalpy, heat of fusion and specific electrical resistivity of pure silver, pure copper and the binary Ag-28Cu alloy

Within the present work, recent investigation carried out with a fast pulse-heating technique on silver, copper and the Ag-28Cu binary alloy in the solid and the molten states are presented.Properties like enthalpy or electrical resistivity of a pulse-heated sample can be obtained for a wide temperature range (solid state up into the liquid state) from the directly measured base quantities, namely: current through the sample, voltage drop across the specimen and pyrometric determined temperature. As a further result, enthalpy of fusion is computable from the enthalpy values at the melting transition or the solidus/liquidus transition. These thermophysical properties (mainly of the melting transition and the subsequent liquid phase) are commonly used as input data for numerical casting simulations.The measurements presented within this work deal with group¹ 11 elements silver, copper and the binary eutectic 72-28 (wt.%) alloy of the two elements, respectively. One of the main goals of this work is to investigate to which extent the thermophysical properties of the two pure materials influence or determine the properties of its corresponding alloy. It is to proof if data for pure materials can be used to predict the thermophysical properties of simple alloys. For this specific copper-silver alloy, there is a certain mutual solid solubility with a quite large miscibility gap. Ag-28Cu is not a single phase alloy but an eutectic alloy with two phases.     

Determination of the temperature and enthalpy of the solid-solid phase transition of caesium nitrate by differential scanning calorimetry

The equilibrium temperature of the solid-solid phase transition of high purity caesium nitrate has been measured accurately by stepwise heating and by the extrapolation to zero heating rate method. A mean value of 154.3 ± 0.1 °C was obtained using two different heat flux DSC instruments. A value of 3.44 ± 0.04 kJ mol⁻¹ was determined for the enthalpy of transition.     

Liquid chromatography of polyoxyethylenes under critical conditions: a thermodynamic study

Polyethylene glycols (PEG), fatty alcohol ethoxylates (FAE) and fatty acid polyglycol esters were analyzed by liquid chromatography under critical conditions (LCCC) on typical reversed phase columns in mobile phases consisting of methanol-water and acetone-water in the region of the critical adsorption point (CAP) for the oxyethylene unit. Critical conditions can be adjusted by varying the mobile phase composition or temperature. In methanol-water the temperature dependence is almost negligible, while it is much more pronounced in acetone-water. Critical conditions for the oxyethylene unit were realized on octadecyl phases in methanol-water containing 85.8 wt.% methanol and in acetone-water at 89.6 wt.% acetone. In the van't Hoff plots the logarithm of the distribution coefficient was plotted versus the reciprocal temperature. In all plots straight lines were found, from slope and intercept of which the entropy and enthalpy changes were calculated. The relation of the thermodynamic parameters -deltaG/RT, -deltaH/RT, and deltaS/R to the numbers of A and B chain units in block copolymers AB and BAB at the CAP for A is studied both theoretically and experimentally. Various approaches for obtaining the critical temperature are discussed.     

不同结晶度的乙二醇及其水溶液玻璃化转变与焓松弛

为了考察晶体成分对无定形成分玻璃化转变和结构松弛行为的影响,利用差示扫描量热法(DSC),结合低温显微技术,研究了乙二醇(EG)及其50％水溶液在不同结晶度时的玻璃化转变和焓松弛行为.采用等温结晶方法控制骤冷的部分结晶玻璃体中的晶体份额.DSC结果表明,对于部分结晶的EG,只有单一的玻璃化转变过程,而对于50％EG,当结晶度不同时,不同程度地表现出两次玻璃化转变（无定形相Ⅰ和无定形相Ⅱ）.相Ⅰ的玻璃化转变温度和完全无定形态的含水EG的玻璃化转变温度相一致;相Ⅱ的玻璃化转变温度要比此温度约高6 ℃.低温显微观察结果印证了DSC实验结果.DSC等温退火的实验和KWW(Kohlrausch-Williams-Watts)衰变函数分析结果表明,EG无定形和50％EG中的两种无定形有不同的焓松弛行为.     

Enthalpies of addition of radicals to aldehydes, ketones, acids and esters

Enthalpies of the addition of radicals HO^•, HO₂ ^•, CH₃ ^•, CH₃O^•, CH₃O₂ ^• to the C=0 bond of model aldehydes, ketones, acids and esters have been calculated by thermodynamic and quantum chemical methods. It has been shown that the exothermic effect of these reactions decreases in the row HO^•>CH₃O^•>CH₃ ^•>HOO^•>CH₃OO^•.     

小功率等离子体射流的流特性

采用焓探针对小功率(5kW)热喷涂等离子体射流的焓、温度和速度进行了测量和计算。研究了气体成分、流量、电弧电压和电流对等离子流体的焓、温度和速度分布的影响。结果表明,对于单一氩气等离子体,当使用新喷嘴时,增大氩气流量能够使喷嘴内部电弧弧根向出口方向移动,从而增加等离子体射流的焓、温度和速度。对于Ar-N2等离子体,增加气体中氮气的含量,会提高等离子电弧电压,在同样的输入功率下,改变等离子电流和电压对等离子体的焓、温度和速度影响较小。对于Ar-N2等离子体,增加氢气含量会明显地提高等离子射流的速度和热传递。     

Colloidal chemistry as a guide to design intended dispersions of carbon nanomaterials

In this review, some established concepts from Colloidal Science and their application to graphene and carbon nanotubes dispersions in organic or aqueous media are highlighted to rationalize alternatives for some issues in terms of colloidal properties. Recent applications for carbon-based dispersions are presented, as well as van der Waals interactions in carbon materials and strategies to overcome these interactions, such as increasing electrostatic repulsion between dispersed particles, surface functionalization, or adsorption of passivation agents such as macromolecules, which are the basis of many dispersion and exfoliation procedures. The demonstration of how knowledge and fine control of colloidal interactions have been used to overcome several limitations, such as the preparation of stable and concentrated dispersions of carbon materials and keeping appreciable electrical conductivity, is presented. It is also showed that the same knowledge can help the development of more environmentally friendly carbon-based colloids as well as the improvement of similar systems as dispersions of two-dimensional materials.     

Enthalpies of Solution of Organic Compounds inWater/Octan-1-ol Mixtures. A Rationale Based ona Model of Structural Organization of the SolventMedium

Limiting enthalpies of solution _solnH°(oct/w) of several monofunctionalcompounds (tetrahydropyran, diethylamine, pyrrolidine, piperidine,1-methylpiperidine) in water–octan-1-ol mixtures with water content ranging from zero tosaturation have been determined at 25°C. The observed phenomenology hasbeen interpreted by supposing that the solvent medium undergoes a microphasetransition at water mole fraction of about 0.08. In the water-poor region theexperimental behavior is consistent with the presence of water molecules inprevailingly monodispersed form, while in the water-rich region the formationof organized pseudomicellar water aggregates is suggested. Two different simplemodels have also been proposed to describe quantitatively the observed trendsof _solnH°(oct/w) vs. mole fraction of water.Deceased while this research was in progress. The coauthors wish to dedicate this work to his memory