Excess volumes of ternary mixtures of N,N-dimethylformamide-diethyl ketone-1-alkanols at 303.15K

Volume changes on mixing of ternary liquid mixtures of N,N-dimethylformamide and diethyl ketone with 1-alkanols have been measured as a function of composition at 303.15 K. The alkanols include 1-propanol, 1-butanol, 1-pentanol and 1-hexanol. The measured V^E values are negative in the mixtures of N,N-dimethylformamide, diethyl ketone and 1-propanol, or 1-butanol. The V^E data exhibits an inversion in sign in the mixture containing 1-pentanol and positive excess volumes are observed in the mixture containing 1-hexanol. The measured data are compared with predicted values based upon empirical relations. The excess volume for the binary mixture of N,N-dimethylformamide with diethyl ketone has been measured over the entire range of composition at 303.15 K. The V^E values are negative for the binary mixture.     

Multilayer adsorption of alcohols from benzene/n-heptane mixtures on silica gel

An equation for multilayer adsorption from multicomponent liquid mixtures on solid surfaces¹ has been examined. For this purpose experimental adsorption data for four alcohols from benzene/n-heptane mixture on silica gel have been measured. Average number of the adsorbed layers, heterogeneity parameter and capacity of the surface phase have been evaluated by using the equation mentioned above.

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Mehrschichten-Adsorption von Alkoholen aus Benzol/n-Heptan-Mischung an Silica Gel

Zusammenfassung Eine Gleichung für Mehrschichten-Adsorption an festen Oberflächen¹ aus Mehrkomponentenlösungen wurde getestet. Zu diesem Zweck wurden experimentelle Daten für die Adsorption von vier Alkoholen aus Benzol/n-Heptan-Mischung an Silica Gel herangezogen. Der Mittelwert für die Anzahl der Adsorptionsschichten, der Heterogenitätsparameter und die Kapazität der Oberflächenphase wurde aus dieser Gleichung berechnet.

     

Monte Carlo simulation of a lattice model for ternary polymer mixtures

Monte Carlo studies of symmetrical polymer mixturesAB, modelled by selfavoiding walks withN _A =N _B =N steps on a simple cubic lattice, are presented for arbitrary concentrations of vacancies _v in the range from _v =0.2 to _v =0.8 and chain lengthsN64. We obtained the phase diagrams and the equation of state for three choices of the ratio / _AB ( being the energy between monomers of the same kind, _AB being the energy between different monomers). Flory-Huggins theory provides only a qualitative understanding of these results. If the equation of state is fitted with an effective Flory-Huggins parameter _eff , the latter turns out to be strongly dependent on both concentration and temperature.Contributed paper delivered at the Tagung der Deutschen Physikalischen Gesellschaft, Fachausschuß Polymerphysik, Berlin, March 30–April 3, 1987.     

Rapid determination of desorption efficiency, and analysis of solvent mixtures for occupational exposure studies

Summary An analytical procedure has been developed for simultaneous determination of solvent mixture vapors to enable evaluation of occupational exposure. To determine the desorption efficiency the volatile components of the solvent mixtures were generated from a glass tube filled with glass wool. This device is easy to prepare and use. These vapors were then collected in activated charcoal tubes and analyzed by capillary gas chromatography. The method was tested with a mixture of 22 solvents, including aliphatic and aromatic hydrocarbons, alcohols, ethers, esters, and ketones, all at low concentrations. All the components were detected. When a 99∶1 mixture of carbon disulfide-dimethylformamide was used for desorption the efficiency was>75% for most of the solvents.     

Effect of solvent composition on free release static coating of capillary columns

Summary Three aspects with respect to the selection of solvents for static coating of capillary columns, i.e. coating speed, occurrence of bumping and solubility of stationary phases are discussed. Hypotheses are proposed in an attempt to explain the observed facts that mixed solvents result in much higher coating speeds than those obtained from pure solvents, that a proper choice of solvents together with a good and uniform deactivitation of the column inner wall is needed to prevent bumping. Stationary phase solubility vs. solvent composition is also briefly discussed.     

Effect of Solvent on Competitive Bulk Membrane Transport of Transition and Post Transition Metal Cations Using Decyl-18-crown-6

A series of competitive metal ion transport experiments have been performed. Each involved transport from an aqueous source phase across an organic membrane phase into an aqueous receiving phase. The source phase contained equimolar concentrations of cobalt(II), nickel(II), cupper(II), zinc(II), cadmium(II), silver(I) and lead(II) metal cations. The membrane phase incorporated ionophore, decyl-18-crown-6. The membrane solvents include: chloroform, dichloromethane, 1,2-dichloroethane, nitrobenzene and chloroform–nitrobenzene binary solvents. A good transport efficiency and selectivity of Pb²⁺ transport from aqueous solutions are observed in this investigation. The selectivity order for competitive bulk liquid membrane transport of the studied transition and post transition metal cations through chloroform is: Pb²⁺>Co²⁺>Ni²⁺>Ag⁺>Cd²⁺, but in the case of dichloromethane, 1,2-dichloroethane and nitrobenzene as liquid membranes, the selectivity sequences were found to be: Pb²⁺>Co²⁺>Cd²⁺>Cu²⁺>Ag⁺>Ni²⁺>Zn²⁺, Pb²⁺>Co²⁺>Ag⁺>Ni²⁺>Zn²⁺ and Pb²⁺>Co²⁺>Ni²⁺>Zn²⁺>Cd²⁺>Ag⁺, respectively. The transport rate of the metal cations in chloroform–nitrobenzene binary solvents is sensitive to the solvent composition. The transport processes were studied in absence and presence of the stearic acid and the results show that the sequence of selectivities and ion transport rates change in the presence of stearic acid.     

Extractability of Curcuminoids Is Enhanced with Milk and Aqueous-Alcohol Mixtures

In this study, we evaluated the extractability of three curcuminoids (curcumin, demethoxycurcumin, and bisdemethoxycurcumin) from turmeric powder in several solvents using high-performance liquid chromatography (HPLC) with the diode-array detection method. These solvents include water, milk (homogenized, 2% reduced fat, low fat, fat free, soy, almond, coconut, and milkadamia), and aqueous ethanols (0%, 4%, 10%, 20%, 30%, 40%, 50%, and 100%). Ambient water was able to extract only 0.55 mg/g of curcuminoids, whereas warm water extracted more than four-fold higher amounts (2.42 mg/g). Almond, coconut, and milkadamia milk were able to extract only small amounts of curcuminoids at ambient temperatures (0.01–0.07 mg/g). The extractability of curcuminoids in these milk types did not improve, even in warm conditions (0.08–0.37 mg/g). Whereas dairy and soy milk extracted 6.76–9.75 mg/g of curcuminoids under ambient conditions, their extractability increased significantly in warm conditions by 30–100% higher (11.7–14.9 mg/g). The solubility of curcuminoids also varied remarkably in different proportions of aqueous-alcohol mixtures. With 4% ethanol, only 1.7 mg/g of curcuminoids were extracted, and the amounts improved with the increase in ethanol content up to 50% (32.2 mg/g), while 100% ethanol extracted a similar amount as 50% ethanol (34.2 mg/g). This study suggests that the extractability of curcuminoids from turmeric will be dependent on the type of diets consumed with the turmeric supplements.     

非共沸制冷剂R417A在水平光滑管内的沸腾传热

应用一种快速、准确的隐式格式迭代数值计算方法 ,对非共沸制冷剂 R41 7A在水平光滑管内的蒸发过程进行了数值模拟。通过应用纯质的传热公式计算后与实验值相比较 ,数值计算结果高于实验值。     

成分无序颗粒体系中切向力的分布

采用离散元模拟研究成分无序颗粒体系中切向力的几率分布.将切向力分为主切向力和次切向力分别进行统计,结果表明主切向力与次切向力服从不同的分布.随着缺陷率的增加,主切向力由近似的正态分布变为双峰状的分布,最后变为单峰状的分布;而次切向力总是指数型分布.通过理论计算和模拟讨论了切向力分布,说明缺陷率较大的成分无序体系与结构无序体系有类似的力分布规律.     

离散颗粒层被横向推移过程中的力学行为研究

研究发现,颗粒物质层被匀速推移挤压过程中,所需推移力先以线性规律增加,在某一确定点后,则会以指数规律增加.而颗粒物质是由众多离散颗粒组成的软凝聚态物质,其宏观上反映的是离散颗粒的个体性质和凝聚态物质的集体效应.颗粒与颗粒之间以及颗粒与边界之间的细观尺度接触力链的构成以及演变规律将会直接影响各种宏观受力情况,其摩擦力与挤压力便是力链的主要构成形式.围绕着定量描述细观力链特征,从而揭示力的变化规律这一目标,采用计算机模拟的方法,依照球形颗粒Hertz法向接触理论和Mindlin-Deresiewicz切向接触理论,对重力作用下不同数目的三维等径球体颗粒层的推移情况进行了离散元仿真模拟,量化分析了推移力变化规律、各摩擦力变化规律以及力链分布规律,发现摩擦力与挤压力在颗粒堆积的不同阶段对力链的构成起到了不同的主次作用,使得力链发生强弱演变,从而发现了推移颗粒物质层时推移力的变化规律及原因.这些结果有利于从力链角度揭示颗粒内部和颗粒与各边界之间的受力情况.