基于乙醇/水体系的Fmoc-L-亮氨酸化学结构鉴定

基于乙醇/水溶液体系结晶纯化制备了Fmoc-L-亮氨酸.通过HRMS,IR和1 H NMR对该化合物进行了化学结构分析.被测化合物相对分子质量与Fmoc-L-亮氨酸理论相对分子质量一致,含有芴环、酰胺键和苯环等Fmoc-L-亮氨酸特征基团,其结构与目标化合物的分子结构一致.

Measurement of Liquid Diffusion Coefficients of Aqueous Solutions of Glycine, L-Alanine, L-Valine and L-Isoleucine by Holographic Interferometry

The diffusion coefficients of aqueous solutions ofglycine, L-alanine, L-valine and L-isoleucine at 298.15 K were determined by holographic interferometry with accuracy and promptness while without disturbance. The density and viscosity of these solutions were also determined. According to original Gordon model, a model for correlating the diffusion coefficients of amino acids in aqueous solutions was developed and applied. The results showed that this model provided significant convenience in correlation of diffusion coefficients for amino acids system.

Copper partitioning between granitic silicate melt and coexisting aqueous fluid at 850°C and 100 MPa

Experiments on the partitioning of Cu between different granitic silicate melts and the respective coexisting aqueous fluids have been performed under conditions of 850 ℃, 100 MPa and oxygen fugacity （fO2） buffered at approaching Ni-NiO （NNO）. Partition coefficients of Cu （Dcu = Cfluid/Cmelt） were varied with different alumina/alkali mole ratios [Al2O3/（Na2O ＋ K2O）, abbreviated as Al/ Alk], Na/K mole ratios, and SiO2 mole contents. The DCu increased from 1.28 ± 0.01 to 22.18 ±0.22 with the increase of Al/Alk mole ratios （ranging from 0.64 to 1.20） and Na/K mole ratios （ranging from 0.58 to 2.56）. The experimental results also showed that Dcu was positively correlated with the HCl concentration of the starting fluid. The Dcu was independent of the SiO2 mole content in the range of SiO2 content considered. No Dcu value was less than 1 in our experiments at 850 ℃ and 100 MPa, indicating that Cu preferred to enter the fluid phase rather than the coexisting melt phase under most conditions in the melt-fluid system, and thus a significant amount of Cu could be transported in the fluid phase in the magmatichydrothermal environment. The results indicated that Cu favored partitioning into the aqueous fluid rather than the melt phase if there was a high Na/K ratio, Na-rich, peraluminous granitic melt coexisting with the high Cl^- fluid.

Influence factors on thermal conductivity of ammonia-water nanofluids

In order to investigate the mechanism of nanoparticles enhancing the heat and mass transfer of the ammonia-water absorption process,several types of binary nanofluids were prepared by mixing Al2O3 nanoparticles with polyacrylic acid(PAA),TiO2 with polyethylene glycol(PEG 1000),and TiN,SiC,hydroxyapatite(noodle-like) with PEG 10000 to ammonia-water solution,respectively.The thermal conductivities were measured by using a KD2 Pro thermal properties analyzer.The influences of surfactant and ammonia on the dispersion stabilities of the binary nanofluids were investigated by the light absorbency ratio index methods.The results show that the type,content and size of nanoparticles,the temperature as well as the dispersion stability are the key parameters that affect the thermal conductivity of nanofluids.For the given nanoparticle material and the base fluid,the thermal conductivity ratio of the nanofluid to the ammonia-water liquid increases as the nanoparticle content and the temperature are increased,and the diameter of nanoparticle is decreased.Furthermore,the thermal conductivity ratio increases significantly by improving the stabilities of nanofluids,which is achieved by adding surfactants or performing the proper ammonia content in the fluid.

Measurement and Correlation on Liquid DifFusion Coefficients of Aqueous L-Threonine Solutions from 298.15K to 328.15 K

The diffusion coefficients of aqueous L-threonine solutions were determined from 298.15 K to 328.15 K by the metallic diaphragm cell method with accuracy, promptness and convenience. Meanwhile, the densities and viscosities of the solutions were also determined and correlated. Based on a semi-empirical model for correlating the diffusion coefficients of some amino acids in their aqueous solutions, a new semi-empirical model for correlating the diffusion coefficients involving temperature was provided, which is more comprehensive and less experiment dependent compared to the previous model. The fitting results are satisfactory. Compared to a former model for correlating the diffusion coefficients of solid organic salts in their aqueous solutions, this model provides significant improvement in correlation of diffusion coefficients with different temperatures avoiding arduous work.

Density and Viscosity of Ternary Systems(Poloxamer 188+Ethanol/ Acetone+Water)at Temperatures from 288.15 K to 308.15 K

The densities and viscosities of ternary systems(Poloxamer 188+ethanol/acetone+water)were meas- ured at 288.15,293.15,298.15,303.15,308.15 K and atmospheric pressure for different mass fractions of Poloxamer 188(0 to 0.02)in aqueous solution and different solvent volume fractions of ethanol/acetone(0 to 0.3)in Poloxamer 188 aqueous solution.The densities were measured by a pycnometer,while the viscosities were measured using two Ubbelohde capillary viscometers.The correlations of density and viscosity of these ternary systems are obtained by fitting the experimental data at different temperatures,mass fractions and volume fractions.

Calculating models of mass action concentrations for structural units or ion couples in RbCl-H_2O binary system and RbCl-RbNO_3-H_2O ternary system

Thermodynamic models of calculating mass action concentrations for structural units or ion couples in RbCl-H2O binary and RbCl-RbNO3-H2O ternary strong electrolyte aqueous solutions were developed based on the ion and molecule coexistence theory at 298.15 K.A transformation coefficient is needed to compare the calculated mass action concentration and the reported activity because they are obtained at different standard states and concentration units.The results show that the transformation coefficients between the calculated mass action concentrations and the reported activities of the same structural units or ion couples in RbCl-H2O binary and RbCl-RbNO3-H2O ternary strong electrolyte aqueous solutions change in a very narrow range.The transformed mass action concentrations of structural units or ion couples in RbCl-H2O binary system are in good agreement with the reported activities. The transformed mass action concentrations of RbCl and RbNO3 in RbCl-RbNO3-H2O ternary solution are also in good agreement with the reported activities,aRbCl and 3RbNOa,with different total ionic strengths as 0.01,0.05,0.1,0.5,1.0,1.5,2.0,3.0 and 3.5 mol/kg,respectively.All those results mean the developed thermodynamic model of strong electrolyte aqueous solutions can reflect structural characteristics of RbCl-H2O binary and RbCl-RbNO3-H2O ternary strong electrolyte aqueous solutions and the mass action concentration also strictly follows the mass action law.

Mechanism of Coalescence Demulsification with Microfiltra- tion Membrane

A study on the membrane coalescence demulsification was carried out with four working systems of water/n-butyl alcohol, water/n-octanol, water/30% TBP(in kerosene) and water/kerosene. The membranes made of polytetrafluoroethylene (PTFE) with 1.0μm pore size were used. The results indicated that the excellent demulsification efficiency for emulsions with various oil contents was obtained. A conductivity probe was used to study the demulsification mechanism. An electrode probe was designed and used to determine the oil content near the membrane surface. The obtained data showed that the oil content in the permeated stream was much higher than that in the feed emulsion. A physical mechanism to explain the membrane demulsification was put forward.

Electrical conductivities for four ternary electrolyte aqueous solutions with one or two ionic liquid components at ambient temperatures and pressure

This work provides a method to explore the transport property of the electrolyte aqueous solutions with one or two ionic liquids, especially focus on their electrical conductivity. The conductivities were measured for the ternary systems Na Cl–[C6mim][Cl](1-hexyl-3-methylimidazolium chloride)–H2O, [C6mim][BF4]–[C6mim][Cl]–H2O,Na NO3–[C6mim][BF4](1-hexyl-3-methylimidazolium tetrafluoroborate)–H2O, and [C4mim][BF4](1-butyl-3-methylimidazolium tetrafluoroborate)–[C6mim][BF4]–H2O, and their binary subsystems NaN O3–H2O, NaC l–H2O,[C6mim][BF4]–H2O, [C6mim][Cl]–H2O, and [C4mim][BF4]–H2O, respectively. The conductivities of the ternary systems were also determined using generalized Young's rule and semi-ideal solution theory in terms of the data of their binary solutions. The comparison showed that the two simple equations provide good predictions for conductivity of mixed electrolyte solutions and the mixed ionic liquid solutions based on the conductivity of their binary subsystems.

Study on the compatibility of cement-superplasticizer system based on the amount of free solution

The changes of free solution amount, fluidity and the time-depended fluidity loss of cement paste were examined by varying the water-cement ratio and the dosages of superplasticizer. The distribution of solution and flocculation microstructure in flesh cement paste was observed with optical microscope. The change of free solution amount and its effect on the fluidity and bleeding of cement paste was studied. The results show that the adsorbed solution amount has a great influence on the com- patibility of cement-superplasticizer system, including the bleeding degree, the fluidity and the time-depended fluidity loss of cement paste. Superplasticizer increases the fluidity of cement paste by destroying the flocculated cement particle structure and increasing the amount of adsorbed solution. Polycarboxylate superplasticizer shows higher ability of adsorption than naphtha- lene superplasticizer. Over dosage of superplasticizer is not the primary cause of bleeding. The principle reason of bleeding is the high water-cement ratio and the insufficient enhancing ability of water adsorption of superplasticizer.

Effect of Abiotic Factors on the Mercury Reduction Process by Humic Acids in Aqueous Systems

As a global pollutant process, the reduction of mercury （Hg） is especially important. One pathway is through an abiotic reduction with humic acids （HAs）, which is controlled by different factors, including initial Hg and HA concentrations, pH, temperature and light. In this study, three humic acids were selected to illustrate the Hg2＋ abiotic reduction mechanisms by HAs, and to identify the key limiting factors for reduction rates and amounts. In addition, the initial status of the HAs as a solid or in an aqueous solution were also compared, to help explain why HAs show different dominant characteristics （e.g. complexation or reduction） in the reaction process with Hg. Results indicated that HAs were able to reduce Hg abiotically. Higher initial Hg, higher HA concentrations and either high （8.1） or low （3.6） solution pH decreased the HA reduction capacity. In addition, Hg~ production rates increased with increasing temperature, and the same trend was observed with light exposure. Humic acids added as an aqueous solution resulted in significantly greater HgO production than addition as a bulk solid. Finally, the Hg reduction rate and capacity varied significantly （P 〈 0.05） with HAs from different sources. These findings helped to explain why HAs showed different dominant characteristics （e.g. complexation or reduction） in the reaction process with of Hg2＋ reduction, which indicated that humic substances in sink or a source for Hg. Hg, and evidentially demonstrated the existence of a possible pathway natural environments, especially in water bodies, could act either as a