双柱气相色谱法测定有机物的正辛醇/水分配系数

通过对烷烃，醇类等有机物在五种不同极性固定相上的气相色谱保留值的测定，提出了从有机物气相色谱保留值测定其正辛醇/分配系数的公式，研究了从不同极性固定相上测得的保留值来测定其分配系数的准确性，得出烷烃类在所有柱上测得的保留值与其分配系数间均具有很好的关联，烷烃醇类在极性相异柱上的保留值之比值与其分配系数间也有很好的相关性，从而为烷烃及醇类等有机物分配系数的测定提供了一种简单、可靠，易行的新方法。     

Measurements of HO2 uptake coefficient on aqueous (NH4)2SO4 aerosol using aerosol flow tube with LIF system

The γ(HO₂) was elevated with increase of Cu(II) concentrations in aqueous (NH₄)₂SO₄ aerosol. The threshold of Cu(II) concentration was 10^-3 mol/L for the dramatic increase of γ(HO₂) to 0.1, suggesting sensitive γ(HO₂) value to concentration of transition metal ions in aerosol.     

Surface structures of adsorption layers of sodium hyaluronate and bovine serum albumin complexes on poly(γ-methyl-l-glutamate) film and their surface properties

Two-dimensional structures and characteristics of the complexes between sodium hyaluronate (NaHA) and bovine serum albumin (BSA) were studied by using a quartz crystal microbalance method and an atomic force microscope (AFM). NaHA did not adsorb on poly(-methyl-l-glutamate) (PMLG) film. On the other hand, the complexes adsorbed on it and the adsorption behaviors were found to be Langmuir types. With increasing weight ratio of BSA to NaHA, W _BSA, the adsorption constants K decreased and the saturated adsorption masses increased. The adsorbed complexes were spherical particles and at saturated adsorption states they covered compactly on the PMLG film. The mean diameters d _AFM estimated from the topographic images decreased from 70 to 54 nm with increasing W _BSA. The adhesion force F _ad and the frictional force F _f between the complex layers and the AFM tip were obtained by using the contact mode of the AFM. With increasing W _BSA, the values of F _ad decreased and the values of F _f increased. Compared with the frictional coefficient of the NaHA adsorption layer on the BSA monolayer, the values for the NaHA–BSA complex layer were found to be much higher.     

Salting coefficients for gases in seawater from scaled-particle theory

Experimental values of the salting coefficients for He, Ne, Ar, O₂, and N₂ in seawater are compared with values calculated from scaled-particle theory. The agreement is reasonably good; the average difference between calculated and observed values at 25°C is 0.007. Scaled-particle theory predicts correctly thatk _s should decrease as the temperature increases and that this effect should be most pronounced at low temperatures. However, the predicted magnitude ofdK _s/dt is only about half of that observed.     

Osmotic and activity coefficients of sodium chloride-sorbitol and potassium chloride-sorbitol solutions at 25°C

Osmotic and activity coefficients are reported for sorbitol over the range 1.8–11.1m with NaCl as the reference and 1.8–7.6m with KCl as the reference electrolyte. The osmotic coefficients over the range 0–3.7m are identical with those reported earlier by Robinson. It was found that the activity coefficients of sorbitol are uniformly about four percent lower than those of dextrose. Activity coefficients of trace quantities of NaCl in concentrated sorbitol solutions are about one-half of their value in pure NaCl solutions while the activity coefficients of trace quantities of sorbitol in concentrated NaCl solutions are about one-third of their value in pure sorbitol solutions. Potassium chloride lowers the activity coefficient of sorbitol less than does sodium chloride in solutions of similar water activity. Sorbitol lowers the activity coefficients of potassium chloride in concentrated solution but actually elevates them in dilute solutions.     

Volumetric properties of ethanol–water mixtures under high temperatures and pressures

The densities of ethanol and ethanol–water mixtures were measured with a vibrating tube densimeter at 25.0, 50.0 and 75.0 °C in the pressure range from 0.10 to 40.00 MPa. Densities were correlated using an empirical model. Partial molar volumes, excess molar volumes, isothermal compressibilities, cubic expansion coefficients and internal pressures were calculated from obtained densities. This study reports the dependence of densities, partial molar volumes, excess molar volumes, isothermal compressibilities, cubic expansion coefficients and internal pressures on composition, temperature and pressure.     

含铅聚合物微凝胶与硫化氢反应前后在良溶剂中的分子扩散行为

用溶液聚合法制备出轻度交联的含铅微凝胶,用光子相关光谱技术测定其在良溶剂中与H2S反应前、后的扩散行为,由外推法得到在浓度无限稀时的分子扩散系数,给出微凝胶的流体力学半径。结果表明:相同量的含铅微凝胶在不同的初始浓度下与H2S反应,生成含PbS纳米微粒的凝胶；但其体积增大不同,这说明H2S与含铅微凝胶的反应既可以在分子内也可以在分子间进行,分子间的反应使含硫化铅微凝胶扩散系数随浓度的变化曲线的线性范围变小。     

固定pH滴定法测定弱酸弱碱性药物

报道一种水溶液吕测定弱酸弱碱性药物的新型滴定分析方法－固定ｐＨ滴定法，其理论基础是弱酸弱碱在水溶液中各种存在形式的分布系数在ｐＨ值固定时为常数，对甲硝唑，盐酸美西律等离散常数在１０＾－８至１０＾－１１范围内的７种弱酸弱碱性药物进行测定。结果与药典法吻合，回收率在９９．４％～１００．６％，方法简便，快速，准确，制剂中的赋形剂及色物不影响测定。     

Amino acid overproduction by analog resistant mutants of the nitrogen fixing cyanobacteriumAnabaena sp 287

Two amino acid analog resistant mutants of the cyanobacteriumAnabaena sp 287 were isolated after MNNG mutagenesis.Anabaena ST 16, a mutant resistant to the alanine analog D-α-aminobutyric acid andAnabaena ST 25, another mutant resistant to the histidine analog l,2,4-triazole-3-alanine, released alanine and histidine, respectively, into the medium upon immobilization in alginic acid during diazotrophic growth in fluidized bed reactors. The rates of amino acid production by the mutants were 4.3 μmol mg chl^-1 h^-1 of D-alanine byAnabaena ST 16 and 16.6 μnol mg chl^-1 h^-1 of L-histidine byAnabaena ST 25. Nitrogen fixation by the mutants was not affected by the extracellular amino acid concentration. While the radioactive carbon flow was followed, the parent strain retained 93% of fixed¹⁴C and released only 7% into the medium. On the other hand,Anabaena ST 16 released 13% andAnabaena ST 25 released 29% into the medium. These mutants are beneficial in the production of radioactive amino acids using diazotrophic photobiotechnology.