An easy pot incubation method for measuring nitrogen mineralization from easily decomposable organic material under well defined conditions

A pot incubation method for measuring mineralization dynamics from fresh plant material was tested. The aim was to develop a method which under well-defined conditions could produce mineralization data suited for estimating model input parameters for nitrogen prediction models. The results showed that the water tension of the soil could be controlled easily and precisely by diffusion through porous ceramic cups, and that nitrogen mineralization or immobilization could be measured already after 15 days at 15°C. The results showed that for the incubated catch crop residues carbon, nitrogen and nitrate-N contents were the most important factors determining mineralization. No significant effects ould be ascribed to other parameters measured.     

2-甲基-1,3-丙二醇水溶液的表面性质研究

采用最大泡压法测定了常压下纯液体2-甲基-1,3-丙二醇(MPO)及不同浓度MPO水溶液在298.15~367.7 K范围的界面张力。实验结果表明,纯MPO及其水溶液的界面张力σ随温度升高而呈线性减小;恒温下σ随浓度的增加呈幂函数递减。MPO水溶液的表面层发生正吸附,与理论上低脂肪醇类表面张力的性质符合。而且低浓度下MPO水溶液的吸附等温线呈直线,与G ibbs吸附等温式描述的规律相吻合。     

无患子表面活性物及其复配体系的性质研究

对天然植物原料无患子提取物中的表面活性物的性质（临界胶束浓度、表面张力和起泡性能）及其影响因素（温度、pH、水硬度和盐度等）进行了系统的研究，结果表明无患子表面活性物具有很低的cmc和γcmc，且在一定范围内受一些因素的影响也不大，是一种理想的香波原料；同时也研究了无患子活性物与其他温和型的阴离子表面活性剂的复配体系，表明具有明显的协同增效效果。     

Paste extrusion of polytetrafluoroethylene (PTFE): Surface tension and viscosity effects

The effects of the lubricant physical properties on the processing of polytetrafluoroethylene (PTFE) fine powder resins are studied. Lubricants having different surface tension and viscosity were used; the two properties changed independently. These effects were studied by using dies of various contraction angle and reduction ratio for resins having a variety of molecular architecture. It was found that the wettability (surface tension) of the lubricant strongly affects the pressure needed to extrude the PTFE pastes. The viscosity of the lubricant was also found to play a significant role in the process since a lubricant with a low viscosity causes the paste to be extruded at a lower pressure. These effects of the physical properties on the extrusion pressure influence significantly the mechanical properties of the final extrudates. The latter are functions of the degree of fibrillation, which is significantly influenced by the wettability and viscosity of lubricants. Finally, the effects of die geometry on extrusion pressure and mechanical properties of extrudates were also assessed in order to determine the geometrical characteristics and operation conditions for the optimization of the process.     

Effectiveness test of alginate‐derived polymeric surfactants

A series of alginate‐derived polymeric surfactants (APSs) with a linear alkyl group (C8, C12, C16) was synthesized by oxidation followed by reductive amination of 2,3‐dialdehydic alginate. The products were characterized by measuring IR spectra, NMR spectra, surface tension and critical micelle concentration (cmc). They were also tested for the solubilization of azobenzene and adsorption of heavy metal. In the case of 40% CHO‐C8 APSs, the lowest interfacial tension value (31.5 m Nm^?1) was obtained at the cmc value of 1.35 g dm^?3. The dissolving capacity of 40% CHO‐C8 APS towards azobenzene was 27 times greater than that of alginate. The overall cobalt (Co²⁺) removal efficiency by adsorption using APSs was high compared with that of sodium alginate at pH 3, 5 and 7. Equilibrium aspects of cobalt adsorption onto 10% CHO‐APSs were studied, and the results show that APSs had high equilibrium capacities for cobalt uptake, 115.5 mgg^?1. © 2002 Society of Chemical Industry     

两亲性无规共聚物MAA-SMA-PEGMA的表面活性研究

利用功能性单体甲基丙烯酸(MAA)、甲基丙烯酸十八烷基酯(SMA)和聚乙二醇甲基丙烯酸酯(PEG-MA)通过自由基共聚,合成了两亲性共聚物Poly(MAA-SMA-PEGMA)。研究了其结构、临界胶束浓度(CMC)和表面张力,探讨了由共聚物与低分子表面活性剂组成的复配体系。结果表明高低分子表面活性剂复配体系在质量比为5∶5后,体系的表面张力和临界胶束浓度都有所降低,接近于低分子表面活性剂。     

伊朗轻质原油减渣馏分油水界面张力的研究

The vacuum residual from Iranian Light crude oil are separated into a series of 16 narrow fractions according to the molecular weight by the supercritical fluid extraction and fractional (SFEF) technology. The chemical element and the UV spectrum of each fraction are analyzed. The effects of several factors on the interfacial tension are investigated, which are the fraction concentration in oil phase, the ratio of oil component, the salts dissolved in the water phase and the pH value. The interfacial tension decreases rapidly as the concentration of the residual fraction in the oil increases, showing a higher interfacial activity of the fraction. The interfacial tension changes, as the amount of absorption or the state of the fractions in the interface changes resulting from different ratios of oil, different kinds or concentrations of salts in water, and different pH values. It is concluded that the intrfacial tension changes regularly, corresponding to the regular molecular parameters of the vacuum residual fractions.     

Synthesis and solution properties of novel nonionic functional polyurethane surfactants

A series of novel nonionic functional polyurethane surfactants were synthesized by the polycondensation of 2,4‐toluene diisocyanate with poly(propylene oxide) (weight‐average molecular weight = 400, 1000, or 2000) and monoallyl‐end‐capped poly(ethylene oxide). The chemical structure of the polyurethane surfactants was determined by Fourier transform infrared and ¹H‐NMR, and the effects of the concentration, salt, rest time, and temperature on the surface tension were investigated. These polymeric surfactants exhibited excellent surface activity. Sample III, which was synthesized with monoallyl‐end‐capped poly(ethylene oxide) (number‐average molecular weight = 1000), poly(propylene oxide) (number‐average molecular weight = 2000), and tolylene diisocyanate, could reduce the surface tension to 37.6 mN/m at a concentration of 0.06 mol/L at 25°C. All polyurethane surfactants synthesized in this study had low critical micelle concentrations (ca. 10^?4 to 10^?5 mol/L) and could reduce the surface tension even at very low concentration levels. Moreover, the surface tension decreased with an increase in the temperature or the concentration of the polyurethane surfactants. The addition of salt resulted in a decrease in the surface tension, and it took some time for the polyurethane surfactants to reach a constant surface tension value. UV spectra were found to be very useful for determining the critical micelle concentration. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2956–2962, 2006     

Polymer/surfactant interaction—Its relevance to detergent systems

The field of polymer/surfactant interaction is reviewed in this work. Results from two investigative methods,viz., dialysis and surface tension, are discussed, illustrating the main behavioral patterns and outlining the principles of the interactions. Next, aspects of the interaction phenomena that appear to have relevance to detergent formulation are presented. These include solution rheology, solubility control and surface conditioning. Lastly, the importance of surface activity of the polymer itself is stressed, culminating in a discussion of the properties of hydrophobically modified water-soluble polymers (“polymeric surfactants”), both alone and in the presence of conventional surfactants. Based on the Samuel Rosen Memorial Award lecture, given at the AOCS Annual Meeting, Anaheim, CA, April 1993.     

Corrosion inhibition of triethanolammonium bromide mono- and dibenzoate as cationic inhibitors in an acidic medium

A weight loss technique was used to determine the corrosion inhibition efficiency of synthesized alkyl mono-and dibenzoate triethanolammonium bromide derivatives (TEAMB, TEADB) in an acidic medium (2 N HCl) at different doses (50, 100, and 200 ppm). The results showed that monoderivatives had a higher corrosion inhibition efficiency than diderivatives. The results were correlated with several factors, including the alkyl chain length of the hydrophobic chains, interfacial tension (IT), critical micelle concentration (CMC), and adsorption free energy of these inhibitors. Increasing the geometric length of the alkyl chains in the synthesized inhibitors had an increasing effect on their corrosion inhibition efficiency, whereas decreasing the CMC and IT had an increasing effect on their tendency toward corrosion inhibition. The number of hydrophobic chains attached to the inhibitor molecules had a vital influence on their efficiency as corrosion inhibitors.