2-十一烷基-N-羧甲基-N-羟乙基咪唑啉与阴离子表面活性剂的协同效应

用最大气泡法测定咪唑啉的表面张力和临界胶束浓度 ,并与N 月桂酸 N 甲基牛磺酸钠 (AMT)复配后测其表面张力及其分子间的相互作用参数。利用正规溶液理论对它们的协同效应进行了讨论 ,表明实验值与计算结果相符。

盐酸氯丙嗪作探针共振瑞利散射法测定环境水样中某些阴离子表面活性剂

在pH3.0～5.0的HAc-NaAc缓冲溶液中,盐酸氯丙嗪与十二烷基苯磺酸钠(SDBS)、十二烷基硫酸钠(SDS)和十二烷基磺酸钠(SLS)等阴离子表面活性剂反应形成离子缔合物时,能导致共振瑞利散射(RRS)的显著增强并产生新的RRS光谱,最大RRS峰分别位于277,369和277nm处,方法对SDBS,SDS和SLS的检出限分别为0.018,0.046和0.200μg/mL,其线性范围分别为0.09～10.0,0.15～15.0和0.67～12.5μg/mL.研究了适宜的反应条件及分析化学性质,提出了一种用RRS技术灵敏、简便并快速测定阴离子表面活性剂的新方法.

阴阳离子混合表面活性剂体系的性质及其应用

综述了阴阳离子混合表面活性剂体系的表面活性、相行为、增溶性及起泡性等一些性质，说明了阴阳离子混合表面活性剂的不同分子比对界面性质的影响以及阴阳离子混合表面活性剂体系的广泛应用前景．

Extraction of Theanine from Waste Liquid of Tea Polyphenol Production in Aqueous Two-phase Systems with Cationic and Anionic Surfactants

Extraction of theanine from waste liquid of tea polyphenol production was studied in aqueous surfactanttwo-phase system （ASTP） with cationic surfactant （CTAB） and anionic surfactant （SDS）. Results indicate that the region of ASTP is narrow and there is only a two-phase region of cationic surfactant. The increase in concentrations of NaBr and Na2SO4 are beneficial to the formation of ASTP. Theanine concentration in the bottom phase increases with increasing concentration of theanine, whereas the Partition coefficient and extraction rate only change a littlewhen the concentration of theanine is above 0.2 g.L-＇. With the increase of SDS concentration, the phase ratio and the partition coefficient decrease, while the extraction efficiency of theanine increases and the concentration of theanine changes a little in the range from 2.4/7.5 to 2.8/7.2 for SDS/CTAB ratio. The temperature has a notable ef- fect on the concentration of theanine in the bottom phase, partition coefficient and extraction rate of theanine. The increase of waste liquid decreases the phase ratio, increases the concentration and extraction rate of theanine in the bottom ohase, since the orotein and the saccharide enter the bottom nhase with theanine.

Interaction of DNA with Cationic Gemini Surfactant Trimethylene-1, 3-bis （dodecyldimethyl-ammonium bromide） and Anionic Surfactant SDS Mixed System

The interaction of DNA with cationic gemini suffactant trimethylene-1,3-bis （dodecyl dimethyl-ammonium bromide） （12-3-12） and anionic surfactant sodium dodecyl sulfate （SDS） mixed system has been investigated by measuring the fluorescence, zeta potential, UV-Vis spectrum, and circular dichroism. In the absence of SDS, owing to the electrostatic and hydrophobic interactions, 12-3-12 forms micelle-like structure on the DNA chain before the micellization in bulk phase. For the mixed system of 12-3-12 and SDS, the negative charges on SDS can compete against DNA to bind with cationic 12-3-12 because of the stronger interaction between oppositely charged surfactants, and thus, the catanionic mixed micelles are formed before the formation of DNA/12-3-12 complexes. There-after, the positive charges on the mixed micelles bind with DNA, and thus, the change of the zeta potential from negative to positive is distinctly different from the system without SDS. Meanwhile, the existence of SDS postpones the exclusion of ethidium bromide （EB） from DNA/EB complexes. The conformation of DNA undergoes a change from native B-form to chiral ψ-phase as binding with 12-3-12 process. Upon adding SDS to the DNA/12-3-12 complex solution, however, DNA is released to the bulk and the ψ-phase returns to B-form again.

Effect of an Anionic Surfactant on Hydraulic Conductivities of Sodium- and Calcium-Saturated Soils

The effect of sodium dodecylbenzenesulfonate (SDBS), an anionic surfactant used widely in household products and industrial processes, on saturated hydraulic conductivities (Ksat) of an Anthrosol saturated with sodium (Na-soil) or calcium (Ca-soil) was analyzed in a laboratory experiment using the constant head method, and adsorption and dispersion experiments were also conducted to infer the possible mechanisms of Ksat fluctuations. The results showed that SDBS was more intensely adsorbed in the Ca-soil than in the Na-soil. With an increase in the SDBS concentration, the stability of the Na-soil suspensions decreased when the SDBS concentration was less than 1.2 mmol L-1 and then above this concentration, increased markedly, while the stability of the Ca-soil suspensions increased gradually at all SDBS concentrations studied. With an increase in the SDBS concentration, the Ksat of the Na-soil increased, which resulted mainly from the increase of water channels in the soil because of the coagulation of the soil particles, while the Ksat of Ca-soil decreased mainly on account of the clogging of partial water channels by precipitated Ca(DBS)2 and the fine soil particles generated.

Effects of Ionic Surfactants on Bacterial Luciferase and α-Amylase

In order to study the effects of ionic surfactants on bacterial luciferase,the cationic surfactant dodecyltrimethylammonium biomide (DTAB) and anionic surfactant sodium dodecylsulfate (SDS) were chosen.For comparison with bacterial luciferase,α-amylase was used since these two enzymes have similar electrostatic potential and charged active sites.After the enzymes were treated with the surfactants,the catalytic properties of bacterial luciferase andα-amylase were assayed,and fluorescence spectroscopy and circular dichroism (CD) were used to analyze the alteration of the protein structure.The results showed that when the DTAB concentration was low,the cationic surfactant DTAB enhanced the enzymatic activities of bacterial luciferase andα-amylase.On the other hand,the anionic surfactant SDS did not alter the enzymatic activity.The main interaction of cationic surfactant DTAB and the negatively charged surface of the proteins was the ionic interaction,which could alter the environment for the enzyme to work when the DTAB/enzyme molar ratio was low.However,at high cationic surfactant concentration,the ionic interaction and hydrophobic interaction might destroy the secondary and tertiary structures of the proteins,leading to the loss of enzymatic activities.

Influence of surfactants on bioleaching of arsenic-containing gold concentrate

To shorten the bioleaching cycle of arsenic-containing gold concentrate, surfactants were used to promote the interaction between bacteria and ore to increase the arsenic leaching rate. Three different kinds of surfactants were used to evaluate the effects of surfactants on the growth of bacteria and arsenic leaching rate of arsenic-containing gold concentrate. The mechanism underlying surfactant enhancement was also studied. Results show that when relatively low-concentration surfactants are added to the medium, no significant difference is observed in the growth and Fe2+ oxidation ability of the bacteria compared with no surfactant in the medium. However, only the anionic surfactant calcium lignosulfonate and the nonionic surfactant Tween 80 are found to improve the arsenic leaching rates. Their optimum mass concentrations are 30 and 80 mg/L, respectively. At such optimum mass concentrations, the arsenic leaching rates are approximately 13.7% and 9.1% higher than those without the addition of surfactant, respectively. Mechanism research reveals that adding the anionic surfactant calcium lignosulfonate improves the percentage of bacterial adhesion on the mineral surface and decreases the surface tension in the leaching solution.

Direct Synthesis of Amine-functionalized Mesoporous Silica for CO_2 Adsorption

Amine-functionalized mesoporous silica was prepared by using lauric acid and N-stearoyl-l-glutamic acid as structure directing agents via the S-N+-I- mechanism and applied to CO2 adsorption at room temperature. With γ-aminopropyltriethoxysilane as co-structure directing agent and due to the direct electrostatic interaction with anionic surfactant, most of the amino groups were uniformly distributed at the inner surface of pores and the per- formance was stable. The amine-functionalized mesoporous silica was characterized by Fourier transform infrared spectrometer, X-ray diffraction, nitrogen physisorption and thermogravimetric analysis. The CO2 adsorption capacity was measured by digital recording balance. At the room temperature and under the atmospheric pressure, the adsorption capacity of LAA-AMS-0.2 for CO2 and N2 is 1.40 mmol·g-1 and 0.03 mmol·g-1, respectively, indicating high separation coefficient of CO2/N2.

Effect of different surfactants on removal efficiency of heavy metals in sewage sludge treated by a novel method combining bio-acidification with Fenton oxidation

The aim of this work was to investigate the effect of different surfactants on the removal efficiency of heavy metals in sewage sludge treated by a method combining bio-acidification with Fenton oxidation. Four surfactants were adopted such as anionic surfactant(sodium dodecyl benzene sulfonate, SDBS), nonionic surfactants(tween-20 and tween-60) and cationic surfactant(hexadecyl trimethyl ammonium chloride, HTAC), respectively. The indigenous sulfur-oxidizing bacteria in bio-acidification phase were enriched and cultured from fresh activated sludge obtained from a wastewater treatment plant. It is shown that different surfactants exhibited distinct effect on the removal efficiency of heavy metals from sewage sludge. The nonionic surfactants,especially tween-60, promotes the solubilization of heavy metals, while the anionic and cationic surfactants hinder the removal of heavy metals. Copper is efficiently leached. The removal efficiency of cadium is relatively lower than that of Cu due to the demand for rigorous p H value. Lead is leached with a low efficiency as the formation of low soluble Pb SO4 precipitates.

Effects of Preparation Parameters on Paraffin Wax Microemulsion

The paraffin wax microemulsion was prepared from fully refined paraffin wax No.58-60 in the presence of a nonionic surfactant and an anionic surfactant.The influence of manufacturing parameters on the particle diameter of paraffin wax microemulsion included the quantity of the emulsifier,the temperature and emulsification time,the stirring speed,the pH value and the auxiliary ingredient(cosurfactant).The test results showed that the temperature of emulsification had little effect on the particle size of paraffin wax microemulsion in a temperature range of 75-85 ℃.Other manufacturing parameters all had a great effect on the particle size of paraffin wax microemulsion.The optimum preparation conditions included:a w(emulsifier) of 6%,an emulsification temperature of 80 ℃,an emulsification time of 40 min,a pH value of about 8,and a stirring speed of 600 r/min,with n-amyl alcohol serving as the co-surfactant.Under these conditions,a translucent and baby blue paraffin wax emulsion was prepared with its particle size equating to 97 nm.

Development of Ru-Decorated Carbon Nanotubes-Supported Catalyst for a Microchannel Methanation Reactor

In this study, MWNT and alumina nanopowder were used as a ruthenium catalyst support for the conversion of carbon monoxide to methane. Metal foam structures were employed to support such catalytic systems, offering interesting possibilities for commercial applications due to low-pressure drop; excellent flow characteristic and heat transfer properties. Prior to the ruthenium impregnation, the MWNT surface was initially modified by means of metal cation activation and surface adsorption of anionic surfactant. The decoration processes using both surface modifications promoted the deposition of ruthenium with a mean 2 nm diameter. The use of nickel as a nucleating center enhanced the Ru nanoparticle density on the CNT surface compared to the Ru/CNT catalyst prepared by excess solution impregnation. As a reducing agent, ethylene glycol completely converted Ru2＋ to Ru0as confirmed by an EDS/TEM analysis. Among the prepared catalysts, Ru/AI203-CNTs prepared by Ni2＋ activation showed the best performance for the hydrogenation reaction. This is interpreted in terms of the higher ruthenium nanoparticle exposure on the nanostructured catalyst, as a result of the better MWNT dispersion in the MWNT/Al2O3 mixture.

Research on solubilization used for micellar enhanced ultrafiltration

Micellar enhanced ultrafiltration （MEUF） is a new effective treatment technology for the filtration removal of organic pollutants through solubilization. The present paper is aimed to study the solubilization of organic compounds such as chlorobenzene （CB）, pyrene and phenol by anionic, cationic and mixed anionic-nonionic surfactants such as sodium dodecyl sulfate （SDS）, cetyltrimethylammonium bromide （CTMAB） and Tween-80 （TW80） and the mixed SDS-TW80 with a batch equilibrium method. This study enables us to supply deeper investigation for MEUF. The results showed that solubilization capacity was not obvious below the critical micellar concentration （CMC）. The apparent solubilities of organic compounds were linearly related to surfactant concentrations over their CMCs. Solubilization capacity by single surfactants follow the order of TW80 〉 CTMAB 〉 SDS. The results also proved that the solubilization of the organic contaminants by the mixed surfactants can significantly be enhanced compared with the single anionic surfactant SDS. Whereas the CMC can be decreased, the solubility can be increased as long as the mass ratio of nonionic surfactant increases. The solubility enhancement efficiency of the different organic compounds follow the order of phenol 〉 CB 〉 pyrene. In addition, the solubilization ratio appears to be positively relative to the intrinsic water solubility of the organic contaminants and negatively correlates to octanol-water coefficients （Kow） of organic compounds and the hydrophile-lypophile balance values （HLB） of the surfactants.

Solvent extraction of thorium(Ⅳ) using W/O microemulsion

The extraction of thorium(IV) was investigated using two types of W/O microemulsion,one of which was formed by a surface-active saponified extractant sodium bis(2-ethylhexyl) phosphate(NaDEHP) and the other was formed by a mixture of an anionic surfactant sodium bis(2-ethylhexyl) sulfosuccinate(AOT) and an extractant bis(2-ethylhexyl)phosphoric acid(HDEHP) as the cosurfactant.The extraction capacities of the above two systems were higher than that of the HDEHP extraction system.High concentration of NaNO 3 showed no influence on the extraction in the NaDEHP based W/O microemulsion system,whilst reduced the extractability in the AOT-HDEHP W/O microemulsion system.The mechanism in acidic condition was demonstrated by the log-log plot method.The structure of the aggregations and the water content in the organic phase after extraction were measured by dynamic light scattering and Karl Fischer water titration,respectively.It was found that NaDEHP based W/O microemulsion broke up after extraction,while AOT-HDEHP W/O microemulsion was reserved.

Anionic surfactant anchoring enables 23.4%efficient and stable perovskite solar cells

Nonradiative recombination losses at defects in metal halide perovskite films are responsible for hindering the improvement of the photovoltaic performance and stability of perovskite solar cells(PSCs).Here,we report a feasible multifunctional additive strategy that uses cesium stearate to passivate defects in perovskite films and simultaneously enhances the tolerance to light and moisture stress.Nonradiative recombination losses are effectively suppressed in target films that exhibit improved crystallinity,low trap-state density,and enhanced carrier separation and transportation.The present strategy hence boosts the power conversion efficiency of the pi-n structured PSC to 23.41%.Our device also shows good stability in ambient air without encapsulation,maintaining 91.6%of the initial efficiency after 720 h.

Structural properties of hydroxyl-substituted alkyl benzenesulfonates at the water/vapor and water/decane interfaces

Molecular dynamics simulations have been performed to investigate the structural properties of hydroxyl-substituted alkyl benzenesulfonate monolayers formed at the water/vapor and water/decane interfaces.We report a detailed study of the interfacial properties-liquid density profile,hydrogen bond structure,surfactant aggregate structure and order parameter-of the novel anionic surfactant,sodium 2-hydroxy-3-decyl-5-octylbenzenesulfonate(C10C8OHphSO3Na).Simulation results show that:with increasing number of surfactant molecules,the average number of intramolecular hydrogen bonds per surfactant molecule in the monolayer decreases,but the structures forming the intramolecular hydrogen bonds still play a dominant role;the hydrophobic part of the alkyl tail chain,especially the decyl substituent on the third carbon atom in the benzene ring,becomes straighter,and more ordered towards the external interface at higher surfactant coverage;two-dimensional radial distribution functions can describe the characteristic of surfactant aggregate structures and highlight the decane phase effect on the orientation of the hydrophobic part of the surfactant;the surfactant molecules readily form long-range hydrogen bonded structures.Our results are an important complement to experimental studies.We used the all-atom model by employing the GROMACS and ffAMBER programs in the simulations,which provides a new way to simulate the interfacial behavior of alkyl benzenesulfonate surfactants.