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Sample records for surfactant solution consisted

  1. Solubilization of Hydrophobic Dyes in Surfactant Solutions

    Directory of Open Access Journals (Sweden)

    Ali Reza Tehrani-Bagha

    2013-02-01

    Full Text Available In this paper, the use of surfactants for solubilization of hydrophobic organic dyes (mainly solvent and disperse dyes has been reviewed. The effect of parameters such as the chemical structures of the surfactant and the dye, addition of salt and of polyelectrolytes, pH, and temperature on dye solubilization has been discussed. Surfactant self-assemble into micelles in aqueous solution and below the concentration where this occurs—the critical micelle concentration (CMC—there is no solubilization. Above the CMC, the amount of solubilized dye increases linearly with the increase in surfactant concentration. It is demonstrated that different surfactants work best for different dyes. In general, nonionic surfactants have higher solubilization power than anionic and cationic surfactants. It is likely that the reason for the good performance of nonionic surfactants is that they allow dyes to be accommodated not only in the inner, hydrocarbon part of the micelle but also in the headgroup shell. It is demonstrated that the location of a dye in a surfactant micelle can be assessed from the absorption spectrum of the dye-containing micellar solution.

  2. Fluorescence emission of pyrene in surfactant solutions.

    Science.gov (United States)

    Piñeiro, Lucas; Novo, Mercedes; Al-Soufi, Wajih

    2015-01-01

    The systematic description of the complex photophysical behaviour of pyrene in surfactant solutions in combination with a quantitative model for the surfactant concentrations reproduces with high accuracy the steady-state and the time resolved fluorescence intensity of pyrene in surfactant solutions near the cmc, both in the monomer and in the excimer emission bands. We present concise model equations that can be used for the analysis of the pyrene fluorescence intensity in order to estimate fundamental parameters of the pyrene-surfactant system, such as the binding equilibrium constant K of pyrene to a given surfactant micelle, the rate constant of excimer formation in micelles, and the equilibrium constant of pyrene-surfactant quenching. The values of the binding equilibrium constant K(TX100)=3300·10³ M⁻¹ and K(SDS)=190·10³ M⁻¹ for Triton X-100 (TX100) and SDS micelles, respectively, show that the partition of pyrene between bulk water and micelles cannot be ignored, even at relatively high surfactant concentrations above the cmc. We apply the model to the determination of the cmc from the pyrene fluorescence intensity, especially from the intensity ratio at two vibronic bands in the monomer emission or from the ratio of excimer to monomer emission intensity. We relate the finite width of the transition region below and above the cmc with the observed changes in the pyrene fluorescence in this region.

  3. Foaming behaviour of polymer-surfactant solutions

    Energy Technology Data Exchange (ETDEWEB)

    Cervantes-MartInez, Alfredo [Departamento de Investigacion en PolImeros y Materiales, Universidad de Sonora, Apartado Postal 130, 83000 Hermosillo, Sonora (Mexico); Maldonado, Amir [Departamento de Fisica, Universidad de Sonora, Apartado Postal 1626, 83000 Hermosillo, Sonora (Mexico)

    2007-06-20

    We study the effect of a non-ionic amphiphilic polymer (PEG-100 stearate also called Myrj 59) on the foaming behaviour of aqueous solutions of an anionic surfactant (sodium dodecyl sulfate or SDS). The SDS concentration was kept fixed while the Myrj 59 concentration was varied. Measurements of foamability, surface tension and electrical conductivity were carried out. The results show two opposite effects depending on the polymer concentration: foamability is higher when the Myrj 59 concentration is low; however, it decreases considerably when the polymer concentration is increased. This behaviour is due to the polymer adsorption at the air/liquid interface at lower polymer concentrations, and to the formation of a polymer-surfactant complex in the bulk at higher concentrations. The results are confirmed by surface tension and electrical conductivity measurements, which are interpreted in terms of the microstructure of the polymer-surfactant solutions. The observed behaviour is due to the amphiphilic nature of the studied polymer. The increased hydrophobicity of Myrj 59, compared to that of water-soluble polymers like PEG or PEO, increases its 'reactivity' towards SDS, i.e. the strength of its interaction with this anionic surfactant. Our results show that hydrophobically modified polymers have potential applications as additives in order to control the foaming properties of surfactant solutions.

  4. Dynamic Surface Tensions of Fluorous Surfactant Solutions

    Institute of Scientific and Technical Information of China (English)

    高艳安; 侯万国; 王仲妮; 李干佐; 韩布兴; 张高勇; 吕锋锋

    2005-01-01

    Dynamic surface properties of aqueous solutions of cationic fluorous surfactant CF3CF2CF20(CF(CF3)CF2O)2CF(CF3)CONH(CHE)3N+(C2H5)2CH3I- (abbrev. FC-4 ) were reported. The critical micelle concentration (cmc)(3.6×10-5 mol/L) and equilibdum surface tensions γeq were measured by Krtlss K12 tension apparatus. Dynamic surface tension γ(t) was measured in the range of 15 ms to 200 s using the MBP tensiometer. The surface excess Γ,as a function of concentration, was obtained from equilibrium tensiometry using the Gibbs equation. Data from these experiments were combined to analyze the γ(t) decays according to the asymptotic Ward and Tordai equation.The results show that at the initial adsorption stage, the dynamic surface tension data were all consistent with this diffusion-controlled mechanism, and at the end of the adsorption process, there were some evidences for an adsorption barrier, suggesting a mixed diffusion-controlled adsorption mechanism. Using measured quantities, the barrier strength was estimated as between 25 and 35 kJ/mol at 25℃. The surface pressure plays an important role in contributing to the barrier.

  5. The Krafft temperature of surfactant solutions

    Directory of Open Access Journals (Sweden)

    Manojlović Jelena Ž.

    2012-01-01

    Full Text Available Our main motivation to revisit the solution properties of cetyltrimethylammonium bromide is related to the clear requirement for better control of the adsorption parameters to form uniform self-assembled monolayers on muscovite mica substrates. To readily monitor the temporal evolution of structural details in cetyltrimethylammonium bromide solutions, we realized a rather simple conductivity experiment. Conductivity measurements were carried out as a function of temperature, to look closer into the Krafft temperature behavior of this surfactant. We measured the electrical conductivity of different concentrations of aqueous cetyltrimethylammonium bromide solutions, below and above the critical micells concentration.

  6. Heat-regulated foaming in surfactant solutions

    Energy Technology Data Exchange (ETDEWEB)

    Pletnev, M.Y.; Eremina, L.D.; Vlasenko, I.G.

    1984-01-01

    This article examines the mechanism of the foam-inhibiting action resulting from the use of propylene oxide derivatives in solutions both of anionic and of nonionic surfactants. The objective is the creation of a detergent composition with heat-regulated foaming, which would foam well at 30-50/sup 0/ and poorly at 80-90/sup 0/, which is the usual temperature of washing machines. It is demonstrated that foaming can be regulated by the variation of the cloud points of solutions with the aid of additions of polypropylene glycols and their alkyl derivatives or block copolymers in solutions of surfactants. Foaming and foam stability decrease sharply above the cloud points of the solutions due to the foam-inhibiting action of the coacervate phase on the coexisting foam-forming solution. The foam inhibition of polypropylene glycols increases and becomes apparent at lower concentrations with the increase of the average molecular weight of the hydrophobic blocks, the increase of their relative content (in block copolymers with oxyethylene groups), and upon the introduction of alkyl groups.

  7. Evaporation of droplets of surfactant solutions.

    Science.gov (United States)

    Semenov, Sergey; Trybala, Anna; Agogo, Hezekiah; Kovalchuk, Nina; Ortega, Francisco; Rubio, Ramón G; Starov, Víctor M; Velarde, Manuel G

    2013-08-13

    The simultaneous spreading and evaporation of droplets of aqueous trisiloxane (superspreader) solutions onto a hydrophobic substrate has been studied both experimentally, using a video-microscopy technique, and theoretically. The experiments have been carried out over a wide range of surfactant concentration, temperature, and relative humidity. Similar to pure liquids, four different stages have been observed: the initial one corresponds to spreading until the contact angle, θ, reaches the value of the static advancing contact angle, θad. Duration of this stage is rather short, and the evaporation during this stage can be neglected. The evaporation is essential during the next three stages. The next stage after the spreading, which is referred to herein as the first stage, takes place at constant perimeter and ends when θ reaches the static receding contact angle, θr. During the next, second stage, the perimeter decreases at constant contact angle θ = θr for surfactant concentration above the critical wetting concentration (CWC). The static receding contact angle decreases during the second stage for concentrations below CWC because the concentration increases due to the evaporation. During the final stage both the perimeter and the contact angle decrease. In what follows, we consider only the longest stages I and II. The developed theory predicts universal curves for the contact angle dependency on time during the first stage, and for the droplet perimeter on time during the second stage. A very good agreement between theory and experimental data has been found for the first stage of evaporation, and for the second stage for concentrations above CWC; however, some deviations were found for concentrations below CWC.

  8. Self-consistent field modeling of non-ionic surfactants at the silica-water interface: Incorporating molecular detail

    NARCIS (Netherlands)

    Postmus, B.R.; Leermakers, F.A.M.; Cohen Stuart, M.A.

    2008-01-01

    We have constructed a model to predict the properties of non-ionic (alkyl-ethylene oxide) (C(n)E(m)) surfactants, both in aqueous solutions and near a silica surface, based upon the self-consistent field theory using the Scheutjens-Fleer discretisation scheme. The system has the pH and the ionic

  9. Solubilization isotherms of aromatic solutes in surfactant aggregates

    Energy Technology Data Exchange (ETDEWEB)

    Gadelle, F.; Koros, W.J.; Schechter, R.S. (Univ. of Texas, Austin, TX (United States). Dept. of Chemical Engineering)

    1995-03-01

    Several factors affecting solubilization of aromatic solutes in surfactant micelles have been investigated. Solubilization isotherms of benzene, toluene, and chlorobenzene in various aqueous micellar solutions were determined using head space gas chromatography. Cationic surfactants such as cetylpyridinium chloride or cetyltrimethylammonium bromide present high solubilization capacities. Comparable anionic surfactants exhibit lower solubilization and a greater tendency to precipitate. It was observed that nonionic surfactants show high solubilization on a molar basis. Solubilization in mixed cationic-anionic micelles was also investigated. It also appears that the molecular size of the solute determines the extent of the solubilization. Finally, the shape of the different isotherms indicates that knowing the amount solubilized at saturation of the micellar solution is not sufficient to estimate solubilization at solute concentrations lower than the solute aqueous solubility. Solubilization of organics in surfactant micelles is of major importance in many applications. One new application is micellar-enhanced ultrafiltration. Another application of interest is the surfactant-enhanced aquifer remediation, a process in which a micellar aqueous solution is flushed into contaminated groundwaters to enhance recovery of pollutants by micellar solubilization.

  10. Enrichment of surfactant from its aqueous solution using ultrasonic atomization.

    Science.gov (United States)

    Takaya, Haruko; Nii, Susumu; Kawaizumi, Fumio; Takahashi, Katsuroku

    2005-08-01

    Dilute aqueous solutions of dodecyl-benzenesulfonic acid sodium salt (DBS-Na) and polyoxyethylenenonylphenyl ethers (PONPEs) were ultrasonically atomized. The surfactants were concentrated in collected mist droplets. The enrichment ratio increased with decreasing surfactant concentration. Depending on the surfactant's molecular weight and affinity to water, different enrichment ratio was observed in the range of low feed concentrations. For anionic surfactant, DBS-Na, the enrichment ratio was significantly improved by KCl addition and a peak appeared on the plot of the ratio against KCl concentration. Addition of NaCl or CaCl2 . 2H2O to the surfactant solution also enhanced the enrichment ratio; however, the effect was relatively small. Such behaviors of the ratio were interpreted as enhanced interfacial adsorption of the surfactant and a lack of supply of surfactant monomers from liquid bulk because of slow breaking of surfactant micelles. Time required for collecting an amount of mist was also observed. Among the three salt systems, the time for KCl system was twice as long as others. This fact suggested that the formation of smaller droplets in KCl system.

  11. Non-ionic surfactants do not consistently improve the enzymatic hydrolysis of pure cellulose.

    Science.gov (United States)

    Zhou, Yan; Chen, Hongmei; Qi, Feng; Zhao, Xuebing; Liu, Dehua

    2015-04-01

    Non-ionic surfactants have been frequently reported to improve the enzymatic hydrolysis of pretreated lignocellulosic biomass and pure cellulose. However, how the hydrolysis condition, substrate structure and cellulase formulation affect the beneficial action of surfactants has not been well elucidated. In this work, it was found that the enzymatic hydrolysis of pure cellulose was not consistently improved by surfactants. Contrarily, high surfactant concentration, e.g. 5 g/L, which greatly improved the hydrolysis of dilute acid pretreated substrates, actually showed notable inhibition to pure cellulose conversion in the late phase of hydrolysis. Under an optimal hydrolysis condition, the improvement by surfactant was limited, but under harsh conditions surfactant indeed could enhance cellulose conversion. It was proposed that non-ionic surfactants could interact with substrates and cellulases to impact the adsorption behaviors of cellulases. Therefore, the beneficial action of surfactants on pure cellulose hydrolysis is influenced by hydrolysis condition, cellulose structural features and cellulase formulation. Copyright © 2015 Elsevier Ltd. All rights reserved.

  12. A supersymmetric consistent truncation for conifold solutions

    CERN Document Server

    Cassani, Davide

    2010-01-01

    We establish a supersymmetric consistent truncation of type IIB supergravity on the T^{1,1} coset space, based on extending the Papadopoulos-Tseytlin ansatz to the full set of SU(2)xSU(2) invariant Kaluza-Klein modes. The five-dimensional model is a gauged N=4 supergravity with three vector multiplets, which incorporates various conifold solutions and is suitable for the study of their dynamics. By analysing the scalar potential we find a family of new non-supersymmetric AdS_5 extrema interpolating between a solution obtained long ago by Romans and a solution employing an Einstein metric on T^{1,1} different from the standard one. Finally, we discuss some simple consistent subtruncations preserving N=2 supersymmetry. One of them is compatible with the inclusion of smeared D7-branes.

  13. The adsorption of surfactant at the amorphous polymer solution interface

    CERN Document Server

    Gilchrist, V A

    2001-01-01

    Adsorption of surfactants onto amorphous polymers at the solid-solution interface is of direct relevance to many industrial sectors ranging from food, pharmaceuticals, paints, paper and photographic colour films. Although it is widely accepted that surfactants play the underpinning role in these applications, little is currently understood about the interactions between surfactants and polymeric materials at the molecular level. This lack of progress is mainly due to the inability of most existing techniques in probing this type of structural information at the wet interface. Specular neutron reflection (SNR) is a recently developed technique capable of detecting structural information with resolution down to a few angstroms (A). When combined with deuterium labeling, it is possible to distinguish the surfactant from the polymeric species at the interface. The aim of this work is to explore the appropriate experimental approach that utilizes the potential of neutron reflection to unravel molecular information...

  14. Experimental study on thermophoresis of colloids in aqueous surfactant solutions

    Science.gov (United States)

    Dong, Ruo-Yu; Zhou, Yi; Yang, Chun; Cao, Bing-Yang

    2015-12-01

    Thermophoresis refers to the motion of particles under a temperature gradient and it is one of the particle manipulation techniques. Regarding the thermophoresis of particles in liquid media, however, many open questions still remain, especially the role of the interfacial effect. This work reports on a systematic experimental investigation of surfactant effects, especially the induced interfacial effect, on the thermophoresis of colloids in aqueous solutions via a microfluidic approach. Two kinds of commonly used surfactants, sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB), are selected and the results show that from relatively large concentrations, the two surfactants can greatly enhance the thermophilic mobilities. Specifically, it is found that the colloid-water interfaces modified with more polar end groups can potentially lead to a stronger thermophilic tendency. Due to the complex effects of surfactants, further theoretical model development is needed to quantitatively describe the dependence of thermophoresis on the interface characteristics.

  15. Model study of enhanced oil recovery by flooding with aqueous surfactant solution and comparison with theory.

    Science.gov (United States)

    Fletcher, Paul D I; Savory, Luke D; Woods, Freya; Clarke, Andrew; Howe, Andrew M

    2015-03-17

    With the aim of elucidating the details of enhanced oil recovery by surfactant solution flooding, we have determined the detailed behavior of model systems consisting of a packed column of calcium carbonate particles as the porous rock, n-decane as the trapped oil, and aqueous solutions of the anionic surfactant sodium bis(2-ethylhexyl) sulfosuccinate (AOT). The AOT concentration was varied from zero to above the critical aggregation concentration (cac). The salt content of the aqueous solutions was varied to give systems of widely different, post-cac oil-water interfacial tensions. The systems were characterized in detail by measuring the permeability behavior of the packed columns, the adsorption isotherms of AOT from the water to the oil-water interface and to the water-calcium carbonate interface, and oil-water-calcium carbonate contact angles. Measurements of the percent oil recovery by pumping surfactant solutions into calcium carbonate-packed columns initially filled with oil were analyzed in terms of the characterization results. We show that the measured contact angles as a function of AOT concentration are in reasonable agreement with those calculated from values of the surface energy of the calcium carbonate-air surface plus the measured adsorption isotherms. Surfactant adsorption onto the calcium carbonate-water interface causes depletion of its aqueous-phase concentration, and we derive equations which enable the concentration of nonadsorbed surfactant within the packed column to be estimated from measured parameters. The percent oil recovery as a function of the surfactant concentration is determined solely by the oil-water-calcium carbonate contact angle for nonadsorbed surfactant concentrations less than the cac. For surfactant concentrations greater than the cac, additional oil removal occurs by a combination of solubilization and emulsification plus oil mobilization due to the low oil-water interfacial tension and a pumping pressure increase.

  16. Study on the Surface Property of Surfactant Ionic Liquids Solutions

    Institute of Scientific and Technical Information of China (English)

    Yan An GAO; Zhong Ni WANG; Jin ZHANG; Wan Guo HOU; Gan Zuo LI; Bu Xing HAN; Feng Feng Lü; Gao Yong ZHANG

    2005-01-01

    The surfactant TX-100 can be dissolved in ionic liquid bmimPF6 and decrease the surface tension of 1-butyl-3-methylimidazolium hexafluorophosphate (bmimPF6) solutions. Here,we confirmed that in this new system, the pure solvents need rearrangement at the air-water interface at the initial stage. The dynamic surface tension (DST) study shows that at the initial adsorption stage, the adsorption model of surfactant accords with the diffusion-controlled adsorption mechanism, and the dilute ionic liquids solutions is further close to the diffusion-controlled adsorption.

  17. Remediation of sandy soils using surfactant solutions and foams.

    Science.gov (United States)

    Couto, Hudson J B; Massarani, Guilio; Biscaia, Evaristo C; Sant'Anna, Geraldo L

    2009-05-30

    Remediation of sandy soils contaminated with diesel oil was investigated in bench-scale experiments. Surfactant solution, regular foams and colloidal gas aphrons were used as remediation fluids. An experimental design technique was used to investigate the effect of relevant process variables on remediation efficiency. Soils prepared with different average particle sizes (0.04-0.12 cm) and contaminated with different diesel oil contents (40-80 g/kg) were used in experiments conducted with remediation fluids. A mathematical model was proposed allowing for the determination of oil removal rate-constant (k(v)) and oil content remaining in the soil after remediation (C(of)) as well as estimation of the percentage of oil removed. Oil removal efficiencies obtained under the central experimental design conditions were 96%, 88% and 35% for aphrons, regular foams and surfactant solutions, respectively. High removal efficiencies were obtained using regular foams and aphrons, demanding small amounts of surfactant.

  18. Foaming and foam stability for mixed polymer-surfactant solutions: effects of surfactant type and polymer charge.

    Science.gov (United States)

    Petkova, R; Tcholakova, S; Denkov, N D

    2012-03-20

    Solutions of surfactant-polymer mixtures often exhibit different foaming properties, compared to the solutions of the individual components, due to the strong tendency for formation of polymer-surfactant complexes in the bulk and on the surface of the mixed solutions. A generally shared view in the literature is that electrostatic interactions govern the formation of these complexes, for example between anionic surfactants and cationic polymers. In this study we combine foam tests with model experiments to evaluate and explain the effect of several polymer-surfactant mixtures on the foaminess and foam stability of the respective solutions. Anionic, cationic, and nonionic surfactants (SDS, C(12)TAB, and C(12)EO(23)) were studied to clarify the role of surfactant charge. Highly hydrophilic cationic and nonionic polymers (polyvinylamine and polyvinylformamide, respectivey) were chosen to eliminate the (more trivial) effect of direct hydrophobic interactions between the surfactant tails and the hydrophobic regions on the polymer chains. Our experiments showed clearly that the presence of opposite charges is not a necessary condition for boosting the foaminess and foam stability in the surfactant-polymer mixtures studied. Clear foam boosting (synergistic) effects were observed in the mixtures of cationic surfactant and cationic polymer, cationic surfactant and nonionic polymer, and anionic surfactant and nonionic polymer. The mixtures of anionic surfactant and cationic polymer showed improved foam stability, however, the foaminess was strongly reduced, as compared to the surfactant solutions without polymer. No significant synergistic or antagonistic effects were observed for the mixture of nonionic surfactant (with low critical micelle concentration) and nonionic polymer. The results from the model experiments allowed us to explain the observed trends by the different adsorption dynamics and complex formation pattern in the systems studied.

  19. CATALYSIS BY SURFACTANT AGGREGATES IN AQUEOUS-SOLUTIONS

    NARCIS (Netherlands)

    ENGBERTS, JBFN

    1992-01-01

    Catalysis of organic reactions by unfunctionalized surfactant aggregates (micelles, vesicles) in aqueous solution is largely determined by medium effects induced at the micellar binding sites and by entropy effects due to compartimentalization. The efficiency of these catalytic effects responds to c

  20. Compatible solutes: ectoine and hydroxyectoine improve functional nanostructures in artificial lung surfactants.

    Science.gov (United States)

    Harishchandra, Rakesh Kumar; Sachan, Amit Kumar; Kerth, Andreas; Lentzen, Georg; Neuhaus, Thorsten; Galla, Hans-Joachim

    2011-12-01

    Ectoine and hydroxyectoine belong to the family of compatible solutes and are among the most abundant osmolytes in nature. These compatible solutes protect biomolecules from extreme conditions and maintain their native function. In the present study, we have investigated the effect of ectoine and hydroxyectoine on the domain structures of artificial lung surfactant films consisting of dipalmitoylphosphatidylcholine (DPPC), dipalmitoylphosphatidylglycerol (DPPG) and the lung surfactant specific surfactant protein C (SP-C) in a molar ratio of 80:20:0.4. The pressure-area isotherms are found to be almost unchanged by both compatible solutes. The topology of the fluid domains shown by scanning force microscopy, which is thought to be responsible for the biophysical behavior under compression, however, is modified giving rise to the assumption that ectoine and hydroxyectoine are favorable for a proper lung surfactant function. This is further evidenced by the analysis of the insertion kinetics of lipid vesicles into the lipid-peptide monolayer, which is clearly enhanced in the presence of both compatible solutes. Thus, we could show that ectoine and hydroxyectoine enhance the function of lung surfactant in a simple model system, which might provide an additional rationale to inhalative therapy.

  1. EXPERIMENTAL CHARACTERIZATION OF FLUOROCARBON-MODIFIED POLYACRYLAMIDE/SURFACTANT AQUEOUS SOLUTIONS

    Institute of Scientific and Technical Information of China (English)

    Huai-tian Bu; Zhen-zhong Yang; Yun-xiang Zhang

    2003-01-01

    The interaction between surfactants and fluorocarbon-modified polyacrylamide (FC-PAM) in aqueous solutions was evaluated by theological means and fluorescence spectroscopy and was found to be strong regardless of the surfactant's nature. Two representative surfactants, anionic sodium dodecyl sulfate (SDS) and nonionic Triton X-100, were used. The origin of the interaction and its dependence on the surfactant concentration were discussed.

  2. Multilayers at the surface of solutions of exogenous lung surfactant: direct observation by neutron reflection.

    Science.gov (United States)

    Follows, D; Tiberg, F; Thomas, R K; Larsson, M

    2007-02-01

    Pharmacy-grade exogenous lung surfactant preparations of bovine and porcine origin, dispersed in physiological electrolyte solution have been studied. The organization and dynamics at the air/water interface at physiological temperature was analysed by neutron reflection. The results show that a well-defined surface phase is formed, consisting of a multilayer structure of lipid/protein bilayers alternating with aqueous layers, with a repetition period of about 70 A and correlation depths of 3 to >25 bilayers, depending on electrolyte composition and time. The experimental surfactant concentration of 0.15% (w/w) is far below that used in therapeutic application of exogenous surfactants and it is therefore likely that similar multilayer structures are also formed at the alveolar surface in the clinical situation during surfactant substitution therapy. Lung surfactant preparations in dry form swell in aqueous solution towards a limit of about 60% (w/w) of water, forming a lamellar liquid-crystalline phase above about 34 degrees C, which disperses into lamellar bodies at higher water concentrations. The lamellar spacings in the surface multilayers at the air/water interface are smaller than those in the saturated limit even though they are in contact with much greater water concentrations. The surface multilayers are laterally disordered in a way that is consistent with fragments of Lalpha-phase lamellae. The near surface layers of the multilayer structure have a significant protein content (only SP-B and SP-C are present in the preparations). The results demonstrate that a multilayer structure can be formed in exogenous surfactant even at very low concentrations and indicate that multilayers need to be incorporated into present interpretations of in vitro studies of similar lung surfactant preparations, which are largely based on monolayer models.

  3. Thermophoresis and thermoelectricity in surfactant solutions.

    Science.gov (United States)

    Vigolo, Daniele; Buzzaccaro, Stefano; Piazza, Roberto

    2010-06-01

    In electrolyte solutions, the differential migration of the ionic species induced by the presence of a thermal gradient leads to the buildup of a steady-state electric field. Similarly to what happens for the Seebeck effect in solids, the sample behaves therefore as a thermocell. Here, we provide clear evidence for the presence of thermoelectric fields in liquids by detecting and quantifying their strong effects on colloid thermophoresis. Specifically, by contrasting the effects of the addition of NaCl or NaOH on the Soret effect of micellar solutions of sodium dodecyl sulfate, we show that the presence of highly thermally responsive ions such as OH(-) may easily lead to the reversal of particle motion. Our experimental results can be quantitatively explained by a simple model that takes into account interparticle interactions and explicitly includes the micellar electrophoretic transport driven by such a thermally generated electric field. The chance of carefully controlling colloid thermophoresis by tuning the solvent electrolyte composition may prove to be very useful in microfluidic applications and field-flow fractionation methods.

  4. Surfactant-free exfoliation of graphite in aqueous solutions.

    Science.gov (United States)

    Ricardo, Karen B; Sendecki, Anne; Liu, Haitao

    2014-03-14

    We report an ultrasound exfoliation of graphite in a weakly basic solution to produce multi-layer graphene dispersion. A unique feature of this process is that no surfactant was added to stabilize the exfoliated graphene in water. The concentration of the graphene dispersion prepared by this approach can be up to 0.02 mg mL(-1) and it was stable at room temperature for several months.

  5. Molecular thermodynamics for micellar branching in solutions of ionic surfactants.

    Science.gov (United States)

    Andreev, Vasily A; Victorov, Alexey I

    2006-09-26

    We develop an analytical molecular-thermodynamic model for the aggregation free energy of branching portions of wormlike ionic micelles in 1:1 salt solution. The junction of three cylindrical aggregates is represented by a combination of pieces of the torus and bilayer. A geometry-dependent analytical solution is obtained for the linearized Poisson-Boltzmann equation. This analytical solution is applicable to saddle-like structures and reduces to the solutions known previously for planar, cylindrical, and spherical aggregates. For micellar junctions, our new analytical solution is in excellent agreement with numerical results over the range of parameters typical of ionic surfactant systems with branching micelles. Our model correctly predicts the sequence of stable aggregate morphologies, including a narrow bicontinuous zone, in dependence of hydrocarbon tail length, head size, and solution salinity. For predicting properties of a spatial network of wormlike micelles, our aggregation free energy is used in the Zilman-Safran theory. Our predictions are compared with experimental data for branching micelles of ionic surfactants.

  6. Conformational and phase transitions in DNA--photosensitive surfactant solutions: Experiment and modeling.

    Science.gov (United States)

    Kasyanenko, N; Lysyakova, L; Ramazanov, R; Nesterenko, A; Yaroshevich, I; Titov, E; Alexeev, G; Lezov, A; Unksov, I

    2015-02-01

    DNA binding to trans- and cis-isomers of azobenzene containing cationic surfactant in 5 mM NaCl solution was investigated by the methods of dynamic light scattering (DLS), low-gradient viscometry (LGV), atomic force microscopy (AFM), circular dichroism (CD), gel electrophoresis (GE), flow birefringence (FB), UV-Vis spectrophotometry. Light-responsive conformational transitions of DNA in complex with photosensitive surfactant, changes in DNA optical anisotropy and persistent length, phase transition of DNA into nanoparticles induced by high surfactant concentration, as well as transformation of surfactant conformation under its binding to macromolecule were studied. Computer simulations of micelles formation for cis- and trans-isomers of azobenzene containing surfactant, as well as DNA-surfactant interaction, were carried out. Phase diagram for DNA-surfactant solutions was designed. The possibility to reverse the DNA packaging induced by surfactant binding with the dilution and light irradiation was shown.

  7. Perstraction of intracellular pigments by submerged cultivation of Monascus in nonionic surfactant micelle aqueous solution.

    Science.gov (United States)

    Hu, Zhiqiang; Zhang, Xuehong; Wu, Zhenqiang; Qi, Hanshi; Wang, Zhilong

    2012-04-01

    "Milking processing" describes the cultivation of microalgae in a water-organic solvent two-phase system that consists of simultaneous fermentation and secretion of intracellular product. It is usually limited by the conflict between the biocompatibility of the organic solvent to the microorganisms and the ability of the organic solvent to secret intracellular product into its extracellular broth. In the present work, submerged cultivation of Monascus in the nonionic surfactant Triton X-100 micelle aqueous solution for pigment production is exploited, in which the fungus Monascus remains actively growing. Permeabilization of intracellular pigments across the cell membrane and extraction of the pigments to the nonionic surfactant micelles of its fermentation broth occur simultaneously. "Milking" the intracellular pigments in the submerged cultivation of Monascus is a perstraction process. The perstractive fermentation of intracellular pigments has the advantage of submerged cultivation by secretion of the intracellular pigments to its extracellular broth and the benefit of extractive microbial fermentation by solubilizing the pigments into nonionic surfactant micelles. It is shown as the marked increase of the extracellular pigment concentration by the submerged cultivation of Monascus in the nonionic surfactant Triton X-100 micelle solution.

  8. TURBULENCE TRANSPORT OF SURFACTANT SOLUTION FLOW DURING DRAG REDUCTION DEGENERATION

    Institute of Scientific and Technical Information of China (English)

    GU Wei-guo; WANG De-zhong

    2012-01-01

    Turbulence transport of surfactant solution flow during drag reduction degeneration is investigated experimentally in a two-dimensional channel.Particle Image Velocimetry (P1V) system is used to take two-dimensional velocity frames in the streamwise and wall-normal plane.The additive of surfactant is cetyltrimethyl ammonium chloride (CTAC) with the mass concentration of 25 ppm.Drag reduction degeneration happens in the CTAC solution flow,exhibiting the maximal drag reduction at Re =25000and losing drag reduction completely at Re =40 000.The velocity frames are statistically analyzed in four quadrants which are divided by the u -axis and v-axis.It is found that the phenomenon of“Zero Reynolds shear stress” is caused by the decrease of wallnormal fluctuations and its symmetrical distribution in quadrants.The increase of Reynolds number leads to the enhancement of turbulence burst phenomenon.During thc drag reduction degeneration,the CTAC solution flow contains both high turbulence intensity and drag reduction states.

  9. Water solubility enhancements of pyrene by single and mixed surfactant solutions

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Water solubility enhancements of pyrene by both single-surfactant and mixed-surfactant solutions were compared andevaluated. The solubility of pyrene in water was greatly enhanced by each of Triton X-100 (TX100), Triton X-405 (TX405), Brij 35 and SDS, in which the water solubility enhancements increased with increasing surfactant concentrations. The extent of solubility enhancements at surfactant concentrations below the CMC is the order of TX100 > Brij 35 > TX405 > SDS; the sequence at surfactantconcentrations above the CMC is TX100 > Brij 35 > SDS > TX405. Pyrene was solubilized synergistically by anionic-nonionic mixed surfactant solutions, especially at low surfactant concentrations. The synergistic power of the mixed surfactants is SDS-TX405 > SDS-Brij 35 > SDS-TX100. The synergism as noted is attributed to increasing Kmc and/or decreasing the CMC of the mixed surfactan solution. For SDS-TX405 and SDS-Brij 35 mixed surfactant solutions, an increase in Kmc is coupled with a decrease in the CMC; for SDS-TX100, only a decreased in the CMC value is noted. Mixed-surfactant solutions may improve the performance of the surfactant-enhanced remediation (SER) of soils by increasing the bioavailability and biodegradation of non-aqueous-phase organic pollutants and reducing the level of surfactant pollution and remediation expenses.

  10. Effect of Dynamic Surface Tension on Droplet Formation of Surfactant Solution Injected from a Capillary Tube

    OpenAIRE

    山本, 剛宏; 加藤, 有樹; 山下, 敦史; Takehiro, YAMAMOTO; Yuki, Kato; Atsushi, Yamashita; 阪大院工; Osaka University

    2008-01-01

    Effects of dynamic surface tension on the droplet formation of surfactant solutions were studied. Aqueous solutions of CTAB at several surfactant concentrations were used as test fluids. A droplet formed when a surfactant solution was injected from a capillary tube was investigated and the relation between the droplet diameter and the injection velocity was measured. The diameter increased with increasing the velocity at relatively low velocities because the dynamic tension also increased. Ho...

  11. Unsteady Motion of a Single Droplet in Surfactant Solutions

    Institute of Scientific and Technical Information of China (English)

    李晓锦; 毛在砂; 费维扬

    2003-01-01

    A numerical investigation of the unsteady motion of a deformed drop released freely in another quiescent liquid contaminated by surfactant is presented in this paper. The finite difference method was used to solve numerically the coupled time-dependent Navier-Stokes and convective-diffusion equations in a body-fitted orthogonal coordinate system. Numerical simulation was conducted on the experimental cases, in which MIBK drops with the size ranging from 1.24 mm to 1.97 mm rose and accelerated freely in pure water and in dilute sodium dodecyl sulphate (SDS) aqueous solution. The applicability of the numerical scheme was validated by the agreement between the simulation results and the experimental data. Both the numerical and experimental results showed that the velocitytime profile exhibited a maximum rising velocity for drops in SDS solutions, which was close to the terminal velocity in pure water, before it dropped down to a steady-state value. The effect of the sorption kinetics of surfactant on the accelerating motion was also evaluated. It is also suggested that introduction of virtual mass force into the formulation improved obviously the precision of numerical simulation of transient drop motion.

  12. Removal of 226Ra and 228Ra from TENORM sludge waste using surfactants solutions.

    Science.gov (United States)

    Attallah, M F; Hamed, Mostafa M; El Afifi, E M; Aly, H F

    2015-01-01

    The feasibility of using surfactants as extracting agent for the removal of radium species from TENORM sludge produced from petroleum industry is evaluated. In this investigation cationic and nonionic surfactants were used as extracting agents for the removal of radium radionuclides from the sludge waste. Two surfactants namely cetyltrimethylammonium bromide (CTAB) and Triton X-100 (TX100) were investigated as the extracting agents. Different parameters affecting the removal of both (226)Ra and (228)Ra by the two surfactants as well as their admixture were studied by the batch technique. These parameters include effect of shaking time, surfactants concentration and temperature as well as the effect of surfactants admixture. It was found that, higher solution temperature improves the removal efficiency of radium species. Combined extraction of nonionic and cationic surfactants produces synergistic effect in removal both (226)Ra and (228)Ra, where the removals reached 84% and 80% for (226)Ra and (228)Ra, respectively, were obtained using surfactants admixture.

  13. Surfactant solutions and porous substrates: spreading and imbibition.

    Science.gov (United States)

    Starov, Victor M

    2004-11-29

    nitrocellulose membranes. J. Colloid Interface Sci. 264 (2003) 481-489]: the overall time of the spreading of drops of SDS solution over dry thin porous substrates decreases with the increase of surfactant concentration; the difference between advancing and hydrodynamic receding contact angles decreases with the surfactant concentration increase; the constancy of the contact angle during the third stage of spreading has nothing to do with the hysteresis of contact angle, but determined by the hydrodynamic reasons. It is shown using independent spreading experiments of the same drops on nonporous nitrocellulose substrate that the static receding contact angle is equal to zero, which supports the conclusion on the hydrodynamic nature of the hydrodynamic receding contact angle on porous substrates. In Section 3, a theory is developed to describe a spontaneous imbibition of surfactant solutions into hydrophobic capillaries, which takes into account the micelle disintegration and the concentration decreasing close to the moving meniscus as a result of adsorption, as well as the surface diffusion of surfactant molecules [N.V. Churaev, G.A. Martynov, V.M. Starov, Z.M. Zorin, Colloid Polym. Sci. 259 (1981) 747]. The theory predictions are in good agreement with the experimental investigations on the spontaneous imbibition of the nonionic aqueous surfactant solution, Syntamide-5, into hydrophobized quartz capillaries. A theory of the spontaneous capillary rise of surfactant solutions in hydrophobic capillaries is presented, which connects the experimental observations with the adsorption of surfactant molecules in front of the moving meniscus on the bare hydrophobic interface [V.J. Starov, Colloid Interface Sci. 270 (2003)]. In Section 4, capillary imbibition of aqueous surfactant solutions into dry porous substrates is investigated from both theoretical and experimental points of view in the case of partial wetting [V. Straov, S. Zhdanov, M. Velarde, J. Colloid Interface Sci. 273 (2004

  14. Solubility limits and phase diagrams for fatty alcohols in anionic (SLES) and zwitterionic (CAPB) micellar surfactant solutions.

    Science.gov (United States)

    Tzocheva, Sylvia S; Danov, Krassimir D; Kralchevsky, Peter A; Georgieva, Gergana S; Post, Albert J; Ananthapadmanabhan, Kavssery P

    2015-07-01

    By analysis of experimental data, a quantitative theoretical interpretation of the solubility limit of medium- and long-chain fatty alcohols in micellar solutions of water-soluble surfactants is presented. A general picture of the phase behavior of the investigated systems is given in the form of phase diagrams. The limited solubility of the fatty alcohols in the micelles of conventional surfactants is explained with the precipitation of their monomers in the bulk, rather than with micelle phase separation. The long chain fatty alcohols (with n=14, 16 and 18 carbon atoms) exhibit an ideal mixing in the micelles of the anionic surfactant sodium laurylethersulfate (SLES) and the zwitterionic surfactant cocamidopropyl betaine (CAPB) at temperatures of 25, 30, 35 and 40 °C. Deviations from ideality are observed for the alcohols of shorter chain (n=10 and 12), which can be explained by a mismatch with the longer chains of the surfactant molecules. Using the determined thermodynamic parameters of the systems, their phase diagrams are constructed. Such a diagram consists of four domains, viz. mixed micelles; coexistent micelles and precipitate (dispersed crystallites or droplets); precipitate without micelles, and molecular solution. The four boundary lines intersect in a quadruple point, Q. For ionic surfactants (like SLES), a detailed theory for calculating the boundary lines of the phase diagrams is developed and verified against data for the positions of the kinks in surface tension isotherms. The theory takes into account the electrostatic interactions in the micellar solutions and the effect of counterion binding. The results can be useful for a quantitative interpretation and prediction of the phase behavior of mixed solutions of two (or more) surfactants, one of them being water soluble and forming micelles, whereas the other one has a limited water solubility, but readily forms mixed micelles with the former surfactant.

  15. Brownian Dynamics Simulation of Microstructures and Elongational Viscosities of Micellar Surfactant Solution

    Institute of Scientific and Technical Information of China (English)

    WEI Jin-Jia; KAWAGUCHI Yasuo; YU Bo; LI Feng-Chen

    2008-01-01

    @@ Brownian dynamics simulation is conducted for a dilute surfactant solution under a steady uniaxial elongational flow.A new inter-cluster potential is used for the interaction among surfactant micelles to determine the micellar network structures in the surfactant solution.The micellar network is successfully simulated.It is formed at low elongation rates and destroyed by high elongation rates.The computed elongational viscosities show elongation-thinning characteristics.The relationship between the elongational viscosities and the microstructure of the surfactant solution is revealed.

  16. Dependence of the solubility of atmospheric oxygen in weakly alkaline aqueous solutions on surfactant concentration

    Science.gov (United States)

    Chistyakova, G. V.; Koksharov, S. A.; Vladimirova, T. V.

    2012-11-01

    The solubility of atmospheric oxygen in solutions of surfactants of different natures at 293 K and pH 8 is determined by gas chromatography. It is found that additives of nonionic surfactants decrease the oxygen content in the solution in the premicellar region and increase its solubility in the micellar region. It is shown that, for anionic surfactants, a decrease in the solubility of O2 is observed over the entire concentration range.

  17. Solubilization and degradation of perchloroethylene (PCE) in cationic and nonionic surfactant solutions

    Institute of Scientific and Technical Information of China (English)

    Sivaram Harendra; Cumaraswamy Vipulanandan

    2011-01-01

    Solubilization of perchloroethylene (PCE) in a nonionic (Triton X-100) and a cationic (cetyltrimethylammonium bromide (CTAB)) surfactant solutions and the degradation of surfactant solubilized PCE using fine to nanosize Fe and bi-metallic Fe-Ni particles were investigated.Micelle partition coefficients (Km) and molar solubility ratio (MSR) for PCE in 10 g/L of surfactant solutions have been quantified and the solubility of PCE (100 mg/L in water) in the surfactant solutions increased by about ten fold.Of the two surfactants studied,Triton X-100 solubilized the higher amount of PCE per gram of surfactant.To degrade solubilized PCE,both iron and bimetallic Fe-Ni particles were used in continuously stirred batch reactors.The iron and bi-metallic particles were synthesized using the solution method and the particles were characterized using the SEM,EDS,TEM and XRD.The PCE solubilized up to 500 mg/L in both surfactant solutions were totally degraded at various rates by 200 g/L of bi-metallic Fe-Ni particles in less than 20 hr,which is the highest concentration of PCE degraded in the shortest time compared to data in the literature.The degradations of PCE solubilized in surfactant solutions were represented by nonlinear kinetic relationships which depended on the type of surfactant used for solubilizing the PCE.

  18. Use of Emulsions with Surfactant Solutions for Viscous Fluids Transportation

    Directory of Open Access Journals (Sweden)

    Erich Martínez Martín

    2015-01-01

    Full Text Available The needs for improving the fluidity of fluids is present in the industry, because of the expenses that it takes and its relation with the achievement of the consumers’ demand according to volumes required for its different uses. In this way, the Oil Industry shows several methods to achieve this purpose, taking into account the characteristics of this substance. A method that can be used is the oil emulsions. Emulsions provide good results if they gather certain requirements for its use. In thispaper are shown the results of a research about the use of surfactant solutions in emulsions W/O. Oil transmission is used in this work because of its similar properties to oil.

  19. Nanofiltration: ion exchange system for effective surfactant removal from water solutions

    Directory of Open Access Journals (Sweden)

    I. Kowalska

    2014-12-01

    Full Text Available A system combining nanofiltration and ion exchange for highly effective separation of anionic surfactant from water solutions was proposed. The subjects of the study were nanofiltration polyethersulfone membranes and ion-exchange resins differing in type and structure. The quality of the treated solution was affected by numerous parameters, such as quality of the feed solution, membrane cut-off, resin type, dose and the solution contact time with the resin. A properly designed purification system made it possible to reduce the concentration of anionic surfactant below 1 mg L-1 from feed solutions containing surfactant in concentrations above the CMC value.

  20. Capillary electrophoresis investigation on equilibrium between polymer-related and surfactant-related species in aqueous polymer-surfactant solutions.

    Science.gov (United States)

    Wu, Yefan; Chen, Miaomiao; Fang, Yun; Zhu, Meng

    2017-03-17

    It was inferred from aqueous solution behavior of nonionic polymers and anionic surfactants that the formation of charged polymer-bound surfactant micelle above critical aggregation concentration (cac) and the formation of free surfactant micelle beyond polymer saturation point (psp), but there was still a lack of direct experimental evidence for the considered equilibrium chemical species. Three modes of capillary electrophoresis are applied in this paper to study the complexation between nonionic polymers, polyvinylpyrrolidone (PVP) or polyethylene glycol (PEG), and sodium dodecylbenzenesulfonate (SDBS) by successfully distinguishing the imaginary charged polymer-bound SDBS micelle from nonionic polymer and SDBS molecule. Perhaps even more important, it is the action of SDBS as both a main surfactant and a UV probe that makes the free surfactant micelle emerged in electropherogram beyond psp, and thus makes it possible for the first time to provide the equilibrium relationship of the polymer-related and the surfactant-related species in the concentration regions divided into by cac and psp. Copyright © 2017 Elsevier B.V. All rights reserved.

  1. Solution behaviour of new cationic surfactants derived from Guerbet alcohols and their use in hair conditioners.

    Science.gov (United States)

    Yahagi, K; Hoshino, N; Hirota, H

    1991-10-01

    Summary The solution behaviour of new cationic surfactants, synthesized by using long-chain Guerbet alcohols, in water was investigated by a polarizing microscopic technique, differential scanning calorimetry, and electric conductivity measurements. These surfactants show the gel-liquid crystalline phase transition to be lower than 0 degrees C and form lamellar liquid crystals even in cold water and at low concentrations of surfactants. The sorption of cationic surfactants from aqueous solutions onto hair was determined as a function of temperature. The effect of adsorbed cationic surfactants on the critical surface tension and kinetic frictional coefficients of hair surface have been investigated. These surface characteristics of hair treated with quaternary ammonium compounds derived from Guerbet alcohols were found to be significantly improved. These results can be explained by the high ability of sorption onto hair. Hair rinses and conditioners having excellent ease of combing or brushing for wet and dry hair can be formulated by the application of these cationic surfactants.

  2. Kinetics of Surfactant Desorption at an Air–Solution Interface

    KAUST Repository

    Morgan, C. E.

    2012-12-18

    The kinetics of re-equilibration of the anionic surfactant sodium dodecylbenzene sulfonate at the air-solution interface have been studied using neutron reflectivity. The experimental arrangement incorporates a novel flow cell in which the subphase can be exchanged (diluted) using a laminar flow while the surface region remains unaltered. The rate of the re-equilibration is relatively slow and occurs over many tens of minutes, which is comparable with the dilution time scale of approximately 10-30 min. A detailed mathematical model, in which the rate of the desorption is determined by transport through a near-surface diffusion layer into a diluted bulk solution below, is developed and provides a good description of the time-dependent adsorption data. A key parameter of the model is the ratio of the depth of the diffusion layer, H c, to the depth of the fluid, Hf, and we find that this is related to the reduced Péclet number, Pe*, for the system, via Hc/Hf = C/Pe*1/2. Although from a highly idealized experimental arrangement, the results provide an important insight into the "rinse mechanism", which is applicable to a wide variety of domestic and industrial circumstances. © 2012 American Chemical Society.

  3. Desorption of two organophosphorous pesticides from soil with wastewater and surfactant solutions.

    Science.gov (United States)

    Hernández-Soriano, M C; Mingorance, M D; Peña, A

    2012-03-01

    A batch test was used to evaluate the extent of desorption of diazinon and dimethoate, preadsorbed on a calcareous agricultural soil, representative of the Mediterranean area. Urban wastewater from a secondary treatment and seven surfactant solutions, at concentrations ranging from 0.75 mg L(-1) to 10 gL(-1), were used. The surfactants assayed were cationic (hexadecyl trimethyl ammonium bromide (HD)), anionic (sodium dodecyl sulfate (SDS), Aerosol 22 (A22) and Biopower (BP)), and nonionic (Tween 80 (TW), Triton X 100 (TX) and Glucopon 600 (G600)). Desorption of dimethoate was either not affected or only slightly by the nonionic and anionic surfactants tested, while desorption of diazinon from the soil was only enhanced by A22, BP and TW. This desorption increase correlated significantly with the surfactant concentration of the solution used for desorption and with the concurrent increase in the supernatant of the dissolved organic carbon, in particular that originating from the surfactant. This parameter did not vary with the use of SDS, G600 and TX. The cationic surfactant HD was retained on the soil surface, as confirmed by an increase in soil organic carbon, resulting in a fall in desorption rate for both pesticides. Comparing treatment by wastewater with control water, there was no difference in desorption rate for either pesticide. Mixed TW/anionic surfactant solutions either did not modify or slightly increased desorption of both pesticides in comparison with individual surfactant solutions.

  4. Evolution of mixed surfactant aggregates in solutions and at solid/solution interfaces

    Science.gov (United States)

    Zhang, Rui

    Surfactant systems have been widely used in such as enhanced oil recovery, waste treatment and metallurgy, etc., in order to solve the problem of global energy crisis, to remove the pollutants and to generate novel energy resources. Almost all surfactant systems are invariably mixtures due to beneficial and economic considerations. The sizes and shapes of aggregates in solutions and at solid/solution interfaces become important, since the nanostructures of mixed aggregates determine solution and adsorption properties. A major hurdle in science is the lack of information on the type of complexes and aggregates formed by mixtures and the lack of techniques for deriving such information. Using techniques such as analytical ultracentrifuge, small angle neutron scattering, surface tension, fluorescence, cryo-TEM, light scattering and ultrafiltration, the nanostructures of aggregates of sugar based n-dodecyl-beta-D-maltoside (DM) and nonionic pentaethyleneglycol monododecyl ether or nonyl phenol ethoxylated decyl ether (NP-10) and their mixtures have been investigated to prove the hypothesis that the aggregation behavior is linked to packing of the surfactant governed by the molecular interactions as well as the molecular structures. The results from both sedimentation velocity and sedimentation equilibrium experiments suggest coexistence of two types of micelles in nonyl phenol ethoxylated decyl ether solutions and its mixtures with n-dodecyl-beta-D-maltoside while only one micellar species is present in n-dodecyl-beta-D-maltoside solutions, in good agreement with those from small angle neutron scattering, cryo-TEM, light scattering and ultrafiltration. Type I micelles were primary micelles at cmc while type II micelles were elongated micelles. On the other hand, the nanostructures of mixed surface aggregates have been quantitatively predicted for the first time using a modified packing index. As a continuation of the Somasundaran-Fuersteneau adsorption model, a

  5. Polymers and surfactants in solution and at interfaces : a model study on detergency

    NARCIS (Netherlands)

    Torn, L.H.

    2000-01-01

    This thesis deals with detergency-related adsorption phenomena of (mixtures of) polymers and surfactants. Both types of molecules play an important role in the removal and subsequent stabilization of soil from a substrate. Starting with a model detergency system consisting of polymers, surfactants,

  6. Thermodynamically consistent description of the hydrodynamics of free surfaces covered by insoluble surfactants of high concentration

    CERN Document Server

    Thiele, Uwe; Plapp, Mathis

    2012-01-01

    In this paper we propose several models that describe the dynamics of liquid films which are covered by a high concentration layer of insoluble surfactant. First, we briefly review the 'classical' hydrodynamic form of the coupled evolution equations for the film height and surfactant concentration that are well established for small concentrations. Then we re-formulate the basic model as a gradient dynamics based on an underlying free energy functional that accounts for wettability and capillarity. Based on this re-formulation in the framework of nonequilibrium thermodynamics, we propose extensions of the basic hydrodynamic model that account for (i) nonlinear equations of state, (ii) surfactant-dependent wettability, (iii) surfactant phase transitions, and (iv) substrate-mediated condensation. In passing, we discuss important differences to most of the models found in the literature.

  7. Comparison of cytotoxicity in vitro and irritation in vivo for aqueous and oily solutions of surfactants.

    Science.gov (United States)

    Czajkowska-Kośnik, Anna; Wolska, Eliza; Chorążewicz, Juliusz; Sznitowska, Małgorzata

    2015-01-01

    The in vivo model on rabbit eyes and the in vitro cytotoxicity on fibroblasts were used to compare irritation effect of aqueous and oily (Miglyol 812) solutions of surfactants. Tween 20, Tween 80 and Cremophor EL were tested in different concentrations (0.1, 1 or 5%) and the in vitro test demonstrated that surfactants in oil are less cytotoxic than in aqueous solutions. In the in vivo study, the aqueous solutions of surfactants were characterized as non-irritant while small changes in conjunctiva were observed after application the oily solutions of surfactants and the preparations were classified as slightly irritant, however this effect was similar when Miglyol was applied alone. In conclusion, it is reported that the MTT assay does not correlate well with the Draize scores.

  8. Semi-quantitative determination of cationic surfactants in aqueous solutions using gold nanoparticles as reporter probes.

    Science.gov (United States)

    Kuong, Chi-Lap; Chen, Wei-Yu; Chen, Yu-Chie

    2007-03-01

    Concentrations of cationic surfactants in aqueous solutions have been estimated on the basis of changes in the color of gold nanoparticles, used as reporter probes. We have shown that the colors of gold nanoparticles with anionic protective groups on their surfaces shift from red to indigo/purple and then back to red in a range of cationic surfactant solutions in which concentrations vary from very low to above the theoretical CMCs. The color changes occur near the theoretical CMCs, presumably because the presence of surfactant micelles in the solution prevents the gold nanoparticles from aggregating. We have used gold nanoparticles as reporter probes to determine the concentrations of cationic surfactants in products such as hair conditioners, which often contain large amounts of alkyltrimethylammonium halides. Although this approach can only provide an estimate, it can be performed simply by addition of a given amount of gold nanoparticles to a series of diluted solutions, without the need for instruments or labor-intensive procedures.

  9. Thermodynamically consistent description of the hydrodynamics of free surfaces covered by insoluble surfactants of high concentration

    OpenAIRE

    Thiele, Uwe; Archer, Andrew J.; Plapp, Mathis

    2012-01-01

    In this paper we propose several models that describe the dynamics of liquid films which are covered by a high concentration layer of insoluble surfactant. First, we briefly review the 'classical' hydrodynamic form of the coupled evolution equations for the film height and surfactant concentration that are well established for small concentrations. Then we re-formulate the basic model as a gradient dynamics based on an underlying free energy functional that accounts for wettability and capill...

  10. Removal of Organic Dyes from Aqueous Solutions with Surfactant-Modified Magnetic Nanoparticles

    Directory of Open Access Journals (Sweden)

    Wybieralska Katarzyna

    2014-06-01

    Full Text Available The paper presents the results of studies on the possibility of using magnetic nanoparticles modified with selected hydrophobic surfactants for model post-production water purification. Colloidal solutions of iron hydroxide (III and iron oxide (II and III were obtained and their particles were subjected to surface modification using surfactants. Thus obtained magnetic fluids were used as active agents in the process of removing selected organic dyes from their aqueous solutions. The effectiveness of the modified compounds was analysed using spectrophotometric methods. It has been shown that the effectiveness of the process depends on the type of surfactant used to modify selected magnetic nanoparticles.

  11. Removal of Organic Dyes from Aqueous Solutions with Surfactant-Modified Magnetic Nanoparticles

    OpenAIRE

    Wybieralska Katarzyna; Wajda Anna

    2014-01-01

    The paper presents the results of studies on the possibility of using magnetic nanoparticles modified with selected hydrophobic surfactants for model post-production water purification. Colloidal solutions of iron hydroxide (III) and iron oxide (II and III) were obtained and their particles were subjected to surface modification using surfactants. Thus obtained magnetic fluids were used as active agents in the process of removing selected organic dyes from their aqueous solutions. The effecti...

  12. Acidic surfactant solutions for tributylphosphate removal in nuclear fuel reprocessing plants: A formulation study

    Energy Technology Data Exchange (ETDEWEB)

    Causse, J.; Faure, S. [CEA Marcoule, LPAD, SPDE, DEN, 30 (France)

    2009-04-15

    The removal of tributylphosphate (TBP), an organic solvent widely used as a complexing agent for uranium and plutonium in nuclear plants, was investigated to understand and adapt the mechanisms involved in TBP detachment and solubilization in acidic surfactant solutions. Two well-known degreasing mechanisms, roll-up and emulsification, should be combined for maximum effect. These mechanisms were characterized with a CCD camera to measure contact angles between a solid substrate and a liquid drop. We measured the contact angles of a TBP drop deposited on a stainless steel plate immersed in an acidic surfactant solution, and quantified the amount of TBP solubilized in the micelles by turbidity measurements. Preliminary results of micelle size characterization by dynamic light scattering are presented. We formulated new acidic surfactant solutions associating two industrial surfactants, Pluronic P123 and Rewopal X1207L, with improvement factors in various fields (total organic matter content, oil detachment and solubilization efficiency, emulsion stability, etc.). (authors)

  13. Surface tension of polytetrafluoroethylene and its wetting by aqueous solution of some surfactants and their mixtures

    Science.gov (United States)

    Mańko, Diana; Zdziennicka, Anna; Jańczuk, Bronisław

    2017-01-01

    Measurements of the contact angle of aqueous solution of rhamnolipid (RL) mixture with n-octyl-β-D-glucopyranoside (OGP), Triton X-100 (TX-100) or/and sodium dodecylsulfate (SDDS) on polytetrafluoroethylene (PTFE) were made. To this aim there was used a plate whose surface topography was analyzed by means of optical profilometry method. Additionally, plate surface chemistry was studied employing the Fourier transform infrared spectroscopy. The obtained values of contact angle were discussed based on the PTFE surface tension (γSV) as well as the Lifshitz-van der Waals component of the water surface tension (γWLW). The contact angle of aqueous solution of several surfactants and their mixtures on PTFE was also considered on the basis of γSV and γWLW . It occured that by using the values of γSV , γWLW and surface tension of the aqueous solution of surfactants and their mixtures, the contact angle on PTFE can be predicted. It also occured that changes of adhesion tension of aqueous solutions of surfactants as a function of their concentration can be determined by the exponential function of the first or second order. Using such functions Gibbs surface excess concentration of surfactants at the PTFE-water interface, mole fraction of surfactant in the mixed monolayer and fraction of the area occupied by given surfactants in the monolayer were determined. Gibbs surface free energy of adsorption of a given surfactant in the presence of another one and adhesion work of the aqueous solution of surfactants to the PTFE surface were also evaluated.

  14. Rheological Properties of the Aqueous Solution for Fluorocarbon-containing Hydrophobically Modified Sodium PolyacrylicAcid with Various Surfactants

    Institute of Scientific and Technical Information of China (English)

    GUO,Jin-Feng(郭金峰); ZHUANG,Dong-Qing(庄东青); ZHOU,Hui(周晖); ZHANG,Yun-Xiang(章云祥)

    2001-01-01

    The interaction of fluorocarbon-containing hydrophobicallymodified sodiun polyacryiic acid (FMPAANa) (0.5 wt% )with various surfactants (anionic,nonionic and cationic) hasbeen investigated by theological measurements.Different rhe-ological behaviors are displayed for ionic surfactants and non-ionic surfactants.Fluorinated surfactants have stronger affini-ty with polyelectrolyte hydrophobes comparing with hydro-genated surfactants.The hydrophobic association of FM-PAANa with a cationic surfactant (CTAB) and a fluorinatednonionic surfactant (FC171) is much stronger than with anonionic surfactant (NP7.5 ) and an anionic surfactant(FC143).Further investigation of the effects of temperatureon solution properties shows that the dissociation energy Em iscorrelated to the strength of the aggregated junctions.``

  15. Desorption of organophosphorous pesticides from soil with wastewater and surfactant solutions

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez-Soriano, M. C.; Mingorance, M. D.; Pena, A.

    2009-07-01

    Surfactants can be introduced in the environment by wastewater discharge, point-charge pollution or deliberate action, e. g. to remediate contaminated soil or groundwater. The irrigation of soil with wastewater containing surfactants may modify pesticide desorption from soil, thus affecting their affecting their environmental fate. Desorption from soil of the plain of Granada (South-eastern Spain) of two organophosphorous pesticides, diazinon and dimethoate, differing in solubility and hydrophobicity, has been evaluated in the presence of different surfactant aqueous solutions and municipal wastewater. (Author)

  16. Alkyl propoxy ethoxylate "graded" surfactants: micelle formation and structure in aqueous solutions.

    Science.gov (United States)

    Sarkar, Biswajit; Alexandridis, Paschalis

    2010-04-08

    The self-assembly of alkyl propoxy ethoxylate surfactants in aqueous solutions has been investigated with a focus on the (i) thermodynamics of micellization (critical micellization concentration; free energy, enthalpy, and entropy of micellization) and (ii) structure of the micelles (overall shape and size; local environment in the micelle core and corona) as affected by the surfactant composition (variation of degree of ethoxylation). The various results are compared to those for alkyl ethoxylate and poly(ethylene oxide)-b-poly(propylene oxide) amphiphiles with the aim to elucidate the role of the middle, propoxy, block in the novel alkyl propoxy ethoxylate surfactants which exhibit a "graded" hydrophobic-hydrophilic character.

  17. Solution Properties of Dissymmetric Sulfonate-type Anionic Gemini Surfactants.

    Science.gov (United States)

    Yoshimura, Tomokazu; Akiba, Kazuki

    2016-01-01

    Dissymmetric and symmetric anionic gemini surfactants, N-alkyl-N'-alkyl-N,N'dipropanesulfonylethylenediamine (CmCnSul, where m and n represent alkyl chain lengths of m-n = 4-16, 6-14, 8-12, 10-10, and 12-12), were synthesized by two- or three-step reactions. Their physicochemical properties were characterized by equilibrium surface tension measurements, steady-state fluorescence spectroscopy of pyrene, and dynamic light scattering. The critical micelle concentration (CMC) of the dissymmetric surfactants C4C16Sul, C6C14Sul, and C8C12Sul was slightly lower than that of the symmetric surfactant C10C10Sul. The occupied area per molecule (A) of C8C12Sul was smaller than that of C10C10Sul, indicating that C8C12Sul has a high surface activity. However, the increase in the degree of dissymmetry from C8C12Sul to C6C14Sul and then to C4C16Sul resulted in high surface tension and large A. Based on the surface tension, the standard free energies of micellization (∆G°mic) and adsorption (∆G°ads), the efficiency of surface adsorption (pC20), and the effectiveness of surface adsorption (CMC/C20) were obtained. These parameters suggested that C8C12Sul formed micelles more readily than the other surfactants. The properties determined from the surface tension indicated that C8C12Sul's ability is intermediate between those of C10C10Sul and C12C12Sul. The pyrene fluorescence and dynamic light scattering results revealed that the micelle size depends on the longer of the two alkyl chains in dissymmetric surfactants.

  18. Spontaneous Vesicle Formation in Mixed Aqueous Solution of Poly-tailed Cationic and Anionic Surfactants

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Spontaneous vesicles from the mixed aqueous solution of poly-tailed cationic surfactant PTA and anionic surfactant AOT are firstly obtained. Vesicle formation and characterizations are demonstrated by negative-staining TEM and dynamic light scattering. A monodisperse vesicle system is obtained with a polydispersity of 0.082. Ultrasonication can promote the vesicle formation. Mechanism of vesicle formation is discussed from the viewpoint of molecular interaction.

  19. Weak solutions to a thin film model with capillary effects and insoluble surfactant

    CERN Document Server

    Escher, Joachim; Laurencot, Philippe; Walker, Christoph

    2011-01-01

    The paper focuses on a model describing the spreading of an insoluble surfactant on a thin viscous film with capillary effects taken into account. The governing equation for the film height is degenerate parabolic of fourth order and coupled to a second order parabolic equation for the surfactant concentration. It is shown that nonnegative weak solutions exist under natural assumptions on the surface tension coefficient.

  20. Heterogeneous photocatalytic degradation of phenanthrene in surfactant solution containing TiO{sub 2} particles

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Yanlin, E-mail: zhangyl@scnu.edu.cn [School of Chemistry and Environment, South China Normal University, Guangzhou (China); Sino-Forest Applied Research Centre for Pearl River Delta Environment and Department of Biology, Hong Kong Baptist University, Kowloon Tong (Hong Kong); Wong, J.W.C. [Sino-Forest Applied Research Centre for Pearl River Delta Environment and Department of Biology, Hong Kong Baptist University, Kowloon Tong (Hong Kong); Liu Peihong [School of Chemistry and Environment, South China Normal University, Guangzhou (China); Yuan Min [Research Resources Center, South China Normal University, Guangzhou (China)

    2011-07-15

    Highlights: {yields} Degradation of phenanthrene in surfactant solution and the role of surfactant have been elucidated. {yields} Possible pathway of phenanthrene degradation in surfactant solution is proposed. {yields} The degradation of phenanthrene follows pseudo-second-order kinetics. {yields} It is proved that applying the surfactants as solubilizing agents to remove contaminants from soils followed by photocatalytic degradation is a promising strategy for soil remediation. - Abstract: Photocatalytic degradation of phenanthrene (PHE) over TiO{sub 2} in aqueous solution containing nonionic surfactant micelles was investigated. All photocatalytic experiments were conducted using a 253.7 nm mercury monochromatic ultraviolet lamp in a photocatalytic reactor. The surfactant micelles could provide a nonaqueous 'cage' to result in a higher degradation rate of PHE than in an aqueous solution, but the higher Triton X-100 concentration (more than 2 g/L) lowered the degradation ratio of PHE because the additional surfactant micelles hindered the movement of micelles containing PHE so as to reduce their adsorption onto titania. Pseudo-second-order kinetics was observed for the photocatalytic degradation of PHE. Alkaline solution environment was beneficial to the photocatalytic degradation of PHE. PHE degradation could mainly be attributed to the formation of hydroxyl radicals as evident from the comparison of degradation efficiencies when O{sub 2}, H{sub 2}O{sub 2} and tert-butyl alcohol (TBA) were applied as oxidants or hydroxyl radical scavenger. Based on the GC/MS analysis of the intermediates, the possible pathways of the photocatalytic degradation of PHE were proposed.

  1. Unsteady motion of receding contact lines of surfactant solutions: the role of surfactant re-self-assembly.

    Science.gov (United States)

    Varanasi, K S; Garoff, S

    2005-10-25

    Re-self-assembly of surfactant molecules must occur at moving contact lines of soluble surfactant solutions. Molecules are transported into and out of the contact line region from four sources: the three interfaces meeting at the contact line and the fluid confined between the solid-liquid and liquid-vapor interfaces. As molecules move among these sources at the contact line, they must rearrange. The dynamics of this re-self-assembly has been shown to have a dominating effect on the structure of advancing contact lines, causing unsteady motion and complex structure of the contact line. It might be assumed that the re-self-assembly for receding contact lines leads to more steady contact line movement. However, in this article we show that for a wide variety of systems this is not true. Quasi-static distortions of the contact line occur as it retreats because of the inability of the surfactant to completely re-self-assemble at localized positions along the contact line.

  2. Interactions between Surfactants in Solution and Electrospun Protein Fibers: Effects on Release Behavior and Fiber Properties.

    Science.gov (United States)

    Stephansen, Karen; García-Díaz, María; Jessen, Flemming; Chronakis, Ioannis S; Nielsen, Hanne M

    2016-03-07

    Intermolecular interaction phenomena occurring between endogenous compounds, such as proteins and bile salts, and electrospun compounds are so far unreported, despite the exposure of fibers to such biorelevant compounds when applied for biomedical purposes, e.g., tissue engineering, wound healing, and drug delivery. In the present study, we present a systematic investigation of how surfactants and proteins, as physiologically relevant components, interact with insulin-loaded fish sarcoplasmic protein (FSP) electrospun fibers (FSP-Ins fibers) in solution and thereby affect fiber properties such as accessible surface hydrophilicity, physical stability, and release characteristics of an encapsulated drug. Interactions between insulin-loaded protein fibers and five anionic surfactants (sodium taurocholate, sodium taurodeoxycholate, sodium glycocholate, sodium glycodeoxycholate, and sodium dodecyl sulfate), a cationic surfactant (benzalkonium chloride), and a neutral surfactant (Triton X-100) were studied. The anionic surfactants increased the insulin release in a concentration-dependent manner, whereas the neutral surfactant had no significant effect on the release. Interestingly, only minute amounts of insulin were released from the fibers when benzalkonium chloride was present. The FSP-Ins fibers appeared dense after incubation with this cationic surfactant, whereas high fiber porosity was observed after incubation with anionic or neutral surfactants. Contact angle measurements and staining with the hydrophobic dye 8-anilino-1-naphthalenesulfonic acid indicated that the FSP-Ins fibers were hydrophobic, and showed that the fiber surface properties were affected differently by the surfactants. Bovine serum albumin also affected insulin release in vitro, indicating that also proteins may affect the fiber performance in an in vivo setting.

  3. Non-autonomous discrete Boussinesq equation: Solutions and consistency

    Science.gov (United States)

    Nong, Li-Juan; Zhang, Da-Juan

    2014-07-01

    A non-autonomous 3-component discrete Boussinesq equation is discussed. Its spacing parameters pn and qm are related to independent variables n and m, respectively. We derive bilinear form and solutions in Casoratian form. The plain wave factor is defined through the cubic roots of unity. The plain wave factor also leads to extended non-autonomous discrete Boussinesq equation which contains a parameter δ. Tree-dimendional consistency and Lax pair of the obtained equation are discussed.

  4. Complexation between dodecyl sulfate surfactant and zein protein in solution.

    Science.gov (United States)

    Ruso, Juan M; Deo, Namita; Somasundaran, P

    2004-10-12

    Interactions between sodium dodecyl sulfate and zein protein, a model system for the understanding of the effect of surfactants on skin, were investigated using a range of techniques involving UV-vis spectroscopy, TOC (total organic carbon analysis), electrophoresis, and static and dynamic light scattering. Zein protein was solubilized by SDS. The adsorption of SDS onto insoluble protein fraction caused the zeta potential of the complex to become more negative. From these values, we calculated the Gibbs energy of absorption, which decreases when the SDS concentration is raised. Finally the structure of the complex, based on the analysis by static and dynamic light scattering, is proposed to be rod like.

  5. Spectral and Acid-Base Properties of Hydroxyflavones in Micellar Solutions of Cationic Surfactants

    Science.gov (United States)

    Lipkovska, N. A.; Barvinchenko, V. N.; Fedyanina, T. V.; Rugal', A. A.

    2014-09-01

    It has been shown that the spectral characteristics (intensity, position of the absorption band) and the acid-base properties in a series of structurally similar hydroxyflavones depend on the concentration of the cationic surfactants miramistin and decamethoxin in aqueous solutions, and the extent of their changes is more pronounced for hydrophobic quercetin than for hydrophilic rutin. For the first time, we have determined the apparent dissociation constants of quercetin and rutin in solutions of these cationic surfactants (pKa1) over a broad concentration range and we have established that they decrease in the series water-decamethoxin-miramistin.

  6. Solution properties and emulsification properties of amino acid-based gemini surfactants derived from cysteine.

    Science.gov (United States)

    Yoshimura, Tomokazu; Sakato, Ayako; Esumi, Kunio

    2013-01-01

    Amino acid-based anionic gemini surfactants (2C(n)diCys, where n represents an alkyl chain with a length of 10, 12, or 14 carbons and "di" and "Cys" indicate adipoyl and cysteine, respectively) were synthesized using the amino acid cysteine. Biodegradability, equilibrium surface tension, and dynamic light scattering were used to characterize the properties of gemini surfactants. Additionally, the effects of alkyl chain length, number of chains, and structure on these properties were evaluated by comparing previously reported gemini surfactants derived from cystine (2C(n)Cys) and monomeric surfactants (C(n)Cys). 2C(n)diCys shows relatively higher biodegradability than does C(n)Cys and previously reported sugar-based gemini surfactants. Both critical micelle concentration (CMC) and surface tension decrease when alkyl chain length is increased from 10 to 12, while a further increase in chain length to 14 results in increased CMC and surface tension. This indicates that long-chain gemini surfactants have a decreased aggregation tendency due to the steric hindrance of the bulky spacer as well as premicelle formation at concentrations below the CMC and are poorly packed at the air/water interface. Formation of micelles (measuring 2 to 5 nm in solution) from 2C(n)diCys shows no dependence on alkyl chain length. Further, shaking the mixtures of aqueous 2C(n)diCys surfactant solutions and squalane results in the formation of oil-in-water type emulsions. The highly stable emulsions are formed using 2C₁₂diCys or 2C₁₄diCys solution and squalane in a 1:1 or 2:1 volume ratio.

  7. Small angle neutron scattering study of two nonionic surfactants in water micellar solutions

    Indian Academy of Sciences (India)

    Rajewska Aldona

    2008-11-01

    Two classic nonionic surfactants – C14E7 (heptaethylene glycol monotetra-decyl ether) and C10E7 (heptaethylene glycol monodecyl ether) were investigated in heavy water solution for concentration = 0.17% (dilute regime) at different temperatures in the range = 10–35°C by small angle neutron scattering (SANS) method. In the case of C14E7 surfactant – for all temperatures at = 0.17% there are two axial ellipsoidal micelles with longer axis 15 nm at 10°C and 49.5 nm at 35°C in investigated solutions. For C10E7 surfactant at the same concentration of solution and temperature – two axial ellipsoidal micelles were observed, too. The longer axis is equal to 7.5 nm at 10°C, 9 nm at 20°C and at 35°C this axis is equal to 12 nm. Micelles of C10E7 nonionic surfactant are smaller than those of C14E7 surfactant in the same experimental conditions.

  8. Spectral studies of safranin-O in different surfactant solutions.

    Science.gov (United States)

    Göktürk, Sinem; Tunçay, Melda

    2003-06-01

    The interaction of Safranin-O (SO), a cationic dye, with various surfactants viz., anionics; Sodiumdodecylsulfate (SDS) and Sodiumdodecylsulfonate (SDSo), nonionics; polyoxyethylenesorbitanmonolaurate (Tween 20) and polyoxyethylenedodecylether (Brij 35), cationic; Dodecyltrimethylammoniumbromide (DTAB) and zwitterionic; Laurylsulfobetaine (LSB) was studied spectrophotometrically as a function of surfactant concentration ranging from premicellar to postmicellar region in aqueous media in the absence and presence of cosolvents. The binding constants (K(b)) and fraction of bound SO to micelles (f), were calculated by means of Benesi-Hildebrand Equation. The binding tendency of SO to micelles followed the order as; Tween 20>Brij 35>SDS>SDSo>LSB. The presence of cosolvents, such as Methanol, Dimethylformamide (DMFA) and 1,4 Dioxan (DX) at various volume percentages, increased the CMC of both SDS and Tween 20 and at a certain concentration totally inhibited the micellization. The binding of SO to micelles decreased as the concentration of the cosolvents increased. This inhibitory effect of cosolvents on binding of SO to micelles followed the order as; Methanol>DMFA>DX.

  9. The Effect of Fluorocarbon Surfactant Additives on the Effective Viscosity of Acetone Solutions of Cellulose Diacetate,

    Science.gov (United States)

    2014-09-26

    34 FOREIGN TECHNOLOGY DIVISION i00 Lfl .. THE EFFECT OF FLUOROCARBON SURFACTANT ADDITIVES ON THE EFFECTIVE VISCOSITY OF ACETONE SOLUTIONS OF CELLULOSE ...ADDITIVES ON TH~ .. t- ’_ ition EFFECTIVE VISCOSITY OF ACETONE SOLUTIONS OF CELLULOSE DIACETATE D~rbt~l By: L.A. Shits, N. Yu. Kal’nova Codesuton English...VISCOSITY OF ACETONE SOLUTIONS OF CELLULOSE DIACETATE L. A. Shits, N. Yu. Kal’nova (Institute of Physical Chemistry of the AS USSR, Moscow) ! - The

  10. CISM Course on Fluid Mechanics of Surfactant and Polymer Solutions

    CERN Document Server

    Ivanov, Ivan

    2004-01-01

    Colloidal systems and dispersions are of great importance in oil recovery, waist water treatment, coating, food and beverage industry, pharmaceutical industry, medicine, environmental protection etc. Colloidal systems and dispersions are always multi-component and multiphase systems. In these systems at least one dimension is in a range of colloidal forces action: colloidal dispersions/emulsions are examples of three dimensional colloidal systems, while thin liquid films are examples of one dimensional colloidal systems. The contribution presented in this issue deals with flow, distribution and redistribution, coating and deposition of surfactant and polymer molecules in colloidal systems. The book presents reviews of recent advances and trends by well-know scientists and engineers in this area.

  11. Performance of Surfactant Methyl Ester Sulphonate solution for Oil Well Stimulation in reservoir sandstone TJ Field

    Science.gov (United States)

    Eris, F. R.; Hambali, E.; Suryani, A.; Permadi, P.

    2017-05-01

    Asphaltene, paraffin, wax and sludge deposition, emulsion and water blocking are kinds ofprocess that results in a reduction of the fluid flow from the reservoir into formation which causes a decrease of oil wells productivity. Oil well Stimulation can be used as an alternative to solve oil well problems. Oil well stimulation technique requires applying of surfactant. Sodium Methyl Ester Sulphonate (SMES) of palm oil is an anionic surfactant derived from renewable natural resource that environmental friendly is one of potential surfactant types that can be used in oil well stimulation. This study was aimed at formulation SMES as well stimulation agent that can identify phase transitions to phase behavior in a brine-surfactant-oil system and altered the wettability of rock sandstone and limestone. Performance of SMES solution tested by thermal stability test, phase behavioral examination and rocks wettability test. The results showed that SMES solution (SMES 5% + xylene 5% in the diesel with addition of 1% NaCl at TJformation water and SMES 5% + xylene 5% in methyl ester with the addition of NaCl 1% in the TJ formation water) are surfactant that can maintain thermal stability, can mostly altered the wettability toward water-wet in sandstone reservoir, TJ Field.

  12. Current applications of foams formed from mixed surfactant-polymer solutions.

    Science.gov (United States)

    Bureiko, Andrei; Trybala, Anna; Kovalchuk, Nina; Starov, Victor

    2015-08-01

    Foams cannot be generated without the use of special foaming agents, as pure liquids do not foam. The most common foaming agents are surfactants, however often for foam stability one active agent is not enough, it is necessary to add other component to increase foam lifetime. Foams on everyday use are mostly made from mixture of different components. Properly chosen combinations of two active ingredients lead to a faster foam formation and increased foam stability. During the last decade polymers (mainly polyelectrolytes and proteins) have become frequently used additives to foaming solutions. Mixtures of surfactants and polymers often demonstrate different foaming properties in comparison to surfactant only or polymer only solutions. The nature of surfactant-polymer interactions is complicated and prediction of resulting foaming properties of such formulations is not straightforward. Properties and foaming of surfactant-polymer mixtures are discussed as well as current applications of foams and foaming agents as foams are widely used in cosmetics, pharmaceutics, medicine and the food industry.

  13. Simultaneous treatment of chlorinated organics and removal of metals and radionuclides with bimetals and complexing acids - application to surfactant solutions

    Energy Technology Data Exchange (ETDEWEB)

    Korte, N.E.; Gu, B. [Oak Ridge National Lab., TN (United States)

    1997-10-01

    Currently available methods for separation and treatment of radioactive mixed waste are typically energy-intensive, and often require high temperatures. Passive methods that operate at ambient temperatures are needed. The purpose of this task is to develop bimetallic substrates, using a base metal such as iron and a promoter metal such as palladium (Pd), to provide a passive, low-energy solution to a substantial portion of DOE`s mixed-waste problem. This technology consists of a porous medium that can simultaneously dechlorinate hazardous organics such as TCE and polychlorinated biphenyls (PCBs) at the same time that it removes metallic and hazardous wastes from a solvent/surfactant solution. The porous medium consists of a bimetallic substrate such as palladized iron (Pd/Fe). Palladium is readily chemically plated on iron and preliminary studies suggest that only 0.05 to 0.1% Pd is needed for an efficient reaction. Thus, the cost of the material is reasonable especially is it is long-lived or can be regenerated. Field implementation would consist of the passage of a surfactant-laden, mixed waste through a column or bed of the bimetallic substrate. The organic component of this mixed waste may contain semivolatile compounds such as PCBs or pesticides and herbicides. The bimetal simultaneously removes radionuclides and metals and degrades halogenated hydrocarbons. Virtually any concentration can be treated. Following reaction of the bimetal with the waste stream, the resulting effluent will consist of an uncontaminated aqueous solution of surfactant or solvent that can be reused. The bimetal would then be rinsed with a dilute mineral acid or a mild complexing acid (e.g., oxalic or citric acid) to regenerate the surface and to remove sorbed metals and non-hazardous organic residue. The latter effluent would be low-level radioactive waste in some cases, but it would now be much easier to manage and be of a lower volume than the original mixed waste.

  14. Effects of Various Surfactants on the Dispersion of MWCNTs-OH in Aqueous Solution.

    Science.gov (United States)

    Cui, Hongzhi; Yan, Xiantong; Monasterio, Manuel; Xing, Feng

    2017-09-06

    Dispersion of carbon nanotubes (CNTs) is a challenge for their application in the resulting matrixes. The present study conducted a comparison investigation of the effect of four surfactants: Alkylphenol polyoxyethylene ether (APEO), Silane modified polycarboxylate (Silane-PCE), I-Cationic polycarboxylate (I-C-PCE), and II-Cationic polycarboxylate (II-C-PCE) on the dispersion of hydroxyl functionalized multi-walled carbon nanotubes (MWCNTs-OH). Among the four surfactants, APEO and II-C-PCE provide the best and the worst dispersion effect of CNTs in water, respectively. Dispersion effect of MWCNTs-OH has been characterized by optical microscope (OM), field emission-scanning electron microscope (FE-SEM), and Ultraviolet-visible spectroscopy (UV-Vis).The OM images are well consistent with the UV-Vis results. Based on the chemical molecular structures of the four surfactants, the mechanism of MWCNTs-OH dispersion in water was investigated. For each kind of surfactant, an optimum surfactant/MWCNTs-OH ratio has been determined. This ratio showed a significant influence on the dispersion of MWCNTs-OH. Surfactant concentration higher or lower than this value can weaken the dispersion quality of MWCNTs-OH.

  15. The interactions between cationic cellulose and Gemini surfactant in aqueous solution.

    Science.gov (United States)

    Zhao, Shaojing; Cheng, Fa; Chen, Yu; Wei, Yuping

    2016-05-05

    Due to the extensive application of cationic cellulose in cosmetic, drug delivery and gene therapy, combining the improvement effect of surfactant-cellulose complexes, to investigate the properties of cellulose in aqueous solution is an important topic from both scientific and technical views. In this study, the phase behavior, solution properties and microstructure of Gemini surfactant sodium 5-nonyl-2-(4-(4-nonyl-2-sulfonatophenoxy)butoxy)phenyl sulfite (9-4-9)/cationic cellulose (JR400, the ammonium groups are directly bonded to the hydroxyethyl substituent with a degree substitution of 0.37) mixture was investigated using turbidity, fluorescence spectrophotometer and shear rheology techniques. As a control, the interaction of corresponding monovalent surfactant, sodium 2-ethoxy-5-nonylbenzenesulfonate (9-2) with JR400 in aqueous solution was also studied. Experimental results showed that 9-4-9/JR400 mixture has lower critical aggregation concentration (CAC) and critical micelle concentration (CMC) (about one order of magnitude) than 9-2/JR400 mixture. A low concentration of Gemini surfactant 9-4-9 appeared to induce an obvious micropolarity and viscosity value variation of the mixture, while these effects required a high concentration of corresponding monovalent one. Furthermore, dynamic light scattering (DLS) and transmission electron microscopy (TEM) measurements illuminated the formation and collapse procedure of network structure of the 9-4-9/JR400 mixture, which resulted in the increase and decrease of viscosity. These results suggest that the molecular structure of the surfactant has a great effect on its interaction with cationic cellulose. Moreover, the Gemini surfactant/cationic cellulose mixture may be used as a potencial stimuli-responsive drug delivery vector which not only load hydrophilic drugs, but also deliver hydrophobic substances.

  16. Absorption and recovery of n-hexane in aqueous solutions of fluorocarbon surfactants.

    Science.gov (United States)

    Xiao, Xiao; Yan, Bo; Fu, Jiamo; Xiao, Xianming

    2015-11-01

    n-Hexane is widely used in industrial production as an organic solvent. As an industrial exhaust gas, the contribution of n-hexane to air pollution and damage to human health are attracting increasing attention. In the present study, aqueous solutions of two fluorocarbon surfactants (FSN100 and FSO100) were investigated for their properties of solubilization and dynamic absorption of n-hexane, as well as their capacity for regeneration and n-hexane recovery by thermal distillation. The results show that the two fluorocarbon surfactants enhance dissolution and absorption of n-hexane, and their effectiveness is closely related to their concentrations in solution. For low concentration solutions (0.01%-0.30%), the partition coefficient decreases dramatically and the saturation capacity increases significantly with increasing concentration, but the changes for both are more modest when the concentration is over 0.30%. The FSO100 solution presents a smaller partition coefficient and a greater saturation capacity than the FSN100 solution at the same concentration, indicating a stronger solubilization for n-hexane. Thermal distillation is a feasible method to recover n-hexane from these absorption solutions, and to regenerate them. With 90sec heating at 80-85°C, the recovery of n-hexane ranges between 81% and 85%, and the regenerated absorption solution maintains its original performance during reuse. This study provides basic information on two fluorocarbon surfactants for application in the treatment of industrial n-hexane waste gases.

  17. Accumulation of yellow Monascus pigments by extractive fermentation in nonionic surfactant micelle aqueous solution.

    Science.gov (United States)

    Xiong, Xu; Zhang, Xuehong; Wu, Zhenqiang; Wang, Zhilong

    2015-02-01

    Monascus species can produce various secondary metabolites of polyketide structure. In the current study, it is found that an interesting phenomenon, i.e., submerged culture of Monascus species in an aqueous solution majorly accumulated intracellular orange Monascus pigments exhibiting one peak at 470 nm with absorbance of 32 OD while extractive fermentation in a nonionic surfactant micelle aqueous solution produced extracellular and intracellular yellow Monascus pigments exhibiting one peak at 410 nm with absorbance 30 OD and 12 OD, respectively. The spectrum profiles of both intracellular and extracellular Monascus pigments were affected by surfactant loading, extractive fermentation time, and surfactant adding time. Meanwhile, the instability of orange Monascus pigments in the extracellular nonionic surfactant micelle aqueous solution was also confirmed experimentally. The mechanism behind this phenomenon is attributed to the export of intracellular yellow Monascus pigments into its broth by extractive fermentation. The transferring of intracellular yellow Monascus pigments into its broth blocks yellow Monascus pigments from further enzymatic conversion or eliminates the feedback inhibition of yellow Monascus pigments based on the biosynthetic pathway of Monascus pigments.

  18. Different behaviours in the solubilization of polycyclic aromatic hydrocarbons in water induced by mixed surfactant solutions.

    Science.gov (United States)

    Sales, Pablo S; de Rossi, Rita H; Fernández, Mariana A

    2011-09-01

    Water solubility of polycyclic aromatic hydrocarbons (PAHs), viz, naphthalene and phenanthrene, in micellar solutions at 25°C was investigated, using two series of different binary mixtures of anionic and nonionic surfactants. Tween 80 and Brij-35 were used as nonionic surfactants whereas fatty acids or amphiphilic cyclodextrins (Mod-β-CD) synthesized in our laboratory were used as anionic ones. Solubilization capacity has been quantified in terms of the molar solubilization ratio and the micelle-water partition coefficient, using UV-visible spectrophotometry. Anionic surfactants exhibited less solubilization capacity than nonionics. The mixtures between Tween 80 and Mod-β-CD did not show synergism to increase the solubilization of PAHs. On the other hand, the mixtures formed by Tween 80 and fatty acids at all mole fractions studied produced higher enhancements of the solubility of naphthalene than the individual surfactants. The critical micellar concentration of the mixtures of Tween 80/sodium laurate was determined by surface tension measurements and spectrofluorimetry using pyrene as probe. The system is characterized by a negative interaction parameter (β) indicating attractive interactions between both surfactants in the range of the compositions studied. Copyright © 2011 Elsevier Ltd. All rights reserved.

  19. Verification of surfactant CHAPS effect using AFM for making biomemory device consisting of recombinant azurin monolayer

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Taek [Department of Chemical and Biomolecular Engineering, Sogang University, 1 Shinsu-dong, Mapo-gu, Seoul 121-742 (Korea, Republic of); Ahmed El-Said, Waleed [Interdisciplinary Program of Integrated Biotechnology, Sogang University, 1 Shinsu-dong, Mapo-gu, Seoul 121-742 (Korea, Republic of); Min, Junhong [College of Bionanotechnology, Kyungwon University, Bokjung-dong, Sujung-gu, Seongnam 461-701 (Korea, Republic of); Oh, Byung-Keun [Department of Chemical and Biomolecular Engineering, Sogang University, 1 Shinsu-dong, Mapo-gu, Seoul 121-742 (Korea, Republic of); Interdisciplinary Program of Integrated Biotechnology, Sogang University, 1 Shinsu-dong, Mapo-gu, Seoul 121-742 (Korea, Republic of); Choi, Jeong-Woo, E-mail: jwchoi@sogang.ac.kr [Department of Chemical and Biomolecular Engineering, Sogang University, 1 Shinsu-dong, Mapo-gu, Seoul 121-742 (Korea, Republic of); Interdisciplinary Program of Integrated Biotechnology, Sogang University, 1 Shinsu-dong, Mapo-gu, Seoul 121-742 (Korea, Republic of)

    2010-05-15

    In this study, a protein-based biomemory device was developed using a surface modified recombinant azurin layer and its surface characteristics were analyzed by atomic force microscopy. The cysteine-modified azurin used for this purpose was a metalloprotein that had redox properties. To immobilize the metalloprotein on the Au substrates, the cysteine-modified azurin layer was self-assembled on the Au surface through a covalent bond between the thiol group on the cysteine and the Au surface. In our previous work, we showed that this protein layer was formed as cohesive clusters on Au surface through physical adsorption. To reduce the formation of these cohesion clusters, a zwitterionic surfactant, (3-[(3-cholamidopropyl) dimethylammonio]-1-propanesulfonate) (CHAPS) was introduced to modify the surface properties. Using this approach, we found that CHAPS significantly reduced the amount of cysteine-modified azurin aggregates that nonspecifically adsorbed to the Au substrate. Atomic force microscopy was used to analyze the modified-surface. Based on this analysis, the size of the recombinant azurin clusters when CHAPS was used were about 15-25 nm whereas aggregates of 150-200 nm were observed in the absence of CHAPS. In addition, Raman spectroscopy was performed to confirm the retention of azurin molecules self-assembled on the Au surface. Electrochemical results using cyclic voltammetry indicated that recombinant azurin was successfully immobilized onto the Au surface with CHAPS and its redox property remained intact. Chronoamperometry was then used to demonstrate the memory characteristics of this azurin-based fabricated memory device. The combined results of this study show that CHAPS can significantly reduce the size of protein aggregates that become immobilized on the surface without a loss of the electrochemical properties of the protein.

  20. The photodegradation of trichloroethylene with or without the NAPL by UV irradiation in surfactant solutions

    Energy Technology Data Exchange (ETDEWEB)

    Jia Juncai [Department of Civil and Structural Engineering, Research Centre for Urban Environmental Technology and Management, Hong Kong Polytechnic University, Hung Hom, Kowloon (Hong Kong); Chu, W. [Department of Civil and Structural Engineering, Research Centre for Urban Environmental Technology and Management, Hong Kong Polytechnic University, Hung Hom, Kowloon (Hong Kong)], E-mail: cewchu@polyu.edu.hk

    2009-01-15

    The photodegradation of trichloroethene (TCE) with or without nonaqueous phase liquids (NAPL) by ultraviolet irradiation in surfactant solutions was examined in this study. The photodecay of TCE was studied at monochromatic 254 nm UV lamps. The effects of the type of surfactants, initial surfactant concentrations, pH levels and NAPL concentrations were examined to explore the photodecay of TCE. All the photodegradation of TCE followed pseudo-first-order decay kinetics at various conditions. It was found that Brij 35 overdose and higher initial pH levels may retard or inhibit the photodecay of TCE, mainly due to protons, intermediate generation and change of surfactant structure in the processes. The optimal condition for TCE photodecay was suggested based on the analysis of kinetics data, from which the reaction mechanism of TCE in the presence of NAPL form was also studied. In general, the reactions of TCE in micellar solution and NAPL pool can be considered as independent pathways due to the low molecule diffusion between the two phases.

  1. Explicit- and implicit-solvent simulations of micellization in surfactant solutions.

    Science.gov (United States)

    Jusufi, Arben; Panagiotopoulos, Athanassios Z

    2015-03-24

    In this article, we focus on simulation methodologies to obtain the critical micelle concentration (cmc) and equilibrium distribution of aggregate sizes in dilute surfactant solutions. Even though it is now relatively easy to obtain micellar aggregates in simulations starting from a fully dispersed state, several major challenges remain. In particular, the characteristic times of micelle reorganization and transfer of monomers from micelles to free solution for most systems of practical interest exceed currently accessible molecular dynamics time scales for atomistic surfactant models in explicit solvent. In addition, it is impractical to simulate highly dilute systems near the cmc. We have demonstrated a strong dependence of the free surfactant concentration (frequently, but incorrectly, taken to represent the cmc in simulations) on the overall concentration for ionic surfactants. We have presented a theoretical framework for making the necessary extrapolations to the cmc. We find that currently available atomistic force fields systematically underpredict experimental cmc's, pointing to the need for the development of improved models. For strongly micellizing systems that exhibit strong hysteresis, implicit-solvent grand canonical Monte Carlo simulations represent an appealing alternative to atomistic or coarse-grained, explicit-solvent simulations. We summarize an approach that can be used to obtain quantitative, transferrable effective interactions and illustrate how this grand canonical approach can be used to interpret experimental scattering results.

  2. Property Changes in Aqueous Solutions due to Surfactant Treatment of PCE: Implications to Geophysical Measurements

    Science.gov (United States)

    Werkema, D. D.

    2007-12-01

    Select physicochemical properties of aqueous solutions composed of surfactants, dye, and perchloroethylene (PCE) were evaluated through a response surface quadratic design model of experiment. Nine surfactants, which are conventionally used in the remediation of PCE, were evaluated with varying concentrations of PCE and indicator dyes in aqueous solutions. Two hundred forty experiments were performed using PCE as a numerical factor (coded A) from 0 to 200 parts per million (ppm), dye type (coded B) as a 3-level categorical factor, and surfactant type (coded C) as a 10-level categorical factor. Five responses were measured: temperature (°C), pH, conductivity (μS/cm), dissolved oxygen (DO, mg/L), and density (g/mL). Diagnostics proved a normally distributed predictable response for all measured responses except pH. The Box-Cox plot for transforms recommended a power transform for the conductivity response with lambda (λ) = 0.50, and for the DO response, λ =2.2. The overall mean of the temperature response proved to be a better predictor than the linear model. The conductivity response is best fitted with a linear model using significant coded terms B and C. Both DO and density also showed a linear model with coded terms A, B, and C for DO; and terms A and C for density. Some of the surfactant treatments of PCE significantly alter the conductivity, DO, and density of the aqueous solution. However, the magnitude of the density response is so small that it does not exceed the instrument tolerance. Results for the conductivity and DO responses provide predictive models for the surfactant treatment of PCE and may be useful in determining the potential for geophysically monitoring surfactant enhanced aquifer remediation (SEAR) of PCE. As the aqueous physicochemical properties change due to surfactant remediation efforts, so will the properties of the subsurface pore water which are influential factors in geophysical measurements. Geoelectrical methods are potentially

  3. Thermal Transport across Surfactant Layers on Gold Nanorods in Aqueous Solution.

    Science.gov (United States)

    Wu, Xuewang; Ni, Yuxiang; Zhu, Jie; Burrows, Nathan D; Murphy, Catherine J; Dumitrica, Traian; Wang, Xiaojia

    2016-04-27

    Ultrafast transient absorption experiments and molecular dynamics simulations are utilized to investigate the thermal transport between aqueous solutions and cetyltrimethylammonium bromide (CTAB)- or polyethylene glycol (PEG)-functionalized gold nanorods (GNRs). The transient absorption measurement data are interpreted with a multiscale heat diffusion model, which incorporates the interfacial thermal conductances predicted by molecular dynamics. According to our observations, the effective thermal conductance of the GNR/PEG/water system is higher than that of the GNR/CTAB/water system with a surfactant layer of the same length. We attribute the enhancement of thermal transport to the larger thermal conductance at the GNR/PEG interface as compared with that at the GNR/CTAB interface, in addition to the water penetration into the hydrophilic PEG layer. Our results highlight the role of the GNR/polymer thermal interfaces in designing biological and composite-based heat transfer applications of GNRs, and the importance of multiscale analysis in interpreting transient absorption data in systems consisting of low interfacial thermal conductances.

  4. [Study on synergistic effect of bactericidal effect of chlorine dioxide solution by surfactant].

    Science.gov (United States)

    Wang, Kuitao; Tian, Vuena; Gu, Na; Zhang, Congjing; Niu, Jiajing

    2013-03-01

    To study the effect of gemini fluorocarbon, sodium p-perfluorous nonenoxybenzene sulfonate and sodium dodecyl sulfate on the chlorine dioxide solution sterilization to object surface. Pure chlorine dioxide solution as the reference disinfectant, carrier quantitative bactericidal test and simulated test on-site were used to carry out laboratory observation according to The disinfection technical specifications (2002). Carrier quantitative bactericidal test showed that the addition dosage of gemini fluoronates, sodium dodecyl sulfate surfactant and perfluorinated the nonene oxy benzene sulfonate in disinfectant solution were 60, 60 and 40 mg/L respectively, the killing log value of Staphylococcus aureus exposed to the disinfectant solution containing chlorine dioxide 50 mg/L for 10 mm were all more than 3; and the addition dosage of gemini fluorinates, sodium dodecyl sulfate and perfluorinated the nonene oxy benzene sulfonate in disinfectant solution were 60 mg/L, the killing log value of Escherichia coli exposed to the disinfectant solution containing chlorine dixoxide 20 mg/L for 10 min were all more than 3. The bactericidal effect of the mixture use of surfactant and chlorine dioxide was better than the single use of chlorine dioxide. The simulated test on-site showed that the killing log value of Escherichia coli exposed to the disinfectant solution containing perfluorinated the nonene oxy benzene sulfonate 40 mg/L and chlorine dioxide 20 mg/L for 15 min was more than 3. Surface active agent on germicidal efficacy of chlorine dioxide solution had synergistic action.

  5. Electrostatic charge on spray droplets of aqueous surfactant solutions

    OpenAIRE

    POLAT, Mehmet; Polat, Hürriyet; Chander, Subhash

    2000-01-01

    Electrostatic charges on individual spray droplets were measured using a refined form of the Millikan oil drop method. The measurement system consisted of three main sections; a droplet generation cell, a settling column and a charge measurement chamber. The trajectories required for calculation of charge were determined using a high-speed motion analyzer coupled to a long-focal-length microscope. Charges on droplets were manipulated by the addition of surface-active agents into the spray sol...

  6. Effect of inorganic additives on solutions of nonionic surfactants VI: Further cloud point relations.

    Science.gov (United States)

    Schott, H; Royce, A E

    1984-06-01

    Disperse dosage forms stabilized with nonionic surfactants frequently contain electrolytes as active ingredients or adjuvants. Salting out of the surfactants by these electrolytes may cause breakdown of the dosage forms. The cloud point of an aqueous solution of octoxynol 9 was used to measure the salt effects. Electrolytes which salt octoxynol 9 out lower its cloud point, while salting-in electrolytes raise it. The observed cloud point effects are discussed according to the mechanisms involved. Salting out by dehydration in competition with octoxynol 9 for the available water was observed with sulfate and phosphate anions, sodium, potassium, and ammonium tribasications, and the nonelectrolyte sorbitol. The extensive self-association of water by hydrogen bonds at and below room temperature weakens its solvent power. Ions which reduce this self-association, breaking the structure of water, increased the cloud point of octoxynol 9. Among them were the iodide, thiocyanate, and nitroprusside anions. Ions which tighten the structure of water and enhance its self-association salted the surfactant out, lowering its cloud point. Among these were the fluoride and hydroxide anions. Complex formation between the ether linkages of octoxynol 9 and the following cations increased its cloud point: hydrogen (from strong acids), silver, magnesium, and zinc. Including published data, the only cations which do not form complexes with polyoxyethylated surfactants (and are, therefore, unable to salt them in) were the alkali metal ions sodium, potassium, and cesium and the ammonium ion.(ABSTRACT TRUNCATED AT 250 WORDS)

  7. Interactions between fluorinated cationic guar gum and surfactants in the dilute and semi-dilute solutions.

    Science.gov (United States)

    Wang, Chen; Li, Xiaorui; Li, Peizhi; Niu, Yuhua

    2014-01-01

    The interactions between the fluorinated cationic guar gum (FCGG) and ionic surfactants including cetyl trimethyl ammonium bromide (CTAB) and sodium lauryl sulfate (SDS) were studied by light scattering, fluorescence spectroscopy, UV-spectrophotometer, (19)F NMR and dynamic rheometer, respectively. The FCGG is prepared with cationic guar gum, isophorone diisocyanate and 2,2,3,4,4,4-hexafluoro-1-butanol. The results show that, with the addition of the surfactants, the stretching degree of the FCGG chains is increased in the FCGG/CTAB solutions, while the dramatical shrinking of FCGG chain, the phase separation and the re-stretched macromolecules appear successively because of the electricity neutralization reaction in the FCGG/SDS system. The mixed hydrophobic domains in all solutions will be reinforced and then dismantled. The solution elasticity shows up the maximum value accordingly. The surfactants can be embedded in the micro-domains and then hinder the fluorinated segmental motions. The interactions between FCGG and SDS are much stronger than those between FCGG and CTAB.

  8. Enhanced Oil Recovery from Oil-wet Carbonate Rock by Spontaneous Imbibition of Aqueous Surfactant Solutions

    Energy Technology Data Exchange (ETDEWEB)

    Standnes, Dag Chun

    2001-09-01

    The main theme of this thesis is an experimental investigation of spontaneous imbibition (SI) of aqueous cationic surfactant solution into oil-wet carbonate (chalk- and dolomite cores). The static imbibition process is believed to represent the matrix flow of oil and water in a fractured reservoir. It was known that aqueous solution of C{sub 12}-N(CH{sub 3}){sub 3}Br (C12TAB) was able to imbibe spontaneously into nearly oil-wet chalk material, but the underlying mechanism was not understood. The present work was therefore initiated, with the following objectives: (1) Put forward a hypothesis for the chemical mechanism underlying the SI of C12TAB solutions into oil-wet chalk material based on experimental data and (2) Perform screening tests of low-cost commercially available surfactants for their ability to displace oil by SI of water into oil-wet carbonate rock material. It is essential for optimal use of the surfactant in field application to have detailed knowledge about the mechanism underlying the SI process. The thesis also discusses some preliminary experimental results and suggests mechanisms for enhanced oil recovery from oil-wet carbonate rock induced by supply of thermal energy.

  9. Heterogeneous photocatalytic degradation of phenanthrene in surfactant solution containing TiO2 particles.

    Science.gov (United States)

    Zhang, Yanlin; Wong, J W C; Liu, Peihong; Yuan, Min

    2011-07-15

    Photocatalytic degradation of phenanthrene (PHE) over TiO(2) in aqueous solution containing nonionic surfactant micelles was investigated. All photocatalytic experiments were conducted using a 253.7 nm mercury monochromatic ultraviolet lamp in a photocatalytic reactor. The surfactant micelles could provide a nonaqueous "cage" to result in a higher degradation rate of PHE than in an aqueous solution, but the higher Triton X-100 concentration (more than 2 g/L) lowered the degradation ratio of PHE because the additional surfactant micelles hindered the movement of micelles containing PHE so as to reduce their adsorption onto titania. Pseudo-second-order kinetics was observed for the photocatalytic degradation of PHE. Alkaline solution environment was beneficial to the photocatalytic degradation of PHE. PHE degradation could mainly be attributed to the formation of hydroxyl radicals as evident from the comparison of degradation efficiencies when O(2), H(2)O(2) and tert-butyl alcohol (TBA) were applied as oxidants or hydroxyl radical scavenger. Based on the GC/MS analysis of the intermediates, the possible pathways of the photocatalytic degradation of PHE were proposed.

  10. Formation of wormlike micelles in anionic surfactant AES aqueous solutions

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The growth and structure of anionic micelles of sodium dodecyl trioxyethylene sulfate (AES) in the presence 3+of multivalent counterion Al were investigated by means of dynamic rheological methods. It has been obtained by the measurements of shear viscosity, complex viscosity and dynamic moduli, as well as the application of Cox-Merz rule and Cole-Cole plot that wormlike micelle and network structure could be formed in AES/AlCl3 aqueous solutions.The structure was of a character of nonlinear viscoelastic fluid and departure from the simple Maxwell model. The technique of freeze-fracture transmission electron microscopy (FF-TEM) was also used to confirm the formation of this interesting structure.``

  11. Visualization of TCE recovery mechanisms using surfactant-polymer solutions in a two-dimensional heterogeneous sand model.

    Science.gov (United States)

    Robert, Thomas; Martel, Richard; Conrad, Stephen H; Lefebvre, René; Gabriel, Uta

    2006-06-30

    This research focused on the optimization of TCE dissolution in a physical two-dimensional model providing a realistic representation of a heterogeneous granular aquifer. TCE was infiltrated in the sand pack where it resided both in pools and in zones of residual saturation. Surfactant was initially injected at low concentration to minimize TCE remobilization at first contact but was incrementally increased later during the experiment. Xanthan gum was added to the injected surfactant solution to optimize the sweep efficiency through the heterogeneous medium. Photographs and digital image analysis illustrated the interactions between TCE and the injected fluids. During the polymer flood, the effects of heterogeneities inside the sand pack were greatly reduced by the increased fluid viscosity and the shear-thinning effects of the polymer. The polymer also improved the contact between the TCE ganglia and the surfactant-polymer solution, thereby promoting dissolution. Surfactants interacted with the polymer reducing the overall viscosity of the solution. At first contact with a 0.5%(mass) surfactant solution, the TCE pools drained and some remobilization occurred. However, no TCE bank was formed and TCE did not penetrate into any previously uncontaminated areas. As a result, TCE surface area was increased. Subsequent surfactant floods at higher surfactant concentrations did not trigger more remobilization. TCE was mainly dissolved by the solution with the highest surfactant concentration. Plugging from bacterial growth or microgel formation associated to the polymer at the inflow screen prevented the full completion of the experiment. However, more than 90% of TCE was recovered with the circulation of less than 6 pore volumes of surfactant-polymer solution.

  12. Composition-insensitive highly viscous wormlike micellar solutions formed in anionic and cationic surfactant systems.

    Science.gov (United States)

    Aramaki, Kenji; Iemoto, Suzuka; Ikeda, Naoaki; Saito, Keitaro

    2010-01-01

    We investigated phase behavior and rheological properties of aqueous micellar phase formed in water/cocoyl glutamate neutralized with triethanol amine (CGT-n)/hexadecyl trimethylammonium salt (CTAB or CTAC) systems, where n is a degree of neutralization. Micellar phase appears in wide composition range with respect to the surfactant mixing fraction in ternary phase diagrams at 25 degrees C. At high mixing fraction of cationic surfactant in the water/CGT-n/CTAB systems, one can observe a highly viscous micellar phase in which worm-like micelles are expected to form. Contrary to conventional systems in which worm-like micelles are formed, the zero-shear viscosity of the micellar solution in the water/CGT-n/CTAB system with n=1.2 increases with the addition of cationic cosurfactant and once decreases after a maximum, then increases again and decreases after the second maximum. At n=1.5 and 2, highly viscous solution is observed in the relatively wide range of surfactant mixing fraction instead of two maxima of the viscosity curve observed at n=1.2. In the case of CTAC instead of CTAB we can observe narrow composition range for the maximum viscosity. Frequency sweep measurements were performed on the highly viscous samples in the water/CGT-1.5/CTAB system. Typical viscoelastic behavior of worm-like micellar solutions is observed; i.e. the curves of storage (G') and loss (G") moduli make a crossover and the data points of G' and G" can be fitted to the Maxwell model. Relaxation time against the mixing fraction of two surfactants behaves similarly to the zero-shear viscosity change, whereas the plateau modulus continuously increases in the plateau region for the zero-shear viscosity curve.

  13. Dynamic contact angles on PTFE surface by aqueous surfactant solution in the absence and presence of electrolytes.

    Science.gov (United States)

    Chaudhuri, Rajib Ghosh; Paria, Santanu

    2009-09-15

    This study presents the experimental results on dynamic contact angles of pure surfactants and surfactants with electrolyte solutions on PTFE (Teflon) surface. Dynamic advancing (theta(A)) and receding (theta(R)) contact angles measurements by the Wilhelmy plate technique were carried out for aqueous solution of three different surfactants Triton X-100 (TX-100), sodium dodecylbenzene sulfonate (SDBS), and cetyltrimethylammonium bromide (CTAB). The same measurements in the presence of different electrolytes NaCl, Na(2)SO(4), and CaCl(2) for ionic surfactants (SDBS and CTAB) were also carried out to see the change in contact angle and wetting behavior. The presence of electrolytes changes the advancing contact angle as well as wetting properties of hydrophobic solid surface significantly even at very low surfactant concentration. Counter ion valency of the electrolyte is more important in reducing advancing contact angle on hydrophobic PTFE surface at very low concentration of ionic surfactants from CMC. Pure surfactants and ionic surfactants in the presence of electrolytes show a linear relationship between the adhesional tension and surface tension at air-water interface with different slope and intercept.

  14. Spontaneous change in trajectory patterns of a self-propelled oil droplet at the air-surfactant solution interface

    Science.gov (United States)

    Tanaka, Shinpei; Sogabe, Yoshimi; Nakata, Satoshi

    2015-03-01

    Trajectory-pattern formation of a self-propelled oil droplet floating on the surface of a surfactant solution in a circular dish is studied both experimentally and by simulation. The Marangoni effect induced by the dissolution of oil in the solution drives the droplet's motion. The trajectories spontaneously organize into several patterns including circular, knot-forming, back-and-forth, and irregular ones. They are either global patterns, whose center corresponds to the dish center, or other local patterns. Our simple model consisting of three forces, the driving force, the viscous resistance, and the repulsion from the boundary, successfully reproduces the global trajectory patterns including the power spectrum of the droplet speed.

  15. Mechanical properties of polyurethane film exposed to solutions of nonoxynol-9 surfactant and polyethylene glycol

    Science.gov (United States)

    McDermott, Martin Kendrick

    Changes in physical properties (tensile strength, strain to failure, elastic modulus, diffusion kinetics and soft segment glass transition temperature (Tg)) were examined for polyetherurethane block copolymers Estane and Tecoflex. These polymer chains consist of 2 mutually incompatible blocks or segments which form microphases consisting of rigid/hard segments in an elastomeric matrix of soft segments. The polyurethanes were exposed to mixtures of nonoxynol 9 (N9) surfactant in polyethylene glycol 400 (PEG) at various concentrations and for various times. The purpose was to estimate the effect of exposure to mixtures of N9 spermicide and PEG lubricant on breakage of condoms made from films of these elastomers. Mechanical properties of Estane varied with direction because of molecular orientation induced during manufacturing, suggesting that condoms should be cut from the film in a way that optimizes this property-orientation relationship. Large amounts of N9 were absorbed from N9/PEG solutions. The polymer fraction of the swollen Estane film versus soak solution composition did not follow a linear rule of mixtures. As the percentage of N9 in the PEG/N9 soak solution increased, Estane absorbed more liquid and its properties decreased more than did Tecoflex. This may not matter for low concentrations of N9 where the mechanical properties of Estane were superior to those of Tecoflex. The loss of mechanical properties with increased N9 concentration was likely due to plasticization of the soft segment domains. Hard segment domain disruption was probably not occurring because the relationship between the elastic modulus and polymer volume fraction followed the Flory-Rehner relationship for swollen elastic rubber networks and diffusion of neat N9 and neat PEG followed a Fickian behavior. This is expected because hard domains are much more difficult to disrupt due to strong hydrogen bonding and/or crystallization. Most of the absorption and decrease in mechanical

  16. Dielectric analysis on phase transition and micelle shape of polyoxyethylene trisiloxane surfactant in dilute aqueous solution

    Institute of Scientific and Technical Information of China (English)

    Ya Wen Zhou; Wei Zhou; Fu Han; Bao Cai Xu

    2011-01-01

    The cloudy Silwet L-77 aqueous solution on the concentration range from 0.5% to 50% was investigated by dielectric relaxation spectroscopy. The concentration dependence of phase microstructure was confirmed by means of analyzing the dielectric parameters of bulk solution. The relaxation behavior was assigned to the interfacial polarization between the micelle and the medium, and the relaxation distribution parameter was used to figure the shape transition from sphere to ellipsoid with the concentration increasing. The synchronous reduction of permittivity and conductivity indicated the formation of the lamellar phase. As compensation, the quantity of the surfactant liquid phase gradually decreased, whose shape constantly kept ellipsoidal.

  17. Ludwig-Soret effect of non-ionic surfactant aqueous solution studied by beam deflection method

    Science.gov (United States)

    Maeda, Kousaku; Kita, Rio; Shinyashiki, Naoki; Yagihara, Shin

    2013-02-01

    We have studied the thermal diffusion of non-ionic surfactant aqueous solutions by a beam deflection method. The thermal diffusion of pentaethylene glycol monododecyl ether (C12E5) and hexaethylene glycol monododecyl ether (C12E6) is studied in the concentration range of 1.0-99.0 wt% and in the temperature range of 20.0-35.0 °C. A stable temperature gradient is applied to the solution, where solute molecules shift to the cold side of the solution for lowconcentration samples. The concentration dependence of the Soret coefficient ST of the C12E6 aqueous solution shows a sign inversion behavior. At all concentrations, the developed concentration gradient is proportionally related to the applied temperature gradient. The results confirm that the magnitude of ST has no temperature gradient dependence under the studied experimental conditions.

  18. Study of the formation and solution properties of worm-like micelles formed using both N-hexadecyl-N-methylpiperidinium bromide-based cationic surfactant and anionic surfactant.

    Directory of Open Access Journals (Sweden)

    Zhihu Yan

    Full Text Available The viscoelastic properties of worm-like micelles formed by mixing the cationic surfactant N-hexadecyl-N-methylpiperidinium bromide (C16MDB with the anionic surfactant sodium laurate (SL in aqueous solutions were investigated using rheological measurements. The effects of sodium laurate and temperature on the worm-like micelles and the mechanism of the observed shear thinning phenomenon and pseudoplastic behavior were systematically investigated. Additionally, cryogenic transmission electron microscopy images further ascertained existence of entangled worm-like micelles.

  19. Factors Affecting the Stability of Crude and Transmission Oil Emulsion Swith Surfactant Solutions

    Directory of Open Access Journals (Sweden)

    Erich Martínez Martín

    2016-04-01

    Full Text Available Crude oil emulsions with surfactant solutions are used to transport this for piping systems. The applicationof this technique requires that the emulsions remain stable during the pumping period and haveseparated after transporting the crude. In this paper, experimental assays were performed using differentconcentrations of surfactant, and mixing types settling conditions. They were employed as the continuousphase two substances: oil transmission and Cuban crude oil. The strong infl uence of the concentrationand type of mixing on the stability of the emulsions was observed. The results demonstrate the similaritiesin thermalhydraulic fl uid parameters objects of study. Allowing infer the approximate behavior of theCuban crude oil from experimental work with transmission oil.

  20. Investigation of extractive microbial transformation in nonionic surfactant micelle aqueous solution using response surface methodology.

    Science.gov (United States)

    Xue, Yingying; Qian, Chen; Wang, Zhilong; Xu, Jian-He; Yang, Rude; Qi, Hanshi

    2010-01-01

    Extractive microbial transformation of L-phenylacetylcarbinol (L-PAC) in nonionic surfactant Triton X-100 micelle aqueous solution was investigated by response surface methodology. Based on the Box-Behnken design, a mathematical model was developed for the predication of mutual interactions between benzaldehyde, Triton X-100, and glucose on L-PAC production. It indicated that the negative or positive effect of nonionic surfactant strongly depended on the substrate concentration. The model predicted that the optimal concentration of benzaldehyde, Triton X-100, and glucose was 1.2 ml, 15 g, and 2.76 g per 100 ml, respectively. Under the optimal condition, the maximum L-PAC production was 27.6 mM, which was verified by a time course of extractive microbial transformation. A discrete fed-batch process for verification of cell activity was also presented.

  1. Wormlike micelles in poly(oxyethylene) surfactant solution: Growth control through hydrophilic-group size variation.

    Science.gov (United States)

    Ahmed, Toufiq; Aramaki, Kenji

    2008-11-01

    Viscoelastic micellar solutions are formed in poly(oxyethylene) cholesteryl ether (ChEO(m), m=15, 30) aqueous solutions on addition of tri(ethyleneglycol) mono n-dodecyl ether (C(12)EO(3)). The steady-shear and dynamic rheological behavior of the systems is characteristic of wormlike micellar solution. In either system, the plateau modulus (G(0)) and relaxation time (tau) are found to increase with increasing cosurfactant mixing fractions. The plateau modulus of the ChEO(30)-C(12)EO(3) system at the maximum viscosity region is found to be higher than that in the ChEO(15)-C(12)EO(3) system at the maximum viscosity region, whereas for the relaxation time the opposite relation is found. The maximum viscosities obtained in the two systems are of the same order of magnitude. In the ChEO(30)-C(12)EO(3) system, the maximum viscosity is obtained at a higher cosurfactant mixing fraction than that in the ChEO(15)-C(12)EO(3) system. It is concluded that decreasing the head-group size of the hydrophilic surfactant favors micellar growth. Monolaurin, another hydrophobic surfactant known to induce growth in some systems, is found to cause phase separation before significant micellar growth occurs in ChEO(m) solutions, although the effect of head-group size of ChEO(m) is found to be similar to the ChEO(m)-C(12)EO(3) systems.

  2. Effects of Surfactant on Zinc Recovery by Solvent Extraction during Leaching in HCl—FeCl3 Solution

    Institute of Scientific and Technical Information of China (English)

    LULizhu; KANGXiaobong; 等

    2002-01-01

    The effects of surfactant on the solvent extraction in leaching sphalerite were investigated. It is found that sodium dodecyl sulfonate is the effective surfactant in improving the zinc recovery from sphalerite in the aqueous FeCl3-HCl-tetrachloroethylene system. Through the measurements of surface tension and viscosity of the sphalerite slurry modified with different surfactants, it is concluded that sodium dodecyl sulfonate in the concentration range of 0.05 to 0.2g·L-1 can improve the viscosity of sphalerite slurry in the water, decrease the surface tension of leaching solution, prevent the aggregation of ore particles, and give very high zinc extraction.

  3. Viscoelasticity Enhancement of Surfactant Solutions Depends on Molecular Conformation: Influence of Surfactant Headgroup Structure and Its Counterion.

    Science.gov (United States)

    Lutz-Bueno, Viviane; Pasquino, Rossana; Liebi, Marianne; Kohlbrecher, Joachim; Fischer, Peter

    2016-05-03

    During the anisotropic growth from globular to wormlike micelles, the basic interactions among distinct parts of the surfactant monomer, its counterion, and additives are fundamental to tune molecular self-assembly. We investigate the addition of sodium salicylate (NaSal) to hexadecyltrimethylammonium chloride and bromide (CTAC and CTAB), 1-hexadecylpyridinium chloride and bromide (CPyCl and CPyBr), and benzyldimethylhexadecylammonium chloride (BDMC), which have the same hydrophobic tail. Their potential to enhance viscoelasticity by anisotropic micellar growth upon salt addition was compared in terms of (i) the influence of the headgroup structure, and (ii) the influence of surfactant counterion type. Employing proton nuclear magnetic resonance ((1)H NMR), we focused on the molecular conformation of surfactant monomers in the core and polar shell regions of the micelles and their interactions with increasing concentration of NaSal. The viscoelastic response was investigated by rotational and oscillatory rheology. We show that micellar growth rates can be tuned by varying the flexibility and size of the surfactant headgroup as well as the dissociation degree of the surfactant counterion, which directly influences the strength of headgroup-counterion pairing. As a consequence, the morphological transitions depend directly on charge neutralization by electrostatic screening. For example, the amount of salt necessary to start the rodlike-to-wormlike micelle growth depends directly on the number of dissociated counterions in the polar shell.

  4. An Asymptotic Theory for the Re-Equilibration of a Micellar Surfactant Solution

    KAUST Repository

    Griffiths, I. M.

    2012-01-01

    Micellar surfactant solutions are characterized by a distribution of aggregates made up predominantly of premicellar aggregates (monomers, dimers, trimers, etc.) and a region of proper micelles close to the peak aggregation number, connected by an intermediate region containing a very low concentration of aggregates. Such a distribution gives rise to a distinct two-timescale reequilibration following a system dilution, known as the t1 and t2 processes, whose dynamics may be described by the Becker-Döring equations. We use a continuum version of these equations to develop a reduced asymptotic description that elucidates the behavior during each of these processes.© 2012 Society for Industrial and Applied Mathematics.

  5. Relationship between Spreading Rate and Wetting Behaviour of Oil on Surface of Surfactant Solution

    Institute of Scientific and Technical Information of China (English)

    YE Xi; CHENG Yang; HUANG Xue-Dong; MA Hong-Ru

    2007-01-01

    @@ We report a systematic investigation of the spreading of a polydimethylsiloxane oil layer on flat surfaces of solution containing anionic surfactant of sodium dodecylsulfate. The experiment reveals that different wetting behaviours of the oil follow different spreading rates. In the case of complete wetting, it obeys a 0. 75 power law, while in the pseudopartial wetting it follows a non-power law. The results can well be explained by a new simple theory of spreading. The theory further predicts that for a complete wetting state there exists another spreading rate.

  6. A rotating disk apparatus for assessing the biodegradation of polycyclic aromatic hydrocarbons transferring from a non-aqueous phase liquid to solutions of surfactant Brij 35

    OpenAIRE

    Bernardez, Letícia Alonso

    2009-01-01

    Texto completo: acesso restrito. p. 415-424 A rotating disk apparatus was used to investigate the biodegradation of PAHs from non-aqueous phase liquids to solutions of Brij 35. The mass transfer of PAHs in absence of surfactant solution was not large enough to replenish the degraded PAHs. The addition of surfactant resulted in an overall enhancement of biodegradation rates compared to that observed in pure aqueous solution. This is because surfactant partition significant amount of PAHs in...

  7. Biosynthesis of Monascus pigments by resting cell submerged culture in nonionic surfactant micelle aqueous solution.

    Science.gov (United States)

    Wang, Bo; Zhang, Xuehong; Wu, Zhenqiang; Wang, Zhilong

    2016-08-01

    Growing cell submerged culture is usually applied for fermentative production of intracellular orange Monascus pigments, in which accumulation of Monascus pigments is at least partially associated to cell growth. In the present work, extractive fermentation in a nonionic surfactant micelle aqueous solution was utilized as a strategy for releasing of intracellular Monascus pigments. Those mycelia with low content of intracellular Monascus pigments were utilized as biocatalyst in resting cell submerged culture. By this means, resting cell submerged culture for production of orange Monascus pigments was carried out successfully in the nonionic surfactant micelle aqueous solution, which exhibited some advantages comparing with the corresponding conventional growing cell submerged culture, such as non-sterilization operation, high cell density (24 g/l DCW) leading to high productivity (14 AU of orange Monascus pigments at 470 nm per day), and recycling of cells as biocatalyst leading to high product yield (approximately 1 AU of orange Monascus pigments at 470 nm per gram of glucose) based on energy metabolism.

  8. Enhanced aqueous solubility of polycyclic aromatic hydrocarbons by green diester-linked cationic gemini surfactants and their binary solutions

    Science.gov (United States)

    Panda, Manorama; Fatma, Nazish; Kabir-ud-Din

    2016-07-01

    Three homologues of a novel biodegradable diester-linked cationic gemini surfactant series, CmH2m+1 (CH3)2N+(CH2COOCH2)2N+(CH3)2CmH2m+1.2Cl- (m-E2-m; m = 12, 14, 16), were used for investigation of the solubilization of polycyclic aromatic hydrocarbons (PAHs) such as naphthalene, anthracene and pyrene in single as well as binary surfactant solutions. Physicochemical parameters of the pure/mixed systems were derived by conductivity and surface tension measurements. Dissolution capacity of the equimolar binary surfactant solutions towards the PAHs was studied from the molar solubilization ratio (MSR), micelle-water partition coefficient (Km) and free energy of solubilization (ΔGs0) of the solubilizates. Influence of hydrophobic chain length of the dimeric surfactants on solubilization was characterized. Aqueous solubility of the PAHs was enhanced linearly with concentration of the surfactant in all the pure and mixed gemini-gemini surfactant systems.

  9. Calculation of the molecular exchanging energy of binary surfactants system on the surface monolayer of aqueous solution

    Institute of Scientific and Technical Information of China (English)

    WANG ZhengWu; YI XiZhang

    2007-01-01

    By using the binary anionic/cationic surfactants system CH3(CH2)nOSO-3/CH3(CH2)nN+(CH3)3 as an example, the molecular exchanging energy (ε) of adsorption on the surface monolayer of aqueous solution has been studied. εcan be obtained with two methods. One is from the relationship between εand the molecule interaction parameter (β). This relationship is founded by considering that the adsorption of mixed surfactants on the surface monolayer of solution satisfies the dimensional crystal model condition under which β can be obtained by testing the surface tension of solution. The other is directly from the molecular structure of surfactants with the Lennard-Jones formula. The results for the studied system show that these two methods coincide well.

  10. Calculation of the molecular exchanging energy of binary surfactants system on the surface monolayer of aqueous solution

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    By using the binary anionic/cationic surfactants system CH3(CH2)nOSO3/CH3(CH2)nN+(CH3)3 as an ex-ample, the molecular exchanging energy (ε) of adsorption on the surface monolayer of aqueous solu-tion has been studied. ε can be obtained with two methods. One is from the relationship between ε and the molecule interaction parameter (β). This relationship is founded by considering that the adsorption of mixed surfactants on the surface monolayer of solution satisfies the dimensional crystal model condition under which β can be obtained by testing the surface tension of solution. The other is directly from the molecular structure of surfactants with the Lennard-Jones formula. The results for the studied system show that these two methods coincide well.

  11. EFFECT OF ANIONIC SURFACTANT UPON THE VISCOSITY OF POLYMER GUAR GUM SOLUTIONS

    Institute of Scientific and Technical Information of China (English)

    Xiao-ming Chen; Hai-yang Yang; Xian You; Ping-ping Zhu; Ping-sheng Hea

    2006-01-01

    The reduced viscosity of polymer guar gum solutions containing a certain concentration of sodium dodecyl benzene sulfonate (SDBS) was measured. It has been found that the Huggins coefficient kH of polymer solutions is verysensitive to the concentration of the surfactant, cSDBS, in solutions. If cSDBS is lower than CMC, the critical micelle concentration of SDBS, kH increases rapidly with cSDBS. On the other hand, if cSDBS is larger than CMC, kH decreases rapidly with cSDBS. Comparatively, the intrinsic viscosity of polymer solution does not show a notable change with cSDBS. The experimental results indicate that the interchain association of polymer guar gum in solution is greatly associated with SDBS interacted with polymer chains through hydrogen bonds. However, the effect of SDBS upon the intrachain association of polymer guar gum solution is negligible, presumably due to the fact that guar gum is a slightly stiffened random-coil chain polymer.

  12. Absorption of gaseous toluene in aqueous solutions of some kinds of fluorocarbon surfactant.

    Science.gov (United States)

    Xiao, Xiao; Yan, Bo; Fu, Jiamo; Xiao, Xianming

    2015-01-01

    A self-designed device was applied to treat a simulated exhaust gas loaded with toluene by aqueous solutions of five kinds of fluorocarbon surfactant (FS-3100, FS-22, FSN-100, FSO-100 and FSG) under the controlled laboratory conditions. The simulated exhaust gas is generated by a mixture of clean air and toluene vapor, and its toluene concentration can be controlled by changing the volume ratio of the inlet air to the vapor. Two mass transfer methods: liquid-liquid transfer and gas-liquid transfer, were compared for their toluene saturation capacities of these absorbent solutions, and it was found that more toluene was dissolved by the liquid-liquid transfer than by the gas-liquid transfer. According to the saturation capacities of these absorbent solutions and their Henry's Constants, FSO-100 is the best absorbent to treat the simulated exhaust gas and was selected for further experiments. The FSO-100 absorbent solution with a concentration of 0.1 % shows an efficient absorption to the simulated exhaust gas, with a toluene saturation capacity of 4.2 mg/g. Heating distillation (90- 95 oC) is highly efficient to recover toluene from the FSO-100 absorbent solution as well as regenerate it. A toluene recovery of about 85 % was achieved. The regenerated absorption solution can keep its initial toluene absorption capacity during the reuse.

  13. Interactions between Surfactants in Solution and Electrospun Protein Fibers: Effects on Release Behavior and Fiber Properties

    DEFF Research Database (Denmark)

    Boutrup Stephansen, Karen; García-Díaz, María; Jessen, Flemming

    2016-01-01

    ), a cationic surfactant (benzalkonium chloride), and a neutral surfactant (Triton X-100) were studied. The anionic surfactants increased the insulin release in a concentration-dependent manner, whereas the neutral surfactant had no significant effect on the release. Interestingly, only minute amounts...... of insulin were released from the fibers when benzalkonium chloride was present. The FSP-Ins fibers appeared dense after incubation with this cationic surfactant, whereas high fiber porosity was observed after incubation with anionic or neutral surfactants. Contact angle measurements and staining...

  14. Effect of inorganic positive ions on the adsorption of surfactant Triton X-100 at quartz/solution interface

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    The electrode-separated piezoelectric sensor (ESPS), an improved setup of quartz crystal microbalance (QCM), has been employed to investigate the adsorption behavior of nonionic surfactant Triton X-100 at the hydrophilic quartz-solution interface in mineralized water medium in situ, which contained CaCl2 0.01 mol·L?1, MgCl2 0.01 mol·L?1, NaCl 0.35 mol·L?1. In a large scale of surfactant concentration, the effects of Ca2+, Mg2+ and Na+ on the adsorption isotherm and kinetics are obviously different. In aque-ous solution containing NaCl only, adsorption of Triton X-100 on quartz-solution interface is promoted, both adsorption rate and adsorption amount increase. While in mineralized water medium, multivalent positive ions Ca2+ and Mg2+ are firmly adsorbed on quartz-solution interface, result in the increasing of adsorption rate and adsorption amount at low concentration of surfactant and the peculiar desorption of surfactant at high concentration of Triton X-100. The results got by solution depletion method are in good agreement with which obtained by ESPS. The "bridge" and "separate" effect of inorganic positive ions on the adsorption and desorption mechanism of Triton X-100 at the quartz- solution interface is discussed with molecular dynamics simulations (MD), flame atomic absorption spectrometry (FAAS) and atomic force microscopy (AFM) methods.

  15. Removal of cationic surfactant (CTAB from aqueous solution on to activated carbon obtained from corncob.

    Directory of Open Access Journals (Sweden)

    S. M. Yakout

    2009-05-01

    Full Text Available Direct and indirect releases of large quantities of surfactants to the environment may result in serious health and environmental problems. Therefore, surfactants should be removed from water before water is released to the environment or delivered for public use. Using powdered activated carbon (PAC as adsorbent may be an effective technique to remove surfactants. In this study, the removal of surfactants by PAC was investigated and the influencesof the operating parameters on the effectiveness on adsorption rate were studied. Cationic surfactant, Cetyl trimethyl ammonium bromide (CTAB was selected for the experiments. A series of batch experiments were performed to determine the sorption isotherms of surfactants to PAC. The results showed that carbon structure affect mainly on the surfactant adsorption. Surfactant equilibrium data fitted very well to the binary langmuir model. The pseudo first-,second- order and intraparticle diffusion kinetic models were applied. Both, the external mass transfer and intraparticle diffusion mechanisms involve in CTAB sorption.

  16. Equilibrium and dynamic interfacial properties of protein/ionic-liquid-type surfactant solutions at the decane/water interface.

    Science.gov (United States)

    Cao, Chong; Lei, Jinmei; Zhang, Lu; Du, Feng-Pei

    2014-11-25

    The interfacial behavior of β-casein and lysozyme solutions has been investigated in the presence of an ionic liquid-type imidazolium surfactant ([C16mim]Br) at the decane/water interface. The dynamic dilational properties of the protein/surfactant solutions are investigated by the oscillating drop method and interfacial tension relaxation method. The interfacial tension isotherms for the mixed adsorption layers indicate that the increased addition of [C16mim]Br to a pure protein changes the properties of the complex formed at the decane/water interface. Whereas the interfacial tension data of the protein/surfactant mixed layers do not clearly show differences with changing bulk composition, the dilational rheology provides undoubted evidence that the structure and, in particular, the dynamics of the adsorbed layers depend on the bulk surfactant concentration. The experiment data for β-casein/[C16mim]Br solutions indicate that at higher bulk [C16mim]Br concentrations, β-casein in the interfacial layer is subject to conformational changes, where it gives space to [C16mim]Br molecules in the form of coadsorb rather than replacement; in contrast, in lysozyme/[C16mim]Br solutions some lysozyme molecules desorb from the interface due to the competitive adsorption of free [C16mim]Br molecules. Experimental results related to the interfacial dilational properties of the protein/surfactant solutions show that the dilational modulus turns out to be more sensitive to the conformation of protein/surfactant mixture at the liquid interface than the interfacial tension.

  17. Impact of Micellar Surfactant on Supersaturation and Insight into Solubilization Mechanisms in Supersaturated Solutions of Atazanavir.

    Science.gov (United States)

    Indulkar, Anura S; Mo, Huaping; Gao, Yi; Raina, Shweta A; Zhang, Geoff G Z; Taylor, Lynne S

    2017-06-01

    The goals of this study were to determine: 1) the impact of surfactants on the "amorphous solubility"; 2) the thermodynamic supersaturation in the presence of surfactant micelles; 3) the mechanism of solute solubilization by surfactant micelles in supersaturated solutions. The crystalline and amorphous solubility of atazanavir was determined in the presence of varying concentrations of micellar sodium dodecyl sulfate (SDS). Flux measurements, using a side-by-side diffusion cell, were employed to determine the free and micellar-bound drug concentrations. The solubilization mechanism as a function of atazanavir concentration was probed using fluorescence spectroscopy. Pulsed gradient spin-echo proton nuclear magnetic resonance (PGSE-NMR) spectroscopy was used to determine the change in micelle size with a change in drug concentration. Changes in the micelle/water partition coefficient, K m/w , as a function of atazanavir concentration led to erroneous estimates of the supersaturation when using concentration ratios. In contrast, determining the free drug concentration using flux measurements enabled improved determination of the thermodynamic supersaturation in the presence of micelles. Fluorescence spectroscopic studies suggested that K m/w changed based on the location of atazanavir solubilization which in turn changed with concentration. Thus, at a concentration equivalent to the crystalline solubility, atazanavir is solubilized by adsorption at the micelle corona, whereas in highly supersaturated solutions it is also solubilized in the micellar core. This difference in solubilization mechanism can lead to a breakdown in the prediction of amorphous solubility in the presence of SDS as well as challenges with determining supersaturation. PGSE-NMR suggested that the size of the SDS micelle is not impacted at the crystalline solubility of the drug but increases when the drug concentration reaches the amorphous solubility, in agreement with the proposed changes in

  18. Determination of the free energy of adsorption on carbon blacks of a nonionic surfactant from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez-Garcia, C.M.; Gonzalez-Martin, M.L.; Gomez-Serrano, V.; Bruque, J.M.; Labajos-Broncano, L.

    2000-04-18

    The adsorption of a nonionic surfactant (Triton X-100) from aqueous solutions has been studied on six carbon blacks with very different specific surface areas. The surface area occupied per surfactant molecule on the carbon black surface and the free energy of adsorption have been evaluated from the adsorption isotherms. Also, the free energy of adsorption has been determined from the free energy of interaction between adsorbent and adsorbate through water. The results obtained from both methods are in good agreement. They indicate that adsorption progresses following two different processes: the first one deals with the direct interaction between carbon black surface and adsorbate molecules, and the second one mainly due to the interaction between surfactant molecules at the adsorbent-solution interphase.

  19. Selective labeling of pulmonary surfactant protein SP-C in organic solution

    DEFF Research Database (Denmark)

    Plasencia, I; Cruz, A; López-Lacomba, J L

    2001-01-01

    Pulmonary surfactant protein SP-C has been isolated from porcine lungs and treated with dansyl isothiocyanate in chloroform:methanol 2:1 (v/v) solutions,under conditions optimized to introduce a single dansyl group covalently attached to the N-terminalamine group of the protein without loss of its...... native thioesther-linked palmitic chains. The resulting derivative Dans-SP-C conserves the secondary structure of native SP-C as well as the ability to promote interfacial adsorption of DPPC suspensions and to affect the thermotropic behavior of DPPC bilayers. This derivative can be used to characterize...... lipid-protein and protein-protein interactions of a native-like SP-C in lipid/protein complexes. Udgivelsesdato: 2001-Sep-1...

  20. Metal ion coordination, conditional stability constants, and solution behavior of chelating surfactant metal complexes.

    Science.gov (United States)

    Svanedal, Ida; Boija, Susanne; Almesåker, Ann; Persson, Gerd; Andersson, Fredrik; Hedenström, Erik; Bylund, Dan; Norgren, Magnus; Edlund, Håkan

    2014-04-29

    Coordination complexes of some divalent metal ions with the DTPA (diethylenetriaminepentaacetic acid)-based chelating surfactant 2-dodecyldiethylenetriaminepentaacetic acid (4-C12-DTPA) have been examined in terms of chelation and solution behavior. The headgroup of 4-C12-DTPA contains eight donor atoms that can participate in the coordination of a metal ion. Conditional stability constants for five transition metal complexes with 4-C12-DTPA were determined by competition measurements between 4-C12-DTPA and DTPA, using electrospray ionization mass spectrometry (ESI-MS). Small differences in the relative strength between the coordination complexes of DTPA and 4-C12-DTPA indicated that the hydrocarbon tail only affected the chelating ability of the headgroup to a limited extent. The coordination of Cu(2+) ions was investigated in particular, using UV-visible spectroscopy. By constructing Job's plots, it was found that 4-C12-DTPA could coordinate up to two Cu(2+) ions. Surface tension measurements and NMR diffusometry showed that the coordination of metal ions affected the solution behavior of 4-C12-DTPA, but there were no specific trends between the studied divalent metal complexes. Generally, the effects of the metal ion coordination could be linked to the neutralization of the headgroup charge of 4-C12-DTPA, and the resulting reduced electrostatic repulsions between adjacent surfactants in micelles and monolayers. The pH vs concentration plots, on the other hand, showed a distinct difference between 4-C12-DTPA complexes of the alkaline earth metals and the transition metals. This was explained by the difference in coordination between the two groups of metal ions, as predicted by the hard and soft acid and base (HSAB) theory.

  1. Determination of Surface Tension of Surfactant Solutions through Capillary Rise Measurements: An Image-Processing Undergraduate Laboratory Experiment

    Science.gov (United States)

    Huck-Iriart, Cristia´n; De-Candia, Ariel; Rodriguez, Javier; Rinaldi, Carlos

    2016-01-01

    In this work, we described an image processing procedure for the measurement of surface tension of the air-liquid interface using isothermal capillary action. The experiment, designed for an undergraduate course, is based on the analysis of a series of solutions with diverse surfactant concentrations at different ionic strengths. The objective of…

  2. Sphere-to-Rod Transitions of Nonionic Surfactant Micelles in Aqueous Solution Modeled by Molecular Dynamics Simulations

    NARCIS (Netherlands)

    Velinova, Maria; Sengupta, Durba; Tadjer, Alia V.; Marrink, Siewert-Jan

    2011-01-01

    Control of the size and agglomeration of micellar systems is important for pharmaceutical applications such as drug delivery. Although shape-related transitions in surfactant solutions are studied experimentally, their molecular mechanisms are still not well understood. In this study, we use coarse-

  3. EFFECTS OF NH4CI ON THE INTERACTION BETWEEN POLY(ETHYLENE OXIDE)AND IONIC SURFACTANTS IN AQUEOUS SOLUTIONS

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    The interaction of poly(ethylene oxide)(PEO)with the ionic surfactants,sodium dodecylsulfate(SDS)and cetyltrimethylammonium chloride(CTAC)respectively,in aqueous solutions containing a certain concentration of NH4Cl,is studied by the viscosity measurement.It has been found that the ion-dipole interaction between PEO and ionic surfactants is changed considerably by the organic salt.For anionic surfactant of SDS,the addition of NH4Cl into solution strengthens the interaction between PEO and the headgroup of SDS.On the other hand,for cationic surfactant of CTAC,the interaction between PEO and the headgroup of CTAC is screened significantly by NH4Cl dissolved in solution.These findings may potentially be attributed to the negative property of the oxygen group of the PEO chain.In the presence of NH4Cl,the cationic ions of the organic salt bind to the oxygen group of the PEO chain so that PEO can be referred to as a pseudopolyelectrolyte in solution.

  4. Absorption of a volatile organic compound by a jet loop reactor with circulation of a surfactant solution: Performance evaluation

    Energy Technology Data Exchange (ETDEWEB)

    Park, Byungjoon; Hwang, Geelsu; Haam, Seungjoo; Lee, Changha [Department of Chemical Engineering, Yonsei University, Seoul 120-749 (Korea, Republic of); Ahn, Ik-Sung [Department of Chemical Engineering, Yonsei University, Seoul 120-749 (Korea, Republic of)], E-mail: iahn@yonsei.ac.kr; Lee, Kyoungjoo [Advanced Biotech Inc., Seoul (Korea, Republic of)

    2008-05-01

    Biofiltration shows high efficiency for the removal of industrial waste gases and reliable operational stability at low investment and operating cost, especially when the VOC concentration is low, such as 100 ppmv ({mu}L L{sup -1}) or less. However, it has been reported that the abrupt change in VOC concentrations leads to the failure of the biofilter. Hence, the pretreatment of waste gases is necessary to ensure the stable operation of the biofilter. The objective of this study is to develop a jet loop reactor (JLR) with circulation of a surfactant solution to lower the concentration of VOCs, especially hydrophobic VOCs. Toluene and Tween 81 were used as a model industrial waste gas and a surfactant, respectively. Among several non-ionic surfactants tested, Tween 81 showed the most rapid dissolution of toluene. When a JLR is replaced with fresh Tween 81 solution (0.3% w/v) every hour, it successfully absorbed for 48 h over 90% of the toluene in an inlet gas containing toluene at 1000 ppmv ({mu}L L{sup -1}) or less. Therefore, JLR with circulation of a surfactant solution is believed to ensure the stable operation of the biofilter even with the unexpected increase in the VOC concentrations.

  5. Hexadecyltrimethylammonium bromide micellization in glycine, diglycine, and triglycine aqueous solutions as a function of surfactant concentration and temperatures

    Science.gov (United States)

    Ali, Anwar; Malik, Nisar Ahmad; Uzair, Sahar; Ali, Maroof; Ahmad, Mohammad Faiz

    2014-06-01

    Micellization behavior of hexadecyltrimethylammonium bromide (HTAB) was investigated conductometrically in aqueous solutions containing 0.02 mol kg-1glycine (Gly), diglycine (Gly-Gly), and triglycine (Gly-Gly-Gly) as a function of surfactant concentration at different temperatures. The critical micelle concentration (CMC) of HTAB exhibits a decreasing trend as the number of carbon atoms increases from Gly to Gly-Gly-Gly, favoring the micelle formation. The values of CMC and the degree of counterion dissociation of the micelles were utilized to evaluate the standard free energy for transferring the surfactant hydrophobic chain out of the solvent to the interior of the micelle, Δ G {HP/○}, free energy associated with the surface contributions, Δ G {S/○}, standard free energy, Δ G {m/○}, enthalpy, Δ H {m/○}, and entropy, Δ S {m/○} of micellization were also calculated. The results show that the micellization of HTAB in aqueous solutions as well as in aqueous Gly/Gly-Gly/Gly-Gly-Gly solutions is primarily governed by the entropy gain due to the transfer of the hydrophobic groups of the surfactant from the solvent to the interior part of the micelle. The CMC obtained by fluorometric method is in close agreement with those obtained conductometrically. Furthermore, decrease in the I 1/ I 3 ratio of pyrene fluorescence intensity suggests the solubilization of the additives by the surfactant micelles and that this solubilization increases as the hydrophobicity increases from Gly to Gly-Gly-Gly.

  6. Study on Gold(Ⅰ) Solvent Extraction from Alkaline Cyanide Solution by TBP with Addition of Surfactant

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    The new solvent extraction system for gold(Ⅰ) from alkaline cyanide solution by TBP with addition of surfactant in aqueous phase was studied. The effect of various factors, such as equilibrium pH, constitution of organic phase, molar ratio of CPB∶Au(CN)2-, extraction time, aqueous/organic phase ratio, different initial gold concentration, equilibrium temperature, different diluent, different types of extractants and surfactants etc., was inspected. The results show that gold(Ⅰ) can be extracted quantitatively by controlling the quantity of surfactant (CPB); both the equilibrium pH and diluent hardly influence percent extraction. Gold(Ⅰ) percent extraction reaches more than 98% under the optimal experimental conditions. 30% vol TBP diluted by sulphonating kerosene can load gold(Ⅰ) to rather high levels. Loading capacity is in excess of 38 g/L. The extraction mechanism is discussed and the overall extraction reaction is deduced.

  7. Dynamics of falling droplet and elongational properties of dilute nonionic surfactant solutions with drag-reducing ability

    Science.gov (United States)

    Tamano, Shinji; Ohashi, Yota; Morinishi, Yohei

    2017-05-01

    The dynamics of the falling droplet through a nozzle for dilute nonionic surfactant (oleyl-dimethylamine oxide, ODMAO) aqueous solutions with viscoelastic and drag-reducing properties were investigated at different concentrations of ODMAO solutions Cs = 500, 1000, and 1500 ppm by weight. The effects of the flow rate and tube outer diameter on the length of the filament, which was the distance between the tube exit and the lower end of a droplet at the instant when the droplet almost detached from the tube, were clarified by flow visualization measurements by a high-speed video camera. Two types of breaking-off processes near the base of the droplet and within the filament were classified by the Ohnesorge number Oh and the Weber number We. In the regime of the higher Oh and We, the length of the filament became drastically larger at Cs = 1000 and 1500 ppm, whose high spinnability represented the strong viscoelasticity of ODMAO solutions. In the case where the filament was broken up near the lower end of the neck and thinning in time, the thinning of the diameter of the filament was measured by a light-emitting diode micrometer. As for the elasto-capillary thinning of dilute nonionic surfactant solutions, the initial necking process was similar to that of Newtonian fluids and then followed the exponential thinning like polymer solutions. The apparent elongational viscosity of the dilute nonionic surfactant solution was evaluated in the elasto-capillary thinning regime, in which the elongation rate was almost constant. At Cs = 1000 and 1500 ppm, the Trouton ratio, which was the ratio of the apparent elongational viscosity to the shear viscosity, was found to be several orders of magnitude larger than that of Newtonian fluids, while the shear viscosity measured by the capillary viscometer was almost the same order of the Newtonian fluids. The higher elongational property would be closely related to the higher drag-reducing ability of dilute nonionic surfactant

  8. The removal of phenol from aqueous solutions by adsorption using surfactant-modified bentonite and kaolinite

    Energy Technology Data Exchange (ETDEWEB)

    Alkaram, Uday F.; Mukhlis, Abduljabar A. [Department of Chemistry, College of Education, Ibn Al-Haitham, University of Baghdad, Baghdad (Iraq); Al-Dujaili, Ammar H., E-mail: ahdujaili@yahoo.com [Department of Chemistry, College of Education, Ibn Al-Haitham, University of Baghdad, Baghdad (Iraq)

    2009-09-30

    The natural bentonite (BC) and kaolinite (KC) were modified with two surfactant of hexadecyltrimethylammonium bromide (HDTMA) and phenyltrimethylammonium bromide (PTMA) to form four kinds of organic-modified clays, i.e., HDTMA-bentonite (BHM), HDTMA-kaolinite (KHM), PTMA-bentonite (KPM) and PTMA-kaolinite (KPM). The modified minerals were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD) and FT-IR spectroscopy. The surface areas were determined using methylene blue adsorption method. Cation-exchange capacity (CEC) was estimated using an ethylenediamine complex of copper method and the modifier loading was calculated from the total carbon analysis. The ability of raw and organo-modified clays to remove phenol from aqueous solutions has been carried out as a function of contact time, pH and temperatures using a batch technique. The removal of phenol from aqueous solutions by modified clays seems to be more effective than unmodified samples. The adsorption capacity was found to increase with increasing temperature indication that the adsorptions were endothermic. The adsorption of phenol onto these clays was found to be increased by increasing of pH value and the adsorption patterns data are correlated well by Langmuir and Freundlich isotherm models and that the adsorption is physical in nature. The experimental data fitted very well with the pseudo-second-order kinetic model. The thermodynamic study of adsorption process showed that the adsorption of phenol with these six adsorbents was carried out spontaneously, and the process was endothermic in nature.

  9. On the predictions and limitations of the Becker–Döring model for reaction kinetics in micellar surfactant solutions

    KAUST Repository

    Griffiths, I.M.

    2011-08-01

    We investigate the breakdown of a system of micellar aggregates in a surfactant solution following an order-one dilution. We derive a mathematical model based on the Becker-Döring system of equations, using realistic expressions for the reaction constants fit to results from Molecular Dynamics simulations. We exploit the largeness of typical aggregation numbers to derive a continuum model, substituting a large system of ordinary differential equations for a partial differential equation in two independent variables: time and aggregate size. Numerical solutions demonstrate that re-equilibration occurs in two distinct stages over well-separated timescales, in agreement with experiment and with previous theories. We conclude by exposing a limitation in the Becker-Döring theory for re-equilibration of surfactant solutions. © 2011 Elsevier Inc.

  10. Removal of para-nitrochlorobenzene from aqueous solution on surfactant-modified nanoscale zero-valent iron/graphene nanocomposites.

    Science.gov (United States)

    Wu, Yan; Luo, Hanjin; Wang, Hou

    2014-01-01

    This study demonstrated a remarkably simple and efficient method for the synthesis of nanoscale zero-valent iron (NZVI)/graphene (GN) nanocomposites. In order to prevent the agglomeration and restack of nanocomposites, chemical functionalization of nanocomposites with cetyltrimethylammonium bromide was proposed. The adsorption performance of surfactant-modified NZVI/GN nanocomposites was evaluated for the removal of para-nitrochlorobenzene (p-NCB) from aqueous solutions. The characteristics of nanocomposites were characterized by X-ray diffraction, BET surface area, Fourier transform infrared spectrum, thermogravimetric analysis and scanning electron microscopy. The effect factors including initial solution pH, contact time, reaction temperature, dosage, initial concentration of humic acid (HA) on the adsorption property of p-NCB onto surfactant-modified nanocomposites were investigated. The adsorption kinetics fitted well with pseudo-second-order model. The adsorption capacity of p-NCB on surfactant-modified nanocomposites inferred from the Langmuir model was 105.15 mg/g at 293 K. The thermodynamic parameters indicated that the adsorption of p-NCB onto surfactant-modified nanocomposites was an exothermic and spontaneous process. HA had a strong suppression effect on p-NCB uptake in the adsorption experiment.

  11. Classification of calorimetric titration plots for alkyltrimethylammonium and alkylpyridinium cationic surfactants in aqueous solutions

    NARCIS (Netherlands)

    Bijma, K; Engberts, J.B.F.N.; Blandamer, M.J; Cullis, P.M.; Last, P.M.; Irlam, K.D.; Soldi, L.G.

    1997-01-01

    Calorimetric titration plots for deaggregation of micelles formed by alkylpyridinium and alkyltrimethylammonium surfactants are classified into three types, A, B and C, depending on the shape of the plot of the enthalpy of dilution as a function of surfactant concentration. For Type A plots the reco

  12. Classification of calorimetric titration plots for alkyltrimethylammonium and alkylpyridinium cationic surfactants in aqueous solutions

    NARCIS (Netherlands)

    Bijma, K; Engberts, J.B.F.N.; Blandamer, M.J; Cullis, P.M.; Last, P.M.; Irlam, K.D.; Soldi, L.G.

    1997-01-01

    Calorimetric titration plots for deaggregation of micelles formed by alkylpyridinium and alkyltrimethylammonium surfactants are classified into three types, A, B and C, depending on the shape of the plot of the enthalpy of dilution as a function of surfactant concentration. For Type A plots the

  13. Effect of Non-Newtonian Viscosity for Surfactant Solutions on Vortex Characteristics in a Swirling Pipe Flow

    Institute of Scientific and Technical Information of China (English)

    Mizue MUNEKATA; Hidefumi TAKAKI; Hideki OHBA; Kazuyoshi MATSUZAKI

    2005-01-01

    Effects of non-Newtonian viscosity for surfactant solution on the vortex characteristics and drag-reducing rate in a swirling pipe flow are investigated by pressure drop measurements, velocity profile measurements and viscosity measurements. Non-Newtonian viscosity is represented by power-law model (τ = kD n). Surfactant solution used has shear-thinning viscosity with n < 1.0. The swirling flow in this study has decay of swirl and vortex-type change from Rankin's combined vortex to forced vortex. It is shown that the effect of shear-thinning viscosity on the decay of swirl intensity is different by vortex category and the critical swirl number with the vortex-type change depends on shear-thinning viscosity.

  14. Effectiveness of nanozeolite modified by cationic surfactant in the removal of disinfection by-product precursors from water solution

    Directory of Open Access Journals (Sweden)

    Amir Mohammadi

    2012-01-01

    Conclusions: This study showed that modification of nanozeolite by cationic surfactants, to reduce its negative surface charge, could markedly improve its efficiency in the adsorption of disinfection by-product precursors from an aqueous solution. The HDTMA-Br/Clinoptilolite nanozeolite (CNZ ratio of 0.07, pH have to coincide in iso-electric point, can be an optimum ratio for the modification.

  15. Removal of crystal violet dye from aqueous solution using triton X-114 surfactant via cloud point extraction

    Directory of Open Access Journals (Sweden)

    Arunagiri Appusamy

    2014-09-01

    Full Text Available In this work, the cloud point extraction (CPE was carried out for the removal of crystal violet dye from aqueous solution using triton X-114 surfactant. Density, refractive index and viscosity of pure components and two different phases of the mixture were measured, and the corresponding excess molar volume was calculated. Most of the dye molecules get solubilized in the coacervate phase, leaving a dye free dilute phase. This experiment was conducted for different sets of surfactant and solute concentration in order to find out the cloud point temperature and their influencing factors such as extraction efficiency, phase volume ratio, distribution coefficient and pre-concentration factor. Furthermore, the thermodynamic parameters like change in Gibbs-free energy (ΔG0, the change in enthalpy (ΔH0 and the change in entropy (ΔS0 were analyzed and found that cloud point extraction with surfactant was a more feasible process in the removal of dyes from aqueous solution.

  16. Thermodynamic properties of micellization of Sulfobetaine-type Zwitterionic Gemini Surfactants in aqueous solutions--a free energy perturbation study.

    Science.gov (United States)

    Liu, Guoyu; Gu, Daming; Liu, Haiyan; Ding, Wei; Luan, Huoxin; Lou, Yanmin

    2012-06-01

    In this article, the validity and accuracy of the free energy perturbation (FEP) model used in a previous article for ionic liquid-type Gemini imidazolium surfactants (ILGISs) is further evaluated by using it to model the Enthalpy-entropy compensation of Sulfobetaine-type Zwitterionic Gemini Surfactants (SZGSs), with different carbon atoms of the hydrophobic group or the spacer chain length, in aqueous solutions. In the FEP model, the Gibbs free energy contributions to the driving force for micelle formation are computed using hydration data obtained from molecular dynamics simulations. According to the pseudo-phase separation model, the thermodynamic properties of micellization in aqueous solutions for SZGS were discussed. The results show that the micellization of SZGS in aqueous solutions is a spontaneous and entropy-driven process. It is linearly Enthalpy-entropy compensated and different from the micelle formation of ILGIS but similar to anionic surfactants. The compensation temperature was found to be (302±3)K which was lower than ILGIS. As the temperature rises, the micellization is easy initially but then becomes difficult with the unusual changes of enthalpy values from positive to negative. The contribution of entropy change to the micellization tends to decrease but the contribution of enthalpy change tends to increase. In particular, as the number carbon atoms in the alkyl chains and spacer chains are increased, the thermodynamic favorability and stability of the micelles both increase.

  17. Solutions and Three-Dimensional Consistency for Nonautonomous Extended Lattice Boussinesq-Type Equations

    Science.gov (United States)

    Feng, Wei; Zhao, Song-lin

    2016-10-01

    In this paper, we investigate the nonautonomous extended lattice Boussinesq-type equations in terms of generalized Cauchy matrix approach. Several kinds of solutions more than multi-soliton solutions to these equations are derived by solving determining equation set. Three-dimensional consistency of these equations is also studied.

  18. SOLUBILIZATION OF DODECANE, TETRACHLOROETHYLENE, AND 1,2-DICHLOROBENZENE IN MICELLAR SOLUTIONS OF ETHOXYLATED NONIONIC SURFACTANTS

    Science.gov (United States)

    Although surfactants have received considerable attention as a potential means for enhancing the recovery of organic compounds from the subsurface, only limited information is available regarding the micellar solubilization of common groundwater contaminants by nonionic surfactan...

  19. Desorption of organo phosphorous pesticides from soil with wastewater and surfactant solution

    OpenAIRE

    Hernandez-Soriano, Maria del Carmen; Mingorance, Maria Dolores; Peña, Aranzazu

    2008-01-01

    Surfactants can be introduced in the environment by wastewater discharge, point-charge pollution or deliberate action, e.g. to remediate contaminated soil or groundwater. The irrigation of soil with wastewater containing surfactants may modify pesticide desorption from soil, thus affecting their environmental fate. Desorption from soil of the plain of Granada (South-eastern Spain) of two organophosphorous pesticides, diazinon and dimethoate, differing in solubility and hydrophobicity...

  20. Electrophoretic and spectroscopic characterization of the protein patterns formed in different surfactant solutions.

    Science.gov (United States)

    Blanco, Elena; Ruso, Juan M; Prieto, Gerardo; Sarmiento, Félix

    2008-01-01

    The complexations between catalase and the sodium perfluorooctanoate/sodium octanoate and sodium perfluorooctanoate/sodium dodecanoate systems have been studied by a combination of electrophoresis and spectroscopy measurements. The numbers of adsorption sites on the protein were determined from the observed increases of the zeta-potential as a function of surfactant concentration in the regions where the adsorption was a consequence of the hydrophobic effect. The Gibbs energies of adsorption of the surfactants onto the protein were evaluated and the results show that for all systems, Gibbs energies are negative and larger, in absolute values, at low values of surfactant concentration where binding to the high energy sites takes place, and become less negative as more surfactant molecules bind, suggesting a saturation process. The role of hydrophobic interactions in these systems has been demonstrated to be the predominant. Spectroscopy measurements suggest conformational changes on catalase depending on the surfactant mixture as well as the mixed ratio. No isosbestic point or shifts have been found showing that catalase has spectrophotometrically one kind of binding site for these surfactant mixtures.

  1. Enhanced Molecular Recognition between Nucleobases and Guanine-5'-monophosphate-disodium (GMP) by Surfactant Aggregates in Aqueous Solution.

    Science.gov (United States)

    Liu, Zhang; Wang, Dong; Cao, Meiwen; Han, Yuchun; Xu, Hai; Wang, Yilin

    2015-07-15

    Only specific base pairs on DNA can bind with each other through hydrogen bonds, which is called the Watson-Crick (W/C) pairing rule. However, without the constraint of DNA chains, the nucleobases in bulk aqueous solution usually do not follow the W/C pairing rule anymore because of the strong competitive effect of water and the multi-interaction edges of nucleobases. The present work applied surfactant aggregates noncovalently functionalized by nucleotide to enhance the recognition between nucleobases without DNA chains in aqueous solution, and it revealed the effects of their self-assembling ability and morphologies on the recognition. The cationic ammonium monomeric, dimeric, and trimeric surfactants DTAB, 12-3-12, and 12-3-12-3-12 were chosen. The surfactants with guanine-5'-monophosphate-disodium (GMP) form micelles, vesicles, and fingerprint-like and plate-like aggregates bearing the hydrogen-bonding sites of GMP, respectively. The binding parameters of these aggregates with adenine (A), uracil (U), guanine (G), and cytosine(C) indicate that the surfactants can promote W/C recognitions in aqueous solution when they form vesicles (GMP/DTAB) or plate-like aggregates (GMP/12-3-12) with proper molecular packing compactness, which not only provide hydrophobic environments but also shield non-W/C recognition edges. However, the GMP/12-3-12 micelles with loose molecular packing, the GMP/12-3-12 fingerprint-like aggregates where the hydrogen bond sites of GMP are occupied by itself, and the GMP/12-3-12-3-12 vesicles with too strong self-assembling ability cannot promote W/C recognition. This work provides insight into how to design self-assemblies with the performance of enhanced molecule recognition.

  2. Multisoliton Solutions for the Isospectral and Nonisospectral BKP Equation with Self-Consistent Sources

    Institute of Scientific and Technical Information of China (English)

    DENG Shu-Fang

    2008-01-01

    The isospectral and nonisospectral BKP equation with self-consistent sources is derived to study the linear problem of the BKP system. The bilinear form of the nonisospectral BKP equation with self-consistent sources is given and the N-soliton solutions are obtained with the Hirota method and Pfaffian technique, respectively.

  3. Spontaneous and forced imbibition of aqueous wettability altering surfactant solution into an initially oil-wet capillary.

    Science.gov (United States)

    Hammond, Paul S; Unsal, Evren

    2009-11-03

    Unforced invasion of wettability-altering aqueous surfactant solutions into an initially oil-filled oil-wet capillary tube has been observed to take place very slowly, and because this system is an analogue for certain methods of improved oil recovery from naturally fractured oil-wet reservoirs, it is important to identify the rate-controlling processes. We used a model for the process published by Tiberg et al. ( Tiberg , F. , Zhmud , B. , Hallstensson , K. and Von Bahr , M. Phys. Chem. Chem. Phys. 2000 , 2 , 5189 - 5196 ) and modified it for forced imbibitions. We show that when applied pressure differences are not too large invasion rates are controlled at large times by the value of the bulk diffusion coefficient for surfactant in the aqueous phase and at early times by the resistance to transfer of surfactant from the oil-water meniscus onto the walls of the capillary. For realistic values of the bulk diffusion coefficient, invasion rates are indeed slow, as observed. The model also predicts that the oil-water-solid contact angle during unforced displacement is close to pi/2, and so, the displacement occurs in a state of near-neutral wettability with the rate of invasion controlled by the rate of surfactant diffusion rather than a balance between capillary forces and viscous resistance. Under forced conditions, the meniscus moves faster, but the same kinds of dynamical balances between the various processes as were found in the spontaneous case operate. Once the capillary threshold pressure for entry into the initial oil-wet tube is exceeded, the effect of pressure on velocity becomes more significant, there is not sufficient time for the surfactant molecules to transfer in great quantity from the meniscus to the solid surface, and wettability alteration is then no longer important.

  4. Thermally cleavable surfactants

    Science.gov (United States)

    McElhanon, James R.; Simmons, Blake A.; Zifer, Thomas; Jamison, Gregory M.; Loy, Douglas A.; Rahimian, Kamyar; Long, Timothy M.; Wheeler, David R.; Staiger, Chad L.

    2006-04-04

    Two new surfactant molecules are reported which contain thermally labile Diels-Alder adducts connecting the polar and non-polar sections of each molecule. The two surfactants possess identical non-polar dodecyl tail segments but exhibit different polar headgroups. The surfactants become soluble in water when anionic salts are formed through the deprotonation of the surfactant headgroups by the addition of potassium hydroxide. When either surfactant is exposed to temperature above about 60.degree. C., the retro Diels-Alder reaction occurs, yielding hydrophilic and hydrophobic fragments and the aqueous solutions of the surfactants subsequently exhibit loss of all surface-active behavior.

  5. Thermally cleavable surfactants

    Energy Technology Data Exchange (ETDEWEB)

    McElhanon, James R. (Manteca, CA); Simmons, Blake A. (San Francisco, CA); Zifer, Thomas (Manteca, CA); Jamison, Gregory M. (Albuquerque, NM); Loy, Douglas A. (Albuquerque, NM); Rahimian, Kamyar (Albuquerque, NM); Long, Timothy M. (Urbana, IL); Wheeler, David R. (Albuquerque, NM); Staiger, Chad L. (Albuquerque, NM)

    2009-09-29

    Two new surfactant molecules are reported which contain thermally labile Diels-Alder adducts connecting the polar and non-polar sections of each molecule. The two surfactants possess identical non-polar dodecyl tail segments but exhibit different polar headgroups. The surfactants become soluble in water when anionic salts are formed through the deprotonation of the surfactant headgroups by the addition of potassium hydroxide. When either surfactant is exposed to temperature above about 60.degree. C., the retro Diels-Alder reaction occurs, yielding hydrophilic and hydrophobic fragments or the aqueous solutions of the surfactants subsequently exhibit loss of all surface-active behavior.

  6. Thermally cleavable surfactants

    Energy Technology Data Exchange (ETDEWEB)

    McElhanon, James R. (Manteca, CA); Simmons, Blake A. (San Francisco, CA); Zifer, Thomas (Manteca, CA); Jamison, Gregory M. (Albuquerque, NM); Loy, Douglas A. (Albuquerque, NM); Rahimian, Kamyar (Albuquerque, NM); Long, Timothy M. (Urbana, IL); Wheeler, David R. (Albuquerque, NM); Staiger, Chad L. (Albuquerque, NM)

    2009-11-24

    Two new surfactant molecules are reported which contain thermally labile Diels-Alder adducts connecting the polar and non-polar sections of each molecule. The two surfactants possess identical non-polar dodecyl tail segments but exhibit different polar headgroups. The surfactants become soluble in water when anionic salts are formed through the deprotonation of the surfactant headgroups by the addition of potassium hydroxide. When either surfactant is exposed to temperature above about 60.degree. C., the retro Diels-Alder reaction occurs, yielding hydrophilic and hydrophobic fragments or the aqueous solutions of the surfactants subsequently exhibit loss of all surface-active behavior.

  7. Thermodynamics on the micellization of CPC/TX-100 mixed surfactant system in aqueous solutions of KCI

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Yung Cheol [Health and Environmental Research Institute, Daegu (Korea, Republic of); Lee, Byung Hwan [Korea University of Technology and Education, Chonan (Korea, Republic of)

    2005-10-15

    The Critical Micelle Concentration (CMC) of the mixed surfactant system of CetylPyridinium Chloride (CPC) with Triton X-100 (TX-100) in aqueous solutions of KCI were determined by using the UV absorbance method from 15 .deg. C to 35 .deg. C. Thermodynamic parameters ({delta} G{sup o}{sub m}, {delta} H{sup o}{sub m}, and {delta} S{sup o}{sub m}), associated with the micelle formation of CPC/TX-100 mixed surfactant system, have been estimated from the temperature dependence of CMC values. The calculated values of {delta} G{sup o}{sub m} are all negative but the values of {delta} S{sup o}{sub m} are positive in the whole measured temperature region. On the other hand, the values of {delta} H{sup o}{sub m} are positive or negative, depending on the measured temperature.

  8. The effect of surfactants on the ozonation of o-cresol in aqueous solutions in a rotating packed contactor.

    Science.gov (United States)

    Ku, Young; Ji, Yan-Shiun; Chen, Hua-Wei; Chou, Yiang-Chen; Chang, Ching-Yuan

    2010-02-01

    Steady-state dissolved ozone concentrations were maintained relatively constant for experiments on ozone dissolution conducted in the presence of various amounts of sodium dodecyl sulphate (SDS) and Triton X-100 (TX-100), an anionic surfactant and a nonionic surfactant, respectively. Ozonation in a rotating packed contactor has been shown to be feasible for achieving nearly complete decomposition of o-cresol within about 10 minutes of reaction time for most experiments conducted. The temporal decomposition behaviour of o-cresol in aqueous solution by ozonation was described by a two-step pseudo-first-order reaction kinetics. Even though the presence of SDS and TX-100 slightly affected the decomposition rate constant of o-cresol by ozonation in the rotating packed contactor, the mineralization of total organic carbon was apparently reduced with the addition of SDS and TX-100.

  9. Temperature dependence of transport and equilibrium properties of alkylpyridinium surfactants in aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Bhat, Mohsin Ahmad; Dar, Aijaz Ahmed; Amin, Adil; Rashid, Peer Irfan [Department of Chemistry, University of Kashmir, Hazratbal Srinagar - 190006, J and K (India); Rather, Ghulam Mohammad [Department of Chemistry, University of Kashmir, Hazratbal Srinagar - 190006, J and K (India)], E-mail: gmrather2002@yahoo.com

    2007-11-15

    Conductivity measurements at varying concentrations and temperatures for two alkyl pyridinium surfactants-dodecylpyridinium chloride (DPC) and cetylpyridinium chloride (CPC) in aqueous medium have been performed. The resulting data in the lower concentration range were used for the determination of limiting transport parameters of the surfactant ions. Temperature dependence of limiting ion conductance {lambda}{sub +(surf.cation)}{sup 0} and limiting ion mobility u{sub +(surf.cation)}{sup 0} of surfactant ions were used for determination of standard partial molar enthalpy of activation for ion migration ({delta}H{sub {lambda}{sub +0}}) and the change in activation energy for translational mobility ({delta}E{sub trans}{sup 0}) of water molecules from surfactant ion hydration shell. The conductivity data at higher concentrations were used for determination of equilibrium micellar parameters, viz. critical micelle concentration (cmc), degree of counter ion dissociation ({alpha}), and aggregation number (n). Comparison of such parameters of the two surfactants at different temperatures was made in the light of molecular structure, ion-solvent, ion-ion, and solvent-solvent interactions.

  10. On relationships between surfactant type and globular proteins interactions in solution.

    Science.gov (United States)

    Blanco, Elena; Ruso, Juan M; Prieto, Gerardo; Sarmiento, Félix

    2007-12-01

    The binding of sodium perfluorooctanoate (C8FONa), sodium octanoate (C8HONa), lithium perfluorooctanoate (C8FOLi), and sodium dodecanoate (C12HONa) onto myoglobin, ovalbumin, and catalase in water has been characterized using electrophoretic mobility. The tendency of the protein-surfactant complexes to change their charge in the order catalase < ovalbumin < myoglobin was observed which was related to the contents of alpha-helices in the proteins. alpha-Helices are more hydrophobic than beta-sheets. The effect of surfactant on the zeta potentials follows C8HONa < C8FONa < C8FOLi < C12HONa for catalase and ovalbumin; and C8HONa < C8FOLi < C8FONa < C12HONa for myoglobin. The numbers of binding sites on the proteins were determined from the observed increases of the zeta-potential as a function of surfactant concentration in the regions where the binding was a consequence of the hydrophobic effect. The Gibbs energies of binding of the surfactants onto the proteins were evaluated. For all systems, Gibbs energies are negative and large at low concentrations (where binding to the high energy sites takes place) and become less negative at higher ones. This fact suggests a saturation process. Changes in Gibbs energies with the different proteins and surfactants under study have been found to follow same sequence than that found for the charge. The role of hydrophobic interactions in these systems has been demonstrated to be the predominant.

  11. All-proportional solid-solution Rh–Pd–Pt alloy nanoparticles by femtosecond laser irradiation of aqueous solution with surfactant

    Energy Technology Data Exchange (ETDEWEB)

    Sarker, Md. Samiul Islam, E-mail: samiul-phy@ru.ac.bd; Nakamura, Takahiro; Sato, Shunichi [Tohoku University, Institute of Multidisciplinary Research for Advanced Materials (Japan)

    2015-06-15

    Formation of Rh–Pd–Pt solid-solution alloy nanoparticles (NPs) by femtosecond laser irradiation of aqueous solution in the presence of polyvinylpyrrolidone (PVP) or citrate as a stabilizer was studied. It was found that the addition of surfactant (PVP or citrate) significantly contributed to reduce the mean size of the particles to 3 nm for PVP and 10 nm for citrate, which was much smaller than that of the particles fabricated without any surfactants (20 nm), and improved the dispersion state as well as the colloidal stability. The solid-solution formation of the Rh–Pd–Pt alloy NPs was confirmed by the XRD results that the diffraction pattern was a single peak, which was found between the positions corresponding to each pure Rh, Pd, and Pt NPs. Moreover, all the elements were homogeneously distributed in every particle by STEM-EDS elemental mapping, strongly indicating the formation of homogeneous solid-solution alloy. Although the Rh–Pd–Pt alloy NPs fabricated with PVP was found to be Pt rich by EDS observation, the composition of NPs fabricated with citrate almost exactly preserved the feeding ratio of ions in the mixed solution. To our best knowledge, these results demonstrated for the first time, the formation of all-proportional solid-solution Rh–Pd–Pt alloy NPs with well size control.

  12. Removal of Hg (II and Mn (II from aqueous solution using nanoporous carbon impregnated with surfactants

    Directory of Open Access Journals (Sweden)

    Mansoor Anbia

    2016-09-01

    Full Text Available Mesoporous carbons were impregnated with the anionic and cationic surfactants to increase adsorbing capacity for heavy metal ions. Prepared samples were characterized by X-ray diffraction (XRD and nitrogen adsorption–desorption isotherms. Batch adsorption studies were carried out to study the effect of various parameters like contact time, pH, metal ion concentration and agitation speed. The mercury removal by cationic surfactant cetyltrimethyl ammonium bromide (CTAB, anionic surfactant sodium dodecyl sulfate (SDS modified mesoporous carbon and unmodified mesoporous carbon were found to be 94%, 81.6% and 54.5%, respectively while the manganese removal for these adsorbents were found to be 82.2%, 70.5% and 56.8%, respectively. The sorption data were fit better with the Langmuir adsorption isotherm than Freundlich isotherm.

  13. Time consistent Pareto solutions in common access resource gameswith asymmetric players

    OpenAIRE

    De-Paz, Albert; Marín Solano, Jesús; Navas, Jorge

    2011-01-01

    In the analysis of equilibrium policies in a di erential game, if agents have different time preference rates, the cooperative (Pareto optimum) solution obtained by applying the Pontryagin's Maximum Principle becomes time inconsistent. In this work we derive a set of dynamic programming equations (in discrete and continuous time) whose solutions are time consistent equilibrium rules for N-player cooperative di erential games in which agents di er in their instantaneous utility functions and a...

  14. The fundamental solution for a consistent complex model of the shallow shell equations

    OpenAIRE

    Matthew P. Coleman

    1999-01-01

    The calculation of the Fourier transforms of the fundamental solution in shallow shell theory ostensibly was accomplished by J. L. Sanders [J. Appl. Mech. 37 (1970), 361-366]. However, as is shown in detail in this paper, the complex model used by Sanders is, in fact, inconsistent. This paper provides a consistent version of Sanders's complex model, along with the Fourier transforms of the fundamental solution for this corrected model. The inverse Fourier transforms are then calculated for th...

  15. Comparison between micro-emulsion and surfactant solution flooding efficiency for enhanced oil recovery in TinFouye Oil Field

    Energy Technology Data Exchange (ETDEWEB)

    Bouabboune, M.; Benhadid, S. [Applied and Theoretical Fluid Mechanical Laboratory, Algiers (Algeria). Faculty of Physics; Hammouch, N. [Sonatrach, Hydra, Algiers (Algeria). Forage Division

    2006-07-01

    The TinFouye (TFY) reservoir is among the largest oil reservoirs discovered in Algeria. The reservoir has been extensively gas lifted for many years, but gas lift is now reaching its economic limits. Therefore, a tertiary enhancement method is needed. This report investigated the technical feasibility of applying a microemulsion flood to TFY reservoir. The purpose of the study was to optimize the concentration of surfactant, in order to obtain a lower interfacial tension between oil and microemulsion phases, and a high viscosity of the microemulsion compared to that of the oil phase. Another objective was to test the effectiveness of the obtained optimum chemical system for the displacement of residual oil saturation after waterflooding (secondary recovery). TinFouye reservoir conditions and samples were used in this study. Geomechanical equipment was used for the displacement experiments in porous media. Two optimum microemulsion compositions were determined through phase behavior studies: 4 wt per cent anionic surfactant, 2.5 wt per cent pentanol, total salinity of 0.5 g/l. Two surfactant solutions were prepared with the same anionic and alcohol concentration as those of the optimized microemulsions. This made it possible to compare the efficiency of displacing residual oil saturation. 12 refs., 5 tabs., 4 figs.

  16. Adsorption at air-water and oil-water interfaces and self-assembly in aqueous solution of ethoxylated polysorbate nonionic surfactants.

    Science.gov (United States)

    Penfold, Jeffrey; Thomas, Robert K; Li, Peixun X; Petkov, Jordan T; Tucker, Ian; Webster, John R P; Terry, Ann E

    2015-03-17

    The Tween nonionic surfactants are ethoxylated sorbitan esters, which have 20 ethylene oxide groups attached to the sorbitan headgroup and a single alkyl chain, lauryl, palmityl, stearyl, or oleyl. They are an important class of surfactants that are extensively used in emulsion and foam stabilization and in applications associated with foods, cosmetics and pharmaceuticals. A range of ethoxylated polysorbate surfactants, with differing degrees of ethoxylation from 3 to 50 ethylene oxide groups, have been synthesized and characterized by neutron reflection, small-angle neutron scattering, and surface tension. In conjunction with different alkyl chain groups, this provides the opportunity to modify their surface properties, their self-assembly in solution, and their interaction with macromolecules, such as proteins. Adsorption at the air-water and oil-water interfaces and solution self-assembly of the range of ethoxylated polysorbate surfactants synthesized are presented and discussed.

  17. Self-consistent approximation to the solution of the Bethe-Salpeter equation

    Energy Technology Data Exchange (ETDEWEB)

    Crawford, G.A. (Department of Physics and Astronomy, University of Massachusetts, Amherst, MA (USA)); Thaler, R.M. (Department of Physics, Case Western Reserve University, Cleveland, OH (USA) Los Alamos National Laboratory, Mail Stop B243, Los Alamos, NM (USA))

    1990-07-01

    A technique for the approximate solution of the Bethe-Salpeter equation is examined. The technique requires the solution of a pair of coupled equations for the relative-momentum and relative-energy dependence of the relativistic {ital T} matrix. The solutions obey a self-consistency requirement as well as the usual elastic-unitarity constraint. It is also shown that the approximate {ital T} matrix is stable under a single iteration in the exact four-dimensional equation at certain kinematic points, including the fully on-shell point. A model problem with an exactly solvable separable interaction is examined and exact, approximate, as well as three-dimensional reduction results are compared. The phase shifts calculated in this self-consistent approximation scheme are found to be in excellent agreement with the exact phase shifts.

  18. Self-consistent approximation to the solution of the Bethe-Salpeter equation

    Science.gov (United States)

    Crawford, G. A.; Thaler, R. M.

    1990-07-01

    A technique for the approximate solution of the Bethe-Salpeter equation is examined. The technique requires the solution of a pair of coupled equations for the relative-momentum and relative-energy dependence of the relativistic T matrix. The solutions obey a self-consistency requirement as well as the usual elastic-unitarity constraint. It is also shown that the approximate T matrix is stable under a single iteration in the exact four-dimensional equation at certain kinematic points, including the fully on-shell point. A model problem with an exactly solvable separable interaction is examined and exact, approximate, as well as three-dimensional reduction results are compared. The phase shifts calculated in this self-consistent approximation scheme are found to be in excellent agreement with the exact phase shifts.

  19. Study of the interactions between lysozyme and a fully-fluorinated surfactant in aqueous solution at different surfactant-protein ratios.

    Science.gov (United States)

    Ruso, Juan M; González-Pérez, Alfredo; Prieto, Gerardo; Sarmiento, Félix

    2003-11-01

    The interactions of a fluorinated surfactant, sodium perfluorooctanoate, with lysozyme, have been investigated by a combination of UV absorbance, electrical conductivity and dynamic light scattering to detect and to characterize the conformational transitions of lysozyme. By using difference spectroscopy, the transition was followed as a function of surfactant concentration, and the data were analyzed to obtain the Gibbs energy of the transition in water (DeltaGw(o)) and in a hydrophobic environment (DeltaGh(o)) for saturated protein-surfactant complexes. Electrical conductivity was used to determine the critical micelle concentration of the surfactant in the presence of different lysozyme concentration. From these results, the average number of surfactant monomer per protein molecule was calculated. Finally, dynamic light scattering show that only changes in the secondary structure of the protein can be observed.

  20. Effect of Anionic Surfactant on the Thermo Acoustical Properties of Sodium Dodecyl Sulphate in Polyvinyl Alcohol Solution by Ultrasonic Method

    Directory of Open Access Journals (Sweden)

    S. Ravichandran

    2011-01-01

    Full Text Available The interaction of sodium dodecyl sulphate (SDS / poly(vinyl alcohol (PVA solution was studied by ultrasonic velocity measurements. Ultrasonic velocity, density, viscosity in mixtures of sodium dodecyl sulphate in polyvinyl alcohol was measured over the entire range of composition. From the experimental data, other related thermodynamic parameters, viz., adiabatic compressibility, intermolecular free length, surface tension, relative association, relaxation time, absorption coefficient and internal pressure were calculated. Formations of rods interfere with velocity of ultrasonic waves. Hence the ultrasonic velocity decreases with concentration. These results were interpreted in terms of polymer-surfactant complex reactions.

  1. Persistence of two neonicotinoid insecticides in wastewater, and in aqueous solutions of surfactants and dissolved organic matter.

    Science.gov (United States)

    Peña, A; Rodríguez-Liébana, J A; Mingorance, M D

    2011-07-01

    Wastewater treatment plants receive organic contaminants, such as pesticides, which reach the sewage system from domestic, industrial or agricultural activities. In wastewater, which is a complex mixture of organic and inorganic compounds, biotic or abiotic degradation of contaminants can be affected by the presence of co-solutes. The photodecomposition in natural sunlight of two neonicotinoid insecticides, thiamethoxam and thiacloprid, was investigated in wastewater, aqueous extracts of sewage sludge and in aqueous surfactant solutions, which are abundant in wastewater. Dissipation in the dark was also studied in wastewater, due to reduction of transmitted sunlight in wastewater ponds. With regard to photolysis, thiamethoxam degraded rapidly in all the aqueous solutions. Among them sewage sludge extracts slightly modified (average half-life 17.6h), wastewater increased (13.7h) and non-ionic surfactants led, as a family, to the highest dissipation rates (average 6.2h), with respect to control water (18.7h). Additionally this pesticide also underwent a slower biodegradation process in wastewater in the dark under anaerobic conditions (around 25d). A metabolite of thiamethoxam from the biological decomposition in wastewater was identified by HPLC/MS. On the other hand thiacloprid was found to be resistant to photo- and biodecomposition and remained almost unchanged during the experimental periods in all the tested media.

  2. Cloud point extraction of vanadium in pharmaceutical formulations, dialysate and parenteral solutions using 8-hydroxyquinoline and nonionic surfactant

    Energy Technology Data Exchange (ETDEWEB)

    Khan, Sumaira, E-mail: skhanzai@gmail.com [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan); Kazi, Tasneem G., E-mail: tgkazi@yahoo.com [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan); Baig, Jameel A., E-mail: jab_mughal@yahoo.com [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan); Young Welfare Society Mughalabad, Near Akri, Taluka Faiz Ganj, District Khairpur Sindh (Pakistan); Kolachi, Nida F., E-mail: nidafatima6@gmail.com [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan); Afridi, Hassan I., E-mail: hassanimranafridi@yahoo.com [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan); Wadhwa, Sham Kumar [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan); Shah, Abdul Q., E-mail: aqshah07@yahoo.com [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan); Kandhro, Ghulam A. [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan); Shah, Faheem, E-mail: shah_ceac@yahoo.com [Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan)

    2010-10-15

    A cloud point extraction (CPE) method has been developed for the determination of trace quantity of vanadium ions in pharmaceutical formulations (PF), dialysate (DS) and parenteral solutions (PS). The CPE of vanadium (V) using 8-hydroxyquinoline (oxine) as complexing reagent and mediated by nonionic surfactant (Triton X-114) was investigated. The parameters that affect the extraction efficiency of CPE, such as pH of sample solution, concentration of oxine and Triton X-114, equilibration temperature and time period for shaking were investigated in detail. The validity of CPE of V was checked by standard addition method in real samples. The extracted surfactant-rich phase was diluted with nitric acid in ethanol, prior to subjecting electrothermal atomic absorption spectrometry. Under these conditions, the preconcentration of 50 mL sample solutions, allowed raising an enrichment factor of 125-fold. The lower limit of detection obtained under the optimal conditions was 42 ng/L. The proposed method has been successfully applied to the determination of trace quantity of V in various pharmaceutical preparations with satisfactory results. The concentration ranges of V in PF, DS and PS samples were found in the range of 10.5-15.2, 0.65-1.32 and 1.76-6.93 {mu}g/L, respectively.

  3. Structure and performance of cationic assembly dispersed in amphoteric surfactants solution as a shampoo for hair damaged by coloring.

    Science.gov (United States)

    Nagahara, Yasuo; Nishida, Yuichi; Isoda, Masanori; Yamagata, Yoshifumi; Nishikawa, Naoki; Takada, Koji

    2007-01-01

    In recent years, hair coloring gains popularity as a trend of consumer's hair care. This coloring frequently damages hair. In response to this, a new shampoo-base was developed for repairing hair damaged by coloring. The new shampoo-base was prepared by dispersing cationic assembly in a solution of amphoteric surfactants. The mixture of behenyl trimethyl ammonium chloride (C22TAC) and behenyl alcohol (C22OH) was applied as the cationic assembly, which are dispersed in amido propyl betaine laurate (LPB) solution. LPB, which behaves as an amphoteric surfactant, was used as the wash-base. It was verified from the results on the measurements of DSC, calorimeter polarization, cryo-SEM and X-ray diffraction that the cationic assembly has a crystalline structure in the LPB solution. The new shampoo-base was highly efficient to change the color-damaged hair from hydrophilic to hydrophobic. The friction level of the hair washed with the new shampoo-base recovered to the same state as that of healthy hair. The exfoliation of cuticle was reduced after washing with the new shampoo-base.

  4. Winds driven by super-star clusters: The self-consistent radiative solution

    CERN Document Server

    Silich, S A; Rodríguez-Gónzalez, A; Silich, Sergiy; Tenorio-Tagle, Guillermo; Rodriguez-Gonzalez, Ary

    2004-01-01

    Here we present a self-consistent stationary solution for spherically symmetric winds driven by massive star clusters under the impact of radiative cooling. We demonstrate that cooling may modify drastically the distribution of temperature if the rate of injected energy approaches a critical value. We also prove that the stationary wind solution does not exist whenever the energy radiated away at the star cluster center exceeds ~ 30% of the energy deposition rate. Finally we thoroughly discuss the expected appearance of super-star cluster winds in the X-ray and visible line regimes. The three solutions here found: the quasi-adiabatic, the strongly radiative wind and the inhibited stationary solution, are then compared to the winds from Arches cluster, NGC 4303 central cluster and to the supernebula in NGC 5253.

  5. Corridor of existence of thermodynamically consistent solution of the Ornstein-Zernike equation.

    Science.gov (United States)

    Vorob'ev, V S; Martynov, G A

    2007-07-14

    We obtain the exact equation for a correction to the Ornstein-Zernike (OZ) equation based on the assumption of the uniqueness of thermodynamical functions. We show that this equation is reduced to a differential equation with one arbitrary parameter for the hard sphere model. The compressibility factor within narrow limits of this parameter variation can either coincide with one of the formulas obtained on the basis of analytical solutions of the OZ equation or assume all intermediate values lying in a corridor between these solutions. In particular, we find the value of this parameter when the thermodynamically consistent compressibility factor corresponds to the Carnahan-Stirling formula.

  6. The fundamental solution for a consistent complex model of the shallow shell equations

    Directory of Open Access Journals (Sweden)

    Matthew P. Coleman

    1999-09-01

    Full Text Available The calculation of the Fourier transforms of the fundamental solution in shallow shell theory ostensibly was accomplished by J. L. Sanders [J. Appl. Mech. 37 (1970, 361-366]. However, as is shown in detail in this paper, the complex model used by Sanders is, in fact, inconsistent. This paper provides a consistent version of Sanders's complex model, along with the Fourier transforms of the fundamental solution for this corrected model. The inverse Fourier transforms are then calculated for the particular cases of the shallow spherical and circular cylindrical shells, and the results of the latter are seen to be in agreement with results appearing elsewhere in the literature.

  7. Polymerizable gemini surfactants at solid/solution interfaces: adsorption and polymerization on melamine formaldehyde particles and capsule fabrication.

    Science.gov (United States)

    Sakai, Kenichi; Izumi, Keiko; Sakai, Hideki; Abe, Masahiko

    2010-03-15

    Organic capsules have been fabricated via three steps, by using the polymerizable gemini surfactant (1,2-bis(dimethyl(11-methacryloyloxy)undecylammonio) hexane dibromide, PC11-6-11) as a single wall component. In the first fabrication step, the surfactant spontaneously adsorbs on acid-dissolvable melamine formaldehyde (MF) particles in aqueous media. The adsorption isotherm data reveal that the adsorbed amount of PC11-6-11 (per chain) is greater than that of the corresponding monomeric surfactant ((11-methacryloyloxy)undecyltrimethylammonium bromide, PC11), resulting from the greater intermolecular association of PC11-6-11 at the solid/solution interface. The closely packed adsorbed layer of PC11-6-11 provides an opportunity to give a polymer thin film, as a result of in situ photo-polymerization on MF particles (in the second fabrication step) and subsequent acid dissolution of the core MF particles (in the third fabrication step). The dynamic light scattering (DLS) measurements have shown that the apparent hydrodynamic diameter of PC11-6-11 capsules is reversibly changed in response to a change in ionic strength: the increased background electrolyte concentration results in deswelling of the capsules, and vice versa. It seems likely that this swelling/deswelling behavior is primarily driven by the electrostatic interaction between quaternary ammonium groups within the polymerized film. We have also studied the capture and release capabilities of glucose into/from the capsule core and found that (i) glucose is encapsulated into the capsule core at high electrolyte concentrations and (ii) the glucose molecules encapsulated into the core are gradually released when the outer electrolyte solution is replaced by pure water. We believe, therefore, that the PC11-6-11 capsules fabricated here are useful as stimulus-responsive smart vehicles.

  8. Fluorescent Ensemble Based on Bispyrene Fluorophore and Surfactant Assemblies: Sensing and Discriminating Proteins in Aqueous Solution.

    Science.gov (United States)

    Fan, Junmei; Ding, Liping; Bo, Yu; Fang, Yu

    2015-10-14

    A particular bispyrene fluorophore (1) with two pyrene moieties covalently linked via a hydrophilic spacer was synthesized. Fluorescence measurements reveal that the fluorescence emission of 1 could be well modulated by a cationic surfactant, dodecyltrimethylammonium bromide (DTAB). Protein sensing studies illustrate that the selected ensemble based on 1/DTAB assemblies exhibits ratiometric responses to nonmetalloproteins and turn-off responses to metalloproteins, which can be used to differentiate the two types of proteins. Moreover, negatively charged nonmetalloproteins can be discriminated from the positively charged ones according to the difference in ratiometric responses. Fluorescence sensing studies with control bispyrenes indicate that the polarity of the spacer connecting two pyrene moieties plays an important role in locating bispyrene fluorophore in DTAB assemblies, which further influences its sensing behaviors to noncovalent interacting proteins. This study sheds light on the influence of the probe structure on the sensing performance of a fluorescent ensemble based on probe and surfactant assemblies.

  9. Tuning the crystal morphology and size of zeolitic imidazolate framework-8 in aqueous solution by surfactants

    KAUST Repository

    Pan, Yichang

    2011-01-01

    Herein we report a facile synthesis method using surfactant cetyltrimethylammonium bromide (CTAB) as a capping agent for controlling the crystal size and morphology of zeolitic imidazolate framework-8 (ZIF-8) crystals in aqueous systems. The particle sizes can be precisely adjusted from ca. 100 nm to 4 μm, and the morphology can be changed from truncated cubic to rhombic dodecahedron. This journal is © The Royal Society of Chemistry.

  10. Lanthanide-surfactant-combined catalysts for the allylation of benzaldehyde with tetraallyltin in aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Deleersnyder, Karen; Shi Danzhao; Binnemans, Koen [Katholieke Universiteit Leuven, Department of Chemistry, Laboratory of Coordination Chemistry, Celestijnenlaan 200F, B-3001 Leuven (Belgium); Parac-Vogt, Tatjana N. [Katholieke Universiteit Leuven, Department of Chemistry, Laboratory of Coordination Chemistry, Celestijnenlaan 200F, B-3001 Leuven (Belgium)], E-mail: Tatjana.Vogt@chem.kuleuven.be

    2008-02-28

    Metal-surfactant-combined catalysts having the general formula M(DOS){sub x} (DOS = dodecylsulfate), x = 1-3, can be used for the efficient allylation of benzaldehyde with tetraallyltin in water. Due to the formation of micelles the reaction proceeds in the absence of organic solvents. Examination of a series of lanthanide(III) and divalent transition-metal dodecylsulfates as catalysts for the reaction between benzaldehyde and tetraallyltin revealed that the highest yields can be obtained when lanthanide(III) and copper(II) salts are used. Within 6 h at room temperature nearly quantitative conversion of benzaldehyde to 1-phenyl-3-buten-1-ol was achieved in the presence of 10 mol% of Cu(DOS){sub 2} or Yb(DOS){sub 3}. The influence of the amount of catalyst and tetraallyltin on the reaction yield was investigated. Different alkylsulfates, alkylsulfonates and arylsulfonates metal salts were prepared and tested as catalysts in the allylation reaction. The highest yields were obtained with ytterbium(III) alkylsulfates and ytterbium(III) arylsulfonates, while ytterbium(III) alkylsulfonates were found to be poor allylation catalysts. The results show that both the nature of the metal cation as well as the length and the nature of anionic surfactant chain are crucial for the activity of the metal-surfactant-combined catalysts in water.

  11. TiO2-assisted degradation of a perfluorinated surfactant in aqueous solutions treated by gliding arc discharge.

    Science.gov (United States)

    Marouf-Khelifa, Kheira; Abdelmalek, Fatiha; Khelifa, Amine; Addou, Ahmed

    2008-02-01

    The plasma-chemical degradation of Forafac 1110, a perfluorinated non-ionic surfactant, in aqueous solutions was investigated using TiO2 catalysts. The considered plasma was the gliding arc in humid air, which results from an electric discharge at atmospheric pressure and quasi-ambient temperature. Two titanium dioxide powders were used and their synergistic effects on the Forafac degradation were compared. The results were discussed through the evolution of the pH, the conductivity, the fluoride ions concentration released in solutions, the surfactant concentration remaining after treatment and the chemical oxygen demand (COD) measurement. The combination of the plasma-chemical treatment with heterogeneous catalysis through the use of TiO2 accelerated the Forafac degradation, since only 60 min was sufficient to remove 96% instead of 360 min needed in the absence of TiO2. The use of anatase and rutile under the trade-name of Rhodia TiO2 and Merck TiO2, respectively, led to different results, because Rhodia TiO2 has proven to be more efficient. It would seem that the crystalline phase as well as the crystallite size, explain the efficiency of anatase. The advantage of the plasma-catalysis is due to the fact that there is a significant production of the OH* radicals not only generated by the gliding arc discharge but also by TiO2.

  12. On Exact Solutions and the Consistency of 3D Minimal Massive Gravity

    CERN Document Server

    Altas, Emel

    2015-01-01

    We show that all algebraic Type-O, Type-N and Type-D and some Kundt-Type solutions of Topologically Massive Gravity are inherited by its holographically well-defined deformation, that is the recently found Minimal Massive Gravity. This construction provides a large class of constant scalar curvature solutions to the theory. We also study the consistency of the field equations both in the source-free and matter-coupled cases. Since the field equations of MMG do not come from a Lagrangian that depends on the metric and its derivatives only, it lacks the Bianchi identity valid for all non-singular metrics. But it turns out that for the solutions of the equations, Bianchi identity is satisfied. This is a necessary condition for the consistency of the classical field equations but not a sufficient one, since the the rank-two tensor equations are susceptible to double-divergence. We show that for the source-free case the double-divergence of the field equations vanish for the solutions. In the matter-coupled case, ...

  13. The in-situ decontamination of sand and gravel aquifers by chemically enhanced solubilization of multiple-component DNAPLS with surfactant solutions. Topical report

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-01-01

    Laboratory, numerical simulation, and field studies have been conducted to assess the potential use of micellar-surfactant solutions to solubilize chlorinated solvents contaminating sand and gravel aquifers. Laboratory studies were conducted at the State University of New York at Buffalo (SUNY) while numerical simulation and field work were undertaken by INTERA Inc. in collaboration with Martin Marietta Energy Systems Inc. at the Paducah Gaseous Diffusion Plant (PGDP) in Kentucky. Ninety-nine surfactants were screened for their ability to solubilize trichloroethene (TCE), perchloroethylene (PCE), and carbon tetrachloride (CTET). Ten of these were capable of solubilizing TCE to concentrations greater than 15,000 mg/L, compared to its aqueous solubility of 1,100 mg/L. Four surfactants were identified as good solubilizers of all three chlorinated solvents. Of these, a secondary alcohol ethoxylate was the first choice for in situ testing because of its excellent solubilizing ability and its low propensity to sorb. However, this surfactant did not meet the Commonwealth of Kentucky`s acceptance criteria. Consequently, it was decided to use a surfactant approved for use by the Food and Drug Administration as a food-grade additive. As a 1% micellar-surfactant solution, this sorbitan monooleate has a solubilization capacity of 16,000 mg TCE/L, but has a higher propensity to sorb to clays than has the alcohol ethoxylate.

  14. Emulsion of aqueous-based nonspherical droplets in aqueous solutions by single-chain surfactants: templated assembly by nonamphiphilic lyotropic liquid crystals in water.

    Science.gov (United States)

    Varghese, Nisha; Shetye, Gauri S; Bandyopadhyay, Debjyoti; Gobalasingham, Nemal; Seo, JinAm; Wang, Jo-Han; Theiler, Barbara; Luk, Yan-Yeung

    2012-07-24

    Single-chain surfactants usually emulsify and stabilize oily substances into droplets in an aqueous solution. Here, we report a coassembly system, in which single types of anionic or non-ionic surfactants emulsify a class of water-soluble nonamphiphilic organic salts with fused aromatic rings in aqueous solutions. The nonamphiphilic organic salts are in turn promoted to form droplets of water-based liquid crystals (chromonic liquid crystals) encapsulated by single-chain surfactants. The droplets, stabilized against coalescence by encapsulated in a layer (or layers) of single chain surfactants, are of both nonspherical tactoid (elongated ellipsoid with pointy ends) and spherical shapes. The tactoids have an average long axis of ∼9 μm and a short axis of ∼3.5 μm with the liquid crystal aligning parallel to the droplet surface. The spherical droplets are 5-10 μm in diameter and have the liquid crystal aligning perpendicular to the droplet surface and a point defect in the center. Cationic and zwitterionic surfactants studied in this work did not promote the organic salt to form droplets. These results illustrate the complex interplay of self-association and thermodynamic incompatibility of molecules in water, which can cause new assembly behavior, including potential formation of vesicles or other assemblies, from surfactants that usually form only micelles. These unprecedented tactoidal shaped droplets also provide potential for the fabrication of new soft organic microcapsules.

  15. Small-angle neutron scattering study of aggregate structures of multi-headed pyridinium surfactants in aqueous solution

    Indian Academy of Sciences (India)

    J Haldar; V K Aswal; P S Goyal; S Bhattacharya

    2004-08-01

    The aggregate structures of a set of novel single-chain surfactants bearing one, two and three pyridinium headgroups have been studied using small-angle neutron scattering (SANS). It is found that the nature of aggregate structures of these cationic surfactants depend on the number of headgroups present in the surfactants. The single-headed pyridinium surfactant forms the lamellar structure, whereas surfactants with double and triple headgroups form micelles in water. The aggregates shrink in size with increase in the number of headgroups in the surfactants. The aggregation number () continually decreases and the fractional charge () increases with more number of headgroups on the surfactants. The semimajor axis () and semiminor axis ( = ) of the micelle also decrease with the increase in the number of headgroups in the surfactants. This indicates that hydrocarbon chains in such micelles prepared from multiheaded surfactants adopt bent conformation and no longer stay in extended conformation.

  16. Molecular Mechanisms of ZnO Nanoparticle Dispersion in Solution: Modeling of Surfactant Association, Electrostatic Shielding and Counter Ion Dynamics.

    Directory of Open Access Journals (Sweden)

    Patrick Duchstein

    Full Text Available Molecular models of 5 nm sized ZnO/Zn(OH2 core-shell nanoparticles in ethanolic solution were derived as scale-up models (based on an earlier model created from ion-by-ion aggregation and self-organization and subjected to mechanistic analyses of surface stabilization by block-copolymers. The latter comprise a poly-methacrylate chain accounting for strong surfactant association to the nanoparticle by hydrogen bonding and salt-bridges. While dangling poly-ethylene oxide chains provide only a limited degree of sterical hindering to nanoparticle agglomeration, the key mechanism of surface stabilization is electrostatic shielding arising from the acrylates and a halo of Na+ counter ions associated to the nanoparticle. Molecular dynamics simulations reveal different solvent shells and distance-dependent mobility of ions and solvent molecules. From this, we provide a molecular rationale of effective particle size, net charge and polarizability of the nanoparticles in solution.

  17. Heat transfer and pressure drop of surfactant solutions at crossflown finned helical tubes. Waermeuebergang und Druckverlust waessriger Tensidloesungen an einer querangestroemten berippten Rohrwendel

    Energy Technology Data Exchange (ETDEWEB)

    Weber, M. (Huels AG, Marl (Germany)); Kleuker, H.H.; Steiff, A.; Weinspach, P.M. (Dortmund Univ. (Germany). Lehrstuhl fuer Thermische Verfahrenstechnik)

    1992-09-01

    The addition of suitable drag reducers to water in district heating networks either reduces the pressure drop significantly or the electrical power consumption of the conveying pump can be reduced at the same flow rate. New surfactant additive systems accomplish the requirements on the thermal and mechanical capacitance of district heating systems. One of the important aspects for the application of surfactant solutions is the influence on the heat transfer in the installed heat exchangers in district heating networks. In earlier publications heat transfer and pressure drop of surfactant solutions in straight pipes and in helical tubes have been discussed. Developing from the scientific findings heat transfer and pressure drop at crossflown finned helical tubes were investigated in this work. The main purpose is the presentation of the occurred effects of drag reducing solutions. Due to the complex flow conditions a prediction could not be developed as yet. (orig.).

  18. Consistent and inconsistent truncations. General results and the issue of the correct uplifting of solutions

    CERN Document Server

    Pons, J M; Pons, Josep M.; Talavera, Pere

    2004-01-01

    We clarify the existence of two different types of truncations of the field content in a theory, the consistency of each type being achieved by different means. A proof is given of the conditions to have a consistent truncation in the case of dimensional reductions induced by independent Killing vectors. We explain in what sense the tracelessness condition found by Scherk and Scharwz is not only a necessary condition but also a {\\it sufficient} one for a consistent truncation. The reduction of the gauge group is fully performed showing the existence of a sector of rigid symmetries. We show that truncations originated by the introduction of constraints will in general be inconsistent, but this fact does not prevent the possibility of correct upliftings of solutions in some cases. The presence of constraints has dynamical consequences that turn out to play a fundamental role in the correctness of the uplifting procedure.

  19. Separation of Methylene Blue Dye from Aqueous Solution Using Triton X-114 Surfactant

    Directory of Open Access Journals (Sweden)

    Arunagiri Appusamy

    2014-01-01

    Full Text Available In this study, the interaction energy between Triton X-114 surfactant + methylene blue or water and methylene blue + water was investigated using Hartree-Fock (HF theory with 6-31G* basis set. The results of structures and interaction energies show that these complexes have good physical and chemical interactions at atom and molecular levels. However, the Triton X-114 surfactant + methylene blue complex shows stronger molecular interaction compared to other complexes systems. The order of the interaction energy is 4303.472023 (Triton X-114 surfactant + water > -1222.962 (methylene blue + water > -3573.28 (Triton X-114 surfactant + methylene blue kJ·mole−1. Subsequently, the cloud point extraction was carried out for 15 ppm of methylene blue in a mixture at 313.15 and 323.15 K over the surfactant concentration range from 0.01 M to 0.1 M. From the measured data, the excess molar volume was calculated for both phases. The results show a positive deviation in the dilute phase and a negative deviation in the surfactant rich phase. It is confirmed that the interaction between Triton X-114 and methylene blue is stronger than other complex systems due to the presence of chemical and structural orientation. The concentration of dyes and surfactant in the feed mixture and temperature effect in both phases has been studied. In addition, the thermodynamics feasibility and efficiency of the process have also been investigated.

  20. Correlation between wetting, adhesion and adsorption in the polymer-aqueous solutions of ternary surfactant mixtures-air systems

    Science.gov (United States)

    Szymczyk, Katarzyna; Zdziennicka, Anna; Krawczyk, Joanna; Jańczuk, Bronisław

    2014-01-01

    The correlation between the wettability of polymers and adsorption of ternary mixtures including CTAB, TX-100 and TX-114 at the polymer-aqueous solution interface as well as the adhesion of aqueous solution of these mixtures to apolar polytetrafluoroethylene (PTFE), monopolar polymethyl methacrylate (PMMA) and nylon 6 was considered on the basis of the contact angle measurements and the literature data of the solutions surface tension. From these considerations it appeared that the efficiency and effectiveness of the adsorption at the PTFE-water interface are comparable to those at the water-air one, but for the PMMA-water and nylon 6-water interfaces they are lower than those for the water-air one for a given series of solutions. The efficiency and effectiveness are reflected in the composition of the mixed monolayer at the polymer-solution interface which even for the PTFE-solution interface is somewhat different from the water-air interface. The properties of the mixed monolayer at these interfaces influence the critical surface tension of polymer wetting which for PTFE is somewhat higher but for PMMA and nylon 6 considerably lower than their surface tension. From these considerations it also appeared that the work of adhesion of aqueous solutions of ternary mixtures of surfactants to the PTFE surface does not depend on the composition and concentration of solution contrary to PMMA and nylon 6. The adhesion work of these solutions to the PMMA and nylon 6 surface can be determined on the basis of van Oss et al. and Neumann et al. equations.

  1. Study of monoprotic acid-base equilibria in aqueous micellar solutions of nonionic surfactants using spectrophotometry and chemometrics.

    Science.gov (United States)

    Babamoradi, Hamid; Abdollahi, Hamid

    2015-10-05

    Many studies have shown the distribution of solutes between aqueous phase and micellar pseudo-phase in aqueous micellar solutions. However, spectrophotometric studies of acid-base equilibria in these media do not confirm such distribution because of the collinearity between concentrations of chemical species in the two phases. The collinearity causes the number of detected species to be equal to the number of species in a homogenous solution that automatically misinterpreted as homogeneity of micellar solutions, therefore the collinearity is often neglected. This interpretation is in contradiction to the distribution theory in micellar media that must be avoided. Acid-base equilibrium of an indicator was studied in aqueous micellar solutions of a nonionic surfactant to address the collinearity using UV/Visible spectrophotometry. Simultaneous analysis (matrix augmentation) of the equilibrium and solvation data was applied to eliminate the collinearity from the equilibrium data. A model was then suggested for the equilibrium that was fitted to the augmented data to estimate distribution coefficients of the species between the two phases. Moreover, complete resolution of concentration and spectral profiles of species in each phase was achieved.

  2. Transient behavior of simultaneous flow of gas and surfactant solution in consolidated porous media

    Energy Technology Data Exchange (ETDEWEB)

    Baghdikian, S.Y.; Handy, L.L.

    1991-07-01

    The main objective of this experimental research was to investigate the mechanisms of foam generation and propagation in porous media. Results obtained give an insight into the conditions of foam generation and propagation in porous media. The rate of propagation of foam is determined by the rates of lamellae generation, destruction, and trapping. Several of the factors that contribute to foam generation have studied with Chevron Chaser SD1000 surfactant. Interfacial tension (IFT) measurements were performed using a spinning drop apparatus. The IFT of two surfactant samples of different concentrations were measured with dodecane and crude oil from the Huntington Beach Field as a function of temperature and time. Foam was used as an oil-displacing fluid. However, when displacing oil, foam was not any more effective than simultaneous brine and gas injection. A series of experiments was performed to study the conditions of foam generation in Berea sandstone cores. Results show that foam may be generated in sandstone at low flow velocities after extended incubation periods. The effect of pregenerating foam before injection into the sandstone was also studied. The pressure profiles in the core were monitored using three pressure taps along the length of the core. A systematic study of foaming with different fluid velocities and foam qualities provides extensive data for foam flow conditions. 134 refs., 57 figs., 2 tabs.

  3. Silver nanocombs and branched nanowires formation in aqueous binary surfactants solution

    Energy Technology Data Exchange (ETDEWEB)

    Umar, Akrajas Ali, E-mail: akrajas@ukm.my [Universiti Kebangsaan Malaysia, Institute of Microengineering and Nanoelectronics (Malaysia); Oyama, Munetaka [Kyoto University, Department of Materials Chemistry, Graduate School of Engineering (Japan); Salleh, Muhamad Mat; Majlis, Burhanuddin Yeop [Universiti Kebangsaan Malaysia, Institute of Microengineering and Nanoelectronics (Malaysia)

    2012-07-15

    Branched nanocrystals, particularly nanocombs, are a unique 1D-morphology that is normally formed in polytypic materials, such as ZnO, and rarely occurs in the highly symmetric fcc metallic system. Here, we report the chemical synthesis of nanocombs of a highly symmetrical fcc silver system that is realized by reducing the silver ions in the presence of a mixture of silver nanoseeds and binary surfactants, namely cetyltrimethylammonium bromide (CTAB) and hexamethylenetetramine (hexamine or HMT), under an alkaline condition. The silver nanocombs feature a high-degree branching orientation toward a single direction with good branch-to-branch spacing. The nanocombs formation was very sensitive to the concentrations of CTAB, HMT and NaOH in the reaction in which, in a typical case, nanocombs or curly nanowires were produced by controlling the concentration of these chemicals in the reaction. We hypothesized that the branching could be due to: (i) a kind of polytypism in such highly symmetrical fcc nanocrystals that was enabled by a selective surfactant adhesion process on the growing crystalline plane and (ii) lattice defects or twinning induced growth redirection in the nanocrystals. The silver nanocombs might generate a peculiar characteristic that is probably superior to those produced by other morphologies, such as nanorods, nanowires, and so on. Thus, it should find extensive use in the currently existing applications.

  4. Self-consistent-field analysis of poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) surfactants: micellar structure, critical micellization concentration, critical micellization temperature, and cloud point

    NARCIS (Netherlands)

    Bruijn, de V.G.; Broeke, van den L.J.P.; Leermakers, F.A.M.; Keurentjes, J.T.F.

    2002-01-01

    The self-assembly of a series of poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) surfactants into spherical micelles has been analyzed by a numerical self-consistent-field model. A united atom description is used in which three segment types are identified, that is,

  5. Self-consistent-field analysis of poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) surfactants: micellar structure, critical micellization concentration, critical micellization temperature, and cloud point

    NARCIS (Netherlands)

    Bruijn, de V.G.; Broeke, van den L.J.P.; Leermakers, F.A.M.; Keurentjes, J.T.F.

    2002-01-01

    The self-assembly of a series of poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) surfactants into spherical micelles has been analyzed by a numerical self-consistent-field model. A united atom description is used in which three segment types are identified, that is, CH2

  6. Removal of natural organic matter (NOM) from an aqueous solution by NaCl and surfactant-modified clinoptilolite.

    Science.gov (United States)

    Niri, Mehdi Vosoughi; Mahvi, Amir Hosein; Alimohammadi, Mahmoud; Shirmardi, Mohammad; Golastanifar, Hafez; Mohammadi, Mohamma Javad; Naeimabadi, Abolfazl; Khishdost, Maria

    2015-06-01

    Zeolitic tuffs are found in different parts of the world. Iranian zeolite is a low-cost material that can be frequently found in nature. Surfactant-modified zeolite (SMZ) can be used for the adsorption of natural organic matter (NOM) from aqueous solutions. The adsorption study was conducted to evaluate the adsorption capacity of SMZ; furthermore, the effects of contact time, initial pH, and the initial adsorbent dose on the adsorption process were investigated in a batch system. The kinetic studies showed that the adsorption of NOM on SMZ was a gradual process. The optimum initial pH values for the adsorption of NOM on SMZ were in the acidic ranges. The batch kinetic experiments showed that the adsorption followed the pseudo-second-order kinetic model with good correlation coefficients. The equilibrium data were well described by the Langmuir isotherm model. The results show that the natural zeolite being modified with NaCl and hexadecyltrimethylammonium bromide as a cationic surfactant was an appropriate adsorbent for the removal of NOM.

  7. The consistent Riccati expansion and new interaction solution for a Boussinesq-type coupled system

    Science.gov (United States)

    Ruan, Shao-Qing; Yu, Wei-Feng; Yu, Jun; Yu, Guo-Xiang

    2015-06-01

    Starting from the Davey-Stewartson equation, a Boussinesq-type coupled equation system is obtained by using a variable separation approach. For the Boussinesq-type coupled equation system, its consistent Riccati expansion (CRE) solvability is studied with the help of a Riccati equation. It is significant that the soliton-cnoidal wave interaction solution, expressed explicitly by Jacobi elliptic functions and the third type of incomplete elliptic integral, of the system is also given. Project supported by the National Natural Science Foundation of China (Grant No. 11275129).

  8. Linear Scaling Solution of the Time-Dependent Self-Consistent-Field Equations

    Directory of Open Access Journals (Sweden)

    Matt Challacombe

    2014-03-01

    Full Text Available A new approach to solving the Time-Dependent Self-Consistent-Field equations is developed based on the double quotient formulation of Tsiper 2001 (J. Phys. B. Dual channel, quasi-independent non-linear optimization of these quotients is found to yield convergence rates approaching those of the best case (single channel Tamm-Dancoff approximation. This formulation is variational with respect to matrix truncation, admitting linear scaling solution of the matrix-eigenvalue problem, which is demonstrated for bulk excitons in the polyphenylene vinylene oligomer and the (4,3 carbon nanotube segment.

  9. Application of Surfactant Micellar Solutions as Extractants and Mobile Phases for TLC-Determination of Purine Bases and Doping Agents in Biological Liquids

    Directory of Open Access Journals (Sweden)

    Daria Victorovna Yedamenko

    2015-04-01

    Full Text Available Separation of caffeine and its metabolites (theophylline and theobromine and doping agents (spironolactone, propranolol, and ephedrine and determination of caffeine in serum sample and propranolol and ephedrine in urine were studied on normal-phase thin layers (“Sorbfil-UV-254”. Aqueous organic solvents and aqueous micellar surfactant solutions were compared as the mobile phases for separation. The acceptable separation of purine bases and doping agents was achieved by micellar Thin Layer Chromatography and normal-phase Thin Layer Chromatography. Anionic surfactant solution with added 1-propanol was the best eluent as for caffeine, theophylline, and theobromine separation, as for doping agents. The best characteristics of caffeine extraction from serum, and propranolol and ephedrine from urine were achieved when micellar eluent based on non-ionic Tween-80 surfactant was used. DOI: http://dx.doi.org/10.17807/orbital.v7i1.632

  10. A Pseudo-Boolean Solution to the Maximum Quartet Consistency Problem

    CERN Document Server

    Morgado, Antonio

    2008-01-01

    Determining the evolutionary history of a given biological data is an important task in biological sciences. Given a set of quartet topologies over a set of taxa, the Maximum Quartet Consistency (MQC) problem consists of computing a global phylogeny that satisfies the maximum number of quartets. A number of solutions have been proposed for the MQC problem, including Dynamic Programming, Constraint Programming, and more recently Answer Set Programming (ASP). ASP is currently the most efficient approach for optimally solving the MQC problem. This paper proposes encoding the MQC problem with pseudo-Boolean (PB) constraints. The use of PB allows solving the MQC problem with efficient PB solvers, and also allows considering different modeling approaches for the MQC problem. Initial results are promising, and suggest that PB can be an effective alternative for solving the MQC problem.

  11. Surfactant-Amino Acid and Surfactant-Surfactant Interactions in Aqueous Medium: a Review.

    Science.gov (United States)

    Malik, Nisar Ahmad

    2015-08-01

    An overview of surfactant-amino acid interactions mainly in aqueous medium has been discussed. Main emphasis has been on the solution thermodynamics and solute-solvent interactions. Almost all available data on the topic has been presented in a lucid and simple way. Conventional surfactants have been discussed as amphiphiles forming micelles and amino acids as additives and their effect on the various physicochemical properties of these conventional surfactants. Surfactant-surfactant interactions in aqueous medium, various mixed surfactant models, are also highlighted to assess their interactions in aqueous medium. Finally, their applied part has been taken into consideration to interpret their possible uses.

  12. Consistent Algorithms Marching Along Characteristics for the Numerical Solution of the Boltzmann Equation

    Directory of Open Access Journals (Sweden)

    Nilson C. Roberty

    2011-01-01

    Full Text Available We introduce algorithms marching over a polygonal mesh with elements consistent with the propagation directions of the particle (radiation flux. The decision for adopting this kind of mesh to solve the one-speed Boltzmann transport equation is due to characteristics of the domain of the transport operator which controls derivatives only in the direction of propagation of the particles (radiation flux in the absorbing and scattering media. This a priori adaptivity has the advantages that it formulates a consistent scheme which makes appropriate the application of the Lax equivalence theorem framework to the problem. In this work, we present the main functional spaces involved in the formalism and a description of the algorithms for the mesh generation and the transport equation solution. Some numerical examples related to the solution of a transmission problem in a high-contrast model with absorption and scattering are presented. Also, a comparison with benchmarks problems for source and reactor criticality simulations shows the compatibility between calculations with the algorithms proposed here and theoretical results.

  13. Consistent robust a posteriori error majorants for approximate solutions of diffusion-reaction equations

    Science.gov (United States)

    Korneev, V. G.

    2016-11-01

    Efficiency of the error control of numerical solutions of partial differential equations entirely depends on the two factors: accuracy of an a posteriori error majorant and the computational cost of its evaluation for some test function/vector-function plus the cost of the latter. In the paper consistency of an a posteriori bound implies that it is the same in the order with the respective unimprovable a priori bound. Therefore, it is the basic characteristic related to the first factor. The paper is dedicated to the elliptic diffusion-reaction equations. We present a guaranteed robust a posteriori error majorant effective at any nonnegative constant reaction coefficient (r.c.). For a wide range of finite element solutions on a quasiuniform meshes the majorant is consistent. For big values of r.c. the majorant coincides with the majorant of Aubin (1972), which, as it is known, for relatively small r.c. (< ch -2 ) is inconsistent and looses its sense at r.c. approaching zero. Our majorant improves also some other majorants derived for the Poisson and reaction-diffusion equations.

  14. Adsorption of polynuclear aromatic hydrocarbons from aqueous solution: Agrowaste-modified kaolinite vs surfactant modified bentonite

    Directory of Open Access Journals (Sweden)

    E. I. Unuabonah

    2017-01-01

    Full Text Available The adsorption efficiency of a new hybrid clay adsorbent for polynuclear aromatic hydrocarbons (PAHs is compared with known modified clay adsorbents. The new hybrid clay adsorbent (HYCA showed far higher adsorption capacities for the adsorption of various PAH molecules compared with sodium dodecyl sulfate modified and humic acid modified Bentonite clay adsorbents. With the new hybrid clay adsorbent (HYCA, the adsorption of some of the larger PAH molecules was complete in the first 1 h as compared with ≈ 62% and ≈ 76% observed for both humic acid modified and sodium dodecyl sulfate modified Bentonite clay adsorbents respectively. In 24 h adsorption of the PAHs was complete for all adsorbents with HYCA adsorbent showing better efficiency in the removal of the PAH molecules from aqueous solutions. No significant change was observed with increase in time up to 48 h. The adsorption was observed to be more spontaneous with HYCA adsorbent than with either modified Bentonite adsorbents. The enthalpy of adsorption did not follow any specific order and were not consistent for all PAH molecules considered.

  15. Temperature sensitivity of wormlike micelles in poly(oxyethylene) surfactant solution: importance of hydrophilic-group size.

    Science.gov (United States)

    Ahmed, Toufiq; Aramaki, Kenji

    2009-08-01

    We have studied the temperature sensitivity of the rheology of the wormlike micellar solutions formed in poly(oxyethylene) cholesteryl ether (ChEO(m), m=15 and 30) upon addition of tri(ethyleneglycol) mono n-dodecyl ether (C(12)EO(3)) and monolaurin. We have found that increasing the poly(oxyethylene) chain length of ChEO(m) greatly reduces the temperature-sensitivity of the viscosity of the solution. In the viscous region small changes in the cosurfactant composition can subtly change the temperature sensitivity depending on the temperature range and type of cosurfactant. For, C(12)EO(3), which is a poly(oxyethylene) surfactant, the temperature sensitivity is lower at lower temperatures and higher at higher temperatures if the cosurfactant mixing fraction is high and vice versa if the mixing fraction is low. For monolaurin, the temperature sensitivity increases with cosurfactant mixing fraction in the viscous region. In the ChEO(30)-monolaurin system viscous solutions are not formed at any temperature that we studied. We have discussed these results in terms of the reduction of the average curvature of micellar interface with temperature due to dehydration of the poly(oxyethylene) chain and formation of branches in long micelles. We indicate the scientific and technical significance of our findings.

  16. Improved discharge capacity and suppressed surface passivation of zinc anode in dilute alkaline solution using surfactant additives

    Science.gov (United States)

    Yang, Hanxi; Cao, Yuliang; Ai, Xinping; Xiao, Lifen

    The capacity utilization of zinc anode is usually very low in dilute alkaline solution or at high rate discharge because of the passivation of zinc surface. This problem can be considerably overcome by use of surfactant additive in electrolyte. In this work, it is found that with addition of 2% sodium dodecyl benzene sulfonate (SDBS) in 20% KOH solution, the discharge capacity of zinc anode increases from 360 to 490 mAh/g at moderate discharge rate of 40 mA/g, corresponding to a 35% increase in the capacity utilization. Based on the electrochemical and morphological observation of the anodic passivation behaviors of zinc electrode, this effect is revealed that due to the SDBS adsorption, the passive layer formed on the zinc surface has a loose and porous structure rather than a dense and compact film. This type of surface layer facilitates the diffusive exchange of the solution reactant and discharged product through the surface deposit layer and therefore effectively suppresses the surface passivation of zinc anode.

  17. Effect of inorganic additives on solutions of nonionic surfactants V: Emulsion stability.

    Science.gov (United States)

    Schott, H; Royce, A E

    1983-12-01

    Electrolytes often break emulsions to which they were added as active ingredients, adjuvants, or impurities. The stability of oil-in-water emulsions containing octoxynol 9 NF as the emulsifier and various added electrolytes was investigated by measuring droplet size, turbidity, and oil separation on storage at various temperatures and in a centrifugal field at 25 degrees. Electrolytes were added to hexadecane emulsions after emulsification (direct addition); alternatively, hexadecane was emulsified in octoxynol 9-electrolyte mixtures (reverse addition). Xylene emulsions were prepared by direct addition only. Hexadecane emulsions containing 0.10% octoxynol 9 were considerably more stable than xylene emulsions containing 0.60% because the surfactant is practically insoluble in hexadecane, but miscible in all proportions with xylene. An emulsifier soluble in the disperse phase as well as the continuous phase evidently forms less stable interfacial films. The electrolytes investigated were sulfuric and hydrochloric acids, magnesium nitrate, and aluminum nitrate, which salt octoxynol 9 in by complexation between its ether groups and their cations; sodium thiocyanate, which salts the surfactant in by destructuring water; and sodium chloride and sodium sulfate, which salt octoxynol 9 out. The addition of these electrolytes at concentrations up to 2 or 3 m to hexadecane emulsions produced fast and extensive creaming, little or no flocculation, no coalescence, and only minor changes in droplet size or turbidity on storage at room temperature. The extent of coalescence during centrifugation was actually reduced by the additives. Such stability is unusual. Droplet size and turbidity depended mainly on octoxynol 9 concentration. The greatest decrease in the former and increase in the latter occurred when the concentration was increased from 0.10 to approximately 0.4%. All emulsions became slightly coarser on storage at 25 degrees. Stability at 50 degrees was impaired by

  18. Competitive adsorption from mixed hen egg-white lysozyme/surfactant solutions at the air-water interface studied by tensiometry, ellipsometry, and surface dilational rheology.

    Science.gov (United States)

    Alahverdjieva, V S; Grigoriev, D O; Fainerman, V B; Aksenenko, E V; Miller, R; Möhwald, H

    2008-02-21

    The competitive adsorption at the air-water interface from mixed adsorption layers of hen egg-white lysozyme with a non-ionic surfactant (C10DMPO) was studied and compared to the mixture with an ionic surfactant (SDS) using bubble and drop shape analysis tensiometry, ellipsometry, and surface dilational rheology. The set of equilibrium and kinetic data of the mixed solutions is described by a thermodynamic model developed recently. The theoretical description of the mixed system is based on the model parameters for the individual components.

  19. Thermodynamically Consistent Algorithms for the Solution of Phase-Field Models

    KAUST Repository

    Vignal, Philippe

    2016-02-11

    Phase-field models are emerging as a promising strategy to simulate interfacial phenomena. Rather than tracking interfaces explicitly as done in sharp interface descriptions, these models use a diffuse order parameter to monitor interfaces implicitly. This implicit description, as well as solid physical and mathematical footings, allow phase-field models to overcome problems found by predecessors. Nonetheless, the method has significant drawbacks. The phase-field framework relies on the solution of high-order, nonlinear partial differential equations. Solving these equations entails a considerable computational cost, so finding efficient strategies to handle them is important. Also, standard discretization strategies can many times lead to incorrect solutions. This happens because, for numerical solutions to phase-field equations to be valid, physical conditions such as mass conservation and free energy monotonicity need to be guaranteed. In this work, we focus on the development of thermodynamically consistent algorithms for time integration of phase-field models. The first part of this thesis focuses on an energy-stable numerical strategy developed for the phase-field crystal equation. This model was put forward to model microstructure evolution. The algorithm developed conserves, guarantees energy stability and is second order accurate in time. The second part of the thesis presents two numerical schemes that generalize literature regarding energy-stable methods for conserved and non-conserved phase-field models. The time discretization strategies can conserve mass if needed, are energy-stable, and second order accurate in time. We also develop an adaptive time-stepping strategy, which can be applied to any second-order accurate scheme. This time-adaptive strategy relies on a backward approximation to give an accurate error estimator. The spatial discretization, in both parts, relies on a mixed finite element formulation and isogeometric analysis. The codes are

  20. Synthesis and Solution Properties of Adamantane Containing Quaternary Ammonium Salt-type Cationic Surfactants: Hydrocarbon-based, Fluorocarbonbased and Bola-type.

    Science.gov (United States)

    Yoshimura, Tomokazu; Okada, Mari; Matsuoka, Keisuke

    2016-10-01

    Quaternary ammonium salt-type cationic surfactants with an adamantyl group (hydrocarbon-type; CnAdAB, fluorocarbon-type; Cm(F)C3AdAB, bola-type; Ad-s-Ad, where n, m and s represent hydrocarbon chain lengths of 8-16, fluorocarbon chain lengths of 4-8, and spacer chain length of 10-12) were synthesized via quaternization of N, N-dimethylaminoadamantane and n-alkyl bromide or 1, n-dibromoalkane. Conductivity and surface tension were measured to characterize the solution properties of the synthesized adamantyl group-containing cationic surfactants. In addition, the effects of hydrocarbon and fluorocarbon chain lengths and spacer chain length between headgroups on the measured properties were evaluated by comparison with those of conventional cationic surfactants. The critical micelle concentration (CMC) of CnAdAB and Ad-s-Ad was 2/5 of that for the corresponding conventional surfactants CnTAB and bola-type surfactants with similar number of carbons in the alkyl or alkylene chain; this was because of the increased hydrophobicity due to the adamantyl group. A linear relationship between the logarithm of CMC and the hydrocarbon chain length for CnAdAB was observed, as well as for CnTAB. The slope of the linear correlation for both surfactants was almost the same, indicating that the adamantyl group does not affect the CMC with variations in the hydrocarbon chain length. Similar to conventional surfactants CnTAB, the hydrocarbon-type CnAdAB is highly efficient in reducing the surface tension of water, despite the large occupied area per molecule resulting from the relatively bulky structure of the adamantane skeleton. On the other hand, the bola-type Ad-s-Ad resulted in increased surface tension compared to CnAdAB, indicating that the curved chain between adamantyl groups leads to poor adsorption and orientation at the air-water interface.

  1. Adsorption of N-decanoyl-N-methylglucamine at the Interface Electrode−NaClO4 Solution. Comparison of Adsorption Properties of Different Surfactants

    Directory of Open Access Journals (Sweden)

    Dorota Gugała-Fekner

    2016-06-01

    Full Text Available The electrosorption behaviour of non-ionic surfactant: N-decanoyl-N-methylglucamine on mercury electrode in 1 mol dm−3 NaClO4 solution was determined. The values of the relative surface excess were determined on the basis of double layer differential capacity. A set of parameters of maximal adsorption and the constants of Frumkin, modified Flory-Huggins and virial adsorption isotherms were obtained. It was stated that the adsorption of this surfactant is determined by the adsorption energy, however here is no simple relation between a surface excess and the values of repulsive interactions parameter A. Adsorption properties of three surfactants: cationic, anionic and non-ionic were compared. This work is licensed under a Creative Commons Attribution 4.0 International License.

  2. Excitation energy transfer in europium chelate with doxycycline in the presence of a second ligand in micellar solutions of nonionic surfactants

    Science.gov (United States)

    Smirnova, T. D.; Shtykov, S. N.; Kochubei, V. I.; Khryachkova, E. S.

    2011-01-01

    The complexation of Eu3+ with doxycycline (DC) antibiotic in the presence of several second ligands and surfactant micelles of different types is studied by the spectrophotometric and luminescence methods. It is found that the efficiency of excitation energy transfer in Eu3+-DC chelate depends on the nature of the second ligand and surfactant micelles. Using thenoyltrifluoroacetone (TTA) as an example, it is shown that the second ligand additionally sensitizes the europium fluorescence, and the possibility of intermediate sensitization of DC and then of europium is shown by the example of 1,10-phenanthroline. In all cases, the excitation energy transfer efficiency was increased due to the so-called antenna effect. The decay kinetics of the sensitized fluorescence of the binary and mixed-ligand chelates in aqueous and micellar solutions of nonionic surfactants is studied and the relative quantum yields and lifetimes of fluorescence are determined.

  3. Dendrimer-surfactant interactions.

    Science.gov (United States)

    Cheng, Yiyun; Zhao, Libo; Li, Tianfu

    2014-04-28

    In this article, we reviewed the interactions between dendrimers and surfactants with particular focus on the interaction mechanisms and physicochemical properties of the yielding dendrimer-surfactant aggregates. In order to provide insight into the behavior of dendrimers in biological systems, the interactions of dendrimers with bio-surfactants such as phospholipids in bulk solutions, in solid-supported bilayers and at the interface of phases or solid-states were discussed. Applications of the dendrimer-surfactant aggregates as templates to guide the synthesis of nanoparticles and in drug or gene delivery were also mentioned.

  4. Interaction of 4-aminosalieylic Acid and Surfactants in Aqueous Solutions Using UV-Vis Spectra and Steady-state Fluorescence Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    XU Dongying; REN Jiaoyan; LIAO Zhengfu; WANG Hui; ZHAO Mouming; LI Guangji

    2011-01-01

    The interactions of 4-aminosalicylic acid (4-ASA) and surfactants in aqueous solutions were investigated by using UV-Vis spectra and steady-state fluorescence spectroscopy.The results showed that the strongest peak at UV-vis spectra of 4-ASA aqueous solution in the presence of cationic surfactant and cetyltrimethyl ammonium bromide (CTAB) appeared at 206 nm and took.a red shift from 206 nm to 221 nm with the increase of 4-ASA concentrations from 0.8× 10-5 to 4.4× 10-4 mol/L.Similarly,the strongest peak at UV-vis spectra of 4-ASA aqueous solution in the presence of nonionic surfactant and polyvinylpyrrolidone (PVP)appeared at 206 nm and took a red shift from 206 nm to 219 nm with the increase of 4-ASA concentrations from 0.8× 10-5 to 4.4x 10-4 mol/L.However,the similar phenomena did not appeared in the presence of anion surfactant,sodium dodecyl sulfate (SDS),the UV-vis spectra of 4-ASA aqueous solution remained the same peak position and the peak value increased with the 4-ASA concentration increase.The results could be attributed to the electrostatic attraction between 4-ASA and CTAB or PVP,as well as the electrostatic repulsion between 4-ASA and SDS.Furthermore,the value of critical micelle concentration (CMC) of surfactants in the presence of 4-ASA was determined with Fluorescence method.The first and second CMC of CTAB was 1.2×10-4 M and 2.4x10-4 M,respectively.The first and second CMC of PVP was 1.2×10 4 M and 2.8x 10 4 M.SDS realized the multiple micellizations to form multiple CMC.

  5. Fabrication of novel microstructures based on orientation-dependent adsorption of surfactant molecules in a TMAH solution

    Science.gov (United States)

    Pal, Prem; Sato, K.; Gosalvez, M. A.; Tang, B.; Hida, H.; Shikida, M.

    2011-01-01

    In this work, the orientation-dependent adsorption of surfactant molecules on the silicon surface during etching in surfactant-added tetramethylammonium hydroxide (TMAH) is investigated. Triton X-100 (C14H22O(C2H4O)n, n = 9-10) and 25 wt% TMAH are used as surfactant and main etchant, respectively. The crystallographic planes affected by the surfactant molecules are determined by analyzing the etching behavior of different mask patterns on Si{1 0 0} wafers and silicon hemispheres in pure and surfactant-added TMAH. Taken together, the shapes of the etched profiles and the analysis of the hemispherical etch rates confirm that thick and dense adsorbed surfactant layers are typically formed on both the exact and vicinal Si{1 1 0} surfaces. In addition, the results indicate that the adsorbed surfactant layer behaves as a permeable mask, partially slowing down the etch rate of the affected surface orientation/s and thus enforcing their appearance on the etching front. The peculiar etching properties of surfactant-added and surfactant-free TMAH are then utilized for the fabrication of advanced micromechanical structures with new shapes on Si{1 0 0} wafers and polydimethylsiloxane based on complex Si{1 0 0} molds.

  6. Properties of aqueous solutions of nonionic surfactants, Triton X-114 and Tween 80, at temperatures from 293 to 318 K: Spectroscopic and ultrasonic studies

    Science.gov (United States)

    Szymczyk, Katarzyna; Taraba, Anna

    2017-02-01

    The speed of sound, density and refractive index of aqueous solutions of the nonionic surfactants, p-(1,1,3,3-tetramethylbutyl) phenoxypoly(ethyleneglycol) Triton X-114 (TX114) and polysorbate 80, Tween 80, have been measured over the entire range of concentration at 293, 298, 303, 308, 313 and 318 K under atmospheric pressure. Steady state fluorescence measurements have been also made using pyrene as a probe. From the experimental data the quantities such as critical micelle concentration (CMC), apparent dielectric constant, hydration number, isentropic compressibility, apparent specific adiabatic compressibility of a solute, intermolecular free length, acoustic impedance and molar sound number were determined. The variation of these parameters with concentration and temperature was discussed in terms of intermolecular interactions in the solution of a given surfactant.

  7. Adsorption properties of the nanozirconia/anionic polyacrylamide system-Effects of surfactant presence, solution pH and polymer carboxyl groups content

    Science.gov (United States)

    Wiśniewska, Małgorzata; Chibowski, Stanisław; Urban, Teresa

    2016-05-01

    The adsorption mechanism of anionic polyacrylamide (PAM) on the nanozirconia surface was examined. The effects of solution pH, carboxyl groups content in macromolecules and anionic surfactant (sodium dodecyl sulfate-SDS) addition were determined. The more probable structure of polymer adsorption layer was characterized based on the data obtained from spectrophotometry, viscosimetry and potentiometric titration methods. The adsorbed amount of polymer, size of macromolecules in the solution and surface charge density of ZrO2 particles in the absence and presence of PAM were assessed, respectively. Analysis of these results indicated that the increase of solution pH and content of carboxyl groups in the polymeric chains lead to more expanded conformations of adsorbing macromolecules. As a result, the adsorption of anionic polyacrylamide decreased. The SDS presence caused the significant increase of PAM adsorbed amount at pH 3, whereas at pH 6 and 9 the surfactant addition resulted in reduction of polymer adsorption level.

  8. Adsorption of proteins at the solution/air interface influenced by added nonionic surfactants at very low concentrations for both components. 3. Dilational surface rheology.

    Science.gov (United States)

    Fainerman, V B; Aksenenko, E V; Lylyk, S V; Lotfi, M; Miller, R

    2015-03-05

    The influence of the addition of the nonionic surfactants C12DMPO, C14DMPO, C10OH, and C10EO5 at concentrations between 10(-5) and 10(-1) mmol/L to solutions of β-casein (BCS) and β-lactoglobulin (BLG) at a fixed concentration of 10(-5) mmol/L on the dilational surface rheology is studied. A maximum in the viscoelasticity modulus |E| occurs at very low surfactant concentrations (10(-4) to 10(-3) mmol/L) for mixtures of BCS with C12DMPO and C14DMPO and for mixtures of BLG with C10EO5, while for mixture of BCS with C10EO5 the value of |E| only slightly increased. The |E| values calculated with a recently developed model, which assumes changes in the interfacial molar area of the protein molecules due to the interaction with the surfactants, are in satisfactory agreement with experimental data. A linear dependence exists between the ratio of the maximum modulus for the mixture to the modulus of the single protein solution and the coefficient reflecting the influence of the surfactants on the adsorption activity of the protein.

  9. Novel Pyridinium Surfactants with Unsaturated Alkyl Chains : Aggregation Behavior and Interactions with Methyl Orange in Aqueous Solution

    NARCIS (Netherlands)

    Kuiper, Johanna M.; Buwalda, Rixt T.; Hulst, Ron; Engberts, Jan B.F.N.

    2001-01-01

    This paper presents the synthesis and a study of the aggregation behavior of 4-undecyl-1-methyl- and 4-undecenyl-1-methylpyridinium iodide surfactants. The effect of the position of the double bond in the alkyl chain of the surfactant on the critical micelle concentration (cmc), degree of counterion

  10. Studies on an ester-modified cationic amphiphile in aqueous systems: behavior of binary solutions and ternary mixtures with conventional surfactants.

    Science.gov (United States)

    Lundberg, Dan; Unga, Johan; Galloway, Ashley L; Menger, Fredric M

    2007-11-06

    The aqueous behavior of an ester-modified cationic amphiphile with the molecular structure CH3CH2O(C=O)(CH2)6(C=O)O(CH2)8N+(CH3)3Br-, in the following referred to as A, has been investigated. Systems with A as the only solute, as well as different aqueous mixtures with conventional cationic surfactants, primarily dodecyltrimethylammonium bromide (DTAB), were included in the study. Isotropic solution samples were characterized using 1H NMR, 13C NMR, NMR diffusometry, and conductivity measurements, whereas liquid crystalline samples were investigated by optical polarization microscopy and small-angle X-ray diffraction. The results are compared to the behavior of the binary system of DTAB and water. A does not exhibit a typical surfactant behavior. When it is present as the only solute in a binary aqueous system, it forms neither conventional micelles nor liquid crystalline phases. However, there is clear evidence that it assembles with lower cooperativity into loose clusters at concentrations above 25-30 mM. When A is mixed with DTAB in solution, the two amphiphiles form mixed assemblies, the structure of which varies with the total amphiphile concentration. In concentrated mixtures with alkyltrimethylammonium surfactants, A can participate in hexagonal liquid crystalline phases even when it constitutes a significant fraction of the total amphiphile content.

  11. Effects of the Biomolecules: Vitamins, Proteins, Amino Acids, and Surfactants: DTAB, MTOAC, TMSOI, Orcinol on Upper Critical Solution Temperatures

    Directory of Open Access Journals (Sweden)

    Vinod Kumar

    2007-09-01

    Full Text Available Upper critical solution temperatures (UCSTS ± 0.05 K and mutual solubilities of phenol + water systems are reported separately with 0.5 millimol kg-1 (mm kg-1 proteins (casein, pepsin, egg-albumin, vitamins (B1-thiamine, B2-riboflavin, B6-pyridoxine, amino acids (glycine, β-alanine, L-leucine and surfactants (dodecyl trimethylammonium bromide- DTAB, trimethylsulphoxonium iodide-TMSOI, methyltrioctylammonium chloride- MTOAC, orcinol. The additives decrease the UCSTs by about 0.50-2 0C with slight enhancement in mutual solubilities but the leucine with two –CH3 (methyl and two - CH2- (methylene groups produce negligible increase in the solubilities. The –CH3 and - CH2- groups develop stronger hydrophobic interactions but the glycine develops stronger hydrophilic interactions due to –N+H3 (amino and –COO- (carboxylic groups and weaker hydrophobic due to single –CH2- group. The leucine increases the solubility by 0.009 mole fractions with a 0.7 0C decrease in USCT as compared to phenol-water. The mole fractions of additives restricted to 0.002 to 0.005 range, the conjugations of casein and vitamins in place of –CH3 groups of amino acids enhance the solubility with lower UCST values.

  12. Photochemical degradation of an anionic surfactant by TiO2 nanoparticle doped with C, N in aqueous solution

    Science.gov (United States)

    Zamiri, M.; Giahi, M.

    2016-12-01

    Novel C,N-doped TiO2 nanoparticles were prepared by a solid phase reaction. The catalyst was characterized by X-ray powder diffraction (XRD), transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDX). The results showed that crystallite size of synthesized C,N-doped TiO2 particles were in nanoscale. UV light photocatalytic studies were carried out using sodium naphthalenesulfonate formaldehyde condensate (SNF) as a model pollutant. The effects of initial concentration of surfactant, catalyst amount, pH, addition of oxidant on the reaction rate were ascertained and optimum conditions for maximum degradation was determined. The results indicated that for a solution of 20 mg/L of SNF, almost 98.7% of the substance were removed at pH 4.0 and 0.44 g/L photocatalyst load, with addition of 1 mM K2S2O8 and irradiation time of 90 min. The kinetics of the process was studied, and the photodegradation rate of SNF was found to obey pseudo-first-order kinetics equation represented by the Langmuir-Hinshelwood model.

  13. Factors affecting size and swelling of poly(ethylene glycol) microspheres formed in aqueous sodium sulfate solutions without surfactants.

    Science.gov (United States)

    Nichols, Michael D; Scott, Evan A; Elbert, Donald L

    2009-10-01

    The LCST behavior of poly(ethylene glycol) (PEG) in aqueous sodium sulfate solutions was exploited to fabricate microspheres without the use of other monomers, polymers, surfactants or organic solvents. Reactive PEG derivatives underwent thermally induced phase separation to produce spherical PEG-rich domains that coarsened in size pending gelation, resulting in stable hydrogel microspheres between approximately 1 and 100 microns in size. The time required to reach the gel point during the coarsening process and the extent of crosslinking after gelation both affected the final microsphere size and swelling ratio. The gel point could be varied by pre-reaction of the PEG derivatives below the cloud point, or by controlling pH and temperature above the cloud point. Pre-reaction brought the PEG derivatives closer to the gel point prior to phase separation, while the pH and temperature influenced the rate of reaction. Dynamic light scattering indicated a percolation-to-cluster transition about 3-5 min following phase separation. The mean radius of PEG-rich droplets subsequently increased with time to the 1/4th power until gelation. PEG microspheres produced by these methods with controlled sizes and densities may be useful for the production of modular scaffolds for tissue engineering.

  14. Exhaustive derivation of static self-consistent multi-soliton solutions in the matrix Bogoliubov-de Gennes systems

    CERN Document Server

    Takahashi, Daisuke A

    2015-01-01

    The matrix-generalized Bogoliubov-de Gennes systems are recently considered by the present author [arXiv:1509.04242], and the time-dependent and self-consistent multi-soliton solutions are constructed based on the ansatz method. In this paper, restricting the problem to the static case, we exhaustively determine the self-consistent solutions using the inverse scattering theory. Solving the gap equation, we rigorously prove that the self-consistent potential must be reflectionless. As a supplementary topic, we elucidate the relation between the stationary self-consistent potentials and the soliton solutions in the matrix nonlinear Schr\\"odinger equation. The asymptotic formulae of multi-soliton solutions for sufficiently isolated solitons are also presented.

  15. Viscous and Surface Properties of Upper Critical Solution Temperatures of Immiscible Solvents with Biomolecules, Surfactants and Polymer Resin

    Directory of Open Access Journals (Sweden)

    Man Singh

    2011-05-01

    Full Text Available

    Viscosity and surface tension of upper critical solutions (UCS of water + phenol with ΔG > 0 are reported. The phenol upper critical solutions within before (B and after (A UCS temperatures range are depicted as BUCS and AUCS respectively and were used for study. Viscous flow times (t, sec and pendant drop numbers (n were measured together with Survismeter for h/N m s-2 and g/mN m-1 respectively. The t and n were repeated for UCS with 0.5 millimol/L proteins (casein, pepsin, EA-Egg, albumin, vitamins [thiamine (B1, riboflavin (B2, pyridoxine (B6], amino acids (glycine, b-alanine, L-leucine, surfactants dodecyltrimethylammoniumbromide (DTAB, trimethylsulphoxoniumiodide (TMSOI, methyltrioctylammoniumchloride (MTOAC, orcinol and melamineformaldehyde-polyvinylpyrrolidone (MFP. Additives formed UCS at lower temperature with about 60% thermal energy saving. The t and n were used to calculate tn sec-1 for density calculation with Mansingh equation. The BUCS, UCS and AUCS as pre UCS and post UCS were obtained at 600C, 700C and 610C respectively. The tn with water were obtained for 25 to 700C and plotted with corresponding densities (± 0.05 kg m-3 for calibration curve used for density calculations. The densities were noted as TMSOI > orcinol > MFP > DTAB > MTOAC, with lower values at 66.5 and higher at 660C.


  16. Effect of varying nonwoven cotton substrate and the properties of the surfactant solution upon the adsorption of aqueous solutions of alkyl-dimethyl-benzyl-ammonium chloride

    Science.gov (United States)

    The adsorption of alkyl-dimethyl-benzyl-ammonium chloride (ADBAC), a cationic surfactant commonly employed as an antimicrobial agent, on greige, alkaline scoured, and bleached nonwoven cotton fabrics was investigated at varying surfactant concentrations and liquor ratios using UV-vis absorption spec...

  17. Interactions of surfactants with a water treatment protein from Moringa oleifera seeds in solution studied by zeta-potential and light scattering measurements.

    Science.gov (United States)

    Kwaambwa, Habauka M; Rennie, Adrian R

    2012-04-01

    Protein extracted from Moringa oleifera (MO) seeds has been advocated as a cheap and environmental friendly alternative to ionic flocculants for water purification. However, the nature and mechanism of its interaction with particles in water, as well as with dissolved surface-active molecules, are not well understood. In this article, we report studies of the protein and its interaction with four surfactants using dynamic light scattering (DLS), zeta-potential and turbidity measurements. Zeta-potential measurements identified points of charge reversal and the turbidity and DLS measurements were used to characterize the microstructure and size of protein-surfactant complexes. From the points of charge reversal, it was estimated that 7 anions are required to neutralize the positive charges of each protein molecule at pH 7. For protein mixtures with sodium dodecyl sulfate and dodecyl di-acid sodium salt, the peak in turbidity corresponds to concentrations with a large change in zeta-potential. No turbidity was observed for protein mixtures with either the nonionic surfactant Triton X-100 or the zwitterionic surfactant N-dodecyl-N,N-dimethyl-3-ammonio-1-propanesulfonate. Changes of pH in the range 4-10 have little effect on the zeta-potential, turbidity, and the hydrodynamic radius reflecting the high isoelectric point of the protein. Addition of small amounts of salt has little effect on the size of protein in solution. These results are discussed in the context of the use of the MO protein in water treatment.

  18. A triplet-triplet annihilation based up-conversion process investigated in homogeneous solutions and oil-in-water microemulsions of a surfactant.

    Science.gov (United States)

    Penconi, Marta; Gentili, Pier Luigi; Massaro, Giuseppina; Elisei, Fausto; Ortica, Fausto

    2014-01-01

    The triplet-triplet annihilation based up-conversion process, involving a platinum octaethyl-porphyrin (PtOEP) as a sensitizer and tetraphenyl-pyrene (TPPy) as an emitter, has been investigated in homogeneous solutions of toluene, bromobenzene and anisole, and oil-in-water microemulsions of the TX-100 surfactant, where toluene constitutes the non-polar phase. In homogeneous solutions, the highest up-conversion quantum yield (of the order of 20%) has been achieved in toluene, being the solvent that has the lowest viscosity among those explored. The up-conversion emission from the PtOEP-TPPy pair has been then investigated in a toluene based oil-in-water microemulsion at three different concentrations of the solutes, showing quantum yields up to the order of 1%, under the same irradiation conditions, but different deoxygenating procedures. The results herein reported might represent a good starting point for a future investigation in microheterogeneous systems. An optimization of the microemulsion composition, in terms of surfactant, co-surfactant and toluene concentrations, could allow us to increase the sensitizer and emitter concentrations and set up the best operative conditions to obtain even higher up-conversion efficiencies.

  19. Equilibrium study of single-solute adsorption of anionic surfactants with polymeric XAD resins

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Delgado, R.A.; Cotoruelo-Minguez, L.M.; Rodriguez, J.J. (Univ. de Malaga (Spain))

    1992-06-01

    Equilibrium data for the adsorption of sodium lauryl sulfate (SLS) and sodium dodecylbenzene sulfonate (SDBS) from aqueous solutions by Amberlite XAD-4 and XAD-7 polymeric resins at temperatures in the 10-40C range have been obtained. The specific surface area of the resins plays a major role in adsorption, and thus the best results have been obtained with XAD-4 resin. A higher adsorption of SDBS over SLS was also observed. Several adsorption isotherm models have been used to fit the experimental data. The best results have been obtained with the Redlich-Peterson and Langmuir-Freundlich equations. Estimations of the isosteric heat of adsorption, free energy, and entropy of adsorption are also reported.

  20. Effect of Surfactants on Association Characteristics of Di- and Triblock Copolymers of Oxyethylene and Oxybutylene in Aqueous Solutions: Dilute Solution Phase Diagrams, SANS, and Viscosity Measurements at Different Temperatures

    Directory of Open Access Journals (Sweden)

    Sanjay H. Punjabi

    2011-01-01

    Full Text Available The interactions in poly(oxyethylene (E – poly(oxybutylene (B of EB or EBE type block copolymers-sodium dodoecyl sulfate (SDS or dodecyltrimethylammonium bromide (DTAB and/or t-octylphenoxy polyethoxyethanol, (TX-100 have been monitored as a function of surfactant concentration and temperature. The addition of ionic surfactants to copolymer micellar solutions in general induced not only shape transition from spherical to prolate ellipsoids at 30∘C in the copolymer micelles but also destabilize them and even suppress the micelle formation at high surfactant loading. DTAB destabilizes the copolymer micelles more than SDS. TX-100, being nonionic, however, forms stable mixed micelles. The block copolymer-surfactant complexes are hydrophilic in nature and are characterized by high turbid and cloud points. Triblock copolymer micelles got easily destabilized than the diblock copolymer ones, indicating the importance of the interaction between the hydrophilic E chains and surfactants. The effects of destabilization of the copolymer micelles are more dominating than the micellar growth at elevated temperatures, which is otherwise predominant in case of copolymer micelles alone.

  1. Solution Properties of Linear Descriptor (Singular Matrix Differential Systems of Higher Order with (Non- Consistent Initial Conditions

    Directory of Open Access Journals (Sweden)

    Athanasios A. Pantelous

    2010-01-01

    Full Text Available In some interesting applications in control and system theory, linear descriptor (singular matrix differential equations of higher order with time-invariant coefficients and (non- consistent initial conditions have been used. In this paper, we provide a study for the solution properties of a more general class of the Apostol-Kolodner-type equations with consistent and nonconsistent initial conditions.

  2. The exact solution of self-consistent equations in the scanning near-field optic microscopy problem

    DEFF Research Database (Denmark)

    Lozovski, Valeri; Bozhevolnyi, Sergey I.

    1999-01-01

    The macroscopic approach that allows one to obtain an exact solution of the self-consistent equation of the Lippmann-Schwinger type is developed. The main idea of our method consist in usage of diagram technque for exact summation of the infinite series corresponding to the iteration procedure fo...

  3. Surfactants as additives for NO{sub x} reduction during SNCR process with urea solution as reducing agent

    Energy Technology Data Exchange (ETDEWEB)

    Ayoub, Muhammad [Department of Environmental Engineering, Kwangwoon University (Korea, Republic of); Irfan, Muhammad Faisal, E-mail: muhammadfipk@um.edu.my [Department of Chemical Engineering, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur (Malaysia); Yoo, Kyung-Seun [Department of Environmental Engineering, Kwangwoon University (Korea, Republic of)

    2011-09-15

    Highlights: {yields} We study SNCR process using urea as a reducing agent for NO{sub x} reduction. {yields} We improve NO{sub x} reduction efficiency by adding the different types of additives. {yields} We introduce new additives: surfactants and blends of alkali metal with organic group. {yields} Anionic surfactants give maximum efficiency and max. range for temperature window. - Abstract: NO{sub x} reduction from gas stream by selective non-catalytic reduction (SNCR) using urea as a reducing agent was performed in this study. A Pilot-scale experimental system was designed and constructed to evaluate the NO{sub x} reduction efficiency and temperature window of the process. Particularly, different types of additives were added during SNCR process to improve NO{sub x} reduction efficiency and enlarge temperature window. The addition of additives was based on organic compounds like alcoholic group (CH{sub 3}OH, C{sub 2}H{sub 5}OH and C{sub 3}H{sub 7}OH) and metallic compounds like alkali metals (NaOH, KOH and LiOH). Some newly introduced additives, such as surfactants and different blends of alkali metal NaOH (1%) with organic group or surfactants were also added to assess the effect of these mixed additives on NO{sub x} reduction efficiency and reaction temperature window during SNCR process. Main focus was laid on surfactants as an additive because of their cost effectiveness and availability. Basically, surfactants have both organic and metallic parts which provide -OH free radicals from both ends (organic and metallic) to enhance the reaction mechanism and improve the NO{sub x} reduction at low temperature. Different types of surfactants (anionic, cationic, amphitricha, long chain, short chain and with different functional groups attached to chains) were tested as an additive during SNCR process. Anionic surfactants (SPES, APS, LAS and SPS) gave maximum efficiency for NO{sub x} reduction and provided maximum range for the temperature window.

  4. Solar neutrino problem accounting for self-consistent magnetohydrodynamics solution for solar magnetic fields

    CERN Document Server

    Rashba, T I; Peña-Garay, C; Semikoz, V B; Valle, José W F

    2001-01-01

    The analysis of the resonant spin-flavour (RSF) solutions to the solar neutrino problem in the framework of simplest analytic solutions to the solar magneto-hydrodynamics (MHD) equations is presented. We performed the global fit of the recent solar neutrino data, including event rates as well as day and night recoil electron spectra induced by solar neutrino interactions in SuperKamiokande. We compare quantitatively our simplest MHD-RSF fit with vacuum oscillation (VAC) and MSW--type (SMA, LMA and LOW) solutions to the solar neutrino problem using a common well-calibrated theoretical calculation and fit procedure and find MHD-RSF fit to be somewhat better than those obtained for the favored neutrino oscillation solutions. We made the predictions for future experiments to disentangle the MHD-RSF scenario from other scenarios.

  5. Adding salt to a surfactant solution: Linear rheological response of the resulting morphologies

    Energy Technology Data Exchange (ETDEWEB)

    Gaudino, Danila; Pasquino, Rossana, E-mail: r.pasquino@unina.it; Grizzuti, Nino [DICMaPI, Università degli Studi di Napoli Federico II, P.le Tecchio 80, 80125 Napoli (Italy)

    2015-11-15

    The micellar system composed of Cetylpyridinium Chloride-Sodium Salicylate (CPyCl-NaSal) in brine aqueous solutions has been studied by systematically changing the salt concentration, in order to investigate the rheology of the arising morphologies. In particular, the zero-shear viscosity and the linear viscoelastic response have been measured as a function of the NaSal concentration (with [CPyCl] = 100 mM). The Newtonian viscosity shows a nonmonotonic dependence upon concentration, passing through a maximum at NaSal/CPyCl ≈ 0.6, and eventually dropping at higher salt concentrations. The progressive addition of salt determines first a transition from a Newtonian to a purely Maxwell-like behavior as the length of the micelles significantly increases. Beyond the peak viscosity, the viscoelastic data show two distinct features. On the one hand, the main relaxation time of the system strongly decreases, while the plateau modulus remains essentially constant. Calculations based on the rheological data show that, as the binding salt concentration increases, there is a decrease in micelles breaking rate and a decrease in their average length. On the other hand, in the same concentration region, a low-frequency elastic plateau is measured. Such a plateau is considered as the signature of a tenuous, but persistent branched network, whose existence is confirmed by cryo-transmission electron microscopy images.

  6. Darboux transformation and exact solutions of the integrable Heisenberg ferromagnetic equation with self-consistent potentials

    Science.gov (United States)

    Yersultanova, Z. S.; Zhassybayeva, M.; Yesmakhanova, K.; Nugmanova, G.; Myrzakulov, R.

    2016-10-01

    Integrable Heisenberg ferromagnetic equations are an important subclass of integrable systems. The M-XCIX equation is one of a generalizations of the Heisenberg ferromagnetic equation and are integrable. In this paper, the Darboux transformation of the M-XCIX equation is constructed. Using the DT, a 1-soliton solution of the M-XCIX equation is presented.

  7. Consistencies and Inconsistencies in Students' Solutions to Algebraic 'Single-Value' Inequalities

    Science.gov (United States)

    Tsamir, Pessia; Bazzini, Luciana

    2004-01-01

    This paper describes students' solutions to a commonly taught and not commonly taught inequality. The findings showed students' difficulties. Participants implicitly and explicitly exhibited two intuitive beliefs: inequalities must result in inequalities and solving inequalities and equations are the same process. Following the analysis of…

  8. 表面活性剂对十六烷基羟乙基纤维素溶液黏度的影响%Effects of surfactant on viscosity of cetyl hydroxyethylcellulose solution

    Institute of Scientific and Technical Information of China (English)

    徐强; 杨成

    2009-01-01

    Effects of surfactant on viscosity of cetyl hydroxyethylcellulose (CHEC) solution were investigated by rheometer. Experimental results indicated that the viscosity of CHEC solution increases with increasing of the surfactant concentration, and after a maximum value, then decreases with further addition of the surfactant. The effect of temperature on the viscosity of surfactant and CHEC solution depends upon the formation of surfactant/CHEC complex. The effect of variety of surfactant on the hydrophobic associate interaction of surfactant and CHEC is in the order of AES >6501 > CAB.%通过流变仪研究了几种表面活性剂对十六烷基羟乙基纤维素(CHEC)溶液黏度的影响.结果表明,CHEC溶液的黏度随表面活性剂质量分数的增加先升高,达到最大值后逐渐下降;温度对表面活性剂和CHEC混合溶液黏度的影响与表面活性剂和CHEC形成的复合物有关;表面活性剂与CHEC的疏水缔合作用强弱顺序是AES>6501>CAB.

  9. VOC removal from contaminated groundwater through membrane pervaporation. (Ⅱ): 1,1,1-trichloroethane- SDS surfactant solution system

    Institute of Scientific and Technical Information of China (English)

    PENG Ming; Sean LIU

    2003-01-01

    The conventional "pump-and-treat" technology for subsurface remediation of groundwater contaminated with volatile organic compounds(VOCs) such as 1,1,1-trichloroethane(TCA), a common chlorinated organic solvent, has limitation of prohibitively long treatment time due to extremely low water solubility of the VOCs. Surfactant-based soil remediation has emerged as the effective technology that substantially reduces the treatment time. In order to make the whole process economical, the surfactant used in soil washing has to be recovered and reused. This study examined the recovery of anionic surfactant, sodium dodecyl sulfate (SDS), from soil remediation fluids containing TCA, using a bench-scale membrane pervaporation unit. The effects of high TCA concentration, surfactant dosage, and flow rate on permeation flux and selectivity( α value) of the process were evaluated. In general, higher surfactant concentration yielded lower TCA flux and constant water flux, resulting in declining α values; higher flow rate of TCA feed stream results in higher VOC flux and selectivity, an indication of the effect of concentration polarization; higher TCA feed concentration produces higher TCA permeation across the membrane, however, the selectivity was virtually unchanged unless the total TCA concentration exceeded 2000 ppm.

  10. Factors affecting protein transfer into surfactant-isooctane solution: a case study of extraction behavior of chemically modified cytochrome c.

    Science.gov (United States)

    Ono, T; Goto, M

    1998-01-01

    The extraction mechanism of proteins by surfactant molecules in an organic solvent has been investigated using a chemically modified protein. We conducted guanidylation on lysine residues of cytochrome c by replacing their amino groups with homoarginine to enhance the protein-surfactant interaction. Results have shown that guanidylated cytochrome c readily forms a hydrophobic complex with dioleyl phosphoric acid (DOLPA) through hydrogen bonding between the phosphate moiety and the guanidinium groups. Although improved protein-surfactant interaction activated the formation of a hydrophobic complex at the interface, it could not improve the protein transfer in isooctane. It has been established that the protein extraction mechanism using surfactant molecules is mainly governed by two processes: formation of an interfacial complex at the oil-water interface and the subsequent solubilization of the complex into the organic phase. In addition, a kinetic study demonstrated that guanidylation of lysine accelerated the initial extraction rate of cytochrome c. This fact implies that the protein transferability from aqueous phase into organic phase depends on the protein-surfactant interaction which can be modified by protein surface engineering.

  11. An explanation of dispersion states of single-walled carbon nanotubes in solvents and aqueous surfactant solutions using solubility parameters.

    Science.gov (United States)

    Ham, Hyeong Taek; Choi, Yeong Suk; Chung, In Jae

    2005-06-01

    Dispersions of single-walled carbon nanotubes in various solvents and aqueous surfactant emulsions were investigated to correlate the degree of dispersion state with Hansen solubility parameters (deltat2=deltad2+deltap2+deltah2). It was found that the nanotubes were dispersed or suspended very well in the solvents with certain dispersive component (deltad) values. They were precipitated in the solvents with high polar component (deltap) values or hydrogen-bonding component (deltah) values. The solvents in the dispersed group occupied a certain region in a 3-dimensional space of three components. The surfactants with a lipophilic group equal to and longer than decyl, containing 9 methylene groups and 1 methyl group, contributed to the dispersion of nanotubes in water. The surfactants in the dispersed group had a lower limit in the dispersive component (deltad) of the Hansen parameter.

  12. Self-consistent solution of the Dyson equation for atoms and molecules within a conserving approximation

    NARCIS (Netherlands)

    Dahlen, NE; Dahlen, Nils Erik

    2005-01-01

    We have calculated the self-consistent Green's function for a number of atoms and diatomic molecules. This Green's function is obtained from a conserving self-energy approximation, which implies that the observables calculated from the Green's functions agree with the macroscopic conservation laws f

  13. A study of the distribution of polymer/surfactant coacervate between solution and foam in archetypal shampoo systems.

    Science.gov (United States)

    Wilgus, Leigh Ann; Davis, Kathleen; Labeaud, Lauren; Gandolfi, Lisa; Lochhead, Robert Y

    2011-01-01

    The research reported here attempted to answer the question, "is the foam important in delivering coacervates from shampoos." In order to answer this question, we have measured the amount of polymer in the foam and in the liquid phases of several cationic polymer/anionic surfactant systems by gravimetry and by FTIR techniques. In all cases studied, we discovered that the concentration of solids and, especially the polymer, in the liquid phase and in the foam phase were essentially the same. We conclude that the foam is unlikely to be an important factor in the topical delivery of polymer/surfactant coacervates.

  14. Self-consistent solution of the Dyson equation for atoms and molecules within a conserving approximation.

    Science.gov (United States)

    Dahlen, Nils Erik; van Leeuwen, Robert

    2005-04-22

    We have calculated the self-consistent Green's function for a number of atoms and diatomic molecules. This Green's function is obtained from a conserving self-energy approximation, which implies that the observables calculated from the Green's functions agree with the macroscopic conservation laws for particle number, momentum, and energy. As a further consequence, the kinetic and potential energies agree with the virial theorem, and the many possible methods for calculating the total energy all give the same result. In these calculations we use the finite temperature formalism and calculate the Green's function on the imaginary time axis. This allows for a simple extension to nonequilibrium systems. We have compared the energies from self-consistent Green's functions to those of nonselfconsistent schemes and also calculated ionization potentials from the Green's functions by using the extended Koopmans' theorem.

  15. 有机硅表面活性剂对水体中多环芳烃的浊点萃取研究%Cloud Point Extraction of Polycyclic Aromatic Hydrocarbons in Aqueous Solution with Silicone Surfactants

    Institute of Scientific and Technical Information of China (English)

    姚炳佳; 杨立; 胡琼; Shigendo Akita

    2007-01-01

    Cloud point extraction (CPE) processes with two silicone suffactants, Dow Corning DC-190 and DC-193, were studied as preconcentration and treatment for the water polluted by three trace polycyclic aromatic hydrocarbons (PAHs): anthracene, phenanthrene and pyrene. For all cases, the volumes of suffactant-rich phase obtained by two silicone suffactants were very small, i.e. a lower water content in the surfactant-rich phase was obtained. For example, less than 3% of the initial solution was obtained in a 1% (by mass) surfactant solution, which was much smaller than that of TX-114 in the same surfactant concentration. And TX-114 is known as a high compact surfactant-rich phase among most nonionic surfactants, thus the comparison showed that an excellent enrichment was ensured in the analysis application by the CPE process with the silicone surfactants, and the lower water content obtained in the surfactant-rich phase is also important in the large scale water treatment. The influences of additives and phase separation methodology on the recovery of PAHs were discussed. Comparing with DC-193,DC-190 has a lower cloud point and a higher recovery (near 100%) of all the three PAHs in same surfactant concentration, which was required for application as a preconcentration process prior to HPLC system. However the DC-190 solution is hard to be phase separated only by heating, whereas DC-193 has a relative higher phase separating speed by heating, but a high cloud point (around 360K) limits its application. Due to the phase separation by heating is the only method of CPE suitable to the large scale water treatment, the mixtures of two silicone surfacrants solutions were investigated in this study. A solution containing 1% of mixed DC-190 and DC-193 (in the ratio of 90∶10) removed anthracene, phenanthrene and pyrene near 100% with a relative low cloud point and quick phase separating speed.

  16. An investigation of bubble coalescence and post-rupture oscillation in non-ionic surfactant solutions using high-speed cinematography.

    Science.gov (United States)

    Bournival, G; Ata, S; Karakashev, S I; Jameson, G J

    2014-01-15

    Most processes involving bubbling in a liquid require small bubbles to maximise mass/energy transfer. A common method to prevent bubbles from coalescing is by the addition of surfactants. In order to get an insight into the coalescence process, capillary bubbles were observed using a high speed cinematography. Experiments were performed in solutions of 1-pentanol, 4-methyl-2-pentanol, tri(propylene glycol) methyl ether, and poly(propylene glycol) for which information such as the coalescence time and the deformation of the resultant bubble upon coalescence was extracted. It is shown in this study that the coalescence time increases with surfactant concentration until the appearance of a plateau. The increase in coalescence time with surfactant concentration could not be attributed only to surface elasticity. The oscillation of the resultant bubble was characterised by the damping of the oscillation. The results suggested that a minimum elasticity is required to achieve an increased damping and considerable diffusion has a detrimental effect on the dynamic response of the bubble, thereby reducing the damping.

  17. INDUCTION OF AGGREGATE FORMATION OF CATIONIC POLYSOAPS AND SURFACTANTS BY LOW CONCENTRATIONS OF ADDITIVES IN AQUEOUS-SOLUTION

    NARCIS (Netherlands)

    WANG, GJ; ENGBERTS, JBFN

    1994-01-01

    The induction of aggregate formation of cationic polysoaps ((CL)-Copol C1-12), cetyltrimethylammonium bromide (CTAB), n-dodecyltrimethylammonium bromide (DTAB), and n-dodecylmethyldiallylammonium bromide (DMDAAB) by low concentrations of Methyl Orange (10(-5)-10(-4) M) and anionic surfactants (conce

  18. Solubilisation of different medium chain esters in zwitterionic surfactant solutions--effects on phase behaviour and structure.

    Science.gov (United States)

    Barth, A; Prévost, S; Popig, J; Dzionara, M; Hedicke, G; Gradzielski, M

    2011-12-01

    We studied the effect of solubilisation of methyl esters with different chains of medium length into the binary surfactant system tetradecyldimethylamine oxide/water at constant surfactant concentration of 200 mM. As esters we employed valeric, capronic, enanthic, and pelargonic methyl ester, thereby decreasing the polarity. Always a phase sequence L(1)-L(α)-L(1) is observed with increasing ester concentration, where the L(α)-phase increases in extent and goes to much lower temperatures with increasing chain length of the ester. Viscosity measurements show a maximum at intermediate concentrations of additive that is independent of the type of ester. From SANS measurements detailed information about the structural changes occurring during the rod-to-sphere transition in the system of the shortest additive is deduced, which proceeds first through a pronounced rod growth. Interestingly, for the different esters an almost constant value of the volumic solubilisation capacity is observed, in agreement with the relatively constant interfacial tension. For the different esters no effect on the radius and the area requirement at the amphiphilic interface is observed at the solubilisation boundary. The microemulsions present here are spherical aggregates where the ester is partitioned between core and shell. From the SANS and interfacial tension data the effective bending constants of the surfactant monolayers were deduced and they show that the extension of the L(α)-phase is directly related to a corresponding increase in the bending constants of the surfactant/ester monolayers. Copyright © 2011 Elsevier Inc. All rights reserved.

  19. Effects of acidity, temperature and surfactants on electrochemical behavior of V5+ ion in sulfuric acid solutions

    Institute of Scientific and Technical Information of China (English)

    易清风; 刘云清; 赵红钢; 周秀林; 刘小平; 宋和付

    2003-01-01

    The effects of sulfuric acid concentration,reaction temperature,potential-scanning rate and surfactants on electrochemical behavior of V5+ ion on platinum electrodes were investigated.In voltammetric curves of V5+ ion there are two reduction peaks corresponding to reductions of V5+ to V4+(R2)and V5+ to V3+(R1),which are irreversible and quasi-reversible processes respectively.Oxidation peak of V3+ to V5+ is intensively affected by pH values on the electrode surface and scanning-potential rates.Only stronger acidity on the electrode surface and faster scanning-potential rates can lead to appearance of this oxidation peak.The neutral surfactant(PCBE)and cationic surfactant(CTAB)retard the V5+ electroreduction.The anionic surfactant(SDS),even at a very low concentration,increases the currents of both the reduction peaks R1 and R2,and the oxidation peak involves with the oxidation of H2 to H+.

  20. Consistent model reduction of polymer chains in solution in dissipative particle dynamics: Model description

    KAUST Repository

    Moreno Chaparro, Nicolas

    2015-06-30

    We introduce a framework for model reduction of polymer chain models for dissipative particle dynamics (DPD) simulations, where the properties governing the phase equilibria such as the characteristic size of the chain, compressibility, density, and temperature are preserved. The proposed methodology reduces the number of degrees of freedom required in traditional DPD representations to model equilibrium properties of systems with complex molecules (e.g., linear polymers). Based on geometrical considerations we explicitly account for the correlation between beads in fine-grained DPD models and consistently represent the effect of these correlations in a reduced model, in a practical and simple fashion via power laws and the consistent scaling of the simulation parameters. In order to satisfy the geometrical constraints in the reduced model we introduce bond-angle potentials that account for the changes in the chain free energy after the model reduction. Following this coarse-graining process we represent high molecular weight DPD chains (i.e., ≥200≥200 beads per chain) with a significant reduction in the number of particles required (i.e., ≥20≥20 times the original system). We show that our methodology has potential applications modeling systems of high molecular weight molecules at large scales, such as diblock copolymer and DNA.

  1. Wave solutions of ion cyclotron heated plasmas with self-consistent velocity distributions in a tokamak

    Science.gov (United States)

    Lee, Jungpyo; Wright, John; Bonoli, Paul; Harvey, Robert

    2015-11-01

    We describe a numerical model for the propagation and absorption of ion cyclotron waves in a tokamak with a non-Maxwellian velocity space distribution function. The non-Maxwellian distribution is calculated by solving Maxwell's equations and the Fokker-Plank equation self-consistently. This approach will be useful to interpret measurements of minority hydrogen tail formation during ICRF heating experiments in Alcator C-Mod. To couple the Maxwell equation solver with Fokker-Plank equation solver, the quasilinear diffusion coefficients for the fundamental ion cyclotron absorption and the first harmonic absorption are calculated. In a previous study, the all-orders spectral algorithm wave solver (AORSA) was coupled with the Fokker-Plank code (CQL3D) to find the self-consistent non-Maxwellian distribution. We derive the modified quasilinear diffusion coefficients for the finite Larmor radius (FLR) approximation using a significantly faster wave solver (TORIC) following the approach by Jaeger. The coupled TORIC-CQL3D model will be compared against results from AORSA-CQL3D in order to verify the accuracy of the reduced FLR physics in TORIC. Work supported by US Department of Energy Contract No. DE-FC02-01ER54648.

  2. A unified nonlinear fractional equation of the diffusion-controlled surfactant adsorption: Reappraisal and new solution of the Ward–Tordai problem

    Directory of Open Access Journals (Sweden)

    Jordan Hristov

    2016-01-01

    Full Text Available The article addresses a reappraisal of the famous Ward–Tordai equation describing the equilibrium of surfactants at air/liquid interfaces under diffusion control. The new derivation is entirely developed in the light of fractional calculus. The unified approach demonstrates that this equation can be clearly reformulated as a nonlinear ordinary time-fractional equation of order 1/2. The work formulates versions with different isotherms. A simple solution of the case with the Henry’s isotherm and a discussion of a Cauchy problem involving the Freundlich isotherm are provided.

  3. Wormlike Micelle Formation and Rheological Behavior in the Aqueous Solutions of Mixed Sulfate Gemini Surfactant without Spacer Group and Dodecyltrimethylammonium Bromide%Wormlike Micelle Formation and Rheological Behavior in the Aqueous Solutions of Mixed Sulfate Gemini Surfactant without Spacer Group and Dodecyltrimethylammonium Bromide

    Institute of Scientific and Technical Information of China (English)

    裴晓梅; 赵剑曦; 游毅; 刘玉芳; 魏西莲

    2011-01-01

    The rheological behavior of the aqueous solutions of mixed sulfate gemini surfactant with no spacer group, referred to as d-C12S, and dodecyltrimethylammonium bromide (C12TABr) at a total concentration of 100 mmol,L-1 but different molar ratios of ClzTABr to d-C12S (a1) was investigated using steady rate and frequency sweep measurements. The wormlike micelles were formed over a narrow a1 range of 0.20-0.27. The viscoelastic solutions exhibited Maxwell fluid behavior. At the optimum molar ratio of 0.25, the zero-shear viscosity was as high as 600 paos and the length of the mixed wormlike micelle was about 0.45-0.85 pm. The present result provides an exam- ple to construct long wormlike micelles by anionic gemini surfactant.

  4. Caractérisation des solutions de tensio-actif utilisées en récupération assistée Characterization of Surfactant Solutions Used in Enhanced Recovery

    Directory of Open Access Journals (Sweden)

    Moulu J. C.

    2006-11-01

    Full Text Available Des solutions de tensio-actif sont étudiées en vue de déterminer celles qui doivent être les plus efficaces pour le déplacement d'huile résiduelle en milieu poreux. Selon les propriétés de ces solutions au moment de leur injection, un banc d'huile se forme rapidement et progresse au niveau du front de tensio-actif, ou au contraire, les globules d'huile sont entraînés avec une vitesse faible dans l'ensemble du bouchon, les échanges entre les phases peuvent alors être importants. On a donc cherché à évaluer les caractéristiques des solutions en tenant compte des échanges qu'elles ont pu avoir avec l'huile et en particulier dans les deux cas extrêmes : solutions aqueuses sans huile et solutions équilibrées avec un grand volume d'huile. Pour ces deux états des solutions aqueuses, on a mis en évidence des comportements rhéologiques et interfaciaux très différents, dus à la migration d'alcool et d'huile entre les phases en présence. Ces propriétés des solutions de tensio-actif ont par ailleurs été reliées à la présence de structures cristallines et à leur transformation au cours des échanges qui se produisent. Research is being done on surfactant solutions to determine the ones that should be the most efficient for driving residual oil in porous media. Depending on the properties of these solutions at the time of their injection, an oil bank is formed quickly and progresses at the level of the surfactant front or, on the contrary, the oil ganglia are displaced slowly in the slug as a whole, and exchanges between the phases may then be great. Therefore, an effort was made to assess the characteristics of solutions while considering the exchanges they may have had with the oil, and particularly in the two extreme cases, i. e. aqueous solutions without oil and equilibrated solutions with a large volume of oil. For these two states of aqueous solutions, very different rheological and interfacial behaviors were found as

  5. The effects of surfactants and solution chemistry on the transport of multiwalled carbon nanotubes in quartz sand-packed columns.

    Science.gov (United States)

    Lu, Yinying; Xu, Xiaopan; Yang, Kun; Lin, Daohui

    2013-11-01

    The effect of different surfactants on the transport of multiwalled carbon nanotubes (MWCNTs) in quartz sand-packed columns was firstly investigated under various conditions. The stable plateau values (C(max)) of the breakthrough curves (BTCs), critical PVs (the number of pore volumes of infusions needed to reach the C(max)), maximum transport distances (L(max)), deposition rate coefficients (kd) and retention rates were calculated to compare the transport and retention of MWCNTs under various conditions. Stability of the MWCNT suspensions as a function of the influencing factors was examined to reveal the underlying mechanism of the MWCNT retention. Results showed that MWCNTs suspended by different surfactants presented different BTCs; the MWCNT transport increased with increasing sand size and MWCNT concentration; high flow velocity was favorable for the MWCNT transport, while high Ca(2+) concentration and low pH were unfavorable for the transport; hetero-aggregation, straining and site blocking occurred during the transport.

  6. Thermodynamic solution properties of pefloxacin mesylate and its interactions with organized assemblies of anionic surfactant, sodium dodecyl sulphate

    Energy Technology Data Exchange (ETDEWEB)

    Usman, Muhammad [Department of Chemistry, Government College University, Faisalabad 38000 (Pakistan); Department of Chemistry, Quaid-i-Azam University, Islamabad 45320 (Pakistan); Rashid, Muhammad Abid [Department of Chemistry and Biochemistry, University of Agriculture, Faisalabad (Pakistan); Mansha, Asim [Department of Chemistry, Government College University, Faisalabad 38000 (Pakistan); Siddiq, Mohammad, E-mail: m_sidiq12@yahoo.com [Department of Chemistry, Quaid-i-Azam University, Islamabad 45320 (Pakistan)

    2013-12-10

    Graphical abstract: - Highlights: • Free energy of adsorption is more negative than free energy of micellization. • Micellization becomes more spontaneous at high temperature. • There is strong interaction between PFM and SDS. - Abstract: This manuscript reports the physicochemical behavior of antibiotic amphiphilic drug pefloxacin mesylate (PFM) and its interaction with anionic surfactant, sodium dodecyl sulfate (SDS). The data of surface tension and electrical conductivity are helpful to detect the CMC as well as to calculate surface parameters, i.e. surface pressure, π, surface excess concentration, Γ, area per molecule of drug and standard Gibbs free energy of adsorption, ΔG{sub ads} and thermodynamic parameters like standard free energy of micellization, ΔG{sub m}, standard enthalpy of micellization, ΔH{sub m} and standard entropy of micellization, ΔS{sub m}. The interaction of this drug with anionic surfactant, sodium dodecyl sulfate (SDS) was studied by electrical conductivity and UV/visible spectroscopy. This enabled us to compute the values of partition coefficient (K{sub x}), free energy of partition, ΔG{sub p}, binding constant, K{sub b}, free energy of binding, ΔG{sub b}, number of drug molecules per micelle, n, and thermodynamic parameters of drug–surfactant interaction.

  7. Surfactant monitoring by foam generation

    Science.gov (United States)

    Mullen, Ken I.

    1997-01-01

    A device for monitoring the presence or absence of active surfactant or other surface active agents in a solution or flowing stream based on the formation of foam or bubbles is presented. The device detects the formation of foam with a light beam or conductivity measurement. The height or density of the foam can be correlated to the concentration of the active surfactant present.

  8. 表面活性剂溶液中单液滴的非稳态运动%Unsteady Motion of a Single Droplet in Surfactant Solutions

    Institute of Scientific and Technical Information of China (English)

    李晓锦; 毛在砂; 费维扬

    2003-01-01

    A numerical investigation of the unsteady motion of a deformed drop released freely in another quiescent liquid contaminated by surfactant is presented in this paper. The finite difference method was used to solve numerically the coupled time-dependent Navier-Stokes and convective-diffusion equations in a body-fitted orthogonal coordinate system. Numerical simulation was conducted on the experimental cases, in which MIBK drops with the size ranging from 1.24 mm to 1.97 mm rose and accelerated freely in pure water and in dilute sodium dodecyl sulphate (SDS) aqueous solution. The applicability of the numerical scheme was validated by the agreement between the simulation results and the experimental data. Both the numerical and experimental results showed that the velocitytime profile exhibited a maximum rising velocity for drops in SDS solutions, which was close to the terminal velocity in pure water, before it dropped down to a steady-state value. The effect of the sorption kinetics of surfactant on the accelerating motion was also evaluated. It is also suggested that introduction of virtual mass force into the formulation improved obviously the precision of numerical simulation of transient drop motion.

  9. Complex Formation Between Polyelectrolytes and Ionic Surfactants

    OpenAIRE

    1998-01-01

    The interaction between polyelectrolyte and ionic surfactant is of great importance in different areas of chemistry and biology. In this paper we present a theory of polyelectrolyte ionic-surfactant solutions. The new theory successfully explains the cooperative transition observed experimentally, in which the condensed counterions are replaced by ionic-surfactants. The transition is found to occur at surfactant densities much lower than those for a similar transition in non-ionic polymer-sur...

  10. Surfactant enhanced volumetric sweep efficiency

    Energy Technology Data Exchange (ETDEWEB)

    Harwell, J.H.; Scamehorn, J.F.

    1989-10-01

    Surfactant-enhanced waterflooding is a novel EOR method aimed to improve the volumetric sweep efficiencies in reservoirs. The technique depends upon the ability to induce phase changes in surfactant solutions by mixing with surfactants of opposite charge or with salts of appropriate type. One surfactant or salt solution is injected into the reservoir. It is followed later by injection of another surfactant or salt solution. The sequence of injections is arranged so that the two solutions do not mix until they are into the permeable regions well away from the well bore. When they mix at this point, by design they form a precipitate or gel-like coacervate phase, plugging this permeable region, forcing flow through less permeable regions of the reservoir, improving sweep efficiency. The selectivity of the plugging process is demonstrated by achieving permeability reductions in the high permeable regions of Berea sandstone cores. Strategies were set to obtain a better control over the plug placement and the stability of plugs. A numerical simulator has been developed to investigate the potential increases in oil production of model systems. Furthermore, the hardness tolerance of anionic surfactant solutions is shown to be enhanced by addition of monovalent electrolyte or nonionic surfactants. 34 refs., 32 figs., 8 tabs.

  11. Electronic structure of PrBa2Cu3O7 within LSDA+U: Different self-consistent solutions

    Directory of Open Access Journals (Sweden)

    M R Mohammadizadeh

    2009-08-01

    Full Text Available  Based on the density functional theory and using the full-potential linearized augmented-plane-waves method the electronic structure of PrBa2Cu3O7 (Pr123 system was calculated. The rotationally invariant local spin density approximation plus Hubbard parameter U was employed for Pr(4f orbitals. One self-consistent solution more stable than the previous solution, which has been proposed by Liechtenstein and Mazin (LM, was found. In contrast to the LM solution, it can explain the results of the 17O NMR spectroscopy study of nonsuperconducting Pr123 samples. This new solution favors the suggestion that the pure Pr123 samples should be intrinsically superconductor and metal similar to the other RBa2Cu3O7 (R=Y or a rare earth element samples. The imperfections cause the superconducting holes are transferred to the nonsuperconducting hole states around the high-symmetry (π/a, π/b, kz line in the Brillouin zone and so, superconductivity is suppressed in the conventional samples. It predicts that the superconducting 2pσ holes in the O2 sites of nonsuperconducting Pr123 samples should be depleted and the ones in the O3 sites should be almost unchanged .

  12. A method of self-consistent three-dimensional solution of the magnetohydrostatic equations using magnetogram data

    CERN Document Server

    Rudenko, G V

    2000-01-01

    A technique is proposed for constructing three-dimensional solutions comlplying with the self-consistent magnetohydrostatic (MHS) equations and with observations along the line of sight of the magnetic field at the photosphere. The technique is a generalization of a paper Rudenko, {\\tt arXiv:astro-ph/0004222} to a potential-field approximation. The solution of the problem under consideration leans a representation of the magnetic field in terms of a scalar function, with its subsequent harmonic expansion in terms of a spherical functional basis that satisfies specified boundary conditions. A numerical realization of the proposed method is expected to permit a real-time modelling of three-dimensional magnetic field, temperature, pressure and density distributions.

  13. Consistent CMT solutions from Harvard University before great earthquakes in Kurile Islands and its significance for earthquake prediction

    Institute of Scientific and Technical Information of China (English)

    WANG Jun-guo; DIAO Gui-ling

    2005-01-01

    In the paper, we use the Central Moment Tensor (CMT) solution acquired by Harvard University for the earthquakes occurred in Kurile Islands to analyze the consistent focal mechanism in the area and propose the idea of making earthquake prediction based on the consistent parameter a of focal mechanism and stress field. The results from the study indicate that before MW≥7.5 earthquakes, the consistent parameter a decreases, which starts about 10~110 days and ends about 30~2 days before the great earthquakes. Although the phenomenon is not totally the same for individual earthquake, the difference is not large. Certainly, the phenomenon should be tested by time for its reliability. However, it should not be random that the focal mechanism of MW≥5.3 earthquakes are consistent successively with the stress field in an area of several hundreds kilometers in length. It should be a phenomenon of predictive significance. When the accumulated earthquake examples are sufficient, uniform judgment criteria and prediction principles can be stipulated then.

  14. SCREENING METHODS FOR SELECTION OF SURFACTANT FORMULATIONS FOR IOR FROM FRACTURED CARBONATE RESERVOIRS

    Energy Technology Data Exchange (ETDEWEB)

    William A. Goddard III; Yongchun Tang; Patrick Shuler; Mario Blanco; Yongfu Wu; Seung Soon Jang

    2005-07-01

    This topical report presents details of the laboratory work performed to complete Task 1 of this project; developing rapid screening methods to assess surfactant performance for IOR (Improved Oil Recovery) from fractured carbonate reservoirs. The desired outcome is to identify surfactant formulations that increase the rate and amount of aqueous phase imbibition into oil-rich, oil-wet carbonate reservoir rock. Changing the wettability from oil-wet to water-wet is one key to enhancing this water-phase imbibition process that in turn recovers additional oil from the matrix portion of a carbonate reservoir. The common laboratory test to evaluate candidate surfactant formulations is to measure directly the aqueous imbibition rate and oil recovery from small outcrop or reservoir cores, but this procedure typically requires several weeks. Two methods are presented here for the rapid screening of candidate surfactant formulations for their potential IOR performance in carbonate reservoirs. One promising surfactant screening protocol is based on the ability of a surfactant solution to remove aged crude oil that coats a clear calcite crystal (Iceland Spar). Good surfactant candidate solutions remove the most oil the quickest from the chips, plus change the apparent contact angle of the remaining oil droplets on the surface that thereby indicate increased water-wetting. The other fast surfactant screening method is based on the flotation behavior of powdered calcite in water. In this test protocol, first the calcite power is pre-treated to make the surface oil-wet. The next step is to add the pre-treated powder to a test tube and add a candidate aqueous surfactant formulation; the greater the percentage of the calcite that now sinks to the bottom rather than floats, the more effective the surfactant is in changing the solids to become now preferentially water-wet. Results from the screening test generally are consistent with surfactant performance reported in the literature.

  15. Corrosion inhibition of aluminum with a series of aniline monomeric surfactants and their analog polymers in 0.5 M HCl solution

    Directory of Open Access Journals (Sweden)

    M.M. El-Deeb

    2015-07-01

    Full Text Available The inhibition effect of 3-(12-sodiumsulfonate dodecyloxy aniline monomeric surfactant (MC12 and its analog polymer Poly 3-(dodecyloxy sulfonic acid aniline (PC12 on the corrosion of aluminum in 0.5 M HCl solution was investigated using weight loss and potentiodynamic polarization techniques. The presence of these two compounds in 0.5 M HCl inhibits the corrosion of aluminum without modifying the mechanism of corrosion process. It was found that these inhibitors act as mixed-type inhibitors with anodic predominance as well as the inhibition efficiency increases with increasing inhibitor concentration, but decreases with raising temperature. Langmuir and Frumkin adsorption isotherms fit well with the experimental data. Thermodynamic functions for both dissolution and adsorption processes were determined. The obtained results from weight loss and potentiodynamic polarization techniques are in good agreement with contact angle measurements.

  16. Adsorption, desorption and condensation of nitrobenzene solution from active carbon: a comparison of two cyclodextrins and two surfactants.

    Science.gov (United States)

    Chen, Ming; Cui, Lei; Li, Chunhui; Diao, Guowang

    2009-02-15

    The adsorption of nitrobenzene on active carbon was researched. The experimental results shown the adsorption of nitrobenzene on active carbon can be described by Freundlich's adsorption model. On the other hand, beta-cyclodextrin (beta-CD) and hydroxypropyl-beta-cyclodextrin (HP-beta-CD) can react with nitrobenzene to form inclusion complex, which will enhance the aqueous solubility of nitrobenzene. By using different concentrations of beta-CD and HP-beta-CD as extractants, nitrobenzene on active carbon has been desorbed statically. As a comparison, surfactant CTAB and SDS were also selected as extractants. The desorbing of mechanism has been discussed. The low concentration of NB was effectively condensed by enrichment of active carbon and desorption of HP-beta-CD. HP-beta-CD is regarded as a potential extractant to deal with soil, sediment or active carbon.

  17. Removal and recovery of molybdenum from aqueous solutions by adsorption onto Surfactant-Modified coir pith, a lignocellulosic polymer

    Energy Technology Data Exchange (ETDEWEB)

    Namasivayam, Chinnaiya [Environmental Chemistry Division, Department of Environmental Sciences, Bharathiar University, Coimbatore (India); Sureshkumar, Molagoundanpalayam Venkatachalam [Department of Chemistry, PARK College of Engineering and Technology, Coimbatore (India)

    2009-01-15

    Coconut coir pith, a lignocellulosic polymer, is an unwanted by-product of the coir fiber industry. The pith was used as a biosorbent for the removal of Molybdenum(VI) after modification with a cationic surfactant, hexadecyltrimethylammonium bromide. The optimum pH for maximum adsorption of Mo(VI) was found to be 3.0. Langmuir, Freundlich and Dubinin Radushkevich isotherms were used to model the adsorption equilibrium data and the system was seen to follow all three isotherms. The Langmuir adsorption capacity of the biosorbent was found to be 57.5 mg g{sup -1}. Kinetic studies showed that the adsorption generally obeyed a second-order kinetic model. Desorption studies showed that the recovery of Mo(VI) from the spent adsorbent was feasible. The effect of foreign anions on the adsorption of Mo(VI) was also examined. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  18. Adsorption of surfactants and polymers at interfaces

    Science.gov (United States)

    Rojas, Orlando Jose

    Surface tension and high-resolution laser light scattering experiments were used to investigate the adsorption of isomeric sugar-based surfactants at the air/liquid interface in terms of surfactant surface packing and rheology. Soluble monolayers of submicellar surfactant solutions exhibited a relatively viscous behavior. It was also proved that light scattering of high-frequency thermally-induced capillary waves can be utilized to study surfactant exchange between the surface and the bulk solution. Such analysis revealed the existence of a diffusional relaxation mechanism. A procedure based on XPS was developed for quantification, on an absolute basis, of polymer adsorption on mica and Langmuir-Blodgett cellulose films. The adsorption of cationic polyelectrolytes on negatively-charged solid surfaces was highly dependent on the polymer ionicity. It was found that the adsorption process is driven by electrostatic mechanisms. Charge overcompensation (or charge reversal) of mica occurred after adsorption of polyelectrolytes of ca. 50% charge density, or higher. It was demonstrated that low-charge-density polyelectrolytes adsorb on solid surfaces with an extended configuration dominated by loops and tails. In this case the extent of adsorption is limited by steric constraints. The conformation of the polyelectrolyte in the adsorbed layer is dramatically affected by the presence of salts or surfactants in aqueous solution. The phenomena which occur upon increasing the ionic strength are consistent with the screening of the electrostatic attraction between polyelectrolyte segments and solid surface. This situation leads to polyelectrolyte desorption accompanied by both an increase in the layer thickness and the range of the steric force. Adsorbed polyelectrolytes and oppositely charged surfactants readily associate at the solid/liquid interface. Such association induces polyelectrolyte desorption at a surfactant concentration which depends on the polyelectrolyte charge

  19. Switchable Surfactants

    National Research Council Canada - National Science Library

    Yingxin Liu; Philip G. Jessop; Michael Cunningham; Charles A. Eckert; Charles L. Liotta

    2006-01-01

    .... We report that long-chain alkyl amidine compounds can be reversibly transformed into charged surfactants by exposure to an atmosphere of carbon dioxide, thereby stabilizing water/alkane emulsions...

  20. Interaction of nonionic surfactant AEO9 with ionic surfactants

    Institute of Scientific and Technical Information of China (English)

    ZHANG Zhi-guo; YIN Hong

    2005-01-01

    The interaction in two mixtures of a nonionic surfactant AEO9 (C12H25O(CH2CH2O)9H) and different ionic surfactants was investigated. The two mixtures were AEO9/sodium dodecyl sulfate (SDS) and AEO9/cetyltrimethylammonium bromide (CTAB) at molar fraction of AEO9, αAEO9 =0.5. The surface properties of the surfactants, critical micelle concentration (CMC),effectiveness of surface tension reduction (γCMC), maximum surface excess concentration (Гmax) and minimum area per molecule at the air/solution interface (Amin) were determined for both individual surfactants and their mixtures. The significant deviations from ideal behavior (attractive interactions) of the nonionic/ionic surfactant mixtures were determined. Mixtures of both AEO9/SDS and AEO9/CTAB exhibited synergism in surface tension reduction efficiency and mixed micelle formation, but neither exhibited synergism in surface tension reduction effectiveness.

  1. The study of furfural removal from aqueous solutions using activated carbon and bentonite modified with cetyltrimethylammonium bromide (CTAB, a cationic surfactant

    Directory of Open Access Journals (Sweden)

    M Leili

    2016-01-01

    Full Text Available Background and Objectives: Furfural is one of the toxic chemical compounds used in many industries such as petrochemical, food, paper products, pharmaceutical, etc., due to having some characteristics. Therefore, furfural could be found at different concentrations in the effluent from these industries and can enter the environment. Hence, the aim of this study was the assessment the efficiency of a low cost bentonite modified with cationic surfactant in the removal of furfural from aqueous solution. Material and Methods: In this experimental study, bentonite was purchased from one of the Mines of Zanjan Province, Iran and then the efficiency of bentonite modified with the cationic surfactant CTAB (CTAB-Bent was assessed in the adsorption of furfural from aqueous solution. Activated carbon (AC was also purchased as commercial grade. Results: Under optimum conditions, the removal efficiency of AC and CTAB-Bent was about 52 and 66%, respectively. For both adsorbents used in this study, the increase of contact time and sorbent dosage resulted in increasing the removal efficiency, but the removal efficiency was decreased with the increase of furfural initial concentrations. Regarding pH, the removal efficiency was the highest in relative acidic and neutral environment, (60 and 69% for AC and CTAB-Bent respectively. The kinetics studies revealed that the highest correlation coefficients were obtained for the pseudo-second order rate kinetic model. Adsorption data from both adsorbents was also fitted with Langmuir isotherm.   Conclusion: It was found that modified bentonite with CTAB as a natural adsorbent could have better efficiencies compared with activated carbon in the furfural removal, although more contact times is needed.

  2. First evaluation of the thermodynamic properties for spheres to elongated micelles transition of some propanediyl-alpha,omega-bis(dimethylalkylammonium bromide) surfactants in aqueous solution.

    Science.gov (United States)

    Fisicaro, Emilia; Compari, Carlotta; Duce, Elenia; Contestabili, Cristina; Viscardi, Guido; Quagliotto, Pierluigi

    2005-02-10

    The apparent and partial molar enthalpies, apparent molar volumes, and adiabatic compressibilities at 298 K of the aqueous solutions of the cationic gemini surfactants propanediyl-alpha,omega-bis(octyldimethylammonium bromide) (8-3-8) and propanediyl-alpha,omega-bis(dodecyldimethylammonium bromide) (12-3-12) have been measured as a function of concentration. The trends of the partial molar enthalpies versus concentration are the first well documented thermodynamic evidence of sphere to rod transition in the micellar phase, involving a detectable quantity of heat, and allow the determination of the change in enthalpy associated with this transition. The changes in enthalpies upon micellization and for the sphere to elongated micelles transition, DeltaH(s)(-->)(r), have been obtained from the experimental data by using a pseudo-phase transition approach: -1.5 kJ mol(-1) for 8-3-8 and -3.9 kJ mol(-1) for 12-3-12. No evidence of the above transition is found in the trends of volumetric properties versus m. The apparent adiabatic molar compressibilities for the compounds under investigation are also reported here for the first time: a negative group contribution for the methylene group is evaluated, when the surfactants are present in solution as a single molecule, reflecting its solvation structure. In the micellar phase, the -CH(2)- group contribution becomes positive. A value of 1.17 x 10(-3) cm(3) bar(-1) mol(-1) for the change in adiabatic molar compressibility upon micellization is obtained. The lower values of the methylene group contributions to the volumetric properties for the monomers support the hypothesis of partial association of the chains before the cmc.

  3. Anionic Polyelectrolyte-Cationic Surfactant Interactions in Aqueous Solutions and Foam Films Stability Interactions entre polyélectrolytes anioniques et tensioactifs cationiques en solutions aqueuses et stabilité des films de mousses

    Directory of Open Access Journals (Sweden)

    Langevin D.

    2006-12-01

    Full Text Available The objective of this work is to study polymer/surfactant interactions in aqueous solution and at the air/water interface. These interations are involved in many physicochemical phenomena, such as colloidal stabilization and wettability which are of major importance in oil application as for exemple drilling muds. More precisely, we have attempted to characterize interactions between a non surface active anionic copolymer (acrylamide/acrylamide sulfonate and an oppositely charged cationic surfactant (C12 TAB. Our results show a synergestic surface tension lowering (coadsorption at extremely low surfactant concentrations (10 to the power of (-3 to 10 to the power of (-1 CMC. At higher concentrations, namely above the so called Critical Aggregation Concentration (CAC, polymer-surfactant complexes form in the bulk and the macromolecules precipitate out of the solution. Foam films made from these mixed solutions are stable while C12TAB films are unstable. Disjoining pressure measurements on mixed films with surfactant concentration two orders of magnitude below the CAC show the existence of long range repulsive forces and a discrete film thickness transition. At the CAC, we obtain mixed films with gel-like networks that are strongly affected by the film thinning rate. L'objectif de cette étude est d'étudier les interactions polymère/tensioactif en solution aqueuse et à l'interface eau/air. Ces interactions interviennent dans de nombreux phénomènes physico-chimiques tels que la stabilisation de suspensions colloïdales et la mouillabilité qui sont d'une importance majeure dans les applications pétrolières comme, par exemple, les boues de forage. Plus précisément, nous avons essayé de caractériser les interactions entre un copolymère anionique n'ayant pas d'activité de surface (acrylamide/acrylamide sulfoné avec un tensioactif de charge opposée cationique (C12TAB. Nos résultats montrent une diminution synergique de la tension

  4. Diester-containing Zwitterionic Gemini Surfactants with Different Spacer and Its Impact on Micellization Properties and Viscosity of Aqueous Micellar Solution.

    Science.gov (United States)

    Patil, Sachin Vasant; Patil, Sanyukta Arun; Pratap, Amit Prabhakar

    2016-09-01

    A series of diester containing zwitterionic gemini surfactants, N,N-dimethyl-N-alkyl-2-[[hydroxy (alkoxy) phosphinyl]oxy]-alkylammonium designated as C8(-)-S-Cn(+), S = 2 and 3, n = 12, 14 and 16, were synthesized and characterized by instrumental techniques namely FT-IR, (1)H NMR, (13)C NMR, (31)P NMR and Mass spectral studies. These new gemini surfactants further investigated for their various surfactant properties. The critical micelle concentration (cmc) and the effectiveness of surface tension reduction (Πcmc) were determined as a function of surfactant concentration by means of surface tension measurement. Micellization and viscosity properties were investigated by surface tension, electrical conductivity, dye micellization and rheology techniques. The findings of the aqueous surfactant system obtained were impacted by polarity, size and the nature of zwitterions as the surface. The thermodynamic and viscosity properties of these surfactants found to be based on the structures of gemini surfactants.

  5. Synthesis and characterization of nano-sized BaSr1–SO4 (0 ≤ ≤ 1) solid solution by a simple surfactant-free aqueous solution route

    Indian Academy of Sciences (India)

    Yu-Feng Li; Jia-Hu Ouyang; Yu Zhou; Xue-Song Liang; Ji-Yong Zhong

    2009-04-01

    A facile aqueous solution route has been employed to synthesize BaSr1–SO4 (0 4 ≤ 1) solid solution nanocrystals at room temperature without using any surfactants or templates. The as-synthesized products were characterized by means of X-ray diffraction (XRD), X-ray fluorescence spectrometer (XRF), scanning electron microscopy (SEM), and differential scanning calorimetry–thermogravimetry (DSC–TG). The BaSr1–SO4 solid solution nanocrystals exhibit an orthorhombic structure and an ellipsoidal-shaped morphology with an average size of 80–100 nm. The lattice parameters of BaSr1–SO4 solid solution crystals increase with increasing x value. However, they are not strictly coincident with the Vegard’s law, which indicates that the as-obtained products are non-ideal solid solutions. The BaSr1–SO4 solid solution nanocrystals have an excellent thermal stability from ambient temperature to 1300°C with a structural transition from orthorhombic to cubic phase at about 1111°C.

  6. Surfactant adsorption kinetics in microfluidics

    Science.gov (United States)

    Riechers, Birte; Maes, Florine; Akoury, Elias; Semin, Benoît; Gruner, Philipp; Baret, Jean-Christophe

    2016-10-01

    Emulsions are metastable dispersions. Their lifetimes are directly related to the dynamics of surfactants. We design a microfluidic method to measure the kinetics of adsorption of surfactants to the droplet interface, a key process involved in foaming, emulsification, and droplet coarsening. The method is based on the pH decay in the droplet as a direct measurement of the adsorption of a carboxylic acid surfactant to the interface. From the kinetic measurement of the bulk equilibration of the pH, we fully determine the adsorption process of the surfactant. The small droplet size and the convection during the droplet flow ensure that the transport of surfactant through the bulk is not limiting the kinetics of adsorption. To validate our measurements, we show that the adsorption process determines the timescale required to stabilize droplets against coalescence, and we show that the interface should be covered at more than 90% to prevent coalescence. We therefore quantitatively link the process of adsorption/desorption, the stabilization of emulsions, and the kinetics of solute partitioning—here through ion exchange—unraveling the timescales governing these processes. Our method can be further generalized to other surfactants, including nonionic surfactants, by making use of fluorophore-surfactant interactions.

  7. Solution strengthened ferritic ductile iron ISO 1083/JS/500-10 provides superior consistent properties in hydraulic rotators

    Institute of Scientific and Technical Information of China (English)

    Dr.Richard Larker

    2009-01-01

    Consistent mechanical and machining properties are essential in many applications where ductile irons offer the most cost-effective way to produce structural parts. In the production of hydraulic rotators, dimensional tolerances are typically 20 μm to obtain designated performance.For castings where intermediate strength and ductility is required, it is common knowledge that conventional ferritic-pearlitic ductile irons such as ISO 1083/500-7 show large hardness variations. These are mainly caused by the notoriously varying pearlite content, both at different locations within a part and between parts in the same or different batches. Cooling rate variations due to different wall thickness and position in the molding box, as well as varying amounts of pearlite-stabilizing elements, all contribute to detrimental hardness variations.The obvious remedy is to avoid pearlite formation, and instead obtain the necessary mechanical properties by solution strengthening of the ferritic matrix by increasing silicon content to 3.7wt% -3.8wt%. The Swedish development in this field 1998 resulted in a national standardization as SS 140725, followed in 2004 by ISO 1083/ JS/500-10.Indexator AB decided 2005 to specify JS/500-10 for all new ductile iron parts and to convert all existing parts. Improvements include reduction by 75% in hardness variations and increase by 30% in cutting tool life, combined with consistently better mechanical properties.

  8. Conductometric study of sodium dodecyl sulfate - nonionic surfactant (Triton X-100, Tween 20, Tween 60, Tween 80 or Tween 85) mixed micelles in aqueous solution

    OpenAIRE

    Ćirin Dejan M; Poša Mihalj M.; Krstonošić Veljko S.; Milanović Maja Lj.

    2012-01-01

    The present study is concerned with the determination of the critical micelle concentration (cmc) of mixed micelles of sodium dodecyl sulfate with one of five nonionic surfactants (Triton X-100, Tween 20, Tween 60, Tween 80 or Tween 85) from conductance measurements. Based on the calculated values of the β parameters we have noticed that SDS-nonionic surfactants mostly showed strong synergistic effect. It was found that nonionic surfactants with mainly longer and more hydrophobic tail s...

  9. Stability of silicon and titanium carbide suspensions in electrolyte, poly(ethylene oxide), and PEO-surfactant solutions.

    Science.gov (United States)

    Barany, Sandor; Eremenko, Boris V; Malysheva, Mariya L

    2004-07-01

    It has been shown that the coagulation values of counterions for SiC and TiC suspensions with particle radius from 0.5 to 5 microm obey a z(2.5-3.5) law and there is an insufficient change in the critical concentration of 1-1 electrolytes (CCE) when the surface potential of particles increases more than two times. Also, the CCE values hardly depend on the position of counterions in the lyotropic sequence. This is explained by aggregation of SiC and TiC particles at a secondary minimum, which is proved by calculations of the potential curves of interparticle interactions using the DLVO theory. The adsorption of poly(ethylene oxide) on the surfaces studied does not cause--in contradiction to dispersions with smaller particles--an unlimited growth in the stability of suspensions. This is due to the aggregation of large particles with adsorbed PEO, as in polymer-free dispersions, under barrierless conditions in which the coordinates of the secondary minimum are determined by superposition of molecular attractive forces and steric repulsive forces of adsorbed polymeric chains, without a contribution from the electric repulsion term. PEO-anionic surfactant complexes possess higher stabilizing capacity compared to the individual components of the mixture. Our results show that the adsorbed polymer layers may hinder the aggregation both in the primary and in the secondary minimum for not very large particles only, the critical size of which depends on the dispersed phase nature and the molecular mass of the polymer.

  10. Micellization of alkyl-propoxy-ethoxylate surfactants in water-polar organic solvent mixtures.

    Science.gov (United States)

    Sarkar, Biswajit; Lam, Stephanie; Alexandridis, Paschalis

    2010-07-06

    The effects of cosolvents (glycerol, ethanol, and isopropanol) on the self-assembly of novel alkyl-propoxy-ethoxylate surfactants in aqueous solutions have been investigated with a focus on the (i) quantification of solvent effects on the critical micelle concentration (cmc), (ii) free-energy contributions to micellization, (iii) local environment in the micellar solution, and (iv) structure of the micelles. The introduction of the polar organic solvents considered in this work into water decreases cohesive forces in the solvent mixture, resulting in an increase in the solubility of the surfactant molecules. As a result, micelle formation becomes less favorable and the cmc increases. The contribution of the cosolvent to the free energy of micellization is positive, and the data for different mixed solvents collapse onto a single straight line when plotted versus a function of the solubility parameters of the surfactant alkyl chains and the mixed solvents. The behavior of the poly(propylene oxide) part of the alkyl-propoxy-ethoxylate surfactants is hydrophilic, albeit less so in the ethanol-water mixed solvent than in plain water. Pyrene fluorescence emission I(1)/I(3) data suggest that the microenvironment in micellar solutions is affected mainly by the cosolvent concentration, not the surfactant degree of ethoxylation. Small-angle X-ray scattering data for both water and ethanol-water surfactant solutions are consistent with oblate ellipsoid micelles and reveal that the introduction of 20% ethanol decreases the micelle long axis by 10-15%.

  11. Characterization, kinetic, and isotherm data for Cr (VI removal from aqueous solution by Populus alba biochar modified by a cationic surfactant

    Directory of Open Access Journals (Sweden)

    Maryam Shahverdi

    2016-12-01

    Full Text Available Populus alba is fast and auto- growing tree which profoundly accessible in around the world. The usage of the wastes of this tree would be admirable from environmental and solid waste management point of view. Thus, herein, this data set presents a facile method for providing an adsorbent from wastes of P. alba tree. The prepared adsorbent was modified by the cationic surfactant of (C16H33N(CH33Br and applied to remove Cr (VI from aqueous solution. The characterization data of the modified adsorbent were analyzed using FTIR and SEM methods. The information regarding kinetics, isotherms, and thermodynamics of chromium ions adsorption were listed. The data implied that the maximum adsorption capacity of adsorbent to uptake Cr (VI from aqueous solution was obtained 52.63 mg/g. The acquired data indicated that the adsorption of Cr (VI by the adsorbent prepared from P. alba is an promising technique for treating Cr-bearing wastewaters.

  12. Remediation using trace element humate surfactant

    Energy Technology Data Exchange (ETDEWEB)

    Riddle, Catherine Lynn; Taylor, Steven Cheney; Bruhn, Debra Fox

    2016-08-30

    A method of remediation at a remediation site having one or more undesirable conditions in which one or more soil characteristics, preferably soil pH and/or elemental concentrations, are measured at a remediation site. A trace element humate surfactant composition is prepared comprising a humate solution, element solution and at least one surfactant. The prepared trace element humate surfactant composition is then dispensed onto the remediation site whereby the trace element humate surfactant composition will reduce the amount of undesirable compounds by promoting growth of native species activity. By promoting native species activity, remediation occurs quickly and environmental impact is minimal.

  13. Self-consistent field theoretic simulations of amphiphilic triblock copolymer solutions: Polymer concentration and chain length effects

    Directory of Open Access Journals (Sweden)

    X.-G. Han

    2014-06-01

    Full Text Available Using the self-consistent field lattice model, polymer concentration φP and chain length N (keeping the length ratio of hydrophobic to hydrophilic blocks constant the effects on temperature-dependent behavior of micelles are studied, in amphiphilic symmetric ABA triblock copolymer solutions. When chain length is increased, at fixed φP, micelles occur at higher temperature. The variations of average volume fraction of stickers φcos and the lattice site numbers Ncols at the micellar cores with temperature are dependent on N and φP, which demonstrates that the aggregation of micelles depends on N and φP. Moreover, when φP is increased, firstly a peak appears on the curve of specific heat CV for unimer-micelle transition, and then in addition a primary peak, the secondary peak, which results from the remicellization, is observed on the curve of CV. For a long chain, in intermediate and high concentration regimes, the shape of specific heat peak markedly changes, and the peak tends to be a more broad peak. Finally, the aggregation behavior of micelles is explained by the aggregation way of amphiphilic triblock copolymer. The obtained results are helpful in understanding the micellar aggregation process.

  14. 离子型双子表面活性剂溶液流变性影响因素比较%The Comparative Study of Influence Factors of Ionic Gemini Surfactant Solution's Rheology

    Institute of Scientific and Technical Information of China (English)

    高大鹏; 于萌

    2012-01-01

    分析离子型双子表面活性剂溶液流变性与其聚集体形态间的依赖关系,阐述分子结构、表面活性剂浓度、无机盐、有机酸盐、温度等因素对阳离子型双子表面活性剂溶液流变性的影响。针对阳离子双子表面活性剂在实际应用中的不足,以硫酸酯盐双子表面活性剂GA12-4-12溶液为例,对阴离子型双子表面活性剂溶液的流变性进行实验研究。研究表明:GA12-4-12浓度升高,溶液黏度则上升;加入质量分数小于0.04%的NaCl有一定增黏效果,而加入浓度超过0.04%的无机盐(NaCl、AlCl3.6H2O)对GA12-4-12溶液有降黏作用,加入较高浓度的CaCl2溶液对GA12-4-12溶液有增黏作用;与少量有机酸盐复合而成的GA12-4-12溶液体系黏度可以增大几倍甚至十几倍;GA12-4-12溶液黏度随温度的升高先升高后下降。%The unique rheology of Gemini surfactant solution in future application of enhanced oil recovery has been discussed, the dependency between Gemini surfactant solution's rheology and its morphology of the aggregate has been analyzed. Application of molecular structure, surfactant concentrations, inorganic salt, organic acid salt, temperature of factors of cationic Gemini surfactant the influence of the solution theological property. For cationic Gemini surfactant in practical application is insufficient, sulfuric acid ester salt Gemini surfactants GA12-4-12 solution. For example, in view of the anion type of Gemini surfactant the rheological properties of solution by experiments and research show that with the GA12-4-12 increased concentration, the solution viscosity rises. Join concentrations more than 0.03% of the inorganic salt (NaC1, A1C13) to GA12-4-12 solution viscosity reduction have role, and to join with high CaC12 solution to the GA12-4-12 solution have viscous role. And a small amount of organic acid salt (salicylic acid, sodium lauryl benzene sulfonic acid sodium) compound and into the GA12

  15. Theoretical modeling of cationic surfactant aggregation at the silica/aqueous solution interface: Effects of pH and ionic strength

    NARCIS (Netherlands)

    Drach, M.; Andrzejewska, A.; Narkiewicz-Michalek, J.; Rudzinski, W.; Koopal, L.K.

    2002-01-01

    A theory of ionic surfactant aggregation on oppositely charged surfaces is presented. In the proposed model the adsorbed phase is considered as a mixture of singly dispersed surfactant molecules, monolayered and bilayered aggregates of various sizes and the ions of simple electrolyte added to the aq

  16. Measurement of resistance to solute transport across surfactant-laden interfaces using a Fluorescence Recovery After Photobleaching (FRAP) technique

    Science.gov (United States)

    Browne, Edward P.; Nivaggioli, Thierry; Hatton, T. Alan

    1994-01-01

    A noninvasive fluorescence recovery after photobleaching (FRAP) technique is under development to measure interfacial transport in two phase systems without disturbing the interface. The concentration profiles of a probe solute are measured in both sides of the interface by argon-ion laser, and the system relaxation is then monitored by a microscope-mounted CCD camera.

  17. Effect of the salt-induced micellar microstructure on the nonlinear shear flow behavior of ionic cetylpyridinium chloride surfactant solutions

    Science.gov (United States)

    Gaudino, D.; Pasquino, R.; Kriegs, H.; Szekely, N.; Pyckhout-Hintzen, W.; Lettinga, M. P.; Grizzuti, N.

    2017-03-01

    The shear flow dynamics of linear and branched wormlike micellar systems based on cetylpyridinium chloride and sodium salicylate in brine solution is investigated through rheometric and scattering techniques. In particular, the flow and the structural flow response are explored via velocimetry measurements and rheological and rheometric small-angle neutron scattering (SANS) experiments, respectively. Although all micellar solutions display a similar shear thinning behavior in the nonlinear regime, the experimental results show that shear banding sets in only when the micelle contour length L ¯ is sufficiently long, independent of the nature of the micellar connections (either linear or branched micelles). Using rheometric SANS, we observe that the shear banding systems both show very similar orientational ordering as a function of Weissenberg number, while the short branched micelles manifest an unexpected increase of ordering at very low Weissenberg numbers. This suggests the presence of an additional flow-induced relaxation process that is peculiar for branched systems.

  18. Electrochemical Oscillations Induced by Surfactants

    Institute of Scientific and Technical Information of China (English)

    翟俊红; 贺占博

    2003-01-01

    A new type of electrochemical oscillation induced by surfactant was observed in experiments. The electrochemical system is a Daniell cell with a copper rod in CuSO4 aqueous and an aluminum rod in Al(NO3)3 aqueous as electrodes. The surfactants are CTAB, TX-100, SLS. The addition of trace surfactant solution by a micro-syringe made the original monotonously changing electrochemical system produce obvious periodic phenomena. At the mean time, the copper ion selective electrode and Hg2SO4 reference electrode were used to monitor the copper electrode reaction and determine its rate constant k of first order reaction. According to the experimental results of electrode reaction kinetics, the possible mechanism was found to be the polarization induced from the directional adsorption of trace surfactant on the electrode surface. That is the electrochemical oscillations.

  19. Electrokinetic investigation of surfactant adsorption.

    Science.gov (United States)

    Bellmann, C; Synytska, A; Caspari, A; Drechsler, A; Grundke, K

    2007-05-15

    Fuerstenau [D.W. Fuerstenau, in: M.L. Hair (Ed.), Dekker, New York, 1971, p. 143] has already discussed the role of hydrocarbon chain of surfactants, the effect of alkyl chain length, chain structure and the pH of the solution on the adsorption process of surfactants. Later Kosmulski [M. Kosmulski, Chemical Properties of Material Surfaces, Surfactant Science Series, vol. 102, Dekker, New York, Basel, 2001] included the effect of surfactant concentration, equilibration time, temperature and electrolyte in his approaches. Certainly, the character of the head groups of the surfactant and the properties of the adsorbent surface are the basis for the adsorption process. Different surfactants and adsorbents cause different adsorption mechanisms described firstly by Rosen [M.J. Rosen, Surfactants and Interfacial Phenomena, second ed., Wiley, New York, 1989]. These adsorption mechanisms and their influencing factors were studied by electrokinetic investigations. Here only changes of the charges at the surfaces could be detected. To control the results of electrokinetic investigations they were compared with results from ellipsometric measurements. In the case of surfactant adsorption the chain length was vitally important. It could be shown by the adsorption of alkyl trimethyl ammonium bromides onto polymer films spin coated at wafer surfaces. The influence of the chain length depending on surface properties of the polymer film was studied. Streaming potential measurements were applied for these investigations. The obtained results enabled us to calculate the molar cohesive free energy per mol of CH2-group in the alkaline chain of the surfactant if all other specific adsorption effects were neglected.

  20. Polymer gels with associating side chains and their interaction with surfactants

    Science.gov (United States)

    Gordievskaya, Yulia D.; Rumyantsev, Artem M.; Kramarenko, Elena Yu.

    2016-05-01

    Conformational behaviour of hydrophobically modified (HM) polymer gels in solutions of nonionic surfactants is studied theoretically. A HM gel contains hydrophobic side chains (stickers) grafted to its subchains. Hydrophobic stickers are capable to aggregate into joint micelles with surfactant molecules. Micelles containing more than one sticker serve as additional physical cross-links of the network, and their formation causes gel shrinking. In the proposed theoretical model, the interior of the gel/surfactant complex is treated as an array of densely packed spherical polymer brushes consisting of gel subchains tethered to the surface of the spherical sticker/surfactant micelles. Effect of stickers length and grafting density, surfactant concentration and hydrophobicity on gel swelling as well as on hydrophobic association inside it is analyzed. It is shown that increasing surfactant concentration can result in a gel collapse, which is caused by surfactant-induced hydrophobic aggregation of stickers, and a successive gel reswelling. The latter should be attributed to a growing fraction of surfactants in joint aggregates and, hence, increasing number of micelles containing only one sticker and not participating in gel physical cross-linking. In polyelectrolyte (PE) gels hydrophobic aggregation is opposed by osmotic pressure of mobile counterions, so that at some critical ionization degree hydrophobic association is completely suppressed. Hydrophobic modification of polymers is shown to open new ways for controlling gel responsiveness. In particular, it is discussed that incorporation of photosensitive groups into gel subchains and/or surfactant tail could give a possibility to vary the gel volume by light. Since hydrophobic aggregation regularities in gels and solutions are common, we hope our findings will be useful for design of polymer based self-healing materials as well.

  1. Anomalous pH dependent stability behavior of surfactant-free nonpolar oil drops in aqueous electrolyte solutions.

    Science.gov (United States)

    Clasohm, Lucy Y; Vakarelski, Ivan U; Dagastine, Raymond R; Chan, Derek Y C; Stevens, Geoffrey W; Grieser, Franz

    2007-08-28

    Recent advances in atomic force microscopy (AFM) force measurement techniques have allowed the direct measurement and theoretical interpretation of the interaction between a liquid droplet and a solid surface or between two liquid droplets. In this study, we investigated the interaction across an aqueous thin film between fluorocarbon (perfluoropentane) droplets, hydrocarbon (tetradecane) droplets, and a droplet and a flat mica surface in the absence of stabilizers. It was found that even at a relatively elevated electrolyte concentration of 0.1 M NaNO3, depending on the solution pH, interactions between two identical droplets or a droplet and a mica surface could be repulsive. A simple theoretical analysis of the magnitude and range of these interactive forces suggests that the DLVO theory cannot explain the observed behavior. The measured force behavior is discussed in the context of ion adsorption, and the arising charging effects, at the bare oil-water interface.

  2. Interaction Study and Reactivity of Zr(IV) -Substituted Wells-Dawson Polyoxometalate towards Hydrolysis of Peptide Bonds in Surfactant Solutions.

    Science.gov (United States)

    Quanten, Thomas; Shestakova, Pavletta; Van Den Bulck, Dries; Kirschhock, Christine; Parac-Vogt, Tatjana N

    2016-03-01

    The interaction between the 1:2 Zr(IV) :Wells-Dawson complex, K15 H[Zr(α2 -P2 W17 O61 )2] (1), and a range of surfactants was studied in detail with the aim of developing metal-substituted POMs as potential artificial proteases for membrane proteins. The surfactants include the positively charged cetyl(trimethyl)ammonium bromide (CTAB), the negatively charged sodium dodecyl sulfate (SDS), the neutral Triton X-100 (TX-100), and zwitterionic 3-[dodecyl(dimethyl)ammonio]-1-propanesulfonate (Zw3-13) and 3-[dimethyl(3-{[(3α,5β,7α,12α)-3,7,12-trihydroxy-24-oxocholan-24-yl]amino}propyl)ammonio]-1-propanesulfonate (CHAPS). A combination of multinuclear (1)H, (13)C, and (31) P NMR spectroscopy, (1)H diffusion-ordered NMR spectroscopy ((1)H DOSY), and nuclear Overhauser effect spectroscopy (NOESY) was used to examine the interaction between 1 and each surfactant on the molecular level. Cationic surfactant CTAB caused precipitation of 1 due to strong electrostatic interactions, while the anionic SDS and neutral TX-100 surfactants did not exhibit any interaction at neutral pD. (1)H DOSY NMR spectroscopy indicated an interaction between 1 and zwitterionic surfactants Zw3-12 and CHAPS, which occurs via the positively charged ammonium group in the surfactant molecule. In the presence of anionic, neutral, and zwitterionic surfactants, 1 preserves its catalytic activity towards the hydrolysis of the peptide bond in the dipeptide glycyl-l-histidine (GH). The fastest hydrolysis was observed at pD 7.0 and could be rationalized by taking into account pD-dependent speciation of 1 and coordination properties of GH.

  3. Chemical modification of a plant origin biomass using cationic surfactant ABDAC and the biosorptive decolorization of RR45 containing solutions.

    Science.gov (United States)

    Akar, Tamer; Ozkara, Esra; Celik, Sema; Turkyilmaz, Serpil; Akar, Sibel Tunali

    2013-01-01

    This study focused on the improvement of the decolorization potential of biomass derived from Pyracantha coccinea. Alkyl benyzldimethyl ammonium chloride (ABDAC) was used as modification agent. Batch mode decolorization potential of modified biosorbent was explored at different operating conditions. ABDAC modification significantly increased the biosorption yield to 97.27%, which was 3.88 times higher than that of natural biomass. The prepared biosorbent was effectively used for the decolorization of Reactive Red 45 contaminated solutions after the optimization of biosorption conditions. The non-linear regression analysis was used to evaluate the isotherm and kinetic model parameters. Process followed the Langmuir isotherm model and the highest monolayer capacity of 152.49 mg g(-1) was obtained with a small amount of modified biosorbent. Kinetic studies indicated fast decolorization rate of the process following the pseudo-first-order model. Biosorption performance of the prepared biosorbent was tested in RR45 containing real wastewater sample. The possible dye biosorbent interactions in the biosorption process were explored by zeta potential, scanning electron microscobe and FTIR analysis.

  4. Adsorption of Orange II dye in aqueous solution onto surfactant-coated zeolite: characterization, kinetic and thermodynamic studies.

    Science.gov (United States)

    Jin, Xiaoying; Yu, Bing; Chen, Zuliang; Arocena, Joselito M; Thring, Ronald W

    2014-12-01

    Adsorption of anionic dye - Orange II - in aqueous solution onto hexadecyltrimethylammonium bromide (HDTMA)-coated zeolite (HCZ) reached 38.96mg/g compared with 8.13mg/g onto natural zeolite. Fourier Transform Infrared (FTIR), scanning electronic microscopy (SEM) and X-ray powder diffraction (XRD) data showed that HDTMA-coated zeolite developed surficial positive charges. The adsorption reaction fits the Freundlich isotherm (R(2)=0.93) and the value of 1/n was less than unity (=0.81) and suggest a multi-layer physi-sorption process. The kinetics of the adsorption is a pseudo-second-order model. The activation energy (Ea) of the reaction is +35.70kJ/mol to further support a physi-sorption process while the ΔH(o) (+82.79kJ/mol) is characteristic for an endothermic reaction. The ΔG(o) values of -2.33, -0.98 and -0.37kJ/mol at 25°C, 30°C and 35°C, respectively implied that the adsorption reaction was feasible and thermodynamically spontaneous. We proposed that both electrostatic interactions and partitioning process are involved in the adsorption mechanisms of Orange II dye onto HCZ. Copyright © 2014 Elsevier Inc. All rights reserved.

  5. The model of a polyelectrolyte solution with explicit account of counterions within a self-consistent field theory

    Science.gov (United States)

    Budkov, Yu. A.; Nogovitsyn, E. A.; Kiselev, M. G.

    2013-04-01

    A theoretical approach to calculating the thermodynamic and structural functions of solutions of polyelectrolytes based on Gaussian equivalent representation for the calculation of functional integrals is proposed. It is noted that a new analytical result of this work is the direct assumption of counterions, along with an equation for the gyration radius of a polymer chain as a function of the concentrations of monomers and added low-molecular salt. An equation of state is obtained within the proposed model. Our theoretical results are used to describe the thermodynamic and structural properties of an aqueous solution of sodium polystyrene sulfonate with additions of NaCl.

  6. Modification of an Iranian clinoptilolite nano-particles by hexadecyltrimethyl ammonium cationic surfactant and dithizone for removal of Pb(II) from aqueous solution.

    Science.gov (United States)

    Anari-Anaraki, Mostafa; Nezamzadeh-Ejhieh, Alireza

    2015-02-15

    Natural clinoptilolite tuff was mechanically converted to micro (MCP) and nano (NCP) particles. The MCP and NCP powders were respectively modified with hexadecyltrimethyl ammonium bromide (HDTMA) and dithizone (DTZ). The raw and modified samples were characterized by X-ray diffraction (XRD), Fourier transformation infra red (FT-IR), scanning electron microscope (SEM), transmission electron microscope (TEM) and thermogravimetry (TG) and used for the removal of Pb(II) from aqueous solution. The results confirm that both ion exchange and complexation processes are responsible for removal of Pb(II) cations in the modified samples, while Pb(II) cations were only removed via an ion exchange process by the raw clinoptilolite. In this sorbent, the anionic removal property of surfactant modified zeolites (SMZs) changed to cationic removal property by an additional modification step. The best removal efficiency was observed by NCP-HDTMA-DTZ at the following experimental conditions: C(Pb(II)): 800 mg L(-1), HDTMA dosage: 0.2 mol L(-1), DTZ dosage: 5 mmol L(-1), contact time of DTZ with NCP-HDTMA: 1800 min and contact time of the sorbent with Pb(II): 360 min. The NCP-HDTMA-DTZ sorbent showed good efficiency for the removal of lead in the presence of different multivalent cations. Adsorption isotherms of Pb(II) ions obey the Langmuir equation that indicate the monolayer sorption of Pb(II). The adsorption kinetics based on the pseudo-second-order rate equation indicates that the rate limiting step involving a chemical reaction. The negative ΔH and ΔG indicate an exothermic and spontaneous process.

  7. Comparative study of hydro soluble polymers solutions and surfactants aiming the polymer-rock interactions in consolidated sandstone; Estudo comparativo de solucoes de polimeros hidrossoluveis e tensoativos visando as interacoes polimero-rocha em arenito consolidado

    Energy Technology Data Exchange (ETDEWEB)

    Valentim, Adriano Cesar M.; Marcelino, Cleuton Pereira; Medeiros, Ana Catarina R.; Garcia, Rosangela Balaban [Universidade Federal do Rio Grande do Norte (UFRN), Natal, RN (Brazil). Lab. de Pesquisa em Petroleo (LAPET)

    2004-07-01

    The polyacrylamide is one of the main polymers used in the petroleum industry. Among its properties, stands out the capacity to alter the permeability of the rock to water. However, the polyacrylamide presents some limitations, such as low tolerance to the presence of salts, what can promote its precipitation resulting in low oil recovery efficiency. The application of the polymer in emulsion can promote a larger stability, due to the presence of a surfactant, which has the capacity to modify the interfacial tension and to form a film between the phases of the emulsion. Thereby, the injection of a polymer emulsion can promote an increase of oil recovery. In this work, a preliminary study of the effect of a anionic surfactant (SDS) and polyacrylamides (anionic and neutral) on the surface tension and rheology is presented in aqueous solutions contend salt (NaCl). The results showed surface tension of the mixtures had been remained constant and low (around 32 mN/m), independent of the polymer concentration. A viscosity reduction was observed at polymeric solutions as much in presence of salt, as in presence of the surfactant. Both the samples showed a pseudo plastic behavior. (author)

  8. Conductometric study of sodium dodecyl sulfate - nonionic surfactant (Triton X-100, Tween 20, Tween 60, Tween 80 or Tween 85 mixed micelles in aqueous solution

    Directory of Open Access Journals (Sweden)

    Ćirin Dejan M.

    2012-01-01

    Full Text Available The present study is concerned with the determination of the critical micelle concentration (cmc of mixed micelles of sodium dodecyl sulfate with one of five nonionic surfactants (Triton X-100, Tween 20, Tween 60, Tween 80 or Tween 85 from conductance measurements. Based on the calculated values of the β parameters we have noticed that SDS-nonionic surfactants mostly showed strong synergistic effect. It was found that nonionic surfactants with mainly longer and more hydrophobic tail show stronger interactions with hydrophobic part of SDS, thus expressing stronger synergism. In SDS-Tween 80 binary system the strongest synergistic effect was noticed. SDS-Tween 85 micellar system showed antagonistic effect, most probably because the presence of the double bond in its three hydrophobic tails (three C18 tails makes it sterically rigid.

  9. Controlling Synthesis of PbS Nanostructures in Surfactant Solutions%表面活性剂溶液中硫化铅纳米结构的可控生长

    Institute of Scientific and Technical Information of China (English)

    于雪莲; 曹传堂; 曹传宝; 朱鹤孙

    2005-01-01

    应用软模板法成功制备了半导体硫化铅树枝状纳米结构.此反应是在非离子表面活性剂Triton X-100存在下进行的,具有条件温和,操作简单等优点.对反应过程中硫化铅各向异性生长的影响因素进行系统的阐述,通过简单地控制反应时间及表面活性剂的加入量就可得到纳米棒、纳米分枝结构以及立方结构.考虑到形貌对半导体性能有重要影响,这一实验结果的取得应具有很高的实际应用价值.%PbS dendritic nanostructures have been successfully synthesized by a facile method from solutions containing a nonionic surfactant, Triton X-100 ( t-octyl-( OCH2CH2 ) xOH ,x = 9,10) under the ambient pressure. The anisotropic structural evolution of semiconductor PbS nanocrystals and the systematically elucidated key growth parameters for their shape control were studied. Through simply programming growth parameters such as aging time and capping molecules in the initial scheme, desired architecture of building blocks including nanorods, nanodendrities and nanocubes can be consistently obtained. Considering that the size and morphology of such semiconductors very strongly affect their applications, there will be significant advances that can be applied to the nanoscale devices.

  10. Molecular-thermodynamic theory of micellization of multicomponent surfactant mixtures: 2. pH-sensitive surfactants.

    Science.gov (United States)

    Goldsipe, Arthur; Blankschtein, Daniel

    2007-05-22

    In article 1 of this series, we developed a molecular-thermodynamic (MT) theory to model the micellization of mixtures containing an arbitrary number of conventional (pH-insensitive) surfactants. In this article, we extend the MT theory to model mixtures containing a pH-sensitive surfactant. The MT theory was validated by examining mixtures containing both a pH-sensitive surfactant and a conventional surfactant, which effectively behave like ternary surfactant mixtures. We first compared the predicted micellar titration data to experimental micellar titration data that we obtained for varying compositions of mixed micelles containing the pH-sensitive surfactant dodecyldimethylamine oxide (C12DAO) mixed with either a cationic surfactant (dodecyltrimethylammonium bromide, C12TAB), a nonionic surfactant (dodecyl octa(ethylene oxide), C12E8), or an anionic surfactant (sodium dodecyl sulfate, SDS) surfactant. The MT theory accurately modeled the titration behavior of C12DAO mixed with C12E8. However, C12DAO was observed to interact more favorably with SDS and with C12TAB than was predicted by the MT theory. We also compared predictions to data from the literature for mixtures of C12DAO and SDS. Although the pH values of solutions with no added acid were modeled with only qualitative accuracy, the MT theory resulted in quantitatively accurate predictions of solution pH for mixtures containing added acid. In addition, the predicted degree of counterion binding yielded a lower bound to the experimentally measured value. Finally, we predicted the critical micelle concentration (cmc) of solutions of two pH-sensitive surfactants, tetradecyldimethylamine oxide (C14DAO) and hexadecyldimethyl betaine (C16Bet), at varying solution pH and surfactant composition. However, at the pH values considered, the pH sensitivity of C16Bet could be neglected, and it was equivalently modeled as a zwitterionic surfactant. The cmc's predicted using the MT theory agreed well with the experimental

  11. Interaction of Fluorocarbon Containing Hydrophobically Modified Polyelectrolyte with Nonionic Surfactants

    Institute of Scientific and Technical Information of China (English)

    GUO,Jin-Feng(郭金峰); ZHUANG,Dong-Qing(庄东青); ZHOU,Hui(周晖); ZHANG,Yun-Xiang(章云祥)

    2002-01-01

    The interaction of fluorocarbon containing hydrophobically modified polyelectrolyte (FMPAANa) with two kinds of nonionic surfactants (hydrogenated and fluorinated) in a semidilute (0.5 wt% ) aqueous solution had been studied by rheological measurements. Association behavior was found in both systems. The hydrophobic interaction of FMPAANa with fluorinated surfactant (FC171) is much stronger than that with hydrogenated surfactant (NP7.5) at low surfactant concentrations. The interaction is strengthened by surfactants being added for the density of active junctions increased. Whereas distinct phenomena for FC171 and NP7. 5 start to be found as the surfactants added over their respective certain concentration. The interaction of polyelectrolyte with fluorinated surfactant increases dramatical ly while that with hydrogenated surfactant decreases.

  12. Polyelectrolyte surfactant aggregates and their deposition on macroscopic surfaces

    CERN Document Server

    Voisin, D

    2002-01-01

    Oppositely charged surfactant and polyelectrolyte are present in hair shampoos and conditioners, together with particles (e.g. anti-dandruff agents for scalp) and droplets (e.g. silicone oil for the hair). These are normally formulated at high surfactant concentrations, beyond the flocculation region for the polyelectrolyte concentration used. However, on dilution with water, during application, flocs are formed which carry the particles and droplets to the scalp and hair. The addition of an anionic surfactant to an aqueous solution of cationic polyelectrolyte, at a given concentration, can lead to the formation of polyelectrolyte-surfactant 'particles', in which the surfactant 'binds' to the polyelectrolyte. This occurs from the critical association concentration (CAC), up to the surfactant concentration corresponding to maximum binding. Within this range of surfactant concentrations, the surfactant bound to the polyelectrolyte is thought to associate to form what might be termed 'internal micelles'. Each po...

  13. Sm doped mesoporous CeO2 nanocrystals: aqueous solution-based surfactant assisted low temperature synthesis, characterization and their improved autocatalytic activity.

    Science.gov (United States)

    Mandal, Bappaditya; Mondal, Aparna; Ray, Sirsendu Sekhar; Kundu, Amar

    2016-01-28

    Mesoporous Sm(3+) doped CeO2 (Ce-Sm) with a nanocrystalline framework, a high content of Ce(3+) and surface area (184 m(2) g(-1)), have been synthesized through a facile aqueous solution-based surfactant assisted route by using inorganic precursors and sodium dodecyl sulphate as a template. The XRD results indicate that the calcined Ce-Sm and even the as-prepared material have a cubic fluorite structure of CeO2 with no crystalline impurity phase. XRD studies along with HRTEM results confirmed the formation of mesoporous nanocrystalline CeO2 at a lower temperature as low as 100 °C. A detailed analysis revealed that Sm(3+) doping in CeO2 has increased the lattice volume, surface area, mesopore volume and engineered the surface defects. Higher concentrations of Ce(3+) and oxygen vacancies of Ce-Sm resulted in lowering of the band gap. It is evident from the H2-TPR results that Sm(3+) doping in CeO2 strongly modified the reduction behavior of CeO2 by shifting the bulk reduction at a much lower temperature, indicating increased oxygen mobility in the sample which enables enhanced oxygen diffusion at lower temperatures, thus promoting reducibility, i.e., the process of Ce(4+)→ Ce(3+). UV-visible transmission studies revealed improved autocatalytic performance due to easier Ce(4+)/Ce(3+) recycling in the Sm(3+) doped CeO2 nanoparticles. From the in vitro cytotoxicity of both pure CeO2 and Sm(3+) doped CeO2 calcined at 500 °C in a concentration as high as 100 μg mL(-1) (even after 120 h) on MG-63 cells, no obvious decrease in cell viability is observed, confirming their excellent biocompatibility. The presence of an increased amount of surface hydroxyl groups, mesoporosity, and surface defects have contributed towards an improved autocatalytic activity of mesoporous Ce-Sm, which appear to be a potential candidate for biomedical (antioxidant) applications.

  14. Atmospheric Chemistry for Astrophysicists: A Self-consistent Formalism and Analytical Solutions for Arbitrary C/O

    CERN Document Server

    Heng, Kevin; Tsai, Shang-Min

    2015-01-01

    We present a self-consistent formalism for computing and understanding the atmospheric chemistry of exoplanets. Starting from the first law of thermodynamics, we demonstrate that the van't Hoff equation (which describes the equilibrium constant), Arrhenius equation (which describes the rate coefficients) and procedures associated with the Gibbs free energy (minimisation, rescaling) have a common physical and mathematical origin. We correct an ambiguity associated with the equilibrium constant, which is used to relate the forward and reverse rate coefficients, and rigorously derive its two definitions. By necessity, one of the equilibrium constants must be dimensionless and equate to an exponential function involving the Gibbs free energy, while the other is a ratio of rate coefficients and must therefore possess physical units. To avoid confusion, we simply term them the dimensionless and dimensional equilibrium constants. We demonstrate that the Arrhenius equation takes on a functional form that is more gene...

  15. Effects of Surfactant on Zinc Recovery by Solvent Extraction during Leaching in HCl-FeCl3 Solution%表面活性剂对HCl-FeCl3溶液中锌精矿在浆萃取浸出率的影响

    Institute of Scientific and Technical Information of China (English)

    卢立柱; 康晓红; 谢慧琴

    2002-01-01

    The effects of surfactant on the solvent extraction in leaching sphalerite were investigated. It is found that sodium dodecyl sulfonate is the effective surfactant in improving the zinc recovery from sphalerite in the aqueous FeCla-HCl-tetrachloroethylene system. Through the measurements of surface tension and viscosity of the sphalerite slurry modified with different surfactants, it is concluded that sodium dodecyl sulfonate in the concentration range of 0.05 to 0.2g@L-1 can improve the viscosity of sphalerite slurry in the water, decrease the surface tension of leaching solution, prevent the aggregation of ore particles, and give very high zinc extraction .

  16. Kinetic analysis of anionic surfactant adsorption from aqueous solution onto activated carbon and layered double hydroxide with the zero length column method

    NARCIS (Netherlands)

    Schouten, Natasja; Ham, Louis G.J. van der; Euverink, Gert-Jan W.; Haan, André B. de

    2009-01-01

    Low cost adsorption technology offers high potential to clean-up laundry rinsing water. From an earlier selection of adsorbents, layered double hydroxide (LDH) and granular activated carbon (GAC) proved to be interesting materials for the removal of anionic surfactant, linear alkyl benzene sulfonate

  17. Protolytic properties and complexation of DL-alpha-alanine and DL-alpha-valine and their dipeptides in aqueous and micellar solutions of surfactants

    NARCIS (Netherlands)

    Chernyshova, O. S.; Boychenko, Oleksandr; Abdulrahman, H.; Loginova, L. P.

    2013-01-01

    In this work we investigated the effect of the micellar media of anionic (sodium dodecylsulfate, SDS), cationic (cetylpiridinium chloride, CPC) and non-ionic (Brij-35) surfactants on the protolytic properties of amino acids DL-alpha-alanine, DL-alpha-valine and dipeptides L-alpha-alanyl-L-alpha-alan

  18. Freely dissolved concentrations of anionic surfactants in seawater solutions: optimization of the non-depletive solid-phase microextraction method and application to linear alkylbenzene sulfonates.

    NARCIS (Netherlands)

    Rico Rico, A.; Droge, S.T.J.; Widmer, D.; Hermens, J.L.M.

    2009-01-01

    A solid-phase microextraction method (SPME) has been optimized for the analysis of freely dissolved anionic surfactants, namely linear alkylbenzene sulfonates (LAS), in seawater. An effect of the thermal conditioning treatment on the polyacrylate fiber coating was demonstrated for both uptake kineti

  19. Experimental study of surfactant transfer in fluid systems in microgravity conditions

    Science.gov (United States)

    Kostarev, K. G.; Levtov, V. L.; Romanov, V. V.; Shmyrov, A. V.; Viviani, A.

    2010-02-01

    The paper presents the results of the space experiment studying the process of surfactant dissolution from a binary fluid drop in microgravity conditions. The experiment was performed during the flight of the space satellite "Foton M-3" in September 2007. Investigation of the surfactant diffusion was made using a new original setup based on the interferometric method. The experimental cuvette represented a thin Hele-Shaw cell filled with water, which surrounded a drop in the form of a short liquid cylinder with a free lateral surface. The drop consisted of a binary mixture, in which one of the components was the surfactant easily dissolved in water. The use of interferometry made it possible to visualize and investigate evolution of the surfactant distributions and the flow structures in the drop and the surrounding liquid. The characteristic stages of the dissolution process were identified, and the rate of the concentration front propagation was defined. It was shown that in microgravity conditions the process of surfactant diffusion through the interface did not initiate an intensive solutal Marangoni convection as contrasted to the case of terrestrial simulation. The observed phenomenon has its origins in the long-lived fields of surfactant concentration formed near the interface due to the absence of the gravitational mechanisms of motion and large characteristic time of admixture diffusion which is hundreds of times longer than the time of thermal diffusion.

  20. ATMOSPHERIC CHEMISTRY FOR ASTROPHYSICISTS: A SELF-CONSISTENT FORMALISM AND ANALYTICAL SOLUTIONS FOR ARBITRARY C/O

    Energy Technology Data Exchange (ETDEWEB)

    Heng, Kevin; Tsai, Shang-Min [University of Bern, Center for Space and Habitability, Sidlerstrasse 5, CH-3012, Bern (Switzerland); Lyons, James R., E-mail: kevin.heng@csh.unibe.ch [Arizona State University, School of Earth and Space Exploration, Bateman Physical Sciences, Tempe, AZ 85287-1404 (United States)

    2016-01-10

    We present a self-consistent formalism for computing and understanding the atmospheric chemistry of exoplanets from the viewpoint of an astrophysicist. Starting from the first law of thermodynamics, we demonstrate that the van’t Hoff equation (which describes the equilibrium constant), Arrhenius equation (which describes the rate coefficients), and procedures associated with the Gibbs free energy (minimization, rescaling) have a common physical and mathematical origin. We address an ambiguity associated with the equilibrium constant, which is used to relate the forward and reverse rate coefficients, and restate its two definitions. By necessity, one of the equilibrium constants must be dimensionless and equate to an exponential function involving the Gibbs free energy, while the other is a ratio of rate coefficients and must therefore possess physical units. We demonstrate that the Arrhenius equation takes on a functional form that is more general than previously stated without recourse to tagging on ad hoc functional forms. Finally, we derive analytical models of chemical systems, in equilibrium, with carbon, hydrogen, and oxygen. We include acetylene and are able to reproduce several key trends, versus temperature and carbon-to-oxygen ratio, published in the literature. The rich variety of behavior that mixing ratios exhibit as a function of the carbon-to-oxygen ratio is merely the outcome of stoichiometric book-keeping and not the direct consequence of temperature or pressure variations.

  1. Coadsorption of low-molecular weight aromatic and aliphatic alcohols and acids with the cationic surfactant, CTAB, on silica surfaces.

    Science.gov (United States)

    Wangchareansak, Thipvaree; Keniry, Max A; Liu, Guangming; Craig, Vincent S J

    2014-06-17

    We have investigated the coadsorption of a range of small molecules with the cationic surfactant CTAB to silica surfaces over a range of concentrations and CTAB to solute ratios and compared the coadsorption with adsorption in the presence of the salicylate ion. We find that molecules with aromatic character and molecules with double bonds are most favorably adsorbed, and we attribute this to cation-π bonding between the surfactant headgroups and the π orbitals of the unsaturated bonds of the solute molecules. The adsorption is complex and depends on chemical interactions between the solute molecules and the surfactant, which are highly specific to the structure of the solute. To improve our understanding of the specifics of these interactions, we have performed one-dimensional rotating frame Overhauser spectroscopy (ROESY) nuclear magnetic resonance experiments. These experiments show the complexity of the intermolecular interactions and can be used to determine the position of the solute molecule with regard to the CTAB molecules in the adsorbed aggregates. The ROESY spectrum for the salicylate anion is distinct from those of the other solute molecules and suggests that the anions are dimerizing. Along with the cation-π bonding between the dimers, this provides a model for the strong influence that salicylate has on adsorption, micellar structure, and viscoelasticity. The ROESY data indicate that the catechol molecule interacts with all parts of the surfactant alkane chains such that they wrap around the molecule, but this has little effect on the interfacial curvature or aggregate shape. More intense isophthalic acid-CTAB intermolecular ROEs compared to those of other aromatic solutes are consistent with an interaction between isophthalic acid and the headgroups of two surfactant molecules that slows the intramicellar motion of isophthalic acid. Differences in interactions between solute molecules and the aliphatic surfactant chains do not result in changes

  2. Use of electrical impedance spectroscopy as a practical method of investigating the formation of aggregates in aqueous solutions of dyes and surfactants.

    Science.gov (United States)

    de Oliveira, Helinando P; de Melo, Celso P

    2011-06-01

    Molecular aggregation plays a key role in the physicochemical properties of dyes and surfactants. In this work, we show that electrical impedance spectroscopy (EIS) provides a practical method for the investigation of processes such as micellization in surfactants and dye dimerization. The electrical characterization of the structural phase transitions associated with aggregation events in these systems allows an accurate and direct determination of relevant parameters such as the corresponding critical concentrations for micelle formation and dimerization of these types of molecules, without the need of recurring to the use of auxiliary probe or reporter molecules. Because of its competitive advantages with respect to currently used methods (such as conductimetry and spectroscopic techniques), we argue that when implemented along the procedures described in this work, EIS becomes a simple and convenient technique for the characterization of aggregation processes in soft matter.

  3. Alkanediyl-α, ω-bis (dimethyl cetylammonium bromide gemini surfactants as novel corrosion inhibitors for mild steel in formic acid

    Directory of Open Access Journals (Sweden)

    Mohammad Mobin

    2012-12-01

    Full Text Available Gemini surfactants, butanediyl 1,4-bis(dimethyl cetylammonium bromide, pentanediyl 1,5 - bis (dimethyl cetylammonium bromide and hexanediyl 1,6 - bis (dimethyl cetylammonium bromide from Alkanediyl-α, ω-bis (dimethyl cetylammonium bromide series were synthesized in laboratory and were characterized by using Nuclear Magnetic Resonance (NMR spectroscopy. The surfactants were tested as corrosion inhibitors for mild steel in 20% formic acid. The influence of surfactants on mild steel corrosion inhibition was investigated by measuring the corrosion rate of mild steel in their absence and presence by weight loss measurements, solvent analysis of iron ions into the test solution and potentiodynamic polarization measurements. The surface morphology of the corroded steel samples in presence and absence of surfactants was evaluated by using Scanning Electron Microscopy (SEM. The synthesized gemini surfactants performed as excellent corrosion inhibitor, the inhibition efficiency (IE being in the range of 76.66-97.41%. The IE of surfactants is slightly affected by the spacer length. The IE increased with increase in surfactant concentration and temperature. The adsorption of gemini surfactants on the steel surface was found to obey Langmuir adsorption isotherm. The results of the potentiodynamic polarization studies are consistent with the results of weight loss studies.

  4. Photoisomerization of merocyanine 540 in polymer-surfactant aggregate

    Indian Academy of Sciences (India)

    Sobhan Sen; Dipankar Sukul; Partha Dutta; Kankan Bhattacharyya

    2002-02-01

    Photoisomerization of merocyanine 540 (MC540) in a polymer-surfactant aggregate is studied using picosecond time resolved emission spectroscopy. The aggregate consists of the polymer, poly(vinylpyrrolidone) (PVP) and the surfactant, sodium dodecyl sulphate (SDS). With increase in the concentration of SDS in an aqueous solution of MC540 containing PVP, the emission quantum yield and lifetime of MC540 increase markedly. This indicates marked retardation in the nonradiative photoisomerization process of MC540, when it binds to the polymersurfactant aggregate. The critical association concentration of SDS for binding to PVP has been found to be 0.5 mM. This is about 16 times lower than the CMC of SDS in pure water (8 mM).

  5. New mechanisms for phase separation in polymer-surfactant mixtures

    NARCIS (Netherlands)

    Currie, E.P.K.; Cohen Stuart, M.A.; Borisov, O.V.

    2000-01-01

    The cooperative association of ionic surfactants with polymer chains leads to quite novel features in the phase behaviour of polymer solutions. Using an analytic mean-field model, we analyze phase equilibria in solutions of neutral polymers mixed with ionic surfactants. We predict the possibilities

  6. On the mesoscopic origins of high viscosities in some polyelectrolyte-surfactant mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Hoffmann, Ingo, E-mail: ingo.hoffmann@tu-berlin.de [Stranski-Laboratorium für Physikalische und Theoretische Chemie, Institut für Chemie, Technische Universität Berlin, Straße des 17. Juni 124, Sekr. TC 7, D-10623 Berlin (Germany); Institut Max von Laue-Paul Langevin (ILL), F-38042 Grenoble Cedex 9 (France); Farago, Bela; Schweins, Ralf; Falus, Peter; Sharp, Melissa [Institut Max von Laue-Paul Langevin (ILL), F-38042 Grenoble Cedex 9 (France); Prévost, Sylvain [Stranski-Laboratorium für Physikalische und Theoretische Chemie, Institut für Chemie, Technische Universität Berlin, Straße des 17. Juni 124, Sekr. TC 7, D-10623 Berlin (Germany); Helmholtz-Zentrum Berlin, D-14109 Berlin (Germany); Gradzielski, Michael, E-mail: michael.gradzielski@tu-berlin.de [Stranski-Laboratorium für Physikalische und Theoretische Chemie, Institut für Chemie, Technische Universität Berlin, Straße des 17. Juni 124, Sekr. TC 7, D-10623 Berlin (Germany)

    2015-08-21

    Oppositely charged polyelectrolyte (PE) surfactant mixtures allow the control of rheological parameters of a solution even at fairly low concentrations. For example, addition of 0.3 wt. % of anionic surfactant to a 1 wt. % solution of the polycation JR 400 increases the viscosity by 4 orders of magnitude. Recently, we could show that this increase is related to the formation of mixed, rod-like PE/surfactant aggregates which interconnect several polyelectrolyte chains [Hoffmann et al., Europhys. Lett. 104, 28001 (2013)]. In this paper, we refine our structural model of the aggregates to obtain a more consistent picture of their internal structure for different anionic surfactants. Combining small angle neutron scattering (SANS) and neutron spin-echo (NSE) allows us to determine the size of the aggregates. By comparing different contrasts, the internal structure of the aggregates can be elucidated and it is seen that the PE in the aggregates retains a relatively high freedom of movement. We proceeded to investigate the influence of the surfactant concentration and the surfactant type on structure and dynamics of the mixed aggregates. It is seen that the structural parameters of the aggregates depend very little on the surfactant concentration and headgroup. However, it is crucial to incorporate a sufficient amount of PE in the aggregates to increase the viscosity of the aggregates. By comparing viscous samples at 1 wt. % PE concentration with samples at a PE concentration of 0.3 wt. %, where no significant increase in viscosity is observed, we find that similar aggregates are formed already at this lower PE concentrations. However, the amount of PE incorporated in them is insufficient to interconnect several PE chains and therefore, they do not increase viscosity. So, our detailed investigation combining contrast variation SANS and NSE does not only allow to explain the viscosity behavior but also to deduced detailed information regarding the structures and

  7. Modeling of surfactant transport and adsorption in porous media

    Energy Technology Data Exchange (ETDEWEB)

    Chung, F.T.H.

    1991-04-01

    When surfactant solution is flowing in a reservoir formation, surfactants will be diluted by flow dispersion, retained in dead-end pores, adsorbed on rock surfaces, or precipitated due to ion exchange. The loss of surfactant will be detrimental to the performance of gas foam. Information of surfactant concentration profiles in reservoir formations is essential for gas foaming technique development. The major objective of this research is to investigate with mathematical models the transport and dynamic adsorption of surfactants in porous media. The mathematical models have taken into account the convection, dispersion, capacitance, and adsorption effects on concentrations of surfactants. Numerical methods and computer programs have been developed which can be used to match experimental results and to determine the characterization parameters in the models. The models can be included in foam simulation programs to calculate surfactant concentration profiles in porous media. A flow experimental method was developed to measure the effluent surfactant concentration, which will be used to determine the model parameters. Commercial foaming agent Alipal CD-128 was used in this study. Equilibrium adsorption and surfactant precipitation have been tested. Tracer solutions with a nonadsorbing solute such as dextrose and sucrose were used to determine the dispersion parameters for the experimental sandpack; thus, the adsorption of the surfactant in the test sand can be identified with an adequate model. 49 refs., 21 figs.

  8. The ability of single-chain surfactants to emulsify an aqueous-based liquid crystal oscillates with odd-even parity of alkyl-chain length.

    Science.gov (United States)

    Varghese, Nisha; Shetye, Gauri S; Yang, Sijie; Wilkens, Stephan; Smith, Robert P; Luk, Yan-Yeung

    2013-12-15

    The physical properties of many organic molecules often oscillate when the number of carbons in their aliphatic chains changes from odd to even. This odd-even effect for single-chain surfactants in solution is rarely observed. Here, we report the ability of single-chain surfactants to emulsify a class of non-amphiphilic organic salts, disodium cromoglycate (5'DSCG) oscillates as a function of the odd or even number of the aliphatic carbons. This system provides a water-in-oil-in-water emulsion, in which aqueous droplets of 5'DSCG in liquid crystal phases are coated with single-chain surfactants in a bulk carrying aqueous solution. For both surfactants of [Formula: see text] and CH3(CH2)nCOO(-)Na(+), the ability to emulsify 5'DSCG molecules in water is stronger for surfactants with an odd number of sp(3)-hybridized carbon atoms in the aliphatic chains than those with an even number. This observed odd-even effect is consistent with the notion that conventional micelles possess a core of randomly arranged surfactant hydrocarbon tails. However, this water-in-oil-in-water resembles a vesicle system in which the surfactants assemble in a highly ordered structure that separates two aqueous systems. These new self-assembled phases have potential application in the formulation and design of new organic soft materials.

  9. Temperature Triggered Structural Transitions in Surfactant organized Self Assemblies

    Science.gov (United States)

    Rose, J. Linet; Balamurugan, S.; Sajeevan, Ajin C.; Sreejith, Lisa

    2011-10-01

    Preparation & characterization of tunable fluids is an emerging area with potential application in many fields. Surfactants self assemble in aqueous solution to give a rich variety of phase structures, the size and shape of which can be tuned by additives like salts, alcohols, amines, aromatics etc or external stimuli such as light, temperature etc. The addition of long chain aliphatic alcohol has significant influence on the surfactant aggregation, as it promotes morphological growth of micelles. The cationic surfactant, Cetyl Trimethyl Ammonium Bromide (CTAB) with nonanol in presence of potassium bromide (KBr) shows thermo tunable viscosity behaviour and optical switching behaviour. The solution is visually observed to transform from a turbid and less viscous phase at low temperature to clear and considerably viscous phase at high temperature. Temperature induced changes in turbidity and viscosity are consistent with the transition from vesicle to worm like micelle. It is also worth emphasizing that the transition is thermo reversible, so that vesicles that are disrupted into micelles upon heating can be reformed upon cooling. The thermo tunable transition from turbid to transparent state and the concomitant changes in viscosity are promising for the use in smart windows, monitoring of tumor growth or in other stimuli based application.

  10. Influence of surfactants in forced dynamic dewetting.

    Science.gov (United States)

    Henrich, Franziska; Fell, Daniela; Truszkowska, Dorota; Weirich, Marcel; Anyfantakis, Manos; Nguyen, Thi-Huong; Wagner, Manfred; Auernhammer, Günter K; Butt, Hans-Jürgen

    2016-09-20

    In this work we show that the forced dynamic dewetting of surfactant solutions depends sensitively on the surfactant concentration. To measure this effect, a hydrophobic rotating cylinder was horizontally half immersed in aqueous surfactant solutions. Dynamic contact angles were measured optically by extrapolating the contour of the meniscus to the contact line. Anionic (sodium 1-decanesulfonate, S-1DeS), cationic (cetyl trimethylammonium bromide, CTAB) and nonionic surfactants (C4E1, C8E3 and C12E5) with critical micelle concentrations (CMCs) spanning four orders of magnitude were used. The receding contact angle in water decreased with increasing velocity. This decrease was strongly enhanced when adding surfactant, even at surfactant concentrations of 10% of the critical micelle concentration. Plots of the receding contact angle-versus-velocity almost superimpose when being plotted at the same relative concentration (concentration/CMC). Thus the rescaled concentration is the dominating property for dynamic dewetting. The charge of the surfactants did not play a role, thus excluding electrostatic effects. The change in contact angle can be interpreted by local surface tension gradients, i.e. Marangoni stresses, close to the three-phase contact line. The decrease of dynamic contact angles with velocity follows two regimes. Despite the existence of Marangoni stresses close to the contact line, for a dewetting velocity above 1-10 mm s(-1) the hydrodynamic theory is able to describe the experimental results for all surfactant concentrations. At slower velocities an additional steep decrease of the contact angle with velocity was observed. Particle tracking velocimetry showed that the flow profiles do not differ with and without surfactant on a scales >100 μm.

  11. Solvent Property Induced Morphological Changes of ABA Amphiphilic Triblock Copolymer Micelles in Dilute Solution: A Self-consistent Field Simulation Study

    Institute of Scientific and Technical Information of China (English)

    Juan-juan Fan; Yuan-yuan Han; Jie Cui

    2014-01-01

    The morphological changes of ABA amphiphilic triblock copolymer micelles in dilute solution were systematically studied by tuning the solvent property using self-consistent field simulation.The solvent property was tuned by changing the Flory-Huggins interaction parameters between each type of blocks and solvent,respectively.The simulation results show that by changing the solvent properties,a series of micelle morphologies such as vesicle,cage-like,ring-shaped,rod-like and spherical micelle morphologies can be obtained.Variations of the free energy of the solution system and the surface area of micelles with the Flory-Huggins interaction parameters were calculated to better understand the effect of solvent property on micelle morphologies.In addition,a phase diagram showing the morphological changes of micelles with the Flory-Huggins interaction parameters is provided.

  12. First- and second-order transitions for a superconducting cylinder in a magnetic field obtained from a self-consistent solution of the Ginzburg-Landau equations

    Energy Technology Data Exchange (ETDEWEB)

    Zharkov, G. F.

    2001-06-01

    Based on self-consistent solution of nonlinear GL equations, the phase boundary is found, which divides the regions of first- and second-order phase transitions to normal state of a superconducting cylinder of radius R, placed in magnetic field and remaining in the state of fixed vorticity m. This boundary is a complicated function of the parameters (m,R,{kappa}) ({kappa} is the GL parameter), which does not coincide with the simple phase boundary {kappa}=1/{radical}2, dividing the regions of first- and second-order phase transitions in infinite (open) superconducting systems.

  13. Solvent dependence of Stokes shift for organic solute-solvent systems: A comparative study by spectroscopy and reference interaction-site model-self-consistent-field theory.

    Science.gov (United States)

    Nishiyama, Katsura; Watanabe, Yasuhiro; Yoshida, Norio; Hirata, Fumio

    2013-09-01

    The Stokes shift magnitudes for coumarin 153 (C153) in 13 organic solvents with various polarities have been determined by means of steady-state spectroscopy and reference interaction-site model-self-consistent-field (RISM-SCF) theory. RISM-SCF calculations have reproduced experimental results fairly well, including individual solvent characteristics. It is empirically known that in some solvents, larger Stokes shift magnitudes are detected than anticipated on the basis of the solvent relative permittivity, ɛr. In practice, 1,4-dioxane (ɛr = 2.21) provides almost identical Stokes shift magnitudes to that of tetrahydrofuran (THF, ɛr = 7.58), for C153 and other typical organic solutes. In this work, RISM-SCF theory has been used to estimate the energetics of C153-solvent systems involved in the absorption and fluorescence processes. The Stokes shift magnitudes estimated by RISM-SCF theory are ∼5 kJ mol(-1) (400 cm(-1)) less than those determined by spectroscopy; however, the results obtained are still adequate for dipole moment comparisons, in a qualitative sense. We have also calculated the solute-solvent site-site radial distributions by this theory. It is shown that solvation structures with respect to the C-O-C framework, which is common to dioxane and THF, in the near vicinity (∼0.4 nm) of specific solute sites can largely account for their similar Stokes shift magnitudes. In previous works, such solute-solvent short-range interactions have been explained in terms of the higher-order multipole moments of the solvents. Our present study shows that along with the short-range interactions that contribute most significantly to the energetics, long-range electrostatic interactions are also important. Such long-range interactions are effective up to 2 nm from the solute site, as in the case of a typical polar solvent, acetonitrile.

  14. Solute partitioning in aqueous surfactant assemblies: comparison of hydrophobic-hydrophilic interactions in micelles, alcohol-swollen micelles, microemulsions, and synthetic vesicles

    Energy Technology Data Exchange (ETDEWEB)

    Russell, J.C.; Whitten, D.G.

    1982-11-03

    The structures of anionic assemblies including sodium lauryl sulfate (SLS) micelles, alcohol-swollen SLS micelles, microemulsions, and vesicles of a mixture of dipalmitoyllecithin and dicetyl phosphate are investigated by using the ground-state complexation of a hydrophilic quencher (methyl viologen) with several hydrophobic fluorescent probes, including surfactant stilbenes and 1,4-diphenylbutadiene. In SLS micelles this complexation can be decreased nearly an order of magnitude by addition of 1-heptanol, indicating that the structure of the micelle can be adjusted from the highly open structure of the pure micelle to a much more closed structure in which hydrophobic solubilizates can be sequestered from hydrophilic reagents bound to the surface. The fluorescence quenching process in anionic vesicles is strongly dependent on temperature; at low temperatures quenching occurs, while at higher temperatures addition of methyl viologen appears to increase the stilbene fluorescence, indicating that the dicationic quencher binds to the vesicle surface, increasing the order of the system. These results indicate that the degree of organization of surfactant systems can be adjusted by simple changes in composition. 33 references.

  15. The hydrophobicity of silicone-based oils and surfactants and their use in reactive microemulsions.

    Science.gov (United States)

    Castellino, Victor; Cheng, Yu-Ling; Acosta, Edgar

    2011-01-01

    In this work, for the first time, the Hydrophilic-Lipophilic Difference (HLD) framework for microemulsion formulation has been applied to silicone oils and silicone alkyl polyether surfactants. Based on the HLD equations and recently introduced mixing rules, we have quantified the hydrophobicity of the oils according to the equivalent alkane carbon number (EACN). We have found that, in a reference system containing sodium dihexyl sulfosuccinate (SDHS) as the surfactant, 0.65 centistoke (cSt) and 3.0 cSt silicone oils behave like n-dodecane and n-pentadecane, respectively. Silicone alkyl polyether surfactants were found to have characteristic curvatures ranging 3.4-18.9, exceeding that of most non-ionic surfactants. The introduction of methacrylic acid (MAA) and hydroxyethyl methacrylate (HEMA) to the aqueous phase caused a significant negative shift in HLD, indicative of an aqueous phase that is less hydrophilic than pure water. The more hydrophobic surfactants (largest positive curvatures) were used in order to compensate for this effect. These findings have led to the formulation of bicontinuous microemulsions (μEs) containing silicone oil, silicone alkyl polyether and reactive monomers in aqueous solution. Ternary phase diagrams of these systems revealed the potential for silicone-containing polymer composites with bicontinuous morphologies. These findings have also helped to explain the phase behavior of formulations previously reported in literature, and could help in providing a systematic, consistent approach to future silicone oil based microemulsion formulation.

  16. The Optimization of Aniline Adsorption from Aqueous Solutions by Raw Bentonite and Bentonite Modified with Cationic Surfactants Using the Taguchi Model

    Directory of Open Access Journals (Sweden)

    F. Taherkhani

    2015-04-01

    Full Text Available Introduction & Objectives: Aniline is an organic compound widely used in various industries. The release of this compound has had various environmental impacts. Thus, the assessment of efficient and practical methods for the removal of aniline from wastewater of these industries is remarkable. Taguchi model is a model for the analysis of experiments, that predicts both the effects of each factors and the optimum level of them using a certain number of experiment. The purpose of this study was the optimization of aniline adsorption on the raw and modified bentonite with a cationic surfactant using Taguchi model. Materials & Methods: In this experimental study, the raw bentonite and modified bentonite was prepared in a few steps. Then, 4 main factors (i.e. pollutant concentration, contact time, pH, and adsorbent dosage on 4 levels were selected by Matrix L16 trials and the experiments were conducted in this matrix. The factors were also ranked based on the R-value. Then , the data were analyzed with Minitab 17 software. Finally, the adsorption of aniline on raw and modified bentonite was determined in optimal conditions. Results: The optimization of adsorption process using Taguchi model showed that the factors of importance for optimizing respectively were: contact time of 360 minutes, pH =10 pH, ani-line initial concentration of 300 mg/L and adsorbent dosages of 40 g/L. The maximum ad-sorption of aniline onto raw bentonite and modified bentonite with cationic surfactant in op-timal conditions were determined 81.86 and 8.75, respectively. The results revealed that Freundlich isotherm and pseudo-second-order kinetic model provided a better ?t to the ex-perimental data. Conclusion: The results showed that the bentonite modified with cationic surfactant is efficient in the removal of aniline. At the same time, since bentonite is cheap and easily accessible ,it is considered a desirable adsorbant. (Sci J Hamadan Univ Med Sci 2015; 22 (1:55-64

  17. Thermodynamic and Spectroscopic Investigation of Interactions between Reactive Red 223 and Reactive Orange 122 Anionic Dyes and Cetyltrimethyl Ammonium Bromide (CTAB Cationic Surfactant in Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Muhammad Irfan

    2014-01-01

    Full Text Available The present study describes the conductometric and spectroscopic study of the interaction of reactive anionic dyes, namely, reactive red 223 and reactive orange 122 with the cationic surfactant cetyltrimethyl ammonium bromide (CTAB. In a systematic investigation, the electrical conductivity data was used to calculate various thermodynamic parameters such as free energy (ΔG, enthalpy (ΔH, and the entropy (ΔS of solubilization. The trend of change in these thermodynamic quantities indicates toward the entropy driven solubilization process. Moreover, the results from spectroscopic data reveal high degree of solubilization, with strong interactions observed in the cases of both dyes and the CTAB. The spontaneous nature of solubilization and binding was evident from the observed negative values of free energies (ΔGp and ΔGb.

  18. Thermodynamic and spectroscopic investigation of interactions between reactive red 223 and reactive orange 122 anionic dyes and cetyltrimethyl ammonium bromide (CTAB) cationic surfactant in aqueous solution.

    Science.gov (United States)

    Irfan, Muhammad; Usman, Muhammad; Mansha, Asim; Rasool, Nasir; Ibrahim, Muhammad; Rana, Usman Ali; Siddiq, Mohammad; Zia-Ul-Haq, Muhammad; Jaafar, Hawa Z E; Khan, Salah Ud-Din

    2014-01-01

    The present study describes the conductometric and spectroscopic study of the interaction of reactive anionic dyes, namely, reactive red 223 and reactive orange 122 with the cationic surfactant cetyltrimethyl ammonium bromide (CTAB). In a systematic investigation, the electrical conductivity data was used to calculate various thermodynamic parameters such as free energy (ΔG), enthalpy (ΔH), and the entropy (ΔS) of solubilization. The trend of change in these thermodynamic quantities indicates toward the entropy driven solubilization process. Moreover, the results from spectroscopic data reveal high degree of solubilization, with strong interactions observed in the cases of both dyes and the CTAB. The spontaneous nature of solubilization and binding was evident from the observed negative values of free energies (ΔG p and ΔG b).

  19. Surfactants in tribology

    CERN Document Server

    Biresaw, Girma

    2014-01-01

    Surface science and tribology play very critical roles in many industries. Manufacture and use of almost all consumer and industrial products rely on the application of advanced surface and tribological knowledge. The fourth in a series, Surfactants in Tribology, Volume 4 provides an update on research and development activities connecting surfactants and tribological phenomena. Written by renowned subject matter experts, the book demonstrates how improved design of surfactants can be harnessed to control tribological phenomena. Profusely illustrated and copiously referenced, the chapters also

  20. The role of surfactants in Köhler theory reconsidered

    Directory of Open Access Journals (Sweden)

    R. Sorjamaa

    2004-05-01

    Full Text Available Atmospheric aerosol particles typically consist of inorganic salts and organic material. The inorganic compounds as well as their hygroscopic properties are well defined, but the effect of organic compounds on cloud droplet activation is still poorly characterized. The focus of the present study is in the organic compounds that are surface active i.e. they concentrate on droplet surface and decrease droplet surface tension. Gibbsian surface thermodynamics were used to find out how partitioning in binary and ternary aqueous solutions affects the droplet surface tension and the droplet bulk concentration in droplets large enough to act as cloud condensation nuclei. Sodium dodecyl sulfate was used as a model compound together with sodium chloride to find out the effect the correct evaluation of surfactant partitioning has on the solute effect (Raoult effect. While the partitioning is known to lead to higher surface tension compared to a case in which partitioning is neglected, the present results show that the partitioning also alters the solute effect, and that the change is large enough to further increase the critical supersaturation and hence decrease the droplet activation. The fraction of surfactant partitioned to droplet surface increases with decreasing droplet size, which suggests that surfactants might enhance the activation of larger particles relatively more thus leading to less dense clouds. Cis-pinonic acid-ammonium sulfate aqueous solution was studied in order to relate the partitioning to more realistic atmospheric situation and to find out the combined effects of dissolution and partitioning behaviour. The results show that correct partitioning consideration alters the shape of the Köhler curve when compared to a situation in which the partitioning is neglected either completely or in the Raoult effect.

  1. Simulation of 3D mesoscale structure formation in concentrated aqueous solution of the triblock polymer surfactants (ethylene oxide)(13)(propylene oxide)(30)(ethylene oxide)(13) and (propylene oxide)(19)(ethylene oxide)(33)(propylene oxide)(19). Application of dynamic mean-field density functional theory

    NARCIS (Netherlands)

    van Vlimmeren, BAC; Maurits, NM; Zvelindovsky, AV; Sevink, GJA; Fraaije, JGEM

    1999-01-01

    We simulate the microphase separation dynamics of aqueous solutions of the triblock polymer surfactants (ethylene oxide)(13)(propylene oxide)(30)(ethylene oxide)(13) and (propylene oxide)(19)(ethylene oxide)(33)(propylene oxide)(19) by a dynamic variant of mean-field density functional theory for

  2. Simulation of 3D mesoscale structure formation in concentrated aqueous solution of the triblock polymer surfactants (ethylene oxide)(13)(propylene oxide)(30)(ethylene oxide)(13) and (propylene oxide)(19)(ethylene oxide)(33)(propylene oxide)(19). Application of dynamic mean-field density functional theory

    NARCIS (Netherlands)

    van Vlimmeren, BAC; Maurits, NM; Zvelindovsky, AV; Sevink, GJA; Fraaije, JGEM

    1999-01-01

    We simulate the microphase separation dynamics of aqueous solutions of the triblock polymer surfactants (ethylene oxide)(13)(propylene oxide)(30)(ethylene oxide)(13) and (propylene oxide)(19)(ethylene oxide)(33)(propylene oxide)(19) by a dynamic variant of mean-field density functional theory for Ga

  3. POLYMERIC SURFACTANT STRUCTURE

    Institute of Scientific and Technical Information of China (English)

    P.M. Saville; J.W. White

    2001-01-01

    Polymeric surfactants are amongst the most widespread of all polymers. In nature, proteins and polysaccharides cause self organization as a result of this surfactancy; in industry, polymeric surfactants play key roles in the food, explosives and surface coatings sectors. The generation of useful nano- and micro-structures in films and emulsions as a result of polymer amphiphilicity and the application of mechanical stress is discussed. The use of X-ray and neutron small angle scattering and reflectivity to measure these structures and their dynamic properties will be described. New results on linear and dendritic polymer surfactants are presented.

  4. Aggregation of sulfosuccinate surfactants in water

    Energy Technology Data Exchange (ETDEWEB)

    Magid, L.J.; Daus, K.A.; Butler, P.D.; Quincy, R.B.

    1983-12-22

    The aggregation of sodium di-n-alkyl sulfosuccinates in water (H/sub 2/O and D/sub 2/O at 45/sup 0/C) has been investigated. A self-consistent picture of the dependence of sodium ion binding on surfactant concentration is obtained from emf measurements, conductimetry, and small-angle neutron scattering (SANS) measurements. The concentration dependence of the micellar agregation number for the sulfosuccinates and related double-tailed surfactants depends markedly on surfactant solubility. A sphere-to-disk transition in micellar shape, which might have been expected as a precursor to formation of a lamellar mesophase, was not observed as the surfactant concentration was increased. 8 figures, 2 tables.

  5. Surfactant Sector Needs Urgent Readjustment

    Institute of Scientific and Technical Information of China (English)

    Huang Hongzhou

    2007-01-01

    @@ Surfactant industrial system has been basically established After 50 years' development, China has already established a surfactant industrial system with a relatively complete product portfolio and can produce 4714 varieties of surfactants in cationic,anionic, nonionic and amphoteric categories.

  6. Interactions in Calcium Oxalate Hydrate/Surfactant Systems.

    Science.gov (United States)

    Sikiric; Filipovic-Vincekovic; Babic-Ivancić Vdović Füredi-Milhofer

    1999-04-15

    Phase transformation of calcium oxalate dihydrate (COD) into the thermodynamically stable monohydrate (COM) in anionic (sodium dodecyl sulfate (SDS)) and cationic (dodecylammonium chloride) surfactant solutions has been studied. Both surfactants inhibit, but do not stop transformation from COD to COM due to their preferential adsorption at different crystal faces. SDS acts as a stronger transformation inhibitor. The general shape of adsorption isotherms of both surfactants at the solid/liquid interface is of two-plateau-type, but differences in the adsorption behavior exist. They originate from different ionic and molecular structures of crystal surfaces and interactions between surfactant headgroups and solid surface. Copyright 1999 Academic Press.

  7. Hydrophobically Modified Polyelectrolytes: V. Interaction of Fluorocarbon Modified Poly (acrylic acid) with Various Added Surfactants

    Institute of Scientific and Technical Information of China (English)

    ZHOU,Hui(周晖); SONG,Guo-Qaiang(宋国强); GUO,Jin-Feng(郭金峰); ZHANG,Yun-xiang (章云祥); DIEING,Reinhold; MA,Lian(马莲); HAEUSSLING,Lukas

    2001-01-01

    The interactions between fiuorocarbon-medified pol(sodium acrylate) and various kinds of added surfactant have been studied by means of viscometric measurement. Association behavior was found in both hydrogenated and fluorinated anionic, nonionic and cationic surfactants. Among them, the interactions between fluorocarbon-modified poly ( sodium acrylate) and cationic surfactants are the strongest, owing to the cooperation of both electrostatic attractions and hydrophobic associations. The anionic surfactants have the weakest effects on the solution properties because of the existence of unfavorable electrostatic repulsion. The hydrophobic interactions between copolymers and fluorinated surfactants are much stronger than those between copolymers and hydrogenated surfactants.

  8. Alkyl-imidazolium glycosides: non-ionic-cationic hybrid surfactants from renewable resources.

    Science.gov (United States)

    Salman, Abbas Abdulameer; Tabandeh, Mojtaba; Heidelberg, Thorsten; Hussen, Rusnah Syahila Duali; Ali, Hapipah Mohd

    2015-08-14

    A series of surfactants combining carbohydrate and imidazolium head groups were prepared and investigated on their assembly behavior. The presence of the imidazolium group dominated the interactions of the surfactants, leading to high CMCs and large molecular surface areas, reflected in curved rather than lamellar surfactant assemblies. The carbohydrate, on the other hand, stabilized molecular assemblies slightly and reduced the surface tension of surfactant solutions considerably. A comparative emulsion study discourages the use of pure alkyl imidazolium glycosides owing to reduced assembly stabilities compared with APGs. However, the surfactants are believed to have potential as component in carbohydrate based surfactant mixtures.

  9. Influence of metacide - surfactant complexes on agricultural crops

    Directory of Open Access Journals (Sweden)

    Orynkul Esimova

    2014-12-01

    Full Text Available The complexes based on surfactants and polyhexamethyleneguanidine hydrochloride (metacide are important for agriculture. This paper considers compositions of known bactericidal metacide with different surfactants: anionic surfactant sodium dodecylsulphate (DDSNa and nonionic surfactant Tween 80 (monooleate of oxyethylenated anhydrosorbitols. The effect of individual components and associates of metacide and surfactants on productivity and infection of cereals was studied. According to the study, the highest productivity and infection rate were shown by the associate of metacide and Tween-80. At concentration of Tween-80 in aqueous solution equal to 0.001% in combination with metacide, efficiency was 98% at 0% infection. The surface tension and the wetting of metacide, DDSNa, Tween-80, and associates of metacide with surfactants were studied. In comparison with individual components, metacide-DDSNa and metacide-Tween-80 associates have higher surface activity.

  10. Gemini imidazolium surfactants: synthesis and their biophysiochemical study.

    Science.gov (United States)

    Kamboj, Raman; Singh, Sukhprit; Bhadani, Avinash; Kataria, Hardeep; Kaur, Gurcharan

    2012-08-21

    New gemini imidazolium surfactants 9-13 have been synthesized by a regioselective epoxy ring-opening reaction under solvent-free conditions. The surface properties of these new gemini surfactants were evaluated by surface tension and conductivity measurements. These surfactants have been found to have low critical micelle concentration (cmc) values as compared to other categories of gemini cationic surfactants and also showed the tendency to form premicellar aggregates in solution at sufficiently low concentration below their cmc values. The thermal degradation of these surfactants was determined by thermograviometry analysis (TGA). These new cationic surfactants have a good DNA binding capability as determined by agarose gel electrophoresis and ethidium bromide exclusion experiments. They have also been found to have low cytotoxicity by MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay on the C6 glioma cell line.

  11. The effects of nonionic surfactants on the tris(2,2'-bipyridyl)ruthenium(II)--tripropylamine electrochemiluminescence system.

    Science.gov (United States)

    Workman, S; Richter, M M

    2000-11-15

    The electrochemistry and electrogenerated chemiluminescence (ECL) of Ru(bpy)3(2+) (bpy = 2,2'-bipyridyl) were studied in the presence of the nonionic surfactants Triton X-100, Thesit, and Nonidet P40. The anodic oxidation of Ru(bpy)3(2+) produces ECL in the presence of tri-n-propylamine in both aqueous and surfactant solutions. Increases in both ECL efficiency (> or =8-fold) and duration of the ECL signal were observed in surfactant media. A shift to lower energies of the Ru(bpy)3(2+) ECL emission by approximately 8 nm was also observed. The one-electron oxidation of Ru(bpy)3(2+) to Ru(bpy)3(3t) occurs at + 1.03 V vs Ag/AgCl in aqueous buffered (0.2 M potassium phosphate) solution as found by square wave voltammetry. This potential did not shift in surfactant systems, indicating that the redshifts in ECL emission are due to stabilization of ligand pi* orbitals in the metal-to-ligand charge-transfer excited state. These results are consistent with hydrophobic interactions between Ru(bpy)3(2+) and the nonionic surfactants.

  12. Performance of some surfactants as wetting agents

    Energy Technology Data Exchange (ETDEWEB)

    Shalaby, M.N.; El-Shanny, O.A.A. [Egyptian Petroleum Research Institute (EPRI), Cairo (Egypt). Evaluation and Analysis Dept.

    2005-12-01

    The wetting power of anionic surfactant: sodium dodecyl sulfate (SDS), and nonionic surfactants: polyoxyethelene(14)monolaurate [La(EO){sub 14}] and polyoxyethelene(14)monoeleate [OI(EO){sub 14}] has been studied to determine their performance as wetting agents. The study reveals that the nonionic compound with a long hydrophobic chain exhibits higher wettability than the shorter one when used at very low cocentrations (below CMC) and the reverse is shown with high concentrations (above CMC). the wetting power of the investigated surfactants increases as the CMC values increases. In case of the nonionic compounds and at surfactant concentrations equal their CMC values, OI(EO){sub 14} shows a higher wetting power than La(EO){sub 14} while is possesses a lower HLB value. The anionic surfactant shows an optimum wetting in comparison with the tested nonionic one. The wettability of all the investigated samples increases as the surface tension of their solutions increases to the allowed limit that can be reached in the presence of surfactant. (orig.)

  13. Investigation of DNA-cationic bolaform surfactants interaction with different spacer length.

    Science.gov (United States)

    Sohrabi, Beheshteh; Khani, Vahid; Moosavi-Movahedi, Ali Akbar; Moradi, Parviz

    2013-10-01

    In this paper interaction of DNA with cationic bolaform surfactants is investigated. The structural formula for synthesized bolaforms is as follows: bolaform B1 with structural formula Br(-)(CH3)3N(+)(CH2)3N(+)(CH3)Br(-) and bolaform B2 with structural formula of Br(-)(CH3)3N(+)(CH2)12N(+)(CH3)Br(-). There are stronger electrostatic interactions in bolaform B1 due to shorter spacer length, while there are stronger hydrophobic interactions in bolaform B2 compared to bolaform B1 due to existence of 12 carbons in hydrocarbonic chain. The structure of bolaforms consists of two polar head groups which play important role in DNA compaction. Surface tension change in aqueous solution of bolaform surfactants is measured using tensiometer. Electrical conductivity of surfactants aqueous solution is examined with and without DNA. DNA compaction is tracked in the presence of bolaforms by dynamic light scattering (DLS) technique. Results of DLS indicate bolaforms with shorter spacer length (dominant electrostatic interactions) are more influential in compressing DNA compared to bolaforms with longer spacer length (stronger hydrophobic interactions). UV-vis and fluorescence spectroscopies specify the binding mechanism of bolaform surfactants to DNA.

  14. Self-Propelled Oil Droplets and Their Morphological Change to Giant Vesicles Induced by a Surfactant Solution at Low pH.

    Science.gov (United States)

    Banno, Taisuke; Tanaka, Yuki; Asakura, Kouichi; Toyota, Taro

    2016-09-20

    Unique dynamics using inanimate molecular assemblies based on soft matter have drawn much attention for demonstrating far-from-equilibrium chemical systems. However, there are no soft matter systems that exhibit a possible pathway linking the self-propelled oil droplets to formation of giant vesicles stimulated by low pH. In this study, we conceived an experimental oil-in-water emulsion system in which flocculated particles composed of a imine-containing oil transformed to spherical oil droplets that self-propelled and, after coming to rest, formed membranous figures. Finally, these figures became giant vesicles. From NMR, pH curves, and surface tension measurements, we determined that this far-from-equilibrium phenomenon was due to the acidic hydrolysis of the oil, which produced a benzaldehyde derivative as an oil component and a primary amine as a surfactant precursor, and the dynamic behavior of the hydrolytic products in the emulsion system. These findings afforded us a potential linkage between mobile droplet-based protocells and vesicle-based protocells stimulated by low pH.

  15. Thermodynamics of non-ionic surfactant Triton X-100-cationic surfactants mixtures at the cloud point

    Energy Technology Data Exchange (ETDEWEB)

    Batigoec, Cigdem [Department of Chemistry, Faculty of Sciences, Trakya University, 22030 Edirne (Turkey); Akbas, Halide, E-mail: hakbas34@yahoo.com [Department of Chemistry, Faculty of Sciences, Trakya University, 22030 Edirne (Turkey); Boz, Mesut [Department of Chemistry, Faculty of Sciences, Trakya University, 22030 Edirne (Turkey)

    2011-12-15

    Highlights: > Non-ionic surfactants are used as emulsifier and solubilizate in such as textile, detergent and cosmetic. > Non-ionic surfactants occur phase separation at temperature as named the cloud point in solution. > Dimeric surfactants have attracted increasing attention due to their superior surface activity. > The positive values of {Delta}G{sub cp}{sup 0} indicate that the process proceeds nonspontaneous. - Abstract: This study investigates the effects of gemini and conventional cationic surfactants on the cloud point (CP) of the non-ionic surfactant Triton X-100 (TX-100) in aqueous solutions. Instead of visual observation, a spectrophotometer was used for measurement of the cloud point temperatures. The thermodynamic parameters of these mixtures were calculated at different cationic surfactant concentrations. The gemini surfactants of the alkanediyl-{alpha}-{omega}-bis (alkyldimethylammonium) dibromide type, on the one hand, with different alkyl groups containing m carbon atoms and an ethanediyl spacer, referred to as 'm-2-m' (m = 10, 12, and 16) and, on the other hand, with -C{sub 16} alkyl groups and different spacers containing s carbon atoms, referred to as '16-s-16' (s = 6 and 10) were synthesized, purified and characterized. Additions of the cationic surfactants to the TX-100 solution increased the cloud point temperature of the TX-100 solution. It was accepted that the solubility of non-ionic surfactant containing polyoxyethylene (POE) hydrophilic chain was a maximum at the cloud point so that the thermodynamic parameters were calculated at this temperature. The results showed that the standard Gibbs free energy ({Delta}G{sub cp}{sup 0}), the enthalpy ({Delta}H{sub cp}{sup 0}) and the entropy ({Delta}S{sub cp}{sup 0}) of the clouding phenomenon were found positive in all cases. The standard free energy ({Delta}G{sub cp}{sup 0}) increased with increasing hydrophobic alkyl chain for both gemini and conventional cationic

  16. SURFACTANTS IN LUBRICATION

    Science.gov (United States)

    Surfactants are one of the most widely applied materials by consumers and industry. The application areas for surfactants span from everyday mundane tasks such as cleaning, to highly complex processes involving the formulation of pharmaceuticals, foods, pesticides, lubricants, etc. Even though sur...

  17. Dynamic covalent surfactants

    NARCIS (Netherlands)

    Minkenberg, C.B.

    2012-01-01

    In this thesis the development of surfactant aggregates with fast exchange dynamics between the aggregated and non-aggregated state is described. Dynamic surfactant exchange plays an important role in natural systems, for instance in cell signaling, cell division, and uptake and release of cargo. Re

  18. Surfactant process for promoting gas hydrate formation and application of the same

    Science.gov (United States)

    Rogers, Rudy E.; Zhong, Yu

    2002-01-01

    This invention relates to a method of storing gas using gas hydrates comprising forming gas hydrates in the presence of a water-surfactant solution that comprises water and surfactant. The addition of minor amounts of surfactant increases the gas hydrate formation rate, increases packing density of the solid hydrate mass and simplifies the formation-storage-decomposition process of gas hydrates. The minor amounts of surfactant also enhance the potential of gas hydrates for industrial storage applications.

  19. Use of surfactants for the remediation of contaminated soils: a review.

    Science.gov (United States)

    Mao, Xuhui; Jiang, Rui; Xiao, Wei; Yu, Jiaguo

    2015-03-21

    Due to the great harm caused by soil contamination, there is an increasing interest to apply surfactants to the remediation of a variety of contaminated soils worldwide. This review article summarizes the findings of recent literatures regarding remediation of contaminated soils/sites using surfactants as an enhancing agent. For the surfactant-based remedial technologies, the adsorption behaviors of surfactants onto soil, the solubilizing capability of surfactants, and the toxicity and biocompatibility of surfactants are important considerations. Surfactants can enhance desorption of pollutants from soil, and promote bioremediation of organics by increasing bioavailability of pollutants. The removal of heavy metals and radionuclides from soils involves the mechanisms of dissolution, surfactant-associated complexation, and ionic exchange. In addition to the conventional ionic and nonionic surfactants, gemini surfactants and biosurfactants are also applied to soil remediation due to their benign features like lower critical micelle concentration (CMC) values and better biocompatibility. Mixed surfactant systems and combined use of surfactants with other additives are often adopted to improve the overall performance of soil washing solution for decontamination. Worldwide the field studies and full-scale remediation using surfactant-based technologies are yet limited, however, the already known cases reveal the good prospect of applying surfactant-based technologies to soil remediation.

  20. Physical principles for developing a synthetic lung surfactant

    Energy Technology Data Exchange (ETDEWEB)

    Jaehnig, F. (Max-Planck-Institut fuer Biologie, Tuebingen (Germany, F.R.)); Obladen, M. (Tuebingen Univ. (Germany, F.R.). Kinderklinik)

    1984-01-01

    The physical principles for developing a synthetic lung surfactant to treat the respiratory distress syndrome are discussed. Requirements for the lipid composition and preparation of the synthetic surfactant are detailed, leading to the conclusion that a suspension of large unilamellar vesicles consisting of dipalmitoylphosphatidylcholine and a small amount of unsaturated lipid is a promising choice.

  1. Colloidal stability influenced by inhomogeneous surfactant assemblies in confined spaces

    NARCIS (Netherlands)

    Jodar-Reyes, A.B.; Leermakers, F.A.M.

    2009-01-01

    Recently, a molecular-level self-consistent field approach was used to show that some surfactants assemblies (with local cylindrical structure) can bridge between two surfaces that in turn are covered by surfactant bilayers. The stability of such a connection is related to a higher end-cap (free) en

  2. Surfactants in the environment.

    Science.gov (United States)

    Ivanković, Tomislav; Hrenović, Jasna

    2010-03-01

    Surfactants are a diverse group of chemicals that are best known for their wide use in detergents and other cleaning products. After use, residual surfactants are discharged into sewage systems or directly into surface waters, and most of them end up dispersed in different environmental compartments such as soil, water or sediment. The toxic effects of surfactants on various aquatic organisms are well known. In general, surfactants are present in the environment at levels below toxicity and in Croatia below the national limit. Most surfactants are readily biodegradable and their amount is greatly reduced with secondary treatment in wastewater treatment plants. The highest concern is the release of untreated wastewater or wastewater that has undergone primary treatment alone. The discharge of wastewater polluted with massive quantities of surfactants could have serious effects on the ecosystem. Future studies of surfactant toxicities and biodegradation are necessary to withdraw highly toxic and non-biodegradable compounds from commercial use and replace them with more environmentally friendly ones.

  3. Pulmonary surfactant and lung transplantation

    NARCIS (Netherlands)

    Erasmus, Michiel Elardus

    1997-01-01

    Pulmonary surfactant lowers the surface tension at the air-water interface inside the alveolus. This is achieved by adsorption of surfactant phospholipids at the air-water interface, a process controlled by surfactant-associated proteins, such as SP-A. In this way, surfactant prevents collapse of th

  4. Bending elasticity of charged surfactant layers: the effect of mixing.

    Science.gov (United States)

    Bergström, L Magnus

    2006-08-01

    Expressions have been derived from which the spontaneous curvature (H(0)), bending rigidity (k(c)), and saddle-splay constant (k(c)) of mixed monolayers and bilayers may be calculated from molecular and solution properties as well as experimentally available quantities such as the macroscopic hydrophobic-hydrophilic interfacial tension. Three different cases of binary surfactant mixtures have been treated in detail: (i) mixtures of an ionic and a nonionic surfactant, (ii) mixtures of two oppositely charged surfactants, and (iii) mixtures of two ionic surfactants with identical headgroups but different tail volumes. It is demonstrated that k(c)H(0), k(c), and k(c) for mixtures of surfactants with flexible tails may be subdivided into one contribution that is due to bending properties of an infinitely thin surface as calculated from the Poisson-Boltzmann mean field theory and one contribution appearing as a result of the surfactant film having a finite thickness with the surface of charge located somewhat outside the hydrophobic-hydrophilic interface. As a matter of fact, the picture becomes completely different as finite layer thickness effects are taken into account, and as a result, the spontaneous curvature is extensively lowered whereas the bending rigidity is raised. Furthermore, an additional contribution to k(c) is present for surfactant mixtures but is absent for k(c)H(0) and k(c). This contribution appears as a consequence of the minimization of the free energy with respect to the composition of a surfactant layer that is open in the thermodynamic sense and must always be negative (i.e., k(c) is generally found to be brought down by the process of mixing two or more surfactants). The magnitude of the reduction of k(c) increases with increasing asymmetry between two surfactants with respect to headgroup charge number and tail volume. As a consequence, the bending rigidity assumes the lowest values for layers formed in mixtures of two oppositely charged

  5. Effects of Surfactant on Solubility and Microbial Conversion of Steroid

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    Enhancing the dispersion and dissolution of substrate particles in substrate/water suspension is a feasible way to improve steroid bioconversion. The aim of the present study is to investigate the effects of applying surfactant to microbial conversion system on the dispersion, solubilization and in turn bioconversion of steroid substrate. The model system is hydroxylation of substrate 16α-,17α-epoxy-4-pregnene-3,20-dine by microbial enzymes from Rhizopus nigricanl. The results show that the presence of substrate leads to an increase in critical micelle concentration (CMC) of surfactant PSE compared with the normal CMC of PSE in aqueous solution. The grinding time during substrate suspension preparation affects the substrate aqueous solubility differently with the varied surfactant concentrations while barely making any difference in substrate solubility in the absence of surfactant. The properly prolonged grinding time can make up for the loss in substrate solubility arising from the reduction in surfactant concentration. The surfactant complexes composed of surfactants PSE and MGE at appropriate ratios are screened out with orthodoxy experiment method, the interaction between PSE and MGE exerts the most prominent effects on substrate bioconversion, and the surfactant complexes show more beneficial effects on steroid bioconversion than the surfactant PSE used alone.

  6. Use of surfactants for the remediation of contaminated soils: A review

    Energy Technology Data Exchange (ETDEWEB)

    Mao, Xuhui, E-mail: clab@whu.edu.cn [School of Resource and Environmental Science, Wuhan University, Wuhan 430072 (China); Jiang, Rui; Xiao, Wei [School of Resource and Environmental Science, Wuhan University, Wuhan 430072 (China); Yu, Jiaguo, E-mail: jiaguoyu@yahoo.com [State Key Laboratory of Advanced Technology for Material Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China)

    2015-03-21

    Highlights: • The recent advances in use of surfactant for soil remediation are reviewed. • The mechanisms of surfactant-based soil remediation are discussed. • A review on the application of different types of surfactants is made. • The future research direction of surfactant-based technologies is suggested. - Abstract: Due to the great harm caused by soil contamination, there is an increasing interest to apply surfactants to the remediation of a variety of contaminated soils worldwide. This review article summarizes the findings of recent literatures regarding remediation of contaminated soils/sites using surfactants as an enhancing agent. For the surfactant-based remedial technologies, the adsorption behaviors of surfactants onto soil, the solubilizing capability of surfactants, and the toxicity and biocompatibility of surfactants are important considerations. Surfactants can enhance desorption of pollutants from soil, and promote bioremediation of organics by increasing bioavailability of pollutants. The removal of heavy metals and radionuclides from soils involves the mechanisms of dissolution, surfactant-associated complexation, and ionic exchange. In addition to the conventional ionic and nonionic surfactants, gemini surfactants and biosurfactants are also applied to soil remediation due to their benign features like lower critical micelle concentration (CMC) values and better biocompatibility. Mixed surfactant systems and combined use of surfactants with other additives are often adopted to improve the overall performance of soil washing solution for decontamination. Worldwide the field studies and full-scale remediation using surfactant-based technologies are yet limited, however, the already known cases reveal the good prospect of applying surfactant-based technologies to soil remediation.

  7. Synthesis and properties of novel gemini surfactant with short spacer

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Cationic gemini surfactant dimethylene-1,2-bis(dodecyldiethylammonium bromide), referred to as C12C2C12(Et) was synthesized, and its surface property and aggregation behavior in aqueous solution were studied. The value of γat the critical micelle concentration (γcmc) is much smaller than that of the surfactant homologues with longer spacer. Spherical and elongated micelles were formed in the aqueous solution of this gemini surfactant,and the spherical micelles were absolutely dominant compared to the elongated micelles at our studied concentration quantitatively.

  8. Complex phase behavior in solvent-free nonionic surfactants

    DEFF Research Database (Denmark)

    Hillmyer, M.A.; Bates, F.S.; Almdal, K.

    1996-01-01

    Unsolvated block copolymers and surfactant solutions are ''soft materials'' that share a common set of ordered microstructures, A set of polyethyleneoxide-polyethylethylene (PEG-PEE) block copolymers that are chemically similar to the well-known alkane-oxyethylene (C(n)EO(m)) nonionic surfactants...... was synthesized here. The general phase behavior in these materials resembles that of both higher molecular weight block copolymers and lower molecular weight nonionic surfactant solutions. Two of the block copolymers exhibited thermally induced order-order transitions and were studied in detail by small...

  9. Metathesis depolymerizable surfactants

    Science.gov (United States)

    Jamison, Gregory M.; Wheeler, David R.; Loy, Douglas A.; Simmons, Blake A.; Long, Timothy M.; McElhanon, James R.; Rahimian, Kamyar; Staiger, Chad L.

    2008-04-15

    A class of surfactant molecules whose structure includes regularly spaced unsaturation in the tail group and thus, can be readily decomposed by ring-closing metathesis, and particularly by the action of a transition metal catalyst, to form small molecule products. These small molecules are designed to have increased volatility and/or enhanced solubility as compared to the original surfactant molecule and are thus easily removed by solvent extraction or vacuum extraction at low temperature. By producing easily removable decomposition products, the surfactant molecules become particularly desirable as template structures for preparing meso- and microstructural materials with tailored properties.

  10. Paramaterization of a coarse-grained model for linear alkylbenzene sulfonate surfactants and molecular dynamics studies of their self-assembly in aqueous solution

    Science.gov (United States)

    He, Xibing; Shinoda, Wataru; DeVane, Russell; Anderson, Kelly L.; Klein, Michael L.

    2010-02-01

    A coarse-grained (CG) forcefield for linear alkylbenzene sulfonates (LAS) was systematically parameterized. Thermodynamic data from experiments and structural data obtained from all-atom molecular dynamics were used as targets to parameterize CG potentials for the bonded and non-bonded interactions. The added computational efficiency permits one to employ computer simulation to probe the self-assembly of LAS aqueous solutions into different morphologies starting from a random configuration. The present CG model is shown to accurately reproduce the phase behavior of solutions of pure isomers of sodium dodecylbenzene sulfonate, despite the fact that phase behavior was not directly taken into account in the forcefield parameterization.

  11. Cost Effective Surfactant Formulations for Improved Oil Recovery in Carbonate Reservoirs

    Energy Technology Data Exchange (ETDEWEB)

    William A. Goddard; Yongchun Tang; Patrick Shuler; Mario Blanco; Yongfu Wu

    2007-09-30

    This report summarizes work during the 30 month time period of this project. This was planned originally for 3-years duration, but due to its financial limitations, DOE halted funding after 2 years. The California Institute of Technology continued working on this project for an additional 6 months based on a no-cost extension granted by DOE. The objective of this project is to improve the performance of aqueous phase formulations that are designed to increase oil recovery from fractured, oil-wet carbonate reservoir rock. This process works by increasing the rate and extent of aqueous phase imbibition into the matrix blocks in the reservoir and thereby displacing crude oil normally not recovered in a conventional waterflood operation. The project had three major components: (1) developing methods for the rapid screening of surfactant formulations towards identifying candidates suitable for more detailed evaluation, (2) more fundamental studies to relate the chemical structure of acid components of an oil and surfactants in aqueous solution as relates to their tendency to wet a carbonate surface by oil or water, and (3) a more applied study where aqueous solutions of different commercial surfactants are examined for their ability to recover a West Texas crude oil from a limestone core via an imbibition process. The first item, regarding rapid screening methods for suitable surfactants has been summarized as a Topical Report. One promising surfactant screening protocol is based on the ability of a surfactant solution to remove aged crude oil that coats a clear calcite crystal (Iceland Spar). Good surfactant candidate solutions remove the most oil the quickest from the surface of these chips, plus change the apparent contact angle of the remaining oil droplets on the surface that thereby indicate increased water-wetting. The other fast surfactant screening method is based on the flotation behavior of powdered calcite in water. In this test protocol, first the calcite

  12. Interface Consistency

    DEFF Research Database (Denmark)

    Staunstrup, Jørgen

    1998-01-01

    This paper proposes that Interface Consistency is an important issue for the development of modular designs. Byproviding a precise specification of component interfaces it becomes possible to check that separately developedcomponents use a common interface in a coherent matter thus avoiding a very...... significant source of design errors. Awide range of interface specifications are possible, the simplest form is a syntactical check of parameter types.However, today it is possible to do more sophisticated forms involving semantic checks....

  13. Study of the micellization and micellar growth in pure alkanediyl-alpha-omega-bis(dodecyldimethylammonium) bromide and MEGA10 surfactant solutions and their mixtures. Influence of the spacer on the enthalpy change accompanying sphere-to-rod transitions.

    Science.gov (United States)

    Martín, Victoria Isabel; Rodríguez, Amalia; Graciani, María del Mar; Robina, Inmaculada; Moyá, María Luisa

    2010-06-17

    The micellization and micellar growth in pure aqueous alkanediyl-alpha-omega-bis(dodecyldimethylammonium) bromide, 12-s-12,2Br(-) (with s = 2,5,6,8,10,12), and N-decanoyl-N-methylglucamide MEGA10 solutions and their mixtures are investigated at 303 K. Application of different theoretical approaches to the binary mixtures shows a nonideal behavior. It also shows that the spacer length does not play an important role in the attractive interactions shown by the mixed systems. The sphere-to-rod morphological transition in the pure dimeric micellar solutions is studied at 303 K. From comparison of these results with those at 298 K the key role played by the spacer in the micellar growth is shown. The spacer length controls not only the surfactant concentration at which the morphological transition happens but also the sign of the enthalpy change accompanying the sphere-to-rod equilibrium. Spacers with an even number of methylenes show smaller C* values than those with an odd number of -CH(2)- units. An endothermic enthalpy change is found for even spacers whereas an exothermic enthalpy change is found for odd spacers. To the authors knowledge, this is the first time this experimental trend has been shown. Addition of MEGA10 diminishes the tendency of the aggregates to grow. An increment in the solution mole fraction of MEGA10 makes the formation of elongated micelles difficult. Microviscosity measurements provide additional information about the influence of the MEGA10 content on the sphere-to-rod transition.

  14. Phosphine oxide surfactants revisited.

    Science.gov (United States)

    Stubenrauch, Cosima; Preisig, Natalie; Laughlin, Robert G

    2016-04-01

    This review summarizes everything we currently know about the nonionic surfactants alkyl dimethyl (C(n)DMPO) and alkyl diethyl (C(n)DEPO) phosphine oxide (PO surfactants). The review starts with the synthesis and the general properties (Section 2) of these compounds and continues with their interfacial properties (Section 3) such as surface tension, surface rheology, interfacial tension and adsorption at solid surfaces. We discuss studies on thin liquid films and foams stabilized by PO surfactants (Section 4) as well as studies on their self-assembly into lyotropic liquid crystals and microemulsions, respectively (Section 5). We aim at encouraging colleagues from both academia and industry to take on board PO surfactants whenever possible and feasible because of their broad variety of excellent properties.

  15. Performance improvement of ionic surfactant flooding in carbonate rock samples by use of nanoparticles

    Directory of Open Access Journals (Sweden)

    Mohammad Ali Ahmadi

    2016-07-01

    Full Text Available Abstract Various surfactants have been used in upstream petroleum processes like chemical flooding. Ultimately, the performance of these surfactants depends on their ability to reduce the interfacial tension between oil and water. The surfactant concentration in the aqueous solution decreases owing to the loss of the surfactant on the rock surface in the injection process. The main objective of this paper is to inhibit the surfactant loss by means of adding nanoparticles. Sodium dodecyl sulfate and silica nanoparticles were used as ionic surfactant and nanoparticles in our experiments, respectively. AEROSIL® 816 and AEROSIL® 200 are hydrophobic and hydrophilic nanoparticles. To determine the adsorption loss of the surfactant onto rock samples, a conductivity approach was used. Real carbonate rock samples were used as the solid phase in adsorption experiments. It should be noted that the rock samples were water wet. This paper describes how equilibrium adsorption was investigated by examining adsorption behavior in a system of carbonate sample (solid phase and surfactant solution (aqueous phase. The initial surfactant and nanoparticle concentrations were 500–5000 and 500–2000 ppm, respectively. The rate of surfactant losses was extremely dependent on the concentration of the surfactant in the system, and the adsorption of the surfactant decreased with an increase in the nanoparticle concentration. Also, the hydrophilic nanoparticles are more effective than the hydrophobic nanoparticles.

  16. Solid consistency

    Science.gov (United States)

    Bordin, Lorenzo; Creminelli, Paolo; Mirbabayi, Mehrdad; Noreña, Jorge

    2017-03-01

    We argue that isotropic scalar fluctuations in solid inflation are adiabatic in the super-horizon limit. During the solid phase this adiabatic mode has peculiar features: constant energy-density slices and comoving slices do not coincide, and their curvatures, parameterized respectively by ζ and Script R, both evolve in time. The existence of this adiabatic mode implies that Maldacena's squeezed limit consistency relation holds after angular average over the long mode. The correlation functions of a long-wavelength spherical scalar mode with several short scalar or tensor modes is fixed by the scaling behavior of the correlators of short modes, independently of the solid inflation action or dynamics of reheating.

  17. Solubilization capacity of nonionic surfactant micelles exhibiting strong influence on export of intracellular pigments in Monascus fermentation

    Science.gov (United States)

    Kang, Biyu; Zhang, Xuehong; Wu, Zhenqiang; Qi, Hanshi; Wang, Zhilong

    2013-01-01

    Summary In this study, perstractive fermentation of intracellular Monascus pigments in nonionic surfactant micelle aqueous solution had been studied. The permeability of cell membrane modified by nonionic surfactant might have influence on the rate of export of intracellular pigments into its extracellular broth while nearly no effect on the final extracellular pigment concentration. However, the solubilization of pigments in nonionic surfactant micelles strongly affected the final extracellular pigment concentration. The solubilization capacity of micelles depended on the kind of nonionic surfactant, the super-molecule assembly structure of nonionic surfactant in an aqueous solution, and the nonionic surfactant concentration. Elimination of pigment degradation by export of intracellular Monascus pigments and solubilizing them into nonionic surfactant micelles was also confirmed experimentally. Thus, nonionic surfactant micelle aqueous solution is potential for replacement of organic solvent for perstractive fermentation of intracellular product. PMID:23425092

  18. Solubilization capacity of nonionic surfactant micelles exhibiting strong influence on export of intracellular pigments in Monascus fermentation.

    Science.gov (United States)

    Kang, Biyu; Zhang, Xuehong; Wu, Zhenqiang; Qi, Hanshi; Wang, Zhilong

    2013-09-01

    In this study, perstractive fermentation of intracellular Monascus pigments in nonionic surfactant micelle aqueous solution had been studied. The permeability of cell membrane modified by nonionic surfactant might have influence on the rate of export of intracellular pigments into its extracellular broth while nearly no effect on the final extracellular pigment concentration. However, the solubilization of pigments in nonionic surfactant micelles strongly affected the final extracellular pigment concentration. The solubilization capacity of micelles depended on the kind of nonionic surfactant, the super-molecule assembly structure of nonionic surfactant in an aqueous solution, and the nonionic surfactant concentration. Elimination of pigment degradation by export of intracellular Monascus pigments and solubilizing them into nonionic surfactant micelles was also confirmed experimentally. Thus, nonionic surfactant micelle aqueous solution is potential for replacement of organic solvent for perstractive fermentation of intracellular product.

  19. Surfactant effects on SF6 hydrate formation.

    Science.gov (United States)

    Lee, Bo Ram; Lee, Ju Dong; Lee, Hyun Ju; Ryu, Young Bok; Lee, Man Sig; Kim, Young Seok; Englezos, Peter; Kim, Myung Hyun; Kim, Yang Do

    2009-03-01

    Sulfur hexafluoride (SF(6)) has been widely used in a variety of industrial processes, but it is one of the most potent greenhouse gases. For this reason, it is necessary to separate or collect it from waste gas streams. One separation method is through hydrate crystal formation. In this study, SF(6) hydrate was formed in aqueous surfactant solutions of 0.00, 0.01, 0.05, 0.15 and 0.20 wt% to investigate the effects of surfactants on the hydrate formation rates. Three surfactants, Tween 20 (Tween), sodium dodecyl sulfate (SDS) and linear alkyl benzene sulfonate (LABS), were tested in a semi-batch stirred vessel at the constant temperature and pressures of 276.2 K and 0.78 MPa, respectively. All surfactants showed kinetic promoter behavior for SF(6) hydrate formation. It was also found that SF(6) hydrate formation proceeded in two stages with the second stage being the most rapid. In situ Raman spectroscopy analysis revealed that the increased gas consumption rate with the addition of surfactant was possibly due to the increased gas filling rate in the hydrate cavity.

  20. Syntheses of surfactants from oleochemical epoxides

    Directory of Open Access Journals (Sweden)

    Warwel Siegfried

    2001-01-01

    Full Text Available Sugar-based surfactants were obtained in good yields (up to 100% under mild conditions (70°C, methanol or mixtures of methanol and water by ring-opening of terminal epoxides with aminopolyols, derived from glucose. Reaction of N-methyl glucamine with epoxides from even-numbered C4-C18 alpha-olefins or from terminal unsaturated fatty acid methyl esters leads to linear products, while corresponding reactions with N-dodecyl glucamine or glucamine yield surfactants with different Y-structures. Products obtained by conversion of omega-epoxy fatty acid methyl esters were saponificated with NaOH or hydrolyzed enzymatically to sodium salts or free acids respectively, which are amphoteric surfactants. Studies of the surfactants at different pH-values demonstrate different surface active properties in aqueous solutions. Critical micelle concentrations (c.m.c. in a range between 2 and 500mg/l and surface tensions of 25-40mN/m were measured for several of the synthesized sugar-based surfactants. The ring-opening products are rather poor foamers, whereas some of the corresponding hydrobromides show good foaming properties.

  1. A novel biosensor method for surfactant determination based on acetylcholinesterase inhibition

    Science.gov (United States)

    Kucherenko, I. S.; Soldatkin, O. O.; Arkhypova, V. M.; Dzyadevych, S. V.; Soldatkin, A. P.

    2012-06-01

    A novel enzyme biosensor based on acetylcholinesterase inhibition for the determination of surfactants in aqueous solutions is described. Acetylcholinesterase-based bioselective element was deposited via glutaraldehyde on the surface of conductometric transducers. Different variants of inhibitory analysis of surfactants were tested, and finally surfactant's concentration was evaluated by measuring initial rate of acetylcholinesterase inhibition. Besides, we studied the effect of solution characteristics on working parameters of the biosensor for direct measurement of acetylcholine and for inhibitory determination of surfactants. The biosensor's sensitivity to anionic and cationic surfactants (0.35 mg l-1) was tested. The high operational stability of the biosensor during determination of acetylcholine (RSD 2%) and surfactants (RSD 11%) was shown. Finally, we discussed the selectivity of the biosensor toward surfactants and other AChE inhibitors. The proposed biosensor can be used as a component of the multibiosensor for ecological monitoring of toxicants.

  2. Phase diagrams of DNA-photosensitive surfactant complexes: effect of ionic strength and surfactant structure.

    Science.gov (United States)

    Zakrevskyy, Yuriy; Titov, Evgenii; Lomadze, Nino; Santer, Svetlana

    2014-10-28

    Realization of all-optically controlled and efficient DNA compaction is the major motivation in the study of interactions between DNA and photosensitive surfactants. In this article, using recently published approach of phase diagram construction [Y. Zakrevskyy, P. Cywinski, M. Cywinska, J. Paasche, N. Lomadze, O. Reich, H.-G. Löhmannsroben, and S. Santer, J. Chem. Phys. 140, 044907 (2014)], a strategy for substantial reduction of compaction agent concentration and simultaneous maintaining the light-induced decompaction efficiency is proposed. The role of ionic strength (NaCl concentration), as a very important environmental parameter, and surfactant structure (spacer length) on the changes of positions of phase transitions is investigated. Increase of ionic strength leads to increase of the surfactant concentration needed to compact DNA molecule. However, elongation of the spacer results to substantial reduction of this concentration. DNA compaction by surfactants with longer tails starts to take place in diluted solutions at charge ratios Z phase diagrams for different DNA-photosensitive surfactant systems allowed explanation and proposal of a strategy to overcome previously reported limitations of the light-induced decompaction for complexes with increasing surfactant hydrophobicity.

  3. Effects of surfactants and salt on Henry's constant of n-hexane.

    Science.gov (United States)

    Yang, Chunping; Chen, Fayuan; Luo, Shenglian; Xie, Gengxin; Zeng, Guangming; Fan, Changzheng

    2010-03-15

    n-Hexane biological removal is intrinsically limited by its hydrophobic nature and low bioavailability. The addition of surfactants could enhance the transport of volatile organic compounds (VOCs) and change the gas-liquid equilibrium of VOCs. In this paper, the effects of four surfactants, sodium dodecyl sulfate (SDS), cetyltrimethylammonium bromide (CTAB), tert-octylphenoxypoly-ethoxyethanol (Triton X-100), polyoxyethylene (20) sorbitan monooleate (Tween 80), and sodium nitrate on apparent Henry's constant of n-hexane in surfactant solutions were investigated. The apparent Henry's constants were significantly reduced when surfactants concentrations exceeded their critical micelle concentrations (cmc's). On a cmc basis, the anionic surfactant SDS was found to have the greatest effect on the apparent Henry's constant with CTAB succeeding, then followed by Triton X-100 and Tween 80. However, the apparent Henry's constant of n-hexane decreased even more rapidly when Triton X-100, a nonionic surfactant, was added than when the ionic surfactant of SDS or CTAB was applied under identical mass concentration and other conditions. These results suggest that Triton X-100 have the biggest solubilization of n-hexane among the four surfactants. Sodium nitrate slightly decreased the apparent Henry's constant of n-hexane in surfactant solutions, and could be considered as a cosolvent in the surfactant-(n-hexane) solution. In addition, the relationship between apparent Henry's constant and surfactant concentration was further developed.

  4. Dilute Surfactant Methods for Carbonate Formations

    Energy Technology Data Exchange (ETDEWEB)

    Kishore K. Mohanty

    2006-02-01

    There are many fractured carbonate reservoirs in US (and the world) with light oil. Waterflooding is effective in fractured reservoirs, if the formation is water-wet. Many fractured carbonate reservoirs, however, are mixed-wet and recoveries with conventional methods are low (less than 10%). The process of using dilute anionic surfactants in alkaline solutions has been investigated in this work for oil recovery from fractured oil-wet carbonate reservoirs both experimentally and numerically. This process is a surfactant-aided gravity drainage where surfactant diffuses into the matrix, lowers IFT and contact angle, which decrease capillary pressure and increase oil relative permeability enabling gravity to drain the oil up. Anionic surfactants have been identified which at dilute concentration of 0.05 wt% and optimal salinity can lower the interfacial tension and change the wettability of the calcite surface to intermediate/water-wet condition as well or better than the cationic surfactant DTAB with a West Texas crude oil. The force of adhesion in AFM of oil-wet regions changes after anionic surfactant treatment to values similar to those of water-wet regions. The AFM topography images showed that the oil-wetting material was removed from the surface by the anionic surfactant treatment. Adsorption studies indicate that the extent of adsorption for anionic surfactants on calcite minerals decreases with increase in pH and with decrease in salinity. Surfactant adsorption can be minimized in the presence of Na{sub 2}CO{sub 3}. Laboratory-scale surfactant brine imbibition experiments give high oil recovery (20-42% OOIP in 50 days; up to 60% in 200 days) for initially oil-wet cores through wettability alteration and IFT reduction. Small (<10%) initial gas saturation does not affect significantly the rate of oil recovery in the imbibition process, but larger gas saturation decreases the oil recovery rate. As the core permeability decreases, the rate of oil recovery reduces

  5. Micellization of monomeric and poly-ω-methacryloyloxyundecyltrimethylammonium surfactants.

    Science.gov (United States)

    FitzGerald, Paul A; Chatjaroenporn, Khwanrat; Zhang, Xiaoli; Warr, Gregory G

    2011-10-04

    We have used small-angle neutron scattering to study how micelle morphology of the tail-polymerizable surfactants MUTAB and MUTAC (ω-methacryloyloxyundecyltrimethylammonium bromide and chloride) is affected by classic self-assembly modifiers such as temperature changes, salt addition, and counterion exchange, as a function of their conversion from monomer into polymer amphiphile in aqueous solution. Contrary to common assumptions about polymerized surfactants, these systems remain in dynamic equilibrium under all conditions examined and at all conversions (except for a small amount of high-molecular-weight precipitation by MUTAC). Counterintuitively, the polymerized methacrylate backbone has little influence on aggregate morphology, except for the formation of rod-like mixed micelles of polymerized and unpolymerized surfactant at intermediate conversions. The addition of salt produces a transition to rod-like micelles at all conversions except in the unpolymerized surfactant, which has some characteristics of an asymmetric bolaform surfactant and retains its spheroidal geometry under almost all conditions.

  6. Aqueous foam surfactants for geothermal drilling fluids: 1. Screening

    Energy Technology Data Exchange (ETDEWEB)

    Rand, P.B.

    1980-01-01

    Aqueous foam is a promising drilling fluid for geothermal wells because it will minimize damage to the producing formation and would eliminate the erosion problems of air drilling. Successful use of aqueous foam will require a high foaming surfactant which will: (1) be chemically stable in the harsh thermal and chemical environment, and (2) form stable foams at high temperatures and pressures. The procedures developed to generate and test aqueous foams and the effects of a 260/sup 0/C temperature cycle on aqueous surfactant solutions are presented. More than fifty selected surfactants were evaluated with representatives from the amphoteric, anionic, cationic, and nonionic classes included. Most surfactants were severely degraded by this temperature cycle; however, some showed excellent retention of their properties. The most promising surfactant types were the alkyl and alkyl aryl sulfonates and the ethoxylated nonionics.

  7. Micellization properties of cardanol as a renewable co-surfactant.

    Science.gov (United States)

    Fontana, Antonella; Guernelli, Susanna; Zaccheroni, Nelsi; Zappacosta, Romina; Genovese, Damiano; De Crescentini, Lucia; Riela, Serena

    2015-09-21

    With the aim to improve the features of surfactant solutions in terms of sustainability and renewability we propose the use of hydrogenated natural and sustainable plant-derived cardanol as an additive to commercial surfactants. In the present study we demonstrated that its addition, in amounts as high as 10%, to commercial surfactants of different charge does not significantly affect surfactant properties. Conversely, the presence of hydrogenated cardanol can strongly affect spectrophotometric determination of CMC if preferential interactions with the dyes used take place. This latter evidence may be profitably exploited in surfactant manufacturing by considering that the concurrent presence of a rigid organic molecule such as Orange OT and 10% hydrogenated cardanol decreases the CMC of CTAB up to 65 times.

  8. Use of a surfactant coacervate phase to extract trichloroethylene from water

    Energy Technology Data Exchange (ETDEWEB)

    Kimchuwanit, W.W.; Scamehorn, J.F.; Osuwan, S. [Univ. of Oklahoma, Norman, OK (United States)] [and others

    1996-10-01

    At temperatures above the cloud point, aqueous nonionic surfactant solutions can separate into two phases: a surfactant-rich coacervate phase and a surfactant-dilute phase. Since the coacervate phase can be a concentrated micellar solution, organic solute tends to concentrate in the coacervate due to solubilization. In this study, up to 90% of trichloroethylene was shown to be extracted into the coacervate phase in one stage. Increasing temperature, surfactant concentration, and added NaCl concentration all improved the fraction of TCE extracted.

  9. Flow Behaviour of Alkali, Surfactant, and Xanthan Solutions Used for Enhanced Oil Recovery Fluidité des solutions d'alcali, de tensio-actif et de xanthane utilisées pour la récupération assistée du pétrole

    Directory of Open Access Journals (Sweden)

    Nasr-El-Din H. A.

    2006-11-01

    Full Text Available An experimental study was conducted to examine the effects of various alkalis, surfactants and brines on the viscosity of dilute aqueous solutions of two xanthan materials containing medium and high pyruvate content, over a wide range of parameters. The effect of alkalis on the flow curves of xanthan solutions depended on alkali type and concentration, shear rate and pyruvate content of xanthan. Strong alkalis caused partial degradation of the xanthan molecules. As a result, a fast and significant reduction in apparent viscosity occurred, especially with the high pyruvate xanthan. This drop was only noticeable at low shear rates. Buffered alkalis were less detrimental to the viscosity of xanthan solutions. Triton X-100 up to 10 wt% had no significant effect on the flow curves of both xanthan materials. Neodol 25-3S caused noticeable changes only in the flow curves of the high pyruvate xanthan. Triton X-100 up to 10 wt% in the presence of alkali had no significant effect on the flow curves of either xanthan material. The addition of anionic surfactants at low concentrations slightly decreased the viscosity of alkali/xanthan solutions. A significant viscosity enhancement was observed at higher surfactant concentrations over a narrow range of alkali concentrations. This behaviour was only observed with anionic surfactants and was due to the formation of surfactant aggregates. The effect of sodium chloride on the apparent viscosity of xanthan solutions depended on polymer concentration and the pyruvate content of xanthan. Only the high pyruvate polymer at high polymer concentrations (= 1 wtO/o showed a dramatic increase in the apparent viscosity upon the addition of sodium chloride. At low polymer concentrations, calcium chloride had a more detrimental effect on the viscosity of the high pyruvate xanthan than sodium chloride. Une étude expérimentale a été effectuée pour examiner les effets de divers alcalis, tensioactifs et saumures sur la

  10. The Nature of Aqueous Solutions of a Cationic Calix[4]arene: A Comparative Study of Dye–Calixarene and Dye–Surfactant Interactions

    Directory of Open Access Journals (Sweden)

    V. I. Kalchenko

    2006-08-01

    Full Text Available Among different types of calixarenes, the water–soluble ones are of especial interestbecause of their possible applications in biochemical research. In order to elucidate the natureof aqueous solutions of a cationic amphiphilic calixarene, substituted tetrapropoxycalix[4]arene bearing hydrophilic choline groups at the upper rim, we studied vis–spectroscopically the influence of the above system on the acid–base behavior of threeindicator dyes, namely, 2,4-dinitrophenol, bromophenol blue, and N,N/-dioctadecylrhodamine,at constant ionic strength of 0.05 M, maintained with NaCl addition. Simultaneously,‘apparent’ ionization constants, Kaa , of the same dyes were determined in the presence ofcommon cationic surfactant micelles. Within the concentration range from 1.0×10–5 to 0.01 M,the aforementioned water–soluble calixarene displays effects similar to those of micelles ofcetyltrimethylammonium bromide (or chloride. The shifts of the absorption and emissionbands in the visible region, as well as the alterations of the Kaa values against the ‘aqueous’ones appeared to be very similar in aqueous solutions of both calix[4]arene and cationicsurfactant. A conclusion can be made about aggregation (or association, i.e., micelleformation of the cationic calix[4]arene under study.

  11. Recovering hydrocarbons with surfactants from lignin

    Energy Technology Data Exchange (ETDEWEB)

    Naae, D.G.; Whittington, L.E.; Ledoux, W.A.; Debons, F.E.

    1988-11-29

    This patent describes a method of recovering hydrocarbons from an underground hydrocarbon formation penetrated by at least one injection well and at least one production well, which comprises: injecting into the formation through an injection well a surfactant slug comprising about 0.1% to about 10% by weight of surfactants produced from lignin, the surfactants produced by placing lignin in contact with water, converting the lignin into low molecular weight lignin phenols by reducing the lignin in the presence of a reducing agent of carbon monoxide or hydrogen creating a reduction reaction mixture comprising oil soluble lignin phenols, the reduction occurring at a temperature greater than about 200/sup 0/C and a pressure greater than about 100 psi, recovering the oil soluble lignin phenols from the reduction mixture, and converting the lignin phenols into lignin surfactants by a reaction selected from the group consisting of alkoxylation, sulfonation, sulfation, aklylation, sulfomethylation, and alkoxysulfation; injecting into the formation through the injection well a drive fluid to push the surfactant slug towards a production well; and recovering hydrocarbons at the production well.

  12. The in-situ decontamination of sand and gravel aquifers by chemically enhanced solubilization of multiple-compound DNAPLs with surfactant solutions: Phase 1 -- Laboratory and pilot field-scale testing and Phase 2 -- Solubilization test and partitioning and interwell tracer tests. Final report

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-10-24

    Laboratory, numerical simulation, and field studies have been conducted to assess the potential use of micellar-surfactant solutions to solubilize chlorinated solvents contaminating sand and gravel aquifers. Ninety-nine surfactants were screened for their ability to solubilize trichloroethene (TCE), perchloroethylene (PCE), and carbon tetrachloride (CTET). The field test was conducted in the alluvial aquifer which is located 20 to 30 meters beneath a vapor degreasing operation at Paducah Gaseous Diffusion Plant. This aquifer has become contaminated with TCE due to leakage of perhaps 40,000 liters of TCE, which has generated a plume of dissolved TCE extending throughout an area of approximately 3 km{sup 2} in the aquifer. Most of the TCE is believed to be present in the overlying lacustrine deposits and in the aquifer itself as a dense, non-aqueous phase liquid, or DNAPL. The objective of the field test was to assess the efficacy of the surfactant for in situ TCE solubilization. Although the test demonstrated that sorbitan monooleate was unsuitable as a solubilizer in this aquifer, the single-well test was demonstrated to be a viable method for the in situ testing of surfactants or cosolvents prior to proceeding to full-scale remediation.

  13. Coupled Transport of PAH and Surfactants in Natural Aquifer Material

    Science.gov (United States)

    Danzer, J.; Grathwohl, P.

    1998-03-01

    Surfactants in aqueous solution adsorb onto mineral surfaces and form micelles above the critical micelle concentration (CMC) due to their physico-chemical properties. Hydrophobic organic compounds such as polycyclic aromatic hydrocarbons (PAHs) have a high affinity for the adsorbed surfactant layers (monomers, hemimicelles and admicelles) and to the micelles in the mobile aqueous phase. The transport of PAHs is controlled by the concentration of the surfactant and the partition coefficients, of the PAHs between water and admicelles (adsolubilization: K adm) and water and micelles (solubilization: K mic), respectively. These partition coefficients were measured in laboratory batch and column experiments using phenanthrene as a chemical probe for the PAHs, a non-ionic surfactant (Terrasurf G50), natural aquifer sand (River Neckar Alluvium: RNA) and its petrographic subcomponents. The sorption of the surfactant can be described by a linear isotherm for concentrations below the CMC and a sorption maximum above the CMC, which both depend on the grain size and the surfactant accessible internal surface area of the particles. K adm was found to be higher than K mic. Both depend on the surfactant's properties, such as alkyl chain length, polar headgroup or ethoxylation. In column experiments an increasing retardation of phenanthrene was observed up to the CMC followed by a facilitated transport at surfactant concentration several times the CMC.

  14. Surfactant-Free Synthesis of Carbon-Supported Palladium Nanoparticles and Size-Dependent Hydrogen Production from Formic Acid-Formate Solution.

    Science.gov (United States)

    Zhang, Shuo; Jiang, Bei; Jiang, Kun; Cai, Wen-Bin

    2017-07-26

    Steerable hydrogen generation from the hydrogen storage chemical formic acid via heterogeneous catalysis has attracted considerable interest given the safety and efficiency concerns in handling H2. Herein, a series of carbon-supported capping-agent-free Pd nanoparticles (NPs) with mean sizes tunable from 2.0 to 5.2 nm are developed due to the demand for more efficient dehydrogenation from a formic acid-formate solution of pH 3.5 at room temperature. The trick for the facile size-controlled synthesis of Pd/C catalysts is the selective addition of Na2CO3, NH3·H2O, or NaOH to a Pd(II) solution to attain initial pH values of 7-9.5. For comparison, cuboctahedron modeling and electrochemical COads stripping methods are applied to evaluate active surface Pd sites for turnover frequency (TOF) calculation. Both mass activity and specific activity (TOF) of hydrogen production are not only time-dependent but also Pd-size-dependent. An initial H2 production rate of 246 L·h(-1)·gPd(-1) is achieved on 2.0 nm Pd/C at 303 K, together with a TOF of 1815 h(-1) on the basis of cuboctahedron modeling of surface-active Pd sites. The initial TOF exhibits a significant rise from 3.5 down to 2.8 nm and then levels off below 2.8 nm and even shows a maxima at ca. 2.2 nm using the electrochemical surface area for calculation. The volcano-shaped dependence of TOF on Pd NP size may be better attributed to the changing ratios of terrace sites to defect sites on Pd NPs.

  15. Thermodynamic Studies of Aqueous m-s-m Gemini Surfactant Systems.

    Science.gov (United States)

    Wettig, S. D.; Verrall, R. E.

    2001-03-15

    The specific conductance, surface tension, and apparent molar volume properties of aqueous solutions of two series of m-s-m gemini surfactants-one having a constant spacer s(=3) with m=8, 10, 12, and 16 and the other having a constant alkyl chain length m(=12) with variable spacer length 2bolaform cation. Poor agreement was obtained with the first method, while good agreement was obtained with the second. The observed variation in the volume change due to micelle formation, DeltaV(φ,M), is consistent with variations in the head group area and critical micelle concentrations and can be rationalized in terms of the location of the spacer-either at the micelle/water interface, or in the micelle interior. Results obtained for the 12-φ-12 surfactant indicate that rigidity of the spacer has no measurable effect on the micellization process for such a short spacerlength. Copyright 2001 Academic Press.

  16. Theory of interfacial phase transitions in surfactant systems

    Science.gov (United States)

    Shukla, K. P.; Payandeh, B.; Robert, M.

    1991-06-01

    The spin-1 Ising model, which is equivalent to the three-component lattice gas model, is used to study wetting transitions in three-component surfactant systems consisting of an oil, water, and a nonionic surfactant. Phase equilibria, interfacial profiles, and interfacial tensions for three-phase equilibrium are determined in mean field approximation, for a wide range of temperature and interaction parameters. Surfactant interaction parameters are found to strongly influence interfacial tensions, reducing them in some cases to ultralow values. Interfacial tensions are used to determine whether the middle phase, rich in surfactant, wets or does not wet the interface between the oil-rich and water-rich phases. By varying temperature and interaction parameters, a wetting transition is located and found to be of the first order. Comparison is made with recent experimental results on wetting transitions in ternary surfactant systems.

  17. Surfactant aggregation and its application to drag reduction

    Energy Technology Data Exchange (ETDEWEB)

    Harwigsson, I.

    1995-09-01

    A number of different drag-reducing (DR) surfactants: nonionics, zwitterionics and ampholytics suitable for use in both cool and hot water solution are described. These surfactants have been tested under various conditions common in district energy distribution. The surfactants described are environmentally more acceptable than the organic salts of quaternary ammonium compounds which have so far dominated as DR surfactants. The micellar phase formed in water by the surfactant system cetylpyridinium chloride/sodium salicylate has been investigated with surfactant self-diffusion (NMR) measurements and cryo-transmission electron microscopy. Results from this study support the hypothesis that worm-like micellar systems form a network before the phase boundary, when the first liquid crystalline phase formed is a bicontinuous cubic phase. A series of surfactants similar to the one used in the DR experiments has been examined in dilute solutions. Critical micellar concentration and the size of these micelles are investigated as a function of the amphiphile concentration, the pH and salt concentration. Adsorption properties on silica of zwitterionic dodecyl-N,N-dimethylammonio alkanoates, with polymethylene interchange arms of different lengths, have been investigated with an in situ ellipsometry technique. The use of two-tone frequency modulation spectroscopy as a general method for the determination of water activity has been initiated. 173 refs, 6 figs

  18. Modeling transport effects of perfluorinated and hydrocarbon surfactants in groundwater by using micellar liquid chromatography

    Energy Technology Data Exchange (ETDEWEB)

    Simmons, Rashad N. [Department of Chemistry and Center for Integrative Toxicology, Michigan State University, East Lansing, MI 48824-1322 (United States); McGuffin, Victoria L. [Department of Chemistry and Center for Integrative Toxicology, Michigan State University, East Lansing, MI 48824-1322 (United States)], E-mail: jgshabus@aol.com

    2007-11-05

    The effects of hydrocarbon and perfluorinated surfactants, above their critical micelle concentration (CMC), on the transport of neutral environmental pollutants are compared. Reversed-phase micellar liquid chromatography is used to model the groundwater system. The octadecylsilica stationary phase serves to simulate soil particles containing organic matter, whereas the aqueous surfactant mobile phases serve to simulate groundwater containing a surfactant at varying concentrations. Sodium dodecyl sulfate and lithium perfluorooctane sulfonate are used as representatives of the hydrocarbon and perfluorinated surfactants, respectively. Benzene, mono- and perhalogenated benzenes, and polycyclic aromatic hydrocarbons are used as models for environmental pollutants. Transport effects were elucidated from the retention factor, k, and the equilibrium constant per micelle, K{sub eq}, of the model pollutants in the individual surfactants. Based on k values, the transport of the model pollutants increased in both surfactant solutions in comparison to pure water. As the concentration of the surfactants increased, the transport of the pollutants increased as well. Notably, the K{sub eq} values of the pollutants in the perfluorinated surfactant were at least an order of magnitude less than those in the hydrocarbon surfactant. Overall, these results suggest that the presence of a perfluorinated surfactant, above its CMC, increases the transport of pollutants in a groundwater system. However, the perfluorinated surfactant exhibits a lesser transport effect than the hydrocarbon surfactant.

  19. Surface tension method for determining binding constants for cyclodextrin inclusion complexes of ionic surfactants

    Energy Technology Data Exchange (ETDEWEB)

    Dharmawardana, U.R.; Christian, S.D.; Tucker, E.E.; Taylor, R.W.; Scamehorn, J.F. (Univ. of Oklahoma, Norman, OK (United States))

    1993-09-01

    A new method has been developed for determining binding constants of complexes of cyclodextrins with surface-active compounds, including water-soluble ionic surfactants. The technique requires measuring the change in surface tension caused by addition of a cyclodextrin (CD) to aqueous solutions of the surfactant; the experimental results lead directly to inferred values of the thermodynamic activity of the surfactant. Surface tension results are reported for three different surfactants sodium dodecyl sulfate (SDS), cetylpyridinium chloride (CPC), and cetyltrimethylammonium bromide (CTAB) in the presence and in the absence of added [beta]-CD. Data for CPC have been obtained at surfactant concentrations below and above the critical micelle concentration. Correlations between surface tension and surfactant activity are expressed by the Szyszkowski equation, which subsumes the Langmuir adsorption model and the Gibbs equation. It is observed that the surface tension increases monotonically as [beta]-cyclodextrin is added to ionic surfactant solutions. At concentrations of CD well in excess of the surfactant concentration, the surface tension approaches that of pure water, indicating that neither the surfactant-CD complexes nor CD itself are surface active. Binding constants are inferred from a model that incorporates the parameters of the Szyszkowski equation and mass action constants relating to the formation of micelles from monomers of the surfactant and the counterion. Evidence is given that two molecules of CD can complex the C-16 hydrocarbon chain of the cetyl surfactants. 30 refs., 5 figs., 1 tab.

  20. Studies on interfacial tension and contact angle of synthesized surfactant and polymeric from castor oil for enhanced oil recovery

    Science.gov (United States)

    Babu, Keshak; Pal, Nilanjan; Bera, Achinta; Saxena, V. K.; Mandal, Ajay

    2015-10-01

    New synthesized polymeric surfactants have immensely attracted the researchers for further development of chemical enhanced oil recovery method particularly in surfactant flooding. Contact angle and interfacial tension measurement tests are the effective ways to identify proper chemicals/surfactants for enhanced oil recovery by chemical/surfactant flooding. In the present study a new polymeric surfactant was synthesized from pre-synthesized sodium methyl ester sulfonate (surfactant) and acrylamide for application in chemical enhanced oil recovery. The synthesized surfactant and polymeric surfactant were used to measure interfacial tension between their aqueous phase and crude oil phase to investigate the efficiency of the surfactants in reduction of interfacial tension. The synthesized polymeric surfactant has also ability to control the mobility because of its viscous nature in aqueous solution. Contact angles of solid-crude oil-surfactant interface were also measured to study the effect of the synthesized surfactant and polymeric surfactant on wettability alteration mechanism. Synergistic effect was studied by using NaCl and synthesized surfactants on interfacial tension. Dynamic interfacial tensions of the surfactant and polymeric surfactant solutions with crude oil were measured at different NaCl concentrations. Interfacial tension was found to be lowered up to 10-2 to 10-3 mN/m which is effective for oil recovery. Measurement of contact angle indicates the wettability change of the quartz surface. Comparative studies on efficiencies of synthesized sodium methyl ester sulfonate surfactant and polymeric surfactant were also carried out with respect to interfacial tension reduction and contact angle change.

  1. Tuning of protein-surfactant interaction to modify the resultant structure.

    Science.gov (United States)

    Mehan, Sumit; Aswal, Vinod K; Kohlbrecher, Joachim

    2015-09-01

    Small-angle neutron scattering and dynamic light scattering studies have been carried out to examine the interaction of bovine serum albumin (BSA) protein with different surfactants under varying solution conditions. We show that the interaction of anionic BSA protein (pH7) with surfactant and the resultant structure are strongly modified by the charge head group of the surfactant, ionic strength of the solution, and mixed surfactants. The protein-surfactant interaction is maximum when two components are oppositely charged, followed by components being similarly charged through the site-specific binding, and no interaction in the case of a nonionic surfactant. This interaction of protein with ionic surfactants is characterized by the fractal structure representing a bead-necklace structure of micellelike clusters adsorbed along the unfolded protein chain. The interaction is enhanced with ionic strength only in the case of site-specific binding of an anionic surfactant with an anionic protein, whereas it is almost unchanged for other complexes of cationic and nonionic surfactants with anionic proteins. Interestingly, the interaction of BSA protein with ionic surfactants is significantly suppressed in the presence of nonionic surfactant. These results with mixed surfactants thus can be used to fold back the unfolded protein as well as to prevent surfactant-induced protein unfolding. For different solution conditions, the results are interpreted in terms of a change in fractal dimension, the overall size of the protein-surfactant complex, and the number of micelles attached to the protein. The interplay of electrostatic and hydrophobic interactions is found to govern the resultant structure of complexes.

  2. Key interactions of surfactants in therapeutic protein formulations: A review.

    Science.gov (United States)

    Khan, Tarik A; Mahler, Hanns-Christian; Kishore, Ravuri S K

    2015-11-01

    Proteins as amphiphilic, surface-active macromolecules, demonstrate substantial interfacial activity, which causes considerable impact on their multifarious applications. A commonly adapted measure to prevent interfacial damage to proteins is the use of nonionic surfactants. Particularly in biotherapeutic formulations, the use of nonionic surfactants is ubiquitous in order to prevent the impact of interfacial stress on drug product stability. The scope of this review is to convey the current understanding of interactions of nonionic surfactants with proteins both at the interface and in solution, with specific focus to their effects on biotherapeutic formulations.

  3. Fibrinogen stability under surfactant interaction.

    Science.gov (United States)

    Hassan, Natalia; Barbosa, Leandro R S; Itri, Rosangela; Ruso, Juan M

    2011-10-01

    Differential scanning calorimetry (DSC), circular dichroism (CD), difference spectroscopy (UV-vis), Raman spectroscopy, and small-angle X-ray scattering (SAXS) measurements have been performed in the present work to provide a quantitatively comprehensive physicochemical description of the complexation between bovine fibrinogen and the sodium perfluorooctanoate, sodium octanoate, and sodium dodecanoate in glycine buffer (pH 8.5). It has been found that sodium octanoate and dodecanoate act as fibrinogen destabilizer. Meanwhile, sodium perfluorooctanoate acts as a structure stabilizer at low molar concentration and as a destabilizer at high molar concentration. Fibrinogen's secondary structure is affected by all three studied surfactants (decrease in α-helix and an increase in β-sheet content) to a different extent. DSC and UV-vis revealed the existence of intermediate states in the thermal unfolding process of fibrinogen. In addition, SAXS data analysis showed that pure fibrinogen adopts a paired-dimer structure in solution. Such a structure is unaltered by sodium octanoate and perfluoroctanoate. However, interaction of sodium dodecanoate with the fibrinogen affects the protein conformation leading to a complex formation. Taken together, all results evidence that both surfactant hydrophobicity and tail length mediate the fibrinogen stability upon interaction. Copyright © 2011 Elsevier Inc. All rights reserved.

  4. Adsorption of anionic and non-ionic surfactants on carbon nanotubes in water with dissipative particle dynamics simulation.

    Science.gov (United States)

    Vo, Minh D; Shiau, Benjamin; Harwell, Jeffrey H; Papavassiliou, Dimitrios V

    2016-05-28

    The morphology of surfactants physically adsorbed on the surface of carbon nanotubes (CNTs) has a significant impact on the dispersion of CNTs in the solution. The adsorption of the surfactants alfoterra 123-8s (AF) and tergitol 15-s-40 (TG) on CNTs was investigated with dissipative particle dynamics (DPD) simulations, as well as the behavior of the binary surfactant system with CNTs. Properties of surfactants (i.e., critical micelle concentration, aggregation number, shape and size of micelle, and diffusivity) in water were determined to validate the simulation model. Results indicated that the assembly of surfactants (AF and TG) on CNTs depends on the interaction of the surfactant tail and the CNT surface, where surfactants formed mainly hemimicellar structures. For surfactants in solution, most micelles had spherical shape. The particles formed by the CNT and the adsorbed surfactant became hydrophilic, due to the outward orientation of the head groups of the surfactants that formed monolayer adsorption. In the binary surfactant system, the presence of TG on the CNT surface provided a considerable hydrophilic steric effect, due to the EO groups of TG molecules. It was also seen that the adsorption of AF was more favorable than TG on the CNT surface. Diffusion coefficients for the surfactants in the bulk and surface diffusion on the CNT were calculated. These results are applicable, in a qualitative sense, to the more general case of adsorption of surfactants on the hydrophobic surface of cylindrically shaped nanoscale objects.

  5. Adsorption of anionic and non-ionic surfactants on carbon nanotubes in water with dissipative particle dynamics simulation

    Science.gov (United States)

    Vo, Minh D.; Shiau, Benjamin; Harwell, Jeffrey H.; Papavassiliou, Dimitrios V.

    2016-05-01

    The morphology of surfactants physically adsorbed on the surface of carbon nanotubes (CNTs) has a significant impact on the dispersion of CNTs in the solution. The adsorption of the surfactants alfoterra 123-8s (AF) and tergitol 15-s-40 (TG) on CNTs was investigated with dissipative particle dynamics (DPD) simulations, as well as the behavior of the binary surfactant system with CNTs. Properties of surfactants (i.e., critical micelle concentration, aggregation number, shape and size of micelle, and diffusivity) in water were determined to validate the simulation model. Results indicated that the assembly of surfactants (AF and TG) on CNTs depends on the interaction of the surfactant tail and the CNT surface, where surfactants formed mainly hemimicellar structures. For surfactants in solution, most micelles had spherical shape. The particles formed by the CNT and the adsorbed surfactant became hydrophilic, due to the outward orientation of the head groups of the surfactants that formed monolayer adsorption. In the binary surfactant system, the presence of TG on the CNT surface provided a considerable hydrophilic steric effect, due to the EO groups of TG molecules. It was also seen that the adsorption of AF was more favorable than TG on the CNT surface. Diffusion coefficients for the surfactants in the bulk and surface diffusion on the CNT were calculated. These results are applicable, in a qualitative sense, to the more general case of adsorption of surfactants on the hydrophobic surface of cylindrically shaped nanoscale objects.

  6. Perfluorinated Alcohols Induce Complex Coacervation in Mixed Surfactants.

    Science.gov (United States)

    Jenkins, Samuel I; Collins, Christopher M; Khaledi, Morteza G

    2016-03-15

    Recently, we reported a unique and nearly ubiquitous phenomenon of inducing simple and complex coacervation in solutions of a broad variety of individual and mixed amphiphiles and over a wide range of concentrations and mole fractions. This paper describes a novel type of biphasic separation in aqueous solutions of mixed cationic-anionic (catanionic) surfactants induced by hexafluoroisopropanol (HFIP). The test cases included mixtures of cetyltrimethylammonium bromide (CTAB) and sodium dodecyl sulfate (SDS) (surfactants with different carbon chain lengths) as well as dodecyltrimethylammonium bromide (DTAB) with SDS (surfactants with the same carbon chain lengths). The CTAB-SDS-HFIP coacervate systems can be produced at many different mole ratios of surfactant, but DTAB-SDS-HFIP formed only coacervates at equimolar (1:1) mole ratios of DTAB and SDS. The phase-transition behavior of both systems was studied over a wide range of surfactant and HFIP concentrations at the stoichiometric (1:1) mole ratio of cationic/anionic surfactants. The chemical compositions of each of the two phases (aqueous-rich and coacervate phases) were studied with regard to the concentrations of HFIP, water, and individual surfactants. It is revealed that the surfactant-rich phase (coacervate phase) contains a large percentage of fluoroalcohol relative to the aqueous phase and is enriched in both surfactants but contains a small percentage of water. Surprisingly, the concentration of water in the coacervate phase increases as the total HFIP concentration is increased while the concentration of HFIP in the coacervate phase remains relatively constant, which means a larger amount of water associated with HFIP molecules is extracted into the coacervate phase, which results in the growth of the phase. The volume of the coacervate phase increases with an increase in surfactant concentration and total HFIP %. The coacervate phase is highly enriched in the two amphiphilic ions (DTA(+) and DS

  7. Application of peptide gemini surfactants as novel solubilization surfactants for photosystems I and II of cyanobacteria.

    Science.gov (United States)

    Koeda, Shuhei; Umezaki, Katsunari; Noji, Tomoyasu; Ikeda, Atsushi; Kawakami, Keisuke; Kondo, Masaharu; Yamamoto, Yasushi; Shen, Jian-Ren; Taga, Keijiro; Dewa, Takehisa; Ito, Shigeru; Nango, Mamoru; Tanaka, Toshiki; Mizuno, Toshihisa

    2013-09-17

    We designed novel peptide gemini surfactants (PG-surfactants), DKDKC12K and DKDKC12D, which can solubilize Photosystem I (PSI) of Thermosynecoccus elongatus and Photosystem II (PSII) of Thermosynecoccus vulcanus in an aqueous buffer solution. To assess the detailed effects of PG-surfactants on the original supramolecular membrane protein complexes and functions of PSI and PSII, we applied the surfactant exchange method to the isolated PSI and PSII. Spectroscopic properties, light-induced electron transfer activity, and dynamic light scattering measurements showed that PSI and PSII could be solubilized not only with retention of the original supramolecular protein complexes and functions but also without forming aggregates. Furthermore, measurement of the lifetime of light-induced charge-separation state in PSI revealed that both surfactants, especially DKDKC12D, displayed slight improvement against thermal denaturation below 60 °C compared with that using β-DDM. This degree of improvement in thermal resistance still seems low, implying that the peptide moieties did not interact directly with membrane protein surfaces. By conjugating an electron mediator such as methyl viologen (MV(2+)) to DKDKC12K (denoted MV-DKDKC12K), we obtained derivatives that can trap the generated reductive electrons from the light-irradiated PSI. After immobilization onto an indium tin oxide electrode, a cathodic photocurrent from the electrode to the PSI/MV-DKDKC12K conjugate was observed in response to the interval of light irradiation. These findings indicate that the PG-surfactants DKDKC12K and DKDKC12D provide not only a new class of solubilization surfactants but also insights into designing other derivatives that confer new functions on PSI and PSII.

  8. Surfactant therapy in late preterm infants

    Directory of Open Access Journals (Sweden)

    Murat Yurdakök

    2013-06-01

    Full Text Available Late preterm (LPT neonates are at a high risk for respiratory distress soon after birth due to respiratory distress syndrome (RDS, transient tachypnea of the newborn, persistent pulmonary hypertension, and pneumonia along with an increased need for surfactant replacement therapy, continuous positive airway pressure, and ventilator support when compared with the term neonates. In the past, studies on outcomes of infants with respiratory distress have primarily focused on extremely premature infants, leading to a gap in knowledge and understanding of the developmental biology and mechanism of pulmonary diseases in LPT neonates. Surfactant deficiency is the most frequent etiology of RDS in very preterm and moderately preterm infants, while cesarean section and lung infection play major roles in RDS development in LPT infants. The clinical presentation and the response to surfactant therapy in LPT infants may be different than that seen in very preterm infants. Incidence of pneumonia and occurrence of pneumothorax are significantly higher in LPT and term infants. High rates of pneumonia in these infants may result in direct injury to the type II alveolar cells of the lung with decreasing synthesis, release, and processing of surfactant. Increased permeability of the alveolar capillary membrane to both fluid and solutes is known to result in entry of plasma proteins into the alveolar hypophase, further inhibiting the surface properties of surfactant. However, the oxygenation index value do not change dramatically after ventilation or surfactant administration in LPT infants with RDS compared to very preterm infants. These finding may indicate a different pathogenesis of RDS in late preterm and term infants. In conclusion, surfactant therapy may be of significant benefit in LPT infants with serious respiratory failure secondary to a number of insults. However, optimal timing and dose of administration are not so clear in this group. Additional

  9. An Unusual Variation of Surface Tension with Concentration of.Mixed Cationic-anionic Surfactants

    Institute of Scientific and Technical Information of China (English)

    肖进新; 暴艳霞

    2001-01-01

    There are two platforms in the surface tension vs. concentration curve (γ-lgC curve) of cationic-anionic surfactant mixtures. The first platform is the same as that of common surfactant solution, and the cross point is the CMC. After the CMC, the mixtures form precipitate. At higher concentration, the mixtures form homogeneous sloution.When the mixtures form homogeneous solution at high concentration. surface tension increases with concentration, the becomes constant.So the γ-lgC curve exhibits the second platform. The surface tension at the second platform increases by increasing molar ratio of two surfactants and polar group size of surfactants, and decreases with adding inorganic salts.

  10. Investigation of the adsorption of anionic surfactants at different pH values by means of active carbon and the kinetics of adsorption

    Directory of Open Access Journals (Sweden)

    SIBEL ZOR

    2004-01-01

    Full Text Available In this study, the effect of pH on the removal of anionic surfactants, such as linear alkyl benzene sulfonate (LABS and dodecyl benzene sulfonate (DBS by means of adsorption by activated carbon was investigated. For this purpose activated carbon was used as adsorbent. Anionic surfactant solutions with initial pH values of 3, 6, 8 and 12 were used. The adsorption isotherms for the adsorption of anionic surfactants by active carbon at different pH were determined. These adsorption isotherms were seen to be consistent with Freundlich’s adsorption isotherm. k and n constants were determined from Freundlich’s linear equation. Adsorption rate constants were determined from the obtained kinetic curves which were suitable for the first order of rate kinetics.

  11. Porous gold nanobelts templated by metal-surfactant complex nanobelts.

    Science.gov (United States)

    Li, Lianshan; Wang, Zhijian; Huang, Teng; Xie, Jinglin; Qi, Limin

    2010-07-20

    Unique, porous gold nanobelts consisting of self-organized nanoparticles were synthesized in a high yield by morphology-preserved transformation from metal-surfactant complex precursor nanobelts formed by a bolaform surfactant dodecane-1,12-bis(trimethylammonium bromide) (N-C(12)-NBr(2)) and HAuCl(4). It was revealed that the precursor nanobelts of the stoichiometric N-C(12)-N(AuCl(4))(2) complex formed through electrostatic combination of the positively charged quaternary ammonium headgroups of N-C(n)-NBr(2) and the negatively charged AuCl(4)(-) ions. They were subsequently converted into porous gold nanobelts with shrunken sizes upon reduction by NaBH(4). The morphology of the produced gold nanostructures could be adjusted by changing the mixing ratio between N-C(12)-NBr(2) and HAuCl(4) in the reaction solution. It was found that the obtained porous Au nanobelts exhibited enhanced catalytic activity toward reduction of 4-nitrophenol compared with solid gold nanobelts, probably owing to their larger surface area and more active sites.

  12. A simplified treatment of surfactant effects on cloud drop activation

    Directory of Open Access Journals (Sweden)

    T. Raatikainen

    2010-07-01

    Full Text Available Dissolved surface active species, or surfactants, have a tendency to partition to solution surface and thereby decrease solution surface tension. Activating cloud droplets have large surface-to-volume ratios, and the amount of surfactant molecules in them is limited. Therefore, unlike with macroscopic solutions, partitioning to the surface can effectively deplete the droplet interior of surfactant molecules.

    Surfactant partitioning equilibrium for activating cloud droplets can be solved numerically from a group of equations. This can be a problem when surfactant effects are examined by using large-scale cloud models. Namely, computing time increases significantly due to the partitioning calculations done in the lowest levels of nested iterations.

    The purpose of this paper is to present analytical equations for surfactant partitioning equilibrium. Some simplifications are needed in deriving the equations, but the numerical errors caused by the simplifications are shown to be very minor. In addition, computing time is decreased roughly by an order of magnitude.

  13. Sizing up surfactant synthesis.

    Science.gov (United States)

    Han, SeungHye; Mallampalli, Rama K

    2014-08-01

    Phosphatidylcholine is generated through de novo synthesis and remodeling involving a lysophospholipid. In this issue of Cell Metabolism, research from the Shimizu lab (Harayama et al., 2014) demonstrates the highly selective enzymatic behavior of lysophospholipid acyltransferases. The authors present an enzymatic model for phosphatidylcholine molecular species diversification that impacts surfactant formation.

  14. Heteroepitaxial formation of aligned mesostructured silica films with large structural periodicities from mixed surfactant systems.

    Science.gov (United States)

    Hayase, Saeko; Kanno, Yosuke; Watanabe, Masatoshi; Takahashi, Masahiko; Kuroda, Kazuyuki; Miyata, Hirokatsu

    2013-06-11

    Liquid-crystal phases consisting of cylindrical micelles of amphiphilic block copolymers and silica precursors are epitaxially built up on aligned surface micelles formed by an alkyl-PEO surfactant, Brij56, irrespective of the large difference in the intrinsic structural periodicities resulting in the formation of fully aligned mesostructured silica films with large lattice constants. Brij56 works as an alignment controlling agent on rubbing-treated polyimide through selective adsorption from a precursor solution containing the two surfactants, a block copolymer and Brij56, through strong hydrophobic interactions to form an anisotropic surface micelle structure. Aligned mesostructured silica layers with larger periodicities, which dominantly consist of block copolymers, form on these aligned surface micelles by gradually changing the vertical periodicity keeping the lateral intermicelle distance constant. This can be regarded as a kind of heteroepitaxy because the lattice constant at the surface is different from that of the bulk of the film. On the basis of this new concept, highly aligned mesostructured silica films with structural periodicities as large as 10 nm are successfully formed, which has never been achieved when the block copolymers are used alone as the structure-directing agent. The periodicity of the aligned films can precisely be controlled by an appropriate choice of block copolymers and the mixing ratio of the two surfactants, which increases the opportunity for applications of these films with highly anisotropic mesoscale structure.

  15. Small-angle neutron scattering study of structural evolution of different phases in protein solution

    Indian Academy of Sciences (India)

    V K Aswal; S Chodankar; J Kohlbrecher; R Vavrin; A G Wagh

    2008-10-01

    Small-angle neutron scattering (SANS) has been used to study the structural evolution of different phases in protein solution leading to crystallization, denaturation and gelation. The protein solution under crystallization mostly consists of monomers and dimers, and higher-mers are not observed as they are perhaps formed in very small numbers. The onset and the rate of crystallization strongly depend on the salt concentration. Protein denaturation on addition of surfactant occurs due to the formation of micelle-like clusters along the unfolded polypeptide chains of the protein. The structure of such protein{surfactant complex is found to be independent of the size of the micelles in their pure surfactant solutions. The structure of temperature-induced protein gels shows a fractal structure. Rheology of these gels shows a strong dependence on varying pH or protein concentration, whereas the structure of such gels is found to be similar.

  16. COUPLING THE ALKALINE-SURFACTANT-POLYMER TECHNOLOGY AND THE GELATION TECHNOLOGY TO MAXIMIZE OIL PRODUCTION

    Energy Technology Data Exchange (ETDEWEB)

    Malcolm Pitts; Jie Qui; Dan Wilson; Phil Dowling

    2004-05-01

    Gelation technologies have been developed to provide more efficient vertical sweep efficiencies for flooding naturally fractured oil reservoirs or more efficient areal sweep efficiency those with high permeability contrast ''thief zones''. The field proven alkaline-surfactant-polymer technology economically recovers 15% to 25% OOIP more oil than waterflooding in the swept pore space of an oil reservoir. However, alkaline-surfactant-polymer technology is not amenable to the naturally fractured reservoirs or those with thief zones because much of the injected solution bypasses the target pore space containing oil. The objective of this work is to investigate whether combining these two technologies could broaden the applicability of alkaline-surfactant-polymer flooding into these reservoirs. Fluid-fluid interaction with different gel chemical compositions and alkaline-surfactant-polymer solution with pH values ranging from 9.2 to 12.9 have been tested. Aluminum-polyacrylamide gels are not stable to alkaline-surfactant-polymer solutions at any pH. Chromium--polyacrylamide gels with polymer to chromium ion ratios of 25 or greater were stable to alkaline-surfactant-polymer solutions if solution pH was 10.6 or less. When the polymer to chromium ion was 15 or less, chromium-polyacrylamide gels were stable to alkaline-surfactant-polymer solutions with pH values up to 12.9. Chromium-xanthan gum gels were stable to alkaline-surfactant-polymer solutions with pH values of 12.9 at the polymer to chromium ion ratios tested. Silicate-polyacrylamide, resorcinol-formaldehyde, and sulfomethylated resorcinol-formaldehyde gels were also stable to alkaline-surfactant-polymer solutions with pH values ranging from 9.2 to 12.9. Iron-polyacrylamide gels were immediately destroyed when contacted with any of the alkaline-surfactant-polymer solutions with pH values of 9.2 to 12.9.

  17. Characterization and control of surfactant-mediated Norovirus interactions.

    Science.gov (United States)

    Mertens, Brittany S; Velev, Orlin D

    2015-11-28

    Understanding of the colloidal interactions of Norovirus particles in aqueous medium could provide insights on the origins of the notorious stability and infectivity of these widespread viral agents. We characterized the effects of solution pH and surfactant type and concentration on the aggregation, dispersion, and disassembly of Norovirus virus-like particles (VLPs) using dynamic light scattering, electrophoretic light scattering, and transmission electron microscopy. Owing to net negative surface charge of the VLPs at neutral pH, low concentrations of cationic surfactant tend to aggregate the VLPs, whereas low concentrations of anionic surfactant tend to disperse the particles. Increasing the concentration of these surfactants beyond their critical micelle concentration leads to virus capsid disassembly and breakdown of aggregates. Non-ionic surfactants, however, had little effect on virus interactions and likely stabilized them additionally in suspension. The data were interpreted on the basis of simple models for surfactant binding and re-charging of the virus capsid. We used zeta potential data to characterize virus surface charge and interpret the mechanisms behind these demonstrated surfactant-virus interactions. The fundamental understanding and control of these interactions will aid in practical formulations for virus inactivation and removal from contaminated surfaces.

  18. Caractérisation des solutions de tensio-actif utilisées en récupération assistée Characterization of Surfactant Solutions Used in Enhanced Recovery

    OpenAIRE

    Moulu J. C.

    2006-01-01

    Des solutions de tensio-actif sont étudiées en vue de déterminer celles qui doivent être les plus efficaces pour le déplacement d'huile résiduelle en milieu poreux. Selon les propriétés de ces solutions au moment de leur injection, un banc d'huile se forme rapidement et progresse au niveau du front de tensio-actif, ou au contraire, les globules d'huile sont entraînés avec une vitesse faible dans l'ensemble du bouchon, les échanges entre les phases peuvent alors être importants. On a donc cher...

  19. Surfactant Enhanced Electroremediation of Phenanthrene

    Institute of Scientific and Technical Information of China (English)

    佘鹏; 杨建刚; 等

    2003-01-01

    Removal of hydrophobic organic contaminants(HOCs) form soil of low permeability by electroremediation was investigated by using phenanthrene and kaolinite as a model system.Tween 80 was added into the purging solution in order to enhance the solubility of phenanthrene.The effects of pH on the adsorption of phenanthrene and Tween 80 on kaolinite and the magnitude of ζ-potential of kaolinite were examined,respectively.The effects of electric field strength indicated by electric current on the electroremediation behavior,including the pH of purging solution,the conductivity,phenanthrene concentration and flow rate of effluent,were experimentally investigated,repectively,In case of an electric field of 25mA applied for 72 hours,over 90% of phenanthrene was removed from 424g(dry mass)of kaolinite at an energy consumption of 0.148kW.h.The experimental results described in present study show that the addition of surfactant into purging solution greatly enhances the removel of HOCs by electroremediation.

  20. Cost Effective Surfactant Formulations for Improved Oil Recovery in Carbonate Reservoirs

    Energy Technology Data Exchange (ETDEWEB)

    William A. Goddard; Yongchun Tang; Patrick Shuler; Mario Blanco; Yongfu Wu

    2007-09-30

    This report summarizes work during the 30 month time period of this project. This was planned originally for 3-years duration, but due to its financial limitations, DOE halted funding after 2 years. The California Institute of Technology continued working on this project for an additional 6 months based on a no-cost extension granted by DOE. The objective of this project is to improve the performance of aqueous phase formulations that are designed to increase oil recovery from fractured, oil-wet carbonate reservoir rock. This process works by increasing the rate and extent of aqueous phase imbibition into the matrix blocks in the reservoir and thereby displacing crude oil normally not recovered in a conventional waterflood operation. The project had three major components: (1) developing methods for the rapid screening of surfactant formulations towards identifying candidates suitable for more detailed evaluation, (2) more fundamental studies to relate the chemical structure of acid components of an oil and surfactants in aqueous solution as relates to their tendency to wet a carbonate surface by oil or water, and (3) a more applied study where aqueous solutions of different commercial surfactants are examined for their ability to recover a West Texas crude oil from a limestone core via an imbibition process. The first item, regarding rapid screening methods for suitable surfactants has been summarized as a Topical Report. One promising surfactant screening protocol is based on the ability of a surfactant solution to remove aged crude oil that coats a clear calcite crystal (Iceland Spar). Good surfactant candidate solutions remove the most oil the quickest from the surface of these chips, plus change the apparent contact angle of the remaining oil droplets on the surface that thereby indicate increased water-wetting. The other fast surfactant screening method is based on the flotation behavior of powdered calcite in water. In this test protocol, first the calcite

  1. Solubilization of pentanol by cationic surfactants and binary mixtures of cationic surfactants

    Energy Technology Data Exchange (ETDEWEB)

    Morgan, M.E.

    1993-12-31

    The research reported here has included studies of the solubilization of pentanol in hexadecylpyridinium chloride (CPC), trimethyletetradecylammonium chloride (C{sub 14}Cl), benzyldimethyltetradecylammonium chloride (C{sub 14}BzCl), benzyldimethylhexadecylpyridinium chloride (C{sub 16}BzCl), hexadecyltrimethylammonium bromide (CTAB), and binary mixtures of CPC + C{sub 16}BzCl and C{sub 14}Cl + C{sub 14}BzCl. Rather than using calorimetric methods, this project will employ headspace chromatography to measure solubilization of pentanol over a wide range of solute concentrations. While not yielding as much thermodynamic data as calorimetry, headspace chromatography is a more direct measure of the extent of solubilization. Using headspace chromatography, is a more direct measure of the extent of solubilization. Using headspace chromatography, this study will seek to determine whether strongly synergistic mixture ratios exist in the case of binary cationic surfactant systems. There are two equilibria in the pentanol-water-surfactant system: (1) The pentanol solubilized in micelles is in equilibrium with the monomeric pentanol in solution, and (2) the monomeric pentanol is in equilibrium with the pentanol in the vapor above the solution. To establish the link between the two equilibria, a sample of the vapor above pure liquid pentanol must be collected, in order to find the activity of pentanol in solution. Also, a calibration curve for various concentrations of pentanol in solution. From this type of data it is possible to infer both the concentration of pentanol solubilized in micelles and the concentrations of pentanol in the ``bulk`` solution outside the micelles. The method is equally applicable to systems containing a single surfactant as well as mixtures of surfactants.

  2. Evaluation of surfactant flushing for remediating EDC-tar contamination

    Science.gov (United States)

    Liang, Chenju; Hsieh, Cheng-Lin

    2015-06-01

    Ethylene dichloride tar (EDC-tar) is a dense non-aqueous phase liquid (DNAPL) waste originated from the process of vinyl chloride production, with major constituents including chlorinated aliphatic and aromatic hydrocarbons. This study investigated the feasibility of Surfactant Enhanced Aquifer Remediation (SEAR) for treating EDC-tar contaminated aquifers. Initial experiments explored the potential to enhance the apparent solubility of EDC-tar using single or mixed surfactants. The results showed that an aqueous solution mixed anionic and non-ionic surfactants (i.e., SDS/Tween 80) exhibited higher EDC-tar apparent solubility and lower surface tension than other surfactant systems tested. Additionally, alkaline pH aids in increasing the EDC-tar apparent solubility. In column flushing experiments, it was seen that the alkaline mixed SDS/Tween 80 solution showed better removal of pure EDC-tar from silica sand porous media. Furthermore, separation of EDC-tar in the surfactant solution was conducted employing a salting-out effect. Significant separation of DNAPL was observed when 13 wt.% or more NaCl was added to the solution. Overall, this study evaluates the feasibility of using SEAR for remediating EDC-tar contaminated subsurface soil and groundwater.

  3. Novel fluorinated gemini surfactants with γ-butyrolactone segments.

    Science.gov (United States)

    Kawase, Tokuzo; Okada, Kazuyuki; Oida, Tatsuo

    2015-01-01

    In this work, novel γ-butyrolactone-type monomeric and dimeric (gemini) surfactants with a semifluoroalkyl group [Rf- (CH2)3-; Rf = C4F9, C6F13, C8F17] as the hydrophobic group were successfully synthesized. Dimethyl malonate was dimerized or connected using Br(CH2)sBr (s = 0, 1, 2, 3) to give tetraesters, and they were bis-allylated. Radical addition of fluoroalkyl using Rf-I and an initiator, i.e., 2,2'-azobisisobutyronitrile for C4F9 or di-t-butyl peroxide for C6F13 and C8F17, was perform at high temperature, with prolonged heating, to obtain bis(semifluoroalkyl)-dilactone diesters. These dilactone diesters were hydrolyzed using KOH/EtOH followed by decarboxylation in AcOH to afford γ-butyrolactonetype gemini surfactants. Common 1 + 1 semifluoroalkyl lactone surfactants were synthesized using the same method. Their surfactant properties [critical micelle concentration (CMC), γCMC, pC20, ΓCMC, and AG] were investigated by measuring the surface tension of the γ-hydroxybutyrate form prepared in aqueous tetrabutylammonium hydroxide solution. As expected, the CMC values of the gemini surfactants were more than one order of magnitude smaller than those of the corresponding 1 + 1 surfactants. Other properties also showed the excellent ability of the gemini structure to reduce the surface tension. These surfactants were easily and quantitatively recovered by acidification. The monomeric surfactant was recovered in the γ-hydroxybutyric acid form, and the gemini surfactant as a mixture of γ-butyrolactone and γ-hydroxybutyric acid forms.

  4. Ranking of aqueous surfactant-humectant systems based on an analysis of in vitro and in vivo skin barrier perturbation measurements.

    Science.gov (United States)

    Ghosh, Saswata; Hornby, Sidney; Grove, Gary; Zerwick, Charles; Appa, Yohini; Blankschtein, Daniel

    2007-01-01

    We propose that skin electrical current measurements can be used in vitro to effectively rank aqueous solutions containing surfactants and humectants (the enhancer) contacting the skin, relative to a PBS aqueous solution (the control) contacting the skin, based on their ability to perturb the skin aqueous pores. Specifically, we develop an in vitro ranking metric using the increase in the skin electrical current induced by an enhancer relative to the control. Aqueous contacting solutions containing (i) surfactants [SDS (sodium dodecyl sulfate)] and C(12)E(6) [dodecyl hexa (ethylene oxide)], (ii) humectants (glycerol and propylene glycol), and (iii) a control (PBS) were studied. Utilizing the new in vitro ranking metric, these aqueous contacting solutions were ranked as follows (from the mildest to the harshest): glycerol aqueous surfactant-humectant solutions described above. The results of these in vivo measurements were found to be consistent with the ranking results obtained using the in vitro ranking metric. To further explore the validity of our model and to verify the skin barrier mitigating effect of glycerol, in vivo soap chamber measurements were carried out for aqueous SDS solutions containing 10 wt% added glycerol. These in vivo measurements support our recent in vitro finding that glycerol reduces the average radius and the pore number density of the skin aqueous pores, such that SDS micelles are hindered from penetrating into the skin and inducing skin barrier perturbation.

  5. Rheology of cellulose nanofibrils in the presence of surfactants.

    Science.gov (United States)

    Quennouz, Nawal; Hashmi, Sara M; Choi, Hong Sung; Kim, Jin Woong; Osuji, Chinedum O

    2016-01-07

    Cellulose nanofibrils (CNFs) present unique opportunities for rheology modification in complex fluids. Here we systematically consider the effect of ionic and non-ionic surfactants on the rheology of dilute CNF suspensions. Neat suspensions are transparent yield-stress fluids which display strong shear thinning and power-law dependence of modulus on concentration, G' ∼ c(2.1). Surfactant addition below a critical mass concentration cc produces an increase in the gel modulus with retention of optical clarity. Larger than critical concentrations induce significant fibril aggregation leading to the loss of suspension stability and optical clarity, and to aggregate sedimentation. The critical concentration was the lowest for a cationic surfactant (DTAB), cc ≈ 0.08%, while suspension stability was retained for non-ionic surfactants (Pluronic F68, TX100) at concentrations up to 8%. The anionic surfactant SDS led to a loss of stability at cc ≈ 1.6% whereas suspension stability was not compromised by anionic SLES up to 8%. Dynamic light scattering data are consistent with a scenario in which gel formation is driven by micelle-nanofibril bridging mediated by associative interactions of ethoxylated surfactant headgroups with the cellulose fibrils. This may explain the strong difference between the properties of SDS and SLES-modified suspensions. These results have implications for the use of CNFs as a rheology modifier in surfactant-containing systems.

  6. Size separation of analytes using monomeric surfactants

    Science.gov (United States)

    Yeung, Edward S.; Wei, Wei

    2005-04-12

    A sieving medium for use in the separation of analytes in a sample containing at least one such analyte comprises a monomeric non-ionic surfactant of the of the general formula, B-A, wherein A is a hydrophilic moiety and B is a hydrophobic moiety, present in a solvent at a concentration forming a self-assembled micelle configuration under selected conditions and having an aggregation number providing an equivalent weight capable of effecting the size separation of the sample solution so as to resolve a target analyte(s) in a solution containing the same, the size separation taking place in a chromatography or electrophoresis separation system.

  7. MICROBIAL SURFACTANTS. I. GLYCOLIPIDS

    Directory of Open Access Journals (Sweden)

    Pirog T. Р.

    2014-02-01

    Full Text Available The review is devoted to surface-active glycolipids. The general characteristics, the physiological role of the rhamnolipids, trehalose lipids, sophorolipids, mannosylerythritol lipids and their traditional producers — the representatives of the genera Pseudozyma, Pseudomonas, Rhodococcus and Candida are given. The detailed analysis of the chemical structure, the stages of the biosynthesis and the regulation of some low molecular glycolipids are done. The own experimental data concerning the synthesis intensification, the physiological role and the practical use of Rhodococcus erythropolis IMV Ac-5017, Acinetobacter calcoaceticus IMV B-7241 and Nocardia vaccinii IMV B-7405 surfactants, which are a complex of the glyco-, phospho-, amino- and neutral lipids (glycolipids of all strains are presented by trehalose mycolates are summarized. It was found that R. erythropolis IMV Ac-5017, A. calcoaceticus IMV B-7241 and N. vaccinii IMV B-7405 surfactants have protective, antimicrobial and antiadhesive properties. It was shown that R. erythropolis IMV Ac-5017, A. calcoaceticus IMV B-7241 and N. vaccinii IMV B-7405 surfactants preparation of cultural liquid intensified the degradation of oil in water due to the activation of the natural petroleum-oxidizing microflora.

  8. MICROBIAL SURFACTANTS. II. LIPOPEPTIDES

    Directory of Open Access Journals (Sweden)

    T. P. Pirog

    2014-04-01

    Full Text Available The classification and the chemical structure of the lipopeptides and their producers (bacteria of the genera Bacillus and Pseudomonas are given. The role of the lipopeptides in cells motility, biofilm formation, metal binding and xenobiotics degradation and their action on the cells of pro- and eukaryotes is summarized. The stages of the nonribosomal lipopeptides synthesis and the role of two-component (GacA/GacS, ComA/ComP and the quorum system regulation of this process are shown. The potential of lactic acid bacteria and marine microorganisms as alternative surfactants producers (glycolipids, lipopeptides, phospholipids and fatty acids, glycolipopeptides are discussed. Their productivity and advantages over traditional producers are given as well. The properties of surfactants synthesized by lactic acid bacteria (the reduction of the surface tension, the critical micelle concentration, the stability in a wide range of pH, the temperature, the biological activity are summarized. Surfactants of nonpathogenic probiotic bacteria could be used as effective antimicrobial agents and antiadhesive and marine producers which able to synthesize unique metabolites that are not produced by other microorganisms.

  9. Surfactant/detergent titration analysis method and apparatus for machine working fluids, surfactant-containing wastewater and the like

    Science.gov (United States)

    Smith, D.D.; Hiller, J.M.

    1998-02-24

    The present invention is an improved method and related apparatus for quantitatively analyzing machine working fluids and other aqueous compositions such as wastewater which contain various mixtures of cationic, neutral, and/or anionic surfactants, soluble soaps, and the like. The method utilizes a single-phase, non-aqueous, reactive titration composition containing water insoluble bismuth nitrate dissolved in glycerol for the titration reactant. The chemical reaction of the bismuth ion and glycerol with the surfactant in the test solutions results in formation of micelles, changes in micelle size, and the formation of insoluble bismuth soaps. These soaps are quantified by physical and chemical changes in the aqueous test solution. Both classical potentiometric analysis and turbidity measurements have been used as sensing techniques to determine the quantity of surfactant present in test solutions. This method is amenable to the analysis of various types of new, in-use, dirty or decomposed surfactants and detergents. It is a quick and efficient method utilizing a single-phase reaction without needing a separate extraction from the aqueous solution. It is adaptable to automated control with simple and reliable sensing methods. The method is applicable to a variety of compositions with concentrations from about 1% to about 10% weight. It is also applicable to the analysis of waste water containing surfactants with appropriate pre-treatments for concentration. 1 fig.

  10. Surfactant/detergent titration analysis method and apparatus for machine working fluids, surfactant-containing wastewater and the like

    Science.gov (United States)

    Smith, Douglas D.; Hiller, John M.

    1998-01-01

    The present invention is an improved method and related apparatus for quantitatively analyzing machine working fluids and other aqueous compositions such as wastewater which contain various mixtures of cationic, neutral, and/or anionic surfactants, soluble soaps, and the like. The method utilizes a single-phase, non-aqueous, reactive titration composition containing water insoluble bismuth nitrate dissolved in glycerol for the titration reactant. The chemical reaction of the bismuth ion and glycerol with the surfactant in the test solutions results in formation of micelles, changes in micelle size, and the formation of insoluble bismuth soaps. These soaps are quantified by physical and chemical changes in the aqueous test solution. Both classical potentiometric analysis and turbidity measurements have been used as sensing techniques to determine the quantity of surfactant present in test solutions. This method is amenable to the analysis of various types of new, in-use, dirty or decomposed surfactants and detergents. It is a quick and efficient method utilizing a single-phase reaction without needing a separate extraction from the aqueous solution. It is adaptable to automated control with simple and reliable sensing methods. The method is applicable to a variety of compositions with concentrations from about 1% to about 10% weight. It is also applicable to the analysis of waste water containing surfactants with appropriate pre-treatments for concentration.

  11. Dielectrophoresis of a surfactant-laden viscous drop

    Science.gov (United States)

    Mandal, Shubhadeep; Bandopadhyay, Aditya; Chakraborty, Suman

    2016-06-01

    The dielectrophoresis of a surfactant-laden viscous drop in the presence of non-uniform DC electric field is investigated analytically and numerically. Considering the presence of bulk-insoluble surfactants at the drop interface, we first perform asymptotic solution for both low and high surface Péclet numbers, where the surface Péclet number signifies the strength of surface convection of surfactants as compared to the diffusion at the drop interface. Neglecting fluid inertia and interfacial charge convection effects, we obtain explicit expression for dielectrophoretic drop velocity for low and high Péclet numbers by assuming small deviation of drop shape from sphericity and small deviation of surfactant concentration from the equilibrium uniform distribution. We then depict a numerical solution, assuming spherical drop, for arbitrary values of Péclet number. Our analyses demonstrate that the asymptotic solution shows excellent agreement with the numerical solution in the limiting conditions of low and high Péclet numbers. The present analysis shows that the flow-induced redistribution of the surfactants at the drop interface generates Marangoni stress, owing to the influence of the surfactant distribution on the local interfacial tension, at the drop interface and significantly alters the drop velocity at steady state. For a perfectly conducting/dielectric drop suspended in perfectly dielectric medium, Marangoni stress always retards the dielectrophoretic velocity of the drop as compared with a surfactant-free drop. For a leaky dielectric drop suspended in another leaky dielectric medium, in the low Péclet number limit, depending on the electrical conductivity and permittivity of both the liquids, the Marangoni stress may aid or retard the dielectrophoretic velocity of the drop. The Marangoni stress also has the ability to move the drop in the opposite direction as compared with a surfactant-free drop. This non-intuitive reverse motion of the drop is

  12. Performance of Hydrophobic Associating Water-solute Polymer/Surfactant System%疏水缔合聚合物/表面活性剂二元体系性能研究

    Institute of Scientific and Technical Information of China (English)

    曹伟佳; 卢祥国; 苏鑫; 杨怀军; 张杰

    2016-01-01

    of Dagang oilfield and the poor development effect of water flooding,the feasibility of the application of hydrophobic associating polymer/surfactant displacement system was probed. The dimension of polymer molecular coil Dh,interfacial tension between the crude oil and the hydrophobic associating polymer AP-P7 solution or“polymer/surfactant”displacement system,compounded of AP-P7 and nonionic surfactant Guan 109PS985,and their influential factors were studied under the experimental conditions,andβ-cyclodextrin(β-cd) was used as the regulator to improve the suitability of polymer with oil reservoir,also the EOR mechanism of polymer flooding and“polymer/surfactant”displacement system in high viscosity and high condensate reservoirs was analyzed. The results showed that,β-cd could change the molecular morphological structure of the hydrophobic associating polymer,and make the matching of the polymer structure and core pore throat stronger,resulting in the reduction of the blockage. The viscosity hydrophobic associating polymer solution and“polymer/surfactant”system prepared with soft water,increased by 35.2%and 20.2%compared to that of the inject water,the viscosity of the polymer solution at the concentration of 2000 mg/L prepared with injected water and soft water, respectively,were 223.4 mPa.s and 302.5 mPa·s,When adding 700 mg/L ofβ-cd,the viscosity decreased to be of 26.5 mPa·s and 35.3 mPa·s,respectively,which indicated that the addition of theβ-cd made the viscosity of AP-P7 solutions decrease obviously. When the concentration of β-cd increased from 10 mg/L to 700 mg/L,the Dh of AP-P7 decreased from 235 nm to 155 nm. In addition,when the concentration ofβ-cd increased from 10 mg/L to 700 mg/L or the concentration of Ca2+and Mg2+decreased from 508 mg/L to 0,the interfacial tension between the polymer system and the simulated reduced to some degree. The 2000 mg/L polymer solution containingβ-cd was injected into the core with permeability

  13. 单一和混合表面活性剂对硫丹的增溶作用研究%Water Solubility Enhancement of Endosulfan by Single and Mixed Surfactant Solutions

    Institute of Scientific and Technical Information of China (English)

    熊佰炼; 张进忠

    2015-01-01

    研究了添加和不添加Na2SiO3两种情况下,单一和非/阴离子混合表面活性剂对硫丹的增溶作用。结果表明,不添加Na2SiO3时,单一表面活性剂中硫丹溶解度顺序为Tween 80>Triton X-100>SDS,与临界胶束浓度(CMCs)呈负相关。非、阴离子表面活性剂的质量比大于或等于4:1时,混合表面Tween 80/SDS和Triton X-100/SDS均对硫丹起协同增溶作用,Tween 80/SDS对硫丹的增溶能力强于Triton X-100/SDS。混合表面活性剂Tween 80/SDS和Triton X-100/SDS对硫丹的质量增溶比(WSR)分别与对应的单一非离子表面活性剂Tween 80和Triton X-100相差不大。添加Na2SiO3可提高单一和混合表面活性剂的增溶能力。Na2SiO3浓度为1000 mg·L-1的Tween 80和Tween 80/SDS溶液是硫丹良好的增溶剂。%The solubilization of endosulfan by single non-ionic surfactants and mixed anionic/non-ionic surfactants in the presence or ab-sence of Na2SiO3 was studied. The results showed that, in the absence of Na2SiO3, the solubilities of endosulfan followed a decreasing order of Tween 80, Triton X-100 and SDS, which were negatively correlated with critical micelle concentrations (CMCs) of these sur-factants. When the mass ratio of anionic and nonionic surfactants was not less than 4:1, the mixed surfactants Tween 80/SDS and Triton X-100/SDS both could synergistically increase the solubility of endosulfan, and the solubilization capacity of the former was stronger than the latter. The weight solubilization ratio (WSR) of mixed surfactants, i.e. Tween 80/SDS and Triton X-100/SDS, were similar to those corresponding single non-ionic surfactant. The addition of Na2SiO3 could increase the solubility of endosulfan in mixed surfactant and single surfactants. Compared with other surfactants, Tween 80/SDS and Tween 80 in the presence of Na2SiO3 have good efficacies for the solubilization to endosulfan.

  14. Surfactants at the Design Limit.

    Science.gov (United States)

    Czajka, Adam; Hazell, Gavin; Eastoe, Julian

    2015-08-04

    This article analyzes how the individual structural elements of surfactant molecules affect surface properties, in particular, the point of reference defined by the limiting surface tension at the aqueous cmc, γcmc. Particular emphasis is given to how the chemical nature and structure of the hydrophobic tails influence γcmc. By comparing the three different classes of surfactants, fluorocarbon, silicone, and hydrocarbon, a generalized surface packing index is introduced which is independent of the chemical nature of the surfactants. This parameter ϕcmc represents the volume fraction of surfactant chain fragments in a surface film at the aqueous cmc. It is shown that ϕcmc is a useful index for understanding the limiting surface tension of surfactants and can be useful for designing new superefficient surfactants.

  15. Effect of Added Surfactants on the Dynamic Interfacial Tension Behaviour of Alkaline/Diluted Heavy Crude Oil System Effet de l’ajout de tensioactifs sur le comportement dynamique de la tension interfaciale du système solution alcaline/brut dilué

    Directory of Open Access Journals (Sweden)

    Trabelsi S.

    2013-02-01

    Full Text Available This study has been undertaken to get a better understanding of the interactions between Enhanced Oil Recovery (EOR surfactants used in chemical flooding and in situ surfactants present in an heavy oil. We report an experimental study of dynamic Interfacial Tension (IFT behaviour of diluted heavy oil/surfactant enhanced-alkaline systems. The dynamic IFT was measured using pendant drop and spinning drop tensiometers. The dynamic IFT between diluted heavy oil and alkaline solution (pH 11 with no added surfactant increased sharply with time, which was attributed to the transfer of the in situ surfactant (produced by saponification of the acids groups present in the crude oil across the oil/water interface. The addition of Sodium Dodecyl Benzene Sulfonate (SDBS above the Critical Micellar Concentration (CMC ~ 0.002%, changed completely the dynamic IFT behaviour of the diluted heavy oil as the IFT strongly decreased and finally reached a plateau, of about 1.5 × 10-3 mN/m at a concentration of only 0.02%. We attributed the efficiency of SDBS to a synergistic effect between the in situ surfactant and the added surfactant that form a mixed interfacial monolayer, which is very efficient in decreasing the IFT to ultra low values and in resisting mass transfer across the oil/water interface. Cette étude a été réalisée pour mieux comprendre les interactions entre les tensioactifs utilisés pour la récupération assistée de pétrole et les tensioactifs in situ présents dans le brut. Nous expérimentons le comportement dynamique des tensions interfaciales (mesurées par les méthodes de goutte pendante et goutte tournante entre le brut lourd dilué et les solutions alcalines avec ajout de tensioactif. La tension interfaciale dynamique entre le brut dilué et une solution alcaline (pH 11 sans ajout de tensioactif croît fortement au cours du temps, cette augmentation est attribuée au transfert des tensioactifs in situ (produits par saponification des

  16. SOLUTIONING

    Directory of Open Access Journals (Sweden)

    Maria de Hoyos Guajardo, Ph.D. Candidate, M.Sc., B.Eng.

    2004-11-01

    Full Text Available The theory that is presented below aims to conceptualise how a group of undergraduate students tackle non-routine mathematical problems during a problem-solving course. The aim of the course is to allow students to experience mathematics as a creative process and to reflect on their own experience. During the course, students are required to produce a written ‘rubric’ of their work, i.e., to document their thoughts as they occur as well as their emotionsduring the process. These ‘rubrics’ were used as the main source of data.Students’ problem-solving processes can be explained as a three-stage process that has been called ‘solutioning’. This process is presented in the six sections below. The first three refer to a common area of concern that can be called‘generating knowledge’. In this way, generating knowledge also includes issues related to ‘key ideas’ and ‘gaining understanding’. The third and the fourth sections refer to ‘generating’ and ‘validating a solution’, respectively. Finally, once solutions are generated and validated, students usually try to improve them further before presenting them as final results. Thus, the last section deals with‘improving a solution’. Although not all students go through all of the stages, it may be said that ‘solutioning’ considers students’ main concerns as they tackle non-routine mathematical problems.

  17. Influence of Watering with an enriched solution of surfactants on the soil properties and vegetation growth. Experimental model with two types of soils: district cambisol and calcaricum cambisol; Influencia del riego con solucion enriquecida en tensoactivos sobre las propiedades del suelo y el desarrollo vigetal

    Energy Technology Data Exchange (ETDEWEB)

    Cruz Caravaca, M. T.; Crespo Alia, M. A. [Universidad Complutense. Madrid (Spain)

    2000-07-01

    A study done on the the influence of watering with an enriched solution of surfactants on the soil properties and vegetation growth using an experimental model with two types of soils, each one with different characteristic: district Cambisol and calcaricum Cambisol. The results show significant differences in conductivity, organic carbon content, clay content and in phosphates. As well, the sodium enrichment of the adjuvants components of the detergent employed significantly influence the content of free clay and the SAR values. The chosen vegetation was seen to be affected in these areas: sprouting, vegetal mass and principally in the amount of calcium foliage. (Author) 18 refs.

  18. 表面活性剂从碱性氰化液中萃取金的微观机理研究(Ⅰ):萃取体系的优化%The Micromechanism of Extracting Gold from Alkaline Cyanide Solution with Surfactants(Ⅰ):The Optimization of Extraction System

    Institute of Scientific and Technical Information of China (English)

    余建民; 李奇伟; 陈景

    2001-01-01

    系统研究了含氧、含磷、含氮及含硫类萃取剂分别在水相中加入及不加入典型表面活性剂的2种情况下,对Au(CN)-2的萃取性能,优选出了适宜的萃取体系。%Extracting gold with extractants containing oxgen,phosphorus,nitrogan or suphur from alkaline cyanide solution with or without typical surfactants has been extensively studied.The optimum extraction system is also given in the present paper.

  19. BINDING ISOTHERMS SURFACTANT-PROTEINS

    Directory of Open Access Journals (Sweden)

    Elena Irina Moater

    2011-12-01

    Full Text Available The interactions between surfactants and proteins shows some similarities with interactions between surfactants and polymers, but the hydrophobic amphoteric nature of proteins and their secondary and tertiary structure components make them different from conventional polymer systems. Many studies from the past about surfactant - proteins bonding used the dialysis techniques. Other techniques used to determine the binding isotherm, included ultrafiltration, ultracentrifugation, potentiometry, ion-selective electrode method and surface tension. High affinity isotherms which are typical of an anionic surfactant - protein bonding, exhibit an initial increase steep followed by a slow growth region and then a vertical growth above a certain concentration. This isotherm is typical of ionic surfactant to protein binding. Often the high affinity initial bond appears at very low concentrations of surfactant and therefore in some protein-surfactant systems, the exact shape of the isotherm in this region may be missing. The surfactant - protein binding is influenced by a number of variables such as the nature and chain length of surfactant, pH, ionic strength, temperature, nature of this protein and additives.

  20. Synthesis and properties of di-n-dodecyl alpha,omega-alkyl bisphosphate surfactants

    NARCIS (Netherlands)

    Duivenvoorde, F.L.; Feiters, M.C.; Van der Gaast, S.J.; Engberts, J.B.F.N.

    1997-01-01

    Three gemini and two bolaform bisphosphate surfactants of the type 12-s-12, with s = 6, 8, 12, 18, and 24 carbon atoms, have been synthesized and their aggregation behavior has been studied. The bolaform surfactants 12-18-12 and 12-24-12 were found to form vesicles in aqueous solution, as indicated

  1. Improving reseeding success after catastrophic wildfire - shifting the paradigm with surfactant seed coatings

    Science.gov (United States)

    The application of soil surfactants in wildfire-affected ecosystems has been limited due to logistical and economic constraints associated with the standard practice of using large quantities of irrigation water as the surfactant carrier. We tested a potential solution to this problem that uses seed...

  2. Improving reseeding success after catastrophic wildfire with surfactant seed coating technology

    Science.gov (United States)

    The application of soil surfactants in wildfire-affected ecosystems has been limited due to logistical and economic constraints associated with the standard practice of using large quantities of irrigation water as the surfactant carrier. We tested a potential solution to this problem that uses seed...

  3. Synthesis and properties of di-n-dodecyl alpha,omega-alkyl bisphosphate surfactants

    NARCIS (Netherlands)

    Duivenvoorde, F.L.; Feiters, M.C.; Van der Gaast, S.J.; Engberts, J.B.F.N.

    1997-01-01

    Three gemini and two bolaform bisphosphate surfactants of the type 12-s-12, with s = 6, 8, 12, 18, and 24 carbon atoms, have been synthesized and their aggregation behavior has been studied. The bolaform surfactants 12-18-12 and 12-24-12 were found to form vesicles in aqueous solution, as indicated

  4. Quantitative Structure-Property Relationship on Prediction of Surface Tension of Nonionic Surfactants

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A quantitative structure-property relationship (QSPR) study has been made for the prediction of the surface tension of nonionic surfactants in aqueous solution.The regressed model includes a topological descriptor,the Kier & Hall index of zero order (KH0) of the hydrophobic segment of surfactant and a quantum chemical one,the heat of formation () of surfactant molecules.The established general QSPR between the surface tension and the descriptors produces a correlation coefficient of multiple determination,=0.9877,for 30 studied nonionic surfactants.

  5. Electrophoretic separations in poly(dimethylsiloxane) microchips using a mixture of ionic and zwitterionic surfactants.

    Science.gov (United States)

    Guan, Qian; Noblitt, Scott D; Henry, Charles S

    2012-01-01

    The use of mixtures of ionic and zwitterionic surfactants in poly(dimethylsiloxane) (PDMS) microchips is reported. The effect of surfactant concentration on electroosmotic flow (EOF) was studied for a single anionic surfactant (sodium dodecyl sulfate, SDS), a single zwitterionic surfactant (N-tetradecylammonium-N,N-dimethyl-3-ammonio-1-propanesulfonate, TDAPS), and a mixed SDS/TDAPS surfactant system. SDS increased the EOF as reported previously while TDAPS showed an initial increase in EOF followed by a reduction at higher concentrations. When TDAPS was added to a solution containing SDS, the EOF decreased in a concentration-dependent manner. The EOF for all three surfactant systems followed expected pH trends, with increasing EOF at higher pH. The mixed surfactant system allowed tuning of the EOF across a range of pH and concentration conditions. After establishing the EOF behavior, the adsorption/desorption kinetics were measured and showed a slower adsorption/desorption rate for TDAPS than SDS. Finally, the separation and electrochemical detection of model catecholamines in buffer and reduced glutathione in red blood cell lysate using the mixed surfactant system were explored. The mixed surfactant system provided shorter analysis times and/or improved resolution when compared to the single surfactant systems.

  6. Inorganic Salts Effect on Adsorption Behavior of Surfactant AEC at Liquid/Liquid Interface

    Directory of Open Access Journals (Sweden)

    Changhua Yang

    2013-07-01

    Full Text Available Behaviors of nonionic-anionic surfactant sodium fatty Alcohol polyoxyethylene Ether Carboxylate (AEC at dodecane/water interface influenced by inorganic salts NaCl, CaCl2 and MgCl2 were investigated by interfacial tension methods and molecular dynamics simulation. Contrasted distributions of various salts at interface and in aqueous solutions and resulting lowering the interfacial tension have been observed. Composition of surfactants-salts complex at interface surrounding different cations within 2.5 Å were found to be in two categories: (i the octahedral complexation of divalent cation was generated by the participation of surfactant head group and water molecule, (ii only water molecules were involved in the complexation. According to the simulation results, all the Na+ involved in type ii, without any direct interaction with surfactant head group, while Ca2+ and Mg2+ involved in type I, following the formula: Ca2++4 (surfactant +2(H2 O⇄ [Ca (surfactant4 [(H2 O]2]2+ M2+g+(surfactant+5 (H2 O⇄[Mg (surfactant [(H2 O]5 ]2+ This strongly chelate interaction between Ca2+ and surfactants makes surfactants more stretched at interface, thus more effective in oil/water interface.

  7. New theoretical framework for designing nonionic surfactant mixtures that exhibit a desired adsorption kinetics behavior.

    Science.gov (United States)

    Moorkanikkara, Srinivas Nageswaran; Blankschtein, Daniel

    2010-12-21

    How does one design a surfactant mixture using a set of available surfactants such that it exhibits a desired adsorption kinetics behavior? The traditional approach used to address this design problem involves conducting trial-and-error experiments with specific surfactant mixtures. This approach is typically time-consuming and resource-intensive and becomes increasingly challenging when the number of surfactants that can be mixed increases. In this article, we propose a new theoretical framework to identify a surfactant mixture that most closely meets a desired adsorption kinetics behavior. Specifically, the new theoretical framework involves (a) formulating the surfactant mixture design problem as an optimization problem using an adsorption kinetics model and (b) solving the optimization problem using a commercial optimization package. The proposed framework aims to identify the surfactant mixture that most closely satisfies the desired adsorption kinetics behavior subject to the predictive capabilities of the chosen adsorption kinetics model. Experiments can then be conducted at the identified surfactant mixture condition to validate the predictions. We demonstrate the reliability and effectiveness of the proposed theoretical framework through a realistic case study by identifying a nonionic surfactant mixture consisting of up to four alkyl poly(ethylene oxide) surfactants (C(10)E(4), C(12)E(5), C(12)E(6), and C(10)E(8)) such that it most closely exhibits a desired dynamic surface tension (DST) profile. Specifically, we use the Mulqueen-Stebe-Blankschtein (MSB) adsorption kinetics model (Mulqueen, M.; Stebe, K. J.; Blankschtein, D. Langmuir 2001, 17, 5196-5207) to formulate the optimization problem as well as the SNOPT commercial optimization solver to identify a surfactant mixture consisting of these four surfactants that most closely exhibits the desired DST profile. Finally, we compare the experimental DST profile measured at the surfactant mixture condition

  8. Vesicle formation and stability in the surfactant sodium 4-(1'-heptylnonyl) benzenesulfonate

    Energy Technology Data Exchange (ETDEWEB)

    Franses, E.I.; Talmon, Y.; Scriven, L.E.; Davis, H.T.; Miller, W.G.

    1982-04-01

    Surfactants composed of a hydrophilic moiety covalently attached to the end of a hydrocarbon chain (e.g., sodium dodecyl sulfate), spontaneously form micelles, equilibrium aggregates, in solution if the surfactant concentration exceeds a critical value called the CMC. Naturally occurring double-tail surfactants (e.g., phospholipids) are not known to form micelles. Over a considerable range in surfactant concentration, 2 phases coexist in equilibrium: a hydrated, multilamellar (smectic) surfactant phase and an aqueous phase saturated with surfactant. In this report the preparation of vesicles, their direct, unstained visualization by electron microscopy, and investigation of their stability and structure by turbidimetry, conductimetry, light microscopy, densitometry, scanning calorimetry, and nuclear magnetic resonance spectroscopy are discussed. Dispersed liquid crystal was studied by the same means. For comparison, parallel studies on bovine lecithin are presented. From the results, it is concluded that these vesicles may be stable for many months, but eventually revert to multilamellar liquid crystals.

  9. EFFECT OF SURFACTANTS ON Ni-TiN NANOCOMPOSITE COATINGS PREPARED BY ULTRASONIC ELECTRODEPOSITION

    Institute of Scientific and Technical Information of China (English)

    XIA Fafeng; JIA Zhenyuan; WU Menghua; LI Zhi

    2008-01-01

    Ni-TiN nanocomposite coatings were prepared by ultrasonic electrodeposition, and the effects of the surfactants on the coatings were investigated and the microstructure and micro rigidity of the coatings were characterized. Samples were also submitted to corrosion tests in 3% NaCl solution. The results showed that the surfactants had great effects on Ni-TiN nanocomposite coatings. The composite coatings prepared by ultrasonic electrodeposition with the surfactants were better than that of the coatings prepared without surfactants. The favorable properties of Ni-TiN nanocomposite coatings were prepared with the mixing of the non-ion and positive ion surfactants. The concentration of the mixing was 80 mg/L, and the ratio of the non-ion and positive ion surfactants was 1: 2.

  10. Enhanced desorption of phenanthrene from contaminated soil using anionic/nonionic mixed surfactant.

    Science.gov (United States)

    Zhou, Wenjun; Zhu, Lizhong

    2007-05-01

    A new approach using an anionic/nonionic mixed surfactant, sodium dodecyl sulphate (SDS) with Triton X-100 (TX100), was utilized for the desorption of phenanthrene from an artificial contaminated natural soil in an aim to improve the efficiency of surfactant remediation technology. The experimental results showed that the presence of SDS not only reduced the sorption of TX100 onto the natural soil, but also enhanced the solubilization of TX100 for phenanthrene, both of which resulted in the distribution of phenanthrene in soil-water systems decreasing with increasing mole fraction of SDS in surfactant solutions. These results can be attributed to the formation of mixed micelles in surfactant solution and the corresponding decrease in the critical micelle concentration of TX100 in mixed solution. The batch desorption experiments showed that the desorption percentage of phenanthrene from the contaminated soil with mixed solution was greater than that with single TX100 solution and appeared to be positively related to the mole fraction of SDS in surfactant solution. Thus, the anionic/nonionic mixed surfactants are more effective for the desorption of phenanthrene from the contaminated soil than a single nonionic surfactant.

  11. INFLUENCE OF CULTIVATION CONDITIONS ON ANTIMICROBIAL PROPERTIES OF Nocardia vaccinii ІMV B-7405 SURFACTANTS

    Directory of Open Access Journals (Sweden)

    Т. P.

    2016-02-01

    Full Text Available The aim of the work was investigation of antimicrobial effect of Nocardia vaccinii ІMV B-7405 surfactants, synthesized in various culture conditions, against phytopathogenic bacteria of genera Pseudomonas, Xanthomonas, and Pectobacterium. The antimicrobial properties of surfactant were determined in suspension culture by Koch method and also by index of the minimum inhibitory concentration. Surfactants were extracted from supernatant of cultural liquid using mixture of chloroform and methanol (2: 1. It has been established that antimicrobial properties of surfactants depend on the nature of the carbon source in the medium (refined vegetable oil, as well as waste oil after frying potatoes and meat, glycerol, the duration of the cultivation (5 and 7 days, the degree of purification of the surfactants (the supernatant of cultural liquid, purified surfactants solution and the test culture type. The highest antimicrobial activity was exhibited by purified surfactants solutions synthesized by microorganisms on the waste oil after potato frying (decreased survival of pathogenic bacteria by 50–95%, and surfactants formed within 7 days of strain B-7405 ІMV cultivation on all test substrates (minimum inhibitory concentration 7–40 µg/mL, which is several times lower than the surfactant, synthesized for 5 days. These data are promising for the development of ecologically friendly biopreparations for the regulation of the number of phytopathogenic bacteria.

  12. Chemoenzymatic synthesis and properties of novel lactone-type anionic surfactants.

    Science.gov (United States)

    Mori, Keisuke; Matsumura, Shuichi

    2012-01-01

    Two series of lactone-type surfactants with and without a hexyl side chain were prepared by the cyclocondensation of dimethyl alkanedioates with unsaturated diols, such as cis-2-butene-1,4-diol and ricinoleyl alcohol, using a lipase, followed by the addition of hydrophilic 3-mercaptopropionic acid in the presence of triethylamine. The lactone-type surfactants showed clear cmc values and surface tension lowering in aqueous solution irrespective of the hexyl side chain. It was found that the cmc values of lactone-type surfactants were lower than that of typical anionics, e.g., sodium laurate, and the cmc value became lower with increasing size of the lactone ring. The adsorption area at the surface of the aqueous lactone-type surfactant solution was larger when compared to the corresponding non-lactone-type surfactants. Lactone-type surfactants without the hexyl side chain aggregated quickly, forming 3-10 nm micelles; on the other hand, lactone-type surfactants with the hexyl side chain formed significantly larger micelles. This is due to the steric hindrance of the hexyl group on the lactone ring. The solubilization ability of the lactone-type surfactants with a hexyl side chain was superior to those without a hexyl side chain. The lactone-type surfactants showed a high foaming power and low foaming stability. They were also biodegraded by activated sludge.

  13. Influência dos Íons Mg, Ca, Fe, Cu e Zn sobre a tensão superficial estática de soluções contendo surfatante Influence of Mg, Ca, Fe, Cu and Zn Ions on static surface tension of surfactant solutions

    Directory of Open Access Journals (Sweden)

    F.M.L. Silva

    2006-09-01

    Full Text Available O objetivo do estudo foi avaliar a influência da presença de cinco íons em uma calda de pulverização contendo o surfatante Aterbane. A tensão superficial foi analisada por meio da medição da massa de um conjunto de 25 gotas, com quatro repetições constituindo um tratamento. O trabalho foi dividido em duas etapas. Na primeira, os tratamentos foram combinados em esquema fatorial 9x5x2, sendo nove concentrações do surfatante Aterbane (0,01; 0,025; 0,05; 0,1; 0,2; 0,5; 1; 2; e 3%, cinco íons (Mg++, Ca++, Fe+++, Cu+++ e Zn+++ e duas concentrações desses elementos (10 e 100 ppm. Na segunda etapa, os tratamentos foram combinados em esquema fatorial 5x5x1, utilizandose os mesmos cinco elementos (Mg++, Ca++, Fe+++, Cu+++ e Zn+++, em cinco concentrações (1, 5, 20, 50 e 200 ppm, com apenas uma concentração do surfatante Aterbane (0,025%. Outros nove tratamentos permitiram avaliar as tensões superficiais das concentrações do surfatante (0,01; 0,025; 0,05; 0,1; 0,2; 0,5; 1; 2; e 3% sem a adição dos íons. Os resultados mostraram que houve interferência dos íons sobre as soluções, já que, com exceção do Fe+++ (na concentração de 10 e 100 ppm e do Cu+++ (na concentração de 100 ppm, todos os íons reduziram a tensão mínima alcançada e aumentaram a eficiência do surfatante, implicando benefícios à ação do surfatante e sobre as características de possíveis soluções de aplicação. Todos os íons avaliados promoveram reduções nas tensões superficiais de soluções do surfatante na concentração de 0,025%.The objective of this study was to evaluate the influence of 5 ions on a spray solution containing the surfactant aterbane. Surface tension was analyzed by measuring the mass of a set of 25 drops, with four repetitions constituting a treatment. The work was divided in two stages. In the first, the treatments were arranged in a 9x5x2 factorial design, nine Aterbane concentrations (0.01; 0.025; 0.05; 0.1; 0.2; 0

  14. COUPLING THE ALKALINE-SURFACTANT-POLYMER TECHNOLOGY AND THE GELATION TECHNOLOGY TO MAXIMIZE OIL PRODUCTION

    Energy Technology Data Exchange (ETDEWEB)

    Malcolm Pitts; Jie Qi; Dan Wilson

    2004-10-01

    Gelation technologies have been developed to provide more efficient vertical sweep efficiencies for flooding naturally fractured oil reservoirs or more efficient areal sweep efficiency for those with high permeability contrast ''thief zones''. The field proven alkaline-surfactant-polymer technology economically recovers 15% to 25% OOIP more oil than waterflooding from swept pore space of an oil reservoir. However, alkaline-surfactant-polymer technology is not amenable to naturally fractured reservoirs or those with thief zones because much of injected solution bypasses target pore space containing oil. This work investigates whether combining these two technologies could broaden applicability of alkaline-surfactant-polymer flooding into these reservoirs. A prior fluid-fluid report discussed interaction of different gel chemical compositions and alkaline-surfactant-polymer solutions. Gel solutions under dynamic conditions of linear corefloods showed similar stability to alkaline-surfactant-polymer solutions as in the fluid-fluid analyses. Aluminum-polyacrylamide, flowing gels are not stable to alkaline-surfactant-polymer solutions of either pH 10.5 or 12.9. Chromium acetate-polyacrylamide flowing and rigid flowing gels are stable to subsequent alkaline-surfactant-polymer solution injection. Rigid flowing chromium acetate-polyacrylamide gels maintained permeability reduction better than flowing chromium acetate-polyacrylamide gels. Silicate-polyacrylamide gels are not stable with subsequent injection of either a pH 10.5 or a 12.9 alkaline-surfactant-polymer solution. Neither aluminum citrate-polyacrylamide nor silicate-polyacrylamide gel systems produced significant incremental oil in linear corefloods. Both flowing and rigid flowing chromium acetate-polyacrylamide gels produced incremental oil with the rigid flowing gel producing the greatest amount. Higher oil recovery could have been due to higher differential pressures across cores. None of

  15. Optimization and mechanism of surfactant accelerating leaching test

    Institute of Scientific and Technical Information of China (English)

    艾纯明; 吴爱祥; 王贻明; 侯春来

    2016-01-01

    To solve the problem of slow leaching speed of copper, surfactant was added into lixivium as leaching agent in the experiment. Based on physical chemistry and seepage flow mechanics, the leaching mechanics of surfactant was analyzed. The solution surface tension and surfactant adsorbing on the surface of ore have a significant impact on the surface wetting effect. With leaching rate for response, the study screened out three main factors by Plackett-Burman design method: the sulfuric acid concentration, surfactant concentration and temperature. Among these three factors, the surfactant concentration is the most important contributor to leaching rate. After obtaining the experiment center by the steepest ascent experiment, a continuous variable surface model was built by response surface methodology. By solving quadratic polynomial equation, optimal conditions for leaching were finally obtained as follows:the sulfuric acid concentration was 60 g/L, the surfactant concentration was 0.00914 mol/L, and the temperature was 45 °C. The leaching rate was 66.81%in the optimized leaching conditions, which was close to the predicted value, showing that regression result was good.

  16. Research on surfactant flooding in high temperature and high-salinity reservoir for enhanced oil recovery

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Ming [Southwest Petroleum Univ., Chengdu, Sichuan (China). State Key Lab. of Oil and Gas Reservoir Geology and Exploitation; Southwest Petroleum Univ., Chengdu, Sichuan (China). School of Material Science and Engineering; Zhao, Jinzhou; Yang, Yan [Southwest Petroleum Univ., Chengdu, Sichuan (China). State Key Lab. of Oil and Gas Reservoir Geology and Exploitation; Wang, Xu [Southwest Petroleum Univ., Chengdu, Sichuan (China). School of Material Science and Engineering

    2013-05-15

    The aim of this work was to research the solution properties of a new surfactant flooding system for high temperature and high salinity reservoir, which include trimeric sulfonate surfactants 1,2,3-tri(2-oxypropyl sulfonation-3-alkylether-propoxyl) propanes (TTSS-n) and anion-nonionic surfactant NPSO [sodium nonyl phenol polyethyleneoxy ether sulfonate, (EO = 10)]. The critical micelle concentrations (CMCs) of five trimeric sulfonate surfactants were smaller than 400 mg L{sup -1}. Furthermore, their interfacial tensions (IFTs) could reach an ultralow value with Tazhong 4 oil at lower concentrations. Through optimized formulation, we found that TTSS-12 had better properties and was selected as the major component of the surfactant flooding system. We designed an optimal formulation of the surfactant flooding system with 1000 mg . L{sup -1} TTSS-12 and 1000 mg . L{sup -1} NPSO surfactant. The system with a very small surfactant concentration could reach ultralow IFT with Tazhong 4 crude oils at high temperature (110 C) and high concentration formation brine (112,228.8 mg/L TDS), which proved that the simpler component surfactant had better reservoir compatibility. NPSO could weaken the disadvantage of the surfactant TTSS-12 in oil/water interface. The stability of this surfactant flooding system was evaluated by aging time, static adsorption and chromatographic separation. All experiments showed that it still keeps ultralow IFT in high temperature and high salinity conditions. Coreflooding experimentation showed that average oil recovery reached 9.8 wt% by surfactant flooding, therefore, it is feasible to use as a surfactant flooding system for enhanced oil recovery (EOR). (orig.)

  17. Synthesis of organic rectorite with novel Gemini surfactants for copper removal

    Energy Technology Data Exchange (ETDEWEB)

    Han, Guocheng; Han, Yang [State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou 510640 (China); Wang, Xiaoying, E-mail: xyw@scut.edu.cn [State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou 510640 (China); Liu, Shijie, E-mail: sjliu@163.com [State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou 510640 (China); Department of Paper and Bioprocess Engineering, State University of New York, College of Environmental Science and Forestry, 1 Forestry Drive, Syracuse, NY 13210 (United States); Sun, Runcang [State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou 510640 (China); China Beijing Key Laboratory of Lignocellulosic Chemistry, Beijing Forestry University, Beijing 100083 (China)

    2014-10-30

    Graphical abstract: Three Gemini surfactants showed stronger rapid intercalation capacity into rectorite and behaved better on Cu{sup 2+} removal than two single-chain surfactants, which were positive to their increasing amount and chain length. - Highlights: • Modification of rectorite (REC) with several surfactants was performed in 1 h. • The arrangement of Gemini surfactants in REC layers was discussed. • All ORECs displayed better adsorption capacities on Cu{sup 2+} than pure REC. • Gemini-REC behaved better than single-chain surfactant modified REC on Cu{sup 2+} removal. • The adsorption capacity was positive to the amount and chain length of surfactant. - Abstract: Three novel Gemini surfactants were used to prepare organic rectorite (OREC) under microwave irradiation, in comparison with single-chain surfactant ester quaternary ammonium salt (EQAS) and cetyltrimethyl ammonium bromide (CTAB). The structure and morphology of OREC were characterized by XRD, BET, FT-IR, TEM and TGA. The removal of Cu{sup 2+} on OREC from aqueous solution was performed. The results reveal that Gemini surfactants modified REC had larger interlayer distance and higher surface area than single-chain surfactants EQAS and CTAB, and the increasing amount or chain length of Gemini surfactants led to larger layer spacing and higher adsorption capacities. The adsorption behavior of Gemini surfactant modified REC can be better described by Freundlich adsorption isotherm model, with a maximum adsorption capacity of 15.16 mg g{sup −1}. The desorption and regeneration experiments indicate good reuse property of Gemini modified REC adsorbent. Therefore, this study may widen the utilization of Gemini surfactants modified layered silicates.

  18. Growth Mechanism of Gold Nanorods in Binary Surfactant System

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Bo-Mi; Seo, Sun-Hwa; Joe, Ara; Shim, Kyu-Dong; Jang, Eue-Soon [Kumoh National Institute of Technology, Gumi (Korea, Republic of)

    2016-06-15

    In order to reveal the growth mechanism of gold nanorods (GNRs) in a binary surfactant system, we synthesized various GNRs by changing the concentration of the surfactants, AgNO{sub 3}, and HBr in the growth solution. We found that the benzyldime thylhexadecylammoniumchloride surfactant had weak interaction with the gold ions, but it could reduce the membrane fluidity. In addition, we could dramatically decrease the cetyltrimethylammonium bromide concentration required for GNR growth by adding an HBr solution. Notably, Ag{sup +} ions were necessary to break the symmetry of the seed crystals for GNR growth, but increasing the concentration of Ag{sup +} and Br{sup -} ions caused a decrease in the template size.

  19. ADSORPTION OF SURFACTANT ON CLAYS

    Science.gov (United States)

    Surfactants used to enhance remediation of soils by soil washing are often lost in the process. Neither the amount nor the cause of this loss is known. It is assumed that clays present in the soil are responsible for the loss of the surfactant. In this papere, adsorption prope...

  20. Lung surfactant protein A (SP-A) interactions with model lung surfactant lipids and an SP-B fragment.

    Science.gov (United States)

    Sarker, Muzaddid; Jackman, Donna; Booth, Valerie

    2011-06-07

    Surfactant protein A (SP-A) is the most abundant protein component of lung surfactant, a complex mixture of proteins and lipids. SP-A performs host defense activities and modulates the biophysical properties of surfactant in concerted action with surfactant protein B (SP-B). Current models of lung surfactant mechanism generally assume SP-A functions in its octadecameric form. However, one of the findings of this study is that when SP-A is bound to detergent and lipid micelles that mimic lung surfactant phospholipids, it exists predominantly as smaller oligomers, in sharp contrast to the much larger forms observed when alone in water. These investigations were carried out in sodium dodecyl sulfate (SDS), dodecylphosphocholine (DPC), lysomyristoylphosphatidylcholine (LMPC), lysomyristoylphosphatidylglycerol (LMPG), and mixed LMPC + LMPG micelles, using solution and diffusion nuclear magnetic resonance (NMR) spectroscopy. We have also probed SP-A's interaction with Mini-B, a biologically active synthetic fragment of SP-B, in the presence of micelles. Despite variations in Mini-B's own interactions with micelles of different compositions, SP-A is found to interact with Mini-B in all micelle systems and perhaps to undergo a further structural rearrangement upon interacting with Mini-B. The degree of SP-A-Mini-B interaction appears to be dependent on the type of lipid headgroup and is likely mediated through the micelles, rather than direct binding.

  1. Jamming dynamics of stretch-induced surfactant release by alveolar type II cells.

    Science.gov (United States)

    Majumdar, Arnab; Arold, Stephen P; Bartolák-Suki, Erzsébet; Parameswaran, Harikrishnan; Suki, Béla

    2012-03-01

    Secretion of pulmonary surfactant by alveolar epithelial type II cells is vital for the reduction of interfacial surface tension, thus preventing lung collapse. To study secretion dynamics, rat alveolar epithelial type II cells were cultured on elastic membranes and cyclically stretched. The amounts of phosphatidylcholine, the primary lipid component of surfactant, inside and outside the cells, were measured using radiolabeled choline. During and immediately after stretch, cells secreted less surfactant than unstretched cells; however, stretched cells secreted significantly more surfactant than unstretched cells after an extended lag period. We developed a model based on the hypothesis that stretching leads to jamming of surfactant traffic escaping the cell, similar to vehicular traffic jams. In the model, stretch increases surfactant transport from the interior to the exterior of the cell. This transport is mediated by a surface layer with a finite capacity due to the limited number of fusion pores through which secretion occurs. When the amount of surfactant in the surface layer approaches this capacity, interference among lamellar bodies carrying surfactant reduces the rate of secretion, effectively creating a jam. When the stretch stops, the jam takes an extended time to clear, and subsequently the amount of secreted surfactant increases. We solved the model analytically and show that its dynamics are consistent with experimental observations, implying that surfactant secretion is a fundamentally nonlinear process with memory representing collective behavior at the level of single cells. Our results thus highlight the importance of a jamming dynamics in stretch-induced cellular secretory processes.

  2. Effect of light on self-assembly of aqueous mixtures of sodium dodecyl sulfate and a cationic, bolaform surfactant containing azobenzene.

    Science.gov (United States)

    Hubbard, F Pierce; Abbott, Nicholas L

    2007-04-24

    We report light and small-angle neutron scattering measurements that characterize microstructures formed in aqueous surfactant solutions (up to 1.0 wt % surfactant) containing mixtures of sodium dodecyl sulfate (SDS) and the light-sensitive bolaform surfactant, bis(trimethylammoniumhexyloxy)azobenzene dibromide (BTHA) as a function of composition, equilibration time, and photostationary state (i.e., solutions rich in cis-BTHA or trans-BTHA). We observed formation of vesicles in both SDS-rich and trans-BTHA-rich regions of the microstructure diagram, with vesicles present over a particularly broad range of compositions for trans-BTHA-rich solutions. Illumination of mixtures of BTHA and SDS with a broadband UV light source leads to formation of photostationary states where the fraction of BTHA present as cis isomer (75-80% cis-BTHA) is largely independent of the mixing ratio of SDS and BTHA. For a relatively limited set of mixing ratios of SDS and BTHA, we observed UV illumination of SDS-rich vesicles to result in the reversible transformation of the vesicles to micellar aggregates and UV illumination of BTHA-rich vesicles to result in irreversible precipitation. Surprisingly, however, for many mixtures of trans-BTHA and SDS that formed solutions containing vesicles, illumination with UV light (which was confirmed to lead to photoisomerization of BTHA) resulted in only a small decrease in the number of vesicles in solution, relatively little change in the sizes of the remaining vesicles, and coexistance of the vesicles with micelles. These observations are consistent with a physical model in which the trans and cis isomers of BTHA present at the photostationary state tend to segregate between the different microstructures coexisting in solution (e.g., vesicles rich in trans-BTHA and SDS coexist with micelles rich in cis-BTHA and SDS). The results presented in this paper provide guidance for the design of light-tunable surfactants systems.

  3. Innovation in surfactant therapy II: surfactant administration by aerosolization.

    Science.gov (United States)

    Pillow, J Jane; Minocchieri, S

    2012-01-01

    Instilled bolus surfactant is the only approved surfactant treatment for neonatal respiratory distress syndrome. However, recent trends towards increased utilization of noninvasive respiratory support for preterm infants with surfactant deficiency have created a demand for a similarly noninvasive means of administering exogenous surfactant. Past approaches to surfactant nebulization met with varying success due to inefficient aerosol devices resulting in low intrapulmonary delivery doses of surfactant with variable clinical effectiveness. The recent development of vibrating membrane nebulizers, coupled with appropriate positioning of the interface device, indicates that efficient delivery of aerosolized surfactant is now a realistic goal in infants. Evidence of clinical effect despite low total administered dose in pilot studies, together with suggestions of enhanced homogeneity of pulmonary distribution indicate that this therapy may be applied in a cost-effective manner, with minimal patient handling and disruption. These studies need to be subjected to appropriately designed randomized controlled trials. Further work is also required to determine the optimum delivery route (mask, intranasal prong, nasopharyngeal or laryngeal), dosing amount and redosing interval.

  4. Tensão superficial dinâmica e ângulo de contato de soluções aquosas com surfatantes em superfícies artificiais e naturais Dynamic surface tension and contact angle of water solutions with spray surfactants in artificial and natural surfaces

    Directory of Open Access Journals (Sweden)

    Cristina A. R. Iost

    2010-08-01

    Full Text Available O trabalho objetivou avaliar o efeito de surfatantes em soluções aquosas sobre a tensão superficial dinâmica e ângulo de contato das gotas em diferentes superfícies: artificiais (lâmina de vidro e de óxido de alumínio e naturais (superfícies adaxiais de folhas de Euphorbia heterophylla, Ipomoea grandifolia e Brachiaria plantaginea. Seis formulações de surfatantes (Antideriva®; Uno®; Pronto 3®; Li-700®; Supersil® e Silwet L-77®, respectivamente nas doses recomendadas do produto comercial (0,050; 0,025; 0,100; 0,250; 0,100 e 0,100 % v v-1 e o dobro delas, foram avaliadas em soluções aquosas. A tensão superficial dinâmica e o ângulo de contato formado sobre as superfícies naturais foram medidos por tensiômetro. Os ângulos de contato formados pelas gotas nas superfícies artificiais foram obtidos por análise de imagens capturadas por uma câmera digital. Os surfatantes influenciam nas propriedades físico-químicas de soluções aquosas. As soluções contendo os surfatantes Silwet L-77® e Supersil®; nas doses de 0,100 e 0,200% v v-1; proporcionaram maiores reduções na tensão superficial dinâmica e menores ângulos de contato das gotas sobre as superfícies artificiais e naturais. Os surfatantes organossiliconados em solução aquosa foram mais eficientes na redução da tensão superficial e proporcionaram maior molhamento de superfícies natural e artificial. Em alvos naturais, essas propriedades obtidas com organossiliconados são dependentes das características de superfície das espécies vegetais.The aim of the work was to evaluate the effect of surfactants in water solutions on dynamic surface tension and contact angle formed by the spray droplets in different surfaces: artificial (glass and aluminum oxide slides and natural (leaves surface of three species of weeds: Euphorbia heterophylla, Ipomoea grandifolia e Brachiaria plantaginea. Were studied six surfactants formulations (AntiderivaTM; UnoTM; Pronto 3TM

  5. Polyelectrolyte surfactant aggregates and their deposition on macroscopic surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Voisin, David

    2002-07-01

    Oppositely charged surfactant and polyelectrolyte are present in hair shampoos and conditioners, together with particles (e.g. anti-dandruff agents for scalp) and droplets (e.g. silicone oil for the hair). These are normally formulated at high surfactant concentrations, beyond the flocculation region for the polyelectrolyte concentration used. However, on dilution with water, during application, flocs are formed which carry the particles and droplets to the scalp and hair. The addition of an anionic surfactant to an aqueous solution of cationic polyelectrolyte, at a given concentration, can lead to the formation of polyelectrolyte-surfactant 'particles', in which the surfactant 'binds' to the polyelectrolyte. This occurs from the critical association concentration (CAC), up to the surfactant concentration corresponding to maximum binding. Within this range of surfactant concentrations, the surfactant bound to the polyelectrolyte is thought to associate to form what might be termed 'internal micelles'. Each polyelectrolyte-surfactant particle in the region of the CAC, and just beyond, contains many polyelectrolyte chains, held together essentially by micelle bridges. These particles, however, remain net positively charged, and therefore stable. At the other end of the binding range of the surfactant, so many internal micelles are present that the polymer-surfactant particles are now net negatively charged. Indeed binding stops since no further micelles can be accommodated. Again, the particles are stable. However, there exists a range of surfactant concentrations, lying within the range referred to above, where the net charge is reduced sufficiently that the polymer-surfactant particles will flocculate to form much larger structures. The onset of this second range might be termed the 'critical flocculation concentration' (CFC), and the end, the 'critical stabilisation concentration' (CSC). In this work, the CFC and

  6. Ecotoxicological characterization of polyoxyethylene glycerol ester non-ionic surfactants and their mixtures with anionic and non-ionic surfactants.

    Science.gov (United States)

    Ríos, Francisco; Fernández-Arteaga, Alejandro; Lechuga, Manuela; Fernández-Serrano, Mercedes

    2017-03-03

    This paper reports on a study that investigated the aquatic toxicity of new non-ionic surfactants derived from renewable raw materials, polyoxyethylene glycerol ester (PGE), and their binary mixtures with anionic and non-ionic surfactants. Toxicity of pure PGEs was determined using representative organisms from different trophic levels: luminescent bacteria (Vibrio fischeri), microalgae (Pseudokirchneriella subcapitata), and freshwater crustaceans (Daphnia magna). Relationships between toxicity and the structural parameters such as unit of ethylene oxide (EO) and hydrophilic-lipophilic balance (HLB) were evaluated. Critical micellar concentration (CMC) in the conditions of the toxicity test was also determined. It was found that the toxicity of the aqueous solutions of PGE decreased when the number of EO units in the molecule, HLB, and CMC increased. PGEs showed lower CMC in marine medium, and the toxicity to V. ficheri is lower when the CMC was higher. Given their non-polar nature, narcosis was expected to be the primary mode of toxic action of PGEs. For the mixture of surfactants, we observed that the mixtures with PGE that had the higher numbers of EO units were more toxic than the aqueous solutions of pure surfactants. Moreover, we found that concentration addition was the type of action more likely to occur for mixtures of PGE with lower numbers of EO units with non-ionic surfactants (alkylpolyglucoside and fatty alcohol ethoxylate), whereas for the mixture of PGE with lower EO units and anionic surfactant (ether carboxylic derivative), the most common response type was response addition. In case of mixtures involving amphoteric surfactants and PGEs with the higher numbers of EO units, no clear pattern with regard to the mixture toxicity response type could be observed.

  7. Interaction of nonionic surfactant AEO9 with ionic surfactants*

    OpenAIRE

    2005-01-01

    The interaction in two mixtures of a nonionic surfactant AEO9 (C12H25O(CH2CH2O)9H) and different ionic surfactants was investigated. The two mixtures were AEO9/sodium dodecyl sulfate (SDS) and AEO9/cetyltrimethylammonium bromide (CTAB) at molar fraction of AEO9, α AEO9=0.5. The surface properties of the surfactants, critical micelle concentration (CMC), effectiveness of surface tension reduction (γ CMC), maximum surface excess concentration (Γ max) and minimum area per...

  8. Bending moduli and spontaneous curvature of the monolayer in a surfactant bilayer

    NARCIS (Netherlands)

    Kik, R.A.; Kleijn, J.M.; Leermakers, F.A.M.

    2005-01-01

    We developed a method to evaluate the mechanical properties of the monolayers in symmetric surfactant bilayers using self-consistent field theory. A specific boundary condition is used to impose the same curvature onto the two opposing monolayers at the surfactant chemical potential equal to that of

  9. Bending moduli and spontaneous curvature of the monolayer in a surfactant bilayer

    NARCIS (Netherlands)

    Kik, R.A.; Kleijn, J.M.; Leermakers, F.A.M.

    2005-01-01

    We developed a method to evaluate the mechanical properties of the monolayers in symmetric surfactant bilayers using self-consistent field theory. A specific boundary condition is used to impose the same curvature onto the two opposing monolayers at the surfactant chemical potential equal to that of

  10. Adsorption and micellization of surfactants : comparison of theory and experiment

    NARCIS (Netherlands)

    Boehmer, M.

    1991-01-01

    The purpose of this thesis is to extend the knowledge of micellization and adsorption of surfactants in aqueous solutions or the solid /electrolyte interface. To this end experimental results for well defined systems have been compared with theoretical calculations.

    The theoretical

  11. SURFACTANT ENHANCED REMEDIATION OF SOIL COLUMNS CONTAMINATED BY RESIDUAL TETRACHLOROETHYLENE

    Science.gov (United States)

    The ability of aqueous surfactant solutions to recover tetrachloroethylene (PCE) entrapped in Ottawa sand was evaluated in four column experiments. Residual PCE was emplaced by injecting 14C-labeled PCE into water-saturated soil columns and displacing the free product ...

  12. Synergetic effect of chelating agent and nonionic surfactant for benzotriazole removal on post Cu-CMP cleaning

    Science.gov (United States)

    Yanlei, Li; Yuling, Liu; Chenwei, Wang; Yue, Li

    2016-08-01

    The cleaning of copper interconnects after chemical mechanical planarization (CMP) process is a critical step in integrated circuits (ICs) fabrication. Benzotriazole (BTA), which is used as corrosion inhibitor in the copper CMP slurry, is the primary source for the formation of organic contaminants. The presence of BTA can degrade the electrical properties and reliability of ICs which needs to be removed by using an effective cleaning solution. In this paper, an alkaline cleaning solution was proposed. The alkaline cleaning solution studied in this work consists of a chelating agent and a nonionic surfactant. The removal of BTA was characterized by contact angle measurements and potentiodynamic polarization studies. The cleaning properties of the proposed cleaning solution on a 300 mm copper patterned wafer were also quantified, total defect counts after cleaning was studied, scanning electron microscopy (SEM) review was used to identify types of BTA to confirm the ability of cleaning solution for BTA removal. All the results reveal that the chelating agent can effectively remove the BTA residual, nonionic surfactant can further improve the performance. Project supported by the Natural Science Foundation of Hebei Province, China (No. F2015202267) and the Scientific Innovation Grant for Excellent Young Scientists of Hebei University of Technology (No. 2015007).

  13. Small-angle neutron scattering from mixtures of sodium dodecyl sulfate and a cationic, bolaform surfactant containing azobenzene.

    Science.gov (United States)

    Hubbard, F Pierce; Santonicola, Gabriella; Kaler, Eric W; Abbott, Nicholas L

    2005-07-05

    This paper reports on the microstructures formed in aqueous solutions containing mixtures of sodium dodecyl sulfate (SDS) and a photosensitive, bolaform surfactant, bis(trimethylammoniumhexyloxy)azobenzene dibromide (BTHA). By using quasi-elastic light scattering and small-angle neutron scattering, we determined that aqueous solutions containing SDS and the trans isomer of BTHA (0.1 wt % total surfactant, 15 mol % BTHA, 85 mol % SDS) form vesicles with average hydrodynamic diameters of 1350 +/- 50 angstroms and bilayer thicknesses of 35 +/- 2 angstroms. The measured bilayer thickness is consistent with a model of the vesicle bilayer in which the trans isomer of BTHA spans the bilayer. Upon illumination with UV light, the BTHA underwent photoisomerization to produce a cis-rich photostationary state (80% cis isomer). We measured this photoisomerization to drive the reorganization of vesicles into cylindrical aggregates with cross-sectional radii of 19 +/- 3 angstroms and average hydrodynamic diameters of 240 +/- 50 angstroms. Equilibration of the cis-rich solution in the dark at 25 degrees C for 12 h or illumination of the solution with visible light leads to the recovery of the trans-rich photostationary state of the solution and the reformation of vesicles, thus demonstrating the potential utility of this system as the basis of a tunable fluid.

  14. MICROBIAL SURFACTANTS IN ENVIRONMENTAL TECHNOLOGIES

    Directory of Open Access Journals (Sweden)

    T. P. Pirog

    2015-08-01

    Full Text Available It was shown literature and own experimental data concerning the use of microbial surface active glycolipids (rhamno-, sophoro- and trehalose lipids and lipopeptides for water and soil purification from oil and other hydrocarbons, removing toxic heavy metals (Cu2+, Cd2+, Ni2+, Pb2+, degradation of complex pollution (oil and other hydrocarbons with heavy metals, and the role of microbial surfactants in phytoremediation processes. The factors that limit the use of microbial surfactants in environmental technologies are discussed. Thus, at certain concentrations biosurfactant can exhibit antimicrobial properties and inhibit microorganisms destructing xenobiotics. Microbial biodegradability of surfactants may also reduce the effectiveness of bioremediation. Development of effective technologies using microbial surfactants should include the following steps: monitoring of contaminated sites to determine the nature of pollution and analysis of the autochthonous microbiota; determining the mode of surfactant introduction (exogenous addition of stimulation of surfactant synthesis by autochthonous microbiota; establishing an optimal concentration of surfactant to prevent exhibition of antimicrobial properties and rapid biodegradation; research both in laboratory and field conditions.

  15. Surfactant Facilitated Spreading of Aqueous Drops on Hydrophobic Surfaces

    Science.gov (United States)

    Kumar, Nitin; Couzis, Alex; Maldareili, Charles; Singh, Bhim (Technical Monitor)

    2001-01-01

    Microgravity technologies often require aqueous phases to spread over nonwetting hydrophobic solid surfaces. Surfactants facilitate the wetting of water on hydrophobic surfaces by adsorbing on the water/air and hydrophobic solid/water interfaces and lowering the surface tensions of these interfaces. The tension reductions decrease the contact angle, which increases the equilibrium wetted area. Hydrocarbon surfactants; (i.e., amphiphiles with a hydrophobic moiety consisting of an extended chain of (aliphatic) methylene -CH2- groups attached to a large polar group to give aqueous solubility) are capable of reducing the contact angles on surfaces which are not very hydrophobic, but do not reduce significantly the contact angles of the very hydrophobic surfaces such as parafilm, polyethylene or self assembled monolayers. Trisiloxane surfactants (amphiphiles with a hydrophobe consisting of methyl groups linked to a trisiloxane backbone in the form of a disk ((CH3)3-Si-O-Si-O-Si(CH3)3) and an extended ethoxylate (-(OCH2CH2)a-) polar group in the form of a chain with four or eight units) can significantly reduce the contact angle of water on a very hydrophobic surface and cause rapid and complete (or nearly complete) spreading (termed superspreading). The overall goal of the research described in this proposal is to establish and verify a theory for how trisiloxanes cause superspreading, and then use this knowledge as a guide to developing more general hydrocarbon based surfactant systems which superspread. We propose that the trisiloxane surfactants superspread because their structure allows them to strongly lower the high hydrophobic solid/aqueous tension when they adsorb to the solid surface. When the siloxane adsorbs, the hydrophobic disk parts of the molecule adsorb onto the surface removing the surface water. Since the cross-sectional area of the disk is larger than that of the extended ethoxylate chain, the disks can form a space-filling mat on the surface which

  16. Network Consistent Data Association.

    Science.gov (United States)

    Chakraborty, Anirban; Das, Abir; Roy-Chowdhury, Amit K

    2016-09-01

    Existing data association techniques mostly focus on matching pairs of data-point sets and then repeating this process along space-time to achieve long term correspondences. However, in many problems such as person re-identification, a set of data-points may be observed at multiple spatio-temporal locations and/or by multiple agents in a network and simply combining the local pairwise association results between sets of data-points often leads to inconsistencies over the global space-time horizons. In this paper, we propose a Novel Network Consistent Data Association (NCDA) framework formulated as an optimization problem that not only maintains consistency in association results across the network, but also improves the pairwise data association accuracies. The proposed NCDA can be solved as a binary integer program leading to a globally optimal solution and is capable of handling the challenging data-association scenario where the number of data-points varies across different sets of instances in the network. We also present an online implementation of NCDA method that can dynamically associate new observations to already observed data-points in an iterative fashion, while maintaining network consistency. We have tested both the batch and the online NCDA in two application areas-person re-identification and spatio-temporal cell tracking and observed consistent and highly accurate data association results in all the cases.

  17. A conductometric investigation of hydroxypropylmethyl cellulose/sodium dodecyl sulfate/nonionic surfactant systems

    Directory of Open Access Journals (Sweden)

    Petrović Lidija B.

    2014-01-01

    Full Text Available Surfactant mixtures are very often used in various cosmetic and pharmaceutical products because they commonly act in synergism and provide more favorable properties than the single surfactants. At the same time, the 9 presence of polymers in mixtures of surfactants may lead to molecular interactions thereby affecting product stability and activity. For these reasons it is very important to determine the surfactant interactions influence on 1micellization and mixed micellization, as well as polymer-surfactants mixed micelles interactions. In this work we examined self-aggregation of nonionic surfactants, polysorbate 20 (Tween 20, polyoxyethylene octylphenyl ether (Triton X100 and polyoxyethylene-polyoxypropylene block copolymer (Pluronic F68 with ionic surfactant, sodium dodecylsulfate, in aqueous solution at 40ºC using conductometric titration method. It was found that concentration region for mixed micelle formation depends on nonionic surfactant characteristics and its concentration. Formation of surfactants mixed micelles in the presence of nonionic polymer, hydroxypropylmethyl cellulose, and their binding to polymer hydrophobic sites, were investigated too. Analysis of obtained results points to different kinds of interactions in investigated systems, which are crucial for their application. [Projekat Ministarstva nauke Republike Srbije, br. III 46010

  18. Reversibly enhanced aqueous solubilization of volatile organic compounds using a redox-reversible surfactant

    Institute of Scientific and Technical Information of China (English)

    Yingjie Li; Senlin Tian; Hong Mo; Ping Ning

    2011-01-01

    Surfactant-enhanced remediation (SER) is an effective method for the removal of volatile organic compounds (VOCs) from contaminated soils and groundwater.To reuse the surfactant the VOCs must be separated from the surfactant solutions.The water solubility of VOCs can be enhanced using reversible surfactants with a redox-acive group,(ferrocenylmethyl)dodecyldimethylammonium bromide (Fc12) and (ferrocenylmethyl)tetradecanedimethylammonium bromide (Fc14),above and below their critical micelle concentrations (CMC) under reducing (I+) and oxidative (I2+) conditions.The CMC values of Fc12 and Fc14 in I+ are 0.94 and 0.56 mmol/L and the solubilization of toluene by Fc12 and Fc14 in I+ for toluene is higher than the solubilization achieved with sodium dodecyl sulfate,cetyltrimethylammonium bromide and Trition X-114.The solubilization capacity of the ferrocenyl surfactants for each tested VOCs ranked as follows:ethylbenzene > toluene > benzene.The solubilities of VOCs by reversible surfactant in I+ were 30% higher than those in 12+ at comparable surfactant concentrations.The effects of Fc14 concentrations on VOCs removal efficiency were as follows:benzene > toluene > ethylbenzene.However,an improved removal efficiency was achieved at low ferrocenyl surfactant concentrations.Furthermore,the reversible surfactant could be recycled through chemical approaches to remove organic pollutants,which could significantly reduce the operating costs of SER technology.

  19. Washing Phenanthrene and Pyrene Contaminated Soil Using Surfactant Solutions%表面活性剂对菲/芘模拟污染黄土的洗脱作用

    Institute of Scientific and Technical Information of China (English)

    刘婷; 钟金魁; 赵保卫; 冉婧媛; 石夏颖

    2013-01-01

    采用聚乙二醇辛基酚基醚(TX100)、聚氧乙烯失水山梨醇单油酸酯(TW80)、十二烷基苯磺酸钠(SDBS)和十二烷基硫酸钠(SDS)4种表面活性剂对菲、芘及其混合物模拟污染黄土进行洗脱实验,研究4种表面活性剂对菲、芘的洗脱作用.结果表明:随着表面活性剂浓度的提高,4种表面活性剂对菲、芘的去除作用均增强.对于单一的菲污染土壤,表面活性剂对菲去除率最大值的大小顺序为TW80>TX100>SDS>SDBS,最高可达92%.表面活性剂条件一定时,100 mg/L菲污染土壤的去除率高于1000 mg/L.对于单一的芘污染土壤,当表面活性剂浓度低于5000 mg/L时,TX100和TW80对芘的去除率高于SDS和SDBS,但浓度高于5000 mg/L时效果截然相反,最高可达66%.菲和芘混合污染土壤中,菲的去除率明显高于单一菲污染土壤,而芘的去除率却低于单一芘污染土壤.芘清洗1h后达到平衡,菲为4h.土水比越小表面活性剂对土壤中菲、芘的洗脱效果越好.%The batch equilibrium washing of phenanthrene and pyrene in the loess soil matrix by four surfactants, octylphenoxypolyethoxyethanol(TX100), ethoxylated anhydrosorbitol esters (TW80), sodium dode-cylbenzyl sulfonate (SDBS)and sodium dodecyl sulfate(SDS) was studied and compared. The influences of surfactant concentrations, shaking time and the ratio of soil to water were investigated. It was shown that the washing efficiency of phenanthrene and pyrene increased sharply with the increase of surfactant concentrations. The maximum washing efficiency of phenanthrene can be found following the order of TW80> TX100>SDS>SDBS, and the efficiency was up to 92 %. For pyrene, when surfactant concentrations were lower than 5000 mg/L, the efficiency by TW80 and TX100 were higher than that by SDS and SDBS. However, when surfactant concentrations were higher than 5000 mg/L, the result was opposite, and the washing efficiency was up to 66 %. Given the surfactant

  20. Effect of a commercial alcohol ethoxylate surfactant (C11-15E7) on biodegradation of phenanthrene in a saline water medium by Neptunomonas naphthovorans.

    Science.gov (United States)

    Li, Jing-Liang; Bai, Renbi

    2005-02-01

    Biodegradation of poorly soluble polycyclic aromatic hydrocarbons (PAHs) has been a challenge in bioremediation. In recent years, surfactant-enhanced bioremediation of PAH contaminants has attracted great attention in research. In this study, biodegradation of phenanthrene as a model PAHs solubilized in saline micellar solutions of a biodegradable commercial alcohol ethoxylate nonionic surfactant was investigated. The critical micelle concentration (CMC) of the surfactant and its solubilization capacity for phenanthrene were examined in an artificial saline water medium, and a type of marine bacteria, Neptunomonas naphthovorans, was studied for the biodegradation of phenanthrene solubilized in the surfactant micellar solutions of the saline medium. It is found that the solubility of phenanthrene in the surfactant micellar solutions increased linearly with the surfactant concentrations, but, at a fixed phenanthrene concentration, the biodegradability of phenanthrene in the micellar solutions decreased with the increase of the surfactant concentrations. This was attributed to the reduced bioavailability of phenanthrene, due to its increased solubilization extent in the micellar phase and possibly lowered mass transfer rate from the micellar phase into the aqueous phase or into the bacterial cells. In addition, an inhibitory effect of the surfactant on the bacterial growth at high surfactant concentrations may also play a role. It is concluded that the surfactant largely enhanced the solubilization of phenanthrene in the saline water medium, but excess existence of the surfactant in the medium should be minimized or avoided for the biodegradation of phenanthrene by Neptunomonas naphthovorans.

  1. Anaerobic Biodegradation of Detergent Surfactants

    Directory of Open Access Journals (Sweden)

    Erich Jelen

    2009-03-01

    Full Text Available Detergent surfactantscan be found in wastewater in relevant concentrations. Most of them are known as ready degradable under aerobic conditions, as required by European legislation. Far fewer surfactants have been tested so far for biodegradability under anaerobic conditions. The natural environment is predominantly aerobic, but there are some environmental compartments such as river sediments, sub-surface soil layer and anaerobic sludge digesters of wastewater treatment plants which have strictly anaerobic conditions. This review gives an overview on anaerobic biodegradation processes, the methods for testing anaerobic biodegradability, and the anaerobic biodegradability of different detergent surfactant types (anionic, nonionic, cationic, amphoteric surfactants.

  2. Direct suppression of phagocytosis by amphipathic polymeric surfactants.

    Science.gov (United States)

    Watrous-Peltier, N; Uhl, J; Steel, V; Brophy, L; Merisko-Liversidge, E

    1992-09-01

    Recent studies have demonstrated that phagocytosis of colloidal particles by the mononuclear phagocytes of the liver and spleen can be controlled by either coating or stabilizing particulate carriers with the amphipathic polymeric surfactants, F108 and T908. These surfactants consist of copolymers of polypropylene oxide (PPO) and polyethylene oxide (PEO) and, when adsorbed to particulate surfaces, significantly decrease sequestration of particulates by the mononuclear phagocytes (MPS) of the liver. To evaluate these observations further, murine peritoneal macrophages were incubated for varying periods with surfactant-coated and noncoated polystyrene particles (PSPs). Phagocytosis was monitored using gamma counting and quantitative fluorescence microscopy. The data show that phagocytosis is decreased when PSPs are coated with F108 and T908. In addition, suppression of phagocytic activity was observed when cells were pretreated with the surfactant and then challenged with noncoated particles. The data confirm previous observations that polymeric surfactants consisting of PEO and PPO protect particulate carriers from rapid uptake by the MPS of the liver. Further, F108 and T908 suppress phagocytosis directly without affecting the integrity, viability, or functional state of the cell.

  3. Treatment with exogenous surfactant stimulates endogenous surfactant synthesis in premature infants with respiratory distress syndrome

    NARCIS (Netherlands)

    Bunt, JEH; Carnielli, VP; Janssen, DJ; Wattimena, JLD; Hop, WC; Sauer, PJ; Zimmermann, LJI

    2000-01-01

    Objective: Treatment of preterm infants with respiratory distress syndrome (RDS) with exogenous surfactant has greatly improved clinical outcome. Some infants require multiple doses, and it has not been studied whether these large amounts of exogenous surfactant disturb endogenous surfactant metabol

  4. MINERAL-SURFACTANT INTERACTIONS FOR MINIMUM REAGENTS PRECIPITATION AND ADSORPTION FOR IMPROVED OIL RECOVERY

    Energy Technology Data Exchange (ETDEWEB)

    P. Somasundaran

    2005-04-30

    The aim of this project is to delineate the role of mineralogy of reservoir rocks in determining interactions between reservoir minerals and externally added reagents (surfactants/polymers) and its effect on critical solid-liquid and liquid-liquid interfacial properties such as adsorption, wettability and interfacial tension in systems relevant to reservoir conditions. Previous studies have suggested that significant surfactant loss by precipitation or adsorption on reservoir minerals can cause chemical schemes to be less than satisfactory for enhanced oil recovery. Both macroscopic adsorption, wettability and microscopic orientation and conformation studies for various surfactant/polymer mixtures/reservoir rocks systems were conducted to explore the cause of chemical loss by means of precipitation or adsorption, and the effect of rock mineralogy on the chemical loss. During this period, the adsorption of mixed system of n-dodecyl-{beta}-D-maltoside (DM) and dodecyl sulfonate (C{sub 12}SO{sub 3}Na) has been studied. The effects of solution pH, surfactant mixing ratio and different salts on surfactant adsorption on alumina have been investigated in detail. Along with these adsorption studies, changes in mineral wettability due to the adsorption of the mixtures were determined under relevant conditions to identify the nano-structure of the adsorbed layers. Solution properties of C{sub 12}SO{sub 3}Na/DM mixtures were also studied to identify surfactant interactions that affect the mixed aggregate formation in solution. Adsorption of SDS on gypsum and limestone suggested stronger surfactant/mineral interaction than on alumina, due to the precipitation of surfactant by dissolved calcium ions. The effects of different salts such as sodium nitrate, sodium sulfite and sodium chloride on DM adsorption on alumina have also been determined. As surfactant hemimicelles at interface and micelles in solution have drastic effects on oil recovery processes, their microstructures in

  5. Rheological Properties Of Some Surfactant-Based Fracturing Fluids

    Directory of Open Access Journals (Sweden)

    Andra Tamas

    2014-02-01

    Full Text Available The paper presents the rheological behavior study of some cationic surfactant-based aqueous solutions that can be used as fracturing fluids. It was followed the influence of salt type and concentration, as well as that of temperature by setting the dependence between the shear stress τ and the shear rate   . The analysis of dependence between τ and   demonstrates that all the studied solutions have non-Newtonian behavior with flow behavior index smaller than 1.

  6. Rapid growth of nanotubes and nanorods of würtzite ZnO through microwave-irradiation of a metalorganic complex of zinc and a surfactant in solution

    Indian Academy of Sciences (India)

    Sanjaya Brahma; Kalya Jagannatha Rao; Srinivasarao Shivashankar

    2010-04-01

    Large quantities of single-crystalline ZnO nanorods and nanotubes have been prepared by the microwave irradiation of a metalorganic complex of zinc, in the presence of a surfactant. The method is simple, fast, and inexpensive (as it uses a domestic microwave oven), and yields pure nanostructures of the hexagonal würtzite phase of ZnO in min, and requires no conventional templating. The ZnO nanotubes formed have a hollow core with inner diameter varying from 140–160 nm and a wall of thickness, 40–50 nm. The length of nanorods and nanotubes varies in the narrow range of 500–600 nm. These nanostructures have been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and selected area electron diffraction (SAED). The ZnO nanorods and nanotubes are found by SAED to be single-crystalline. The growth process of ZnO nanorods and nanotubes has been investigated by varying the surfactant concentration and microwave irradiation time. Based on the various results obtained, a tentative and plausible mechanism for the formation of ZnO nanostructures is proposed.

  7. Mineral-Surfactant Interactions for Minimum Reagents Precipitation and Adsorption for Improved Oil Recovery

    Energy Technology Data Exchange (ETDEWEB)

    P. Somasundaran

    2008-09-20

    Chemical EOR can be an effective method for increasing oil recovery and reducing the amount of produced water; however, reservoir fluids are chemically complex and may react adversely to the polymers and surfactants injected into the reservoir. While a major goal is to alter rock wettability and interfacial tension between oil and water, rock-fluid and fluid-fluid interactions must be understood and controlled to minimize reagent loss, maximize recovery and mitigate costly failures. The overall objective of this project was to elucidate the mechanisms of interactions between polymers/surfactants and the mineral surfaces responsible for determining the chemical loss due to adsorption and precipitation in EOR processes. The role of dissolved inorganic species that are dependent on the mineralogy is investigated with respect to their effects on adsorption. Adsorption, wettability and interfacial tension are studied with the aim to control chemical losses, the ultimate goal being to devise schemes to develop guidelines for surfactant and polymer selection in EOR. The adsorption behavior of mixed polymer/surfactant and surfactant/surfactant systems on typical reservoir minerals (quartz, alumina, calcite, dolomite, kaolinite, gypsum, pyrite, etc.) was correlated to their molecular structures, intermolecular interactions and the solution conditions such as pH and/or salinity. Predictive models as well as general guidelines for the use of polymer/surfactant surfactant/surfactant system in EOR have been developed The following tasks have been completed under the scope of the project: (1) Mineral characterization, in terms of SEM, BET, size, surface charge, and point zero charge. (2) Study of the interactions among typical reservoir minerals (quartz, alumina, calcite, dolomite, kaolinite, gypsum, pyrite, etc.) and surfactants and/or polymers in terms of adsorption properties that include both macroscopic (adsorption density, wettability) and microscopic (orientation

  8. Persurf, a New Method to Improve Surfactant Delivery: A Study in Surfactant Depleted Rats

    OpenAIRE

    2012-01-01

    PURPOSE: Exogenous surfactant is not very effective in adults with ARDS, since surfactant does not reach atelectatic alveoli. Perfluorocarbons (PFC) can recruit atelectatic areas but do not replace impaired endogenous surfactant. A surfactant-PFC-mixture could combine benefits of both therapies. The aim of the proof-of-principal-study was to produce a PFC-in-surfactant emulsion (Persurf) and to test in surfactant depleted Wistar rats whether Persurf achieves I.) a more homogenous pulmonary di...

  9. [Adsorption of phenol chemicals by surfactant-modified zeolites].

    Science.gov (United States)

    Xie, Jie; Wang, Zhe; Wu, De-Yi; Li, Chun-Jie

    2012-12-01

    Two kinds of zeolites were prepared from fly ash and modified by surfactant subsequently. Surfactant-modified zeolites were studied for adsorption of phenol chemicals (phenol, p-chlorphenol, bisphenol A). It showed that the adsorption affinity of zeolite to phenol chemicals was significantly improved after surfactant modification. The adsorption isotherms of phenol chemicals were well fitted by the Langmuir isotherm. For the two surfactant-surfactant modified zeolites, the maximum adsorption amounts of phenol, p-chlorphenol, and bisphenol A calculated from the Langmuir equation were 37.7, 52.36, 90.9 mg x g(-1) and 10.7, 22.83, 56.8 mg x g(-1), respectively. When pH values of solutions were higher than the pK(a) values of phenol chemicals, the removal efficiencies were getting higher with the increase of pH values. The octanol/water partition coefficient (K(ow)) was also found to be an important factor affecting adsorption of phenol chemicals by the modified zeolites. Higher K(ow) value, which means the greater hydrophobicity of the chemicals, resulted in a higher removal.

  10. Controlling block copolymer phase behavior using ionic surfactant

    Science.gov (United States)

    Ray, D.; Aswal, V. K.

    2016-05-01

    The phase behavior of poly(ethylene oxide)-poly(propylene oxide-poly(ethylene oxide) PEO-PPO-PEO triblock copolymer [P85 (EO26PO39EO26)] in presence of anionic surfactant sodium dodecyl sulfate (SDS) in aqueous solution as a function of temperature has been studied using dynamic light scattering (DLS) and small-angle neutron scattering (SANS). The measurements have been carried out for fixed concentrations (1 wt%) of block copolymer and surfactants. Each of the individual components (block copolymer and surfactant) and the nanoparticle-surfactant mixed system have been examined at varying temperature. The block copolymer P85 forms spherical micelles at room temperature whereas shows sphere-to-rod like micelle transition at higher temperatures. On the other hand, SDS surfactant forms ellipsoidal micelles over a wide temperature range. Interestingly, it is found that phase behavior of mixed micellar system (P85 + SDS) as a function of temperature is drastically different from that of P85, giving the control over the temperature-dependent phase behavior of block copolymers.

  11. Flow improvers for water injection based on surfactants

    Energy Technology Data Exchange (ETDEWEB)

    Oskarsson, H.; Uneback, I.; Hellsten, M.

    2006-03-15

    In many cases it is desirable to increase the flow of injection water when an oil well deteriorates. It is very costly in offshore operation to lay down an additional water pipe to the injection site. Flow improvers for the injection water will thus be the most cost-effective way to increase the flow rate. During the last years water-soluble polymers have also been applied for this purpose. These drag-reducing polymers are however only slowly biodegraded which has been an incentive for the development of readily biodegradable surfactants as flow improvers for injection water. A combination of a zwitterionic and an anionic surfactant has been tested in a 5.5 inch, 700 m long flow loop containing sulphate brine with salinity similar to sea water. A drag reduction between 75 and 80% was achieved with 119 ppm in solution of the surfactant blend at an average velocity of 1.9 m/s and between 50 and 55% at 2.9 m/s. The surfactants in this formulation were also found to be readily biodegradable in sea water and low bio accumulating which means they have an improved environmental profile compared to the polymers used today. Due to the self-healing properties of the drag-reducing structures formed by surfactants, these may be added before the pump section - contrary to polymers which are permanently destroyed by high shear forces. (Author)

  12. Migration of a surfactant-laden droplet in non-isothermal Poiseuille flow

    CERN Document Server

    Das, Sayan; Som, S K; Chakraborty, Suman

    2016-01-01

    The motion of a surfactant-laden viscous droplet in the presence of background non-isothermal Poiseuille flow is studied analytically and numerically. Specifically, the effect of interfacial Marangoni stress due to non-uniform distribution of surfactants and temperature at the droplet interface on the velocity and direction of motion of the droplet along the centerline of imposed Poiseuille flow is investigated in the presence of linearly varying temperature field. In the absence of thermal convection, fluid inertia and shape deformation, the interfacial transport of bulk-insoluble surfactants is governed by the surface Peclet number which represents the relative strength of the advective transport of surfactant over the diffusive transport. We obtain analytical solution for small and large values of the surface Peclet number. Numerical solution is obtained for arbitrary surface Peclet number, which compares well with the analytical solution. Depending on the direction of temperature gradient with respect to ...

  13. Structure and Dynamics of Nonionic Surfactant Aggregates in Layered Materials.

    Science.gov (United States)

    Guégan, Régis; Veron, Emmanuel; Le Forestier, Lydie; Ogawa, Makoto; Cadars, Sylvian

    2017-09-26

    The aggregation of surfactants on solid surfaces as they are adsorbed from solution is the basis of numerous technological applications such as colloidal stabilization, ore flotation, and floor cleaning. The understanding of both the structure and the dynamics of surfactant aggregates applies to the development of alternative ways of preparing hybrid layered materials. For this purpose, we study the adsorption of the triethylene glycol mono n-decyl ether (C10E3) nonionic surfactant onto a synthetic montmorillonite (Mt), an aluminosilicate clay mineral for organoclay preparation with important applications in materials sciences, catalysis, wastewater treatment, or as drug delivery. The aggregation mechanisms follow those observed in an analogous natural Mt, with the condensation of C10E3 in a bilayer arrangement once the surfactant self-assembles in a lamellar phase beyond the critical micelle concentration, underlining the importance of the surfactant state in solution. Solid-state (1)H nuclear magnetic resonance (NMR) at fast magic-angle spinning (MAS) and high magnetic field combined with(1)H-(13)C correlation experiments and different types of (13)C NMR experiments selectively probes mobile or rigid moieties of C10E3 in three different aggregate organizations: (i) a lateral monolayer, (ii) a lateral bilayer, and (iii) a normal bilayer. High-resolution (1)H{(27)Al} CP-(1)H-(1)H spin diffusion experiments shed light on the proximities and dynamics of the different fragments and fractions of the intercalated surfactant molecules with respect to the Mt surface. (23)Na and (1)H NMR measurements combined with complementary NMR data, at both molecular and nanometer scales, precisely pointed out the location of the C10E3 ethylene oxide hydrophilic group in close contact with the Mt surface interacting through ion-dipole or van der Waals interactions.

  14. Evaporation of Sessile Droplets Laden with Particles and Insoluble Surfactants.

    Science.gov (United States)

    Karapetsas, George; Chandra Sahu, Kirti; Matar, Omar K

    2016-07-12

    We consider the flow dynamics of a thin evaporating droplet in the presence of an insoluble surfactant and noninteracting particles in the bulk. On the basis of lubrication theory, we derive a set of evolution equations for the film height, the interfacial surfactant, and bulk particle concentrations, taking into account the dependence of liquid viscosity on the local particle concentration. An important ingredient of our model is that it takes into account the fact that the surfactant adsorbed at the interface hinders evaporation. We perform a parametric study to investigate how the presence of surfactants affects the evaporation process as well as the flow dynamics with and without the presence of particles in the bulk. Our numerical calculations show that the droplet lifetime is affected significantly by the balance between the ability of the surfactant to enhance spreading, suppressing the effect of thermal Marangoni stresses-induced motion, and to hinder the evaporation flux through the reduction of the effective interfacial area of evaporation, which tend to accelerate and decelerate the evaporation process, respectively. For particle-laden droplets and in the case of dilute solutions, the droplet lifetime is found to be weakly dependent on the initial particle concentration. We also show that the particle deposition patterns are influenced strongly by the direct effect of the surfactant on the evaporative flux; in certain cases, the "coffee-stain" effect is enhanced significantly. A discussion of the delicate interplay between the effects of capillary pressure and solutal and thermal Marangoni stresses, which drive the liquid flow inside of the evaporating droplet giving rise to the observed results, is provided herein.

  15. Coupling the Alkaline-Surfactant-Polymer Technology and The Gelation Technology to Maximize Oil Production

    Energy Technology Data Exchange (ETDEWEB)

    Malcolm Pitts; Jie Qi; Dan Wilson; Phil Dowling; David Stewart; Bill Jones

    2005-12-01

    Gelation technologies have been developed to provide more efficient vertical sweep efficiencies for flooding naturally fractured oil reservoirs or reservoirs with different sand lenses with high permeability contrast. The field proven alkaline-surfactant-polymer technology economically recovers 15% to 25% OOIP more crude oil than waterflooding from swept pore space of an oil reservoir. However, alkaline-surfactant-polymer technology is not amenable to naturally fractured reservoirs or reservoirs with high permeability contrast zones because much of injected solution bypasses target pore space containing oil. This work investigates whether combining these two technologies could broaden applicability of alkaline-surfactant-polymer flooding into these reservoirs. Fluid-fluid interaction with different gel chemical compositions and alkaline-surfactant-polymer solution with pH values ranging from 9.2 to 12.9 have been tested. Aluminum-polyacrylamide gels are not stable to alkaline-surfactant-polymer solutions at any pH. Chromium-polyacrylamide gels with polymer to chromium ion ratios of 25 or greater were stable to alkaline-surfactant-polymer solutions if solution pH was 10.6 or less. When the polymer to chromium ion was 15 or less, chromium-polyacrylamide gels were stable to alkaline-surfactant-polymer solutions with pH values up to 12.9. Chromium-xanthan gum gels were stable to alkaline-surfactant-polymer solutions with pH values of 12.9 at the polymer to chromium ion ratios tested. Silicate-polyacrylamide, resorcinol-formaldehyde, and sulfomethylated resorcinol-formaldehyde gels were also stable to alkaline-surfactant-polymer solutions with pH values ranging from 9.2 to 12.9. Iron-polyacrylamide gels were immediately destroyed when contacted with any of the alkaline-surfactant-polymer solutions with pH values ranging from 9.2 to 12.9. Gel solutions under dynamic conditions of linear corefloods showed similar stability to alkaline-surfactant-polymer solutions as in

  16. Controlling molecular ordering in solution-state conjugated polymers.

    Science.gov (United States)

    Zhu, J; Han, Y; Kumar, R; He, Y; Hong, K; Bonnesen, P V; Sumpter, B G; Smith, S C; Smith, G S; Ivanov, I N; Do, C

    2015-10-01

    Rationally encoding molecular interactions that can control the assembly structure and functional expression in a solution of conjugated polymers hold great potential for enabling optimal organic optoelectronic and sensory materials. In this work, we show that thermally-controlled and surfactant-guided assembly of water-soluble conjugated polymers in aqueous solution is a simple and effective strategy to generate optoelectronic materials with the desired molecular ordering. We have studied a conjugated polymer consisting of a hydrophobic thiophene backbone and hydrophilic, thermo-responsive ethylene oxide side groups, which shows a step-wise, multi-dimensional assembly in water. By incorporating the polymer into phase-segregated domains of an amphiphilic surfactant in solution, we demonstrate that both chain conformation and degree of molecular ordering of the conjugated polymer can be tuned in hexagonal, micellar and lamellar phases of the surfactant solution. The controlled molecular ordering in conjugated polymer assembly is demonstrated as a key factor determining the electronic interaction and optical function.

  17. Surfactant damages on coastal vegetation in southern Italy

    Directory of Open Access Journals (Sweden)

    2005-01-01

    Full Text Available Coastal vegetation decline caused by seaspray has been reported to affect a variety of species in several countries: Australia, South of France, along the Italian Tyrrhenian coast, Spain and Tunisia. The most serious injury is due to the interaction between sea salt and surfactants, even if surfactants may cause direct damage on cell membranes. The salt uptake is enhanced by the durfactant-induced erosion of the epicuticular wax, which reduces the water surface tension. The symptoms are non-specific and consist in leaf discoloration and necrosis. In needles, necrosis begins from the apex; in leaves, from the edges. Directionality of crown damage is the main symptom for diagnosing the involvement of polluted seaspray. If an obstacle is placed between trees and sea wind, the trees do not show appreciable damage. In Italy, the tree decline caused by seaspray and surfactants has been investigated with special reference to the pinewoods of the San Rossore (Tuscany, Central Italy, or on the Tyrrhenian coastlands of Central Italy, such as the area around Castelporziano in Lazio. This research is aimed at a preliminary assessment of the extent of surfactant damage to the coastal vegetation in four regions in Southern Italy by: i field surveys and mapping of damage caused by surfactants; ii detecting the presence of surfactants on the tree crowns. The damages have been observed in a lot of zones in Apulia, Basilicata, Campania and Calabria, within 500 m inland from the sea, for a maximum length of 5500 m coastline, near the mouth of a river or stream, near the outlet of sewage canals and in any other coastal areas where the surface currents carry a surfactant load.

  18. Emulsification at the Liquid/Liquid Interface: Effects of Potential, Electrolytes and Surfactants.

    Science.gov (United States)

    Chowdhury, Mehrin; Kataky, Ritu

    2016-01-04

    Emulsification of oils at liquid/liquid interfaces is of fundamental importance across a range of applications, including detergency. Adsorption and partitioning of the anionic surface active ions at the interface between two immiscible solutions is known to cause predictable chaos at the transfer potential region of the surfactant. In this work, the phenomenon that leads to the chaotic behaviour shown by sodium dodecylbenzene sulfonate (SDBS) at the water/1,2-dichloroethane interface is applied to commercial surfactants and aqueous/glyceryl trioleate interface. Electrochemical methods, electrocapillary curves, optical microscopy and conductivity measurements demonstrated that at 1.5 mm of SDBS, surfactants are adsorbed at the interface and assemble into micelles, leading to interfacial instability. As the concentration of the anionic surfactant was enhanced to 8 and 13.4 mm, the Marangoni effect and the interfacial emulsification became more prominent. The chaotic behaviour was found to be dependent on the surfactant concentration and the electrolytes present.

  19. Synthesis of nanocrystalline calcium phosphate in microemulsion--effect of nature of surfactants.

    Science.gov (United States)

    Singh, Sujata; Bhardwaj, Pallavi; Singh, V; Aggarwal, S; Mandal, U K

    2008-03-01

    Nanosized calcium phosphate (CP) powders have been synthesized by an inverse microemulsion system using kerosene as the oil phase, a cationic surfactant Aliquat 336, a non-ionic surfactant Tween 20 and their mixture and aqueous solutions of calcium nitrate tetrahydrate and biammonium hydrogen phosphate as the water phase. It has been found that the nature of surfactants played an important role to regulate the size and morphologies of the calcium phosphate nanoparticles. The cationic surfactant Aliquat 336 has been found to regulate the nucleation and crystal growth. The synthesized powders have been comprehensively characterized using transmission electron microscopy (TEM), scanning electron microscopy (SEM), powder X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). Our results show that the brushite (DCPD) is the major phase comprising the calcium phosphate nanoparticles. In mixed surfactants mediated system a morphological controlled highly crystalline particles have been synthesized. Further, the role of Aliquat 336 has been established and a plausible synthetic mechanism has been proposed.

  20. Interactions of short chain phenylalkanoic acids within ionic surfactant micelles in aqueous media

    Directory of Open Access Journals (Sweden)

    Naeem Kashif

    2012-01-01

    Full Text Available % SDS KR nema Solubilization and interactions of phenylalkanoic acids induced by cationic surfactant, cetyltrimethylammonium bromide (CTAB and an anionic surfactant, sodium dodecyl sulfate (SDS was investigated spectrophotometrically at 25.0°C. The UV spectra of the additives (acids were measured with and without surfactant above and below critical micelle concentration (cmc of the surfactant. The presence of alkyl chain in phenylalkanoic acids is responsible for hydrophobic interaction resulting in shift of the spectra towards longer wavelength (red shift. The value of partition coefficient (Kx between the bulk water and surfactant micelles and in turn standard free energy change of solubilization (ΔGpº were also estimated by measuring the differential absorbance (ΔA of the additives in micellar solutions.

  1. Structural characterisation of human proteinosis surfactant protein A

    DEFF Research Database (Denmark)

    Leth-Larsen, Rikke; Holmskov, U; Højrup, P

    2000-01-01

    Human surfactant protein-A (SP-A) has been purified from a proteinosis patient and characterised by a combination of automated Edman degradation and mass spectrometry. The complete protein sequence was characterised. The major part of SP-A was shown to consist of SP-A2 gene product, and only...

  2. Spontaneous surface self-assembly in protein-surfactant mixtures: interactions between hydrophobin and ethoxylated polysorbate surfactants.

    Science.gov (United States)

    Tucker, Ian M; Petkov, Jordan T; Penfold, Jeffrey; Thomas, Robert K; Li, Peixun; Cox, Andrew R; Hedges, Nick; Webster, John R P

    2014-05-01

    The synergistic interactions between certain ethoxylated polysorbate nonionic surfactants and the protein hydrophobin result in spontaneous self-assembly at the air-water interface to form layered surface structures. The surface structures are characterized using neutron reflectivity. The formation of the layered surface structures is promoted by the hydrophobic interaction between the polysorbate alkyl chain and the hydrophobic patch on the surface of the globular hydrophobin and the interaction between the ethoxylated sorbitan headgroup and hydrophilic regions of the protein. The range of the ethoxylated polysorbate concentrations over which the surface ordering occurs is a maximum for the more hydrophobic surfactant polyoxyethylene(8) sorbitan monostearate. The structures at the air-water interface are accompanied by a profound change in the wetting properties of the solution on hydrophobic substrates. In the absence of the polysorbate surfactant, hydrophobin wets a hydrophobic surface, whereas the hydrophobin/ethoxylated polysorbate mixtures where multilayer formation occurs result in a significant dewetting of hydrophobic surfaces. The spontaneous surface self-assembly for hydrophobin/ethoxylated polysorbate surfactant mixtures and the changes in surface wetting properties provide a different insight into protein-surfactant interactions and potential for manipulating surface and interfacial properties and protein surface behavior.

  3. Biomimicry of surfactant protein C.

    Science.gov (United States)

    Brown, Nathan J; Johansson, Jan; Barron, Annelise E

    2008-10-01

    Since the widespread use of exogenous lung surfactant to treat neonatal respiratory distress syndrome, premature infant survival and respiratory morbidity have dramatically improved. Despite the effectiveness of the animal-derived surfactant preparations, there still remain some concerns and difficulties associated with their use. This has prompted investigation into the creation of synthetic surfactant preparations. However, to date, no clinically used synthetic formulation is as effective as the natural material. This is largely because the previous synthetic formulations lacked analogues of the hydrophobic proteins of the lung surfactant system, SP-B and SP-C, which are critical functional constituents. As a result, recent investigation has turned toward the development of a new generation of synthetic, biomimetic surfactants that contain synthetic phospholipids along with a mimic of the hydrophobic protein portion of lung surfactant. In this Account, we detail our efforts in creating accurate mimics of SP-C for use in a synthetic surfactant replacement therapy. Despite SP-C's seemingly simple structure, the predominantly helical protein is extraordinarily challenging to work with given its extreme hydrophobicity and structural instability, which greatly complicates the creation of an effective SP-C analogue. Drawing inspiration from Nature, two promising biomimetic approaches have led to the creation of rationally designed biopolymers that recapitulate many of SP-C's molecular features. The first approach utilizes detailed SP-C structure-activity relationships and amino acid folding propensities to create a peptide-based analogue, SP-C33. In SP-C33, the problematic and metastable polyvaline helix is replaced with a structurally stable polyleucine helix and includes a well-placed positive charge to prevent aggregation. SP-C33 is structurally stable and eliminates the association propensity of the native protein. The second approach follows the same design

  4. Cationic surfactants derived from lysine: effects of their structure and charge type on antimicrobial and hemolytic activities.

    Science.gov (United States)

    Colomer, A; Pinazo, A; Manresa, M A; Vinardell, M P; Mitjans, M; Infante, M R; Pérez, L

    2011-02-24

    Three different sets of cationic surfactants from lysine have been synthesized. The first group consists of three monocatenary surfactants with one lysine as the cationic polar head with one cationic charge. The second consists of three monocatenary surfactants with two amino acids as cationic polar head with two positive charges. Finally, four gemini surfactants were synthesized in which the spacer chain and the number and type of cationic charges have been regulated. The micellization process, antimicrobial activity, and hemolytic activity were evaluated. The critical micelle concentration was dependent only on the hydrophobic character of the molecules. Nevertheless, the antimicrobial and hemolytic activities were related to the structure of the compounds as well as the type of cationic charges. The most active surfactants against the bacteria were those with a cationic charge on the trimethylated amino group, whereas all of these surfactants showed low hemolytic character.

  5. Use of Viscosity to Probe the Interaction of Anionic Surfactants with a Coagulant Protein from Moringa oleifera Seeds

    Directory of Open Access Journals (Sweden)

    Raymond Maikokera

    2009-01-01

    Full Text Available The intrinsic viscosity of the coagulant protein was evaluated from the flow times of the protein solutions through a capillary viscometer, and the results suggested the coagulant protein to be globular. The interactions of the coagulant protein with anionic surfactant sodium dodecyl sulphate (SDS and sodium dodecyl benzene sulfonate (SDBS were also investigated by capillary viscometry. We conclude that there is strong protein-surfactant interaction at very low surfactant concentrations, and the behavior of the anionic surfactants in solutions containing coagulant protein is very similar. The viscometry results of protein-SDS system are compared with surface tension, fluorescence, and circular dichroism reported earlier. Combining the results of the four studies, the four approaches seem to confirm the same picture of the coagulant protein-SDS interaction. All the physical quantities when studied as function of surfactant concentration for 0.05% (w/v protein solution either exhibited a maximum or minimum at a critical SDS concentration.

  6. Effect of surfactant hydrophile-lipophile balance (HLB) value on mineral oxide charging in apolar media.

    Science.gov (United States)

    Gacek, Matthew Michael; Berg, John C

    2015-07-01

    The current work examines the role of surfactant hydrophile-lipophile balance (HLB) on the ability for surfactant reverse micelles to impart charge to particles dispersed in an apolar medium, a study motivated by a number of applications that seek to maximize particle charge in such systems. Previous investigations have shown that relative acid-base properties of the particles and surfactants, as well as surfactant concentration and trace water content, all play a major role in the particle charge obtained. However, the ability of a surfactant to stabilize charge in reverse micelles is also an important aspect of creating charge on a particle surface. It has been previously shown that surfactant HLB value is an important parameter in assessing the size of the polar core of the reverse micelles, thereby impacting the total charge that is generated in the bulk solution as determined by conductivity. In the current study, this theory is extended to investigate the impact on particle charging. To accomplish this, the electrophoretic mobility is determined for a series of mineral oxides dispersed in Isopar-L with either Span 20, Span 80, or Span 85. These three surfactants all have the same head group chemistry, but their HLB value ranges from 1.8 to 8.6. It is found that the maximum observed particle electrophoretic mobility does scale directly with the HLB of the accompanying surfactant. This indicates that there is a direct correlation between a surfactant's ability to stabilize charge and its ability to impart charge to a particle. However, the largest HLB surfactant, Span 20, also exhibited a large amount of charge screening or neutralization at larger surfactant concentrations. This highlights the competition between particle charging and micelle-micelle charging that remains one of the largest obstacles to maximizing particle charge in apolar systems.

  7. Evaluation of therapeutic pulmonary surfactants by thin liquid film methods.

    Science.gov (United States)

    Todorov, Roumen; Exerowa, Dotchi; Platikanov, Dimo; Bianco, Federico; Razzetti, Roberta

    2015-08-01

    An example of the application of the Black Foam Film (BFF) Method and the Wetting Film Method, using the Microinterferomertric and the Pressure Balance Techniques, for characterization interfacial properties of the animal derived therapeutic pulmonary surfactant preparations (TSP), is presented. BFF thickness, probability of black film formation, and disjoining pressure for foam films from TSP aqueous solutions are measured as well as the wetting properties of TSP solutions on solid surfaces with different hydrophobicity have been studied. Interfacial characteristics such as minimal surfactant concentration to obtain black film (critical concentration) and concentration at which a black film is 100% obtained (threshold concentration) are determined. An evaluation of the four widely used TSP – Curosurf, Infasurf, Survanta, and Alveofact – by these methods has been carried out. Thus the methods of the thin liquid films are useful tools for studying the interfacial properties of TSP solutions, as well as for their improvement.

  8. Surfactant for pediatric acute lung injury.

    Science.gov (United States)

    Willson, Douglas F; Chess, Patricia R; Notter, Robert H

    2008-06-01

    This article reviews exogenous surfactant therapy and its use in mitigating acute lung injury (ALI) and the acute respiratory distress syndrome (ARDS) in infants, children, and adults. Biophysical and animal research documenting surfactant dysfunction in ALI/ARDS is described, and the scientific rationale for treatment with exogenous surfactant is discussed. Major emphasis is placed on reviewing clinical studies of surfactant therapy in pediatric and adult patients who have ALI/ARDS. Particular advantages from surfactant therapy in direct pulmonary forms of these syndromes are described. Also discussed are additional factors affecting the efficacy of exogenous surfactants in ALI/ARDS.

  9. Modification of Deeply Buried Hydrophobic Interfaces by Ionic Surfactants

    Energy Technology Data Exchange (ETDEWEB)

    L Tamam; D Pontoni Z Sapir; S Yefet; S Sloutskin; B Ocko; H Reichert; M Deutsch

    2011-12-31

    Hydrophobicity, the spontaneous segregation of oil and water, can be modified by surfactants. The way this modification occurs is studied at the oil-water interface for a range of alkanes and two ionic surfactants. A liquid interfacial monolayer, consisting of a mixture of alkane molecules and surfactant tails, is found. Upon cooling, it freezes at T{sub s}, well above the alkane's bulk freezing temperature, T{sub b}. The monolayer's phase diagram, derived by surface tensiometry, is accounted for by a mixtures-based theory. The monolayer's structure is measured by high-energy X-ray reflectivity above and below T{sub s}. A solid-solid transition in the frozen monolayer, occurring approximately 3 C below T{sub s}, is discovered and tentatively suggested to be a rotator-to-crystal transition.

  10. Solubilization and separation of p-tert-butylphenol using polyelectrolyte/surfactant complexes in colloid-enhanced ultrafiltration

    Energy Technology Data Exchange (ETDEWEB)

    Uchiyama, Hirotaka; Christian, S.D.; Tucker, E.E.; Scamehorn, J.F. (Univ. of Oklahoma, Norman, OK (United States))

    1994-03-15

    Water-soluble polyelectrolyte/surfactant complexes, involving oppositely charged species, can form at quite low thermodynamic activities of the surfactant. This fact can be exploited in colloid-enhanced ultrafiltration separations, where both molecular organic pollutants and toxic ions are to be removed from contaminated aqueous streams. Investigations have been made of (a) the solubilization and ultrafiltration of solutions of organic solutes in polymer/surfactant solutions, for comparison with studies of micellar surfactant solutions in the absence of added polymers; (b) the penetration of surfactant through the membrane (leakage of monomer) in dialysis and ultrafiltration experiments; and (c) the utility of polyelectrolytes as scavengers'' for surfactant species that-enter the permeate or filtrate in colloid-enhanced ultrafiltration separations. The polyelectrolyte chosen for the studies is sodium poly(styrenesulfonate) and the surfactant is cetylpyridinium chloride (hexadecylpyridinium chloride). A detailed study has been made of the solubilization and separation of p-tert-butylphenol in aqueous mixtures of sodium poly(styrenesulfonate) and cetylpyridinium chloride, at polyelectrolyte to surfactant mole ratios of two to one and three to one.

  11. Non-covalent bonding interaction of surfactants with functionalized carbon nanotubes in proton exchange membranes for fuel cell applications.

    Science.gov (United States)

    Sayeed, M Abu; Kim, Young Ho; Park, Younjin; Gopalan, A I; Lee, Kwang-Pill; Choi, Sang-June

    2013-11-01

    Dispersion of functionalized multiwalled carbon nanotubes (MWCNTs) in proton exchange membranes (PEMs) was conducted via non-covalent bonding between benzene rings of various surfactants and functionalized MWCNTs. In the solution casting method, dispersion of functionalized MWCNTs in PEMs such as Nafion membranes is a critical issue. In this study, 1 wt.% pristine MWCNTs (p-MWCNTs) and oxidized MWCNTs (ox-MWCNTs) were reinforced in Nafion membranes by adding 0.1-0.5 wt.% of a surfactant such as benzalkonium chloride (BKC) as a cationic surfactant with a benzene ring, Tween-80 as a nonanionic surfactant without a benzene ring, sodium dodecylsulfonate (SDS) as an anionic surfactant without a benzene ring, or sodium dodecylben-zenesulfonate (SDBS) as an anionic surfactant with a benzene ring and their effects on the dispersion of nanocomposites were then observed. Among these surfactants, those with benzene rings such as BKC and SDBS produced enhanced dispersion via non-covalent bonding interaction between CNTs and surfactants. Specifically, the surfactants were adsorbed onto the surface of functionalized MWCNTs, where they prevented re-aggregation of MWCNTs in the nanocomposites. Furthermore, the prepared CNTs reinforced nanocomposite membranes showed reduced methanol uptake values while the ion exchange capacity values were maintained. The enhanced properties, including thermal property of the CNTs reinforced PEMs with surfactants, could be applicable to fuel cell applications.

  12. Degradation of Surfactants in Hydroponic Wheat Root Zones

    Science.gov (United States)

    Monje, Oscar; McCoy, Lashelle; Flanagan, Aisling

    Hygiene water recycling in recirculating hydroponic systems can be enhanced by plant roots by providing a substrate and root exudates for bacterial growth. However, reduced plant growth can occur during batch mode additions of high concentrations of surfactant. An analog hygiene water stream containing surfactants (Steol CS330, Mirataine CB) was added to a hydroponically-grown wheat plant root zone. The plants were grown at 700 mol mol-1 CO2, a photosynthetic photon flux of 300 mol m-2 s-1, and a planting density of 380 plants m-2. Volumetric oxygen mass transfer coefficients were determined using the fermentative/dynamic outgassing method to maintain adequate oxygen mass transfer rates in the root zone. This analysis suggested an optimal flow rate of the hydroponic solution of 5 L min-1. The hydroponic system was inoculated with biofilm from a bioreactor and rates of surfactant degradation were measured daily based on reduction in chemical oxygen demand (COD). The COD decreased from 400 to 100 mg L-1 after 2 days following batch addition of the analog hygiene water to the hydroponic system. Measurements of dissolved oxygen concentration and solution temperature suggest that the root zone was provided adequate aeration to meet both oxygen demands from plant and microbial respiration during the degradation of the surfactant. Results from this study show that hydroponic systems can be used to enhance rates of hygiene water processing.

  13. Phase behavior and shear alignment in SWNT-surfactant dispersions.

    Science.gov (United States)

    Nativ-Roth, Einat; Yerushalmi-Rozen, Rachel; Regev, Oren

    2008-09-01

    The effect of single-walled carbon nanotubes (SWNT) on the phase behavior of the cationic surfactant cetyltrimethylammonium bromide (CTAB) in aqueous solutions is investigated at room temperature. Small-angle X-ray scattering (SAXS) and cryogenic transmission electron microscopy (cryo-TEM) are used for characterization of bulk dispersions and nanometrically thin films. Additional carbonaceous additives (fullerenes, multi-walled carbon nanotubes, and carbon black) serve as reference systems. It is found that dispersions of carbonaceous additive (excluding fullerenes) at intermediate surfactant concentrations (below the liquid-crystalline region of the native surfactant) induce demixing and macroscopic phase separation in otherwise homogeneous solutions of CTAB. Two coexisting liquid phases of similar CTAB concentrations are observed, with the carbonaceous species residing within the lower phase. At high CTAB concentrations (liquid-crystal region) the SWNTs are found to incorporate into the ordered lyotropic liquid-crystalline phase while preserving the native d-spacing. Investigation of nanometrically thin films at intermediate surfactant concentrations under external shear reveals shear-induced structure (SIS) in the presence of minute amounts of SWNTs. The effect is found to be exclusive to SWNT and does not occur in dispersions of other carbonaceous additives.

  14. A study of polymer-surfactant interactions by neutron reflectivity

    CERN Document Server

    Warren, N

    1999-01-01

    surfactants and their relative levels of interaction with the polymer. The surface behaviour of these systems was observed to be in many ways more remarkable than that of the bulk solution. In the high total surfactant concentration range, once all polymer molecules were associated with bound micelles, the extent of adsorption at the air-liquid interface was found to be dominated largely, as might be expected, by the solution monomer concentrations of the two surfactants. Prior to this, however, adsorption was dominated by the presence of a very surface active polymer-SDS complex which gave rise to enhanced SDS adsorption and low surface tensions compared with those found in polymer-free systems. The origin of this effect, being the stabilisation of the adsorbed SDS monolayer due to a reduction in the inter-headgroup repulsions through screening, by the charged polymer segments, suggests that this may be a characteristic feature of systems continuing a polyelectrolyte and an oppositely charged surfactant. In ...

  15. Synthesis and characterization of mesostructured ceria-zirconia solid solution

    Institute of Scientific and Technical Information of China (English)

    LI Changlin; GU Xin; WANG Yanqin; WANG Yaojun; WANG Yangang; LIU Xiaohui; LU Guanzhong

    2009-01-01

    Mesostructured Ce0.6Zr0.4O2 solid solutions were synthesized by coprecipitation combined with evaporation-induced self-assembly process. The obtained materials were characterized by X-ray diffractometer (XRD), Raman, transmission electron microscopy (TEM), N2 sorption, and hydrogen temperature programmed reduction (H2-TPR). The results showed that the solid solutions consisted of uniform nanocrystals, which piled homogeneous mesopores of about 4 nm. Furthermore, different surfactants had little influence on the mesoporous structures. All these samples exhibited high thermal stability.

  16. Phase behavior and molecular thermodynamics of coacervation in oppositely charged polyelectrolyte/surfactant systems: a cationic polymer JR 400 and anionic surfactant SDS mixture.

    Science.gov (United States)

    Li, Dongcui; Kelkar, Manish S; Wagner, Norman J

    2012-07-17

    Coacervation in mixtures of polyelectrolytes and surfactants with opposite charge is common in nature and is also technologically important to consumer health care products. To understand the complexation behavior of these systems better, we combine multiple experimental techniques to systematically study the polymer/surfactant binding interactions and the phase behavior of anionic sodium dodecyl sulfate (SDS) surfactant in cationic JR 400 polymer aqueous solutions. The phase-behavior study resolves a discrepancy in the literature by identifying a metastable phase between the differing redissolution phase boundaries reported in the literature for the surfactant-rich regime. Isothermal titration calorimetry analyzed within the framework of the simple Satake-Yang model identifies binding parameters for the surfactant-lean phase, whereas a calculation for polymer-bound micelles coexisting with free micelles is analyzed in the surfactant-rich redissolution regime. This analysis provides a preliminary understanding of the interactions governing the observed phase behavior. The resulting thermodynamic properties, including binding constants and the molar Gibbs free energies, enthalpies, and entropies, identify the r