Influence Of Sodium Dodecyl Sulfate Research Articles

Influence of alkyl sulfates on waste activated sludge fermentation at ambient temperature

Alkyl sulfates (AS), such as sodium dodecyl sulfate (SDS), are widely used in household and industrial products, and can be found in some wastewater and waste activated sludge (WAS). The effect of SDS on the fermentation of WAS at ambient temperature was investigated in this paper. Experimental results showed that the concentrations of protein and carbohydrate in aqueous phase increased with the amount of SDS. The concentrations of both NH 4 +-N and PO 4 3−-P in fermentation liquor also increased in the presence of SDS. In addition, it was observed that the fermentative short-chain fatty acids (SCFAs) concentration was affected by SDS. With the increase of SDS dosage, the maximum SCFAs concentration increased, and the fermentation time before reaching the maximum SCFAs concentration also increased. Further investigation showed that the produced SCFAs consisted of acetic, propionic, n-butyric, iso-butyric, n-valeric and iso-valeric acids, and acetic, iso-valeric and propionic acids were the three main products. The influence of SDS on methanogenesis was also investigated, and the inhibitory effect of SDS on methanogens activity was observed.

Application of a partial filling technique to electrophoretic analysis on microchip with T-cross channel configuration

To achieve a high performance sample injection, we designed microchips with both T- and cross-type channel geometry (T-cross chip), which enables two sample solutions to be introduced into a separation channel simultaneously with desired volumes by a combination of gated and pinched injection techniques. The developed microchips were applied to microchip micellar electrokinetic chromatography (MCMEKC) using a partial filling (PF) technique. In the PF technique, to suppress the increase in the background noise due to the presence of a pseudostationary phase (PSP), e.g., ionic surfactant micelles in MCMEKC with mass spectrometric (MS) detection, in a background solution (BGS), the separation channel is partially filled with a PSP while the rest of the channel including the detection point is filled with the BGS without a PSP. As a result, both sodium dodecyl sulfate (SDS) micellar and sample solutions were simultaneously injected into the separation channel on the T-cross chip with a good repeatability of the injection lengths by applying programmed voltages, and a baseline separation of rhodamine derivatives was achieved within 40 s by MCMEKC, in which the micellar zone was partially injected with the PF technique. It was confirmed that the detection could be performed without any influence of SDS by the fluorescence imaging measurements. These results demonstrated that the developed T-cross chips will allow a combination of the MCMEKC separation with the MS detection by employing the PF technique for high performance analysis of biogenic compounds. In the PF–MCMEKC analysis, furthermore, the resolution of two rhodamines clearly increased from 1.30 to 1.73 with the increase of the injection length of PSP from 0.16 to 0.89 mm, whereas at the injection length of 1.47 mm the resolution decreased. Therefore, the selection of an optimal injection length on the T-cross chip is very important and the effects of the injection length on the separation processes in PF–MCMEKC were discussed on the basis of theoretical calculations.

Influence of sodium dodecyl sulfate on colloidal fouling potential during ultrafiltration

The influence of sodium dodecyl sulfate (SDS) on colloidal interactions in the cake layer on a membrane surface was investigated with colloidal fouling tests. Fouling experiments of silica colloids were carried out in a bench scale ultrafiltration (UF) device under various SDS concentrations in waters of different ionic strengths. Addition of small amounts of SDS (0.3 mM) was found to reduce the colloidal fouling potential by 15–18.5%. This reduction was brought about by masking of heterogeneities on the colloidal silica surface thus increasing their repulsion in the cake layer and thereby resulting in a more porous cake layer. At intermediate concentrations of SDS, the colloidal fouling potential of the feed water increased with the SDS concentration and reached a peak at the critical micelle concentration (CMC). SDS additions in this range were shown to function similar to indifferent electrolytes that compress the electric double layer around the colloidal particles to form a tighter cake layer. Concentrations of SDS beyond the CMC resulted in a decline of the colloidal fouling potential. Co-deposition of micelles with colloidal particles on the membrane surface resulted in an additional structural interaction energy to the Derjaguin–Landau–Verway–Overbeek (DLVO) interaction energy between the silica particles. The structuring of micelles between silica particles facilitated a more porous cake layer. The same general trends were observed in all waters tested.

Soy Protein Isolate Based Films: Influence of Sodium Dodecyl Sulfate and Polycaprolactone‐triol on Their Properties

AbstractSummary: We report on the preparation and properties of soy protein isolate (SPI)‐sodium dodecyl sulfate (SDS)‐polycaprolactone‐triol (PCL‐T) films obtained by solvent casting from solutions containing variable amounts of SDS or SDS/PCL‐T. It is shown that the mechanical and thermal properties, and the morphology of SPI‐based biofilms can be easily controlled by changing SDS, PCL‐T, and moisture contents, enabling the fabrication of rigid and flexible materials as pure SPI films [Young's modulus ∼ 1 400 MPa, elongation at break (E) ∼ 2%, and glass transition temperature (Tg) ∼ 150 °C] and SPI/SDS/PCL‐T films with [PCL‐T] ≥ 18% (Young's modulus ∼ 50 MPa, E ∼ 90%, and Tg ∼ 135 °C), respectively. Micrographs taken at the cross‐section of biofilms whose [PCL‐T] ≥ 18% revealed the occurrence of a porous matrix, whereas a dense bulk phase was otherwise observed (pure SPI, SPI/SDS, and SPI/SDS/PCL‐T films with [PCL‐T] < 18%).

Influence of Sodium Dodecyl Sulfate and Static Magnetic Field on the Properties of Freshly Precipitated Calcium Carbonate

Properties of calcium carbonate precipitated from aqueous solutions of CaCl(2) and Na(2)CO(3) in the presence of sodium dodecyl sulfate (SDS) and S-S 0.1 T magnetic field (MF) were studied. The nucleation and precipitation processes of CaCO(3) were investigated by pH and zeta potential measurements at 20 +/- 1 degrees C up to 2 h after mixing the solutions. Also the amounts of calcium carbonate deposited on the glass surfaces and its structure were examined. It was found that SDS influences the kinetics of precipitation, crystallographic forms, and crystal size of CaCO(3). The SDS effects are more pronounced in MF presence. A small amount of SDS accelerates transformation of vaterite into calcite, whereas increasing surfactant concentration moderates such a transformation. On the other hand, in all the systems, MF in the presence of SDS causes a slower transformation of vaterite into calcite. These effects are reflected in pH and zeta potential changes, although there is no clear dependence between the SDS amount present during the precipitation and changes of the parameters investigated. It seems that MF effect is most significant at a defined optimal SDS concentration. The results, however, do not allow suggestion of any detailed mechanism of the field interaction.

Preparation of Hollow Polymer Particles with a Single Hole in the Shell by SaPSeP

The influence of sodium dodecyl sulfate (SDS) on the shell formation of hollow polymer particles prepared by the SaPSeP method, which was proposed by the authors for the preparation of micrometer-sized hollow polymer particles, was investigated. A single hole was observed in the shell of the hollow particles prepared by seeded polymerization of micrometer-sized, monodisperse divinylbenzene/p-xylene droplets in aqueous medium in the presence of SDS at concentrations above 43.3 mM, which were prepared by the dynamic swelling method. The fraction of the hollow particles having a single hole in the shell and the area of the hole increased with the SDS concentration.

Morphological control of calcium carbonate crystallized in reverse micelle system with anionic surfactants SDS and AOT

The influence of a surfactant over water on the polymorphism and crystal size of calcium carbonate produced by reaction crystallization in microemulsion systems was investigated in a mixing tank reactor. The crystallization was induced by the reaction between two aqueous micelle solutions (Na 2CO 3–CaCl 2) stabilized by anionic surfactants, SDS (sodium dodecyl sulfate) or AOT (sodium bis(2-ethylhexyl) sulfosuccinate). With increasing surfactant ratio to water, the water-in-oil microemulsion was stably developed and the morphology of the calcium carbonate crystallized in the micelles sharply transformed from calcite to vaterite. The influence of SDS on the polymorphism and crystal size of calcium carbonate was much clearer than that of AOT. In addition, with AOT, certain step changes in the morphology and crystal size occurred around a surfactant ratio to water ( R = [ H 2 O ] / [ surfactant ] ) of 15 due to a two-phase separation of the microemulsion.

Cationic Amphiphilic Polyelectrolytes and Oppositely Charged Surfactants at the Silica−Aqueous Interface

The influence of sodium dodecyl sulfate (SDS) on the interfacial behavior of two amphiphilic polyelectrolytes, which are copolymers of the cationic monomers triethyl(vinylbenzyl)ammonium chloride and dimethyldodecyl(vinylbenzyl)ammonium chloride, at the silica-aqueous interface was studied. The fraction of amphiphilic monomers was varied, where 0DT, 40DT, and 80DT contained 0, 40, and 80 mol % monomers with dodecyl side chains, respectively. We used in situ ellipsometry to follow the kinetics of adsorption, in terms of adsorbed amount and adsorbed layer thickness, as well as the response of the adsorbed layers to changes in ionic strength and surfactant concentration. Different results were obtained when surfactant was added to the preadsorbed layers compared to the cases when complexes were preformed in the solution prior to the adsorption. In the whole range of concentrations studied, SDS interacts with 40DT and 80DT noncooperatively, whereas for 0DT cooperativity of binding is observed. The amount adsorbed increased significantly as the SDS concentration was close to the cmc. At high SDS concentrations, a lowering of the layer density was observed. For the amphiphilic polyelectrolytes, 40 DT and 80DT, no desorption from the interface was detected for the range of SDS concentrations studied, while 0DT features a maximum in adsorbed amount at concentrations close to the cmc of SDS. Adsorption of 40DT and 80DT from their mixtures with SDS is found to be path dependent with respect to the variation in SDS concentration, where the reversibility decreases with increasing SDS concentration above the expected charge neutralization point. The coadsorption of 80DT and SDS is highly irreversible with respect to changes in the ionic strength within the time scale of the experiment. In this study, we attempt to illustrate both general mechanisms and specific effects. With regard to the general behavior, it is important to note the charge regulation of both the silica surfaces and the polyion/surfactant complexes; an interplay between the two charge-regulating effects is the key to understanding our observations.

Investigation of the state of 8-hydroxyquinoline in aqueous sodium dodecyl sulfate solutions

The influence of sodium dodecyl sulfate on the dissociation of protonated 8-hydroxyquinoline in aqueous solutions is investigated by potentiometric titration at 293 K. The constants of direct binding of 8-hydroxyquinoline with the monomers and micelles of sodium dodecyl sulfate are determined by the computer simulation of the most probable processes. The role of electrostatic and hydrophobic interactions in the studied system is discussed.

The interfacial dilational properties of hydrophobically modified associating polyacrylamide studied by the interfacial tension relaxation method at an oil-water interface.

The interfacial dilational viscoelastic properties of hydrophobically associating block copolymer composed of acrylamide (AM) and a low amount of 2-phenoxylethyl acrylate (POEA) (<1.0 mol%) at the octane-water interfaces were studied by means of the interfacial tension relaxation method. The dependencies of interfacial dilational elasticity and viscous component on the dilational frequency were investigated. The interaction of hydrophobically associating block copolymer [P(AM/POEA)] with sodium dodecyl sulfate (SDS) has been explored. The results show that at lower frequency, the dilational elasticity for different concentration copolymer is close to zero; at higher frequency, the dilational elasticity shows no change with increased frequency; At moderate frequency (10(-3)-1 Hz), the dilational elasticity decreased with a decrease in the dilational frequency. The results show that the hydrophobic groups of [P(AM/POEA)] chains can be associated by inter- or intrachain liaisons in water solution. The dilational viscous component for P(AM/POEA) comes forth a different maximum value at different frequencies when the polymer concentration is different. It is generally believed that the dilational viscous component reflects the summation of the various microscopic relaxation processes at and near the interface and different relaxation processes have different characteristic frequencies. The spectrum of dilational viscous component may appear more than once maximum values at different frequencies. The influence of SDS on the limiting dilational elasticity and viscous component for polymer solution was elucidated. For 5000 ppm polymer solution, the limiting dilational elasticity decreased with an increase in SDS concentration. The dilational viscous component passed through a maximum value with a rise in the dilational frequency, which appeared at different frequency when SDS concentration is different; and the higher is the concentration, the lower is the dilational frequency. It can be explained that macromolecules may be substituted by SDS molecules in the interface and the interaction of molecules decrease, which makes the limiting dilational elasticity decrease. For 200 ppm polymer solution, the limiting dilational elasticity increased firstly and then decreased with SDS concentration increasing. This may be explained that the interfacial polymer concentration is so low that SDS molecules absorbed in the interface dominate dilational properties of the interfacial film even at very low SDS concentration. However, SDS molecules can gradually substitute the polymer molecules in the interface with a rise in SDS concentration, which results in the decrease in the limiting dilational elasticity.

Influence of sodium dodecyl sulphate and Dowfroth frothers on froth stability

Surfactants significantly influence froth stability. Detailed theoretical analysis of this influence is deficient at present. This paper presents an experimental investigation into the influence of surfactants on froth stability measured by the foam lifetime. The surfactants studied include sodium dodecyl sulphate (SDS) and the Dowfroth frothers. The foaming experiments were carried out in a laboratory flotation column by blowing air through a sparger. The physical properties of the foaming systems versus the surfactant concentration were experimentally determined for the surface tension, bubble size, and interfacial viscosity. The pendant drop method was used for surface tension measurement for various concentrations of SDS and Dowfroth frothers. The bubble size was determined using a photography technique. The interfacial viscosity was determined with a deep-channel interfacial viscometer. The obtained physical parameters of foams were not able to describe the dependence of the foam lifetime on the surfactant concentration. As the interfacial shear viscosity, which significantly influences the liquid drainage in foam, is not directly correlated with the foam lifetime it is possible that the froth stability is to a great extent controlled by the rupture of the intervening liquid films residing between bubbles.

Surfactant-enhanced transdermal delivery by electroporation

The objective of the experiment was to study the influence of sodium dodecyl sulfate (SDS) on transdermal transport of diffusants by electroporation. The resistance of porcine epidermis in contact with SDS solution (0.2% w/v) dropped by 40% within 24 h. SDS improved the efficiency of transdermal delivery of glucose, dextrans of molecular weight (MW) 4 kDa (FD4K) and 10 kDa (FD10K) by electroporation. However, the transport of dextran MW 35 kDa (FD35K) was not influenced significantly. Pretreatment of epidermis with SDS solution reduced its electroporation threshold from 80 to 60 V. It appears that presence of SDS during electroporation helps in achieving the desired transport with less electrical exposure dose. SDS enhanced the transdermal delivery of molecules by electroporation most likely by facilitating the barrier disruption during pulse application and also by prolonging the lifetime of electropores created by the pulse.

Voltammetric behavior of ethopropazine and the influence of sodium dodecylsulfate on its accumulation on gold electrodes

Surfactants are sometimes used to improve the accumulation of some electroactive organic compounds, but anionic surfactants have seldom been utilized for such a purpose yet. In this paper, the influence of the anionic surfactant sodium dodecylsulfate (SDS) on the accumulation of ethopropazine (EPZ) at a polycrystalline gold electrode has been studied. EPZ exhibits an anodic peak at about 0.67 V (vs. SCE) and a shoulder in pH 3.5 citric acid–biphthalate buffer solution. In the absence of SDS, the peak is small and ill defined, but it becomes high and well shaped when SDS is added. This results from the adsorption of EPZ in the SDS membrane, which forms spontaneously on the gold electrode surface. For both cases EPZ shows the same electrode reaction mechanism, which is similar to that of promethazine (PMZ). The influence of other factors, such as pH value, variety and concentration of buffers, other surfactants, accumulation potential and time etc has been discussed. It was found that only the anionic surfactants had an enhancement effect on the EPZ accumulation. Also, the solution should be acidic or neutral so as to maintain the interaction due to its electrostatic nature. The optimum SDS concentration for EPZ accumulation is about 0.1 mM regardless of whether or not an accumulation potential is adopted. When all the experiment conditions are optimized, the peak current of the anodic peak changes linearly with the concentration of EPZ over the range 0.4–4 μM, and is thus of analytical significance.

Hydrophobically Modified Associating Polyacrylamide Solutions: Relaxation Processes and Dilational Properties at the Oil−Water Interface

The interfacial dilational viscoelastic properties of hydrophobically associating block copolymer composed of acrylamide (AM) and a low amount of 2-phenoxylethyl acrylate (POEA) (<1.0 mol %) at the octane−water interfaces were investigated by means of two methods: the interfacial tension response to sinusoidal area variations and the relaxation of an applied stress. The dependencies of interfacial dilational modulus and phase angle on the polymer concentration were explored. The influence of sodium dodecyl sulfate (SDS) on the dilational viscoelastic properties of polymer solutions was studied. The results obtained by oscillating barriers method showed that the dilational modulus passed through a maximum value with increasing polymer concentration, while the phase angle decreased with increasing concentration below 200 ppm, then showed very low concentration dependence up to 3000 ppm, and increased dramatically above it. When SDS was added to the aqueous phase, the dilational modulus passed through a maximum with increasing SDS concentration, while the change of phase angle depended on the polymer bulk concentration. The results obtained by the relaxation of an applied stress show that two main relaxation processes exist in the interface at low bulk concentration below the critical aggregation concentration: one is the fast process involving the exchange of hydrophobic microdomains between the proximal region and distal region in the interface with a characteristic time value from several tens of seconds to several seconds at different bulk concentration; the other is the slow relaxation process involving conformational changes of polymer chain in the interface with characteristic time value from 1000 s to several tens of seconds, depending on the bulk concentration. However, there is only one main relaxation process controlling the dilational properties above c*: a fast relaxation process with the characteristic relaxation time of less than 1 s, which is believed to be related to the associations formed by hydrophobic microdomains. Anionic surfactant SDS can influence the dilational properties of polymer solutions by the following ways: first, SDS can absorb onto the interface and bind to the hydrophobic microdomains to change the characteristic times and contributions of the existed relaxation processes of polymer chains; second, SDS can provide a new fast relaxation process involving the exchange of SDS molecules between monomers and mixed micelles in interface. The information on relaxation processes obtained from interfacial tension relaxation measurements can explain the results from dilational viscoelasticity measurements very well. The negative phase angles have been obtained in some case. It is believed that the in-interface slow relaxation process, which sometimes dominates the dilational viscoelasticity of polymer film, is responsible for this phenomenon in our employed experimental method.

Influence of Sodium Dodecyl Sulfate and Tween 20 on Fungal Growth and Toluene Degradation in a Vapor-Phase Bioreactor

Biofiltration, a process in which contaminated air is passed through a biologically active bed, can be used to remove volatile organic pollutants from air streams. While most biofilters rely on bacteria to degrade organic pollutants, biofilters utilizing a fungal biofilm have the potential to be an efficient and robust treatment alternative. In this study, two surfactants were evaluated for their ability to activate the spores of the fungus Exophiala lecanii-corni and reduce the start-up period typically observed in fungal vapor-phase bioreactors. Sodium dodecyl sulfate, an anionic surfactant, was found to inhibit growth of E. lecanii-corni. Polyoxyethylene sorbitan monolaurate (Tween 20), a nonionic surfactant, stimulated bud formation and enhanced toluene degradation in E. lecanii-corni cultures. Tween 20 was also found to enhance inoculum development by shortening the lag period during culture growth. However, when bioreactors were presoaked in medium containing Tween 20, washout of the fungal cells occurred during inoculation, inhibiting the initial fungal biofilm development. After a seven-day start-up period, no detrimental effects on reactor performance due to residual Tween 20 were observed, and toluene elimination capacities of up to 150g/m3⋅h were achieved.

Conformation of Poly(ethylene oxide) in Polymer−Surfactant Aggregates

The influence of sodium dodecyl sulfate (SDS) on the conformation of poly(ethylene oxide) (PEO) in water is studied using viscosity measurements and small-angle neutron scattering (SANS). The behav...

Influence of Sodium Dodecyl Sulfate on the Protolytic Properties of N,N-Dimethyl-N′-(2-hydroxybenzyl) Ethylenediamine and Its Complexation with Copper(II)

To investigate the effect of sodium dodecyl sulfate (concentration Cs = 5 and 10 mM) on the acid–base properties of N,N-dimethyl-N′-(2-hydroxybenzyl) ethylenediamine and its complexation with copper(II) (Cs = 10 mM) was studied using the methods of potentiometry, spectrophotometry (at 298 K), and mathematical simulation of equilibria in solutions. The sodium dodecyl sulfate contributes to the formation of a monomeric form of N,N-dimethyl-N′-(2-hydroxybenzyl)ethylenediamine, while this compound exists in 40% isopropyl alcohol predominantly in the form of a dimer. The acidic properties of protonated monomeric and dimeric species are weaker than those in an aqueous alcohol solution. Sodium dodecyl sulfate facilitates the coordination of the deprotonated form of ligand. The region of the predominant accumulation of an uncharged complex of 1 : 2 composition is shifted to lower pH values (11.0 and 7.5, respectively), whereas the molar absorption coefficient of the complex increases by approximately 1.7 times. The apparent stability constants of complexes of the same type increase.

Influence of sodium dodecyl sulfate on the kinetics of complex formation between [PdCl(dien)] + and sulfur containing ligands l-cysteine and glutathione

The effect of sodium dodecyl sulfate (SDS) micelles on the kinetics of the complex formation between [PdCl(dien)] + and sulfur containing ligands l-cysteine and glutathione (GSH) was investigated by using the stopped-flow technique under pseudo-first order conditions (ligand in excess) in the acidity range from pH 1 to 6. The presence of anionic micelles induced the acceleration of the complex formation in the entire acidity range with the maxima corresponding to the first protolytic constant of the ligands. This effect was interpreted in terms of the attractive electrostatic interaction between reacting species and the micellar surface and their effective concentration in the vicinity of micelles. An increase of the ionic strength leads to a decrease of the rate of complex formation in the presence of anionic micelles due to competition of reactive species with cations originating from inert salt for the micellar surface. The calculation of activation parameters revealed that the entropy of activation is strongly negative in the presence and in the absence of micelles, which is compatible with an associative reaction mechanism.

The Influence of Surfactant (SDS) on the Adsorption Properties of Polyvinyl Alcohol and Polyethylene Glycol in an Alumina/Solution System

The influence of sodium dodecyl sulphate (SDS) on the adsorption properties of non-ionic polymers, i.e. polyethylene glycol (PEG) and polyvinyl alcohol (PVA), at the Al2O3/solution interface was studied. Measurements for various molecular weights and for various amounts of functional groups on the polymer macromolecules were undertaken and the results obtained discussed in the light of these variations. Studies of the mutual interactions of the polymer–surfactant system in aqueous solution were helpful in explaining the equilibria involved in the Al2O3/polymer solution system in the presence of SDS. The thickness of the adsorption layer was determined by viscometric methods and the influence of the degree of hydrolysis of PVA on the structure of the adsorption layer demonstrated.

Influence of sodium dodecyl sulfate on the physicochemical properties of whey protein-stabilized emulsions

The influence of sodium dodecyl sulfate (SDS) on the flocculation of droplets in 20 wt.% soybean oil-in-water emulsions stabilized by whey protein isolate (WPI) was investigated by light scattering, rheology and creaming measurements. The SDS concentrations used were low enough to prevent depletion flocculation by surfactant micelles and extensive protein displacement. In the absence of SDS, emulsions were prone to droplet flocculation near the isoelectric point of the proteins (4<pH<6), but were stable at a higher and lower pH. Flocculation led to an increase in emulsion viscosity, pronounced shear thinning behavior and accelerated creaming. When the surfactant-to-protein molar ratio was increased from 0 to 10, the emulsion instability range shifted to lower pH values due to binding of the negatively charged SDS molecules to the droplets. Our results indicate that the physicochemical properties of protein-stabilized emulsions can be modified by utilizing surfactant–protein interactions.