Experimental investigation of the effects of oil asphaltene content on CO_(2) foam stability in the presence of nanoparticles and sodium dodecyl sulfate

Foam stability tests were performed using sodium dodecyl sulfate(SDS)surfactant and SiO2 nanoparticles as foaming system at different asphaltene concentrations,and the half-life of CO_(2) foam was measured.The mechanism of foam stability reduction in the presence of asphaltene was analyzed by scanning electron microscope(SEM),UV adsorption spectrophotometric concentration measurement and Zeta potential measurement.When the mass ratio of synthetic oil to foam-formation suspension was 1:9 and the asphaltene mass fraction increased from 0 to 15%,the half-life of SDS-stabilized foams decreased from 751 s to 239 s,and the half-life of SDS/silica-stabilized foams decreased from 912 s to 298 s.When the mass ratio of synthetic oil to foam-formation suspension was 2:8 and the asphaltene mass fraction increased from 0 to 15%,the half-life of SDS-stabilized foams decreased from 526 s to 171 s,and the half-life of SDS/silica-stabilized foams decreased from 660 s to 205 s.In addition,due to asphaltene-SDS/silica interaction in the aqueous phase,the absolute value of Zeta potential decreases,and the surface charges of particles reduce,leading to the reduction of repulsive forces between two interfaces of thin liquid film,which in turn,damages the foam stability.

Sodium dodecyl sulfate (SDS) as an effective corrosion inhibitor for Mg-8Li-3Al alloy in aqueous NaCl: A combined experimental and theoretical investigation

The corrosion inhibition behavior of Mg-8Li-3Al alloy in NaCl solution with sodium dodecyl sulfate(SDS)was investigated by hydrogen analysis,scanning electron microscopy(SEM),electrochemical test,scanning Kelvin probe force microscopy(SKPFM)and computational methods.Results showed that the corrosion resistance of Mg-8Li-3Al alloy in NaCl solution was effectively improved with SDS.The SEM and SKPFM results confirmed a dense,200 nm-thick SDS-adsorbed layer had formed on the alloy surface.The separation energy ΔE_(gap) and adsorption energy E_(ads) of SDS on the Mg surface were calculated by density functional theory and molecular dynamics simulations,respectively.And the corrosion inhibition mechanism was hypothesized and described.

Curing of the Bacillus subtilis Plasmid Using Sodium Dodecyl Sulfate

Curing of Bacillus subtilis plasmid using sodium dodecyl sulfate (SDS)was studied in order to obtain a host strain. An overnight culture of Bacillus subtilis 24/pMX45 was used to inoculate fresh LB containing SDS (0-0.008%). No growth of 24/pMX45 was observed when LB contained an SDS concentration of 0.006% or greater, and the sublethal concentration (w/v) of SDS was 0.005% with a killing rate of 99%. Samples were diluted and plated on LB agar, individual colonies were randomly picked to a selective agar medium by tooth to screen for loss of plasmid-encoded erythomycin resistance. CsCl-EtBr gradient centrifugation and plasmid DNA profile demonstrated that plasmid-cured derivative A7 has completely lost its plasmid. A7 had a shorter lag, and its cell concentration was consistently higher than that of the 24/pMX45. Elimination of the plasmid was first observed after 24/pMX45 had been treated with SDS for 8 h. The percent elimination then continued to increase until about 22 h, after which the fraction of cured cell in the population remained constant. Plasmid cured cell numbers were measured in a separate control culture of 24/pMX45 untreated by SDS. No spontaneous loss of pMX45 was observed after 24/pMX45 were incubated for 24 h and 48 h with shaking at 37 ℃.These results suggested that SDS can be used as curing agent to eliminate the plasmid of Bacillus subtilis.

Enhancing the leaching effect of an ion-absorbed rare earth ore by ameliorating the seepage effect with sodium dodecyl sulfate surfactant

Ameliorating the problem of low leaching efficiency,long leaching period,and high agent consumption should be studied to efficiently exploit ion-absorbed rare earth ore resources.In this study,the surfactant sodium dodecyl sulfate(SDS) is used to enhance the leaching effect of an ion-absorbed rare earth ore by ameliorating the seepage effect for the first time.The effects of surfactant concentration,leaching agent dosage,solution flow velocity,and solution pH on the leaching rate were explored,and the mechanism of SDS was discussed.Under the optimum conditions,the addition of a small amount of SDS(mass fraction0.04%) can increase the leaching rate by about 5%,shorten the leaching period,and reduce the consumption of the leaching agent.SDS significantly ameliorates the seepage effect of the ore body by reducing the surface tension of the leaching agent and ameliorating the wettability of the mineral surface.This effect is the main factor that improves the leaching efficiency.DFT(density functional theory) calculation results show that SDS can react with rare earth ions,which reduces the adsorption strength on clay mineral surfaces.Hence,rare earth ions are easily exchanged by ammonium ions,and mass transfer is enhanced.

Intermolecular Interactions in Self-Assembly Process of Sodium Dodecyl Sulfate by Vertically Polarized Raman Spectra

Molecular self-assembly is extremely important in many fields, but the characterization of their corresponding intermolecular interactions is still lacking. The C-H stretching Raman band can reflect the hydrophobic interactions during the self-assembly process of sodium dodecyl sulfate （SDS） in aqueous solutions. However, the Raman spectra in this region are seriously overlapped by the OH stretching band of water. In this work, vertically polarized Raman spectra were used to improve the detection sensitivity of spectra of C-H region for the first time. The spectral results showed that the first critical micelle concentration and the second critical micelle concentration of SDS in water were 8.5 and 69 mmol/L, respectively, which were consistent with the results given by surface tension measurements. Because of the high sensitivity of vertically polarized Raman spectra, the critical micelle concentration of SDS in a relatively high concentration of salt solution could be obtained in our experiment. The two critical concentrations of SDS in 100 mmol/L NaCl solution were recorded to be 1.8 and 16.5 mmol/L, respectively. Through comparing the spectra and surface tension of SDS in water and in NaCl solution, the self-assembly process in bulk phase and at interface were discussed. The interactions among salt ions, SDS and water molecules were also analyzed. These results demonstrated the vertically polarized Raman spectra could be employed to study the self-assembly process of SDS in water.

Phase Behavior of Sodium Dodecyl Sulfate-n-Butanol-Kerosene-Water Microemulsion System

Experiments were carried out to investigate the influences of cation from electrolytes and acidity/alkalinity on the phase behavior of sodium dodecyl sulfate-n-butanol-organics-water （with electrolytes） microemulsion sys-tem. The organics used is commercial kerosene. The volume ratio of water to organics is 1︰1. The results show that the type and valence of electrolyte cations are important factors influencing the microemulsion behavior. Biva-lent Ca2＋is more effective than monovalent K＋and Na＋for the formation of Winsor type III and II microemulsion. For electrolytes with the same monovalent cation Na＋, i.e. NaCl and Na2CO3, anions in the electrolyte have some effect. Bivalent anion 23CO - leads to a lower activity of cation Na＋than monovalent anion Cl-. NaOH （or KOH） behaves similar with NaCl （or KCl）. When HCl is used as electrolyte, its acidity plays an important role. Phase in-version of microemulsion from type III （or II） to type I is observed through precipitation of Ca2＋using Na2CO3, neutralization of HCl by NaOH, and addition of water to the system, which releases the oil from the microemulsion.

Molecular Dynamics Simulation of Effect of Salt on the Compromise of Hydrophilic and Hydrophobic Interactions in Sodium Dodecyl Sulfate Micelle Solutions

The presence of salt has a profound effect on the size,shape and structure of sodium dodecyl sulfate(SDS)micelles.There have been a great number of experiments on SDS micelles in the presence and absence of salt to study this complex problem.Unfortunately,it is not clear yet how electrolyte ions influence the structure of micelles.By describing the compromise between dominant mechanisms,a simplified atomic model of SDS in presence of salt has been developed and the molecular dynamics(MD)simulations of two series of systems with different concentrations of salt and charges of ion have been performed.Polydispersity of micelle size is founded at relatively high concentration of SDS and low charge of cation.Although the counter-ion pairs with head groups are formed,the transition of micelle shape is not observed because the charge of cation is not enough to neutralize the polar of micelle surface.

Molecular dynamics simulations of the effects of sodium dodecyl sulfate on lipid bilayer

Molecular dynamics simulations have been performed on the fully hydrated lipid bilayer with different concentrations of sodium dodecyl sulfate （SDS）. SDS can readily penetrate into the membrane. The insertion of SDS causes a decrease in the bilayer area and increases in the bilayer thickness and lipid tail order, when the fraction of SDS is less than 28%. Through calculating the binding energy, we confirm that the presence of SDS strengthens the interactions among the DPPC lipids, while SDS molecules act as intermedia. Both the strong hydrophilic interactions between sulfate and phosphocholine groups and the hydrophobic interactions between SDS and DPPC hydrocarbon chains contribute to the tight packing and ordered alignment of the lipids. These results are in good agreement with the experimental observations and provide atomic level information that complements the experiments.

Effect of β-Cyclodextrin Upon the Sol-gel Transition of Methylcellulose Solutions in the Presence of Sodium Dodecyl Sulfate

The sol-gel transition temperature of methylcellulose （MC） solution in the presence of sodium dodecyl sulfate （SDS） as well as the mixtures of SDS and β-cyclodextrin （β-CD） was mea- sured, and the effect of the two competing interactions, the hydrophobic interaction between SDS and MC and the inclusion interaction between SDS and β-CD, upon the sol-gel transition of MC solution was studied. It has been found that the inclusion interaction between SDS and β-CD is much greater than the hydrophobic interaction between SDS and MC. As a result, in the coexistence of SDS and β-CD, the sol-gel transition temperature of MC solution keeps the same value, independent of the concentration of SDS in solution on con- dition that the concentration of SDS is less than β-CD. Our experimental results not only suggest that the effect of SDS upon the sol-gel transition of MC solution can be screened by β-CD completely but also indicate the inclusion ratio of SDS to β-CD can be determined quantitatively by using rheological measurement. The inclusion ratio of SDS to β-CD is 1：1, which is in good agreement with the inclusion ratio of SDS to β-CD in the presence of poly（vincyl pyrrolidone） determined by the viscosity measurement but is critically different from the inclusion ratio of SDS to β-CD in the presence of the oppositely charged polyelec-trolyte by using the rheological measurement, mainly due to the reason that the mechanism of the interaction between SDS and MC is critically different from the mechanism of the interaction between SDS and the oppositely charged polyelectrolyte.

The Electrooxidation of Tetracycline at Acetylene Black Electrode in the Presence of Sodium Dodecyl Sulfate

The electrooxidation of tetracycline (TC) at acetylene black electrode has been studied in the presence of sodium dodecyl sulfate (SDS). Tetracycline (TC) exhibited very sensitive oxidation peak in this system. The peak current was proportional to TC concentration, and the detection limit was 1.2×10-8 mol/L. The system was used to the determination of TC in Pharmaceuticals.

Effects of Sodium Dodecyl Sulfate on a Single Cavitation Bubble

Dynamics of a single cavitation bubble in sodium dodecyl sulfate（SDS） aqueous solutions is investigated experimentally and theoretically. The bubble pulsation is measured by a phase-locked integrated imaging technique,and the ambient radius is obtained by fitting the numerical calculation based on the Rayleigh–Plesset bubble dynamics model to the experimental data. The results show that, under the same driving condition, the ambient radius of the cavitation bubble decreases correspondingly with the increase of SDS concentration within the critical micelle concentration, while the compression ratio of the radius increases, which indicates that the addition of SDS decreases the internal molecular number of the cavitation bubble and increases the power capability of the cavitation bubble. In addition, bubble oscillation increases the concentration of the surfactant molecules on the bubble wall, so that the effect of SDS on a single cavitation bubble is reduced when the SDS concentration is greater than 0.8 m M.

Adsorption of Cr(III) from an Aqueous Solution by Chitosan Beads Modified with Sodium Dodecyl Sulfate (SDS)

This study is to prepare chitosan beads modified with sodium dodecyl sulfate (SDS) to effectively remove Cr(III) from an aqueous solution. The characterizations of SDS-chitosan by scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS), Fourier transform-infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS) proved the successful synthesis of the adsorbent. The adsorption of Cr(III) on the SDS material was investigated by varying experimental conditions such as pH, contact time and adsorbent dosage. The maximum adsorption capacity of SDS-chitosan for Cr(III) was estimated to be 3.42 mg?g-1. The results of adsorption kinetics and isothermal models show that the adsorption process conforms to the pseudo-second-order and Langmuir isotherm models, indicating that the adsorption is single-layer chemical adsorption. Thermodynamic analyses indicate that the adsorption of Cr(III) is an endothermic reaction. These results show that the new adsorbent has obvious application prospect to eliminate Cr(III).

Observations on the Function of Mucous Cells in the Epidermis of the Cat-fish Clarias batrachus Exposed to Sodium Dodecyl Sulfate

Response of mucous cells, in the epidermis of the catfish Clarias batrachus, to a sublethal concentration of sodium dodecyl sulfate was studied and correlated with the alteration in the status of their secretory activity after different durations of the treatment. At 4h, 8h, 24h,48h and 72h of the detergent treatment, most mucous cells attained voluminous dimensions and appeared closely approximating to or even overlapping the adjacent ones. At 12h, 36h, and 60h, in contrast, the mucous cells appeared small and slender, and seemed to be located at greater intervals. These changes in dimensions were responsible for the apparent increase or decrease in the density of mucous cells after different durations of detergent treatment. Statistically, however, no significant change was observed in the total number of the mucous cells throughout the experiment.The mucous cells appeared enlarged towards the end of the experiment signifying increased mucus production. This is considered as an adaptation, for protection, assisting the fish to adjust to the changed environment.A shift in the histochemical nature of the secretory contents at the middle and basal parts of the mucous cells, from a mixture of neutral and acid glycoproteins to neutral glycoproteins, during the early stages of the treatment suggests that acid moities could not simultaneously be synthesized as an immediate response to enhanced mucous secretion. The apical parts of the mucous cells, however, showed no histochemical change throughout the experiment.

Room Temperature Synthesis of Gold Nanokites in Polyvinyl Alcohol-Sodium Dodecyl Sulfate Aggregations Aqueous Solution

Controlled synthesis of asymmetrical gold nanokites was realized by reducing HAuCl4 with polyvinyl alcohol （PVA） in PVA-sodium dodecyl sulfate （SDS） aggregations aqueous solution at room temperature without any addi- tional reducing agents. The crystal structures, optical property and growth process of the gold nanokites were inves- tigated by X-ray diffraction （XRD）, Vis-NIR spectrum and transmission electron microscope （TEM）. HAuCl4 con- centration dramatically influenced the morphologies of the products. When HAuCl4 concentration was increased from 0.5 mmol·L^-1 to 2.2 mmol·L^-1, the products changed from network-like nanostructures to nanokites, nanoleaves and microplates. SDS was indispensable for the formation of gold nanokites and without SDS su- per-branched structures became the dominant products.

Sodium dodecyl sulfate sensitized electrochemical method for subnanomole level determination of ortho-phenylphenol at a novel disposable electrode

The electrochemical behavior of ortho-phenylphenol （OPP） at a disposable electrode （an improved wax-impregnated graphite electrode） in the presence of sodium dodecyl sulfate （SDS） was studied for the first time. The results demonstrated that the electrocatalytic oxidation process of OPP was accompanied with two-charge-two-proton transference. The electronic transmission coefficient （a） and diffusion coefficient （DR） for OPP were calculated to be 0.8126 and 3.61× 10^-2 cm2/s, respectively. The electrochemical signal was apparently improved by SDS at the disposable electrode and the oxidative peaks current was proportional to the concentration of OPP over the range from 1.0 ×10^-9 to 4.0 × 10^-6 mol/L with the detection limit of 8.7× 10^-10 mol/L. This novel and highly sensitive method can be successfully applied to detect OPP in the orange rind sample.

Sodium dodecyl sulfate sensitized electrochemical method for sub-picomole level determination of topotecan hydrochloride at a novel disposable electrode

A sub-picomole level topotecan hydrochloride determination method was first proposed using sodium dodecyl sulfate (SDS) as a sensitized reagent at a novel disposable electrode (an improved wax-impregnated graphite electrode).The effects of different kinds of surfactants on the electrochemical response to topotecan hydrochloride were examined.The results indicate the electrochemical signal was apparently improved by SDS.At optimal conditions,the oxidative peak current increased linearly with the logarithm of concentrations for topotecan hydrochloride in the ranges of 2.0 × 10-12 to 1.0 × 10-11 mol/L and 8.0 × 10-11 to 8.0 × 10-10 mol/L with a detection limit of 6.4 × 10-13 mol/L.The proposed method could be applied in determining topotecan hydrochloride in urine.

Atomic force microscopy imaging of dialyzed single-walled carbon nanotubes dispersed with sodium dodecyl sulfate

The existence of excess sodium dodecyl sulfate(SDS)molecules in a single-walled carbon nanotube(SWNT)solution dispersed by hybridization with SDS leads to unstable atomic force microscopy(AFM)imaging.In this study,we demonstrate sequential dialysis against pure water in order to remove excess SDS molecules from an SDS-SWNT hybrid dispersion.A 1:102 volume ratio of SDS-SWNT dispersion to water in the dialysis was found to be effective in realizing stable AFM observations of the SDS-SWNT hybrids despite imperfect filtering of SDS via dialysis.On the other hand,the SDS-SWNT hybrids were stable even when this volume ratio was 1:106.Further,the SDS-SWNT hybrids were present in the solution even when the dialyzed samples were stored for 14 days.Our results reveal that dialysis under optimal conditions enables improved handling of SDS-SWNT hybrids,particularly for stable AFM observations.

Effects of additives on nickel electrowinning from sulfate system

In order to eliminate the pitting and improve the surface morphology of cathode nickel,the influence of additives of boric acid and dodecyl sodium sulfate(SDS)on the process of nickel electrowinning from sulfate system was studied by cathode polarization tests and nickel electrodeposition experiments.The experimental results show that the addition of boric acid can increase the cathode polarization while SDS can decrease the cathode polarization.Both boric acid and SDS are useful to eliminate the pitting on nickel deposits and improve the morphology of surface.Good deposit morphology with rare pitting and high current efficiency is favored by adding 10 g/L boric acid and 40 mg/L SDS in the electrolyte under the condition of nickel ion concentration of 80 g/L, sodium ion concentration of 10 g/L,pH of 3,current density of 220 A/m 2 and temperature of 70℃.

Anionic surfactant sulfate dodecyl sodium (SDS)-induced thermodynamics and conformational changes of collagen by ultrasensitive microcalorimetry

In this communication,sulfate dodecyl sodium(SDS)-induced thermodynamics and conformational changes of collagen were studied.We used ultrasensitive differential scanning calorimetry(US-DSC)to directly monitor the thermal transition of collagen in the presence of SDS.The results show that SDS affects the conformation and thermal stability of collagen very differently depending on its concentrations.At C SDS≤0.05mM,the enhanced thermal stability of collagen indicates the stabilizing effect by SDS.However,a further increase of SDS leads to the denaturation of collagen,verifying the well-known ability of SDS to unfold proteins.This striking difference in thermodynamics and conformational changes of collagen caused by SDS concentrations can be explained in terms of their interactions.With increasing SDS,the binding of SDS to collagen can be dominated by electrostatic interaction shifting to hydrophobic interaction,and the latter plays a key role in loosening and unfolding the triple-helix structure of collagen.The important finding in the present study is the stabilizing effect of SDS on collagen molecules at extreme low concentration.

Surface plasmon resonance-induced visible-light photocatalytic performance of silver/silver molybdate composites

Novel silver/silver molybdate（Ag/Ag2MoO4） composites with surface plasmon resonance（SPR）-enhanced photocatalytic performance were successfully fabricated via a facile one-pot hydrothermal route with the presence of sodium dodecyl sulfate（SDS） in this study.The as prepared silver/silver molybdate（Ag/Ag2MoO4） composites were systematically characterized by X-ray diffraction（XRD）,scanning electron microscopy（SEM） and ultraviolet-visible diffuse reflectance absorption spectroscopy（DRS） in order to investigate their crystal structure,morphology and optical property as well.The photocatalytic activities of the composites were subsequently evaluated by their ability to degrade rhodamine B（RhB） under visible-light irradiation.Varies of controlled experiments were then carefully operated to gain a deep insight into the assembling of Ag/Ag2MoO4composites.It was found that preparation conditions such as pH,reaction time,and the amount of surfactant played important roles in the formation of composites with octahedral microstructures.And the composite obtained at 160 ℃ using 0.5 g of sodium dodecyl sulfate exhibited the highest photocatalytic performance under visible-light irradiation.Capture experiments were also conducted to clarify the function of different active species generated on the surface of Ag/Ag2MoO4during the photocatalytic process,in which both holes and ·OH radicals were found to play crucial role in photocatalytic removal of RhB under visible light irradiation.A possible photocatalytic mechanism of Ag/Ag2MoO4 was finally proposed on the basis of all the results to explain the higher photocatalytic activity of the octahedral Ag/Ag2MoO4 composites.It was inferred that the photoinduced ＂hot＂ electrons can quickly transfer from the Ag NPs to the conduction band of Ag2MoO4 and react with oxygen and H2O to generate a large quality of active radicals such as ·OH and ·O2^- because of the SPR effects.Besides,this SPR effects of Ag nanoparticles deposited on the surface of Ag2MoO4 can not only dramatically amplify its light absorption,especially in the visible region,but also promote the separation of photoexcited electron-hole pairs and effectively decrease electron-hole recombination.