• Journal of Soil and Groundwater Environment
• /
• v.17 no.1
• /
• pp.13-21
• /
• 2012

This study reports a surfactant-enhanced in-situ remediation treatment at a test site which is located in a hilly terrain. The leakage oils from a storage tank situated on the top of the hill contaminated soils and groundwater in the lower elevation. Sixteen vertical injection wells (11 m deep) were installed at the top of the hill to introduce 0.1-0.5 vol.% of non-ionic Tween-80 surfactant. The contaminated area that required remediation treatment was about $1,650\;m^2$. Two cycles of injecting surfactant solution followed by water were repeated over approximately 7.5 months: first cycle with 0.5 month of surfactant injection followed by 3 months of water injection, and second cycle with 1 month of surfactant followed by 3 months of water injection. The seasonal fluctuation in groundwater table was also considered in the selection of periods for surfactant and water injection. The results showed that the initial Total Petroleum Hydrocarbon (TPH) concentration of 1,041 mg/kg (maximum 3,605 mg/kg) was reduced significantly down to 76.6 mg/kg in average. After 2nd surfactant injection process finished, average TPH concentration of soils was reduced to 7.5% compared to initial concentration. Also, average BTEX concentration of soils was reduced to 10.8%. This resultes show that the surfactant enhanced in-situ remediation processes can be applicable to LNAPL contaminated site in field scale.

• Applied Chemistry for Engineering
• /
• v.20 no.1
• /
• pp.15-20
• /
• 2009

In this study, solubilization experiments of n-octane oil were performed by micellar solutions of polymeric nonionic surfactant Pluronic L64 ($EO_{13}PO_{30}EO_{13}$) at room temperature. A single spherical drop of n-octane was injected into aqueous surfactant solution using an oil drop contacting technique and solubilization rate of n-octane was measured by observing the size of oil drop with time. It was found that solubilization rate was independent of initial oil drop size but inversely proportional to the initial surfactant concentration. These results revealed that solubilization of n-octane oil by L64 micellar solution is controlled by interface-controlled mechanism rather than diffusion-controlled mechanism. Dynamic interfacial tension measurements showed that interfacial tension decreases such as from $2.59{\times}10^{-2}$ to $2.45{\times}10^{-2}$, and further to $2.13{\times}10^{-2}mN/m$ as surfactant concentration increases from 8 to 9 and further to 10 wt% respectively. The equilibration time was also found to decrease slightly with an increase in surfactant concentration. All three systems reached an equilibrium within 7 minutes.

• Korean Chemical Engineering Research
• /
• v.47 no.1
• /
• pp.24-30
• /
• 2009

In this study, solubilization experiments of n-decane, n-undecane and n-dodecane oil were performed by micellar solutions of polymeric nonionic surfactant Pluronic L64($EO_{13}PO_{30}EO_{13}$) at room temperature. A single spherical drop of hydrocarbon oil was injected into aqueous surfactant solution using an oil drop contacting technique and solubilization rate of hydrocarbon oil was measured by observing the size of oil drop with time. It was shown that solubilization rate decreased with the alkane carbon number(ACN) of the hydrocarbon oil. The solubilization rate was also found to be independent of initial oil dorp size and almost linearly proportional to the initial surfactant concentration. These results revealed that solubilization of n-decane, n-undecane and n-dodecane oils by L64 micellar solution is controlled by interface-controlled mechanism but not by diffusion-controlled mechanism. The equilibrium solubilization capacity(ESC) was measured by a turbidimeter and the result showed that EAC decreased with an increase in ACN but increased with both increases in surfactant concentration and solubilization rate. Dynamic interfacial tension measurements showed that interfacial tension and equilibrium time increased with an increase in ACN of hydrocarbon oil but decreased with an increase in surfactant concentration.

• Transactions of the Korean Society of Mechanical Engineers B
• /
• v.27 no.5
• /
• pp.604-611
• /
• 2003

This study was concerned with the enhancement of mass transfer by surfactant added to the aqueous solution of LiBr. Different vertical inner tubes were tested with and without an additive of normal octyl alcohol. The test tubes were a bare tube, groove tube, corrugate tube and inserted spring tubes. The additive concentration of normal octyl alcohol as a surfactant is about 0.08mass%. The Sherwood number was measured as a function of film Reynolds number 20~200. The experimental results were compared with those which use no surfactant. The enhancement of mass transfer by Marangoni convection effect which was generated by addition of the surfactant is proved for each testing tube Especially, it is clarified that the tube with the spring has the highest enhancement effect. A correlation of the experimental mass transfer data for the bare, groove, corrugate and insert spring tubes results expressed as the form of Sh=cㆍ Re$_{f}$ $^{n}$ .

• Journal of the Korean Society of Clothing and Textiles
• /
• v.25 no.8
• /
• pp.1465-1474
• /
• 2001

The dispersion stability of particles and the adsorption of surfactant were examined as a fundamental environment to adhesion of particulate soil to fabric. The adsorption of surfactant on the PEF fabrics decreased with the addition of electrolytes and decreased with increasing the ionic strengths showed similar tendency to PET fabric. And the dispersion force of $\alpha$-Fe$_2$O$_3$particles decreased with the addition of electrolyte. The adhesion of particulate soil to fabric, increased with decreasing the adsorption of surfactant the correlation between the two was high at low ionic strength. The correlation between the adsorption of surfactants on $\alpha$-Fe$_2$O$_3$ particles and the adhesion of particles to fabric was smaller as shown in the correlation between the adsorption of surfactants on fiber substrate and the adhesion of particles on fabric. However, the correlation between the adhesion of particles to fabric and the stability of particle dispersion was relatively more significant.

• Bulletin of the Korean Chemical Society
• /
• v.10 no.4
• /
• pp.339-343
• /
• 1989

The interaction of cationic surfactants, n-alkyltrimethylammonium bromide ($C_nTAB$; n = 12, 14, 16) with anionic polyelectrolyte, poly(styrenesulfonate) (PSS) has been studied by surface tension measurement. In the absence of added salt, the cationic surfactants bind to PSS quantitatively up to ca. 60% coverage of anionic sites of the polyanion and the complexes were surface inactive. Further binding of the surfactant cations on PSS caused a sharp conformational transition of the surfactant/ PSS complexes to surface active complexes and accompanied precipitation. The binding showed a biphasic behavior in the presence of NaCl and cooperativity of the binding became less as the concentration of NaCl increased. Binding of the cationic surfactants on poly(vinylsulfonate) also showed the biphasic behavior and the cooperativity of the binding was much less even in the absence of NaCl. The binding of surfactant to PSS provided hydrophobic environment to solubilized pyrene and reduced the viscosity of the solution greatly even at surfactant concentrations well below cmc. This study indicated that the surfactant bound to PSS up to $60{\%}$ coverage of PSS sites are present as surfactant aggregates which are wrapped up with PSS chains, and hydrophobic interaction is an important factor in the binding of the surfactants to PSS.

• Korea-Australia Rheology Journal
• /
• v.14 no.3
• /
• pp.129-138
• /
• 2002

A cationic surfactant, cetyltrimethylammonium $\rho$-toluenesufonate (CTA$\rho$TS), forms long threadlike micelles in aqueous solution. The threadlike micelles make concentrated entanglement networks, so that the solution shows pronounced viscoelastic behavior as concentrated polymer systems do. However, a mechanism for a process responsible for the longest relaxation time of the threadlike micellar system is different from that of semi-dilute to concentrated polymer systems. The threadlike micellar system exhibits unique viscoelasticity described by a Maxwell model. The longest relaxation time of the threadlike micellar system is not a function of the concentration of CTA$\rho$TS, but changes with that of $\rho$-toluenesufonate ($\rho$$TS^{-}$) ions in the bulk aqueous phase supplied by adding sodium $\rho$-toluenesulfonate (NapTS). The rates of molecular motions in the threadlike micelles are not influenced by the concentration of $\rho$$TS^{-}$ anions, therefore, molecular motions in the threadlike micelles (micro-dynamics) are independent of the longest relaxation mechanism (macro-dynamics). A nonionic surfactant, oleyldimethylamineoxide (ODAO), forms long threadlike micelles in aqueous solution without any additives. The aqueous threadlike micellar system of ODAO also shows Maxwell type viscoelastic behavior. However, the relaxation mechanism for the longest relaxation process in the system should be different from that in the threadlike micellar systems of CTA$\rho$TS, since the system of ODAO does not contain additive anions. Because increase in the average degree of protonation of head groups of ODAO molecules in micelles due to adding hydrogen bromide causes the relaxation time remarkably longer, changes in micro-structure and micro-dynamics in the threadlike micelle are closely related to macro-dynamics in contrast with the threadlike micellar system of CTA$\rho$TS.

• Korean Journal of Materials Research
• /
• v.15 no.5
• /
• pp.340-347
• /
• 2005

Silver nanoparticles were synthesized by chemical reduction method from aqueous silver nitrate solution ana hydrazine as a reduction agent. The morphology, particle size and shape were dependent on the mixing method, reaction temperature and time, molar ratio of hydrazine and silver nitrate, the kind of surfactant, and the addition of surfactant. The stability of the colloidal silver was achieved by the adsorption of surfactant molecules onto the particle. Silver nanoparticles have a characteristic absorption maximum at 430 nm under UV irradiation. It was found that the colloid was nanometer m size and formed very stable dispersion of silver. The Ag nanoparticles obtained showed the spherical shape with the size range of 10-30 nm.

• Korean Journal of Air-Conditioning and Refrigeration Engineering
• /
• v.4 no.2
• /
• pp.65-71
• /
• 1992

In most absorption machines, absorption enhancement has been achieved by adding small amount of surfactant additive, which introduced the surface tension difference between absorbent and surfactant droplets in the vapor absorption. The aim of this study is to understand a basic mechanism of Marangoni convection and its effectiveness in the vapor absorption enhancement. In this study, nonflowing aqueous solution of LiBr 60 mass% was exposed to saturated water vapor under the condition that two dropwises surfactant were fixed on the absorbent surface. Our experiments achieved to visualize the enhanced heat and mass transfer phenomena by the effect of Marangoni convection through the laser holographic interferometry. Also, Marangoni convection behavior was obtained by using tracer method.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
• /
• 2000.11a
• /
• pp.119-123
• /
• 2000

In-situ treatment technologies have been proposed to transform or remove pollutants from contaminated groundwater. Zero-valent iron(Fe$^{0}$ ), metallic iron, is being evaluated as a permeable reactive material to retard the transport of wide array of highly mobile contaminants in groundwater. In this research, tetrachloroethylene(PCE) dechlorination by powdered zero-valent iron in buffered aqueous solution was studied with and without the presence of surfactants. The rate of dechlorination of PCE by zero-valent iron with surfactant was much higher than without surfactant. The presence of surfactant increased the apparent rate of dechlorination because the surfactants influenced the dissolution of PCE into the aqueous phase.