Understanding and Modeling the Effect of Surfactants in Enhanced Particle Removal from Surfaces in Aqueous Media

The removal of particulate contamination is a critical issue for many manufacturing processes. It is particularly critical to the electronics industry in which small pieces of microscopic debris remaining after chemical mechanical planarization (cmp) using submicron polishing particles can cause device failure. One way to enhance particle removal following the cmp process is to utilize surfactants. Recent research has shown ways to model the effect of surfactants on enhanced particle removal. However, previous research has not demonstrated the effect of ionic strength on enhanced particle removal associated with surfactant use. Past research has also not shown the combined effects of ionic strength and surfactant concentration on enhanced particle removal using surfactants. This article summarizes the parameters affecting particle removal, and it provides data and analysis on the effect of ionic strength as well as the combined effects of ionic strength and surfactant concentration on particle removal following cmp processing.     

Understanding and Modeling the Effect of Surfactants in Enhanced Particle Removal from Surfaces in Aqueous Media

The removal of particulate contamination is a critical issue for many manufacturing processes. It is particularly critical to the electronics industry in which small pieces of microscopic debris remaining after chemical mechanical planarization (cmp) using submicron polishing particles can cause device failure. One way to enhance particle removal following the cmp process is to utilize surfactants. Recent research has shown ways to model the effect of surfactants on enhanced particle removal. However, previous research has not demonstrated the effect of ionic strength on enhanced particle removal associated with surfactant use. Past research has also not shown the combined effects of ionic strength and surfactant concentration on enhanced particle removal using surfactants. This article summarizes the parameters affecting particle removal, and it provides data and analysis on the effect of ionic strength as well as the combined effects of ionic strength and surfactant concentration on particle removal following cmp processing.     

Effects of surfactants on size and structure of amylose nanoparticles prepared by precipitation

The present work investigated the influence of surfactants on size and structure of amylose nanoparticles (ANPs) prepared through precipitation. ANPs were fabricated using absolute ethanol containing surfactants (Tween80, Span80 and mixtures of Tween80 and Span80 with ratios of 25/75, 50/50 and 75/25, respectively) as non-solvents. The obtained ANPs were characterized using dynamic light scattering (DLS), scanning electron microscopy and X-ray diffraction. The results showed that surfactant type, concentration and hydrophilic–lipophilic balance (HLB) value had great impact on size of precipitated ANPs. The smallest ANPs with mean size of 155 nm determined by DLS were obtained by using 0.5% (in proportion of the amylose solution volume) of Tween80/Span80 mixture (HLB = 12.33). The precipitated ANPs possessed the V-type crystalline structure no matter whether using the surfactants or not.     

Silicone emulsion-enhanced recovery of chlorinated solvents: batch and column studies

Batch and column experiments were conducted to investigate the feasibility of flushing with silicone oil emulsion for the removal of chlorinated solvents, including trichloroethylene (TCE), perchloroethylene (PCE) and 1,2-dichlorobenzene (DCB). In the batch experiments, solubilization potentials of emulsion and effects of surfactants as additives were examined. The emulsion prepared with 2% (v/v) silicone oil could solubilize 90.7% of 10,000 ppm TCE, 97.3% of 4000 ppm PCE and 99.7% of 7,800 ppm DCB. Results of one-dimensional column studies indicated that aqueous solubility and sorption of contaminants determined the flushing efficiency. The addition of surfactants below their critical micelle concentration (CMC) did not affect the removal of chlorinated solvents in batch and column experiments. The results of this study show that flushing with oil-based emulsion can be applied to treat the chlorinated solvents.     

Soil washing using various nonionic surfactants and their recovery by selective adsorption with activated carbon

The performance of activated carbon in soil washing and subsequent selective adsorption for surfactant recovery from the washed solution was investigated. Sandy loam soil contaminated with phenanthrene at 200 mg kg(-1) was washed with four different nonionic surfactants: Tween 40, Tween 80, Brij 30 and Brij 35. The efficiency of soil washing was highest when using Brij 30 with the highest solubilizing ability for phenanthrene and low adsorption onto soil. In the selective adsorption step, surfactant recovery was quite effective for all surfactants ranging from 85.0 to 89.0% at 1 g L(-1) of activated carbon (Darco 20-40 mesh). Phenanthrene removal from the solution washed with Brij 30 was only 33.9%, even though it was 54.1-56.4% with other surfactants. The selectivity was larger than 7.02 except for Brij 30 (3.60). The overall performance considering both the washing and surfactant recovery step was effective when using Tween 80 and Brij 35. The results suggest that higher solubilizing ability of surfactants is a requirement for soil washing but causes negative effects on phenanthrene removal in the selective adsorption. Therefore, if a surfactant recovery process by selective adsorption is included in soil remediation by washing, the overall performance including the two steps should be considered for properly choosing the surfactant.     

Effect of different extraction agents on metal and organic contaminant removal from a field soil

This paper presents an evaluation of different extracting solutions for the removal of phenanthrene, lead and zinc from a contaminated soil obtained from a former manufactured gas plant site. The field soil contained 50%-88% sand, 11%-35% fines, 2.7%-3.7% organic matter and high concentrations of phenanthrene (260 mg/kg), lead (50.6 mg/kg) and zinc (84.4 mg/kg). A series of batch extraction experiments were conducted using the field soil with different extracting solutions at various concentrations to investigate the removal efficiency and to optimize the concentration of each extractant. The results showed that removal efficiencies of different flushing systems were significantly influenced by their affinity and selectivity for the contaminants in the soil matrix. Non-ionic surfactants (Igepal CA720 and Tween 80) were found to be effective in removing phenanthrene, but they were ineffective in removing lead and zinc. Chelating agents (ethylenediamine tetra acetic acid, EDTA and diethylene triamine penta acetic acid, DTPA) and selected acids were effective in removing lead and zinc, but they were ineffective for the phenanthrene removal. Co-solvents and cyclodextrins were not effective for removal of any of the contaminants. A sequential use of the 0.2 M EDTA followed by 5% Tween 80 or 5% Tween 80 followed by 1 M citric acid was found to be effective for the removal of lead, zinc, and phenanthrene. Overall, it can be concluded that sequential use of different extracting solutions is required for the removal of both heavy metals and organics from field contaminated silty sand soils.     

表面活性剂对超滤膜表面改性的研究

采用三类表面活性剂对聚砜超滤膜进行表面改性．实验结果表明，非离子表面活性剂Ｔｗｅｅｎ２０效果最明显，改善了膜表面的亲水性，提高了通量．     

表面活性剂对壳聚糖成膜体系物理特性的影响

目的 为研究不同表面活性剂对壳聚糖成膜体系物理与力学性能的影响,以期制备性能优良的壳聚糖膜。方法 文中配制质量分数为1%的壳聚糖膜液,以壳聚糖质量分数为30%的甘油为增塑剂,分别以质量分数为0.05%的吐温20、40、80,司盘20、40、80为表面活性剂,采用流延法制备可食膜。考察膜液流变性质、表面张力、Zeta电位,成膜力学性能、水分敏感性（水蒸气透过率、溶胀性、溶解性）、透光性,并利用AHP–CRITIC联合评价法对膜性能进行综合评价。结果 在质量分数为1%时,壳聚糖膜液表现为弱胀塑性;表面活性剂的加入能够有效降低膜液表面张力,使其保持稳定状态（Zeta电位>30 mV）;成膜均为淡黄色半透明状,透光范围为45%～77%;对同一系列表面活性剂,随着亲水亲油平衡值（HLB）的增加,成膜力学性能下降,但阻水能力增强,同时,吐温添加组膜的力学性能均优于司盘添加组,而阻水性能则相反。结论 综合评价膜体系性能发现,加入司盘20的壳聚糖膜得分最高,吐温系列最高分为吐温20。研究结果为成膜体系中表面活性剂的选择提供了理论依据。     

Effects of concentration, head group, and structure of surfactants on the degradation of phenanthrene

The effects of concentration, polar/ionic head group, and structure of surfactants on the biodegradation of polycyclic aromatic hydrocarbons (PAHs) in the aqueous phase, as well as their effects on the bacterial activity were investigated. The toxicity ranking of studied surfactants is: non-ionic surfactants (Tween 80, Brij30, 10LE and Brij35)相似文献   

Effect of different polysorbates on development of self-microemulsifying drug delivery systems using medium chain lipids

The primary objective of this study was to develop lipid-based self-microemulsifying drug delivery systems (SMEDDS) without using any organic cosolvents that would spontaneously form microemulsions upon dilution with water. Cosolvents were avoided to prevent possible precipitation of drug upon dilution and other stability issues. Different polysorbates, namely, Tween 20, Tween 40, Tween 60, and Tween 80, were used as surfactants, and Captex 355 EP/NF (glycerol tricaprylate/caprate) or its 1:1 mixture with Capmul MCM NF (glycerol monocaprylocaprate) were used as lipids. Captex 355-Tween-water ternary phase diagrams showed that oil-in-water microemulsions were formed only when the surfactant content was high (80–90%) and the lipid content low (10–20%). Thus, mixtures of Tweens with Captex 355 alone were not suitable to prepare SMEDDS with substantial lipid contents. However, when Captex 355 was replaced with the 1:1 mixture of Captex 355 and Capmul MCM, clear isotropic microemulsion regions in phase diagrams with sizes in the increasing order of Tween 20?相似文献   

Application of surfactant enhanced permanganate oxidation and bidegradation of trichloroethylene in groundwater

The industrial solvent trichloroethylene (TCE) is among the most ubiquitous chlorinated solvents found in groundwater contamination. The main objectives of this study were to evaluate the feasibility of using non-ionic surfactant Simple Green™ (SG) to enhance the oxidative dechlorination of TCE by potassium permanganate (KMnO₄) employing a continuous stir batch reactor system (CSBR) and column experiments. The effect of using surfactant SG to enhance the biodegradation of TCE via aerobic cometabolism was also examined. Results from CSBR experiments revealed that combination of KMnO₄ with surfactant SG significantly enhanced contaminant removal, particularly when the surfactant SG concentrated at its CMC. TCE degradation rates ranged from 74.1% to 85.7% without addition of surfactant SG while TCE degradation rates increased to ranging from 83.8% to 96.3% with presence of 0.1 wt% SG. Furthermore, results from column experiments showed that TCE was degraded from 38.1 μM to 6.2 μM in equivalent to 83.7% of TCE oxidation during first 560 min reaction. This study has also demonstrated that the addition of surfactant SG is a feasible method to enhance bioremediation efficiency for TCE contaminated groundwater. The complete TCE degradation was detected after 75 days of incubation with both 0.01 and 0.1 wt% of surfactant SG addition. Results revealed that surfactant enhanced chemical oxidation and bioremediation technology is one of feasible approaches to clean up TCE contaminated groundwater.     

Selection of surfactants for enhancing diesel hydrocarbons-contaminated media bioremediation

The use of surfactants represents a valuable method to enhance the access of the microorganisms to low-soluble and recalcitrant compounds in bioremediation techniques. The choice of surfactants is the first step of feasibility studies for this application. So far, no defined procedures are present in literature to select the most suitable surfactant for the treatment of a specific contaminated site. Furthermore, the characterisation of physico-chemical parameters is important to understand the reason of successes and failures. In this paper a step procedure to select and characterise a commercial surfactant to be used in bioremediation enhancement of hydrocarbon-contaminated media was developed. Among the commercial surfactants, the procedure was applied to alkyl polyethoxylates (Brij family) and sorbitan derivates (Tween family). The selection resulted in the application of Brij 56 and Tween 80 as biodegradation-enhancer in different lab scale systems for remediation of diesel contamination. In liquid systems, Tween 80 greatly increased biodegradation of highly branched and high-molecular weight hydrocarbons, while Brij 56 enhanced degradation of highly branched hydrocarbons. Based on these results, the potential applications and the limitations of these surfactants at full scale level were estimated.     

Effects of pure and dyed PCE on physical and interfacial properties of remedial solutions

Hydrophobic dyes have been used to visually distinguish dense non-aqueous phase liquid (DNAPL) contaminants from background aqueous phases and soils. The objective of this study was to evaluate the effects of a dyed DNAPL, 0.5 g Oil-Red-O/l of PCE, on the physical properties of remedial solutions: water, co-solvents (50, 70, and 90% (v/v) ethanol), and surfactants (4% (w) sodium dihexyl sulfosuccinate). This study compared the densities, viscosities, and interfacial tensions (IFTs) of the remedial solutions in contact with both dyed and undyed PCE. The presence of the dye in PCE substantially alters the IFTs of water and ethanol solutions, while there is no apparent difference in IFTs of surfactant solutions. The remedial solutions saturated with PCE showed higher viscosities and densities than pure remedial solutions. Solutions with high ethanol content exhibited the largest increases in liquid density. Because physical properties affect the flow of the remedial solutions in porous media, experiments using dyed DNAPLs should assess the influence of dyes on fluid and interfacial properties prior to remediation process analysis.     

Effects of mixed surfactants on the volatilization of naphthalene from aqueous solutions

The effects of mixed anionic-nonionic surfactants, Tween40-SDS (sodium dodecyl sulfate), Tween40-SDBS (sodium dodecylbenzene sulfonate), Tween20-SDS and Tween20-SDBS, on the solubility and volatilization of naphthalene from static aqueous solutions were investigated. The experiment results indicated that mixed anionic-nonionic surfactants can solubilize naphthalene synergistically, which was resulted from the reduction in critical micelle concentration (CMC) of the mixed surfactant and the increase in micellar partition coefficient (K(mc)) of naphthalene between micelles and aqueous phase. The synergistic effects of mixed surfactants resulted in further reduction in volatilization of naphthalene than that induced by single surfactant. A positive linear correlation was found between the synergistic solubilization ratio (DeltaS) and the synergistic inhibitory capacity on naphthalene volatilization (DeltaC) in the presence of mixed surfactants. Results from this study imply that mixed surfactants can be employed in environmental remediation to formulate the needed solubility and volatilization of volatile and semivolatile compounds in aqueous solutions.     

Physicochemical Characterization of Rutaecarpine-Loaded Microemulsion System

To develop an o/w microemulsion system containing poorly water-soluble rutaecarpine, the solubility of rutaecarpine in water, ethanol, various oils, and surfactants were investigated. Among the surfactants and oils tested, Tween 20/PEG 400 and castor oil were chosen as the surfactant system and oil phase of the microemulsion, as rutaecarpine was most soluble in them, respectively. Pseudoternary phase diagrams were constructed to obtain the concentration range of oil, surfactant, and cosurfactant for microemulsion formation, and the stability test of rutaecarpine delivered by microemulsion formation was then evaluated. Pseudoternary phase diagrams show that the areas of microemulsion appeared at those with 0–20% Smix (PEG 400/Tween80 = 60/40), 64–81% water, and 10–20% oil. The rutaecarpine (300 µg/g)-loaded microemulsion composed of 10.8% PEG 400, 7.2% Tween 80, 20% caster oil, and 72% water was physically and chemically stable for at least 6 months. Thus, the microemulsion system composed of castor oil, PEG 400, Tween 80, and water could be a stable dosage form for rutaecarpine.     

Solubilization of pyrene by anionic-nonionic mixed surfactants

Surfactant-enhanced remediation (SER) is an effective approach for the removal of sorbed hydrophobic organic compounds from contaminated soils. The solubilization of pyrene by four anionic-nonionic mixed surfactants, sodium dodecyl sulfate (SDS) with Triton X-405 (TX405), Brij35, Brij58, and Triton X-100 (TX100), has been studied from measurements of the molar solubilization ratio (MSR), the micelle-water partition coefficient (Kmc), and the critical micelle concentration (CMC). The MSRs of pyrene in mixed surfactants are found to be larger than those predicted according to an ideal mixing rule. The mixing effect of anionic and nonionic surfactants on MSR for pyrene follows the order of SDS-TX405 > SDS-Brij35 > SDS-Brij58 > SDS-TX100 and increases with an increase in the hydrophile-lipophile balance (HLB) value of nonionic surfactant in mixed systems. In addition, the mixture of anionic and nonionic surfactants cause the Kmc value for pyrene to be greater than the ideal value in SDS-TX405 mixed system, but to be smaller than the ideal value in SDS-Brij35, SDS-Brij58, and SDS-TX100 mixed systems. Meanwhile, in the four mixed systems, the experimental CMCs are lower than the ideal CMCs at almost all mixed surfactant solution compositions. The mixing effect of anionic and nonionic surfactants on MSR for pyrene can be attributed to the conjunct or the net result of the negative deviation of the CMCs from ideal mixture and the increasing or decreasing Kmc.     

The effect of component of microemulsion for transdermal delivery of nicardipine hydrochloride

Purpose: Nicardipine hydrochloride has been used widely for the treatment of angina pectoris and hypertension. Because of its extensive first pass metabolism after oral administration, the transdermal administration of nicardipine microemulsions was developed in this study. Methods: Microemulsions consisted of isopropyl myristate (IPM), surfactant mixture of Tween 80/Span 80 and/or Tween 80/Span 20, co-surfactant (ethanol) and aqueous phase. Pseudo-ternary phase diagrams were constructed using water titration method. The effect of component of microemulsion on the percutaneous absorption of drug was evaluated by in vitro permeation study. Results: The area of microemulsion isotropic region in the presence of ethanol was comparably larger in the absence of ethanol. The mean droplet size of nicardipine microemulsions ranged from 70 to 123 nm. With addition of ethanol, the droplet size became smaller. The permeation rate and extent of nicardipine microemulsion transport across rat skin was affected by the components of microemulsion. Nicardipine microemulsion had higher flux at surfactant mixture with lower hyrophile-lipophile balance (HLB) value and Tween content. Conclusions: The microemulsion consisted of 52% IPM, 35% surfactant mixture and 13% water had higher permeation rate through rat skin above 122.53±1.87 μg/cm2/h and was expected to develop a transdermal delivery system.     

Effect of non-ionic surfactant concentration and type on the formation and stability of W/O/W multiple emulsions: Microscopic and conductometric evaluations

W/O/W multiple emulsions with sodium salicylate as a model drug were prepared and evaluated for the effect of surfactant concentration and type on stability using microscopic and conductometric methods. Primary (W/O) emulsions were prepared with lipophilic surfactants (2-31% W/W relative to the oily phase). W/O/W emulsions were formed by mixing the primary emulsions with solutions containing 0.5 to 2% W/V hydrophilic surfactants. Optimum concentration of the lipophilic surfactant was 26% W/W. The optimum hydrophilic surfactant concentration was 1% W/V. Best stability was achieved with HLB 3.7 lipophilic and HLB 15.6 hydrophilic surfactants.     

Stability of orange oil/water nanoemulsions prepared by the PIT method

This article reports the preparation and characterization of orange oil/water nanoemulsions stabilized by commercial nonionic surfactants based on ethoxylated lauryl ether (Ultrol line), by the phase inversion temperature (PIT) method. The orange oil/surfactant/water dispersions were prepared at different HLB values, by varying the concentrations of the surfactants as well as the concentration of the oil phase. The stability of the o/w nanoemulsions and the size distribution of the dispersed particles in these systems in general depended on the concentration of the oil phase used: the emulsions prepared with an oil phase of 14 wt% had smaller droplet size in the dispersed phase than the emulsions prepared in the presence of oil phases of 20 and 30 wt%. The nanoemulsions prepared with pure surfactants were more stable in the presence of Ultrol L60, but the surfactants' cloud point had a strong influence on the stability of the emulsions formed when this was very near room temperature. Because of this, we prepared systems containing mixtures of surfactants. Among these systems, the most stable nanoemulsions were those prepared with a Ultrol L100/Ultrol L20 mixture with HLB of 12.40. This behavior can be attributed to the complete solubilization in mixed micelles of the more hydrophobic surfactant.     

In situ investigation of surfactants’ effect onto electrochemical synthesis and properties of polyfurans

Polyfuran (PFu) films were electrochemically deposited onto gold electro-quartz crystal microbalance (EQCM) electrodes using acetonitrile (ACN)/LiClO₄ solvent-electrolyte in presence of dodecylbenzenesulfonic acid (anionic, DBSA) and polyethylene glycol sorbitan monolaurate (non-ionic, Tween 20) surfactants. The effect of surfactants on structural and conductivity properties of the polymer films was investigated using Fourier transform-infrared spectroscopy (FT-IR) and four-probe conductivity measurements. The doping effects of surfactants onto the properties of PFu were correlated with mass gain using in situ EQCM. The conductivity of PFu polymer was measured for PFu with no surfactant and for PFu in presence of two surfactants (Tween 20 and DBSA). Our data indicate that although a fast polymerization, a sharp shift in the frequency and mass changes of the polymer films as well as the highest recorded conductivity of 0.048 S cm^?1 were all obtained for the PFu/Tween 20-2 sample, significantly more PFu films formed with PFu/DBSA than with PFu/Tween 20 samples. We concluded that more PFu films can be obtained when an oxidant and an anionic surfactant (DBSA) are used than when an oxidant is used alone, or when an oxidant is used with a non-ionic surfactant (Tween 20). A part of an anionic surfactant can be incorporated into a PFu structure like an oxidant anion and can act as co-dopant.