Pentachlorophenol interactions with soil

Pentachlorophenol (PCP) adsorption and desorption equilibrium was studied with two Menfro silt loam soils — upper horizon and lower horizon. For the adsorption studies the variables were: temperature (10 and 30 °C) and the amount of organic matter. The variables for the desorption studies were: temperature (10 and 30 °C), pH and the presence of an anionic and a cationic surfactant. The results from these studies confirmed the importance of soil organic matter for adsorption of PCP on the soils. The adsorption data at different temperatures indicated the physical nature of the adsorption process. The desorption data produced non-singularity and some PCP was irreversibly adsorbed onto the soil despite repeated washings. Increased pH increased the desorption of PCP from the soil. The anionic surfactant, sodium dodecylbenzene sulfonate (SDS) was able to desorb significant amounts of PCP from the soil at doses equal to critical micelle concentration (CMC). But, the nonionic surfactant, surfactant, Triton X-405 required a much higher dose (twice the CMC) to cause a significant desorption of PCP from the soil.     

Influence of surfactant charge on antimicrobial efficacy of surfactant-stabilized thyme oil nanoemulsions

Thyme oil-in-water nanoemulsions stabilized by a nonionic surfactant (Tween 80, T80) were prepared as potential antimicrobial delivery systems (pH 4). The nanoemulsions were highly unstable to droplet growth and phase separation, which was attributed to Ostwald ripening due to the relatively high water solubility of thyme oil. Ostwald ripening could be inhibited by incorporating ≥75% of corn oil (a hydrophobic material with a low water solubility) into the nanoemulsion droplets. The electrical characteristics of the droplets in the nanoemulsions were varied by incorporating ionic surfactants with different charges after homogenization: a cationic surfactant (lauric arginate, LAE) or an anionic surfactant (sodium dodecyl sulfate, SDS). The antifungal activity of nanoemulsions containing positive, negative, or neutral thymol droplets was then conducted against four strains of acid-resistant spoilage yeasts: Zygosaccharomyces bailli, Saccharomyces cerevisiae, Brettanomyces bruxellensis, and Brettanomyces naardenensis. The antifungal properties of the three surfactants (T80, LAE, SDS) were also tested in the absence of thymol droplets. Both ionic surfactants showed strong antifungal activity in the absence of thymol droplets, but no antimicrobial activity in their presence. This effect was attributed to partitioning of the antimicrobial surfactant molecules between the oil droplet and microbial surfaces, thereby reducing the effective concentration of active surfactants available to act as antimicrobials. This study shows oil droplets may decrease the efficacy of surfactant-based antimicrobials, which has important consequences for formulating effective antimicrobial agents for utilization in emulsion-based food and beverage products.     

Isothermal titration calorimetry study of pectin-ionic surfactant interactions

Isothermal titration calorimetry (ITC) was used to measure enthalpy changes resulting from injection of anionic (sodium dodecyl sulfate, SDS) or cationic (dodecyl trimethylammonium bromide, DTAB) surfactants into aqueous 1 wt % pectin solutions (30, 60, or 90% methoxylated). In the absence of pectin, the critical micelle concentrations (cmc) determined by ITC were 14.7 mM for DTAB and 7.7 mM for SDS. Binding of DTAB to pectin was endothermic and was attributed to electrostatic attraction between the cationic surfactant and anionic biopolymer. Binding of SDS to pectin was exothermic and was attributed to hydrophobic interactions. Pectin reduced the cmc of SDS, probably because of long-range electrostatic repulsion between the molecules. Above a particular concentration, which depended on pectin and surfactant type, both ionic surfactants promoted pectin aggregation (monitored by turbidity increase). This study demonstrates the potential of ITC for providing valuable information about interactions between polysaccharides and amphiphiles.     

Effect of soil components on the surfactant-enhanced soil sorption of PAHs

Purpose  

The use of cationic surfactants was proposed to enhance the soil retention of hydrophobic organic contaminants (HOCs). However, due to the complexity of soil composition, the effect of cationic surfactants on the soil sorption of HOCs was limited to a qualitative understanding. To gain further insight into the mechanism of the surfactant and predict its efficiency, a comparative study on the HOCs sorption capacities of the surfactants sorbed on pure typical soil components was investigated.     

Cosorption of atrazine and a lauryl polyoxyethylene oxide nonionic surfactant on smectite

Commercial atrazine formulations commonly contain nonionic surfactants that serve as solubilizing and wetting agents for enhancing the stability and efficacy of the herbicide. The fate of atrazine in soils has been extensively investigated; yet, few studies have considered the effects of formulation components on the fate of atrazine in soils. In this study, we investigated the influence of the nonionic surfactant, Brij 35 (Brij), on the sorption of atrazine on Ca- and K-saturated samples of a reference smectite, Panther Creek (PC). In general, Brij concentrations of 50 and 200 mg L(-1) had little effect on atrazine sorption, but sorption was substantially inhibited by Brij concentrations of 2100 mg L(-1). For Brij concentrations of 6300 mg L(-1), atrazine sorption was intermediate between that observed for the 200 and 2100 mg L(-1) Brij systems. Brij molecules themselves were very strongly sorbed by PC, with sorption maxima exceeding 200 g kg(-1). X-ray diffraction analysis of Brij-treated PC indicated that the sorbed Brij was intercalated into interlayers of the smectite. At Brij concentrations of 2100 mg L(-1), Brij competed with atrazine for interlayer sorption sites. In contrast, at the initial Brij concentration of 6300 mg L(-1), the clay interlayers were largely filled with Brij, and excess Brij probably accumulated on external surfaces of the clay as surface micelles. We hypothesize that atrazine partitioning into surfactant micelles on external surfaces of the clay led to enhanced retention by the solid phase.     

Characterization of interactions between chitosan and an anionic surfactant

Chitosan is a cationic biopolymer that has many potential applications in the food industry because of its unique nutritional and physiochemical properties. Many of these properties depend on its ability to interact with anionic surface-active molecules, such as phospholipids, surfactants, and bile acids. The purpose of this study was to characterize the interaction between chitosan and a model anionic surfactant (sodium dodecyl sulfate, SDS) using isothermal titration calorimetry (ITC), surfactant-selective electrode (SSE), and turbidity measurements. ITC and SSE indicated that SDS bound strongly to chitosan via a highly exothermic interaction. The turbidity measurements indicated that chitosan formed insoluble complexes with SDS that strongly scattered light. The chitosan bound approximately 4 mM of SDS per 0.1 wt % chitosan before becoming saturated with surfactant. The SDS-chitosan interaction was weakened appreciably by the presence of 100 mM NaCl, which suggested that it was electrostatic in origin. This study provides information about the origin and characteristics of molecular interactions between chitosan and anionic surface-active lipids that may be useful for the rational design of chitosan-based food ingredients with specific nutritional and functional characteristics, e.g., cholesterol lowering or fat replacement.     

复合表面活性剂（SDS/Tw-80）对长链烷烃的增溶和柴油污染土壤的洗脱作用

表面活性剂能够快速高效处理石油污染土壤,但由于所选用表面活性剂的类型和配比、土壤性质、污染物种类的差异,洗脱效果和作用原理不尽相同。通过研究复合表面活性剂SDS/Tw-80对石油烷烃的表观增溶和从受试土壤中的洗脱过程,探讨和阐释影响洗脱过程的各种因素。结果表明,复合表面活性剂对污染土壤中的石油烷烃洗脱效果较单一表面活性剂更好,且随复合表面活性剂SDS/Tw-80中的组分配合比例的增大而显著提高,同时能够降低胶束的成束浓度要求,扩大目标物在单位胶束内的容纳量,促使各目标长链烷烃进入胶束内部的趋势加大。复合表面活性剂的适用不仅能够改善胶束构成,且组分间表现出显著的协同作用,从而使在保证较高洗脱效率的同时能够大幅降低试剂用量,有效地克服土壤的吸附作用,把对土壤性状的影响降低,对土壤质量的恢复具有积极意义。     

Removal of Nickel by Means of Micellar-Enhanced Ultrafiltration (MEUF) Using Two Anionic Surfactants

Micellar-enhanced ultrafiltration (MEUF) is an effective separation technique for removing metal ions from aqueous environments. The critical micellar concentration (CMC) of two anionic surfactants, sodium dodecyl sulfate (SDS) and linear alkylbenzene sulfonate (LAS), was determined by means of conductometry. The effects of pH, conductivity, and surfactant concentration on the permeate flow, retention of surfactants and nickel by MEUF, was studied. Results showed that for surfactant concentrations beyond the CMC, Ni(II) retention with SDS was slightly higher than with LAS (S/M?=?45: Ni(II) retention was 70% and 55% for SDS and LAS, respectively). LAS surfactant was always retained in higher quantities than SDS. An increase in conductivity produced large reduction in Ni(II) retention and slightly increased surfactant retention. pH values between 4 and 8 did not affect nickel retention but enhanced the SDS and LAS surfactant retentions.     

Factors affecting lycopene oxidation in oil-in-water emulsions

Evidence that dietary lycopene decreases the risk for a number of health conditions has generated new opportunities for the addition of lycopene to functional foods. This work examined the potential of oil-in-water emulsions as a lycopene delivery system for foods. Oil-in-water emulsions containing lycopene were prepared using different kinds of surfactant (cationic, anionic, and nonionic) and oil types (corn oil, stripped corn oil, and hexadecane). The formation of fatty acid oxidation products and the degradation of lycopene and tocopherol were then monitored. Fatty acids and lycopene had greater stability in oil-in-water emulsions stabilized by cationic dodecyltrimethylammonium bromide (DTAB) or nonionic polyoxyethylene (23) lauryl ether than by anionic sodium dodecyl sulfate (SDS). Oxidative stability in the corn oil-in-water emulsions stabilized by SDS was in the following order: tocopherolhexadecane>tocopherol-stripped corn oil. Lycopene degradation rates were similar in emulsions with and without fatty acids, suggesting that lycopene loss was independent of the presence of fatty acids. These results suggest that the stability of lycopene in oil-in-water emulsions could be inhibited by altering the emulsion droplet interface and by the presence of tocopherols.     

Selenite adsorption by a variety of oxides

Abstract

Selenite adsorption by a variety of oxides consisting of iron (Fe), aluminum (Al), titanium (Ti), manganes (Mn), and silicon (Si), and by two humic acids were investigated in order to grasp selenite behavior and fixation mechanisms in soil. It was found that selenite was apparently adsorbed even by the Mn oxides on which surface negative charge was dominant in normal pH range (pH <4). No selenite adsorption was observed in the silicon dioxide (SiO₂) and the two humic acids. A sequential extraction of adsorbed selenite with competitive anions showed the differences of binding force or stability of adsorbed selenite among the minerals. While the goethite fixed selenite strongly, selenite adsorbed on the Mn oxide was easily released to the liquid phase with other anions, such as phosphate. Each mineral had its inherent characteristic in ligand exchange reactions accompanied with selenite sorption. Selenite sorption by the Mn and the Ti oxides resulted in large increase of surface negative charge, while only a little increase in the Fe and Al oxides. Proton consumption with selenite sorption was extremely smaller for the Mn oxide than for the others.     

Maltodextrin-anionic surfactant interactions: isothermal titration calorimetry and surface tension study

Interactions between maltodextrin (DE = 10) and an anionic surfactant (sodium dodecyl sulfate, SDS) were studied in a buffer solution (pH 7.0, 10 mM NaCl, 20 mM Trizma, 30.0 degrees C) using isothermal titration calorimetry (ITC), surface tension, differential scanning calorimetry (DSC), and turbidity techniques. ITC measurements indicated that the binding of SDS to maltodextrin was exothermic and that, on average, one SDS monomer bound per 24 glucose units of maltodextrin at saturation. Surface tension measurements indicated that there was a critical surfactant concentration ( approximately 0.05 mM SDS) below which surfactant and maltodextrin did not interact and that the amount of surfactant bound to the maltodextrin above this concentration increased with increasing maltodextrin concentration. Turbidity measurements indicated that the solutions remained transparent at all maltodextrin (0-1 wt %) and SDS (0-20 mM) concentrations studied, which suggested that phase separation did not occur. DSC measurements indicated that no phase transitions occurred between 10 and 110 degrees C for maltodextrin solutions (0.5 wt %) in the presence or absence of surfactant. A phase diagram was developed to describe the interactions between SDS and maltodextrin.     

Surfactant Enhanced Desorption of TNT from Soil

Surfactant enhanced desorption of 2,4,6-trinitrotoluene (TNT) from contaminated soils at a military site was investigated. Anionic (SDS and DOWFAX 8390), cationic (CTAC and CTAB), and nonionic (Tween 80 and Brij 35) surfactants were first tested at concentrations ranging from 0.1 to 1%. The anionic and nonionic surfactants were further tested at concentrations of up to 10%. Anionic surfactants, particularly SDS, provided the best desorption of TNT from the soil. There was not any increase in TNT desorption for both the nonionics and cationics at concentrations ranging between 0.1 to 1% and the extent of desorption was found to be lower than the TNT desorption only by water. The competition of the negatively charged soil surfaces for the positively charged cationics and the neutral nonionic surfactants may constitute the underlying reason. TNT was significantly desorbed when the concentrations of Tween 80, DOWFAX 80 and SDS were increased up to 10%.     

Effects of ionic surfactants on the aggregate stability and water repellency of silt loam soil

Purpose

With the increase of surfactant usages, more and more concerns were paid on their effects on the physicochemical characteristics of soils. Up to now, only few researches have examined the effects of ionic surfactants on the stability of soil structure and soil water repellency.

Materials and methods

Cetyltrimethyl ammonium bromide (CTAB) as cationic surfactant and sodium dodecyl sulfate (SDS) as anionic surfactant were adopted to investigate their effects on the aggregate stability and water repellency of a silt loam soil which was sampled in Corn High-Tech Park, Huang-Huai-Hai region, China. (1) Aggregate stability: 50 g soil was mixture with 100 mL surfactant solution in a beaker. The concentrations of surfactant solutions were 0 (the blank), 200, 400, 600, 800, 1000, and 2000 mg L^?1, respectively. After 30 min, the soil was sieved and divided into four fraction aggregates. (2) Soil water repellency: the concentrations of surfactant solutions were the same as experiment 1. Forty grams of soil was blended with 80 mL surfactant solution in an aluminum specimen. Drying the water by oven of 40 °C firstly and then by air, the whole period was about 1 week. After that, soil water infiltration and sorptivity were measured.

Results and discussion

Compared to the blank, surfactants increased the amounts of 2–0.25 and <0.053 mm aggregates of the soil and decreased the amounts of 0.25–0.053 mm aggregates of the soil. Surfactants also increased the mean weight diameter (MWD) of the soil. Except the 200 mg L^?1 treatment, CTAB promoted the soil water infiltration. All SDS treatments impeded the soil water infiltration. The soil repellency factor (R) value of the blank was 1.22, lower than the critical value of 1.95, which implied that the soil of blank treatment was free of soil water repellency. For CTAB, only 200 and 400 mg L^?1 treatment’s R were higher than 1.95 while for SDS, all the treatment’s R were higher than 1.95.

Conclusions

Surfactants improved the stability of soil aggregates. Soil treated with CTAB did not show the repellency, whereas SDS treatment resulted in intense water repellency compared with the wettable blank soil. Findings of this study can be used to explain the role of ionic surfactants on soil structure stability as well as on the development of water repellency in lower soil depths.

     

Toxicity of Synthetic Surfactants to the Marine Macroalga, Ulva lactuca

The toxicities of three synthetic surfactants to the marine macroalga, Ulva lactuca, have been examined by monitoring chlorophyll a fluorescence quenching. The anionic surfactant, sodium dodecyl sulphate (SDS), exerted no measurable toxicity over the concentration range 0?C10 mg L^?1, while presence of the non-ionic surfactant, Triton X-100 (TX), elicited a small reduction in photochemical efficiency that was independent of concentration. The cationic surfactant, hexadecyltrimethylammonium bromide (HDTMA), incurred a dose-dependent response to ??3 mg L^?1 (EC₅₀?=?2.4 mg L^?1), but a reduction in toxicity thereafter. Presence of TX had little effect on the toxicity of HDTMA but an equimolar concentration of SDS directly offset the impact of HDTMA on photochemical efficiency. Relative toxicities of the surfactants are attributed to differences in affinity for the algal surface and tendencies to disrupt cell membranes and interact with intracellular macromolecules. Non-linear dose responses and antagonistic effects are attributed to non-specific interactions between molecules of the same surfactant and electrostatic interactions between molecules of different amphiphilic character.     

不同pH、电解质浓度条件下草酸对针铁矿吸附Cd(II)的影响及机制

用吸附平衡法研究了不同草酸浓度、体系pH对针铁矿 (G)吸附Cd2+的影响与机制以及电解质 (KNO3)浓度对针铁矿、草酸化针铁矿 (G+40 )吸附Cd2+的影响差别及原因。结果表明 ,低浓度草酸 (1mmolL-1 )促进Cd2+的吸附 ;高浓度草酸 (1mmolL-1/sup )抑制Cd2+的吸附。已吸附在针铁矿表面的草酸对Cd2+ 吸附的影响与液相中草酸的影响不同 ,这主要与草酸引起的针铁矿表面电荷性质的变化、草酸在固液两相间的分配、草酸与Cd2+的配合作用和竞争作用有关。电解质 (KNO3)浓度对针铁矿和草酸化针铁矿吸附Cd2+的影响明显不同 ,随KNO3 浓度的提高 ,针铁矿的Cd吸附率由 44.5%增至 95%以上 ,而草酸化针铁矿吸附率由 29%降至6.2% ,这主要决定于二者的电荷零点 (PZC)和体系pH变化的不同。     

Affinity constants and behavior of Cd sorption in some acid soils

Cadmium sorption was studied in several acidic soils in a pH range from 4.5 to 6.5. The soils had two classes of surfaces with acidity constants (pKa₁ = 4.09 and pKa₂ = 6.39) similar to those for weakly and very weakly cidic carboxyls, and N-containing groups in fulvic acid. Titratable H and acidity constants were used to estimate the number of exchange sites at each pH level. Sorption of Cd was closely related to Cd concentration, pH, and soil type. Although the inclusion of pH and organic C contents in a regression accounted for some variations in the Cd distribution coefficient defined as the ratio of the quantity of Cd sorbed to the solution Cd concentration, the number of sorption sites was a more appropriate factor to explain the variability. Because of a negligible contribution to the number of exchange sites from Fe oxides, the sorption of Cd at pH = 4.5 was considered to be of a one-surface Langmuir type. A two-surface Langmuir equation was considered to model sorption at higher pH values. The average affinity constants (log K) were 3.61 and 4.89 for Cd sorption by the two classes of surfaces.     

Removal of Malachite Green from Aqueous Medium Employing Polyurethane Foam as Adsorbent and Sodium Dodecylsulfate as Carrier

The present work describes a detailed study about the adsorption of malachite green (MG) by a polyether-type polyurethane foam (PUF) using sodium dodecylsulfate (SDS) as a carrier. The adsorption process was based on the formation of a hydrophobic ionic-pair between the MG cationic dye and the dodecylsulfate anion, which presented high affinity for the PUF. The manifold employed in the study was built up by adjusting a cylinder of PUF with 200 mg in the arm of an overhead stirrer, which was soaked (and stirred) in the solution containing the dye and SDS. The adsorption process was characterized in relation to equilibrium and kinetic aspects. Langmuir (r ² = 0.842) and Freundlich (r ² = 0.996) isotherms were also employed for modeling the system as well as the Nernst partition law (r ² = 0.999). A study about the recovery of MG and the PUF regeneration was conducted, and the acetonitrile was the most efficient solvent for the desorption of the adsorbed ionic pair. The obtained results showed that the concentration of SDS added to the medium plays an important role on the adsorption process, which can be better described by employing a second-order kinetic model.     

Sulfentrazone adsorbed on micelle-montmorillonite complexes for slow release in soil

Interactions of the herbicide sulfentrazone with the cationic surfactants octadecyltrimethylammonium (ODTMA), hexadecyltrimethylammonium (HDTMA), and benzyldimethylhexadecylammonium (BDMHDA) have been studied for the design of slow-release formulations based on sulfentrazone adsorbed on a micelle-montmorillonite complex. Adsorbed amounts of sulfentrazone on ODTMA- and BDMHDA-montmorillonite complexes were 99.2-99.8% of that added, and desorption of herbicide in water during 24 h was low. After 10 washings in funnels with soil, only 2.6% of herbicide was released from ODTMA-montmorillonite formulations versus 100% release from the commercial formulation. The strong binding of sulfentrazone to micelles was confirmed by pH and spectroscopic measurements and was explained by the formation of ionic pairs between cationic surfactant and anionic herbicide. The ODTMA-clay and commercial formulations of sulfentrazone yield almost complete and 40% growth inhibition of green foxtail, respectively, at 700 g of active ingredient/ha. Hence, the slow release from micelle-clay formulations of sulfentrazone promotes its biological activity and reduces environmental contamination.     

Equilibrium and spectroscopic studies of lead retention in smectite

Abstract

Heavy metal pollution of soils and water is a serious environmental problem. Sorption onto solid surfaces from aqueous solutions is an important process influencing transport and accumulation of heavy metals in the environment. Lead (Pb) sorption in smectite SWy‐2 was investigated by equilibrium sorption studies, coupled with spectroscopic methods. The isotherm and pH‐edge of lead sorption in the smectite were measured in batch experiments. The sorption isotherms under uncontrolled pH were best‐fitted with the Langmuir equation, while those with a fixed pH 5.5 were best‐fitted with the Freundlich equation. The pH‐edge of lead sorption shifted to a higher pH as the Pb concentration increased. The ionic strength only affected Pb sorption in the low pH range. The effects of associated nitrate and perchlorate anions were significant only for the Pb sorption at high Pb concentration (>2 mM). FTIR and XRD spectroscopies were performed with oriented clay samples. In the infrared spectra, apeak with a maximum near 1398 cm^‐1 and a shoulder centered near 1470 cm^‐1 was significant for the samples treated with >1 mM Pb at pH >5.6. This peak may be composed of several IR bands, including an OH bending band from Pb hydroxides and CO₃ ^2‐ stretching bands from Pb carbonates. The basal spacing of Pb‐treated smectites increased with increasing Pb content in the clay and correlated well with the intensity of OH bending band (around 1621 cm^‐1) of adsorbed water. The increase of basal spacing at low pH (pH <3.3) was poorly correlated with the intensity of water OH bending band. The comprehensive studies provided many evidences for revealing the structure of various lead complexes on clay surfaces.