Sources, transport and reactivity of anionic and non-ionic surfactants in several aquatic ecosystems in SW Spain: a comparative study

Presence, distribution and transport mechanisms of the four major synthetic surfactants -linear alkylbenzene sulfonates (LAS), alkyl ethoxysulfates (AES), nonylphenol ethoxylates (NPEOs) and alcohol ethoxylates (AEOs)- have been simultaneously studied in different aquatic ecosystems. Urban wastewater discharges and industrial activities were identified as the main sources for these compounds and their metabolites. LAS, AES and carboxylic metabolites remained in the dissolved form (87–99%). However, NPEOs and AEOs were mostly associated with particulate matter (65–86%), so their degradation in the water column was limited due to their lower bioavailability. It was also observed that sorption to the particulate phase was more intense for longer homologs/ethoxymers for all surfactants. With respect to surface sediments, AES levels were considerably below (<0.25 mg/kg) the values detected for LAS and NPEOs. Concentrations of AEOs, however, were occasionally higher (several tens of ppm) than those found for the rest of the target compounds in several sampling stations.     

Influence of surfactant-facilitated interfacial tension reduction on chlorinated solvent migration in porous media: observations and numerical simulation

The ability of a multiphase flow model to capture the migration behavior of chlorinated solvents under conditions of surfactant-facilitated interfacial tension (IFT) reduction is assessed through comparison of model predictions with observations from controlled laboratory experiments. Tetrachloroethene (PCE) was released in two-dimensional saturated systems, packed with sandy media that incorporated rectangular lenses of capillary contrast. Spatially uniform interfacial tension conditions were created in the tanks by pre-flushing the porous medium with either Milli Q water or an aqueous surfactant solution. Experimental observations showed that surfactant-facilitated IFT reductions substantially lowered capillary resistance to the vertical downward migration of PCE and enabled PCE to enter finer grained, less permeable lenses that were not penetrated in the absence of surfactant. An immiscible flow model was used to simulate the conditions of the laboratory experiments. Under higher IFT conditions (47.5 and 5 dyn/cm), the model could successfully predict the general migration behavior of the organic liquid. Model predictions, however, exhibited poorer agreement with observed migration pathways under low IFT conditions (0.5 dyn/cm). In all cases, the predicted PCE distributions were influenced by selection of the parametric model for capillary retention and relative permeability. Simulated migration rates were more consistent with observed behavior when the Brooks-Corey/Burdine model was employed. For low interfacial tensions, improved predictions of migration pathways were obtained through grid refinement and incorporation of small-scale packing variability. Simulations highlight the substantial sensitivity of model predictions to the capillary pressure-scaling factor, grid resolution, and small-scale porosity variations at interfaces of permeability contrast under reduced IFT conditions.     

叶轮气浮机用浮选剂研究

采用阳离子聚合物的表面活性剂作浮选剂，能增强气泡与絮粒的粘附能力，提高气浮分离效果，用该浮选剂对南充炼油厂的南阳油田稠油污水进行处理，去浊率达到９０％左右，处理效果与美国埃克森公司产３３９０浮选剂相当。     

Dispersibility of crude oil in fresh water

The effects of surfactant composition on the ability of chemical dispersants to disperse crude oil in fresh water were investigated. The objective of this research was to determine whether effective fresh water dispersants can be designed in case this technology is ever considered for use in fresh water environments. Previous studies on the chemical dispersion of crude oil in fresh water neither identified the dispersants that were investigated nor described the chemistry of the surfactants used. This information is necessary for developing a more fundamental understanding of chemical dispersion of crude oil at low salinity. Therefore, we evaluated the relationship between surfactant chemistry and dispersion effectiveness. We found that dispersants can be designed to drive an oil slick into the freshwater column with the same efficiency as in salt water as long as the hydrophilic-lipophilic balance is optimum.     

Characterization of seawater and aerosol particle surfactants using solid phase extraction and mass spectrometry

Surface-active organic molecules (surfactants) may influence the ability of an aerosol particle to act as a cloud condensation nuclei by reducing its surface tension. One source of organic mass in aerosol particles, which may also contain surfactants, is bubble bursting on the sea surface. In order to directly compare these molecules in the ocean and aerosol particles, we developed a method using multiple solid phase extractions and high resolution mass spectrometry to characterize surface active organic molecules in both. This method has extraction efficiencies greater than 85%, 75%, and 60% for anionic, cationic, and nonionic surfactant standards, respectively. In this study, we demonstrate the presence of three ionic classes of surface active organics in atmospheric aerosol particles and estuarine water from Skidaway Island, GA. With this extraction method, organic molecules from both estuarine water and atmospheric aerosol particles significantly reduced surface tension of pure water (surface tension depression of ~ 18 mN/m) and had high ratios of hydrogen to carbon (H/C) and low ratios of oxygen to carbon (O/C), indicative of surfactants. While previous work has observed a larger fraction of anionic surface active organics in seawater and marine aerosol particles, here we show cationic surface active organics may make up a large fraction of the total surface active molecules in estuarine water (43%–47%).     

An assessment of the toxicity of pyridinium chlorides and their biodegradation intermediates

Toxicity investigations were conducted for four pyridinium chlorides belonging to cationic surface-active substances (CSAS), which differed from each other in the numbers of methyl groups (CH(3)) in pyridinium ring.The crustacean Daphnia magna, the fish Lebistes reticulatus and the alga Scenedesmus quadricauda were chosen as biotests. Toxicity of examined preparations appeared to be very high but did not depend on their chemical structure. S. quadricauda was the most sensitive organism. Toxicity of intermediate products obtained in biological oxidation process was also examined. Biodegradation was conducted according to the "river water test". It was found that only partial degradation took place while pyridinium chlorides constituted main energy and carbon source. Presence of biodegradation intermediate products was shown on the basis of 1H NMR analysis. Intermediates were not toxic to any biotests.     

Alcohol-assisted dyeing processes: a chemical substitution study

Dyeing processes of various yarns (wool, cotton, polyester, nylon 6 and acrylic) were studied with the aim to substitute some auxiliary agents with ethanol at low concentration. The results observed in isothermal dyeing showed a favorable effect of alcohol addition, at about 1-3% v/v, on the dye uptake, with some differences depending on fiber nature and dye class. This effect was correlated with contact angle measurements of water-ethanol solutions on the mentioned yarns, which confirmed a lower surface tension in the same concentration range. Then, laboratory tests with dye triads at programmed temperature were carried out comparing the results of standard dyeing recipes with those obtained by replacing wetting, retardant and leveling agents with ethanol. Good color imitations were generally shown with respect to standard processes. A wetting effect of ethanol was shown for all the tested yarns and dye classes, while in wool dyeing with acid, pre-metallized and reactive dyes, ethanol was suitable to replace also leveling and retarding agents. Light and wash fastnesses were also compared. Finally the environmental benefits arising from chemical substitution of auxiliary agents with ethanol were highlighted and the cost of alcohol introduction was compared with the cost saving of auxiliary substitution. A positive economic balance was obtained.     

Impacts of surfactants on the ecotoxicological effects of TiO2-NP and/or Cd contamination in sediments北大核心CSCD

Surfactants may alter the interaction between engineered nanoparticles (ENP) and coexisting pollutants, and further influence the ecotoxicity of these pollutants. This research aimed to evaluate the impacts of the surfactant sodium dodecyl benzene sulfonate (SDS) on the ecotoxicological effects of TiO2-NP and Cd combined contamination in freshwater sediments by deposit-feeding gastropoda Bellamya aeroginosa. We investigated the effects of TiO2-NP and/or Cd contamination in the presence of different concentrations of SDS on DNA damage, Na+, K+-ATPase activities, malondialdehyde (MDA) levels, and protein carbonyl (PCO) levels in the hepatopancreas of B. aeroginosa following 21-d chronic sediment bioassay. The results showed that low concentration (5 μg g-1) of Cd had no toxicity to B. aeroginosa, while relatively high concentration (25 μg g-1) displayed obvious toxicity, and that SDS could significantly enhance the toxicity of Cd to B. aeroginosa. TiO2-NP with nontoxic concentration could enhance the toxicity of Cd with low concentration to B. aeroginosa, but had no effects on the toxicity of Cd with high concentration. SDS could significantly enhance the toxicity of TiO2-NP and Cd combined contamination to B. aeroginosa in a SDS-concentration-dependent manner. When assessing the potential environmental risk of ENP, we should not only focus on the toxicity of ENP itself, or the interaction between ENP and coexisting contaminants, but also should consider the potential impacts of surfactants and other environmental factors.     

Chemical indicators of anthropogenic impacts in sediments of the pristine karst lakes

The anthropogenic impact on the pristine karst lakes was investigated using combination of specific parameters, including multielemental analysis of major inorganic constituents (Al, K, Fe) and trace metals (Li, Ag, Cd, Sn, Pb, Bi, Cr, Co, Ni, Cu, Zn and Sb), polycyclic aromatic hydrocarbons (PAHs) and anionic surfactants of linear alkylbenzene sulfonate (LAS) type. The study was performed in the Plitvice Lakes National Park, situated in a sparsely populated area of the northwestern Dinarides, central Croatia. Dated cores of recent sediments from the two biggest lakes, Lake Prosce and Lake Kozjak, were analysed for the selected contaminants using highly specific methods, involving inductively coupled plasma mass spectrometry (ICP/MS), gas chromatography/mass spectrometry (GC/MS) and liquid chromatography/tandem mass spectrometry (LC/MS/MS). The concentration of inorganic constituents reflected primarily the geological background of the area as well as geomorphological and geochemical characteristics of the Plitvice Lakes. Due to the higher terrigenous input, the concentration of all elements was significantly higher in the Lake Prosce. The concentration of toxic metals was relatively low in both lakes, except for Cd (>1 mg kg⁻¹) and Pb (up to 40 mg kg⁻¹). The vertical profiles of these metals suggested that elevated concentrations of Cd were of natural origin, derived from the erosion of the Jurassic dolomite bedrock, while Pb was predominately of recent anthropogenic origin. A similar distribution pattern, suggesting the same prevailing mechanism of input, was observed for pyrolytic PAHs. The characteristic diagnostic PAH ratios revealed that higher PAHs prevailingly originated from the combustion of biomass and fossil fuels. LAS, which represent highly specific indicators of untreated wastewaters, were found in rather high concentrations in the recent sediment layers (up to 4.7 mg kg⁻¹), suggesting that contaminated household and hotel wastewaters reach the Lakes, very probably by leaking through the porous karst rocks.     

Surfactive stabilization of multi-walled carbon nanotube dispersions with dissolved humic substances

Soil humic substances (HS) stabilize carbon nanotube (CNT) dispersions, a mechanism we hypothesized arose from the surfactive nature of HS. Experiments dispersing multi-walled CNT in solutions of dissolved Aldrich humic acid (HA) or water-extractable Catlin soil HS demonstrated enhanced stability at 150 and 300 mg L⁻¹ added Aldrich HA and Catlin HS, respectively, corresponding with decreased CNT mean particle diameter (MPD) and polydispersivity (PD) of 250 nm and 0.3 for Aldrich HA and 450 nm and 0.35 for Catlin HS. Analogous trends in MPD and PD were observed with addition of the surfactants Brij 35, Triton X-405, and SDS, corresponding to surfactant sorption maximum. NEXAFS characterization showed that Aldrich HA contained highly surfactive domains while Catlin soil possessed a mostly carbohydrate-based structure. This work demonstrates that the chemical structure of humic materials in natural waters is directly linked to their surfactive ability to disperse CNT released into the environment.