The well-known toxicity of conventional chemical oil spill dispersants demands the development of alternative and environmentally friendly dispersant formulations. Therefore, in the present study we have developed a pair of less toxic and green dispersants by combining lactonic sophorolipid (LS) biosurfactant individually with choline myristate and choline oleate ionic liquid surfactants. The aggregation behavior of resulted surfactant blends and their dispersion effectiveness was investigated using the baffled flask test. The introduction of long hydrophobic alkyl chain with unsaturation (attached to choline cation) provided synergistic interactions between the binary surfactant mixtures. The maximum dispersion effectiveness was found to be 78.23% for 80:20 (w/w) lactonic sophorolipid-choline myristate blends, and 81.15% for 70:30 (w/w) lactonic sophorolipid-choline oleate blends at the dispersant-to-oil ratio of 1:25 (v/v). The high dispersion effectiveness of lactonic sophorolipid-choline oleate between two developed blends is attributed to the stronger synergistic interactions between surfactants and slower desorption rate of blend from oil-water interface. The distribution of dispersed oil droplets at several DOR were evaluated and it was observed that oil droplets become smaller with increasing DOR. In addition, the acute toxicity analysis of developed formulations against zebra fish (Danio rerio) confirmed their non-toxic behavior with LC₅₀ values higher than 400 ppm after 96 h. Overall, the proposed new blends/formulations could effectively substitute the toxic and unsafe chemical dispersants.

The dispersion effectiveness of dispersants containing Tween 80, Span 80, and dioctyl sodium sulfosuccinate (DOSS) was characterized using a modified Swirling Flask test, and was correlated with both initial and dynamic interfacial tension produced by those dispersants at an oil–water interface. Compositional trends in effectiveness were shown to be governed by: (1) initial oil–water interfacial tension observed upon dispersant–oil–saltwater contact; (2) rate of increase (or decrease) from the initial interfacial tension as DOSS was rapidly lost to the aqueous phase; and (3) gradually slowing kinetics of dispersant adsorption to the oil–water interface as Span 80 concentration was increased, which ultimately diminished dispersion effectiveness considerably even as dynamic interfacial tension remained <10−3mN/m. It is proposed that this third phenomenon results not only from the hydrophobicity of Span 80, but also from the dependence of mixed Tween–Span–DOSS reverse micelles’ stability in crude oil on dispersant composition.

Effective emulsification plays an important role in the treatment of marine oil spills. The negative effects of chemical surfactants have necessitated a search for alternative dispersant that are sustainable and environmentally-friendly. To identify alternate dispersants, oil-in-seawater emulsions stabilized by hydrocarbon-degrading bacteria were investigated. After individual immobilization and surface-modification, the hydrocarbon-degrading bacteria, Bacillus cereus S-1, was found to produce a stable oil-in-seawater Pickering emulsion, which was similar to particle emulsifiers. The individual immobilization and surface-modification process improved the surface hydrophobicity and wettability of the bacterial cells, which was responsible for their effective adsorption at the oil–water interface. Through effective emulsification, the biodegradation of oil was remarkably facilitated by these treated bacteria, because of the increased interfacial area. By combining the emulsification and biodegradation, the results of this reported work demonstrated a novel approach for developing environmentally-friendly bioremediation technology in the field of oil treatment.

A sorbent for oil spill cleanup was prepared through a novel strategy by treating polyurethane sponges with silica sol and gasoline successively. The oil sorption capacity, oil/water selectivity, reusability and sorption mechanism of prepared sorbent were studied. The results showed that the prepared sorbent exhibited high sorption capacity and excellent oil/water selectivity. 1g of the prepared sorbent could adsorb more than 100g of motor oil, while it only picks up less than 0.1g of water from an oil–water interface under both static and dynamic conditions. More than 70% of the sorption capacity remained after 15 successive sorption–squeezing cycles, which suggests an extraordinary high reusability. The prepared sorbent is a better alternative of the commercial polypropylene sorbent which are being used nowadays.

Effectiveness of oil spill dispersants containing lecithin/Tween 80 (L/T) blends in ethanol was measured as a function of L:T ratio, surfactant:solvent ratio, solvent composition, and dispersant:oil ratio (DOR) using baffled flask dispersion effectiveness tests. Optimal L:T ratios are between 60:40 and 80:20 (w/w); at higher L:T ratios, effectiveness is limited by high interfacial tension, while at lower L:T ratios, insufficient lecithin is present to form a well-packed monolayer at an oil–water interface. These optimal L:T ratios retain high effectiveness at low DOR: 80:20 (w/w) L:T dispersant is 89% effective at 1:25 DOR (v/v) and 77% effective at 1:100 DOR (v/v). Increasing surfactant:solvent ratio increases dispersant effectiveness even when DOR is proportionally reduced to keep total surfactant concentration dosed into the oil constant. Replacing some of the ethanol with octane or octanol also increases dispersant effectiveness, suggesting that ethanol's hydrophilicity lowers dispersant–oil miscibility, and that more hydrophobic solvents would increase effectiveness.

The hydrolysis of 4-Nitrophenylphosphate (NPP) in the presence of Ferrous and Ferric ions in Oil in water microemulsion media was investigated. The reaction was monitored by measuring the absorbance of the nitrophenolate ion produced in the reaction aliquots with time. The order of effectiveness of the microemulsion system towards the hydrolysis of NPP was found to be cationic > anionic> aqueous in the presence of Ferrous, Ferric and Turnbull's blue at neutral pH. The result of the present investigation enriches our understanding of the possible roles polymetallic ions play in hydrolysis reactions. The reactions mimic the roles of purple acid phosphatases in the hydrolysis of phosphate esters. The application of the above systems for environmental decontamination of organophosphates is also envisoned.

Although the potential corrosive microbial communities of the refined oil pipelines can cause pipeline failure which directly threatens on soil and water environment, few studies have been published in this field. Therefore, the long-distance on-site internal corrosion detection and high-throughput sequencing techniques were employed in this study to investigate the distribution shifts of the corrosive microbial communities on the inner wall of a refined oil pipeline and its impact on the internal corrosion. The microorganisms colonizing on the inner wall of the pipeline showed significant distribution differences between the axial direction of the relative elevation and radial direction of the cross-section. On the inner wall, the high diversity and the abundance of the corrosive microbial communities induced serious microbiologically influenced corrosion (MIC), while the chemical corrosion and the synergy of the corrosive microbial communities accelerated the internal corrosion of the refined oil pipeline. A corrosion zone model has been proposed, which divides the pipeline cross-section into the sediment, the water–oil interface, the gas-oil interface, and the oil fully immersed zones. Therefore, the relationships between the environment, corrosion degree, and distribution characteristics of the corrosive microbial communities in the pipeline were analyzed. This research exhibited the importance of the distribution characteristics of the corrosive microorganisms on the inner wall of the refined oil pipelines. Its internal corrosion behavior was accurately explored, while providing a basis for controlling the corrosive microbial communities.

Oil slicks occurring during petroleum transportation or production are major sources of surface water pollution, and spread over large areas. Herders are interfacially active species that reduce the spread of oil slicks on water surfaces, facilitating slick recovery. Here, octanol (a readily biodegradable fatty alcohol) is used as a herder to facilitate the recovery of diluted bitumen and conventional crude oil spilled onto the surface of fresh and synthetic marine water. While octanol promptly decreases the area of simulated oil slicks in Petri dishes, over time it partitions into the oil phase and lowers its interfacial tension. As a result, low-viscosity hydrocarbons (toluene and conventional crude oil) re-spread. This study uses charcoal to suppress re-spreading and facilitate the mechanical recovery of oil slicks. Charcoal partitions into the crude oil phase and does not stabilize crude oil in water emulsions upon mixing, as demonstrated using optical microscopy. This ensures that charcoal particles are not lost to the water phase and do not promote hydrocarbon dispersion. Charcoal prevents herded slicks from re-expanding by rigidifying the crude oil–water interface (demonstrated using a Langmuir trough) and potentially due to the affinity of crude oil for charcoal. Therefore, charcoal facilitates the physical removal of crude oil slicks after herding, as qualitatively assessed by retrieving them from Petri dishes with the aid of a spatula. While charcoal also facilitates the recovery of herded low-viscosity conventional crude oil, it has only a marginal effect on the recovery of herded bitumen, which has high viscosity.

In the context of an oil spill accident and the following oil spill response, much attention is given to the use of dispersants. Dispersants are used to disperse an oil slick from the sea surface into the water column generating a cloud of dispersed oil droplets. The main consequence is an increasing of the sea water–oil interface which induces an increase of the oil biodegradation. Hence, the use of dispersants can be effective in preventing oiling of sensitive coastal environments. Also, in case of an oil blowout from the seabed, subsea injection of dispersants may offer some benefits compared to containment and recovery of the oil or in situ burning operation at the sea surface. However, biological effects of dispersed oil are poorly understood for deep-sea species. Most effects studies on dispersed oil and also other oil-related compounds have been focusing on more shallow water species. This is the first approach to assess the sensitivity of a macro-benthic deep-sea organism to dispersed oil. This paper describes a toxicity test which was performed on the macro-benthic deep-sea amphipod (Eurythenes gryllus) to determine the concentration causing lethality to 50 % of test individuals (LC₅₀) after an exposure to dispersed Brut Arabian Light (BAL) oil. The LC₅₀ (24 h) was 101 and 24 mg L⁻¹ after 72 h and 12 mg L⁻¹ at 96 h. Based on EPA scale of toxicity categories to aquatic organisms, an LC₅₀ (96 h) of 12 mg L⁻¹ indicates that the dispersed oil was slightly to moderately toxic to E. gryllus. As an attempt to compare our results to others, a literature study was performed. Due to limited amount of data available for dispersed oil and amphipods, information on other crustacean species and other oil-related compounds was also collected. Only one study on dispersed oil and amphipods was found, the LC₅₀ value in this study was similar to the LC₅₀ value of E. gryllus in our study. Since toxicity data are important input to risk assessment and net environmental benefit analyses, and since such data are generally lacking on deep-sea species, the data set produced in this study is of interest to the industry, stakeholders, environmental management, and ecotoxicologists. However, studies including more deep-sea species covering different functional groups are needed to evaluate the sensitivity of the deep-sea compartments to dispersed oil relative to other environmental compartments.

Polypropylene (PP) and poly(butylmethacrylate-co-hydroxyethylmethacrylate) (PBMA-co-HEMA) nonwoven materials as oil absorbents have been fabricated for the first time via melt blown method. As-prepared nonwovens were investigated in terms of mass per unit area, density, air permeability, contact angle, and morphology observations for fiber diameter distribution and single fiber surface by a field emission scanning electron microscope. The nonwovens are demonstrated as fast and efficient absorbents for various kinds of oils with oil absorbency up to seven to ten times their own weight. The nonwovens show excellent water repulsion but superoleophilic properties. The measured contact angles for water and toluene are more than 127° and ca. 0°, respectively. The addition of PBMA-co-HEMA makes the nonwoven surface more hydrophobic while conserving superoleophilicity. Compared with PP nonwoven, broad diameter distribution of the blend nonwoven is attributed to poor melt fluidity of PBMA-co-HEMA. In terms of single fiber, coarse surface and the presence of point-like convexities lead to the fibers being more readily wetted by oil. More interesting, oil–water separation and oil recovery can be easily carried out by filter and absorption–desorption process, the recovered materials contained hardly any oil droplet and could be reused for next cycles.