Impact of Microplastics on Oil Dispersion Efficiency in the Marine Environment

Oil spill and microplastics (MPs) pollution has raised global concerns, due to the negative impacts on ocean sustainability. Chemical dispersants were widely adopted as oil-spill-treating agents. When MPs exist during oil dispersion, MP/oil-dispersant agglomerates (MODAs) are observed. This study explored how MPs affect oil-dispersion efficiency in oceans. Results showed that, under dispersant-to-oil volumetric ratio (DOR) 1:10 and mixing energy of 200 rpm, the addition of MPs increased the oil droplet size, total oil volume concentration, and oil-dispersion efficiency. Under DOR 1:25 and mixing energy of 120 rpm, the addition of MPs increased the oil droplet size but resulted in a decrease of total oil volume concentration and dispersion efficiency. Compared with the oil volume concentration, the oil droplet size may no longer be an efficient parameter for evaluating oil-dispersion efficiency with the existence of MODAs. A machine learning (ML)-based XGBRegressor model was further constructed to predict how MPs affected oil volume concentration and oil-dispersion efficiency in oceans. The research outputs would facilitate decision-making during oil-spill responses and build a foundation for the risk assessment of oil and MP co-contaminants that is essential for maintaining ocean sustainability.

Aggregation and Degradation of Dispersants and Oil by Microbial Exopolymers (ADDOMEx): Toward a Synthesis of Processes and Pathways of Marine Oil Snow Formation in Determining the Fate of Hydrocarbons

Microbes (bacteria, phytoplankton) in the ocean are responsible for the copious production of exopolymeric substances (EPS) that include transparent exopolymeric particles. These materials act as a matrix to form marine snow. After the Deepwater Horizon oil spill, marine oil snow (MOS) formed in massive quantities and influenced the fate and transport of oil in the ocean. The processes and pathways of MOS formation require further elucidation to be better understood, in particular we need to better understand how dispersants affect aggregation and degradation of oil. Toward that end, recent work has characterized EPS as a function of microbial community and environmental conditions. We present a conceptual model that incorporates recent findings in our understanding of the driving forces of MOS sedimentation and flocculent accumulation (MOSSFA) including factors that influence the scavenging of oil into MOS and the routes that promote decomposition of the oil post MOS formation. In particular, the model incorporates advances in our understanding of processes that control interactions between oil, dispersant, and EPS in producing either MOS that can sink or dispersed gels promoting microbial degradation of oil compounds. A critical element is the role of protein to carbohydrate ratios (P/C ratios) of EPS in the aggregation process of colloid and particle formation. The P/C ratio of EPS provides a chemical basis for the “stickiness” factor that is used in analytical or numerical simulations of the aggregation process. This factor also provides a relative measure for the strength of attachment of EPS to particle surfaces. Results from recent laboratory experiments demonstrate (i) the rapid formation of microbial assemblages, including their EPS, on oil droplets that is enhanced in the presence of Corexit-dispersed oil, and (ii) the subsequent rapid oil oxidation and microbial degradation in water. These findings, combined with the conceptual model, further improve our understanding of the fate of the sinking MOS (e.g., subsequent sedimentation and preservation/degradation) and expand our ability to predict the behavior and transport of spilled oil in the ocean, and the potential effects of Corexit application, specifically with respect to MOS processes (i.e., formation, fate, and half-lives) and Marine Oil Snow Sedimentation and Flocculent Accumulation.

Biodegradation of crude oil by immobilized Exiguobacterium sp. AO-11 and shelf life evaluation

Exiguobacterium sp. AO-11 was immobilized on bio-cord at 109 CFU g−1 carrier for the removal of crude oil from marine environments. To prepare a ready-to-use bioremediation product, the shelf life of the immobilized cells was calculated. Approximately 90% of 0.25% (v/v) crude oil removal was achieved within 9 days when the starved state of immobilized cells was used. The oil removal activity of the immobilized cells was maintained in the presence of oil dispersant (89%) and at pH values of 7–9. Meanwhile, pH, oil concentration and salinity affected the oil removal efficacy. The immobilized cells could be reused for at least 5 cycles. The Arrhenius equation describing the relationship between the rate of reaction and temperature was validated as a useful model of the kinetics of retention of activity by an immobilized biocatalyst. It was estimated that the immobilized cells could be stored in a non-vacuum bag containing phosphate buffer (pH 7.0) at 30 °C for 39 days to retain the cells at 107 CFU g−1 carrier and more than 50% degradation activity. These results indicated the potential of using bio-cord-immobilized crude oil-degrading Exiguobacterium sp. AO-11 as a bioremediation product in a marine environment.

Experimental investigation of effect of biodiesel fatty acid methyl ester on performance of engine oil dispersant additive

In the present work, blends of methyl oleate (MO), polyisobutylene-bis-succinimide (PIBSI) and a mineral lubricant base oil were oxidized and some of their physicochemical properties were evaluated to understand the effects of biodiesel fatty acid methyl esters on the performance of the engine oil dispersant additive PIBSI. The oxidation experimentations of blends were conducted under elevated temperatures. Thereafter, the viscosity and acidity of fresh and oxidized blends were determined. The dispersancy, thermal stability and chemical species of oxidized samples were tested and analyzed by the blotter spot method, a TGA, and a GC/MS, respectively. Results showed that the viscosity and acidity of blends containing MO increased significantly after oxidation. The dispersing ability of PIBSI was markedly impaired by only a small amount of MO in a blend. In addition, the thermal characteristics of blends were altered by MO. Many varieties of oxygenated chemicals in the oxidized blend containing MO were detected. The negative impact of MO on performances of PIBSI was attributed to the accelerated oxidation caused by MO, and to the chemical interactions between MO and PIBSI. The present results demonstrated that PIBSI was incompatible with MO.