Conventional in-situ light non-aqueous phase liquid (LNAPL) remediation techniques often face challenges of high costs and limited efficiency, leaving residual hydrocarbons trapped in soil pores. This study investigates the efficiency of an alcohol-in-biopolymer emulsion for enhancing diesel-contaminated soil remediation. The emulsion, formulated with xanthan gum biopolymer, sodium dodecyl sulfate surfactant, and the oil-soluble alcohol 1-pentanol, was evaluated through rheological tests, interfacial tension measurements, and onedimensional sand-column experiments under direct injection and post-waterflooding scenarios. The emulsion exhibited non-Newtonian shear-thinning behavior with high viscosity, ensuring stable propagation and efficient delivery of 1-pentanol to mobilize trapped diesel ganglia. It achieved 100 % diesel recovery within 1.2 PV during direct injection, outperforming shear-thinning polymer-only and polymer-surfactant solutions, which achieved recovery factors of 83.4-92.9 %. Post-waterflooding experiments also demonstrated 100 % diesel recovery within 1.3 PV, regardless of initial diesel saturation. Key mechanisms include reduced interfacial tension, diesel swelling and mobilization induced by 1-pentanol, and uniform displacement facilitated by the emulsion's viscosity. Additionally, the emulsion required lower injection pressures compared to more viscous alternatives, enhancing its injectability into the soil and reducing energy demands. These findings highlight the emulsion's potential to overcome conventional remediation limitations, offering a highly effective and sustainable solution for diesel-contaminated soils and groundwater.

Conventional pump-and-treat technologies have demonstrated limited effectiveness in remediating soils contaminated with light non-aqueous phase liquids (LNAPLs), such as petroleum hydrocarbons. Nonconventional in-situ flushing with shear-thinning fluids, such as polymers, offers a promising alternative. However, even with polymer flushing, residual LNAPL ganglia may remain trapped in porous media, requiring further improvement of the flushing fluid to enhance remediation efficiency. In this study, we present a novel alcohol-in-biopolymer emulsion developed to enhance the recovery of residual diesel oil from porous media. Batch experiments were conducted to evaluate the partitioning behavior of fifteen different alcohols between the aqueous and diesel phases. The results revealed that 1-pentanol preferentially partitions into the diesel phase rather than the aqueous phase, leading to an increase in diesel oil volume via a swelling mechanism. Furthermore, 1-pentanol forms a stable and homogeneous emulsion when combined with an aqueous solution of the biopolymer xanthan gum, and the surfactant sodium dodecyl sulfate. The emulsion demonstrated high stability for over 30 days, ensuring its suitability for prolonged remediation processes. Rheological experiments confirmed the emulsion's shear-thinning behavior, which ensures stable and uniform displacement within porous media. A two-dimensional cell packed with silica sand was used to evaluate the efficiency of the emulsion in removing residual diesel oil. The results demonstrated that the emulsion propagates uniformly throughout the porous media, effectively achieving complete removal of residual diesel within 1.15 pore volumes of injection. Porescale visualizations revealed the swelling and subsequent mobilization of entrapped diesel ganglia induced by the emulsion, further confirming its efficacy. These findings highlight the potential of this novel alcohol-inbiopolymer emulsion to significantly improve diesel oil recovery from contaminated soils.

Since the beginning of their production and use, fossil fuels have affected ecosystems, causing significant damage to their biodiversity. Bacterial bioremediation can provide solutions to this environmental problem. In this study, the new species Isoptericola peretonis sp. nov. 4D.3T has been characterized and compared to other closely related species in terms of hydrocarbon degradation and biosurfactant production by in vitro and in silico analyses. Biosurfactants play an important role in microbial hydrocarbon degradation by emulsifying hydrocarbons and making them accessible to the microbial degradation machinery. The tests performed showed positive results to a greater or lesser degree for all strains. In the synthesis of biosurfactants, all the strains tested showed biosurfactant activity in three complementary assays (CTAB, hemolysis and E24%) and rhamnolipid synthesis genes have been predicted in silico in the majority of Isoptericola strains. Regarding hydrocarbon degradation, all the Isoptericola strains analyzed presented putative genes responsible for the aerobic and anaerobic degradation of aromatic and alkane hydrocarbons. Overall, our results highlight the metabolic diversity and the biochemical robustness of the Isoptericola genus which is proposed to be of interest in the field of hydrocarbon bioremediation.

Biosurfactants are one of the recently investigated biomolecules that have enormous applications in many fields including agriculture. As there is a need to develop less toxic, and environmentally friendly surfactants, therefore, amino acid-based biosurfactants that are produced from renewable raw materials are of great demand nowadays and can be used as an alternative to conventional chemical surfactants. The negative effects of chemical surfactants present in agrochemicals and modern detergents can damage human health and the environment, thus there is a crucial requirement to explore innovative, well planned, as well as cost-effective natural products for the welfare of humanity. Biodegradable surfactants created through green chemistry, specifically amino acid-based surfactants, are a favourable alternative to avoid these risks. Since amino acids (AAs) are inexhaustible compounds, therefore biosurfactants based on AAs have abundant potential as eco-friendly and environmentally friendly substances. Their higher biodegradation ability, low or even no toxicity, temperature stability, and tolerance to pH fluctuations make these biosurfactants preferable over chemical surfactants. In modern agriculture, most chemical pesticides and fertilizers used are frequently associated with numerous environmental issues. Hence, the development of green molecules as biosurfactants has a promising role in this regard to ensure agricultural sustainability. Biosurfactants can be harnessed for plant pathogen management, plant growth elevation, improving the quality of agricultural soil by soil remediation, degradation of complex hydrocarbons, increasing bioavailability of nutrients for advantageous plant-microbe interactions, and improving plant immunity, hence, they can supersede the grim synthetic surfactants which are presently being used.

Fusarium is genetically diverse and widely distributed geographically. It is one of the genera with more endophytes (which cause no damage to the host plants). This review highlights the capability of Fusarium species to degrade environmental pollutants and describes the biodegradation pathways of some of the emerging environmental contaminants. Some Fusarium species use metabolic strategies enabling them to efficiently mineralize high concentrations of toxic environmental pollutants. These fungi can degrade hydrocarbons, pesticides, herbicides, dyes, pharmaceutical compounds, explosives, plastics, and plastic additives, among other pollutants, and possess high metal biosorption capabilities. According to data from consulted reports, Fusarium strains showed a percentage of biodegradation of a variety of contaminants ranging between 30 % and 100 % for different tested concentrations (from 1 mg to 10 g/L) in a time range between 10 hand 90 d. Enzymes such as esterase, cutinase, laccase, lignin peroxidase, manganese peroxidase, dehydrogenase, lipase, dioxygenase, and phosphoesterase were detected during the pollutant biodegradation process. Fusarium oxysporum, Fusarium solani, and Fusarium culmorum are the most studied species of this genus. Owing to their metabolic versatility, these fungal species and their enzymes represent promising tools for bioremediation applications to mitigate the adverse effects of environmental pollution.

PurposeA of in-service PE gas pipeline in Guocun, Beijing, was found to appear gas leaking at the electrofusion (EF) joint. This study is dedicated to reveal the material cause of EF joint failure to help with a more accurate prediction of service life of PE gas pipe and further normalize the construction of PE gas pipeline.Design/methodology/approachDefect detection was carried out on the leaking EF joint using ultrasonic phased array. The mechanical degradation and structural aging behavior was studied by tension test, FTIR technology, TG test and DSC test. The organic components in the soil surrounding the PE gas pipe failure area were qualitatively identified.FindingsThe results showed that the organic surfactants in the soil environment could accelerate the aging behavior of PE material, leading to a deterioration of mechanical properties and a serious reduction in the ability of the PE pipe and EF joint, especially at the welding defect, to resist external force.Originality/valueA novel study was conducted to investigate the failure cause of the EF joint of in-service PE gas pipe, incorporating the analysis of environmental factors and structural deterioration.

This study investigates the synthesis and characterization of four non-ionic surfactants of different spacer lengths derived from Brassica Juncea (mustard oil) and explore their potential applications. The chemical structures of the surfactants were confirmed by FTIR, 1HNMR spectroscopy and GC. Surface tension values of the surfactants were measured at various temperatures, unveiling temperature-dependent behaviour and associated thermodynamics. The critical micelle concentrations (CMC) of different surfactants were found to be very low (0.064-0.096 mmol/l at 303 K) compared to conventional surfactants. The CMC and the surface tension further decrease significantly with an increase in temperature. Surface-active thermodynamic parameters of the surfactants demonstrate their lower interfacial characteristics and enhanced self-aggregation capability. At CMC, the synthesized surfactants effectively decrease the interfacial tension (IFT) between water and dodecane to a notably low range of 9.5 to 12.1 mN/m, which is further reduced to a range of 3.2 to 6.1 mN/m at optimal salinity. The surfactants also show good emulsification properties, the emulsions formed in the water-dodecane system using the gemini surfactants as emulsifiers were extensively characterized, encompassing phase behaviour and droplet size distribution analysis. These emulsions exhibit favourable viscous properties, with viscosities ranging from 5 to 20 mPa.s at a 5 s-1 shear rate. This study establishes that the synthesized Gemini surfactants are viable candidates for Enhanced Oil Recovery (EOR), showcasing robust stability, interfacial activity, and favourable rheological properties, alongside biodegradability.

Carbonate minerals are ubiquitous in nature, and their dissolution impacts many environmentally relevant processes including preferential flow during geological carbon sequestration, pH buffering with climate-change induced ocean acidification, and organic carbon bioavailability in melting permafrost. In this study, we advance the atomic level understanding of calcite dissolution mechanisms to improve our ability to predict this complex process. We performed high pressure and temperature (1300 psi and 50 degrees C) batch experiments to measure transient dissolution of freshly cleaved calcite under H2O, H+, and H(2)CO(3)(-)dominated conditions, without and with an inhibitory anionic surfactant present. Before and after dissolution experiments, we measured dissolution etch-pit geometries using laser profilometry, and we used density functional theory to investigate relative adsorption energies of competing species that affect dissolution. Our results support the hypothesis that calcite dissolution is controlled by the ability of H2O to preferentially adsorb to surface Ca atoms over competing species, even when dissolution is dominated by H+ or H2CO3. More importantly, we identify for the first time that adsorbed H+ enhances the role of water by weakening surface Ca-O bonds. We also identify that H2CO3 undergoes dissociative adsorption resulting in adsorbed HCO3- and H+. Adsorbed HCO3- that competes with H2O for Ca acute edge sites inhibits dissolution, while adsorbed H+ at the neighboring surface of CO3 enhances dissolution. The net effect of the dissociative adsorption of H2CO3 is enhanced dissolution. These results will impact future efforts to more accurately model the impact of solutes in complex water matrices on carbonate mineral dissolution.

The effect of several prevalent cations (including Na+, K+, Mg2+, Ca2+, Al3+, and Fe3+) on the adsorption of monochlorobenzene (MCB) onto bentonite was investigated at the coexistence of nonionic surfactant Tween 80 (T80) in surfactant-enhanced remediation (SER). They are all favorable for MCB and T80 adsorption, especially Mg2+ and Ca2+. Adsorption of MCB is strongly depended on T80 micelles. When its concentration exceeds the solubility, MCB is easier to bind with T80 micelles and be adsorbed by bentonite. Acidic environment can facilitate MCB and T80 adsorption, but the effect of cations on the adsorption is most significant under alkaline conditions. Adsorption capacity of MCB increases first followed by a slight decrease with increasing cations concentrations. The maximum adsorption rate of MCB determined is about 68.4% in a solution containing Mg2+ in the isothermal adsorption of MCB, while it is only 6.8% in a cation -free solution. Various characterizations showed that cations mainly changed the repulsion between bentonite particles and T80 micelles and the agglomeration and structure of bentonite, thus affecting the adsorption of MCB and T80 micelles. Our research demonstrated the nonnegligible promotion of MCB adsorption on bentonite by cations and acidic environment, which will adversely affect SER efficiency.

Large numbers of contaminants such as polycyclic aromatic hydrocarbons, pesticides and chlorophenols pass through sediments and soil, causing a giant danger to human health and ecosystem. To remediate the soil contaminated with these pollutants, various methods have been proposed including coupled soil washing with Fenton or Sono-Fenton process. In this study, non-ionic surfactants [Tween 85 AND linear alkylbenzene sulfonates (LASs)] were used for the removal of chlorpyrifos (organophosphate pesticide). The optimal conditions for LAS surfactant were found to be a concentration of 2.5 g/L with 20/1.5 ratio (liquid/solid), 360 min operation time and 120 rpm washing speed in room temperature; while 1 g/L Tween 85 concentration was more effective at 20:1 ratio (liquid solid), 360 min operation time and 60 rpm washing speed in room temperature, respectively. The results imply that combining both Tween 85 and LAS can be an effective way to remove large amounts of contaminants from soils quickly without damaging them further or harming humans who might come into contact with it afterward. The results of the experimental study on soil washing and Fenton/Sono-Fenton suggest that these two processes combined can be an effective way to remediate soils contaminated with chlorpyrifos. This combination was shown to provide superior results for both remediation and recovery of surfactants used in the cleaning process.