Surface Tension Reduction Research Articles

Exploring the potential of biosurfactants produced by fungi found in soil contaminated with petrochemical wastes

Biosurfactants are a diverse group of compounds derived from microorganisms, possessing various structures and applications. The current study was seeking to isolate and identify a new biosurfactant-producing fungus from soil contaminated with petrochemical waste. The bioprocess conditions were optimized to maximize biosurfactant production for Aspergillus carneus OQ152507 using a glucose peptone culture medium with a pH of 7.0 and a temperature of 35 °C. The carbon source was glucose (3%), and ammonium sulfate (0.25%) was utilized as the nitrogen source. For Aspergillus niger OQ195934, the optimized conditions involved a starch nitrate culture medium with a pH of 7.0 and a temperature of 30 °C. The carbon source used was sucrose (3.5%), and ammonium sulfate (0.25%) served as the nitrogen source. The phenol-H2SO4 and phosphate tests showed that the biosurfactants that were extracted did contain glycolipid and/or phospholipid molecules. They showed considerable antimicrobial activity against certain microbes. The obtained biosurfactants increased the solubility of tested polyaromatic hydrocarbons, including fluoranthene, pyrene, anthracene, and fluorine, and successfully removed the lubricating oil from contaminated soil and aqueous media surface tension reduction. Based on the obtained results, A. carneus and A. niger biosurfactants could be potential candidates for environmental oil remediation processes.

Behavior of Microbubbles on Air-Aqueous Interfaces.

Animal-derived lung surfactants have saved millions of lives of preterm neonates with neonatal Respiratory Distress Syndrome (nRDS). However, a replacement for animal-derived lung surfactants has been sought for decades due to its high manufacturing cost, inaccessibility in low-income countries, and failure to show efficacy when nebulized. This study investigated the use of lipid-coated microbubbles as potential replacements for exogenous lung surfactants. Three different formulations of microbubbles (DPPC with/out PEG40-stearate and poractant alfa) were prepared, and their equilibrium and dynamic surface tensions were tested on a clean air-saline interface or a simulated air-lung fluid interface using a Langmuir-Blodgett trough. In dynamic surface measurements, microbubbles reduced the minimum surface tension compared with the equivalent composition lipid suspension: e.g., PEG-free microbubbles had a minimum surface tension of 4.3 mN/m while the corresponding lipid suspension and poractant alfa had 20.4 (p ≤ 0.0001) and 21.8 mN/m (p ≤ 0.0001), respectively. Two potential mechanisms for the reduction of surface tension were found: Fragmentation of the foams created by microbubble coalescence; and clustering of microbubbles in the aqueous subphase disrupting the interfacial phospholipid monolayer. The predominant mechanism appears to depend on the formulation and/or the environment. The use of microbubbles as a replacement for exogenous lung surfactant products thus shows promise and further work is needed to evaluate efficacy in vivo.

Structure, orientation, and dynamics of per- and polyfluoroalkyl substance (PFAS) surfactants at the air-water interface: Molecular-level insights

HypothesisUnderstanding the intricate molecular-level details of toxic per- and polyfluoroalkyl substances (PFAS) partitioning to the air–water interface holds paramount importance in evaluating their fate and transport, as well as for finding safer alternatives for various applications, including aqueous film forming foams. The behavior of these substances at interfaces strongly depends on molecular architecture, chemistry, and concentration, which define molecular packing, self-assembly, interfacial diffusion, and the surface tension. SimulationsModeling of three PFAS surfactants, namely, longer-tail (perfluorooctanoate (PFOA)) and shorter-tail (perfluorobutanoate (PFBA) and 2,3,3,3-tetrafluoro-2-(heptafluoropropoxy) propanoate (GenX)) has been conducted using atomistic molecular dynamics simulations. A systematic comparison between these representative PFAS of different sizes and structure reveals factors influencing their association behavior, mechanism of surface tension reduction, and interfacial mobility as a function of surface coverage. FindingsShorter-chain PFAS surfactants (GenX or PFBA) require lower surface coverage compared to longer chain (PFOA) PFAS to achieve the same decrease in surface tension. However, a higher concentration of GenX and PFBA is necessary in the bulk aqueous solution to achieve the same surface coverage as PFOA, due to their higher solubility in water. The PFAS molecular orientation and mobility at the interface are found to be vastly influenced by the length and architecture of the hydrophobic fluorocarbon tail. A significant ordering of the water dipole moment near the anionic headgroup is apparent at high surface concentration. A direct correlation is established between the PFAS interfacial properties and PFAS-PFAS, PFAS-counterion, and PFAS-water interactions.

The surfactant protein B polymorphisms (rs7316 and rs1130866) and their correlation with disease progression of COVID-19

BackgroundIt is critical to examine the pathogenic pathways in coronavirus disease 2019 (COVID-19) that resulted in the development of severe lung injury. Surfactant protein B (SFTPB) is a vital component for sustaining life and serves pivotal functions in the host’s defensive mechanisms and alveolar surface tension reduction. Our study aimed to determine the effect of SFTPB rs7316 and rs1130866 variants on the course of disease in COVID-19 patients. MethodsThe study cohort comprised 3,184 individuals diagnosed with COVID-19. We employed the RFLP approach to determine the variations of the SFTPB genes. ResultsSFTPB rs7316 did not exhibit a statistically significant correlation with COVID-19 mortality across different inheritance models. But, after making more changes for SARS-CoV-2 variants, it was found that there was a strong link between the TT and TC genotypes of SFTPB rs7316 and death rates, especially for the Delta variant. Furthermore, our study’s findings indicate a significant association between the SFTPB rs1130866 G allele and an elevated risk of mortality in COVID-19 across all variants of SARS-CoV-2. ConclusionsThe use of the SFTPB rs1130866 marker has the potential to facilitate the prediction of COVID-19 severity. On the other hand, for SFTPB rs7316, this kind of prediction seems to depend on the particular SARS-CoV-2 variants.

Modelling and impact of tensiometer plate geometry and sample volume on biosurfactant surface activity assessment

Biosurfactants are molecules with hydrophilic and hydrophobic moieties with the capacity to reduce the surface tension of water. Given the limited quantity of biosurfactant extracts in laboratories, it is recommended to use equipment that requires minimal sample quantities for detecting the presence of biosurfactants. In this work, commercial glycolipids biosurfactants (rhamnolipids or sophorolipids) were diluted in water and subjected to different analyses to obtain their minimum surface tension (ST) reduction and their critical micellar concentration (CMC). The independent variables of the study were: the geometry of platinum plate (rectangular or cylindrical), the sample volume (2, 4 and 20 mL) and the container material consisting of either glass or polytetrafluoroethylene (PTFE). The variation of ST with biosurfactant concentration was studied based on the isotherm model proposed by Li & Lu. It was observed that the profile of ST values did not vary so much using the different independent variables described, observing that platinum rectangular plate can be used for volumes of 4 mL biosurfactants instead of cylindrical plate usually recommended for volumes lower than 20 mL, the container material was also not significant based on the Pearson and Spearman statistical treatment. Moreover, well-fitting regression model results were obtained for a non-commercial biosurfactant extract obtained from a residual stream of the dairy industry, predicting values close to the observed data.

Use of corncob and pineapple peel as associated substrates for biosurfactant production.

Biosurfactants are amphiphilic biomolecules with promising tensoative and emulsifying properties that find application in the most varied industrial sectors: environment, food, agriculture, petroleum, cosmetics, and hygiene. In the current work, a 23 full-factorial design was performed to evaluate the effect and interactions of pineapple peel and corncob as substrates for biosurfactant production by Bacillus subtilis LMA-ICF-PC 001. In a previous stage, an alkaline pretreatment was applied to corncob samples to extract the xylose-rich hydrolysate. The results indicated that pineapple peel extract and xylose-rich hydrolysate acted as partial glucose substitutes, minimizing production costs with exogenous substrates. Biosurfactant I (obtained at 8.11% pineapple peel extract, 8.11% xylose-rich hydrolysate from corncob, and 2.8109g/L glucose) exhibited a significant surface tension reduction (52.37%) and a promising bioremediation potential (87.36%). On the other hand, biosurfactant III (obtained at 8.11% pineapple peel extract, 31.89% xylose-rich hydrolysate from corncob, and 2.8109g/L glucose) exhibited the maximum emulsification index in engine oil (69.60%), the lowest critical micellar concentration (68mg/L), and the highest biosurfactant production (5.59g/L). These findings demonstrated that using pineapple peel extract and xylose-rich hydrolysate from corncob effectively supports biosurfactant synthesis by B. subtilis, reinforcing how agro-industrial wastes can substitute traditional carbon sources, contributing to cost reduction and environmental sustainability.

Nanoemulgel: A Comprehensive Review of Formulation Strategies, Characterization, Patents and Applications

<p>Background: Delivering hydrophobic or poorly soluble drugs has become increasingly challenging, with issues like stability and bioavailability complicating the process. Among various strategies devised to address these problems, nanoemulgels have proven effective. Nanoemulgels combine a gel base and an emulsion at the nanoscale, making them excellent for drug delivery. The nanoemulsion component protects the active ingredient from degradative reactions like hydrolysis and enzymatic degradation. Meanwhile, the gel base enhances the emulsion's thermodynamic stability by increasing the viscosity of the aqueous phase and reducing surface and interfacial tension. </p><p> Objective: The primary objective of this review was to explore nanoemulgels as a drug delivery system in the pharmaceutical industry. It delves into the advantages and applications of nanoemulgels in various medical fields, compares them with conventional emulgel, and examines formulation strategies, preparation methods, patent trends, future prospects, and evaluation methods in detail. </p><p> Method: An exhaustive literature survey was conducted keeping in view the various aspects of nanoemulgel. Information from various resources, such as books, review articles, scientific reports, research articles, and patents, were searched, read, analyzed, and summarized. </p><p> Conclusion: This review article thoroughly examines nanoemulgels, discussing their formulation strategies, characterization techniques, and applications in various fields. It highlights their benefits, such as enhanced drug solubility, controlled release, improved stability, and targeted delivery. The article also covers patents related to nanoemulgel technology and explores its future prospects, emphasizing potential applications in pharmaceuticals, cosmetics, dermatology, and other industries.</p>

A Study on Two-Phase Flow with High Viscosity and Low Surface Tension Liquid in a 40-Degree Inclined Mini Channel

There are numerous applications of two-phase flow in mini pipes, including electronics cooling systems, microreactors in the chemical industry, and material development and manufacturing. This application requires a thorough understanding and is supported by complete data and information. However, the data and information are currently limited. Experimental research has been carried out on flow patterns, void fractions, and two-phase flow pressure gradients in small pipes. This study aims to obtain primary data on the subject. Dry air and a mixture of 67% distilled water, 30% glycerin, and 3% butanol represent the gas and liquid phases, respectively. The addition of butanol and glycerin each aims to reduce surface tension and improve the viscosity of the liquid phase, respectively. The density, kinematic viscosity, and surface tension of the liquid were 1,080.4 kg/m3, 2,368 mm2/s, and 38.6 mN/m, respectively. The test section was a 1.6 mm diameter glass pipe equipped with an optical correction box. The gas superficial velocity (JG) ranged from 0.025 to 66.3 m/s, whereas liquid superficial velocity (JL) varied from 0.033 to 4.935 m/s. The experiment was conducted under adiabatic conditions. Plug, slug-annular, annular, disperse bubbly, and churn flow patterns emerged, while separated flow was not discovered. For plug, slug-annular, and dispersed bubbly flows, the increase of JG proportionally affected the void fraction. However, for churn and annular flows, no particular relationship existed between JG and void fraction due to the slip between the real velocities of the gas and the liquid. The pressure gradient rose as JG and JL increased.

Promoting sustainability: Micellization and surface dynamics of recycled monoethanolamine surfactants

The purpose of this work is to explore the micellization and surface characteristics of recycled monoethanolamine (MEA) surfactants, designated as MK-1, MK-2, and MK-3, and to assess their potential in promoting sustainability. Traditional surfactants contribute to environmental pollution due to their non-renewable sources and persistence in nature. This study addresses the knowledge gap in sustainable surfactant development by investigating the efficacy of recycled MEA surfactants. Its novelty lies in its innovative recycling process, which not only reduces waste, but also produces surfactants with superior properties. This study also investigates the distillation-based separation of MEA from degraded compounds, showcasing its potential in waste management. It was found that a maximum MEA separation of 17 % was achieved with a resulting purity of 83 %. Optimal conditions, including the use of catalysts and a temperature of 393K, led to enhanced oleic acid conversion. Similarly, reactions conducted with catalysts at 433K for 3 h demonstrated favorable outcomes. Surfactant MK-1 exhibited superior foam and emulsifying abilities, generating a foam height of 60 cm with only 8 cm lost after 10 min. Regarding emulsifying properties, the sunflower oil/water system with a 0.1% MK-1 solution exhibited delayed water separation from the emulsion. MK-3 displayed the highest pC20 value at 2.91. Among the MEA-based surfactants, MK-1 reduced surface tension to 33.1 mN/m. The maximum surface excess concentration (Γmax) for all surfactants was consistent. This demonstrates that recycled MEA surfactants exhibited favorable micellization properties, with a critical micelle concentration (CMC) comparable to that of virgin counterparts. Over ten cycles of use and regeneration, the performance of recycled MEA surfactants remained stable. Surface tension measurements indicated improved interfacial activity, while emulsification capacity tests revealed an enhanced performance in forming stable emulsions. This implies the potential of recycled MEA surfactants to produce high-performance surfactants, thereby promoting sustainability in the chemical industry.

Yarrowia lipolytica growth, lipids, and protease production in medium with higher alkanes and alkenes

Two strains of Yarrowia lipolytica (CBS 2075 and DSM 8218) were first studied in bioreactor batch cultures, under different controlled dissolved oxygen concentrations (DOC), to assess their ability to assimilate aliphatic hydrocarbons (HC) as a carbon source in a mixture containing 2 g·L−1 of each alkane (dodecane and hexadecane), and 2 g·L−1 hexadecene. Both strains grew in the HC mixture without a lag phase, and for both strains, 30 % DOC was sufficient to reach the maximum values of biomass and lipids. To enhance lipid-rich biomass and enzyme production, a pulse fed-batch strategy was tested, for the first time, with the addition of one or three pulses of concentrated HC medium. The addition of three pulses of the HC mixture (total of 24 g·L−1 HC) did not hinder cell proliferation, and high protease (> 3000 U·L−1) and lipids concentrations of 3.4 g·L−1 and 4.3 g·L−1 were achieved in Y. lipolytica CBS 2075 and DSM 8218 cultures, respectively. Lipids from the CBS 2075 strain are rich in C16:0 and C18:1, resembling the composition of palm oil, considered suitable for the biodiesel industry. Lipids from the DSM 8218 strain were predominantly composed of C16:0 and C16:1, the latter being a valuable monounsaturated fatty acid used in the pharmaceutical industry. Y. lipolytica cells exhibited high intrinsic surface hydrophobicity (> 69 %), which increased in the presence of HC. A reduction in surface tension was observed in both Y. lipolytica cultures, suggesting the production of extracellular biosurfactants, even at low amounts. This study marks a significant advancement in the valorization of HC for producing high-value products by exploring the hydrophobic compounds metabolism of Y. lipolytica.

The effect of temperature and breathing pattern on the surface activity of ground squirrel pulmonary surfactant.

This study investigates how hibernation affects the surface activity of pulmonary surfactant with respect to temperature and breathing pattern. Surfactant was isolated from a hibernating species, the 13-lined ground squirrel, and a homeotherm, the rabbit, and analysed for biophysical properties on a constrained sessile drop surfactometer. The results showed that surfactant from ground squirrels reduced surface tension better at low temperatures, including when mimicking episodic breathing, as compared with rabbit surfactant. In addition, low temperature adaptation was also observed using only the hydrophobic components of surfactant from ground squirrels. Overall, the data support the conclusion that ground squirrel surfactant has adapted to maintain surface activity during low temperature episodic breathing patterns, and that temperature adaptation is maintained with the hydrophobic components of the surfactant.

The Role of Pulmonary Collectins, Surfactant Protein A (SP-A) and Surfactant Protein D (SP-D) in Cancer.

Surfactant proteins A and D (SP-A and SP-D) belong to the collectin subfamily of C-type oligomeric lectins. They are pattern-recognition molecules (PRMs), able to recognise pathogen- or danger-associated molecular patterns (PAMPs, DAMPs) in the presence of Ca2+ cations. That property enables opsonisation or agglutination of non-self or altered/abnormal self cells and contributes to their clearance. Like other collectins, SP-A and SP-D are characterised by the presence of four distinct domains: a cysteine-rich domain (at the N-terminus), a collagen-like region, an α-helical neck domain and a globular carbohydrate-recognition domain (CRD) (at the C-terminus). Pulmonary surfactant is a lipoprotein complex, preventing alveolar collapse by reducing surface tension at the air-liquid interface. SP-A and SP-D, produced by type II alveolar epithelial cells and Clara cells, are not only pattern-recognition molecules but also contribute to the surfactant structure and homeostasis. Moreover, they are expressed in a variety of extrapulmonary sites where they are involved in local immunity. The term "cancer" includes a variety of diseases: tumours start from uncontrolled growth of abnormal cells in any tissue which may further spread to other sites of the body. Many cancers are incurable, difficult to diagnose and often fatal. This short review summarises anti- and pro-tumorigenic associations of SP-A and SP-D as well as perspectives of their usefulness in cancer diagnosis and therapy.

Secondary utilization of self-suspending proppant's coating polymer: Enhance oil recovery

Fracturing is associated with significant economic costs, and the loss of the utility of the self-suspending proppants' coating polymer after fracturing appears highly wasteful. To enhance the utilization of the self-suspending proppant's coating polymer, we propose a novel concept: the secondary utilization of coating polymer, enabling the coating polymer to gel-breaking within the reservoir and generate surface-active substances, thereby enhancing the oil recovery efficiency. To realize this concept, this study designed and synthesized a hydrophobic associative polymer, which was combined with ceramic proppant to form self-suspending proppant. Using the surface-active monomer octadecyl dimethyl allyl ammonium chloride (DMDAAC-18), acrylamide (AM), acrylic acid (AA), and 2-acrylamido-2-methylpropane sulfonic acid (AMPS) via aqueous free-radical copolymerization synthesized the PAAAD (Polymer (AM/AA/AMPS/DMDAAC-18)). PAAAD has demonstrated excellent thickening properties, with a viscosity of 240.01 mPa s at a concentration of 6 g/L in shear rate 170s−1. Its solution exhibits high viscoelasticity, and a loss factor (tan δ) < 1 over the frequency range of 0–20 Hz at a shear stress of 0.56 Pa indicates that it behaves like a viscoelastic solid with gel-like characteristics, which is beneficial for proppant suspension. The gel-breaking solution of PAAAD reduced surface tension (29.33 mN/m at a PAAAD concentration of 6 g/L), converted oil-wet rocks to water-wet conditions (reducing the contact angle of oil-wet shale to 46.7° and of oil-wet sandstone to 19.9°), and enhanced shale imbibition oil recovery efficiency in 16.5%. The basic properties of self-suspending proppants meet the Chinese Petroleum Industry Standard SY/T 5108-2014 and exhibit good suspension properties, with sedimentation of 1.7 mm in 40 min at a sand ratio of 15%. This study is the first to propose the secondary utilization of the self-suspending proppant's coating polymer, significantly enhancing their utilization value.

Interface properties and applications in laundry of the BS12-SAS mixed systems

In the BS12/SAS mixed systems, the solution exhibits acidity. BS12 can act as a cationic surfactant to form anionic-cationic complexes with SAS. In this study, the surface properties and application characteristics of the BS12/SAS mixed systems were investigated. The static surface tension, dynamic surface tension, and contact angle of BS12, SAS, and their different mixed molar ratios were measured at 25 °C to evaluate interaction parameters, activity coefficient, molar fraction, and thermodynamic variables of surfactants in the mixed micelles. The results demonstrated that the BS12/SAS mixed systems deviated from the ideal state due to the strong molecular attraction between the two components, resulting in a synergistic effect. The mixed systems exhibited higher surface activity and lower critical micelle concentration. Thermodynamic analysis indicated that the spontaneous micellization of binary mixtures of BS12 and SAS occurred through both enthalpy-driven and entropy-driven processes. The adsorption kinetics data revealed that the mixed systems followed a diffusion-adsorption process. Contact angle measurements demonstrated that BS12/SAS possesses superior ability to reduce surface tension, which facilitated rapid droplet diffusion and efficient wetting of the matrix within a short time period. Furthermore, the aggregation behavior of individual surfactants and the two composite systems in aqueous solutions was analyzed using DLS and TEM to investigate their effects on the wetting, emulsification stability, foaming stability, and decontamination capability of liquid paraffin.

Leaching process assisted by cetyltrimethylammonium chloride for weathered crust elution-deposited rare earth ores: Leaching behavior, kinetic analysis and interfacial regulation

Magnesium salts are commonly employed as ammonium-free leaching agents in the extraction of weathered crust elution-deposited rare earth ores (WCE-REO). Nonetheless, these salts frequently face technical challenges, including relatively low leaching rates and inadequate permeability in the in-situ leaching process. In this study, cetyltrimethylammonium chloride (CTAC) was used as a novel leaching aid agent to improve the rare earth leaching process. The effects of CTAC and pH on the rare earth leaching behavior and permeability was investigated. The leaching kinetic model was established and the regulation mechanism by which CTAC interacts with clay mineral surfaces was revealed for rare earth leaching process enhanced by CTAC. The results indicate that the appropriate amount of CTAC can increase the permeation velocity by 1.16×10−4 cm·s−1. Moreover, the rare earth leaching rate increased from 83.75 % to 95.65 %, accompanied by a reduction in leaching equilibrium time under optimal conditions. However, a higher concentration of CTAC results in a lower permeation velocity due to the increasing viscosity and the hydrophilicity. The relatively low pH will affect permeability of composite leaching agent in the ore pillar, diminishing its beneficial impact on rare earth leaching. The kinetic equation, fitted by the shrinking core model, suggests that the leaching adheres to an internal diffusion control mechanism, underscoring mass transfer as the pivotal limiting factor in rare earth leaching. CTAC reduces surface tension and viscosity, facilitating the permeation of the leaching solution into the rare earth ore. Furthermore, CTAC can be adsorbed on the surface of rare earth mineral particles, increasing the contact angle of clay minerals, elevating the Zeta potential, and diminishing the thickness of the diffusion layer, thus promoting mass transfer during leaching. The results of atomic force microscopy (AFM) analysis shows that the appropriate amount of CTAC adsorbed on rare earth ores can decreases the thickness of the hydration film on the particles’ surface, further improving the mass transfer efficiency during the leaching process. The findings of this study offer new insights into the green and efficient extraction of rare earth resources from both theoretical and technical perspectives.

Achieving the hydrophobic alteration by functionalized nano-silica for improving shale hydration inhibition

Shale hydration is the primary cause of wellbore instability during drilling processes. In this study, two non-fluorinated silane-coupling agents, octyltriethoxysilane (OTES) and (3-Aminopropyl) triethoxysilane (APTES), were grafted onto the nano-silica surface to develop a hydrophobic material (SHM). Various performance characterizations, including infrared spectroscopy, thermogravimetric analysis, surface tension, wetting alteration, capillary self-suction height, bentonite expansion, and shale dispersion, were employed to investigate the shale inhibition properties of SHM comprehensively. Experimental results revealed that SHM could significantly improve shale hydration inhibition. For instance, in a 2 % SHM liquids, the shale hot rolling recovery rate increased from 25.39 % to 83.78 %, and the bentonite expansion height decreased from 7.65 mm to 2.80 mm. The inhibition performance was notably superior to potassium chloride (KCl) and polyether amine (PEA). Inhibition mechanisms analysis unveiled that the outstanding inhibitory effect of SHM was achieved through electrostatic adsorption, wettability alteration, and surface tension reduction. Firstly, SHM contained numerous amine groups that could demonstrate strong adsorption on the clay surface through electrostatic and hydrogen bonding interactions. Secondly, with long hydrophobic alkyl chains, it formed a highly hydrophobic film enveloping the shale surface, effectively preventing water from invading. Thirdly, it reduced liquid surface tension, further minimizing the water infiltration. As a result, the use of SHM significantly enhanced shale hydration inhibition during the shale drilling process.

The Use of Electrochemical Cells to Generate Nanobubbles As Innovative Agents for Alleviating Eutrophication in Aquatic Environments

Eutrophication, characterized by the excessive accumulation of nutrients, notably nitrogen and phosphorus, in aquatic environments, represents a growing concern in contemporary environmental science. Specifically, eutrophication is intricately associated with the proliferation of algae, giving rise to the development of dense populations known as algal blooms. Harmful Algal Blooms (HABs), primarily composed of cyanobacteria and green algae, pose a threat to aquatic ecosystems by diminishing water clarity, depleting oxygen levels, and, in certain instances, generating detrimental toxins. The global incidence of HABs is increasing, and their frequency is anticipated to further rise due to the impacts of climate change.Conventional methods of water management often encounter significant challenges in effectively addressing and mitigating occurrences of algae blooms. HAB present a multifaceted challenge, influenced by nutrient pollution, climate factors, and diverse algal species. The intricate interactions among these elements contribute to the complexity of the issue. Additionally, the varying responses of algae to environmental conditions and the potential toxicity of certain species further complicate mitigation efforts. To address this challenge effectively, a nuanced understanding of these interconnected factors is essential. Implementing targeted strategies for sustainable water management is crucial for mitigating the impact of algae blooms on aquatic ecosystems and human health.Nanobubble technology represents a revolutionary approach to gas exchange, generating ultrafine bubbles with distinctive properties. These bubbles, with diameters smaller than 1000 nm, are non-buoyant, negatively charged, and exhibit remarkable longevity. These attributes allow them to spontaneously form at the interface between solid surfaces and aqueous solutions. Moreover, their small size enhances mass transport at the electrode-electrolyte interface, impacting reaction rates and catalytic activity. These electrochemical properties position nanobubbles as promising candidates for applications in electrosynthesis, energy storage, and water treatment, with ongoing research aiming to further understand their intricate interplay in diverse electrochemical processes. Nanobubbles play a pivotal role in improving water quality by reducing surface tension, preventing the escape of gas molecules into the atmosphere. This action effectively enhances the concentration of dissolved oxygen in bodies of water. By mitigating the adverse effects of HABs, nanobubbles emerge as a transformative technology with the potential to revolutionize water management strategies.Our research entails a thorough investigation into the formation mechanisms and diverse applications of nanobubbles. The work presented here specialized focuses on nanobubble generation using electrochemical cells. We aim to present how nanobubbles are generated using customized and portable electrochemical cells and the unique properties of these generated nanobubbles. Preliminary results will also be presented to compare the nanobubbles generated using electrochemical cells to the nanobubbles generated using conventional approaches currently employed in the industry. By delving into the details of nanobubble formation, we seek to understand their effectiveness at addressing the challenges associated with eutrophication and HABs in aquatic environments. This comparative analysis will shed light on the advantages and limitations of generating nanobubbles using electrochemical cells in the context of restoration of bodies of water, offering valuable insights for future applications and guiding decisions in environmental management practices.

A novel approach to produced water management using surfactants for water-wise energy production

Evaporation can become a prominent solution for management of the large volumes of contaminated water produced each year in the energy industry. However, improvements to the evaporation rates are needed which can be accomplished through the use of surfactants. In this paper, organic and inorganic compounds commonly found in produced water were studied in a controlled, laboratory oven to understand their effect on water evaporation rate. Organic compounds were classified in three ways: as either miscible or immiscible, as having a density less than or greater than water for immiscible compounds, and by their volatility. For each sample, the evaporation rate and surface tension were measured, and correlations were made between the two. As the cationic charges of salts added to water increased from +1 to +3, the evaporation rates decreased and the surface tension increased. Monovalent cationic charges were 60% higher than solutions containing divalent or trivalent cations. From the organic compounds tested, the addition of surfactants to deionized water increased evaporation rates by more than 50% while the addition of immiscible organic compounds hindered these rates. Surfactants reduced the surface tension of these samples thus positively affecting the evaporation rates. Applying surfactants to basic salt solutions showed evaporation rates increased with the greatest being that of sodium chloride, the most common salt in produced water. Increases in salt concentrations lowered evaporation rates and increased surface tension while increases in surfactant concentrations did not necessarily continue to reduce surface tension and increase evaporation rates. When surfactants were added to produced water samples, up to a 27% increase in the rates of evaporation were observed. The quality of produced water varies from region to region and therefore some surfactants may have a greater effect in one type of water than another.

Effect of physicochemical properties on critical sinking and attachment of respirable coal mine dust impacting on a water surface

Respirable coal mine dust (RCMD) inhalation is identified as the main cause of the resurgence of coal worker’s pneumoconiosis (CWP) since the mid-1990s. At present, the predominant dust control technology is the water spray system. However, in practice, the capture efficiency of RCMD by this technology is relatively low. To understand the capturing mechanism and develop improvement strategies, this research is focused on the surface chemistry study of RCMD and its impact on a water surface using a dynamic model. Proximate analysis, chemical, and mineral composition of a run-of-mine (ROM) coal sample from Appalachian region were analyzed using a proximate analyzer, Inductively Coupled Plasma Mass Spectrometry (ICP-MS), and X-ray Diffraction (XRD), respectively. Contact angles were measured by capillary rise test using the Washburn equation. Based on the dynamic model, the effects of particle size, density, contact angle, and surface tension on the critical sinking were investigated. It was pointed out in this work that reducing surface tension, in turn, decreases contact angle, which has been neglected in the literature. Regime maps for different minerals were created and showed that organic matter has the highest critical velocity due to its low density and high contact angle. Reducing water surface tension to the critical solid surface tension of coal around 30 mN/m could maximize the attachment efficiency. Scaling laws, constructed by force balance, led to the criteria of critical sinking: Ucr∼61-cosθ2D+1γlvρlR, i.e., Wecr∼121-cosθ2D+1. A semi-empirical formula for critical velocity was obtained by fitting the simulation data, Ucr=1.0961-cosθ2D+1γlvρlR. Attachment efficiency was defined and formulated as Pa=U02Ucr2=We0Wecr, establishing relationships between attachment efficiency and the physicochemical properties of RCMD and water droplets.

Production of Lipopeptide Biosurfactant Using Wastewater from Parboiled Paddy Rice and Evaluation of Antifungal Property of the Biosurfactant Against Two Dermatophyte Fungi.

A previously isolated lipopeptide biosurfactant-producing bacterium Bacillus licheniformis SCV1 was investigated for the production of the biosurfactant using wastewater from parboiled paddy rice. The biosurfactant thus produced was evaluated for its antifungal property against dermatophyte fungi Trichophyton ajelloi and Microsporum fulvum. Results revealed that the bacterial strain reduced surface tension of the media from 56.16 ± 1 mN/m to 35 ± 0.9 mN/m within 12h, which further shrank to 29.3 ± 1 mN/m in 24h of incubation. The yield of the biosurfactant was 3.15 ± 0.25g/L at 48h of incubation. The obtained biosurfactant exhibited efficient emulsifying activity against a wide range of hydrophobic substrates such as crude oil, olive oil, engine oil, and kerosene oil used in the study. The critical micelle concentration of the biosurfactant was found to be 80mg/L. Structural characterization using FT-IR and TLC revealed that the biosurfactant produced by the strain in the wastewater is a lipopeptide consisting of surfactin and iturin. LCMS analysis revealed that the surfactin homologs range from C12 to C17-surfactin while the iturin contains C13 to C17-iturin homologs. It also revealed an in vitro study that the biosurfactant has antifungal properties against dermatophyte fungi Trichophyton ajelloi and Microsporum fulvum. Microscopic observation of the hyphae of the treated dermatophyte revealed disruption and fissure of the mycelia. The chemical composition of the wastewater revealed that it contains adequate nutritional composition and micronutrients to support bacterial growth. This is the first report that the wastewater of parboiled paddy could be used as a low-cost substrate for the production of lipopeptide biosurfactant, and the biosurfactant could be used for preventing dermatophytes fungi.