Sulfate Surfactant Research Articles

Investigation of the synergistic effects of SiO2 and Al2O3 nanoparticles with SDS and CTAB surfactants on the stability and improving phase behavior of water-oil emulsions

The stability of emulsions is a significant challenge across various industries, including food, pharmaceutical, and petroleum. Surface-active agents utilized for enhanced oil recovery often exhibit inadequate performance under high salinity reservoir conditions, presenting a critical barrier to effective emulsion stabilization. Furthermore, due to the extreme hydrophilic or hydrophobic nature of nanoparticles (NPs), they are not effective in stabilizing emulsions on their own. To address this limitation, a minimal quantity of surfactant was introduced into the NPs to improve their wettability and achieve dual wettability. This research has examined the synergistic effects of SiO₂ and Al₂O₃ NPs combined with sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB) surfactants on water-oil emulsion stability. This approach enhanced emulsion stability by combining the stabilizing effects of both the NPs and the surfactants, an aspect that has not been previously addressed in phase behavior studies through the examination of the interactions and surface behavior of surfactant-nanoparticle complexes at the oil-water interface. Several experiments, including phase behavior, FT-IR, zeta potential, contact angle, and interfacial tension (IFT) tests, were performed to evaluate the interaction of surfactants with NPs. The results demonstrate that combining NPs with surfactants, especially those with opposite charges, significantly reduces IFT to the order of 10−6 mN/m, which can overcome capillary pressure, and enhances optimal salinity levels even up to 75000 ppm. Interactions between CTAB-SiO₂ and SDS-Al₂O₃ notably improve the hydrophobicity of NPs, resulting in IFT reductions of 11.4 and 7 mN/m, respectively, compared to NPs alone.

Synergistic enhancement of oil recovery: Integrating anionic-nonionic surfactant mixtures, SiO2 nanoparticles, and polymer solutions for optimized crude oil extraction

Enhanced oil recovery (EOR) methods are essential for optimizing oil extraction from modern reservoirs. This research delved into the synergistic impact of combining anionic and nonionic surfactant mixtures with silica (SiO2) nanoparticles (NPs) in sodium chloride (NaCl) solutions, alongside the added enhancement of polymers, to improve crude oil recovery. The study comprehensively evaluated stability, rheological characteristics, interfacial tension (IFT) behavior, wettability alterations, and EOR experiments using mixtures of sodium dodecyl sulfate (SDS) and triton X-100 (TX-100) surfactants. Scenarios both with and without SiO2 NPs in a base solution containing 3000 ppm NaCl and 2000 ppm xanthan gum (XG) polymer were examined. Core flooding tests were carried out on San-Saba sandstone core specimens with low permeability. The stability tests and dynamic light scattering (DLS) analysis were performed to assess the stability of NPs in low saline-surfactant-polymer solution. It was observed that NPs significantly reduced the IFT between the test solutions and crude oil, with nanofluids exhibiting satisfactory stability at a 0.4 wt% SiO2 NPs concentration. Core flooding studies demonstrated a synergistic interaction between NPs and the binary surfactant-polymer mixture, resulting in substantially greater incremental recovery of oil in comparison with the case of using binary surfactant-polymer combination alone. The mechanisms contributing to EOR with nanofluids, such as IFT reduction and wettability alteration, were explored. Incorporating NPs at concentrations of 0.1, 0.2, and 0.4 wt% led to incremental oil recoveries of 4.01 %, 12.35 %, and 12.73 % of the original oil in place (OOIP), respectively, as opposed to the recovery achieved using only SDS + TX-100 + XG. Consequently, these findings advance the understanding of the potential application of SiO2 NPs in combination with the binary surfactant-polymer mixture as effective chemical EOR agents. Additionally, these insights aid in identifying suitable sandstone reservoirs for nanofluid application, contributing to the optimization of oil recovery strategies.

Performance evaluation of hybrid electrochemical oxidation and ultraviolet light-based persulfate process for the abatement of sodium dodecyl sulfate from wastewater.

The application of hybrid advanced oxidation processes (AOPs) is an efficacious way to remediate emerging contaminants from wastewater. In the present research work, a hybrid electrochemical oxidation and ultraviolet light-based persulfate activation processes (EO-UV/PS) were used to efficiently degrade sodium dodecyl sulfate (SDS) surfactant from synthetic and municipal wastewater. By operating the EO-UV/PS at optimum operating conditions at pH of 7.0, NaCl of 0.02M, current density of 6.4mA/cm2, persulfate dose of 2.5mM, and operating period of 180min, about 94.5 ± 2.8% of SDS (20mg/L) removal was achieved from synthetic wastewater. The abetment of SDS in both EO and UV/PS obeyed pseudo-first-order kinetics with a rate constant of 0.012 and 0.019min-1, respectively. Moreover, the economic analysis revealed 0.23 $ m-3order-1 as the operating cost for degrading SDS in EO-UV/PS. The degradation pathway experimentation suggested the generation of lauric acid by-product during SDS abatement. Besides, nearly 89.3 ± 2.9% of SDS and 58.7 ± 2.4% of total organic carbon reduction was also achieved from real municipal wastewater. Phytotoxicity test on Vigna radiata affirms the non-toxic nature of the EO-UV/PS effluent.

Temperature dependence of the near infrared absorption spectrum of single-wall carbon nanotubes dispersed by sodium dodecyl sulfate in aqueous solution: experiments and molecular dynamics study.

Single-wall carbon nanotubes (SWCNT) dispersed in water with the help of sodium dodecyl sulfate (SDS) surfactants exhibit a temperature dependent near infrared (NIR) exciton spectrum. Due to their biocompatibility and NIR spectrum falling within the transparent window for biological tissue, SWCNTs hold potential for sensing temperature inside cells. Here, we seek to elucidate the mechanism responsible for this temperature dependence, focusing on changes in the water coverage of the SWCNT as the surfactant structure changes with temperature. We compare optical absorption spectra in the UV-Vis-IR range and fully atomistic molecular dynamics (MD) simulations. The observed temperature dependence of the spectra for various SWCNTs may be attributed to changes in the dielectric environment and its impact on excitons. MD simulations reveal that the adsorbed SDS molecules effectively shield the SWCNT, with ~ 70% of water molecules removed from the first two adlayers; this coverage shows a modest temperature dependence. Although we are not able to directly demonstrate how this influences the NIR spectrum, this represents a potential pathway given the strong influence of the water environment on the excitons in SWCNTs. Optical absorption measurements were carried out in the UV-Vis-NIR range using a Varian Cary 5000 spectrophotometer in a temperature-controlled environment. PeakFit™ v. 4.06 was used as peak-fitting program in the spectral range 900-1400nm (890-1380meV) as a function of the temperature. Fully atomistic molecular dynamics simulations were conducted using the NAMD2 package. The CHARMM force field comprising two-body bond stretching, three-body angle deformation, four-body dihedral angle deformation, and nonbonded interactions (electrostatic and Lennard-Jones 6-16 potentials) was employed.

The impact of sodium lauryl sulfate on hydrogen evolution reaction in water electrolysis

This study confirms the sodium lauryl sulfate (SLS) surfactant is effective to enhance water electrolysis performance especially when combined with NaCl. The water electrolysis experiment on different concentrations of SLS and SLS-NaCl mixture electrolyte were performed. The results indicate the presence of NaCl is more effective to enhance the SLS containing electrolyte performance instead of adding more SLS concentration. More SLS concentration is effective to enhance hydrogen evolution reaction (HER) when NaCl is added. The effectiveness of NaCl is shown by the order of final HER SLS 0.5 M + NaCl 3.9212 × 10−7 Mol. L−1, SLS 0.3 M + NaCl 3.8789 × 10−7 Mol. L−1, and, SLS 0.5 M 3.6758 × 10−7 Mol. L−1. The SLS creates positively charged micelles which increases ion mobility and HER. The NaCl accelerates the HER due to the formation of smaller ion clusters that react more quickly with the cathode. Therefore, this study reveals the mechanism of electrolysis enhancement by surfactant mixed electrolyte.

Salt-Induced Linker Dehydration Modulates Micellar Structure in Ether-Linked Sulfate Surfactants.

Ether-linked surfactants are widely used in formulations such as liquid soaps, but despite their ubiquity, it is unclear how n-ethylene glycol linkers in surfactants, such as sodium lauryl n-(ethylene glycol) sulfate (SLEnS), influence micellar packing in the presence of NaCl. In the present work, we probe the structure and hydration of ether linkers in micelles comprising monodisperse SLEnS surfactants using contrast-variation small-angle neutron scattering (CV-SANS) and small-angle X-ray scattering (SAXS). Using SAXS, changes in micellar structure were observed for SLEnS (n = 1, 2, or 3) arising from the extent of ethoxylation. Scattering profiles indicated a clear transition from elongated cylindrical micelles to shorter ellipsoidal micelles with increasing ethoxylation. With CV-SANS, micellar structure and linker geometries of SLE3S were able to be resolved, indicating that a change in micellar architecture is modulated by dehydration of the tri(ethylene glycol) linker, offering new insights into the role of water and ions in the self-assembly of this key class of surfactants.

Green and sensitive detection of olopatadine in aqueous humor using a signal-on fluorimetric approach: GREEnness assessment.

Olopatadine (OLP) is widely utilized as an effective antihistaminic drug for alleviating ocular itching associated with allergic conjunctivitis. With its frequent usage in pharmacies, there arises a pressing need for a cost-effective, easily implementable, environmentally sustainable detection method with high sensitivity. This study presents a novel signal-on fluorimetric method for detecting OLP in both its pure form and aqueous humor. The proposed approach depends on enhancing the weak intrinsic fluorescence emission of OLP, achieving a remarkable increase of up to 680% compared to its intrinsic fluorescence. This enhancement is achieved by forming micelles around protonated OLP using an acetate buffer (pH 3.6) and incorporating a solution of sodium dodecyl sulfate (SDS) surfactant. A strong correlation (R = 0.9996) is observed between the concentration of OLP and fluorescence intensities ranging from 1.0 to 100.0 ng mL-1 with a limit of detection of 0.22 ng mL-1. This described method is successfully employed for quantifying OLP in both its powder form and pharmaceutical eye drops. Furthermore, it demonstrates robust performance in determining OLP in artificial aqueous humor with a percentage recovery of 99.05 ± 1.51, with minimal interference from matrix interferents. Moreover, the greenness of the described method was evaluated.

Mesoporous pineapple crown-derived activated carbon modified matrix for the detection of carbendazim in the presence of anionic surfactant

Carbon paste electrodes (CPEs) are commonly employed in electroanalysis because of their chemical stability, broad electrochemical window, low capacitive current, ease of fabrication, and surface renewability. Electrocatalysts can easily be embedded into CPEs to make them suitable for a variety of applications. Poor biowaste management presents a significant challenge in the agro-industry and agriculture due to the rapid decomposition of biowaste, driven by its high water content and limited biological stability, which leads to pest attraction and greenhouse gas emissions. Consequently, this green waste can be utilized for the development of electrocatalysts. Activated carbon (AC) has been utilized in progressive electrochemical applications as it exhibits high conductivity and porosity that help to enhance electrocatalytic activity. Herein, pineapple fruit crown (PC) peel-derived AC (PCAC) is utilized as the sensing material for the determination of fungicide, carbendazim (CBM). The synthesized material was characterized using SEM, FT-IR, XRD, EDX, AFM, CV and EIS. Besides, to enhance the surface properties, Sodium dodecyl sulfate (SDS) surfactant is used as a mediator in detecting CBM. The CV and SWV approaches were employed to assess the electrochemical response of the developed electrodes for the CBM determination. Under optimum experimental conditions, the SDS/PCAC/CPE exhibits low DLim and QLim values of 32.0 nM and 128.0 nM with considerable selectivity. Furthermore, the SDS/PCAC/CPE was employed in real-time analysis of CBM in spiked environmental samples, which showed satisfying recovery results. Moreover, the electrode showed good stability over multiple measurements, and these results demonstrate that SDS/PCAC/CPE is a promising sensor for CBM detection.

Effect of the mixed micelles of zwitterionic-anionic surfactant on efficiency of antibiotic azithromycin dihydrate

The study highlights the importance of mixed micelles in enhancing the binding and solubilization properties of partially water-soluble medications, using zwitterionic cocoamidopropyl betaine (CAPB) and anionic sodium tetradecyl sulfate surfactants. Surface tension and fluorescence spectroscopy evaluated the critical micelle concentration (CMC) of CAPB-STS mixed micelle. The thermodynamic parameters were assessed using Clint, Rubingh, and Motomura’s approach, which showed a synergistic interaction between the CAPB and STS. UV spectroscopy technique was used to evaluate the applicability of mixed micelle to enhance the solubility and binding constant (Kb) of antibiotic azithromycin dihydrate (AZI). Kb values of AZI were increased from 2.301 to 3.415 and molar solubilization ratio (MSR) values of AZI were increased from 0.228 to 0.801 by decreasing αCAPB from 0.9 to 0.1. The result indicated that zwitterionic CAPB was an electrostatic interaction consisting of both attractive (−CH2COO¯ group) and repulsive (−N+ group) interactions with AZI (−NH+ group), causing AZI molecules to reside in the Stern layer. While STS consisted of a negative −SO4¯ head group, it caused increased electrostatic interaction, and AZI penetrated the palisade layer of mixed micelles. At 7.00 mmolL-1 concentration of αCAPB 0.1, the solubility of AZI in water was increased to 2.77 mmol/L from 0.0032 mmol/L. Additionally, after 8 h, the controlled release of AZI in PBS at pH 7.4 was 95.58 % and decreased up to 30.77 % at αCAPB 0.1 mixed micelles. The observation of controlled AZI release from αCAPB 0.9 to 0.1 indicates that AZI molecules were strongly bound to mixed micelles by both hydrophobic and electrostatic interactions. In the end, a mixed micelle of CAPB-STS could serve as a useful drug-solubilizing agent in pharmaceutical applications.

GO and surfactant assisted regulation of polyamide nanofiltration membranes for improved separation performance

Fabricating nanofiltration membranes with high water permeance and selectivity by tailoring the structure and morphology is crucial to efficient water purification. In this work, the fabrication of thin film nanocomposite (TFN) nanofiltration membranes by combining two methods, the surfactant-assembly interfacial polymerization (SARIP) and the addition of graphene oxide (GO) or ionic liquid functionalized graphene oxide (GO-IL) for the preparation of the selective PA layer on a novel porous substrate is reported. For the preparation of the porous substrate, mechanically robust, aromatic polyethers containing polar pyridine units (PDSPP) were chosen targeting to improved hydrophilicity and thus enhanced water permeability. The anionic sodium dodecyl sulfate (SDS) surfactant was used to regulate the interfacial polymerization thereby enabling the formation of dense PA layers with high cross-linking degree and consequently high salt rejections. On the other hand, the addition of GO/GO-IL nanosheets could impart hydrophilicity and antifouling properties. The novel porous PDSPP substrate was selected for the fabrication of TFN membranes due to its improved water permeability and superior salt rejection and increased hydrophilicity compared to commercial PSf substrate. The detailed study of the fabricated TFN membranes by ATR-FT-IR, SEM, AFM, XPS, contact angle measurements revealed the formation of polyamide selective layers with rougher surfaces, increased hydrophilicity and high cross-linking degrees (from 44 % to 94 %), resulted from the synergistic effect of SDS and GO incorporation. Moreover, the prepared TFN membranes exhibited high salt rejections while maintaining a moderate water permeability. In particular, the membrane containing the neat GO (TFNGO50) displayed excellent Na2SO4 and MgSO4 rejections (98.8 % and 99.5 %, respectively) while the NaCl rejection was 47.0 % and a water permeability value of 4.2 L m-2h−1 bar−1. The divalent salt rejections were among the highest values reported in the literature in comparison with commercial NF membranes and TFN membranes containing GO/functionalized GO. When GO-IL nanosheets were embedded in the PA layer, the water permeability was slightly improved while the salt rejections were significantly reduced compared to TFNGO50. Lastly, the incorporation of GO enhanced the anti-fouling properties of the prepared membranes due to increased hydrophilicity of the PA surface.

Surface modification for enhanced Anti‐Wetting properties of electrospun omniphobic membranes in membrane distillation

AbstractMembrane wetting caused by substances in the feed solution with low surface tension has posed serious issues for membrane distillation (MD). Omniphobic membranes could be helpful when dealing with this problem because they strongly repel liquids with a wide range of surface tensions. We fabricated electrospun omniphobic membranes containing PVDF‐TEOS‐PFDTMS, PVDF‐HFP‐TMOS‐PFDTMS, and PVDF‐HFP‐TEOS‐PFDTMS. All electrospun membranes have shown contact angles >90°, but the electrospun membrane containing PVDF‐HFP‐TEOS‐PFDTMS has shown super repellence with a contact angle >150° and maintains stable salt rejection and water flux in direct contact MD processes in the presence of sodium dodecyl sulfate surfactant (up to 0.3 mM). Furthermore, the morphology and crystallinity of the electrospun membranes were studied by scanning electron microscopy and Fourier‐transform infrared spectroscopy, and the percentage composition of elements was analyzed by x‐ray photoelectron spectroscopy. liquid entry pressure, mechanical strength, and the porosity of the electrospun omniphobic membranes were also studied.

Formulation and Antibacterial Activity Testing of Eco-Soap Based on Sodium Lauryl Sulfate Surfactant

Pineapple is a fruit that is often used only for its flesh, while the skin remains waste. As a form of dealing with pineapple waste, one way is to use it as an eco-enzyme. Making soap with added eco-enzyme can be used as an alternative for washing dishes. Therefore, this research aims to determine the formulation and test the antibacterial activity of eco-soap based on the surfactant Sodium Lauryl Sulphate. This research is experimental research, which was carried out in July-October 2023. The research results showed that the pH of eco-Soap was 3.46; foam height 1.5 cm; viscosity testing 14.9 mPas; fatty acids 1.44%; and 6 mm antibacterial activity testing. Based on the research results, it was concluded that the surfactant-based eco-soap formulation had good stability in the eco-soap foam height test. The diameter of the zone of inhibition of eco-soap's antibacterial activity showed that bacterial inhibition was moderate.

A Janus membrane with silica nanoparticles interlayer for treating coal mine water via membrane distillation

The use of membrane distillation (MD) technology to treat coal mine water content has great potential, and the Janus membrane is very resistant to scaling and wetting during MD. In this work, SiO2 nanoparticles were electrostatically adsorbed onto the surface of a polyvinylidene fluoride (PVDF) membrane, followed by the construction of a polyamide (PA) layer through interfacial polymerization (IP). The intermediate layer of SiO2 nanoparticles can promote the enrichment of amine monomers during the subsequent IP process as well as slow its entry into the organic phase to regulate the PA layer. The addition of SiO2 nanoparticles was increased from 0 to 0.10 %, and the thickness of the polyamide layer was also reduced from 225.1 nm to 102.3 nm. Compared with the original membrane vapor flux of 40.9 ± 1.0LMH, the modified membrane vapor flux slightly increased to 46.2 ± 0.9LMH, but excessive SiO2 nanoparticles blocked the membrane pore, resulting in a decrease in flux. MD experiments show that the Janus membrane is wettability and scaling resistance when passing through the salt solution containing sodium dodecyl sulfate (SDS) surfactant or simulated wastewater as feed. At the same time, the interface thermodynamics of the simulated wastewater and the membrane are calculated to understand the anti-scaling mechanism of the membrane, offering a theoretical foundation for the application of real mine water.

Impact of surfactant polydispersity on the phase and flow behavior in water: the case of Sodium Lauryl Ether Sulfate

This study delves into the impact of molecular polydispersity on the phase behavior of Sodium Lauryl Ether Sulfate (SLES) surfactant, aiming to deepen understanding of its implications for fundamental science and industrial applications. SLE3S is utilized as a model compound: a comprehensive characterization of molecular polydispersity is conducted using Gas Chromatography–Mass Spectrometry and Nuclear Magnetic Resonance spectroscopy, juxtaposing the findings with those for SLE1S.Our comprehensive investigative approach entails: (i) employing Time-Lapse dissolution experiments in microchannel geometries to observe the dissolution and phase transitions; (ii) utilizing polarized light microscopy, confocal microscopy, and Small Angle X-ray Scattering for microstructure identification assessments; (iii) conducting rheological evaluations at various concentrations and temperatures to determine their effects on the surfactant properties.The findings reveal that SLE3S, being more polydisperse, demonstrates complex phase behavior not observed in the less polydisperse SLE1S. Notably, SLE3S exhibits a unique concentration domain, corresponding to a concentration of about 60 %wt, where hexagonal (H), cubic, and lamellar (Lα) phases coexist, resulting in highly viscoelastic heterogeneous mixtures. This behavior is attributed to the local segregation of surfactant components with varying polarity, underscoring the crucial role of molecular polydispersity in the phase behavior of SLES surfactants.

Energy storage density enhancement in paraffin phase change material emulsions: A comparative study with two different base fluids

This investigation examined the thermophysical properties of emulsions comprising paraffin 56/58 phase change material (PCM) dispersed in water and ethylene glycol (60 wt%) aqueous solution to optimize energy storage density for low-temperature thermal applications. Dynamic Light Scattering analysis revealed a uniform dispersion of paraffin 56/58 PCM droplets in the basefluids, with an average diameter of approximately 150 nm achieved by incorporating sodium dodecyl sulfate surfactant. The latent heat of fusion for emulsions containing paraffin 56/58 PCM in ethylene glycol (60 wt%) exhibited values of 37.5/41.7, 58.5/63.9, 73.8/75.43, and 93/90.25 J/g for concentrations of 20, 30, 40, and 50 wt%, respectively, during melting/solidification phases. Furthermore, the highest energy storage densities of 306.95 and 361.3 kJ/kg were attained at a PCM concentration of 50 wt% in ethylene glycol (60 wt%) and water-based emulsions, respectively, surpassing those of similar working fluids. It is also indicated that water-based paraffin 56/58 PCMs offer superior energy storage density. However, under severe operating conditions such as extreme temperatures, ethylene glycol (60 wt%) based paraffin 56/58 emulsions demonstrate greater suitability, as the evaporation and freezing points of the basefluid can be adjusted by modulating the ethylene glycol concentration ratio.

Waste to fuel: A detailed combustion, performance, and emission characteristics of a CI engine fuelled with sustainable fish waste management augmentation with alcohols and nanoparticles

All over the world, 130 million tonnes of fish waste have been generated per annum. Improper disposal of such waste leads to environmental pollution, habitat degradation, oxygen depletion, spread of pathogens, parasites, and diseases. From this point of view, this research motivated to benefit from such fish waste by converting an alternative fuel along with various additives for diesel engines. Fish wastes gathered from the fish market are used as feedstock for producing fish waste biodiesel (FWBD) through the transesterification process. The derived fish waste biodiesel (FWBD) 60 %, 20 % diesel, and 20 % n-butanol (C4H9OH) by volume were blended (60FWBD+20Bu+20D) to form the test fuels. Then the fuel blends were used to convert two nano fuels by separately adding zinc oxide and graphene nanoparticles of 100 ppm along with sodium dodecyl sulphate surfactant, and the nanoparticles-added test fuels were exposed to sound waves of 50 kHz in an ultrasonicator for 1 h. These fuels were characterized to derive and ensure the fuel properties for diesel engines and tested such fuels in a 5.2 kW CI engine to do a comparative study. The experiments were conducted at the constant engine speed of 1500 rpm, and varying engine loads from 25 % to 100 % with intervals of 25 %. When the fish waste biodiesel was added to diesel fuel, the engine performance worsened in a given engine load, but it started to improve with the existence of nanoparticles. Compared to 60FWBD+20Bu+20D, graphene-based nano fuel blend recorded 1.99 % higher BTE, but 15.03 % higher NOx. Similarly, compared to 60FWBD+20Bu+20D, zinc oxide-based nano fuel blends recorded 6.75 % higher BTE and reduced NOx, CO, HC, and smoke emissions by 29.97 %, 15.98 %, 22.0 %, and 16.03 % respectively. In conclusion, the present research reveals that fish wastes can be used in diesel engines without any modification on the vehicular system, and this may contribute to both slowing down the rate of depletion of fossil reserves and the waste management of the fish wastes from nature in a useful way.

Diffusiophoretic Transport of Charged Colloids in Ionic Surfactant Gradients Entirely below versus Entirely above the Critical Micelle Concentration.

When placed in an ionic surfactant gradient, charged colloids will undergo diffusiophoresis at a velocity, uDP = MDP∇ ln S, where MDP is the diffusiophoretic mobility and S is the surfactant concentration. The diffusiophoretic mobility depends in part on the charges and diffusivities of the surfactants and their counterions. Since micellization decreases surfactant diffusivity and alters charge distributions in a surfactant solution, MDP of charged colloids in ionic surfactant gradients may differ significantly when surfactant concentrations are above or below the critical micelle concentration (CMC). The role of micelles in driving diffusiophoresis is unclear, and a previously published model that accounts for micellization suggests the possibility of a change in the sign of MDP above the CMC [Warren, P. B.; . Soft Matter 2019, 15, 278-288]. In the current study, microfluidic channels were used to measure the transport of negatively charged polystyrene colloids in sodium dodecyl sulfate (SDS) surfactant gradients established at SDS concentrations that are either fully above or fully below the CMC. Interpretation of diffusiophoresis was aided by measurements of the colloid electrophoretic mobility as a function of SDS concentration. A numerical transport model incorporating the prior diffusiophoretic mobility model for ionic surfactant gradients was implemented to elucidate signatures of positive and negative diffusiophoretic mobilities and compare with experiments. The theoretically predicted sign of the diffusiophoretic mobility below the CMC was determined to be particularly sensitive to uncertainty in colloid and surfactant properties, while above the CMC, the mobility was consistently predicted to be positive in the SDS concentration range considered in the experiments conducted here. In contrast, experiments only showed signatures of a negative diffusiophoretic mobility for these negatively charged colloids with no change of sign. Colloid diffusiophoretic transport measured in micellar solutions was more extensive than that below the CMC with the same ∇ ln S.

Experimental and Molecular Dynamics Simulation to Investigate Oil Adsorption and Detachment from Sandstone/Quartz Surface by Low-Salinity Surfactant Brines.

In this study, we explore the impact of monovalent (NaCl) and divalent (CaCl2) brines, coupled with sodium dodecyl sulfate (SDS) surfactant at varying low concentrations, on the detachment and displacement of oil from sandstone rock surfaces. Employing the sessile drop method and molecular dynamics simulations, we scrutinize the behavior of the brine solutions. Our findings reveal that both low salinity and low-salinity surfactant solutions induce a gradual shift in rock wettability toward a more water-wet state. This wettability transformation is not instantaneous but evolves over time, as observed through meticulous molecular motion analyses. Through contact angle measurements and molecular dynamics simulations, we delve into the molecular motion at subpore and micropore scales on sandstone/quartz surfaces. The adsorption of surface-active agents from the oil to the oil-brine interface results in a reduced interfacial tension, significantly contributing to oil displacement. Notably, low salinity concentrations ranging from 1000 to 10,000 ppm exhibit the lowest contact angles within 30 min across all solutions. However, higher concentrations deviate from this declining trend, especially with divalent ions like Ca2+, which bridge polar molecules onto the rock surface, resulting in an increased oil-wetting state. This research unveils the intricate molecular motions involved in employing low-salinity surfactant solutions for oil detachment from surfaces. Furthermore, it provides valuable insights into the underlying forces driving oil detachment and wettability alteration.

Synthesis of carbon quantum dots via electrochemically-induced carbon dioxide nanobubbles exfoliation of graphite for heavy metal detection in wastewater

Carbon quantum dots (CQDs) offer significant promise across industries due to their distinctive optical properties and strong biocompatibility. However, conventional synthesis methods frequently need more precision in controlling nanoparticle size, shape, and uniformity, limiting their versatility in diverse applications. Therefore, this study introduced an innovative approach to synthesising CQDs by combining electrochemical techniques with carbon dioxide (CO2) nanobubbles, circumventing the need for conventional surfactant-based exfoliation. According to the findings, the synthesised CQDs exhibited remarkable properties, including a high quantum yield of 26.17% and an average particle size of 2.24 ± 1.07 nm. Such characteristics render them exceptionally suitable for portable sensors for heavy metal detection in wastewater. Moreover, the investigation revealed the outstanding selectivity of the synthesised CQDs, particularly towards iron (Fe3+) ions, but demonstrated limited reactivity towards lead (Pb2+) and copper (Cu2+) ions. The novel approach also generated non-toxic CQD under the supply of CO2 nanobubbles, which offers a scalable avenue for developing advanced materials for various applications, including sensors for heavy metal ion detection in wastewater. The conventional synthesis method that relied on sodium dodecyl sulphate (SDS) surfactants without CO2 nanobubbles yielded CQDs with a significantly lower quantum yield of 11.2%. In short, incorporating CO2 nanobubbles with electrochemical techniques enhanced quantum yield and superior control over the size and shape of the synthesized CQDs. This novel method successfully produced CQDs with scalable distinct morphologies and provided a new understanding of the CQD synthesis mechanism, with potential applications in portable sensing for environmental monitoring and water quality management.

Ultrasonication‐assisted alkali treatment of hemp fibers to improve the fiber/matrix interface of hemp/epoxy composites: The influence of sodium dodecyl sulfate surfactant

AbstractAlkali pretreatment of fibers is an efficient technique to enhance fiber/matrix bonding in natural fiber composites. This study investigates if the addition of sodium dodecyl sulfate (SDS) surfactant increases the efficacy of alkali treatment of hemp fibers. SDS concentrations ranging between 2 and 10% wt/wt were used with a constant (10% wt/wt) NaOH concentration. Fiber surfaces were observed with scanning electron microscopy (SEM). Fiber surfaces were cleaner when SDS was used compared with alkali treatment with no SDS added indicating the elimination of substances such as lignin, waxes, hemicelluloses, and pectin. Fourier‐transform infrared spectroscopy and TGA studies also confirmed the removal of these substituents. Mechanical performance of the composites was evaluated via static and dynamic tests. The tensile strength and modulus improved 24.9% and 13.6% respectively with the addition of 10 wt% SDS. The flexural strength and modulus also showed an improvement of 22.4% and 26.3% respectively when 10 wt% SDS was added to alkali solution. Dynamic mechanical tests showed that the storage and loss modulus of the composites increase with SDS/alkali treatment. Results indicated that the use of SDS in alkali treatment notably improves the composite performance which is attributable to more efficient elimination of noncellulosic constituents from fiber structure.Highlights Sodium dodecyl sulfate (SDS) improves the efficacy of NaOH treatment of hemp. Removal of noncellulosic substances from fibers was facilitated by SDS. Ultrasound/SDS assisted alkalization of fibers improved composite properties.