Dodecylbenzenesulfonate Research Articles

Precipitation–Flotation Process for Molybdenum and Uranium Separation from Wastewater

The mining of molybdenum and uranium ores inevitably results in the generation of large volumes of wastewater containing low concentrations of metals, which poses significant threats to the environment. This study presents a novel precipitation–flotation process for the simultaneous separation of molybdenum and uranium from wastewater. A systematic investigation was conducted on the impacts of the type of precipitant, flotation reagent type, and flotation parameters on the experimental results. Ferric salt served better as a precipitant than aluminum salt and humic acid did, and sodium dodecyl sulfate (SDS) was more suitable than sodium dodecyl benzene sulfonate for acting as a surfactant and foaming agent. Under specific conditions, including a pH of 6.6, an Fe3+ dosage of 0.6 mmol·L−1, an SDS dosage of 40 mg·L−1, an air flow rate of 25 mL·min−1, and a flotation time of 10 min, the removal efficiencies of molybdenum and uranium reached 96.6% and 93.6%, respectively. After flotation, the molybdenum concentration, uranium concentration, chemical oxygen demand, and turbidity of the treated water all meet the emission standards. Furthermore, the metal removal mechanisms, including the particle size distribution, functional group structure, surface element composition, microstructure, and element distribution, were elucidated on the basis of characterization of the precipitation–flotation products.

A comparative study of extraction free detection of HBV DNA using sodium dodecyl sulfate, N-lauroylsarcosine sodium salt, and sodium dodecyl benzene sulfonate

This study aimed to develop an extraction-free method for quantitative and qualitative detection of HBV DNA compared to traditional nucleic acid extraction. Paired serum and dried blood spot (DBS) samples from 67 HBsAg-positive and 67 HBsAg-negative individuals were included. Two samples with known HBV DNA titers (~ 109 copies/mL) were examined by extraction-free detection using three surfactants (0.2 to 1% of Sodium dodecyl sulfate:SDS, N-Lauroylsarcosine sodium salt:NL, Sodium dodecyl benzene sulfonate:SDBS), two stabilizing agents (0.1 or 0.01% 2-Mercaptoethanol:2ME and 3.5 or 7% Bovine Serum Albumin:BSA) and two Taq polymerases (Fast Advanced and Prime Direct Probe). HBV DNA in all 67 HBsAg-positive and 67 HBsAg-negative serum and DBS samples was directly quantified by Rt-PCR using 0.4% SDS or 0.4% NL with Fast Advance or Prime Direct Probe Taq. Extraction-free amplification was also performed. Detection limits were varied by different surfactants and Taq. SDS combined with Fast Advanced Taq showed lower detection limits, while SDS with Prime Direct Probe Taq outperformed NL or SDBS-based detection. Adding 2ME to SDS improved detection limit with Prime Direct Probe Taq but not significantly compared to SDS alone. BSA did not significantly enhance detection limits but provided insights into sample stability. The senitivity and specificity of 0.4% SDS and NL in combination with either Fast advanced or Prime Direct Probe Taq polymerase in serum samples were > 90% and 100% resepctively, while it was > 80% and 100% respectively in DBS samples. Extraction-free HBV DNA amplification provided 100% identity with original genomes. Our study suggests that SDS, NL or SDBS-based extraction-free HBV DNA detection strategies using Prime Direct Probe Taq have potential to simplify and accelerate HBV DNA detection with high sensitivity and specificity in both serum and DBS samples, with implications for resource-limited settings and clinical applications. Utilizing surfactants with 2ME is optional, and further research and validation are necessary to broaden its application in real-world diagnostics.

Enhancing mechanical properties of carbonated steel slag through surfactant-assisted CaCO3 crystallization

This study investigates the enhancement of mechanical properties in carbonated steel slag through surfactant-assisted CaCO3 crystallization. Sodium dodecyl benzene sulfonate (SDBS) was employed at various concentrations (0.1–0.4 mol/L) and temperatures (20–60 °C) to modulate the carbonation process. Optimal performance was achieved with 0.2 mol/L SDBS at 40 °C, resulting in a maximum CO2 uptake of 8.51 % and a compressive strength of 62.89 MPa, 81.66 % higher than unmodified steel slag. Characterization techniques confirmed the formation of crystalline calcite, vaterite, and aragonite, contributing to improved microstructure and strength. SDBS micelles act as templates for CaCO3 nucleation and growth, with low concentrations facilitating carbonation and high concentrations inhibiting it. This research offers new insights into surfactant-assisted crystallization for enhancing carbonated steel slag properties, paving the way for high-performance, eco-friendly building materials from industrial waste.

Silver-Doped Reduced Graphene Oxide/PANI-DBSA-PLA Composite 3D-Printed Supercapacitors.

This study presents a novel approach to the development of high-performance supercapacitors through 3D printing technology. We synthesized a composite material consisting of silver-doped reduced graphene oxide (rGO) and dodecylbenzenesulfonic acid (DBSA)-doped polyaniline (PANI), which was further blended with polylactic acid (PLA) for additive manufacturing. The composite was extruded into filaments and printed into circular disc electrodes using fused deposition modeling (FDM). These electrodes were assembled into symmetric supercapacitor devices with a solid-state electrolyte. Electrochemical characterization, including cyclic voltammetry (CV) and galvanostatic charge-discharge (GCD) tests, demonstrated considerable mass-specific capacitance values of 136.2 F/g and 133 F/g at 20 mV/s and 1 A/g, respectively. The devices showed excellent stability, retaining 91% of their initial capacitance after 5000 cycles. The incorporation of silver nanoparticles enhanced the conductivity of rGO, while PANI-DBSA improved electrochemical stability and performance. This study highlights the potential of combining advanced materials with 3D printing to optimize energy storage devices, offering a significant advancement over traditional manufacturing methods.

SDBS-AEO Mixture for Triton X-100 Replacement: Surface Activity and Application in Biosensors.

Triton X-100 (TX-100) is a commonly used surfactant in the manufacture of biosensors. The factors limiting the use of TX-100 in biosensors are environmental concerns. In this study, the binary system of sodium dodecyl benzene sulfonate (SDBS) and fatty alcohol-polyoxyethlene ether (AEO) was investigated from the physicochemical principle of surfactant interaction and its application in biosensors. The results demonstrated that a mixture of SDBS and AEO at an appropriate molar ratio had a comparable activity to TX-100 in terms of surface activity, micelle formation, dynamic adsorption, foaming, emulsifying, and cell permeability. Theory and experimentation support the idea that SDBS-AEO might take the place of TX-100 in the manufacturing of biosensors. This study contributes to the development of alternatives to TX-100 and provides a new perspective for an in-depth study of the interaction mechanism of additives in biosensor design.

Preparation of novel nanoparticle demulsifier and its demulsification for surfactant-stabilized crude oil emulison

The application of nanoparticle (NP) demulsifiers in processing the emulsified crude oil production fluid is of great significance for improving production efficiency and reducing energy consumption in crude oil extraction. In this work, a novel NP demulsifier (PPA@KAO) was prepared by chemically modifying the mineral kaolinite (KAO) nanoparticles using γ-Methacryloyl propyltrimethoxysilane (MPS) and polyether-polyquaternium (PPA). The morphology and structure of the PPA@KAO demulsifiers were characterized by FT-IR, SEM, TG, XPS and Zeta potential. The contact angle measurements, interfacial tension (IFT) characterization, and the distribution of nanoparticles in the oil-water phase showed that PPA@KAO have good amphiphilicity and interfacial activity. The demulsification performance of PPA@KAO demulsifiers for a sodium dodecyl benzene sulfonate (SDBS) stabilized crude oil emulsion was studied with bottle method. It was found that the oil-water separation could be completed within 20 min, with a demulsification efficiency of 96.75 % at a dosage of 3 g L−1，pH of 6 and temperature of 30°C. Such a result indicates that the PPA@KAO NP demulsifier can achieve rapid and efficient demulsification for the surfactant-stabilized crude oil emulsion at room temperature. The demulsification mechanism of PPA@KAO for the SDBS-stabilized crude oil emulsion was well revealed, which provides an important synthetic strategy of how obtaining an effective NP demulsifiers by regulating the amphiphilicity and surface functional groups of the nanoparticles.

Study on the effect of spatial adsorption orientation on the preferential selection mechanism of dust suppression surfactants

Surfactants are widely used in the field of coal dust control. However, the dust suppression effect of different surfactants varies significantly, and the preferential selection mechanism of dust suppressants for mining is not clear. In this study, the water/surfactant/lignite system was constructed by molecular simulation to investigate the adsorption behavior of surfactants with different structures on the lignite surface at the molecular level. The reasons for the differences in the wettability adsorption of sodium dodecyl sulfate (SDS), sodium dodecyl benzene sulfonate (SDBS), fatty alcohol polyoxyethylene ether-9 (AEO-9), and alkyl polyglycoside (APG1214) on the lignite surface were also investigated based on the quantum chemical calculations and macroscopic experimental analysis. The results showed that the adsorption orientation of surfactant molecules at the solid–liquid interface exerted a pivotal influence on the surface wettability of lignite. According to molecular orbital and electrostatic potential analysis, surfactant molecules with LUMO distributed in the tail chain were more inclined to form a positive adsorption orientation than that concentrated in the polar headgroups; and the stronger the interaction between the polar headgroups and the coal surface with the like charge, the more stable the adsorption of surfactant molecules with the positive arrangement at the interface was. Furthermore, the stronger potential difference between SDS molecules and the hydroxyl-rich structure of the APG1214 molecules are conducive to the formation of hydrogen bonds with water molecules. Wettability experiments showed that the ability of surfactants to improve the wettability of coal dust was positively correlated with the adsorption orientation.

Novel benzene sulfonate surfactants: Alkyl-tetralin sulfonates synthesized via coal chemical route

Benzene sulfonate surfactants are crucial anionic surfactants, commonly derived from petrochemical sources. Herein, we present a new method for synthesizing alkyl-tetralin sulfonate anionic surfactants using α-olefins (n-hexene, n-octene, n-decene) and tetralin sourced from the coal chemical industry as raw materials. The three-resulting alkyl-tetralin sulfonates (C6-THNS, C8-THNS and C10-THNS), obtained by alkylation and sulfonation of tetralin were characterized through HPLC, FTIR, LCMS and 1H NMR techniques. Their surfactant properties were also investigated and compared with commercially applied linear alkylbenzene sulfonate (LAS). We observed that C6 alkyl-tetralin sulfonate (C6-THNS) exhibited smaller critical micelle concentration (CMC=0.60 mM) and lower equilibrium surface tension (γCMC=33.43 mN/m). Similarly, C6-THNS also showed comparable foaming, wetting and emulsifying properties with LAS, which can be used as a substitute for LAS surfactants. This study shows that the synthesized alkyl-tetralin sulfonates is a potential surfactant, providing a route for efficiently using coal-based chemicals to synthesize surfactants.

Efficient and Sustainable Removal of Linear Alkylbenzene Sulfonate in a Membrane Biofilm: Oxygen Supply Dosage Impacts Mineralization Pathway

Linear alkylbenzene sulfonate (LAS) can be thoroughly mineralized within sufficient oxygen (O2), but which is energy intensive and may causes serious foaming problem. Although cometabolism can achieve efficient LAS removal within a wide range of O2 dosages, how O2 dosage systematically affects LAS metabolic pathway is still unclear. Here, membrane aerated biofilm reactor (MABR) enabled accurate O2 delivery and bulk dissolved oxygen (DO) control. MABR achieved efficient removal of LAS (> 96.4%), nitrate (> 97.8%) and total nitrogen (> 96.2%) at the three target DO conditions. At high DO condition (0.6 mg/L), LAS was efficiently removed by aerobic mineralization (predominant) coupled with aerobic denitrification biodegradation with the related functional enzymes. Pseudomonas, Flavobacterium, Hydrogenophaga, and Pseudoxanthomonas were dominant genus contributing to four possible LAS aerobic metabolic pathways. As O2 dosage reduced to only 29.7% of the demand for LAS mineralization, O2 facilitated LAS activation, benzene-ring cleavage and a portion of respiration. NO- 3-N respiration-induced anaerobic denitrification also contributed to ring-opening and organics mineralization. Desulfomicrobium and Desulfonema related two possible anaerobic metabolic pathways also contributed to LAS removal. The findings provide a promising strategy for achieving low-cost high LAS-containing greywater treatment.

Effect of salt ions (Na+, Ca2+ and Mg2+) and EOR anionic and nonionic surfactants on the dispersion stability of cellulose nanocrystals

The application of cellulose nanocrystals (CNCs) in enhanced oil recovery (EOR) is a developing hotspot. To improve the stability of CNCs in salt environments, the effects of sodium dodecylbenzene sulfonate (SDBS) and polyoxyethylene sorbitan monooleate (Tween 80) on the stability of CNCs in the presence of sodium (Na+), calcium (Ca2+) and magnesium (Mg2+) were investigated. The range of salt ions and the stability mechanism for improving the CNCs stability in the presence of SDBS and Tween 80 were pointed out. SDBS improved the stability of CNCs in the presence of 30–100 mM Na+, 1–2 mM Ca2+ and 2 mM Mg2+, respectively. Tween 80 improved the stability of CNCs in the presence of Na+ ≤ 300 mM, Ca2+ ≤ 10 mM and Mg2+ ≤ 10 mM, respectively. The mechanism was explained by the bridging effect of salt ions, electrostatic effect and spatial stability effect. The combined systems of surfactants (SDBS and Tween 80) with CNCs exhibited strong emulsifying properties, low interfacial tension (0.023 mN/m and 1.85 mN/m), and the ability to alter the wettability of oil wet rocks. This made the combined systems have better oil displacement performance.

Mussel-inspired co-deposition of catechol-amine and graphene oxide (GO) modified anion exchange membranes (AEMs) for antifouling

Mussel-inspired co-deposition has many applications in surface modification of polymer membranes. Organic fouling of ion exchange membranes is one of the common issues that hinder electrodialysis treatment of industrial wastewater. In this work, anion exchange membranes were surface-modified by the mussel-inspired co-deposition of catechol-amine and graphene oxide (GO) nanosheets. Results showed that co-deposition with catechol (CA) and m-phenylenediamine (MPD) as reactant monomers rapidly generated modifying layer on the AEM surface. And the addition of GO into co-deposition helped improve the homogeneity and reduce polymer particle aggregation. The synergistic effect of catechol-amine and GO nanosheets was beneficial to form uniform modifying layer with improved hydrophilicity and negative charge density of membrane surface. In eletrodialysis experiments with sodium dodecyl benzene sulfonate (SDBS) as model foulants, GO-CA-MPD-3h modified AEM maintained high desalination rate close to that without folants, indicating good modifying antifouling performance. Mussel-inspired co-deposition of catecholamines and functional materials give new insights into membrane modificatin through a feasible and cost-effective method

Multi-scale evaluation of surfactant effects on asphalt desorption behavior from oil sand surfaces

This study created a hydrophobic oil sand model to investigate the impact of surfactants on the desorption behavior of asphalt from solid surface. Cationic surfactant cetyl trimethyl ammonium bromide (CTAB) and anionic surfactant sodium dodecyl benzene sulfonate (SDBS) were used to soak the model to observe the effect of surfactants on asphalt desorption. The effect of surfactant pretreatment on the wettability of the substrate was evaluated by measuring the contact angle of ultrapure water on the substrate and observing the morphological changes of the solid surface by atomic force microscopy. The results show that the contact angle of the model treated with SDBS decreases to 10° after 3 days, which significantly improves the wettability of the substrate surface and promotes the desorption of asphalt. However, CTAB has no obvious effect on asphalt desorption. The standard deviation of the gray value of the sand surface image is significantly reduced to 38.693 after the SDBS treatment, which can be seen by binarizing the image. This suggests that the asphalt and solution are evenly distributed and that there is hardly any discernible boundary. Nevertheless, neither of the two surfactants can improve the water-based extraction efficiency of oil sands after soaking treatment. The asphalt yield is less than 5% after 30 days of pretreatment with CTAB solution, while only 45% asphalt yield is obtained after 30 days of pretreatment with SDBS solution. Despite these variations, the quality of asphalt foam remains relatively the same. This may be related to the failure of surfactants to improve the surface wettability of hydrophobic sand. Therefore, the surface wettability of the sand is considered to be a key factor affecting the asphalt desorption and final yield. This study can provide a scientific basis for oil sand recovery to a certain extent.

Effect of novel non-inhibitor slurry on chemical mechanical polishing properties of copper interconnect copper film based on experiments and theoretical calculations

In order to simplify the component of copper slurry during chemical mechanical polishing (CMP) and improve the surface corrosion inhibition efficiency, anionic surfactant dodecylbenzene sulfonic acid (DBSA) and nonionic surfactant decyl glucoside (DG) as mixed surfactants were used instead of inhibitors, and the corrosion inhibition properties were thoroughly studied by experiments and theoretical calculations. Polishing experiments and surface morphology tests show that the mixed surfactants can effectively enhance the surface quality after CMP compared with traditional inhibitor TAZ. Electrochemical experiments show that DG and DBSA can form a dense passivation film on the Cu surface to prevent corrosion. The inhibition efficiency of mixed surfactants is as high as 95 %. The theoretical calculations indicate that DBSA and DG form a stable long-chain structure, which leads to a higher adsorption energy, a denser passivation film, and stronger corrosion inhibition, in agreement with the experimental findings. These studies confirmed the stronger inhibitory effect of mixed surfactant on Cu film CMP and provided a new reference for the design of simplified slurry without inhibitor components.

Solvent-induced modulation of sensitivity and selectivity in the self-assembly of tetracationic cyclophanes with cholesterol sulphate, sodium dodecyl sulfate, and sodium dodecyl benzene sulfonate: Observations of significant shifts

Cyclophane CP-1 demonstrates markedly distinct sensitivities toward Cholesterol sulfate (CH-S), Sodium Dodecyl Sulfate (SDS), and Sodium Dodecyl Benzene Sulfonate (SDBS) when the solvent is shifted minimally from a 95 % to a 98 % HEPES-DMSO mixture. In a 98:2 HEPES-DMSO mixture, CP-1 engages in highly selective self-assembly with CH-S, which is characterized by aggregation-induced emission enhancement (AIEE) in contrast to other steroidal sulfates such as pregnenolone sulfate (PRG-S), dehydroisoandrosterone sulfate (DIAND-S), taurocholic acid (TACH-S), and the surfactants SDS and SDBS. This assembly results in an approximate 40-fold increase in fluorescence intensity with three equivalents of CH-S and allows for the detection of concentrations as low as 200 nM under physiological conditions. Dynamic light scattering (DLS) studies illustrate the aggregation of CP-1 and CH-S, with the zeta potential of each shifting from negative values to nearly zero in a 1:2 CP-1:CH-S mixture, indicating self-assembly. This aggregation behavior is reversible, as demonstrated by a corresponding decrease and then increase in fluorescence intensity with temperature variations from 25 °C to 70 °C and back to 25 °C. Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) analyses show that CP-1 forms aggregates ranging from 100 to 180 nm, which increase to 150–250 nm upon interaction with CH-S. In a 95:5 HEPES-DMSO mixture, CP-1 exhibits a stronger AIEE response with SDS and SDBS compared to CH-S. Cyclophane CP-2, when dissolved in binary DMSO-water mixtures with water content exceeding 80 %, shows similar AIEE phenomena and undergoes selective fluorescence quenching with SDS and only a 50 % increase in fluorescence intensity with CH-S, irrespective of the HEPES concentration (95 % or 98 %).

Stabilization strategies for granite waste powder applied in sustainable pavement subgrade: Mechanical and durability performance

The sustainable and efficient treatment of massive granite waste powder (GWP) has received increasing attention. This study proposes a novel method for recycling GWP cemented by inorganic binder-stabilized materials (IBSM) for sustainable pavement subgrade filler, i.e., IBSM-stabilized GWP (ISG). IBSM consists of Portland cement (PC), quicklime (QL), ground granulated blast furnace slag (GGBS), and sodium dodecyl benzene sulfonate (SDBS). Response surface methodology (RSM) and microstructure analysis were employed to analyze the effects of IBSM components on ISG mechanical properties and durability. The 56d compressive strength of ISG is above 2.62 MPa, meeting the minimum criterion of 1 MPa. The residual strength coefficient after 5 freezing-drawing cycles is generally greater than 65 %, except for the groups with high QL content. Both PC and GGBS are positively correlated with the performance of ISG. Moreover, multi-objective optimization identifies the optimal mix ratio: 3.03 % PC, 0.83 % QL, 3.47 % GGBS, and 0.18 % SDBS. The optimal ISG presents excellent strength and durability performance, with S7d of 1.61 MPa, S56d of 3.88 MPa, Sw of 3.35 MPa, Rftc of 90 %, Rwdc of 92.01 %. These findings provide insight into the stabilization strategies of GWP using in highway subgrade filler, which can alleviate the environmental pollution induced by GWP waste.

Surfactant-Assisted Regulation of WS2/Tourmaline Microstructures for Excellent Photocatalytic Performance

The controllable electrical and optical properties of two-dimensional tungsten disulfide (WS2) attracted much attention in photocatalysis, but commercial development has been severely restricted by their restacking properties. Surfactant-assisted synthesis techniques can be considered as an effective option to break this bottleneck. In this work, the effect of surfactants including sodium dodecylbenzene sulfonate (SDBS), hexadecyltrimethylammonium bromide (CTAB), and polyvinylpyrrolidone (PVP) on the microstructure of WS2/tourmaline composites prepared by coupled hydrothermal and calcination methods was explored. The WS2 nanosheets were uniformly deposited on the tourmaline surface with the assistance of 1.0 mmol/L SDBS. Meanwhile, WS2/Tour-SDBS exhibited the highest rhodamine B (RhB) degradation activity, which was 1.8 and 2.3 times higher than that of photocatalysts prepared with CTAB and PVP under the same conditions, respectively. This study provides a new tactic for the fabrication of high-performance WS2-based composites.

New insights into the inhibition performance and mechanisms of sodium dodecyl benzene sulfonate (SDBS) on nitrogen removal in activated sludge-biofilm system

To investigate the effect of sodium dodecyl benzene sulfonate (SDBS) on nitrogen (N) removal performance and biological mechanisms, a gradient of SDBS concentrations was introduced into a set of sequencing batch biofilm reactors (SBBRs). The results indicated that a negative correlation was observed between SDBS concentration and the removal efficiencies of chemical oxygen demand (COD), ammonia nitrogen (NH4+-N), and nitrate nitrogen (NO3−-N). Compared to the control group, their removal efficiencies were the lowest (decreases of 11.83 %, 12.15 %, and 8.11 %) when SDBS concentration was 1.67 mg (g MLSS) -1 (5 mg L−1). High-throughput sequencing showed that the abundance of Proteobacteria remained stable with SDBS addition, while the abundances of Patescibacteria and Actinobacteria decreased by 0.67–0.70 % and 0.69–3.06 %, respectively. Moreover, SDBS reduced both microbial diversity and richness and hindered the interspecific relationships among microorganisms. It also inhibited N metabolic activities and led to a decrease in the expression of key functional genes involved in N transformation (nifD, nifH, nasA, norB, norC, and nosZ). Additionally, the abundances of key enzymes (EC:1.7.99.1, EC:1.7.2.4, and EC:1.1.1.42) in the N and tricarboxylic acid (TCA) cycles decreased following the addition of SDBS. This study provided insights into the effects of SDBS on N removal in activated sludge-biofilm systems and the adaptive responses of microbial communities to SDBS exposure.

Exploring the Recognition Mechanism of Surfactant-Cyclodextrin Complex Formation: Insights from SPR Studies on Temperature and Ionic Liquid Influence.

This study examines the kinetics and thermodynamics of the inclusion complex (IC) formation between sodium dodecylbenzenesulfonate (SDBS) and amine-modified β-cyclodextrin (βCD-NH2) using surface plasmon resonance (SPR) and theoretical analysis. We determined a binding constant of 103 L mol-1 for the thermodynamically stable complex ([βCD-NH2/SDBS]°) within the temperature range of 285.2-301.2 K. The thermodynamic analysis revealed a transition from entropy-driven to enthalpy-driven behavior with increasing temperature. The rate constant for IC formation was approximately 102 M-1 s-1, with the residence time decreasing from 14.08 s at 285.2 K to 6.13 s at 301.2 K. We observed the formation of an activated complex ([βCD-NH2/SDBS]‡), with energetic parameters indicating temperature dependence. At 285.2 K, the activated enthalpy change was positive, while at 301.2 K, it was negative. The dissociation energetic parameters remained temperature-independent. Additionally, increasing concentrations of the ionic liquid 1-butyl-3-methylimidazolium chloride influenced the SDBS tail's conformation and penetration into the βCD-NH2 cavity at the activated state. These findings provide insights into the complexation mechanism and the effects of the temperature and ionic liquids on IC formation.

Hydrophobic and positively charged magnetic nanoparticles for enhanced oil recovery from concentrated emulsion wastewaters

With the development of petroleum industry, a large amount of oil-in-water (O/W) emulsion wastewaters were produced, resulting in serious environmental pollution and resource waste. Up till now, magnetic nanoparticles (MNPs) were frequently reported in emulsion wastewater treatment and mainly focused on the water purification, but little effort was devoted to the facile recovery of oil resource. In the present work, a class of hydrophobic and positively charged MNPs, namely dimethyloctadecyl [3-(trimethoxysilyl) propyl] ammonium chloride (DOTAC)-coated MNPs (M−DOTAC), was carefully synthesized by regulating DOTAC anchoring density on Fe3O4@SiO2, and then employed to treat the concentrated emulsion wastewaters stabilized by anionic sodium dodecyl benzene sulfonate (SDBS) or nonionic Tween-80. M−DOTAC with relatively high DOTAC density (M−DOTAC 1.8) exhibited higher positive charge density and hydrophobicity, and hence could significantly promote the oil droplet coalescence and mergence via the electrostatic attraction and hydrophobic adsorption bridging as well as the hydrophilic-lipophilic transition of interfacial adsorption layer. Accordingly, with addition of moderate dosage of M−DOTAC 1.8, the emulsion was broken and divided into three layers: (1) a continuous oil layer was formed in the upper layer which could be directly recycled; (2) the middle layer was composed of MNPs-tagged oil droplets/flocs; (3) the bottom layer was the clearer water phase. The optimal recovery rate of oil resource reached ∼ 60 % in SDBS stabilized system, and further increased to ∼ 98 % in Tween-80 stabilized system. However, the oil recovery rate was declined at an excessive dosage of M−DOTAC 1.8 due the formation of double emulsion. Besides, M−DOTAC 1.8 exhibited good reusability. These results indicated the fabricated M−DOTAC had great application prospect in treating emulsion wastewaters containing high oil content.

Management of zooplanktonic predations for efficient and sustainable production of Arthrospira

Arthrospira, commonly known as Spirulina in the commercial sector, is the most produced algae globally. A significant challenge in Arthrospira mass cultivation is zooplankton contamination, which might result in an annual loss of up to 30 % in biomass productivity if the zooplanktonic predation is not managed. This study, based on comprehensive field tests conducted in 1000 m2 raceway ponds, demonstrates the feasibility of using sodium dodecyl benzene sulfonate (SDBS) as a pesticide for managing zooplanktonic predators in Arthrospira mass cultivation. Under compensatory SDBS application, planktonic predators such as rotifers and ciliates are completely eliminated. This involves an initial application of SDBS at 15 mg L−1 followed by an additional enhancement of 5 mg L−1 after 24 h. Early detection of the contamination and apply the SDBS pesticide as soon as possible by a compensatory manner is beneficial for a better management of the contaminations. The findings provide a novel approach for managing zooplanktonic predations and ensuring efficient and sustainable production of Arthrospira.