Insights into Zwitterionic Surfactant Interactions at the Oil-Water Interface by Interferometry Experiments and MDS Calculations.

In this work, the interaction performance of zwitterionic surfactant [dodecyl dimethyl sulfopropyl betaine (DSB-12) and hexadecyl dimethyl sulfopropyl betaine (DSB-16)] at the n-octadecane oil surface is investigated from experimental and simulation insights. For a macroscopic experiment, interfacial interferometry technology was developed for real-time monitor interaction performances and to obtain the quantitative interfacial thickness and mass results. The Langmuir model was characterized by thermodynamic analysis, deducing the aggregation spontaneity of DSB-16 > DSB-12 with ΔGagg(DSB-16) = -5.94 kJ mol-1 < ΔGagg(DSB-12) = 24.08 kJ mol-1. A three-step dynamic model (adsorption, arrangement, and aggregation) was characterized by kinetic analysis, indicating arrangement process as slow-limiting step with k2(arr) < k1(ads), k3(agg). For microscopic simulation, and molecular dynamic (MD) method was utilized to theoretically investigate interaction performances and obtain the interfacial configuration and energy results. The interaction stability and interaction strength were indicated to be DSB-16 > DSB-12 with differences of final energy ΔEfin = 48-88 kcal mol-1. The interaction mechanism was explained by proposing the model of "response enhancement" and "deposition activity" for DSB-16 interactions, and "response decrease" and "elution activity" for DSB-12 interactions. The different performances can be attributed to the different interaction forms and forces of surfactants. This work provided a platform for performance and mechanism investigation between the surfactant molecule and oil surface, which is of great significance in reservoir exploitation and enhanced oil recovery (EOR).

Investigation of Oil-Water Separation on an F-SiO2/TiO2-Based Superhydrophobic/Superoleophilic Surface: Experiment Evaluation and MD Simulation.

Experiment evaluation and mechanism analysis of separation performance are crucial for oily wastewater treatment. In this work, a fluorinated superhydrophobic/superoleophilic (F-SHPB/SOPL) surface was fabricated on a steel mesh substrate by double depositions of SiO2-TiO2 nanoparticles for high-roughness improvement and composite modification of fluorine-alkyl groups for low-energy achievement. Measurements of SEM, XPS, FTIR, laser scanning confocal microscope (LSCM), and excitation-emission matrix (EEM) were carried out for surface property characterization. The oil-water separation performances at the prepared F-SHPB/SOPL surface were investigated from experimental and simulation aspects. Separation tests, flux tests, and anti-contamination tests were performed by experimental methods. The results indicated that the surface showed excellent separation efficiencies (>99.2%) for oil-water mixture and oil-in-water emulsion, high permeate flux (>3000 L·m-2·h-1) for organic oils, and perfect anti-pollution/self-cleaning capacity for liquid and solid contaminations. The interaction energies and interaction distances were measured by ab initio molecular dynamics simulation (AIMD) simulations. With lower interaction energy (Eoil = -456.52∼-1044.22 eV) than that of water molecules (Ewater = -172.73 eV) and shorter distance (Doil = 4.42∼5.13 Å) than that of water molecules (Dwater = 11.49 Å), oil molecules showed higher interaction stability than water molecules on the F-SHPB/SOPL surface. The calculation revealed the essence of the oil-water separation phenomenon. This work not only proposes the fabrication methodology of the SHPB/SOPL material but also elucidates the intermolecular interaction for oil-water separation. The results can provide a fundamental basis for separation operation and removal treatment in industrial and domestic applications.

Insight into Organic Pollutant Adsorption Characteristics on a g-C3N4 Surface by Attenuated Total Reflection Spectroscopy and Molecular Dynamics Simulation.

Herein the adsorption characteristics of zwitterionic dye pollutant Rhodamine B (Rh+B-) on a g-C3N4 surface were investigated by both an attenuated total reflection spectroscopy (ATRS) experiment and a molecular dynamics simulation (MDS). For experimental investigation, g-C3N4 was coated on a silica optical fiber (SOF) surface to fabricate an adsorption film. According to the ATRS response, adsorption thermodynamics and thermodynamics results were in situ obtained and evaluated. The isothermal Langmuir model was used to calculate the adsorption equilibrium constants (Kads) and adsorption energies (ΔGads) for Rh+B- as 27.25 × 104 M-1 and -31.01 kJ mol-1, respectively, which indicated the spontaneous adsorption behavior of Rh+B- at the g-C3N4 surface. Using dynamic Elovich modeling, the rate constants of Rh+B- were found to be k1 = 0.0063 min-1 and k2 = 0.0004 min-1, which indicated two-stage adsorption at the g-C3N4 surface. For theoretical simulation, adsorption configurations and adsorption energies were systematically calculated by a molecular dynamics simulation (MDS) . Rh+B- molecules were inclined to orient in a parallel position at the g-C3N4 surface during low concentration but a perpendicular position at the g-C3N4 surface during high concentration. Combined with experimental and calculation results, this work revealed the microscopic adsorption performance and elucidated the intermolecular interaction between localized interfaces of g-C3N4 and hazardous dye pollutant. We propose an adsorption model to explain the process of surface interaction, which is based on molecular orientation and a force-driven mechanism. Electrostatic attraction and π-π interaction dominated the adsorption interaction with an adsorption energy of ΔGlow(ads) = -38.96 kJ mol-1 for low Rh+B- concentration, and electrostatic attraction dominated the adsorption interaction with an adsorption energy of ΔGhigh(ads) = -25.76 kJ mol-1 for high Rh+B- concentration. This work can provide a fundamental basis for a dye-pollutants removal application by g-C3N4 in both adsorption and photocatalyzation.

Insight into the Synergistic Effect of Adsorption-Photocatalysis for the Removal of Organic Dye Pollutants by Cr-Doped ZnO.

The adsorption of dye molecules is an important process for the photodegradation removal of dye pollutants. In this work, a semiconductor photocatalyst of Cr-doped ZnO nanorods (Cr-ZnO NRs) was synthesized, and its adsorption-photocatalysis synergy (APS) effect was investigated for anionic methyl orange (MO-) and cationic methylene blue (MB+). The detailed thermodynamic information (including adsorption maximum capacity qmax, adsorption equilibrium constant Kads and adsorption efficiency AE %) and dynamic information (including adsorption rate constant ka, degradation rate constant kd and degradation efficiency DE %) were obtained to evaluate the different reaction performances for MO- and MB+. With qmax(MB+) = 40.59 mg g-1 > qmax(MO-) = 15.95 mg g-1, ka(MB+) = 20.61 min-1 > ka(MO-) = 4.62 min-1, and AE(MB+) = 40% > AE(MO-) = 9%, Cr-ZnO NRs showed much superior adsorption performance for MB+ than MO-. With kd (MB+) = 0.0430 min-1 > kd (MO-) = 0.0014 min-1 and DE(MB+) = 98% > AE(MO-) = 20%, Cr-ZnO NRs also showed much superior photodegradation performance for MB+ than MO-. The APS mechanism of Cr-ZnO NRs is revealed to be multiple π-π interactions and stronger electrostatic attractions dominant for enhanced adsorption of MB+ and higher AE and more photocatalytic active species dominant for enhanced photodegradation of MB+. The APS was furthermore characterized and verified by zeta potential analysis, Fourier transform infrared investigation, and fluorescence imaging. The results indicate that Cr-ZnO NRs are promising adsorbent and photocatalyst candidates favorable for positive MB+ than negative MO-. Such an APS investigation can effectively help to improve the photodegradation treatment performance of photocatalysts for dye pollutant removal.

Preparation of poly-dopamine-silk fibroin sponge and its dye molecular adsorption.

This paper proposes a process for fabricating a poly-dopamine-silk fibroin sponge (PDA-SF) by using dopamine self-assembly and coating the skeleton of a silk fibroin sponge. The PDA-SF sponge was characterized by SEM, TEM, XPS, XRD and FT-IR. It was found that the sponge exhibits sheet structures with a pore size of 60 ± 20 µm and poly-dopamine adhered to the surface of pure silk fibroin through noncovalent bond forces. With a hierarchical porous structure, the derived sponge provides fast flow channels and abundant active sites, which will benefit the diffusion and removal of cationic dyes. Batch adsorption and dynamic adsorption of crystal violet (CV) were studied. The batch adsorption capacity of the PDA-SF sponge for CV increased with its PDA content. Under a dynamic adsorption mode, the adsorption efficiency of the PDA-SF sponge for CV (5 mg/L, 200 mL) can reach up to 98.2% after 12 min, whereas it is only 90.2% under stationary mode after 72 h. Furthermore, the sponge shows an outstanding smart adsorption performance. More importantly, the composite sponge still keeps high separation and adsorption efficiencies after 20 cycles, and the appearance remains good.

In Situ Measurement of Depletion Caused by SDBS Micelles on the Surface of Silica Particles Using Optical Tweezers.

Dual-trap optical tweezers have been used to directly measure the interaction forces between two silica particles upon controlling the concentration of the ionic surfactant sodium dodecylbenzenesulfonate (SDBS). By capturing two silica particles in one spot optical trap and one linear optical trap and controlling the linear trap to bring one particle to approach another sufficiently closer, the interaction forces between these two particles can be measured as the separation distance changes. Results showed that with increasing concentrations of SDBS, the interaction force between the two silica particles emerges at closer surface distance between two silica particles. Only repulsive force exists between silica particles below the critical micelle concentration (cmc) of SDBS and it could be well-fitted using the classical Derjaguin-Landau-Verwey-Overbeek (DLVO) theory. However, the depletion attraction force appears above the cmc of SDBS which is induced by the generation of SDBS micelles. By in situ measurement of the interaction force between two silica particles in the presence of different concentrations of SDBS, the depletion force can be quantitatively calculated.

Insight into the Adsorption-Interaction Mechanism of Cr(VI) at the Silica Adsorbent Surface by Evanescent Wave Measurement.

The investigation of adsorption performance at the adsorbent surface can help to reveal the treatment mechanism and improve the treatment efficiency of adsorption technology for heavy metal ions (HMIs). This work developed a methodology to investigate the adsorption behavior of HMI Cr(VI) at the silica surface by confined near-field evanescent wave (CNFEW) measurement. A silica optical fiber (SOF) was used as the adsorption substrate and light waveguide element to integrate both Cr(VI) adsorption and CNFEW production on its surface. According to the sensitive CNFEW response, the adsorption behavior of Cr(VI) was in situ monitored and real-time evaluated. The thermodynamic information of adsorption equilibrium constant (Kads) and adsorption free energy (ΔG) and dynamic information of the apparent adsorption rate (vads) and adsorption time (tads) were obtained through Langmuir isotherm and kinetic fitting, respectively. Different reaction performances between Cr(VI) and adsorption sites were successfully differentiated, evaluated, and characterized. A site-decided-mechanism was therefore presented to describe the surface interaction process for Cr(VI), which including fast adsorption on type I Si-O- site through electrostatic attraction with [Formula: see text] and slow adsorption on type II Si-OH site through coordinative interaction with ΔGSiOH-Cr(VI)II = -26.18 kJ mol-1. The adsorption mechanism of Cr(VI) at the SOF silica surface was furthermore verified by zeta potential analysis, Fourier transform infrared investigation, and fluorescence imaging. Unlike conventional ex situ or in bulk detection, the present CNFEW-based approach targets the "localized" adsorption of Cr(VI) adsorbed to the solid adsorbent surface. Consequently, our work favorably constructs a surface platform and provides new insights on understanding the adsorption mechanism for HMIs.

Preparation of a selective flocculant for treatment of oily wastewater produced from polymer flooding and its flocculant mechanism.

There are residual polymers in the oily wastewater produced from polymer flooding (OWPF); keeping the residual polymer in the water during the flocculation is meaningful and challenging. In this paper, a selective flocculant (denoted as PDC10) which can remove the oil while keeping partially hydrolyzed polyacrylamide (HPAM) in water was prepared by copolymerization of decyl two methyl vinylbenzyl ammonium chloride (C10MVBA) and dimethyl aminopropyl methacryamide (DMAPMA). By using oil removal and HPAM retention as evaluation indexes, the synthesis condition of PDC10 was optimized. The optimum PDC10 exhibited oil removal of 98.0% and HPAM retention of 80.5%. Its HPAM retention is much higher than that of a regular cationic flocculant. Measurements of zeta potential, interfacial tension, interfacial dilational modulus and a dual polarization interferometry (DPI) test were carried out for investigating the flocculation mechanism of PDC10. The mechanism of PDC10 was that it can bridge and flocculate oil droplets by electrostatic interaction and hydrophobic interaction. It also preferred to distribute at the interface, and its interaction with HPAM in bulk water was weak, which confirms its selective flocculation properties.

Real-Time Monitoring of Azo Dye Interfacial Adsorption at Silica-Water Interface by Total Internal Reflection-Induced Surface Evanescent Wave.

An interface research method based on total internal reflection induced evanescent wave (TIR-EW) is developed to monitor the adsorption behavior of azo dye at the silica-water interface. The monitoring system is constructed by employing silica optical fiber (SOF) as both charged substrate for dye adsorption and light transmission waveguide for evanescent wave production. According to the change of evanescent wave intensity and followed by Beer's law, the methylene blue (MB) adsorption behavior can be real-time monitored at the silica-water interface. Langmuir adsorption model and pseudo-first-order model are applied to obtain the related thermodynamic and kinetic data. The adsorption equilibrium constant ( Kads) and adsorption free energy (Δ G) of MB at the silica-water interface are determined to be (3.3 ± 0.5) × 104 M-1 and -25.7 ± 1.7 kJ mol-1. Meanwhile, this method is highlighted to isolate elementary processes of adsorption and desorption under steady-state conditions, and gives adsorption rate constant ( ka) and desorption rate constant ( kd) of 8585 ± 19.8 min-1 and 0.26 ± 0.0006 min-1 for 15 r/min flow rate. The surface interaction process is revealed and adsorption mechanism is proposed, indicating MB first adsorbed on Si-O- sites through electrostatic attraction and then on Si-OH sites through hydrogen bond with increasing MB concentrations. Our findings from this study provided molecular-level interpretation of azo dye adsorption at silica-water interface, and the results provide important insight into how MB adsorption can be controlled at the interface.

Characterization and differentiation of the adsorption behavior of crystal violet and methylene blue at the silica/water interface using near field evanescent wave.

Different molecular structures lead to different adsorption performances. In this work, the adsorption behavior of two organic dyes, namely, crystal violet (CV, triphenylmethane dye of symmetric structure) and methylene blue (MB, azo dye of linear structure), were investigated, characterized and differentiated at the silica/water interface using the total internal reflection induced near field evanescent wave (TIR-NFEW) platform. According to the change in the evanescent wave intensity and following Beer's law, the adsorption behaviors of CV and MB can be monitored real time and sensitively. On one hand, the Langmuir adsorption model was applied to obtain the related thermodynamic data (including adsorption equilibrium constant (Kads) and adsorption free energy (ΔG)). With ΔG(MB) = -25.7 ± 1.7 kJ mol-1 < ΔG(CV) = -21.5 ± 0.6 kJ mol-1 < 0, the linear MB showed a higher spontaneous adsorption ability than the symmetric CV at the silica/water interface. On the other hand, a two-step adsorption kinetic model was applied to obtain the dynamics data including the linear adsorption rate constant (k1) and the exponential adsorption rate constant (k2). With k1(CV) < k1(MB) and k2(CV) ≈ k2(MB), MB diffused faster than CV at the first diffusion step but had nearly the same interaction speed as CV in the second adsorption step. A molecular-aligned-mechanism was successfully proposed to describe the interfacial interaction process for both CV and MB that includes molecular reactions involving electrostatic attraction of type I SiO- and H-bonds of type II SiOH. This work provides new insights into the molecular-level interpretation of the adsorption of the azo and triphenylmethane dyes at the silica-water interface.

Real-time measurement of the crystal violet adsorption behavior and interaction process at the silica-aqueous interface by near-field evanescent wave.

The interfacial adsorption and interaction of crystal violet (CV) at the silica-water interface was real-time measured based on a total-internal-reflection-induced near-field evanescent wave (TIR-NFEW). A silica optical fiber (SOF) was employed as a charged substrate for CV adsorption and as a light transmission waveguide for evanescent wave production for the investigation system. According to the change of evanescent wave intensity, the CV adsorption behavior could be real-time monitored at the silica-aqueous interface. The Langmuir adsorption model and two kinetic models were applied to obtain the related thermodynamic and kinetic data, including the adsorption equilibrium constant (Kads) of (5.9 ± 1.5) × 104 M-1 and adsorption free energy (ΔG) of -21.6 ± 0.6 kJ mol-1. Meanwhile, this method was shown to be able to isolate the elementary processes of adsorption and desorption under steady-state conditions, and gave an adsorption rate constant (ka) and desorption rate constant (kd) of 2089 ± 6.96 M min-1 and 0.35 ± 0.0012 min-1 for a 15 rpm flow rate. The surface interaction process was revealed and the adsorption mechanism proposed by a molecular orientation adsorption model with three-stage-concentration, indicating that CV first adsorbed on Si-O- sites through electrostatic attraction, then on Si-OH sites through hydrogen bonding, and lastly on the surface through van der Waals forces with different CV concentrations. This study can provide a molecular-level interpretation of CV adsorption and provides important insights into how CV adsorption can be controlled at the silica-water interface.

Amphiphilic nanosheet self-assembly at the water/oil interface: computer simulations.

In this paper, dissipative particle dynamics simulations are performed to study the interfacial and emulsion stabilizing properties of various systems of amphiphilic nanosheets (ANs) self-assembled at the oil/water (O/W) interface. The ANs have a dimensional symmetry structure that encompasses a triangular-plate at the center and two soft comb-like shells constructed with hydrophilic and hydrophobic polymers. As the simulation results show, the AN molecules are highly oriented in interfacial films with their triangular nanosheets parallel to the O/W interface, while their hydrophobic and hydrophilic segments attempt to immerse into the oil phase and aqueous phase, respectively. These results reveal that the rotation of ANs at oil/water interfaces is greatly restricted, meanwhile, their nanosheet (or planar) configuration facilitates their favorable orientation thereby, thus making the emulsion more stable. At higher concentrations, a wrapped-like or micelle morphology is observed. The O/W emulsions stabilized by ANs were also simulated, and it is interesting to find AN 'patches' at the O/W interface which resembles the leather patches on a football. By introducing the "amphiphilic nanosheet balance" concept, the hydrophilic-lipophilic balance (HLB) values of ANs were calculated. Due to their properties of two-dimensional symmetry, the HLB values of ANs tend to approximately 1 which reveals a stronger stability for emulsions.

Mesoscopic Simulations of Adsorption and Association of PEO-PPO-PEO Triblock Copolymers on a Hydrophobic Surface: From Mushroom Hemisphere to Rectangle Brush.

The dissipative particle dynamics (DPD) method is used to investigate the adsorption behavior of PEO-PPO-PEO triblock copolymers at the liquid/solid interface. The effect of molecular architecture on the self-assembled monolayer adsorption of PEO-PPO-PEO triblock copolymers on hydrophobic surfaces is elucidated by the adsorption process, film properties, and adsorption morphologies. The adsorption thicknesses on hydrophobic surfaces and the diffusion coefficient as well as the aggregation number of Pluronic copolymers in aqueous solution observed in our simulations agree well with previous experimental and numerical observations. The radial distribution function revealed that the ability of self-assembly on hydrophobic surfaces is P123 > P84 > L64 > P105 > F127, which increased with the EO ratio of the Pluronic copolymers. Moreover, the shape parameter and the degree of anisotropy increase with increasing molecular weight and mole ratio of PO of the Pluronic copolymers. Depending on the conformation of different Pluronic copolymers, the morphology transition of three regimes on hydrophobic surfaces is present: mushroom or hemisphere, progressively semiellipsoid, and rectangle brush regimes induced by decreasing molecular weight and mole ratio of EO of Pluronic copolymers.

A miniaturized fiber-optic colorimetric sensor for nitrite determination by coupling with a microfluidic capillary waveguide.

A microfluidic-capillary-waveguide-coupled fiber-optic sensor was developed for colorimetric determination of hazardous nitrite based on the Griess-Ilosvay reaction. The sensor was modularly designed by use of a light-emitting diode as the light source, silica fiber as the light transmission element, and a capillary waveguide tube as the light reaction flow cell. With the light interacting with the azo dye generated by the Griess-Ilosvay reaction between nitrite and Griess reagents, nitrite could be determined by a colorimetric method according to Beer's law. By use of the inexpensive and micro-sized elements mentioned above, the sensor provided a new low-cost and portable method for in situ and online measurement of nitrite. The sensor had a wide linear range for nitrite from 0.02 to 1.8 mg L(-1) and a low detection limit of 7 µg L(-1) (3σ), with a relative standard deviation of 0.37% (n = 10). With a low reagent demand of 200 µL, a short response time of 6.24 s, and excellent selectivity, the sensor is environmentally friendly and has been applied to nitrite determination in different water samples. The results were compared with those obtained by conventional spectrophotometry and ion chromatography, indicating the sensor's potential for practical applications.

Empirical Relationship among the Parameters in HLD Equation of Block Polyether Water Clarifier.

In this work, the empirical relationship among three apparent parameters in the hydrophilic-lipophilic deviation (HLD) equation was studied to provide help in using the HLD equation to design a block polyether water clarifier for treating produced water in an oilfield. Ten block polyethers (including six linear polyethers and four branched polyethers) were prepared, and their HLD equations were measured. By curve fitting, the empirical relationship among apparent hydrophobicity characteristic (K), apparent characteristic curvature (Cc n ), and apparent temperature coefficient (c t) of block polyether were obtained: K = 9.32c t, Cc n = 18e-24.5K (for linear polyether), and Cc n = 3.7e-20.8K (for branched polyether). By introducing these relationships into the HLD equation and combining an empirical relationship between propylene oxide/ethylene oxide (mole ratio) in a block polyether and K/Ccn, a new block polyether was designed to treat the produced water. The treatment result confirmed the reliability of these empirical relationships. The results expand the practical application of HLD theory and are useful for the development of a block polyether water clarifier.

Study on the structure-activity relationship of cationic polyacrylates for the treatment of oilfield produced water.

Cationic polyacrylates exhibit both reverse demulsification and flotation performance, which can avoid incompatibility between the reverse demulsifier and flotation agent during treatment of produced water from offshore oilfields. In our previous work, the effect of the structure of the cationic unit on the reverse demulsification and flotation performance of cationic polyacrylates was studied. However, the structure-activity relationship of cationic polyacrylates has not been systematically studied. In this study, the relationships between the structure (acrylate type, tertiary amine type, mass ratio of acrylate to tertiary amine, and degree of cationicity), interfacial properties (surface tension, interfacial tension, zeta potential, interfacial elastic modulus, interaction force between oil droplets, and film drainage time of an oil-covered bubble), and reverse demulsification and flotation performance of cationic polyacrylates were investigated. A reduction in the elastic modulus of the oil-water interface was the key factor for good reverse demulsification performance, whereas a decrease in the film drainage time of an oil-covered bubble was the key factor for good flotation performance. Ethyl acrylate (EA) was superior to methyl acrylate (MA), and dimethylaminopropyl methacrylamide (DPM) was superior to dimethylaminoethyl methacrylate (DEM). Increases in the mass ratio of ethyl acrylate to dimethylaminopropyl methacrylamide and the degree of cationicity were beneficial for reducing the elastic modulus of the oil-water interface and the film drainage time of an oil-covered bubble. This is the first time that the structure-property-performance relationship of cationic polyacrylates has been systematically studied. A cationic polyacrylate that exhibited both good reverse demulsification performance and good flotation performance is recommended.

Effect of the Surfactant Type on the Demulsification of the W/O Crude Oil Emulsion Produced by Surfactant-Polymer Flooding.

At present, there are many works on the influences of partially hydrolyzed polyacrylamide (HPAM) and surfactant on the stability and treatment of O/W emulsion produced by surfactant-polymer (SP) flooding. However, there are few related reports on the effects of HPAM and surfactant on the demulsification of W/O crude oil emulsion produced by SP flooding. Especially, there is no report on the effect of the surfactant type. In this paper, sodium dodecyl sulfate (SDS), octylphenol polyoxyethylene ether (OP-10), and alkyl C16-18 hydroxypropyl sulfobetaine (HSB1618) were selected as representatives of the anionic surfactant, nonionic surfactant, and zwitterionic surfactant, respectively. Demulsification experiments and interface behavior experiments were conducted to investigate their influences on the demulsification performance of a demulsifier D1. The results showed that the order of the negative effect of the surfactant type on dehydration speed and the dehydration rate of D1 was HPAM + OP-10 > HPAM + HSB1618 > HPAM + SDS. There is no difference in the effect of three surfactants on the conformation adjustment of D1 at the W/O interface, but the properties of the composite W/O interface formed by them and D1 were different. The coalescence time was longest when there were HPAM and OP-10 in water, while the lg(G 1'/G demulsifier')/lgG 1' was the smallest, which led to the most difficult demulsification of W/O emulsion. This work can guide surfactant selection during SP flooding from the perspective of produced fluid treatment.

Treatment of oil-based drilling cuttings by floatation-advanced oxidation two-step process.

In this paper, a floatation-advanced oxidation two-step process was proposed for deep oil removal of oil-based drilling cuttings (OBDC). In the first stage, a novel and simple degreasing solution was prepared and most of the base oil contained by OBDC was removed by flotation; in the second stage, the oil content of OBDC was further reduced by combined ultrasound + ozone (US + O3) advanced oxidation. The recommended degreasing solution was a mixture of methanol, ammonium chloride, and water with a mass ratio of 1.48.1 : 0.25. The best flotation process was as follows: a mass ratio of OBDC to degreasing solution of 1 : 10, stirring speed of 400 rpm and N2 flotation with a flow rate of 400 mL min-1 for 60 min. The oil content of OBDC can be reduced from 14.57% to 1.42% after flotation treatment and the degreasing solution can be reused more than five times. The optimal process of US + O3 advanced oxidation was as follows: a mass ratio of OBDC to water of 1 : 10, ultrasonic power of 1000 W, and an ozone flow rate of 4.0 L min-1 for 100 min. The oil content of OBDC can be reduced from 1.42% to 0.14% after US + O3 treatment at room temperature. The results of this paper provide a new method and idea for OBDC treatment.

Ultrasonication-flotation-advanced oxidation tertiary treatment of oil-based drilling cuttings.

The treatment of oil-based drilling cuttings (OBDCs) with high oil content is difficult. In this study, a tertiary treatment of ultrasonication-flotation-advanced oxidation for treating OBDCs with a high oil content of 20.10 wt% was proposed for the first time. All stages of the treatment processes were optimised. The recommended parameters for ultrasonication at room temperature were a mass ratio of OBDCs to the degreaser of 1:8, an ultrasonication power of 600 W and treatment time of 30 min. After the ultrasonication treatment, the oil content of the OBDCs decreased from 20.10 wt% to 5.00 wt%. Flotation was performed at room temperature with a mass ratio of OBDCs to the degreaser of 1:10, a stirring speed of 400 rpm, an aeration head aperture of 3 µm and airflow rate of 400 mL/min under N2 injection for 60 min. After the flotation treatment, the oil content of the OBDCs decreased from 5.00 wt% to 2.01 wt%. Advanced oxidation was performed at room temperature with a mass ratio of OBDCs to water of 1:10, 3.57 wt% sodium persulphate in water, 4.17 wt% ferrous sulphate heptahydrate in water and ultrasonication power of 1000 W for 100 min. Following the advanced oxidation treatment, the oil content of the OBDCs decreased from 2.01 wt% to 0.58 wt%. The results of this study provide a new method and idea for treating OBDCs with high oil content.

Liquid Metal-Tailored PEDOT:PSS for Noncontact Flexible Electronics with High Spatial Resolution.

Electric field-based noncontact flexible electronics (EF-NFEs) allow people to communicate with intelligent devices through noncontact human-machine interactions, but current EF-NFEs with limited detections (usually <20 cm) distance often lack a high spatial resolution. Here, we report a versatile material for preparing EF-NFE devices with a high spatial resolution to realize everyday human activity detection. Eutectic gallium-indium alloy (EGaIn) was introduced into poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) chains to fabricate this material, named Ga-PP. The introduction of EGaIn successfully regulates the intra- and interchain interactions of PEDOT chains and thus increases the π-electron accumulation on Ga-PP chains, which facilitates improvement of the electron storage of Ga-PP and its noncontact sensing ability. The water solubility of the obtained Ga-PP can reach approximately 15 mg/mL, comparable to that of commercial PEDOT:PSS, thus making Ga-PP suitable for various design strategies to prepare EF-NFE devices. We demonstrate that a conductive textile with a noncontact sensing ability can be achieved by immersing a commercial silk fabric into a Ga-PP solution for 5 min. With a detection distance exceeding 1 m, the prepared Ga-PP-based conductive textile (Ga-PP-CT) possesses outstanding noncontact sensing sensitivity, showing advantages in tracing the locations of signal sources and distinguishing motion states. Surprisingly, even when placed in water, Ga-PP-CT can be used to monitor the movement signals of athletes in different sporting events and output specific noncontact response signals for different sports. Intriguingly, the Ga-PP solution itself can be used to construct noncontact sensing conductive circuits, displaying the potential to be incorporated into smart electronics.