Octylphenol Polyoxyethylene Ether Research Articles

Hydrophilic Chain Length for Octylphenol Polyoxyethylene Ether Adsorption at the n-Hexadecane-Water Interface: Theoretical and Experimental Study.

With the advancement of technologies for developing tight and shale reservoirs, nonionic surfactants have garnered significant attention due to their remarkable properties. The structure of these surfactants plays a crucial role in determining the characteristics of the oil-water interface, particularly influencing emulsification behavior and crude oil recovery. This study investigates the effect of varying the number of hydrophilic polar groups (n = 10, 20, 30, 50) in octylphenol polyoxyethylene ether (OP-n) on its adsorption behavior at the n-hexadecane-water interface using molecular dynamics simulation. The impact of these variations on interfacial properties was further analyzed through measurements of interfacial tension and observations of emulsion droplet morphology. The study results indicate that variations in the number of hydrophilic polar groups significantly affect interfacial properties. Increasing the number of hydrophilic polar groups led to a notable increase in the thickness of the n-hexadecane or water phase, as well as the thickness of the water or oil layer and the surfactant layer. Moreover, when the number of hydrophilic polar groups reached 20, the OP-n molecules exhibited a more curled conformation at the interface, enhancing their ability to encapsulate water and resulting in a decrease in the diffusion coefficient of the molecules in each phase. Additionally, interfacial tension was found to be positively correlated with the number of hydrophilic polar groups and remained unchanged beyond a certain emulsion diameter. This study provides a theoretical basis and reference data for optimizing surfactant structures to improve crude oil recovery.

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.

Effect of Polyoxyethylene-Based Nonionic Surfactants on Chemical–Mechanical Polishing Performance of Monocrystalline Silicon Wafers

The use of surfactants is crucial in the chemical–mechanical polishing fluid system for silicon wafers. This paper examines the impact of the functional group structure of polyoxyethylene-based nonionic surfactants and the variation in the polyoxyethylene (EO) addition number on the polishing performance of monocrystalline silicon wafers, to achieve the appropriate material removal rate and surface quality. The results demonstrated that the straight-chain structure of fatty alcohol polyoxyethylene ether (AEO-9) exhibited superior performance in wafer polishing compared to octylphenol polyoxyethylene ether (OP-9) and isoprenol polyoxyethylene ether (TPEG) and polyethylene glycol (PEG). By varying the number of EO additions of AEO-type surfactants, this study demonstrated that the polishing performance of monocrystalline silicon wafers was affected by the number of EO additions. The best polishing effect was achieved when the number of EO additions was nine. The mechanism of the role of polyoxyethylene-type nonionic surfactants in silicon wafer polishing was derived through polishing experiments, the contact angle, abrasive particle size analysis, zeta potential measurement, XPS, and other means of characterization.

Effect of guar gum on dynamic wetting the fat coal surface with octyl phenol polyoxyethylene ether solution

To study the effect of guar gum (GG) on the surface of octyl phenol polyoxyethylene ether dynamic wetting fat coal, the effect of GG addition concentration on physical parameters, sedimentation rate, contact angle, maximum dimensionless wetting length (Ldw(max)) and maximum dimensionless wetting area (Adw(max)) in mixed dust suppression solutions was studied by experimental and molecular dynamic simulation methods. The results show that adding GG does not significantly alter the mixed dust suppression solution surface tension, but it increases the solution viscosity. When the GG concentration is greater than 0.1%, the viscosity of the mixed dust suppression solution increasing extent becomes larger. The impact wetting experiment and contact angle experiment show that when GG concentration is 0.01%, the mixed dust suppression solution contact angle is the smallest, the Ldw(max) and Adw(max) are the largest, and the solution wettability is the best. Compared with the Ldw(max), the Adw(max) has a smaller standard deviation and higher repeatability. Molecular dynamics simulation shows that after adding a trace amount of GG to the water/OP surfactant/fat coal system, the relative concentration coincidence area and interaction energy absolute value between coal and water in the system increases, the water molecules diffusion coefficient decreases, and the system wettability is further enhanced, which further illustrates the experimental results accuracy.

Adsorption mechanism of alkylphenol ethoxylates surfactants (APEO) on anthracite surface: A combined experimental, DFT and molecular dynamics study

The serious hazards posed by inhalable coal dust to the safety, air purity, and health of coal miners can be effectively alleviated through the use of appropriate dust suppressants. The wetting enhancement capabilities of two dust suppressants, octylphenol polyoxyethylene ether (OP-10) and nonylphenol polyoxyethylene ether (NP-10), were examined in this study through experimental and simulation methods. Macroscopic experiments (surface tension, contact angle, coal dust settling time, and water retention) indicate that the shorter the alkyl chain attached to the benzene ring in the surfactant and the lower the surface tension, the more conducive it is to improving the fluidity and suspension stability of anthracite particles in the wetting solution and further improving the interfacial properties and wetting effect between coal dust and the liquid medium. Mesoscopic experiments (laser particle size, FTIR, XPS, UV–visible spectroscopy, BET, and SEM) showed that the relevant properties of APEO-modified coals were greatly changed, especially the anthracite modified with short-chain alkyl groups of OP-10, which exhibited a stronger aggregation effect on the coal dust particles and increased the pore structure and specific surface area of the coal dust. Additionally, the hydrophilic functional groups are augmented, leading to a notable enhancement in the adsorption capacity of OP-10 on the coal surface. Microscopic simulations (Density Functional Theory calculations, Molecular Dynamics simulations) reveal that APEO surfactants with longer alkyl side chains attached to benzene rings hinder the π-π interactions between the coal's aromatic ring structures and the benzene rings in the surfactants. The surface polarity of coal modified with OP-10 is significantly enhanced, resulting in a more pronounced improvement in wetting performance and an increased water retention capability. The study systematically explores surfactant microstructure effects on anthracite wetting, laying essential groundwork for advanced dust suppression system development.

Synergistic effect of surfactant and 1,10-decanedithiol as corrosion inhibitor for zinc anode in alkaline electrolyte of zinc-air batteries

The self-discharge by corrosion of zinc-air batteries (ZABs) will result in the reduced coulombic efficiency and lower energy efficiency. The additives in electrolyte should not only inhibit the occurrence of self-corrosion during battery dormancy, but also achieve a stable cycle of adsorption–desorption during battery operation, improving the durability of discharge cycles. But the former requires strong binding between additives and zinc to form a dense protective film, while the latter requires easy desorption of additives and zinc without affecting discharge power, which is contradictory to balance. In this study, a dynamic combination of additives and zinc, as well as a design of multi-channel strategy for the corresponding protective layer, have been proposed to solve the issues of self-corrosion and discharge cycle stability. Specifically, the surfactant (octylphenol polyoxyethylene ether phosphate (OP-10P)) and 1,10-decanedithiol (DD) have been selected as the combined anti-corrosion additives in ZABs with concentrated alkaline solution. The synergistic inhibition mechanism and the stabilization mechanism in zinc-air full cells have been studied systematically. The results indicated that the combined inhibitors inhibited the self-corrosion of Zn efficiently in the dormancy, and the inhibition efficiency reached 99.9 % at the optimized proportion. OP-10P achieve the preferential adsorption on the zinc surface, and then the chelates of DD with Zn2+ deposit on the outer layer to form the protective film with fine hydrophobic performance. The stability of ZABs in discharge and charging cycles has been improved owing to the multilayer adsorption film on zinc surface, which retains ion transport channels with the homogeneously pores to weaken the dendrites and side reactions during galvanostatic cycles. A probable model on zinc surface was established to discuss the actual working mechanism.

High-efficiency mechanism of enhancement of spreading performance of oil involving surfactant-laden oil droplet spreading over water surface

This study clarified the high-efficiency mechanism of enhancement of the spreading performance of oil by allowing a droplet of an organic solvent to spread over the surface of water with the addition of oil-soluble surfactants. Firstly, the effect of Span 85, Span 80, Span 20, octylphenol polyoxyethylene (4) ether (OP-4), and sodium dioctyl sulfosuccinate (AOT) on the interfacial parameters of an n-decane droplet was evaluated by measuring the surface tension and interfacial tension. Then the spreading coefficient was calculated to determine whether the surfactant-laden oil droplets could spread at the air–water interface. Moreover, the law governing the spreading of the surfactant-laden oil droplets over water was systematically studied. Furthermore, the characteristics of the dynamic behavior of the surfactants were investigated by molecular dynamics simulations to elucidate the spreading mechanism. The results of the experiments and simulations explained how the oil-soluble surfactants Span 85, Span 80, Span 20, OP-4, and AOT significantly improved the spreading performance of oil droplets over the water surface.

Molecular Mechanism Study on the Effect of Microstructural Differences of Octylphenol Polyoxyethylene Ether (OPEO) Surfactants on the Wettability of Anthracite.

Inhalable coal dust poses a serious threat to coal mining safety, air quality, and the health of miners. Therefore, the development of efficient dust suppressants is crucial for addressing this issue. This study evaluated the ability of three high-surface-active OPEO-type nonionic surfactants (OP4, OP9, and OP13) to improve the wetting properties of anthracite via extensive experiments and a molecular simulation and determined the micro-mechanism of different wetting properties. The surface tension results show that OP4 has the lowest surface tension (27.182 mN/m). Contact angle tests and wetting kinetics models suggest that OP4 exhibits the strongest wetting improvement ability on raw coal with the smallest contact angle (20.1°) and the fastest wetting rate. In addition, FTIR and XPS experimental results also reveal that OP4-treated coal surfaces introduce the most hydrophilic elements and groups. UV spectroscopy testing shows that OP4 has the highest adsorption capacity on the coal surface, reaching 133.45 mg/g. The surfactant is adsorbed on the surface and pores of anthracite, while the strong adsorption ability of OP4 results in the least amount of N2 adsorption (8.408 cm3/g) but the largest specific surface area (1.673 m2/g). In addition, the filling behavior and aggregation behavior of surfactants on the anthracite coal surface were observed using SEM. The MD simulation results indicate that OPEO reagents with overly long hydrophilic chains would produce spatial effects on the coal surface. Under the influence of the π-π interaction between the hydrophobic benzene ring and the coal surface, OPEO reagents with fewer ethylene oxide quantities are more prone to adsorb onto the coal surface. Therefore, after the adsorption of OP4, both the polarity and the water molecule adhesion ability of the coal surface are greatly enhanced, which helps to suppress dust production. These results provide important references and a foundation for future designs of efficient compound dust suppressant systems.

Electromagnetic Shielding Enhancement of Butyl Rubber/Single-Walled Carbon Nanotube Composites via Water-Induced Modification.

Electromagnetic properties of polymer composites strongly depend on the loading amount and the completeness of the filler's dispersive structure. Improving the compatibility of single-walled carbon nanotubes (SWCNTs) with isobutylene butyl rubber (IIR) is a good solution to mitigate aggregation. The change in configuration of poly-oxyethylene octyl phenol ether (OP-10) was induced using water as the exposed hydrophilic groups linking with water molecules. The SWCNT and IIR/SWCNT composites were then prepared via wetly-melt mixing at a relatively high temperature to remove water, and they were then mixed with other agents after vacuum drying and cured. The SWCNTs were dispersed uniformly to form a good network for a lower percolation threshold of the wave-absorbing property to 2 phr from 8 phr. With 8 phr SWCNTs, the tensile strength of the material improved significantly from 7.1 MPa to 15.1 MPa, and the total electromagnetic shielding effectiveness of the material was enhanced to 23.8 dB, a 3-fold increase compared to the melt-mixed material. It was demonstrated that water-induced modification achieved good dispersion of SWCNTs for electromagnetic shielding enhancement while maintaining a wide damping temperature range from -55 °C to 40 °C with a damping factor over 0.2.

Insights into the relation of crude oil components and surfactants to the stability of oily wastewater emulsions: Influence of asphaltenes, colloids, and nonionic surfactants

Large amounts of asphaltenes, colloids, and surfactants in the oily wastewater emulsions produced during the resource utilization of oily sludge make the treatment of oily wastewater emulsions difficult. In this study, the crude oil components were separated by solvent separation method, characterized by SEM, XRD, FT-IR, and EDS for crude oil components, suspended solids, and “oil-particulate aggregates”, and compared the emulsification performance of each crude oil component according to the oil–water wetting angle. In addition, the static stability and coalescence stability of different surfactant emulsions were determined, and the kinetic parameters of emulsion decomposition and oil–water interfacial film strength parameters were calculated based on the stability model of emulsion two-phase separation. The mechanisms of active components such as asphaltenes and colloids in crude oil and surfactants on the emulsion stability of oily wastewater were analyzed. It was found that the polar components in crude oil consisted of asphaltenes and colloids, and with the increase of asphaltenes and colloids, the oil–water wetting angle decreased significantly and the emulsion stability increased, and the emulsion stability of nonionic surfactants was better than that of cationic and anionic surfactants, among which octylphenol polyoxyethylene ether (10) (OP-10) had the best emulsion stability. The results of the study provide a theoretical basis for the demulsification and oil removal of oily wastewater emulsions.

The attraction between like-charged oil-in-water emulsion droplets induced by ionic micelles

Although extensive work has been reported that micelles can induce depletion attraction between two solid spheres or a sphere and a plate, the effect of different micelles on the depletion between two soft surfaces has been rarely reported. Optical tweezers were used to measure the forces between two oil-in-water emulsions in solutions of sodium dodecylbenzenesulfonate (SDBS), cetyltrimethylammonium bromide (CTAB), and octylphenol polyoxyethylene ether with ten oxyethylene glycol ether (OP-10) at varying concentrations. When the concentration of surfactant below their critical micelle concentration (cmc), force profiles between two emulsion droplets were purely repulsive. As the concentration of SDBS or CTAB above its cmc, the attraction between like-charged O/W emulsion droplets was dominant. The coalescence of the like-charged O/W emulsion droplets is observed. For nonionic surfactants OP-10, even if the cmc had been reached, the attractive force between O/W emulsion droplets couldn’t be measured. Results shows that attractive forces between two like-charged emulsion droplets of several microns in solution can also be induced by ionic micelles and the depletion was enhanced by counterion osmotic pressure. Our work suggests that the effect of micelle-induced depletion on the force between two solid surfaces can be used to predict forces between several micrometers of emulsion droplets.

Promoting the removal of fine particles by surfactants in a novel cyclone with heterogeneous-condensation agglomeration: A combined experimental and molecular dynamics study

Using heterogeneous-condensation agglomeration to enhance removal of fine particles by conventional equipment is an economical and efficient method. Recently proposed Cloud-Air-Purifying (CAP) technology, which combines heterogeneous-condensation agglomeration with a centrifugal field, has significantly improved the removal efficiency of fine particles in gas cyclones. In this work, surfactants were used to further enhance the removal of fine particles. The effect of three surfactants on promoting the removal of fine particles was investigated experimentally. The results indicated that non-ionic surfactant octylphenol polyoxyethylene ether (10) (OP-10) had the best effect on promoting the removal of methylated silica (SiO2-CH3) particles, because it improved heterogeneous condensation of fine particles and collision agglomeration between particles by improving the surface wettability, resulting in the formation of larger aggregates. Furthermore, the interaction energy, mean square displacement and hydrogen bond interactions in different simulation systems were calculated by molecular dynamics simulation to study the mechanism of surfactants on improving the surface wettability. The simulation results demonstrated the hydrophobic tail chains of OP-10 molecules spontaneously adsorbed on the nonpolar SiO2(001)–CH3 surface through the Van der Waals interaction, which changed the surface polarity and reduced the solid–liquid interaction energy. Meanwhile, hydrogen bonds were formed between polar head groups and water molecules, which enhanced the interaction between water molecules and the surface. Moreover, the mobility of water molecules is enhanced by surfactant molecules. The spatial distribution of the head group and tail chain of surfactant is an important factor affecting the surface wettability. This work is of great importance for enhancing the removal of fine particles in the dedusting system with heterogeneous-condensation agglomeration technology.

Enhancement of heat and mass transfer of potassium carbonate-based thermochemical materials for thermal energy storage

Salt hydrates are ideal for long-term thermochemical heat storage in a built environment, where K2CO3 is considered a promising thermochemical heat storage material. This class of materials continues to encounter certain technical bottlenecks in practical applications, and the enhancement of heat and mass transfer is a key challenge. Composite materials are a promising method to address this challenge because heat and mass transfer are coupled and material-dependent. In this study, a novel K2CO3-based composite material was synthesized from expanded graphite (EG), K2CO3, and octylphenol polyoxyethylene(10) ether (OP-10), and its structural information, reaction kinetic properties, thermodynamic properties, and cycling stability were determined. The results showed that the use of EG with OP-10 significantly enhanced mass and heat transfer. Compared to pure K2CO3, the thermal conductivities of the composites were increased by 9–15 times and their half-conversion time was shortened by approximately 3/4–4/5, indicating that their mass and heat transfer capacities were effectively improved. The mass and volume energy storage densities (ESDs) of K2CO3-based composites reached 429–563 kJ⋅kg−1 and 138–216 kWh⋅m−3, respectively, and these values depended on the content of K2CO3. In addition, the cycling stability results indicated that these K2CO3-based composites performed well and were suitable for medium-to-low-temperature thermochemical thermal storage applications.

Molecular interaction between sodium dodecylbenzene sulfonate and octylphenol polyoxyethylene ether and effect of hydrophilic chain

The micellization behavior of two binary mixtures of an anionic sodium dodecylbenzene sulfonate with a nonionic surfactant octylphenol polyethoxylated ether (including OP-10 or OP-7) was investigated in aqueous solution at 298.15 K using the tensiometry, and the effect of hydrophilic chain of nonionic surfactant was discussed. In the framework of pseudophase separation model and based on the regular solution theory, the related micellization parameters and thermodynamic parameters were estimated by some models including Clint’s model, Rubingh’s model, etc. The two mixtures exist some differences in the micellization behavior. The synergistic effect, the antagonism, nonideal mixing and ideal mixing are observed in the two mixtures. The dependence of the mixed critical micelle concentration, the composition in mixed micelle, the interaction parameter between molecules on the composition in aqueous solution is explained by the electrostatic interaction, the steric effect and the shell structure of mixed micelle, etc. Thermodynamic parameters are adopted to account for the difference in energy and verify the micellization behavior. The two binary mixtures show different contributions of energy to the process of micellization. These findings help with understanding the nature on the interaction between two surfactants and the effect of the length of hydrophilic chain of nonionic surfactant so as to obtain some information in theoretical and practical investigations.

A simple and green approach to the preparation of super tough IIR/SWCNTs nanocomposites with tunable and strain responsive electrical conductivity

Abstract Nanocomposites of single-wall carbon nanotubes in isobutylene isoprene rubber (IIR/SWCNTs) were successfully prepared by a simple and green wet process. The traditional melt mixing process and organic solvent dissolution suffered from unable to effectively disperse the SWCNTs of tangled structure, and degradation of polymer molecules, respectively. Our process very well avoided these two problems. The SWCNTs aqueous solutions emulsified by polyoxyethylene octyl phenol ether (OP-10) were firstly mixed and compounded with IIR rubber at a relatively high temperature, followed by the second step of melt compounding process with the addition of cross-linking agent and accelerators. The SWCNTs were dispersed uniformly, and a fine network was constructed in the matrix of the obtained IIR/SWCNTs nanocomposite with a low percolation threshold. With the concentration of SWCNTs as low as 2 phr, the IIR/SWCNTs nanocomposite received an electrical conductivity of 10−6∼10−3 S/cm, and a 71% improvement of tensile strength. By varying the loadings of SWCNTs in a certain range, the tensile strength, electrical conductivity, and dielectric property were found tunable. Besides, the nanocomposites also presented strain responsive specific resistance, excellent elongation (600–740%), and better heat resistance.

Preparation and Properties of a New Type of Coal Dust Suppressant

A new type of water-soluble coal dust suppressant (later called MA) with excellent performance was prepared by modified starch, styrene, methyl methacrylate, Butyl acrylate (as the main monomers) and acrylic acid (as the functional monomer) via mixed the emulsifiers of Sodium dodecyl sulfate (SDS)/octylphenol polyoxyethylene(10)ether (OP-10) and ammonium persulfate served as initiator. The properties of anti-wind erosion, water retention and coal quality impact were investigated. The MA was characterized by viscosity measurements and scanning electron microscopy. The results show that the spraying of MA has no effect on coal quality, and the water loss rate of MA is slightly lower than that of water, which has certain moisture retention. After spraying MA on the surface of coal sample for 120 hours, the coal sample is swept by six-stage wind (wind speed is 10.8-13.8 m/s), and the erosion rate is only 1.8%. The MA and coal samples are closely bonded to form a dense soft film, which has a excellent dust suppression effect.

Phase separation phenomena and thermodynamics of octylphenol polyoxyethylene ether in micellar solutions: Effect of high concentration of inorganic salts and linear correlation

The phase separation phenomena or cloud points (CP) behavior of nonionic octylphenol polyoxyethylene ether with oxyethylene glycol ether unit of 15 (OP-15) were investigated in aqueous micellar solutions containing high concentrations of inorganic salts including NaCl, KCl, MgCl2, CaCl2, BaCl2, AlCl3, FeCl3, Na2SO4 and Na2SiO3. The change in CP induced by salts and its mechanism are discussed theoretically. In aqueous solutions containing high concentration of salt, for the first time the linear relationship between CP and salt concentration is well established to characterize the depression of CP. Based on pseudo phase separation model, thermodynamic parameters are estimated and adopted to further describe the phase separation process and the interactions between OP-15 molecules or the OP-15/water interactions. Thermodynamic parameters including standard Gibbs energy change (ΔGCP0), enthalpy change (ΔHCP0) and entropy change (ΔSCP0) indicate that the additions of different salts result in the change in entropy-driven nonspontaneous process of phase separation. These data, which are from the compensation temperatures and the change of molar heat capacity, also prove that different ions induce the change in the interactions between surfactant molecules or the surfactant–water interaction and thus affect the depression of CP. These findings help with understanding the effect of inorganic salts, especially the high concentration of salt, on CP of nonionic surfactant and then broadening the application of nonionic surfactant based on CP such as the extraction of biomaterials in biological samples derived from animals or plants, etc.

Improved antifouling performance of a polyamide composite reverse osmosis membrane by surface grafting of dialdehyde carboxymethyl cellulose (DACMC)

Antifouling properties are considered to be essential to polyamide (PA) composite reverse osmosis (RO) membranes for their industrial applications. In this work, an antifouling material, dialdehyde carboxymethyl cellulose (DACMC), was prepared by the oxidation of carboxymethyl cellulose (CMC) and then grafted onto the surface of a nascent PA RO membrane to improve its antifouling properties. The results showed that DACMC grafting could endow the membrane with improved hydrophilicity, surface smoothness and NaCl retention, while the permeability was decreased slightly after DACMC grafting. The zeta potentials of the membrane could be adjusted by changing the DACMC concentration. In addition, three typical surfactants with various charge properties, including sodium dodecyl sulfate (SDS), polyoxyethylene octylphenol ether (OP-10) and cetyltrimethylammonium bromide (CTAB), were used as feed foulants to evaluate the antifouling property of membranes. The results showed that, for the anionic SDS and nonionic OP-10 surfactants, the modified membranes with more DACMC had better antifouling performance because the membrane hydrophilicity dominated the interaction between foulants and the membrane surface. For the cationic CTAB, however, the pristine membrane showed better antifouling performance than the modified membrane with low DACMC grafting concentrations (5 and 10 g/L). This difference was attributed to the stronger electrostatic adsorption between the cationic CTAB and the modified membranes with more negative charges. The modified membrane with high DACMC grafting concentrations (20 g/L) exhibited the best antifouling performance for all the surfactants thanks to its high hydrophilicity and low negative charge. Therefore, the charge and hydrophilic properties of the RO membrane must be designed rationally to enhance the antifouling performance of the RO membrane when treating surfactant-containing wastewater.

Synthesis and Characterization of Water-Based Epoxy-Acrylate/Graphene Oxide Decorated with Fe3O4 Nanoparticles Coatings and Its Enhanced Anticorrosion Properties

ABSTRACT In this article, water-based epoxy–acrylate (EP/AC) emulsion coatings and its nanocomposites with Fe3O4 nanoparticles, graphene oxide nanosheets and graphene oxide which was decorated with Fe3O4 nanoparticles were synthesized. This was executed by means of a pre-emulsion seeded semi-batch emulsion polymerization handle with a blend of conventional anionic surfactant (Polyalkylene glycol ether sulfate, ammonium salt-EXOSEL 20 S) and typical nonionic type emulsifier (Octylphenol polyoxyethylene ether OP-10) for emulsion polymerization (schematic 1). Prepared nanoparticles were investigated with different analyzing methods like FT-IR, XRD, SEM-EDAX and TGA. The impact of the distinctive nanostructures in an (EP/AC) resin, on coated steel panels with the features of corrosion conservation, was investigated by the test of electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization. Morphology of surface and thermal behavior of nanocomposite tests were executed using surface filtering electron microscopy (FE-SEM) and thermal gravimetric analysis (TGA). Different analyses resulted from nanostructures and nanocomposites approved very good dispersion of fillers in nanocomposite beads. Besides, they indicate the effective role of nanoparticles especially graphene oxide which was decorated with Fe3O4 nanoparticles in corrosion resistance of water-based EP/AC coatings and other properties of coated instances.

Preparation and Characterization of Soap-Free Vinyl Acetate/Butyl Acrylate Copolymer Latex.

The soap-free emulsion of vinyl acetate (VAc)/butyl acrylate (BA) copolymer was prepared by a semi-continuous and pre-emulsification polymerization method, using ammonium sulfate allyloxy nonylphenoxy poly(ethyleneoxy) (10) ether (DNS-86) as a reactive emulsifier. The effects of DNS-86 on the stability of the emulsion and the properties of the latex film were investigated. The infrared spectrum, thermal stability, glass transition temperature and micromorphology of latex were also studied. The results showed that the emulsion had the best stability and the conversion rate reached a maximum of 98.46% when the DNS-86 amount was 4 wt % of the total amount of monomers. Compared with the PVAc latex synthesized with octylphenol polyoxyethylene ether (10) (OP-10), the latex prepared with DNS-86 has higher thermal stability and ionic stability, whereas the latex film has better water resistance.