Hydrocarbon Surfactants Research Articles

Evaporation, spreading, and possible uptake of droplets on sorghum (Sorghum bicolor) and cowpea (Vigna unguiculata) leaves using an imaging-based technology.

Sprayed agrochemical droplets have a dynamic evolution on the leaf surface, undergoing changes in shape and volume due to spreading, evaporation, and adsorption. To better understand these processes, an accessible imaging-based experimental methodology is presented to precisely measure droplet spreading, evaporation, and potential uptake by a leaf within a controlled relative humidity environment. Laboratory experiments were conducted to determine the effect of hydrocarbon surfactants, accelerators (light mineral oil), and humectants (high fructose corn syrup) on droplet spread, evaporation, and potential uptake when applied to sorghum (Sorghum bicolor 'Tricker') and cowpea (Vigna unguiculata) leaves. Experiments on cowpea leaves showed uniform spreading and no change in evaporation compared to the predicted rate. In contrast, on sorghum leaves, results suggest that the volume loss rate exceeds the predicted evaporation rate (up to 23%), indicating a potential uptake by the leaves. Some accelerated dynamics on sorghum can be attributed to the lateral spreading observed on hairy leaves along the veins, increasing the contact area by an average of 65%. However, samples containing light mineral oil, typically considered an accelerant to aid in uptake, demonstrated the highest rate but exhibited minimal spreading. The study demonstrates how droplet composition affects droplet dynamics on waxy and hairy leaves by using an imaging-based methodology to measure evaporation rates, volume loss, contact angle, wetted area, and spreading behavior. The findings highlight some of the complex coupling between the crop protection product composition and droplet life cycle on a leaf. © 2024 The Author(s). Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Effect of nano-aluminum hydroxide on the liquid phase properties and fire-fighting foam performance of the mixed surfactants solution

Short-chain fluorocarbon surfactants show synergistic effects with hydrocarbon surfactants in foaming and foam stability. Nano-aluminum hydroxide (nano-ATH) was added as an additive to the short-chain fluorocarbon surfactant mixture solution, which was found to increase the surface tension and viscosity of the surfactant mixture solution, and decrease the foaming properties of the solution, as measured by Wilhelmy method, Waring Blender method and viscometer. By measuring zeta potential experiments, surfactant molecules were found to be adsorbed on nano-ATH through charge gravity, which increased the desorption energy of nano-ATH. Measuring the visco-elastic modulus of the solution by rheometer, it was found that nano-ATH increased the visco-elastic modulus of the surfactant mixture solution, which improved the foam's resistance to the external disturbances. Observed by the image analysis system on the foam, the uniform distribution of nano-ATH in the liquid film reduced the coarsening and coalescence speed of foam .Through the self-developed oil resistance test, nano-ATH enhanced the oil resistance stability and inhibition of fuel vapour diffusion of the foam by about 12%; through self-developed foam fire extinguishing and anti-burning tests, nano-ATH shortened the fire extinguishing time of the two-phase foam by 25%, and showed better fire extinguishing and anti-burning performance than the foam.

Tuning thermal stability of fluorine-free foam by nano-MDH inorganic flame retardant

Foams enhanced by nanoparticles (NPs) have become an important way to develop new type of fluorine-free firefighting foams. This study focuses on thermal stability of foams generated by the mixed dispersion of CoatOsil-77 silicone and BS-12 hydrocarbon surfactants as foaming agent and nano-magnesium hydroxide (nano-MDH) as foam stabilizer. The interaction between nano-MDHs and surfactants were studied. Thermal stability of nano-MDH enhanced foam was explored by investigating drainage and volume attenuation of foam and heat transfer in vertical foam blanket. Stabilization mechanism of nano-MDH enhanced foam under heat was clarified. Results show that nano-MDHs have a weak interaction with the BS-12 molecules and almost has no interaction with the CoatOsil-77 molecules. Initial foam height of mixed dispersion increases at the presence of nano-MDHs, but further increase in the concentration of nano-MDH decreases its foaming ability. At room temperature, foam drainage and coarsening are accelerated by low concentration nano-MDH (1 wt%) and delayed by high concentration nano-MDH (>1 wt%). Meanwhile, foam was strengthened by rising nano-MDH content after exceeding 1 wt%. Drainage and volume attenuation of foam and heat transfer in vertical foam blanket were significantly delayed and the corresponding thermal stability was strengthened by nano-MDHs. This study can offer a possibility for tuning thermal stability of fluorine-free foams based on nano-MDHs.

Effect of fluorocarbons and inorganic salts on wetting and foaming characteristics of hydrocarbon surfactants

To improve the wetting and foaming properties of anionic SDS foam on coal dust, we experimentally investigated the effects of short-chain fluorocarbon surfactant FS-50 and inorganic salt NaCl on the wetting and foaming properties of SDS foam and the synergistic effect of the mixed system. The experimental results show that SDS and FS-50 can effectively improve the wetting properties of coal dust in a concentration of 0.05–0.16 wt% and a ratio of 3:1–1:2. In the mixed system, SDS provides sufficient hydrophilic base, FS-50 can effectively reduce the surface tension and have a certain agglomeration effect on coal dust to accelerate the settlement of coal dust and improve the wetting properties of coal dust. When the mixed ratio is lower than 1:1, the foaming volume and foam half-life of the surfactant solution are significantly reduced. The number of SDS molecules at the solution gas-liquid interface is reduced due to electronegative repulsion, and the FS-50 replenishes to the liquid surface faster due to stronger hydrophobicity, and it is difficult to form hydrogen bonds with water molecules, which reduces the foam stability. Low concentrations of inorganic salts can significantly improve the wetting performance of the SDS/FS-50 mixed system to coal dust, and high concentrations will reduce the foam stability of the mixed system.

Surface activity and wetting behavior of branched short‐chain anionic perfluorinated/cationic hydrocarbon surfactant blends in dilute solutions

Surface activity and wetting behavior of branched short‐chain anionic perfluorinated/cationic hydrocarbon surfactant blends in dilute solutions

Oil resistivity of fluorine-free foams stabilized by silica nanoparticles and mixture of silicone and hydrocarbon surfactants

Oil resistivity of fluorine-free foams stabilized by silica nanoparticles and mixture of silicone and hydrocarbon surfactants

Coomassie Brilliant Blue G for Smart Colorimetric Determination of the Ionic Surfactants in Triton X-100 Solutions.

The conditions for the smart colorimetric determination of cetylpyridinium chloride and sodium dodecyl sulfate by reaction with Coomassie brilliant blue G (CBBG) have been proposed. The nature of the absorption and fluorescence spectra of aqueous solutions of CBBG as a function of acidity has been investigated. A variety of reagent forms and associations with ionic surfactants have been demonstrated. The composition of the associates formed in the CBBG-cationic surfactant system has been established. The increase in the analytical signal of the cationic surfactant and the stabilization of the colloid-chemical state of the system during reactions in the organized medium of the nonionic surfactant Triton X-100 has been demonstrated. These effects are realized through association in premicellar solutions and as a result of the solubilization of components in Triton X-100 micellar solutions. The addition of long-chain cationic surfactants to the reagent occurs with the replacement of the heteroatom proton. The absorption of CBBG-cationic surfactant associates solutions increases with the length of the cationic surfactant hydrocarbon chain. Ethanol additives decrease the aggregation of CBBG. The technique of cationic surfactant determination has been tested in the analysis of the pharmaceutical. The results show that the simplicity of analytical signal registration with satisfactory correctness and acceptably high sensitivity of determination is an advantage of the developed technique.

The performance of hydrophilic moieties in synthesized fluorinated cationic surfactants on corrosion inhibition of carbon steel pipelines

Compared with traditional hydrocarbon surfactants, fluorinated surfactants exhibit unique characteristics such as reduced surface tension, enhanced efficacy in reducing interfacial tension, dual hydrophobic and oleophobic nature, increased thermal stability, and superior chemical resistance. These characteristics make them a favorite material for many kinds of applications. This study aims to highlight the synthetic route for three novel cationic fluorinated surfactants (CFS) and applied them in the oilfield as corrosion inhibitors. Characterization of the prepared surfactants took place using different spectroscopic techniques. The influence of hydrophilic moieties on the micellar characteristics of ionic surfactants that have the same hydrophobic fluorinated chains are investigated in this research. Also, an evaluation of the influence of these groups on thermodynamic parameters was carried out.The metal corrosion inhibition efficiency of the CFS was studied in acidic medium by three different techniques, including potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), and weight loss procedures, at three different temperature ranges (25, 40, and 60 °C).The achieved results displayed the inhibition efficiency of the metal corrosion that was elevated by increasing both the CFS's concentration and the applied temperature values. The highest level of inhibition, reaching 97.48 %, was achieved at a concentration of 700 parts per million (ppm) and a temperature of 60 °C. Furthermore, it was noticed that the charge transfer resistance value was raised; however, the constant phase element was decreased with increasing the CFS concentrations. The CFS regards an excellent and mixed-type corrosion inhibitor. The adsorption of CFS has agreed the Langmuir's adsorption isotherm and was related to chemisorption. SEM photos show a good CS surface in the presence of CFS versus the absence of them.

Tuning stability, rheology, and fire-extinguishing performance of advanced firefighting foam material by inorganic nanoparticle flame retardants

HypothesisNanoparticle-stabilized foams are extremely stable, and flame retardant inorganic nanoparticles should be able to add sealing capacity of firefighting foams on flammable liquid fuels, and hence enhance fire extinguishment performance on liquid fuel fire. In practice, how do flame retardant nanoparticles resist the destructive effect of oil molecules on foam and tune foam properties? ExperimentsWe have prepared a nanoparticle-enhanced foam comprising of hydrocarbon surfactant, short-chain fluorocarbon surfactant, and nanoparticles. The interactions among nanoparticles and surfactant molecules were characterized by using dynamic surface tension and conductivity. Stability, rheology, and oil resistivity on liquid fuel of the nanoparticle-enhanced foam were evaluated systematically. Fire suppression effectiveness of the foams was verified based on a standard experiment. FindingsFoam stability and oil resistivity were enhanced due to self-assembled network structures formed by jammed aggregates composed by nanoparticles and surfactants in Plateau borders and bubble films, providing structural recoverability and enhanced viscoelasticity within foam. Foams containing nano-SiO2, nano-CaCO3, nano-Al(OH)3, and nano-Mg(OH)2 show difference in fire extinguishment due to different ability to enhance foam properties. Foam containing nano-Al(OH)3 shows the strongest adaptation and could shorten fire extinguishing time by 2 times and prolong burn-back time by 2.3 times compared with commercial product.

Synergistic enhancement of foam stability by nanocellulose and hydrocarbon surfactants

Synergistic effects and stability mechanism of carboxylated cellulose nanofiber (CCNF) and hydrocarbon surfactants on the environmentally friendly foam are investigated in this work. Higher concentrations of CCNF decelerate the bubble coarsening and liquid drainage processes, consequently enhancing foam stability. Increasing viscosity is the primary cause of foam stability enhancement for all surfactant solutions. However, the generation of aggregates is still another reason for the enhanced stability of CTAB/CCNF foam. In addition, CCNF diminishes the foaming ability of all surfactants. Furthermore, as CCNF exceeds 0.8 wt.%, the foaming ability of all surfactants diminishes noticeably, with CTAB solution experiencing a more pronounced reduction. In SDS solutions, the foaming ability is governed by viscosity, whereas in CTAB solutions, it is influenced by adsorption kinetics and viscosity.

Vesicle Hydrogels Formed from the Perfluorononanoic Acid/Tetradecyl Dimethylaminoxide Oxide System.

Vesicle hydrogels are supramolecular structures formed by the self-assembly of surfactant molecules in solution, which have great application prospects. The phase behavior of perfluorononanoic acid (C8F17COOH) and an amphoteric hydrocarbon surfactant, tetradecyl dimethylaminoxide (C14DMAO), in an aqueous solution has been studied. By changing the mixing ratio and concentration of C8F17COOH and C14DMAO, the phase diagram of the system was drawn, and interestingly, a hydrogel composed of polyhedral and spherical vesicles was successfully constructed. The formation mechanism of the polyhedral and spherical vesicle hydrogel was studied by differential scanning calorimetry (DSC), small-angle X-ray diffraction (XRD), wide-angle X-ray scattering (WAXS), and 1H nuclear magnetic resonance (1H NMR) measurements, and the rheological properties and influencing factors of the hydrogel were systematically investigated. The formation of the vesicle hydrogels in this system was considered to be caused by the "cocrystallization" of two surfactant molecular chains.

Experimental Study on Foam Properties of Mixtures of Organic Silicon and Hydrocarbon Surfactants Regulated by Nano-SiO2 Particles

Experimental Study on Foam Properties of Mixtures of Organic Silicon and Hydrocarbon Surfactants Regulated by Nano-SiO2 Particles

Identification of Hydrocarbon Sulfonates as Previously Overlooked Transthyretin Ligands in the Environment.

Incidences of thyroid disease, which has long been hypothesized to be partially caused by exposure to thyroid hormone disrupting chemicals (TDCs), have rapidly increased in recent years. However, known TDCs can only explain a small portion (∼1%) of in vitro human transthyretin (hTTR) binding activities in environmental samples, indicating the existence of unknown hTTR ligands. In this study, we aimed to identify the major environmental hTTR ligands by employing protein Affinity Purification with Nontargeted Analysis (APNA). hTTR binding activities were detected in all 11 indoor dust and 9 out of 10 sewage sludge samples by the FITC-T4 displacement assay. By using APNA, 31 putative hTTR ligands were detected including perfluorooctanesulfonate (PFOS). Two of the most abundant ligands were identified as hydrocarbon surfactants (e.g., dodecyl benzenesulfonate). Moreover, another abundant ligand was surprisingly identified as a disulfonate fluorescent brightener, 4,4'-bis(2-sulfostyryl)biphenyl sodium (CBS). CBS was validated as a nM-affinity hTTR ligand with an IC50 of 345 nM. In total, hydrocarbon surfactants and fluorescent brighteners explain 1.92-17.0 and 5.74-54.3% of hTTR binding activities in dust and sludge samples, respectively, whereas PFOS only contributed <0.0001%. Our study revealed for the first time that hydrocarbon sulfonates are previously overlooked hTTR ligands in the environment.

Surface activity, foamability, and foam stability of binary mixed systems based on siloxane-based Gemini and hydrocarbon surfactants

Aiming to explore the potential of siloxane-based Gemini surfactants in the development of environmentally friendly foam extinguishing agent to address the pollution caused by traditional fluorinated ones. A crucial step is to study the performance of binary mixed systems of siloxane-based Gemini and hydrocarbon surfactants in terms of surface activity, foamability, and foam stability. In this study, binary mixed systems of two types of siloxane-based Gemini surfactants and one siloxane surfactant with four different hydrocarbon surfactants are prepared. Parameters such as surface tension, foam height, drainage time, and coarsening rate are tested. The results show that the siloxane-based Gemini surfactant HY-4000 with double silane chains could effectively reduce the surface tension of hydrocarbon surfactants. In addition, the two types of Gemini surfactants performed better in enhancing the foamability of hydrocarbon surfactants. The siloxane OFX0193 even inhibits the foaming of cationic hydrocarbon surfactant CATC. Besides the HY-4000/APG0180 mixed system, the binary mixed systems of three silicone surfactants with AOS and APG0180 exhibit better foam stability, particularly the systems containing TEGO4100. For the coarsening process of foam bubbles, we develop a predictive model based on previous studies, where the relationship between bubble area and time follows a power function law. The findings of this study could provide guidance for the development of green foam extinguishing agent with siloxane-based Gemini and hydrocarbon surfactants as core components.

Environmentally friendly fluorine-free fire extinguishing agent based on the synergistic effect of silicone, hydrocarbon surfactants and foam stabilizers

The environmentally friendly fluorine-free fire extinguishing agent based on the silicone surfactant was developed in order to solve the environmental hazards and bio-accumulative of traditional aqueous film-forming foam (AFFF). The carboxyl modified polyether polysiloxane surfactant (CMPS) was an efficient alternative to fluorocarbon surfactant, which was firstly synthesized via the esterification reaction using hydroxyl-containing polyether modified polysiloxane (HPMS) and maleic anhydride (MA) as raw materials. Then the surface activity, foam properties, micellar morphology of the CMPS and four hydrocarbon surfactants, as well as their mixture are evaluated by surface tension, Ross-Miles and cryo-transmission electron microscopy (Cryo-TEM). And the suitable key amount of CMPS and hydrocarbon surfactants added to the extinguishing agent were optimized by orthogonal tests. Moreover, the effect of foam stabilizer on the surface activity, foam property and fire extinguishing performance of fire extinguishing agent are also analyzed. Consequently, a new environmentally friendly fluorine-free fire extinguishing agent was prepared and the surface tension, the interfacial tension, foam properties, bubble morphology, spreading behavior and fire extinguishing mechanism were systematically characterized. The Cryo-TEM results illustrate that the intense interaction among silicone and hydrocarbon molecules exists in the the mixture of CMPS and hydrocarbon surfactants, which is produced through the change of micellar morphology, i.e. microscopic larger spheroidal micelles of CMPS transited to smaller spheroidal micelles and wormlike micelles in the mixed system. The surface tension of synthesized foam extinguishing agent is 22.3 mN/m and the spread coefficient is 0.9 mN/m, which has excellent surface activity and spreading property. The prepared foam extinguishing agent exhibits superior fire-fighting property, which can be attributed to the high surface activity, good foam property and superior foam stability. The research results of this paper lay a theoretical foundation for the research and development of efficient environmentally friendly foam extinguishing agent.

Design of fluorine-free foam extinguishing agent with high surface activity, foam stability and pool fire suppression by optimization of surfactant composition and foam system

To meet the environmental requirement of foam extinguishing agent, a novel fluorine-free surfactant named amino-terminated polyether modified silicone (ATPMS) was successfully synthesized, and then in combination with hydrocarbon surfactant prepared fluorine-free foam extinguishing agent. The study carefully investigated surface tension, foamability, foam stability and fire extinguishing performance of fluorine-free foam extinguishing agent. The results indicate that ATPMS has a low surface tension of 21.17 mN/m, which combined with hydrocarbon surfactant at the mass concentration ratio of 1:1 imparts high surface activity. The sodium lauryl ether sulfate (AES)/ATPMS system owes the optimal comprehensive performance with an initial foam height value of 85.8 mm, a surface tension value of 24.76 mN/m and a foam stability value (the ratio of foam height between initial foam and five-minute foam) of 64.0 % at critical micelle concentration (CMC), respectively. Fire suppression test shows that the obtained fluorine-free foam extinguishing agent is effective in fighting diesel pool fires. The firefighting efficiency of foam agent links to the mixing chamber structure of compressed air foam fire extinguishing system (CAFS). When the mixing chamber of CAFS has a recurrent segment length of 50 mm and the filled particle size of 10 mm, the firefighting efficiency of fluorine-free foam extinguishing agent is optimal with a fire extinguishing time of 33 s and a temperature drop rate of 6.49 °C/s.

Influence of typical liquid fuels on foam properties of critical components of environmentally friendly aqueous film-forming foams

In this study, the influence mechanism of typical fuels (oils) on the foam properties of mixture of hydrocarbon and fluorocarbon surfactants was investigated. A mixed solution was prepared based on a nonionic hydrocarbon surfactant (APG-0810) and a zwitterionic C6 fluorocarbon surfactant (short-chain). The effect of different oils (heptane, kerosene, diesel, and transformer oil) on the physical property parameters, foamability, oil resistivity of foam and single vertical liquid film of the mixture are systematically investigated. Results indicate that the viscosity of mixture increases, but the conductivity, surface activity, and initial foam height decreases with addition of the four oils. The drainage and volume decay of the foam are accelerated by the presence of oils. In addition, the presence of oils accelerates liquid film thinning through affecting drainage, especially for the oil with higher density, water solubility, and volatility. The four oils showed different effect on foam properties due to the difference in nature and emulsification of them. Among them, the foam properties under the action of heptane is the best, and the oil resistivity of foams is the best. This study can provide theoretical guidance for oil resistivity of hydrocarbon and fluorocarbon surfactant stabilized foams.

Molecular Dynamics Simulations of the Short-Chain Fluorocarbon Surfactant PFHXA and the Anionic Surfactant SDS at the Air/Water Interface.

The research and development of alternatives to long-chain fluorocarbon surfactants are desperately needed because they are extremely toxic, difficult to break down, seriously harm the environment, and limit the use of conventional aqueous film-forming foam fire extinguishing agents. In this study, mixed surfactant systems containing the short-chain fluorocarbon surfactant perfluorohexanoic acid (PFHXA) and the hydrocarbon surfactant sodium dodecyl sulfate (SDS) were investigated by molecular dynamics simulation to investigate the microscopic properties at the air/water interface at different molar ratios. Some representative parameters, such as surface tension, degree of order, density distribution, radial distribution function, number of hydrogen bonds, and solvent-accessible surface area, were calculated. Molecular dynamics simulations show that compared with a single type of surfactant, mixtures of surfactants provide superior performance in improving the interfacial properties of the gas-liquid interface. A dense monolayer film is formed by the strong synergistic impact of the two surfactants. Compared to the pure SDS system, the addition of PFHXA caused SDS to be more vertically oriented at the air/water interface with a reduced tilt angle, and a more ordered structure of the mixed surfactants was observed. Hydrogen bonding between SDS headgroups and water molecules is enhanced with the increasing PFHXA. The surface activity is arranged in the following order: PFHXA/SDS = 1:1 > PFHXA/SDS = 3:1 > PFHXA/SDS = 1:3. These results indicate that a degree of synergistic relationship exists between PFHXA and SDS at the air/water interface.

Rheological properties of fluorine-free foams stabilized by aluminum hydroxide nanoparticles and mixture of siloxane and hydrocarbon surfactants

Fluorine-free foam stabilized by nanoparticle (NP) is expected to become a new generation of environmental-friendly firefighting foam. Many problems on properties of NP-stabilized fluorine-free foams remain to be studied. The present paper focuses on the rheology and foam stability of fluorine-free foam stabilized by aluminum hydroxide NPs. The surface tension, conductivity, foamability, viscosity, and viscoelasticity of mixed dispersions were measured. The stability, viscosity, viscoelasticity, and thixotropy of foam was analyzed deeply by model fitting and mechanism explanation. The results show that the rheological properties and foam stability of mixed dispersions are both enhanced by the presence of NPs, and the enhancement amplitude increased with NP concentration. Both dispersions and NP-stabilized foams exhibit shear thinning behavior, and the viscosity variations in dispersions conform to the Cross model well. As NP concentration increases, the linear viscoelastic range of foam becomes wider, the flow point of NP foam is delayed, demonstrated enhanced viscoelasticity. The thixotropic recovery of foam decreases with the increasing NP concentration, and foam thixotropic recovery decreases with the increase of irreversible deformation degree. This study can provide design idea for the development of fluorine-free firefighting foam.

Experimental study on thermal stability and burn-back performance of aqueous film forming foam agent(AFFF) with short-chain fluorocarbon surfactant or flame retardant

Long-chain fluorocarbon surfactant is widely used in aqueous film-forming AFFF due to its excellent interfacial property. It can effectively improve the extinguishing efficiency of foam by improving the stability of foam. However, due to its severity environmental damage, some studies in recent years have focused on using short-chain fluorocarbon surfactants or flame retardants to replace long-chain fluorocarbon surfactants. However, the stability mechanism of foam after adding new additives and its performance in high-temperature thermal radiation environment are still unclear and require further clarification. Therefore, in this work, the effect of different additives on the interfacial properties of foam solution, foaming ability and foam stability, thermal stability and burn-back performance under the heat radiation environment are discussed. The results indicate that the thermal stability and burn-back performance of AFFF mixed with long-chain fluorocarbon surfactant (FS-30) or flame retardant (APP and MCA) was not significantly improved. However, the foam mixed with FS-50 exhibits excellent thermal stability and burn-back performance, it could be a proper substitute for long-chain fluorocarbon surfactants to be used in the AFFF mixed system. Through exploring the adsorption behavior of surfactant molecules on the liquid-air interface of the foam, FS-50 molecules and hydrocarbon surfactant molecules have a strong synergistic effect, which making it more difficult for water molecules to enter the surface of the mixed system. and the stability of foam will be enhanced. Besides, the proper mass concentration will also affect the interfacial properties of foam solution, foaming ability and foam stability, thermal stability and burn-back performance of the foam in fire environment, the mass concentration of additive in the foam solution should be remained at 0.3 wt%.