Search Results (14)

Nanomaterials play a beneficial role in regulating the function of cement-based materials. The effects and mechanism of graphene oxide (GO) on foam behavior in solutions and air-entraining behavior of cement mortar were studied, and its effect on the microstructure of cement mortar was also investigated. The results show that a synergy between GO’s hydrophobicity and the air-entraining agent’s hydrophobic chains drove more agent molecules to adsorb onto the GO surface, subsequently spreading and aggregating across the bubbles. GO effectively assisted the air entraining agent to refine the bubble size, improved the bubble stability of aqueous solutions, and had excellent air entraining performance in the fresh cement mortar, as well as the optimum air-void adjustment performance of hardened cement mortars. With the addition of 0.4‰ GO, the loss rate of gas content in the GO mixed mortar was 10.3%, which was 55.8% lower than that when only using AEA. The addition of 0.4‰ of GO effectively increased the volume fraction of the cement mortar system. GO reduced the pore volume in the mortar through the filling effect and nucleation effect to reduce the total porosity and refine the microstructure of the mortar. Full article

When a liquid film is thinning, the charge and the potential of its surfaces change simultaneously due to the interaction between the two surfaces. This phenomenon is an example for charge regulation and has been known for half a century for systems featuring aqueous solutions in contact with metals, salts, biological surfaces covered by protolytes, etc. Few studies, however, investigated regulation in foam and emulsion films, where the charge is carried by soluble ionic surfactants. This work presents an analysis of the phenomenon for surfactants that follow the classical Davies adsorption isotherm. The electrostatic disjoining pressure Π_el was analyzed, and the Davies isotherm was shown to lead to Π_el ∝ h^−1/2 behavior at a small film thickness h. As usual, the charge regulation regime (constant chemical potential of the surfactant) corresponded to a dependence of Π_el on h between those for constant charge and constant electric potential regimes. The role of the background electrolyte was also studied. At the water–air interface, many ionic surfactants exhibit a surface phase transition. We show that the interaction between the two surfaces of a foam film can trigger the phase transition (i.e., the film changes its charge abruptly), and two films of different h values can coexist in equilibrium with each other—one covered by surfactant in the 2D gaseous state and another in the 2D liquid state. Full article

For years, cold plasma processing has been used as a non-thermal technology in industries such as food. As interfacial properties of protein play a remarkable role in many processes, this study investigates the effect of cold plasma on the foaming and interfacial behavior of WPI. The objective of this study is to evaluate the effect of different gases (air, 1:1 argon–air mixture, and sulfur hexafluoride (SF6)) used in low-pressure cold plasma (VCP) treatments of whey protein isolate (WPI) on the surface and foaming behavior of aqueous WPI solutions. Dynamic surface dilational elasticity, surface tension isotherms, surface layer thickness, and the foamability and foam stability were investigated in this study. VCP treatment did not significantly affect the adsorption layer thickness. However, an increase in induction time, surface pressure equilibrium value, and aggregated size is observed after SF₆VCP treatment, which can be attributed to the reaction of WPI with the reactive SF₆ species of the cold plasma. The surface dilational elastic modulus increased after VCP treatment, which can be related to the increased mechanical strength of the protein layer via sulfonation and aggregate formation. VCP treatment of WPI increases the foam stability, while the average diameter of foam bubbles and liquid drainage in the foam depends on the gas used for the cold plasma. Full article

It is well known that the type of counter-ion affects the state of the adsorption layer of ionic surfactants and, consequently, its surface potential. Yet, it is not clear how they affect the foamability, the rate of foam decay or foam production. How is the surface potential of the air/water interface related to the properties of the foam? This work aims to answer these questions. Foam films, stabilized by 0.5 mmol/L sodium dodecyl sulfate (SDS) in the presence of added LiCl, NaCl, and KCl, were studied by means of the interferometric experimental setup of Scheludko–Exerowa. The surface potential values were derived from the equilibrium film thickness by means of the DLVO theory. A linear relation between the values of the surface potential and specific adsorption energy of the counter-ions on the air/water interface was established. The slope of this linear relation depends on the salt concentration. The foamability, the rate of foam decay, and the foam production of the same aqueous solutions of SDS and added salts were studied by means of the shaking method. A correlation was found between the derived surface potential of the foam film’s surfaces and the properties of the foam. The foam production, which is the ratio between the initial foam volume and the rate of foam decay, increases with the decrease in the surface potential. Previous studies in the literature confirm that the lower surface potential promotes higher surfactant adsorption, thus boosting more foam and vice versa. It was also confirmed that the dual effect of KCl on foam production involves converting the best foam stabilizer into a foam suppressor at the highest salt concentration. Full article

Per- and polyfluorinated alkyl substances (PFAS) are an environmentally persistent group of chemicals that can pose an imminent threat to human health through groundwater and surface water contamination. In this review, we evaluate the subsurface behavior of a variety of PFAS chemicals with a focus on aqueous film forming foam (AFFF) discharge sites. AFFF is the primary PFAS contamination risk at sites such as airports and military bases due to use as a fire extinguisher. Understanding the fate and transport of PFAS in the subsurface environment is a multifaceted issue. This review focuses on the role of adsorbent, adsorbate, and aqueous solution in the fate and transport of PFAS chemicals. Additionally, other hydrogeological, geochemical, ecological factors such as accumulation at air–water interfaces, subsurface heterogeneity, polyfluorinated PFAS degradation pathways, and plant interactions are discussed. This review also examines several case studies at AFFF discharge sites in order to examine if the findings are consistent with the broader PFAS literature. We present the most crucial future research directions and trends regarding PFAS and provide valuable insights into understanding PFAS fate and transport at AFFF discharge sites. We suggest a more comprehensive approach to PFAS research endeavors that accounts for the wide variety of environmental variables that have been shown to impact PFAS fate and transport. Full article

Hardystonite-based (HT) bioceramic foams were easily obtained via thermal treatment of silicone resins and reactive oxide fillers in air. By using a commercial silicone, incorporating strontium oxide and magnesium oxide precursors (as well as CaO and ZnO), and treating it at 1100 °C, a complex solid solution (Ca_1.4Sr_0.6Zn_0.85Mg_0.15Si₂O₇) that has superior biocompatibility and bioactivity properties compared to pure hardystonite (Ca₂ZnSi₂O₇) can be obtained. Proteolytic-resistant adhesive peptide mapped on vitronectin (D2HVP), was selectively grafted to Sr/Mg-doped HT foams using two different strategies. Unfortunately, the first method (via protected peptide) was unsuitable for acid-sensitive materials such as Sr/Mg-doped HT, resulting in the release of cytotoxic levels of Zinc over time, with consequent negative cellular response. To overcome this unexpected result, a novel functionalization strategy requiring aqueous solution and mild conditions was designed. Sr/Mg-doped HT functionalized with this second strategy (via aldehyde peptide) showed a dramatic increase in human osteoblast proliferation at 6 days compared to only silanized or non-functionalized samples. Furthermore, we demonstrated that the functionalization treatment does not induce any cytotoxicity. Functionalized foams enhanced mRNA-specific transcript levels coding IBSP, VTN, RUNX2, and SPP1 at 2 days post-seeding. In conclusion, the second functionalization strategy proved to be appropriate for this specific biomaterial and was effective at enhancing the material’s bioactivity. Full article

Biocompatible and biodegradable ingredients of natural origin are widely used in the design of foam and emulsion systems with various technological applications in the food, cosmetics and pharmaceutical industries. The determination of the precise composition of aqueous solution formulations is a key issue for the achievement of environmentally-friendly disperse systems with controllable properties and reasonable stability. The present work is focused on the investigation of synergistic interactions in aqueous systems containing Quillaja saponins and Apple pectins. Profile analysis tensiometer (PAT-1) is applied to study the surface tension and surface dilational rheology of the adsorption layers at the air/solution interface. The properties and the foam films (drainage kinetics, film thickness, disjoining pressure isotherm, critical pressure of rupture) are investigated using the thin-liquid-film (TLF) microinterferometric method of Scheludko–Exerowa and the TLF-pressure-balance technique (TLF-PBT). The results demonstrate that the structure and stability performance of the complex aqueous solutions can be finely tuned by changing the ratio of the bioactive ingredients. The attained experimental data evidence that the most pronounced synergy effect is registered at a specific saponin:pectin ratio. The obtained information is essential for the further development of aqueous solution formulations intended to achieve stable foams based on mixtures of Quillaja saponins and Apple pectins in view of future industrial, pharmaceutical and biomedical applications. Full article

In the framework of the industry of secondary aluminum, the chemical neutralization of highly reactive materials that come from the pre-treatment screening processes of scraps (beverage cans and domestic appliances) was investigated through experiments in aqueous alkaline solutions. Metallic aluminum-rich by-products are classified, according to EU law, as dangerous waste, as they can potentially develop flammable gases capable of forming explosive mixtures with air. In this way they cannot be disposed of in landfills for non-hazardous wastes if chemical neutralization is not planned and performed beforehand. In this way, these experiments were mainly aimed at unraveling the oxidation rate and at quantifying the production of hydrogen-rich gases from the reactions of the metallic aluminum-rich by-products in a water-rich alkaline (liquid or vapor) environment. Reactions were carried out in a stainless-steel batch mini-reactor with metering and sampling valves, with the resulting gases analyzed by gas-chromatography (GC). The experimental setup was planned to avoid the following issues: (i) the corrosion of the reactor by the alkaline solution and (ii) the permeability of the system to hydrogen (i.e., possible leaks of H₂), related to the fast kinetics and short duration of the reactions (which may hinder a pile-up-effect) between the solid by-products and the liquid. The procedure was defined by a controlled interaction process between metals and liquid, using NaOH to increase reaction rates. The experimental runs performed in the mini-reactor proved to be effective for eliminating the reactive metallic aluminum, reaching a maximum hydrogen production of 96% of the total gases produced in the experiments. The relations between gas generation (up to 55 bar of H₂ in the experiments, which lasted for four days) and each specific parameter variation are discussed. All the obtained results can be transferred and applied to (i) the possible industrialization of the method for the chemical neutralization of these dangerous by-products, increasing sustainability and workplace safety, (ii) the use of the resulting hydrogen as a source of energy for the furnaces of the secondary aluminum industry itself, and (iii) new technological materials (e.g., “foamed geopolymers”), by using hydrogen as a foaming agent, coupled with aluminosilicate materials, during geopolymeric reactions. Full article

The intensive mechanical stirring of suspensions of recycled glass and inorganic waste powders in ‘weakly alkaline’ aqueous solutions (e.g., 2.5–3 NaOH), followed by viscous flow sintering at 800–1000 °C, easily yields highly porous glass-ceramic foams. The firing determines just the consolidation of powders with concurrent incorporation of pollutants from iron-rich waste, such as fly ash from coal combustion (FA). Engineered mixtures allow for the obtainment of chemically stable foams from treatments in air. Treatments in nitrogen are even more significant since they extend the conditions for stabilization and promote novel functionalities. In addition, the change in the atmosphere favors the formation of magnetite (Fe₃O₄), in turn enabling ultra-high dielectric permittivity and semiconductivity. Such a condition was further evidenced by preliminary tests on recycled glass combined with residues from the Bayer processing of aluminum ores or red mud (RM). Full article

Flexible pressure sensors have attracted tremendous research interests due to their wide applications in wearable electronics and smart robots. The easy-to-obtain fabrication and stable signal output are meaningful for the practical application of flexible pressure sensors. The graphene/polyurethane foam composites are prepared to develop a convenient method for piezo-resistive devices with simple structure and outstanding sensing performance. Graphene oxide was prepared through the modified Hummers method. Polyurethane foam was kept to soak in the obtained graphene oxide aqueous solution and then dried. After that, reduced graphene oxide/polyurethane composite foam has been fabricated under air phase reduction by hydrazine hydrate vapor. The chemical components and micro morphologies of the prepared samples have been observed by using FT-IR and scanning electron microscopy (SEM). The results predicted that the graphene is tightly adhered to the bare surface of the pores. The pressure sensing performance has been also evaluated by measuring the sensitivity, durability, and response time. The results indicate that the value of sensitivity under the range of 0–6 kPa and 6–25 kPa are 0.17 kPa⁻¹ and 0.005 kPa⁻¹, respectively. Cycling stability test has been performed 30 times under three varying pressures. The signal output just exhibits slight fluctuations, which represents the good cycling stability of the pressure sensor. At the same stage, the response time of loading and unloading of 20 g weight turned out to be about 300 ms. These consequences showed the superiority of graphene/polyurethane composite foam while applied in piezo-resistive devices including wide sensitive pressure range, high sensitivity, outstanding durability, and fast response. Full article

Nano/submicron particles can be activated by surfactants and aggregate at the air-water interface to generate and stabilize foams. Such systems have been applied extensively in the food, medicine, and cosmetic industries. Studying particle charging behavior in a particle/surfactant/water system is a fundamental way to understand the activation of the particle surface. This paper presents an investigation of the charging behavior of polystyrene (PS) particles dispersed in aqueous solutions of the surfactant sodium di-2-ethylhexylsulfosuccinate (AOT). The results showed that zeta potential of PS was related to the AOT concentration with two different concentration regions. Below the critical micelle concentration (CMC), the charging of PS particles was effected by AOT ions; while above the CMC, it came from both AOT ions and AOT micelles. This behavior was different from that observed for PS in aqueous salt solutions. Additionally, the particle concentration and size were found to affect the zeta potential differently in the two AOT concentration regions. By analyzing these results, the charging mechanism of the PS/AOT/water system was revealed to be preferential adsorption. In summary, the study disclosed the internal connection between the PS charging in aqueous AOT solution and the activation of PS particles, as well as their influence to foam formation and stability. Full article

In the oil industry, oil foams can be found at different steps from the crude oil treatment to the gas stations. Their lifetime can sometimes reach several hours and be much longer than the residence times available for gas/liquid separation. However, the conditions of formation and stability of such foams have been poorly studied in the literature, in contrast to the foamability of aqueous systems. On the fields, it is currently observed that crude oils enriched with asphaltenes form particularly stable foams. In this work, we have studied the influence of asphaltenes on the foamability of oil mixtures. All the experiments were performed on model systems of crude oils, that-is-to-say decane/toluene mixtures containing asphaltenes at concentrations ranging from 0.01 to 5 wt%. We in particular demonstrate that, within the investigated concentration range, asphaltenes from two different wells do not have any significant surface active properties despite their contribution to the foamability of oil mixtures. We show that the formation of an asphaltene layer at the interface with air that has been evidenced in the past results from solvent evaporation. Using a recently developed experiment based on the Marangoni effect with our model oils, we demonstrate that asphaltenes are not surface active in those oils. We further characterize the oil foamability by measuring the lifetime of the foam formed by blowing nitrogen through the liquid in a column. At concentrations larger than 1 wt%, asphaltenes significantly enhance the foamability of the oil mixtures. Moreover, the closer the asphaltenes are to their limit of precipitation the larger the foamability. However, we evidence that the oil mixtures themselves foam and we show the importance to consider that effect on the foamability. In addition, we observe that the foamability of the asphaltenes solutions unexpectedly varies with the initial height of the liquid in the column. We suggest that, although not significantly modifying the surface tension, the asphaltenes could be trapped at the oil/gas interface and thus prevent bubble coalescence. Full article

The influence of salinity on the characteristics of individual bubbles (2–4 mm in diameter) in fresh and saline water (up to 40 practical salinity units) was investigated. Bubbles were produced by forcing air through capillary tubes. Aqueous solutions in distilled and filtered tap waters with minimized presence of organic additives were used. Salinity, surface tension, and water temperature were monitored. Parameters measured were the bubble surface lifetime, diameter, and rise velocity. The surface lifetime varies widely (in the range of 0.4–35 s) depending on the salinity concentration and the purity of the solutions. Variations with salinity of size and rise velocity of large individual bubbles are discussed. Interpretation of the results in terms of anti-foaming (negative adsorption), as well as the Marangoni and the Gibbs effects, is helpful in understanding the results. Full article

The purpose of this research is to evaluate the fire-extinguishing performance of a compressed air foam system at different mixing ratios of pressurized air. In this system, compressed air is injected into an aqueous solution of foam and then discharged. The experimental device uses an exclusive fire-extinguishing technology with compressed air foam that is produced based on the Canada National Laboratory and UL (Underwriters Laboratories) 162 standards, with a 20-unit oil fire model (Class B) applied as the fire extinguisher. Compressed air is injected through the air mixture, and results with different air-to-aqueous solution foam ratios of 1:4, 1:7, and 1:10 are studied. In addition, comparison experiments between synthetic surfactant foam and a foam type which forms an aqueous film are carried out at an air-to-aqueous solution foam ratio of 1:4. From the experimental results, at identical discharging flows, it was found that the fire-extinguishing effect of the aqueous film-forming foam is greatest at an air-to-aqueous solution foam ratio of 1:7 and weakest at 1:10. Moreover, the fire-extinguishing effect of the aqueous film-forming foam in the comparison experiments between the aqueous film-forming foam and the synthetic surfactant foam is greatest. Full article