Aqueous Foam Research Articles

Non-target screening reveals 124 PFAS at an AFFF-impacted field site in Germany specified by novel systematic terminology.

The uncontrolled release of aqueous film-forming foam (AFFF) ingredients during a major fire incident in Reilingen, Germany, in 2008 led to significant soil and groundwater contamination. As the identity of fluorochemical surfactants in AFFF are often veiled due to company secrets, it is important to characterize AFFF contaminations and their impact on the environment comprehensively. In this study, we adapted a systematic approach combining a suitable extraction method with liquid chromatography high-resolution quadrupole time-of-flight mass spectrometry (LC-QTOF-MS) for an extensive non-targeted analysis. Our analysis identified 124 per- and polyfluoroalkyl substances (PFAS) from 42 subclasses in the contaminated soil (confidence levels of identification between 1 and 3). Typical for AFFF-impacted field sites, these included anionic, cationic, and zwitterionic substances with perfluoroalkyl chains spanning from 3 to 14 carbon atoms. Furthermore, we identified 1 previously unreported substance, and detected 9 PFAS subclasses for the first time in soil. AFFFs have long been employed to extinguish large hydrocarbon fires, yet their environmental consequences remain a concern. This study sheds light on the complex composition of AFFFs at this particularly contaminated area, emphasizing the necessity for extensive contaminant characterization as sound basis for informed management strategies to mitigate their adverse effects. AFFF PFAS are often named differently in the literature, leading to inconsistency in terminology. To address this issue, we introduced partially new terminology for AFFF-related PFAS to establish consistent terminology, to facilitate communication of identified compounds, and to ensure that the chemical structure can be directly derived from acronyms.

Shift from legacy to emerging per- and polyfluoroalkyl substances for watershed management along the coast of China

Per- and polyfluoroalkyl substances and their short-chain alternatives have attracted world-wide attention due to their widespread presence and persistence in the environment. However, the sources, environmental fate, and driving forces of PFAS in coastal ecosystems remain poorly understood. In this study, the spatial distribution, source apportionment, and driving mechanisms of PFAS were investigated through a comprehensive analysis of water samples collected along the China's coastline. The concentrations of Σ25PFAS in water samples followed a general pattern, with higher levels observed in northern coastal zones of China than the south, ranging from 0.72 to 1872.21 ng L−1. PFOA and PFBA were dominant. Emerging short-chain PFAS, such as PFBS, PFBA, F-53B and GenX, were frequently detected, with detection rates of 97%, 99%, 95% and 77%, respectively. This indicated a shift in coastal PFAS contamination from legacy compounds to emerging short-chain alternatives. Source apportionment using the Positive Matrix Factorization model identified key contributors to PFAS pollution, including textile production, volatile precursors, precious metal industries, aqueous film-forming foam, metal-plating, electrochemical fluorination, and fluoropolymer manufacturing. Additionally, PFAS concentrations were significantly positively correlated with cultivated land, urban area, and wastewater discharge, while negatively correlated with annual precipitation and woodland coverage (p < 0.05). Socio-economic development was identified as a major driver of PFAS emissions, while the hydrological factors and vegetation coverage can significantly enhance watershed resilience against PFAS pollution.

Characterizing the Areal Extent of PFAS Contamination in Fish Species Downgradient of AFFF Source Zones.

Most monitoring programs next to large per- and polyfluoroalkyl substances (PFAS) sources focus on drinking water contamination near source zones. However, less is understood about how these sources affect downgradient hydrological systems and food webs. Here, we report paired PFAS measurements in water, sediment, and aquatic biota along a hydrological gradient away from source zones contaminated by the use of legacy aqueous film-forming foam (AFFF) manufactured using electrochemical fluorination. Clustering analysis indicates that the PFAS composition characteristic of AFFF is detectable in water and fishes >8 km from the source. Concentrations of 38 targeted PFAS and extractable organofluorine (EOF) decreased in fishes downgradient of the AFFF-contaminated source zones. However, PFAS concentrations remained above consumption limits at all locations within the affected watershed. Perfluoroalkyl sulfonamide precursors accounted for approximately half of targeted PFAS in fish tissues, which explain >90% of EOF across all sampling locations. Suspect screening analyses revealed the presence of a polyfluoroketone pharmaceutical in fish species, and a fluorinated agrochemical in water that likely does not accumulate in biological tissues, suggesting the presence of diffuse sources such as septic system and agrochemical inputs throughout the watershed in addition to AFFF contamination. Based on these results, monitoring programs that consider all hydrologically connected regions within watersheds affected by large PFAS sources would help ensure public health protection.

Determination of Toxicity at Different Trophic Levels of Aqueous Film-Forming Foams (AFFF) Used in Fire Fighting.

Aqueous film-forming foams (AFFF), containing perfluorinated surfactants, can reach the environment. The objective of this study was to determine the ecotoxicity of AFFF, according to the type of fire to be fought (A1: 1.05g.L- 1, A2: 3.15g.L- 1 and A3: 6.30g.L- 1), to bioindicators of different trophic levels. For Artemia salina a toxic effect was observed at sample A1 (at concentrations of 100%), A2 (at concentrations above 25%) and A3 (at concentrations above 12.5%). For Lactuca sativa all samples affected the number of germinated seeds, speed and percentage of germination and root length. To the Eisenia fetida earthworm, samples A2 and A3 were considered toxic due to the percent avoidance being 70% and 100%, respectively. In Macaca mullata renal cell culture test, none of the samples were toxic by the MTT test. Therefore, it is necessary to develop methods for the safe use of AFFF by professionals.

Making Waves: The Progress of Management Strategies for Cleaning and Rinsing of PFAS-Impacted Fire Suppression Systems

Aircraft rescue firefighting (ARFF) vehicles often contain residual levels of per- and polyfluoroalkyl substances (PFAS) due to the global use of legacy and current use of aqueous film-forming foam (AFFF) for class B firefighting. However, numerous countries are transitioning to fluorine-free foam (F3) alternatives. There is, thus, an urgent need to develop efficient methods to rinse and clean interior ARFF surfaces thereby avoiding expensive replacement costs and preventing further discharge of PFAS to the environment. However, the unique self-assembly behavior of amphiphilic PFAS is a complicating factor that can result in measurable levels of PFAS within replacement F3s following cleanout efforts (i.e., the rebound effect). This Making Waves article aims to elucidate the emerging challenges associated with cleanout of impacted ARFF vehicles and introduce the current efforts for PFAS management of rinsate derived from cleanout of impacted fire suppression infrastructure.

PFAS: The Journey from Wonder Chemicals to Environmental Nightmares and the Search for Solutions

Per- and polyfluoroalkyl substances (PFAS) are diverse synthetic chemicals manufactured over seven decades. It is an aliphatic molecule with a basic hydrophobic structure of carbon and fluorine linked to a hydrophilic end group. Due to their physicochemical properties associated with the unique structure, PFAS has been used in a wide variety of applications including aqueous film-forming foams (AFFF), paper, carpets, non-stick cookware, etc. as they make products resistant to water, heat, and stains. These molecules have drawn great attention recently for their unique properties, high stability and low degradability, and so-called “Forever Chemicals”. PFAS has the strongest carbon-fluorine bond which makes them persistent in the environment. Hence it contaminates natural resources and endangers public health. This review discusses the discovery, development, and evolution of PFAS from the wonder chemical era to a nightmare chemical era, exposure and its impacts on human health and the environment, current remediation techniques, and future trends of PFAS molecules and related products. The primary objective of this review is to identify knowledge gaps on PFAS contamination, remediation methods, and possible PFAS alternatives.

Synthesis of carboxyl group functionalized polyhedral oligomeric silsesquioxane for fabricating ultrastable foams driven by high temperature and salinity

Aqueous foams are thermodynamically unstable systems, and their instability increases with temperature and salinity. In this study, we successfully synthesized an amphiphilic polyhedral oligomeric silsesquioxane, POSS-NH2-BTCA, featuring phenyl and carboxyl groups, through a substitution reaction. Highly stable foams were prepared under temperatures conditions ranging from 50 to 90 °C and salinity levels between 20 and 80 g/L. Rheological tests and scanning electron microscopy analysis show that the interactions between divalent ions and carboxyl groups improve the film strength. However, the half-life of the drainage only increased from 38 s to 55 s. Therefore, the enhancement in foam stability is believed to be caused by the inhibition of coarsening and coalescence rather than the suppression of drainage. The strategy for fabricating amphiphilic nanoparticles can serve as a reference for designing new foam stabilizers for high temperature and salinity conditions.

Spectral induced polarization (SIP) measurements across a PFAS-contaminated source zone

There is a need to develop field-scale, in situ screening technologies for assessing variations in aqueous film-forming foam (AFFF) concentrations in soils at former fire training and storage sites. Field-scale Spectral Induced Polarization (SIP) geophysical measurements were acquired on a transect crossing an AFFF source zone. Soil samples were acquired to determine variations in poly- and per-fluoroalkyl substances (PFAS) concentrations in soils, characterize soil texture, and create triplicate soil columns for laboratory SIP measurements. Field and laboratory observations show that SIP measurements are sensitive to the concentration of AFFF constituents associated with soil pore surface area. The specific polarizability and the phase of the SIP measurements for the laboratory samples were linearly correlated with total soil-sorbed PFAS concentration. The phase from the field SIP measurements was highest over the location of maximum PFAS concentration measured on the laboratory samples. However, a significant correlation between field-measured phase and laboratory-measured total PFAS concentration still needs to be established. These observations, along with the demonstrated sensitivity of the SIP response to the removal of soil PFAS using a methanol wash procedure, support the case for SIP characterization of AFFF source zones.

Closing PFAS analytical gaps: Inter-method evaluation of total organofluorine techniques for AFFF-impacted water

Multiple poly- and perfluoroalkyl substances (PFASs) are present in aqueous film-forming foams (AFFF) used for firefighting activities. Currently, no single analytical technique provides a complete accounting of total PFASs or total organofluorine content in AFFF-contaminated samples. To provide insight into the performance of existing methods, we compared ten previously described PFAS measurement techniques. In AFFF-amended tap water, US EPA Methods 533 and 1633, adsorbable organic fluorine with particle induced gamma emission spectroscopy (AOF-PIGE) and fluorine-19 nuclear magnetic resonance (19F NMR) provided similar estimates of total fluorine. The total oxidizable precursor (TOP) assay, suspect screening, and adsorbable organic fluorine with combustion ion chromatography (AOF-CIC) yielded estimates of total organic fluorine that were about two to three times higher than the other techniques. Proximate to AFFF sources, suspect screening and modified EPA Method 1633 yielded higher results, while the TOP assay results were between the other two sets of analyses. Further from sources, suspect screening, modified EPA Method 1633, and the TOP assay yielded similar results that were 4-fold higher than results from targeted quantification methods, such as EPA Method 1633. These results are consistent with expectations about PFAS behavior and inform the selection of analytical techniques used for PFAS contamination characterization efforts.

Pickering Foam Stabilized by Diacylglycerol-Based Solid Lipid Nanoparticles: Effect of Protein Modification.

Pickering foams have great potential for applications in aerated foods, but their foaming ability and physical stability are still far from satisfactory. Herein, solid lipid particles (SLNs) were fabricated by using diacylglycerol of varying acyl chain lengths with modification by a protein. The SLNs showed different crystal polymorphisms and air-water interfacial activity. C14-DAG SLN with a contact angle ∼ 79° formed aqueous foam with supreme stability and high plasticity. Whey protein isolate and sodium caseinate (0.1 wt %) considerably enhanced the foamability and interfacial activity of SLNs and promoted the packing of particles at the bubble surface. However, high protein concentration caused foam destruction due to the competitive adsorption effect. β-sheet increased in protein after adsorption and changed the polymorphism and thermodynamic properties of SLN. The foam collapsing behaviors varied in the presence of protein. The results gave insights into fabricating ultrastable aqueous foams by using high-melting DAG particles. The obtained foams demonstrated good temperature sensitivity and plasticity, which showed promising application prospects in the food and cosmetic fields.

Assessing the effects of fluorine-free and PFAS-containing firefighting foams on development and behavioral responses using a zebrafish-based platform

Significant progress has been made in developing fluorine-free firefighting foams (F3) as alternatives to perfluoroalkyl substances (PFAS)-containing aqueous film-forming foams (AFFF) to help eliminate the health and environmental concerns linked to PFAS exposure. However, developing viable F3 options hinges on a thorough assessment of potential risks alongside the technical performance evaluations. This study showcases the capability of a zebrafish-based platform to discern the developmental and behavioral toxicities associated with exposure to one AFFF and two F3 formulations. To facilitate direct exposure to the chemicals, embryos were enzymatically dechorionated and then exposed to the diluted formulations (6–120 hours post fertilization (hpf)) at concentrations folding from 0.1% of the manufacturer-recommended working concentrations. The exposure regimen also included daily automated media changes (50%) and mortality assessments (24 and 120 hpf). At 120 hpf, a comprehensive assessment encompassing overall development, prevalence of morphological defects, and behavioral responses to acute stressors (visual, acoustic, and peripheral irritant) was conducted. Exposure to both F3s significantly increased larval mortalities to percentages exceeding 90%, whereas AFFF exposures did not cause any significant effect. Overall development, marked by total larval length, was significantly impacted following exposures to all foams. Behavioral responses to acute stressors were also significantly altered following exposures to both F3s, whereas the AFFF did not alter behavior at the concentrations tested. Our findings demonstrate toxicities associated with tested F3 formulations that encompass several endpoints and highlight the utility of the proposed platform in evaluating the developmental toxicities of current and future foam formulations.

One-step preparation and characterization of an imidazolium-contained fluorocarbon surfactant and its potential application in aqueous film-forming foam

One-step preparation and characterization of an imidazolium-contained fluorocarbon surfactant and its potential application in aqueous film-forming foam

Consolidating two-dimensional liquid chromatography–high-resolution tandem mass spectrometry (LC×LC-HRMS/MS) technique for the non-targeted analysis of poly- and perfluorinated substances: A trial on aqueous film-forming foams

To date, poly- and perfluoroalkyl substances (PFAS) represent a real threat for their environmental persistence, wide physicochemical variability, and their potential toxicity. Thus far a large portion of these chemicals remain structurally unknown. These chemicals, therefore, require the implementation of complex non-targeted analysis workflows using liquid chromatography coupled with high-resolution mass spectrometry (LC-HRMS) for their comprehensive detection and monitoring. This approach, even though comprehensive, does not always provide the much-needed analytical resolution for the analysis of complex PFAS mixtures such as fire-fighting aqueous film-forming foams (AFFFs). This study consolidates the advantages of the LC×LC technique hyphenated with high-resolution tandem mass spectrometry (HRMS/MS) for the identification of PFAS in AFFF mixtures. A total of 57 PFAS homolog series (HS) were identified in 3M and Orchidee AFFF mixtures thanks to the (i) high chromatographic peak capacity (n’2D,c ~ 300) and the (i) increased mass domain resolution provided by the “remainder of Kendrick Mass” (RKM) analysis on the HRMS data. Then, we attempted to annotate the PFAS of each HS by exploiting the available reference standards and the FluoroMatch workflow in combination with the RKM defect by different fluorine repeating units, such as CF2, CF2O, and C2F4O. This approach resulted in 12 identified PFAS HS, including compounds belonging to the HS of perfluoroalkyl carboxylic acids (PFACAs), perfluoroalkyl sulfonic acids (PFASAs), (N-pentafluoro(5)sulfide)-perfluoroalkane sulfonates (SF5-PFASAs), N-sulfopropyldimethylammoniopropyl perfluoroalkane sulfonamides (N-SPAmP-FASA), and N-carboxymethyldimethylammoniopropyl perfluoroalkane sulfonamide (N-CMAmP-FASA). The annotated categories of perfluoroalkyl aldehydes and chlorinated PFASAs represent the first record of PFAS HS in the investigated AFFF samples.

Exploring the Prospects and Challenges of Fluorine-Free Firefighting Foams (F3) as Alternatives to Aqueous Film-Forming Foams (AFFF): A Review.

This review provides a comparative analysis of the performance, toxicity, environmental impact, and health risks associated with fluorotelomer-based/short-chain AFFF and F3. Despite notable progress in F3 development, achieving comparable performance remains challenging in some cases. F3 formulations, while promising, are yet to be considered a direct replacement for AFFF in all Class B fire suppression scenarios due to variations in their performance across different fuel types and test conditions. Available studies indicate that commercially available F3 exhibit greater biodegradability and reduced environmental persistence compared to AFFF. However, some alternatives may still pose similar environmental impacts. Limited ecotoxicity studies suggest that some F3 may exhibit equal or even higher toxicity to aquatic species than short-chain (C6) AFFF. Toxicological assessments and risk evaluations of F3 should consider factors beyond environmental persistence, including acute and chronic ecotoxicity, potential endocrine disruption, and the full toxicological profile of foam formulations and their individual components. Further research is necessary to understand the fate, transport, bioaccumulation, and toxicity of F3 degradation products. Addressing these knowledge gaps is crucial to ensure the safe and sustainable implementation of F3 as an alternative fire suppression solution.

Phytoremediation Potential of Azolla filiculoides: Uptake and Toxicity of Seven Per- and Polyfluoroalkyl Substances (PFAS) at Environmentally Relevant Water Concentrations.

Environmental contamination of aquatic systems by per- and polyfluoroalkyl substances (PFAS) has generated significant health concerns. Remediation of contaminated sites such as the fire-fighting emergency training grounds that use aqueous film-forming foams is a high priority. Phytoremediation may help play a part in removing PFAS from such contaminated waters. We investigated the potential of the water fern Azolla filiculoides, which is used for phytoremediation of a wide range of contaminants, to uptake seven common PFAS (perfluorobutanoic acid [PFBA], perfluorobutane sulfonic acid [PFBS], perfluoroheptanoic acid [PFHpA], perfluorohexanoic acid [PFHxA], perfluorohexane sulfonic acid [PFHxS], perfluorooctanoic acid [PFOA], and perfluoropentanoic acid [PFPeA]), during a 12-day exposure to environmentally relevant concentrations delivered as equimolar mixtures: low (∑PFAS = 0.0123 ± 1.89 μmol L-1), medium (∑PFAS = 0.123 ± 2.88 μmol L-1), and high (∑PFAS = 1.39 μmol L-1) treatments, equivalent to approximately 5, 50, and 500 µg L-1 total PFAS, respectively. The possible phytotoxic effects of PFAS were measured at 3-day intervals using chlorophyll a content, photosystem II efficiency (Fv/Fm), performance index, and specific growth rate. The PFAS concentrations in plant tissue and water were also measured every 3 days using ultra-high-performance liquid chromatography-tandem mass spectrometry. Treatments with PFAS did not lead to any detectable phytotoxic effects. All seven PFAS were detected in plant tissue, with the greatest uptake occurring during the first 6 days of exposure. After 12 days of exposure, a maximum bioconcentration factor was recorded for PFBA of 1.30 and a minimum of 0.192 for PFBS. Consequently, the application of Azolla spp. as a stand-alone system for phytoremediation of PFAS in aquatic environments is not sufficient to substantially reduce PFAS concentrations. Environ Toxicol Chem 2024;00:1-12. © 2024 The Author(s). Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.

Anomalous diffusion of hydrocarbon vapor through an aqueous foam bubble structure

Hydrocarbons are known as “anti-foamers” because they cause bubble rupture, coalescence, and reduce foaming. We show that the dynamics of bubble structure allows hydrocarbon vapors permeate rapidly when an aqueous foam is placed on a hydrocarbon pool. Two distinct foam layers are formed. Vapor accumulates in an expanding bottom layer at the foam-pool interface where bubbles grow rapidly, rupture, and coalesce. Simultaneously, vapor diffuses through a top layer having small bubble structure, which changes slowly due to Ostwald-ripening. Very little vapor accumulates in the top layer, which has a constant thickness equal to the initial foam thickness. Surprisingly, both accumulation in the bottom layer and diffusion through top layer occur at constant rates, which are independent of time and initial foam thickness. The vapor diffusion rate in the top layer should have decreased, inversely proportional to the initial foam thickness, based on classical diffusion theory; only the fluorosurfactant containing foam (RefAFFF) placed on gasoline follows the classical theory where the bottom foam layer is absent. Therefore, we propose a theory to show a linear increase in diffusion time with initial foam thickness using an effective diffusion-coefficient. Experiments show that this variation could be because of increased liquid drainage, drying, and bubble coarsening, which are not considered explicitly in the theory. We also describe a theory for the expanding bottom layer to show that most vapor formed at the pool surface accumulates for very volatile hydrocarbons. The vapor diffusion controls foam ignition. We show that the measured foam ignition time also increases linearly with initial foam thickness, qualitatively consistent with the predicted diffusion time. By employing different hydrocarbons, we show that the measured foam ignition times decrease inversely proportion to square root of hydrocarbon vapor concentration for a given surfactant. This could be because a surfactant exhibits different degrees of oleophobicity towards different hydrocarbons that can reduce vapor adsorption, solubility, and diffusion at a bubble surface. Different surfactants also exhibit different degrees of oleophobicity towards a given hydrocarbon (n-pentane) and increase ignition times by a factor of six: RefAFFF having the longest ignition time, followed by siloxane-polyoxyethylene formulation, and its individual surfactant components.

Characterization of aqueous foams of alkyl polyglycoside, GreenZyme, alpha-olefin sulfonate, and cetyltrimethylammonium bromide in the presence of divalent ions

In this study, the impacts of divalent ions (calcium and magnesium) on aqueous foam stability and its rheological properties are investigated. A biodegradable surfactant of alkyl polyglycoside, (APG) and a commercial enzyme (GreenZyme, GZ) are used and their performance were compared with synthetic surfactants of alpha-olefin sulfonate (AOS) and cetyltrimethylammonium bromide (CTAB). The findings of the study revealed that the stability of all foams decreased with increasing concentrations of divalent ions, GZ recorded the lowest foam stability in the presence of the two ions and precipitation occurred in the AOS solution. On the other hand, foams generated by APG achieved the highest stability and the foams generated by CTAB showed the second highest stability among the foaming agents. Through rheological analyses, APG and CTAB exhibited shear thinning behaviour and their behaviour were modelled using a power law model in which the model can incorporate the effects of temperature and salinity.

Biotransformation of PFAA Precursors by Oxygenase-Expressing Bacteria in AFFF-Impacted Groundwater and in Pure-Compound Studies with 6:2 FTS and EtFOSE.

Numerous US drinking water aquifers have been contaminated with per- and polyfluoroalkyl substances (PFAS) from fire-fighting and fire-training activities using aqueous film-forming foam (AFFF). These sites often contain other organic compounds, such as fuel hydrocarbons and methane, which may serve as primary substrates for cometabolic (i.e., nongrowth-linked) biotransformation reactions. This work investigates the abilities of AFFF site relevant bacteria (methanotrophs, propanotrophs, octane, pentane, isobutane, toluene, and ammonia oxidizers), known to express oxygenase enzymes when degrading their primary substrates, to biotransform perfluoroalkyl acid (PFAA) precursors to terminal PFAAs. Microcosms containing AFFF-impacted groundwater, 6:2 fluorotelomer sulfonate (6:2 FTS), or N-ethylperfluorooctane sulfonamidoethanol (EtFOSE) were inoculated with the aerobic cultures above and incubated for 4 and 8 weeks at 22 °C. Bottles were sacrificed, extracted, and subjected to target, nontarget, and suspect screening for PFAS. The PFAA precursors 6:2 FTS, N-sulfopropyldimethyl ammoniopropyl perfluorohexane sulfonamide (SPrAmPr-FHxSA), and EtFOSE transformed up to 99, 71, and 93%, respectively, and relevant daughter products, such as the 6:1 fluorotelomer ketone sulfonate (6:1 FTKS), were identified in quantities previously not observed, implicating oxygenase enzymes. This is the first report of a suite of site relevant PFAA precursors being transformed in AFFF-impacted groundwater by bacteria grown on substrates known to induce specific oxygenase enzymes. The data provide crucial insights into the microbial transformation of these compounds in the subsurface.

High-performance lightweight foam concrete enabled by compositing ultra-stable hydrophobic aqueous foam

The major limitations of lightweight foam concrete are inferior mechanical properties and durability. This study designs a novel high-modulus hydrophobic foam to produce high-strength and durable foam concrete. Poly (methyl hydrogen)siloxane (PMHS) was employed to construct a hydrophobic boundary of hydroxypropyl methylcellulose (HPMC) foam. The produced hydrophobic foam bubbles exhibit a high modulus, fine bubble size, and exceptional thermodynamic stability. A dense foam wall of 8 μm in thickness functions as a structure for chemical loadings of inorganic-organic particles onto the viscoelastic bubble film. This facilitates their interaction effect of adsorption and chemical bonding, contributing to the hydrophobic nature of the foam wall. The resulting hydrophobic foam concrete shows low water adsorption and high mechanical strength. The hydrophobic foam concrete demonstrates superior chemical resistance and anti-chloride diffusion compared with normal concrete. This study might provide a practical strategy for designing high-performance lightweight foam concrete with significant potential as structural elements.

Air‐laid and foam‐laid nonwoven composites: The effect of carrier medium on mechanical properties

AbstractThermoplastic nonwoven composites were produced with the air‐laying and foam‐forming processes from cellulosic and plastic fibers. The two raw material combinations were (1) PP/PE (fiber length 3 mm), PP/PE (12 mm), fluff pulp fibers (2 mm) and (2) PP/PE (3 mm), fluff pulp fibers, viscose (10 mm). After forming, the fibrous sheets (400 gsm) were bonded with heat pressing (145°C). The effect of the carrier medium, air or aqueous foam, on the tensile and impact properties and sheet structure was explored. The air‐laids differed from the foam‐laids by sheet anisotropy, density, and the lack of an additional bonding regime between wood fibers due to the dry forming process. The PP/PE bonding fibers gave the air‐laids a good capacity to elongate compared to the foam‐laids. The advantage was lost when nonbonding viscose was added. The impact strength was dependent on the PP/PE dosage and the sheet density, rather than the moisture‐induced bonding between wood fibers. The changing long/short fiber ratios caused gradual shifts in sheet properties, usually a reduction in a mechanical property as the share of short fiber increased in the mix. Economic analysis revealed that increasing fluff content can reduce raw material costs, providing a possibility for cost optimization in total production costs.