Short-chain Carboxylic Acids Research Articles

Phytoscreening for Per- and Polyfluoroalkyl Substances at a Contaminated Site in Germany.

The aim of this study was to perform a phytoscreening of per- and polyfluoroalkyl substances (PFAS) at a contaminated site in Germany, to investigate the applicability of this technique for PFAS contaminations. Foliage of three species, namely, white willow (Salix alba L.), black poplar (Populus nigra L.), and black alder (Alnus glutinosa L.), were sampled to evaluate seasonal and annual variations in PFAS concentrations. The results of the phytoscreening clearly indicated species and specific differences, with the highest PFAS sum concentrations ∑23 observed in October for white willow (0-1800 μg kg-1), followed by black poplar (6.7-32 μg kg-1) and black alder (0-13 μg kg-1). The bulk substances in leaves were highly mobile short-chain perfluoroalkyl carboxylic acids (PFCAs). In contrast, the PFAS composition in soil was dominated by long-chain PFCAs, perfluorooctanoic acid (PFOA) and perfluorodecanoic acid (PFDA), as a result of the lower mobility with ∑23PFAS ranging between 0.18 and 26 μg L-1 (eluate) and between 66 and 420 μg kg-1 (solid). However, the PFAS composition in groundwater was comparable to the spectrum observed in leaves. Spatial interpolations of PFAS in groundwater and foliage correspond well and demonstrate the successful application of phytoscreening to detect and delineate the impact of the studied PFAS on groundwater.

Enhanced degradation of sulfamethazine in FeCeOx Fenton-like system by tea polyphenols as reducing agents: Performance, mechanism and pathway

In this study, we constructed a Fenton-like system with FeCeOx nanocomposite, tea polyphenols (TP) and H2O2 for the degradation of sulfamethazine (SMT). Compared with other reducing agents (RAs), the addition of TP had a strong promoting effect on SMT degradation of FeCeOx/H2O2/RAs system, then FeCeOx/H2O2/TP system could realize the complete degradation of SMT within 90 min under optimized conditions of 150 mg·L−1 of catalyst dosage, 2.12 mmol·L−1 of H2O2 concentration, 115 mg·L−1 of TP dosage and 5.2 of initial pH. The main active species in FeCeOx/H2O2/TP system and their corresponding contributions to the SMT degradation were ranked as following: ∙OH (52.5%) > 1O2 (31.9%) > ∙O2- (15.6%). The reduction mechanism (heterogeneous catalysis) and chelation mechanism (homogeneous catalysis) of FeCeOx/H2O2/TP system were proposed. The addition of TP not only achieved the circulation of Fe/Ce species and the formation of oxygen vacancies on the catalyst surface, but also could accelerated the formation of various chelate structure in solution, which both contributed to the generation of active species. SMT was mineralized into CO2, H2O2 and some short chain carboxylic acids through five degradation pathways. Finally, FeCeOx/H2O2/TP system exhibited favorable degradation rate (>90%) towards SMT after six recycling times, and it could work effectively in different water sources. This study provided a new insight into Fenton-like process for improving pollutant degradation.

Competitive Reactions during Ethanol Chain Elongation Were Temporarily Suppressed by Increasing Hydrogen Partial Pressure through Methanogenesis Inhibition.

Organic waste streams can be converted into high-value platform chemicals such as medium-chain carboxylic acids (MCCAs) using mixed microbial communities via chain elongation. However, the heterogeneity of waste streams and the use of complex microbial communities can lead to undesirable reactions, thus decreasing process efficiency. We explored suppressing excessive ethanol oxidation to acetate (EEO) by increasing the hydrogen partial pressure (PH2) through hydrogenotrophic methanogenesis inhibition by periodically adding 2-bromoethanesulfonate (2-BES) to an MCCA-producing bioreactor to reach 10 mM of 2-BES upon addition. The bioreactor was fed with pretreated food waste and brewery waste containing high concentrations of short-chain carboxylic acids and ethanol, respectively. While 2-BES addition initially reduced EEO, some methanogens (Methanobrevibacter spp.) persisted and resistant populations were selected over time. Besides changing the methanogenic community structure, adding 2-BES also changed the bacterial community structure due to its impact on PH2. While we demonstrated that PH2 could be manipulated using 2-BES to control EEO, methods that do not require the addition of a chemical inhibitor should be explored to maintain optimum PH2 for long-term suppression of EEO.

Development of a Transformation System for Nitratireductor sp.

Nitratireductor sp. OM-1 can accumulate butenoic acid, which is a short-chain unsaturated carboxylic acid utilized for chemical products. So far, we have predicted the thioesterase gene, te, as a candidate gene for butenoic acid biosynthesis, based on comparative transcriptome analysis. To confirm the function of te, the gene transfer system in Nitratireductor sp. OM-1 was required. Thus, in this study, we used electroporation as a transformation system and pRK415, a broad host range plasmid, and optimized the conditions. As a result, a maximum transformation efficiency of 7.9 × 104 colonies/µg DNA was obtained at 22.5 kV/cm. Moreover, an expression vector, pRK415-te, was constructed by insertion of te, which was successfully transferred into strain OM-1, using electroporation. The recombinant OM-1 strain produced butenoic acid at 26.7 mg/g of dried cell weight, which was a 254% increase compared to transformants harboring an empty vector. This is the first report of a gene transfer system for Nitratireductor sp., which showed that the te gene was responsible for butenoic acid production.

Hydrochar coupled with iodide for efficient photodegradation of perfluorooctanoic acid and perfluorooctane sulfonic acid under ultraviolet light

Perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS) are typical emerging persistent organic pollutants that are raising concerns regarding their environmental persistence. The photodegradation of these chemicals in water can be promoted by generating hydrated electrons (eaq−). The present work demonstrates a highly efficient process combining ultraviolet (UV) radiation, hydrochar (H-BC) and KI that is capable of decomposing PFOA and PFOS. After 60 min of photolysis using this technique, 99.5 % and 94.1 % of the initial amounts of PFOA and PFOS in aqueous solution were degraded, respectively, with corresponding defluorination percentages of 87.8 % and 71.7 %, respectively. These degradation values were higher than the sum of those obtained using UV radiation with only H-BC or KI, implying a synergistic effect from the combination of H-BC and KI. This effect can be attributed to the unique structure and numerous oxygen-containing functional groups of the H-BC. This material was able to absorb PFOA and PFOS, reduce iodide oxidation products back to I−, act as an electron shuttle and shorten the diffusion distance to the target substrate. These factors all increased the probability of reactions between the contaminants and eaq−. Analyses by liquid chromatography/electrospray ionization/tandem mass spectrometry showed that short-chain perfluoroalkyl carboxylic acids with less than seven carbons were the primary degradation intermediates, suggesting that the photodegradation proceeded stepwise. These results confirmed the cooperative effect of the H-BC and iodide, leading to effective eaq− generation. This work is expected to facilitate the development of new strategies for the treatment of water systems contaminated with PFOA and PFOS.

Occurrence and implications of per and polyfluoroalkyl substances in animal feeds used in laboratory toxicity testing

The exceptional thermal and chemical stability and the amphiphilicity of per- and polyfluoroalkyl substances (PFAS) have resulted in widespread use and subsequent contamination in environmental media and biota. Concerns surrounding toxicity have led to numerous animal-based toxicity studies. Due to the ubiquity of PFAS and the low parts per trillion (ppt) health advisory levels for drinking water, several contamination elimination protocols have been implemented. In addition, it is urgently necessary to perform low-dose experiments, but due to unknown pathways for entry of unwanted PFAS, low-dose studies are extremely challenging to conduct. However, animal feed sources are a likely route that could introduce unwanted PFAS into experiments, yet investigations of PFAS in common animal feeds are lacking. Here, we report the examination of PFAS levels in eighteen different animal feeds, representing a range of diets fed to diverse taxa. We evaluated whether PFAS levels in feeds were correlated with ingredient composition (plant versus animal-based) or dietary habits of lab animals (amphibian, fish, invertebrate, mammal). PFOS, PFHxS, PFOA, and short-chain perfluoroalkyl carboxylic acids had the highest detection levels and frequencies across all samples. Different food ingredients led to different PFAS profiles. No meaningful levels of PFAS precursors were detected. We demonstrate that PFAS contamination in animal feed is pervasive. Reducing food-sourced PFAS is a critical, albeit challenging task to improve interpretability of in vivo exposures.

Electrochemical conversion of lignin to short-chain carboxylic acids

A method for direct electrochemical conversion of lignin to short-chain carboxylic acids is developed.

Fast and Complete Destruction of the Anti-Cancer Drug Cytarabine from Water by Electrocatalytic Oxidation Using Electro-Fenton Process

The fast and complete removal of the anti-cancer drug cytarabine (CYT) from water was studied, for the first time, by the electro-Fenton process using a BDD anode and carbon felt cathode. A catalytic amount (10−4 M) of ferrous iron was initially added to the solution as catalyst and it was electrochemically regenerated in the process. Complete degradation of 0.1 mM (24.3 mg L−1) CYT was achieved quickly in 15 min at 300 mA constant current electrolysis by hydroxyl radicals (●OH) electrocatalytically generated in the system. Almost complete mineralization (91.14% TOC removal) of the solution was obtained after 4 h of treatment. The mineralization current efficiency (MCE) and energy consumption (EC) during the mineralization process were evaluated. The absolute (second order) rate constant for the hydroxylation reaction of CYT by hydroxyl radicals was assessed by applying the competition kinetics method and found to be 5.35 × 109 M−1 s−1. The formation and evolution of oxidation reaction intermediates, short-chain carboxylic acids and inorganic ions were identified by gas chromatography-mass spectrometry, high performance liquid chromatography and ion chromatography analyses, respectively. Based on the identified intermediate and end-products, a plausible mineralization pathway for the oxidation of CYT by hydroxyl radicals is proposed.

Corrosion Behavior of Aluminum in some Short-chain Carboxylic Acid solutions as a Simulant for Cooling Water in HVDC Transmission

Corrosion Behavior of Aluminum in some Short-chain Carboxylic Acid solutions as a Simulant for Cooling Water in HVDC Transmission

Short-chain carboxylic acids in the scent gland secretions of the eastern small-scaled burrowing asp (Atractaspis fallax: Lamprophiidae, Serpentes, Reptilia)

Embedded in the tail base of all snakes is a pair of scent glands that open through ducts at the margin of the cloaca. Scent gland secretions (SGS), which typically are discharged when snakes are disturbed, are thought to deter predators. Previous chemical analyses have indicated carboxylic acids as the chief lipid constituents of SGS. We examined by GC-MS the SGS of the eastern small-scaled burrowing asp (Atractaspis fallax), a venomous, fossorial species in the Lamprophiidae, a diverse family containing more than 60 genera of mostly non-venomous African snakes. Our results confirm that acetic, propionic, 2-methylpropanoic, n-butanoic, and 3-methylbutanoic acids are the major constituents in the SGS samples of A. fallax. These compounds are widespread in the SGS of the Alethinophidia (‘typical snakes’). Some of these short-chain acids also occur in the anal glands of mammals and the uropygial (preen) glands of birds, where they arise via microbial activity. Whether these compounds in SGS have a similar origin is unknown.

The Effect of Short Chain Carboxylic Acids as Additives on the Crystallization of Methylammonium Lead Triiodide (MAPI)

Due to their exceptional properties, the study of hybrid perovskite (HyP) structures and applications dominate current photovoltaic prospects. Methylammonium lead tri-iodide perovskite (MAPI) is the model compound of the HyP class of materials that, in a few years, achieved, in photovoltaics, a power conversion efficiency of 25%. The attention on HyP has recently moved to large single crystals as emerging candidates for photovoltaic application because of their improved stability and optoelectronic properties compared to polycrystalline films. To control the quality and symmetry of the large MAPI single crystals, we proposed an original method that consisted of adding short-chain carboxylic acids to the inverse temperature crystallization (ICT) of MAPI in γ-butyrolactone (GBL). The crystals were characterized by single-crystal X-ray diffraction (SC-XRD), X-ray powder diffraction (XRPD) and Raman spectroscopy. Based on SC-XRD analysis, MAPI crystals grown using acetic and trifluoroacetic acids adopt a tetragonal symmetry “I4cm”. MAPI grown in the presence of formic acid turned out to crystallize in the orthorhombic “Fmmm” space group demonstrating the acid’s effect on the crystallization of MAPI.

Studying the influence of different parameters on the electrochemical oxidation of tannery dyes using a Ti/IrO2-SnO2-Sb2O5 anode

Electrochemical oxidation directly converts organic compounds into simple inorganic molecules like carboxylic acids, H2O and CO2, and it is considered an efficient method for treating highly polluted wastewater. In this study, MMO (Ti/IrO2-SnO2-Sb2O5) was tested for the electrochemical oxidation of mono-azo (Violet RL), diazo (Green A), and tetra-azo (Brown DR) dyes used in the tannery industry. The study focused on understanding the effect of different parameters such as supporting electrolyte, dye concentration, azo dye type, pH, and current density, on the performance of the electrochemical oxidation process of individual dyes and their mixture. Under 50 mM of Na2SO4 at pH 3 and j = 50 mA cm−2 close to 100% electrochemical oxidation was achieved when 50 mg L−1 Violet RL solution was tested. Using the best conditions of 35 mM NaCl + 25 mM Na2SO4 supporting electrolyte at pH 3.0 and 50 mA cm−2 current density, a rapid and complete discoloration of a mixture of the three azo dyes at 80 mg L−1 each, with about 92% COD decay and low energy consumption, with an acceptable low ECCOD value of 0.08 kWh (g COD)−1. To assess the complete level of dye oxidation, the evolution of nontoxic short-chain carboxylic acids was evaluated.

Using Au NPs anchored on ZrO2/carbon black toward more efficient H2O2 electrogeneration in flow-by reactor for carbaryl removal in real wastewater

In the present study, we designed a highly efficient catalyst for H2O2 production using gold nanoparticles (Au NPs) anchored on hybrid substrate composed of ZrO2 and Printex L6 carbon (Au-ZrO2/PL6C). The higher selectivity of Au-ZrO2/PL6C (97%) toward H2O2 electrogeneration and its improved activity in terms of ORR onset potential (140 mV for more positive values) compared to Au/PL6C (80%) were attributed to the synergism between Au NPs anchored on ZrO2/PL6C hybrid support. The results obtained from the application of the catalysts for H2O2 generation on gas diffusion electrode (GDE) after 120 min of electrolysis reflected the following order of efficiency: PL6C (∼140 mg L−1) < ZrO2/PL6C (∼235 mg L−1) < Au/PL6C (∼374 mg L−1) < Au-ZrO2/PL6C (∼600 mg L−1). Given that Au-ZrO2/PL6C exhibited the highest catalytic efficiency, this catalyst was employed for the removal of carbaryl (CBR) using different electrochemical advanced oxidation processes. The CBR degradation tests exhibited pseudo first-order kinetics, with the electro-Fenton (EF) and photoelectro-Fenton (PEF) processes recording the fastest removal kinetics (3.5 × 10−2 s−1 and 4.1 × 10−2 s−1, respectively). The PEF process exhibited the highest efficiency in terms of organic by-products mineralization; this was attributed to the additional photodecarboxylation of the Fe(III)-RCOOH complexes by UVC light. The aromatic by-products, short chain carboxylic acids, and ionic nitrogen species produced during the mineralization process contributed to the successful degradation of CBR. Apart from the analysis with synthetic water, the study also analyzed the treatment of urban wastewater spiked with CBR using a pre-pilot flow plant.

Electrochemical Advanced Oxidation of Perfluorooctanoic Acid: Mechanisms and Process Optimization with Kinetic Modeling.

Electrochemical advanced oxidation processes (EAOPs) are promising technologies for perfluorooctanoic acid (PFOA) degradation, but the mechanisms and preferred pathways for PFOA mineralization remain unknown. Herein, we proposed a plausible primary pathway for electrochemical PFOA mineralization using density functional theory (DFT) simulations and experiments. We neglected the unique effects of the anode surface and treated anodes as electron sinks only to acquire a general pathway. This was the essential first step toward fully revealing the primary pathway applicable to all anodes. Systematically exploring the roles of valence band holes (h+), hydroxyl radicals (HO•), and H2O, we found that h+, whose contribution was previously underestimated, dominated PFOA mineralization. Notably, the primary pathway did not generate short-chain perfluoroalkyl carboxylic acids (PFCAs), which were previously thought to be the main degradation intermediates, but generated other polyfluorinated alkyl substances (PFASs) that were rapidly degraded upon formation. Also, we developed a simplified kinetic model, which considered all of the main processes (mass transfer with electromigration included, surface adsorption/desorption, and oxidation on the anode surface), to simulate PFOA degradation in EAOPs. Our model can predict PFOA concentration profiles under various current densities, initial PFOA concentrations, and flow velocities.

Ultrasound-sodium percarbonate effectively promotes short-chain carboxylic acids production from sewage sludge through anaerobic fermentation

Short-chain carboxylic acids (SCCAs) production from sewage sludge via anaerobic fermentation is usually restricted by low substrates availability and rapid products consumption. Therefore, the ultrasound (US)-sodium percarbonate (SPC) technique was proposed to effectively break the bottlenecks. Results showed the total SCCAs yield, acetate yield and particulate organics reduction respectively attained 392.8 mg COD/g VSS, 204.6 mg COD/g VSS and 47.4 % under the optimal condition. Mechanistic explorations disclosed that US + SPC largely reduced biodegradation resistances of particulate organics and improved sludge biodegradability. The destruction of spatial structure was the inherent mechanisms for initial solubilization and further degradation of solid-phase sludge. Besides, US + SCP up-regulated hydrolytic and SCCAs-forming enzymes, but downregulated the key enzyme for methanation. Meanwhile, US + SPC altered the microbial structure and stimulated functional microorganism enrichment, well correlated with substrate biotransformation and products output. Overall, this strategy could effectively enhance SCCAs production from WAS and reduce the environmental risk for subsequent sludge disposal.

Improved quantitation of short-chain carboxylic acids in human biofluids using 3-nitrophenylhydrazine derivatization and liquid chromatography with tandem mass spectrometry (LC-MS/MS)

Short-chain carboxylic acids (SCCAs) produced by gut microbial fermentation may reflect gastrointestinal health. Their concentrations in serum and urine are indicative of specific metabolic pathway activity; therefore, accurate quantitation of SCCAs in different biofluids is desirable. However, it is often challenging to quantitate SCCAs since matrix effects, induced by the presence of a vast variety of other compounds other than SCCAs in complex biofluids, can suppress or enhance signals. Materials used for sample preparation may introduce further analytical challenges. This study reports for the first time a LC-MS/MS-based method to quantitate ten SCCAs (lactate, acetate, 2-hydroxybutyrate, propionate, isobutyrate, butyrate, 2-methylbutyrate, isovalerate, valerate and hexanoate) and evaluates the matrix effects in five human biofluids: serum, urine, stool, and contents from the duodenum and intestinal stoma bags. The optimized method, using 3-Nitrophenylhydrazone as a derivatization agent and a Charge Surface Hybrid reverse phase column, showed clear separation for all SCCAs at a concentration range of 0.1−100 µM, in a 10.5 min run without carry-over effects. The validation of the method showed a good linearity (R2 > 0.99), repeatability (CV ≤ 15%) assessed by intra- and inter-day monitoring. The lowest limit of detection (LLOD) was 25 nM and lowest limit of quantitation (LLOQ) was 50 nM for nine SCCA except acetate at 0.5 and 1 µM, respectively. Quantitative accuracy in all biofluids for most compounds was < ±15%. In summary, this methodology has the advantages over other techniques for its simple and fast sample preparation and a high level of selectivity, repeatability and robustness for SCCA quantification. It also reduced interferences from the matrix or sample containers, making it ideal for use in high-throughput analyses of biofluid samples from large-scale studies.

Effect of solution chemistry on the transport of short-chain and long-chain perfluoroalkyl carboxylic acids (PFCAs) in saturated porous media.

Perfluorocarboxylic acids (PFCAs) are one of the most widely detected classes of PFAS in the global environment after decades of intensive use. This study investigated the impact of perfluorinated carbon chain length on the transport behavior of PFCAs by testing and modeling two short-chain (PFPeA and PFHxA) and two long-chain PFCAs (PFOA and PFDA) in laboratory water-saturated columns. Moreover, their transport behavior was examined under different solution chemistry conditions, including pH, ionic strength, and cationic type. The experimental and simulation results indicated that the chain length had a limited impact on transport behaviors of PFPeA, PFHxA, and PFOA under various pH and ionic strengths, evidenced by their tracer-like breakthrough curves. In contrast, the mobility of PFDA was significantly affected by pH and ionic strengths. Additionally, the transport of all four PFCAs was inhabited in the presence of the divalent cation Ca2+. This study could help predict migration behavior and assess the potential risk of PFCAs in the subsurface system.

Micellar and sub-micellar chromatography with a cocamidopropyl betaine surfactant

We have coated a typical C18 column with the pH cationic charge controllable zwitterionic synthetic surfactant, cocamidopropyl betaine (CAPB), in order to generate a mixed mode reversed phase weak ion exchange column. As determined by the Thomas model, the column has an adsorbed surfactant capacity of 0.557 mmoles. The addition of 8.8 × 10–4 M CAPB to the totally aqueous mobile phase ensured stability of the surfactant on the column and permitted separation of the four component sulfonamide mixture with micellar liquid chromatography (MLC) in under 11 min. Comparatively, with a dilute H2SO4 mobile phase with no CAPB, the separation time for the sulfonamide mixture reached an excessive run time of an hour on the bare C18 chains. With CAPB in the mobile phase (no organic solvent present), a seven component sulfonamide mixture could be separated in less than 45 min. A five component short chain carboxylic acid mixture, separated in 20 min, was used to examine the ion exchange character of the column in pH environments of 2.3 and 4.6. Three phase MLC equilibrium analysis was also done in these pH environments with the sulfa drug and carboxylic acid mixtures to determine partition coefficients. Finally, a quite high molecular weight (70,000) anionic polystyrene sulfonate polymer was characterized by MLC with only CAPB and variable pH mobile phases; the optimal pH was determined to be 5.6. A totally aqueous mobile phase without CAPB was not suitable for profiling this polymer.

The potential of caproate (hexanoate) production using Clostridium kluyveri syntrophic cocultures with Clostridium acetobutylicum or Clostridium saccharolyticum.

Caproate (hexanoate) and other medium-chain fatty acids are valuable platform chemicals produced by processes utilizing petroleum or plant oil. Clostridium kluyveri, growing on short chain alcohols (notably ethanol) and carboxylic acids (such as acetate) is noted for its ability to perform chain elongation to produce 4- to 8-carbon carboxylates. C. kluyveri has been studied in monoculture and coculture conditions, which lead to relatively modest carboxylate titers after long fermentation times. To assess the biosynthetic potential of C. kluyveri for caproate production from sugars through coculture fermentations, in the absence of monoculture data in the literature suitable for our coculture experiments, we first explored C. kluyveri monocultures. Some monocultures achieved caproate titers of 150 to over 200 mM in 40–50 h with a production rate of 7.9 mM/h. Based on that data, we then explored two novel, syntrophic coculture partners for producing caproate from sugars: Clostridium acetobutylicum and Clostridium saccharolyticum. Neither species has been cocultured with C. kluyveri before, and both demonstrate promising results. Our experiments of C. kluyveri monocultures and C. kluyveri—C. saccharolyticum cocultures demonstrate exceptionally high caproate titers (145–200 mM), fast production rates (3.25–8.1 mM/h), and short fermentation times (18–45 h). These results represent the most caproate produced by a C. kluyveri coculture in the shortest known fermentation time. We also explored the possibility of heterologous cell fusion between the coculture pairs similar to the results seen previously in our group with C. acetobutylicum and Clostridium ljungdahlii. Fusion events were observed only in the C. acetobutylicum—C. kluyveri coculture pair, and we offer an explanation for the lack of fusion between C. saccharolyticum and C. kluyveri. This work supports the promise of coculture biotechnology for sustainable production of caproate and other platform chemicals.

Environmentally-friendly short-chain perfluoropolyether polyacrylates emulsion films for high water barrier coating applications

Water-based protective coatings have gained wide popularity because of their low toxicity and volatile organic compounds (VOCs) emissions. However, improving water barrier performance is a significant challenge. An environmentally friendly short-chain perfluoropolyether carboxylic acid (PFPE-MMA) material has been synthesized in this study, and a series of PFPE-based polyacrylates were prepared using RAFT miniemulsion copolymerization. The impact of PFPE chains and crystalline stearyl methacrylate (SMA) on the wettability of copolymer latex films and their use in protective coatings were studied. Based on the surface and bulk morphology of latex films, the addition of SMA to PFPE-based polyacrylates promoted PFPE chains to migrate toward the air/film interface, leading to exceptional wettability and water resistance through the matrix, resulting in remarkable water barrier properties. After 192 h, the water absorption ratio of 25% PFPE-7% SMA latex film was 3.98%, while that of 25% PFPE latex film was 6.03%. Not only are PFPE-based polyacrylates excellent protective materials with potential applications, but they are also an effective preparation strategy for improving the high barrier property in waterborne protective coatings.