Latex Films Research Articles

Deformation Behavior of Microparticle-Based Polymer Films Visualized by AFM Equipped with a Stretching Device.

Understanding the structural changes and property alterations at the nanoscale and microscopic levels is critical to clarifying the deformation behavior and mechanical properties of polymer materials. Especially, in latex films composed of polymer nanoparticles, it is widely accepted that the remaining interfaces between microparticles in the film affect their brittleness. However, detailed information on nanoscale changes of latex films during deformation remains unclear due to technical difficulties in analyzing the microstructures under mechanical stress. In this study, we employed atomic force microscopy equipped with a uniaxial stretching device to visualize the surface structures of films composed of slightly cross-linked microparticles under elongation strain. The observations revealed that the latex film deforms in a nonaffine manner, which is attributed to the concurrent deformation of individual microparticles and the pull-out of interpenetration between them. Furthermore, by introducing a load-strain measurement mechanism to the stretching device, we compared the relationships between nanostructural changes, local property changes, and macroscopic deformation of microparticle-based films. The results suggest that loads are dominated by the deformation of microparticles and dissipate as the interpenetration of surface polymer chains between microparticles is pulled out.

Synthesis and properties of superhydrophobic monomer stearyl methacrylate-modified polyacrylate latex pressure sensitive adhesives

Hybrid surfactants of long carbon chain hydrophobic nonionic emulsifier N-390 and conventional anionic emulsifier CO-436 were utilized in this study to enable successful emulsion polymerization of super-hydrophobic monomer stearyl methacrylate (SMA) together with butyl acrylate (BA), acrylic acid (AA), and 2-hydroxyethyl acrylate (HEA). The influences of SMA on the resulting latex and film properties were thoroughly investigated. Both FTIR and 1H NMR were used to confirm the successful participation of SMA in the emulsion polymerization. The results indicated that with introduction of SMA, the roughness of the latex film increases, while the light transmission decreases. It was also found that with the addition of SMA, contact angle of the latex PSA film increased from 115.1° to 127.2°, while water absorption decreased from 5.76 to 2.89 wt%. DSC curves demonstrated that SMA has participated more in the homopolymerization reaction than in the copolymerization reaction. TGA results showed that the initial decomposition temperature (T5%) of the latex film was increased from 302.8 to 332.7 °C with the increase of SMA dosage from 0 to 20 wt%. Finally, adhesion properties results indicated that loop tack and 180° peel force of the PSA films were decreased from 11.51 to 1.88 N/25 mm and 6.36 to 3.44 N/25 mm, respectively, while shear strength was increased from 732 to 2865 min.

Preparation and properties of fluorinated VAc-VeoVa10 latex emulsified with allyl nonyl phenoxy propyl alcohol polyoxyethylene ether ammonium sulphate

Purpose The traditional VeoVa10-VAc copolymer latex, which prepared via the emulsion polymerization of the mixed monomers of VAc and VeoVa10, has the poor water resistance and thermal stability because of the migration of the conventional emulsifier molecules and the low bond energy of C-C bond. The purpose of this work is that the fluorinated monomer is used to modify the latex. The film of the resultant latex has the C-F bond with high bond energy and low surface energy, which can effectively improve the heat resistance and water resistance of the resultant film. In addition, the reactive emulsifier is used to replace the conventional emulsifier. The drawbacks of the conventional emulsifier molecules migrate and desorb can be avoided when the polymer latex is stored, thereby also improving the water resistance. Design/methodology/approach The modified VAc-VeoVa10 latex has been successfully synthesized via the semi-continuous seeded emulsion polymerization, which VAc and VeoVa10 is used as the main monomers and HFMA was used as the functional monomer. KPS and reactive surfactants of SE-10 were used as the initiator and emulsifier, respectively. The structure of resultant latex film was characterized by Fourier transform infrared spectroscopy (FTIR). The latex films were tested by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and contact angle (CA). The particle size and its distribution of the latex were measured by the nano particle size analyzer. Findings The factors that had an influence on the properties of the latex and the film were investigated in detail. The stability of the resultant latex is good. The average particles of the latex and its distribution are small and uniform, respectively. In comparison with the conventional latex film, the thermal stability and hydrophobicity of the resultant latex film are improved obviously. Practical implications The resultant latex can be used in both the waterborne interior and exterior wall coatings, pickering stabilized waterborne polymer dispersions, polymer powders, environmentally friendly polymer-modified waterproof mortar and other fields, which can be satisfied with the high demand of thermal stability and hydrophobicity. Originality/value The modification of poly (VAc-VeoVa10) by reactive surfactant and fluorinated monomer is seldom reported. In this study, the fluorinated poly (VAC-VeoVa) latex is prepared via the reactive surfactants, which VAc and VeoVa10 is used as the main monomers and hexafluorobutyl methacrylate is used as the functional monomer. Potassium persulfate (KPS) and allyl nonyl phenoxy propyl alcohol polyoxyethylene ether ammonium sulfate are used as the initiator and emulsifier, respectively.

Visible light-induced self-healing fluorinated polyurethane-acrylate containing aromatic Schiff base

Light-induced self-healing materials are of great practical value due to their precise local modulation. Aromatic Schiff bases with imine bonds have self-healing property due to their fast dynamic bond exchange properties under visible light. In this paper, we prepared a fluorinated polyurethane-acrylate containing aromatic Schiff base with visible light-induced self-healing ability by Pickering emulsion polymerization. The effect of the aromatic Schiff base content on the particle size of the fluorinated polyurethane-acrylate emulsion, the hydrophobic and oleophobic, mechanical and self-healing properties of the latex films was systematically investigated. The maximum water contact angle and tensile strength of fluorinated polyurethane-acrylate latex film could reach 113.25° and 8.64 MPa, respectively. The tensile strength could be restored to 88.64 % of the original one under visible light irradiation after damage. This work is the first report on visible light-induced self-healing fluorinated polyurethane-acrylate containing aromatic Schiff base, and provides a new design idea for the development of sustainable waterborne polyurethane-acrylate.

Self-healing cellulose nanocrystals/fluorinated polyacrylate with double dynamic interactions of coumarin groups and multiple hydrogen bonds

In this work, self-healing cellulose nanocrystals/fluorinated polyacrylate with dual dynamic networks of photoreversible crosslinking network and high-density hydrogen bonds was prepared by Pickering emulsion polymerization. The main work was to study the effects of 7-(2-methacryloyloxy)-4-methylcoumarin (CMA) and 2-ureido-4[1H]-pyrimidinone methyl methacrylate (UPyMA) monomer dosage on emulsion polymerization and latex film properties. The monomer conversion increased first and then decreased as the CMA and UPyMA monomer dosage increased, while a reverse trend was noted for the particle size and particle size distribution. Incorporating UPyMA allowed the rapid formation of hydrogen bonds at the crosslinking sites, which increased the interaction force between the healing surfaces. Besides, reversible photocrosslinking reaction of coumarin groups provided another support for self-healing performance. Moreover, the influence of self-healing temperature, self-healing time and UV irradiation on the self-healing ability was also systematically investigated The tensile strength of the prepared cellulose nanocrystals/fluorinated polyacrylate latex film exhibited a self-healing efficiency of 91.4 % under 365 nm UV irradiation and 80 °C for 12 h. The latex film had excellent thermal stability as was shown by TG and DTG analyses. The outstanding self-healing capability of latex film was attributed to the reversible photodimerization of coumarin groups and multiple hydrogen bonds. In addition, the water-oil repellent and mechanical properties of the latex films were improved as the CMA and UPyMA monomer dosage increased.

Synergistic effects of chitosan and gamma irradiation on enhanced fungal growth inhibition and biodegradability of natural rubber latex film

Developing novel formulations and processes to improve the fungal growth inhibition and biodegradability of NR products has become a major challenge for the scientific community, given the health risks associated with fungi in natural rubber (NR) products and the environmental concerns regarding NR waste. Consequently, this study comprehensively investigated the synergistic effects of chitosan and gamma irradiation on enhancing fungal growth inhibition and biodegradability in natural rubber latex (NRL) films. The research involved incorporating varying chitosan contents (0, 3, 6, or 9 phr) into NRL composites and exposing them to different gamma doses (0, 5, 10, or 15 kGy). The results showed that increasing the chitosan content and the gamma dose improved the ability of the NRL samples to inhibit fungal growth on their surfaces. This was evidenced by the absence of fungal colonies after 7 days of incubation on potato dextrose agar (PDA) plates for NRL samples irradiated at 5–15 kGy with 9 phr of chitosan. This determination was based on isolating fungi from the film surfaces, followed by serial dilution and a viable plate count. The biodegradability tests also revealed that the NRL films irradiated at 15 kGy with 9 phr of chitosan had the highest weight loss, reaching as high as 10.42 ± 0.62 % after soil burial for 8 weeks. However, the results indicated that gamma irradiation on the pristine NRL and chitosan/NRL films did not substantially alter the thermal stabilities, density, morphology, and functional groups of the samples. Lastly, by comparing the tensile properties of all the NRL films to the ASTM D3578-01a standard for examination gloves, the optimum conditions for the NRL films were 5 kGy of gamma irradiation with 9 phr of chitosan. This combination resulted in gloves with sufficient tensile strength and complete fungal growth inhibition.

Unveiling the Hidden Networks: AFM Insights into Pre‐Vulcanized Hevea Latex and Its Profound Impact on Latex Film Mechanical Properties

AbstractNatural rubber (NR) films with different natural networks—concentrated NR (CNR), deproteinized NR (DPNR), and small rubber particles (SRP)—are investigated to explore the relationship between network structure and film properties using atomic force microscopy (AFM) in PeakForce Quantitative Nanomechanics (QNM) mode. Nitrogen content, gel content, and particle size distribution analyses reveal distinct network topologies in each latex type. Mechanical testing shows variations in tensile strength and crosslink density. AFM analysis provides insights into the crosslink network structures within the pre‐vulcanized latex film. It is found that DPNR and CNR films have a uniform distribution of crosslink networks, with DPNR exhibiting higher Young's modulus values. In contrast, SRP shows varying Young's modulus values, suggesting poor coalescence arising from a harder particle surface and a softer rubber core in an inhomogeneous network structure intrinsic to the non‐rubber components (NRCs) make‐up of SRP latex. This study highlights the pivotal role of natural network structures formed by NRCs in determining the ultimate properties of latex films, which has significant implications for the rubber industry, particularly in the production of latex‐dipped products, medical devices, and bioengineering applications.

Synergistic Effects of the Superhydrophilic and Superhydrophobic Components on the Antifreezing Performances of Latex Particles and Anti-Icing Properties of Latex Films.

The development of new materials for antifreezing and anti-icing applications is a big challenge in industry and academic area. Inspired by the antifreeze proteins, latex particles with superhydrophilic zwitterionic shells and superhydrophobic cores are synthesized by reversible addition-fragmentation chain transfer emulsion polymerization, and the applications of the latex particles in antifreezing and anti-icing applications are investigated. In antifreezing study, the critical aggregate temperature (CAT) of the latex particles decreases, and the separation of the melting and freezing temperature of ice increases with the particle concentration. Enzyme molecules can be cryopreserved in the particle solution, andtheir bioactivities are well maintained. Latex particles are casted into latex films with dynamic surfaces. Anti-icing performances, including antifrosting properties, freezing delay time, and ice adhesion strengths, are studied; and the water-treated latex films present stronger anti-icing properties than other films, due to the synergistic effects of the superhydrophilic and superhydrophobic components. In addition, latex particles with zwitterionic shells and poly(n-butyl methacrylate) cores, and latex particles with small molecular surfactant on the surfaces are synthesized. The antifreezing performances of the latex particles and anti-icing properties of the latex films are compared.

Synergistic Effect of Natural Rubber Latex Film Filled with Corn Starch

Synergistic Effect of Natural Rubber Latex Film Filled with Corn Starch

Colloidal and thermal properties of poly(hydroxyethyl caprolactone acrylate‐co‐methyl methacrylate)‐g‐pullulan latex obtained by seeded semi‐batch emulsion polymerization

AbstractIn this study, the influence that the monomer composition of hydroxyethyl caprolactone acrylate/methyl methacrylate (HECLA/MMA) has on the properties of the latex films, including contact angle, thermogravimetric analysis, and mechanical properties was evaluated. The polymerization process to obtain small particle sizes, good colloidal stability, and polymer films was optimized through the use of pullulan (Pull) and different ratios of HECLA and MMA. The results revealed a substantial impact of the monomer composition and polymerization processes on the particle size and latex film properties. The use of seed latex obtained in situ reduces particle size and particle size distribution. Additionally, it was observed that the contact angle of the polymer films increased as the concentration of HECLA increased. Furthermore, the water absorption of the polymer films exhibited a decreasing trend after reaching an 80/20 monomer composition of HECLA/MMA. An increase in HECLA contents in the recipe showed a reduction in tensile strength, elastic modulus, hardness, and elongation at break. Conversely, higher HECLA contents contributed to improving the thermal properties of the polymer films. Finally, the optimal ratio of HECLA/MMA to improve the thermal degradation and tensile mechanical properties of the polymer film was 50/50 wt%. The results found in this work allow additional data for producing poly(HECLA‐co‐MMA)‐g‐Pull latexes by manipulating the ratios of HECLA and MMA, which can create new potential applications in various industrial settings for a wide range of polysaccharides.Highlights Poly(HECLA‐co‐MMA)‐g‐Pull with different ratios of HECLA/MMA were successfully obtained. The use of Pull after molar mass reduction had a significant effect on colloidal stability. A reduction in tensile strength and elongation at break was obtained by increasing the amount of HECLA. Thermal stability of the latex films showed a direct relationship with the content of HECLA. Poly(HECLA‐co‐MMA)‐g‐Pull latexes can be used in agricultural applications.

Effectiveness of Starch Nanocrystals on Mechanical and Shape Memory Behaviour of Smart Rubber

Shape memory rubber (SMR) is a type of smart rubber that can undergo reversible changes when exposed to external stimuli such as temperature, solvent, pH, light, magnetic field and oxidation. Lightly crosslinked rubber demonstrated shape memory behaviour without any initial heat treatment. However, the strength of lightly crosslinked natural rubber latex (NRL) film cured by sulphur is relatively low. With the concept of sustainability in mind, the idea of fabricating green smart material for continuous development has motivated researchers to explore the realms of sustainable materials. This research aims to investigate the mechanical behaviour of starch nanocrystals (SNC) reinforced rubber composite films. To this end, the emphasis is laid on evaluating the effectiveness of SNC on shape memory effect (SME) of rubber nanocomposite films. In the current work, up to 8 wt% of SNC synthesized by acid hydrolysis was incorporated into NRL and the mixture was cast to form rubber nanocomposite films. SNC effectively increased the modulus and energy-storing potential of the rubber nanocomposite films. Moreover, the shape memory behaviour of the rubber nanocomposite films improved significantly with SNC content, leading to increased shape fixity (Sf) and full shape recovery (Sr).

Preparation and Characterization of Poly(Methyl Methacrylate) Grafted Natural Rubber Latex Films

Poly(methyl methacrylate) (PMMA) grafted natural rubber (NR) latex was successfully prepared and solely exploited even at high MMA concentration (1.5 mol/kg-rubber) to make coherent and uniform vulcanized films without blending with other polymer to achieve excellent physical properties. High ammonia natural rubber (HANR) latex was subjected to graft-copolymerization with methyl methacrylate (MMA) monomer in the presence of tert-butyl hydroperoxide (TBHP) and tetraethylenepentamine (TEPA). High conversion, i.e., 85.12 mol%, and grafting efficiency, i.e., 92.70 mol%, were obtained at 1.5 mol/kg-rubber MMA. The resulting gross PMMA grafted NR (1.5PMMA) latex was then compounded, dipped, and vulcanized to produce thin films. The tensile strength and modulus at 300 percent (M300) of vulcanized 1.5PMMA film were superior to vulcanized HANR film by 1-fold. While elongation at break (EB) was identical to each other due to the high gel content in both vulcanized films. Besides, the vulcanized 1.5PMMA film absorbed less oil compared to HANR film. The thermal stability of vulcanized 1.5PMMA film was found to be higher than that of vulcanized HANR film. Hence, it can be deduced that controlling the graft-copolymerization of PMMA in NR latex is the key to produce coherent thin films with improved properties at higher PMMA content.

The effects of silver nitrate as antimicrobial agent in rubber latex films to reduce hospital acquired infections

The effects of silver nitrate as antimicrobial agent in rubber latex films to reduce hospital acquired infections

Preparation and Application of CO2-Resistant Latex in Shale Reservoir Cementing

With the application of CO2 fracturing, CO2 huff and puff, CO2 flooding, and other stimulation technologies in shale reservoirs, a large amount of CO2 remained in the formation, which also lead to the serious corrosion problem of CO2 in shale reservoirs. In order to solve the harm caused by CO2 corrosion, it is necessary to curb CO2 corrosion from the cementing cement ring to ensure the long-term stable exploitation of shale oil. Therefore, a new latex was created using liquid polybutadiene, styrene, 2-acrylamide-2-methylpropanesulfonic acid, and maleic anhydride to increase the cement ring’s resistance to CO2 corrosion. The latex’s structure and characteristics were then confirmed using infrared, particle size analyzer, thermogravimetric analysis, and transmission electron microscopy. The major size distribution of latex is between 160 and 220 nm, with a solid content of 32.2% and an apparent viscosity of 36.8 mPa·s. And it had good physical properties and stability. Latex can effectively improve the properties of cement slurry and cement composite. When the amount of latex was 8%, the fluidity index of cement slurry was 0.76, the consistency index was 0.5363, the free liquid content was only 0.1%, and the water loss was reduced to 108 mL. At the same time, latex has a certain retarding ability. With 8% latex, the cement slurry has a specific retarding ability, is 0.76 and 0.5363, has a free liquid content of just 0.1%, and reduces water loss to 108 mL. Moreover, latex had certain retarding properties. The compressive strength and flexural strength of the latex cement composite were increased by 13.47% and 33.64% compared with the blank cement composite. A long-term CO2 corrosion experiment also showed that latex significantly increased the cement composite’s resilience to corrosion, lowering the blank cement composite’s growth rate of permeability from 46.88% to 19.41% and its compressive strength drop rate from 27.39% to 11.74%. Through the use of XRD and SEM, the latex’s anti-corrosion mechanism, hydration products, and microstructure were examined. In addition to forming a continuous network structure with the hydrated calcium silicate and other gels, the latex can form a latex film to attach and fill the hydration products. This slows down the rate of CO2 corrosion of the hydration products, enhancing the cement composite’s resistance to corrosion. CO2-resistant toughened latex can effectively solve the CO2 corrosion problem of the cementing cement ring in shale reservoirs.

A Study on the Preparation of a Vulcanizing Mixture and Its Application in Natural Rubber Latex.

The traditional preparation process of natural rubber latex requires tedious treatment of a variety of rubber additives. In this paper, a new process of wet mixed grinding was used to prepare a reinforced vulcanization mixture and a rapid vulcanization effect. The effect of different amounts of vulcanization mixtures on the mechanical properties of natural latex film was studied, and the pre-vulcanization process of latex and the vulcanization process of film were optimized. The results showed that with the increase in the amount of vulcanization mixture, the tensile strength increased from 5.96 MPa to 29.28 MPa, and the tear strength increased from 7.59 kN/m to 52.81 kN/m. When the vulcanization temperature of the latex film is heated from 80 °C to 100 °C, the vulcanization time is shortened by 5~6 times. The new vulcanization mixture prepared in this work has the characteristics of simple production and fast vulcanization speed, which provides a new solution for the development of the latex product industry.

Fabrication of core-shell polyacrylate latex pressure sensitive adhesives modified by fluorinated monomer and film properties

In this work, a series of fluorinated core-shell polyacrylate latex pressure sensitive adhesives (PSAs) were successfully synthesized through monomer-starved seeded semi-continuous emulsion polymerization. Specifically, (meth)acrylate monomers were employed as the main materials, with dodecafluoroheptyl methacrylate (DFMA) were used as modified monomer. The impact of fluorine monomer DFMA on the resulting core-shell latex and PSA properties was thoroughly examined. FTIR analysis confirmed the successful incorporation of DFMA into the latex copolymer through emulsion polymerization. TEM images illustrated that the morphology of latex particles exhibit a distinct core-shell structure. The results also showed that with the addition of DFMA, the water absorption and water whitening of the latex films decreased, while the water contact angle and thermal stability are improved. Interestingly, the latex films with DFMA added to the shell phase exhibit a larger WCA value when compared to those with DFMA in the core phase, further confirmed by XPS results. Finally, the adhesive properties of the fluorinated core-shell acrylate PSA were evaluated. The results of shear strength and gel content demonstrate that the prepared PSA exhibits excellent cohesive properties. Thus, this work could present a feasible strategy for optimizing the comprehensive properties of acrylate latex PSAs.

Hierarchical nanoengineered emulsion with robust adhesion enables superior self-cleaning cotton fabrics

Self-cleaning treatment is of vital importance for the practical application of functional cotton fabrics. However, developing highly efficient, eco-friendly, and durable hydrophobic and oleophobic treatment agents still remains a great challenge. Herein, inspired by the design of the inorganic–organic nanonetwork, we successfully synthesized a novel core–shell structured emulsion of nano-SiO2/fluorine-silicon polyacrylate through semi-continuous emulsion polymerization. The introduction of long-chain alkyl methacrylate octadecyl ester within the shell phase results in a more organized arrangement of fluorine atoms on the surface of cotton fabrics, leading to a rapid reduction in the surface free energy of latex film. The sample is optimized with 20 wt% dodecafluoroheptyl methacrylate and 1 wt% SiO2. The nanoengineered emulsion exhibits strong adhesion and effectively transforms the hydrophilic cotton fabrics into hydrophobic (143.2°) and oleophobic (121.6°) materials. Besides, the self-cleaning characteristic can withstand 25 laundering cycles and 800 abrasion cycles with enhanced robustness. This work opens up a pathway to develop effective, green but long-lasting amphiphobic agents for functional fabrics and sustainable textiles.

Block copolymers hybrid latex coatings with environment-friendly short-chain perfluoroalkyl: From sequence structure to surface properties

Block copolymers (BCs) of perfluorocarbons (PFCs) show a well-ordered phase separation morphology on the surface that is an ideal structure to fabricate low surface free energy (SFE) environment-friendly short-chained PFCs based coating materials. In this study, a series of block copolymers of 2-(perfluorobutyl) ethyl acrylate hybrid latex coating materials were synthesized via soap-free RAFT emulsion polymerization. The impact of copolymers sequence structure on the surface properties and surface micro-nano structure of hybrid latex films were investigated. The results revealed that the functional chain segments of short-chain perfluorinated were preferentially arranged in the outermost chain segments of the BCs, thereby leading to the stacking of trifluoromethyl (-CF3) groups on the hybrid latex film surfaces and the decrease of SFE. The SFE of BCs latex films were significantly reduced from 21.83 mN/m to 16.03 mN/m compared to that of the random copolymer. Additionally, the SFE of the hybrid latex film can be reduced to 15.32 mN/m under the action of the modified silica crosslinking. Ultimately, the hybrid latex films show excellent superhydrophobic and oleophobic properties on cotton fabrics with water and oil contact angles of 152.5° and 142.4°, respectively, reaching the level of commercial water and oil repellent finishing agents with six fluorocarbon atoms. This study of BCs hybrid latex coatings provides important insights into the mechanism of the sequence structure and surface properties of BCs and offers an environment-friendly superhydrophobic and oleophobic coating material.

Dual cross‐linking of XNBR latex with epoxy‐functional calcium silicate particles for the production of accelerator‐free medical gloves

AbstractIn this work, an innovative dual cross‐linking strategy for carboxylated nitrile butadiene rubber (XNBR) latex using epoxy‐modified calcium silicate particles is presented. In their role as dual cross‐linker, the particles are able to form covalent bonds (nucleophilic ring opening of epoxy moieties) as well as ionic cross‐links (calcium ions of the inorganic core) across the carboxylic acid groups of the rubber. To characterize the curing efficiency, thin elastomer films are prepared by using a conventional coagulant dipping process and their cross‐link densities, curing kinetics, and tensile properties are investigated as a function of the concentration of the cross‐linker and curing time. The results show that latex films containing 5 phr of epoxy‐functional particles give the highest tensile strength, which is further improved by pre‐vulcanizing the liquid latex compound at 60°C for 30 min. The latex formulations are stable over 3 days and the pre‐cured films exhibit a high resistance against gamma sterilization and subsequent accelerated aging. Moreover, sterile films do not cause any skin irritation or skin sensitization reactions, showing the high potential of epoxy‐functional particles in the production of accelerator‐free hypoallergenic gloves.

Self‐healing waterborne fluorinated polyurethane‐acrylate based on photoreversible reaction and hydrogen bonds

AbstractThe development of self‐healing materials is an effective strategy to improve the service life of polymer materials. In this study, self‐healing waterborne fluorinated polyurethane‐acrylate (WFPUA) containing UV‐responsive coumarin groups was prepared by Pickering emulsion polymerization using modified cellulose nanocrystal as a stabilizer. The effect of double bond‐terminated waterborne polyurethane content on emulsion polymerization and latex film properties was mainly studied. Due to the dynamic reversibility of the coumarin groups and the synergistic effect of hydrogen bonds, the optimized sample (WFPUA‐30) had excellent mechanical properties and self‐healing properties. The tensile strength was 5.24 MPa and the elongation at break was 267%. The self‐healing efficiency of tensile strength and elongation at break after 6 h of repair was 86.52% and 93.20%, respectively. In addition, due to the presence of fluorine‐containing groups, the water and oil contact angles of the latex film could reach 101.7° and 82.1°, respectively. This work broadens the way for the manufacture of self‐healing and multifunctional waterborne polyurethane‐acrylates. © 2024 Society of Industrial Chemistry.