Search Results (48)

In the field of water-based inks, the use of alkali-soluble resins (ASRs) as polymeric surfactants for synthesizing polyacrylate latexes has become a mainstream method. This study first designed and prepared crosslinkable ASRs with a diacetone acrylamide (DAAM) crosslinking monomer via emulsion polymerization. These ASRs were then employed as surfactants to synthesize self-crosslinking polyacrylate latexes through an in situ one-pot method, systematically investigating the influence of crosslinkable ASRs on the properties of the corresponding polyacrylate latexes. The research revealed that all prepared polyacrylate latexes exhibited a core–shell structure. With increasing DAAM content in the ASRs, the latex particle size gradually increased while the particle size distribution narrowed. All latexes demonstrated excellent stability, with absolute ζ-potential values exceeding 30 mV. The introduction of DAAM into ASRs significantly increased the glass transition temperature in the high-temperature region of the corresponding latex films, with the tensile strength reaching a maximum of 7.96 MPa. Moderate crosslinking in ASRs substantially improved the water resistance of latex films. Crosslinking degree tests indicated that latex films prepared through either single shell-layer crosslinking or single core-layer crosslinking showed relatively low crosslinking degrees, while only the dual core–shell crosslinking strategy could effectively enhance the film crosslinking degree. However, excessively crosslinked shell layers significantly hindered the crosslinking reaction of DAAM in the core layer, leading to reduced overall film crosslinking. Additionally, incorporating a certain number of DAAM crosslinking groups in ASRs was found to improve the adhesion of corresponding water-based inks on PE and BOPP substrates, with adhesion on BOPP substrates reaching up to 100%. Full article

Traditional approaches to constructing thermally conductive networks typically necessitate costly equipment and intricate processes, rendering them unsuitable for mass production and commercialization. Here, we propose a facile strategy to construct highly oriented boron nitride/polyacrylate pressure-sensitive adhesive frameworks by a calendering process. A UV light-based bulk polymerization method is adopted to prepare the pressure-sensitive adhesives (PSAs), which makes the preparation process solvent-free and volatile organic compound (VOC)-free, and environmentally friendly compared to emulsion and solvent-based pressure-sensitive adhesives. This simple, economical and scalable method provides new ideas and ways for the preparation of advanced thermal conductive networks. The highly oriented and flexible m-BNNSs/polyacrylate pressure-sensitive adhesive composites (m-BNNSs/PSAs-Ori) exhibited a significantly high thermal conductivity (TC) of 0.9552 W/(m·K) at 25 wt% filler content. Significantly, m-BNNSs/PSAs-Ori composites showed a better thermal response than the single-layer thermally conductive pressure-sensitive adhesive. Moreover, the composites also possess excellent electrical insulation and mechanical properties. This exploration not only provides a reasonable design scheme for thermal interface materials, but also promotes the practical application of polyacrylate pressure-sensitive adhesive composites in thermal management. Full article

Superabsorbent core/shell composite materials are a type of advanced materials presenting enhanced water absorption and retention capabilities. The central core material can swell and absorb water covered by a shell that serves a specific function. The composition and functionality of each layer can be tailored to improve the material’s performance. The core is typically fabricated from superabsorbent polymers such as sodium polyacrylate, poly(acrylic acid) or other hydrophilic materials. The shell can be either inorganic polymers or organic polymers such as poly(methyl methacrylate), biodegradable polymers, polysaccharides or other functionalized materials in order to enhance biodegradability, mechanical strength or responsiveness to stimuli (e.g., temperature, pH). These materials present enormous potential to address issues for versatile applications in various fields, including biomedical applications, hygiene products and agriculture, due to their tailored structure. The common synthesis techniques for these advanced materials are emulsion polymerization, in situ polymerization, suspension polymerization with respect to the core material, layer-by-layer assembly and the sol–gel technique with respect to the shell formation. The techniques that are usually utilized for the characterization of the aforementioned materials and the validation of their functionalities are based on thermal analysis, morphology studies and swelling behavior and water retention and release mechanical properties, respectively. This review offers an in-depth examination of recent advancements in synthesis methods, structural engineering approaches and emerging applications of superabsorbent core/shell composites, highlighting the critical importance of material design in boosting their performance and broadening their practical use. Finally, special attention is devoted to the future perspectives of superabsorbent core/shell composites, exploring potential innovations in material design and multifunctionality. Emerging trends such as stimuli-responsive behavior, sustainability and scalability are discussed as key factors for next-generation applications. The review also outlines challenges and opportunities that could guide future research and industrial implementation. Full article

This work aims to investigate the synergistic effects of hybrid bio-fillers and compatibilizers on the properties of natural rubber composites. Rice husk silica (RSi) and hydroxyapatite (HA), derived from rice husk ash and seabass fish scales, respectively, were successfully prepared and used as bio-fillers. Poly(acrylic acid-co-acrylamide)-grafted deproteinized natural rubber (gDPNR) was synthesized via emulsion graft copolymerization, achieving a grafting efficiency and grafting percentage of 15.94 and 4.23%, respectively. The gDPNR was utilized as a compatibilizer in the preparation of natural rubber composites. The addition of hybrid bio-fillers at an RSi-to-HA ratio of 25:75 exhibited superior mechanical properties compared to composites containing a single filler. The incorporation of gDPNR improved filler dispersion and interfacial adhesion between the NR matrix and the bio-fillers, further enhancing the mechanical, thermal, and dielectric properties. The composite with hybrid bio-fillers and 10 phr of gDPNR exhibited the highest tensile strength, showing a 2.10-fold and 1.06-fold improvement over neat natural rubber composite and hybrid filler composite without compatibilizer, respectively. The presence of polar functional groups in gDPNR enhanced the dielectric constant of the natural rubber composites. These composites could have potential in sustainable industrial applications, including flexible electronics and eco-friendly devices. Full article

This paper describes the synthesis of a viscosity-reducing agent using butyl acrylate (BA), ethyl methacrylate (EMA), acrylic acid (AA) and N-hydroxymethylacrylamide (N-MAM) monomers through emulsion polymerization. A series of viscosity-reducing agents were developed by incorporating varying amounts of glycidyl methacrylate (GMA) monomers. The reaction mechanism of epoxy acrylate viscosity reducer was analyzed by Fourier transform infrared spectroscopy (FTIR). Additionally, the particle size and Zeta potential were used to analyze the stability of the polymer and the difference in the polymer after adding GMA monomer. Thermogravimetric (TG) analysis indicated a significant improvement in the thermal stability of the resin due to GMA modification. The viscosity reduction test results demonstrated a substantial decrease in the viscosity of heavy oil, along with a notable increase in the viscosity reduction rate. The FTIR analysis results confirmed that GMA successfully introduced polyacrylate molecular chains. Furthermore, particle size and Zeta potential measurements showed that the average particle size of the emulsion increased from 132 nm to 187 nm, while the Zeta potential changed from −43 mV to −40 mV with the addition of 15% GMA. Compared with W0, the final thermal degradation temperature of W15 increased from 450 °C to 517 °C. When the GMA content reached 15 wt%, the maximum weight loss temperature increased by approximately 12 °C compared to the sample without GMA. Specifically, adding 8% W15 epoxy acrylate resulted in an 89% viscosity reduction rate for heavy oil, demonstrating an excellent viscosity reduction effect. This study successfully developed a novel epoxy acrylate viscosity reducer using a simple synthesis method, showcasing excellent stability, cost-effectiveness and remarkable viscosity reduction. Full article

Previously we suggested a new pharmaceutical derived from coordination complex of Co³⁺ with polyacrylic acid (PAA) exhibiting hemostatic and microbicidal activity, namely Hestatin. Differences in the physiological activity of Hestatin synthesized from PAA 10 kDa (Hestatin 10) and 200 kDa (Hestatin 200) were shown. We tested the acute toxicity of Hestatin and its effect on the healing rate of sterile wounds in rats. Free 10 kDa PAA, emulsion wax, emulsion wax carrying resveratrol, and dexpanthenol were tested for comparison. Hestatin 10 exhibited no acute toxicity when administered intragastrically at dosages of 5 g per kg. Hestatin 10 surpassed all tested drugs in its wound healing ability. Histological analysis of skin sections of rats in the area of healing defects showed an increased rate of synthesis of reticular fibers compared to the placebo. In the early stages of wound healing (inflammatory phase), Hestatin 10 stimulated taxis of mast cells (MCs) to the wound bottom but not to the wound perimeter. At the final stage of wound healing (remodeling phase), Hestatin 10 promoted MC evacuation from the skin defect area. This effect is the opposite of the well-known wound-healing agents (dexpanthenol and resveratrol), which enhance MC infiltration into the defect area in the remodeling phase. Full article

Understanding the adsorption features of polymer microgels with different chemical compositions and structures is crucial in studying the mechanisms of respective emulsion stabilization. Specifically, the use of stimuli-responsive particles can introduce new properties and broaden the application range of such complex systems. Recently, we demonstrated that emulsions stabilized by microgels composed of interpenetrating networks (IPNs) of poly-N-isopropylacrylamide (PNIPAM) and polyacrylic acid (PAA) exhibit higher colloidal stability upon heating compared to PNIPAM homopolymer and other relevant PNIPAM-based copolymer counterparts. In the present work, using pendant drop tensiometry, we studied the evolution of water–tetradecane interfacial tension during the adsorption of PNIPAM-PAA IPN particles, comparing them with single-network P-(NIPAM-co-AA) and PNIPAM microgels. The results showed that, despite having the same chemical composition, copolymer particles exhibit completely different adsorption behavior in comparison to other microgel architectures. The observed disparity can be attributed to the nonuniform distribution of charged acrylic acid groups within the P-(NIPAM-co-AA) network obtained through precipitation polymerization. Oppositely, the presence of IPN architecture provides a uniform distribution of different monomers inside respective microgels. Additionally, hydrogen bonding between PNIPAM and PAA subchains appears to reduce the electrostatic energy barrier, enhancing the ability of IPN particles to successfully cover the liquid interface. Overall, our findings confirm the efficiency of using PNIPAM-PAA IPN microgels for the preparation of oil-in-water emulsions and their stability, even when the temperature rises above the lower critical solution temperature of PNIPAM. Full article

In this study, the use of surfactant-free water-in-oil gelled emulsions containing benzyl alcohol (BAl/w) is proposed as an alternative to the more traditional use of organic solvents for removing varnishes. To mitigate the strong swelling and solvent action of benzyl alcohol and protect the paint and the underlying layers, temporary hydrophobization with cyclomethicone D5 has been proposed. The aim of this study was to evaluate the application of BAl/w surfactant-free, constructed with three different gelling agents of the aqueous dispersing phase (xanthan gum, agar-agar, and polyacrylate) on the surface of an oil painting varnished with and without preliminary saturation with D5. The role of pH, which can influence the ionization, and therefore the water solubility of terpene molecules and all other acid species present on the surface, was also studied. Fourier transform infrared (FT-IR) and Raman spectroscopies were used to characterize the pigments and the surface before and after varnish removal. Elemental analysis and any morphological changes were evaluated using scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM-EDS). The leaching efficiency of each surfactant-free emulsion applied on the paint surface was evaluated using a gas chromatography/mass spectroscopy (GC/MS) analysis: the fatty acid content was established in each sample before and after the treatments. Full article

This work deals with the coating properties of synthetic latices comprising two kinds of polymers, specifically polyacrylate and polypyrrole, which were simultaneously formed by semi-continuous emulsion polymerization using a “one-pot” synthesis strategy. In this procedure, both the emulsion polymerization of acrylate monomers and the oxidative polymerization of pyrrole occurred concurrently in one reactor. Polyacrylate latices differing in polypyrrole loading were prepared by applying various dosages of pyrrole, specifically 0, 0.25, and 0.50, based on the fraction of acrylate monomers. The effect of the in situ incorporated polypyrrole component (having the nature of submicron composite polypyrrole-coated polyacrylate latex particles) on the physico-mechanical properties and chemical resistance of the resulting heterogeneous coating films was investigated. The interaction of incorporated polypyrrole and anti-corrosion pigments (see ZnS, Zn₃(PO₄)₂, ZnFe₂O₄, MoS₂, and ZnO) on the corrosion resistance of coatings was evaluated by using the electrochemical linear polarization technique. The polyacrylate latex prepared with the lowest polypyrrole loading (achieved by polymerizing 0.25 wt. % of pyrrole related to acrylic monomers) was found to be the optimum binder for waterborne anticorrosive coatings based on their properties and protective function. Their compatibility with the selected types of pigments was studied for these latex binders. In addition, their influence on the anti-corrosion efficiency of polyacrylate paint films was evaluated using the linear polarization electrochemical technique. For high corrosion resistance, the ZnS and MoS₂ pigments, showing compatibility with polyacrylate latices containing the polypyrrole component, proved to be advantageous. Full article

Waterborne polyurethane, with a mechanical strength comparable to solvent-based types, is eco-friendly and safe, using water as a dispersion medium. Polyacrylate excels in film formation and weather resistance but suffers from “hot stickiness and cold brittleness”. Merging polyurethane and polyacrylate creates advanced hybrids, while organosilicon enhances properties but is restricted due to hydrolytic crosslinking. In this paper, a series of polyurethane–polyacrylate hybrid latexes with high organosilicon content were prepared using phase inversion emulsion polymerization technology. Even when the monomer content of 3-(methacryloyloxy)propyltrimethoxysilane (MPS) was increased to 10%, the polymerization process was stable, without the formation of a gel precipitate. The resulting latexes could remain stable for at least 6 months without significant changes in the properties of their films. The effects of MPS content on the mechanical and thermal properties of latex films were systematically researched. The study showed that with an increase in MPS dosage, the hardness and elastic modulus of the latex films increased, while the elongation at break and water absorption decreased, together with the increased glass transition temperature and surface hydrophilicity. This work aims to provide new theoretical guidance for the preparation of silicone-modified hybrid latexes, enabling their safe and stable production and storage. Full article

This study developed three composite slurries for coating recycled aggregate by incorporating polyacrylate emulsion, fly ash, and gypsum into a cement-based mixture. The filling and pozzolanic effects of fly ash help to improve microcracks in the recycled aggregates. The polyacrylate emulsion forms a strong bonding layer between the cement matrix and the aggregates, enhancing the interfacial bond strength. Based on relevant studies, the following mix designs were developed: Slurry 1 consists of pure cement paste; Slurry 2 contains 15% fly ash and 3% gypsum added to the cement paste; Slurry 3 adds 22% polyacrylate emulsion to the slurry. The study first compared the effects of the three composite slurries on the crushing value and water absorption of recycled aggregates, and then analyzed their impact on the mechanical properties, permeability, and drying shrinkage of concrete. Finally, the mechanisms behind the enhancement were investigated using the Vickers Hardness Test (HV), Mercury Intrusion Porosimetry (MIP), and scanning electron microscopy–energy-dispersive spectroscopy (SEM-EDS). The results showed that the polyacrylate emulsion composite slurry had the most significant improvement effect. For recycled aggregate AL, the crushing value decreased from 28.8% to 22.5% and the saturated surface–dry water absorption decreased from 15.1% to 13.8% after cement slurry modification. After coating with the composite slurry, the crushing value further dropped to 18.2% and the water absorption to 9.5%. Two aspects of the performance of recycled aggregates are enhanced with the polymer composite slurry: first, fly ash provides nucleation sites for CH, reducing the tendency for directional CH alignment. Second, the long chains of PAE (polyacrylic ester) encapsulate cementitious particles, effectively filling surface defects on the recycled aggregates, improving the bonding strength at the new-to-old interface, and significantly enhancing the performance of both recycled aggregates and recycled concrete. Full article

This article presents the results of research work devoted to improving the characteristics of paint and varnish coatings based on aqueous dispersions of polyacrylates; it is proposed to modify them by introducing mineral raw materials as fillers and hydrated lime, with subsequent processing in a vortex layer apparatus. The introduction of activated diatomite does not cause the deterioration of covering power, adhesion or an increase in the porosity of the paint material. The modification of coatings contributes to an increase in their operational properties, which can be associated with a reduction in the free volume in the composite and the formation of polymer boundary layers with modified physical and chemical properties. The aim of this study is to obtain a water-dispersion paint and varnish composition containing modified diatomite on a polyacrylate basis and, subsequently, study its main physical and mechanical parameters. The work has been carried out by the following method: determination of porosity, adhesion, elasticity and covering power of the control composition; determination of porosity, adhesion, elasticity and covering power of the obtained composites using modified filler; investigation of the influence of radiation on the infrared spectrum of the paint coating surface using a FLIRB620 thermal imager. As a result of this research work, it was noticed that the modification of water dispersions with silica-activated diatomite helps to eliminate the main disadvantages of materials and coatings based on acrylate binders—low water resistance and low physical and mechanical characteristics. The introduction of modified diatomite into water-emulsion paint on an acrylate base does not lead to the deterioration of the main performance characteristics of paint coatings—porosity, adhesion, elasticity and covering. Full article

For polyacrylate latex pressure-sensitive adhesives (PSAs), high peel strength is of crucial significance. It is not only a key factor for ensuring the long-lasting and effective adhesive force of polyacrylate latex PSAs but also can significantly expand their application scope in many vital fields, such as packaging, electronics, and medical high-performance composite materials. High peel strength can guarantee that the products maintain stable and reliable adhesive performance under complex and variable environmental conditions. However, at present, the peel strength capacity of polyacrylate latex PSAs is conspicuously insufficient, making it difficult to fully meet the urgent market demand for high peel strength, and severely restricting their application in many cutting-edge fields. Therefore, based on previous experimental studies, and deeply inspired by the adhesion mechanism of natural marine mussels, in this study, a traditional polyacrylate latex PSA was ingeniously graft-modified with 3,4-dihydroxybenzaldehyde (DHBA) through the method of monomer-starved seeded semi-continuous emulsion polymerization, successfully synthesizing novel high-peel-strength polyacrylate latex pressure-sensitive adhesives (HPSAs) with outstanding strong adhesion properties, and the influence of DHBA content on the properties of the HPSAs was comprehensively studied. The research results indicated that the properties of the modified HPSAs were comprehensively enhanced. Regarding the water resistance of the adhesive film, the minimum water absorption rate was 4.33%. In terms of the heat resistance of the adhesive tape, it could withstand heat at 90 °C for 1 h without leaving residue upon tape peeling. Notably, the adhesive properties were significantly improved, and when the DHBA content reached 4.0%, the loop tack and 180° peel strength of HPSA₄ significantly increased to 5.75 N and 825.4 gf/25 mm, respectively, which were 2.5 times and 2 times those of the unmodified PSA, respectively. Such superior adhesive performance of HPSAs, on the one hand, should be attributed to the introduction of the bonding functional monomer DHBA with a rich polyphenol structure; on the other hand, the acetal structure formed by the grafting reaction of DHBA with the PSA effectively enhanced the spatial network and crosslink density of the HPSAs. In summary, in this study, the natural biological adhesion phenomenon was ingeniously utilized to increase the peel strength of pressure-sensitive adhesives, providing a highly forward-looking and feasible direct strategy for the development of environmentally friendly polyacrylate latex pressure-sensitive adhesives. Full article

To decrease the lipid content in water-in-oil (W/O) emulsions, high internal phase Pickering W/O emulsions (HIPPE) were fabricated using magnetic stirring using a combination of monoglyceride (MAG) oleogel and polyglycerol polyacrylate oleate (PGPR) as stabilizers. Effects of MAGs (glyceryl monostearate-GMS, glycerol monolaurate-GML and glycerol monocaprylate-GMC) and internal phase components on the formation and properties of HIPPEs were investigated. The results showed that milky-white stabilized W/O HIPPE with up to 85 wt% aqueous phase content was successfully prepared, and the droplet interfaces presented a network of MAG crystals, independent of the MAG type. All HIPPEs exhibited great stability under freeze–thaw cycles but were less plastic. Meanwhile, GML-oleogel-based HIPPEs had larger particle size and were less thermal stable than GMS and GMC-based HIPPEs. Compared to guar gum, the internal phase components of sodium chloride and sucrose were more effective in reducing the particle size of HIPPEs, improving their stability and plasticity, and stabilizing them during 100-day storage. HIPPEs presented great spreadability, ductility and plasticity after whipping treatment. This knowledge provides a new perspective on the use of oleogels as co-stabilizers for the formation of W/O HIPPEs, which can be used as a potential substitute for creams. Full article

In this research, the influence of titanium dioxide (TiO₂) nanoparticles and their modifications on the weathering resistance of untreated and heat-treated wood was studied. The wood samples were coated with polyacrylate waterborne emulsion coatings that contain nano-TiO₂ in the amount of 0.75 wt.%. Two types of modifiers were used to modify the nano-TiO₂ surface: 2,2′-azobis(2-methylpropionamide) dihydrochloride (AIBA) and 3-aminopropyltrimethoxy silane (AMPTS). Coated and uncoated wood samples were exposed to accelerated weathering by application of sunlight, water and moisture for 360 h. During the research, the dry film thickness, color, gloss and hardness of the surface of the samples were measured. The obtained results showed that the effect of the addition and surface modification of nano-TiO₂ on the color and gloss stability was different on untreated and heat-treated ash wood, and that accelerated weathering causes an increase in surface hardness and a decrease in thickness of the dry coating. Full article