Search Results (80)

In this work, monodisperse carbon microspheres with an average diameter of approximately 900 nm were successfully synthesized via a hydrothermal method. To further tailor their surface properties, the layer-by-layer (LbL) self-assembly technique was employed, where the cationic polyelectrolyte poly(diallyldimethylammonium chloride) (PDDA) and the anionic polyelectrolyte poly(styrene sulfonate) (PSS) were alternately deposited on the microsphere surface, forming two and four bilayer assemblies, respectively. The resulting composite microspheres exhibited remarkable adsorption performance toward representative dyes in water solution, such as rhodamine B (RhB) and methylene blue (MB). Experimental results demonstrated that the incorporation of a single bilayer significantly reduced the specific surface area but introduced additional active adsorption sites, thereby enhancing dye removal efficiency. However, when the number of bilayers was further increased to two, partial pore coverage and blockage occurred, leading to a reduced surface area and consequently diminished adsorption capacity. These findings highlight that in LbL surface modification, more layers do not necessarily yield better performance, but rather an optimal assembly thickness exists. This insight provides valuable guidance for the rational design of advanced adsorbent materials for wastewater treatment. Full article

This study builds on previous research into the surface modification of beech wood with polyethyleneimine (PEI) prior to finishing it with a waterborne coating. Poly(diallyldimethylammonium chloride) (PDADMAC) is introduced as an alternative cationic polyelectrolyte for the pretreatment of beech wood surfaces. Wood samples were treated with aqueous 1% PDADMAC solutions of low (LMW—8000 g mol⁻¹) and high (HMW—100,000–200,000 g mol⁻¹) molecular weights, with or without NaCl addition. The effects of the treatments on wood surface chemistry, wettability, surface energy, water absorption, coating penetration, coating adhesion strength, and surface roughness of coated wood were analysed using FTIR, fluorescence microscopy, SEM/EDS, and standardised tests commonly used in wood surface finishing. The results showed that polyelectrolyte pretreatment modified the surface properties of wood, reducing water absorption and surface roughness without significantly affecting coating adhesion strength. PDADMAC formed a more uniform surface layer of wood with limited coating penetration, and NaCl addition improved wood surface smoothness (reducing surface roughness parameters of coated wood by 23%–29%, in samples treated with PDADMAC LMW with 0.01 M NaCl). These findings confirm that cationic polyelectrolyte pretreatment enhances the compatibility and performance of waterborne coatings, offering an environmentally friendly approach to improving wood–waterborne coating interactions. Full article

To mitigate the attenuation of color-change sensitivity in cholesteric liquid crystals (CLCs) post-microencapsulation, this study developed MXene-reinforced thermochromic textiles. Monolayer/few-layer MXene nanosheets were fabricated via an etching-intercalation-dispersion approach, while cholesteric liquid crystal microcapsules (CLCMs) were synthesized through a solvent evaporation method. Cotton fabrics were pretreated with polydopamine (PDA), followed by the fabrication of poly(diallyldimethylammonium chloride) (PDAC)/MXene composite coatings via layer-by-layer (LbL) self-assembly and subsequent hydrophobic modification. Systematic characterizations (scanning electron microscopy, SEM; atomic force microscopy, AFM) and performance evaluations revealed that MXene nanosheets have an average thickness of 1.54 nm, while CLCMs display a uniform spherical morphology. The resultant textiles exhibit a reversible red-green-blue color transition over the temperature range of 26.5–29.5 °C, with sensitivity comparable to pristine CLCs and excellent hydrophobicity. This work overcomes the long-standing bottleneck of inadequate color-change sensitivity in conventional liquid crystal microcapsule textiles, offering a novel strategy for the advancement of smart wearable color-changing materials. Full article

Cationic polyelectrolytes, characterized by positively charged functional groups, play an essential role in industries ranging from food solutions, water treatment, medical, cosmetic, textiles and agriculture due to their electrostatic interactions, biocompatibility, and functional versatility. This paper critically examines the transition from petroleum-based synthetic polymers such as poly(diallyldimethylammonium chloride) and cationic polyacrylamides to sustainable natural alternatives derived from agri-forestry resources like starch derivatives and cellulose. Through a cradle-to-gate life cycle assessment, we highlight the superior renewability, biodegradability, and lower carbon footprint of bio-based polycations, despite challenges in agricultural sourcing and processing. This study examines cationization processes by comparing the environmental limitations of traditional chemical methods, such as significant waste production and limited scalability, with those of second-generation reactive extrusion (REX), which enables solvent-free and rapid modification. REX also allows for adjustable degrees of substitution and ensures uniform charge distribution, thereby enhancing overall functional performance. Groundbreaking research and optimization achieved through the integration of artificial intelligence and machine learning for parameter regulation and targeted mechanical energy management underscore REX’s strengths in precision engineering. By methodically addressing current limitations and articulating future advancements, this work advances sustainable innovation that contributes to a circular economy in materials science. Full article

A modified activated carbon (AC) was developed by modifying with poly(diallyldimethylammonium) chloride (PDADMAC) to enhance its adsorption performance for water treatment applications. Different PDADMAC concentrations were explored and evaluated using methyl red as a model contaminant, with 8 w/v% PDADMAC yielding the best adsorption performance. The kinetics data were well described by the pseudo-first-order equation and homogeneous surface diffusion model. The Freundlich isotherm fit the equilibrium data well, indicating multilayer adsorption and diverse interaction types. The removal efficiency remained similar across a pH range of 5–9 and in the presence of background inorganic (NaCl)/organic compounds (sodium acetate) at different concentrations. Rapid small-scale column tests were performed to simulate continuous flow conditions, and the PDADMAC-modified AC effectively delayed the breakthrough of the contaminant compared to raw AC. Regeneration experiments showed that 0.1 M NaOH with 70% methanol effectively restored the adsorption capacity, retaining 80% of the initial efficiency after five cycles. Quantum chemical analysis revealed that non-covalent interactions, including electrostatic and Van der Waals forces, governed the adsorption mechanism. Overall, the results of this study prove that PDADMAC-AC shows great potential for enhanced organic contaminant removal in water treatment systems. Full article

Anion exchange membrane fuel cells (AEMFCs) have garnered significant attention for their potential to advance fuel cell technology. In this study, we developed and characterized anion exchange membranes (AEMs) composed of quaternized poly(vinyl alcohol) (QPVA) electrospun nanofiber mats with poly(acrylamide-co-diallyldimethylammonium chloride) (PAADDA) as a matrix filler for interfiber voids. The objective was to investigate the effect of varying PAADDA concentrations as a matrix filler for interfiber voids on the structural, mechanical, and electrochemical properties of QPVA-based electrospun AEMs. Membranes with various concentrations of PAADDA were fabricated and extensively characterized using FTIR, SEM, tensile strength, water uptake, swelling degree, ion exchange capacity (IEC), and hydroxide ion conductivity (σ). FTIR confirmed the successful incorporation of PAADDA into the membrane structure, while SEM images showed that PAADDA effectively filled the voids between the QPVA fibers, resulting in denser membranes. The results indicated that the eQPAD5.0 membrane, with the highest PAADDA content, exhibited the best overall performance. The incorporation of PAADDA into QPVA-based electrospun AEMs significantly enhanced their mechanical strength, achieving a tensile strength of 23.9 MPa, an IEC of 1.25 mmol g⁻¹, and hydroxide conductivity of 19.49 mS cm⁻¹ at 30 °C and 29.29 mS cm⁻¹ at 80 °C, making them promising candidates for fuel cell applications. Full article

A novel, eco-friendly and cost-effective adsorbent, poly(diallyldimethylammonium) chloride (PDADMAC)-modified clay was developed to enhance its efficacy in removing Methyl Red (MR) from water. Different concentrations of PDADMAC solutions were evaluated during the synthesis and the effects of different operating conditions were investigated. The kinetic data closely followed the pseudo-first-order model, while equilibrium data were well described by Freundlich isotherm. MR removal efficiency decreased as solution pH or NaCl concentration increased, suggesting that electrostatic interaction plays a key role in the adsorption process. Regeneration studies using NaCl solutions revealed that a 1% NaCl solution effectively restored the adsorbent’s capacity. The findings indicate that PDADMAC clay is a promising and sustainable adsorbent for MR removal. Additionally, a three-layer backpropagation artificial neural network (ANN) was developed to predict the MR removal efficiency based on the initial MR concentration, pH, NaCl concentration, and adsorption time. Among these variables, pH was identified as the most influential factor. This approach provides valuable insight into the outcome prediction of a given adsorption process. Full article

This study explores the layer-by-layer (LBL) modification of polyacrylonitrile (PAN) hollow fibers for effective Mg²⁺/Li⁺ separation. It employs an LBL method of surface modification using polyelectrolytes, specifically aiming to enhance ion selectivity and improve the efficiency of lithium extraction from brines or lithium battery wastes, which is critical for battery recycling and other industrial applications. The modification process involves coating the hydrolyzed PAN fibers with alternating layers of positively charged polyelectrolytes, such as poly(allylamine hydrochloride) (PAH), polyethyleneimine (PEI), or poly(diallyldimethylammonium chloride) (PDADMAC) and negatively charged polyelectrolytes, such as poly(styrene sulfonate) (PSS), to form polyelectrolyte multilayers (PEMs). This study evaluates the modified membranes in Mg²⁺ and Li⁺ salt solutions, demonstrating significant improvements in selectivity for Mg²⁺/Li⁺ separation. PAH was identified as the optimal positively charged polyelectrolyte. PAN hollow fibers modified with ten bilayers of PAH/PSS achieved rejection rates of 95.4% for Mg²⁺ ions and 34.8% for Li⁺ ions, and a permeance of 0.39 LMH/bar. This highlights the potential of LBL techniques for effectively addressing the challenges of ion separation across a variety of applications. Full article

The rapid expansion of medical nanotechnology has significantly broadened the potential applications of cellulose nanocrystals (CNCs). While CNCs were initially developed for drug delivery, they are now being investigated for a range of advanced biomedical applications. As these applications evolve, it becomes crucial to understand the physicochemical behavior of CNCs in biologically relevant media to optimize their design and ensure biocompatibility. Functionalized CNCs can adsorb biomolecules, forming a “protein corona” that can impact their physicochemical properties, including alterations in particle size, zeta potential, and overall functionality. In this study, CNCs were coated with low (8500 Da)- and high (400,000–500,000 Da)-molecular-weight cationic polymer (poly(diallyldimethylammonium chloride—(PDDA) via non-covalent grafting, and their physicochemical characteristics, as well as their biological effects, were assessed in physiologically relevant media after sterilization. Our findings show that autoclaving significantly alters the physicochemical properties of CNC-PDDA, particularly when coated with low-molecular-weight (LMW) polymer. Furthermore, we observed that CNC-PDDA of a high molecular weight (HMW) has a greater impact on cell viability and blood biocompatibility than its LMW counterpart. Moreover, cellular immune responses to both CNC-PDDA LMW and HMW vary in the presence or absence of serum, implying that protein adsorption influences cell-nanomaterial recognition and their biological activity. This study provides valuable insights for optimizing CNC-based nanomaterials for therapeutic applications. Full article

Highly alkaline hydrogels are gaining increasing attention in building materials research. Specifically, cationic alkaline hydrogels based on diallyldimethylammonium hydroxide (DADMAOH) as the monomer have been effectively used to seal water-bearing cracks or serve as coupling media for electrochemical chloride extraction. However, the residual halogen content and challenges in scaling up monomer production have hindered broader application. Attempts to use a commercially available cation-selective membrane for ion exchange achieved up to 90% chloride-to-hydroxide switch, but the approach proved ineffective due to significant monomer decomposition during the process. By contrast, neutral gels and gel particles can be readily prepared from diallyldimethylammonium chloride (DADMAC) in large quantities and with a wide range of compositions. It is demonstrated here that these neutral gel particles undergo inverse static anion exchange when suspended in NaOH solution, generating DADMAOH particles with residual halide contents of <0.3%, without the need for ion-selective or dialysis membranes. This corresponds to an up to 100-fold reduction in residual chloride content compared to particles produced directly from alkaline monomer solutions, thereby significantly enhancing the efficiency of hydroxide ion release. The swelling behaviour of the particles is primarily influenced by the initial monomer concentration, while conductivity remains largely unaffected, indicating that charge transport occurs mainly along the particle surface. Despite the pronounced increase in swelling with decreasing particle radii, the specific conductivity of 2.8 Ω⁻¹ m⁻¹ is still sufficient for their use as coupling media in concrete applications. In summary, the alkaline particles prepared via inverse static anion exchange meet all necessary requirements for building materials applications, offering a broader range of tuneable properties and greater ease of production compared to gels or particles derived from DADMAOH. Full article

The hybrid flocculant P(aluminum chloride-co-diallyldimethylammonium chloride) was synthesized in this study. Diallyldimethylammonium chloride monomers were used and ammonium persulfate served as the initiator. The structure of P(aluminum chloride-co-diallyldimethylammonium chloride) was characterized using Fourier-transform infrared spectroscopy, scanning electron microscopy, an electrical conductivity test, and thermogravimetric analysis. Single-factor experiments were conducted to optimize the synthetic conditions of the hybrid flocculant. An optimized product with an intrinsic viscosity of 926.36 mL/g and a flocculation decolorization rate of 99% was obtained under the following reaction conditions: the total monomer concentration was 30%, the initiator concentration was 0.7%, the reaction temperature was 60 °C, and the reaction time was 3 h. The results demonstrated that the PAC-PDMDAAC hybrid flocculant exhibited covalent bonding between its organic–inorganic components and displayed enhanced stability properties due to its high intrinsic viscosity and spatial structure. Moreover, this hybrid flocculant showed superior decolorization performance in disperse-violet-H-FRL-dye wastewater. Full article

Mercury (Hg) is a toxic element which impacts on biological systems and ecosystems. Because the toxicity of Hg species is highly dependent on their concentration levels and chemical forms, the sensitive identification of the chemical forms of Hg—i.e., Hg speciation—is of major significance in providing meaningful information about the sources of Hg exposure. In this study, a microfluidic-based device made of high-clarity poly(methyl methacrylate) (PMMA) was fabricated. Then, titanium dioxide nanoparticles (nano-TiO₂s) were attached to the treated channel’s interior with the aid of poly(diallyldimethylammonium chloride) (PDADMAC). After coupling the nano-TiO₂-coated microfluidic-based photocatalyst-assisted reduction device (the nano-TiO₂-coated microfluidic-based PCARD) with high-performance liquid chromatography (HPLC) and inductively coupled plasma mass spectrometry (ICP-MS), a selective and sensitive, hyphenated system for Hg speciation was established. Validation procedures demonstrated that the method could be satisfactorily applied to the determination of mercury ions (Hg²⁺) and methylmercury ions (CH₃Hg⁺) in both human urine and water samples. Remarkably, the zeta potential measured clearly indicated that the PDADMAC-capped nano-TiO₂s with a predominance of positive charges indeed provided a steady force for firm attachment to the negatively charged device channel. The cause of the durability of the nano-TiO₂-coated microfluidic-based PCARD was clarified thus. Full article

The main purpose of this paper was to reveal the effect of aluminum (Al)-based coagulants on enhanced coagulation for the removal of algae and the synergistic optimization mechanism among different Al species. The formation, breakage, and regrowth processes of algal coagulation flocs formed by a series of monomeric Al-based coagulants (Al₂(SO₄)₃, Al₁₃, and Al₃₀), Al₁₃/Al₃₀ composite coagulant and poly(diallyldimethylammonium chloride)/Al₁₃ (PDADMAC/Al₁₃) composite coagulant were studied. Results indicated that Al₁₃ mainly employed a charge neutralization mechanism, which was conducive to the destabilization of algae and the regeneration of flocs, while Al₃₀ mainly employed a sweep flocculation mechanism, which was conducive to the formation of algae and the strength of flocs. Meanwhile, the charge neutralization was the main mechanism during the algae coagulation process because it could effectively remove the soluble microbial products (SMP) component in the extracellular organic matter (EOM). Therefore, Al₁₃ could achieve a higher coagulation performance than other monomeric Al-based coagulants. The Al₁₃/Al₃₀ composite coagulant could make up for the deficiency of the sweep flocculation mechanism in Al₁₃ and charge neutralization mechanism in Al₃₀, and achieve the best synergistic optimization performance at Al₁₃:Al₃₀-7:3. Additionally, PDADMAC, as a polymer, could further enhance the charge neutralization ability of Al₁₃ at low dosages and the sweep flocculation ability of Al₁₃ at high dosages, respectively. However, an excessive dosage would lead to charge reversal and thus reduce the coagulation effect. Therefore, controlling the dosage was key when using Al-composite coagulants. The findings of our research could offer a certain theoretical foundation for the development of inorganic polymer flocculants. Full article

Van der Waals heterostructures with incommensurate contact interfaces show excellent tribological performance, which provides solutions for the development of new solid lubricants. In this paper, a facile electrostatic layer-by-layer self-assembly (LBL) technique was proposed to prepare multi-layer van der Waals heterostructures tungsten disulfide/hexagonal boron nitride (vdWH WS₂/h-BN). The h-BN and WS₂ were modified with poly (diallyldimethylammonium chloride) (PDDA) and sodium dodecyl benzene sulfonate (SDBS) to obtain the positively charged PDDA@h-BN and the negatively charged SDBS@WS₂, respectively. When the mass ratio of PDDA to h-BN and SDBS to WS₂ were both 1:1 and the pH was 3, the zeta potential of PDDA@h-BN and SDBS@WS₂ were 60.0 mV and −50.1 mV, respectively. Under the electrostatic interaction, the PDDA@h-BN and SDBS@WS₂ attracted each other and stacked alternately along the (002) crystal plane forming the multi-layer (four-layer) vdWH WS₂/h-BN. The addition of the multi-layer vdWH WS₂/h-BN (1.0 wt%) to the base oil resulted in a significant reduction of 33.8% in the friction coefficient (0.104) and 16.8% in the wear rate (4.43 × 10⁻⁵ mm³/(N·m)). The excellent tribological property of the multi-layer vdWH WS₂/h-BN arose from the lattice mismatch (26.0%), a 15-fold higher interlayer slip possibility, and the formation of transfer film at the contact interface. This study provided an easily accessible method for the multi-layer vdWH with excellent tribological properties. Full article

Swine wastewater (SW) was treated using industrial wastes as raw materials in a pre-treatment process (coagulation or adsorption), followed by a continuous heterogeneous Fenton reaction. Before the treatment conducted as a continuous operation, two different batch optimization strategies were evaluated, in which the effects of H₂O₂ concentration and pH were studied. The results show that using excessive H₂O₂ results in the same behavior, regardless of whether the pH is 3 or 7.5, while at low H₂O₂ concentrations, the acidic pH improves the chemical oxygen demand (COD) removal due to a higher solubility of iron. The partial addition of H₂O₂ after 60 min of the reaction proved to be unbeneficial. Considering other perspectives, a continuous Fenton process using iron filings (IF) as the iron source ([H₂O₂] = 50 mg/L) was applied after the SW pre-treatment, consisting of adsorption with red mud (RM) or coagulation with poly-diallyldimethylammonium chloride (PDADMAC). The RM adsorption presented higher COD removal and lower toxicity than the PDADMAC coagulation, revealing to be a suitable material for this purpose, but for both pre-treatments, the application of a subsequent continuous Fenton process revealed to be essential to achieve the COD discharge limits imposed by the Portuguese law. In addition, high amounts of dissolved iron were present in the samples (55–58 mg/L) after the Fenton process. However, after the overall treatment, the samples showed no harmful characteristics for Lepidium sativum, being classified as “non-toxic”, contrary to the initial wastewater. Full article