Epoxy Monomer Research Articles

Enhancement of Moisture‐Resistant Performance of Epoxy Resins via Introduction of Hydrophobic and Flexible Chains

AbstractThe introduction of long and flexible polyether chains in epoxy resins is an effective method to improve their toughness. However, using the hydrophilicity/hydrophobicity of polyether chains to tune their moisture resistance has been overlooked currently. In this work, two types of polyether‐based diglycidyl ethers with hydrophilic poly(oxyethylene) (DGEPOE) and relatively hydrophobic poly(oxybutylene) segments (DGEPOB) are synthesized and then binary‐cured with commercial diglycidyl ether of bisphenol A (DGEBA), respectively, yielding the corresponding DGEPOE:DGEBA‐m:ns and DGEPOB:DGEBA‐m:ns based on various ratios. For comparison, pure DGEPOEr, DGEPOBr, and DGEBAr resins are also prepared. Results show that the equilibrium water uptake of DGEPOB:DGEBA‐m:ns is at least less than one‐fifth of that of DGEPOE:DGEBA‐m:ns; meanwhile, the diffusion coefficients of water molecules in DGEPOB:DGEBA‐m:ns are also 1–2 orders of magnitude lower than those in DGEPOE:DGEBA‐m:ns, demonstrating that the incorporation of hydrophobic POB chains can significantly reduce the hygroscopicity of resins. Moreover, DGEPOB:DGEBA‐m:ns not only exhibit superior flexibility and ductility relative to pure DGEBAr, but display exceptional strength and toughness in comparison with pure DGEPOBr. These findings suggest that tuning the hydrophilicity/hydrophobicity of building units of epoxy monomers offers a promising strategy for developing high‐performance epoxy materials, especially suitable for humid environments.

Synthesis of polymeric nanoparticles with different functionalities to produce new biocatalysts

AbstractThis study aimed to synthesize functionalized nanosupports via emulsion polymerization to develop new promising nanobiocatalyts via enzyme immobilizations. The co‐monomers methyl methacrylate, divinylbenzene and the epoxy monomer glycidyl methacrylate (GMA) were used. The performance of the nanobiocatlysts was evaluated in hydrolysis and esterification reactions after the immobilization of lipase B from Candida antarctica (CAL B). Firstly, the nanosupports functionalized in situ with 25% and 50% w/w of GMA were successfully synthesized. In esterification reactions, the nanobiocatalysts containing 25% (w/w) of GMA were more active, achieving 254 U.g−1, or an enzyme activity per area of 2.8 U.m−2; such value was higher than the one obtained when the commercial matrix Octadecyl Sepabeads was used (328 U.g−1, 2.4 U.m−2). Such results point out that there is an optimum concentration of GMA epoxide groups that should be incorporated into the supports. The greater enzymatic activity obtained for 25% of GMA nanobiocatalyst was achieved not only because of their textural properties, but also due to a favorable interaction between the epoxide groups and CAL B. These results highlight the potential use of the heterofunctional matrices for the synthesis of new market‐competitive biocatalysts.

Design of epoxy composites via molecular orbital modulation and enhanced π-πF interactions achieving synchronous improvement of electrical and mechanical performance

The stacked aromatic rings in bisphenol A epoxy resins provide good mechanical properties and thermal stability while leading to the transport of conjugated delocalized electrons, which dramatically affects the insulation properties of the material. This contradiction leads to performance bottlenecks in epoxy-based encapsulation materials, further limiting the development of high-voltage semiconductor devices. In this study, fluorophenyl-modified epoxy monomers (FPMEPs) are designed to enrich the intermolecular interactions in an aromatic system while inhibiting the charge transport process, thereby solving the contradiction between the electrical and mechanical properties. Firstly, FPMEP with high insulation properties was designed by theoretical calculations and then synthesized by highly selective click chemistry. The fluorophenyl modulates the molecular orbitals of epoxy monomers and acts as a deep trap to inhibit charge injection and transport processes. Further, the π-πF stacking between the aromatic system and fluorophenyl enhances the interaction of the matrix molecules and solves the dispersion problem of fluorinated graphene (FG) fillers. The FPMEP/FG composites thus exhibit a considerable improvement in electrical and mechanical properties (breakdown strength of 39.8 kV/mm, dielectric loss of 0.011@50 Hz, tensile strength of 68.8 MPa, and adhesive strength of 2.15 MPa), and demonstrate good water repellency and aging durability. This matrix-filler synergistic modification strategy provides new insights into the design of insulation material.

Epoxy resin-based polymer-wall stabilized liquid crystal films with low driving voltages and improved mechanical performance for smart window applications

Polymer stabilized liquid crystals (PSLCs) have wide applications in smart windows and light shutters. However, for most applications, it requires low driving voltages and high mechanical performance, which is arduous to achieve both. Herein, a novel epoxy resin-based PSLC device is prepared showing improved electro-optical and mechanical properties simultaneously. This is benefited from the construction of a period polymer wall structure in liquid crystal matrix through cationic polymerization of epoxy monomers and preparation of multi-functional surfaces through self-assembly of silane mixtures. The multi-functional surfaces could ensure homeotropic alignment of liquid crystals and photo-polymerize with the polymer networks. As a result, the polymer-wall stabilized liqduid crystal (PWSLC) film with multi-functional surfaces shows lower (24%) saturation voltage, higher (20%) contrast ratio and improved (2.4 times) peel strength than the PSLC film with only vertical alignment surfaces. This research provides important reference to experiment and manufacture of reverse-mode dimming films for smart windows applications.

Exploring strategies for valorizing wood processing waste: advancing sustainable, fully lignocellulosic biocomposites

This study presents the design and synthesis of bio-composites exhibiting high properties, wherein both the matrix and filler originate from wood biomass. Notably, no additional hardener compounds or treatments/modifications of the lignocellulosic filler were employed. Thermosetting materials were developed by homopolymerizing a bio-based aromatic epoxy monomer, the resorcinol diglycidyl ether (RDGE), with different percentages, from 1 wt% to 30 wt% of natural wood processing side-product, such as spruce bark powder (SB), which was used as such without additional treatments and modifications. The DSC analyses revealed enhanced reactivities with the bio-filler content, resulting in a reduced reaction temperature range and maximum reaction temperature. These findings provide evidence of the chemical interaction between the functional groups from spruce bark and the epoxides groups. The obtained fully based lignocellulosic materials show high E' values from 2.4 GPa to 2.5–3.5 GPa (glassy state) and from 64 MPa to 99–156 MPa in the rubbery region. The damping factor of the bio-composites with 1–10 wt% SB have shown an increase of the α transition temperature from 92 °C to 94–97 °C. The excellent filler/matrix interface and optimal adhesion between them were confirmed by SEM analysis.

Recent Development of Functional Bio-Based Epoxy Resins.

The development of epoxy resins is mainly dependent on non-renewable petroleum resources, commonly diglycidyl ether bisphenol A (DGEBA)-type epoxy monomers. Most raw materials of these thermoset resins are toxic to the health of human beings. To alleviate concerns about the environment and health, the design and synthesis of bio-based epoxy resins using biomass as raw materials have been widely studied in recent decades to replace petroleum-based epoxy resins. With the improvement in the requirements for the performance of bio-based epoxy resins, the design of bio-based epoxy resins with unique functions has attracted a lot of attention, and bio-based epoxy resins with flame-retardant, recyclable/degradable/reprocessable, antibacterial, and other functional bio-based epoxy resins have been developed to expand the applications of epoxy resins and improve their competitiveness. This review summarizes the research progress of functional bio-based epoxy resins in recent years. First, bio-based epoxy resins were classified according to their unique function, and synthesis strategies of functional bio-based epoxy resins were discussed, then the relationship between structure and performance was revealed to guide the synthesis of functional bio-based epoxy resins and stimulate the development of more types of functional bio-based epoxy resins. Finally, the challenges and opportunities in the development of functional bio-based epoxy resins are presented.

Recyclable fully biobased high-performance epoxy thermosets

Thermosetting polymeric materials play a pivotal role in numerous sectors due to their versatility in tailoring physicochemical and mechanical properties and their exceptional performances. The aim of this study is to design 100 % bio-based high performant and recyclable thermosets. To achieve this goal, a natural and renewable-based epoxy monomer, triglycidyl ether of phloroglucinol (TGPh), was crosslinked with biobased anhydrides to create novel polymeric resins. Through detailed investigations, it was found that the designed materials have storage moduli values at room temperature ranging from 2.1 to 3.4 GPa, with damping factors spanning from 86 °C to 163 °C depending on the nature of the anhydride. Tensile tests corroborated the performant mechanical properties of the designed bio-resins, showing Young's modulus values ranging from 1.2 to 1.5 GPa. Furthermore, the water absorption values are very low, ranging from 0.25 % to 0.35 %. Besides, the designed bio-resins exhibited rapid dissolution in TBD/EG solution, as well as thermo-mechanical reprocessability.

Novel phosphorous-containing epoxy thermosets with improved anti-flammability, smoke suppression, and dielectric properties

As one of the most commonly used thermosetting resins, the flammability of epoxy resins (EPs) has become a key factor limiting the expansion of their application range. Herein, a novel phosphorous-containing epoxy monomer (EDPPO) was synthesized using diallyl amine and diphenyl phosphoryl chloride as the starting materials. Subsequently, EDPPO was thermally cured with two diamine hardeners, 4, 4′-diaminodiphenyl sulfone (DDS) and 4,4′-dithiodianiline (DTDA). Additionally, commercial diglycidyl ether of bisphenol A (DGEBA)-type epoxy pre-polymers were cured with DDS and DTDA as comparative samples. The cured EDPPO-based thermosets showed excellent flame-retardant properties coupled with smoke suppression. Specifically, the limiting oxygen index (LOI) for the EDPPO/DDS (P content 6.4 wt.%) reached 32.0 %, and the UL-94 vertical burning test reached a V-0 rating. In addition, the PHRR, THR, and TSP values of EDPPO/DDS were 61.6 %, 49.1 %, and 58.5 % lower than those of DGEBA/DDS, respectively. The flame retardant mechanism analysis indicated that the excellent flame retardancy for cured EDPPO-based thermosets was attributed to the combined modes of action in condensed (promoting the charring capacity) and gaseous phases (quenching the active radicals). More importantly, EDPPO/DDS and EDPPO/DTDA exhibited lower dielectric constant and dielectric loss than DGEBA/DDS and DGEBA/DTDA. This work provided novel phosphorous-containing epoxy thermosets with improved anti-flammability, smoke suppression, and dielectric properties.

Controlling Hybrid Polyhydroxyurethane Adhesive and Rheological Properties by Partial Carbonation of Biobased Epoxy Monomer.

Controlling hybrid material properties by simple monomer design offers an elegant pathway to prepare thermoset adhesives with tunable properties. Herein, biobased hybrid polyhydroxyurethane/polyepoxy is prepared starting from partially carbonated cashew nut shell epoxy derivatives (NC514) and m-xylene diamine (MXDA). The curing reactions, that is, epoxy-amine and cyclic carbonate aminolysis, monitored by ATR-IR spectroscopy at 50°C are found to be concomitant yielding highly homogeneous materials. Hybrid networks are extensively characterized by swelling tests, TGA, DMA, DSC, tensile tests, rheology, and lap-shear-test on aluminum substrates. The introduction of hydroxyurethane moieties within the epoxy-amine networks enhanced the adhesion properties (up to 20% compare to neat epoxy resins) by combining hydrogen bonding capability and vitrimeric properties (thermoset able to flow). Rheological characterizations and reprocessing tests demonstrated that hybrid adhesives with up to 47 mol% of cyclic carbonate groups are capable of covalent exchange (internally catalyzed by tertiary amine) while keeping similar thermomechanical properties and enhanced adhesion strength compare to the permanent epoxy network.

Development of a quaternary photocurable system for 3D printing based on the addition of acrylate monomers to an epoxy/thiol‐Ene system

AbstractThe exothermic nature of acrylate photopolymerizations enables room temperature 3D printing of a quaternary formulation that incorporates an acrylate monomer, and an epoxy/thiol‐ene system (ETES). The latter comprises an epoxy monomer, a multifunctional thiol and a tetraallyl functionalized ditertiary amine curing agent. Pristine ETES necessitates temperatures of 85–95 °C for curing. Several mechanisms operate simultaneously during this process: homopolymerization of acrylates, thiol‐acrylate photopolymerization, thiol‐ene photopolymerization between the double bonds of curing agent and the multifunctional thiol, the Michael addition between thiolates derived from ETES and the double bonds of acrylates, and the anionic polymerization of the epoxy resin via the tertiary amine groups. To optimize the quaternary formulations for printing, parameters, such as reactivity, exothermicity, and viscosity, was explored. Subsequently, the thermal and viscoelastic properties of the printed cross‐linked polymers derived from these formulations were analyzed using Differential Scanning Calorimetry (DSC), Dynamic Mechanical Analysis (DMA) and Thermogravimetric Analysis (TGA). The polymers derived from quaternary formulations exhibited lower crosslinked density compared to those obtained from the pristine acrylates. This reduction in crosslink density contributes to the improved toughness of the hybrid polymers.

Effect of crosslinking density on the self-healing and self-reporting properties of epoxy anti-corrosion coatings

This work developed a novel coating with self-healing and self-reporting performance by embedding polyurethane/poly-(urea-formaldehyde) (PU/UF) microcapsules in a shape memory epoxy polymer. 2’7’-Dichlorofluorescein (DCF) and linseed oil were applied as the coloring agent and healing agent, respectively, which are encapsulated into the PU/UF microcapsules (DL@PU/UF microcapsules) via a facile one-step method. To adjust the shape memory effect and the self-reporting performance of epoxy system, two kinds of curing agents (D230 and D400) were reacted with bisphenol A diglycidyl ether epoxy monomer to design a series of coating samples, finally the optimal coating system was selected by three indexes including barrier performance, residual amino content and coating hardness. When the composite coating was damaged, DCF can flow out of the broken microcapsules and react with the residual amino groups in the epoxy coating matrix, which can be recognized red signals in natural light and yellow fluorescent signals under ultraviolet light irradiation. More importantly, the excellent self-reporting property of the coating can be achieved on various metal substrates that broaden the application range of the coating. As for self-healing performance, the damaged coating can be healed quickly due to the shape memory effect of the coating as well as the filling of linseed oil in the scratched region. The Rct value of the healed coating containing 6 % DL@PU/UF microcapsules after immersing in 3.5 wt% NaCl solution for 5 days was more than 3 times that of the scratched coating, and the Rc value was about 16 times that of the scratched coating, indicating its corrosion protection performance. The novel coting not only achieve timely self-reporting ability of color and fluorescence, but also rapidly repair the coating damage, which is essential to practical applications.

Investigating Cross-Linking Parameters and Molecular Arrangement in Liquid Crystalline Epoxy Monomer with Aromatic Diamine: DSC-TOPEM® and WAXS Analysis.

This study presents the characterization of cross-linking parameters of a liquid crystalline epoxy monomer with an aromatic diamine as a curing agent. The mixture tested consisted of bis [4-(10,11-epoxyundecanoyloxy)benzoate] p-phenylene (LCEM) and 1,3-phenylenediamine (1,3-PDA). This paper focuses on the structural characterization of such systems using X-ray analysis. To investigate this, a comprehensive analysis was conducted using Differential Scanning Calorimetry (DSC) and Wide-Angle X-ray Scattering (WAXS). Through DSC analysis, the curing behavior and transition temperature of the liquid crystal epoxy system were established. To fully characterize the cross-linking of the system, a novel technique called DSC-TOPEM® was employed. The use of this technique enabled real-time monitoring of the curing process and provided precise information on the cross-linking energy, which resulted in the finding that the mixture was cross-linking faster than expected. WAXS analysis was performed to assess the structural changes formed during the cross-linking. The results of this analysis confirm that lower cross-linking temperatures of the mixture cause better ordering of mesogens than higher ones.

Chemical and Solvent‐Based Recycling of High‐Performance Epoxy Thermoset Utilizing Imine‐Containing Secondary Amine Hardener

AbstractEpoxy thermosets are indispensable in various industrial applications due to their exceptional material properties. However, their limited recyclability poses a significant challenge for sustainability. To address this issue, integrating recyclable imine moieties into epoxy systems has emerged as a promising strategy. Despite recent advancements, challenges persist concerning the hydrolytic stability of imine‐based epoxy thermosets and the formation of irregular oligomeric structures upon depolymerization. In this study, these shortcomings are solved by designing a liquid imine monomer with secondary amine functionalities, which is subsequently reacted with commercially available epoxy monomers to produce high‐performance epoxy thermosets. Remarkably, the developed imine‐based epoxy system shows no sign of hydrolysis even under high‐temperature aqueous conditions, underscoring its potential for various industrial applications. Only the treatment with aqueous HCl results in the selective formation of exclusively well‐defined molecules, in high isolated yields after depolymerization. Crosslinking these building blocks once again yields recycled polymers with properties identical to pristine material. Moreover, it is discovered that, despite the crosslinked nature of the epoxy thermoset, the complete dissolution of the intact polymer in dichloromethane allowed for simple solvent‐based recycling. Through design on the molecular level, the recycling of imine‐based epoxy polymers is achieved via chemical and solvent‐based techniques.

Synthesis of a syringaldehyde derivative to enhance the fire resistance and structural strength of epoxy resin

AbstractIn light of growing environmental apprehensions, the threat of global warming, and the depletion of oil reserves, it is advisable to opt for bio‐epoxy resins sourced from sustainable materials. In response to these issues, syringaldehyde (SH) flame retardant epoxy resin derivatives have been formulated and synthesized. Initially, SH was reacted with 4, 4‐diaminodiphenylmethane (DDM) to yield an intermediate compound, DDM‐SH. Subsequently, the inherently flame‐retardant curing agent (DDM‐SH‐DOPO) and the bio‐based epoxy monomer (DDM‐SH‐EP) were produced by reacting with DOPO and epichlorohydrin, respectively. These resulting compounds were then integrated into bisphenol A epoxy resin, enhancing its flame retardant and mechanical characteristics. The flammability was assessed through limiting oxygen index (LOI), UL‐94, and cone calorimeter tests. The DDM‐SH‐EP‐20/5 sample exhibits notable improvements. It elevates the LOI to 25.3%, achieving a UL‐94 rating to V‐0 and effectively reducing smoke and heat release from the epoxy resin. The ternary cross‐linking network formed between DGEBA, DDM‐SH‐EP, and DDM‐SH‐DOPO primarily contributes to this mechanical enhancement, DDM‐SH‐EP‐20/5 has excellent overall performance, bending strength and bending modulus are 103% and 108% higher than DGEBA/DDM. This study offers a viable solution for producing flame‐retardant epoxy resin with superior mechanical properties.

Scalable Synthesis of Thymol-Based Bisphenol E Epoxy Monomer and Related Thermosets with Low Dielectric Constant and Density and Improved Resistance to Hygrothermal Aging

Scalable Synthesis of Thymol-Based Bisphenol E Epoxy Monomer and Related Thermosets with Low Dielectric Constant and Density and Improved Resistance to Hygrothermal Aging

High seminal BPA in IVF patients correlates with lower sperm count and up-regulated miR-21 and miR-130a

Bisphenol A (BPA) is a widespread industrial chemical, used as the key monomer of polycarbonate plastics and epoxy resins. BPA has been detected in human seminal fluid and has been correlated with changes in sperm parameters, crucial in determining male fertility. In this study, semen samples were collected from 100 patients aged 29–47 years undergoing fertility assessment between 2021 and 2023 and analyzed according to WHO guidelines. BPA levels in the seminal plasma were then measured through an enzyme-linked immunosorbent assay (ELISA) and compared to sperm quality metrics. The relative mRNA/miRNA expression of key genes associated to male reproduction, including androgen receptor, miR-34c, miR-21, miR-130a, was then quantified and compared between groups with high or low BPA content. Our results revealed that BPA levels were increased with age and were negatively correlated with sperm counts (p<0.05). The negative correlation remained significant when patients were age-matched. No other relationships between seminal BPA and motility, morphology or DNA fragmentation levels were observed. qPCR analysis showed that androgen receptor mRNA expression was significantly greater in sperm with high seminal BPA (p<0.05). Moreover, we found that the expression of miR-21 and miR-130a was also upregulated in the higher BPA group (p<0.05). These results display a relationship between BPA content in the semen and male fertility parameters, and provide insights into the molecular mechanisms through which BPA may be affecting male reproductive capability. Ultimately, this research can potentially drive changes to guidelines and exposure limits for BPA exposure.

Review of Recyclable Bio-based Epoxy Resins with Dynamic Chemical Bonds

Epoxy thermosetting resins are usually reliant on fossil fuel-based resources, commonly diglycidyl ether bisphenol A (DGEBA) type epoxy monomers. Most raw materials of these thermoset resin are toxic to the health of human, and their eternal cross-links make them difficult to reuse and recycle. To alleviate concerns about the environment and human health, it is an effective way to design new bio-based epoxy thermosetting materials to replace petroleum based thermosetting materials. The introduction of cleavable and dynamic bonds for bio-based thermosetting materials can also realize the recycling of bio-based epoxy resin. In this way, the damaged thermosetting materials can be recovered to prolong their service lifetime and reduce the thermosetting waste. This review article aims to outline the latest improvements in intrinsically recyclable bio-based epoxy thermosetting materials. This review first describes the synthesis method of recyclable bio-based epoxy, then reviews the structure, recyclable and other properties of bio-based epoxy containing different dynamic bonds, and finally summarizes the challenges and opportunities for the recyclable bio-based epoxy.

Recyclable Technology of Thermosetting Resins for High Thermal Conductivity Materials Based on Physical Crushing

Epoxy resin, characterized by prominent mechanical and electric‐insulation properties, is the preferred material for packaging power electronic devices. Unfortunately, the efficient recycling and reuse of epoxy materials with thermally cross‐linked molecular structures has become a daunting challenge. Here, we propose an economical and operable recycling strategy to regenerate waste epoxy resin into a high‐performance material. Different particle size of waste epoxy micro‐spheres (100–600 μm) with core‐shell structure is obtained through simple mechanical crushing and boron nitride surface treatment. By using smattering epoxy monomer as an adhesive, an eco‐friendly composite material with a “brick‐wall structure” can be formed. The continuous boron nitride pathway with efficient thermal conductivity endows eco‐friendly composite materials with a preeminent thermal conductivity of 3.71 W m−1 K−1 at a low content of 8.5 vol% h‐BN, superior to pure epoxy resin (0.21 W m−1 K−1). The composite, after secondary recycling and reuse, still maintains a thermal conductivity of 2.12 W m−1 K−1 and has mechanical and insulation properties comparable to the new epoxy resin (energy storage modulus of 2326.3 MPa and breakdown strength of 40.18 kV mm−1). This strategy expands the sustainable application prospects of thermosetting polymers, offering extremely high economic and environmental value.

Characterization of dental light-curing resin composites incorporating multiple modified low-shrink monomers

ObjectivePolymerization shrinkage poses a significant challenge in dental resin composites. The objective of this study is to introduce spiroorthocarbonate monomer 3,9-dimethylene-1,3,5,7-tetraoxa-spiro[5,5]undecane (BMSOC) and epoxy resin monomer 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate (ECHM-ECHC) into bisphenol-S-bis(3-methacrylato-2-hydroxy propyl)ether (BisS-GMA) based resin composites to develop composites with reduced shrinkage properties. MethodsBMSOC and BisS-GMA were synthesized and thoroughly mixed with ECHM-ECHC, followed by inorganic fillers and photoinitiators. Based on the composition of the resin matrix, five groups of experimental composites were prepared, with traditional bisphenol A-dimethacrylate glycidyl ester (Bis-GMA)/triethylene glycol dimethacrylate (TEGDMA) based composite serving as the control. The polymerization properties, including degree of conversion (DC) and polymerization shrinkage (PS), as well as marginal microleakage, wettability, flexural strength (FS), flexural modulus (FM), and biocompatibility were evaluated. ResultsThe results demonstrated that compared with the control group, the PS of BisS-GMA based composites containing BMSOC and ECHM-ECHC were significantly reduced (P < 0.05), and the lowest PS (0.96 ± 0.08 %) was observed when the ratio of BisS-GMA: (Epoxy + BMSOC) was 4:6. Additionally, the experimental composites also exhibited improved DC, minimal microleakage, low hydrophilicity, enhanced mechanical properties, qualified in vivo biocompatibility, and slight/moderate in vitro biocompatibility. SignificanceThe resin composites incorporating multiple modified low-shrink monomers are promising for dental applications to prevent various clinical problems caused by PS and extend restoration longevity.

Novel Crosslinked Anion Exchange Membranes Based on Thermally Cured Epoxy Resin: Synthesis, Structure and Mechanical and Ion Transport Properties.

Limitations in existing anion exchange membranes deter their use in the efficient treatment of industrial wastewater effluent. This work presents an approach to fabricating novel anion-conducting membranes using epoxy resin monomers like hydrophobic or hydrophilic diglycidyl ether and quaternized polyethyleneimine (PEI). Manipulating the diglycidyl ether nature, the quantitative composition of the copolymer and the conditions of quaternization allows control of the physicochemical properties of the membranes, including water uptake (20.0-330%), ion exchange capacity (1.5-3.7 mmol/g), ionic conductivity (0.2-17 mS/cm in the Cl form at 20 °C), potentiostatic transport numbers (75-97%), as well as mechanical properties. A relationship was established between copolymer structure and conductivity/selectivity trade-off. The higher the quaternized polyethyleneimine, diluent fraction, and hydrophilicity of diglycidyl ether, the higher the conductivity and the lower the permselectivity. Hydrophobic diglycidyl ether gives a much better conductivity/selectivity ratio since it provides a lower degree of hydration than hydrophilic diglycidyl ether. Different mesh and non-woven reinforcing materials were also examined. The developed membranes demonstrate good stability in both neutral and acidic environments, and their benchmark characteristics in laboratory electrodialysis cells and batch-mode dialysis experiments are similar to or superior to, commercial membranes such as Neosepta© AMX, FujiFilm© Type1, and Fumasep FAD-PET.