Diglycidyl Ether Of Bisphenol A Research Articles

Preparation of UV curable acrylamide modified epoxy resin and performance in 3D printing

A novel UV-curable 3D printing resin was synthesized by combining diglycidyl ether of bisphenol A (DGEBA) and acrylamide (AAM) to create a UV-curable acrylamide-modified epoxy resin prepolymer. This prepolymer was then uniformly mixed with the photoinitiator TPO and the reactive diluent hydroxyethyl methacrylate (HEMA). By adjusting the prepolymer content, UV-curable 3D printing resins were formulated with prepolymer concentrations of 30 wt%, 40 wt%, and 50 wt%, respectively. Infrared spectroscopy and nuclear magnetic resonance studies indicated that the amino groups in acrylamide reacted with the epoxy groups. When the prepolymer was added at concentrations of 30 wt% and 40 wt%, the viscosity met the requirements for UV-curable 3D printing. Upon completion of curing, these three distinct resins exhibited high mechanical strength, with tensile strength reaching up to 59.42 MPa and flexural strength peaking at 72.25 MPa. The elongation at break ranged from 2.60 % to 4.91 %. Scanning electron microscopy was used to examine the UV-cured 3D printed samples, and comparison with the design files revealed that the printed samples exhibited excellent dimensional stability. The study results indicated that this novel UV-curable epoxy vinyl resin formulation possessed excellent mechanical properties, suitable curing characteristics, and high resolution, making it a highly promising prepolymer for UV-curable 3D printing.

Biocidal polymer coatings based on porphyrin-modified epoxy-amine networks

For the first time, a pronounced biocidal activity of modified polymers with a porphyrin content of 21.4 μM (0.002 wt%) against Staphylococcus aureus was demonstrated. In order to develop new biocidal polymer coatings, a study was carried out on diglycidyl ether of bisphenol A (DGEBA) and porphyrin-modified oligomeric diamine systems. The study investigated the solubility of porphyrins in oligomers through experimental and theoretical means, using Van Krevelen's approach of additive group contributions. Fully cured epoxy-amine polymer materials modified with varied free-base tetraarylporphyrins were obtained. The materials were studied by means of thermogravimetry, differential scanning calorimetry, UV–Vis and fluorescence spectroscopy. The proposed approach to the formation of modified epoxy-amine materials allows preservation of the photophysical properties of porphyrins, including their photostability. The addition of modifiers in 4.28–21.4 μM range of concentrations makes it possible to keep the thermophysical and thermochemical properties of the polymer matrix.

Development and performance evaluation of a mechanically triggered release microcapsule based on in-situ polymerization for lost circulation control

Lost circulation is a critical technical challenge in the drilling and production process of underground oil and gas energy. In this study, a mechanically triggered release microcapsule for lost circulation control was designed and prepared with an in-situ polymerization using melamine, urea, formaldehyde, and diglycidyl ether of bisphenol A (healing agent) as raw materials. The structure and properties of the microcapsule were characterized by different techniques. The results show that the healing agent was successfully encapsulated by the resin shell, the median particle size (D50) of the microcapsules is 120.3 μm, and the thermal stability is excellent. The compatibility experiments show that the surface wettability and shear stability of the microcapsules are good in water-based drilling fluid. The compressive strength test reveals that the healing agent in the microcapsule is released and filled in the gap of the plugging zone under the contact pressure. The concentration of microcapsules and the size distribution of rigid particles are critical for the in-situ reinforcement effect. In addition, the fracture plugging performance of the microcapsule was studied. The results show that the pressure-bearing capacity of the plugging zone increases as the irregularity of the fracture surface increases. These findings indicate the microencapsulated healing agent is an effective lost circulation material (LCM), and provide a new technical idea for lost circulation control.

Study curing of epoxy resin by Isophoronediamine/ Triethylenetetramine and reinforced with montmorillonite and effect on compressive strength

Epoxy is a widely used thermosetting resin recognized for its exceptional performance in adhesives, coatings, and various other applications, attributed to its high tensile strength, stiffness, electrical performance, and chemical resistance. Epoxy-clay nanocomposites are extensively employed across diverse industries. The physical and chemical properties of these nanocomposites are influenced by the processing methods, clay modifiers, and curing agents used during their preparation. In this study, epoxy/nanoclay composites based on Diglycidyl Ether Bisphenol-A (DGEBA) will be cross-linked using Isophorone Diamine (IPD), a cycloaliphatic amine, and Triethylenetetramine (TETA), a linear aliphatic amine. The initial phase of the research will assess the impact of different types of cross-linkers, both individually and in combination at various molar ratios (such as Isophorone Diamine: Triethylenetetramine (IPA: TETA) / 25:75 and 75:25), on the compressive strength of the epoxy mortar. In the subsequent phase, the epoxy formulation with an Isophorone Diamine: Triethylenetetramine (IPD: TETA / 75:25), which demonstrates the highest compressive strength, will be selected for further investigation. This formulation will be used to evaluate the effects of different weight percentages (3%, 5%, and 7%) of organically modified montmorillonite (OMMT). The prepared epoxy composites will be characterized using a range of techniques, including Fourier Transform Infrared Spectroscopy (FT-IR), Transmission Electron Microscopy (TEM), and Scanning Electron Microscopy (SEM). The epoxy/nanoclay composite with an IPD: TETA / 75:25 and 3 wt % OMMT is expected to show the highest compressive strength, which is 94 MPa.

Non-Stoichiometric Effects on Viscoelasticity in DGEBA-EDA Systems: Insights from Brillouin Light Scattering.

The initial and final stages of the isothermal curing reaction between diglycidyl ether of bisphenol A and ethylenediamine were investigated by using Brillouin light scattering spectroscopy. High-frequency acoustic parameters were measured for these stages as a function of the diamine molar fraction, ranging from the pure prepolymer to the pure cross-linker. Significant differences in the concentration dependencies of the mechanical parameters are interpreted in relation to changes in the system's viscoelastic properties. At the final stage of the reaction, the concentration dependencies exhibit notable changes at two characteristic nonstoichiometric compositions─one corresponding to amine excess and the other to epoxy excess. While these concentrations align well with Flory's critical gel points, experimental evidence suggests they should instead be interpreted as vitrification points.

Optimising Nanoparticle Dispersion Time for Enhanced Thermomechanical Properties in DGEBA-Based Shape Memory Polymer Composites

Shape-memory polymers (SMPs) are smart materials that can change shape upon an external stimulus. This phenomenon is called the shape memory effect (SME), which is caused by entropy change due to rapid molecular motion in the polymer segments. Due to the inherently weak thermomechanical properties, use of SMPs is limited in many engineering applications. Therefore, SMPs are often reinforced with fibres and nanoparticles (NPs). NPs offered greater flexibility due to their superior physical, chemical, electrical, mechanical, and thermal properties. However, the homogeneous distribution of NPs is crucial for composition’s stability and enhancement of the base material’s properties. Among the different techniques used for dispersing NPs, ultrasonic irradiation has shown excellent emulsifying and crushing performance. The sonication process is essential for mitigating agglomerates; however, prolonged sonication time probably increases epoxy temperature, micro-bubbles, cavitation, breaking apart molecules and finally degrading the epoxy resin performances. This paper provides critical insight of nanoparticle dispersion into diglycidyl ether of bisphenol A epoxies (DGEBA). DGEBA epoxy resin was added to TiO2 NPs and sonicated for 60 min with 5 min intervals while the temperature of epoxy was maintained below 60oC by using a water cooling throughout the sonication process. The process parameters such as amplitude, mode, epoxy volume and the weight percentage of NPs were kept constant. After each sonication step, Fourier-transform infrared spectroscopy (FTIR) was performed using Thermo Scientific™ and analysed through OMNIC™ Professional quantitation software. In accordance with FTIR results, until 30 min of the sonication, DGEBA resin was not degraded. In order to confirm the performances and the reinforcing effect of NPs, thermo-mechanical and shape memory properties were compared with the neat specimen. The outcomes of this research have suggested quick guidance to find optimum NP dispersion time for DGEBA resins, which has been hardly studied before.

Density Functional Theory Study of Adhesion Mechanism between Epoxy Resins Cured with 4,4'-Diaminodiphenyl Sulfone and 4,4'-Diaminodiphenylmethane and Carboxyl Functionalized Carbon Fiber.

The molecular mechanism of adhesion of two epoxy resins based on diglycidylether of bisphenol A (DGEBA) cured with 4,4'-diaminodiphenyl sulfone (DDS) and 4,4'-diaminodiphenylmethane (DDM) to the carbon fiber (CF) surface is investigated by employing density functional theory (DFT) calculations. The CF surface was modeled by the armchair-edge structure of graphite functionalized with carboxyl (COOH) groups. Two adhesion interfaces were constructed using the CF surface: one with the DGEBA-DDS molecule (CF/DGEBA-DDS interface) and the other with the DGEBA-DDM molecule (CF/DGEBA-DDM interface). The interfacial properties were analyzed by calculating the maximum adhesion stress (Smax) at the interface. The adhesion stress-displacement curve revealed that Smax is 1160.37 MPa, higher for the CF/DGEBA-DDS interface compared to the CF/DGEBA-DDM interface, which is 1060.48 MPa. The energy decomposition analysis showed a similar DFT contribution to adhesion stress for both interfaces, but the dispersion contribution is more significant at the CF/DGEBA-DDS interface. The crystal orbital Hamilton population (COHP) analysis revealed distinct interfacial interactions despite similar DFT contributions. Hydrogen bonding (H-bonding) between the functional groups at both interfaces including feeble OH-π interactions between the benzene rings of epoxy resins and COOH groups on the CF surface were observed. The orbital interaction energies calculated from integrated COHP, i.e., IpCOHP, revealed that the CF/DGEBA-DDS interface has six H-bonding interactions with large absolute IpCOHP values (>1 eV), whereas the CF/DGEBA-DDM interface has five. The interaction between the amine group of the DGEBA-DDM molecule and the CF surface has a large IpCOHP value among all interactions. The sulfone group being at the center of the DDS molecule and its strong surface interaction positioned the DGEBA-DDS molecule closer to the CF surface than the DGEBA-DDM molecule, enhancing dispersion interaction at the CF/DGEBA-DDS interface. Hence, the CF surface exhibits a stronger affinity toward the DGEBA-DDS molecule than the DGEBA-DDM molecule through dispersion interaction.

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.

Investigation on Polyether Sulfone Toughening Epoxy Vitrimer: Curing and Dynamic Properties.

Diglycidyl ether of bisphenol A crosslinking with glutaric anhydride is used to form the conventional "covalent adaptive network", polyether sulfone (PES) by coiling and aggregating on the adaptive network is used to significantly increase the uncured resin viscosity for improving the processability of epoxy resin, but inevitably affecting the curing reaction and dynamic transesterification reaction. This study investigates the crucial roles of PES in curing dynamics and stress relaxation behavior. The results indicate that although PES does not directly participate in the crosslinking reaction of polyester-based epoxy vitrimers. Moreover, the isothermal curing studies reveal that the addition of PES can greatly bring forward the reaction rate peak from conversion α = 0.6 to α = 0.2, meaning that the curing mechanism transfers from chemical control to diffusion control. Dynamic property analysis shows that the addition of PES significantly accelerates stress relaxation, especially at lower temperatures, leading to low viscous flow activation energy Eτ and relatively insensitive stress relaxation behavior to temperature. Introducing PES into vitrimer resin greatly improves crosslinking density (2.31×10⁴molm- 3), enhancing glass transition temperature (82.68°C), tensile strength (68.66MPa), and fracture toughness (6.25%). Additionally, the modified vitrimer resin exhibits satisfying shape memory performance and reprocessing capability.

Synergistic Effects of Liquid Rubber and Thermoplastic Particles for Toughening Epoxy Resin

This study aims to investigate the toughening effects of rubber and thermoplastic particles on epoxy resin (EP), and to understand the mechanism underlying their synergistic effect. For this purpose, three EP systems were prepared using diglycidyl ether of bisphenol-A (DGEBA) epoxy resin (E-54) and 4,4-Diamino diphenyl methane (Ag-80) as matrix resin, 4,4-diaminodiphenyl sulfone (DDS) as a curing agent, and phenolphthalein poly (aryl ether ketone) particles (PEK-C) and carboxyl-terminated butyl liquid rubber (CTBN) as toughening agents. These systems are classified as an EP/PEK-C toughening system, EP/CTBN toughening system, and EP/PEK-C/CTBN synergistic toughening system. The curing behavior, thermal properties, mechanical properties, and phase structure of the synergistic-toughened EP systems were comprehensively investigated. The results showed that PEK-C did not react with EP, while CTBN reacted with EP to form a flexible block polymer. The impact toughness of EP toughened by PEK-C/CTBN was improved obviously without significantly increasing viscosity or decreasing thermal stability, flexural strength, and modulus, and the synergistic toughening effect was significantly higher than that of the single toughening system. The notable improvement in toughness is believed to be due to the synergistic energy dissipation effect of PEK-C/CTBN.

Preparation of Alkali-Resistant Lignin Nanospheres Loaded with Silver Nanoparticles and Their Applications Toward Antibiosis and Printing.

Lignin nanoparticles (LNPs) loaded with silver nanoparticles have exhibited significant application potential in antibacterial and catalytic fields. However, the high solubility of LNPs in silver ammonia solution makes it difficult to achieve the reduction of Ag+ and the adsorption of silver nanoparticles. In this study, a protecting agent, terephthalic aldehyde (TA) is used to block lignin condensation and introduce aldehyde groups onto the lignin molecular backbone during lignin extraction. Furthermore, the TA stabilized lignin (TASL) is cross-linked with bisphenol A diglycidyl ether (BADGE) to enhance its alkali resistance performance and subsequently prepared into alkali-resistance BADGE- TASL hybrid LNPs (BADGE- TASL hy-LNPs) by anti-solvent precipitation and self-assembly. Because the presence of a large number of aldehyde groups in TASL compensates for the loss of phenolic hydroxyl groups caused by crosslinking reactions, a high loading of silver nanoparticles of 54.00% is obtained after redox reaction and adsorption in silver ammonia solution. When the BADGE-TASL hy-LNPs@Ag is used as an antibacterial agent, its inhibition efficiency reached ≈99%. Besides, the BADGE-TASL hy-LNPs@Ag can serve as a printing material for the preparation of conductive printing ink. Therefore, this study provides a strategy for lignin functionalization and application in printed electronics and antimicrobial fields.

Ionic Liquid-Modified Copper for the Enhanced Thermal Conductivity and Mechanical Properties of Epoxy Resin/Expanded Graphite Composites.

In this study, diglycidylether of bisphenol A (DGEBA)/expanded graphite (EG)/copper (Cu) powder composites with high thermal conductivity were prepared for use as thermal interface materials. To construct an excellent thermally conductive network, the Cu surface was modified using the ionic liquid 1-ethyl-3-methyl imidazolium dicyanamide. In addition, the effect of the Cu content on the thermal conductivity, thermal stability, flexural properties, impact strength, and morphologies of the DGEBA/EG/Cu composites was investigated. The results indicated that the addition of 10 wt % Cu increased the thermal conductivity of the composites from 7.35 to 9.86 W/(m·K). Conversely, the thermal stability of the composites decreased with the addition of Cu. The flexural strength and impact strength of the composites increased from 27.9 MPa and 0.81 kJ/m2 to 39.6 MPa and 0.96 kJ/m2, respectively, as the Cu content increased from 0 to 10 wt %. Moreover, the flexural modulus of the composites increased from 9632 to 11,309 MPa with the addition of 10 wt % Cu. Scanning electron microscopy analysis of the DGEBA/EG/Cu composites revealed sheet-shaped blocks with numerous microcracks on the fracture surfaces.

Synthesis and characterization of epoxy resin‐polydicyclopentadiene interpenetrating polymer networks by UV‐initiated simultaneously frontal polymerization

AbstractBy combination of UV curing and frontal polymerization, interpenetrating polymer networks (IPNs) based on diglycidyl ether of bisphenol‐A (DGEBA) epoxy resin and polydicyclopentadiene (PDCPD) were prepared by UV‐induced simultaneously frontal polymerization in this paper. Compared with the net DGEBA cured polymer, the tensile strength, elongation at break and impact strength of the IPNs were simultaneously improved. The maximum tensile strength and elongation at break of the IPNs reached 100 MPa and 4.64%, respectively, and the maximum impact strength reached 7.34KJ/m2 with an improvement of 115.2% over that of the net DGEBA cured polymer. Thermogravimetric analysis (TGA) results revealed that the IPNs could enhance the thermal stability. Data of the differential scanning calorimetry (DSC) and TGA testing shows that the IPN shows a single glass transition temperature (Tg) which is between the Tg of DGEBA and DCPD, indicating homogeneous phase and highly cross‐linked IPN formed. Morphologies and molecular structure of the IPNs polymer were observed by scanning electron microscope (SEM) and characterized by Fourier transform infrared spectroscopy (FTIR), respectively, whose results also proved the formation of ideal IPNs structures.

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.

Potansiyel bisphenol-A ikameleri sucul yaşam için gerçekten güvenli mi? Birincil üreticiler üzerindeki etkisi

Bisphenol A threat to environmental health and human health and has been added to the Candidate List as Very High Concern Substances by the European Chemicals Agency. This led to the replacement of bisphenol A (BPA) with bisphenol analogues, which were considered "safer". However, there are very few scientific studies on the impact of BPA analogues on the environment. In this study, three analogues bisphenol B (BPB), bisphenol A diglycidyl ether (BADGE) and bisphenol F diglycidyl ether (BFDGE) were selected to investigate their ecotoxicological effects on the marine phytoplankton species Phaeodactylum tricornutum, which is representative of primary producers. Phaeodactylum tricornutum was exposed to different concentrations (0.5, 0.8, 1.0, 1.5, 2.0 mg/L) of BPB, BADGE and BFDGE analogues for 72 hours and the toxicity values of three BPA analogues were calculated by OECD 201 algal growth inhibition assay (IC50/EC50). In the light of the data obtained, algal growth inhibition (IC50/EC50) values for marine phytoplankton Phaeodactylum tricornutum were determined as 3.91 mg-BPA/L, 7.83 mg-BPB/L, 5.69 mg-BFDGE/L, 11.71 mg-BADGE/L. The results revealed that BPB, BFDGE and BADGE showed lower toxicity to Phaeodactylum tricornutum compared to BPA algal growth inhibition (3.91 mg-BPA/L). Therefore, it is necessary to share the results of the adverse effects of BPA analogues on aquatic organisms and to conduct ecotoxicological risk assessments.

Bio-Epoxy Resins Based on Lignin and Tannic Acids as Wood Adhesives-Characterization and Bonding Properties.

The possibility of producing and designing bio-epoxides based on the natural polyphenol lignin/epoxidized lignin and tannic acids for application as wood adhesives is presented in this work. Lignin and tannic acids contain numerous reactive hydroxyl phenolic moieties capable of being efficiently involved in the reaction with commercial epoxy resins as a substitute for commercial, non-environmentally friendly, toxic amine-based hardeners. Furthermore, lignin was epoxidized in order to obtain an epoxy lignin that can be a replacement for diglycidyl ether bisphenol A (DGEBA). Cross-linking of bio-epoxy epoxides was investigated via FTIR spectroscopy and their prospects for wood adhesive application were evaluated. This study determined that the curing reaction of epoxy resin can be conducted using lignin/epoxy lignin or tannic acid. Tensile shear strength testing results showed that lignin and tannic acid can effectively replace amine hardeners in epoxy resins. Examination of the failure of the samples showed that all samples had a 100% fracture through the wood. All samples of bio-epoxy adhesives displayed significant tensile shear strength in the range of 5.84-10.87 MPa. This study presents an innovative approach to creating novel cross-linked networks of eco-friendly and high-performance wood bio-adhesives.

Monolithic Polyepoxide Membranes for Nanofiltration Applications and Sustainable Membrane Manufacture.

The present work details the development of carbon fiber-reinforced epoxy membranes with excellent rejection of small-molecule dyes. It is a proof-of-concept for a more sustainable membrane design incorporating carbon fibers, and their recycling and reuse. 4,4'-methylenebis(cyclohexylamine) (MBCHA) polymerized with either bisphenol-A-diglycidyl ether (BADGE) or tetraphenolethane tetraglycidylether (EPON Resin 1031) in polyethylene glycol (PEG) were used to make monolithic membranes reinforced by nonwoven carbon fibers. Membrane pore sizes were tuned by adjusting the molecular weight of the PEG used in the initial polymerization. Membranes made of BADGE-MBCHA showed rejection of Rose Bengal approaching 100%, while tuning the pore sizes substantially increased the rejection of Methylene Blue from ~65% to nearly 100%. The membrane with the best permselectivity was made of EPON-MBCHA polymerized in PEG 300. It has an average DI flux of 4.48 LMH/bar and an average rejection of 99.6% and 99.8% for Rose Bengal and Methylene Blue dyes, respectively. Degradation in 1.1 M sodium hypochlorite enabled the retrieval of the carbon fiber from the epoxy matrix, suggesting that the monolithic membranes could be recycled to retrieve high-value products rather than downcycled for incineration or used as a lower selectivity membrane. The mechanism for epoxy degradation is hypothesized to be part chemical and part physical due to intense swelling stress leading to erosion that leaves behind undamaged carbon fibers. The retrieved fibers were successfully used to make another membrane exhibiting similar performance to those made with pristine fibers.

Partially bio-derived phosphazene-tannic acid microspheres as fire retardant additives for an epoxy tannic acid resin system

In this work, partially bio-derived colloidal microspheres are synthesised from tannic acid (TA) and hexachloro-cyclophosphazene (HCCP), then investigated for their effectiveness as a fire-retardant additive to a partially bioderived epoxy resin system. The epoxy resin system is based upon diglycidyl ether of bisphenol A (DGEBA) and tannic acid (TA), a bio-derived highly aromatic phenolic curative noted for its inherent fire retardancy. This study presents the impact of increasing the concentration of the phosphazene-TA microspheres (TAPZ) and varying the DGEBA-TA stoichiometry to determine the optimum formulation required to achieve the greatest improvement in fire retardancy. At 15 wt% TAPZ addition, the DGEBA-TA resin system easily achieves a V-0 rating according to the UL-94 vertical burn test, measures 29 % for the limiting oxygen value (LOI) and displays a 62 % reduction in peak heat release rate (PHRR) compared with the unmodified DGEBA-TA network. TAPZ addition however reduces the glass transition temperature (Tg) from 187 °C to 155 °C, flexural strength by up to 30 % and increases viscosity significantly. Varying the stoichiometry between DGEBA and TA shows that additional surface hydroxyl groups from the TAPZ microspheres accelerate the DGEBA-TA reaction through enhancing interfacial reaction between residual epoxide groups of the cured epoxy network. Overall, these results present a promising approach to the development of a highly fire retardant, high performance, and highly bio-derived epoxy network and composite.

Preparation and characterization of cardanol based vinyl ester resins as cross‐linker units

AbstractIn this study, two cardanol based epoxidized resins, NC514 with less than two epoxies per molecule and side chain epoxidized cardanol glycidyl ether (SCECGE) with approximately 2.45 epoxies (1.0 phenolic+1.45 aliphatic epoxies) per molecule were methacrylated. The methacrylated versions of cardanol based NC514 (NC514VE) and SCECGE (SCECGEVE) epoxy resins were used as cross‐linker units in vinyl ester formulations with methacrylated lauric acid (MFA) and styrene (ST) as bio‐based and synthetic based reactive diluents respectively, at various concentrations (10–40 wt%). The curing reactions of the resins were studied via FTIR and the extent of polymerization was determined for different cross‐linker units in the presence of ST and MFA. Our mechanical and thermomechanical characterizations showed that VER formulations prepared with cardanol based SCECGEVE cross‐linker unit have significantly improved properties than the samples prepared with commercially available counterpart NC514VE using either reactive diluent. These properties of SCECGEVE were also comparable with to that of methacrylated petroleum‐based diglycidyl ether of bisphenol A vinyl ester (DGEBAVE) formulations unlike NC514VE formulations due to more effective side chain functionalization and cross‐linking.

Effect of Temperature and Initiator Concentration on the Curing Reaction of an Epoxy/Amine System

AbstractEpoxy blends of diglycidyl ether of bisphenol A (DGEBA) and 2‐[2‐(dimethylamino) ethoxy] ethanol (DMAEE) were prepared. The effect of DMAEE concentration on the rheological properties of the epoxy blends were investigated through oscillatory rheometry under isothermal conditions. A novel technique was developed to study the rheological behavior of the epoxy blends by using a Rubber Process Analyzer (RPA). The rheological study enabled analyzing the variations in the storage modulus (G’), loss modulus (G’’) and torque during the progress of the curing reaction. Additionally, the theoretical cross‐linking density (νe) and the degree of conversión of the curing reaction (α). The gel time (tgel) was determined at different temperatures, and the activation energy (Ea) was calculated by using Arrhenius‐type equation based on the gel time results. The activation energy values found are 24.79 kJ/mol and 23.01 kJ/mol. The results obtained are consistent with the values described in the literature. It was demonstrated that the proposed methodology is valid and, the use of the tertiary amine DMAEE curing agent for epoxy resins was confirmed.