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Synthesis, Curing, and Thermal Stability of Low-Temperature-Cured Benzoxazine Resins Based on Natural Renewable Resources

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1099-0488(20001215)38:24<3289::aid-polb110>3.0.co;2-xopenalex-snapshot
Improved thermal and mechanical properties of polybenzoxazines based on alkyl-substituted aromatic amines
inferredcites →https://doi.org/10.1002/app.11466openalex-snapshot
Molar group contributions to polymer flammability
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Bio‐based benzoxazines based on sesamol: Synthesis and properties
inferredcites →https://doi.org/10.1002/cssc.201600577openalex-snapshot
Smart, Sustainable, and Ecofriendly Chemical Design of Fully Bio‐Based Thermally Stable Thermosets Based on Benzoxazine Chemistry
inferredcites →https://doi.org/10.1002/pi.5957openalex-snapshot
Synthesis and properties of a novel bio‐based benzoxazine resin with excellent low‐temperature curing ability
inferredcites →https://doi.org/10.1002/pola.26918openalex-snapshot
Renewable benzoxazine monomers from “lignin-like” naturally occurring phenolic derivatives
inferredcites →https://doi.org/10.1007/s10973-011-2015-6openalex-snapshot
Thermal degradation of pentaerythritol phosphate alcohol
inferredcites →https://doi.org/10.1016/0032-3861(75)90157-3openalex-snapshot
Some basic aspects of flame resistance of polymeric materials
inferredcites →https://doi.org/10.1016/j.eurpolymj.2015.03.050openalex-snapshot
Vanillin, a key-intermediate of biobased polymers
inferredcites →https://doi.org/10.1016/j.eurpolymj.2016.06.018openalex-snapshot
Chavicol benzoxazine: Ultrahigh Tg biobased thermoset with tunable extended network
inferredcites →https://doi.org/10.1016/j.eurpolymj.2018.09.031openalex-snapshot
Sustainability and antimicrobial assessments of bio based polybenzoxazine film
inferredcites →https://doi.org/10.1016/j.eurpolymj.2019.04.014openalex-snapshot
Towards bio-based high-performance polybenzoxazines: Agro-wastes as starting materials for BPA-free thermosets via efficient microwave-assisted synthesis
inferredcites →https://doi.org/10.1016/j.eurpolymj.2020.109706openalex-snapshot
Biobased high-performance tri-furan functional bis-benzoxazine resin derived from renewable guaiacol, furfural and furfurylamine
inferredcites →https://doi.org/10.1016/j.eurpolymj.2020.109770openalex-snapshot
Intrinsically noncombustible polymers without flame retardant additives: Sulfur-containing and bio-based benzoxazines
inferredcites →https://doi.org/10.1016/j.ijbiomac.2020.12.087openalex-snapshot
Development of sustainable and antimicrobial film based on polybenzoxazine and cellulose
inferredcites →https://doi.org/10.1016/j.polymer.2016.05.053openalex-snapshot
Synthesis of an intrinsically flame retardant bio-based benzoxazine resin
inferredcites →https://doi.org/10.1016/j.polymer.2018.09.061openalex-snapshot
Non-flammable thiazole-functional monobenzoxazines: Synthesis, polymerization, thermal and thermomechanical properties, and flammability studies
inferredcites →https://doi.org/10.1016/j.polymer.2020.122534openalex-snapshot
Novel full bio-based phloroglucinol benzoxazine resin: Synthesis, curing reaction and thermal stability
inferredcites →https://doi.org/10.1016/j.polymer.2020.122673openalex-snapshot
Preparation of high performance bio-based benzoxazine resin through a green solvent-free strategy for shape memory application
inferredcites →https://doi.org/10.1016/j.progpolymsci.2019.101168openalex-snapshot
Natural-sourced benzoxazine resins, homopolymers, blends and composites: A review of their synthesis, manufacturing and applications
inferredcites →https://doi.org/10.1016/j.reactfunctpolym.2017.06.009openalex-snapshot
Adapting benzoxazine chemistry for unconventional applications
inferredcites →https://doi.org/10.1016/s0032-3861(99)00074-9openalex-snapshot
Cationic ring-opening polymerization of benzoxazines
inferredcites →https://doi.org/10.1016/s0141-3910(02)00060-5openalex-snapshot
Flame retardance and thermal degradation of new epoxy containing silicon and phosphorous hybrid ceramers prepared by the sol-gel method
inferredcites →https://doi.org/10.1021/acs.jpca.7b05249openalex-snapshot
Oxazine Ring-Related Vibrational Modes of Benzoxazine Monomers Using Fully Aromatically Substituted, Deuterated, 15N Isotope Exchanged, and Oxazine-Ring-Substituted Compounds and Theoretical Calculations
inferredcites →https://doi.org/10.1021/acs.macromol.8b00741openalex-snapshot
How Does the Hydrogen Bonding Interaction Influence the Properties of Polybenzoxazine? An Experimental Study Combined with Computer Simulation
inferredcites →https://doi.org/10.1021/acs.macromol.8b02033openalex-snapshot
Enhanced Thermal Property and Flame Retardancy via Intramolecular 5-Membered Ring Hydrogen Bond-Forming Amide Functional Benzoxazine Resins
inferredcites →https://doi.org/10.1021/acsapm.8b00083openalex-snapshot
Design and Preparation of Benzoxazine Resin with High-Frequency Low Dielectric Constants and Ultralow Dielectric Losses
inferredcites →https://doi.org/10.1021/acsapm.9b00668openalex-snapshot
Thermally Activated Structural Changes of a Norbornene–Benzoxazine–Phthalonitrile Thermosetting System: Simple Synthesis, Self-Catalyzed Polymerization, and Outstanding Flame Retardancy
inferredcites →https://doi.org/10.1021/acsapm.9b01079openalex-snapshot
Photoresponsive Azobenzene Materials Based on Pyridine-Functionalized Benzoxazines as Surface Relief Gratings
inferredcites →https://doi.org/10.1021/acssuschemeng.0c02773openalex-snapshot
Advanced Thermosets from Sulfur and Renewable Benzoxazine and Ionones via Inverse Vulcanization
inferredcites →https://doi.org/10.1021/acssuschemeng.7b00062openalex-snapshot
Renewable Cardanol-Based Phosphate as a Flame Retardant Toughening Agent for Epoxy Resins
inferredcites →https://doi.org/10.1021/acssuschemeng.7b02657openalex-snapshot
Eco-Friendly Halogen-Free Flame Retardant Cardanol Polyphosphazene Polybenzoxazine Networks
inferredcites →https://doi.org/10.1021/acssuschemeng.8b00340openalex-snapshot
Development of Fully Biobased High-Performance Bis-Benzoxazine under Environmentally Friendly Conditions
inferredcites →https://doi.org/10.1021/acssuschemeng.8b03631openalex-snapshot
Harvesting the Benefits of Inherent Reactive Functionalities in Fully Biosourced Isomeric Benzoxazines
inferredcites →https://doi.org/10.1021/acssuschemeng.9b00603openalex-snapshot
Design and Synthesis of Bio-Based High-Performance Trioxazine Benzoxazine Resin via Natural Renewable Resources
inferredcites →https://doi.org/10.1021/acssuschemeng.9b00607openalex-snapshot
Making Benzoxazine Greener and Stronger: Renewable Resource, Microwave Irradiation, Green Solvent, and Excellent Thermal Properties
inferredcites →https://doi.org/10.1021/ma8013178openalex-snapshot
Selective Formation of Poly(N,O-acetal) by Polymerization of 1,3-Benzoxazine and Its Main Chain Rearrangement
inferredcites →https://doi.org/10.1039/c2gc35796hopenalex-snapshot
Synthesis and copolymerization of fully bio-based benzoxazines from guaiacol, furfurylamine and stearylamine
inferredcites →https://doi.org/10.1039/c4py00914bopenalex-snapshot
Polybenzoxazines: new players in the bio-based polymer arena
inferredcites →https://doi.org/10.1039/c4ta06636gopenalex-snapshot
Eugenol-based benzoxazine: from straight synthesis to taming of the network properties
inferredcites →https://doi.org/10.1039/c5ra12076dopenalex-snapshot
Synthesis and characterization of novel biobased benzoxazines from cardbisphenol and the properties of their polymers
inferredcites →https://doi.org/10.1039/c6gc01229aopenalex-snapshot
Arbutin-based benzoxazine: en route to an intrinsic water soluble biobased resin
inferredcites →https://doi.org/10.1039/c6nj02242aopenalex-snapshot
Replacing bisphenol-A with bisguaiacol-F to synthesize polybenzoxazines for a pollution-free environment
inferredcites →https://doi.org/10.1039/c7gc02348kopenalex-snapshot
Phloretic acid as an alternative to the phenolation of aliphatic hydroxyls for the elaboration of polybenzoxazine
inferredcites →https://doi.org/10.1039/c8py01823eopenalex-snapshot
Coumarines as masked phenols for amide functional benzoxazines
inferredcites →https://doi.org/10.1039/d0py00983kopenalex-snapshot
An apigenin-based bio-benzoxazine with three polymerizable functionalities: sustainable synthesis, thermal latent polymerization, and excellent thermal properties of its thermosets
inferredcites →https://doi.org/10.1080/00222348.2010.502495openalex-snapshot
Effect of Interaction between Transition Metal Oxides and Nitrogen Atoms on Thermal Stability of Polybenzoxazine
inferredcites →https://doi.org/10.3389/fchem.2020.00711openalex-snapshot
Cardanol and Eugenol Sourced Sustainable Non-halogen Flame Retardants for Enhanced Stability of Renewable Polybenzoxazines
inferredcites →https://doi.org/10.3390/polym11081341openalex-snapshot
Synthesis of Highly Thermally Stable Daidzein-Based Main-Chain-Type Benzoxazine Resins

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4688349openalex-extracted
Studies on Catalyst Assisted Low-Temperature Curing of Benzoxazines
inferred← citeshttps://doi.org/10.1002/adfm.202515814openalex-snapshot
Designing Thermally Compatible Template‐Coating Pairs Toward Dimensionally Stable 3D Porous Carbons with Tunable Density
inferred← citeshttps://doi.org/10.1002/adsu.202300372openalex-snapshot
Research Progress of Bio‐Based Polybenzoxazine Materials
inferred← citeshttps://doi.org/10.1002/app.54421openalex-snapshot
A facile method to fabricate thermally stable methacrylate‐terminated oligo(2,6‐dimethyl‐1,4‐phenylene oxide)/benzoxazine thermosetting resins with low dielectric constants and losses at 10 GHz
inferred← citeshttps://doi.org/10.1002/app.57414openalex-snapshot
Sustainable Aqueous‐Based Poly(Geo‐Benzoxazine) Composites for High‐ k Dielectrics
inferred← citeshttps://doi.org/10.1002/app.71023openalex-snapshot
Flame‐Retardant Eugenol‐Based Polymers via Inverse Vulcanization on Sulfur and Selenium
inferred← citeshttps://doi.org/10.1002/asia.202401777openalex-snapshot
Synthesis and Characterization of Bio‐based Polybenzoxazine Hybrids From Vanillin, Thymol, and Carvacrol
inferred← citeshttps://doi.org/10.1002/pat.6321openalex-snapshot
Synergistic effect of activated carbon from disposed plastics and polybenzoxazine composite coating on corrosion inhibition
inferred← citeshttps://doi.org/10.1002/pat.70704openalex-snapshot
Towards Bio‐Based Benzoxazines (2015–2025): A Critical Review of Renewable Building Blocks, Formaldehyde‐Free Aldehydes, and ECHA Hazard Landscape
inferred← citeshttps://doi.org/10.1002/pol.20220744openalex-snapshot
Synthesis of new biobased benzoxazine through green strategy and its polybenzoxazine resin with high thermal resistance and mechanical strength
inferred← citeshttps://doi.org/10.1007/978-981-99-4580-1_9openalex-snapshot
Producing N-Containing Chemicals from Biomass for High Performance Thermosets
inferred← citeshttps://doi.org/10.1007/s10853-023-08671-5openalex-snapshot
Nonylphenol-based polybenzoxazine composites: hydrophobic coating, ultra-low-k and anticorrosion applications
inferred← citeshttps://doi.org/10.1007/s10904-024-03182-5openalex-snapshot
Boron Doped Graphitic Carbon Nitride Reinforced Phenylenebis(Azomethine)Diphenol and Bio-Phenol Based Hybrid Polybenzoxazine Composites for High Dielectric Application
inferred← citeshttps://doi.org/10.1007/s10965-023-03520-0openalex-snapshot
Preparation of high-performance thermosetting films from novel diallyl bisphenol A/furfurylamine type benzoxazine and oligo(phenylene oxide)
inferred← citeshttps://doi.org/10.1007/s10965-025-04499-6openalex-snapshot
Curing kinetics and surface properties of bio-based polybenzoxazine prepared from monomers synthesized via continuous flow
inferred← citeshttps://doi.org/10.1016/j.diamond.2026.113895openalex-snapshot
Engineered metal/carbon hybrid composites from polybenzoxazine precursors for electromagnetic shielding applications
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2021.110871openalex-snapshot
Room-temperature fast-curing polybenzoxazine hybrid thermosets via UV irradiation
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2022.111320openalex-snapshot
Developing thermally resistant and strong biobased resin from benzoxazine synthesized using green solvents
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2022.111581openalex-snapshot
Developing intrinsic halogen-free and phosphorus-free flame retardant biobased benzoxazine resins with superior thermal stability and high strength
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2022.111722openalex-snapshot
Novel polybenzoxazine and polybenzoxazine/epoxy thermosetting copolymers containing polysilsesquioxane nanostructures for high-performance thermal protection systems
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.135935openalex-snapshot
Drying temperature effect on the characteristics of cationically polymerized kraft lignin
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2026.152161openalex-snapshot
Fabrication of a bio-based benzoxazine-modified hydrophobic cellulose aerogel for efficient oil-water separation
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.123277openalex-snapshot
Cationic lignin derivatives with enhanced antibacterial and functional properties for sustainable PU-based packaging
inferred← citeshttps://doi.org/10.1016/j.mtcomm.2022.103645openalex-snapshot
Natural fiber reinforced polybenzoxazine composites: A review
inferred← citeshttps://doi.org/10.1016/j.polymdegradstab.2025.111912openalex-snapshot
High performance intrinsically flame-retardant bio-benzoxazine resin derived from 2,5-furandimethylene amine and sesamol: Synthesis and investigations of structure-property relationship
inferred← citeshttps://doi.org/10.1016/j.polymer.2022.125613openalex-snapshot
Improvement of thermal properties of polybenzoxazines synthesized from an oligonuclear phenolic compound without sacrificing toughness by introducing crosslinkable groups separated by rigid biphenyl linkers
inferred← citeshttps://doi.org/10.1016/j.polymer.2024.127745openalex-snapshot
Investigating UV light and ziram catalyst as alternative activators for sulfur-promoted benzoxazine curing
inferred← citeshttps://doi.org/10.1016/j.polymer.2025.128888openalex-snapshot
Degradable thermosetting polybenzoxazine with diacetal structure from renewable xylitol
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Biobased benzoxazine monomers with low melting point: incorporation of hydroxyethyl and ethynyl groups to achieve excellent thermal stability and flame retardancy
inferred← citeshttps://doi.org/10.1016/j.polymertesting.2023.107933openalex-snapshot
Liquid crystalline polybenzoxazines for manufacturing of technical textiles: Water repellency and ultraviolet shielding
inferred← citeshttps://doi.org/10.1016/j.reactfunctpolym.2024.105880openalex-snapshot
Studies on catalyst assisted low-temperature curing of benzoxazines
inferred← citeshttps://doi.org/10.1016/j.reactfunctpolym.2025.106434openalex-snapshot
Research progress and application of solvent-free technology, green catalysis and biomass resource strategy for the synthesis of benzoxazine
inferred← citeshttps://doi.org/10.1016/j.reactfunctpolym.2025.106491openalex-snapshot
Rational design and synthesis of novel benzoxazine resins with excellent thermal and flame - Retardant properties
inferred← citeshttps://doi.org/10.1016/j.susmat.2025.e01387openalex-snapshot
Research progress on properties and applications of bio-based polybenzoxazine materials
inferred← citeshttps://doi.org/10.1021/acs.iecr.3c01289openalex-snapshot
Kinetic Modeling of Ring-Opening Polymerization of Benzoxazines Using MIL-53-Al as a Potent Catalyst
inferred← citeshttps://doi.org/10.1021/acs.macromol.6c00027openalex-snapshot
A Fully Biobased Benzoxazine-Modified Waterborne Two-Component Polyurethane with High Adhesion, Self-Healing, and Hydrophobic Properties
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Benzoxazine Monomers with Antibacterial Property and Polybenzoxazines for Preventing Adhesion to Bacteria
inferred← citeshttps://doi.org/10.1021/acsapm.3c01902openalex-snapshot
Catalytic Role of Nanoconfinement inside MIL-125 (Ti) on the Ring-Opening Polymerization of Simple Benzoxazines
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Properties and Curing Kinetics of a Processable Binary Benzoxazine Blend
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Multifunctional Biobased Benzoxazines: Synthesis, Copolymerization, and Thermal Stability Studies
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Self-Healing Catechol-Based Polybenzoxazine Vitrimers Containing Disulfide Bonds
inferred← citeshttps://doi.org/10.1021/acsapm.6c00405openalex-snapshot
High-Temperature Adhesive Based on Polybenzoxazine for Fabricating Outermost Aluminized Glass Fabric in Fire Proximity Clothing
inferred← citeshttps://doi.org/10.1021/acsapm.6c02134openalex-snapshot
Benzoxazine-Modified Phenolic Triazine Resin with Improved Curing, Toughness, and Balanced Thermomechanical Properties, Enabling Hot-Melt Processing
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Preparation of Thermally Resistant and Mechanically Strong Biomass Benzoxazine Resins via Green Strategy
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Biobased Polybenzoxazine Vitrimer with Imine Bonds: Shape Memory, Reprocessing, and Degradation
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m-Guaiacol-Derived Benzoxazine Resins as Surprising Heterogeneous Photocatalysts for the Photocatalytic Production of Hydrogen Peroxide under Visible Light
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Recent advances in the development of green furan ring-containing polymeric materials based on renewable plant biomass
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Sesamol-based polybenzoxazines for ultra-low- k , high- k and hydrophobic coating applications
inferred← citeshttps://doi.org/10.1039/d3nj05576kopenalex-snapshot
Role of magnolol embedded fully bio-based benzoxazines for hydrophobic, anti-microbial and anti-corrosion applications
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Advancing coatings with polybenzoxazines: insights into molecular design, synthesis, and modification
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Chemistry, Structural Design, Properties and Future Perspectives of High-Performance Polymers from Renewable Biomass
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Renewable bis-benzoxazine from symmetrical vanillin-based dimer
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M -Guaiacol Derived Benzoxazine Resins as Surprising Heterogeneous Photocatalysts for Photocatalytic Production of Hydrogen Peroxide Under Visible Light
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Metal Ion-Catalyzed Low-Temperature Curing of Urushiol-Based Polybenzoxazine
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A Phosphorous-Containing Bio-Based Furfurylamine Type Benzoxazine and Its Application in Bisphenol-A Type Benzoxazine Resins: Preparation, Thermal Properties and Flammability
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