Feng Li
Associate Research ScientistCards
About
Research
Publications
2024
Poly(butylene succinate) reinforced by small amount of grafted nanofibrillated bacterial cellulose: Toughness variability based on nanocomposites preparation method
Hashim H, Xia X, Kani H, Seno S, Li F, Isono T, Yamamoto T, Tani H, Satoh T, Tajima K. Poly(butylene succinate) reinforced by small amount of grafted nanofibrillated bacterial cellulose: Toughness variability based on nanocomposites preparation method. Composites Part A Applied Science And Manufacturing 2024, 185: 108341. DOI: 10.1016/j.compositesa.2024.108341.Peer-Reviewed Original ResearchMelt-kneadedNanofibrillated bacterial cellulosePolybutylene succinateSolvent castingHydroxypropyl celluloseNanocomposite preparation methodBacterial celluloseLow mechanical performanceMechanical performanceFlexural strengthPoly(butylene succinateReinforcing agentYoung's modulusNanocompositesBiodegradable polymersToughnessCompost biodegradation testsSurface compatibilityBiodegradation testsModulusPreparation methodDispersing agentHydrophobic moietiesCellulose-producing bacteriumCelluloseOrganobase-Catalyzed Ring-Opening Copolymerization of Cyclic Anhydrides and Oxetanes: Establishment and Application in Block Copolymer Synthesis
Ota I, Suzuki R, Mizukami Y, Xia X, Tajima K, Yamamoto T, Li F, Isono T, Satoh T. Organobase-Catalyzed Ring-Opening Copolymerization of Cyclic Anhydrides and Oxetanes: Establishment and Application in Block Copolymer Synthesis. Macromolecules 2024, 57: 3741-3750. DOI: 10.1021/acs.macromol.3c02483.Peer-Reviewed Original ResearchRing-opening copolymerizationCyclic anhydridesTrimethylene oxideCyclic ethersRing-opening copolymerization of phthalic anhydridePhthalic anhydrideRing-opening polymerization of trimethylene carbonatePolymerization of trimethylene carbonatePolymerization processBlock copolymer synthesisRing-opening polymerizationSelf-switchable polymerizationPredictable molecular weightGlass transition temperatureControlled/living natureSynthesized polyestersCopolymer synthesisBlock copolymersOxetaneAnhydridePolymer materialsFunctional groupsL-lactidePolymerizationTransition temperatureAcetyl Cellooligosaccharide-Based Block Copolymers for Toughening Cellulose Triacetate/Poly(ε-caprolactone) Biodegradable Blends
Katsuhara S, Tsuji Y, Sunagawa N, Igarashi K, Takahashi K, Yamamoto T, Li F, Tajima K, Isono T, Satoh T. Acetyl Cellooligosaccharide-Based Block Copolymers for Toughening Cellulose Triacetate/Poly(ε-caprolactone) Biodegradable Blends. ACS Sustainable Chemistry & Engineering 2024, 12: 3025-3033. DOI: 10.1021/acssuschemeng.3c06411.Peer-Reviewed Original ResearchPoly(e-caprolactoneBlock copolymersBlend filmsCellulose triacetateImproved interfacial adhesionTernary blend filmsBinary blend filmsImproved mechanical performanceCellulose acetateCellulose triacetate matrixApplication of cellulose acetateAtomic force microscopyInterfacial adhesionHot pressingMechanical performanceEnvironmentally benign materialsMechanical propertiesSolvent castingBlend partnersForce microscopyBenign materialsTriacetateFilmsCopolymersPotential applicationsChemically Recyclable Unnatural (1→6)-Polysaccharides from Cellulose-Derived Levoglucosenone and Dihydrolevoglucosenone
Mizukami Y, Kakehi Y, Li F, Yamamoto T, Tajima K, Isono T, Satoh T. Chemically Recyclable Unnatural (1→6)-Polysaccharides from Cellulose-Derived Levoglucosenone and Dihydrolevoglucosenone. ACS Macro Letters 2024, 13: 252-259. PMID: 38334272, DOI: 10.1021/acsmacrolett.3c00720.Peer-Reviewed Original ResearchClosed-loop chemical recyclingTransparent self-standing filmsCationic ring-opening polymerizationRing-opening polymerizationSelf-standing filmsUnnatural polysaccharidesSubstituent patternChemical spaceAcid catalystMonomer synthesisSynthetic complexesChemical synthesisPolymer materialsLevoglucosenoneThermal stabilityPolymerization kineticsChemical recyclingAmbient conditionsCellulose-derivativesAmorphous solidsDihydrolevoglucosenonePolymerizationMonomerPolymerMaterial properties
2022
Size Control and Enhanced Stability of Silver Nanoparticles by Cyclic Poly(ethylene glycol)
Wang Y, Quinsaat J, Li F, Isono T, Tajima K, Satoh T, Sato S, Yamamoto T. Size Control and Enhanced Stability of Silver Nanoparticles by Cyclic Poly(ethylene glycol). Polymers 2022, 14: 4535. PMID: 36365529, PMCID: PMC9657728, DOI: 10.3390/polym14214535.Peer-Reviewed Original ResearchMeO-PEGUV-vis absorption intensityPoly(ethylene glycolHO-PEG-OHCyclic poly(ethylene glycolMeO-PEG-OMeMethoxy chainUV–visSize controlSilver nanoparticlesStabilization of silver nanoparticlesAbsorption intensityAqueous NaCl solutionMolar ratioEnhanced stabilityNanoparticlesMolecular weightParticle sizeNaCl solutionGlycolCyclizationChain