Journal of Polymer Science最新文献

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Self-Healing Sericin/MXene Composite Hydrogel With Low Hysteresis for Sensing Applications 自修复丝胶/MXene低滞后复合水凝胶传感应用
IF 3.9 3区 化学
Journal of Polymer Science Pub Date : 2026-09-02 Epub Date: 2026-07-13 DOI: 10.1002/pola.70266
Fangrong Sun, Xiang Li, Jingyu Chen, Kunlin Chen
{"title":"Self-Healing Sericin/MXene Composite Hydrogel With Low Hysteresis for Sensing Applications","authors":"Fangrong Sun,&nbsp;Xiang Li,&nbsp;Jingyu Chen,&nbsp;Kunlin Chen","doi":"10.1002/pola.70266","DOIUrl":"https://doi.org/10.1002/pola.70266","url":null,"abstract":"<div>\u0000 \u0000 <p>Conductive hydrogels often suffer from structural damage, fatigue, and signal drift under repeated deformation, limiting their long-term performance in flexible sensing. To overcome these challenges, this study developed a sericin-MXene/phenylboronic acid-polyacrylamide (PADS-MXene) composite hydrogel by copolymerizing 3-acrylamidophenylboronic acid with acrylamide and incorporating polydopamine-modified sericin-functionalized MXene. In this system, the polydopamine-modified sericin (PDA-SS) not only expanded the interlayer spacing of MXene and prevented nanosheet aggregation but also introduced polar functional groups, strengthening hydrogen bonding between MXene and the polyacrylamide network. The resulting hydrogel exhibits excellent mechanical properties, with a fracture strength of 60 kPa and a fracture strain of 380%, coupled with low hysteresis (1.65% after 30 cycles), and efficient self-healing ability. MXene also enhances its high electrical conductivity and photothermal response, enabling rapid 20°C within 300 s under near-infrared light. Functioning as a wearable strain sensor, the hydrogel can reliably monitor movements across various parts of the human body and maintain stable performance even after 2000 cycles at 50% strain. It also enables handwriting posture correction via pressure distribution and Morse code messaging via short/long presses for emergency communication. These features highlight its potential for durable, multifunctional flexible sensing systems.</p>\u0000 </div>","PeriodicalId":16888,"journal":{"name":"Journal of Polymer Science","volume":"64 17","pages":"3743-3758"},"PeriodicalIF":3.9,"publicationDate":"2026-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148862409","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Reactive Modification of Propylene–Ethylene Copolymer With Amine-Dye for Enhanced Melt Strength and Fade Resistance 胺染料对丙烯-乙烯共聚物的活性改性提高熔体强度和抗褪色性能
IF 3.9 3区 化学
Journal of Polymer Science Pub Date : 2026-09-02 Epub Date: 2026-07-10 DOI: 10.1002/pola.70261
Lucia N. Schmidt, Lidia M. Quinzani, Marcelo D. Failla, Jorge Guapacha
{"title":"Reactive Modification of Propylene–Ethylene Copolymer With Amine-Dye for Enhanced Melt Strength and Fade Resistance","authors":"Lucia N. Schmidt,&nbsp;Lidia M. Quinzani,&nbsp;Marcelo D. Failla,&nbsp;Jorge Guapacha","doi":"10.1002/pola.70261","DOIUrl":"https://doi.org/10.1002/pola.70261","url":null,"abstract":"<div>\u0000 \u0000 <p>Melt strength and fade resistance of a random propylene–ethylene copolymer (PEC) were enhanced by generating long-chain branched (LCB) structures using two amine-polyfunctional chain-linking agents (CAs). A maleic-anhydride-grafted copolymer (PECg) was first obtained as a precursor to the LCB polymers that were obtained by reactive melt mixing using various concentrations of m-xylylenediamine (XDA) and Basic Fuchsin (BF). The resulting changes in molecular structure were analyzed using FTIR and shear and extensional rheometry, while color characteristics and fastness were studied using UV–visible spectroscopy, colorimetry, and solvent extraction. The results demonstrate that both CAs react with PECg to form polymers with LCBs and complex molecular structures, being BF being less efficient than XDA. However, the simultaneous use of both CAs produces a significant synergistic effect. For example, the rate of change of the strain-hardening coefficient with CA concentration (SHI<sub>exp</sub> ~ 36.5 <i>c</i>\u0000 <sub>CA</sub>) is greater than the value predicted by a Linear Mixing Rule based on Xi and Fi data (SHI<sub>LMR</sub> ~ 27.8 <i>c</i>\u0000 <sub>CA</sub>). All colored materials exhibit excellent fade resistance, as demonstrated by the color permanence of films exposure to solvents for 10 days. Altogether, the selected approach allows for the generation of dye-grafted polyolefins with improved melt strength and fade resistance.</p>\u0000 </div>","PeriodicalId":16888,"journal":{"name":"Journal of Polymer Science","volume":"64 17","pages":"3648-3658"},"PeriodicalIF":3.9,"publicationDate":"2026-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148862251","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
One-Pot Synthesis of Superparamagnetic Nanocomposites by Melt Polycondensation of Aromatic Diamines and 1,1′-Diacetylferrocene 芳香二胺与1,1′-二乙酰二茂铁熔融缩聚一锅合成超顺磁纳米复合材料
IF 3.9 3区 化学
Journal of Polymer Science Pub Date : 2026-09-02 Epub Date: 2026-07-15 DOI: 10.1002/pola.70270
Ilya G. Beregovsky, Raisa A. Dvorikova, Mikhail I. Buzin, Zinaida S. Klemenkova, Vasilina A. Zakharova, Mikhail I. Bannikov, Mikhail V. Motyakin, Alexander A. Korlyukov, Victor N. Khrustalev, Yaroslav O. Mezhuev
{"title":"One-Pot Synthesis of Superparamagnetic Nanocomposites by Melt Polycondensation of Aromatic Diamines and 1,1′-Diacetylferrocene","authors":"Ilya G. Beregovsky,&nbsp;Raisa A. Dvorikova,&nbsp;Mikhail I. Buzin,&nbsp;Zinaida S. Klemenkova,&nbsp;Vasilina A. Zakharova,&nbsp;Mikhail I. Bannikov,&nbsp;Mikhail V. Motyakin,&nbsp;Alexander A. Korlyukov,&nbsp;Victor N. Khrustalev,&nbsp;Yaroslav O. Mezhuev","doi":"10.1002/pola.70270","DOIUrl":"https://doi.org/10.1002/pola.70270","url":null,"abstract":"<div>\u0000 \u0000 <p>A one-pot synthesis of superparamagnetic nanocomposites via polycondensation of phenylenediamine isomers and 1,1′-diacetylferrocene in the melt is described. Obtained nanocomposites were characterized by IR spectroscopy, XPS, XRD, EPR, SEM, TGA/DTA, and magnetization curves. The formation of oligomeric azomethines in the melt was accompanied by side hydrothermolysis of 1,1′-diacetylferrocene, even at 140°C under an argon atmosphere. According to XRD and IR spectroscopy, hydrothermolysis of 1,1′-diacetylferrocene led to the formation of magnetite nanoparticles with an average size of around 10 nm, and a mixture of diacetyldicyclopentadiene isomers, presumably acting as crosslinking agents via reaction with terminal groups of oligomeric azomethines. XPS and IR spectroscopy demonstrated the formation of C=N bonds with retention of a fraction of unreacted keto and amino groups. The possibility of C=N bond formation was established in experiments on low-molecular-weight model compounds, and the synthesized monoimines and diimines of 1,1′-diacetylferrocene and aniline were characterized by NMR, IR spectroscopy, and X-ray diffraction. XPS revealed the presence of Fe<sup>3+</sup> on the surface of the nanocomposites, which, according to EPR spectroscopy and magnetization curves, exhibit superparamagnetism. The obtained nanocomposites are promising materials for cores of high-frequency inductors, as well as other devices requiring magnetization without energy dissipation due to hysteresis.</p>\u0000 </div>","PeriodicalId":16888,"journal":{"name":"Journal of Polymer Science","volume":"64 17","pages":"3759-3772"},"PeriodicalIF":3.9,"publicationDate":"2026-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148862253","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bio-Based Azine-Functional Polyurethane Networks as Multifunctional Coatings: Nonconventional Luminescence and High-Efficiency Corrosion Protection of Steel 生物基氮-功能聚氨酯网络作为多功能涂料:钢的非常规发光和高效防腐
IF 3.9 3区 化学
Journal of Polymer Science Pub Date : 2026-09-02 Epub Date: 2026-07-11 DOI: 10.1002/pola.70262
Marwa M. Sayed, Abd Elrahman M. Salama, Mohamed Abdel-Hakim, Kamal I. Aly
{"title":"Bio-Based Azine-Functional Polyurethane Networks as Multifunctional Coatings: Nonconventional Luminescence and High-Efficiency Corrosion Protection of Steel","authors":"Marwa M. Sayed,&nbsp;Abd Elrahman M. Salama,&nbsp;Mohamed Abdel-Hakim,&nbsp;Kamal I. Aly","doi":"10.1002/pola.70262","DOIUrl":"https://doi.org/10.1002/pola.70262","url":null,"abstract":"<div>\u0000 \u0000 <p>Developing sustainable polymer networks that integrate robust barrier performance with additional functional responses is an important goal in contemporary polymer science. In this work, bio-based segmented polyurethane networks (PUPH1–PUPH3) are prepared from castor-oil-derived polyols and an azine-modified castor-oil derivative, crosslinked with poly(hexamethylene diisocyanate) (pHMDI), to elucidate how network architecture governs thermal stability, anticorrosion behavior, and nonconventional luminescence. By systematically varying the hard/soft segment ratios, the crosslink density and segmental packing are tuned. Fourier-transform infrared spectroscopy and X-ray diffraction confirm complete urethane formation and predominantly amorphous segmented networks, while scanning electron microscopy reveals smooth, defect-poor morphologies for the most crosslinked compositions. Thermogravimetric analysis shows 5 wt% weight-loss temperatures of 307°C–314°C, evidencing enhanced thermal robustness. Electrochemical measurements in 1.0 M H<sub>2</sub>SO<sub>4</sub> demonstrate that the optimized network markedly suppresses the corrosion current density of mild steel, achieving an inhibition efficiency of 99.55% and a significant increase in charge-transfer resistance, attributed to a dense, highly resistive interfacial barrier. Solid-state photoluminescence measurements further reveal excitation-dependent, cluster-type emission arising from densely packed heteroatom-rich segments. These findings establish clear correlations between molecular/network design and multifunctional properties in castor-oil-based polyurethane networks, highlighting a renewable platform for advanced polymeric coatings.</p>\u0000 </div>","PeriodicalId":16888,"journal":{"name":"Journal of Polymer Science","volume":"64 17","pages":"3659-3674"},"PeriodicalIF":3.9,"publicationDate":"2026-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148862338","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Additive Manufacturing of Continuous Fiber Reinforced Thermosetting Composites: Research Progress on Application Challenges, Process Exploration, Material Development, and Performance Tailoring 连续纤维增强热固性复合材料的增材制造:应用挑战、工艺探索、材料开发和性能定制研究进展
IF 3.9 3区 化学
Journal of Polymer Science Pub Date : 2026-09-02 Epub Date: 2026-07-13 DOI: 10.1002/pola.70234
Chao Chen, Xin Wang, Junchi Jiang, Peng Li, Dongyun Zhang
{"title":"Additive Manufacturing of Continuous Fiber Reinforced Thermosetting Composites: Research Progress on Application Challenges, Process Exploration, Material Development, and Performance Tailoring","authors":"Chao Chen,&nbsp;Xin Wang,&nbsp;Junchi Jiang,&nbsp;Peng Li,&nbsp;Dongyun Zhang","doi":"10.1002/pola.70234","DOIUrl":"https://doi.org/10.1002/pola.70234","url":null,"abstract":"<p>Continuous fiber reinforced thermosetting composites (CFRTCs) are important structural materials for lightweight and high-performance applications, but conventional manufacturing routes remain constrained by mold dependence, long processing cycles, and limited freedom in fabricating complex fiber-reinforced architectures. Additive manufacturing (AM) provides an emerging route for mold-free fabrication of CFRTC components with locally tailored fiber paths and integrated geometries. Rather than presenting the literature as isolated case studies, this review organizes current progress through a process-material-interface-performance framework. Representative AM routes are compared in terms of fiber delivery, resin impregnation, in situ curing, defect formation, achievable fiber volume fraction, and structural performance. Particular attention is given to unresolved trade-offs, including printability versus high fiber loading, rapid curing versus impregnation quality, interfacial strengthening versus fiber damage, and laboratory-scale performance versus industrial reproducibility. By distinguishing AM-enabled applications from conventional composite applications, this review identifies the major barriers and promising research directions for advancing CFRTCs-AM toward reliable structural deployment.</p>","PeriodicalId":16888,"journal":{"name":"Journal of Polymer Science","volume":"64 17","pages":"3687-3715"},"PeriodicalIF":3.9,"publicationDate":"2026-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/pola.70234","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148862440","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synergistic Effects of Phenolic Resin and Polymer Architecture on Crosslink Density and Damping in Poly(Epichlorohydrin-Co-Ethylene Oxide-Co-Allyl Glycidyl Ether) (GECO) Elastomers 酚醛树脂和聚合物结构对聚环氧氯丙烷-环氧乙烷-烯丙基缩水甘油醚(GECO)弹性体交联密度和阻尼的协同效应
IF 3.9 3区 化学
Journal of Polymer Science Pub Date : 2026-08-16 Epub Date: 2026-07-03 DOI: 10.1002/pola.70249
Yalçın Yalaki, Murat Şen
{"title":"Synergistic Effects of Phenolic Resin and Polymer Architecture on Crosslink Density and Damping in Poly(Epichlorohydrin-Co-Ethylene Oxide-Co-Allyl Glycidyl Ether) (GECO) Elastomers","authors":"Yalçın Yalaki,&nbsp;Murat Şen","doi":"10.1002/pola.70249","DOIUrl":"https://doi.org/10.1002/pola.70249","url":null,"abstract":"<p>Epichlorohydrin-based poly(epichlorohydrin-co-ethylene oxide-co-allyl glycidyl ether) (GECO) elastomers are widely used in applications requiring chemical resistance and vibration damping. This study investigates the combined effects of phenolic resin (PR) content and GECO molecular architecture on curing behavior, network structure, and viscoelastic performance. Four GECO elastomers with different monomer compositions, molecular weights, and branching architectures were compounded with varying amounts of novolac-type phenolic resin. Cure kinetics were evaluated by moving die rheometry (MDR), while network structure and viscoelastic behavior were characterized using rubber process analysis (RPA), temperature-scanning stress relaxation (TSSR), cyclic compression, rebound resilience, and dynamic mechanical analysis. Increasing PR content reduced torque and crosslink density, producing softer networks and enhanced energy dissipation, as evidenced by higher tan δ values, greater hysteresis losses, and lower rebound resilience. Correlation analysis demonstrated that elastic recovery is primarily governed by network density, whereas damping behavior is additionally influenced by polymer architecture. Among the investigated materials, T3108 exhibited a more elastic response, while T3100 showed a more dissipative viscoelastic character. The results demonstrate that damping performance is governed by the combined effects of network density and polymer architecture rather than resin content alone, providing a framework for designing advanced vibration-isolation elastomers.</p>","PeriodicalId":16888,"journal":{"name":"Journal of Polymer Science","volume":"64 16","pages":"3471-3491"},"PeriodicalIF":3.9,"publicationDate":"2026-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/pola.70249","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148752472","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Long-Chain Fatty Acid–Modified Cu-MOFs for Constructing Multifunctional PBAT/PLA Composite Films: Interfacial Regulation, Intelligent Responsiveness, and Hydrothermal Stability 长链脂肪酸修饰cu - mof用于构建多功能PBAT/PLA复合膜:界面调节、智能响应和水热稳定性
IF 3.9 3区 化学
Journal of Polymer Science Pub Date : 2026-08-16 Epub Date: 2026-06-22 DOI: 10.1002/pola.70229
Jing Xu, Hui Liu, Pengpeng Huang, Pingbo Zhang, Mingming Fan, Pingping Jiang, Shijun Chen
{"title":"Long-Chain Fatty Acid–Modified Cu-MOFs for Constructing Multifunctional PBAT/PLA Composite Films: Interfacial Regulation, Intelligent Responsiveness, and Hydrothermal Stability","authors":"Jing Xu,&nbsp;Hui Liu,&nbsp;Pengpeng Huang,&nbsp;Pingbo Zhang,&nbsp;Mingming Fan,&nbsp;Pingping Jiang,&nbsp;Shijun Chen","doi":"10.1002/pola.70229","DOIUrl":"https://doi.org/10.1002/pola.70229","url":null,"abstract":"<div>\u0000 \u0000 <p>The Poly (butylene adipate-co-terephthalate) (PBAT) and Poly (lactic acid) (PLA) blend system has garnered significant attention due to its excellent biodegradability and complementary properties. However, the inherent incompatibility between the two polymers has somewhat limited its further development. In this study, Cu-MOF was successfully synthesized via a hydrothermal method. It was surface-modified using organic acids with different carbon chain lengths and incorporated into the PBAT/PLA polymer matrix to enhance interfacial compatibility. Results indicate that incorporating M-Cu-MOF as a functional filler into PBAT/PLA composite films enhances multiple properties. Among these, SA-Cu-MOF composite films exhibit optimal comprehensive performance: a water contact angle of 101°, and reduced water vapor and oxygen transmission rates by 30.75% and 62.19%, respectively. Additionally, the films exhibited excellent antibacterial activity, ammonia visualization response capability, and enhanced hydrothermal degradation rates. Long-chain organic acids influenced the macroscopic properties of M-Cu-MOF/PBAT/PBAT composite films by affecting the microstructure and dispersion of Cu-MOF. These results demonstrate that the Cu-MOF surface modification strategy based on regulating the carbon chain length of organic acids provides an effective approach for constructing high-performance, multifunctional, and controllably degradable PBAT/PLA green packaging films.</p>\u0000 </div>","PeriodicalId":16888,"journal":{"name":"Journal of Polymer Science","volume":"64 16","pages":"3341-3351"},"PeriodicalIF":3.9,"publicationDate":"2026-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148754238","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthesis of Carboxyl Terminated Polymyrcene by Anionic Polymerization Using CO2 as a Terminating Agent 以CO2为终止剂阴离子聚合合成端羧基多桃金娘烯
IF 3.9 3区 化学
Journal of Polymer Science Pub Date : 2026-08-16 Epub Date: 2026-06-26 DOI: 10.1002/pola.70230
Trishna K. Chengappa, Juan Marin Angel, Kevin A. Cavicchi
{"title":"Synthesis of Carboxyl Terminated Polymyrcene by Anionic Polymerization Using CO2 as a Terminating Agent","authors":"Trishna K. Chengappa,&nbsp;Juan Marin Angel,&nbsp;Kevin A. Cavicchi","doi":"10.1002/pola.70230","DOIUrl":"https://doi.org/10.1002/pola.70230","url":null,"abstract":"<p>Carboxyl terminated polymyrcene was successfully synthesized by anionic polymerization. The terminating carboxyl groups were introduced into the system using high purity CO<sub>2</sub> gas. Characterization of the degree of end functionalization was done by titration and gel permeation chromatography using refractive index and UV–vis detectors and a dye functionalized chain. Different reaction conditions were investigated (i.e., temperature, mode of addition of CO<sub>2</sub>, stirring vs. not stirring) to determine their influence on the degree of functionalization. The introduction of CO<sub>2</sub> at −78°C through the headspace of the reactor without stirring proved to be the best reaction condition to achieve the highest amount of end functionalization of 86%–87% at a molecular weight of 20–25 kg/mol.</p>","PeriodicalId":16888,"journal":{"name":"Journal of Polymer Science","volume":"64 16","pages":"3382-3390"},"PeriodicalIF":3.9,"publicationDate":"2026-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/pola.70230","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148754285","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fabrication of Chitosan-Derived Microspheres With Superhydrophobicity and Antibacterial Activity for Functional Coating Applications 具有超疏水性和抗菌活性的壳聚糖微球的制备及其在功能涂层中的应用
IF 3.9 3区 化学
Journal of Polymer Science Pub Date : 2026-08-16 Epub Date: 2026-06-23 DOI: 10.1002/pola.70231
Chenghua Yu, Xueyi Huang, Junjiang Teng, Hao Ma, Yanhui Qiao, Chaochao Yue, Yating Wang
{"title":"Fabrication of Chitosan-Derived Microspheres With Superhydrophobicity and Antibacterial Activity for Functional Coating Applications","authors":"Chenghua Yu,&nbsp;Xueyi Huang,&nbsp;Junjiang Teng,&nbsp;Hao Ma,&nbsp;Yanhui Qiao,&nbsp;Chaochao Yue,&nbsp;Yating Wang","doi":"10.1002/pola.70231","DOIUrl":"https://doi.org/10.1002/pola.70231","url":null,"abstract":"<div>\u0000 \u0000 <p>In this work, superhydrophobic chitosan microspheres were fabricated via spray drying of chitosan aqueous solution followed by surface silanization modification. Characterization methods, namely laser particle size analysis, SEM, and FTIR, were adopted to systematically investigate the particle size distribution, micromorphology, and chemical composition of chitosan microspheres. Experimental results revealed the dissolution medium exerted a remarkable effect on the microscopic morphology of as-prepared microspheres. Hydrophobicity characterization verified the silanized chitosan microspheres possessed excellent hydrophobic performance with a water contact angle of 153.3°. Antibacterial assays confirmed that the modified chitosan microspheres exhibited an antibacterial efficiency of 95.42% against \u0000 <i>Escherichia coli</i>\u0000 . Furthermore, functional composite coatings were constructed by uniformly spraying the modified chitosan microspheres onto filter paper substrates. The coated filter paper presented a water contact angle of 152.1°, which enabled it to achieve efficient separation of oil–water mixtures. Notably, the modified filter paper retained a water contact angle over 150.0° after immersion in acidic, neutral, and weakly alkaline solutions and maintained stable superhydrophobicity even after 90 cycles of weighted friction tests. This study proposes feasible technical strategies for the functional modification of chitosan microspheres and offers valuable references for their practical deployment as coating materials in functional filter paper fabrication.</p>\u0000 </div>","PeriodicalId":16888,"journal":{"name":"Journal of Polymer Science","volume":"64 16","pages":"3352-3363"},"PeriodicalIF":3.9,"publicationDate":"2026-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148754082","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nanostructured Hybrid Binders: Enhancing HTPB–Polyurethane Elastomers Through Precise Q-Siloxane Grafting 纳米结构杂化粘合剂:通过精确q -硅氧烷接枝增强htpb -聚氨酯弹性体
IF 3.9 3区 化学
Journal of Polymer Science Pub Date : 2026-08-16 Epub Date: 2026-06-30 DOI: 10.1002/pola.70242
Noel C. Migliaccio, Nathan J. Weeks, Scott T. Iacono
{"title":"Nanostructured Hybrid Binders: Enhancing HTPB–Polyurethane Elastomers Through Precise Q-Siloxane Grafting","authors":"Noel C. Migliaccio,&nbsp;Nathan J. Weeks,&nbsp;Scott T. Iacono","doi":"10.1002/pola.70242","DOIUrl":"https://doi.org/10.1002/pola.70242","url":null,"abstract":"<div>\u0000 \u0000 <p>The strategic synthesis of polyhedral oligomeric silsesquioxane (POSS) functionalized hydroxyl-terminated polybutadiene (gHTPB) and its integration into segmented polyurethane (PU) elastomers is reported. A two-step platinum-catalyzed hydrosilylation protocol was developed, utilizing precise equivalents of 1-octene to partially functionalize octakis(dimethylsiloxy)silsesquioxane (Q<sub>8</sub>M<sub>8</sub>\u0000 <sup>H</sup>) and isolate the mono-functional intermediate Q<sub>8</sub>M<sub>7</sub>\u0000 <sup>O</sup>M<sub>1</sub>\u0000 <sup>H</sup>. This intermediate was subsequently grafted onto the vinyl pendants of an HTPB backbone, facilitating the high-fidelity incorporation of the inorganic POSS cages while maintaining terminal hydroxyl functionality. Subsequent curing with isophorone diisocyanate (IPDI) yielded a series of nanostructured PU hybrid copolymers and terpolymers. This methodology provides a robust route for tailoring the inorganic content and architecture of liquid rubber pre-polymers, offering a versatile platform for the development of high-performance elastomeric binders with enhanced thermal and rheological properties.</p>\u0000 </div>","PeriodicalId":16888,"journal":{"name":"Journal of Polymer Science","volume":"64 16","pages":"3420-3426"},"PeriodicalIF":3.9,"publicationDate":"2026-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148754265","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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