{"title":"Synthesis of Polyether Ester Plasticizer and Its Application Performance in Hydrogenated Nitrile Butadiene Rubber","authors":"Hui Li, Zhibin Wang, Yuqing Song, Xiao Jian-bin, Qi Chen","doi":"10.1002/pat.70090","DOIUrl":"https://doi.org/10.1002/pat.70090","url":null,"abstract":"ABSTRACT Four polyether ester plasticizers containing both ester groups and ether bonds were synthesized using 1,4‐butanediol, adipic acid, and alkyl ether alcohols as raw materials. By varying the type of end‐capping alcohol ether, the following plasticizers were prepared: poly (butylene adipate dibutyl ether) (PBADBE), poly (butylene adipate butyl ether) (PBABE), poly (butylene adipate dimethyl ether) (PBADME), and poly (butylene adipate methyl ether) (PBAME). These plasticizers were characterized by Fourier transform infrared (FTIR) spectroscopy, proton nuclear magnetic resonance spectroscopy ( 1 H‐NMR), and thermogravimetric (TG) analysis. Furthermore, their differences in cold resistance, heat resistance, and physical‐mechanical properties in hydrogenated nitrile‐butadiene rubber (HNBR) were investigated. The results showed that among the rubber compounds containing the four polyether‐ester plasticizers, the compound with PBADME demonstrated superior heat resistance and low‐temperature performance. Specifically, the PBADME‐containing compound exhibited a TR 10 temperature of −39.9°C and a brittleness temperature of −54°C. This significantly broadened the operating temperature range of the plasticizer, making it suitable for applications requiring both high‐temperature and low‐temperature performance.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"36 2","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147331937","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Tribological Behavior of Self‐Lubricating <scp>PEEK</scp>/Graphite/<scp>Ti<sub>3</sub>SiC<sub>2</sub></scp> Composites Under Dry Sliding Friction","authors":"Zhang Yang, Qingsong Li, Xi Xie, Guoxin Sui","doi":"10.1002/pat.70128","DOIUrl":"https://doi.org/10.1002/pat.70128","url":null,"abstract":"ABSTRACT Most polymers and composites suffer from high friction and wear due to their inherent lack of self‐lubrication under dry sliding friction. Herein, the lamellar Ti 3 SiC 2 MAX material is prepared via vacuum sintering of a powder mixture containing Ti, Si, and TiC in the molar ratio of 1:1.1:1.8 at 1500°C under a pressure of 30 MPa for 2 h. Combined with a soft graphite phase (5 wt%), self‐lubricating PEEK/Graphite/Ti 3 SiC 2 (PG‐T) composites are successfully prepared, dependent on Ti 3 SiC 2 (5 and 15 wt%) as a hard reinforced phase and lubrication additive. PG‐T composites are fabricated via a multistep compounding approach using a twin‐screw extruder. The incorporation of Ti 3 SiC 2 and graphite within the PEEK matrix manifests a highly pronounced synergistic effect, which not only facilitates effective lubrication but also significantly enhances the load‐bearing capability, thereby effectively circumventing direct contact between the counterface and the polymeric matrix. The sliding tests are conducted on the pins (diameter: 6.0 mm, height: 17.0 mm) and friction pair (45#steel, roughness Ra: 148 nm) under dry friction. In terms of PV‐condition (up to 6 MPa and 3 m/s) (PV is a parameter that reflects the load‐bearing capacity of polymer materials, which is defined by multi‐plying the pressure P by the sliding speed V), PG5‐T15 exhibits self‐lubricating properties, featured by an average coefficient of friction (ACOF) as low as 0.119 for the pin‐plate test and a specific wear rate (SWR) of only 0.58 × 10 −6 mm 3 /Nm. Meanwhile, PG‐T composites present excellent thermal properties based on the thermal expansion coefficients (CTEs) and storage moduli (G′) during friction and wear. Considering the practical applications of tribo‐composites, these findings highlight the potential of PG‐T composite as a candidate for demanding tribological applications.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"36 2","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/pat.70128","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147917970","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Study on the Preparation and Separation Performance of Microwave‐Assisted Ru(<scp>IV</scp>)‐<scp>TIIP</scp>","authors":"Bingqian Wang, Ting Huo, Wan Xu, Xiaojian Ou, Yuanjun Sun, Yanjun Cui, Yongsheng Xiang, Zhenbin Chen","doi":"10.1002/pat.70110","DOIUrl":"https://doi.org/10.1002/pat.70110","url":null,"abstract":"ABSTRACT The porous thermosensitive imprinted polymer of MW‐Ru(IV)‐TIIP was prepared in a short time with the aid of a microwave. The structure and morphology of MW‐Ru(IV)‐TIIP were characterized by ATR‐FTIR, SEM‐EDS, and BET. The thermosensitive block PDEA‐ b ‐P(DEA‐ co ‐AM) was introduced into the imprinted polymer preparation system. N‐MAM and AA were selected as functional monomers, and stable HIPE Pickering emulsions were prepared under high‐speed stirring, combined with multi‐field coupling technology. The synthesis process of MW‐Ru(IV)‐TIIP was studied, and the dosages of template ion, functional monomer, and cross‐linking agent, as well as microwave power, polymerization temperature, and polymerization time, were optimized. Under optimal technological conditions, the maximum adsorption capacity of MW‐Ru(IV)‐TIIP reached 0.20 mmol L −1 at 33°C, and adsorption equilibrium was reached within 240 min. Theoretical studies showed that the adsorption of MW‐Ru(IV)‐TIIP conformed to the quasi‐first‐order kinetic model and the Langmuir model. When MW‐Ru(IV)‐TIIP was applied to a diluted platinum group catalyst leaching solution, its adsorption capacity for MW‐Ru(IV)‐TIIP to Ru was 0.23 mmol L −1 , and the purity of platinum group metals increased from 53.72% to 76.43% after one adsorption/desorption cycle. After 11 reuses, the adsorption capacity maintained 70.06% of the original capacity, indicating that MW‐Ru(IV)‐TIIP had good potential in industrial applications.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"36 2","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/pat.70110","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147914956","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Ag‐Deposited Pitch‐Based Carbon Fiber/Silicone Composites With Enhanced Thermal Conductivity Through Reducing Interfacial Thermal Resistance","authors":"Jingbo Shen, Yakai Feng","doi":"10.1002/pat.70106","DOIUrl":"https://doi.org/10.1002/pat.70106","url":null,"abstract":"ABSTRACT Thermal interface materials are crucial for the thermal management of modern electronic devices. The thermal conductivity of polymer‐based composites, as the widely used thermal interface materials, is still limited by the high interfacial thermal resistance between the polymer matrix and the filler. Herein, pitch‐based carbon fibers co‐modified with silane coupling agent and Ag nanoparticles were developed and used as thermally conductive fillers to prepare silicone composites with the purpose of improving interfacial compatibility and reducing interfacial thermal resistance. Under scanning electron microscope observation, the modified carbon fibers dispersed uniformly, and they were adhered to by a number of Ag nanoparticles. The thermal conductivity of the silicone composite with a 20 wt% filling amount of modified carbon fibers reached up to 1.624 W m −1 K −1 , which was 1.46 times higher than that of the unmodified carbon fiber filled silicone composite. The silicone composite with a 20 wt% filling amount of modified carbon fibers also exhibited a relatively high heat transfer rate and excellent mechanical properties. The electrical insulation and dielectric properties of silicone composites filled with modified carbon fibers also satisfied the requirements for the use of thermal interface materials. This approach provided an effective strategy for the development of thermal interface materials with high thermal conductivity in the thermal management field.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"36 2","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147910136","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Danni Yang, Tao Luo, Tao Zhang, Li Lv, Zongpeng Zou, Shengwei Tang
{"title":"Miscible Polymer Blend Membranes Bearing Pyrrolidone for Fractioning Sulfuric Acid and Sulfates","authors":"Danni Yang, Tao Luo, Tao Zhang, Li Lv, Zongpeng Zou, Shengwei Tang","doi":"10.1002/pat.70079","DOIUrl":"https://doi.org/10.1002/pat.70079","url":null,"abstract":"ABSTRACT Ion exchange membranes of new chemistry based on polymer blends are proposed through a convenient solution‐blending process using the hydrophobic commodity polymer polyvinyl chloride (PVC) and the hydrophilic polyvinylpyrrolidone (PVP), which are completely miscible. The pyrrolidone groups can be protonated to form oxonium ions, functioning as transient fixed positive charges for fractioning sulfuric acid and sulfates via diffusion. The influence of PVC molecular weight and the membrane composition on the physical, chemical properties, and mass transfer performance of PVC‐PVP blend membranes was systematically investigated. After equilibrium in 2.68 mol/L sulfuric acid, the sulfuric acid, and water contents in the blend membranes increase with the increase of the membrane PVP contents (20–75 wt%). The permeability coefficients of sulfuric acid and ferrous sulfate for the blend membranes also exhibit a gradual increase. Membranes of mass transfer properties comparable to commercial ones can be easily obtained by tuning the membrane PVP contents. It is proved that the larger sulfuric acid permeability over sulfates (FeSO 4 as an example) is due to both larger solubility and diffusion coefficient of sulfuric acid in the membrane phase. The optimal PVC‐PVP blend membranes have shown nice performance in fractioning sulfuric acid from sulfates, when treating titania waste acid. This study provides valuable guidance for the design of high‐performance yet low‐cost ion exchange membranes with pyrrolidone chemistry from commodity polymers for resource recovery.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"36 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147896592","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Mechanism Insights Into High‐Performance Cu<sup>2+</sup> Adsorption by <scp>ZIF</scp>‐8/<scp>PAN</scp> Nanocomposite Fibers: Coordination and Ion Exchange Dynamics","authors":"Hailong Zhang, Ruimeng Li, Haishui Xu, Ling Quan, Chengyu Zhan, Peng Han, Kehan Xu, Yuping Tong","doi":"10.1002/pat.70068","DOIUrl":"https://doi.org/10.1002/pat.70068","url":null,"abstract":"ABSTRACT The accumulation of copper ions in the environment can devastate the ecological systems and threaten the health of organisms. Consequently, the development of effective adsorbents to extract Cu 2+ from aqueous solutions is urgently needed. Here, the Zeolitic Imidazolate Framework‐8 (ZIF‐8)/polyacrylonitrile (PAN) nanocomposite fibers were synthesized by electrospinning and further characterized using X‐ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR). ZIF‐8 powders were uniformly distributed on the surface of the nanocomposite fibers, and amide CONH bonds were formed between the NH 2 groups of ZIF‐8 and the CO groups of PAN. The ZIF‐8/PAN nanocomposite fibers demonstrated an exceptional Cu 2+ adsorption capacity of 275.7 mg g −1 at pH = 4.0. The adsorption process adhered to the pseudo‐second‐order kinetics and the Langmuir isotherm model. The adsorption mechanism, as conformed by FTIR and X‐ray photoelectron spectroscopy (XPS) analysis, involves the coordination of the NH 2 and CO groups with Cu 2+ and the ion exchange processes between Cu 2+ and Zn 2+ for the nanocomposite fibers. This study provides a novel approach for the removal of Cu 2+ from aqueous solutions and addresses the challenge of recovering powder materials in wastewater treatment.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"36 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147332844","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Synthesis of a Novel Derivative Containing Phosphaphenanthrene and Phenyl Propargyl Ether Groups Toward Enhanced Flame Retardance and Mechanical Properties of Epoxy Resin","authors":"Qinqin Luo, Yulin Sun","doi":"10.1002/pat.70059","DOIUrl":"https://doi.org/10.1002/pat.70059","url":null,"abstract":"ABSTRACT To achieve effective flame retardancy and improved toughness in epoxy resin (EP) without compromising strength and modulus, a new derivative containing phosphaphenanthrene and phenyl propyl ether groups (HPMD) has been developed and used as an additive. The structure of HPMD has been fully characterized, and the properties of HPMD and modified EP have been thoroughly studied. The phenyl propyl ether group in HPMD can undergo Claisen type rearrangement to form benzopyran during heat treatment and subsequently polymerize by curing via the CC bond in the benzopyran. The unique rigid and flexible structures of HPMD allow it to disperse in the EP matrix through melting. Dynamic mechanical analysis suggests that HPMD has a high degree of interpenetration in the EP matrix, resulting in a single‐phase structure for the epoxy resins containing HPMD. Notably, incorporating only 4 wt% HPMD content into the polymer matrix yields a flame‐retarded, toughened, and strengthened EP. EP containing 4 wt% HPMD (EP4; phosphorus content of only 0.33%) displays a limiting oxygen index value of 31.1% and exhibits a UL94 V‐0 rating. Compared with that of EP, the combustion of EP4 exhibits a decrease in the peak of heat release rate, maximum average heat rate emission, average heat release rate, and total heat release, along with an increase in the char yield, further indicating that HPMD effectively retards the combustion of EP. Moreover, EP4 displays improvements in tensile strength, elongation at break, flexural strength, flexural modulus, and impact strength of 18.4%, 9.7%, 14.9%, 19.1%, and 26.7%, respectively, compared with unmodified EP. Analysis of HPMD's flame‐retardant action suggests that it exhibits flame‐retardant activity simultaneously in the gas and condensed phases. Significant progress has been demonstrated toward the development of a meltable epoxy resin additive that combines flame‐retardant, toughening, and strengthening functions while avoiding phase separation from the epoxy resin.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"36 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147902023","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jiahao Duan, Congling Shi, Ling Yang, Xiaodong Qian, Mei Wan, Hongqing Zhu, Houwang Wang
{"title":"Green Preparation of Ammonium Polyphosphate With Shell–Core Structure for Enhancing Fire Safety of Thermoplastic Polyurethane","authors":"Jiahao Duan, Congling Shi, Ling Yang, Xiaodong Qian, Mei Wan, Hongqing Zhu, Houwang Wang","doi":"10.1002/pat.70045","DOIUrl":"https://doi.org/10.1002/pat.70045","url":null,"abstract":"ABSTRACT In the recent years, the development of high‐performance flame retardants (FRs) for thermoplastic polyurethane (TPU) has become increasingly important due to its wide applications in various industries and the growing demand for fire safety. In this study, ammonium polyphosphate (APP) was used as the core, whereas chitosan (CS) and nano‐silica (SiO 2 ) served as the shell to create a shell–core‐structured FR through a self‐assembly process in an aqueous phase. APP, APP@CS, and APP@CS@SiO 2 were incorporated into TPU at a concentration of 20 wt%, and their effects on TPU properties were compared. The findings showed that APP@CS@SiO 2 exhibited superior flame retardancy for TPU. Compared to pure TPU, the TPU/APP@CS@SiO 2 showed reductions in peak heat release rate, total heat release, peak smoke production rate, total smoke production, peak CO production rate, and peak CO 2 production rate by 58%, 80%, 80.5%, 89.1%, 20.4%, and 60.1%, respectively. Additionally, APP@CS@SiO 2 effectively inhibited the thermal degradation of TPU and enhanced its thermal stability, resulting in the residual carbon content of the composite rising to 28.5%, which is about 20 times higher than that of pure TPU. In conclusion, APP@CS@SiO 2 significantly improved the fire safety of TPU by efficiently catalyzing char formation in the condensed phase, diluting flammable gases, and hindering gas‐phase free radical chain reactions, thereby opening new avenues for the practical application of TPU composites.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"36 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147902256","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Preparation of Porous Novel <scp>QuEChERS</scp> Adsorbent <scp>ZIF</scp>‐67/<scp>PAA</scp>/<scp>PES</scp> Composite Microspheres and Their Application for Rapid Adsorption of Triphenylmethane Dyes in Wastewater and Fish","authors":"Xiaotian Wang, Yeerken Aheyeli‐kai, Hao Ying, Jiangli Lin, Yulu Luo, Hongying Ma, Zhongyang Li, Zhen Su","doi":"10.1002/pat.70031","DOIUrl":"https://doi.org/10.1002/pat.70031","url":null,"abstract":"ABSTRACT Triphenylmethane dyes have a wide range of applications in textiles, pharmaceuticals, food, and other fields. Malachite green (MG), fuchsin acid (FA), and crystalline violet (CV) were typical representatives of triphenylmethane dyes, and they are carcinogenic and mutagenic to aquatic organisms and environment. However, they need to be separated and enriched for their accurate quantification due to their low content. Therefore, it is important to develop a rapid and accurate enrichment method to monitor these dyes in aquatic systems for human health. In this paper, a novel QuEChERS adsorbent porous ZIF67/PAA/PES composite microspheres were prepared and applied for the rapid adsorption of triphenylmethane dyes in wastewater and fish samples, which improved the adsorption capacity and the analytical sensitivity of the targets. The experimental results demonstrated that the porous ZIF‐67/PAA/PES composite microspheres exhibited excellent selective adsorption capacity of MG, FA, and CV, and after six adsorption–desorption cycles, the material adsorption amount can reach more than 90% of its original adsorption amount in wastewater. In addition, the porous ZIF67/PAA/PES composite microspheres were applied as QuEChERS adsorbents for the enrichment of MG and CV dyes in fish, and the adsorption rates of the dyes were 99.11% and 99.03%, with the RSDs of 1.58% and 1.27%, respectively. The limits of detection were 0.0093 and 0.0127 mg/L for MG and CV. Through the Langmuir adsorption isotherm models to predict the MG, FA, and CV of the maximum adsorption capacity were 5417.3622, 2119.9011, and 1654.1026 mg/g, respectively. Thus, the novel porous ZIF67/PAA/PES composite microspheres are more advantageous as QuEChERS adsorbents for sample pre‐treatment and have very important research significance.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"36 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147330838","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yawen Li, Guoyang Ma, Shaohong Xu, Zaheer Ahmad, Muhammad Ali, Saad Ahmed, Naveed Ahmed
{"title":"Enhancing Thermal and Mechanical Properties of Soft <scp>PVC</scp> Composites With Phosphorylated Boron Nitride","authors":"Yawen Li, Guoyang Ma, Shaohong Xu, Zaheer Ahmad, Muhammad Ali, Saad Ahmed, Naveed Ahmed","doi":"10.1002/pat.70063","DOIUrl":"https://doi.org/10.1002/pat.70063","url":null,"abstract":"ABSTRACT In the present study, hexagonal boron nitride (h‐BN) nanosheets were first functionalized with hydroxyl groups (h‐BN‐OH), and then phosphonic acid groups were grafted onto the h‐BN surface (BNP) using aminotris(methylenephosphonic acid) (ATMP) through a condensation reaction. The BNP was then incorporated into a polyvinyl chloride (PVC) matrix to prepare PVC/BNP composites. Thermogravimetric analysis showed an increase in thermal stability, with BNP/PVC composites exhibiting greater resistance to degradation at elevated temperatures. The addition of BNP improved the dispersion and interfacial adhesion within the PVC matrix, as confirmed by Scanning Electron Microscopy (SEM). Furthermore, the PVC/BNP composites exhibited a 22.5% increase in tensile strength (21.2 MPa) and an 82% improvement in elongation at break (464%) compared to pristine PVC composites, which showed a tensile strength of 17.3 MPa and an elongation at break of 255%. Moreover, the addition of BNP notably improved the thermal conductivity from 0.18 to 1.50 W/m K as the BNP content increased from BNP‐0 to BNP‐4. These improvements in thermal stability and mechanical strength, as well as excellent migration resistance, make BNP/PVC composites highly promising for advanced applications.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"36 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/pat.70063","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147912720","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}