Pub Date : 2024-10-24DOI: 10.1080/1023666X.2024.2410746
Pragnesh N. Dave , Pradip M. Macwan , Bhagvan Kamaliya
In this work, Gum ghatti-cl-poly(acrylic acid)/CoFe2O4 (GGAACF) hydrogels were synthesized using a free radical polymerization technique, with CoFe2O4 nanoparticles incorporated via a co-precipitation method using nitrates as precursors. Thermal gravimetric analysis (TGA) revealed that the inclusion of CoFe2O4 nanoparticles enhanced the thermal stability of the hydrogels. Swelling studies indicated that the addition of 30 mg of CoFe2O4 nanoparticles maximized water retention. Rheological assessments demonstrated non-Newtonian behavior, with flow curves fitted best by the Power Law model. The incorporation of CoFe2O4 nanoparticles significantly improved the hydrogel’s elasticity and viscosity, as evidenced by a higher storage modulus (G′) compared to the loss modulus (G″) across all frequencies, indicating the elastic nature of the hydrogels. The decrease in complex viscosity with increasing frequency confirmed the pseudoplastic properties of the hydrogels, attributed to the random alignment of CoFe2O4 nanoparticles within the matrix. Tan δ values were below unity at all tested frequencies, underscoring the hydrogels’ strong elastic properties. These findings highlight the effectiveness of rheological analysis in characterizing the viscoelastic behavior of polymer hydrogels, which can be tailored for various applications.
{"title":"Synthesis, rheological and thermal studies of Gum ghatti-cl-poly(acrylic acid) hydrogels containing CoFe2O4 nanoparticles","authors":"Pragnesh N. Dave , Pradip M. Macwan , Bhagvan Kamaliya","doi":"10.1080/1023666X.2024.2410746","DOIUrl":"10.1080/1023666X.2024.2410746","url":null,"abstract":"<div><div>In this work, Gum ghatti-cl-poly(acrylic acid)/CoFe<sub>2</sub>O<sub>4</sub> (GGAACF) hydrogels were synthesized using a free radical polymerization technique, with CoFe<sub>2</sub>O<sub>4</sub> nanoparticles incorporated via a co-precipitation method using nitrates as precursors. Thermal gravimetric analysis (TGA) revealed that the inclusion of CoFe<sub>2</sub>O<sub>4</sub> nanoparticles enhanced the thermal stability of the hydrogels. Swelling studies indicated that the addition of 30 mg of CoFe<sub>2</sub>O<sub>4</sub> nanoparticles maximized water retention. Rheological assessments demonstrated non-Newtonian behavior, with flow curves fitted best by the Power Law model. The incorporation of CoFe<sub>2</sub>O<sub>4</sub> nanoparticles significantly improved the hydrogel’s elasticity and viscosity, as evidenced by a higher storage modulus (G′) compared to the loss modulus (G″) across all frequencies, indicating the elastic nature of the hydrogels. The decrease in complex viscosity with increasing frequency confirmed the pseudoplastic properties of the hydrogels, attributed to the random alignment of CoFe<sub>2</sub>O<sub>4</sub> nanoparticles within the matrix. Tan δ values were below unity at all tested frequencies, underscoring the hydrogels’ strong elastic properties. These findings highlight the effectiveness of rheological analysis in characterizing the viscoelastic behavior of polymer hydrogels, which can be tailored for various applications.</div></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 8","pages":"Pages 658-674"},"PeriodicalIF":1.7,"publicationDate":"2024-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142592607","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}
Pub Date : 2024-10-17DOI: 10.1080/1023666X.2024.2410754
Hakki Cenker Kucukesmen , Mehmet Fahri Sarac
This study was carried out to investigate the chemical, mechanical, and structural properties of increasing amounts of fumed silica added to PMMA denture base material. The effect of adding fumed silica at three different concentrations (0.5%, 1%, and 2% by weight) to PMMA was studied using Fourier transform infrared spectroscopy (FTIR), dynamic mechanical analysis (DMA), density, flexural strength, hardness, atomic force microscopy (AFM), and scanning electron microscopy (SEM). The results showed that the highest flexural strength values (105.64 MPa) and hardness (20.07 microvickers) were obtained with 1% wt. of fumed silica material. According to DMA results, fumed silica samples containing 1% wt. had the highest energy storage (3.24 GPa at 30 °C) and glass transition temperature. As a result, fumed silica in PMMA denture base material reached its maximum saturation limit at 1% wt. A more brittle behavior was observed in samples containing 2% fumed silica, which accumulated on the surface, as confirmed by AFM. The molecular bonds at the resin-fumed silica interface weaken due to the agglomeration of fumed silica. Consequently, the flexural strength and hardness decrease, along with the glass transition temperature and storage modulus. The potential applications of this research are vast, inspiring further exploration and innovation in denture-based materials.
{"title":"Preparation and characterization of fumed silica added PMMA denture base materials","authors":"Hakki Cenker Kucukesmen , Mehmet Fahri Sarac","doi":"10.1080/1023666X.2024.2410754","DOIUrl":"10.1080/1023666X.2024.2410754","url":null,"abstract":"<div><div>This study was carried out to investigate the chemical, mechanical, and structural properties of increasing amounts of fumed silica added to PMMA denture base material. The effect of adding fumed silica at three different concentrations (0.5%, 1%, and 2% by weight) to PMMA was studied using Fourier transform infrared spectroscopy (FTIR), dynamic mechanical analysis (DMA), density, flexural strength, hardness, atomic force microscopy (AFM), and scanning electron microscopy (SEM). The results showed that the highest flexural strength values (105.64 MPa) and hardness (20.07 microvickers) were obtained with 1% wt. of fumed silica material. According to DMA results, fumed silica samples containing 1% wt. had the highest energy storage (3.24 GPa at 30 °C) and glass transition temperature. As a result, fumed silica in PMMA denture base material reached its maximum saturation limit at 1% wt. A more brittle behavior was observed in samples containing 2% fumed silica, which accumulated on the surface, as confirmed by AFM. The molecular bonds at the resin-fumed silica interface weaken due to the agglomeration of fumed silica. Consequently, the flexural strength and hardness decrease, along with the glass transition temperature and storage modulus. The potential applications of this research are vast, inspiring further exploration and innovation in denture-based materials.</div></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 8","pages":"Pages 675-684"},"PeriodicalIF":1.7,"publicationDate":"2024-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142592676","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}
The hunt for sustainable and efficient energy harvesting and storage devices has driven significant interest in triboelectric nanogenerators (TENGs) as potential alternatives to traditional batteries for powering electronic devices. However, the development of biodegradable TENGs remains a formidable challenge. This study presents the preparation of a tribopositive material entirely composed of biodegradable poly(butylene adipate-co-terephthalate) (PBAT) polymer enhanced with CoFe2O4 (CF) nanoparticles. The CF nanoparticles, synthesized via the combustion method, were incorporated into the PBAT matrix through solvent casting to form films with varied filler content (0.2, 0.4, 0.6, 0.8, and 1 g). The CF nanoparticles structural, surface, and electrical properties were characterized using XRD and FTIR spectroscopy. At the same time, the morphology of the nanomaterials and their composites was analyzed by scanning electron microscopy. Specifically, the 0.8 g PBAT-CF TENG demonstrated superior performance, achieving an output voltage of 45.45 V and a current of 4.5 µA. Subsequent electrical studies, including charging commercial capacitors (1.0 to 47 μF) and powering LEDs and calculators, underscored the device’s efficiency. The PBAT-CF TENG also effectively generated voltage and current signals from physical activities like walking and jumping. This innovative approach highlights the potential for biodegradable, high-performing, self-powered flexible electronics, and wearable devices, paving the way for sustainable technological advancements.
对可持续和高效能源采集和存储设备的追求,促使人们对三电纳米发电机(TENGs)产生了浓厚的兴趣,并将其作为传统电池的潜在替代品,为电子设备供电。然而,开发可生物降解的 TENGs 仍然是一项艰巨的挑战。本研究介绍了一种完全由可生物降解的聚己二酸丁二醇酯(PBAT)聚合物和 CoFe2O4(CF)纳米颗粒组成的摩擦正极材料的制备方法。通过燃烧法合成的 CF 纳米粒子通过溶剂浇铸法加入到 PBAT 基质中,形成不同填料含量(0.2、0.4、0.6、0.8 和 1 克)的薄膜。利用 XRD 和傅立叶变换红外光谱对 CF 纳米粒子的结构、表面和电学特性进行了表征。同时,利用扫描电子显微镜分析了纳米材料及其复合材料的形态。具体而言,0.8 克 PBAT-CF TENG 表现出卓越的性能,输出电压达到 45.45 V,电流为 4.5 µA。随后进行的电学研究,包括为商用电容器(1.0 至 47 μF)充电以及为 LED 和计算器供电,都凸显了该器件的效率。PBAT-CF TENG 还能有效地从步行和跳跃等身体活动中产生电压和电流信号。这种创新方法凸显了可生物降解、高性能、自供电柔性电子器件和可穿戴设备的潜力,为可持续技术进步铺平了道路。
{"title":"High-performance biodegradable triboelectric nanogenerators using CoFe2O4 filled poly (butylene adipate-co-terephthalate)","authors":"Vishnu Kadabahalli Thammannagowda , Kariyappa Gowda Guddenahalli Shivanna , Smitha Ankanahalli Shankaregowda , Prashantha Kalappa","doi":"10.1080/1023666X.2024.2410762","DOIUrl":"10.1080/1023666X.2024.2410762","url":null,"abstract":"<div><div>The hunt for sustainable and efficient energy harvesting and storage devices has driven significant interest in triboelectric nanogenerators (TENGs) as potential alternatives to traditional batteries for powering electronic devices. However, the development of biodegradable TENGs remains a formidable challenge. This study presents the preparation of a tribopositive material entirely composed of biodegradable poly(butylene adipate-co-terephthalate) (PBAT) polymer enhanced with CoFe<sub>2</sub>O<sub>4</sub> (CF) nanoparticles. The CF nanoparticles, synthesized via the combustion method, were incorporated into the PBAT matrix through solvent casting to form films with varied filler content (0.2, 0.4, 0.6, 0.8, and 1 g). The CF nanoparticles structural, surface, and electrical properties were characterized using XRD and FTIR spectroscopy. At the same time, the morphology of the nanomaterials and their composites was analyzed by scanning electron microscopy. Specifically, the 0.8 g PBAT-CF TENG demonstrated superior performance, achieving an output voltage of 45.45 V and a current of 4.5 µA. Subsequent electrical studies, including charging commercial capacitors (1.0 to 47 μF) and powering LEDs and calculators, underscored the device’s efficiency. The PBAT-CF TENG also effectively generated voltage and current signals from physical activities like walking and jumping. This innovative approach highlights the potential for biodegradable, high-performing, self-powered flexible electronics, and wearable devices, paving the way for sustainable technological advancements.</div></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 8","pages":"Pages 685-698"},"PeriodicalIF":1.7,"publicationDate":"2024-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142592610","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}
Pub Date : 2024-10-02DOI: 10.1080/1023666X.2024.2378890
Amit Agarwal , Vikas Upadhyay
Recently, bio-composites have attracted much attention due to their potential applications in various industries. The most notable benefits are the product’s low cost, biodegradability, lightweight, availability, and ability to solve environmental issues. The present research utilizes ash gourd (Benincasa hispida) peel, a food waste, as a filler material to produce epoxy (EP) composites. The effect of ash gourd peel particle percentage (ranging from 0 to 25 wt.%) was studied on the developed composites’ mechanical and thermal properties and water absorption behavior. The maximum tensile strength, flexural strength, and shore D hardness were 47.52 MPa, 2409.17 MPa, and 79.6respectively, when the ash gourd peel was 5% by weight in the composite. It was observed that the mechanical characteristics of manufactured bio-composites are negatively affected by the high concentration of ash gourd peel particles in the epoxy matrix. Also, increasing ash gourd peel particle fraction increases the water absorption of composites when immersed in distilled, sea, and tap water. The composite with 5% filler by weight absorbs water at a minimal rate when immersed in seawater. Thermogravimetric analysis was conducted to investigate the newly developed composite’s thermal behavior. In addition, a morphological examination of the fractured surfaces was carried out with assistance from a scanning electron microscope. The work presents ash gourd peel particles as the potential alternative to be used as filler in composites.
{"title":"Mechanical, Thermal, and Water Absorption Behavior of Ash Gourd (Benincasa Hispida) Peel Particles Filled Epoxy Composites","authors":"Amit Agarwal , Vikas Upadhyay","doi":"10.1080/1023666X.2024.2378890","DOIUrl":"10.1080/1023666X.2024.2378890","url":null,"abstract":"<div><div>Recently, bio-composites have attracted much attention due to their potential applications in various industries. The most notable benefits are the product’s low cost, biodegradability, lightweight, availability, and ability to solve environmental issues. The present research utilizes ash gourd (<em>Benincasa hispida</em>) peel, a food waste, as a filler material to produce epoxy (EP) composites. The effect of ash gourd peel particle percentage (ranging from 0 to 25 wt.%) was studied on the developed composites’ mechanical and thermal properties and water absorption behavior. The maximum tensile strength, flexural strength, and shore D hardness were 47.52 MPa, 2409.17 MPa, and 79.6respectively, when the ash gourd peel was 5% by weight in the composite. It was observed that the mechanical characteristics of manufactured bio-composites are negatively affected by the high concentration of ash gourd peel particles in the epoxy matrix. Also, increasing ash gourd peel particle fraction increases the water absorption of composites when immersed in distilled, sea, and tap water. The composite with 5% filler by weight absorbs water at a minimal rate when immersed in seawater. Thermogravimetric analysis was conducted to investigate the newly developed composite’s thermal behavior. In addition, a morphological examination of the fractured surfaces was carried out with assistance from a scanning electron microscope. The work presents ash gourd peel particles as the potential alternative to be used as filler in composites.</div></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 7","pages":"Pages 465-477"},"PeriodicalIF":1.7,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141807387","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}
Pub Date : 2024-10-02DOI: 10.1080/1023666X.2024.2391802
K. Umashankar , G. Kamala Vasanth , R. Krishna Prasad
Polymer composites containing poly (methyl methacrylate) (PMMA) and barium titanate (BaTiO3) were synthesized using the solution mixing method. The electrical conductivity of PMMA is 6 × 10−9 S/cm, and adding 2% fillers reduces to 5 × 10−9 S/cm. The melting point of PMMA is 373 °C, and adding 2% and 4% fillers increased it to 376 °C and 379 °C, respectively. The polymer chains become less mobile and block macromolecules on the filler surface. The modulus of elasticity and mechanical tensile stress of the polymer composites with a 5-wt% of BaTiO3 are 759.3 MPa and 75.6 MPa, respectively. The breakdown strength of PMMA is 203 KV and reduces with the addition of 5% filler to 144 KV. The values of E c/E m evaluated using the Tsai-Pagano, Christensen-Waals, ROM, Mori-Tanaka, and Halpin-Tsai models underpredict the modulus compared to experimental E c/E m values. Fourier spectroscopy confirmed the presence of Ti-O and BaTiO3 bonds in the polymer composite. Scanning electron microscope images reveal spherical aggregates of BaTiO3 coated with PMMA and an interparticle network. The dielectric constant of PMMA is 3 and increased with the addition of 2% and 4% fillers to 4 and 4.3, respectively.
{"title":"Micromechanical modeling, thermal, and dielectric studies of poly (methyl methacrylate)-barium titanate composites","authors":"K. Umashankar , G. Kamala Vasanth , R. Krishna Prasad","doi":"10.1080/1023666X.2024.2391802","DOIUrl":"10.1080/1023666X.2024.2391802","url":null,"abstract":"<div><div>Polymer composites containing poly (methyl methacrylate) (PMMA) and barium titanate (BaTiO<sub>3</sub>) were synthesized using the solution mixing method. The electrical conductivity of PMMA is 6 × 10<sup>−9</sup> S/cm, and adding 2% fillers reduces to 5 × 10<sup>−9</sup> S/cm. The melting point of PMMA is 373 °C, and adding 2% and 4% fillers increased it to 376 °C and 379 °C, respectively. The polymer chains become less mobile and block macromolecules on the filler surface. The modulus of elasticity and mechanical tensile stress of the polymer composites with a 5-wt% of BaTiO<sub>3</sub> are 759.3 MPa and 75.6 MPa, respectively. The breakdown strength of PMMA is 203 KV and reduces with the addition of 5% filler to 144 KV. The values of <em>E c</em>/<em>E m</em> evaluated using the Tsai-Pagano, Christensen-Waals, ROM, Mori-Tanaka, and Halpin-Tsai models underpredict the modulus compared to experimental <em>E c</em>/<em>E m</em> values. Fourier spectroscopy confirmed the presence of Ti-O and BaTiO<sub>3</sub> bonds in the polymer composite. Scanning electron microscope images reveal spherical aggregates of BaTiO<sub>3</sub> coated with PMMA and an interparticle network. The dielectric constant of PMMA is 3 and increased with the addition of 2% and 4% fillers to 4 and 4.3, respectively.</div></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 7","pages":"Pages 521-532"},"PeriodicalIF":1.7,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142359454","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}
Pub Date : 2024-10-02DOI: 10.1080/1023666X.2024.2383460
Dharmendra Kumar , Shweta Mukherjee , Avirup Das
In the present work, a novel ‘doped ceramic-polymer composite’-based solid polymer electrolytes (SPEs) has been synthesized using Zr (LAZTP) and Nb (LANbTP)-doped LATP as a ceramic filler and polyacrylonitrile (PAN) as a host polymer via the solution cast method. A series of SPEs with different ceramic loadings ranging from 10, 20, 30, 40, and 80 wt. % have been investigated using XRD, SEM, and impedance analysis. XRD spectra show the presence of crystalline ceramic peaks in composite solid polymer electrolyte. Further, the homogeneous distribution of the filler has been confirmed by SEM images. For SPEs, the highest conductivity of 5.31 × 10−5 S cm−1 has been obtained for PAN + LANbTP30 at room temperature. Whereas, the optimized conductivity for LATP-incorporated PAN shows 1.79 × 10−5 S cm−1, and the LAZTP-incorporated sample shows a conductivity of 3.03 × 10−5 S cm−1 at room temperature. Also, LANbTP-contained SPE shows excellent voltage stability of 4.90 V w.r.t. pure PAN.
本研究采用掺杂 Zr (LAZTP) 和 Nb (LANbTP) 的 LATP 作为陶瓷填料,以聚丙烯腈 (PAN) 作为主聚合物,通过溶液浇铸法合成了一种新型的 "掺杂陶瓷-聚合物复合材料 "型固体聚合物电解质 (SPE)。我们使用 XRD、SEM 和阻抗分析法研究了一系列具有不同陶瓷负载量(10、20、30、40 和 80 重量百分比)的 SPE。XRD 光谱显示,在复合固体聚合物电解质中存在结晶陶瓷峰。此外,SEM 图像也证实了填料的均匀分布。对于 SPE,PAN + LANbTP30 在室温下的最高电导率为 5.31 × 10-5 S cm-1。而加入 LATP 的 PAN 的最佳电导率为 1.79 × 10-5 S cm-1,加入 LAZTP 的样品在室温下的电导率为 3.03 × 10-5 S cm-1。此外,与纯 PAN 相比,含有 LANbTP 的 SPE 显示出 4.90 V 的出色电压稳定性。
{"title":"Enhanced performance in a NASICON-incorporated solid polymer electrolyte","authors":"Dharmendra Kumar , Shweta Mukherjee , Avirup Das","doi":"10.1080/1023666X.2024.2383460","DOIUrl":"10.1080/1023666X.2024.2383460","url":null,"abstract":"<div><div>In the present work, a novel ‘doped ceramic-polymer composite’-based solid polymer electrolytes (SPEs) has been synthesized using Zr (LAZTP) and Nb (LANbTP)-doped LATP as a ceramic filler and polyacrylonitrile (PAN) as a host polymer via the solution cast method. A series of SPEs with different ceramic loadings ranging from 10, 20, 30, 40, and 80 wt. % have been investigated using XRD, SEM, and impedance analysis. XRD spectra show the presence of crystalline ceramic peaks in composite solid polymer electrolyte. Further, the homogeneous distribution of the filler has been confirmed by SEM images. For SPEs, the highest conductivity of 5.31 × 10<sup>−5</sup> S cm<sup>−1</sup> has been obtained for PAN + LANbTP30 at room temperature. Whereas, the optimized conductivity for LATP-incorporated PAN shows 1.79 × 10<sup>−5</sup> S cm<sup>−1</sup>, and the LAZTP-incorporated sample shows a conductivity of 3.03 × 10<sup>−5</sup> S cm<sup>−1</sup> at room temperature. Also, LANbTP-contained SPE shows excellent voltage stability of 4.90 V w.r.t. pure PAN.</div></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 7","pages":"Pages 573-587"},"PeriodicalIF":1.7,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141926439","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}
Pub Date : 2024-10-02DOI: 10.1080/1023666X.2024.2397392
B. M. Alotaibi , Reem Altuijri , A. Atta , E. Abdeltwab , M. M. Abdelhamied
The films of P(4ClAni)/CuO, which formed of mixing poly 4-chloroaniline P(4ClAni) by CuO, were fabricated by the casting solution method. The XRD confirmed the successful prepration of the P(4ClAni)/CuO films. Additionally, the effect of CuO on the optical characteristics was determined. The CuO increased the refractive index from 1.09 for P(4ClAni) to 1.11 for P(4ClAni)/CuO-1, and 1.19 for P(4ClAni)/CuO-3, respectively, while the oscillation energy E0 dropped from 4.29 eV for P(4ClAni) to 3.57 eV for P(4ClAni)/CuO-1, 3.12 eV for P(4ClAni)/CuO-2, and 3.06 eV for P(4ClAni)/CuO-3. The charge transfer between P(4ClAni) and CuO increased optical conductivity as the CuO ratios increased. This suggests that modifications in the electronic structure of the composite due to the interactions between P(4ClAni) and CuO. Also, the plasma frequency increased from 0.87 x 1012 s−1 to 2.32 x 1012 s−1. These changes in optical parameters occurred when the polarization of the P(4ClAni)/CuO was altered. The study elucidated the advantages of incorporating CuO nanoparticles as fillers in improving the properties of P(4ClAni) structures. The obtained results indicate the P(4ClAni)/CuO composites were sucessfuly fabricated with novel characteristics that can be applied in flexible optical devices.
{"title":"Fabrication, structure and optical characteristics of CuO/polymer nanocomposites materials for optical devices","authors":"B. M. Alotaibi , Reem Altuijri , A. Atta , E. Abdeltwab , M. M. Abdelhamied","doi":"10.1080/1023666X.2024.2397392","DOIUrl":"10.1080/1023666X.2024.2397392","url":null,"abstract":"<div><div>The films of P(4ClAni)/CuO, which formed of mixing poly 4-chloroaniline P(4ClAni) by CuO, were fabricated by the casting solution method. The XRD confirmed the successful prepration of the P(4ClAni)/CuO films. Additionally, the effect of CuO on the optical characteristics was determined. The CuO increased the refractive index from 1.09 for P(4ClAni) to 1.11 for P(4ClAni)/CuO-1, and 1.19 for P(4ClAni)/CuO-3, respectively, while the oscillation energy E<sub>0</sub> dropped from 4.29 eV for P(4ClAni) to 3.57 eV for P(4ClAni)/CuO-1, 3.12 eV for P(4ClAni)/CuO-2, and 3.06 eV for P(4ClAni)/CuO-3. The charge transfer between P(4ClAni) and CuO increased optical conductivity as the CuO ratios increased. This suggests that modifications in the electronic structure of the composite due to the interactions between P(4ClAni) and CuO. Also, the plasma frequency increased from 0.87 x 10<sup>12</sup> s<sup>−1</sup> to 2.32 x 10<sup>12</sup> s<sup>−1</sup>. These changes in optical parameters occurred when the polarization of the P(4ClAni)/CuO was altered. The study elucidated the advantages of incorporating CuO nanoparticles as fillers in improving the properties of P(4ClAni) structures. The obtained results indicate the P(4ClAni)/CuO composites were sucessfuly fabricated with novel characteristics that can be applied in flexible optical devices.</div></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 7","pages":"Pages 562-572"},"PeriodicalIF":1.7,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142359456","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}
Pub Date : 2024-10-02DOI: 10.1080/1023666X.2024.2387605
Hijran S. Ibrahimova , Tahir D. Ibragimov
Charge states, thermophysical and mechanical properties of polypropylene doped with zirconium oxide nanoparticles, and their changes during heat treatment at temperatures 60 °C, 100 °C, and 140 °C are studied. The methods used are thermal stimulated depolarization (TSD), scanning differential calorimetry (SDC), and mechanical life assessment. It is shown that with an increase in the concentration of the filler, the intensity of the TSD peaks increases up to 3 vol.%. A further increase in concentration leads to a decrease in the intensity of the peaks. The activation energy of charge release from traps, temperature of maximum of the peaks, and the magnitude of the accumulated charge in the traps have also maximal value at nanoparticle concentration of 3 vol.%. The study of charge characteristics of the nanocomposite with concentration of 3 vol.% after heat treatment shows that the intensity of TSD peaks, the temperature of peak maxima, and the activation energy of charge release increase with increasing pretreatment temperature. The magnitude of the charge accumulated in traps has a maximal value at treatment temperature of 140 °C owing to the increase in the number of traps. The melting point of the composite is 149.38 °C and shifts to 146.88 °C after heat treatment at 140 °C. It indicates that the high temperature of heat treatment leads to partial destruction of polymer chains, leading to a decrease in the critical melting temperature. The mechanical durability of PP + 3%ZrO2 nanocomposite decreases with increase in pretreatment temperature.
{"title":"Effect of heat treatment on charge states, thermophysical and mechanical properties of polypropylene doped with ZrO2 nanoparticles","authors":"Hijran S. Ibrahimova , Tahir D. Ibragimov","doi":"10.1080/1023666X.2024.2387605","DOIUrl":"10.1080/1023666X.2024.2387605","url":null,"abstract":"<div><div>Charge states, thermophysical and mechanical properties of polypropylene doped with zirconium oxide nanoparticles, and their changes during heat treatment at temperatures 60 °C, 100 °C, and 140 °C are studied. The methods used are thermal stimulated depolarization (TSD), scanning differential calorimetry (SDC), and mechanical life assessment. It is shown that with an increase in the concentration of the filler, the intensity of the TSD peaks increases up to 3 vol.%. A further increase in concentration leads to a decrease in the intensity of the peaks. The activation energy of charge release from traps, temperature of maximum of the peaks, and the magnitude of the accumulated charge in the traps have also maximal value at nanoparticle concentration of 3 vol.%. The study of charge characteristics of the nanocomposite with concentration of 3 vol.% after heat treatment shows that the intensity of TSD peaks, the temperature of peak maxima, and the activation energy of charge release increase with increasing pretreatment temperature. The magnitude of the charge accumulated in traps has a maximal value at treatment temperature of 140 °C owing to the increase in the number of traps. The melting point of the composite is 149.38 °C and shifts to 146.88 °C after heat treatment at 140 °C. It indicates that the high temperature of heat treatment leads to partial destruction of polymer chains, leading to a decrease in the critical melting temperature. The mechanical durability of PP + 3%ZrO<sub>2</sub> nanocomposite decreases with increase in pretreatment temperature.</div></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 7","pages":"Pages 508-520"},"PeriodicalIF":1.7,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141943869","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}
Pub Date : 2024-10-02DOI: 10.1080/1023666X.2024.2394226
Elsayeda F. Salem , Walaa Abd-Elmonem Elkatan , Nesreen R. Abdel Wahab
Polymers play an essential role in both industry and medical fields due to their diverse and adaptable properties. In this work, prepared crosslinking polyethylene (XLPE) samples with hydrophilic bentonite nanoclay fillers (H2Al2O6Si) at concentrations of 0, 1, 2.5, 4, and 5 wt% enhance their flame-retardant and radiation shielding efficiency. The research investigated flame retardancy and thermal stability parameters. The XLPE/H2Al2O6Si nanocomposite polymer sheets were exposed to a collimated beam of fast neutrons using an Am/Be neutron source (5 Ci) and to gamma radiation using a 137Cs point source (5 μCi) to assess their radiation shielding properties. The study found that uniform dispersion of nanoclay particles enhanced the thermal properties of the composite, forming a char layer that acted as a barrier, slowing thermal decomposition and reducing the heat release rate. Limiting oxygen index (LOI) increased from 28% to 34%, and burning rate improved with higher nanoclay concentrations. Additionally, absorption and optical band gap calculations decreased with increasing filler concentrations. Radiation attenuation capabilities increased by approximately 40% for neutrons and 30% for gamma radiation compared to pure XLPE. The study concluded that incorporating nanoclay fillers into XLPE enhances its shielding capabilities and improves flame resistance properties, making the prepared samples suitable for various industrial applications.
{"title":"Improving flame resistance and shielding properties for cross-linked polyethylene (XLPE) using nanoclay filler","authors":"Elsayeda F. Salem , Walaa Abd-Elmonem Elkatan , Nesreen R. Abdel Wahab","doi":"10.1080/1023666X.2024.2394226","DOIUrl":"10.1080/1023666X.2024.2394226","url":null,"abstract":"<div><div>Polymers play an essential role in both industry and medical fields due to their diverse and adaptable properties. In this work, prepared crosslinking polyethylene (XLPE) samples with hydrophilic bentonite nanoclay fillers (H<sub>2</sub>Al<sub>2</sub>O<sub>6</sub>Si) at concentrations of 0, 1, 2.5, 4, and 5 wt% enhance their flame-retardant and radiation shielding efficiency. The research investigated flame retardancy and thermal stability parameters. The XLPE/H<sub>2</sub>Al<sub>2</sub>O<sub>6</sub>Si nanocomposite polymer sheets were exposed to a collimated beam of fast neutrons using an Am/Be neutron source (5 Ci) and to gamma radiation using a <sup>137</sup>Cs point source (5 μCi) to assess their radiation shielding properties. The study found that uniform dispersion of nanoclay particles enhanced the thermal properties of the composite, forming a char layer that acted as a barrier, slowing thermal decomposition and reducing the heat release rate. Limiting oxygen index (LOI) increased from 28% to 34%, and burning rate improved with higher nanoclay concentrations. Additionally, absorption and optical band gap calculations decreased with increasing filler concentrations. Radiation attenuation capabilities increased by approximately 40% for neutrons and 30% for gamma radiation compared to pure XLPE. The study concluded that incorporating nanoclay fillers into XLPE enhances its shielding capabilities and improves flame resistance properties, making the prepared samples suitable for various industrial applications.</div></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 7","pages":"Pages 547-561"},"PeriodicalIF":1.7,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208273","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}
The increase in the use of plastics during the past few decades has caused environmental pollution due to the non-biodegradable and recalcitrance nature of the plastics. This has caused great problems for the solid waste management efforts. The development of biodegradable polymers from natural and renewable ingredients can address the challenges caused by plastic pollution. The present work deals with the optimization of the preparation process of sago starch-based biodegradable bioplastic films. The sago starch, glycerol-sorbitol mixture, and chitosan were used as polysaccharides, plasticizers, and antimicrobial agents, respectively. The factors screening and design optimization were performed using response surface methodology and Box-Behnken Design to investigate the interactions between all components in the film preparation. Furthermore, the developed bioplastic films were characterized through field emission scanning electron microscopy and Fourier transform infrared spectroscopy. The antimicrobial susceptibility assay showed the inhibition of the growth of Bacillus pumilus and Alcaligenes faecalis XF1 by incorporation of cinnamon essential oil into the film. Moreover, the developed films successfully reduced the proliferation of fungal growth on packaged bread samples. The microbial analysis found that the shelf life of the wheat bread was improved from 3 to 15 days. The sago starch bioplastic films developed in this study can potentially meet the requirements for food packaging films.
{"title":"Response surface methodology-based preparation of sago starch bioplastic film for food packaging","authors":"Shikha Guleria , Harpreet Singh , Atul Jain , Shailendra Kumar Arya , Sanjeev Puri , Madhu Khatri","doi":"10.1080/1023666X.2024.2383480","DOIUrl":"10.1080/1023666X.2024.2383480","url":null,"abstract":"<div><div>The increase in the use of plastics during the past few decades has caused environmental pollution due to the non-biodegradable and recalcitrance nature of the plastics. This has caused great problems for the solid waste management efforts. The development of biodegradable polymers from natural and renewable ingredients can address the challenges caused by plastic pollution. The present work deals with the optimization of the preparation process of sago starch-based biodegradable bioplastic films. The sago starch, glycerol-sorbitol mixture, and chitosan were used as polysaccharides, plasticizers, and antimicrobial agents, respectively. The factors screening and design optimization were performed using response surface methodology and Box-Behnken Design to investigate the interactions between all components in the film preparation. Furthermore, the developed bioplastic films were characterized through field emission scanning electron microscopy and Fourier transform infrared spectroscopy. The antimicrobial susceptibility assay showed the inhibition of the growth of <em>Bacillus pumilus</em> and <em>Alcaligenes faecalis XF1</em> by incorporation of cinnamon essential oil into the film. Moreover, the developed films successfully reduced the proliferation of fungal growth on packaged bread samples. The microbial analysis found that the shelf life of the wheat bread was improved from 3 to 15 days. The sago starch bioplastic films developed in this study can potentially meet the requirements for food packaging films.</div></div>","PeriodicalId":14236,"journal":{"name":"International Journal of Polymer Analysis and Characterization","volume":"29 7","pages":"Pages 478-495"},"PeriodicalIF":1.7,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141925027","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}