Pub Date : 2024-08-13DOI: 10.1007/s00396-024-05307-1
Vu Viet Linh Nguyen, Thi Kieu Tien Vu, Dai Phu Huynh, Van-Tien Bui
Triboelectric nanogenerators (TENGs) made from biocompatible materials serve as promising integrated power sources for portable wearable electronics due to many advantages such as lightweight, high flexibility, simple technique, and excellent breathability. In this work, we report the fabrication of electrospun polycaprolactone micro-nanofiber films (s-PCL) and convex-microdome-patterned polydimethylsiloxane (c-PDMS) utilizing electrospinning and micromolding techniques. These materials, s-PCL and c-PDMS, are utilized as positively and negatively charged tribosurfaces, respectively, in the development of a bioTENG device. The developed TENG device can generate a superior power output of 2 mW with an open-circuit voltage (VOC) of 188 V and short-circuit current (ISC) of 18.5 µA, even under a low triggering frequency of 5 Hz. In addition, TENG possesses outstanding durability and output performance stability over a continuous operation of nearly 16,000 cycles. Furthermore, the TENG demonstrates its capacity to harvest mechanical energy and convert it into electricity, capable of directly illuminating more than 100 LEDs. The electrospun s-PCL- and c-PDMS-based TENG can be considered for self-powdered wearable devices attached to fingers, wrists, feet, and other human body parts.
{"title":"High-performance triboelectric nanogenerator based on biocompatible electrospun polycaprolactone nanofiber and counter convex PDMS for low-frequency mechanical energy harvesting","authors":"Vu Viet Linh Nguyen, Thi Kieu Tien Vu, Dai Phu Huynh, Van-Tien Bui","doi":"10.1007/s00396-024-05307-1","DOIUrl":"https://doi.org/10.1007/s00396-024-05307-1","url":null,"abstract":"<p>Triboelectric nanogenerators (TENGs) made from biocompatible materials serve as promising integrated power sources for portable wearable electronics due to many advantages such as lightweight, high flexibility, simple technique, and excellent breathability. In this work, we report the fabrication of electrospun polycaprolactone micro-nanofiber films (<i>s-</i>PCL) and convex-microdome-patterned polydimethylsiloxane (<i>c-</i>PDMS) utilizing electrospinning and micromolding techniques. These materials, <i>s-</i>PCL and <i>c-</i>PDMS, are utilized as positively and negatively charged tribosurfaces, respectively, in the development of a bioTENG device. The developed TENG device can generate a superior power output of 2 mW with an open-circuit voltage (<i>V</i><sub>OC</sub>) of 188 V and short-circuit current (<i>I</i><sub>SC</sub>) of 18.5 µA, even under a low triggering frequency of 5 Hz. In addition, TENG possesses outstanding durability and output performance stability over a continuous operation of nearly 16,000 cycles. Furthermore, the TENG demonstrates its capacity to harvest mechanical energy and convert it into electricity, capable of directly illuminating more than 100 LEDs. The electrospun <i>s</i>-PCL- and <i>c</i>-PDMS-based TENG can be considered for self-powdered wearable devices attached to fingers, wrists, feet, and other human body parts.</p><h3 data-test=\"abstract-sub-heading\">Graphical abstract</h3>","PeriodicalId":520,"journal":{"name":"Colloid and Polymer Science","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142180973","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-06DOI: 10.1007/s00396-024-05304-4
Meng Zhao, Hao Duan, Linfeng Han, Lin Zhang, Keyu Peng, Yuan Jing, Jyotishmoy Borah, Guangyi Lin
Glycidyl methacrylate (GMA) was grafted onto diatomite (DE) to improve the interfacial bonding between GMA and rubber using “one-step”/“two-step” methods, respectively. The hydroxyl group on DE and the amine group on γ-aminopropyltriethoxysilane (KH550) react with the epoxy group on GMA in a ring-opening reaction during the process. The modified diatomite was characterized and analyzed by using Fourier transform infrared spectroscopy (FT-IR), X-ray fluorescence spectrometer (XRF), X-ray diffraction patterns, scanning electron microscopy (SEM), and thermogravimetric analysis (TGA). Natural rubber/diatomite (NR/DE) composites were also prepared using a wet mixing method and investigated the interfacial interactions between different DE and NR in detail using dynamic mechanical analysis (DMA) and rubber process analyzer (RPA). The result showed the improved mechanical properties of NR/DE composites for both “one-step” and “two-step” methods; however, the “two-step” method is found to be more effective. Compared with the unmodified NR/DE composites, the “two-step” modified NR/DE composites exhibited an increase in 37.8% tensile strength, 25.1% tear strength, 11.7% abrasion resistance, and 24% wet slip resistance, respectively. In addition to these, GMA has minimal effect on the elongation at break retention of the rubber composites after aging. These results showed valuable insights for the further application of diatomite in rubber.
{"title":"Glycidyl methacrylate-modified diatomite as reinforcing filler for natural rubber composite","authors":"Meng Zhao, Hao Duan, Linfeng Han, Lin Zhang, Keyu Peng, Yuan Jing, Jyotishmoy Borah, Guangyi Lin","doi":"10.1007/s00396-024-05304-4","DOIUrl":"https://doi.org/10.1007/s00396-024-05304-4","url":null,"abstract":"<p>Glycidyl methacrylate (GMA) was grafted onto diatomite (DE) to improve the interfacial bonding between GMA and rubber using “one-step”/“two-step” methods, respectively. The hydroxyl group on DE and the amine group on γ-aminopropyltriethoxysilane (KH550) react with the epoxy group on GMA in a ring-opening reaction during the process. The modified diatomite was characterized and analyzed by using Fourier transform infrared spectroscopy (FT-IR), X-ray fluorescence spectrometer (XRF), X-ray diffraction patterns, scanning electron microscopy (SEM), and thermogravimetric analysis (TGA). Natural rubber/diatomite (NR/DE) composites were also prepared using a wet mixing method and investigated the interfacial interactions between different DE and NR in detail using dynamic mechanical analysis (DMA) and rubber process analyzer (RPA). The result showed the improved mechanical properties of NR/DE composites for both “one-step” and “two-step” methods; however, the “two-step” method is found to be more effective. Compared with the unmodified NR/DE composites, the “two-step” modified NR/DE composites exhibited an increase in 37.8% tensile strength, 25.1% tear strength, 11.7% abrasion resistance, and 24% wet slip resistance, respectively. In addition to these, GMA has minimal effect on the elongation at break retention of the rubber composites after aging. These results showed valuable insights for the further application of diatomite in rubber.</p><h3 data-test=\"abstract-sub-heading\">Graphical Abstract</h3>","PeriodicalId":520,"journal":{"name":"Colloid and Polymer Science","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141968886","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-05DOI: 10.1007/s00396-024-05302-6
Mengdie Yu, Hechang Shi, Yancun Yu, Hongda Cheng, Ye Zhang, Changyu Han
In order to overcome the drawback of poor mechanical and rheological properties and potentially extend the poly(butylene adipate-co-butylene terephthalate) (PBAT) application market, in this work, we developed PBAT blend with excellent comprehensive performance through blending with biodegradable poly(L-lactide) (PLLA) and poly(D-lactide) (PDLA). Two-step melt blending and constant polylactide (PLA) content were devised to prepared PBAT blend. The effect of PDLA on the crystallization properties, rheological properties, miscibility, morphological structure, and mechanical properties of blend was investigated. According to torque-time curve and DSC results, PLA stereocomplex (SC-PLA) crystallites were formed in blend system. DMA results confirmed that the compatibility between PBAT and PLLA was not changed when PDLA was introduced. SEM results showed that the phase morphology of PBAT/20PLLA/0PDLA blend displayed typical sea-island structure and the particle size of dispersed phase decreased accompanying by agglomeration when PDLA was added. Rheological results showed that percolation SC-PLA network structure had formed and a much denser crystallite network could be formed with high PDLA content, which significantly enhanced rheological properties of blend. The mechanical results demonstrated that the addition of PDLA could significantly enhance mechanical properties. The blend with 6 wt% PDLA presented yield strength, elongation at break, and modulus about 13.3 MPa, 307%, and 221.2 MPa, respectively, the yield strength and modulus increased by 141.7% and 54.7% compared with the pure PBAT.