Startseite Fabrication of polylactic acid nanofibrous yarns for piezoelectric fabrics
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Fabrication of polylactic acid nanofibrous yarns for piezoelectric fabrics

  • Xin Meng , Xiaoyu Jia , Yuanzhang Qi , Dagang Miao und Xu Yan EMAIL logo
Veröffentlicht/Copyright: 15. Mai 2023
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e-Polymers
Aus der Zeitschrift e-Polymers Band 23 Heft 1

Abstract

With the rapid development of smart wearable devices and the urgent demands for new energy resources, fibrous flexible power supply units had attracted a lot of interest. Here, we reported the fabrication of polylactic acid (PLA) piezoelectric nanofibrous yarn-based fabric through conjugated electrospinning and weaving process. Five kinds of PLA yarns including poly(l-lactide) (PLLA), poly(d-lactide) (PDLA), PLLA positive/PDLA negative, PDLA positive/PLLA negative, and PLLA/PDLA mixture (1:1 w/w) ones were prepared and investigated. Among these, the PLLA/PDLA yarn had more uniform and oriented structure with 301 MPa tensile strength, which could meet the requirement of weaving. A 4 cm × 4 cm woven PLLA/PDLA fabric could provide a maximum current of 90.86 nA and a voltage of 8.69 V under 5 N force, and the piezoelectricity could be enhanced by the fabric area and the applied force. This approach may be helpful for the design of wearing generators.

1 Introduction

Nowadays, under the background of carbon neutralization, the development of renewable and environmentally friendly energy technologies was urgently needed to replace the traditional fossil energy (1,2,3,4,5,6,7,8). In addition to the rapid development of intelligent wearable technology, light and wearable power supply units were also a urgent demand (9,10,11).

Recently, various materials were developed to collect energy based on different working mechanisms, such as piezoelectricity (12,13,14) and triboelectricity (15,16). Specifically, piezoelectric nanogenerators (PENGs) which convert mechanical energy into electrical energy through piezoelectric materials had attracted a lot of interest since 2006 (13). Piezoelectric materials were expanded from inorganic materials such as ZnO (13), BaTiO3 (17), and perovskite lead zirconate titanate (18) to polymers including poly(vinylidene fluoride) (PVDF) (19), poly(lactide) (PLA) (20), and their copolymers. To obtain flexible PENGs for wearing, these materials had been isolated or blended electrospun into nanofibrous films (21,22,23). Among these electrospun piezoelectric films, the PLA-based ones had been paid much attention due to its low cost, biodegradability, and biocompatibility (24,25). Generally, PLA had two isomers, namely poly(l-lactide) (PLLA) and poly(d-lactide) (PDLA) (26). Both PLLA and PDLA exhibited weak piezoelectricity (27,28). It had been reported that the PDLA/PLLA multilayer films could generate a larger piezoelectric resonance (28,29,30).

However, the flexible piezoelectric films still had some shortcomings in wearable applications, such as poor air permeability and being less comfortable to wear (31). To overcome these challenges, various self-powered yarns and fabrics were developed (32,33,34). Dai et al. had prepared poly(vinylidene fluoride-co-tri-fluoroethylene) P(VDF-TrFE) piezoelectric yarns by electrospinning, and the woven fabrics achieved 38 nA current and 2.7 V voltage under 15 N pressure (32). However, PLA nanofibrous yarns were rarely mentioned in that study.

In this article, we reported the fabrication of PLA yarns by conjugated electrospinning, which had two spinnerets with opposite polarity. Here, five types of PLA yarns were prepared including pure PLLA yarn, pure PDLA yarn, PLLA positive/PDLA negative yarn, PLLA negative/PDLA positive yarn, and PDLA/PLLA yarn. The morphology of the prepared yarns was examined by scanning electron microscope (SEM). The crystalline properties and mechanical properties of the yarns were also investigated. The yarns were woven into fabrics, and the piezoelectric properties of the fabrics were examined.

2 Materials and methods

2.1 Materials

PLLA (Dongguan Wanda Plastic Raw Materials Co., Ltd, 4032D), PDLA (Dongguan Wanda Plastic Raw Materials Co., Ltd, 4043D), and the mixture of PLLA and PDLA (1:1 w/w) were dissolved into N,N-dimethylformamide (Shanghai Sinopharm Chemical Reagent) at ambient temperature, humidity, and stirring for 24 h at room temperature. The PLLA, PDLA, and the PLLA/PDLA solution concentrations were all 8 wt%. A copper wire with a diameter of 0.05 mm (B&R Company, China) was selected as the core yarn and conductive electrode.

2.2 Preparation of continuous PLA nanofiber yarns and fabric

The conjugate electrospinning process is illustrated in Figure 1. Before electrospinning, the prepared solution was loaded into a 5 mL nozzle with a 25-gauge flat metal nozzle and placed in the nozzle holder of the conjugate spinning machine, using the Cu fiber as the core electrode, and the spinning parameters were set as follows: the distance between the nozzle and the trumpet collector of 12 cm, the positive and negative voltage of ±6.5 kV, the solution feeding rate of 0.4 mL·h−1, the yarn winding speed rate of 1 mm·min−1, and the speed of the trumpet of 300 rpm.

Figure 1 
                  Preparation process of conjugated electrospun PLA nanofiber yarns and fabrics: (a) schematic diagram of conjugated electrospun Cu core/PLA shell yarn, (b) devices for conjugated electrospun PLA nanofiber yarn, (c) the twisting trumpet during electrospinning process, (d) the obtained PLA nanofiber yarn and the cross section images of the yarn, (e) home-made weaving device, (f) hand-weaving process, and (g) the prepared PLA fabric.
Figure 1

Preparation process of conjugated electrospun PLA nanofiber yarns and fabrics: (a) schematic diagram of conjugated electrospun Cu core/PLA shell yarn, (b) devices for conjugated electrospun PLA nanofiber yarn, (c) the twisting trumpet during electrospinning process, (d) the obtained PLA nanofiber yarn and the cross section images of the yarn, (e) home-made weaving device, (f) hand-weaving process, and (g) the prepared PLA fabric.

During the electrospinning process, the positive and negative high-voltage power supply connected to the two spinnerets and the positive- and negative-charged jets were spayed and flied onto the trumpet to form a fiber bundle (32,34), as suggested in Figure 1a and b. Here, we chose five combinations of spinning solutions connected to the positive/negative power supply, which were pure PLLA, pure PDLA, PLLA positive/PDLA negative, PDLA positive/PLLA negative, and PLLA/PDLA mixture. With the rotating of the trumpet, the as-spun fibers were twisted onto the core Cu wire (Figure 1c) and then the continuous core-spun PLA/Cu yarns were obtained, as shown in Figure 1d. Through a small home-made spinning device shown in Figure 1e, the continuous flexible PLA nanofiber yarns were woven into 1/1 plain fabric with warp and weft yarns of the same type. Moreover, during the hand-weaving process as suggested in Figure 1f, the warp yarn density was 17 cm−1 and the weft yarn density was 4 cm−1. The obtained fabric is displayed in Figure 1g.

2.3 Characterization

The real images of the prepared yarns and fabrics were taken using a mobile phone camera (Huawei, Honor 20). The morphology of the prepared nanofiber yarns was observed by a desktop SEM (Phenom Pro, Thermo Fisher Scientific). The crystalline melting behavior of the prepared PLA fibers was examined by a differential scanning calorimeter (DSC, Mettler Toledo, Switzerland) under the protection of nitrogen and at a room temperature of 23–250°C with a ramp-up rate of 10°C·min−1. The chemical structures of the as-spun PLA fibers were characterized by infrared spectroscopy (Nicolet 5700; Thermo Fisher Scientific, USA) in the range of 500–4,000 cm−1. The mechanical properties of the yarns and fabrics were tested by a universal tensile strength machine (Instron 3382, Instron, USA) with a length of 70 mm and a 4 cm × 4 cm area at a stretching speed of 10 mm·min−1, respectively.

The PLA fabric samples were completely wrapped with polyimide tape, and the twisted Cu cores of the warp yarns were used as the electrode. The piezoelectricity of the fabric was examined by a laboratory-assembled piezoelectric test equipment with a picoammeter (Keithley 6487), current amplifier (SR570), and digital oscilloscope (GDS-2102; GW Instek). The pressure was provided by a circulation device (ds-400) with a reciprocating telescopic linear speed regulator and checked by a tensimeter (HG-100; HBO instrument, China).

3 Results and discussion

3.1 Morphology of the prepared PLA nanofiber yarns

Figure 2 shows the morphology of the prepared PLA as-spun yarns and fibers with different combinations, including pure PLLA yarn (Figure 2a and a1), pure PDLA yarn (Figure 2b and b1), PLLA/PDLA yarn (Figure 2c and c1), PLLA positive/PDLA negative (Figure 2d and d1), and PDLA positive/PLLA negative (Figure 2e and e1). It could be found that in each case, the electrospun PLA fibers twined round the Cu core tightly forming a relatively uniform covering yarn without any obvious nodules and defects. The surface fibers of the yarns generally had a directional arrangement due to the twisting process.

Figure 2 
                  SEM images of as-spun PLA yarns and fibers. (a) PLLA yarn, (b) PDLA yarn, (c) PLLA/PDLA yarn, (d) PLLA positive/PDLA negative yarn, (e) PDLA positive/PLLA negative yarn, and the SEM images of corresponding fibers (a1–e1), as well as the fiber diameter distribution (a2–e2).
Figure 2

SEM images of as-spun PLA yarns and fibers. (a) PLLA yarn, (b) PDLA yarn, (c) PLLA/PDLA yarn, (d) PLLA positive/PDLA negative yarn, (e) PDLA positive/PLLA negative yarn, and the SEM images of corresponding fibers (a1–e1), as well as the fiber diameter distribution (a2–e2).

Moreover, from Figure 2a1–e1, it was found that when the positive and negative power supply connected to the same solution (Figure 2a1–c1), the as-spun fibers were more smooth, uniform, and better oriented than the different solution cases (Figure 2d1 and e1). This may be due to the following reasons: the uneven charge distribution in the different solution jets, the as-spun fibers with larger difference in diameter being interspersed with each other, and the adhesion phenomenon would have affected the fibers’ morphology.

The distribution of the fiber diameters is shown in Figure 2a2–e2. It could be found that the electrospun pure PLLA fibers had smaller diameters of about 562 ± 22 nm (Figure 2a2), and the as-spun pure PDLA fibers had average diameters of about 661 ± 19 nm (Figure 2b2). However, when the PLLA and PDLA were mixed in the solution, the as-spun fibers had a larger average diameter of about 666 ± 20 nm (Figure 2c2). When the PLLA and PDLA were electrospun with different power polarity, the average fiber diameters were located in the range of pure PLLA and PDLA ones.

3.2 FTIR and DSC analysis of electrospun PLA fibers

Figure 3 shows the fourier transform infrared (FTIR) spectra and DSC curves of the PLA raw materials and the as-spun PLA fibers. From the FTIR spectra in Figure 3a, we found that the characteristic absorption peaks of all PLA species were almost the same, with C–H stretching vibration absorption peaks at around 3,002–2,932 cm−1 and C═H stretching vibration absorption peaks at 1,750 cm−1, bending vibration absorption peaks of C–H of –CH3 at 1,452 cm−1, 1,380 cm−1, C═H bending vibration absorption peaks at 1,180 cm−1, and the asymmetric stretching and symmetric stretching vibrational peaks of C–O–C at 1,085 cm−1. This suggested that none of the characteristic peaks of the various PLA was changed after electrospinning.

Figure 3 
                  (a) FTIR spectra of PLLA, PDLA powders, and the different types of electrospun PLA fibers and (b) DSC curves of the as-spun PLA fibers.
Figure 3

(a) FTIR spectra of PLLA, PDLA powders, and the different types of electrospun PLA fibers and (b) DSC curves of the as-spun PLA fibers.

Figure 3b displays the DSC results for different types of electrospun PLA nanofibers (PLLA, PDLA, PDLA/PLLA). It was suggested that with the increase of temperature, all PLA fibers showed an exothermic peak at around 70°C. When the temperature raised to more than 150°C, melt peaks appeared in the pure PLLA, pure PDLA, PLLA positive/PDLA negative, and PLLA negative/PDLA positive samples. For pure PLLA electrospun fiber, there were two higher peaks, and PDLA fiber had one peak; both the PLLA positive/PDLA negative and PLLA negative/PDLA positive fibers also had two weaker peaks due to the mixture of PLLA and PDLA fibers (28,30). However, for the electrospun PDLA/PLLA (1:1 w/w) fibers, the melting point shifted to approximately 220°C with a melting point increase of approximately 50°C and better heat resistance (35,36), which might result from the formation of stereocomplex crystal in the mixture of PDLA and PLLA (26,35,36).

3.3 Mechanical properties of PLA yarns and fabrics

The mechanical properties of the as-spun PLA yarns were first investigated to ensure that they could meet the weaving requirements. As shown in Figure 4a, the crystallinity of the samples affected its tensile properties, so there was a large difference in mechanical properties between the different types of PLA yarns. The semi-crystalline pure PLLA yarn had a tensile strain of 16.2% and a tensile strength of 265 MPa, which were much less than the crystalline pure PDLA yarn with a tensile strain of 23.2% and a tensile strength of 285 MPa; the yarn formed by spinning PLLA and PDLA at different polarity charges had the expected tensile strain and strength between PLLA and PDLA. Remarkably, the tensile strain of the PLLA/PDLA yarns was 24.9% and the tensile strength was 301 MPa, which were consistent with the previously assumed results. These results suggested that the PLLA/PDLA yarn could meet the requirements for weaving.

Figure 4 
                  (a) Stress–strain curves of the as-spun PLA yarns, (b) the prepared PLA fabrics of 4 cm × 4 cm with different PLA yarns, (c) stress–strain curves of the PLA fabrics, and (d) the flexibility of the PLLA/PDLA fabrics.
Figure 4

(a) Stress–strain curves of the as-spun PLA yarns, (b) the prepared PLA fabrics of 4 cm × 4 cm with different PLA yarns, (c) stress–strain curves of the PLA fabrics, and (d) the flexibility of the PLLA/PDLA fabrics.

By home-made weaving tools, the prepared PLA yarns were woven into fabrics, as displayed in Figure 4b. The mechanical properties of the fabrics were also examined and shown in Figure 4c. Similar to the PLA yarns, the PLLA/PDLA fabric had the highest tensile strength. Obviously, the stress–strain curves of the fabric were not straight lines but a stepwise variation. The reason was that the yarns in the fabric did not break in the ideal way (all yarns break at the same time), but partly and in sequence. Therefore, the stretching device did not stop immediately at the start of breaking, but continued to stretch until the stress dropped by 30% before defaulting to complete breaking. These test results proved that the prepared PLLA/PDLA fabrics had excellent mechanical properties for wearing.

Nowadays, the wearing power supply required flexibility to adapt to various use environments. As shown in Figure 4d, the flexibility of the prepared fabrics was examined by bending, deformation, and restoration. It was found that the PLLA/PDLA fabric could be bent over 180° and even after applying strong external forces, it could recover fast from deformation with structural stability. The flexibility and stability of the PLLA/PDLA fabric ensured it could be potentially applied for wearing.

3.4 Piezoelectric properties of flexible PLA fabrics

It had been reported that electrospun PLA could enhance orientation and result piezoelectricity under the polarizing effect of the external electric field (27). Accordingly, we examined the piezoelectric properties of the prepared fabrics. First, the piezoelectric voltages of the different PLA fabrics suggested in Figure 4b were tested. As shown in Figure 5a and b, all the prepared PLA fabrics showed piezoelectricity under 5 N forces, and the PLLA/PDLA fabric had the highest open circuit charge of 8.69 V and a short circuit current of 90.86 nA (Figure 5b), which were higher than the PVDF nanofibrous fabric (32). Compared with the pure PLLA fabric, the generated voltage and current increased about 228% and 210%, respectively. The increasing of the piezoelectricity of the PLLA/PDLA one may be attributed to the forming of a stereocomplex crystal in the mixture of PDLA and PLLA, as suggested in Figure 3b.

Figure 5 
                  The piezoelectric voltages (a) and currents (b) of 4 cm × 4 cm PLA fabrics under 5 N forces, the voltages (c) and currents (d) of 4 cm × 4 cm PLLA/PDLA fabric under different forces, and the voltages (e) and currents (f) of PLLA/PDLA fabric with different areas under 5 N forces.
Figure 5

The piezoelectric voltages (a) and currents (b) of 4 cm × 4 cm PLA fabrics under 5 N forces, the voltages (c) and currents (d) of 4 cm × 4 cm PLLA/PDLA fabric under different forces, and the voltages (e) and currents (f) of PLLA/PDLA fabric with different areas under 5 N forces.

Moreover, the piezoelectric properties of the PLLA/PDLA fabrics were examined under different forces and different areas, as displayed in Figure 5c–f. It was found that with the increasing forces and areas, the generated voltages and currents were also improved. These results indicated that the prepared PLLA/PDLA nanofibrous fabric had potential application in flexible power supply for wearing.

4 Conclusions

In summary, we had successfully prepared various PLA nanofibrous yarns by conjugate electrospinning. Since the conjugate electrospinning contained two spinnerets connected to opposite polarity power supply, we designed five types of PLA nanofibrous yarns including pure PLLA, pure PDLA, PLLA positive/PDLA negative, PDLA positive/PLLA negative, and PLLA/PDLA mixture (1:1 w/w) ones. It was found that the two spinnerets with the same solutions would produce more uniform and oriented yarns. The DSC examination suggested that the PLLA/PDLA yarns would raise the melt point temperature due to the formation of stereocomplex crystallization in the mixture of PDLA and PLLA. Moreover, the PLLA/PDLA yarns showed 301 MPa tensile strength, which was higher than the other yarns. Furthermore, a 4 cm × 4 cm woven PLLA/PDLA fabric could generate 8.69 V voltage and 90.86 nA current under 5 N forces, which is much higher than the other PLA nanofibrous fabrics. These results indicated that the PLLA/PDLA nanofibrous fabric could be used as a piezoelectric nanogenerator and had potential application in self-powered wearing textile fields.

  1. Funding information: This work was supported by the Postdoctoral Science Foundation of China (2020M671998), the National Natural Science Foundation of China (51703102), Shandong Province Higher Education Youth Innovation Technology Support Program (2021KJ013), and the State Key Laboratory of Bio-Fibers and Eco-Textiles (Qingdao University) no. ZKT35.

  2. Author contributions: Xin Meng: writing – original draft, writing – review and editing, methodology, formal analysis, investigation; Xiaoyu Jia: formal analysis, conceptualization, writing – review and editing; Yuanzhang Qi: formal analysis, visualization; Dagang Miao: formal analysis, resources; Xu Yan: writing – review and editing, supervision, project administration.

  3. Conflict of interest: The authors state no conflict of interest.

  4. Data availability statement: The raw/processed data required to reproduce these findings are available from the corresponding author on a reasonable request.

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Received: 2023-04-06
Revised: 2023-04-21
Accepted: 2023-04-26
Published Online: 2023-05-15

© 2023 the author(s), published by De Gruyter

This work is licensed under the Creative Commons Attribution 4.0 International License.

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  17. Effect of different proportions of CNTs/Fe3O4 hybrid filler on the morphological, electrical and electromagnetic interference shielding properties of poly(lactic acid) nanocomposites
  18. Doping silver nanoparticles into reverse osmosis membranes for antibacterial properties
  19. Melt-blended PLA/curcumin-cross-linked polyurethane film for enhanced UV-shielding ability
  20. The affinity of bentonite and WO3 nanoparticles toward epoxy resin polymer for radiation shielding
  21. Prolonged action fertilizer encapsulated by CMC/humic acid
  22. Preparation and experimental estimation of radiation shielding properties of novel epoxy reinforced with Sb2O3 and PbO
  23. Fabrication of polylactic acid nanofibrous yarns for piezoelectric fabrics
  24. Copper phenyl phosphonate for epoxy resin and cyanate ester copolymer with improved flame retardancy and thermal properties
  25. Synergistic effect of thermal oxygen and UV aging on natural rubber
  26. Effect of zinc oxide suspension on the overall filler content of the PLA/ZnO composites and cPLA/ZnO composites
  27. The role of natural hybrid nanobentonite/nanocellulose in enhancing the water resistance properties of the biodegradable thermoplastic starch
  28. Performance optimization of geopolymer mortar blending in nano-SiO2 and PVA fiber based on set pair analysis
  29. Preparation of (La + Nb)-co-doped TiO2 and its polyvinylidene difluoride composites with high dielectric constants
  30. Effect of matrix composition on the performance of calcium carbonate filled poly(lactic acid)/poly(butylene adipate-co-terephthalate) composites
  31. Low-temperature self-healing polyurethane adhesives via dual synergetic crosslinking strategy
  32. Leucaena leucocephala oil-based poly malate-amide nanocomposite coating material for anticorrosive applications
  33. Preparation and properties of modified ammonium polyphosphate synergistic with tris(2-hydroxyethyl) isocynurate for flame-retardant LDPE
  34. Thermal response of double network hydrogels with varied composition
  35. The effect of coated calcium carbonate using stearic acid on the recovered carbon black masterbatch in low-density polyethylene composites
  36. Investigation of MXene-modified agar/polyurethane hydrogel elastomeric repair materials with tunable water absorption
  37. Damping performance analysis of carbon black/lead magnesium niobite/epoxy resin composites
  38. Molecular dynamics simulations of dihydroxylammonium 5,5′-bistetrazole-1,1′-diolate (TKX-50) and TKX-50-based PBXs with four energetic binders
  39. Preparation and characterization of sisal fibre reinforced sodium alginate gum composites for non-structural engineering applications
  40. Study on by-products synthesis of powder coating polyester resin catalyzed by organotin
  41. Ab initio molecular dynamics of insulating paper: Mechanism of insulating paper cellobiose cracking at transient high temperature
  42. Effect of different tin neodecanoate and calcium–zinc heat stabilizers on the thermal stability of PVC
  43. High-strength polyvinyl alcohol-based hydrogel by vermiculite and lignocellulosic nanofibrils for electronic sensing
  44. Impacts of micro-size PbO on the gamma-ray shielding performance of polyepoxide resin
  45. Influence of the molecular structure of phenylamine antioxidants on anti-migration and anti-aging behavior of high-performance nitrile rubber composites
  46. Fiber-reinforced polyvinyl alcohol hydrogel via in situ fiber formation
  47. Preparation and performance of homogenous braids-reinforced poly (p-phenylene terephthamide) hollow fiber membranes
  48. Synthesis of cadmium(ii) ion-imprinted composite membrane with a pyridine functional monomer and characterization of its adsorption performance
  49. Impact of WO3 and BaO nanoparticles on the radiation shielding characteristics of polydimethylsiloxane composites
  50. Comprehensive study of the radiation shielding feature of polyester polymers impregnated with iron filings
  51. Preparation and characterization of polymeric cross-linked hydrogel patch for topical delivery of gentamicin
  52. Mechanical properties of rCB-pigment masterbatch in rLDPE: The effect of processing aids and water absorption test
  53. Pineapple fruit residue-based nanofibre composites: Preparation and characterizations
  54. Effect of natural Indocalamus leaf addition on the mechanical properties of epoxy and epoxy-carbon fiber composites
  55. Utilization of biosilica for energy-saving tire compounds: Enhancing performance and efficiency
  56. Effect of capillary arrays on the profile of multi-layer micro-capillary films
  57. A numerical study on thermal bonding with preheating technique for polypropylene microfluidic device
  58. Development of modified h-BN/UPE resin for insulation varnish applications
  59. High strength, anti-static, thermal conductive glass fiber/epoxy composites for medical devices: A strategy of modifying fibers with functionalized carbon nanotubes
  60. Effects of mechanical recycling on the properties of glass fiber–reinforced polyamide 66 composites in automotive components
  61. Bentonite/hydroxyethylcellulose as eco-dielectrics with potential utilization in energy storage
  62. Study on wall-slipping mechanism of nano-injection polymer under the constant temperature fields
  63. Synthesis of low-VOC unsaturated polyester coatings for electrical insulation
  64. Enhanced apoptotic activity of Pluronic F127 polymer-encapsulated chlorogenic acid nanoparticles through the PI3K/Akt/mTOR signaling pathway in liver cancer cells and in vivo toxicity studies in zebrafish
  65. Preparation and performance of silicone-modified 3D printing photosensitive materials
  66. A novel fabrication method of slippery lubricant-infused porous surface by thiol-ene click chemistry reaction for anti-fouling and anti-corrosion applications
  67. Development of polymeric IPN hydrogels by free radical polymerization technique for extended release of letrozole: Characterization and toxicity evaluation
  68. Tribological characterization of sponge gourd outer skin fiber-reinforced epoxy composite with Tamarindus indica seed filler addition using the Box–Behnken method
  69. Stereocomplex PLLA–PBAT copolymer and its composites with multi-walled carbon nanotubes for electrostatic dissipative application
  70. Enhancing the therapeutic efficacy of Krestin–chitosan nanocomplex for cancer medication via activation of the mitochondrial intrinsic pathway
  71. Variation in tungsten(vi) oxide particle size for enhancing the radiation shielding ability of silicone rubber composites
  72. Damage accumulation and failure mechanism of glass/epoxy composite laminates subjected to repeated low velocity impacts
  73. Gamma-ray shielding analysis using the experimental measurements for copper(ii) sulfate-doped polyepoxide resins
  74. Numerical simulation into influence of airflow channel quantities on melt-blowing airflow field in processing of polymer fiber
  75. Cellulose acetate oleate-reinforced poly(butylene adipate-co-terephthalate) composite materials
  76. Radiation shielding capability and exposure buildup factor of cerium(iv) oxide-reinforced polyester resins
  77. Recyclable polytriazole resins with high performance based on Diels-Alder dynamic covalent crosslinking
  78. Adsorption and recovery of Cr(vi) from wastewater by Chitosan–Urushiol composite nanofiber membrane
  79. Comprehensive performance evaluation based on electromagnetic shielding properties of the weft-knitted fabrics made by stainless steel/cotton blended yarn
  80. Review Articles
  81. Preparation and application of natural protein polymer-based Pickering emulsions
  82. Wood-derived high-performance cellulose structural materials
  83. Flammability properties of polymers and polymer composites combined with ionic liquids
  84. Polymer-based nanocarriers for biomedical and environmental applications
  85. A review on semi-crystalline polymer bead foams from stirring autoclave: Processing and properties
  86. Rapid Communication
  87. Preparation and characterization of magnetic microgels with linear thermosensitivity over a wide temperature range
  88. Special Issue: Biodegradable and bio-based polymers: Green approaches (Guest Editors: Kumaran Subramanian, A. Wilson Santhosh Kumar, and Venkatajothi Ramarao)
  89. Synthesis and characterization of proton-conducting membranes based on bacterial cellulose and human nail keratin
  90. Fatigue behaviour of Kevlar/carbon/basalt fibre-reinforced SiC nanofiller particulate hybrid epoxy composite
  91. Effect of citric acid on thermal, phase morphological, and mechanical properties of poly(l-lactide)-b-poly(ethylene glycol)-b-poly(l-lactide)/thermoplastic starch blends
  92. Dose-dependent cytotoxicity against lung cancer cells via green synthesized ZnFe2O4/cellulose nanocomposites
Heruntergeladen am 10.9.2025 von https://www.degruyterbrill.com/document/doi/10.1515/epoly-2023-0030/html
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