Poly Lactic Acid Research Articles

Flat biofilms extrusion of poly(lactic acid)/poly(butylene adipate‐co‐terephthalate) grafted with glycidyl methacrylate blends: Toward ecological packaging for sustainability

AbstractBlends of poly(lactic acid) (PLA)/poly(butylene adipate‐co‐terephthalate) grafted with glycidyl methacrylate (PBAT‐g‐GMA) were developed to produce flat and flexible biofilms through extrusion. The PLA/PBAT‐g‐GMA (90%/10%, 80%/20%, 70%/30%, and 60%/40% by mass) blends were processed in the internal mixer, injection molded, and manufactured into flat films. The optimal composition to produce flexible biofilms was PLA/PBAT‐g‐GMA (60/40%), as it demonstrated a decrease in elastic modulus of 53.2% and a significant gain in elongation at a break of 4923% about pure PLA. The incorporation of 40% PBAT‐g‐GMA in PLA increased the torque (Z) by 208%, while the melt flow index (MFI) decreased by 51.57%, compared to PLA. Additionally, the degradation rate (Rz) and molar mass loss (Rm) during processing were minimized, indicating that 40% PBAT‐g‐GMA enhanced stability of the PLA matrix. Fourier transform infrared spectroscopy indicated interactions between the GMA of PBAT‐g‐GMA and PLA, justifying the increase in viscosity and elongation at break. The PLA/PBAT‐g‐GMA (60/40%) composition showed a transmittance in the range of 20%–48% (400–800 nm) and an oxygen gas permeability of 1.56 × 10−5 cm3 STP/cm−2 h bar, indicating its potential for applications in packaging with optical barrier properties. Scanning electron microscopy (SEM) revealed ligaments in the interfacial region between PLA and PBAT‐g‐GMA, confirming the good performance in elongation at break. The results presented are essential for the plastics processing sector, aiming to develop eco‐friendly packaging.

Effect of Fiber Cross-Sectional and Surface Properties on the Degradation of Biobased Polymers

Biobased polymers such as polylactic acid (PLA) and polybutylene succinate (PBS) break down naturally under certain environmental conditions. The efficiency of degradation can be linked directly to fiber surface properties, which influence polymer accessibility. Here, the degradation of PLA and PBS fibers with six different cross-sections was investigated. The fibers were aged by hydrolysis and UV exposure in an accelerated weathering test, followed by an ISO 20200 laboratory-scale disintegration test with non-aged fibers as controls. The polymers were analyzed by differential scanning calorimetry, Fourier transform infrared spectroscopy, and gel permeation chromatography, comparing the polymer granulate, virgin fibers, and UV-exposed fibers. It was found that the molecular mass and crystallinity of PBS changed more than PLA during spinning. Several PLA samples were completely degraded, whereas all the PBS samples remained intact. Furthermore, surface openings appeared on the PLA fibers during weathering, suggesting greater sensitivity to UV exposure and hydrolysis than PBS. A clear correlation between the fiber surface area and the degradation rate was observed for all samples, but the correlation was positive for PLA and negative for PBS. The slower degradation of PBS fibers with a larger surface area may reflect the ability of PBS to preserve itself by further crystallization during degradation processes at temperatures higher than the glass transition point. The data clearly show that the analysis of single degradation mechanisms is insufficient to predict the behavior of material under real-world conditions, where different degradation mechanisms may work in parallel or consecutively, and may show interdependencies.

Fabrication of Cellulose Nanofiber-Reinforced Polylactic Acid Nanocomposite Containing Anthocyanidin-Based Red Cabbage Extract For Anti-counterfeiting Thermochromic Ink

Fabrication of Cellulose Nanofiber-Reinforced Polylactic Acid Nanocomposite Containing Anthocyanidin-Based Red Cabbage Extract For Anti-counterfeiting Thermochromic Ink

Preparation of environmentally friendly ionic liquids-toughened polylactic acid/nanofibrillated cellulose composites with high strength and precipitation resistance

Polylactic acid (PLA) is one of the most promising biodegradable materials, but poor toughness severely limits its application. Ionic liquids (ILs) have excellent plasticizing effects on PLA, but strength reduction and plasticizer precipitation remain worrisome. Herein, nanofibrillated cellulose (NFC), with excellent morphology, high modulus and strength, was prepared to reinforce PLA plasticization systems. Moreover, its numerous surface hydroxyl groups were tailored to bond with ILs, reducing plasticizer precipitation. The different sulfonation degrees of NFCs (low LSNFC, medium MSNFC, high HSNFC) and the influence of NFC amounts (0–7 wt%) on the mechanical, thermal and plasticizer precipitation properties of PLA composites were investigated. The results indicate that network-like C2/C3-sulfonated NFCs were successfully prepared through simple processing steps. Noteworthy, the tensile elongations of PLA composites increased with the addition of IL-XSNFC (all three degrees), with no significant reduction in tensile strength and modulus. The addition of 7 wt% IL-HSNFC resulted in an elongation of 25.01 % for PLA composites, which is 3.6 times that of pure PLA. Adding 3 wt% IL-MSNFC achieved ultra-high impact toughness of 3.19 kJ/m2, nearly double that of pure PLA. Interestingly, with increasing sulfonation degree, the amount of ILs precipitation in PLA composites significantly decreased. The precipitation rate of the PLA composite with IL-HSNFC is only 24 % of the counterparts with IL-NFC. This work presents an innovative method to improve interface compatibility, providing a new strategy to reduce plasticizer precipitation and broaden the application scope of PLA.

A new strategy to prepare bio-based polylactic acid modifier for multi-functionality: Dopamine-grafted modified lignin

Currently, to address the performance deficiencies associated with high brittleness, inadequate thermal stability, and susceptibility to hydrolysis in polylactic acid (PLA), it is common practice to incorporate multiple or high proportions of additives. However, this approach raises concerns regarding interface compatibility, energy consumption, and environmental impact. In this context, we introduce an environmentally friendly, bio-based PLA modifier that is facile to prepare and facilitates multi-functional applications at a minimal dosage. The presence of a benzene ring structure in lignin endows the material with ultraviolet (UV) resistance, thermal stability, and hydrophobic characteristics, while the exceptional adhesion properties of polydopamine (PDA) enhance interfacial compatibility. A novel biomass polylactic acid modifier, designated as OL@PDA, has been synthesized by modifying low-molecular-weight lignin (OL) with PDA. Comparative analysis of OL@PDA/PLA composite materials reveals a 14.08 % increase in tensile strength and a 42.00 % enhancement in elongation at break relative to pure PLA. The incorporation of the lignin-derived benzene ring structure effectively transforms PLA from a hydrophilic to a hydrophobic material. Furthermore, the UV transmittance at 400 nm (T400 nm%) is recorded at 65.8 % for pure PLA, which significantly decreases to below 5 % for OL@PDA/PLA composites. The integration of OL@PDA as a modifier in PLA materials yields comprehensively performance enhancements while maintaining a low additive concentration.

The use of chain extenders as processing aids in the valorization of single-use polylactide (PLA) products by rotomolding

Biodegradable plastics in single-use products have increased in popularity as a way to reduce the negative environmental impact of conventional plastics and meet the tightening law regulations. However, their recyclability needs to be assessed, as the environmental behavior of single-use plastics, even if compostable, is not negligible. Polylactide (PLA) is susceptible to thermal, oxidative, hydrolytic, and mechanical degradation during reprocessing, so the conditions of such cycles must be accurately controlled. The necessity of using additives to reduce such degradations during rotational molding, a process with long cycle times and oxidizing atmosphere, has been demonstrated. Chain extenders based on a carbodiimide (Bioadimide® 100 - KI), a methylene diphenyl diisocyanate (MDI), and a polystyrene-acrylic copolymer (Joncryl® ADR-4368c - J) have been added to post-consumer PLA wastes. It has been demonstrated that these three chain extenders enabled obtaining a higher molecular weight of the reprocessed polymer, compared to the ∼50% reduction for the neat PLA. The use of carbodiimide yielded the most similar performance to that of unprocessed raw material. All samples provided adequate thermal stability and processing parameters for the rotational molding. Carbodiimide is considered the most efficient additive, as it increases the molecular mass of the polymer as it remains unchanged after processing. Similarly, KI-modified PLA rheological behavior remains unchanged after processing, which means this compound can reduce thermooxidative and hydrolytic degradation reactions. Thus contributing to the achievement of improved processability and better performance; in particular, impact strength increased from 1.06 ± 0.56 for PLA to 8.12 ± 2.28 kJ/m2 for KI-modified PLA, and toughness of 5.36 ± 1.61 to 61.49 ± 8.01 J/mm3, respectively, leading to rotomolded items without structural defects. On the opposite, the use of Joncryl® and MDI led to structural defects in the rotomolded parts despite a higher molecular weight of the polymer, which resulted in poor mechanical properties, although better than PLA without any additive. All three chain extenders resulted in an amorphous PLA structure with increased glass transition temperature and improved thermal stability, which correlated with the reduced emissions of volatile compounds compared to neat recycled PLA. The presented findings significantly contribute to a better understanding of PLA and its modifications at a molecular scale required for its efficient and possibly environmentally burden-free reprocessing. Gathered knowledge will be crucial for optimizing its environmental performance and widening its applications, particularly in a process with long cycle times and oxidative character, such as rotational molding.

Innovative technology for microalgal cell preservation through immobilization in polylactic acid nanofibers

Microalgae are of great biotechnological importance. Thus, it is essential to apply maintenance methods for the utilization of microalgae at any time. Facilitating microalgae adsorption processes on nanofibers may be a promising approach for microalgae preservation. Thus, the objective of this study was to apply poly (lactic acid) nanofibers in the preservation of microalgae Chlorella fusca LEB 111 cells. The nanofibers were characterized regarding their morphology, thermal properties, structural characteristics and wettability. The microalgae cells were immobilized on the nanofibers and stored for 30 days at room temperature, refrigeration and thermostated chamber. Free microalgae cells were also maintained for the same period under the same conditions of the traditional method of microalgae preservation, continuous replication. The cell viability of the free and immobilized cells on the nanofibers was analyzed by Neutral Red (NR) and Trypan Blue (TB). At the end of the experiment, the immobilized cells showed greater viability (94 and 100 %) compared to the free cells (84 %). The cultivation of immobilized cells showed significant cell growth on the 25th day of cultivation for the evaluated storage conditions (3.6, 3.6 and 2.8 g L−1 for refrigeration, room temperature and thermostatted chamber, respectively). Therefore, poly (lactic acid) nanofibers (PLA) are characterized as an innovative technology for microalgae maintenance.

Developing novel hybrid bilayer nanofibers based on polylactic acid with impregnation of chamomile essential oil and gallic acid-stabilized silver nanoparticles

This study presents fabrication and characterization of novel chamomile essential oil (CMO)/gallic acid-stabilized silver nanoparticles (gallic acid-nanosilver, GNS), embedded into polylactic acid (PLA)-based hybrid bilayer nanofibers (NFs). Where CMO was impregnated into polyvinyl alcohol (PVA)-polyethylene glycol (PEG) solution and electrospun simultaneously with PLA to obtain PLA/PVA-PEG-CMO NFs (PLA/CMO A2). Meanwhile, GNS were added to PVA-PEG-CMO and electrospun to obtain PLA/PVA-PEG-CMO-GNS NFs (PLA/CMO-GNS A3). Where pure PLA/PVA-PEG NFs were coded pure PLA/A1. Physicochemical properties of fabricated bilayer-NFs were performed using various approaches. Besides, porosity%, swelling, biodegradability, CMO release pattern, antioxidant, antibacterial activity and cytotoxicity were investigated. Study investigation revealed PLA-based bilayer NFs exhibited a biphasic release profile for impregnated CMO. Due to presence of GA, antioxidant property and biocompatibility of PLA/CMO-GNS A3 was superior compared to pure PLA/A1 and PLA/CMO A2. Antibacterial activity was enhanced in presence of CMO in PLA/CMO A2 than pure PLA/A1. Furthermore, addition of GNS in PLA/CMO-GNS A3 displayed highest antibacterial activity due to synergy of CMO/GNS. Finally, MTT assay with HFB4 fibroblasts demonstrated absence of cytotoxicity of bilayer-based NFs. Thus, study suggests that developed PLA/PVA-PEG NFs could be a promising candidate for tissue regeneration and food edible packaging in particular when impregnated with both CMO/GNS.

Breaking mechanical performance trade-off in 3D-printed complex lattice-inspired multi-cell tubes under axial compression

It is a long-standing challenge to balance the structural load capacity and toughness in the design of lightweight multi-cell tubes. To tackle this challenge, we provide two kinds of complex lattice-inspired composite multi-cell tubes. The composite multi-cell tubes consist of inner polylactic acid (PLA) complex lattice-inspired multi-cell tubes and outside aluminum tubes. The energy absorption capacity of these multi-cell tubes was evaluated under quasi-static axial compression. The effect of cross-sectional topology and thermal exposure were considered in the experiment. The results show that the integration of PLA tubes within aluminum tubes significantly enhances their energy absorption performance, effectively addressing the limitations posed by the low fracture strain of PLA. The synergistic effect between the aluminum and PLA tubes mitigates the fracture instability and distributes the load more evenly, resulting in improved specific energy absorption (SEA) and mean crushing force (MCF) up to 103.32% and 184.38%, respectively. In these composite tubes, a global self-similar layout can markedly enhance its energy absorption. However, their mechanical properties decrease significantly at 323K compared to room temperature. Overall, this research provides a novel approach to enhancing the mechanical performance of PLA tubes, paving the way for their application in engineering fields requiring lightweight and high-strength structures.

Full bio-based flame retardant towards multifunctional polylactic acid: Crystallization, flame retardant, antibacterial and enhanced mechanical properties

The preparation of flame-retardant high-performance polylactic acid (PLA) composites by adding green flame retardants have always been a challenge. In this work, an intumescent flame-retardant PCR based on phytic acid, chitosan, and resveratrol was successfully designed. Adding 4 wt% of PCR, the PLA-PCR composite was classified as UL-94 V-0 grade, with a LOI value increasing from 19.7 % (pure PLA) to 26.0 %, a peak heat release rate decreasing from 433 to 344 kW/m2. Owing to excellent compatibility of PCR, the mechanical strength and toughness of PLA-PCR composites have been improved, as reflected by a ~ 16 % increase in tensile strength, a ~ 73 % increase in impact strength and a ~ 57 % increase in toughness. In addition, PCR also presented plasticization effect on PLA, making it easier to process. This work provided a highly efficient and environmental-friendly modification approach for the development of multifunctional polymers.

Fabrication of composite RGD-tagged poly(lactic acid)-graphene oxide nanofiber containing bone-forming peptide-3 loaded-dendritic silica nanoparticles for bone regeneration in rabbit

In the current study, polylactic acid (PLA)/graphene oxide (GO) based composite scaffolds were fabricated by electrospinning method and then covalently modified with bone-forming peptide-3 (BFP-3)-loaded thiol-functionalized dendritic mesoporous silica nanoparticles (BFP-3@HS-DMSNs) and RGD. In this regard, PLA electrospinning nanofibers and composite of PLA/GO electrospinning nanofibers containing 0.02, 0.01, 0.04, 0.1, 0.2 % of GO were prepared and characterized in terms of mechanical strength, nanofibers diameter, thermal stability, crystallinity, specific surface area, total pore volume and cell adhesion properties. Among the prepared composites, PLA nanofibers containing 0.02 % GO demonstrated superior mechanical and morphological characteristics along with better cell adhesion for mesenchymal stem cell. Then, the PLA/0.02 %GO nanofiber was treated with plasma and consequently modified with N-(2-aminoethyl)maleimide linker which was applied for Cys-RGD and BFP-3@HS-DMSNs conjugation. The obtained results showed desirable adhesion of PLA/0.02 %GO nanofiber after incorporation of RGD (5 % of maleimide groups of the linker) and DMSNs which significantly increase cell adhesion potency (1.53 folds). By incorporation of BFP-3@HS-DMSNs (equivalent to 0.1 µg of BFP-3) to the RGD-tagged PLA/0.02 %GO nanofiber, the scaffold demonstrated better cytocompatibility and MSC differentiation to osteoblast based on biomineralization assay via alizarin red (4.2 folds) and alkaline phosphatase activity (1.7 folds) tests. In preclinical stage, after skull defect creation in rabbits, 5 treatments groups comprising PLA/0.02 %GO nanofiber, PLA/0.02 %GO/DMSNs, PLA/0.02 %GO/DMSNs/Cys-RGD, PLA/0.02 %GO/BFP-3@DMSNs and PLA/0.02%GO/BFP-3@DMSNs/Cys-RGD were used for bone regeneration in skull defects. After 3 months, the implantation of PLA/0.02GO/BFP-3@DMSNs/Cys-RGD showed higher bone regeneration based on CBCT imaging (18.875 mm2 bone formed area) in comparison with other treatment groups. This hybrid multimodal platform is purposely organized interactive processes which lead to potential bone regeneration.

CARACTERIZACIÓN DE LAS PROPIEDADES MECÁNICAS DEL ÁCIDO POLILÁCTICO (PLA) EN IMPRESIÓN 3D: PERSPECTIVAS A PARTIR DE TÉCNICAS AVANZADAS DE ANÁLISIS Y ORIENTACIONES DE IMPRESIÓN

This research examines the mechanical characteristics of polylactic acid (PLA) using a variety of experimental approaches, including analyses of printing orientations and the application of advanced methodologies such as digital image correlation (DIC) for accurate assessment of deformation, along with scanning electron microscopy (SEM) to evaluate fracture properties. Tensile strength, flexural, impact strength, compressive and shear strength were characterized in detail, highlighting the critical impact of layer deposition direction. These findings provide valuable information for optimizing orientation selection in specific additive manufacturing contexts, emphasizing the need to address anisotropy in 3D printed materials engineering. Keywords: Polymer; PLA; 3D-print; industrial process; Digital Image Correlation (DIC).

Utilizing foxtail millet husk waste for sustainable new bioplastic composites with enhanced thermal stability and biodegradability

Foxtail millet husk (FMH) is a byproduct that is not suitable for consumption and is often discarded as solid waste. However, it can be used as a raw material to develop novel bioplastic composites that transform agro-based leftovers into value-added goods. Herein, new bioplastic composites were developed from poly(lactic acid), poly(butylene adipate-co-terephthalate) and FMH based granules by Injection Molding. The required granules were generated via a solvent evaporation method. The resulted bioplastic composites were analyzed for their morphologies, mechanical properties, crystal structures, thermal stability, and melting and crystallization behaviors using various techniques, such as scanning electron microscopy, universal testing machine, X-ray diffraction, thermogravimetric analysis, and differential scanning calorimetry. Expressly, chemical bonding between FMH fibers and poly(lactic acid)/poly(butylene adipate-co-terephthalate) PLA/PBAT was confirmed through Fourier Transform infrared spectroscopy analysis. The inclusion of FMH lowered the impact strength of the PLA/PBAT combination, which was confirmed by mechanical analysis. Morphological findings confirmed that the PLA/PBAT combination had FMH aggregation. DSC thermograph revealed negligible differences in glass transition and melting temperatures of PLA/PBAT blend with and without FMH. The thermogravimetry results exhibit that the FMH can improve bioplastic thermal stability. The addition of FMH improved the biodegradability of the PLA/PBAT bioplastic composites. Overall, FMH waste can be repurposed for bioplastic composites with enhanced thermal stability and biodegradability. This reduces solid waste from agricultural practices and creates eco-friendly products. Further research could lead to more sustainable alternatives.

Superhydrophobic poly(lactic acid) membrane prepared with the induction of modified carbon dots for efficient separation of water-in-oil emulsions

Superhydrophobic separation membranes are considered to be one of the most promising technologies for oil-water separation. However, the plastic waste generated from discarded membranes poses a challenge to the preparation of degraded superhydrophobic separation membranes for achieving eco-friendly separation. In this study, superhydrophobic poly(lactic acid) (PLA) membranes were fabricated using a non-solvent induced phase separation method assisted by l-cysteine modified carbon dots (Cys-CDs). The synergistic effect of Cys-CDs-induced crystallization behavior of PLA and the phase separation process results in the evolution of the surface of the PLA-based membrane from a pistil-like structure to a multi-level micro-nano structure composed of dense lamellar nanofibers and microspheres with an increase in Cys-CDs content. At a Cys-CDs content of 5 wt%, the surface roughness of PLA-based separation membrane reached its maximum, and the water contact angle was as high as 159°. Remarkably, the superhydrophobic Cys-CDs/PLA membrane exhibited promising performance in the separation of water-in-oil emulsions, with a rejection rate of 99.98 % and a flux of 315.74 L·m−2·h−1·bar−1. Additionally, the superhydrophobic Cys-CDs/PLA separation membrane also demonstrates impressive properties such as acid-alkali resistance and rapid recycling into high-value chemicals. Consequently, this rapidly recoverable superhydrophobic porous Cys-CDs/PLA membrane shows great potential for practical applications in actual oil-water separation.

Development of puerarin-loaded poly(lactic acid) microspheres for sustained ocular delivery: In vitro/vivo evaluation

Diabetic retinopathy, an ocular complication of diabetes, is an important cause of blindness in adults. Puerarin is considered to have promising potential for clinical use in treating diabetic retinopathy. In this study, we designed a novel puerarin-loaded poly(lactic acid) sustained-release microspheres suitable for ocular administration, and we assessed itsin vitro and in vivo properties. The preparation of puerarin-loaded microspheres was optimized by Box-Behnken response surface design. The encapsulation efficiency and drug loading of microspheres were 35.71% and 3.85%, respectively. The microspheres exhibited good dispersion and high safety, making it suitable for ocular drug delivery. In vitro release demonstrated that microspheres had a well-sustained release effectiveness, and its release behavior complied with the zero-order kinetic characteristics. The results of ocular tissue distribution revealed that the CmaxandAUC0-∞ of the microspheres group in the retina and choroid were considerably higher than those of the solution group and the intravenous injection group. This research revealed that intravitreal injection of microspheres can significantly prolong the half-life of puerarin in eye tissues and achieve sustained drug release. Therefore, intravitreal injection of microspheres has positive implications for the treatment of diabetic retinopathy.

Design of toughed bio-based polylactide/polyamide 11 blends with regulatable size of dispersed phase and spherulites by interfacial stereocomplex crystallites

Enhancing the ductility of polylactide (PLA) through toughening modification to expand the application range of PLA aligns with the requirements of green development. In this study, eco-friendly bio-based plastic polyamide 11 (PA11) was chosen to modify poly(l-lactide) (PLLA). PA11 and poly(d-lactide) (PDLA) were grafted onto the main chain of ADR via simple reactive processing and utilized as reactive compatibilizers to improve toughening efficiency of PA11. The successful preparation of the graft copolymer was confirmed through 1H NMR, FT-IR and DSC, and a detailed investigation was conducted on how the composition and concentration of the compatibilizer influence the mechanical properties, phase morphology, crystallization, and nucleation behaviors of PLLA/PA11 blends. Elongation at break of the 5 % PDLA/PA11 graft copolymers toughed PLLA was as high as 222 % at 30 % PA11 content, which was 17 times greater than the PLLA toughened by pristine PA11 without compromising the strength. PLLA and PA11 were immiscible binary blends with PA11 droplet/PLLA matrix phase separated morphologies in the molten state. Based on the calculation of interfacial tension, the grafted copolymer would be mainly distributed at the interface between the two phases. The dispersion of PA11 droplet in PLLA matrix was improved since the interfacial interaction force was enhanced through in-situ reaction. The increase of the nucleation site and decrease of the spherulites size were worked synergistically by stereocomplex (SC) crystallites and PA11. Under the impact of reducing the size of the dispersed phase and spherulites, the toughness of blends was enhanced. This study provided valuable insights into the control of PLLA immiscible blend morphology and elucidated the relationship between the size of dispersed phase and spherulites and the ultimate mechanical performance of bio-based PLA materials.

Contact Antibacterial and Biocompatible Polymeric, Composite with Copper Zeolite Filler and Copper Oxide, Nanoparticles: A Step Towards New Raw Materials for the Biomedical Industry

This paper introduces a simple procedure for developing composite materials with antibacterial and biocompatible properties using polylactic acid (PLA) and polypropylene (PP). These composites incorporate three variants of zeolites in different percentages as filler agents: pure zeolite (PZ), copper ion-saturated zeolite (LZ), and copper-ion-saturated zeolite with copper oxide nanoparticles (LZ-nCu). The composites were prepared by the extrusion method and manufactured by injection molding. The impact of these zeolites on various material properties was evaluated, including morphology, thermal stability, mechanical properties, antibacterial capacity, biocompatibility, water absorption, and chemical resistance. The results demonstrated that (i) the incorporation of zeolite into the PP matrix improved thermal stability and increased the tensile modulus of the composites. For PLA-based composites, although there was a slight decrease in these values compared to pure PLA, they remained within acceptable ranges; (ii) zeolite LZ and LZnCu composites at 5 and 10% by weight effectively inhibited the growth of Gram-positive and Gram-negative bacteria within a maximum of 2 hours of contact; and (iii) composites containing 10% by weight of PZ, LZ, or LZ-nCu showed reduced mechanical properties due to a tendency to form agglomerates. Additionally, LZ and LZ-nCu composites with the same percentage proved highly toxic to human gingival fibroblast cells (HGFs). PLA/LZ-nCu at 5% and PP/LZ at 5% composites exhibited antibacterial properties with bactericidal effects upon contact, high biocompatibility, and lower water absorption compared to the pure polymeric matrix. These results highlight the operational effectiveness of the procedure and suggest the potential of these composites in biomedical applications, such as in vitro dentistry, without contamination risks.

Natural filter: Adjustable hydrophobicity from biodegradable zein nanofiber membrane for high efficiency air purification

Faced with the fact that air filtration materials prepared from traditional petroleum-based materials do not have good biodegradability and have the risk of causing secondary pollution to the environment, a kind of nanofiber membrane with biodegradable polylactic acid (PLA) and zein was prepared by electrospinning method. The morphology of as-prepared membrane was carried out along with filtration performance and degradation performance both experimentally and theoretically. The results showed that the hydrophobicity of nanofiber membrane can be adjusted by changing the ratio of PLA and zein. In addition, the highest filtration efficiency for PM2.5 and PM10 was achieved when the ratio of PLA to zein was 1:1, and it could be stabilized at 98.14 % and 97.39 %, and had the highest quality factor (QF) of 0.00738 Pa−1. Moreover, the fiber membrane has excellent adsorption effect on aqueous particles as well as oily particles. Notably, the as-prepared composite filter can be easily biodegraded thus contributing to green ecological environment.

A novel sustainable wood-based negative air anion generator utilizing in-situ polymerization of polylactic acid to reinforce the cellulose framework

The generation of negative air ions (NAI) by furniture contributes to indoor air purification and enhances the living environment. However, commercially available furniture typically relies on surface coatings to release NAI. Over time, the degradation of these coatings leads to a significant decline in NAI release performance, presenting a persistent challenge for sustained effectiveness. Here, a novel sustainable wood-based negative air anion generator (SWNG) had been developed, utilizing a cellulose framework as the substrate. The in-situ synthesis of polylactic acid (PLA) within the wood incorporated titanium dioxide (TiO2), tourmaline (TL), and cellulose acetate, firmly anchoring these materials within the wood structure. Compared to the cellulose framework alone, the NAI production of the SWNG had increased by 406.67 %. The impregnation with PLA enhanced the enduring photocatalytic activity of TiO2 and TL in this innovative wooden NAI generator. After undergoing 200 cycles of testing between −40 °C and 50 °C, it continued to sustain NAI production, demonstrating exceptional antibacterial performance. Overall, this study introduced a novel sustainable wood-based negative air ion generator as a highly stable material with sustainable properties, offering significant potential for applications in improving indoor air quality and in the domain of home construction.

Fast kinetics for lithium storage rendered by Li3VO4 nanoparticles/porous N-doped carbon nanofibers

Li3VO4 (LVO) has been recognized as an alternative anode material for lithium-ion batteries (LIBs) because of its appropriate lithium storage potential and capacity merits. However, its practical application is seriously hindered by slow reaction kinetics stemming from poor electronic conductivity. Herein, Li3VO4/porous N-doped carbon nanofibers (LVO/PNC NFs) are firstly designed and fabricated via an electrospinning method, utilizing the thermal decomposition characteristics of polylactic acid (PLA). The porous N-doped carbon nanofibers provide efficient electrolyte diffusion paths and facilitate ion transport. In addition, LVO nanoparticles are uniformly dispersed along the nanofibers to effectively inhibit particle aggregation. The obtained LVO/PNC NFs are evaluated as anodes for LIBs and deliver high reversible capacity of 768 mAh g−1 after 300 cycles at 0.2 A g−1, along with excellent rate capability (average capacity of 355 mAh g−1 at 8 A g−1 after 6 periodic rate testing) and long cycling life (286 mAh g−1 after 2000 cycles at 4 A g−1). The special porous nanofiber represents an effective strategy for improving the electronic conductivity, inhibiting particle aggregation, and ensuring rapid ion/charge transport towards advanced energy storage technologies.