ABSTRACT
The growing popularity of poly(lactic acid) (PLA) can be attributed to its favorable attributes, such as excellent compostability and robust mechanical properties. Two notable limitations of PLA are its high brittleness and slow biodegradation rate. Both of blending and copolymerization strategies work well to improve PLA's toughness while sacrificing the good tensile strength and modulus properties of PLA. One of the most effective and economical approaches to address this challenge is to incorporate natural reinforcing agents into the toughened PLA system, thereby simultaneously promoting the biodegradation rate of PLA. Nevertheless, the enhancement of tensile strength and modulus is accompanied by a notable decrease in elongation. Therefore, this review provides comprehensive information on the literature works related to the tensile strength, modulus, elongation at break and impact strength of the toughened PLA and its natural fiber reinforced composites. The impact of natural reinforcing agent on the tensile fracture mechanism as well as the synergistic effect on strengthening and toughening performance will be discussed. This review also focuses on the factors boosting the biodegradability of toughened PLA blend by using natural reinforcing fiber. Review presents potential future insights into the development of biodegradable and balanced strengthened-toughened PLA based advanced materials.
ABSTRACT
Over the last few decades, processing and compatibility have become challenging and interesting investigation areas of polymer matrix nanocomposites. This study investigated the addition of maleic anhydride (MAH) at different ratios with graphene nanoplatelets (GnPs) in poly(lactic acid)/modified natural rubber/polyaniline/GnP (PLA/m-NR/PANI/GnP) nanocomposites via two processing methods: a two-step technique and a one-pot technique. The former technique involved first preparing a master batch of PLA grafted with MAH, followed by a second step involving the melt blending of the nanocomposite (T1) using MAH-g-PLA. On the other hand, the one-pot technique involved the direct mixing of MAH during the melt-blending process (T2). The mechanical, morphological and thermal properties of the prepared nanocomposites were investigated. The findings showed that adding MAH significantly improved the tensile strength and elongation at break by about 25% for PLA/m-NR/PANi/GnP nanocomposites, with an optimal ratio of 1:1 of MAH-g-PLA to GnP loading using the T1 technique. FTIR analysis confirmed the chemical interaction between MAH and PLA for T1 nanocomposites, which exhibited improved phase morphology with smoother surfaces. MAH-compatibilized nanocomposites had enhanced thermal stabilities when compared to the sample without a compatibilizer. The findings show that the compatibilized PLA nanocomposite is potentially suitable for bio-inspired materials.
ABSTRACT
This study highlights the potential use of cellulose nanocrystals (CNCs) from kenaf fiber as a dominant phase for aerogel application. CNCs were modified with methyltrimethoxysilane (MTMS) using the sol-gel method and bound with gamma-irradiated cross-linked gelatin. The properties of the aerogel were studied using Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), and water contact angle (WCA). Compression and oil absorption tests were performed to study the aerogels' mechanical and oil absorption properties. A decrease in the OH peak and improved hydrophobicity of CNCs in CNC-MTMS suggested the successful grafting of MTMS onto CNCs, as shown in the FTIR and WCA analyses. Several absorption peaks in the FTIR spectrum shifted, disappeared, or reduced, implying a formation of crosslink between gelatin molecules and hydrogen bonding between CNC and gelatin. FESEM micrographs showed well-organized pores in the gamma-irradiated aerogel, which contribute to increased compressive strength. The oil absorption test indicated that gamma-irradiated CNC-MTMS/gelatin could be a good oil absorbent. Furthermore, this aerogel showed good reusability, where only 4 % of crude oil absorption reduction occurred by the eighth cycle. The combined properties of these aerogel materials can provide good mechanical and oil absorption performance.
Subject(s)
Nanoparticles , Petroleum , Cellulose/chemistry , Gelatin , Gels/chemistry , Hydrophobic and Hydrophilic Interactions , Nanoparticles/chemistry , Silanes , Water/chemistryABSTRACT
Poly(lactic acid) (PLA), a bio-based polyester, has been extensively investigated in the recent past owing to its excellent mechanical properties. Several studies have been conducted on PLA blends, with a focus on improving the brittleness of PLA to ensure its suitability for various applications. However, the increasing use of PLA has increased the contamination of PLA-based products in the environment because PLA remains intact even after three years at sea or in soil. This review focuses on analyzing studies that have worked on improving the degradation properties of PLA blends and studies how other additives affect degradation by considering different degradation media. Factors affecting the degradation properties, such as surface morphology, water uptake, and crystallinity of PLA blends, are highlighted. In natural, biotic, and abiotic media, water uptake plays a crucial role in determining biodegradation rates. Immiscible blends of PLA with other polymer matrices cause phase separation, increasing the water absorption. The susceptibility of PLA to hydrolytic and enzymatic degradation is high in the amorphous region because it can be easily penetrated by water. It is essential to study the morphology, water absorption, and structural properties of PLA blends to predict the biodegradation properties of PLA in the blends.
Subject(s)
Enzymes/chemistry , Polyesters/chemistry , Polymers/chemistry , Water/chemistry , Hydrolysis , KineticsABSTRACT
Eco-friendly materials such as poly(lactic acid) (PLA) and cellulose are gaining considerable interest as suitable substitutes for petroleum-based plastics. Therefore, amorphous cellulose (AC) was fabricated as a new reinforcing material for PLA biocomposites by modifying a microcrystalline cellulose (MCC) structure via milling. In this study, the mechanical properties, thermal properties, and degradability of PLA were analysed to compare the effects of both MCC and AC on PLA. The tensile and impact properties improved at an optimum value with AC at 8 wt% and 4 wt% fibre loading, respectively. Notably, a scanning electron micrograph analysis revealed improved AC fibre-matrix adhesion, compared with MCC fibre-matrix adhesion, as well as excellent interaction between AC and PLA. Both MCC and AC improved the hydrolytic degradation of PLA. Moreover, the biocomposites with AC exhibited superior degradation when the incorporation of AC improved the water absorption efficiency of PLA. These findings can expand AC applications and improve sustainability.
ABSTRACT
In this study, modified agave cellulose fibre combined by graft copolymerisation with methylmethacrylate was tested as a potential reinforcement for polylactic acid (PLA)-natural rubber/liquid natural rubber blends. Mechanical, morphological, thermal, wetting, and biodegradation characterisations were performed to assess the influence of cellulose-graft-polymethylmethacrylate (cell-g-PMMA) content on the properties of biocomposites. The addition of cell-g-PMMA improved the mechanical properties of the composites because of the chemical interaction between PLA and PMMA. Thermal stability decreased slightly upon cell-g-PMMA addition because of the low thermal stability of PMMA. A soil burial test revealed that the degradation of composites decreased with an increase in the cell-g-PMMA content. However, the weight loss after burial, which directly affected the water absorption capacity, was still higher for the cell-g-PMMA composites than for the polymer alone.
ABSTRACT
pH-sensitive poly(acrylic acid) (PAA) hydrogel reinforced with cellulose nanocrystals (CNC) was prepared. Acrylic acid (AA) was subjected to chemical cross-linking using the cross-linking agent MBA (N,N-methylenebisacrylamide) with CNC entrapped in the PAA matrix. The quantity of CNC was varied between 0, 5, 10, 15, 20, and 25 wt %. X-ray diffraction (XRD) data showed an increase in crystallinity with the addition of CNC, while rheology tests demonstrated a significant increase in the storage modulus of the hydrogel with an increase in CNC content. It was found that the hydrogel reached maximum swelling at pH 7. The potential of the resulting hydrogels to act as drug carriers was then evaluated by means of the drug encapsulation efficiency test using theophylline as a model drug. It was observed that 15% CNC/PAA hydrogel showed the potential to be used as drug carrier system.
ABSTRACT
Graft copolymerisation of methyl methacrylate (MMA) onto Agave angustifolia was conducted with ceric ammonium nitrate (CAN) as the redox initiator. The maximum grafting efficiency was observed at CAN and MMA concentrations of 0.91 × 10(-3) and 5.63 × 10(-2)M, respectively, at 45°C for 3h reaction time. Four characteristic peaks at 2995, 1738, 1440, and 845 cm(-1), attributed to PMMA, were found in the IR spectrum of grafted cellulose. The crystallinity index dropped from 0.74 to 0.46, while the thermal stability improved upon grafting. The water contact angle increased with grafting yield, indicating increased hydrophobicity of cellulose. SEM images showed the grafted cellulose to be enlarged and rougher. The changes in the physical nature of PMMA-grafted cellulose can be attributed to the PMMA grafting in the amorphous regions of cellulose, causing it to expand at the expense of the crystalline component.
