Abstract:Antimicrobial films of poly (lactic acid) (PLA)/D‐limonene/zinc oxide (ZnO)‐based bio‐nanocomposites were prepared via melt compounding and subsequent thermocompression. D‐limonene was incorporated at concentrations of 10 or 20 wt%, and ZnO pure nanoparticles and those organically modified with oleic acid (O‐ZnO), with an average diameter of 13.5 nm, were included at concentrations of 3, 5, and 8 wt%. The plasticizing effect of D‐Limonene was corroborated by a decrease in the glass transition temperature compa… Show more
“…According to the literature, nanocomposites based on limonene, including poly (lactic acid)/D-limonene/ZnO bio-nanocomposites [ 33 ], Pt, Ru and Ni/graphene nanocomposites [ 34 ] and V-MCM-41 nanocomposites [ 35 ], but the use of natural clay as a catalyst in the synthesis of copolymers based on limonene and styrene is almost non-existent. The main goal of this research is to look into the catalytic properties of a natural clay (Mag-H + ) as a new non-toxic catalyst for the copolymerization of limonene and styrene and Mag-CTA + as a new nano-reinforcing filler for the fabrication of nanocomposites based on styrene-limonene copolymer (lim-co-sty) using an ultrasonic assisted approach to improve the copolymer’s thermal and mechanical properties.…”
In the present work, we report a simple synthesis method for preparation of copolymers and nanocomposites from limonene and styrene using clay as a catalyst. The copolymerization reaction is carried out by using a proton exchanged clay as a catalyst called Mag-H+. The effect of temperature, reaction time and amount of catalyst were studied, and the obtained copolymer structure (lim-co-sty) is characterized by Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic resonance spectroscopy (1H-NMR) and differential scanning calorimetry (DSC). The molecular weight of the obtained copolymer is determined by gel permeation chromatography (GPC) and is about 4500 g·mol−1. The (lim-co-sty/Mag 1%, 3%, 7% and 10% by weight of clay) nanocomposites were prepared through polymer/clay mixture in solution method using ultrasonic irradiation, in the presence of Mag-CTA+ as green nano-reinforcing filler. The Mag-CTA+ is organophilic silicate clay prepared through a direct exchange process, using cetyltrimethylammonuim bromide (CTAB). The prepared lim-co-sty/Mag nanocomposites have been extensively characterized by FT-IR spectroscopy, X-ray diffraction (XRD), scanning electronic microscopy (SEM) and transmission electronic microscopy (TEM). TEM analysis confirms the results obtained by XRD and clearly show that the obtained nanocomposites are partially exfoliated for the lower amount of clay (1% and 3% wt) and intercalated for higher amounts of clay (7% and 10% wt). Moreover, thermogravimetric analysis (TGA) indicated an enhancement of thermal stability of nanocomposites compared with the pure copolymer.
“…According to the literature, nanocomposites based on limonene, including poly (lactic acid)/D-limonene/ZnO bio-nanocomposites [ 33 ], Pt, Ru and Ni/graphene nanocomposites [ 34 ] and V-MCM-41 nanocomposites [ 35 ], but the use of natural clay as a catalyst in the synthesis of copolymers based on limonene and styrene is almost non-existent. The main goal of this research is to look into the catalytic properties of a natural clay (Mag-H + ) as a new non-toxic catalyst for the copolymerization of limonene and styrene and Mag-CTA + as a new nano-reinforcing filler for the fabrication of nanocomposites based on styrene-limonene copolymer (lim-co-sty) using an ultrasonic assisted approach to improve the copolymer’s thermal and mechanical properties.…”
In the present work, we report a simple synthesis method for preparation of copolymers and nanocomposites from limonene and styrene using clay as a catalyst. The copolymerization reaction is carried out by using a proton exchanged clay as a catalyst called Mag-H+. The effect of temperature, reaction time and amount of catalyst were studied, and the obtained copolymer structure (lim-co-sty) is characterized by Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic resonance spectroscopy (1H-NMR) and differential scanning calorimetry (DSC). The molecular weight of the obtained copolymer is determined by gel permeation chromatography (GPC) and is about 4500 g·mol−1. The (lim-co-sty/Mag 1%, 3%, 7% and 10% by weight of clay) nanocomposites were prepared through polymer/clay mixture in solution method using ultrasonic irradiation, in the presence of Mag-CTA+ as green nano-reinforcing filler. The Mag-CTA+ is organophilic silicate clay prepared through a direct exchange process, using cetyltrimethylammonuim bromide (CTAB). The prepared lim-co-sty/Mag nanocomposites have been extensively characterized by FT-IR spectroscopy, X-ray diffraction (XRD), scanning electronic microscopy (SEM) and transmission electronic microscopy (TEM). TEM analysis confirms the results obtained by XRD and clearly show that the obtained nanocomposites are partially exfoliated for the lower amount of clay (1% and 3% wt) and intercalated for higher amounts of clay (7% and 10% wt). Moreover, thermogravimetric analysis (TGA) indicated an enhancement of thermal stability of nanocomposites compared with the pure copolymer.
“…coli ATCCC 25922 were used for the analysis. Our group has already reported this procedure. ,,,− In brief, the initial number of bacteria present after incubation was calculated by counting the number of colonies in a tenfold dilution. First, a microbial suspension of 1 × 10 7 CFU·mL –1 (CFU: colony-forming units) by a densimat bioMérieux was prepared in a BHI broth plus Triton X-100 in a humid chamber.…”
Section: Methodsmentioning
confidence: 99%
“…PLA/DL/ZnO nanocomposites reached 99.9% effectiveness against Escherichia coli with contents above 5 wt %, regardless of the irradiation source. 29 Alternatively, calcium oxide (CaO) nanoparticles are of great interest for developing antimicrobial materials 30−32 as they are nontoxic to the human body, noncorrosive, recyclable, low-cost bactericidal, economically affordable, and easy to synthesize. 33,34 Silva et al prepared low-density polyethylene (LDPE) films with 3, 5, and 10 wt % CaO nanoparticles (25 and 50 nm).…”
Section: Introductionmentioning
confidence: 99%
“…9% compared with the neat PLA. PLA/DL/ZnO nanocomposites reached 99.9% effectiveness against Escherichia coli with contents above 5 wt %, regardless of the irradiation source …”
Antimicrobial films based on poly(lactic acid) (PLA)/Dlimonene/calcium oxide (CaO)-based nanocomposites were prepared by extrusion and successive thermocompression. D-Limonene was incorporated into PLA at a concentration of 5 or 10 wt %. Venus antiqua clamshell-derived calcium oxide (CaO) nanoparticles with an average diameter of 11.2 ± 9.9 nm were added at concentrations of 3 and 5 wt %. A decrease in the glass transition temperature (T g ) by ca. 20% corroborated the plasticizing effect of D-limonene compared to pure PLA. The incorporation of 5 wt % CaO in PLA composites promoted a ca. 15% decrease in T cc . Although CaO induced a lower Young's modulus and a lower thermal stability in nanocomposites, excellent antimicrobial performance was demonstrated. Both PLA/limonene and PLA/ limonene/CaO films reached 99.99% efficiency against Escherichia coli, regardless of the source of irradiation, D-limonene, and nanoparticle loading. Therefore, these nanocomposites establish significant progress in developing sustainable antimicrobial materials in the fields of medicine or food packaging.
“…Acetylation of NFC can improve the interphase between the PLA matrix and the fibres, to obtain a better and more uniform dispersion [9,10]. At present PLA-based materials can be utilised in packaging [21][22][23][24][25][26][27], medicine [28][29][30], agriculture [31][32][33], electronics [34][35][36],…”
In this study, bionanocomposite films based on poly(lactide) (PLA) plasticised with poly(ethylene glycol) (PEG) (7.5 wt%) and reinforced with various contents of nanofibrillated cellulose (NFC) (1, 3, 5 wt%) were prepared. The hydrothermal degradation was investigated through immersion in several aqueous environments at temperatures of 8, 23, 58, and 70 °C as a function of time (7, 15, 30, 60, 90 days). The effect of water immersion on the physicochemical properties of the materials was assessed by monitoring the changes in the morphology, thermo-oxidative stability, thermal properties, and molar mass through field emission scanning electron microscopy (FE-SEM), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and gel permeation chromatography (GPC). The hydrothermal degradation behaviour was not critically affected regardless of the nanofibrillated cellulose content. All the materials revealed certain integrity towards water immersion and hydrolysis effects at low temperatures (8 and 23 °C). The low hydrothermal degradation may be an advantage for using these PLA biocomposites in contact with water at ambient temperatures and limited exposure times. On the other hand, immersion in water at higher temperatures above the glass transition (58 and 70 °C), leads to a drastic deterioration of the properties of these PLA-based materials, in particular to the reduction of the molar mass and the disintegration into small pieces. This hydrothermal degradation behaviour can be considered a feasible option for the waste management of PLA/PEG/NFC bionanocomposites by deposition in hot aqueous environments.
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