Biocomposites of Poly(Lactic Acid) and Cellulose Nanofibers from Cassava Pulp

2017 ◽  
Vol 753 ◽  
pp. 13-17
Author(s):  
Chi Nguyen Thanh ◽  
Ruksakulpiwat Chaiwat ◽  
Ruksakulpiwat Yupaporn

Cellulose nanofibers (CNFs) were used as biobased fillers to prepare poly(lactic acid) (PLA)-based biocomposites. Cellulose nanofibers were extracted from cassava pulp (CP) by acid hydrolysis method. Before submitted to acid treatment, CP was pre-treated by alkali and bleaching treatments. The biocomposites were prepared by melt mixing, followed by hot melt pressing. In order to improve the compatibility of CNFs with PLA matrix, glycidyl methacrylate (GMA) grafted poly (lactic acid) (PLA-g-GMA) was used as a compatibilizer. PLA-g-GMA was prepared by grafting of GMA onto PLA chain via melt mixing using an internal mixer. Transmission electron microscopy (TEM) micrograph shows that most nanofibers with the diameter in the range of 10-30 nm and immeasurable length were obtained. The appearance of two new peaks at 49.07 and 44.71 ppm in the carbon-13 nuclear magnetic resonance (13C-NMR) spectrum of PLA-g-GMA, which represent the carbons of the epoxy group of GMA, confirms that GMA was successfully grafted onto PLA chain. The morphology of biocomposites, characterized by scanning electron microscopy (SEM), reveals that without using PLA-g-GMA, the poor dispersion of CNFs in PLA matrix was observed. In contrast to that, with using PLA-g-GMA, the dispersion of CNFs in PLA matrix was improved. Moreover, the impact strength results show that by incorporating 1.0 wt% CNFs into PLA matrix and using PLA-g-GMA as a compatibilizer, the impact strength of biocomposites was slightly enhanced compared to that of pure PLA.

2019 ◽  
Vol 33 (8) ◽  
pp. 1094-1108
Author(s):  
Thanh Chi Nguyen ◽  
Chaiwat Ruksakulpiwat ◽  
Yupaporn Ruksakulpiwat

Biocomposites of poly(lactic acid) (PLA) and cellulose nanofibers (CNFs) extracted from cassava pulp were successfully prepared by melt mixing in an internal mixer. CNFs were prepared from cassava pulp by submitting to alkali hydrolysis, bleaching treatment, and acid hydrolysis. The compatibility between CNFs and PLA matrix was improved using glycidyl methacrylate (GMA) grafted PLA (PLA-g-GMA) as an effective compatibilizer. Higher elongation at break and impact strength of PLA/PLA-g-GMA/CNFs biocomposites was achieved compared to that of neat PLA. PLA-g-GMA shows a strong effect on the crystallization behavior of the biocomposites. The PLA/PLA-g-GMA/CNFs biocomposites induce cold crystallization to take place at lower temperature. Higher degree of crystallinity of PLA/PLA-g-GMA/CNFs biocomposites was obtained compared to PLA/CNFs biocomposites. The mechanical and thermal properties of PLA/CNFs biocomposites at various ratios were investigated. With increasing CNFs contents, the modulus of the biocomposites increases. Thermal stability of PLA/CNFs and PLA/PLA-g-GMA/CNFs biocomposites did not change significantly compared to that of neat PLA.


2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Wei Kit Chee ◽  
Nor Azowa Ibrahim ◽  
Norhazlin Zainuddin ◽  
Mohd Faizal Abd Rahman ◽  
Buong Woei Chieng

Poly(lactic acid) (PLA)/poly(ε-caprolactone) (PCL) blends were prepared via melt blending technique. Glycidyl methacrylate (GMA) was added as reactive compatibilizer to improve the interfacial adhesion between immiscible phases of PLA and PCL matrices. Tensile test revealed that optimum in elongation at break of approximately 327% achieved when GMA loading was up to 3wt%. Slight drop in tensile strength and tensile modulus at optimum ratio suggested that the blends were tuned to be deformable. Flexural studies showed slight drop in flexural strength and modulus when GMA wt% increases as a result of improved flexibility by finer dispersion of PCL in PLA matrix. Besides, incorporation of GMA in the blends remarkably improved the impact strength. Highest impact strength was achieved (160% compared to pure PLA/PCL blend) when GMA loading was up to 3 wt%. SEM analysis revealed improved interfacial adhesion between PLA/PCL blends in the presence of GMA. Finer dispersion and smooth surface of the specimens were noted as GMA loading increases, indicating that addition of GMA eventually improved the interfacial compatibility of the nonmiscible blend.


RSC Advances ◽  
2017 ◽  
Vol 7 (73) ◽  
pp. 46183-46194 ◽  
Author(s):  
Jia Yang ◽  
Hongwei Pan ◽  
Xin Li ◽  
Shulin Sun ◽  
Huiliang Zhang ◽  
...  

PPCU was prepared by using PPC and polyols as the raw materials and diphenyl-methane-diisocyanate (MDI) as the extender chain. The impact strength and elongation at break of PLA were remarkably enhanced by blending with PPCU.


Materials ◽  
2021 ◽  
Vol 14 (18) ◽  
pp. 5346
Author(s):  
Daniel Kaczor ◽  
Kacper Fiedurek ◽  
Krzysztof Bajer ◽  
Aneta Raszkowska-Kaczor ◽  
Grzegorz Domek ◽  
...  

To assess the impact of graphite fillers on the thermal processing of graphite/poly(lactic acid) (PLA) composites, a series of the composite samples with different graphite of industrial grade as fillers was prepared by melt mixing. The average size of the graphite grains ranged between 100 µm and 6 µm. For comparative purposes, one of the carbon fillers was expandable graphite. Composites were examined by SEM, FTIR, and Raman spectroscopy. As revealed by thermogravimetric (TG) analyses, graphite filler slightly lowered the temperature of thermal decomposition of the PLA matrix. Differential scanning calorimetry (DSC) tests showed that the room temperature crystallinity of the polymer matrix is strongly affected by the graphite filler. The crystallinity of the composites determined from the second heating cycle reached values close to 50%, while these values are close to zero for the neat polymer. The addition of graphite to PLA caused a slight reduction in the oxidation induction time (OIT). The melt flow rate (MFR) of the graphite/PLA composites was lower than the original PLA due to an increase in flow resistance associated with the high crystallinity of the polymer matrix. Expandable graphite did not cause changes in the structure of the polymer matrix during thermal treatment. The crystallinity of the composite with this filler did not increase after first heating and was close to the neat PLA MFR value, which was extremely high due to the low crystallinity of the PLA matrix and delamination of the filler at elevated temperature.


2019 ◽  
Vol 972 ◽  
pp. 178-184
Author(s):  
Sirirat Wacharawichanant ◽  
Chawisa Wisuttrakarn ◽  
Kasana Chomphunoi ◽  
Manop Phankokkruad

This research prepared poly(lactic acid) (PLA) and PLA/acrylonitrile-butadiene rubber (NBR) blends before and after adding polyethylene-g-maleic anhydride with 3 wt% of maleic anhydride (PE-g-MA3) 3 phr. The effects of NBR and PE-g-MA3 on morphological, mechanical and thermal properties of PLA and PLA blends were discussed. The morphological analysis observed the two-phase morphology of PLA/NBR blends, and it was observed the cavities generated due to NBR phase detachment during sample fracture, and droplets of NBR phase at higher NBR content. The PE-g-MA3 addition could improve adhesion between PLA and NBR phases due to the decrease of cavities in PLA matrix and droplet size of NBR. The mechanical properties showed the impact strength and strain at break of PLA/NBR blends dramatically increased when the amount of NBR increasing. The addition of PE-g-MA3 significantly improved the impact strength of PLA/NBR blends. The thermal properties showed the NBR addition had effect slightly on the melting temperature of PLA/NBR blends. The filling of NBR and PE-g-MA3 greatly decreased the percent crystallinity of PLA more than two times. The thermal degradation of pure PLA and NBR proceeds by one step, while the thermal degradation process of PLA/NBR and PLA/PE-g-MA3 proceeds by two steps. Which the first step showed a large mass loss of PLA degradation and the second step showed a small mass loss of PE-g-MA and NBR degradation.


2018 ◽  
Vol 773 ◽  
pp. 51-55
Author(s):  
Jasmine Pongkasem ◽  
Saowaroj Chuayjuljit ◽  
Phasawat Chaiwutthinan ◽  
Amnouy Larpkasemsuk ◽  
Anyaporn Boonmahitthisud

In this study, poly(lactic acid) (PLA) was melt mixed with three weight percentages (10–30wt%) of ethylene vinyl acetate copolymer (EVA) in an internal mixer, followed by a compression molding. According to a better combination of mechanical properties, the 90/10 (w/w) PLA/EVA was selected for preparing hybrid nanocomposites with three loadings (1, 3 and 5 parts per hundred of resin , phr) of poly(methyl methacrylate)-encapsulated nanosilica (PMMA-nSiO2). The nanolatex of PMMA-nSiO2 was synthesized via in situ differential microemulsion polymerization. The obtained PMMA-nSiO2 showed a core-shell morphology with nSiO2 as a core and PMMA as a shell, having an average diameter of 43.4nm. The influences of the EVA and PMMA-nSiO2 on the impact strength and the tensile properties of the PLA/EVA nanocomposites were studied and compared. It is found that the impact strength and the tensile properties of the 90/10 (w/w) PLA/EVA were improved with the appropriate amounts of the EVA and PMMA-nSiO2.


Polymers ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 465
Author(s):  
Masrat Rasheed ◽  
Mohammad Jawaid ◽  
Bisma Parveez ◽  
Aamir Hussain Bhat ◽  
Salman Alamery

The present study aims to develop a biodegradable polymer blend that is environmentally friendly and has comparable tensile and thermal properties with synthetic plastics. In this work, microcrystalline cellulose (MCC) extracted from bamboo-chips-reinforced poly (lactic acid) (PLA) and poly (butylene succinate) (PBS) blend composites were fabricated by melt-mixing at 180 °C and then hot pressing at 180 °C. PBS and MCC (0.5, 1, 1.5 wt%) were added to improve the brittle nature of PLA. Field emission scanning electron microscopy (FESEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscope (FTIR), thermogravimetric analysis (TGA), differential thermogravimetry (DTG), differential scanning calorimetry (DSC)), and universal testing machine were used to analyze morphology, crystallinity, physiochemical, thermal, and tensile properties, respectively. The thermal stability of the PLA-PBS blends enhanced on addition of MCC up to 1wt % due to their uniform dispersion in the polymer matrix. Tensile properties declined on addition of PBS and increased with MCC above (0.5 wt%) however except elongation at break increased on addition of PBS then decreased insignificantly on addition of MCC. Thus, PBS and MCC addition in PLA matrix decreases the brittleness, making it a potential contender that could be considered to replace plastics that are used for food packaging.


2018 ◽  
Vol 916 ◽  
pp. 19-23 ◽  
Author(s):  
Sirirat Wacharawichanant ◽  
Nisarat Wimonsupakit ◽  
Sasithorn Kuhaudomlap

The objective of this study is to fabricate the polyoxymethylene (POM)/microcrystalline cellulose (MCC) and poly(lactic acid) (PLA)/MCC composites, and to compare the effect of MCC on the morphology and mechanical properties of POM and PLA. The polymer composites were prepared by melt mixing in an internal mixer and molded by compression molding. The MCC concentrations were 1, 3, 5, 7, 10, 15 and 10% by weight. From scanning electron microscopy study observes the fracture surface of POM and PLA composites is much rough and the roughness increases with increasing MCC content. This observation indicates MCC induces the ductile fracture characteristic of POM and PLA. The addition of MCC can improve the impact strength of PLA composite and improve Young’s modulus of both POM and PLA composites. While the tensile strength and strain at break decrease after adding MCC. In summary, MCC can enhance the morphology and mechanical properties of PLA composites is better than POM composites.


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