Modelling of photodegradation effect on elastic–viscoplastic behaviour of amorphous polylactic acid films (original) (raw)
Related papers
2009
In this work, the impact of ultraviolet (UV) irradiation on the mechanical behaviour of amorphous biodegradable poly(lactic acid) (PLA) films is analysed. PLA films were submitted to UV irradiation for increasing exposure time. Two kinds of experiments were conducted, chemical and mechanical. The chemical degradation was measured by gel permeation chromatography technique. The PLA films were mechanically investigated by stretching experiments before and after UV exposure. Their mechanical properties were obtained by a video-controlled system. Our purpose is to establish the relationship between macroscopic mechanical response and molecular parameters such as the molecular weight, and external solicitations such as temperature, strain rate and UV irradiation. The interactions between photodegradation and changes in polymer properties are discussed. Kljucne reci • polilaktid – poli(lakticna kiselina) • ultraljubicasto (UV) zracenje • molekularna teina • mehanicke karakteristike
The mechanical behavior of polylactic acid (PLA) films: fabrication, experiments and modelling
Mechanics of Time-Dependent Materials
Polylactic acid (PLA) is one of the highly applicable bio-polymers in a wide variety of applications including medical fields and packaging. In order to quantitatively model the mechanical behavior of PLA and PLA based bio-composite materials, and also tailor new bio-composites, it is required to characterize the mechanical behavior of PLA. In this study, thin films of PLA are fabricated via hot-pressing, and tensile experiments are performed under different strain rates. To model the mechanical behavior, an elasto-viscoplastic constitutive model, developed in a finite strain setting, is adopted and calibrated. Using the physically-based constitutive model, all regimes of deformation under uniaxial stress state, including post-yield softening, were adequately captured in the simulations. Also, the rate dependency of the stress–strain behavior was properly modelled.
Effects of Electron-Beam Irradiation and Ultraviolet Light (365 nm) on Polylactic Acid Plastic Films
1999
Strips of Ca-I [polylactic acid (PLA) monolayer plastic films from Cargill Dow Polymers LLC, Minnetonka, MN] cut in the machine and nonmachine directions were irradiated with an electron beam using a CIRCLE III Linear Accelerator (MeV Industries S.A., Jouy-en-Josas, Cedex, France). The effects of 33-kGy irradiation on the physical properties of the Ca-I strips were studied. In addition, the effects of ultraviolet (UV) light (365-nm) illumination on the degradation of three PLA plastic films, Ch-I (PLA monolayer plastic films from Chronopol, Golden, CO), GII (PLA trilayer plastic films from Cargill Dow Polymers LLC), MN), and Ca-I (PLA monolayer plastic films from Cargill Dow Polymers LLC) were analyzed by a modified ASTM D5208-91 method. Results showed that irradiation had decreased the weight-average molecular weight (M w ), stress at break, percentage of elongation, and strain energy of Ca-I by 35.5, 26.7, 32.3, and 44.8%, respectively (P < 0.01). The shelf life of the irradiated Ca-I strips at 5°C and <20 ± 5% RH was about 6 months. The degradation rate of Ch-I, GII, and Ca-I with no UV light treatment at 55°C and 10% RH was 2512, 5618, and 3785 M w /week, respectively. Under the UV light illumination (365 nm), the degradation rate of Ch-I, GII, and Ca-I, was 2982, 8722, and 7467 M w /week, respectively. Hence, the degradation rate of GII and Ca-I was increased 55 and 97% by UV light (P < 0.008), respectively. This trend was not observed in Ch-I because its starting M w (78,000 g/mol) was close to the tensile strength lost range (50,000 to 75,000 g/mol) of PLA films. To our knowledge, this is the first study to demonstrate that UV light does further enhance the degradation of PLA films.
The effect of ultraviolet light on the mechanical properties of polyethylene and polypropylene films
Journal of Applied Polymer Science, 1982
Measurements were made of dynamic mechanical response spectra and stress-strain properties at room temperature on films of isotactic polypropylene and low-density polyethylene prior and after ultraviolet irradiation in a Xenotest 450 apparatus. The period of irradiation that caused a deep deterioration of ultimate mechanical properties influenced the dynamic mechanical properties only insignificantly. This is attributed to the heterogeneous nature of the photo-oxidative degradation process which is concentrated in a finite number of sites, thus forming crack precursors rather than changing the material properties in bulk. For a biaxially oriented tubular film of low-density polyethylene, anisotropic embrittlement after exposure in Xenotest 450 was observed. This even reversed the order of strain-at-break values in the two main directions of the film. This is remarkably similar to the effect of artificial incisions introduced into the specimens.
Effect of annealing and orientation on microstructures and mechanical properties of polylactic acid
Polymer Engineering and Science, 2008
Two types of polylactic acid (PLA) films (one amorphous and one semi-crystalline) were produced by sheet extrusion. Talc was used as a nucleation agent for the semi-crystalline PLA. The films were annealed above their Tg or were uniaxially orientated in two ways: (1) via a drawing system in front of the extruder and die or (2) via a three-roller stretching system. The slower crystallization rate and lower melting stress of the PLA resulted in amorphous film using the drawing system. Annealing above Tg increased crystallinity and polymer chain relaxation, which resulted in increases in both strength and toughness. Stretching above Tg also produced simultaneous crystallization and chain relaxation, which resulted in increases in both modulus and toughness. Both modulus and tensile strength in the stretching direction were higher than in the crosswise direction. Talc acted not only as a rigid filler to reinforce the PLA, but also as a nucleation agent for the PLA, especially during annealing. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers
Properties and weldability of plasticized polylactic acid films
Journal of Applied Polymer Science, 2014
The objectives of the presented work were to investigate films based on polylactic acid (PLA) and polyethylene glycol (PEG) in order to improve ductility and weldability of PLA films. The effect of plasticizer amount on the thermal, rheological, and mechanical properties of PLA plasticized films was investigated. The PEG content does affect the glass transition and the cold crystallization temperature of PLA in blends, while the melting temperature was not affected by the addition of PEG. The complex viscosity of the neat PLA granules and of plasticized films showed strong temperature and angular velocity dependence. The Young's modulus and tensile strength of plasticized films were improved with increasing plasticizer concentration, while the elongation at break stays rather constant. Plasticized PLA films were furthermore heat welded. These investigations showed that plasticized PLA films can be welded by heat welding. The obtained weld strength is strongly depending on the PEG amount as well as on selected welding parameters. V
Polyethylene (PE) films are widely used in packaging. PE is a thermoplastic manufactured from nonrenewable petroleum resources. Due to its non–biodegradability, its films have posed serious pollution problems e.g. visual pollution, blockage of gutters and drains, choking of animals etc. Suitable replacements for PE films especially for single use only, are the starch based thermoplastics such as Polylactic acid (PLA) which are fully biodegradable. This paper reports a comparison of the viscoelastic properties of commercially obtained PLA and PE films, and the degradation of the same under a composting environment. The storage and loss moduli of PLA and PE films were determined using the Dynamic mechanical analyzer (DMA) model 2980. The elastic modulus of PLA was found to be 2222.87 MPa at 50˚C and amplitude of 10 μm. This is higher than that of PE which was found to be 236.69 MPa at the same temperature and amplitude. Analysis of composting samples over a time span of 36 days indicated a rapid loss of storage modulus of PLA with that of PE remaining fairly constant. Overall, the results suggest that PLA is a suitable substitute for PE in as far as technical performance and degradability is concerned.
Ageing of poly(lactic acid) films plasticized with commercial polyadipates
Polymer International, 2009
BACKGROUND: Amorphous poly(lactic acid) (PLA) was plasticized with two polyadipates with different molar masses. Some physical properties were studied over time to evaluate the stability of these blends. The aim of this study was to improve PLA ductility and consider the feasibility of its use in flexible films for food packaging. RESULTS: The addition of polyadipates caused a decrease of the glass transition temperature (T g) and an increase of PLA chain mobility. Samples with T g values above the storage temperature suffered physical ageing with a reduction in free volume. All the unaged blends were mainly amorphous, but samples with T g below the storage temperature developed crystallinity during ageing leading to phase separation. Ductile properties of films improved with plasticizer content immediately after blending, but there was a deterioration in such properties upon ageing due to matrix densification and crystallization of PLA chains. CONCLUSION: PLA can be efficiently plasticized by polyadipates and the results have shown that some of the prepared films remain flexible with no phase separation after 150 days.
Enzymatic Degradation of Poly(l-Lactic Acid): Effects of UV Irradiation
Journal of Polymers and the Environment, 2006
Amorphous and crystallized poly(L-lactic acid) (PLLA-A and PLLA-C, respectively) films were prepared, and the proteinase K-catalyzed enzymatic degradation of UV-irradiated and non-irradiated PLLA-A and PLLA-C films was investigated for periods up to 10 h (PLLA-A) and 60 h (PLLA-C). The molecular weights of both the PLLA-A and PLLA-C films can be manipulated by altering the UV irradiation time. The enzymatic weight loss values of the UVirradiated PLLA films were higher than or similar to those of the non-irradiated PLLA film, when compared with the specimens of same crystallinities. UV irradiation is expected to cause the PLLA films to undergo chain cleavage (a decrease in molecular weight) and the formation of C=C double bonds. It seems that the acceleration effects from decreased molecular weight on enzymatic degradation were higher than or balanced with the disturbance effects caused by the formation of C=C double bonds. After enzymatic degradation, a fibrous structure appeared on the spherulites of the UV-irradiated PLLA-C film. This structure may have arisen from chains containing or neighboring on the C=C double bonds, which were enzymatically undegraded and assembled on the film surface during enzymatic degradation. The results of this study strongly suggest that UV irradiation will significantly affect the biodegradation behavior of PLLA materials in the environment.