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Polylactic acid, or polylactide (PLA) is a thermoplasticpolyester with backbone formula or , formally obtained by condensation of lactic acid with loss of water (hence its name). It can also be prepared by ring-opening polymerization of lactide , the cyclic dimer of the basic repeating unit.
PLA has become a popular material due to it being economically produced from renewable resources. In 2010, PLA had the second highest consumption volume of any bioplastic of the world, although it is still not a commodity polymer. Its widespread application has been hindered by numerous physical and processing shortcomings. PLA is the most widely used plastic filament material in 3D printing.
The name "polylactic acid" does not comply with IUPAC standard nomenclature, and is potentially ambiguous or confusing, because PLA is not a polyacid (polyelectrolyte), but rather a polyester.
Several industrial routes afford usable (i.e. high molecular weight) PLA. Two main monomers are used: lactic acid, and the cyclic di-ester, lactide. The most common route to PLA is the ring-opening polymerization of lactide with various metal catalysts (typically tin octoate) in solution or as a suspension. The metal-catalyzed reaction tends to cause racemization of the PLA, reducing its stereoregularity compared to the starting material (usually corn starch).
The direct condensation of lactic acid monomers can also be used to produce PLA. This process needs to be carried out at less than 200 °C; above that temperature, the entropically favored lactide monomer is generated. This reaction generates one equivalent of water for every condensation (esterification) step. The condensation reaction is reversible and subject to equilibrium, so removal of water is required to generate high molecular weight species. Water removal by application of a vacuum or by azeotropic distillation is required to drive the reaction toward polycondensation. Molecular weights of 130 kDa can be obtained this way. Even higher molecular weights can be attained by carefully crystallizing the crude polymer from the melt. Carboxylic acid and alcohol end groups are thus concentrated in the amorphous region of the solid polymer, and so they can react. Molecular weights of 128-152 kDa are obtainable thus.
Polymerization of a racemic mixture of L- and D-lactides usually leads to the synthesis of poly-DL-lactide (PDLLA), which is amorphous. Use of stereospecific catalysts can lead to heterotactic PLA which has been found to show crystallinity. The degree of crystallinity, and hence many important properties, is largely controlled by the ratio of D to L enantiomers used, and to a lesser extent on the type of catalyst used. Apart from lactic acid and lactide, lactic acid O-carboxyanhydride ("lac-OCA"), a five-membered cyclic compound has been used academically as well. This compound is more reactive than lactide, because its polymerization is driven by the loss of one equivalent of carbon dioxide per equivalent of lactic acid. Water is not a co-product.
Another method devised is by contacting lactic acid with a zeolite. This condensation reaction is a one-step process, and runs about 100 °C lower in temperature.
Due to the chiral nature of lactic acid, several distinct forms of polylactide exist: poly-L-lactide (PLLA) is the product resulting from polymerization of L,L-lactide (also known as L-lactide). PLA is soluble in solvents, hot benzene, tetrahydrofuran, and dioxane.
Physical and mechanical properties
PLA polymers range from amorphous glassy polymer to semi-crystalline and highly crystalline polymer with a glass transition 60-65 °C, a melting temperature 130-180 °C, and a tensile modulus 2.7-16 GPa. Heat-resistant PLA can withstand temperatures of 110 °C. The basic mechanical properties of PLA are between those of polystyrene and PET. The melting temperature of PLLA can be increased by 40-50 °C and its heat deflection temperature can be increased from approximately 60 °C to up to 190 °C by physically blending the polymer with PDLA (poly-D-lactide). PDLA and PLLA form a highly regular stereocomplex with increased crystallinity. The temperature stability is maximised when a 1:1 blend is used, but even at lower concentrations of 3-10% of PDLA, there is still a substantial improvement. In the latter case, PDLA acts as a nucleating agent, thereby increasing the crystallization rate. Biodegradation of PDLA is slower than for PLA due to the higher crystallinity of PDLA. The flexural modulus of PLA is higher than polystyrene and PLA has good heat sealability.
Several technologies such as annealing, adding nucleating agents, forming composites with fibers or nano-particles, chain extending and introducing crosslink structures have been used to enhance the mechanical properties of PLA polymers. Polylactic acid can be processed like most thermoplastics into fiber (for example, using conventional melt spinning processes) and film. PLA has similar mechanical properties to PETE polymer, but has a significantly lower maximum continuous use temperature. With high surface energy, PLA has easy printability which makes it widely used in 3-D printing. The tensile strength for 3-D printed PLA was previously determined.
There is also poly(L-lactide-co-D,L-lactide) (PLDLLA) - used as PLDLLA/TCP scaffolds for bone engineering.
PLA is soluble in a range of organic solvents.Ethylacetate, due to its ease of access and low risk of use, is of most interest. PLA 3D printer filament dissolves when soaked in ethylacetate, making it a useful solvent for cleaning 3D printing extruder heads or removing PLA supports. The boiling point of ethylacetate is low enough to also smooth PLA in a vapor chamber, similar to using acetone vapor to smooth ABS.
Other safe solvents to use include propylene carbonate, which is safer than ethylacetate but is difficult to purchase commercially. Pyridine can also be used however this is less safe than ethylacetate and propylene carbonate. It also has a distinct bad fish odor.
PLA can degrade into innocuous lactic acid, so it is used as medical implants in the form of anchors, screws, plates, pins, rods, and as a mesh. Depending on the exact type used, it breaks down inside the body within 6 months to 2 years. This gradual degradation is desirable for a support structure, because it gradually transfers the load to the body (e.g. the bone) as that area heals. The strength characteristics of PLA and PLLA implants are well documented.
PLA can also be used as a decomposable packaging material, either cast, injection-molded, or spun. Cups and bags have been made from this material. In the form of a film, it shrinks upon heating, allowing it to be used in shrink tunnels. It is useful for producing loose-fill packaging, compost bags, food packaging, and disposable tableware. In the form of fibers and nonwoven fabrics, PLA also has many potential uses, for example as upholstery, disposable garments, awnings, feminine hygiene products, and diapers. Thanks to its bio-compatibility and biodegradability, PLA has also found ample interest as a polymeric scaffold for drug delivery purposes.
Racemic and regular PLLA has a low glass transition temperature, which is undesirable. A stereocomplex of PDLA and PLLA has a higher glass transition temperatures, lending it more mechanical strength. It has a wide range of applications, such as woven shirts (ironability), microwavable trays, hot-fill applications and even engineering plastics (in this case, the stereocomplex is blended with a rubber-like polymer such as ABS). Such blends also have good form stability and visual transparency, making them useful for low-end packaging applications. Pure poly-L-lactic acid (PLLA), on the other hand, is the main ingredient in Sculptra, a long-lasting facial volume enhancer, primarily used for treating lipoatrophy of cheeks. Progress in biotechnology has resulted in the development of commercial production of the D enantiomer form, something that was not possible until recently.
PLA is degraded abiotically by three mechanisms:
Hydrolysis: The ester groups of the main chain are cleaved, thus reducing molecular weight.
Thermal degradation: A complex phenomenon leading to the appearance of different compounds such as lighter molecules and linear and cyclic oligomers with different Mw, and lactide.
Photodegradation: UV radiation induces degradation. This is a factor mainly where PLA is exposed to sunlight in its applications in plasticulture, packaging containers and films.
The hydrolytic reaction is:
The degradation rate is very slow in ambient temperatures. A 2017 study found that at 25 °C in seawater, PLA showed no degradation over a year. As a result, it is poorly degraded in landfills and household composts, but is effectively digested in hotter industrial composts.
Pure PLA foams are selectively hydrolysed in Dulbecco's modified Eagle's medium (DMEM) supplemented with fetal bovine serum (FBS) (a solution mimicking body fluid). After 30 days of submersion in DMEM+FBS, a PLLA scaffold lost about 20% of its weight.
PLA samples of various molecular weights were degraded into methyl lactate (a green solvent) by using a metal complex catalyst.
Four possible end of life scenarios are the most common:
Recycling: which can be either chemical or mechanical. Currently, the SPI resin identification code 7 ("others") is applicable for PLA. In Belgium, Galactic started the first pilot unit to chemically recycle PLA (Loopla). Unlike mechanical recycling, waste material can hold various contaminants. Polylactic acid can be chemically recycled to monomer by thermal depolymerization or hydrolysis. When purified, the monomer can be used for the manufacturing of virgin PLA with no loss of original properties  (cradle-to-cradle recycling).[dubious – discuss] End-of-life PLA can be chemically recycled to methyl lactate by transesterification.
Composting: PLA is biodegradable under industrial composting conditions, starting with chemical hydrolysis process, followed by the microbial digestion, to ultimately degrade the PLA.
Incineration: PLA can be incinerated, leaving no residue and producing 19.5 MJ/kg (8,368 btu/lb) of energy.
Landfill: the least preferable option is landfilling because PLA degrades very slowly in ambient temperatures.
^Martin, O; Avérous, L (2001). "Poly(lactic acid): plasticization and properties of biodegradable multiphase systems". Polymer. 42 (14): 6209-6219. doi:10.1016/S0032-3861(01)00086-6.
^ abSödergård, Anders; Mikael Stolt (2010). "3. Industrial Production of High Molecular Weight Poly(Lactic Acid)". In Rafael Auras; Loong-Tak Lim; Susan E. M. Selke; Hideto Tsuji (eds.). Poly(Lactic Acid): Synthesis, Structures, Properties, Processing, and Applications. pp. 27-41. doi:10.1002/9780470649848.ch3. ISBN9780470649848.
^Jung, Yu Kyung; Kim, Tae Yong (2009). "Metabolic Engineering of Escherichia coli for the production of Polylactic Acid and Its Copolymers". Biotechnology and Bioengineering. 105 (1): 161-71. doi:10.1002/bit.22548. PMID19937727. S2CID205499487.
^Södergård, Anders; Mikael Stolt (February 2002). "Properties of lactic acid based polymers and their correlation with composition". Progress in Polymer Science. 27 (6): 1123-1163. doi:10.1016/S0079-6700(02)00012-6.
^Gina L. Fiore; Feng Jing; Victor G. Young Jr.; Christopher J. Cramer; Marc A. Hillmyer (2010). "High Tg Aliphatic Polyesters by the Polymerization of Spirolactide Derivatives". Polymer Chemistry. 1 (6): 870-877. doi:10.1039/C0PY00029A.
^Nugroho, Pramono; Mitomo, Hiroshi; Yoshii, Fumio; Kume, Tamikazu (1 May 2001). "Degradation of poly(l-lactic acid) by ?-irradiation". Polymer Degradation and Stability. 72 (2): 337-343. doi:10.1016/S0141-3910(01)00030-1. ISSN0141-3910.
^Urayama, Hiroshi; Kanamori, Takeshi; Fukushima, Kazuki; Kimura, Yoshiharu (1 September 2003). "Controlled crystal nucleation in the melt-crystallization of poly(l-lactide) and poly(l-lactide)/poly(d-lactide) stereocomplex". Polymer. 44 (19): 5635-5641. doi:10.1016/S0032-3861(03)00583-4. ISSN0032-3861.
^Tsuji, H. (1 January 1995). "Properties and morphologies of poly(l-lactide): 1. Annealing condition effects on properties and morphologies of poly(l-lactide)". Polymer. 36 (14): 2709-2716. doi:10.1016/0032-3861(95)93647-5. ISSN0032-3861.
^Urayama, Hiroshi; Ma, Chenghuan; Kimura, Yoshiharu (July 2003). "Mechanical and Thermal Properties of Poly(L-lactide) Incorporating Various Inorganic Fillers with Particle and Whisker Shapes". Macromolecular Materials and Engineering. 288 (7): 562-568. doi:10.1002/mame.200350004. ISSN1438-7492.
^Trimaille, T.; Pichot, C.; Elaïssari, A.; Fessi, H.; Briançon, S.; Delair, T. (1 November 2003). "Poly(d,l-lactic acid) nanoparticle preparation and colloidal characterization". Colloid and Polymer Science. 281 (12): 1184-1190. doi:10.1007/s00396-003-0894-1. ISSN0303-402X. S2CID98078359.
^Hu, Xiao; Xu, Hong-Sheng; Li, Zhong-Ming (4 May 2007). "Morphology and Properties of Poly(L-Lactide) (PLLA) Filled with Hollow Glass Beads". Macromolecular Materials and Engineering. 292 (5): 646-654. doi:10.1002/mame.200600504. ISSN1438-7492.
^Li, Bo-Hsin; Yang, Ming-Chien (2006). "Improvement of thermal and mechanical properties of poly(L-lactic acid) with 4,4-methylene diphenyl diisocyanate". Polymers for Advanced Technologies. 17 (6): 439-443. doi:10.1002/pat.731. ISSN1042-7147.
^Di, Yingwei; Iannace, Salvatore; Di Maio, Ernesto; Nicolais, Luigi (4 November 2005). "Reactively Modified Poly(lactic acid): Properties and Foam Processing". Macromolecular Materials and Engineering. 290 (11): 1083-1090. doi:10.1002/mame.200500115. ISSN1438-7492.
^Giordano, R.A.; Wu, B.M.; Borland, S.W.; Cima, L.G.; Sachs, E.M.; Cima, M.J. (1997). "Mechanical properties of dense polylactic acid structures fabricated by three dimensional printing". Journal of Biomaterials Science, Polymer Edition. 8 (1): 63-75. doi:10.1163/156856297x00588. PMID8933291.
^Lam, C. X. F.; Olkowski, R.; Swieszkowski, W.; Tan, K. C.; Gibson, I.; Hutmacher, D. W. (2008). "Mechanical and in vitro evaluations of composite PLDLLA/TCP scaffolds for bone engineering". Virtual and Physical Prototyping. 3 (4): 193-197. doi:10.1080/17452750802551298. S2CID135582844.
^Nazre, A.; Lin, S. (1994). Harvey, J. Paul; Games, Robert F. (eds.). Theoretical Strength Comparison of Bioabsorbable (PLLA) Plates and Conventional Stainless Steel and Titanium Plates Used in Internal Fracture Fixation. p. 53. ISBN978-0-8031-1897-3.
^Pavia FC; La Carrubba V; Piccarolo S; Brucato V (August 2008). "Polymeric scaffolds prepared via thermally induced phase separation: tuning of structure and morphology". Journal of Biomedical Materials Research Part A. 86 (2): 459-466. doi:10.1002/jbm.a.31621. PMID17975822.
^McKeown, Paul; Román-Ramírez, Luis A.; Bates, Samuel; Wood, Joseph; Jones, Matthew D. (2019). "Zinc Complexes for PLA Formation and Chemical Recycling: Towards a Circular Economy". ChemSusChem. 12 (24): 5233-5238. doi:10.1002/cssc.201902755. ISSN1864-564X. PMID31714680.