Research Article | Open Access
Synthesis of Poly(L-lactide) via Solvothermal Method
Poly(L-lactide) was obtained from the ring-opening polymerization of L-lactide through a solvothermal process. Tin (II) chloride () was used as the catalyst for the polymerization reaction. The focus of this paper was on the effect of solvents, catalyst usage, temperature, time, and antioxidants on the ring-opening reaction in the solvothermal synthesis. Ubbelohde viscometer, FTIR, GPC, and DSC were used to characterize the products. It is found that the optimal reaction condition for the highest molecular weight of PLA is at for 10 hour with 0.4% SnC in 10 mL toluene as solvent, and the high crystallinity can be obtained. The addition of antioxidant prior to the polymerization is conducive to obtaining high molecular weight and augment , and values of PLA.
Biodegradable polymers have recently been gained much more attention as the potential replacement for conventional synthetic (petroleum-based) materials [1, 2]. Among the new biodegradable polymers that have been developed during the last decade [3–5], polylactides (PLAs) are of particular interest . Moreover, because of their excellent mechanical properties [7, 8], they are widely used in surgery (sutures, orthopaedic applications, tissue engineering). For the same reason, they are also applicable in packaging field as an environmental friendly substitute . Furthermore, PLAs are easily synthesized from lactide, which is produced from renewable resources (corn, sugar beet). The degradation of PLAs depends on both external conditions (temperature, pH, ionic strength) and intrinsic structural parameters (molecular weight, polydispersity index, tacticity, chain ends) .
The synthesis of PLAs is carried out through a direct condensation polymerization or a ring-opening polymerization of lactide. The benefit from the direct polymerization is the ease of process but it is difficult to get the PLAs with a high molecular weight. There were three important factors to get the high molecular weight, including the dynamic control, the removal of water, and the control of degradation . To avoid the disadvantage of the direct condensation, poly(lactide) is usually synthesized by the ring-opening polymerization in bulk or solution . Cationic, anionic, and insertion-coordination mechanisms [13–20] are involved in the ring-opening polymerization of PLAs. The shortcomings of the ring-opening polymerization include high reaction temperature and long vacuum duration which may risk precisely controlling the polymerization process.
Our previous research mainly involved the synthesis of new materials using the solvothermal method and characterization of the structure and properties of the as-made products. The solvothermal synthesis is normally carried out in a pressure vessel where the common-used solvents like toluene and alcohol will be stable beyond their boiling points under a high pressure. This technique was widely used in the synthesis of inorganic compounds such as NiO, ZnO, and . Due to the increased solubility and reactivity of compounds and complexes under elevated temperatures and high pressures, solvothermal approaches are preferred to synthesize chemical compounds or copolymers that are extremely difficult to produce by traditional methods. Our previous works [22, 23] revealed that the solvothermal method was rather promising to prepare the grafting copolymer of high grafting degree because the reaction precursors in solvents were sealed in the vessel [24, 25]. Evaporation of the solvents and the monomers was prevented, which was favorable for the reactive environment.
This paper focuses on the synthesis of PLAs using the solvothermal synthesis. The effect of catalyst usage, reaction temperature, time, solvent, and antioxidant on the polymerization of L-lactide as systematically investigated.
L-lactide (95%) and were purchased from Nanjing Lihan Chemical Co., Ltd. (China). L-lactide (LA) was recrystallized three times from distilled ethyl acetate and dried under vacuum at for 4 hours to remove the water before use. Antioxidant agents IRGANOX 1010 and IRGAFOS 168 were purchased from Ciba Specialty Chemicals (Switzerland). Trichloromethane, toluene, acetone, and alcohol (Yonghua Fine Chemical Factory, China) of analytical grade were used as received.
The reactions were performed in a sealed vessel (50 mL) under various conditions. In a typical process, 15 g L-lactide, appropriate amount of , and other reactants were mixed and purged with nitrogen for more than 3 minutes to remove the oxygen, and then poured into a sealed autoclave. Then the sealed vessel was put into an isothermal oven. After a certain time, the product was taken out of the vessel and dissolved in chloroform and precipitated in ethanol, and subsequently the solid residue was washed several times with ethanol to remove the unreacted reactants. The purified polymer was collected and dried in a vacuum oven at for 6 hours to a constant weight.
2.3. Viscometric Average Molecular Weight ()
The viscometric average molecular weight () of PLAs was determined according to solution intrinsic viscosity  using Ubbelohde viscometer (Shanghai Liangjin Glass Instrument Company, Shanghai, China). is calculated as follows: The solvent was chloroform and the test temperature was (, Polymer Handbook) .
NMR spectra were recorded on a Varian Mercury Plus-400 MHZ spectrometer at 400 MHZ; was used as solvent and tetramethylsilane (TMS) as internal standard.
The PLA samples were dissolved in chloroform and cast the film on KBr for Fourier transform infrared (FTIR) characterization. Infrared spectroscopy of PLA sample was obtained on a Perkin Elmer Paragon 1000 FT-IR spectrophotometer (Waltham, USA) ranging from 450 to 4000 at a resolution of 2 and 1 scan.
The thermal properties such as glass transition temperature (), melting temperature () and enthalpies of fusion () were measured using a Perkin-Elmer DSC-7 differential scanning calorimeter (DSC) (Waltham, USA). Transition temperatures were calibrated using indium and zinc standards. Samples (about 5 mg) were heated from the room temperature to at a rate of /min and held for 3 minutes to eliminate the thermal history of samples before being cooled to room temperature at /min, and then reheated to at a rate of /min.
3. Results and Discussion
The solvothermal reaction was carried out at for 12 hours in an autoclave which contained 15 g PLA, 10 mL toluene, and 0.06 g . The autogenous pressure in the autoclave far exceeded the ambient pressure at . Furthermore, the high temperature and the autogenous pressure out of heating greatly increased reactivity of LA, which is favorable to the polymerization within shorter time than that needed in the traditional process. The FTIR and 1H NMR spectra of the sample were shown in Figure 1.
(a) FTIR spectrum
(b) NMR spectrum
As seen in FTIR spectra (Figure 1(a)), the strong absorb peaks at 1758~1763 and 2994~2997 are corresponding to the characteristic peaks of C = O and –CH2, the absorption peak at 1184~1190 for C–O–C ester group proves the formation of –COO–, the peak at 1452~1457 and 1382~1389 reveals the presence of –CH(), and all of those FTIR characteristic peaks indicate that the PLA was successfully obtained . The typical peak of the –CH bond on the ring of lactide at 932~934 was not observed for all the samples, indicating that the lactide was fully ring-opened. The NMR result (Figure 1(b)) further proves that PLA was successfully prepared [12, 28, 29] through the precisely controlled solvothermal process.
3.1. Effect of Solvents on the Molecular Weight of PLAs
The solvent is one of the important factors to the formation of PLAs because it can promote the higher solubility and reactivity of compounds and complexes at elevated temperatures under a high pressure. In other words, the above-mentioned solvothermal method could be an effective approach to the synthesis of chemical compounds or copolymers that are hard to obtain using traditional methods. It is worth mentioning that in a hermetic system at high temperature, the pressure went up quickly when a volatile organic solvent was heated, which was suspected to affect the final polymerization. Therefore, two typical solvents chloroform and toluene representing the good solvent and the poor solvent, respectively, were chosen for further clarification. The optimal reaction condition for normal lactide open-ring polymerization was at for 24 hours with 0.8 wt% (as catalyst) . Considering the faster reaction speed of solvothermal reaction, we shortened the initial reaction time to 12 hours. Figure 2 gives the effect of solvent types and their amount on the molecular weight. It can be seen from Figure 2 that of PLA increases with the increasing amount of toluene, while of PLA hardly changes with the increase of chloroform content.
It is very clear that more toluene in the system can be conducive to raising the system pressure and thus accelerating the polymerization while a good solvent like chloroform has a negative impact. The possible explanation for this phenomenon includes two points. The first is due to the depolymerization caused by the trace amount of water and the solvent. The second cames from the fact that the lone-pair electrons of chlorine could coordinate with the empty orbit of and reduce the catalysis of catalyst.
3.2. The Effect of Catalyst Usage on the Molecular Weight of PLAs
The catalysts used in the ring-opening polymerization of lactide include Bronsted acids, halides, and anionic species. was used as the catalyzer for PLA formation due to its high efficiency, good solubility in molten lactide, and thermal stability at elevated temperatures. The reaction mechanism was illustrated in Scheme 1. It can be seen from Figure 3 that the molecular weight of PLA initially increases with increasing the amount of catalyst and reaches a maximum when the amount of catalyst is 0.4 wt% and then decreases with higher catalyst content, indicating that the optimized amount of catalyst is close to 0.4 wt% of the total weight. In other words, the different molecular weight of PLAs can be obtained through the effective control of the amount of the catalyst.
The acceptable explanation for the above phenomena include the following: the catalyst is more active to initiate the polymerization of L- lactide when its content is less than 0.4 wt%, more insertion-coordinative centers form while the loading is more than 0.4 wt%, which increases the reactive polymer quantity and in the meantime shortens the polymer chain length, and tin salt catalyzer not only initiates the polymerization of L-lactide but also accelerates the depolymerization at high temperature.
3.3. The Effect of Reaction Temperature on the Molecular Weight of PLAs
In general, the temperature plays an important role in PLA polymerization because the polymerization and depolymerization of PLA take place simultaneously. The relationship between the polymerization temperature and the final PLA molecular weight was investigated in this work (Figure 4).
As shown in Figure 4, the molecular weight of PLAs increased with the temperature increasing from to . When the reaction temperature was beyond , the PLA’s molecular weight reduced remarkably. The major reason for such phenomena came from the mutual competition between the catalytic polymerization and thermal degradation. When the temperature is low, the catalyzed polymerization is dominant. With the temperature increases to certain point, the molecules become active enough to assist the growth of insertion-coordinative center and lead to high molecular weight products. Once the temperature exceeds the critical point, the polymerization speed cannot catch up with the thermal degradation speed, and triggers the thermal degradation, and thus reduces the polymer molecular weight.
3.4. The Effect of Reaction Time on PLAs Molecular Weight
Based on the same dosage of catalyzer and reaction temperature, the relationship between the different reaction times and PLA’s molecular weights was also evaluated. Figure 5 showed that the highest molecular weight was obtained when the reaction lasted for 10 hours. The impact of the reaction time on polymerization is reflected into three stages. First, the longer the reaction time, the longer the polymer chain and the higher molecular weight can be obtained. Second, with the reaction carrying on, less monomer remains for further reaction which leads to slower polymerization while the competitive depolymerization is accelerated. Finally, the PLAs are also easily degraded at elevated temperatures. When the reaction time varied, the low molecular weight and wide molecular weight distribution of PLAs can be obtained. The results prove that the optimal reaction duration is 8–10 hours.
3.5. The Effect of Antioxidants on PLAs Polymerization
The presence of moisture, lactic acid residues, and metal catalysts is known to accelerate the thermal degradation of PLA. Quinone or tropolone compounds were used to stabilize PLA . Oxidative stabilizers were added in order to improve the stability of PLA during molding or extrusion. The incorporation of antioxidants affects the solvothermal polymerization on different stages. The effect of antioxidant on the polymerization and PLA properties was investigated on basis of the optimal reaction condition ( for 10 hours with 0.4 wt% and in 10 mL toluene solvent). The antioxidant mixtures of IRGANOX 1010 and IRGAFOS 168 as 50/50 blending ratio were used due to their excellent oxidation-resistant performance as revealed in general plastic industry. Total 0.5 wt% antioxidants were added during the polymerization. The FTIR was used to identify the polymerization reaction. It can be seen from Figure 7 that FTIR spectra of all samples are almost identical in terms of characteristic absorption of functional groups, which indicates that the molecular structure of PLA does not change with the antioxidant. The effect of antioxidant additives on PLA molecular weight was also studied. The results were given in Figure 6.
It is well known that the disconnection of ester linkage can lead to the degradation of PLA. Apart from the well-known biological degradation, temperature, pH value, water, oxygen, and polymer structure are also responsible for the PLA degradation. From Figure 6, it can be shown that the added antioxidant can help to improve the molecular weight of PLAs. As mentioned earlier, without antioxidant, the degradation of PLAs generates the lactide and blocks the chain growth of PLA. In the presence of antioxidants, the degradation of PLAs is hampered effectively and thus enables the better control of molecular weight and its distribution.
3.6. Melting and Crystallization Behavior
The thermal property of final PLA products by the solvothermal method was studied using DSC. The crystallinity was determined as the ratio of of actual samples to the standard of ideal crystallized PLA. The standard is 93.1 J/g . The crystallinity () was calculated by (2):
The results were summarized in Figure 8 and Table 1. The crystallinity of all the samples is higher than 48%, which indicates that the solvothermal polymerization is favorable to the formation of PLA crystal. Compared to the three samples, it can be found that both and increase with the addition of antioxidant, which means that the anioxidant can effectively inhibit the degradation of PLA in polymerization processing. This is in agreement with the above results. It is interesting to find that the sample with antioxidant before polymerization could get the highest , , and . So adding antioxidant prior to the polymerization is the best option for improved values of , , and .
In this paper, the solvothermal method was introduced for macromolecular polymerization. PLA from the polymerization of L-lactide has been successfully obtained through solvothermal synthesis. The effect of the amount of catalyzer, reaction temperature, time, solvent, and antioxidant on the polymerization of L-lactide was systematically investigated. The optimal reaction condition for the highest molecular weight of PLA is at for 10 hours with 0.4% in 10 mL toluene solvent, and the high crystallinity can be obtained. The addition of antioxidant prior to the polymerization helps to obtain high molecular weight and augment , , and values of PLA.
This work was financially supported by Shanghai Leading Academic Discipline Project (no. B202).
- R. E. Drumright, P. R. Gruber, and D. E. Henton, “Polylactic acid technology,” Advanced Materials, vol. 12, no. 23, pp. 1841–1846, 2000.
- S. Mecking, “Nature or petrochemistry? Biologically degradable materials,” Angewandte Chemie. International Edition, vol. 43, no. 9, pp. 1078–1085, 2004.
- O. Dechy-Cabaret, B. Martin-Vaca, and D. Bourissou, “Controlled ring-opening polymerization of lactide and glycolide,” Chemical Reviews, vol. 104, no. 12, pp. 6147–6176, 2004.
- H. R. Kricheldorf and I. Kreiser-Saunders, “Polylactides—synthesis, characterization and medical application,” Macromolecular Symposia, vol. 103, pp. 85–102, 1996.
- M. Vert, “Lactide polymerization faced with therapeutic application requirements,” Macromolecular Symposia, vol. 153, pp. 333–342, 2000.
- D. W. Grijpma, A. J. Nijenhuis, P. G. T. van Wijk, and A. J. Pennings, “High impact strength as-polymerized PLLA,” Polymer Bulletin, vol. 29, no. 5, pp. 571–578, 1992.
- S. Jacobsen, H.-G. Fritz, P. Degée, P. Dubois, and R. Jérôme, “New developments on the ring opening polymerisation of polylactide,” Industrial Crops and Products, vol. 11, no. 2-3, pp. 265–275, 2000.
- G. Montaudo, M. S. Montaudo, C. Puglisi et al., “Evidence for ester-exchange reactions and cyclic oligomer formation in the ring-opening polymerization of lactide with aluminum complex initiators,” Macromolecules, vol. 29, no. 20, pp. 6461–6465, 1996.
- A.-C. Albertsson and I. K. Varma, “Recent developments in ring opening polymerization of lactones for biomedical applications,” Biomacromolecules, vol. 4, no. 6, pp. 1466–1486, 2003.
- O. Dechy-Cabaret, B. Martin-Vaca, and D. Bourissou, “Controlled ring-opening polymerization of lactide and glycolide,” Chemical Reviews, vol. 104, no. 12, pp. 6147–6176, 2004.
- R. Bhardwaj and A. K. Mohanty, “Advances in the properties of polylactide based materials: a review,” Journal of Biobased Materials & Bioenergy, vol. 1, no. 2, p. 191, 2007.
- M. Jalabert, C. Fraschini, and R. E. Prud'Homme, “Synthesis and characterization of poly(L-lactide)s and poly(D-lactide)s of controlled molecular weight,” Journal of Polymer Science Part A, vol. 45, no. 10, pp. 1944–1955, 2007.
- S. Li and M. Vert, “Synthesis, characterization, and stereocomplex-induced gelation of block copolymers prepared by ring-opening polymerization of L(D)-lactide in the presence of poly(ethylene glycol),” Macromolecules, vol. 36, no. 21, pp. 8008–8014, 2003.
- H. Ma and J. Okuda, “Kinetics and mechanism of L-lactide polymerization by rare earth metal silylamido complexes: effect of alcohol addition,” Macromolecules, vol. 38, no. 7, pp. 2665–2673, 2005.
- V. Simic, N. Spassky, and L. G. Hubert-Pfalzgraf, “Ring-opening polymerization of D,L-lactide using rare-earth μ-oxo isopropoxides as initiator systems,” Macromolecules, vol. 30, no. 23, pp. 7338–7340, 1997.
- H. Otsuka, Y. Nagasaki, and K. Kataoka, “Surface characterization of functionalized polylactide through the coating with heterobifunctional poly(ethylene glycol)/polylactide block copolymers,” Biomacromolecules, vol. 1, no. 1, pp. 39–48, 2000.
- H. R. Kricheldorf and R. Dunsing, “Polylactones, 8. Mechanism of the cationic polymerization of L,L-dilactide,” Die Makromolekulare Chemie, vol. 187, no. 7, pp. 1611–1625, 1986.
- H. Tsuji and Y. Ikada, “Properties and morphologies of poly(l-lactide): 1. Annealing condition effects on properties and morphologies of poly(l-lactide),” Polymer, vol. 36, no. 14, pp. 2709–2716, 1995.
- J. Coudane, C. Ustariz-Peyret, G. Schwach, and M. Vert, “More about the stereodependence of DD and LL pair linkages during the ring-opening polymerization of racemic lactide,” Journal of Polymer Science Part A, vol. 35, no. 9, pp. 1651–1658, 1997.
- A. Bhaw-Luximon, D. Jhurry, N. Spassky, S. Pensec, and J. Belleney, “Anionic polymerization of D,L-lactide initiated by lithium diisopropylamide,” Polymer, vol. 42, no. 24, pp. 9651–9656, 2001.
- E. Beach, S. Brown, K. Shqau, M. Mottern, Z. Warchol, and P. Morris, “Solvothermal synthesis of nanostructured NiO, ZnO and microspheres,” Materials Letters, vol. 62, no. 12-13, pp. 1957–1960, 2008.
- R. Qi, Z. Chen, and C. Zhou, “Solvothermal preparation of maleic anhydride grafted onto acrylonitrile-butadiene-styrene terpolymer (ABS),” Polymer, vol. 46, no. 12, pp. 4098–4104, 2005.
- R. Qi, J. Qian, and C. Zhou, “Modification of acrylonitrile-butadiene-styrene terpolymer by grafting with maleic anhydride in the melt. I. Preparation and characterization,” Journal of Applied Polymer Science, vol. 90, no. 5, pp. 1249–1254, 2003.
- X. F. Qian, J. Yin, X. X. Guo, Y. F. Yang, Z. K. Zhu, and J. Lu, “Polymer-inorganic nanocomposites prepared by hydrothermal method: PVA/ZnS, PVA/CdS, preparation and characterization,” Journal of Materials Science Letters, vol. 19, no. 24, pp. 2235–2237, 2000.
- X. F. Qian, J. Yin, Y. F. Yang, Q. H. Lu, Z. K. Zhu, and J. Lu, “Polymer-inorganic nanocomposites prepared by hydrothermal method: preparation and characterization of PVA-transition-metal sulfides,” Journal of Applied Polymer Science, vol. 82, no. 11, pp. 2744–2749, 2001.
- E. J. Mark, Polymer Data Handbook, Oxford University Press, Oxford, UK.
- C.-S. Wu and H.-T. Liao, “A new biodegradable blends prepared from polylactide and hyaluronic acid,” Polymer, vol. 46, no. 23, pp. 10017–10026, 2005.
- A. J. Ro, S. J. Huang, and R. A. Weiss, “Synthesis and thermal properties of telechelic poly(lactic acid) ionomers,” Polymer, vol. 49, no. 2, pp. 422–431, 2008.
- D. Lu, L. Yang, T. Zhou, and Z. Lei, “Synthesis, characterization and properties of biodegradable polylactic acid-β-cyclodextrin cross-linked copolymer microgels,” European Polymer Journal, vol. 44, no. 7, pp. 2140–2145, 2008.
- Z. Yang and Y. Chen, “Study on selection of solvents in the synthesis of polylactic acid through solution polycondensation,” Applied Chemical Industry, vol. 36, no. 7, pp. 644–645, 2007.
- I. Pillin, N. Montrelay, A. Bourmaud, and Y. Grohens, “Effect of thermo-mechanical cycles on the physico-chemical properties of poly(lactic acid),” Polymer Degradation and Stability, vol. 93, no. 2, pp. 321–328, 2008.
- T. Ke and X. Sun, “Effects of moisture content and heat treatment on the physical properties of starch and poly(lactic acid) blends,” Journal of Applied Polymer Science, vol. 81, no. 12, pp. 3069–3082, 2001.
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